JPH0129361B2 - - Google Patents

Info

Publication number: JPH0129361B2
Authority: JP; Japan
Prior art keywords: reaction; cellulose material; anhydride; powder; cellulose
Prior art date: 1983-12-27
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

JP24469483A

Other languages

English (en)

Japanese (ja)

Other versions

JPS60137901A (ja

Inventor

Minoru Ueda

Hideaki Matsuda

Noryuki Myoshi

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Okura Industrial Co Ltd

Original Assignee

Okura Industrial Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-12-27

Filing date

1983-12-27

Publication date

1989-06-09

1983-12-27 Application filed by Okura Industrial Co Ltd filed Critical Okura Industrial Co Ltd

1983-12-27 Priority to JP24469483A priority Critical patent/JPS60137901A/ja

1985-07-22 Publication of JPS60137901A publication Critical patent/JPS60137901A/ja

1989-06-09 Publication of JPH0129361B2 publication Critical patent/JPH0129361B2/ja

Status Granted legal-status Critical Current

Links

239000000463 material Substances 0.000 claims description 56
239000001913 cellulose Substances 0.000 claims description 55
229920002678 cellulose Polymers 0.000 claims description 55
238000006243 chemical reaction Methods 0.000 claims description 42
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 28
150000008065 acid anhydrides Chemical class 0.000 claims description 20
150000007519 polyprotic acids Polymers 0.000 claims description 20
239000002904 solvent Substances 0.000 claims description 9
238000004519 manufacturing process Methods 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
239000000843 powder Substances 0.000 description 25
241000209094 Oryza Species 0.000 description 15
235000007164 Oryza sativa Nutrition 0.000 description 15
238000005886 esterification reaction Methods 0.000 description 15
235000009566 rice Nutrition 0.000 description 15
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 13
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 12
239000010902 straw Substances 0.000 description 12
239000003054 catalyst Substances 0.000 description 9
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 9
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 8
238000003756 stirring Methods 0.000 description 8
229940014800 succinic anhydride Drugs 0.000 description 8
229910000029 sodium carbonate Inorganic materials 0.000 description 6
230000032050 esterification Effects 0.000 description 5
238000010438 heat treatment Methods 0.000 description 5
238000005979 thermal decomposition reaction Methods 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
239000007795 chemical reaction product Substances 0.000 description 4
238000001035 drying Methods 0.000 description 4
239000000203 mixture Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
238000005406 washing Methods 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
239000002154 agricultural waste Substances 0.000 description 3
-1 linters Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000010893 paper waste Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
238000004566 IR spectroscopy Methods 0.000 description 2
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
241000209140 Triticum Species 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
239000003431 cross linking reagent Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000002699 waste material Substances 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
HEGLMCPFDADCAQ-UHFFFAOYSA-N 4,7-dichloro-2-benzofuran-1,3-dione Chemical compound ClC1=CC=C(Cl)C2=C1C(=O)OC2=O HEGLMCPFDADCAQ-UHFFFAOYSA-N 0.000 description 1
ULSOWUBMELTORB-UHFFFAOYSA-N 5,6-dichloro-2-benzofuran-1,3-dione Chemical compound C1=C(Cl)C(Cl)=CC2=C1C(=O)OC2=O ULSOWUBMELTORB-UHFFFAOYSA-N 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
QHWKHLYUUZGSCW-UHFFFAOYSA-N Tetrabromophthalic anhydride Chemical compound BrC1=C(Br)C(Br)=C2C(=O)OC(=O)C2=C1Br QHWKHLYUUZGSCW-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
125000004018 acid anhydride group Chemical group 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
239000004566 building material Substances 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
238000012993 chemical processing Methods 0.000 description 1
239000003245 coal Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
230000007423 decrease Effects 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
239000002657 fibrous material Substances 0.000 description 1
238000009408 flooring Methods 0.000 description 1
ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
239000011487 hemp Substances 0.000 description 1
238000007731 hot pressing Methods 0.000 description 1
239000010903 husk Substances 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
239000002440 industrial waste Substances 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
238000012545 processing Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000002522 swelling effect Effects 0.000 description 1
SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
230000004580 weight loss Effects 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1

Landscapes

Polysaccharides And Polysaccharide Derivatives (AREA)

JP24469483A 1983-12-27 1983-12-27 カルボキシル基含有セルロ−ス材料の製造方法 Granted JPS60137901A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP24469483A JPS60137901A (ja)	1983-12-27	1983-12-27	カルボキシル基含有セルロ−ス材料の製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP24469483A JPS60137901A (ja)	1983-12-27	1983-12-27	カルボキシル基含有セルロ−ス材料の製造方法

Publications (2)

Publication Number	Publication Date
JPS60137901A JPS60137901A (ja)	1985-07-22
JPH0129361B2 true JPH0129361B2 (ru)	1989-06-09

Family

ID=17122543

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP24469483A Granted JPS60137901A (ja)	1983-12-27	1983-12-27	カルボキシル基含有セルロ−ス材料の製造方法

Country Status (1)

Country	Link
JP (1)	JPS60137901A (ru)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2006316191A (ja) *	2005-05-13	2006-11-24	National Institute Of Advanced Industrial & Technology	セルロース系高分子の選別除去方法および装置
US7772391B2 (en) *	2005-06-16	2010-08-10	The Procter & Gamble Company	Ethersuccinylated hydroxyl polymers
JP5757779B2 (ja) *	2011-04-27	2015-07-29	国立大学法人京都大学	樹脂組成物
JP5828288B2 (ja) *	2011-08-08	2015-12-02	王子ホールディングス株式会社	微細繊維状セルロースの製造方法、不織布の製造方法、微細繊維状セルロース、微細繊維状セルロース含有スラリー、不織布、および複合体
JP7350570B2 (ja) *	2019-08-29	2023-09-26	大阪瓦斯株式会社	修飾セルロースナノファイバーおよびその製造方法

1983
- 1983-12-27 JP JP24469483A patent/JPS60137901A/ja active Granted

Also Published As

Publication number	Publication date
JPS60137901A (ja)	1985-07-22

Publication	Publication Date	Title
Thiebaud et al.	1995	Solvent-free wood esterification with fatty acid chlorides
US6605715B1 (en)	2003-08-12	Process for the preparation of a starch ester
US5693786A (en)	1997-12-02	Esterfied, polyester-grafted starch
Mayumi et al.	2006	Partial substitution of cellulose by ring‐opening esterification of cyclic esters in a homogeneous system
US5639865A (en)	1997-06-17	Thermoplastic biodegradable polysaccharide derivatives, process for the manufacture thereof and use thereof
US4048435A (en)	1977-09-13	Method for the preparation of highly substituted granular starches
JPH0129361B2 (ru)	1989-06-09
US4480091A (en)	1984-10-30	Process for preparing cellulose sulfate esters
Gardea-Hernández et al.	2008	Fast wood fiber esterification. I. Reaction with oxalic acid and cetyl alcohol
JPH0337490B2 (ru)	1991-06-05
US6160111A (en)	2000-12-12	Process for preparing cellulose esters using a sulfonic acid resin catalyst
US3535308A (en)	1970-10-20	Process for the preparation of partially esterified polyhydroxylic polymers
JPS6146001B2 (ru)	1986-10-11
JPH0436844B2 (ru)	1992-06-17
JPH0358881B2 (ru)	1991-09-06
US3634395A (en)	1972-01-11	Preparation of starch derivatives containing both carboxyl and carbonyl groups
US2862922A (en)	1958-12-02	Method of making sodium cellulose sulfate
US3479336A (en)	1969-11-18	Production of cellulose esters from particulate lignocellulosic material
US3045006A (en)	1962-07-17	Preparation of cellulose derivatives
JP2657244B2 (ja)	1997-09-24	化学修飾木質材の製造方法
US2399455A (en)	1946-04-30	Process for preparing starch acetate
JP2646307B2 (ja)	1997-08-27	熱流動性に優れた化学的変性木質材の製造方法
JP2640604B2 (ja)	1997-08-13	化学修飾木質材の製造法
US3554775A (en)	1971-01-12	Production of cellulose esters
JP2636072B2 (ja)	1997-07-30	熱流動性に優れた熱可塑性木質材組成物の製造方法