JPS6243418A - 反応性高分子組成物 - Google Patents

反応性高分子組成物

Info

Publication number: JPS6243418A
Authority: JP; Japan
Prior art keywords: composition; dialkylamine; epihalohydrin; present; reaction
Prior art date: 1985-08-21
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.): Granted

Application number

JP18444685A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0420931B2 (de

Inventor

Hironobu Fukuzaki

裕延福崎

Takao Okada

隆雄岡田

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.)

Taki Chemical Co Ltd

Original Assignee

Taki Chemical 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.)

1985-08-21

Filing date

1985-08-21

Publication date

1987-02-25

1985-08-21 Application filed by Taki Chemical Co Ltd filed Critical Taki Chemical Co Ltd

1985-08-21 Priority to JP18444685A priority Critical patent/JPS6243418A/ja

1987-02-25 Publication of JPS6243418A publication Critical patent/JPS6243418A/ja

1992-04-07 Publication of JPH0420931B2 publication Critical patent/JPH0420931B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 55
229920000642 polymer Polymers 0.000 title abstract description 13
-1 (meth)acrylic acid aminoalkyl ester Chemical class 0.000 claims abstract description 33
125000005265 dialkylamine group Chemical group 0.000 claims abstract description 17
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 11
229920013730 reactive polymer Polymers 0.000 claims description 11
238000006243 chemical reaction Methods 0.000 abstract description 25
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract description 12
239000010802 sludge Substances 0.000 abstract description 11
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract description 10
230000000694 effects Effects 0.000 abstract description 7
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 4
239000012024 dehydrating agents‎ Substances 0.000 abstract description 4
239000011248 coating agent Substances 0.000 abstract description 2
238000000576 coating method Methods 0.000 abstract description 2
150000001875 compounds Chemical class 0.000 abstract 1
239000002861 polymer material Substances 0.000 abstract 1
239000002994 raw material Substances 0.000 abstract 1
230000018044 dehydration Effects 0.000 description 14
238000006297 dehydration reaction Methods 0.000 description 14
238000000034 method Methods 0.000 description 8
239000000243 solution Substances 0.000 description 7
238000003756 stirring Methods 0.000 description 7
239000003973 paint Substances 0.000 description 6
DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 5
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
229910052794 bromium Inorganic materials 0.000 description 5
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 5
239000007788 liquid Substances 0.000 description 5
239000000178 monomer Substances 0.000 description 5
230000009257 reactivity Effects 0.000 description 5
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
230000007423 decrease Effects 0.000 description 4
SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 3
JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 3
125000002091 cationic group Chemical group 0.000 description 3
GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
229920000620 organic polymer Polymers 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
239000010865 sewage Substances 0.000 description 3
238000004448 titration Methods 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
VIONNPZPKYKMMN-UHFFFAOYSA-N [1-(dimethylamino)-2-methylpropyl] prop-2-enoate Chemical compound C(C=C)(=O)OC(C(C)C)N(C)C VIONNPZPKYKMMN-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000007334 copolymerization reaction Methods 0.000 description 2
239000003431 cross linking reagent Substances 0.000 description 2
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 2
239000000835 fiber Substances 0.000 description 2
229910052740 iodine Inorganic materials 0.000 description 2
239000000047 product Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000126 substance Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
QHVBLSNVXDSMEB-UHFFFAOYSA-N 2-(diethylamino)ethyl prop-2-enoate Chemical compound CCN(CC)CCOC(=O)C=C QHVBLSNVXDSMEB-UHFFFAOYSA-N 0.000 description 1
XUYDVDHTTIQNMB-UHFFFAOYSA-N 3-(diethylamino)propyl prop-2-enoate Chemical compound CCN(CC)CCCOC(=O)C=C XUYDVDHTTIQNMB-UHFFFAOYSA-N 0.000 description 1
HBTKQKFURUBIHW-UHFFFAOYSA-N 4-(diethylamino)butyl prop-2-enoate Chemical compound CCN(CC)CCCCOC(=O)C=C HBTKQKFURUBIHW-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229920001661 Chitosan Polymers 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
241000238557 Decapoda Species 0.000 description 1
229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
XOTCXWQAPVALFW-UHFFFAOYSA-N N,N-dimethylacetamide N-methylmethanamine Chemical compound C(C)(=O)N(C)C.CNC XOTCXWQAPVALFW-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000001253 acrylic acids Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
229920006317 cationic polymer Polymers 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229910001919 chlorite Inorganic materials 0.000 description 1
229910052619 chlorite group Inorganic materials 0.000 description 1
QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
230000006835 compression Effects 0.000 description 1
238000007906 compression Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical class CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
239000011790 ferrous sulphate Substances 0.000 description 1
235000003891 ferrous sulphate Nutrition 0.000 description 1
239000008394 flocculating agent Substances 0.000 description 1
238000004108 freeze drying Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
230000005484 gravity Effects 0.000 description 1
150000003944 halohydrins Chemical class 0.000 description 1
229920006158 high molecular weight polymer Polymers 0.000 description 1
239000010800 human waste Substances 0.000 description 1
230000005660 hydrophilic surface Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
159000000014 iron salts Chemical class 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 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
239000004571 lime Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
125000005395 methacrylic acid group Chemical class 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
UXJXCZLHRLBCLF-UHFFFAOYSA-N n-ethylethanamine;ethyl 2-methylprop-2-enoate Chemical compound CCNCC.CCOC(=O)C(C)=C UXJXCZLHRLBCLF-UHFFFAOYSA-N 0.000 description 1
239000005416 organic matter Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000003504 photosensitizing agent Substances 0.000 description 1
238000000053 physical method Methods 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000001294 propane Substances 0.000 description 1
NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000003507 refrigerant Substances 0.000 description 1
238000007665 sagging Methods 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
DBKCLWTWMFVXQN-UHFFFAOYSA-M sodium sulfuric acid chloride Chemical compound [Na+].[Cl-].OS(O)(=O)=O DBKCLWTWMFVXQN-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
238000010998 test method Methods 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1

Landscapes

Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Macromonomer-Based Addition Polymer (AREA)
Separation Of Suspended Particles By Flocculating Agents (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

JP18444685A 1985-08-21 1985-08-21 反応性高分子組成物 Granted JPS6243418A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP18444685A JPS6243418A (ja)	1985-08-21	1985-08-21	反応性高分子組成物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP18444685A JPS6243418A (ja)	1985-08-21	1985-08-21	反応性高分子組成物

Publications (2)

Publication Number	Publication Date
JPS6243418A true JPS6243418A (ja)	1987-02-25
JPH0420931B2 JPH0420931B2 (de)	1992-04-07

Family

ID=16153288

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP18444685A Granted JPS6243418A (ja)	1985-08-21	1985-08-21	反応性高分子組成物

Country Status (1)

Country	Link
JP (1)	JPS6243418A (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2012219173A (ja) *	2011-04-07	2012-11-12	Mitsui Chemicals Inc	ポリアクリルアミド系吸水性ポリマー及びその製造方法

1985
- 1985-08-21 JP JP18444685A patent/JPS6243418A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2012219173A (ja) *	2011-04-07	2012-11-12	Mitsui Chemicals Inc	ポリアクリルアミド系吸水性ポリマー及びその製造方法

Also Published As

Publication number	Publication date
JPH0420931B2 (de)	1992-04-07

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JPH03203916A (ja)	1991-09-05	３―メタクリロイルオキシ―２―ヒドロキシプロピルトリメチルアンモニウムクロリドモノマーとビニルモノマーのコポリマー
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CN1122051C (zh)	2003-09-24	室温聚合高吸水树脂的合成方法
JPH0420931B2 (de)	1992-04-07
JPS58154708A (ja)	1983-09-14	高吸水性樹脂の製造方法
US5525692A (en)	1996-06-11	Dewatering agent for sludge
JPH08283349A (ja)	1996-10-29	両性高分子凝集剤
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JP3565415B2 (ja)	2004-09-15	水溶性重合体の製造方法

JPS6243418A - 反応性高分子組成物 - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=16153288

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Also Published As

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