575 results about "Glycerite" patented technology

A process for purifying glycerin recovered as a byproduct of biodiesel production comprises heating a glycerin effluent stream containing a low molecular weight alcohol, water and fatty acid esters of the low molecular weight alcohol to cause transesterification of the fatty acid esters to glycerides and additional low molecular weight alcohol. The reaction mixture is sparged with nitrogen to help remove water and low molecular weight alcohol, which drives the transesterification reaction towards glyceride formation. A wash water stream may also be added to the recovered glycerin stream from biodiesel production. Either before or following the transesterification reaction, an oil layer can be separated from the recovered glycerin stream by reducing the pH of the stream to below 7. Following separation of the oil layer and transesterification the glycerin stream is flash distilled to separate glycerin from water, salts, and glycerides.

The invention provides a method for preparing normal propyl alcohol by glycerol hydrogenation, wherein glycerite or biodiesel byproduct glycerol which is diluted by glycerol or solvent reacting with hydrogen or gaseous mixture containing hydrogen to generatenormal propyl alcohol, which provides a new way for synthesizing normal propyl alcohol. The present invention can enhance activity of glycerol hydrogenation and selectively generates normal propyl alcohol, also can make normal propyl alcohol united generating with 1,2-propanediol, ethandiol, methylic alcohol and ethyl hydrate, thus its product process program is very flexible. The present invention is characterized in that its technological condition is geniality, raw material is cheap and can be obtained easily and the cost of manufacture is low, which belongs to environment friendly green chemical industry technique.

The present invention relates to a new vegetable-based composition for liquid to be vaporized in electronic cigarettes, comprising water and propylen glycol of vegetable origin and/or glycerol and/or nicotine and/or natural flavors.

The invention relates to an electronic cigarette smoke solution with the herbal tea flavor. The electronic cigarette smoke solution comprises, by weight, 35-70 parts of propylene glycol, 10-45 parts of edible glycerinum, 0.5-10 parts of a tobacco extract, 0.005-5 parts of a flavoring agent, 0.5-15 parts of a herbal tea flavor agent, 0-5 parts of edible alcohol and 0-10 parts of water. The electronic cigarette smoke solution with the herbal tea flavor contains a herbal tea flavor agent capable of clearing heat of the whistle, the appropriate strength and the full-bodied cigarette fragrance can be provided, the herbal tea flavor is added, a certain health care effect of clearing heat to reduce fire is achieved, and the shortcomings on taste of an electronic cigarette are overcome.

A pre-vaporization formulation pre-vaporization formulation for an e-vaping device, the pre-vaporization formulation including a vapor former including a combination of propylene glycol and glycerol, and an additive including at least one of capsicum, allyl isothiocyanate, piperine, isoeugenol, carvacrol, thymol, menthol, monomenthyl succinate, N-(2-hydroxyethyl)-2,3-dimethyl-2-isopropyl butanamide, horseradish oil, garlic extract, onion oil, black pepper, cayenne pepper, ginger oil, thyme oil, cinnamon bark oil, turmeric, fenugreek, cardamom, rosemary extract, grapefruit oil and andrographis extract.

The invention discloses an alcohol-free printing fountain solution and a preparation method of the alcohol-free printing fountain solution. The alcohol-free printing fountain solution comprises, by weight, 10-15% of propylene glycol monomethyl ether, 2-4% of ethylene glycol, 4-8% of a citric acid, 0.5-1.5% of sodium hydroxide, 15-25% of glycerinum, 0.1-0.3% of sodium carboxymethyl cellulose, 0.05-0.1% of lauroyl diethanol amine, 0.4-0.6% of liquid tea saponin, 0.3-0.6% of dodecyl dimethyl benzyl ammonium chloride, 0.5-1% of dodecyl glucoside, 0.05-0.1% of 2-ethyl hexanol and 50-55% of water. The alcohol-free printing fountain solution does not contain isopropyl alcohol and is low in toxicity, safe, environmentally friendly, good in printing effect and low in cost, thereby having huge economic benefit and social benefit.

The invention provides a method for preparing 1, 2- methyl glycol through glycerin hydrogenation. The glycerin, diluted glycerin or side product coarse glycerin of biodiesel mixes with hydrogen gas or hydrogen gas- containing gas, and reacts under catalyst action to produce 1, 2- methyl glycol. The conversion rate is high.

The present invention provides a refining process of biodiesel byproduct crude glycerol, and relates to the technical field of chemical product production. The refining process includes diluting, desalting, removing impurity, distilling, decoloring and deflavouring. The high-quality refined glycerine is produced by employing the technologies of sodium oxalate complexing impurity removal and active carbon decoloring and deflavouring. The refining process is simple, high in glycerin yield, high in finished refined glycerin purity, and good in product quality.

A method of producing biodiesel through the trans-esterification of a triglyceride, comprising mixing a triglyceride, an alcohol, and a catalyst to form a mixture, where said catalyst is non-metal quaternary ammonium hydroxide or non-metal quaternary phosphonium hydroxide, removing volatile components from said mixture, and allowing the remaining mixture to separate into a biodiesel-rich layer and a glycerol-rich layer.

The invention discloses a preparation method for chitosan composite membrane, which aims at providing a preparation method for the composite membrane with great toughness and less water and air permeability. The invention comprises the following steps that: the chitosan is dissolved by dilute acetum; the feed liquid ratio of the chitosan and the dilute acetum is 1:40 to 100 (weight/volume), and the chitosan is added with plasticiser, and then water-bath heating is implemented so as to make the chitosan dissolve completely, after that, the room temperature is lowered, so that the membrane solution is obtained; the plasticiser is a combination of the glycerin which accounts for 0.2 percent to 1.0 percent of the acetum in volume percent and the stearic acid which accounts for 0.3 percent to 0.8 percent of the acetum in mass percent. The prepared membrane solution is filtered for removing impurity, and is deaerated for half an hour, and then the membrane solution is poured into a clean glass plate, and is dried to form a membrane at the constant temperature of 40 to 80 DEG C; after the membrane is formed, and then stripping is implemented for generating the chitosan composite membrane. The invention adopts the glycerol and the stearic acid as the plasticiser, the composite membrane is prepared through the use selection, and the composite membrane not only has certain toughness and can keep a lower water and air permeability.

The invention relates to a method for using molecular distillation to extract nervonic acid from acer truncatum buge oil, which obtains the acer truncatum buge oil with acer truncatum buge seeds as raw materials by extracting and pressing; absolute ethyl alcohol or methanol and the acer truncatum buge oil are mixed, then the catalyst is added for reaction, unreacted ethyl alcohol or methanol is removed, glycerine is separated, and fatty acid ester of the acer truncatum buge oil is obtained by rinsing; five-grade molecular distillation is carried out to the fatty acid ester of the acer truncatum buge oil under the condition of different vacuum degrees and temperature so as to obtain the fatty acid ester with the content of nervonic acid ester of more than 80 wt percent; the fatty acid ester is saponated, acid is added to adjust pH value to be 2 to 3, rinsing is carried out so as to lead the fatty acid ester to be neutral, petroleum ether is used for extracting the fatty acid, the petroleum ether is then removed and the product with the content of nervonic acid of more than 80 wt percent is obtained. The invention has the advantages of low operating temperature, simple technique and high content of nervonic acid.

The invention relates to liquor-fragrance E-cigarette nicotine liquid. The liquor-fragrance E-cigarette nicotine liquid is made by mixing, by weight, 1 to 30% of tobacco extract, 0.5 to 10% of tobacco flavor, 0.5 to 15% of Chinese liquor, 0.5 to 10% of taste fragrance conditioner, 1 to 15% of deionized water, 1 to 25% of edible glycerin and the balance of propylene glycol. The defect that the existing E-cigarette is unable to meet the needs of consumers for taste and fragrance is overcome; the liquor-fragrance E-cigarette nicotine liquid has fragrant aroma, has the tobacco fragrance and the liquor fragrance, has fine and soft taste, has lingering liquor charm and tobacco fragrance, feels good and can substantially meet the needs of consumers.

The invention relates to a preparation method of a health-care product having a function of assisting blood-fat reduction, in particular to a preparation method of a sea-buckthorn perilla seed oil soft capsule having a function of assisting the blood-fat reduction. The sea-buckthorn perilla seed oil soft capsule consists of a capsule casing and contents and is characterized in that the capsule casing consists of, by weight, edible gelatine 40%-45%, glycerol 18%-25% and pure water 35%-40%, and the contents include, by weight, sea-buckthorn seed oil 30%-50% and perilla seed oil 50%-70%. In addition, the preparation method comprises the steps of firstly adopting a supercritical CO2 fluid extraction technology to respectively extract the sea-buckthorn seed oil and the perilla seed oil, evenly mixing the sea-buckthorn seed oil and the perilla seed oil according to formula amount and manufacturing a mixture into soft capsules in a dropping-pill mode, wherein the sea-buckthorn perilla seed oil soft capsule does not contain solvents and other impurities and contains abundant unsaturated fatty acid, vitamin E and various nutritional health-care ingredients. A health-care food functional experiment and a toxicology safety evaluation test prove that the sea-buckthorn perilla seed oil soft capsule has the function of assisting the blood-fat reduction and is suitable for long-term taking of people with high blood fat.

The invention discloses polyvinyl chloride synthetic leather for a luggage. The leather comprises a surface layer, a foaming layer, a bonding layer and fluffing cloth. The surface layer is slurry prepared from the following raw materials in parts by weight: 40-50 parts of SG-3 PVC (Polyvinyl Chloride) resin, 70-80 parts of SG-5 PVC resin, 30-35 parts of glycerol triacetate, 10-15 parts of epoxidized soybean oil, 20-25 parts of glycerol triglycerate, 5-6 parts of PVC color cream, 1-2 parts of bimercapto iso-octyl acetate di-n-octyl tin, 5-10 pats of zinc oxide and 5-10 parts of modified attapulgite. Through improvement of formula and process provided by the invention, the flexibility of the synthetic leather is enhanced, and the synthetic leather has a natural and comfortable handfeel similar to that of natural leather. The synthetic leather is not easy to damage or tear within 3-5 years, and suitable for use in lug gages.

Disclosed are anhydrous antiperspirant and deodorant compositions that comprise from about 0.1% to about 30% by weight of an antiperspirant or deodorant active; from about 0.01% to about 20% by weight of a solid, water-soluble Vitamin B3 material; from about 0.1% to about 40% by weight of a suspending agent; from about 0.1% to about 2.0% by weight of glycerin; and from about 10% to about 99% by weight of an anhydrous carrier liquid other than and in addition to the glycerin. The anhydrous compositions have lower visible residue on the applied areas of the skin even though they also contain relatively high residue solids in the form of solid, water-soluble, Vitamin B3 materials. The compositions also provide for a dry, silky feeling during or after application.

A rosin modified mixed alkylphenol-phenolic resin is prepared from reaction between p-tert-octylphenol, p-nonylphehnol, dodecylphenol and formaldehyde in alkaline condition, modifying by rosin, and esterifying by glycerin and then trihydroxymethyl propane. Its advantages are high soft point, good viscoelasticity, and excellent solubility in fatty hydrocarbon band oil. It can be used for high-speed print color ink.

The embodiment of the invention discloses a method for manufacturing biodiesel, which is characterized in that the method comprises the following steps: filtering food and beverage waste oil by an oil filter; then, heating the waste oil for dewatering; carrying out esterification reaction on the pretreated food and beverage waste oil and methanol or ethanol in the existence of catalysts of basic ionic liquid; carrying out distillation for recovering the rest methanol in the reaction; separating the basic ionic liquid catalysts and the glycerin phase in the reaction lower layer liquid to obtain coarse ester; washing obtained materials by hot water to neutral materials after the coarse ester is washed by saturated sodium chloride solution water; and finally, carrying out heating, stirring and dewatering to obtain finished products of biodiesel. The basic ionic liquid catalysts have the molecular formula as the accompanying drawing.

The invention discloses PET (polyethylene glycol terephthalate) fiber/ceramic fiber composite sound absorbing cotton, which is prepared from the following ingredients in parts by weight: 70 to 80 parts of PET fibers, 40 to 50 parts of ceramic fibers, 10 to 15 parts of emulsifying agents OP-4, 5 to 10 parts of peregal O-15, 80 to 100 parts of PP (propene polymer), 30 to 40 parts of SBR (styrene butadiene rubber), 15 to 20 parts of nanometer bauxite, 10 to 15 parts of modified kieselguhr, 2 to 3 parts of stearic acid, 5 to 8 parts of glycerol triglycerin acid ester, 4 to 6 parts of triphenyl phosphate, 2 to 3 parts of microcrystalline wax, 1 to 2 parts of vinyl (beta-methoxyethoxy) trisilane, 2 to 3 parts of zinc stearate, 1 to 2 parts of lead sulfate tribasic, 0.5 to 1.5 parts of anti-aging agents ODA (octyl decyl adipate) and 1 to 2 parts of antioxidants 168. The sound absorbing cotton prepared by the invention has the advantages that the appearance evenness is good, the thickness is uniform, the hand feeling is soft, the product bonding degree is good, the tensile performance is high, the sound absorbing performance is excellent, the flame retardant effect is good, and the like.

The invention belongs to dosage form technology of functional additives, and particularly relates to a water-dispersible transparent astaxanthin emulsion and a preparation method. The astaxanthin emulsion comprises an oil phase, a water phase and an emulsifier, the oil phase is an astaxanthin solution and comprises astaxanthin and a solvent, mass-volume concentration of the astaxanthin solution is 1-30 mg/mL, the water phase is water or a mixture of glycerin and water, the solvent is edible oil, a volume ratio of the oil phase to the emulsifier is 1:3:3:1, and a volume ratio of the water phase to mixed liquid of the oil phase and the emulsifier is greater than or equal to 1:9. The preparation method includes: preparing the oil phase, preparing the water phase, and preparing the emulsion. The water-dispersible astaxanthin emulsion has high solubility and water dispersity, bioavailability of the water-dispersible astaxanthin emulsion is improved, and various physiological active functions of the water-dispersible astaxanthin emulsion are brought into effective play.

The invention provides a method for preparing high thermal stability microporous polymer electrolyte from imidazole cation intercalation montmorillonite. In the method, firstly, the imidazole cation intercalation montmorillonite is used to prepare high thermal stability montmorillonite; secondly, by the phase transition method, polyvinylidene fluoride, polyethylene glycol and the imidazole cation intercalation montmorillonite are added to the mixed solution of N,N-dimethylformamide and glycerin and violently stirred at a temperature of between 70 and 85 DEG C for 6 to 10 hours, the obtained evenly mixed solution is poured on a clean and preheated glass plate and vacuum dried at a temperature of between 100 and 130 DEG C for 30 t0 40 hours to obtain a polymer membrane with the thickness of between 100 and 300 micrometers; and finally the polymer membrane is soaked in electrolyte in a simple glass box for 24 to 72 hours to obtain the microporous polymer electrolyte. Tests show that the electrical conductivity of the microporous polymer electrolyte prepared by the method reaches 1.6 to 6.15mS/cm, and the residual mass of the dry membrane at a temperature of 400 DEG C(N2) is between 60 and 70 percent.