CA2110366A1 - Polyvinylamines quaternarisees pour sequestrants - Google Patents

Polyvinylamines quaternarisees pour sequestrants

Info

Publication number: CA2110366A1
Authority: CA; Canada
Prior art keywords: polymer; polyvinylamine; retention; quaternized; grams
Prior art date: 1993-01-04
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.): Abandoned

Application number

CA 2110366

Other languages

English (en)

Inventor

John C. Harrington, Iv

Jen-Chi Chen

Fu Chen

Michael A. Schuster

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.)

Veolia WTS USA Inc

Original Assignee

Betz Laboratories Inc

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.)

1993-01-04

Filing date

1993-11-30

Publication date

1994-07-05

1993-11-30 Application filed by Betz Laboratories Inc filed Critical Betz Laboratories Inc

1994-07-05 Publication of CA2110366A1 publication Critical patent/CA2110366A1/fr

Status Abandoned legal-status Critical Current

Links

230000014759 maintenance of location Effects 0.000 title claims abstract description 31
238000000034 method Methods 0.000 claims description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
125000000129 anionic group Chemical group 0.000 claims description 9
150000001450 anions Chemical class 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims 1
229920000642 polymer Polymers 0.000 description 45
239000000243 solution Substances 0.000 description 19
239000007787 solid Substances 0.000 description 12
239000000701 coagulant Substances 0.000 description 10
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 9
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 8
ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 8
238000005956 quaternization reaction Methods 0.000 description 8
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
125000002091 cationic group Chemical group 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
239000000463 material Substances 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 5
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 4
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
238000009833 condensation Methods 0.000 description 4
230000005494 condensation Effects 0.000 description 4
239000008367 deionised water Substances 0.000 description 4
229910021641 deionized water Inorganic materials 0.000 description 4
230000009977 dual effect Effects 0.000 description 4
230000007246 mechanism Effects 0.000 description 4
229940050176 methyl chloride Drugs 0.000 description 4
238000012360 testing method Methods 0.000 description 4
NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 3
LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
239000000654 additive Substances 0.000 description 2
-1 amine salts Chemical class 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000003999 initiator Substances 0.000 description 2
239000000203 mixture Substances 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
230000008569 process Effects 0.000 description 2
238000004448 titration Methods 0.000 description 2
238000004834 15N NMR spectroscopy Methods 0.000 description 1
208000030507 AIDS Diseases 0.000 description 1
102100022704 Amyloid-beta precursor protein Human genes 0.000 description 1
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
101000823051 Homo sapiens Amyloid-beta precursor protein Proteins 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
229920006322 acrylamide copolymer Polymers 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
DZHSAHHDTRWUTF-SIQRNXPUSA-N amyloid-beta polypeptide 42 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 DZHSAHHDTRWUTF-SIQRNXPUSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
235000011089 carbon dioxide Nutrition 0.000 description 1
229960004424 carbon dioxide Drugs 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000008394 flocculating agent Substances 0.000 description 1
239000013538 functional additive Substances 0.000 description 1
239000011121 hardwood Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
230000006872 improvement Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000011707 mineral Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
229940088417 precipitated calcium carbonate Drugs 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000003134 recirculating effect Effects 0.000 description 1
IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000004513 sizing Methods 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000011122 softwood Substances 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
238000010998 test method Methods 0.000 description 1
229950003937 tolonium Drugs 0.000 description 1
HNONEKILPDHFOL-UHFFFAOYSA-M tolonium chloride Chemical compound [Cl-].C1=C(C)C(N)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 HNONEKILPDHFOL-UHFFFAOYSA-M 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1

Landscapes

Paper (AREA)

CA 2110366 1993-01-04 1993-11-30 Polyvinylamines quaternarisees pour sequestrants Abandoned CA2110366A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US42293A	1993-01-04	1993-01-04
US08,000,422		1993-01-04

Publications (1)

Publication Number	Publication Date
CA2110366A1 true CA2110366A1 (fr)	1994-07-05

Family

ID=21691470

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2110366 Abandoned CA2110366A1 (fr)	1993-01-04	1993-11-30	Polyvinylamines quaternarisees pour sequestrants

Country Status (1)

Country	Link
CA (1)	CA2110366A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US8771578B2 (en)	2007-04-17	2014-07-08	Kemira Chemicals, Inc.	Acidified polyamidoamine adhesives, method of manufacture, and use for creping and ply bond applications
CN105754022A (zh) *	2016-03-15	2016-07-13	福州大学	3-乙烯胺基-2-羟丙基三甲基氯化铵共聚物及其制备和应用

1993
- 1993-11-30 CA CA 2110366 patent/CA2110366A1/fr not_active Abandoned

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US8771578B2 (en)	2007-04-17	2014-07-08	Kemira Chemicals, Inc.	Acidified polyamidoamine adhesives, method of manufacture, and use for creping and ply bond applications
CN105754022A (zh) *	2016-03-15	2016-07-13	福州大学	3-乙烯胺基-2-羟丙基三甲基氯化铵共聚物及其制备和应用

Legal Events

Date	Code	Title	Description
2000-11-30	FZDE	Dead

Publication	Publication Date	Title
US8518215B2 (en)	2013-08-27	Quaternary vinylamine-containing polymers as additives in papermaking
US4749444A (en)	1988-06-07	Production of paper and cardboard
US6071379A (en)	2000-06-06	Papermaking process utilizing hydrophilic dispersion polymers of diallyldimethyl ammonium chloride and acrylamide as retention and drainage aids
AU2003211701B2 (en)	2007-09-06	Water-soluble polymer dispersion, process for producing the same and method of use therefor
EP2820189B2 (fr)	2024-05-15	Procédé de fabrication de papier et de carton
US5324787A (en)	1994-06-28	Modification of poly (vinylamine)
US20150299961A1 (en)	2015-10-22	Modified vinylamine containing polymers and their use in papermaking
AU2012242609B2 (en)	2015-06-11	Process to produce an acylated vinylamine-containing polymer and its application as a papermaking additive
US3976824A (en)	1976-08-24	Treating agent useful for fibrous materials and preparation thereof
US9303359B2 (en)	2016-04-05	Method for manufacturing paper using a cationic polymer obtained by hofmann degradation
CA2110365A1 (fr)	1994-07-05	Polyvinylamines quaternarisees pour la clarification de l'eau dans un procede de desencrage
JP4238945B2 (ja)	2009-03-18	製紙用添加剤および紙の製造方法
CA2110366A1 (fr)	1994-07-05	Polyvinylamines quaternarisees pour sequestrants
AU2025203271A1 (en)	2025-05-29	Method for the hydrolysis of a polymer
EP1082493B1 (fr)	2005-03-23	Procede de fabrication de papier utilisant des polymeres a dispersion hydrophile de chlorure d'ammonium diallyldimethyle et d'acrylamide comme auxiliaires de retention et d'egouttage
US5382324A (en)	1995-01-17	Method for enhancing paper strength
JP3291506B2 (ja)	2002-06-10	製紙用薬剤
JP7634831B2 (ja)	2025-02-25	歩留向上システムを用いた抄紙方法
JP3092694B2 (ja)	2000-09-25	填料歩留り向上剤
JPS6363678B2 (fr)	1988-12-08
CA1276376C (fr)	1990-11-13	Polymeres, et leur production
JP2983713B2 (ja)	1999-11-29	紙力増強剤
CA1278904C (fr)	1991-01-15	Papier a forte resistance a l'etat humide, et sa fabrication
JP3294015B2 (ja)	2002-06-17	中性サイズ定着剤
EP0245702A2 (fr)	1987-11-19	Polymères, papier ayant une résistance élevée à l'état humide et leurs procédés de préparation

CA2110366A1 - Polyvinylamines quaternarisees pour sequestrants - Google Patents

Info

Links

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=21691470

Family Applications (1)

Country Status (1)

Cited By (2)

Cited By (2)

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Legal Events