JPH0457684B2 - - Google Patents
Info
- Publication number
- JPH0457684B2 JPH0457684B2 JP57138009A JP13800982A JPH0457684B2 JP H0457684 B2 JPH0457684 B2 JP H0457684B2 JP 57138009 A JP57138009 A JP 57138009A JP 13800982 A JP13800982 A JP 13800982A JP H0457684 B2 JPH0457684 B2 JP H0457684B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- polymer
- emulsion
- acid
- monomer
- 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 - Lifetime
Links
- 239000000839 emulsion Substances 0.000 claims description 23
- 239000000178 monomer Substances 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 150000003839 salts Chemical class 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 12
- 229920003169 water-soluble polymer Polymers 0.000 claims description 12
- 230000014759 maintenance of location Effects 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 238000004090 dissolution Methods 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 3
- 229920003176 water-insoluble polymer Polymers 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims 2
- 229920000642 polymer Polymers 0.000 description 21
- -1 acrylic ester Chemical class 0.000 description 7
- 239000007787 solid Substances 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 229920006317 cationic polymer Polymers 0.000 description 4
- 239000008394 flocculating agent Substances 0.000 description 4
- 150000007522 mineralic acids Chemical class 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000003756 stirring Methods 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000007865 diluting Methods 0.000 description 3
- 238000007720 emulsion polymerization reaction Methods 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 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 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000013054 paper strength agent Substances 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000013055 pulp slurry Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000002351 wastewater Substances 0.000 description 2
- QHVBLSNVXDSMEB-UHFFFAOYSA-N 2-(diethylamino)ethyl prop-2-enoate Chemical compound CCN(CC)CCOC(=O)C=C QHVBLSNVXDSMEB-UHFFFAOYSA-N 0.000 description 1
- OBMRSUNAEQGDLK-UHFFFAOYSA-N 2-(dipropylamino)ethyl 2-methylprop-2-enoate Chemical compound CCCN(CCC)CCOC(=O)C(C)=C OBMRSUNAEQGDLK-UHFFFAOYSA-N 0.000 description 1
- HPGIOSOCXHTQGW-UHFFFAOYSA-N 2-(dipropylamino)ethyl prop-2-enoate Chemical compound CCCN(CCC)CCOC(=O)C=C HPGIOSOCXHTQGW-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- QLIBJPGWWSHWBF-UHFFFAOYSA-N 2-aminoethyl methacrylate Chemical compound CC(=C)C(=O)OCCN QLIBJPGWWSHWBF-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- GXWNNGGUTQVSAR-UHFFFAOYSA-N 5-(dipropylamino)-2-methylidenepentanamide Chemical compound CCCN(CCC)CCCC(=C)C(N)=O GXWNNGGUTQVSAR-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007922 dissolution test Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- NHIYRUPWLYKBNL-UHFFFAOYSA-N methylsulfonyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OS(C)(=O)=O NHIYRUPWLYKBNL-UHFFFAOYSA-N 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- VNLHOYZHPQDOMS-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-2-methylprop-2-enamide Chemical compound CCN(CC)CCCNC(=O)C(C)=C VNLHOYZHPQDOMS-UHFFFAOYSA-N 0.000 description 1
- PTQOQKRUWKRZTR-UHFFFAOYSA-N n-[3-(dipropylamino)propyl]-2-methylprop-2-enamide Chemical compound CCCN(CCC)CCCNC(=O)C(C)=C PTQOQKRUWKRZTR-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 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
- 239000001294 propane Substances 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paper (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Polymerisation Methods In General (AREA)
Description
本発明は、新規な水溶性重合体およびその凝集
剤又は濾水・歩留向上剤としての使用方法に関す
る。
水溶性重合体は、凝集剤、濾水・歩留向上剤、
その他の用途に広く利用されている。これらは、
一般に、数10万ないし数千万の分子量を有し、粉
末状、ペースト状あるいは、油中水型(W/O
型)エマルジヨンとして、通常提供されている。
粉末状重合体は、溶解が難しく、溶解設備に多
大の投資を必要とする。又微粉末の粉塵が起こ
り、作業環境上好ましくない。又、ペースト状製
品は、高粘度となる為、高濃度で提供することが
難しいため、経済的に不利であるだけでなく、製
品の安定性も一般に良好でない。油中水型エマル
ジヨンは、前2者に比較して水への分散、溶解が
迅速なること、溶解設備が簡単で済む等の利点を
有するが、有機溶剤を比較的多量に使用する為、
取扱い上難点があるばかりでなく、経済的にも不
利である。又、凝集剤等の用途に使用する際に有
機溶剤の処理の問題が生ずることもある。又、製
品の安定性も長期保存での二層分離、クリーミン
グ化等一般には良好でない。
本発明者は、最近凝集剤等の水溶性重合体の使
用分野で特に需要の大きなカチオン性重合体の探
索に努めたところ、経済的に有利で、かつ取扱い
が容易で、製品の安定性も良好なカチオン性重合
体の製造方法を見出し本発明に到達した。
すなわち本発明は、一般式
で表わされる単量体()、又はこれと共重合可
能な他のビニル単量体との混合物を水不溶性重合
体が得られる単量体組成で水中で乳化重合した
後、酸又は塩を含有する水に溶解して得られた10
万ないし3000万の分子量を有する水溶性重合体、
および凝集剤、濾水・歩留向上剤として使用する
方法に関する。
以下更に詳しく本発明を説明する。本発明の水
溶性重合体の必須成分となる一般式()で表わ
される単量体としては、たとえば、ジエチルアミ
ノエチルアクリレート、ジエチルアミノエチルメ
タアクリレート、ジプロピルアミノエチルアクリ
レート、ジプロピルアミノエチルメタアクリレー
ト、ジブチルアミノエチルメタアクリレート、ジ
エチルアミノプロピルメタクリルアミド、ジプロ
ピルアミノプロピルメタクリルアミド、ジプロピ
ルアミノプロピルアクリルアミド、ジブチルアミ
ノプロピルメタクリルアミド、ジプチルアミノプ
ロピルアクリルアミドなどが挙げられる。
単量体()と共重合可能な他のビニル単量体
()としては、アクリル酸エステル、メタクル
ル酸エステル、アクリロニトリル及びスチレンか
ら選ばれた1種又は2種以上の疎水性単量体が用
いられる。単量体()の使用割合としては、得
られた重合体が酸又は塩を含有する水に溶解する
範囲で選ばれる。たとえばジエチルアミノエチル
メタクリレートとメシルメタクリレートと共重合
体では、メチルメタクリレートは、全単量体に対
して、0〜30重量%の範囲で水溶性重合体が得ら
れる。
乳化重合に際し使用する界面活性剤としては、
アニオン型、ノニオン型、カチオン型などの通常
の界面活性剤が使用でき、たとえば、アルキルベ
ンゼンスルホン酸ソーダ、アルキルサルフエー
ト、アルキルスルホン酸ソーダ、ポリオキシエチ
レンアルキルエーテルサルフエート、ポリオキシ
エチレンアルキルフエニルエーテルサルフエー
ト、ポリオキシエチレンアルキルエーテル、ポリ
オキシエチレンアルキルフエニルエーテル、アル
キルアミン、ベタイン型などが挙げられる。一般
的には界面活性剤としてはアニオン型、ノニオン
型の併用が凝固物の少いより安定した乳化重合対
を与える。
使用する重合触媒としては、過酸化物、アゾ化
合物などの一般的なラジカル重合開始剤が用いら
れるが、水溶性の重合開始剤が特に好ましい。水
溶性の重合開始剤としては、過硫酸アンモニウ
ム、過硫酸カリウム、過酢酸、過酸化水素などの
過酸化物、および2、2′−アゾビス−2−アミノ
ジノプロパン塩酸塩、4、4′−アゾビス−4−シ
アノペンタノイツクアシツドなどのアゾ化合物が
挙げられる。過酸化物を開始剤として使用する場
合、必要に応じて、適当な還元剤と共存させてレ
ドツクス系の開始剤として使用することも可能で
ある。
得られた重合体は10万ないし300万の分子量を
有し、用途により、各種程度のものを調製でき
る。
本発明者は、かくして得られたエマルジヨン
は、そのままでは水不溶性であるが、無機酸又は
有機酸又は、それらの塩を含有する水に対して水
溶性となることを見出した。溶解する方法として
は、あらかじめ酸を加えた水中にエマルジヨンを
添加してもよく、逆に水にエマルジヨンを添加し
た乳化物に対し、酸を加えても良い。好ましい酸
としては、塩酸、硫酸、硝酸、酢酸、ギ酸、マレ
イン酸、フマル酸、クエン酸、酒石酸、アジピン
酸、スルフアミン酸、トルエンスルホン酸などが
あり、好ましい塩としては、硫酸アルミニウム、
塩化アルミニウム、塩化第2鉄などの強酸弱塩基
塩がある。酸又は塩の使用量としては、重合体が
水溶性となる量が必要であり、一般的には、カチ
オン性単量体に対して、当量以上である。
エマルジヨンの溶解は、得られた水溶性重合体
の各種用途への使用に先立つて行えばよい。溶解
が、粉状品に比べて容易なこと、エマルジヨン状
態での重合体の安定性が良好であることから、保
管はエマルジヨン状態で行い、使用に先立つて水
溶化することは好ましい製品の一態様である。
得られる水溶性重合体の用途として先ず、凝集
剤がある。従来、市販されている凝集剤は、粉末
型、ペースト型が大部分で、又、油中水滴型
(W/O)エマルジヨンも提案されている。しか
し、これらは、前述の如く、溶解性、取扱性等に
おいて、欠点があつたが、本発明の水溶性重合体
を使用する凝集剤は、水中油型(O/W)エマル
ジヨンを使用して製造されるので、水溶性への調
整が容易であり、溶解に当つても粉末型のごとく
特別な溶解装置を必要とすることがない。
一般にカチオン性凝集剤の場合、塩タイプによ
り、性能の変わることがあるが、本発明のO/W
エマルジヨンは、溶解時に廃水等懸濁水の種類に
よりある程度塩タイプを変えることが可能であ
る。
凝集剤として用いる場合、水溶性重合体の使用
量は廃水や被処理水の種類によつても異なるが、
一般に浮遊懸濁物(ss)に対して、固形分換算で
0.05〜2%程度である。
製紙工業における濾水・歩留向上剤としても本
発明重合体は、有効である。濾水・歩留り向上剤
として、使用する場合、通常0.1〜0.5重量%に溶
解して使用する。添加量は、原料、マシン特性に
より、またその目的により相当異なるが、対パル
プあたり、0.005〜0.5%(固形分換算)の範囲で
使用される。本発明重合体を使用すると、微細繊
維、填料の歩留りが向上し、サイズ剤、紙力増強
剤の定着も向上する。又濾水性が向上し、抄速を
上げることが可能となり、ウエブ含水率を低下さ
せ、消費スチームの低減効果が大である。
濾水・歩留向上剤として用いる時エマルジヨン
を水溶化するのに用いる酸又は塩として、各種有
基、無機酸の他、抄紙系に一般に用いられる硫酸
アルミニウムを用いられることは、作業性の点の
みならず、白水中の硫酸イオン等陰イオンの蓄積
防止にもなり、PH低下によるマシンの腐食、成紙
強度低下、サイズ度低下を防ぎ、また抄紙系の白
水クローズドシステム化が可能で、用水の節減、
廃水処理負担の低減等の利益がある。
以上詳述したように、本発明重合体はその製造
が容易で又、凝集剤、濾水・歩留向上剤、等多く
の産業上有用な用途を有するものである。
以下、実施例により本発明をさらに説明する
が、本発明はこれらに限定されるものではない。
なお実施例中の%は、ことわりのない限り重量%
を示す。
実施例 1
撹拌棒、冷却管、チツ素導入管および温度計を
付帯した14つ口フラスコに、
ジエチルアミノエチルメタアクリレート 180g
脱イオン水 120g
エマール10(花王石鹸(株)) 1%(対単量体)
エマルゲン930(花王石鹸(株)) 2%(対単量体)
を仕込み、撹拌下、チツ素ガスを通じて脱酸素し
た後、フラスコ内容物を15℃に保つた。次に過硫
酸アンモニウム0.36gと亜硫酸水素ナトリウム
0.09gを添加して、15〜20℃で4時間重合を行な
い、乳白色のカチオン性重合体のO/W型エマル
ジヨン(A)を得た。生成したエマルジヨンをポリマ
ー濃度2%となるように希釈したのち、種々の無
機、有機酸、及び塩を重量体に対して当量加えた
ところ、容易に溶解し、無色透明の分子量300万
の重合体水溶液を得ることができた。その結果を
表1に示した。
実施例 2
実施例1の方法において、脱酸素までは同様に
行い、その後フラスコ内容物を50℃に保ち、2,
2′−アゾビス−2−アミノジノプロパン塩酸塩を
1.08g添加し、50〜55℃で5時間重合して、カチ
オン性重合体のO/W型エマルジヨン(B)を得た。
得られたエマルジヨンを重合体濃度として、2
%になるように水道水で希釈したのち種々の無
機、有機酸及び塩を重合体に対して、当量加えた
ところ容易に溶解し、分子量83万の重合体水溶液
を得ることができた。その結果を表1に示した。
実施例 3
実施例1において、単量体を、表2に示す、ジ
エチルアミノエチムメタアクリレート/メチルメ
タアクリレートの混合物(90/10及び70/30
(%))とした以外は実施例1の方法でエマルジヨ
ン(C)及び(D)を得た。分子量はそれぞれ、174万及
び26万であつた。実施例1と同様な方法で溶解テ
ストをした結果を表2に示す。
実施例 4
実施例1〜3で得られた、エマルジヨンを凝集
剤として使用した。懸濁濃度2.5%の下水処理場
消化汚泥500mlをビーカーに採り、150rpmで撹拌
しながら、表3に示す酸で処理して溶解した。
0.2%の重合体水溶液を固形分に対して0.2〜0.3%
添加し1分間撹拌した。
形成したフロツクの状態を観察した後、実験用
遠心脱水試験機により、脱水テストを行いケーキ
含水率を測定した。その結果を表3に示す。
The present invention relates to a novel water-soluble polymer and its use as a flocculant or drainage/retention aid. Water-soluble polymers include flocculants, drainage and retention aids,
Widely used for other purposes. these are,
Generally, it has a molecular weight of several hundred thousand to tens of millions, and is in the form of powder, paste, or water-in-oil (W/O).
type) as an emulsion. Powdered polymers are difficult to melt and require significant investment in melting equipment. In addition, fine powder dust is generated, which is unfavorable in terms of the working environment. Further, since paste-like products have high viscosity and are difficult to provide in high concentrations, they are not only economically disadvantageous, but also generally have poor product stability. Water-in-oil emulsions have advantages over the former two, such as rapid dispersion and dissolution in water, and simple dissolution equipment, but because they use relatively large amounts of organic solvents,
Not only is it difficult to handle, but it is also economically disadvantageous. Furthermore, when used as a coagulant, problems may arise in the treatment of organic solvents. In addition, the stability of the product is generally not good, such as separation of two layers and creaming during long-term storage. The present inventor has recently endeavored to search for cationic polymers, which are in particular demand in the field of use of water-soluble polymers such as flocculants, and found that they are economically advantageous, easy to handle, and have good product stability. The present invention was achieved by finding a method for producing a good cationic polymer. That is, the present invention is based on the general formula After emulsion polymerization of the monomer represented by () or a mixture of this and other copolymerizable vinyl monomers in water with a monomer composition that yields a water-insoluble polymer, an acid or salt containing 10 obtained by dissolving in water
a water-soluble polymer having a molecular weight of 10,000 to 30,000,000
and a method for using it as a flocculant, drainage/retention aid. The present invention will be explained in more detail below. Examples of monomers represented by the general formula () that are essential components of the water-soluble polymer of the present invention include diethylaminoethyl acrylate, diethylaminoethyl methacrylate, dipropylaminoethyl acrylate, dipropylaminoethyl methacrylate, and dibutyl Examples include aminoethyl methacrylate, diethylaminopropyl methacrylamide, dipropylaminopropyl methacrylamide, dipropylaminopropylacrylamide, dibutylaminopropyl methacrylamide, diptylaminopropylacrylamide, and the like. As the other vinyl monomer () that can be copolymerized with the monomer (), one or more hydrophobic monomers selected from acrylic ester, methacryl ester, acrylonitrile, and styrene are used. It will be done. The proportion of the monomer () to be used is selected within a range such that the resulting polymer is soluble in water containing the acid or salt. For example, in a copolymer of diethylaminoethyl methacrylate and mesyl methacrylate, a water-soluble polymer is obtained in which methyl methacrylate is present in a range of 0 to 30% by weight based on the total monomers. Surfactants used during emulsion polymerization include:
Usual surfactants such as anionic, nonionic, and cationic surfactants can be used, such as sodium alkylbenzene sulfonate, alkyl sulfate, sodium alkyl sulfonate, polyoxyethylene alkyl ether sulfate, and polyoxyethylene alkyl phenyl ether. Examples include sulfates, polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenyl ethers, alkyl amines, and betaine types. Generally, a combination of anionic and nonionic surfactants provides a more stable emulsion polymerization pair with less coagulation. As the polymerization catalyst used, common radical polymerization initiators such as peroxides and azo compounds are used, but water-soluble polymerization initiators are particularly preferred. Examples of water-soluble polymerization initiators include peroxides such as ammonium persulfate, potassium persulfate, peracetic acid, hydrogen peroxide, and 2,2'-azobis-2-aminodinopropane hydrochloride, 4,4'-azobis Examples include azo compounds such as -4-cyanopentanoid acid. When a peroxide is used as an initiator, it can be used as a redox-based initiator in the presence of a suitable reducing agent, if necessary. The obtained polymer has a molecular weight of 100,000 to 3,000,000, and various grades can be prepared depending on the purpose. The present inventors have discovered that the emulsion thus obtained is water-insoluble as it is, but becomes water-soluble in water containing an inorganic or organic acid or a salt thereof. As a method for dissolving the emulsion, the emulsion may be added to water to which an acid has been added in advance, or conversely, an acid may be added to an emulsion obtained by adding the emulsion to water. Preferred acids include hydrochloric acid, sulfuric acid, nitric acid, acetic acid, formic acid, maleic acid, fumaric acid, citric acid, tartaric acid, adipic acid, sulfamic acid, and toluenesulfonic acid. Preferred salts include aluminum sulfate,
There are salts of strong acids and weak bases such as aluminum chloride and ferric chloride. The amount of acid or salt used must be such that the polymer becomes water-soluble, and is generally at least equivalent to the amount of the cationic monomer. The emulsion may be dissolved before the resulting water-soluble polymer is used for various purposes. One aspect of the product is that it is preferable to store it in an emulsion state and to make it water-soluble before use because it is easier to dissolve than powdered products and the stability of the polymer in an emulsion state is good. It is. The first use of the resulting water-soluble polymer is as a flocculant. Conventionally, most commercially available flocculants are powder type or paste type, and water-in-oil (W/O) emulsions have also been proposed. However, as mentioned above, these had drawbacks in solubility, handling, etc. However, the flocculant using the water-soluble polymer of the present invention uses an oil-in-water (O/W) emulsion. Since it is manufactured, it is easy to adjust the water solubility, and unlike powder type, special dissolving equipment is not required for dissolution. Generally, in the case of cationic flocculants, the performance may vary depending on the salt type, but the O/W of the present invention
When dissolving the emulsion, it is possible to change the salt type to some extent depending on the type of suspended water such as waste water. When used as a flocculant, the amount of water-soluble polymer used varies depending on the type of wastewater or water to be treated;
In general, for suspended solids (ss), in terms of solid content
It is about 0.05 to 2%. The polymer of the present invention is also effective as a drainage and retention aid in the paper industry. When used as a drainage/retention improver, it is usually dissolved in a concentration of 0.1 to 0.5% by weight. The amount added varies considerably depending on the raw material, machine characteristics, and purpose, but it is used in the range of 0.005 to 0.5% (in terms of solid content) based on the pulp. When the polymer of the present invention is used, the retention of fine fibers and fillers is improved, and the retention of sizing agents and paper strength agents is also improved. In addition, the freeness is improved, making it possible to increase the papermaking speed, reducing the web moisture content, and greatly reducing the amount of steam consumed. In addition to various organic and inorganic acids, aluminum sulfate, which is commonly used in papermaking systems, can be used as the acid or salt used to water-solubilize the emulsion when used as a drainage/retention aid, from the point of view of workability. In addition, it prevents the accumulation of anions such as sulfate ions in white water, prevents corrosion of the machine due to a decrease in pH, a decrease in paper strength, and a decrease in size. savings,
There are benefits such as a reduction in the burden of wastewater treatment. As detailed above, the polymer of the present invention is easy to produce and has many industrially useful uses such as a flocculant, drainage/retention aid, and the like. The present invention will be further explained below with reference to Examples, but the present invention is not limited thereto.
In addition, % in the examples is weight % unless otherwise specified.
shows. Example 1 In a 14-necked flask equipped with a stirring bar, cooling tube, nitrogen introduction tube, and thermometer, 180 g of diethylaminoethyl methacrylate, 120 g of deionized water, and 1% (based on monomer) Emar 10 (Kao Soap Co., Ltd.) were added. ) Emulgen 930 (Kao Soap Co., Ltd.) 2% (based on monomers) was charged, and after deoxidizing by passing nitrogen gas under stirring, the contents of the flask were kept at 15°C. Next, ammonium persulfate 0.36g and sodium bisulfite
0.09 g was added and polymerization was carried out at 15 to 20° C. for 4 hours to obtain a milky white O/W type emulsion (A) of a cationic polymer. After diluting the resulting emulsion to a polymer concentration of 2%, various inorganic and organic acids and salts were added in equivalent amounts to the weight of the emulsion, which easily dissolved and resulted in a colorless and transparent polymer with a molecular weight of 3 million. An aqueous solution could be obtained. The results are shown in Table 1. Example 2 In the method of Example 1, deoxidation was carried out in the same manner, and then the contents of the flask were kept at 50°C and 2.
2'-azobis-2-aminodinopropane hydrochloride
1.08g was added and polymerized at 50 to 55°C for 5 hours to obtain an O/W type emulsion (B) of a cationic polymer. The polymer concentration of the obtained emulsion is 2
After diluting the polymer with tap water so that the polymer had a molecular weight of 830,000 %, various inorganic and organic acids and salts were added in equivalent amounts to the polymer. The results are shown in Table 1. Example 3 In Example 1, the monomers were a mixture of diethylaminoethim methacrylate/methyl methacrylate (90/10 and 70/30) shown in Table 2.
(%)) Emulsions (C) and (D) were obtained by the method of Example 1. The molecular weights were 1,740,000 and 260,000, respectively. Table 2 shows the results of a dissolution test conducted in the same manner as in Example 1. Example 4 The emulsion obtained in Examples 1 to 3 was used as a flocculant. 500 ml of sewage treatment plant digested sludge with a suspension concentration of 2.5% was taken into a beaker and treated with the acids shown in Table 3 to dissolve it while stirring at 150 rpm.
0.2% polymer aqueous solution 0.2~0.3% based on solid content
and stirred for 1 minute. After observing the state of the formed flocs, a dehydration test was conducted using an experimental centrifugal dehydration tester to measure the moisture content of the cake. The results are shown in Table 3.
【表】【table】
【表】【table】
【表】【table】
【表】
クリレート
MMA:メチルメタアクリレート
[Table] Acrylate
MMA: Methyl methacrylate
【表】
実施例 5
実施例1で得られたエマルジヨンを重合体濃度
0.2%になるように水道水で希釈した後、2N−
HClを重合体に対して当量添加して、0.2%をポ
リマー水溶液を得た。
400mlカナデイアンスタンダードフリーネス
(C.S.F.)に叩解したLBKPを1%濃度に希釈す
る。得られたパルプスラリーにロジンサイズ対パ
ルプ0.3%、硫酸バンド対パルプ3%、アニオン
系紙力増強対パルプ0.3%、タルク対パルプ20%、
上述した0.2%重合体水溶液を0.005〜0.002%(対
パルプ、固形分換算)加えTAPPI手抄抄紙機に
より抄紙した。得られたシート中のタルク含有量
を測定することにより、タルクの歩留りを測定し
た。その結果を表4に示す。
実施例 6
実施例5で得た、0.2%重合体水溶液を用いて、
漏水向上剤として評価した。
350mlCSF(カナデイアンフリーネス)に叩解し
た段ボール故紙を工業用水を用いて1%に希釈し
た。得られたパルプスラリーにロジンサイズ剤対
パルプ0.3%、硫酸バンド対パルプ3%、アニオ
ン系紙力増強剤対パルプ0.5%を夫々撹拌下に添
加する。最後に上述した、重合体水溶液を対パル
プ0.02〜0.1%(固形分換算)添加した後、
TAPPI標準法によりフリーネスを測定した。そ
の結果を表5に示す。[Table] Example 5 The emulsion obtained in Example 1 was
After diluting with tap water to 0.2%, 2N−
An equivalent amount of HCl was added to the polymer to obtain a 0.2% aqueous polymer solution. Dilute beaten LBKP in 400 ml Canadian Standard Freeness (CSF) to a 1% concentration. The resulting pulp slurry contains 0.3% pulp for rosin size, 3% pulp for sulfate band, 0.3% pulp for anionic paper strength enhancement, 20% pulp for talc,
0.005 to 0.002% (based on pulp, solid content) of the above-mentioned 0.2% polymer aqueous solution was added and paper was made using a TAPPI hand paper machine. The yield of talc was measured by measuring the talc content in the obtained sheet. The results are shown in Table 4. Example 6 Using the 0.2% aqueous polymer solution obtained in Example 5,
It was evaluated as a water leak improver. Waste cardboard beaten in 350 ml CSF (Canadian Freeness) was diluted to 1% using industrial water. To the obtained pulp slurry, 0.3% of rosin sizing agent to pulp, 3% of sulfuric acid band to pulp, and 0.5% of anionic paper strength agent to pulp are respectively added with stirring. Finally, after adding the above-mentioned aqueous polymer solution to the pulp at 0.02 to 0.1% (in terms of solid content),
Freeness was measured by the TAPPI standard method. The results are shown in Table 5.
【表】【table】
【表】【table】
1 (A) 少なくともチタン、マグネシウムおよび
塩素からなる触媒成分を細孔半径75〜5000Åの
範囲の細孔容量が0.25c.c./g以上である多孔質
担体に含浸させた固体触媒成分と、
(B) 有機アルミニウム化合物を少なくとも含む触
媒系を用い、
第1工程でエチレンをプロパンおよび/または
ブタン溶媒中でスラリー重合するか、またはエチ
レンを気相中で重合した後、第2工程で気相中で
エチレンとα−オレフインのランダム共重合を、
該工程で生成する共重合体中のエチレン含量が15
〜90モル%、テトラリン135℃における極限粘度
が0.3〜10であつて且つ該工程で生成する共重合
体が全重合体量に対して60〜97重量%になるよう
に重合することを特徴とする粒状熱可塑性エラス
トマーの製造法。
1 (A) A solid catalyst component in which a porous carrier having a pore radius of 75 to 5000 Å and a pore volume of 0.25 cc/g or more is impregnated with a catalyst component consisting of at least titanium, magnesium, and chlorine, and (B) Using a catalyst system containing at least an organoaluminum compound, ethylene is slurry polymerized in a propane and/or butane solvent in a first step, or ethylene is polymerized in a gas phase, and then ethylene is polymerized in a gas phase in a second step. Random copolymerization of and α-olefin,
The ethylene content in the copolymer produced in this process is 15
~90 mol%, tetralin has an intrinsic viscosity of 0.3 to 10 at 135°C, and is polymerized so that the copolymer produced in the step is 60 to 97% by weight based on the total polymer amount. A method for producing a granular thermoplastic elastomer.
Claims (1)
はCnH2n+lで表わされるアルキル基を、nは
正の整数を、Aは−O−CH2−、又は−NH−
CH2−CH2−を示し、R1、R2、R3は単量体が水
に対し難溶性、又は不溶性である範囲で選ばれ
る。)で表わされる単量体()、又はこれとアク
リル酸エステル、メタクリル酸エステル、アクリ
ロニトリル及びスチレンから選ばれた1種又は2
種以上の全単量体に対し30重量%以下のビニル単
量体との混合物を水不溶性重合体が得られる単量
体組成で、水中で乳化重合した後、酸又は塩を含
有する水に溶解して得られた10万ないし3000万の
分子量を有する水溶性重合体を凝集剤として使用
する方法。 3 一般式 (ただし、式中、R1はHまたはCH3を、R2、R3
はCnH2n+lで表わされるアルキル基を、nは
正の整数を、Aは−O−CH2−、又は−NH−
CH2−CH2−を示し、R1、R2、R3は単量体が水
に対し難溶性、又は不溶性である範囲で選ばれ
る。)で表わされる単量体()、又はこれとアク
リル酸エステル、メタクリル酸エステル、アクリ
ロニトリル及びスチレンから選ばれた1種又は2
種以上の全単量体に対し30重量%以下のビニル単
量体との混合物を水不溶性重合体が得られる単量
体組成で、水中で乳化重合した後、酸又は塩を含
有する水に溶解して得られた10万ないし3000万の
分子量を有する水溶性重合体を濾水・歩留向上剤
として使用する方法。 (However, in the formula, R 1 is H or CH 3 , R 2 , R 3
is an alkyl group represented by CnH 2 n+l, n is a positive integer, and A is -O-CH 2 - or -NH-
It represents CH2 - CH2- , and R1 , R2 , and R3 are selected within a range in which the monomer is poorly soluble or insoluble in water. ), or one or two monomers selected from acrylic esters, methacrylic esters, acrylonitrile, and styrene.
A mixture of 30% by weight or less of vinyl monomer based on the total monomers is emulsion polymerized in water with a monomer composition that yields a water-insoluble polymer, and then immersed in water containing acid or salt. A method in which a water-soluble polymer with a molecular weight of 100,000 to 30 million obtained by dissolution is used as a flocculant. 3 General formula (However, in the formula, R 1 is H or CH 3 , R 2 , R 3
is an alkyl group represented by CnH 2 n+l, n is a positive integer, and A is -O-CH 2 - or -NH-
It represents CH2 - CH2- , and R1 , R2 , and R3 are selected within a range in which the monomer is poorly soluble or insoluble in water. ), or one or two monomers selected from acrylic esters, methacrylic esters, acrylonitrile, and styrene.
A mixture of 30% by weight or less of vinyl monomer based on the total monomers is emulsion polymerized in water with a monomer composition that yields a water-insoluble polymer, and then immersed in water containing acid or salt. A method in which a water-soluble polymer with a molecular weight of 100,000 to 30 million obtained by dissolving is used as a drainage and retention aid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13800982A JPS5927903A (en) | 1982-08-10 | 1982-08-10 | Water-soluble polymer, its production and its use |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13800982A JPS5927903A (en) | 1982-08-10 | 1982-08-10 | Water-soluble polymer, its production and its use |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5927903A JPS5927903A (en) | 1984-02-14 |
JPH0457684B2 true JPH0457684B2 (en) | 1992-09-14 |
Family
ID=15211924
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13800982A Granted JPS5927903A (en) | 1982-08-10 | 1982-08-10 | Water-soluble polymer, its production and its use |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5927903A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0651761B2 (en) * | 1985-04-17 | 1994-07-06 | 中央理化工業株式会社 | Method for producing cationic emulsion |
JPH02269715A (en) * | 1989-04-11 | 1990-11-05 | Sumitomo Chem Co Ltd | cationic emulsion |
JP2721566B2 (en) * | 1989-12-20 | 1998-03-04 | 花王株式会社 | Water disintegration paper, method for producing the same, and water disintegratable cleaning articles using the same |
JP4786569B2 (en) * | 2006-03-29 | 2011-10-05 | 三洋化成工業株式会社 | Organic coagulant |
JP4786558B2 (en) * | 2007-01-16 | 2011-10-05 | 三洋化成工業株式会社 | Polymer flocculant |
JP5967705B2 (en) * | 2012-06-11 | 2016-08-10 | ハイモ株式会社 | Coagulation treatment agent and sludge dewatering method using the same |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5019894A (en) * | 1973-05-17 | 1975-03-03 | ||
JPS5077496A (en) * | 1973-10-02 | 1975-06-24 | ||
JPS5898304A (en) * | 1981-12-07 | 1983-06-11 | Sumitomo Chem Co Ltd | Manufacturing method of cationic resin |
-
1982
- 1982-08-10 JP JP13800982A patent/JPS5927903A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5019894A (en) * | 1973-05-17 | 1975-03-03 | ||
JPS5077496A (en) * | 1973-10-02 | 1975-06-24 | ||
JPS5898304A (en) * | 1981-12-07 | 1983-06-11 | Sumitomo Chem Co Ltd | Manufacturing method of cationic resin |
Also Published As
Publication number | Publication date |
---|---|
JPS5927903A (en) | 1984-02-14 |
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