Patent Application
20150031804
1. Field of the Invention
The present invention relates to cellulose nanofibers and a method for producing the same, a composite resin composition, and a molded body.
2. Description of the Related Art
Cellulose nanofibers are used as a reinforcing material of a polymer composite material in the related art. Specifically, cellulose nanofibers are used as a reinforcing material of, for example, medical instruments, OA apparatuses, acoustic instruments, or cameras.
Typically, the cellulose nanofibers are obtained by mechanically shearing of cellulose fibers such as pulp. For example, Japanese Unexamined Patent Application, First Publication No. 2000-17592 discloses microfibrillated cellulose obtained by treating an aqueous cellulose pulp suspension with a high-pressure homogenizer.
In addition, Japanese Unexamined Patent Application, First Publication No. H9-291102 discloses ultra-fine fibers of acetyl cellulose obtained by acetylating cellulose ultra-fine fibers produced by bacteria. The cellulose ultra-fine fibers produced by bacteria have a polymerization degree of 1700 or higher in a mass average and thus are superior in Young's modulus and tensile strength.
According to a first aspect of the present invention, cellulose nanofibers includes: a linear portion; and a curved portion, in which an average of a length of the linear portion and an average of a maximum diameter of the linear portion have a relationship that satisfies the following Equation (a):
(The average of the length of the linear portion)/(The average of the maximum diameter of the linear portion)≧10 Equation (a)
According to a second aspect of the present invention, in the cellulose nanofibers according to the first aspect, the maximum diameter of the linear portion may be 1 nm to 800 nm.
According to a third aspect of the present invention, in the cellulose nanofibers according to the first or second aspect, an X-ray diffraction pattern, which has a 2θ range of 0° to 30°, may have one or two peaks in 14°≦2θ≦18°, the X-ray diffraction pattern may have one or two peaks in 20≦2θ≦24°, and the X-ray diffraction pattern may have no peak in the other 2θ range.
According to a fourth aspect of the present invention, in the cellulose nanofibers according to any one of the first to third aspects, an average polymerization degree of the cellulose nanofibers may be 600 to 30000.
According to a fifth aspect of the present invention, in the cellulose nanofibers according to any one of the first to fourth aspects, a part or all of hydroxyl groups of the cellulose nanofibers may be chemically modified.
According to a sixth aspect of the present invention, in the cellulose nanofibers according to any one of the first to fifth aspects, cotton may be used as a raw material of the cellulose nanofibers.
According to a seventh aspect of the present invention, in the cellulose nanofibers according to any one of the first to sixth aspects, a saturated absorptivity of the cellulose nanofibers in an organic solvent which has an SP value of 8 to 13, may be 300 mass % to 30000 mass %.
According to an eighth aspect of the present invention, cellulose nanofibers are obtained from a method including: a first process of defibrating a cellulose by swelling and/or partially dissolving the cellulose in a cellulose-containing raw material, by using a solution which contains a tetraalkylammonium acetate and an aprotic polar solvent; and a second process of performing a chemical modification at 20° C. to 65° C.
According to a ninth aspect of the present invention, in the cellulose nanofibers according to the eighth aspect, the chemical modification may be performed at 50° C. to 65° C. in the second process.
According to a tenth aspect of the present invention, in the cellulose nanofibers according to the eighth or ninth aspect, the chemical modification may be performed between 15 minutes to 2 hours in the second process.
According to an eleventh aspect of the present invention, in the cellulose nanofibers according to the tenth aspect, the chemical modification may be performed between 30 minutes to 60 minutes in the second process.
According to a twelfth aspect of the present invention, a composite resin composition containing the cellulose nanofibers according to any one of the first to eleventh aspects is provided.
According to a thirteenth aspect of the present invention, a molded body formed by molding the composite resin composition according to the twelfth aspect is provided.
According to a fourteenth aspect of the present invention, a method for producing the cellulose nanofibers is provided according to any one of the first to sixth aspects, the method including: a first process of defibrating a cellulose by swelling and/or partially dissolving the cellulose in a cellulose-containing raw material, by using a solution containing a tetraalkylammonium acetate and an aprotic polar solvent; and a second process of performing a chemical modification at 20° C. to 65° C.
According to a fifteenth aspect of the present invention, in the method for producing the cellulose nanofibers according to the fourteenth aspect, the chemical modification may be performed at 50° C. to 65° C. in the second process.
According to a sixteenth aspect of the present invention, in the method for producing the cellulose nanofibers according to the fourteenth or fifteenth aspect, the chemical modification may be performed between 15 minutes to 2 hours in the second process.
According to a seventeenth aspect of the present invention, in the method for producing the cellulose nanofibers according to the sixteenth aspect, the chemical modification may be performed between 30 minutes to 60 minutes in the second process.
Cellulose nanofibers according to a first embodiment of the present invention include a linear portion and a curved portion, in which an average of a length of the linear portion and an average of a maximum diameter of the linear portion have a relationship that satisfies the following Equation (a). As a result, cellulose nanofibers according to a first embodiment of the present invention can obtain a sufficient reinforcing effect.
(The average of the length of the linear portion)/(The average of the maximum diameter of the linear portion)≧10 Equation (a)
The cellulose nanofibers according to the first embodiment of the present invention are shown as a cellulose nanofiber A illustrated in
In the cellulose nanofibers according to the first embodiment of the present invention, it is preferable that the maximum diameters of the linear portions be 1 nm to 800 nm. The average diameter is preferably 1 nm to 300 nm and more preferably 1 nm to 100 nm. When the average diameter is 1 nm or more, the manufacturing cost is low. When the average diameter is 800 nm or less, the LAVG/DAVG is unlikely to decrease. As a result, the cellulose nanofibers according to the first embodiment of the present invention can obtain a sufficient reinforcing effect at a low cost.
Cellulose type I is a composite of Iα-type crystals and Iβ-type crystals. Cellulose derived from higher plants, such as cotton, contains much Iβ-type crystal components. On the other hand, bacterial cellulose contains much Iα-type crystal components.
The cellulose nanofibers according to the first embodiment of the present invention have an Iβ-type crystal peak in an X-ray diffraction pattern. Therefore, as illustrated in
In addition, since the cellulose nanofibers according to the first embodiment of the present invention contain Iβ-type crystals as a major component, the reinforcing effect thereof is superior to that of bacterial cellulose that contains much Iα-type crystal components.
The average polymerization degree of the cellulose nanofibers according to the first embodiment of the present invention is preferably 600 to 30000, more preferably 600 to 5000, and most preferably 800 to 5000. When the average polymerization degree is 600 or more, a sufficient reinforcing effect can be obtained.
In the cellulose nanofibers according to the first embodiment of the present invention, a part or all of the hydroxyl groups may be chemically modified to improve functionality. In order to use the cellulose nanofibers in a composite material, it is preferable that hydroxyl groups on the surfaces of the cellulose nanofibers be chemically modified with a modification group to reduce the number of the hydroxyl groups. By preventing the cellulose nanofibers from strongly adhering to each other by a hydrogen bond, the cellulose nanofibers can be easily dispersed in a polymer material and can form a superior interface bond. In addition, the cellulose nanofibers according to the first embodiment of the present invention have high heat resistance according to the chemical modification. Therefore, it is possible to provide a composite resin composition having high heat resistance.
A ratio of hydroxyl groups, which are chemically modified by a modification group, to all of the hydroxyl groups in the cellulose nanofibers is preferably 0.01 to 50 and more preferably 0.5 to 10 in the method described below.
The modification group only needs to be a group which is reactive with a hydroxyl group. The cellulose nanofibers which are etherified and esterified by the chemical modification are preferable because they can be easily and efficiently modified.
As an etherifying agent, for example, alkyl halides such as methyl chloride and ethyl chloride; dialkyl carbonate such as dimethyl carbonate and diethyl carbonate; dialkyl sulfate such as dimethyl sulfate and diethyl sulfate; and alkylene oxides such as ethylene oxide and propylene oxide are preferable. In addition, the etherification is not limited to alkyl etherification, and etherification caused by benzyl bromide, silyl etherification, and the like are also preferable. For example, in silyl etherification, alkoxysilanes are preferable. More specifically, alkoxy silanes such as n-butoxytrimethylsilane, tert-butoxytrimethylsilane, sec-butoxytrimethylsilane, isobutoxytrimethylsilane, ethoxytriethylsilane, octyldimethylethoxysilane, and cyclohexyloxytrimethylsilane; alkoxysiloxanes such as butoxypolydimethylsiloxane; and silazanes such as hexamethyldisilazane, tetramethyldisilazane, and diphenyltetramethyldisilazane are preferable. In addition, silyl halides such as trimethylsilyl chloride and diphenylbutyl chloride; and silyl trifluoromethane sulfonates such as t-butyldimethylsilyl trifluoromethane sulfonate can also be used.
As an esterifying agent, an acid chloride, an acid anhydride, or an acid vinyl ester is preferable. Examples of the acid chloride include propionyl chloride, butyl chloride, octanoyl chloride, stearoyl chloride, benzoyl chloride, and p-toluenesulfonic acid chloride. In a reaction of the acid chloride, an alkaline compound may be added so as to function as a catalyst and to neutralize an acidic material which is a by-product. Specific examples of the alkaline compound include tertiary amine compounds such as triethyl amine and trimethyl amine; and nitrogen-containing aromatic compounds such as pyridine and dimethylaminopyridine. However, the alkaline compound is not limited to these examples.
In addition, examples of the acid anhydride include aliphatic acid anhydrides such as acetic anhydride, propionic anhydride, and butyric anhyride; and dibasic acid anhydrides such as maleic anhydride, succinic anhydride, and phthalic anhydride. As a catalyst in a reaction of the acid anhydride, an acid catalyst such as sulfuric acid, hydrochloric acid, or phosphoric acid; or an alkaline compound such as triethyl amine or pyridine may be used.
Among acid vinyls esters, vinyl carboxylate is preferable. As the vinyl carboxylate, vinyl acetate, vinyl propionate, vinyl butyrate, vinyl valerate, vinyl pivalate, vinyl caproate, vinyl caprate, vinyl laurate, vinyl myristate, vinyl palmitate, vinyl stearate, vinyl cyclohexane carboxylate, vinyl octylate, vinyl methacrylate, vinyl crotonate, vinyl sorbate, vinyl benzoate, or vinyl cinnamate is more preferable; vinyl acetate, vinyl propionate, vinyl butyrate, vinyl valerate, vinyl pivalate, vinyl caproate, vinyl caprate, vinyl laurate, vinyl myristate, vinyl palmitate, vinyl stearate, vinyl cyclohexane carboxylate, or vinyl octylate is still more preferable; and vinyl acetate, vinyl propionate, or vinyl butyrate is most preferable.
Among the types of etherification and the esterification, alkyl etherification, alkyl silylation, and alkyl esterification are preferable since dispersibility in a resin is improved.
A raw material of the cellulose nanofibers is not particularly limited, and examples thereof include natural cellulose raw materials such as cotton, hemp, and ascidian; pulp obtained by chemically treating wood, such as kraft pulp and sulfide pulp; and semi-chemical pulp; used paper or recycled pulp thereof. From the viewpoint of obtaining a high reinforcing effect, filter paper or cotton is preferable. Among these, cotton is particularly preferable, because by using cotton as a raw material, the molecular weight of the acquired cellulose nanofibers becomes large, so a reinforcing effect increases. In addition, fine crystal cellulose or cellulose nanofibers produced using other production methods are also preferable as a raw material. This is because when a production method according to a second embodiment of the present invention is further used, the reinforcing effect of cellulose nanofibers is improved.
The form of the raw material of the cellulose nanofibers is not particularly limited. However, from the viewpoint of easiness of treatment and promotion of solvent permeation, it is preferable that the raw material be used after appropriate pulverization.
In the cellulose nanofibers according to the first embodiment of the present invention which are chemically modified as described above, the saturated absorptivity in an organic solvent having a solubility parameter (hereinafter, referred to as “SP value”) of 8 to 13 is preferably 300 mass % to 30000 mass % and more preferably 5000 mass % to 30000 mass %. The cellulose nanofibers which are dispersed in the organic solvent having the above-described SP value have high affinity with a lipophilic resin and have a high reinforcing effect.
Examples of the organic solvents having an SP value of 8 to 13 include acetic acid, ethyl acetate, butyl acetate, isobutyl acetate, isopropyl acetate, methyl propyl ketone, methyl isopropyl ketone, xylene, toluene, benzene, ethyl benzene, dibutyl phthalate, acetone, isopropanol, acetonitrile, dimethyl formamide, ethanol, tetrahydrofuran, methyl ethyl ketone, cyclohexane, carbon tetrachloride, chloroform, methylene chloride, carbon disulfide, pyridine, n-hexanol, cyclohexanol, n-butanol, and nitromethane.
As the organic solvent, a water-insoluble solvent (solvent that is not mixed with water at 25° C. at any ratio) is more preferable, and examples thereof include xylene, toluene, benzene, ethylbenzene, dichloromethane, cyclohexane, carbon tetrachloride, methylene chloride, ethyl acetate, carbon disulfide, cyclohexanol, and nitromethane. Accordingly, the cellulose nanofibers according to the first embodiment of the present invention which are chemically modified as described above can be dispersed in a water-insoluble solvent and can be easily dispersed in a lipophilic resin in which cellulose nanofibers of the related art have difficulty being dissolved.
The cellulose nanofibers according to the first embodiment of the present invention can be produced using the production method according to the fourth embodiment of the present invention described below.
The cellulose nanofibers according to the first embodiment of the present invention are produced using a method including: a process (hereinafter, referred to as “Process 1”) of swelling and/or partially dissolving cellulose contained in a cellulose-containing raw material in a solution containing tetraalkylammonium acetate and an aprotic polar solvent to defibrate the cellulose; and a process (hereinafter, referred to as “Process 2”) of performing chemical modification at 20° C. to 65° C.
Process 1 (first process) includes: a process (hereinafter, referred to as “Process 1-1”) of swelling and/or partially dissolving cellulose contained in a cellulose-containing raw material in a solution containing tetraalkylammonium acetate and an aprotic polar solvent; and a process (hereinafter, referred to as “Process 1-2”) of defibrating the cellulose.
In natural cellulose, an amorphous component, which is present between fibers, functions as a binding agent, and thus the cellulose fibers are present in a state where a fiber diameter thereof is large.
In this specification, “cellulose is swollen” represents that an amorphous component, which is contained in cellulose, is swollen. According to this swelling of amorphous component, the cellulose nanofibers are loosened and easily split by an external force.
In addition, in this specification, “cellulose is partially dissolved” represents that an amorphus component, which functions as a binding agent of the cellulose nanofibers, is dissolved. By swelling and/or partially dissolving the cellulose, a binding between the cellulose nanofibers becomes weakened, and the defibration of the cellulose nanofibers can be easily performed.
Process 1-1 can be performed using a well-known method of the related art, except that the solution containing tetraalkylammonium acetate and an aprotic polar solvent is used. For example, cellulose can swollen and/or partially dissolved by dispersing a cellulose-containing raw material in the solution and leaving the dispersion to stand or stirring the dispersion. In addition, Process 1-1 and Process 1-2 may be performed at the same time.
As an alkyl group of tetraalkylammonium acetate, an alkyl group having 3 to 6 carbon atoms is preferable. When the number of carbon atoms of the alkyl group in tetraalkylammonium acetate is 3 to 6, cellulose can be sufficiently swollen and/or partially dissolved.
Specific examples of tetraalkylammonium acetate include tetrapropylammonium acetate, tetrabutylammonium acetate, tetrapentylammonium acetate, and tetrahexylammonium acetate. Among these, tetrabutylammonium acetate is more preferable. As tetraalkylammonium acetate, one kind may be used, or two or more kinds may be used in combination.
As the aprotic polar solvent, at least one solvent selected from among amide-based solvents, sulfoxide-based solvents, and pyridine-based solvents is preferable.
Specific example of the aprotic polar solvent include N,N-dimethylformamide, N,N-diethylformamide, N,N-dimethylacetamide, N,N-diethylacetamide, dimethylsulfoxide, N-methyl-2-pyrrolidone, N,N′-dimethylpropyleneurea, N,N′-dimethylethyleneurea, tetramethylurea, tetraethylurea, N,N,N′,N′-tetramethylurea, pyridine, 4-methylpyridine, 2,6-dimethylpyridine, 2,4,6-trimethylpyridine, and derivatives thereof. Among these, N,N-diethylacetamide is preferable. As the aprotic polar solvent, one kind may be used, or two or more kinds may be used in combination.
By using the aprotic polar solvent, the permeation of the solution into cellulose nanofibers is promoted, and Process 1-1 can be efficiently performed. In addition, the destruction of a crystal structure of the cellulose nanofibers can be prevented.
As cellulose to be dissolved in the above-described solution, for example, the same cellulose as that of the cellulose raw material described in the first embodiment may be used.
In addition, a ratio of the cellulose-containing raw material to be added to the solution is preferably 0.5 mass % to 30 mass % and more preferably 1.0 mass % to 20 mass %. By controlling the ratio of the cellulose-containing raw material to be in the above-described range, a slurry of uniformly defibrated cellulose nanofibers is effectively produced.
A processing temperature of Process 1-1 is not particularly limited, but is preferably 10° C. to 120° C. When the processing temperature is lower than 10° C., the viscosity of a process liquid is increased, and a defibrating effect is decreased. On the other hand, when the processing temperature is higher than 120° C., even nanofibers are dissolved and damaged. As a result, a reinforcing effect is decreased, and the yield of nanofibers tends to be decreased.
Process 1-2 can be performed by applying an external force to the cellulose treated in Process 1-1. Specifically, for example, well-known methods such as mechanical shearing, pulverizing, polishing, homogenizing, and ultrasonication may be used. As this means, one kind may be used alone, or two or more kinds may be used in combination.
Process 1-2 may be performed in parallel with Process 1-1 or in parallel with Process 2 described below. Alternatively, Process 1-2 may be performed after Process 2.
In Process 2 (second process), it is necessary that the above-described chemical modification be performed at 20° C. to 65° C. As a result, cellulose nanofibers having a LAVG/DAVG value of 10 or higher can be obtained.
In Process 2, it is preferable that the chemical modification be performed at 55° C. to 65° C. It is preferable that the above-described temperature condition be satisfied because the value of “Average lengths of Linear Portions/Average maximum diameters of Linear Portions” is likely to be increased.
In addition, in Process 2, the chemical modification is performed preferably between 15 minutes to 2 hours and more preferably between 30 minutes to 60 minutes. By controlling the time condition of the chemical modification to be in the above-described range, cellulose nanofibers having a LAVG/DAVG value of 10 or higher can be more reliably obtained.
A composite resin composition according to a second embodiment of the present invention contains the cellulose nanofibers in a resin.
An example of the above-described lipophilic resin, in which the cellulose nanofibers according to the first embodiment of the present invention can be dispersed, only needs to be water-insoluble, and a resin which is widely used as an industrial material which is required to have water resistance is preferable. The lipophilic resin may be a thermoplastic resin or a thermosetting resin. Examples of the lipophilic resin include a plant-derived resin, a resin formed of carbon dioxide as a raw material, an ABS resin, alkylene resins such as polyethylene and polypropylene, a styrene resin, a vinyl resin, an acrylic resin, an amide resin, an acetal resin, a carbonate resin, a urethane resin, an epoxy resin, an imide resin, a urea resin, a silicone resin, a phenol resin, a melamine resin, an ester resin, a fluororesin, a styrol resin, and an engineering plastic. In addition, as the engineering plastic, polyamide, polybutylene terephthalate, polycarbonate, polyacetal, modified polyphenylene oxide, modified polyphenylene ether, polyphenylene sulfide, polyether ether ketone, polyether sulfone, polysulfone, polyamide imide, polyether imide, polyimide, polyarylate, polyallyl ether nitrile, and the like are preferable. In addition, among these resins, two or more kinds may be used as a mixture.
Among these resins, polycarbonate is particularly preferable due to its high impact strength.
As the polycarbonate, polycarbonate which is typically used can be used. For example, aromatic polycarbonate produced from a reaction between an aromatic dihydroxy compound and a carbonate precursor can be preferably used.
Examples of the aromatic dihydroxy compound include 2,2-bis(4-hydroxyphenyl)propane (“bisphenol A”), bis(4-hydroxyphenyl)methane, 1,1-bis(4-hydroxyphenyl)ethane, 2,2-bis(4-hydroxy-3,5-dimethylphenyl)propane, 4,4′-dihydroxydiphenyl, bis(4-hydroxyphenyl)cycloalkane, bis(4-hydroxyphenyl)sulfide, bis(4-hydroxyphenyl)sulfone, bis(4-hydroxyphenyl)sulfoxide, bis(4-hydroxyphenyl)ether, and bis(4-hydroxyphenyl)ketone.
Examples of the carbonate precursor include carbonyl halides, carbonyl esters, and haloformates. Specific examples of the carbonate precursor include phosgene, dihaloformate of a divalent phenol, diphenyl carbonate, dimethyl carbonate, and diethyl carbonate.
In addition, the polycarbonate which is used in the second embodiment of the present invention may be polycarbonate not containing an aromatic group. Examples of the polycarbonate not containing an aromatic group include alicyclic polycarbonate and aliphatic polycarbonate. The polycarbonate resin may be linear or branched. In addition, the polycarbonate resin may also be copolymer of a polymer, which is obtained by polymerizing the aromatic dihydroxy compound and the carbonate precursor, with another polymer.
The polycarbonate resin may be produced using a well-known method of the related art. For example, various methods such as interfacial polymerization, melt transesterification, and a pyridine method may be used.
Examples of the kind of the resin of the composite resin composition according to the second embodiment of the present invention include a hydrophilic resin in addition to the above-described lipophilic resin. As the hydrophilic resin, non-modified cellulose nanofibers or cellulose nanofibers chemically modified with hydrophilic functional groups such as a sulfonic acid group, a carboxylic acid group, or a salt thereof have high dispersibility in a hydrophilic resin and can be suitably used.
Examples of the hydrophilic resin include resins subjected to a hydrophilic treatment, such as polyvinyl alcohol. Among these, polyvinyl alcohol is particularly preferable because it is inexpensive and has high dispersibility for cellulose nanofibers.
In addition, the composite resin composition according to the second embodiment of the present invention may further contain additives such as a filler, a flame retardant promoter, a flame retardant, an antioxidant, a release agent, a colorant, and a dispersant.
As the filler, for example, carbon fibers, glass fibers, clay, titanium oxide, silica, talc, calcium carbonate, potassium titanate, mica, montmorillonite, barium sulfate, a balloon filler, a bead filler, carbon nanotubes, and the like can be used.
As the flame retardant, a halogen-based flame retardant, a nitrogen-based flame retardant, metal hydroxide, a phosphorus-based flame retardant, an organic alkali metal salt, an organic alkaline earth metal salt, a silicone-based flame retardant, expandable graphite, and the like can be used.
As the flame retardant promoter, polyfluoroolefin, antimony oxide, and the like can be used.
As the antioxidant, a phosphorus-based antioxidant, a phenol-based antioxidant, and the like can be used.
As the release agent, a higher alcohol, carboxylic acid ester, polyolefin wax, polyalkylene glycol, and the like can be used.
As the colorant, any colorants such as carbon black and phthalocyanine blue can be used.
The dispersant only needs to enable the cellulose nanofibers to be dispersed in a resin, and for example, surfactants such as anionic surfactants, cationic surfactants, nonionic surfactants, and amphoteric surfactants and polymeric dispersants can be used, and a combination thereof can also be used.
The cellulose nanofibers according to the first embodiment of the present invention have a reinforcing effect as described above. Therefore, the composite resin composition according to the second embodiment of the present invention containing the cellulose nanofibers is superior in strength. Accordingly, the composite resin composition according to the second embodiment of the present invention can be desirably used in a field where strength is required.
In addition, the cellulose nanofibers according to the first embodiment of the present invention have high dispersibility in a resin. Therefore, the composite resin composition according to the second embodiment of the present invention containing the cellulose nanofibers is superior in transparency. Accordingly, the composite resin composition according to the second embodiment of the present invention can secure its transparency and thus can be desirably used in a field where transparency is required.
In addition, the cellulose nanofibers according to the first embodiment of the present invention have higher heat resistance than that of the cellulose nanofibers of the related art. Therefore, the composite resin composition according to the second embodiment of the present invention containing the cellulose nanofibers is superior in heat resistance. Accordingly, the composite resin composition according to the second embodiment of the present invention can be desirably used in a field where heat resistance is required while maintaining transparency.
A molded body according to a third embodiment of the present invention is formed by molding the composite resin composition according to the second embodiment of the present invention. The molded body according to the third embodiment of the present invention also contains the cellulose nanofibers and thus is superior in strength and heat resistance. The molded body is not particularly limited and can be used in medical instruments, OA apparatuses, acoustic instruments, or cameras. In particular, the molded body can be desirably used in molded bodies or lens frames for cameras where strength is required.
The method for producing cellulose nanofibers according to the fourth embodiment of the present invention is a method for producing the cellulose nanofibers according to the first embodiment which is the same as the production method including Process 1 and Process 2 which is described in the cellulose nanofibers according to the first embodiment.
Hereinafter, the present invention will be described in more detail using Examples and Comparative Examples but is not limited to the following examples.
2.2 g of absorbent cotton, 92.5 g of N,N-dimethylacetamide, and 7.5 g of tetrabutylammonium acetate were added to a flask, followed by stifling at 65° C. for 60 minutes to allow cellulose contained in the absorbent cotton to swell.
Next, 16 g of acetic anhydride was added to a solution in which the cellulose swelled, followed by further stirring at 65° C. for 90 minutes.
After stirring, the obtained solid content was washed until tetrabutylammonium acetate was not detected.
N,N-dimethylacetamide was added to the obtained solid content, followed by a treatment with a homogenizer. As a result, a slurry of cellulose nanofibers was obtained.
The obtained slurry of cellulose nanofibers was dried, and the form thereof was observed using FE-SEM (manufactured by JEOL Ltd., product name: JSM-6700f, measurement condition: 20 mA, 60 seconds). Before the observation, the cellulose nanofibers were coated with Pt. The average of diameters of linear portions of the obtained cellulose nanofibers was about 30 nm. Through the IR analysis of the obtained cellulose nanofibers, it was confirmed that hydroxyl groups on the surface of the cellulose nanofibers were modified. The results are shown in Table 1 together.
The cellulose nanofiber slurry was mixed with polycarbonate (manufactured by Teijin Ltd.; PANLITE L-1225L) dissolved in a solvent, followed by drying. As a result, a composite resin composition was prepared.
7.5 g of filter paper (manufactured by Toyo Roshi Kaisha Ltd., FILTER PAPER of ADVANTEC (registered trademark)), which was cut into a size of 3 mm×3 mm with scissors, 90 g of N,N-dimethylacetamide, and 10 g of tetrabutylammonium acetate were added to a flask, followed by stirring at 65° C. for 60 minutes to allow cellulose contained in the filter paper to swell (swelling process).
Next, 40 g of acetic anhydride was added to a solution in which the cellulose swelled, followed by further stirring at 65° C. for 60 minutes.
After stirring, the obtained solid content was washed until tetrabutylammonium acetate was not detected (chemical modification process).
N,N-dimethylacetamide was added to the obtained solid content, followed by a treatment with a homogenizer. As a result, a slurry of cellulose nanofibers was obtained.
The obtained slurry of cellulose nanofibers was dried, and the form thereof was observed using FE-SEM (manufactured by JEOL Ltd., product name: JSM-6700f, measurement condition: 20 mA, 60 seconds). Before the observation, the cellulose nanofibers were coated with Pt. The average of diameters of linear portions of the obtained cellulose nanofibers was about 30 nm. Through the IR analysis of the obtained cellulose nanofibers, it was confirmed that hydroxyl groups on the surface of the cellulose nanofibers were modified. The results are shown in Table 1 together.
The cellulose nanofiber slurry was mixed with polycarbonate (manufactured by Teijin Ltd.; PANLITE L-1225L) dissolved in a solvent, followed by drying. As a result, a composite resin composition was prepared.
Cellulose nanofibers were obtained with the same method as that of Example 2, except that the solution was stirred at 50° C. for 3 hours in the swelling process and was stirred at a solution temperature of 50° C. for 30 minutes in the chemical modification process.
The average of diameters of linear portions of the obtained cellulose nanofibers was about 30 nm. Through the IR analysis of the obtained cellulose nanofibers, it was confirmed that hydroxyl groups on the surface of the cellulose nanofibers were modified. The results are shown in Table 1 together.
Cellulose nanofibers were obtained with the same method as that of Example 2, except that the solution was stirred at a solution temperature of 20° C. for 120 minutes in the chemical modification process.
The average of diameters of linear portions of the obtained cellulose nanofibers was about 30 nm. Through the IR analysis of the obtained cellulose nanofibers, it was confirmed that hydroxyl groups on the surface of the cellulose nanofibers were modified. The results are shown in Table 1 together.
Cellulose nanofibers were obtained with the same method as that of Example 2, except that the solution was stirred at room temperature for 20 minutes in the swelling process and was stirred at a solution temperature of 65° C. for 15 minutes in the chemical modification process.
The average of diameters of linear portions of the obtained cellulose nanofibers was about 30 nm. Through the IR analysis of the obtained cellulose nanofibers, it was confirmed that hydroxyl groups on the surface of the cellulose nanofibers were modified. The results are shown in Table 1 together.
Bacterial cellulose obtained by drying NATA DE COCO (manufactured by Fujicco Co., Ltd., average polymerization degree: 3000 or higher, average aspect ratio: 1000 or higher, average diameter: 70 nm) was prepared. The bacterial cellulose was mixed with polycarbonate (manufactured by Teijin Ltd.; PANLITE L-1225L) dissolved in a solvent, followed by drying. As a result, a composite resin composition was prepared.
Fine crystal cellulose (manufactured by Merck KGaA, average polymerization degree: 250, average aspect ratio: 10, diameter: mixed in a range of 1 μm to 10 μm) was prepared. Using this fine crystal cellulose, a composite resin composition was prepared with the same method as that of Comparative Example 1.
The cellulose nanofibers and the composite resin compositions obtained in the respective Examples and the respective Comparative Examples were measured using the following test methods, and the results thereof are shown in Table 1.
The molded bodies obtained in the respective Examples and the respective Comparative Examples were measured using the following test method, and the results thereof are shown in Table 1.
The molecular weight of the cellulose nanofibers was evaluated by viscometry (reference: Macromolecules, 18, 2394-2401, 1985).
The number average lengths of linear portions of the cellulose nanofibers and the number average maximum diameters of the linear portions were evaluated by SEM analysis.
Specifically, the slurry of cellulose nanofibers was cast on a wafer and was observed by SEM to obtain an image. Per image, the lengths 1 and the maximum diameters d of the linear portions were read for more than 20 fibers which have a linear portion. The largest 10 values were selected from among values of “Lengths 1 of Linear Portions/Maximum Diameters d of Linear Portions” to obtain information regarding the maximum diameters and the lengths.
From the above-obtained data regarding the lengths 1 and the maximum diameters d of the linear portions, the number average LAVG of the lengths of the linear portions and the number average DAVG of the maximum diameters of the linear portions were able to be calculated, and a ratio of the number average LAVG of the lengths of the linear portions to the number average DAVG of the maximum diameters of the linear portions was calculated by the following equation (a). A case where the ratio was 10 or higher was determined as “Good”, and a case where the ratio was lower than 10 was determined as “Poor”.
Average lengths of Linear Portions/Average maximum diameters of Linear Portions≧10 (a)
A crystal structure of the cellulose nanofibers was analyzed using a powder X-ray diffractometer Rigaku Ultima IV. A case where an X-ray diffraction pattern had one or two peaks in 14° 2018° and had one or two peaks in 21°≦2θ≦24° was determined as “Good” in which the crystal structure was Iβ-type. The other cases were determined as “Poor”.
The cellulose nanofibers were measured using a thermal analysis instrument THERMO plus TG 8120. A graph in which the vertical axis represents the weight loss ratio and the horizontal axis represents the temperature was drawn, and a temperature at an intersection between a tangent line during a large weight loss and a tangent line before the weight loss was set as a heat decomposition temperature.
The modification degree of hydroxyl groups was calculated from a ratio of an intensity of corresponding characteristic band to an intensity of CH in cellulose ring (Around 1367 cm−1), which are obtained from FT-IR. That is, for example, when a C═O group (around 1736 cm−1) is obtained by modification, the modification degree of hydroxyl groups can be obtained by dividing this strength by the strength of CH.
Cellulose nanofibers having a weight (W1) were dispersed in N,N-dimethylacetamide (SP value: 11.1) to prepare 2 wt % of a dispersion. The dispersion was put into a centrifugal flask to be treated with a centrifuge (HITACHI CR22G III) at 10000 G for 30 minutes. Next, after an upper transparent solvent layer was removed, the weight (W2) of a lower gel layer was measured. Then, a saturated absorptivity was calculated from the following equation.
R=W2/W1×100%
A case where the saturated absorptivity was 5000 mass % to 30000 mass % was determined as “Good”, a case where the saturated absorptivity was 300 mass % to less than 5000 mass % was determined as “Fair”, and a case where the saturated absorptivity was less than 300 mass % was determined as “Poor”.
The molded bodies obtained in the respective Examples and the respective Comparative Examples were measured using the following test methods, and the results thereof are shown in Table 2.
The composite resin composition was pressed into a sheet-like molded body having a thickness of 0.3 mm at 260° C. for 30 seconds, and the external appearance of the sheet-like molded body was observed by visual inspection. A case where the overall color is lighter than DIC color guide DIC-647 was determined as “Good”, and a case where the overall color is deeper than DIC color guide DIC-647 was determined as “Poor”.
The bending strength of the composite resin composition was measured according to ISO 178 using an autograph AG-X PLUS (manufactured by Shimadzu Corporation).
A case where the bending strength was 100 MPa or higher was determined as “Good”, and a case where the bending strength was lower than 100 MPa was determined as “Poor”.
As shown in Table 2, all the molded bodys according to the third embodiment of the present invention obtained in Examples were superior in heat resistance and bending strength.
According to the above-described embodiments, cellulose nanofibers having a superior reinforcing effect can be provided. Moreover, a method for producing the cellulose nanofibers, a composite resin composition containing the cellulose nanofibers, and a molded body formed by molding the composite resin composition can be provided.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2012-223686 | Oct 2012 | JP | national |
This application is a continuation application based on PCT/JP2013/077078, filed on Oct. 4, 2013, claiming priority based on Japanese Patent Application No. 2012-223686, filed in Japan on Oct. 5, 2012. The contents of both the Japanese Patent Application and the PCT Application are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2013/077078 | Oct 2013 | US |
| Child | 14509283 | US |
