Process for the synthesis of bio-1,2-alkanediols

Abstract

The present disclosure includes a process for synthesizing bio-1,2-alkanediols, comprising providing a bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%, at least about 92%, and / or at least about 95%; and converting the bio-alkene to a bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms. Also included herein are methods for treating catalysts that can be incorporated into the process for synthesizing bio-1,2-alkanediols. Such bio-1,2-alkanediols can be used as antimicrobial materials in compositions and products, either alone or in conjunction with existing bio-compounds and / or antimicrobial agents, preservatives, alternative preservation systems, and / or hard technology components. Bio-1,2-alkanediols incorporate natural and bio-based pathways for antimicrobial effects into various compositions, such as cosmetics, pharmaceuticals, industrial products, and household products.

Description

[Technical Field]

[0001] The invention described herein relates to the field of natural, renewable, or sustainable antimicrobial ingredients that enable alternative preservation systems for use in compositions, particularly personal care compositions, applicable in a variety of industries, including personal care, household and institutional or industrial cleaning products, medical or other related uses. More specifically, the invention relates to the preparation of natural, renewable 1,2-alkanediols, methods for making natural, renewable 1,2-alkanediols, and compositions comprising such 1,2-alkanediols prepared from natural, renewable ("sustainable") feedstocks. [Background technology]

[0002] In most countries, including the United States, cosmetics and / or personal care (“personal care products”) and other consumer products are manufactured and packaged under clean conditions but are typically not sterile, and many are sold in non-sterile form. As a result, small amounts of (usually harmless) bacteria, mold, and yeast spores (collectively “microorganisms”) can become contaminated in the products. Moreover, once a consumer purchases, opens, and begins using such products, further contamination can occur. For example, in personal care products, small amounts of microorganisms from the air or on the consumer's skin can further contaminate the product.

[0003] Over time, initial microbial populations that were negligible during transportation, storage, or use can increase to levels severe enough to result in product discoloration or staining, including the visible appearance of mold, which can affect the usability or performance of the product. When personal care products or other consumer products are applied or ingested (such as vitamins), it can similarly affect health and, in some cases, can cause adverse skin reactions, including infection, upon application.

[0004] To address the problem of microbial growth, manufacturers in the personal care and other industries commonly add chemical preservatives, typically petrochemical-based, to such products and compositions. However, the types and amounts of preservatives that can be used are limited in several ways: (1) legal (the use of certain preservatives is prohibited in some countries); (2) technical (the type / amount of preservative must demonstrate efficacy by meeting certain empirically evaluated criteria ("challenge tests")); (3) consumer preference (consumers may find certain preservative chemicals, such as petroleum-based or non-sustainable products, objectionable, making products containing them commercially unviable); (4) logistical (e.g., the selected preservative must be effective in the relevant chemical environment (where parameters such as pH, hydrophobicity / hydrophilicity, etc. may vary) and be cost-friendly to manufacture); and (5) sustainability, i.e., they should be manufactured using sustainable processes and raw material sourcing, as further described herein.

[0005] There is also a desire to develop alternatives to traditional preservatives and to find more user-friendly chemical ingredient combinations derived from sustainable and renewable resources (i.e., "raw materials"). These natural, renewable antimicrobial ingredients and alternatives to traditional preservatives ("alternative preservatives") should provide equal or better protection and performance to consumers.

[0006] To solve the problems of traditional preservatives, the present applicant has developed a prior art preservative for personal care compositions that does not contain parabens, formaldehyde donors, or chlorinated compounds and can be used in all types of personal care formulations (e.g., both "leave-on" and "rinse-off" products). Such paraben-free or other non-petroleum-based alternative preservative products are attractive to consumers. This paraben-free preservative exhibits efficacy against a wide range of microorganisms at various pH levels, particularly near the neutral pH level typically present in or on the human body. This preservative is described in U.S. Patent No. 5,929,999, and one of the components in this preservative system is a 1,2-alkanediol.

[0007] Another attempt in the art to reduce the use of traditional preservatives is the application of "hurdle technology." Hurdle technology involves applying some type of restrictive or preservative material or process so that microorganisms have a "hurdle" they must overcome before they can grow to spoilage levels (e.g., adding something that changes the pH to reduce growth, and adding small amounts of preservatives or other compounds that together slow or create a "hurdle" for microbial growth). The use of alternative preservatives can be one step or "hurdle" in hurdle technology.

[0008] There is a need in the art for further development of additives that are "alternative preservatives." These alternative preservative systems include consumer-friendly, paraben-free materials that move away from traditional preservatives or antimicrobial agents toward "natural" and "sustainable" ("renewable") formulations and ingredients, as defined below.

[0009] Applicant believes that one diol used in preservation, caprylyl glycol, is the fastest growing alternative preservative ingredient in the world. Other 1,2-alkanediols, such as 1,2-hexanediol, 1,2-decanediol, and 1,2-dodecanediol, are also gaining popularity and functioning in alternative preservative formulations.

[0010] An example of one reaction sequence for the synthesis of caprylyl glycol (1,2-octanediol) using an alkene as the key starting material is shown below. The starting material used is petrochemically derived 1-octene:

[0011] [ka]

[0012] In the above reaction sequence, petrochemically derived 1-octene is reacted in the presence of formic acid and peroxide to form an intermediate chemical mixture, which is further ring-opened with, for example, sodium hydroxide in water to fully form 1,2-octanediol. While this provides an excellent alternative preservative additive and is paraben-free, the starting material (i.e., 1-octene) is derived from fossil-based (petrochemical) resources and, importantly, represents a non-renewable feedstock, i.e., an unsustainable resource.

[0013] Therefore, as mentioned above, there is a need for alternative preservative systems (used alone or as part of hurdle technology) that are more consumer- and environmentally friendly, including paraben-free ones. Additionally, there is a need in the art for materials that can be used as alternative preservatives or in alternative preservative systems that are 100% natural, renewable ("sustainable") sources to generate antimicrobials that can be used as or in alternative preservative systems. An example of a "natural" antimicrobial is one that is prepared from biologically derived feedstocks (e.g., those prepared from current sustainable agricultural practices such as non-GMO-based fermentation, algae, plant, or vegetable origin, e.g., derived from vegetable sources or biomass, and not petrochemically derived (e.g., derived from sustainable tree and plant farms operating in the 21st century). Such materials are referred to herein as "natural" and "renewable" (i.e., "sustainable") and are known as non-petroleum-derived feedstocks. Furthermore, such materials are formed from "new" carbon, rather than from petroleum or other fossil fuel sources ("old" carbon). Such products are referred to herein as "natural" products and are known in the art as non-petrochemically derived or "bio" products. By "sustainable" herein, Applicant refers to materials that are derived from renewable sources rather than from depleting limited natural resources such as fossil fuels or other non-renewable resources such as oil. Thus, natural or bio products that are not petrochemically derived and / or made from non-petrochemically derived feedstocks are sustainable and renewable.

[0014] True natural products (bio-compounds) are formed using biomass (e.g., material stored from the carbon cycle process, such as living plants and roots, or material released by animal respiration or decomposition). When carbon decomposes and breaks down under pressure over millions of years, fossil fuels (petrochemical-derived sources of carbon) are produced. Bio-compounds herein are intended to include materials derived from carbon from plant sources / biomass that are recent, sustainable, and not derived from fossil fuels.

[0015] These bio-based or "natural" ingredients can be used to manufacture alternative preservative formulations. Bio-based or "natural" products from such materials can be tested to determine that they are derived from true, natural, and sustainable sources (as these terms are defined herein). Some products are known or advertised as being derived from natural resources, even though they may not actually be prepared from truly natural and / or sustainable materials. Natural organic products are typically defined as compounds naturally produced by living organisms. To distinguish petroleum-based products from truly natural and / or sustainable products, authenticity must be tested using established, reliable testing methods. Modern methods use mass spectrometry to perform detailed stable isotope analysis and evaluate carbon-12 / carbon-13 and / or hydrogen-1 / hydrogen-2 ratios. Such testing is available through several analytical service laboratories and is much faster, cost-effective, and provides more detailed information than radiocarbon testing.

[0016] Stable isotope analysis is based on the principle of kinetic isotope effect. The latter effect is well known in the field of chemical kinetics. In the broadest sense, heavier isotopes of certain elements react more slowly than their lighter isotopes (e.g., carbon-12 vs. carbon-13). Therefore, when plants incorporate carbon dioxide into biomass, the ratio of carbon-12 to carbon-13 varies depending on the type of chemicals the plant uses to make the biomass (e.g., whether the plant undergoes the C3 or C4 photosynthetic pathway). This is generally expressed as δ 13 C / 12 C ratio (i.e., δ 13 C), referring to the current carbon dioxide standard. Furthermore, a similar isotope kinetic effect is observed when water is incorporated into new biomass, which is also related to δ 2 H / 1 H ratio (i.e., δ 2 H). 13 C and δ 2 By using the combination of H ratios, one skilled in the relevant art can readily identify and confirm the nature of the raw material used to prepare the product being analyzed (i.e., whether it is petrochemically derived or derived from recently living or living algae, plants, or similar biological sources).

[0017] In Figure 2, we can see in general terms how isotope ratios can be used to determine the source of various detergents that have a strong relationship to the raw materials described herein, such as 1-octanol. From the plot in Figure 2, we can see that δ 2 H values ​​have a more clearly defined difference between petroleum-based and renewable feedstocks, therefore, in this case, δ 13 It turns out to be more valuable and clear than the C value. However, 2 H and δ 13 Combining the use of C values ​​together is the preferred technique employed in this invention to prove that the raw materials are indeed natural and renewable.

[0018] Radiocarbon is an unstable isotope of carbon,14 Known as C. 14 C emits radiation energy in the form of beta particles at a very constant rate, eventually forming into more stable 14 It is an unstable isotope that decays to N (i.e., the half-life of radiocarbon is 5730 years). Because petroleum-based (i.e., petrochemical-derived) feedstocks are obtained from plants and animals buried millions of years ago, the radiocarbon (i.e., 14 C) is lost through decay. ASTM International Standards specify test criteria for determining the authenticity of "bio-based compounds" using radiocarbon, which is described in ASTM D6866-16. This standard distinguishes new carbon from carbon derived from fossil fuel or petroleum and petrochemical-derived sources, i.e., "old carbon." 14 Because the amount of carbon is known, the percentage of carbon from renewable sources can be estimated from total organic carbon analysis, which provides the data necessary to determine whether a compound is truly derived from a "natural" and / or "sustainable" ("renewable") source, or conversely, whether it is derived from an "old" sequestration compound (i.e., petrochemical-derived or petroleum-based source). The use of petroleum-based or often labeled fossil-based feedstocks is non-sustainable, i.e., old carbon is non-sustainable, not a renewable source, and, furthermore, is generally recognized in the art as not being considered "natural" and "sustainable." As defined herein, it is not considered a "natural" product or useful in "natural" formulations. Therefore, the use of such feedstocks does not represent a path toward the development of "natural" and "renewable" alternative preservatives.

[0019] Dehydration of terminal alcohols using conventional methods to form alkene starting materials chemically produces a mixture of 1-alkenes, 2-alkenes, and 3-alkenes due to rearrangement and migration of the 1-alkene product during the dehydration process. The use of such a mixture of alkenes ultimately results in a mixture of diols upon dihydroxylation, resulting in low yields of the desired terminal 1,2-diol material and undesirable contaminants.

[0020] In one known pathway to produce caprylyl glycol (1,2-octanediol) starting from 1-octanol produced from petrochemical-derived (i.e., petroleum- or fossil-fuel-derived) feedstocks, the following reaction is known to occur:

[0021] [ka]

[0022] [Table 1]

[0023] [ka]

[0024] As can be seen from the reaction scheme above, the use of heat and conventional acid catalysts converts 1-octanol to an alkene, i.e., octene. Upon exposure to the acid sites of the catalyst, the more thermodynamically stable 2-octene forms along with 1-octene. The 2-octene regioisomers formed (including the 3-octene and 4-octene (not shown) shown above) are very difficult to separate from 1-octene, resulting in a lower net chemical yield of the desired 1-octene. Therefore, increased or higher regioselectivity is an important factor and a goal to achieve in the catalytic dehydration of 1-octanol to 1-octene. When using renewable and natural feedstocks, reaction efficiency (i.e., chemical yield) of the desired product (i.e., 1-alkene) is important. There remains a need in the art for a highly regioselective dehydration of 1-octanol that also has high chemical conversion, uses efficient process equipment, and operates in a rapid and energy-efficient manner.

[0025] Therefore, the conventional route using the regioisomeric mixture of octenes as shown above for conversion to the desired terminal 1,2-octanediol is reduced and yields are also reduced. This makes the ability to form the desired alternative preservative material chemically inefficient, less cost-effective, and results in high process waste, reducing the sustainability of the overall process. There is a significant need in the art for a highly regioselective, high chemical conversion rate process for producing bio-1-octene from bio-1-octanol.

[0026] Patent Document 2 uses γ-alumina without additional promoters, instead endowed with very large pore size and volume, to enhance regioselectivity for the dehydration of 1-octanol. In this study, regioselectivity was high (97.7%), but the chemical conversion was 65%, and the product selectivity to octenes was only 25%. Therefore, the chemical yield of 1-octene from 1-octanol using this catalyst system was only about 15.9%.

[0027] In another example, U.S. Patent No. 5,949,663 describes the formation of 1-octene by decomposing an ether derivative of 1-octanol. This patent requires first converting 1-octanol to a methyl ether (i.e., methyl octyl ether) and then passing the ether over a gamma-alumina catalyst. This involves extra chemicals and additional costs to produce the ether, and the loss of methanol in the process makes it a highly inefficient and atom-inefficient process. Most notably, the catalysts start out with good conversion and regioselectivity in the first few hours, but then, after only 20 hours of time-on-stream (TOS), all catalysts disclosed in the art show a constant and significant decrease in chemical conversion, with a concomitant loss of regioselectivity. This type of short catalyst life is unacceptable for commercial production efforts.

[0028] Lead-containing alumina catalysts are described in U.S. Patent No. 5,623,499, in which plumbite-pseudoboehmite exhibited high apparent selectivity and conversion. The catalyst had a carbon deposition rate of approximately 0.04% / h, which is highly undesirable and insufficient for continuous operation for approximately 1000 hours. A further limitation is that these catalysts contain a hazardous heavy metal, namely, lead. The use of these catalysts requires costly environmental control and worker safety precautions when used on an industrial scale for commercial production.

[0029] One method of producing "natural" alkanediols is to ferment biomass to form straight-chain, linear alkanediols. For example, U.S. Patent No. 5,629,999 teaches the formation of 1,3-propanediol from a fermentation broth. However, 1,3-propanediol is not a 1,2-alkanediol. Fermentation processes to form long-chain diols are chemically inefficient (i.e., have poor life cycle analysis values) and, furthermore, require the use of GMO bacteria or yeast, especially when attempting to produce long-chain carbon 1,2-alkanediols.

[0030] Another example of a natural bio-alcohol described in the art is bio-1-butanol, a known substance that has been used for commercial production since 1862, when Pasteur discovered the acetone-butanol-ethanol fermentation process carried out by Clostridium bacteria (non-GMO bacteria), although currently only in very limited quantities. These bacteria ferment both C5 and C6 sugars, producing a mixture of acetone, 1-butanol, and ethanol (i.e., ABE). Since the discovery of ABE, advances in fermentation processes have provided optimization for bio-1-butanol production over acetone and ethanol production. While production has improved, purifying bio-1-butanol from the fermentation broth and other impurities involved in the fermentation process, such as ethanol and acetone, is difficult and energy-intensive. Furthermore, applicant is unaware of any non-GMO bacterial or yeast processes capable of forming longer-chain alcohols (i.e., six or more chains, such as 1-hexanol or 1-octanol).

[0031] Bio-1-butanol is known as a feedstock for producing biofuels. This method provides a route to converting linear, primary four-carbon alcohols into bio-1-alkenes with very high yields to improve biofuel production. It can also be used, for example, in the production of environmentally friendly tires. In this method, bio-1-alcohol was dehydrated to bio-1-alkenes with high selectivity and chemical yield. The resulting bio-1-alkenes are useful for preparing high-flashpoint diesel and jet biofuels, useful for civilian and military applications. Bio-1-butanol is dehydrated using a solid-phase dehydration catalyst containing an inorganic support, such as γ-alumina or zinc aluminate (ZnAl2O4), treated / modified with an aqueous base solution. The support can be further treated with an organosilane diluted in at least one hydrocarbon solvent. This process can convert bio-1-butanol from fermentation processes containing 0.1 to approximately 90% water by weight, producing the corresponding 1-alkene with 92-99% regioselectivity. A single pass over the solid-phase catalyst achieves reaction conversions of over 95% and produces a chemical yield of bio-1-butene of over 90%. However, even though such results are obtained for bio-1-butene, it should be noted that the conversion of 1-octanol to 1-octene is not equivalent to the conversion of simply 1-butanol to bio-1-butene. Indeed, the comparative example described below illustrates that silanization of the catalyst results in a loss of regioselectivity for the dehydration chemistry of 1-octanol. [Prior art documents] [Patent documents]

[0032] [Patent Document 1] US Patent Application Publication No. 2017 / 0360035Al [Patent Document 2] International Publication No. WO2004 / 078336A2 [Patent Document 3] U.S. Patent No. 7,576,250 [Patent Document 4] Chinese Patent No. 105312044B Specification [Patent Document 5] US Patent Application Publication No. 2005 / 0069997A1 Summary of the Invention [Problem to be solved by the invention]

[0033] While progress has been made based on the above, there remains a need in the art for continuous improvements to consumer products, such as personal care products, household products, industrial products, and pharmaceuticals, that avoid traditional preservatives and rely on natural, biologically-sourced ingredients for consumer product compositions to keep products safe from contamination and fresh during storage and use, particularly to provide additives for antimicrobial applications, or to enhance the effectiveness of known preservatives or alternative preservative systems. More specifically, there exists a need for natural, preferably renewable / sustainable, raw material sources for producing natural bio-caprylyl glycol (i.e., natural or bio-1,2-octanediol) and related bio-1-alkene intermediates. [Means for solving the problem]

[0034] The present invention provides an efficient route to achieving 100% "natural" or "bio-compounds" that are authentic "natural" materials, preferably comprising bio-1,2-alkanediols with carbon lengths of about 5 to about 20, preferably 5 to about 14, which can be used alone, in combination with different types of bio-1,2-alkanediols, or in blends with other natural or traditional antimicrobial agents and other cosmetic additives.

[0035] The present invention includes a process for the synthesis of bio-1,2-alkanediols, comprising providing a bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%; and converting the bio-alkene to a bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms.

[0036] In one embodiment of the process, the bio-alkene and bio-1,2-alkanediol each have a carbon chain length of about 6 to about 14 carbon atoms. The bio-alkene and bio-1,2-alkanediol may each have a carbon chain length of about 6 to about 10 carbon atoms. The bio-alkene and bio-1,2-alkanediol may each have a carbon chain length of about 6 to about 8 carbon atoms. For example, the bio-alkene may be bio-octene and the bio-1,2-alkanediol may be bio-1,2-octanediol.

[0037] In a further embodiment of the process, the bio-alkene preferably results from a process in which bio-1-alcohol is dehydrated by heating the bio-1-alcohol in a reactor equipped with a catalyst. The reactor may be a fixed-bed reactor. The fixed-bed reactor may also be, for example, a fluidized fixed-bed reactor. In such an embodiment, the catalyst may be selected from ZnAl2O4 and γ-alumina catalysts.

[0038] In a preferred embodiment, the bio-alkenes have a regioselectivity of about 92% to about 99%, preferably about 95% to about 99%, of bio-1-alkene. The process also preferably produces at least about 92% to about 99% bio-1,2-alkanediol.

[0039] As noted above, in one embodiment, catalytic treatment can be used. The catalyst can be a γ-alumina catalyst that is treated with a base to form a modified γ-alumina catalyst. The base can include a Group I or Group II metal. The γ-alumina catalyst can be treated with, for example, a calcium promoter to form the modified γ-alumina catalyst. The modified γ-alumina catalyst can then be calcined to obtain the calcined γ-alumina catalyst. In one embodiment in which a calcium promoter is used, the calcium promoter can be used in an amount of about 0.01 weight percent to about 4 weight percent based on the weight of CaO determined after calcination, preferably about 1 weight percent to about 2 weight percent based on the weight of CaO determined after calcination.

[0040] The preferred temperature during calcination is about 400°C to about 500°C, more preferably about 420°C to about 480°C, and most preferably about 440°C to about 460°C. Calcination can be carried out in an oven. Calcination can be carried out in air or under an atmosphere of nitrogen or other inert gas.

[0041] The bio-alkene is preferably subjected to a distillation step to purify the bio-alkene before converting the bio-alkene to bio-1,2-alkenediol. The bio-1,2-alkanediol produced from the bio-alkene may be subjected to a final distillation step to purify the bio-1,2-alkanediol.

[0042] In another embodiment of the process, bio-alkenes can result from a process in which bio-1-alcohol in water is dehydrated by catalytically heating the bio-1-alcohol without or under a purge gas. The purge gas is preferably nitrogen, although other inert gases may be used within the scope of the present invention.

[0043] The bio-alkene in the process can also be converted to bio-1,2-alkanediol by reacting the bio-alkene in the presence of at least one of a peracid, such as formic acid or acetic acid, and hydrogen peroxide to form a mixture of bio-1,2-epoxyalkanes having epoxy rings and bio-1,2-alkanediols, and contacting this mixture with water and sodium hydroxide to complete the formation of the bio-1,2-alkanediol.

[0044] The overall process preferably yields at least about 60% to about 99% bio-1,2-alkanediol, and more preferably at least about 72% to about 99% bio-1,2-alkanediol.

[0045] The present invention further includes a process for producing bio-1,2-alkanediol, the process comprising: providing a bio-1-alcohol and a base-treated catalyst; dehydrating the bio-1-alcohol in the presence of the catalyst to produce a bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%; and converting the bio-alkene to a bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms. Preferably, the catalyst is calcined after treatment with a promoter.

[0046] The catalyst in this process may also be a gamma-alumina catalyst, and the base may include calcium. The gamma-alumina catalyst is preferably treated with a calcium promoter and then calcined at a temperature of about 400°C to about 500°C. This process preferably produces about 92% to about 99% bio-1,2-alkanediol.

[0047] The present invention further includes a method for treating a catalyst for use in alcohol dehydration, comprising providing a γ-alumina catalyst; treating the γ-alumina catalyst with a base containing a Group I or Group II metal, preferably a promoter as described herein; and heating the γ-alumina catalyst to a temperature of about 400°C to about 500°C, preferably in a very controlled and deliberate manner. The base may contain calcium, preferably the base may be a calcium promoter, and the heating occurs during calcination. The calcium promoter may be used in an amount of about 0.01% to about 4% by weight based on the weight of CaO measured after calcination, more preferably about 1% to about 2% by weight based on the weight of CaO measured after calcination, preferably after careful calcination. In a preferred embodiment, the temperature during calcination may be about 420°C to about 480°C, more preferably about 440°C to about 460°C. Beneficial results are achieved based on Applicant's process, including the preferred ranges described above. Applicants have determined that high calcination temperatures reduce the regioselectivity of the catalyst and therefore reduce the chemical yield of bio-1-alkene.

[0048] The present invention further includes a composition comprising at least one first bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms, synthesized by converting a first bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and having a bio-1-alkene regioselectivity of at least about 80%.

[0049] The composition may be a personal care composition, such as a hair care composition, an oral care composition, a skin care composition or a cosmetic composition. The composition may also be a composition for household products such as fabric care or cleaning products.

[0050] The composition may also be an industrial composition, or a pharmaceutical composition, a vitamin composition, or a health care composition. In one embodiment of the compositions described herein, the composition can include a second bio-1,2-alkanediol different from the first bio-1,2-alkanediol, the second bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms, preferably regioselectively synthesized by conversion of a second bio-1,2-alkanediol, such that the resulting bio-alkene of about 5 to about 20 carbon atoms has a terminal bio-alkene content of at least about 80% and a bio-1-alkene regioselectivity of at least about 80%. The composition can also include at least one other bio-compound different from the first and second bio-1,2-alkanediols. In another embodiment, the composition can include an antimicrobial compound different from the first and second bio-1,2-alkanediols and different from the other bio-compounds. The composition may also further comprise at least one other bio-compound different from the at least one bio-1,2-alkanediol. In another embodiment, such a composition may also further comprise at least one antimicrobial compound different from the at least one bio-1,2-alkanediol and different from the other bio-compounds. The first bio-1-alkene in such a composition preferably has a regioselectivity of about 92% to about 99%, more preferably about 95% to about 99%. The first bio-alkene may be bio-octene, and the at least one first bio-1,2-alkanediol may be bio-1,2-octanediol.

[0051] The present invention also includes a method of providing an antimicrobial effect to a composition, comprising incorporating into the composition an antimicrobial system, the antimicrobial system comprising at least one first bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms, the first bio-1,2-alkanediol synthesized by conversion of at least one first bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%. The antimicrobial system may further comprise a second bio-1,2-alkanediol different from the first bio-1,2-alkanediol, the first bio-1,2-alkanediol being formed by regioselectively converting a second bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and different from the first bio-alkene, the second bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%. The composition may further comprise at least one other bio-compound different from the first and second bio-1,2-alkanediols. In another embodiment, the composition may comprise at least one other preservative compound different from the first and second bio-1,2-alkanediols and different from the other bio-compounds. Such compositions may also comprise at least one other bio-compound different from the at least one first bio-1,2-alkanediol. The antimicrobial agent may also comprise at least one other antimicrobial and / or preservative compound different from the at least one first bio-1,2-alkanediol and different from the other bio-compounds. The antimicrobial system may be configured to exhibit antimicrobial efficacy. Preferably, the first bio-1-alkene has a regioselectivity of about 92% to about 99%, preferably about 95% to about 99%. The first bio-alkene may be bio-octene, and the at least one first 1,2-alkanediol may be bio-1,2-octanediol.

[0052] In one embodiment, the present invention further includes a method of increasing the antimicrobial efficacy of an antimicrobial agent and / or preservative in a composition, comprising incorporating into the composition an antimicrobial system, wherein the second antimicrobial system comprises at least one first bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms, the first bio-1,2-alkanediol being synthesized by regioselective conversion of a first bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and a regioselectivity of at least about 80% bio-1-alkene. In this method, the antimicrobial system may further comprise a second bio-1,2-alkanediol different from the first bio-1,2-alkanediol, the second bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms and formed by conversion of a second bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%, different from the first bio-1,2-alkanediol. The composition may further comprise at least one other bio-compound different from the antimicrobial agent and / or preservative and different from the first and second bio-1,2-alkanediols. The composition may also further comprise at least one other bio-compound different from the at least one first bio-1,2-alkanediol. The first bio-1-alkene preferably has a regioselectivity of about 92% to about 99%, more preferably about 95% to about 99%. In one embodiment, the antimicrobial system exhibits antimicrobial efficacy. The first bio-alkene may be a bio-octene and the at least one first bio-1,2-alkanediol may be a bio-1,2-octanediol.

[0053] In yet another embodiment, the invention includes an antimicrobial product comprising at least one first bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms, synthesized by conversion of a first bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and with a bio-1-alkene regioselectivity of at least about 80%. The product further comprises a second bio-1,2-alkanediol different from the at least one first bio-1,2-alkanediol, the second bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms, formed by conversion of a second bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and with a bio-1-alkene regioselectivity of at least about 80%, the second bio-1,2-alkanediol being different from the first bio-alkene.

[0054] The antimicrobial product may further comprise at least one other bio-compound different from the at least one first and second bio-1,2-alkanediol. In one embodiment, the product may further comprise a second antimicrobial agent and / or preservative different from the antimicrobial product. The product may also further comprise at least one other bio-compound different from the at least one first bio-1,2-alkanediol, and may also further comprise a second antimicrobial agent and / or preservative different from the antimicrobial product. The first bio-1-alkene preferably has a regioselectivity of about 92% to about 99%.

[0055] The antimicrobial product preferably also exhibits antimicrobial efficacy.The first bio-alkene may be bio-octene and the at least one first 1,2-alkanediol may be bio-1,2-octanediol.

[0056] The present invention also includes a product for enhancing the efficacy of an antimicrobial and / or preservative agent in a composition, the product comprising at least one first bio-1,2-alkanediol synthesized by conversion of a first bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and with at least about 80% bio-1-alkene regioselectivity, the first bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms. Such product further comprises a second bio-1,2-alkanediol different from the at least one first bio-1,2-alkanediol, the second bio-1,2-alkanediol formed by conversion of a second bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms, different from the first bio-alkene, and having a carbon chain length of about 5 to about 20 carbon atoms and at least about 80% bio-1-alkene regioselectivity. The product composition may also further include at least one other bio-compound different from the at least one first and second bio-1,2-alkanediol, and may also further include at least one other bio-compound different from the at least one first bio-1,2-alkanediol. The first bio-1-alkene preferably has a regioselectivity of about 92% to about 99%. The first bio-alkene may be bio-octene, and the at least one first bio-1,2-alkanediol may be bio-1,2-octanediol. The antimicrobial product preferably also exhibits antimicrobial efficacy. [Brief explanation of the drawings]

[0057] [Figure 1] 1 is a process flow chart of steps in a preferred embodiment of the process described herein. [Figure 2] 1 is a graphical representation of the δH and δC values ​​of petroleum-based alcohols, alkenes, and acids, and the corresponding natural and renewable analogues. [Figure 3]1 is a gas chromatograph (GC) chromatogram of the reactor output where bio-1-octanol was dehydrated using the catalyst prepared in Example 4 and heated to 315° C. with 0.2 ml of bio-1-octanol feed. [Figure 4] GC chromatogram of bio-1-octene obtained from the reactor after distillation. [Figure 5] GC chromatogram of bio-1,2-octanediol obtained by dehydration of bio-1-octene, conversion to 1,2-octanediol, and subsequent fractional distillation of the 1,2-octanediol. [Figure 6] GC chromatogram of petro-1,2-octanediol, which is currently approved for use in cosmetic formulations. [Figure 7] This photo compares a 1400-hour TOS catalyst (left) and a new catalyst (right). DETAILED DESCRIPTION OF THE INVENTION

[0058] The foregoing summary, as well as the following detailed description of preferred embodiments of the invention, will be better understood when read in conjunction with the accompanying drawings. For the purpose of illustrating the invention, there are shown in the drawings embodiments which are presently preferred. It being understood, however, that the invention is not limited to the precise arrangements and instrumentalities shown.

[0059] The present invention includes a process for synthesizing bio-1,2-alkanediols. As used herein, "bio" when used with "alkanediol," or any specific alkanediol compound described within this class of compounds, is intended to mean, as described above, that the compound, preferably a compound within this class of compounds, is an authentic, natural compound derived from a botanical source (algae, plant, animal, or biomass-derived), and that all carbon in the compound is non-petrochemically derived (i.e., not obtained from non-renewable resources such as fossil fuels, petroleum, or other "old" carbon sources), as further described below. In this sense, it is also a sustainable compound, since it is derived from renewable materials. It also means that such a material is formed from a bio-alkene. When used in the terms "bio-alcohol" or "bio-alkene" and similar compounds herein, "bio" is also intended to have the same meaning as described above to describe "bio-1,2-alkanediol." Such materials should preferably meet the requirement of having and being derived from a true or "new" carbonaceous (non-petrochemically derived) source, as can be confirmed by testing such compounds using conventional methods such as mass spectrometry and / or gas chromatography, as described above, current ASTM D6866-16 standards, or specific stable isotope analysis (CSIA). The present invention further includes bio-1-alkenes and bio-1,2-alkanediols obtained from the synthetic process, as well as various products incorporating them. The present invention further includes catalysts that can be used in the embodiments described herein, and methods for treating the catalyst to form bio-alkenes used in the processes described herein for dehydrating bio-1-alcohols to form bio-1,2-alkanediols.

[0060] The present invention provides an efficient route to 100% "natural" or "bio" compounds that are not petrochemically derived and that are preferably used in compositions and products that can be manufactured for a wide variety of end uses and compositions, such as ingredients in antimicrobial compositions and as cosmetic additives, among other uses described herein, from novel carbon or true carbon materials.

[0061] Also disclosed herein are methods for using bio-1,2-alkanediols as antimicrobial agents in compositions, for example, in or in combination with alternative preservation systems and / or as hurdle technologies. Also disclosed are various compositions containing bio-1,2-alkanediols, including those used as antimicrobial agents. Also disclosed are methods for enhancing the antimicrobial efficacy of compositions already containing a preservative or alternative preservation system, and the resulting compositions with enhanced antimicrobial efficacy. Each of these methods involves incorporating into a composition a bio-1,2-alkanediol, a combination of at least two different bio-1,2-alkanediols, or a combination of at least one bio-1,2-alkanediol and at least one other bio-compound different from the at least one bio-1,2-alkanediol, where the bio-1,2-alkanediol acts as an antimicrobial agent or enhances the efficacy of another antimicrobial agent, preservative, or other alternative preservation system already present in the composition. The bio-1,2-alkanediols, whether used alone, in combination with one or more different bio-1,2-alkanediols, or in combination with one or more different bio-1,2-alkanediols and at least one other bio-compound different from the bio-1,2-alkanediol, and / or with any different antimicrobial agent, preservative, or alternative preservative system, may themselves be antimicrobial products and / or antimicrobial-potentiated products. The bio-1,2-alkanediols, when used in the compositions herein, exhibit antimicrobial efficacy.

[0062] In one embodiment herein, a process for synthesizing bio-1,2-alkanediols is described herein. As noted above, herein, materials referred to as "natural" are intended to include materials that are non-petrochemically derived and sustainable, whether synthesized from natural materials or formed from natural, preferably truly natural or bio-based, sources.

[0063] The method includes providing a bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms, preferably about 6 to about 14 carbon atoms, and more preferably about 6 to about 10 carbon atoms, with bio-1-octene being preferred. The bio-alkene is preferably a bio-1-alkene having a traditional α-olefin structure, and when prepared, preferably has a regioselectivity of at least about 80%, more preferably at least about 92%, and most preferably at least about 95%-99%.

[0064] Such bio-alkenes can be bio-1-pentene, bio-1-isopentene, bio-1-hexene, bio-1-heptene, bio-1-octene, bio-1-nonene, bio-1-decene, bio-1-dodecene, and related bio-1-alkenes with chain lengths up to 20 carbons. While larger or smaller bio-alkenes can be produced, preferred bio-alkenes for use herein are those with sufficient chain length to function as effective antimicrobial agents when converted to bio-1,2-alkanediols without losing desired properties. Such bio-alkenes can be linear or branched chain molecules, with linear molecules being preferred, and can include one or more functional groups or substituents, such as, but not limited to, sulfonate, hydroxyl, ether, amide, carbonyl, carboxylic acid, amine, fluorinated, aryl or arene groups, and similar functional groups for a desired end effect in the end use. Preferably, such functional groups or substituents do not interfere with conversion to an alkanediol or end use for the antimicrobial properties desired for the particular alkanediol.

[0065] Bio-alkenes, such as bio-1-hexene and bio-1-octene, produced according to the present invention can be used to produce bio-1,2-alkanediols as described herein and can also be used to synthesize other bio-based compounds and polymers, such as bio-based olefin copolymers. The bio-1-alkenes described herein can be used, for example, in free-radical or catalytic polymerization processes known in the art to produce a variety of bio-polyalphaolefin homopolymers and copolymers useful as lubricants and cosmetic ingredients. As a further example, bio-linear low-density polyethylene (bio-LLDPE) can be prepared by copolymerizing bio-ethylene (obtained by dehydration of sugarcane-derived bio-ethanol to bio-ethylene) with a copolymer of bio-1-alkene, producing a 100% renewable bio-LLDPE, a thermoplastic resin useful for film applications such as food and non-food packaging and shrink / stretch films.

[0066] The process of the present invention includes an embodiment for producing bio-1,2-alkanediol, which process includes providing a bio-1-alcohol and a catalyst treated with a base, preferably a promoter, followed by calcination; dehydrating the bio-1-alcohol in the presence of the catalyst to produce a bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%; and converting the bio-alkene to a bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms.

[0067] An overall flow diagram of a preferred process for producing bio-1,2-alkanediols, incorporating a preferred method of treating the catalyst as further described below, is provided as embodiment 100 as shown in FIG.

[0068] In the process of FIG. 1, generally referred to herein as process 100, a catalyst is prepared prior to the introduction of bio-1-alcohol. A suitable γ-alumina catalyst, e.g., Al2O3 110, is introduced into reactor 101, into which is introduced a calcium promoter or other base-treated material 102, as described further below. After appropriate treatment, as described in detail below, the modified catalyst 103 exits reactor 101 and enters a heated chamber 104, such as an oven, for heat treatment. For example, if a catalyst promoter is used, the calcination step is performed at a preferred and controlled temperature range to increase the level of regioselectivity in the resulting bio-alkene in the next step. For example, after calcination in chamber 104, the calcined or otherwise heat-treated catalyst 105 is introduced into reactor 107 along with a bio-1-alcohol 106, such as bio-1-hexanol or bio-1-octanol, to promote intimate contact of the alcohol with the catalyst. Suitable reactors included fixed-bed reactors, fluidized-bed reactors, tubular reactors, and other suitable reactors. After a sufficient time has elapsed to dehydrate the bio-1-alcohol to bio-1-alkene 109 (which is highly regioselective for the bio-1-alkene), an optional further distillation or other purification or purification step in a column or other apparatus 110 can be performed. The purified or otherwise purified, highly regioselective bio-alkene (which should be the bulk of the bio-1-alkene) is then introduced into reactor 112 to convert the bio-1-alkene to bio-1,2-alkanediol 113. Such bio-1,2-alkanediol 113 may be further purified, as needed, by distillation in a column or through other steps in the apparatus 114. After purification or distillation, a final high yield, up to 99%, is removed as final bio-1,2-alkanediol 115.

[0069] Bio-1-alkene can be produced using a catalytic process, preferably a catalyst treated according to the methods described herein. In one embodiment, bio-1-alcohol is heated in the presence of a catalyst to dehydrate it, thereby forming bio-1-alkene (preferably, a highly regioselective bio-1-alkene, as used herein). This can be done, for example, by passing bio-1-alcohol through a fixed-bed reactor or a fluidized-bed reactor. The fixed bed can be packed with a catalyst, preferably a treated catalyst treated using the techniques described below.

[0070] For example, bio-1-alcohol derived from plant sources includes biomass capable of producing related acids (e.g., 1-octanol derived from coconut, palm, or other plant sources or biomass capable of producing octanoic acid, followed by catalytic dehydrogenation to 1-octanol). The bio-1-alcohol is then regioselectively dehydrated by feeding the material at elevated temperatures, for example, into a fixed-bed reactor or other suitable reactor that provides intimate contact between the bio-1-alcohol and the catalyst. The fixed bed may be packed with catalyst or otherwise positioned to provide sufficient contact with the catalyst. Other suitable reactors may be provided for this purpose, provided that adequate contact to support dehydration can be achieved. Examples include tubular reactors, fixed and fluidized bed reactors, etc.

[0071] The reactor can be designed as a simple heated reaction tube packed with catalyst, and the flow of gaseous bio-1-alcohol over the catalyst preferably provides a conversion of greater than about 95% in a single pass, and in preferred embodiments, greater than about 98%; in all cases, no recycle stream is used in the overall process flow. In one embodiment, the reaction tube is isothermally heated, with one to ten reaction zone temperatures along the tube length, each heated in the range of about 240°C to about 360°C, to optimize catalyst performance. In a preferred embodiment, the reaction tube has one to four reaction zone temperatures in the range of about 260°C to about 340°C.

[0072] In one embodiment, the process is carried out in a fluidized bed reactor operating in a temperature range of about 240° C. to about 360° C. Other continuous flow reactor designs can be used according to procedures and practices used by those skilled in the art of chemical engineering.

[0073] The catalyst used can be prepared by treating γ-alumina (e.g., Porocel® CatGuard®) with at least one base, preferably a promoter, such as sodium hydroxide, potassium hydroxide, calcium acetate, etc., to form a second catalyst. This second catalyst is then calcined to form a third catalyst. The calcination temperature has been found to be most unexpectedly important for creating the most effective catalyst. As shown below, calcination at about 500°C significantly reduces regioselectivity compared to catalysts calcined at lower temperatures. In one embodiment, the preferred calcination temperature is about 400°C to about 480°C, with a more preferred calcination temperature being about 440°C to 460°C, as shown in Table 1 below.

[0074] [Table 2]

[0075] Various catalysts can be used to support the bio-1-alcohol in the dehydration step. However, it is preferred to use a suitable catalyst capable of achieving a high level of regioselectivity as described herein. Suitable catalysts include γ-alumina-based catalysts and ZnAl2O4. Preferably, the catalyst is treated with a base such as sodium hydroxide, potassium hydroxide, or calcium acetate. In one preferred example, the catalyst is a γ-alumina catalyst treated with a base containing a Group I or Group II metal. In a more preferred embodiment, calcium may be included in the base and the calcium promoter used. After treatment with the calcium promoter to form the modified γ-alumina catalyst, in a further preferred embodiment, the modified γ-alumina catalyst is calcined using various calcination techniques, but preferably at temperatures much lower than those used in standard calcination methods, to provide a calcined γ-alumina catalyst. The initial treatment provides a modified γ-alumina catalyst, which is then calcined for use in various processes, including the dehydration step of the process of the present invention to produce bio-1-alkene and its subsequent conversion to bio-1,2-alkanediol.

[0076] If a calcium promoter is used, it may be used in the above process in an amount of about 0.01% to about 4% by weight based on the amount of CaO measured after calcination. In a preferred embodiment, about 1% to about 2% by weight of calcium promoter is used based on the amount of CaO measured after calcination.

[0077] In another embodiment, if desired, the alumina-based treated catalyst can be further organosilaned with an organosilane, for example, by treatment with diethoxydiphenylsilane, to form an organosilaned base-treated γ-alumina catalyst. The organosilanzized base can be, for example, diethoxydiphenylsilane, dichlorodiphenylsilane, and similar materials.

[0078] In one embodiment, the catalyst support may comprise ZnAlO and may be modified with a base, for example, by reaction with a promoter and similar catalysts, and any modified catalyst material known or to be developed that is capable of performing the processes described herein in a manner similar to the catalysts described herein that are capable of producing high levels of regioselectivity may also be used.

[0079] In addition to being suitable when treated with base, the above catalysts may alternatively be treated with organosilanes or organosilane-modified materials to produce promoter-modified catalysts. This promoted catalyst can be further organosilanized by treatment with diethoxydiphenylsilane to produce a third, organosilanized, promoter-modified γ-alumina catalyst. The organosilanes used to modify the catalyst can be, for example, diethoxydiphenylsilane, dichlorodiphenylsilane, and similar materials. As seen in Example 10 herein, silanization of the catalyst results in a decrease in bio-1-octene selectivity, again demonstrating a departure from the prior art and a direct and proven difference in the dehydration catalyst structure required for the highly regioselective dehydration of 1-butanol or 1-octanol.

[0080] In another treatment technique described herein, γ-alumina catalysts may be modified by an incipient wetting impregnation technique. A solution of base is used to modify a solid support, avoiding excessive moisture, which can damage and chemically alter the support. In one embodiment, the incipient wetting impregnation solution (IWS) is about 40% to about 100% of the weight of the solid support, which may be, for example, an untreated γ-alumina catalyst. In one embodiment, the untreated γ-alumina catalyst is selected from commercially available Porocel® CatGuard® catalysts. Preferably, the IWS is about 50% to about 60% of the catalyst support weight.

[0081] γ-alumina is about 50 to about 400 m 2 The γ-alumina may be provided in powder form with a surface area of ​​1 / 4 sq. m / g. The γ-alumina in one embodiment is shaped by a suitable extrusion process, as known to those skilled in the art of solid-state catalysis. In one example, the γ-alumina is in the form of 1 / 16" (0.16 cm) to 1 / 8" (0.32 cm) cylindrical rods with a length-to-diameter ratio of about 20:1, preferably about 5:1. The extrudates can be spheres, stars, hollow cylinders, or any three-dimensional shape that can ultimately deliver γ-alumina with sufficient surface area, pore volume, mechanical strength, and physical size for use in continuous-flow reactor systems.

[0082] Once prepared, the γ-alumina catalyst, for example, base-treated, preferably with a promoter, as described above, is preferably calcined at a carefully controlled temperature. This is done at an elevated temperature, preferably in a suitable chamber such as an oven, and the temperature range is elevated to heat the material, but not as high as the calcination temperatures typically used in conventional catalytic processes. Instead, the temperature for calcination is maintained at about 400°C to about 500°C, preferably about 420°C to about 480°C, and most preferably about 440°C to about 460°C. Typically, conventional standard calcination processes are performed at temperatures above 500°C, with no set or specified limits for effectiveness. However, Applicant has discovered that by controlling this temperature, and in the specific catalytic treatment process described herein, regioselectivity can be unexpectedly controlled to disproportionately favor the production of bio-1-alkene when dehydrating bio-1-alcohol using a calcined catalyst resulting from the combination of catalytic treatment and a carefully controlled calcination process.

[0083] In the dehydration step herein, bio-1-alcohol may be fed neat to the reactor or into the reactor in water. An optional inert gas (e.g., nitrogen) can be used as a purge gas to maintain consistency and avoid contamination during the process. Bio-1-alcohol is preferably fed via a pump (such as an HPLC pump) or pressurized gas source at a temperature of about 200°C to about 400°C, although the temperature can be adjusted for different bio-1-alcohols depending on the reaction time and flow rate, the selected catalyst, and the desired results. The product removal from the reactor is preferably monitored to determine not only the regioselectivity but also the content, product identity, and rate of bio-1-alkene conversion. In a preferred embodiment, bio-1-alkene has a regioselectivity of at least about 80%, more preferably about 92% to about 99%, and even more preferably about 95% to about 99%.

[0084] In one embodiment, the dehydration process described in FIG. 1 can be shut down using the catalyst of the present invention, i.e., the catalyst obtained from the preferred treatment and calcination process described above, and the catalyst can be maintained under an inert gas flow for an extended period of time. This shutdown period can last for hours, days, or weeks, and can be with or without the application of heat. The catalyst of the present invention can be reheated and the dehydration process can be restarted without adversely affecting catalytic activity or regioselectivity. Thus, the catalyst of the present invention is not only robust in continuous operation, but can also withstand periods of downtime (inactivity) without adversely affecting catalytic performance when returned to the line.

[0085] Bio-1-alkene can also be formed using a process for dehydrating bio-1-alcohol in water in a bulk process or other continuous reactor by heating the bio-1-alcohol with a catalyst under a purge gas as described above. A base and optional organosilane treatment can also be used, as well as the catalyst and reaction conditions as described above, most preferably using the calcined γ-alumina catalyst formed by the process described above.

[0086] Bio-1-alcohol may be formed using a process in which bio-1-alcohol in water is dehydrated by heating with a catalyst under a purge, but as noted above, it can also be formed in a bulk process or some other continuous reactor. Similar to the catalysts and reaction conditions described above, a base and optional organosilane treatment may also be used.

[0087] Once the bio-1-alcohol is dehydrated to form a highly regioselective terminal bio-1-alkene, the material is then converted to a bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms. Prior to conversion, the bio-1-alkene can optionally be further purified, such as by distillation, vacuum distillation, fractionation, or a similar purification process, to further purify the bio-alkene and remove trace impurities and minor undesirable fractions. For example, in forming bio-1-octene, a C8 olefin content of about 90% to about 99% by weight can be achieved, with at least about 95% by weight, preferably about 97% by weight or greater, of the C8 olefins in the form of n-α-olefins (i.e., 1-octene). Furthermore, in forming bio-1-hexene, a C6 content of about 95% by weight to about 99.8% by weight can be achieved, with at least about 96% by weight to about 99% by weight of the C8 olefin having the 1-hexene structure.

[0088] Various chemical reactions can be used for this conversion, as are known for use in the conversion of standard alkenes to alkanediols using petrochemically derived starting materials and / or for shorter-chain bio-alkanes. For example, the bio-1-alkene can be reacted in the presence of at least one of formic acid or acetic acid and a peroxide, such as hydrogen peroxide, to form an intermediate solution containing bio-1,2-epoxyalkane, bio-1,2-alkanediol, and other components. This is then further contacted with a base solution, such as sodium hydroxide or another suitable base solution, to complete the formation of bio-1,2-alkanediol. The above process preferably produces bio-1,2-alkanediol at a purity of about 60% to about 99%, more preferably about 70% to about 99%, or about 75% to about 99%.

[0089] Bio-1-alkanols can also be converted to bio-1-alkenes for use in this process by dehydrating the bio-1-alkanols using heat and an acid catalyst, according to other prior art.

[0090] A bio-1,2-alkanediol having a chain length of about 5 to about 20 carbon atoms is synthesized by converting a first bio-alkene having a carbon chain length of about 5 to about 20 carbon atoms and a regioselectivity of the bio-1-alkene of at least about 80%, more preferably 92% to about 99%, and most preferably about 95% to about 99%. In one embodiment, a bio-1-alkanol having a carbon chain length of about 5 to about 20 carbon atoms is preferably first regioselectively converted to a bio-alkene, and the resulting bio-alkene contains at least about 80% or more bio-1-alkene content, as described above. The bio-1-alkene is then converted to a 1,2-alkanediol by any method known in the art. The resulting converted bio-1,2-alkanediol can be further purified by distillation, vacuum distillation, fractionation, or other similar steps as described above to purify the bio-1-alkene and obtain the final purified bio-1,2-alkanediol.

[0091] The resulting bio-1,2-alkanediols having chain lengths of about 5 to about 20 carbon atoms are preferably synthesized by first dehydrating a bio-1-alkanol having a carbon chain length of about 5 to about 20 carbon atoms to a bio-1-alkene with a regioselectivity of at least about 80%, more preferably about 92% to about 99%, and most preferably about 95% to about 99%, followed by treatment of the bio-1-alkene with formic acid or acetic acid in the presence of hydrogen peroxide, followed by treatment with aqueous base. The bio-1,2-alkanediols can then be separated from the aqueous solution by any suitable technique known to those skilled in the art for producing dihydroxyalkanes in general, and more specifically, 1,2-alkanediols. In a preferred embodiment, a distillation step is included for this purpose.

[0092] The bio-1,2-alkanediols described above can be used in a variety of compositions, whether used alone or in combination with other different bio-1,2-alkanediols according to the present invention. Such compositions can include one, two, or more different bio-1,2-alkanediols according to the present invention that can function within an antimicrobial system. Such bio-1,2-alkanediols can be used alone as antimicrobial additives or in antimicrobial systems incorporating other bio-compounds (i.e., any suitable naturally occurring, preferably true natural product, tested using mass spectrometry, gas chromatography, and / or ASTM standards, as described above), such as bio-organic acids, bio-diols such as 1,3-propanediol, bio-1,2-butanediol, and 1,2-pentanediol, extracts from fermentation products of bio-based starting materials, and / or other antimicrobial substances, alternative preservatives, traditional preservatives, or hard technology components known in the art or yet to be developed. An example of a preferred source of bio-compounds for use within the present invention is triglycerides. In yet another example, another chemical group of bio-compounds that can be used in preparing alternative preservatives are generally described as terpenoids. These naturally occurring terpenoids can have 5 to 20 carbon atoms, are readily available through sustainable agricultural practices, and can be used in combination with bio-1,2-alkanediols within the scope of the term "bio-compounds" as used herein.

[0093] When used in compositions, the bio-1,2-alkanediols of the present invention are preferably present in an amount of about 0.1 to about 10% by weight, preferably 0.3 to about 2% by weight, of the total composition. This amount can vary depending on whether the bio-1,2-alkanediols are used alone for their antimicrobial effect or together with other components of an antimicrobial system. In the latter example, the bio-1,2-alkanediols are preferably present in the antimicrobial system in a ratio of about 99:1 to about 1:99, preferably about 75:25 to about 25:75, of bio-1,2-alkanediol to any other antimicrobial components (wherein the system may include the bio-1,2-alkanediols described herein and / or any other antimicrobials, traditional preservatives, alternative preservatives, and / or hurdle technology components in the composition).

[0094] The 1,2-bio-alkanediols of the present invention, when used in certain compositions that are themselves considered "antimicrobial products" for provision to other formulators in various industries, can first be prepared as antimicrobial products that include one or more of the 1,2-bio-alkanediol materials produced according to the present invention as described above and incorporate one or more of the compositions as described above, where such antimicrobial products may also include other bio-compounds, known antimicrobial agents, preservatives, alternative preservative materials or hurdle technology materials.

[0095] Examples of known preservatives and compounds used in alternative preservative materials or systems that can be used with the bio-1,2-alkanediols of the present invention include those suitable for use in various industries that may benefit from the present invention. For example, in the cosmetics and personal care industries, the bio-1,2-alkanediols formed according to the present invention can be used alone, in combinations of two or more such materials, and / or in combination with other biocompounds and / or known cosmetic preservatives and alternative preservative materials and / or hard technology ingredients. Examples of preservative materials include (i) conventional preservatives such as parabens (methyl, ethyl, propyl, and butyl), quaternium 15 (also known as "Dowicil™"), diazolidinyl urea, imidazolidinyl urea, DMDM ​​hydantoin, 2-bromo-2-nitropropane-1,3-diol (also known as "bronopol"), sodium hydroxyglycinate, phenoxyethanol, sorbic acid, potassium sorbate, methylisothiazolinone (also known as "MI"), methylchloroisothiazoline (also known as "CMI," often used in combination with MI as Caison® CG), sodium benzoate, caprylyl glycol, sodium dehydroacetate, and formaldehyde; (ii) ) non-traditional or alternative preservatives such as plant extracts, organic acids, alcohols and glycerol, fermentation products, glyceryl caprylate, levulinic acid, p-anisic acid, eucalyptus, licorice, licorice root extract, salvia grandis (organic grapefruit) extract, arnica montana (organic arnica) extract, boraxis seed extract, leuconostoc / radish root ferment filtrate, gold seal (hydrastis root extract), citrus medicinal, limonium (lemon) peel extract, caprylhydroxamic acid; (iii) so-called "self-preserving" materials such as ethanol (when present at 15% or more), butylene glycol (when present at 10% or more), and propylene glycol (when present at 20% or more);(iv) Other ingredients used in alternative or conventional preservative systems in cosmetics, such as MDM hydantoin, sodium hydroxymethylglycinate, benzisothiazolinone, benzyl alcohol, dehydroacetic acid, benzoic acid, salicylic acid, iodopropynyl butylcarbamate, chloroxylenol, methyldibromoglutaronitrile, chlorphenesin, triclosan, benzalkonium chloride, chlorhexidine, polyaminopropyl biguanide, 5-bromo-5-nitro-1,3-dioxane (bronidox®), hexamidine diisethionate, pentylene glycol, ethylhexylglycerin, triclocarban, glyceryl caprylate, o-cymen-5-ol, chlorphenesin, and glyceryl monolaurate, and 1,2-alkanediols traditionally derived from petrochemicals, such as 1,2-hexanediol and 1,2-octanediol, are listed by the FDA in the United States.

[0096] Other countries have similar lists, and there are variations in the nature and type of preservatives, alternative preservatives or preservative systems, or hurdle technology additives that may be used in those countries. However, the bio-1,2-alkanediols of the present invention can be used in such other materials as well. In each of the above systems and compositions, the preferred bio-alkene used in the present invention is bio-octene, and the at least one first bio-1,2-alkanediol is bio-1,2-octanediol.

[0097] Examples of compositions that could benefit from an antimicrobial system comprising one or more bio-1,2-alkanediols formed according to the above processes and / or compositions include personal care compositions, such as hair care, oral care, skin care or cosmetic compositions; household product compositions, such as fabric care products or cleaning products; industrial compositions; and pharmaceutical, vitamin, dietary supplement or other health care compositions, any of which could benefit from an antimicrobial system, ingredient or product derived from true, natural, bio-based materials.

[0098] The bio-1,2-alkanediol is preferably incorporated into the cosmetic or personal care composition (on a wet or total weight basis) to comprise from about 0.001% to about 25% by weight of the composition, more preferably from about 0.01% to about 10% by weight of the composition. The amount used may vary depending on whether other hard technology ingredients or other preservatives are also used in the composition.

[0099] Such bio-1,2-alkanediols can also be used alone, in combination with two or more different bio-1,2-alkanediols, and / or in antimicrobial systems incorporating bio-1,2-alkanediols alone or with other bio-compounds and / or other preservatives, alternative preservatives, or hurdle technology components, in methods of imparting antimicrobial efficacy to compositions, which may be any of the various types of compositions described above. The bio-1,2-alkanediols described herein preferably impart antimicrobial efficacy and efficacy to personal care compositions, household compositions, industrial compositions, pharmaceutical compositions, vitamin compositions, nutraceutical compositions, or other health care compositions into which the bio-1,2-alkanediols are incorporated. Such antimicrobial efficacy can be demonstrated using a variety of appropriate antimicrobial efficacy tests (AETs). Such tests include, for example, compendial tests conducted during formulation development and stability testing of parenteral formulations intended for multi-dose formulations. Appropriate test methods and acceptance criteria are found in the United States Pharmacopoeia, AET, European Pharmacopoeia (antimicrobial preservative effectiveness), and Japanese Pharmacopoeia (preservative effectiveness testing). Other suitable challenge tests may be used. FDA also recommends suitable challenge tests.

[0100] One group of antimicrobial agents (some of which belong to the above group) is other alcohols, preferably at least one other alcohol, preferably at least one other diol, most preferably one or more other vicinal diols that may be petrochemically derived. Such materials are preferably used as diluents or in small amounts to provide some antimicrobial effect, but not so great as to reduce the impact of the natural bio-based 1,2-alkanediols of the present invention. The term "vicinal diol" refers to materials having hydroxyl groups attached to adjacent atoms in the molecule, i.e., two atoms each bearing a hydroxyl group are bonded to each other. Examples of vicinal diol compounds suitable for use in the present invention include, but are not limited to, ethylene glycol and propylene glycol. Such materials are used as moisturizers and solvents in the personal care, cosmetic, and pharmaceutical fields, and are used to have some mild antimicrobial activity, as described in U.S. Patent Application Publication No. 2007-0207105A1.

[0101] Preferred vicinal diols for use with the bio-1,2-alkanediols described herein in compositions described for use in personal care and pharmaceutical compositions are medium-chain linear vicinal diols, including petrochemically derived 1,2-pentanediol, 1,2-hexanediol, 1,2-octanediol, and 1,2-decanediol, which exhibit some antimicrobial activity. Other vicinal diols useful in the compositions described herein include molecules derived from glycerin. Glycerin can react with other molecules at its 1- or 3-position, leaving two vicinal hydroxyl groups. For example, glyceryl monoethers such as ethylhexylglycerin [3-(2-ethylhexyloxy)propane-1,2-diol], commercially available from Schulke & Mayr as SENSIVA® SC50, are useful traditional liquid vicinal diols with antimicrobial properties. Glyceryl monoesters such as glyceryl monolaurate, glyceryl monocaproate, or glyceryl monocaprylate (the latter commercially available from Inolex Chemical Company, Philadelphia, Pennsylvania) are also useful antimicrobial vicinal diols. With regard to the preservation of cosmetics, toiletries, and pharmaceuticals, vicinal diols are known to be effective against bacteria and yeasts but weak against fungi, and to date there are limited natural options, none of which, to the applicant's knowledge, are bio-derived natural 1,2-alkanediols having 5 to 20 carbon atoms.

[0102] The compositions described herein preferably do not contain or contain only small amounts of any preservative materials, such as parabens, or other known preservative materials, that may be considered harmful to the user.

[0103] Such personal care and pharmaceutical compositions may optionally further comprise a solubilizing agent in an amount of about 1% to about 70% by weight of the combination of solubilizing agent and bio-1,2-alkanediol (or, if used with other preservative components, the total antimicrobial system together with the solubilizing agent). Suitable solubilizing agents include vicinal diols and other conventional diols.

[0104] Useful in any antimicrobial system, along with bio-1,2-alkanediols, are hydroxamic acids, which can be used in a variety of industries. Suitable hydroxamic acids include alkylhydroxamic acids and bio-alkylhydroxamic acids containing at least one alkyl group with a chain length of about 2 to about 22 carbon atoms, which may be structurally branched or linear, substituted or unsubstituted, and saturated or unsaturated, as described above. Preferred alkylhydroxamic acids contain alkyl groups with a chain length of about 6 to about 12 carbon atoms, most preferably linear chains of that length. The most preferred alkylhydroxamic acids are caprylohydroxamic acid, which has a linear terminal chain of 8 carbon atoms, and caprohydroxamic acid, which has a linear chain of 10 carbon atoms. Such alkylhydroxamic acids can be used alone or in combination with any of the solubilizing agents in the amounts described above.

[0105] Formulations prepared for personal care applications, and pharmaceutical compositions depending on the end use (topical or oral), can include any other colorants, fragrances, active ingredients, or other additives typically used and / or to be developed in the art for use in personal care and pharmaceutical formulations, where the additives are selected from the group consisting of: preferred bio-1,2-alkanediols, or antimicrobial products or systems containing bio-1,2-alkanediols; topical skin cosmetics, skin cleansers, night creams, skin creams, shaving creams, skin care lotions, or other cosmetic preparations; foundations, liquid-based and makeup such as powder-based makeup, mascara, lipstick, blush, gloss, eyeliner, etc.; or other personal care and / or pharmaceutical compositions, such as sunscreen, lip balm, perfume, massage oil, shampoo, conditioner, conditioning shampoo, hair styling gel, hair repair agent, hair growth agent, hair fixative, hair mousse, bath and shower gel, liquid soap, moisturizing spray, makeup, pressed powder formulations, bath additives, ophthalmic preparations, foaming soap and body wash, disinfecting wipes, hand sanitizer, medications (tablets and liquids), towelettes and wipes, etc. Based on the present disclosure, a wide variety of personal care and pharmaceutical compositions can benefit from the properties of the bio-1,2-alkanediols of the present invention, where it is to be understood that, as used herein, a pharmaceutical composition is one having at least one active pharmaceutical ingredient (API).

[0106] When liquid-based (gels, hydrogels, lotions, shampoos, liquid medications, etc.), personal care and pharmaceutical formulations preferably include water as part of the liquid base. Depending on the desired final formulation, the formulations and compositions may also include other additives, such as, but not limited to, at least one humectant, at least one emulsifier and / or thickener, chelating agents, gelling agents, amino acids, emollients, various solvents, free radicals and initiators, sunscreen UVA and / or UVB blockers, antioxidants, other preservatives, waxes, polymers and copolymers, inorganic and organic pigments and / or one or more fragrances, flavors, colorants, herbs, natural extracts, essential oils, pharmaceuticals, other active pharmaceutical ingredients, and other additives commonly used in such formulations.

[0107] Personal care and pharmaceutical compositions using the bio-1,2-alkanediols herein may be lotion-based, oil-in-water emulsions, water-in-oil emulsions, water-in-silicone emulsions, silicone-in-water emulsions, gels, solids, liquids, cream-based, oil-based, aqueous / alcoholic or glycolic solution-based, dispersions, suspensions or syrups, microemulsions or liposome-based formulations.

[0108] In water-based formulations other than solids and thicker gels, it is preferred that from about 20% to about 95% by weight of water (on a wet basis) be incorporated therein. Various additives other than water and the preferred antimicrobial system described herein will make up the remainder of various personal care and pharmaceutical compositions. Preferably, each additive is present in an amount up to about 75 weight percent, more preferably up to about 40 weight percent, of the total formulation, and preferably the combined amount of such additives is present in no more than about 50 weight percent.

[0109] Antimicrobial agents are also useful additives in household products. Household product compositions can include household cleaners and fabric care compositions. Cleaning compositions (whether solid or solution) can incorporate detergents (such as bleach, vinegar, ammonia, citric acid, etc.) that are active ingredients for cleaning. For liquid detergents, aqueous solutions of quaternary ammonium compounds, bleach, vinegar, or basic or acidic detergents, known or to be developed in the art, can be used. Commercially available quaternary ammonium-based cleaning products include various well-suited antimicrobial all-purpose cleaners intended for disinfecting or sanitizing effects, but such compositions still contain antimicrobial agents and other preservatives for shelf life and to prevent the growth of foreign substances. Therefore, such compositions also benefit from the use of the natural bio-1,2-alkanediols described herein.

[0110] For more natural cleaning solutions, such as citric acid-based agents or other green cleaning agents, consumers may be interested in additional additives that are also natural, in this case derived from biological sources. Therefore, such compositions benefit from the natural bio-based 1,2-alkanediols described herein, as well as antimicrobial systems and products incorporating the bio-1,2-alkanediols. Such natural cleaning compositions, as well as standard cleaning compositions, can also incorporate various optional additives in varying amounts, as described below. Citric acid-based cleaning products may also include lemon, orange, or grapefruit-based detergents. Other suitable ingredients include vegetable oils in combination with one or more of grapeseed oil, mild peroxide agents, surfactants, etc., as well as pigment or colorant additives to provide a visual warning when a cleaning agent is present; traditional or alternative preservative compounds; antimicrobial, bactericidal, or antifungal agents (each of which can be used alongside or in combination with the bio-1,2-alkanediols of the present invention in antimicrobial systems or products); thixotropic and rheology modifiers; pH-adjusting or buffering additives; and fragrance additives to impart a clean odor (pine, lemon, orange, floral, etc.). Additionally, other agents for foaming, color change, or foaming (bubbling) can be provided as needed to demonstrate cleaning action. Solid cleaning agents can incorporate similar additives but can also be compressed, incorporated, or formed with various inert agents (hardeners, gelling agents, mineral powders, etc.) to deposit the cleaning material on a substrate (sponge, scrubber, mop head, etc.) and hold the solid cleaning material together. Other additives for household cleaning compositions include pH buffers, perfume encapsulants or carriers, fluorescent agents, hydrotropes, soil release agents, polyelectrolytes, enzymes, optical brighteners, antioxidants, UV absorbing compounds, propylene glycol, dipropylene glycol, opacifiers, pearlescent agents and combinations thereof, as well as other cleaning products known or to be developed.

[0111] The fabric care compositions can include any fabric cleaning active ingredient, as well as various conditioning ingredients known in the art or to be developed. Such compositions can include ingredients used in fabric care compositions such as fabric cleaning or laundering, fabric conditioning or softening, fabric dyes, water conditioners, and / or spot removers or stain treatments. Such ingredients include, but are not limited to, antifoam agents, anti-adherents, fragrances and their carriers or encapsulants, traditional or conventional diols (although if bio-1,2-alkanediols are useful at comparable, improved, or enhanced capacity over existing diols, such diols may be omitted), colorants such as pigments or dyes, and co-softeners. Other additives for fabric care compositions include, but are not limited to, other traditional preservatives, antimicrobial agents, bactericides, and / or mildewcides (each of which may be used alone or in the antimicrobial products or systems described herein), pH modifiers or buffers, fluorescent agents, hydrotropes, soil release agents, polyelectrolytes, enzymes, optical brighteners, anti-shrinkage agents, anti-wrinkle agents, anti-spotting agents, antioxidants, UV absorbing compounds, anti-corrosion agents, drape imparting agents, antistatic agents, ironing aids, odor control compounds, perfume encapsulating agents, cottonseed oil, tea oil, aloe extract, propylene glycol, dipropylene glycol, opacifiers, pearlizing agents, and combinations of these ingredients.

[0112] The antimicrobial bio-1,2-alkanediols described herein can also be used in the treatment of finished textiles and / or the treatment of fibers or yarns that will be used to produce textiles to achieve desired benefits. Textiles can include woven and nonwoven textiles, such as felt and tapa and other bark textiles, or blends and combinations thereof. Textile fibers (whether present in finished textile form, threadlike or fibrous form, or both) can be any known or developed in the art, including synthetic fibers, "natural" fibers (e.g., animal-derived fibers or cellulose / plant-derived fibers), and any blends or combinations thereof.

[0113] Animal-derived fibers include and can be derived from animal hair or fur, including, but not limited to, lamb's or sheep's wool, alpaca, angora wool, azulon, byssus, camel hair, cashmere wool, chiengora, chatgora, llama, mohair wool, qiviut, rabbit, silk, vicuña, yak, pashmina wool, and combinations thereof. Cellulosic or plant-derived fibers include, but are not limited to, those derived from flax (linen fiber), cotton, ramie, jute, kenaf, beach hibiscus, roselle, urena, hemp (e.g., Crotalaria juncea, Cannabis sativa, Apocynum cannabinum), hoop vine, sisal, enneke, yucca, Manila hemp, Hemp spp., New Zealand flax, cotton, coir, milkweed, kapok, floss silk, Proboscidea parviflora, bamboo, bast, fiecke, banana, modal, lyocell, piña, raffia, rayon, soy protein, acetate, and combinations thereof. Synthetic fibers include, but are not limited to, any known or to be developed, such as acrylic, Kevlar®, modacrylic, Nomex®, nylon, polyester, Lycra®, spandex, rayon, and combinations thereof.

[0114] Fabric treatment compositions can be applied to textiles or fibers.The compositions can be applied as either wet or dry compositions, and during the washing cycle or drying cycle with water.Such fabric treatment materials can be used to soften and / or condition textiles or fibers; reduce and / or prevent wrinkles; impart fragrance to textiles or fibers; shorten ironing time; improve softness, etc.

[0115] The present invention also includes the use of 1,2-bio-alkanediol materials formed in accordance with the present invention as materials to enhance the antimicrobial efficacy of existing antimicrobial agents, preservatives, alternative preservative materials and / or hurdle technologies.

[0116] By enhancing antimicrobial efficacy, the antimicrobial efficacy of existing antimicrobial agents and / or preservatives (including alternative preservative materials and hurdle technologies) can be improved by more than substantial improvements, i.e., at least about 5%, preferably at least about 10%, and more preferably at least about 20%, when combined with 1,2-bioalkanediols, while providing a natural booster. Boosting and antimicrobial efficacy in formulations are evaluated by measuring performance using preservative efficacy tests (PET) or challenge tests. Preservatives and antimicrobial agents used in cosmetics, toiletries, and pharmaceuticals must pass microbiological testing protocols established by government regulations and industry associations, known as "challenge tests." Challenge tests are performed by adding known amounts of microorganisms to the product and measuring the increase or decrease in microbial counts over time. Microorganisms include gram-positive and gram-negative bacteria, yeasts, and molds. The Cosmetic, Toiletries, and Fragrance Association (CTFA) has defined challenge tests that are widely accepted in the cosmetics, toiletries, and pharmaceutical industries. The test requires a 99% reduction in bacterial counts in seven days and a 90% reduction in yeast and fungi (mold) counts in seven days. To pass the challenge test, the product must contain the appropriate amount and type of preservative compound to provide antimicrobial effectiveness against a wide range of microorganisms in a short period of time.

[0117] In addition to providing antimicrobial efficacy, when used as an enhancing material to improve the effectiveness of existing antimicrobial agents, etc., as described above, 1,2-bioalkanediols are preferably incorporated in an amount of about 0.1 to about 10% by weight, preferably 5.0 to about 3.0% by weight, of the total composition; and preferably in a ratio of about 99.999:0.001 to about 0.001:99.999, preferably about 99.9:0.1 to about 0.1:99.9, of the total amount of antimicrobial agent, preservative, alternative preservative and / or hard technology component already present in the composition.

[0118] The invention will now be described with reference to the following non-limiting examples. [Example]

[0119] Bio-1-octanol is formed from the hydrogenation of bio-octanoic acid (a suitable source of which may be from coconut, palm, or any other renewable source or process capable of producing octanoic acid). Bio-1-octanol is regioselectively dehydrated by feeding bio-1-octanol at elevated temperature to a fixed-bed reactor containing a catalyst according to the invention described herein.

[0120] Gas chromatography (GC) has been an important method used to characterize both petroleum derivatives and natural renewable derivatives. Products (e.g., octene) were characterized using a Thermo Scientific Trace® 1310 gas chromatograph equipped with an FID detector and Chromeleon™ software (version 7.2.4.8525). For dehydration reaction products, GC was performed using a Restek® MXT-5 column (30 m length, 0.5 μm membrane, 0.53 ID), helium carrier gas (3.0 mL / min), CT split injection at 45 mL / min (5.0 mL / min purge flow), injector at 250 °C, detector at 300 °C, and oven at 70 °C, held for 8 min, followed by a ramp to 300 °C (15 °C / min) with a final hold of 6.67 min. For alkanediol products, GC analysis used a Restek® MXT-WAX column (30 m length, 0.5 μm membrane, 0.53 ID), helium carrier gas (5.0 mL / min), CT split injection 10 mL / min (5.0 mL / min purge flow), injector 220°C, detector 250°C, oven 70°C, held for 0.25 min, then ramped to 250°C (10°C / min) with a final hold of 6.67 min.

[0121] Example 1 γ-alumina powder was treated with an aqueous calcium acetate solution using the technique of incipient wetting to give a catalyst containing 1.50% calcium (based on CaO) after calcination at 440°C in air for 12 hours.

[0122] Example 2 Gamma-alumina powder was treated with an aqueous calcium acetate solution using the technique of incipient wetting to give a catalyst containing 1.50% calcium (based on CaO) after calcination at 500°C in air for 12 hours.

[0123] Example 3 The catalysts prepared in Examples 1 and 2 were loaded into separate 75 mL (Sigma-Aldrich part number Z173592) reactors, each wrapped in heating tape and covered with fiberglass insulation. The temperature was controlled by a thermocouple attached to the reactor shell, and this input was used for the temperature controller. Bio-1-octanol was fed to the reactor, which was maintained at 315°C, using an HPLC pump. The feed rate of bio-1-octanol was adjusted to obtain a conversion rate greater than 95% but less than 100%. After 1 hour of continuous operation, samples were collected and analyzed for the chemical conversion of bio-1-octanol and the regioselectivity of bio-1-octene. The results are as follows:

[0124] [Table 3]

[0125] Example 4 Porocel® CatGuard® gamma-alumina in the form of 1 / 16 inch (0.16 cm) extrudates was cut to have a length-to-diameter ratio ranging from 2 to 4. The extrudates were modified with an aqueous solution of calcium acetate. The weight of the solution to the alumina was 0.55 by weight, and the calcium acetate concentration was at a level to provide 1.50% CaO (after calcination). The catalyst was calcined in air at 440°C for 12 hours.

[0126] Example 5 48 g of the catalyst prepared in Example 4 was loaded into a 75 mL (Sigma-Aldrich part number Z173592) reactor, wrapped in heating tape, and covered with fiberglass insulation. Temperature was controlled by a thermocouple attached to the reactor shell, and this input was used for the temperature controller. Bio-1-octanol was fed at 0.2 mL / min to the reactor, which was maintained at 35°C. After over 1,400 hours of TOS, including periodic shutdowns and startups, catalyst performance remained unchanged in terms of 1) chemical conversion of bio-1-octanol, 2) product selectivity, and 3) regioselectivity of bio-1-octene. A GC chromatogram of the crude product recovered from the reactor is shown in Figure 3. The octene selectivity was 96%, and the chemical yield of bio-1-octene was 94%.

[0127] Example 6 The product of Example 5 was subjected to simple distillation at atmospheric pressure. The resulting product was analyzed by GC, and the chromatogram is shown in Figure 4. The product from the distillation was 99.9% bio-octene and 96.7% bio-1-octene.

[0128] Example 7 The product of Example 6 was converted to bio-1,2-octanediol by treatment with formic acid and peroxide, followed by base hydrolysis, and finally purified by fractional distillation. The GC chromatogram is shown in Figure 5. The chemical purity of the bio-1,2-octanediol obtained in this example was 98.7% as determined by GC analysis. A representative GC chromatogram of petro-1,2-octanediol currently used in commercially available cosmetics is shown in Figure 6.

[0129] Example 8 Stable isotope analysis was performed on the petroleum-based and natural renewable feedstock-prepared samples in Examples 6 and 7. The values ​​are shown below:

[0130] [Table 4]

[0131] Example 9 The bio-1,2-octanediol prepared in Example 7 was subjected to tests currently used to certify petroleum, non-renewable, non-natural equivalents. The bio-1,2-octanediol prepared in Example 7 was found to meet all batch analytical test requirements:

[0132] [Table 5]

[0133] Example 10 In a comparative example, bio-1-octanol was fed into a 75 mL reactor packed with a catalyst prepared as follows: γ-alumina powder was modified with sodium hydroxide solution (5 wt.% NaOH) to prepare the second catalyst. The second catalyst was dried in an oven and then treated with diethoxydiphenylsilane (1 wt.% based on alumina) dissolved in ethanol. The solvent was removed, the catalyst was washed with ethanol, and dried in an oven to prepare the third catalyst. This third catalyst was calcined at 400 °C for 12 h. The catalyst was loaded into a 75 mL reactor and heated to a target temperature of 325 °C. The bio-1-octanol feed rate was adjusted to optimize both conversion and regioselectivity.

[0134] Example 11 Petro-1-hexanol was fed to a 75 mL reactor packed with the catalyst prepared in Example 4. The catalyst used in this example had a TOS of over 1400 hours for use in the dehydration of bio-1-octanol to bio-1-octene. In this example dehydration series, the temperature was varied from 330°C to 370°C, and the feed rate was adjusted so that the amount of hexanol passing through the reactor was 1-2%. The results for hexanol dehydration are shown below.

[0135] [Table 6]

[0136] In Example 11C, when the reactor is maintained at 370°C, a new peak in the GC chromatogram appears with an area % of 3.6, thus indicating a low chemical yield of 1-hexene and the formation of other products.

[0137] Example 12 After 1400 hours of TOS for the dehydration of bio-1-octanol, some catalyst was removed at the inlet side of the tubular reactor. In Figure 7, the used catalyst is photographed next to the catalyst from the 0 hour TOS. The used catalyst shows slight discoloration, but does not indicate a loss of chemical conversion or regioselectivity, as described herein.

[0138] Those skilled in the art will appreciate that changes could be made to the embodiments described above without departing from the broad inventive concept thereof. It is understood, therefore, that the invention is not limited to the particular embodiments disclosed, but that it is intended to cover modifications within the spirit and scope of the invention as defined by the appended claims.

Claims

1. A process for the synthesis of bio-1,2-alkanediols, said process comprising: providing a bio-alkene having a carbon chain length of 5 to 20 carbon atoms and a bio-1-alkene regioselectivity of at least 80% by dehydrating bio-1-alcohol in a reactor containing a base-treated and calcined gamma-alumina catalyst, the gamma-alumina catalyst being unsilanized; converting the bio-alkene into a bio-1,2-alkanediol having 5 to 20 carbon atoms; Including, The process produces at least 72% to 99% of the bio-1,2-alkanediol.

2. The process described in claim 1, wherein the bio-1-alcohol, the bio-alkene and the bio-1,2-alkanediol each have 6 to 14 carbon atoms.

3. The process described in claim 2, wherein the bio-1-alcohol, the bio-alkene and the bio-1,2-alkanediol each have 6 to 10 carbon atoms.

4. The process described in claim 3, wherein the bio-1-alcohol, the bio-alkene and the bio-1,2-alkanediol each have 6 to 8 carbon atoms.

5. The process described in claim 1, wherein the bio-1-alcohol is bio-1-octanol, the bio-alkene is bio-octene, and the bio-1,2-alkanediol is bio-1,2-octanediol.

6. 10. The process of claim 1, wherein the reactor is a fixed bed reactor.

7. 7. The process of claim 6, wherein the fixed bed reactor is a fluidized fixed bed reactor.

8. 2. The process of claim 1, wherein the bio-alkene has a bio-1-alkene regioselectivity of 92% to 99%.

9. 9. The process of claim 8, wherein the bio-alkene has a bio-1-alkene regioselectivity of 95% to 99%.

10. 10. The process of claim 1, wherein the process produces at least 92% to 99% bio-1,2-alkanediols.

11. 10. The process of claim 1, wherein the catalyst is a gamma alumina catalyst calcined at a temperature of 400°C to 480°C.

12. 10. The process of claim 1, wherein the treatment with a base comprises treatment with a Group I or Group II metal.

13. The process of claim 12, wherein the treatment with a base includes treatment with a calcium promoter.

14. 14. The process of claim 13, wherein the calcium promoter is used in an amount of 0.01 weight percent to 4 weight percent based on the weight of CaO determined after calcination.

15. 15. The process of claim 14, wherein the calcium promoter is used in an amount of 1 weight percent to 2 weight percent based on the weight of CaO determined after calcination.

16. The process of claim 11, wherein the temperature during calcination is between 420°C and 480°C.

17. 17. The process of claim 16, wherein the temperature during calcination is between 440°C and 460°C.

18. 10. The process of claim 1, wherein the baking is carried out in an oven.

19. 10. The process of claim 1, wherein the calcination is carried out in an atmosphere of air or an inert gas.

20. 10. The process of claim 1, wherein the bio-alkene undergoes a distillation process to purify the bio-alkene before converting the bio-alkene to a bio-1,2-alkanediol.

21. 10. The process of claim 1, further comprising distilling the bio-1,2-alkanediol.

22. The process of claim 1, wherein the dehydration is carried out in water under a purge gas.

23. 2. The process of claim 1, wherein the bio-alkene is converted to a bio-1,2-alkanediol by reacting the bio-alkene in the presence of at least one of formic acid or acetic acid and a peroxide to form a bio-1,2-epoxyalkane having an epoxy ring, and contacting the 1,2-epoxyalkane with water and sodium hydroxide to form a bio-1,2-alkanediol.

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