JPS62280B2 - - Google Patents

Info

Publication number: JPS62280B2
Authority: JP; Japan
Prior art keywords: acrylamide; monomer; acrylonitrile; monomers; paper strength
Prior art date: 1977-05-27
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

JP52061000A

Other languages

English (en)

Japanese (ja)

Other versions

JPS53147804A (en

Inventor

Einosuke Higashimura

Ichiro Watanabe

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.)

Nitto Chemical Industry Co Ltd

Original Assignee

Nitto Chemical Industry 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.)

1977-05-27

Filing date

1977-05-27

Publication date

1987-01-07

1977-05-27 Application filed by Nitto Chemical Industry Co Ltd filed Critical Nitto Chemical Industry Co Ltd

1977-05-27 Priority to JP6100077A priority Critical patent/JPS53147804A/ja

1978-12-22 Publication of JPS53147804A publication Critical patent/JPS53147804A/ja

1987-01-07 Publication of JPS62280B2 publication Critical patent/JPS62280B2/ja

Status Granted legal-status Critical Current

Links

HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 78
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 39
239000000178 monomer Substances 0.000 claims description 38
241000894006 Bacteria Species 0.000 claims description 37
102000004190 Enzymes Human genes 0.000 claims description 27
108090000790 Enzymes Proteins 0.000 claims description 27
229920000642 polymer Polymers 0.000 claims description 23
239000013054 paper strength agent Substances 0.000 claims description 17
229920001577 copolymer Polymers 0.000 claims description 16
239000003623 enhancer Substances 0.000 claims description 14
229920002401 polyacrylamide Polymers 0.000 claims description 9
241000186361 Actinobacteria <class> Species 0.000 claims description 7
238000006243 chemical reaction Methods 0.000 claims description 7
239000004480 active ingredient Substances 0.000 claims description 4
241001446247 uncultured actinomycete Species 0.000 claims 2
239000000123 paper Substances 0.000 description 30
238000000034 method Methods 0.000 description 18
239000000047 product Substances 0.000 description 15
238000006116 polymerization reaction Methods 0.000 description 11
230000001580 bacterial effect Effects 0.000 description 10
239000000243 solution Substances 0.000 description 10
239000007864 aqueous solution Substances 0.000 description 9
239000011347 resin Substances 0.000 description 8
229920005989 resin Polymers 0.000 description 8
230000000694 effects Effects 0.000 description 7
238000003756 stirring Methods 0.000 description 7
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 5
238000000354 decomposition reaction Methods 0.000 description 5
239000000203 mixture Substances 0.000 description 5
-1 vinyl compound Chemical class 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
239000012736 aqueous medium Substances 0.000 description 4
238000010790 dilution Methods 0.000 description 4
239000012895 dilution Substances 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000012263 liquid product Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
229920006322 acrylamide copolymer Polymers 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
230000009467 reduction Effects 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
MTPJEFOSTIKRSS-UHFFFAOYSA-N 3-(dimethylamino)propanenitrile Chemical compound CN(C)CCC#N MTPJEFOSTIKRSS-UHFFFAOYSA-N 0.000 description 2
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
241001467565 Microbacterium imperiale Species 0.000 description 2
241000187654 Nocardia Species 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 2
229910001870 ammonium persulfate Inorganic materials 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
238000007334 copolymerization reaction Methods 0.000 description 2
230000000593 degrading effect Effects 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
238000007865 diluting Methods 0.000 description 2
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 2
FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
125000005670 ethenylalkyl group Chemical group 0.000 description 2
238000000605 extraction Methods 0.000 description 2
238000005259 measurement Methods 0.000 description 2
150000002825 nitriles Chemical class 0.000 description 2
239000003505 polymerization initiator Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000011002 quantification Methods 0.000 description 2
238000004513 sizing Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
150000003460 sulfonic acids Chemical class 0.000 description 2
NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 2
VKKTUDKKYOOLGG-UHFFFAOYSA-N 1-(diethylamino)propan-1-ol Chemical compound CCC(O)N(CC)CC VKKTUDKKYOOLGG-UHFFFAOYSA-N 0.000 description 1
CBQFBEBEBCHTBK-UHFFFAOYSA-N 1-phenylprop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)C(C=C)C1=CC=CC=C1 CBQFBEBEBCHTBK-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
VMSBGXAJJLPWKV-UHFFFAOYSA-N 2-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=C VMSBGXAJJLPWKV-UHFFFAOYSA-N 0.000 description 1
QENRKQYUEGJNNZ-UHFFFAOYSA-N 2-methyl-1-(prop-2-enoylamino)propane-1-sulfonic acid Chemical compound CC(C)C(S(O)(=O)=O)NC(=O)C=C QENRKQYUEGJNNZ-UHFFFAOYSA-N 0.000 description 1
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
241000590020 Achromobacter Species 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
241000588986 Alcaligenes Species 0.000 description 1
241000193830 Bacillus <bacterium> Species 0.000 description 1
241000186146 Brevibacterium Species 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
241000186216 Corynebacterium Species 0.000 description 1
201000004624 Dermatitis Diseases 0.000 description 1
239000002211 L-ascorbic acid Substances 0.000 description 1
235000000069 L-ascorbic acid Nutrition 0.000 description 1
241000192041 Micrococcus Species 0.000 description 1
208000028389 Nerve injury Diseases 0.000 description 1
241000589516 Pseudomonas Species 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
241000589634 Xanthomonas Species 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
125000005263 alkylenediamine group Chemical group 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
229960005070 ascorbic acid Drugs 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000007869 azo polymerization initiator Substances 0.000 description 1
238000010009 beating Methods 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
230000007423 decrease Effects 0.000 description 1
DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
229940008406 diethyl sulfate Drugs 0.000 description 1
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
230000002255 enzymatic effect Effects 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
235000003891 ferrous sulphate Nutrition 0.000 description 1
239000011790 ferrous sulphate Substances 0.000 description 1
239000008394 flocculating agent Substances 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
229920006158 high molecular weight polymer Polymers 0.000 description 1
MHAJPDPJQMAIIY-UHFFFAOYSA-M hydroperoxide group Chemical group [O-]O MHAJPDPJQMAIIY-UHFFFAOYSA-M 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000003999 initiator Substances 0.000 description 1
BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
239000002655 kraft paper Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
238000012704 multi-component copolymerization Methods 0.000 description 1
230000008764 nerve damage Effects 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
230000007096 poisonous effect Effects 0.000 description 1
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
230000002265 prevention Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000000746 purification Methods 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000012966 redox initiator Substances 0.000 description 1
238000007717 redox polymerization reaction Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
239000012488 sample solution Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
238000011282 treatment Methods 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
230000002747 voluntary effect Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1
235000020681 well water Nutrition 0.000 description 1
239000002349 well water Substances 0.000 description 1

Landscapes

Paper (AREA)

JP6100077A 1977-05-27 1977-05-27 Novel paper strength enhancing agent and paper making method by using said agent Granted JPS53147804A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP6100077A JPS53147804A (en)	1977-05-27	1977-05-27	Novel paper strength enhancing agent and paper making method by using said agent

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP6100077A JPS53147804A (en)	1977-05-27	1977-05-27	Novel paper strength enhancing agent and paper making method by using said agent

Publications (2)

Publication Number	Publication Date
JPS53147804A JPS53147804A (en)	1978-12-22
JPS62280B2 true JPS62280B2 (ko)	1987-01-07

Family

ID=13158651

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP6100077A Granted JPS53147804A (en)	1977-05-27	1977-05-27	Novel paper strength enhancing agent and paper making method by using said agent

Country Status (1)

Country	Link
JP (1)	JPS53147804A (ko)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2903852A1 (de) *	1979-02-01	1980-08-14	Bayer Ag	Mikrobiologischer abbau von acrylnitril in waessrigen dispersionen
CA2066378C (en) *	1991-04-24	2000-09-19	David J. Hardman	Dehalogenation of organohalogen-containing compounds
JP6943047B2 (ja) *	2016-07-12	2021-09-29	荒川化学工業株式会社	紙力増強剤の製造方法、および紙の製造方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5040689A (ko) *	1973-06-29	1975-04-14
JPS50155706A (ko) *	1974-06-05	1975-12-16
JPS51144777A (en) *	1975-06-07	1976-12-13	Tadashi Arai	A method for degrading acrylamide monomer by the use of bacteria

1977
- 1977-05-27 JP JP6100077A patent/JPS53147804A/ja active Granted

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5040689A (ko) *	1973-06-29	1975-04-14
JPS50155706A (ko) *	1974-06-05	1975-12-16
JPS51144777A (en) *	1975-06-07	1976-12-13	Tadashi Arai	A method for degrading acrylamide monomer by the use of bacteria

Also Published As

Publication number	Publication date
JPS53147804A (en)	1978-12-22

Publication	Publication Date	Title
CA1294721C (en)	1992-01-21	Paper size based on finely divided aqueous dispersions
EP1309636B1 (de)	2006-12-06	Stärkehaltige polymerdispersionen
CO4440536A1 (es)	1997-05-07	Metodo para la preparacion de una dispersion acuosa de poli- mero
KR970703373A (ko)	1997-07-03	중합체 수분산액의 제조 방법(Method of Producing an Aqueous Polymer Dispersion)
JPS61211319A (ja)	1986-09-19	陽イオン性グラフトでん粉共重合体
EP0494554B1 (fr)	1995-03-15	Nouveaux copolymères cationiques, de nouvelles émulsions et leur application
EP0118327B1 (fr)	1987-04-22	Latex cationiques de copolymères à base de diènes conjugués
JPS5968315A (ja)	1984-04-18	第四級アンモニウムモノマ−のホモポリマ−及びコポリマ−の製造法
CN104098747A (zh)	2014-10-15	一种荧光消除剂的制备方法
JP2001525892A (ja)	2001-12-11	紙、板紙および厚紙の乾燥強度を増加させるための薬剤としての加水分解されたｎ―ビニルカルボン酸アミドポリマーの使用
JPS62280B2 (ko)	1987-01-07
TW438843B (en)	2001-06-07	Bipopulated latex of vinyl chloride copolymers, process for the manufacture thereof and applications thereof
JPH06299494A (ja)	1994-10-25	製紙用サイズ剤組成物およびそれを用いる紙の製造方法
US4306045A (en)	1981-12-15	Process for producing acrylamide polymers
JPH11502575A (ja)	1999-03-02	紙サイズ剤混合物
GB766534A (en)	1957-01-23	New copolymers of acrylonitrile and process of preparing them
JP3452505B2 (ja)	2003-09-29	抄紙用粘剤、抄紙方法および紙
EP0645429A1 (fr)	1995-03-29	Dispersions eau dans huile épaississantes, leur procédé de préparation et leur application en impression textile
JP4675471B2 (ja)	2011-04-20	Ｎ−ビニルカルボン酸アミド系共重合体の製造方法および得られたｎ−ビニルカルボン酸アミド系共重合体の用途
JPS5845730A (ja)	1983-03-17	置換コハク酸無水物の水性分散液、その製造方法、及び該置換コハク酸無水物の水性分散液からなる製紙用サイズ剤
JP2622965B2 (ja)	1997-06-25	製紙用添加剤
US4950748A (en)	1990-08-21	Polysaccharides
JPH08512352A (ja)	1996-12-24	ポリマーからニトリル基含有不純物を除去するための方法
US5538723A (en)	1996-07-23	Method for suppressing the viscosity of bioinsecticide slurries and related slurries
GB910136A (en)	1962-11-07	Acrylonitrile and methacrylonitrile copolymers