JPS6160841B2 - - Google Patents
Info
- Publication number
- JPS6160841B2 JPS6160841B2 JP8194678A JP8194678A JPS6160841B2 JP S6160841 B2 JPS6160841 B2 JP S6160841B2 JP 8194678 A JP8194678 A JP 8194678A JP 8194678 A JP8194678 A JP 8194678A JP S6160841 B2 JPS6160841 B2 JP S6160841B2
- Authority
- JP
- Japan
- Prior art keywords
- polymerization
- acrylamide
- amount
- peroxide
- aqueous solution
- 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
- 238000006116 polymerization reaction Methods 0.000 claims description 33
- 239000000178 monomer Substances 0.000 claims description 17
- 150000002978 peroxides Chemical class 0.000 claims description 16
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 12
- -1 azo compound Chemical class 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 230000000379 polymerizing effect Effects 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 13
- 239000003999 initiator Substances 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 230000007774 longterm Effects 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229920002401 polyacrylamide Polymers 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000008394 flocculating agent Substances 0.000 description 3
- 230000006698 induction Effects 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 239000012966 redox initiator Substances 0.000 description 3
- 150000003839 salts Chemical group 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 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 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- BLKRGXCGFRXRNQ-SNAWJCMRSA-N (z)-3-carbonoperoxoyl-4,4-dimethylpent-2-enoic acid Chemical compound OC(=O)/C=C(C(C)(C)C)\C(=O)OO BLKRGXCGFRXRNQ-SNAWJCMRSA-N 0.000 description 1
- UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- RCLLINSDAJVOHP-UHFFFAOYSA-N n-ethyl-n',n'-dimethylprop-2-enehydrazide Chemical compound CCN(N(C)C)C(=O)C=C RCLLINSDAJVOHP-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000007717 redox polymerization reaction Methods 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000003911 water pollution Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8194678A JPS559629A (en) | 1978-07-07 | 1978-07-07 | Polymerization of acrylamide monomer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8194678A JPS559629A (en) | 1978-07-07 | 1978-07-07 | Polymerization of acrylamide monomer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS559629A JPS559629A (en) | 1980-01-23 |
JPS6160841B2 true JPS6160841B2 (de) | 1986-12-23 |
Family
ID=13760660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8194678A Granted JPS559629A (en) | 1978-07-07 | 1978-07-07 | Polymerization of acrylamide monomer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS559629A (de) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4801643A (en) * | 1987-03-30 | 1989-01-31 | Hercules Incorporated | Small particle size non-surface active protective colloid-stabilized latexes derived from monomers of high aqueous phase grafting tendencies |
FR2700771B1 (fr) * | 1993-01-28 | 1995-03-17 | Snf Sa | Procédé perfectionné pour polymériser l'acrylamide en milieu aqueux. |
-
1978
- 1978-07-07 JP JP8194678A patent/JPS559629A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS559629A (en) | 1980-01-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1099423A (en) | Method for producing acrylamide polymers | |
US3975341A (en) | Water in oil emulsion process for preparing gel-free polyelectrolyte particles | |
US3336269A (en) | Preparation of acrylamide-type water-soluble polymers | |
JPH0214364B2 (de) | ||
JP2008544107A5 (de) | ||
JPS63234007A (ja) | 水溶性が良好なカチオン性重合体 | |
US4622356A (en) | Polyacrylamide and polyacrylic acid polymers | |
CN107325213B (zh) | 一种分子量可调节的甲基丙烯酰氧乙基三甲基氯化铵聚合物制备方法 | |
JPS5814425B2 (ja) | 不飽和第3級アミンまたはその第4級アンモニウム塩の安定化法 | |
JPS6160841B2 (de) | ||
EP2617742B1 (de) | N-vinyl-lactam-polymer und verfahren zu seiner herstellung | |
US3803104A (en) | High molecular weight and low viscosity vinylpyrrolidone polymer flocculants and catalyst and process producing the same | |
JPS6154805B2 (de) | ||
JPS6160842B2 (de) | ||
CN106317306B (zh) | 一种阳离子聚丙烯酰胺的制备方法 | |
JP4108491B2 (ja) | アクリルアミド系水溶性重合体の製造方法 | |
CN110036045B (zh) | 聚丙烯腈的生产方法 | |
JPH0441686B2 (de) | ||
CA1155139A (en) | PREPARATION OF WATER-IMMISCIBLE, ACID-SOLUBLE N- (AMINOMETHYL)-.alpha.,.beta.-ETHYLENICALLY UNSATURATED CARBOXAMIDES, QUATERNARY DERIVATIVES AND POLYMERS THEREOF | |
JPH0361687B2 (de) | ||
JPH062779B2 (ja) | モノアリルアミン又はn−置換モノアリルアミンの無機酸塩の重合体の製造方法 | |
JP4889237B2 (ja) | カチオン性共重合体の製造方法 | |
JP5461978B2 (ja) | アクリルアミド系水溶性重合体の製造方法 | |
JPS5940842B2 (ja) | カチオン系重合体の製造方法 | |
SU927802A1 (ru) | Способ получени волокнообразующих (со)полимеров акрилонитрила |