Method for producing modified lignin, modified lignin, and modified lignin-containing resin composition

Abstract

The present invention provides a method for producing modified lignin from abundant and inexpensive raw materials such as second-generation ethanol fermentation residues and second-generation ethanol saccharification residues, which has improved reactivity with existing plastic materials, and the modified lignin, and further provides a modified lignin-containing resin composition material that can give molded products with improved physical properties such as bending strength. The present invention provides a method for producing modified lignin, which comprises a step of reacting at least one of a second-generation ethanol fermentation residue and a second-generation ethanol saccharification residue with a phenolic compound; 31 The modified lignin and modified lignin-containing resin composition material have a ratio [(2H+G) / S] of 2.5 or more, which is the sum of twice the relative abundance rate H (%) of H-type skeletons and the relative abundance rate G (%) of G-type skeletons to the relative abundance rate S (%) of S-type skeletons, as determined from the integral value measured by P-NMR, and in which the abundance rate of aliphatic hydroxyl groups measured by the same method is less than 20%.

Description

[Technical field]

[0001] The present invention relates to a method for producing modified lignin, a modified lignin, and a modified lignin-containing resin composition. [Background technology]

[0002] From the viewpoint of reducing greenhouse gas emissions, carbon-neutral plant-derived substances are expected to be used as plastic materials. Plant-derived substances mainly include cellulose and hemicellulose derived from sugar, as well as lignin. Of these, lignin has aromatic rings, aliphatic hydroxyl groups, and aromatic hydroxyl groups, and is therefore expected to be useful as a plastic material. However, due to two problems, namely, a simple and economical method for separating and purifying lignin has not been established, and lignin is not only difficult to handle due to its high softening point, but also has poor reactivity with existing plastic materials, and therefore lignin has hardly been used as a plastic material. Therefore, in order to make lignin suitable as a plastic material, appropriate separation and purification are being carried out, modification is being carried out, and a technology for using the modified lignin is being studied.

[0003] In the past, the separation of lignin from biomass residues was done by separating lignin from black liquor, which is a residue from the pulp industry. However, since black liquor contains a lot of impurities such as inorganic salts, it was used for fuel and other products with low industrial value. Recently, as shown in Patent Document 1, efforts have been made to improve the industrial value of black liquor by separating the lignin by modifying it with PEG (polyethylene glycol) or the like. Furthermore, regarding the use of the separated lignin, for example, Patent Document 2 discloses a technology relating to modified lignin in which a benzoxazine skeleton is introduced into lignin to impart reactivity without lowering the molecular weight of the lignin, and a molding material containing the modified lignin to improve the mechanical strength, etc. of the molded product. Furthermore, Patent Document 3 discloses a technique in which lignin is reacted with phenols in the presence of a catalyst to form phenols, which are then heated together with an alkali to form alkalized lignin, and aldehydes are added to the alkalized lignin to form hydroxymethylated lignin, thereby increasing the reactivity of the lignin, and a technique in which the lignin with increased reactivity is used in a binder composition. Furthermore, Patent Document 4 discloses a phenol-modified lignin resin having improved curability and resin strength, which is produced by reacting lignin, phenols, and aldehydes in the presence of an acid. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Special Publication No. 2015-519452 [Patent Document 2] Patent No. 5671430 [Patent Document 3] Special Publication No. 2016-540058 [Patent Document 4] International Publication No. 2015 / 147165 Summary of the Invention [Problem to be solved by the invention]

[0005] When aiming to reduce greenhouse gases as described above by using lignin as a resin material, there is a drawback that the following four conditions must be satisfied: (i) it is inexpensive, (ii) it can be prepared in large quantities, (iii) it can be easily mixed with resin, and (iv) it can easily react with resin. However, sulfite lignin, kraft lignin, and soda lignin obtained from black liquor discharged from the pulp industry, which are currently considered to be lignin raw materials, can satisfy the conditions (i) and (ii). However, since sulfite lignin contains a high sulfur concentration, it is difficult to achieve (iv), and since it is water-soluble, (iii) is not satisfactory. In addition, since kraft lignin and soda lignin have high molecular weights, they cannot achieve (iii) and (iv). Recently, organosolv lignin soluble in organic solvents (PEG lignin in Patent Document 1 is one example) has been reported, which is said to overcome the above drawbacks, but there are problems in solving (i) and (ii).

[0006] In addition to the above-mentioned problem of lignin supply, there are other problems. According to the conventional technology, it is possible to improve the curing reactivity of materials containing lignin to some extent. However, when considering high-quality materials such as metal component replacements, the performance of the formed material, such as bending strength, is insufficient with the conventional technology. Therefore, it is necessary to further improve the reactivity of lignin.

[0007] Therefore, the present invention aims to provide a method for producing modified lignin that has improved reactivity with existing plastic materials from inexpensive raw materials that exist in large quantities, such as biomass residues such as second-generation ethanol fermentation residues and second-generation ethanol saccharification residues, and to provide such modified lignin, as well as a modified lignin-containing resin composition material that can give molded products with improved physical properties, such as bending strength. [Means for solving the problem]

[0008] As a result of intensive research to solve the above problems, the inventors have discovered that the above problems can be solved by treating second-generation ethanol fermentation residues, second-generation ethanol saccharification residues, etc. with phenolic compounds to separate lignin in high yield as modified lignin, while also achieving, in a single reaction, a skeletal ratio conversion of the basic skeleton of lignin, a reduction in aliphatic hydroxyl groups, and a reduction in molecular weight. That is, the present invention is as follows.

[0009] [1] A method for producing modified lignin, comprising a step of reacting one or more of second-generation ethanol fermentation residue and second-generation ethanol saccharification residue with a phenolic compound. [2] 31 the ratio [(2H+G) / S] of the sum of twice the relative abundance H (%) of the H-type skeleton to the relative abundance S (%) of the S-type skeleton determined from the integral value measured by P-NMR and the relative abundance G (%) of the G-type skeleton is 2.5 or more; 31 A modified lignin in which the proportion of aliphatic hydroxyl groups relative to the total proportion of aliphatic hydroxyl groups and aromatic hydroxyl groups, as determined from the integrated value measured by P-NMR, is less than 20%. [3] A modified lignin-containing resin composition material containing a modified lignin produced by the modified lignin production method or the modified lignin. Effect of the Invention

[0010] According to the present invention, a method for producing modified lignin in high yield from inexpensive raw materials such as second-generation ethanol fermentation residues and second-generation ethanol saccharification residues, which are biomass residues, can be provided. Furthermore, the resulting modified lignin has improved reactivity with existing plastic materials and can be easily mixed and reacted with existing resins, so that a modified lignin-containing resin composition material can be provided that can give molded products with improved physical properties such as bending strength. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0011] <Production method of modified lignin and modified lignin> The method for producing modified lignin of the present invention includes a step of reacting one or more of a second-generation ethanol fermentation residue and a second-generation ethanol saccharification residue with a phenolic compound. The second-generation ethanol fermentation residue and the second-generation ethanol saccharification residue contain lignin, and the lignin, the modified lignin of the present invention, the second-generation ethanol fermentation residue, the second-generation ethanol saccharification residue, and the phenolic compound, as well as the reaction step, are described below.

[0012] [Lignin] Lignin is a polymer compound formed by polymerization of three types of lignin monomers, which are p-hydroxycinnamic alcohols, and has a basic skeleton represented by the following formula (2).

[0013] [ka]

[0014] In the above formula (2), the substituent R 3 and R 4 R represents a hydrogen atom or a methoxy group. 3 and R 4 When both are hydrogen atoms, it is a p-hydroxyphenyl nucleus (H-type skeleton), and R 3 and R 4 When either one of the above is a hydrogen atom, the guaiacyl nucleus (G-type skeleton) is formed, and R 3 and R 4 When neither of these is a hydrogen atom, it is called a syringyl nucleus (S-type skeleton). In the above formula (2), X represents a carbon element, and Y represents a bond to a hydrogen or carbon atom.

[0015] In the basic structure of lignin, R 3 and R 4 The carbon atom bonded to R is a highly reactive site (hereinafter, simply referred to as the "reactive site"). 3 and R 4 If R is a methoxy group, the reactivity of that carbon atom is poor. Therefore, in order to react with lignin, R 3 and R 4must be a hydrogen atom. Furthermore, lignin contains not only the aromatic moieties mentioned above but also aliphatic moieties, and since the hydroxyl groups present in the aliphatic moieties have poor oxidation stability (they change to aldehydes or carboxylic acids upon oxidation), the fewer the number of hydroxyl groups, the better the reactivity with existing plastic materials. Furthermore, by lowering the molecular weight without significantly lowering the softening point, the mixability is improved, and the reactivity with existing plastic materials is improved. In other words, lignin has few aliphatic hydroxyl groups and is rich in two types of skeletons, H-type and G-type, which are highly reactive, and more preferably, if it can be made low in molecular weight without significantly lowering the softening point, it will be highly reactive and suitable as a plastic material.

[0016] However, the abundance of each of the above basic skeletons and the aliphatic hydroxyl groups vary depending on the type of plant from which the lignin is made. In addition, natural lignin is originally a gigantic molecule whose molecular weight cannot be measured, and existing separation methods have the disadvantage that reducing the molecular weight also significantly reduces the softening point. For example, in woody biomass, the lignin derived from broadleaf trees contains the above G-type and S-type skeletons, while the lignin derived from coniferous trees contains the above G-type and S-type skeletons, but the G-type skeleton is more prevalent. Furthermore, the lignin derived from broadleaf trees and coniferous trees contains almost no H-type skeletons. In addition, in lignin derived from herbaceous biomass, the above-mentioned H-type skeleton, G-type skeleton and S-type skeleton are present, but the occurrence rate of the H-type skeleton is low. In addition, coniferous lignin has many aliphatic hydroxyl groups, while broadleaf lignin and herbaceous lignin have fewer aliphatic hydroxyl groups. Therefore, in order to increase the reactivity of lignin, it is necessary to increase the proportion of H-type and G-type skeletons, reduce the aliphatic hydroxyl groups, and modify lignin using a low-molecular-weight method that does not significantly lower the softening point.

[0017] [Modified lignin] The modified lignin of the present invention is 31The ratio of the sum of the relative abundance rate H (%) of the H-type skeleton to the relative abundance rate S (%) of the S-type skeleton determined from the integral value measured by P-NMR and the relative abundance rate G (%) of the G-type skeleton [(2H+G) / S] is 2.5 or more, and 31 The percentage of aliphatic hydroxyl groups relative to the total percentage of aliphatic hydroxyl groups and aromatic hydroxyl groups, as determined from the integrated value measured by P-NMR, is less than 20%. In addition, as an embodiment of the modified lignin of the present invention, it is preferable that the number average molecular weight is further reduced to less than 1,000 and the softening point is 90°C or higher.

[0018] <Ratio of the abundance of reactive sites (H-type skeleton × 2 + G-type skeleton) to non-reactive sites (S-type skeleton) [(2H+G) / S] and the abundance of aliphatic hydroxyl groups> The lignin in the second-generation ethanol fermentation residue and the second-generation ethanol saccharification residue is converted into the above R by a substitution reaction described later in the production method of the present invention. 3 and R 4 becomes a hydrogen atom, which increases the reaction points of the modified lignin and reduces the aliphatic hydroxyl groups, thereby enabling the molecular weight to be reduced without significantly lowering the softening point. As mentioned above, H type has two reactive sites and G type has one, and as the above ratio [(2H+G) / S] shows, the modified lignin of the present invention has many reactive sites and has good reactivity. However, in the case of lignin derived from coniferous trees such as cedar, it has been analytically proven that the above ratio [(2H+G) / S] is 3 or more before modification, but aliphatic hydroxyl groups account for 20% or more of the total hydroxyl groups (the sum of the abundance of aliphatic hydroxyl groups and aromatic hydroxyl groups), which is undesirable for use as a plastic material. Therefore, if the above ratio is less than 2.5 or the amount of aliphatic hydroxyl groups is 20% or more, the reactivity as a modified lignin is insufficient, making it unsuitable as a plastic material, and it cannot be expected to give molded products with improved physical properties such as bending strength.

[0019] In contrast, the modified lignin of the present invention has a ratio of the abundance ratios [(2H+G) / S] of 2.5 or more, and the abundance ratio of aliphatic hydroxyl groups relative to the total abundance ratios of aliphatic hydroxyl groups and aromatic hydroxyl groups is less than 20%. In addition, from the viewpoint of further improving the reactivity of the modified lignin and expecting to give a molded product with improved physical properties such as bending strength, the ratio [(2H+G) / S] is preferably 2.8 or more, more preferably 3.0 or more, even more preferably 4.0 or more, even more preferably 5.0 or more, even more preferably 6.0 or more, and even more preferably 7.0 or more. In addition, from the same viewpoint, the abundance ratio of aliphatic hydroxyl groups is preferably less than 15%, more preferably less than 12%, and even more preferably less than 10%.

[0020] The relative abundance of S-type skeleton, H-type skeleton, and G-type skeleton and the amount of aliphatic hydroxyl groups are as follows: 31 This is a value calculated from the integral value measured by P-NMR. 31 More details about the P-NMR measurement are as described in MAGNETIC RESONANCE IN CHEMISTRY, VOL. 33, 375-382 (1995). In the present invention, more specifically, the measurement can be performed by the method described in the examples below.

[0021] <Lower molecular weight and softening point> The modified lignin of the present invention can be obtained by the substitution reaction described below. 3 and R 4 In this way, the molecular chain of lignin is modified, and the molecular weight is reduced. By reducing the molecular weight of lignin, it is possible to extract modified lignin with high efficiency, and at the same time, it is expected to improve the mixability (kneadability or stirrability) with other plastic materials and provide molded products with improved physical properties such as bending strength. In addition, since the modified lignin of the present invention always has a phenol compound inserted at the substitution site, the softening point does not decrease significantly even if the molecular weight is reduced. Therefore, the modified lignin of the present invention can have a softening point of preferably 90°C or higher, more preferably 130°C or higher, and even more preferably 160°C or higher. If the softening point is 90°C or higher, defects such as swelling are unlikely to occur during molding and post-curing of the resin composition material containing the modified lignin. In addition, the softening point of the modified lignin is preferably 200°C or lower, more preferably 190°C or lower, even more preferably 180°C or lower, and even more preferably 170°C or lower. If the softening point is 200°C or lower, the resin composition material containing the modified lignin becomes easier to handle. Furthermore, in the modified lignin of the present invention, for example, when the number average molecular weight is 800 or more and 1,200 or less, the weight average molecular weight is preferably 2,100 or more and 2,700 or less; when the number average molecular weight is 600 or more and less than 800, the weight average molecular weight is preferably 1,200 or more and less than 2,100; and when the number average molecular weight is 400 or more and less than 600, the weight average molecular weight is preferably 700 or more and less than 1,200.

[0022] The modified lignin of the present invention has, for example, a molecular weight distribution (Mw / Mn) of usually about 1.2 to 3.2, preferably 1.3 to 2.7, more preferably 1.5 to 2.6, even more preferably 1.5 to 2.5, and even more preferably 1.5 to 2.3.

[0023] Furthermore, the modified lignin of the present invention preferably has a softening point of 140°C or higher and 200°C or lower if the number average molecular weight is 800 or higher and 1,200 or lower; preferably has a softening point of 120°C or higher and 190°C or lower if the number average molecular weight is 600 or higher and less than 800; preferably has a softening point of 100°C or higher and 170°C or lower if the number average molecular weight is 400 or higher and less than 600; and preferably has a softening point of 90°C or higher and 170°C or lower if the number average molecular weight is 300 or higher and less than 400.

[0024] In addition, the modified lignin of the present invention preferably has a softening point of 140 ° C. or more and 200 ° C. or less if the number average molecular weight is 800 or more and 1,200 or less and the weight average molecular weight is 2,100 or more and 2,700 or less, and preferably has a softening point of 120 ° C. or more and 190 ° C. or less if the number average molecular weight is 600 or more and less than 800 and the weight average molecular weight is 1,200 or more and less than 2,100, and preferably has a softening point of 100 ° C. or more and 170 ° C. or less if the number average molecular weight is 400 or more and less than 600 and the weight average molecular weight is 700 or more and less than 1,200, and preferably has a softening point of 90 ° C. or more and 170 ° C. or less if the number average molecular weight is 300 or more and less than 400 and the weight average molecular weight is 600 or more and less than 700. These can be used depending on the properties of the existing plastic material to be reacted, and it is expected that the reactivity of the modified lignin can be improved by improving the mixability, and a molded product with improved physical properties such as bending strength can be obtained. The number average molecular weight and weight average molecular weight can be measured by the method described in the Examples section below.

[0025] Furthermore, since the modified lignin of the present invention necessarily has a phenolic compound inserted at the substitution site as described above, the method for producing modified lignin of the present invention makes it possible to increase the amount (mass) of modified lignin obtained relative to the amount (mass) of lignin in one or more of second-generation ethanol fermentation residue and second-generation ethanol saccharification residue. Note that the amount (mass) of lignin in one or more of second-generation ethanol fermentation residue and second-generation ethanol saccharification residue refers to the total amount of lignin in one or more of second-generation ethanol fermentation residue and second-generation ethanol saccharification residue.

[0026] (Degree of modification) The method for producing modified lignin of the present invention makes it possible to obtain modified lignin that has more H-type and G-type skeletons than the basic skeleton of lignin contained in second-generation ethanol fermentation residue and second-generation ethanol saccharification residue, and at the same time, has fewer aliphatic hydroxyl groups and more reactive sites. Furthermore, the molecular weight of the obtained modified lignin is reduced, improving the mixability. Specifically, the modified lignin produced by the method of the present invention has the following characteristics: 31 The total amount of reaction sites [2H+G] based on the relative abundance H (%) of H-type skeletons and the relative abundance H (%) of G-type skeletons determined from the integral values ​​measured by P-NMR can be increased, and the abundance of aliphatic hydroxyl groups can be reduced. The increase in [2H+G] is preferably 4% or more. Furthermore, by the method for producing modified lignin of the present invention, it is preferable that 50 mass% or more of the lignin content contained in the second-generation ethanol fermentation residue or the second-generation ethanol saccharification residue is extracted as modified lignin, more preferably 70 mass% or more, and even more preferably 90 mass% or more. A method for calculating the lignin content in the second-generation ethanol fermentation residue or the second-generation ethanol saccharification residue will be specifically explained in the Examples described later.

[0027] [Second-generation ethanol fermentation residue and second-generation ethanol saccharification residue] The second-generation ethanol fermentation residue used as a raw material in the method for producing modified lignin of the present invention is derived from plant biomass such as herbaceous biomass and contains lignin. Second-generation ethanol fermentation residues and second-generation ethanol saccharification residues are residues obtained by removing cellulose and hemicellulose from woody and herbaceous plants, which are non-edible plant biomass containing lignin, through saccharification or saccharification / fermentation. Examples of non-edible plant biomass include woody biomass and herbaceous biomass. Woody biomass includes coniferous and broadleaf trees such as cedar, cypress, Japanese cypress, cherry blossom, eucalyptus, beech, and bamboo. Examples of herbaceous biomass include palm trunks and empty bunches, palm fruit fiber and seeds, bagasse (sugar cane and high-biomass sugar cane residue), cane tops (sugar cane tops and leaves), energy cane, rice straw, wheat straw, corn cobs, stems and leaves, and residues (corn stover, corn cobs, corn hulls), sorghum residues (including sweet sorghum), jatropha seed husks and shells, cashew husks, switchgrass, erianthus, high-biomass yield crops, and energy crops. Among these, from the viewpoints of availability and compatibility with the production method applied in the present invention, herbaceous biomass is preferred, with empty palm bunches, wheat straw, corn cobs, stems and leaves, residues (corn stover, corn cob, corn hull), bagasse, cane tops, energy cane, and residues thereof after useful component extraction being more preferred, with corn cobs, stems and leaves, residues (corn stover, corn cob, corn hull), bagasse, cane tops, and energy cane being even more preferred. The above useful components include, for example, hemicellulose, carbohydrates, minerals, moisture, etc. Bagasse contains about 5 to 30 mass % of lignin, and the lignin in bagasse contains all of the H, G and S nuclei as basic skeletons. The plant biomass may be in the form of a pulverized material, or may be in the form of a block, chip, powder, or a water-containing material.

[0028] Bagasse, corn stover, etc. are treated with organosolv method, pressurized hot water method, steam explosion method, ammonia treatment method, ammonia explosion method, acid treatment method, alkali treatment method, oxidative decomposition method, thermal decomposition, microwave heating method, etc., preferably acid treatment, ammonia explosion, steam explosion, etc., to separate hemicellulose into the solution side, and then cellulose is separated into the solution side as glucose by enzymes, or hemicellulose is not separated and saccharified together with cellulose and separated into the solution side, and the remaining solid is the second generation ethanol saccharification residue. Alternatively, sugars are not separated, but are separated into the solution side as ethanol by fermentation, and the remaining solid is the second generation ethanol fermentation residue. The second generation ethanol saccharification residue is mainly composed of lignin and contains decomposed organic matter, catalysts, enzymes, ash, cellulose, etc. The second generation ethanol fermentation residue is mainly composed of lignin and contains decomposed organic matter, catalysts, enzymes, yeast, ash, cellulose, etc.

[0029] It is not impossible to extract lignin directly from the second-generation ethanol fermentation residue or the second-generation ethanol saccharification residue because they contain low-molecular-weight lignin in part. However, the production method of the present invention reduces the molecular weight and makes it possible to obtain lignin in high yields. A more specific embodiment of the production method of the present invention will be described in the Examples below, but for example, it is as follows. Using one or more of the second generation ethanol fermentation residue and the second generation ethanol saccharification residue as the raw material, first adjust the pH of the raw material in a water-containing state to acidic. Add a phenolic compound to the raw material in an amount equal to or greater than the amount of lignin contained in the raw material by weight. Heat the mixture and remove the water while it is hot (phenolic compounds have a high boiling point, and water can be removed by providing an appropriate oil-water separator such as Dean-Stark). After removing the water, continue heating for 1 to 2 hours. The heated liquid contains insoluble matter and is filtered while it is hot using 5C filter paper. The filtered solid is unreacted matter and inorganic impurities. The filtrate is distilled under reduced pressure to remove unreacted phenolic compounds. Phenol compounds that cannot be completely removed by distillation are dissolved in acetone as necessary and are removed by repeatedly re-precipitating with water, which is a poor solvent. The separated solid is modified lignin that has already been modified. If the phenolic compounds remaining during distillation do not cause problems in subsequent reactions, they can be used as they are.

[0030] [Phenol compounds] The phenolic compound that reacts with lignin (hereinafter may be simply referred to as "lignin") in one or more of the second-generation ethanol fermentation residue and the second-generation ethanol saccharification residue is preferably a phenolic compound (hereinafter may be simply referred to as "phenolic compound") in which at least one of the 2-, 4-, and 6-positions, which are the positions of the substituents relative to the hydroxyl group, is a hydrogen atom. The phenolic compound having hydrogen atoms at the 2-, 4-, and 6-positions (i.e., ortho- and para-positions) is particularly suitable as a receptacle for a substituent in a substitution reaction due to its orientation. By mixing the lignin with the phenolic compound, the R 3 and R 4 This is because the substituent of R of the lignin is transferred to the 2-position, 4-position, or 6-position of the phenol compound. 3 or R 4 Alternatively, both may be hydrogen atoms, resulting in a modified lignin with an increased number of the aforementioned reaction sites. Therefore, the substitution reaction reduces the S-type skeleton in the lignin and increases the G-type and H-type skeletons, improving the reactivity. As described above, the substitution reaction also modifies the molecular chain of the lignin, resulting in a decrease in molecular weight, which leads to a high yield and improved mixability of the modified lignin. The phenol compounds may be used alone or in combination of two or more.

[0031] The phenol compound is preferably a compound represented by the following formula (1): By using the phenol compound, the substitution reaction can proceed smoothly since there are at least three positions for accepting the above-mentioned substituents.

[0032] [ka]

[0033] In the above formula (1), R 1 and R 2 each independently represents a hydrogen atom, a hydroxyl group, or an alkyl group having 1 to 15 carbon atoms; R 1 and R 2 may be the same or different. The alkyl group having 1 to 15 carbon atoms may be linear or branched. It is preferably a linear or branched alkyl group having 1 to 15 carbon atoms, more preferably a linear or branched alkyl group having 1 to 5 carbon atoms, and further preferably a linear alkyl group having 1 to 3 carbon atoms.

[0034] Examples of the phenol compound represented by the above formula (1) include 3-alkylphenols such as phenol, resorcinol, phloroglucinol, meta-cresol, 3-ethylphenol, and 3-propylphenol; 5-alkylresorcinols such as 5-methylresorcinol, 5-ethylresorcinol, and 5-propylresorcinol; and 3,5-dialkylphenols such as 3,5-dimethylphenol, 3-methyl-5-ethyl-phenol, and 3,5-diethylphenol.

[0035] In addition, since the phenolic compound has multiple hydroxyl groups, the acidity of the compound increases, and it is expected that the reaction will proceed without the need for a catalyst. 1 and R 2 It is more preferable that at least one of the above groups is a hydroxyl group. Specific examples of such phenolic compounds include resorcinol, phloroglucinol, and 5-alkylresorcinols (5-methylresorcinol, 5-ethylresorcinol, etc.).

[0036] [Reaction process] <Mass ratio [phenolic compounds / lignin]> In the production method of the present invention, the mass ratio of the phenolic compounds to the lignin in one or more of the second-generation ethanol fermentation residue and the second-generation ethanol saccharification residue [phenolic compounds / lignin] is usually about 0.1 to 15, preferably 0.3 to 15, more preferably 0.5 to 15, even more preferably 1 to 15, even more preferably 1 to 13, even more preferably 1 to 12, even more preferably 1 to 10, even more preferably 1 to 6, and even more preferably 1 to 5. When the mass ratio of the phenolic compounds to the lignin is within the above range, the substitution reaction described above can proceed well.

[0037] <Acid catalyst> In the production method of the present invention, the reaction between lignin in one or more of the second-generation ethanol fermentation residue and the second-generation ethanol saccharification residue and phenolic compounds is preferably carried out without a catalyst or in the presence of an acid catalyst, preferably in an amount of more than 0 to 3.0 mass%, and even more preferably 0.2 to 3.0 mass%, based on the total amount of the lignin and the phenolic compounds. As described above, the reaction can proceed without a catalyst depending on the phenol compound used in the reaction. By proceeding without a catalyst, for example, it is possible to omit post-treatment (purification process) after the reaction process, and it is expected that the physical properties such as bending strength of molded products using the obtained modified lignin as a plastic material will be improved.

[0038] Examples of the acid catalyst include inorganic acids such as phosphoric acid, phosphoric acid esters, hydrochloric acid, sulfuric acid, and sulfuric acid esters, and organic acids such as acetic acid, formic acid, oxalic acid, and p-toluenesulfonic acid. One or more types of acid catalysts may be used in combination. When an acid catalyst is used in the above reaction, the amount of the acid catalyst used relative to the total amount of lignin and phenolic compounds contained in the biomass residue is usually not particularly limited as long as it is more than 0, but the effect of adding the acid catalyst can be exhibited well, and the reaction is usually carried out in the presence of 0.01 to 3.0 mass% of the acid catalyst from the viewpoint of impurities remaining in the modified lignin, preferably 0.1 to 3.0 mass%, more preferably 0.2 to 3.0 mass%, and even more preferably 0.4 to 2.6 mass%. If the amount of the acid catalyst used is within the above range, the above-mentioned substitution reaction can be smoothly progressed.

[0039] <Reaction temperature and time> The reaction temperature is not particularly limited as long as it is usually 100° C. or higher, but is usually about 140° C. or higher and 350° C. or lower, preferably 140° C. or higher and 300° C. or lower, more preferably 140° C. or higher and 270° C. or lower, even more preferably 140° C. or higher and 250° C. or lower, even more preferably 150 to 230° C., and even more preferably 150 to 200° C. If it is above 140° C., most of the phenol compounds can be dissolved to allow the reaction to proceed, and if it is 300° C. or lower, the proceeding of the reverse reaction can be prevented. The reaction time is usually about 0.1 to 15 hours, but from the viewpoint of allowing the reaction to proceed sufficiently and modifying the lignin, it is preferably 0.5 hours or more, and more preferably 1 hour or more. Also, from the viewpoint that the reaction cannot be expected to proceed if the reaction time is too long, the upper limit is preferably 10 hours or less, and more preferably 2 to 8 hours.

[0040] <solvent> The reaction of one or more of the second-generation ethanol fermentation residue and the second-generation ethanol saccharification residue with the phenolic compound can be carried out without a solvent. In addition, one or more of organic solvents such as alcohols such as methanol, ethanol, and isopropyl alcohol, ketones such as acetone and methyl ethyl ketone, ethers such as tetrahydrofuran, and aromatics, and water may be used, and it is preferable to use one or more of ethanol, acetone, and water. From the viewpoint of preventing the solvent from being mixed into the modified lignin and of making it efficient without requiring a step of removing the solvent after the reaction, it is preferable to carry out the reaction without a solvent.

[0041] [Refining process] The modified lignin of the present invention is produced by carrying out the above-mentioned reaction process. Therefore, the modified lignin-containing material obtained by the reaction process can be used as it is as a plastic material, but a purification process may be carried out after the reaction process. <Solid-liquid separation> After the above reaction, the modified lignin is dissolved in the phenol compound, but unreacted substances and inorganic residues are present in the liquid as solids. These are preferably removed by filtration (hot). For example, the reaction liquid is placed in a pressurized hot filter equipped with filter paper such as No. 5C or No. 2, and pressure-filtered at about 20 to 150°C, about 40 to 90°C, usually about 60 to 90°C, and about 0.1 to 0.99 MPa, usually about 0.1 to 0.4 MPa. The filtered solid may be appropriately diluted and / or washed with a phenol compound and filtered. In the filtration, the modified lignin is contained in the filtrate. In addition, for example, the reaction product liquid may be diluted and / or washed with any one or more of low-boiling point general-purpose hydrophilic solvents such as water, ketones such as acetone and methyl ethyl ketone, alcohols such as methanol, ethanol, and isopropyl alcohol, and ethers such as tetrahydrofuran, and separated into solid and liquid. In the solid-liquid separation, the modified lignin is contained in the solution. The method for performing solid-liquid separation is not particularly limited, but examples thereof include filtration, a filter press, centrifugation, and a dehydrator. <distillation> The distillation can be carried out, for example, by distilling the solution containing the modified lignin under reduced pressure at a temperature of about 40 to 200°C, usually about 80 to 150°C, and a reduced pressure of about 3 to 20 kPa, usually about 5 to 10 kPa, to remove the phenolic compounds. In this distillation, the modified lignin is obtained as a solid. In addition, for example, when a dilution solvent other than the phenolic compounds is used, the solvent other than the phenolic compounds is distilled under reduced pressure at an appropriate temperature taking into account the boiling point of the solvent to remove the low-boiling point general-purpose hydrophilic solvent, and then the phenolic compounds are removed by the same method as above. In this distillation, the modified lignin is obtained as a solid. <Drying under reduced pressure> The modified lignin obtained by distillation may be purified by removing the phenolic compounds after the reaction by heating it to typically 50 to 200° C. and vacuum drying it in a solid or molten state. Alternatively, the modified lignin in a heated and fluid state after distillation may be similarly vacuum dried as it is to remove the phenolic compounds after the reaction. <Reprecipitation> If phenolic compounds remain in the modified lignin obtained by distillation or drying under reduced pressure, the modified lignin obtained by the above distillation may be further purified by dissolving the modified lignin in a solvent such as acetone and adding ion-exchanged water, which is a poor solvent for the modified lignin, to cause reprecipitation and remove the phenolic compounds after the reaction. In the purification step, the above-mentioned filtration, distillation, evaporation to dryness under reduced pressure, and reprecipitation may be repeated, or any one or two or more of them may be combined. The amount of phenol compounds remaining in the modified lignin is not particularly limited, but is usually less than 30%, preferably less than 10%, more preferably less than 5%, and even more preferably less than 1%.

[0042] <Modified lignin-containing resin composition materials and molded products> The present invention also provides a modified lignin-containing material, particularly a modified lignin-containing resin composition material, containing the modified lignin or the modified lignin produced by the above-mentioned production method, and a molded product using the same. In addition to the modified lignin obtained by the above-mentioned production method, resin components such as thermosetting resins and thermoplastic resins may be included. The components other than the modified lignin are described below. (thermosetting resin) The modified lignin-containing resin composition may further contain a thermosetting resin. Examples of the thermosetting resin include other general thermosetting resins such as phenolic resins, epoxy resins, polyurethane resins, melamine resins, urea resins, unsaturated polyester resins, silicone resins, and alkyd resins. Among these, phenolic resins are preferred because, like modified lignin, they have phenolic hydroxyl groups, can react with modified lignin, and can be used as a diluent for modified lignin. Among phenolic resins, novolac-based phenolic resins and resol-based phenolic resins are more preferred. These thermosetting resins may be used alone or in combination of two or more.

[0043] The content of the thermosetting resin in the modified lignin-containing resin material may be determined according to the purpose, but from the viewpoint of obtaining good physical properties and moldability, it is preferably 100 to 300 parts by mass, more preferably 150 to 250 parts by mass, per 100 parts by mass of the modified lignin.

[0044] (Aldehydes) The modified lignin-containing molding material may further contain aldehydes. A self-curing molding material can be produced by using a modified lignin-containing resin composition material that contains modified lignin and aldehydes. Examples of aldehydes include formaldehyde, paraformaldehyde, acetaldehyde, propionaldehyde, furfural, benzaldehyde, phenylacetaldehyde, salicylaldehyde, and the like, and among these, formaldehyde is preferred.

[0045] The molar ratio of the phenol group to formaldehyde contained in the modified lignin [formaldehyde / phenol group] is preferably 1.0 to 2.5, more preferably 1.2 to 2.0. If the molar ratio is within the above range, there is no risk of a decrease in the curing rate during the reaction. In order to accelerate the hardening reaction between the modified lignin and aldehydes, it is preferable to use an alkali, such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, ammonia, tetramethylammonium hydroxide, or an alkylamine. There are no limitations on the temperature and reaction time during the curing reaction of the modified lignin and the aldehydes, but it is usually about 60 to 130° C., and the reaction time is usually about 0.5 to 5 hours. The modified lignin-containing resin composition may further contain one or more selected from the group consisting of thermosetting resins and aldehydes.

[0046] (Filler) The modified lignin-containing resin composition may further contain a filler, which may be an inorganic filler or an organic filler. Examples of inorganic fillers include spherical or crushed fused silica, silica powder such as crystalline silica, alumina powder, glass powder, glass fiber, glass flake, mica, talc, calcium carbonate, alumina, hydrated alumina, boron nitride, aluminum nitride, silicon nitride, silicon carbide, titanium nitride, zinc oxide, tungsten carbide, magnesium oxide, and the like. Examples of organic fillers include carbon fiber, aramid fiber, paper powder, wood powder, cellulose fiber, cellulose powder, rice husk powder, fruit shell / nut powder, chitin powder, and starch.

[0047] The inorganic filler and the organic filler may be used alone or in combination of two or more, and the content is determined according to the purpose. When the inorganic filler and / or the organic filler are contained, it is desirable that the content of the inorganic filler and / or the organic filler is appropriate in order to obtain good physical properties and moldability. From this viewpoint, the content of the inorganic filler and / or the organic filler is preferably 50 to 200 parts by mass, more preferably 80 to 150 parts by mass, based on 100 parts by mass of the modified lignin.

[0048] (hardening agent) The modified lignin-containing resin composition may further contain a curing agent. Examples of the curing agent include hexamethylenetetramine, hexaformaldehyde, paraformaldehyde, etc. These may be used alone or in combination of two or more kinds. In addition to the curing agent, in order to further increase the curing speed and degree of curing, inorganic bases such as calcium hydroxide, sodium hydroxide, potassium hydroxide, calcium oxide, and magnesium oxide, Lewis acids such as zinc chloride and zinc acetate, and catalysts such as triethylamine may be used. These may be used alone or in combination of two or more.

[0049] (Other additives) Various additives can be added to the resin composition material according to the present embodiment within the range that does not impair the properties of the molded product obtained from the resin composition material. In addition, a compatibilizer, a surfactant, etc. can be further added depending on the purpose. As the compatibilizer, a resin obtained by adding maleic anhydride or epoxy to a thermoplastic resin to introduce a polar group, such as a maleic anhydride-modified polyethylene resin or a maleic anhydride-modified polypropylene resin, or various commercially available compatibilizers may be used in combination. Examples of surfactants include, but are not limited to, straight-chain fatty acids such as stearic acid, palmitic acid, and oleic acid, and branched or cyclic fatty acids with rosins. In addition to the above, other additives that can be added include flexibilizers, heat stabilizers, ultraviolet absorbers, flame retardants, antistatic agents, antifoaming agents, thixotropic agents, release agents, antioxidants, plasticizers, stress reducing agents, coupling agents, dyes, light scattering agents, small amounts of thermoplastic resins, etc. These may be used alone or in combination of two or more.

[0050] (thermoplastic resin) The thermoplastic resin that can be blended in the modified lignin-containing resin composition is preferably an amorphous thermoplastic resin having a glass transition temperature of 200°C or less, or a crystalline thermoplastic resin having a melting point of 200°C or less. Examples of thermoplastic resins include polycarbonate resins, styrene resins, polystyrene elastomers, polyethylene resins, polypropylene resins, polyacrylic resins (polymethyl methacrylate resin, etc.), polyvinyl chloride resins, cellulose acetate resins, polyamide resins, low-melting-point polyester resins (PET, PBT, etc.) typified by polyesters formed from combinations of terephthalic acid and ethylene glycol, and terephthalic acid and 1,4-butanediol, polylactic acid and / or copolymers containing polylactic acid, acrylonitrile-butadiene-styrene resins (ABS resins), polyphenylene oxide resins (PPO), polyketone resins, polysulfone resins, polyphenylene sulfide resins (PPS), fluororesins, silicone resins, polyimide resins, polybenzimidazole resins, polyamide elastomers, and copolymers of these with other monomers.

[0051] When using modified lignin as an additive for a thermoplastic resin, for example, a conventionally known method such as those described in JP 2014-15579 A, ​​WO 2016 / 104634 A, etc. can be used. From the viewpoint of obtaining remarkable fluidity and strength, the content of the thermoplastic resin in the modified lignin resin composition material is preferably 30% by mass or more and 99.9% by mass or less, more preferably 40% by mass or more and 99.9% by mass or less, even more preferably 45% by mass or more and 99.9% by mass or less, and particularly preferably 50% by mass or more and 99.9% by mass or less, based on the total amount of the resin composition material. The modified lignin-containing resin composition material may contain, in addition to the above-mentioned cellulose-containing solid matter and thermoplastic resin, a resin compatible with the thermoplastic resin composition material, an additive, and a filler.

[0052] (Mixing and molding) The blending and kneading of each component used in the modified lignin-containing resin composition material can be carried out by premixing using commonly used equipment such as a ribbon blender, drum tumbler, etc., and then using a Henschel mixer, Banbury mixer, single screw extruder, twin screw extruder, multi-screw extruder, roll kneader, co-kneader, etc. The heating temperature during kneading is usually appropriately selected in the range of 100 to 300 ° C. The method for molding the modified lignin-containing resin composition is not particularly limited. For example, press molding, injection molding, transfer molding, medium-sized molding, FRP molding, etc. can be mentioned. In addition, when the resin composition is a thermoplastic resin composition, the method for molding into a predetermined shape can be extrusion molding, injection molding, etc.

[0053] Examples of molded products using modified lignin-containing resin compositions include those obtained by curing a resin composition material obtained by blending modified lignin with a curing agent, those obtained by further blending various fillers or industrially obtained general phenolic resins as necessary, molding into a predetermined shape, and then curing, or those obtained by molding after curing, and those obtained by molding a resin composition material obtained by mixing modified lignin with a thermoplastic resin, etc. Examples of molded products using such modified lignin-containing resin compositions include, for example, insulation materials for housing, electronic parts, resins for frac sand, resins for coated sand, resins for impregnation, resins for lamination, resins for FRP molding, automobile parts, reinforcing materials for automobile tires, office automation equipment, machinery, information and communication equipment, industrial materials, etc.

[0054] Modified lignin can be used for modified lignin-containing materials other than resin composition materials. Examples of modified lignin-containing materials other than modified lignin-containing resin composition materials include carbon materials such as carbon black and carbon fiber, lubricants such as grease base materials, foods and cosmetics with antioxidant and antibacterial properties, cement additives, concrete additives, binders, rubber compositions, packaging materials such as gas barrier films, agricultural materials such as plant activators and soil conditioners, inks and toners, adhesives, surfactants, ultraviolet absorbers, storage battery electrode materials, growth promoters for marine organisms, and food discoloration inhibitors. EXAMPLES

[0055] The present invention will be specifically described below with reference to examples and comparative examples, but the present invention is not limited to these.

[0056] <Calculation of lignin content in second-generation ethanol fermentation residue and second-generation ethanol saccharification residue (raw material)> The lignin content of the biomass residue used in the examples was calculated by analyzing the constituent sugars after pretreatment as described below. The same applies when using second-generation ethanol saccharification residue as a raw material. [Preprocessing] As a pretreatment, the raw material samples were pulverized using a Willey mill and dried at 105°C. [Constituent sugar analysis] An appropriate amount of the above raw material sample was weighed out, 72% by mass sulfuric acid was added, and the mixture was left at 30°C for 1 hour while stirring from time to time. The reaction liquid was transferred completely to a pressure bottle while being mixed with pure water, and treated in an autoclave at 120°C for 1 hour, after which the filtrate and the residue were separated by filtration. The monosaccharides in the filtrate were quantified by high performance liquid chromatography. C6 polysaccharides (mainly glucan) were defined as cellulose, and C5 polysaccharides (mainly xylan) were defined as hemicellulose. [Lignin] The residue obtained by filtration during the sugar content analysis was dried at 105°C and weighed to calculate the decomposition residue rate. Furthermore, the lignin content was calculated by correcting for the ash content.

[0057] <Properties of modified lignin and raw lignin> In addition, the modified lignin or raw lignin obtained in each example was subjected to various measurements by the following methods. [Molecular weight measurement] The number average molecular weight (Mn), weight average molecular weight (Mw), and molecular weight distribution (Mw / Mn) of the modified lignin and the raw lignin obtained in each example were determined in terms of standard polystyrene by GPC (gel permeation chromatography). The measuring device and conditions are as follows. Separation column: 2 columns of TSKgel SuperMultiporeHZ-M manufactured by Tosoh Corporation Eluent: Tetrahydrofuran ·Eluent flow rate: 1.0mL / min Detector: Index of Refraction (RI) ·Measurement temperature: 40℃

[0058] [Relative abundance of basic structure (%) and hydroxyl group ratio (%)] (1) A mixture of deuterated chloroform, pyridine, and cyclohexanol (internal standard) was added to the modified lignin or raw lignin obtained in each example, and 2-chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane was added as a derivatization reagent, followed by heating at 50°C for 1 hour. 31 P-NMR measurements were carried out. Pulse width: 30° Repeat time: 2 seconds Measurement range: -60~200ppm -Number of times: 200 The signal derived from cyclohexanol, the internal standard, was set at 145.2 ppm, 144.0 to 142.0 ppm was identified as the S-type skeleton, and 141.0 to 136.6 ppm was identified as the G-type skeleton, and the relative abundance percentage of each basic skeleton was calculated from the integral value. The relative abundance percentage of the H-type skeleton was calculated by subtracting the relative abundance percentages of the S-type skeleton and the G-type skeleton from the total amount of aromatic hydroxyl groups. Furthermore, 150.0 to 145.5 ppm was identified as aliphatic hydroxyl groups, and 144.7 to 136.6 ppm as aromatic hydroxyl groups. The amount of aliphatic hydroxyl groups (mol / g) and the amount of aromatic hydroxyl groups (mol / g) were calculated from the integral curve to determine the percentage of each hydroxyl group. (2) Abundance ratio and reaction point Based on the relative abundance percentage of each basic skeleton above, The ratio of the sum of twice the relative abundance of the H-type skeleton H (%) and the relative abundance of the G-type skeleton G (%) to the relative abundance of the S-type skeleton S (%) [(2H+G) / S], The sum of reaction sites based on the relative abundance of H-type skeletons (H) (%) and the relative abundance of G-type skeletons (G) (2H+G), was calculated.

[0059] [Softening point (℃)] The modified lignin or raw lignin (solid sample) obtained in each example was crushed in a mortar, sieved (40 mesh) to remove large particles, and the crushed sample was placed in an aluminum cup (circular upper φ60, lower φ53 × depth 15 mm) of 10 to 20 mg. The aluminum cup containing the sample was placed on a hot plate (ASONE ND-2A) and covered with a glass plate (thickness 0.5 mm). After heating to 80 °C, the temperature was increased in 10 °C increments, and visual observation was made through the glass. The temperature at which it melted visually was adopted as the softening point.

[0060] [Modified lignin] [Example 1] (1) Reaction process 29.5 parts by mass (29.5 g, 19.5 g as lignin) of second generation ethanol saccharification residue (lignin content: 66% by mass), 180 parts by mass of phenol, and 1 part by mass of phosphoric acid were placed in a 1.0 L pressure-resistant container with stirring and heated. When the phenol had dissolved, stirring was started. Heating was continued at 200°C for 4 hours. (2) Purification process (2-1) Filtration A 1.0 L hot pressure filter incorporating 5C filter paper was assembled and heated with warm water at 60 to 90°C. The entire amount of the reaction liquid obtained in the above reaction step was placed in the filter, pressurized to 0.1 to 0.4 MPa with compressed air or nitrogen, and filtered. The filtered solid was washed with phenol. (2-2) Distillation The filtrate obtained above was distilled under reduced pressure (5 to 10 kPa) and heated (100 to 130° C.) using a Kugelrohr to remove phenol, thereby obtaining 21.77 g of modified lignin. The phenol after the reaction could not be completely removed by the Kugelrohr, and remained at 6.5 mass% for the modified lignin 1. From this result, the amount of modified lignin obtained by the above distillation was calculated to be 20.3 g. The yield was calculated as the amount of modified lignin (20.3 g) relative to the amount of lignin charged (calculated value 19.5 g) using the following formula, which was 104.5%. Note that since phenol is added to the modified lignin, the yield is more than 100%. Yield (%) = [(amount of modified lignin) / (amount of charged lignin)] × 100

[0061] (Reprecipitation) Furthermore, 2 parts by mass of acetone was added to 1 part by mass (5.0 g) of the modified lignin from which the phenol had been distilled off to dissolve the modified lignin, and 40 parts by mass of ion-exchanged water was added thereto to precipitate the modified lignin. The precipitated modified lignin was centrifuged and collected. This operation was repeated 3 to 4 times to further remove the phenol after the reaction, and modified lignin 1 (4.7 g) was obtained.

[0062] [Example 2] The same procedure as in Example 1 was carried out except that 78 parts by mass of phenol was used, no acid catalyst was used, and the reaction time was 2 hours, to obtain modified lignin 2 (amount of modified lignin: 17.7 g, yield: 91.4%). [Example 3] The same procedure as in Example 2 was carried out except that the reaction time was changed to 4 hours, and modified lignin 3 (amount of modified lignin: 18.9 g, yield: 97.2%) was obtained. [Example 4] The same procedure as in Example 2 was carried out except that the reaction temperature was set to 220° C., and modified lignin 4 (amount of modified lignin: 15.8 g, yield: 80.9%) was obtained. [Example 5] The same procedure as in Example 4 was carried out except that the reaction time was changed to 4 hours, and Modified Lignin 5 (amount of modified lignin: 19.7 g, yield: 100.7%) was obtained. [Example 6] The same procedure as in Example 2 was carried out except that the reaction temperature was 230° C., and modified lignin 6 (amount of modified lignin: 18.9 g, yield: 96.6%) was obtained. [Example 7] The same procedure as in Example 2 was carried out except that the reaction temperature was 250° C., and modified lignin 7 (amount of modified lignin: 20.3 g, yield: 104.2%) was obtained. [Example 8] The same procedure as in Example 7 was carried out except that the reaction time was changed to 4 hours, and modified lignin 8 (amount of modified lignin: 23.0 g, yield: 117.7%) was obtained. [Example 9] The same procedure as in Example 7 was carried out except that the reaction time was changed to 6 hours, and Modified Lignin 9 (amount of modified lignin: 22.2 g, yield: 114.1%) was obtained. [Example 10] The same procedure as in Example 8 was carried out except that the reaction temperature was 300° C., and modified lignin 10 (amount of modified lignin: 20.8 g, yield: 106.2%) was obtained.

[0063] [Example 11] The same procedure as in Example 2 was carried out except that the acid catalyst was changed to 0.2 parts by mass of sulfuric acid, and modified lignin 11 (amount of modified lignin: 18.9 g, yield: 96.9%) was obtained. [Example 12] The same procedure as in Example 11 was carried out except that the amount of phenol was 102 parts by mass, the reaction temperature was 220° C., and the reaction time was 1 hour, to obtain modified lignin 12 (amount of modified lignin: 20.5 g, yield: 104.6%). [Example 13] The same procedure as in Example 12 was carried out except that the reaction time was changed to 2 hours, and modified lignin 13 (amount of modified lignin: 22.0 g, yield: 112.5%) was obtained. [Example 14] The same procedure as in Example 12 was carried out except that the reaction time was changed to 4 hours, and modified lignin 14 (amount of modified lignin: 23.4 g, yield: 119.7%) was obtained. [Example 15] The same procedure as in Example 11 was carried out except that the reaction temperature was set to 220° C., and modified lignin 15 (amount of modified lignin: 20.5 g, yield: 105.2%) was obtained. [Example 16] The same procedure as in Example 15 was carried out except that the reaction time was changed to 4 hours, and modified lignin 16 (amount of modified lignin: 23.4 g, yield: 119.6%) was obtained. [Example 17] The same procedure as in Example 13 was carried out except that the reaction temperature was 250° C., and modified lignin 17 (amount of modified lignin: 24.2 g, yield: 124.3%) was obtained. [Example 18] The same procedure as in Example 15 was carried out except that the acid catalyst was changed to 0.4 parts by mass of oxalic acid, and modified lignin 18 (amount of modified lignin: 19.5 g, yield: 100.5%) was obtained.

[0064] [Example 19] The same procedure as in Example 4 was performed except that the raw lignin was a second-generation ethanol fermentation residue, and modified lignin 19 (modified lignin amount 16.4 g, yield 83.6%) was obtained. [Example 20] The same procedure as in Example 19 was carried out except that the reaction time was changed to 4 hours, to obtain modified lignin 20 (amount of modified lignin: 16.8 g, yield: 86.3%). [Example 21] The same procedure as in Example 19 was carried out except that the acid catalyst was changed to 0.2 parts by mass of sulfuric acid, and modified lignin 21 (amount of modified lignin: 17.2 g, yield: 88.3%) was obtained.

[0065] The properties of modified lignins 1 to 21 obtained in Examples 1 to 21 above were measured by the methods described above, and the results are shown in Tables 1 and 2.

[0066] [Comparative Example 1] In Comparative Example 1, the properties of lignin in the raw material, second-generation ethanol saccharification residue, were analyzed. However, since the lignin in the second-generation ethanol saccharification residue is only slightly soluble in various organic solvents, it was not possible to analyze it using the above-mentioned method.

[0067] [Reference example 1] (1) Reference raw material lignin 500 g of bagasse (dried sugarcane residue) was heat treated at 200°C for 4 hours in the presence of 2100 mL of 1-butanol and 3300 mL of water, and the 1-butanol layer was extracted. The extracted 1-butanol layer was filtered (Whatman No. 2 filter paper) to remove cellulose-containing solids. The filtrate was concentrated and dried to obtain 90 g of reference raw lignin. (2) Reaction process 19.5 parts by mass (19.5 g) of the above-mentioned reference raw material lignin, 180 parts by mass of phenol, and 1 part by mass of phosphoric acid were placed in a 1.0 L pressure-resistant container capable of stirring and heated. When the phenol was dissolved, stirring was started. Heating was continued at 200°C for 4 hours. (3) Refining process (distillation) The reaction liquid was removed from the pressure vessel and distilled under reduced pressure (5-10 kPa) by heating (100-130°C) using a Kugelrohr to remove phenol, yielding 29.42 g of a black solid (reference modified lignin). The phenol after the reaction could not be completely removed by the Kugelrohr method, and 16.9% by mass of the modified lignin remained. From this result, the reference amount of modified lignin was calculated to be 24.5 g. The yield was calculated as the amount of the reference modified lignin (24.5 g) relative to the amount of the lignin charged (calculated value 19.5 g) using the following formula, which was 128.9%. Note that since phenol is added to the reference modified lignin, the yield is more than 100%. Yield = [recovered modified lignin / calculated value of lignin] x 100 (Reprecipitation) Reprecipitation was carried out in the same manner as in Example 1 to obtain reference modified lignin 1 (4.5 g). The properties of the obtained Reference Modified Lignin 1 were measured by the above-mentioned methods, and the results are shown in Tables 1 and 2.

[0068] [Reference example 2] As Reference Example 2, the properties of the above-mentioned reference raw material lignin were also measured by the above-mentioned method, and the results are shown in Tables 1 and 2.

[0069] [Table 1]

[0070] [Table 2]

[0071] As can be seen from Tables 1 and 2, the modified lignins of the Examples were modified in molecular weight and composition, demonstrating their applicability as modified lignin-containing materials, particularly as resin composition materials. In addition, the yield in Reference Example 1 was 128.9%, and since isolated lignin was used originally, the increase of 28.9% is thought to be due to the addition of phenol by the reaction. The isolated yield in the examples is lower than that of Reference Example 1, but this is based on a calculated lignin (including high molecular weight substances), and the actual isolated yield requires more detailed analysis. However, while the raw material second-generation ethanol saccharification residue cannot be used as it is as a resin composition material, the production method of the present invention can obtain modified lignin that can actually be used as a resin composition material. In addition, there are examples in which the yield of modified lignin was higher than the input amount, and high yields are also possible.

[0072] [Cured product] Next, using modified lignins 1, 15, 17, and 21 of Examples 1, 15, 17, and 21, second-generation ethanol saccharification residue as raw material (comparative raw material lignin), reference modified lignin of Reference Example 1, and reference raw material lignin of Reference Example 2, resin composition materials and molded bodies using the same were produced in each of the following examples. The resin composition and the molded article were evaluated by the following methods. (Easy to mix) In Examples 22 to 25, Comparative Example 2, and Reference Examples 3 and 4, the ease of kneading was evaluated based on the following index. ○: Easy to knead △: Difficult but possible to knead ×: Unable to knead

[0073] (stirrability) In Examples 26 to 29, Comparative Example 3, and Reference Examples 5 and 6, the ease of stirring during the reaction was evaluated based on the following index. ○: Easy to stir △: Difficult but possible to mix ×: Stirring not possible

[0074] (Bending strength) A sample of 5 mm x 50 mm x 1 mm was cut out from the molded body obtained in each example, and the bending strength was measured using an Instron 5566 manufactured by Instron Japan under conditions of a three-point bending mode, a span of 30 mm, and a speed of 2 mm / min, and evaluated based on the index. ○: The sample was not easily broken. △: The sample was broken. ×: The sample broke immediately. -:Poor molding

[0075] [Examples 22 to 25] 100 parts by mass of novolac-type phenolic resin (PR-53195, manufactured by Sumitomo Bakelite Co., Ltd.), 50 parts by mass of wood flour, 50 parts by mass (50.0 g) of each of modified lignins 1, 15, 17, and 21 of Examples 1, 15, 17, and 21 above, 20 parts by mass of hexamethylenetetramine as a curing agent, and 1 part by mass of zinc stearate as an internal release agent were mixed and kneaded in a two-roll kneader at 100 to 110°C for 3 minutes to obtain a modified lignin-containing resin composition material. The modified lignin-containing resin composition material obtained above was pressed into a heated mold cavity and molded by transfer molding at 170°C for 5 minutes, and then cured in an oven at 180°C for 8 hours to obtain a molded product. The results of the evaluation of the resin composition and the molded article are shown in Table 3.

[0076] [Comparative Example 2] A resin composition material and a molded body were obtained in the same manner as in Example 22, except that a second-generation ethanol saccharification residue (comparative raw lignin) was used as the raw material instead of the modified lignin. The results of the evaluation of the resin composition and the molded article are shown in Table 3. [Reference example 3] A resin composition material and a molded body were obtained in the same manner as in Example 25, except that the reference modified lignin was used instead of the modified lignin. The results of the evaluation of the resin composition and the molded article are shown in Table 3. [Reference example 4] A resin composition material and a molded body were obtained in the same manner as in Example 25, except that a reference raw lignin was used instead of the modified lignin. The results of the evaluation of the resin composition and the molded article are shown in Table 3.

[0077] [Table 3]

[0078] [Examples 26 to 29] In a 0.5L separable flask equipped with a reflux device and a stirring blade, 50 parts by mass (50.0 g) of each of the modified lignins 1, 15, 17, and 21 of the above Examples 1, 15, 17, and 21, and 30 parts by mass of a 40% by mass aqueous formaldehyde solution were added and stirred. The molar ratio of formaldehyde to phenol in the modified lignin was 1.5. While gradually dropping 35 parts by mass of a 50% by mass aqueous sodium carbonate solution, the mixture was heated at 100°C for 2 hours to obtain a liquid composition. Furthermore, 54 parts by mass of wood flour was added and stirred until homogenous, to obtain a modified lignin-containing resin composition material. The modified lignin-containing resin composition material obtained above was decompressed to remove moisture, and press-molded at a surface pressure of 0.2 MPa, 180° C., and 10 minutes, and then cured in an oven at 200° C. for 4 hours to obtain a molded product. The results of the evaluation of the resin composition and the molded article are shown in Table 4.

[0079] [Comparative Example 3] A resin composition material and a molded body were obtained in the same manner as in Example 26, except that a second-generation ethanol saccharification residue (comparative raw lignin) was used as the raw material instead of the modified lignin. The results of the evaluation of the resin composition and the molded article are shown in Table 4. [Reference example 5] A molded body was obtained in the same manner as in Example 26, except that the reference modified lignin was used instead of the modified lignin. The results of the evaluation of the resin composition and the molded article are shown in Table 4. [Reference example 6] A molded body was obtained in the same manner as in Example 26, except that a reference raw lignin was used instead of the modified lignin. The results of the evaluation of the resin composition and the molded article are shown in Table 4.

[0080] [Table 4]

[0081] From Tables 3 and 4, it can be seen that the raw material second-generation ethanol saccharification residue cannot be used as it is as a resin composition material, whereas the modified lignin obtained in the present invention has improved mixability, since it has excellent kneading properties and stirrability during reaction equivalent to the reference modified lignin. In addition, the bending properties of the molded bodies obtained in the examples were evaluated to be equivalent to those of Reference Examples 3 and 5, which used the reference modified lignin, and it can be seen that the molded bodies have good properties. [Industrial Applicability]

[0082] The modified lignin of the present invention has a lower molecular weight, which improves its mixability with other plastic materials and increases the number of reaction sites. The improved mixability and increased reaction sites are expected to improve the physical properties of molded products, and the ease of mixing makes it possible to eliminate the need for large-scale equipment that is costly when producing hardened parts. In addition, since lignin, which has been almost entirely discarded until now, can be effectively utilized, it is also effective in protecting the environment.

Claims

1. A method for producing modified lignin which does not use aldehyde, comprising a step of reacting one or more types of residues obtained by removing cellulose and hemicellulose from non-edible plant biomass containing lignin through saccharification or saccharification / fermentation with a phenolic compound in which at least one of the 2-, 4- and 6-positions, which are the positions of the substituents relative to the hydroxyl groups, is a hydrogen atom, at a temperature above 140°C and not exceeding 350°C, followed by a solid-liquid separation step of removing solids, a mass ratio of the phenolic compound to lignin in one or more residues obtained by removing cellulose and hemicellulose from the lignin-containing non-edible plant biomass through saccharification or saccharification / fermentation [phenolic compound / lignin] is 1 to 10; The modified lignin produced is ３１ the ratio [(2H+G) / S] of the sum of twice the relative abundance H(%) of the H-type skeleton to the relative abundance S(%) of the S-type skeleton determined from the integral value measured by P-NMR and the relative abundance G(%) of the G-type skeleton is 2.5 or more; The modified lignin produced is ３１ A method for producing modified lignin, in which the proportion of aliphatic hydroxyl groups relative to the total proportion of aliphatic hydroxyl groups and aromatic hydroxyl groups, as determined from an integrated value measured by P-NMR, is less than 20%.

2. The method for producing modified lignin according to claim 1, wherein the phenol compound is represented by the following formula (1): 【Chemistry 1】 (In formula (1), R １ and R ２ each independently represents a hydrogen atom, a hydroxyl group, or an alkyl group having 1 to 15 carbon atoms; R １ and R ２ may be the same or different.)

3. The method for producing modified lignin according to claim 1 or 2, wherein the reaction is carried out without a catalyst.

4. The method for producing modified lignin according to claim 1 or 2, wherein the reaction is carried out in the presence of an acid catalyst in an amount of more than 0 to 3.0 mass% relative to the total amount of lignin and the phenolic compounds in one or more residues obtained by removing cellulose and hemicellulose from non-edible plant biomass containing the lignin by saccharification or saccharification / fermentation.

5. The method for producing modified lignin according to any one of claims 1 to 4, wherein the reaction is carried out at a reaction temperature above 140 ° C. and below 250 ° C.

6. The method for producing modified lignin according to any one of claims 1 to 5, wherein the reaction is carried out for a reaction time of 1 hour or more and 8 hours or less.

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