GB812140A - Improvements in linear copolymers - Google Patents
Improvements in linear copolymersInfo
- Publication number
- GB812140A GB812140A GB18486/55A GB1848655A GB812140A GB 812140 A GB812140 A GB 812140A GB 18486/55 A GB18486/55 A GB 18486/55A GB 1848655 A GB1848655 A GB 1848655A GB 812140 A GB812140 A GB 812140A
- Authority
- GB
- United Kingdom
- Prior art keywords
- copolymer
- group
- quaternary ammonium
- aminolysis
- polymers
- Prior art date
- 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
Links
- 229920005684 linear copolymer Polymers 0.000 title 1
- 229920001577 copolymer Polymers 0.000 abstract 18
- 229920000642 polymer Polymers 0.000 abstract 10
- 238000007098 aminolysis reaction Methods 0.000 abstract 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 6
- 150000001412 amines Chemical class 0.000 abstract 6
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 4
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract 4
- 125000002947 alkylene group Chemical group 0.000 abstract 4
- 238000005956 quaternization reaction Methods 0.000 abstract 4
- -1 vinyl aromatic hydrocarbons Chemical class 0.000 abstract 4
- 229920002319 Poly(methyl acrylate) Polymers 0.000 abstract 3
- 229940100198 alkylating agent Drugs 0.000 abstract 3
- 239000002168 alkylating agent Substances 0.000 abstract 3
- 239000002216 antistatic agent Substances 0.000 abstract 3
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 abstract 3
- 239000000463 material Substances 0.000 abstract 3
- 150000002734 metacrylic acid derivatives Chemical class 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 abstract 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 2
- 240000000111 Saccharum officinarum Species 0.000 abstract 2
- 235000007201 Saccharum officinarum Nutrition 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 238000007792 addition Methods 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 239000004927 clay Substances 0.000 abstract 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000000284 extract Substances 0.000 abstract 2
- 230000000855 fungicidal effect Effects 0.000 abstract 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 102000004169 proteins and genes Human genes 0.000 abstract 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- 239000000454 talc Substances 0.000 abstract 2
- 229910052623 talc Inorganic materials 0.000 abstract 2
- 125000000391 vinyl group Chemical class [H]C([*])=C([H])[H] 0.000 abstract 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 1
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- HYQMXMHBGXBEHS-UHFFFAOYSA-N 1-chlorononylbenzene Chemical compound CCCCCCCCC(Cl)C1=CC=CC=C1 HYQMXMHBGXBEHS-UHFFFAOYSA-N 0.000 abstract 1
- MIOZXHSALLZYTG-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]ethanamine Chemical compound CN(C)CCOCCN MIOZXHSALLZYTG-UHFFFAOYSA-N 0.000 abstract 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 abstract 1
- UIKUBYKUYUSRSM-UHFFFAOYSA-N 3-morpholinopropylamine Chemical compound NCCCN1CCOCC1 UIKUBYKUYUSRSM-UHFFFAOYSA-N 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- RIQDFVDDFSZOCO-UHFFFAOYSA-N N',N'-bis(2-butoxyethyl)ethane-1,2-diamine Chemical compound C(CCC)OCCN(CCOCCCC)CCN RIQDFVDDFSZOCO-UHFFFAOYSA-N 0.000 abstract 1
- 239000004677 Nylon Substances 0.000 abstract 1
- 239000004902 Softening Agent Substances 0.000 abstract 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- 239000006096 absorbing agent Substances 0.000 abstract 1
- 238000009825 accumulation Methods 0.000 abstract 1
- 150000003926 acrylamides Chemical class 0.000 abstract 1
- 150000008360 acrylonitriles Chemical class 0.000 abstract 1
- 230000004931 aggregating effect Effects 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 235000011114 ammonium hydroxide Nutrition 0.000 abstract 1
- 238000004873 anchoring Methods 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 239000003899 bactericide agent Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- 230000000536 complexating effect Effects 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 239000000835 fiber Substances 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 239000008394 flocculating agent Substances 0.000 abstract 1
- 230000003311 flocculating effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 150000002485 inorganic esters Chemical class 0.000 abstract 1
- 150000002500 ions Chemical class 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- 239000012528 membrane Substances 0.000 abstract 1
- ATVQWEFDRXEDFX-UHFFFAOYSA-N n',n'-dimethyldecane-1,10-diamine Chemical compound CN(C)CCCCCCCCCCN ATVQWEFDRXEDFX-UHFFFAOYSA-N 0.000 abstract 1
- DILRJUIACXKSQE-UHFFFAOYSA-N n',n'-dimethylethane-1,2-diamine Chemical compound CN(C)CCN DILRJUIACXKSQE-UHFFFAOYSA-N 0.000 abstract 1
- NXBBFAKHXAMPOM-UHFFFAOYSA-N n,n-dimethylprop-1-en-1-amine Chemical group CC=CN(C)C NXBBFAKHXAMPOM-UHFFFAOYSA-N 0.000 abstract 1
- CIIXPUZIJPZIOO-UHFFFAOYSA-N n-butyl-n',n'-dimethylethane-1,2-diamine Chemical compound CCCCNCCN(C)C CIIXPUZIJPZIOO-UHFFFAOYSA-N 0.000 abstract 1
- 229920001778 nylon Polymers 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 230000001172 regenerating effect Effects 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 230000003068 static effect Effects 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- 229920002994 synthetic fiber Polymers 0.000 abstract 1
- 229920001567 vinyl ester resin Chemical class 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/44—Preparation of metal salts or ammonium salts
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US812140XA | 1954-07-06 | 1954-07-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB812140A true GB812140A (en) | 1959-04-22 |
Family
ID=22162788
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB18486/55A Expired GB812140A (en) | 1954-07-06 | 1955-06-27 | Improvements in linear copolymers |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE539555A (enrdf_load_stackoverflow) |
| DE (1) | DE1061076B (enrdf_load_stackoverflow) |
| GB (1) | GB812140A (enrdf_load_stackoverflow) |
| NL (1) | NL91808C (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5496104A (en) * | 1978-01-10 | 1979-07-30 | Rei Tech Inc | Neutral paper making method |
| GB2171108A (en) * | 1982-12-23 | 1986-08-20 | Procter & Gamble | Detergent compositions |
| US4664848A (en) | 1982-12-23 | 1987-05-12 | The Procter & Gamble Company | Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3842201C1 (enrdf_load_stackoverflow) * | 1988-12-15 | 1990-05-03 | Th. Goldschmidt Ag, 4300 Essen, De | |
| DE3842202C1 (enrdf_load_stackoverflow) * | 1988-12-15 | 1990-05-03 | Th. Goldschmidt Ag, 4300 Essen, De | |
| DE102004009930B4 (de) * | 2004-02-26 | 2008-07-24 | Schott Ag | Blei- und arsenfreie optische Lanthan-Flint-Gläser sowie deren Verwendung |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2582194A (en) * | 1946-02-19 | 1952-01-08 | American Cyanamid Co | Anion exchange resins which are polyamine-polyacrylate reaction products |
| US2484420A (en) * | 1946-12-31 | 1949-10-11 | Eastman Kodak Co | Process of preparing quaternized salts of resinous organic polymers containing a basic tertiary nitrogen atom |
-
0
- BE BE539555D patent/BE539555A/xx unknown
- NL NL91808D patent/NL91808C/xx active
-
1955
- 1955-06-27 GB GB18486/55A patent/GB812140A/en not_active Expired
- 1955-07-04 DE DER16961A patent/DE1061076B/de active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5496104A (en) * | 1978-01-10 | 1979-07-30 | Rei Tech Inc | Neutral paper making method |
| GB2171108A (en) * | 1982-12-23 | 1986-08-20 | Procter & Gamble | Detergent compositions |
| US4664848A (en) | 1982-12-23 | 1987-05-12 | The Procter & Gamble Company | Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties |
Also Published As
| Publication number | Publication date |
|---|---|
| BE539555A (enrdf_load_stackoverflow) | |
| NL91808C (enrdf_load_stackoverflow) | |
| DE1061076B (de) | 1959-07-09 |
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