JP2007111666A - Method of preventing flow out of activated sludge - Google Patents
Method of preventing flow out of activated sludge Download PDFInfo
- Publication number
- JP2007111666A JP2007111666A JP2005307973A JP2005307973A JP2007111666A JP 2007111666 A JP2007111666 A JP 2007111666A JP 2005307973 A JP2005307973 A JP 2005307973A JP 2005307973 A JP2005307973 A JP 2005307973A JP 2007111666 A JP2007111666 A JP 2007111666A
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- JP
- Japan
- Prior art keywords
- water
- activated sludge
- group
- general formula
- soluble polymer
- 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.)
- Granted
Links
- 239000010802 sludge Substances 0.000 title claims abstract description 65
- 238000000034 method Methods 0.000 title claims abstract description 31
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 40
- 238000005273 aeration Methods 0.000 claims abstract description 31
- 239000007788 liquid Substances 0.000 claims abstract description 21
- 125000002091 cationic group Chemical group 0.000 claims abstract description 20
- 239000010419 fine particle Substances 0.000 claims abstract description 19
- 239000002245 particle Substances 0.000 claims abstract description 17
- 239000000178 monomer Substances 0.000 claims description 41
- 239000001257 hydrogen Substances 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000004815 dispersion polymer Substances 0.000 claims description 15
- 238000001556 precipitation Methods 0.000 claims description 15
- 125000003545 alkoxy group Chemical group 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 claims description 11
- 230000002265 prevention Effects 0.000 claims description 9
- 150000001450 anions Chemical class 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 150000002431 hydrogen Chemical group 0.000 claims description 8
- 230000001376 precipitating effect Effects 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 125000000129 anionic group Chemical group 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 239000002699 waste material Substances 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 238000012674 dispersion polymerization Methods 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims 1
- 238000004062 sedimentation Methods 0.000 abstract description 26
- 239000002351 wastewater Substances 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 4
- 239000013049 sediment Substances 0.000 abstract 2
- 238000004065 wastewater treatment Methods 0.000 abstract 2
- 150000002466 imines Chemical class 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 238000006116 polymerization reaction Methods 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 10
- 238000003756 stirring Methods 0.000 description 9
- 229920002873 Polyethylenimine Polymers 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- -1 and the like Chemical compound 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000003505 polymerization initiator Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
- 239000000701 coagulant Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 150000007522 mineralic acids Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 239000000243 solution Substances 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
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- DWSMBORYMHSAEA-UHFFFAOYSA-N 3-[(4-amino-4-iminobutan-2-yl)diazenyl]butanimidamide;dihydrochloride Chemical compound Cl.Cl.NC(=N)CC(C)N=NC(C)CC(N)=N DWSMBORYMHSAEA-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 125000001174 sulfone group Chemical group 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 description 1
- ZVUAMUKZHFTJGR-UHFFFAOYSA-N 1-piperazin-1-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCNCC1 ZVUAMUKZHFTJGR-UHFFFAOYSA-N 0.000 description 1
- VBZBISQOWJYWCC-UHFFFAOYSA-N 2-(2-carboxypropan-2-yldiazenyl)-2-methylpropanoic acid Chemical compound OC(=O)C(C)(C)N=NC(C)(C)C(O)=O VBZBISQOWJYWCC-UHFFFAOYSA-N 0.000 description 1
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 description 1
- 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
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- STCKMQSKUYGCQX-UHFFFAOYSA-M 2-chlorooxyethyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOCl STCKMQSKUYGCQX-UHFFFAOYSA-M 0.000 description 1
- VMSBGXAJJLPWKV-UHFFFAOYSA-N 2-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=C VMSBGXAJJLPWKV-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- RIAVQNCBHNMYFJ-UHFFFAOYSA-M 2-hydroxypropyl-dimethyl-[phenyl(prop-2-enoyloxy)methyl]azanium;chloride Chemical compound [Cl-].CC(O)C[N+](C)(C)C(OC(=O)C=C)C1=CC=CC=C1 RIAVQNCBHNMYFJ-UHFFFAOYSA-M 0.000 description 1
- IDUXQGPRIVFLOY-UHFFFAOYSA-M 3-aminopropyl-dimethyl-(2-oxo-1-phenylbut-3-enyl)azanium chloride Chemical compound [Cl-].C(C=C)(=O)C(C1=CC=CC=C1)[N+](C)(C)CCCN IDUXQGPRIVFLOY-UHFFFAOYSA-M 0.000 description 1
- VFXXTYGQYWRHJP-UHFFFAOYSA-N 4,4'-azobis(4-cyanopentanoic acid) Chemical compound OC(=O)CCC(C)(C#N)N=NC(C)(CCC(O)=O)C#N VFXXTYGQYWRHJP-UHFFFAOYSA-N 0.000 description 1
- MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-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
- IRQWEODKXLDORP-UHFFFAOYSA-N 4-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=C(C=C)C=C1 IRQWEODKXLDORP-UHFFFAOYSA-N 0.000 description 1
- RTANHMOFHGSZQO-UHFFFAOYSA-N 4-methoxy-2,4-dimethylpentanenitrile Chemical compound COC(C)(C)CC(C)C#N RTANHMOFHGSZQO-UHFFFAOYSA-N 0.000 description 1
- ZFSPZXXKYPTSTJ-UHFFFAOYSA-N 5-methyl-2-propan-2-yl-4,5-dihydro-1h-imidazole Chemical compound CC(C)C1=NCC(C)N1 ZFSPZXXKYPTSTJ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-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
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- KJRCEJOSASVSRA-UHFFFAOYSA-N Propane-2-thiol Natural products CC(C)S KJRCEJOSASVSRA-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
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- KYIKRXIYLAGAKQ-UHFFFAOYSA-N abcn Chemical compound C1CCCCC1(C#N)N=NC1(C#N)CCCCC1 KYIKRXIYLAGAKQ-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 239000012935 ammoniumperoxodisulfate Substances 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 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
- ZGCZDEVLEULNLJ-UHFFFAOYSA-M benzyl-dimethyl-(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C=CC(=O)OCC[N+](C)(C)CC1=CC=CC=C1 ZGCZDEVLEULNLJ-UHFFFAOYSA-M 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GYCUTPICSQQWKP-UHFFFAOYSA-N bis[2-(5-methyl-4,5-dihydro-1h-imidazol-2-yl)propan-2-yl]diazene Chemical compound N1C(C)CN=C1C(C)(C)N=NC(C)(C)C1=NCC(C)N1 GYCUTPICSQQWKP-UHFFFAOYSA-N 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 150000001767 cationic compounds Chemical group 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920001002 functional polymer Polymers 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000000977 initiatory effect Effects 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229940050176 methyl chloride Drugs 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
- 239000011259 mixed solution Substances 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
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- WGESLFUSXZBFQF-UHFFFAOYSA-N n-methyl-n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCN(C)CC=C WGESLFUSXZBFQF-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
- 229920000333 poly(propyleneimine) Polymers 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
- 238000012545 processing Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007717 redox polymerization reaction Methods 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000001370 static light scattering Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- FZGFBJMPSHGTRQ-UHFFFAOYSA-M trimethyl(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)C=C FZGFBJMPSHGTRQ-UHFFFAOYSA-M 0.000 description 1
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 description 1
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 239000007883 water-soluble azo polymerization initiator Substances 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/10—Biological treatment of water, waste water, or sewage
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Activated Sludge Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
本発明は活性汚泥の流出防止方法に関する。さらに詳しくは活性汚泥を保持する曝気槽に排液を導入して生物処理する活性汚泥法において、混合液を沈殿槽に導いて沈殿分離し、分離汚泥の一部を曝気槽に返送する排液処理方法において、曝気槽から沈殿槽に至る系路に沈降剤としてカチオン性あるいは両性からなる粒径100μm以下の水溶性重合体微粒子とポリアルキレンイミン酸中和物とが共存する水溶性重合体分散液を添加することからなる活性汚泥流出防止方法に関する。 The present invention relates to a method for preventing activated sludge from flowing out. More specifically, in the activated sludge method in which waste liquid is introduced into an aeration tank holding activated sludge and biologically treated, the liquid mixture is guided to the settling tank for precipitation separation, and a part of the separated sludge is returned to the aeration tank. In the treatment method, a water-soluble polymer dispersion in which a water-soluble polymer fine particle having a particle size of 100 μm or less having a particle size of 100 μm or less as a precipitating agent and a neutralized polyalkylenimine acid coexists as a precipitating agent in a system route from an aeration tank to a precipitation tank. The present invention relates to an activated sludge prevention method comprising adding a liquid.
活性汚泥の混合液を沈降槽に送り沈殿分離する場合、沈降不良を起こす場合がある。原因は種々考えられるが、排水の変動によるBOD負荷の増加などにより活性汚泥がバルキングあるいはバルキングに近い状態を起こしている。このような状況の際、従来バルキング防止剤を添加していたが、添加量の調節が難しく、添加量が不足すると効果が全く認められず、過剰に添加すると活性汚泥微生物を死滅あるいは活性度の低下を起こす。これを改良するためバルキング防止剤とカチオン性凝集剤との混合物を適用する方法が試みられている(特許文献1)。一方、バルキング防止よりも汚泥の沈降を中心に対応する方法も試みられている。すなわちカチオン性の水溶性高分子を活性汚泥バッキ槽から沈殿槽間に添加し沈降を促進させ、活性汚泥の流出を防止する方法である(特許文献2)。この場合は比較的高分子量の重合系カチオン性高分子のみを使用しているため親水性の微細な粒子を補足したフロックを形成しにくいと推定され、汚泥の沈降が不完全になると予想される。 When the activated sludge mixed solution is sent to a sedimentation tank for sedimentation, sedimentation failure may occur. There are various causes, but activated sludge is caused to be in a bulking or near-bulking state due to an increase in BOD load due to fluctuations in drainage. In such a situation, a bulking agent has been conventionally added, but it is difficult to adjust the addition amount, and if the addition amount is insufficient, no effect is observed at all. Cause a drop. In order to improve this, an attempt has been made to apply a mixture of a bulking inhibitor and a cationic flocculant (Patent Document 1). On the other hand, a method that responds mainly to sludge sedimentation rather than bulking prevention has also been attempted. That is, it is a method for preventing the outflow of activated sludge by adding a cationic water-soluble polymer from the activated sludge buckling tank to the settling tank to promote sedimentation (Patent Document 2). In this case, since only a relatively high molecular weight cationic polymer is used, it is estimated that it is difficult to form flocs supplemented with hydrophilic fine particles, and sludge sedimentation is expected to be incomplete. .
本発明の活性汚泥の流出防止方法は、活性汚泥を保持する曝気槽に排液を導入して生物処理する活性汚泥法において、混合液を沈殿槽に導いて沈殿分離し、分離汚泥の一部を曝気槽に返送する排液処理方法において、曝気槽から沈殿槽に至る系路に沈降剤としてカチオン性あるいは両性からなる粒径100μm以下の水溶性重合体微粒子とポリエチレンイミン酸中和物とが共存する水溶性重合体分散液を添加することからなる。前記水溶性重合体微粒子はカチオン性水溶性単量体5〜90モル%、特定のアニオン性水溶性単量体5〜50モル%、特定の非イオン性水溶性単量体0〜90モル%からなる。 The activated sludge spill prevention method of the present invention is an activated sludge method in which waste liquid is introduced into an aeration tank holding activated sludge and biologically treated. In the drainage treatment method for returning the water to the aeration tank, a water-soluble polymer fine particle having a particle size of 100 μm or less and a neutralized product of polyethylenimic acid is used as a precipitating agent in the system from the aeration tank to the precipitation tank. It consists of adding a coexisting water-soluble polymer dispersion. The water-soluble polymer fine particles are 5 to 90 mol% of a cationic water-soluble monomer, 5 to 50 mol% of a specific anionic water-soluble monomer, and 0 to 90 mol% of a specific nonionic water-soluble monomer. Consists of.
すなわち活性汚泥法は通常連続的に排水を曝気槽に流入させ、一定の滞留時間を設定することにより水中のBOD(生物化学的酸素要求量)成分を微生物的に分解している。そのため一端汚泥の沈降性が低下した際早急な対応が要求される。すなわち溶解性が速いこと、汚泥への分散性が良く、汚泥沈降性を即改善できることが必要である。 That is, in the activated sludge method, the waste water is usually continuously flowed into the aeration tank, and the BOD (biochemical oxygen demand) component in the water is microbially decomposed by setting a certain residence time. For this reason, an immediate response is required when the settleability of sludge is reduced. That is, it is necessary that the solubility is fast, the dispersibility in sludge is good, and the sludge settling can be improved immediately.
本発明で使用するカチオン性あるいは両性からなる粒径100μm以下の水溶性重合体微粒子とポリエチレンイミンの酸中和物とが共存する水溶性重合体分散液は、分子量として相対的に低いポリアルキレンイミンの酸中和物を分散媒に用いているため分散性が良い。この際、分散液の状態で添加すると相対的に分子量の高い重合系高分子微粒子がポリエチレンイミンの分散後溶解し、フロック成長に寄与し活性汚泥の沈降を促進する。また分散液を溶解して添加すると、相対的に分子量の低いポリエチレンイミン酸中和物と相対的に分子量の高い重合系高分子は並行して分散していくが、分子量の高い重合系高分子粒子は溶解が相対的に遅く、ポリエチレンイミン酸中和物による親水性粒子の電荷中和後に架橋吸着的に作用し、フロックの増大に寄与する。そのため本発明で使用する水溶性重合体微粒子とポリエチレンイミン酸中和物とが共存する水溶性重合体分散液は、沈降性が低下した活性汚泥でも確実に沈降性を促進し活性汚泥の流出を防止することができる。 The water-soluble polymer dispersion in which the water-soluble polymer fine particles having a particle size of 100 μm or less and the neutralized product of polyethyleneimine used in the present invention coexist is a polyalkyleneimine having a relatively low molecular weight. Dispersibility is good because the acid neutralized product is used as a dispersion medium. At this time, when added in the state of a dispersion, polymer-based polymer fine particles having a relatively high molecular weight are dissolved after the dispersion of polyethyleneimine, contributing to floc growth and promoting sedimentation of activated sludge. When the dispersion is dissolved and added, the relatively low molecular weight polyethyleneiminate neutralized product and the relatively high molecular weight polymer are dispersed in parallel, but the high molecular weight polymer. The particles dissolve relatively slowly, and act as a cross-linking adsorbent after neutralizing the charge of the hydrophilic particles with the neutralized polyethyleneiminate, contributing to an increase in flocs. Therefore, the water-soluble polymer dispersion in which the water-soluble polymer fine particles and the neutralized polyethyleneiminate used in the present invention coexist reliably promotes sedimentation even with activated sludge having a lowered sedimentation property, and the activated sludge flows out. Can be prevented.
本発明の目的は、活性汚泥を保持する曝気槽に排液を導入して生物処理する活性汚泥法において、混合液を沈殿槽に導いて沈殿分離し、分離汚泥の一部を曝気槽に返送する排液処理方法において、汚泥の沈降性が低下した場合に即対応可能であり、しかも確実に活性汚泥の沈降を促進する方法を提供することである。 The object of the present invention is to introduce the waste liquid into the aeration tank holding the activated sludge and biologically treat it in the activated sludge method. The mixed liquid is introduced into the precipitation tank for precipitation separation, and a part of the separated sludge is returned to the aeration tank. In the drainage treatment method to be performed, it is possible to immediately cope with the case where the sedimentation property of the sludge is lowered, and to provide a method for surely promoting the sedimentation of the activated sludge.
本発明者らは、上記課題を解決すべく鋭意検討を行った結果、以下のような発明に到達した。すなわち請求項1の発明は、活性汚泥を保持する曝気槽に排液を導入して生物処理する活性汚泥法において、混合液を沈殿槽に導いて沈殿分離し、分離汚泥の一部を曝気槽に返送する排液処理方法において、曝気槽から沈殿槽に至る系路に沈降剤としてカチオン性あるいは両性からなる粒径100μm以下の水溶性重合体微粒子とポリエチレンイミン酸中和物とが共存する水溶性重合体分散液を添加することを特徴とする活性汚泥流出防止方法である。 As a result of intensive studies to solve the above problems, the present inventors have reached the following invention. That is, the invention of claim 1 is an activated sludge method in which waste liquid is introduced into an aeration tank holding activated sludge and biologically treated, and the mixed liquid is guided to the precipitation tank for precipitation separation, and a part of the separated sludge is aerated tank. In the drainage treatment method to be returned to the water solution, water soluble polymer fine particles having a particle size of 100 μm or less and having a particle size of 100 μm or less as a precipitating agent and a neutralized polyethylenimic acid coexist as a precipitating agent in the system from the aeration tank to the precipitation tank. An activated sludge outflow prevention method characterized by adding a functional polymer dispersion.
請求項2の発明は、前記水溶性重合体微粒子とポリアルキレンイミン酸中和物とが共存する水溶性重合体分散液が、下記一般式(1)及び/又は(2)で表わされるカチオン性水溶性単量体5〜100モル%、下記一般式(3)で表わされるアニオン性水溶性単量体0〜50モル%、非イオン性水溶性単量体0〜95モル%からなる単量体(混合物)を攪拌下、ポリアルキレンイミン酸中和物水溶液中で分散重合し製造されたものであることを特徴とする請求項1に記載の活性汚泥流出防止方法である。
R1は水素又はメチル基、R2、R3は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、R4は水素、炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基であり、同種でも異種でも良い。Aは酸素またはNH、Bは炭素数2〜4のアルキレン基またはアルコキシレン基、X1は陰イオンをそれぞれ表わす
R5は水素又はメチル基、R6、R7は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、X2は陰イオンをそれぞれ表わす。
R8は水素、メチル基またはカルボキシメチル基、QはSO3、C6H4SO3、CONHC(CH3)2CH2SO3、C6H4COOあるいはCOO、R9は水素またはCOOY2、Y1あるいはY2は水素または陽イオン。
In the invention of claim 2, the water-soluble polymer dispersion in which the water-soluble polymer fine particles and the polyalkyleneiminate neutralized product coexist is a cationic compound represented by the following general formula (1) and / or (2). A single amount comprising 5 to 100 mol% of a water-soluble monomer, 0 to 50 mol% of an anionic water-soluble monomer represented by the following general formula (3), and 0 to 95 mol% of a nonionic water-soluble monomer 2. The activated sludge outflow prevention method according to claim 1, wherein the body (mixture) is produced by dispersion polymerization in an aqueous solution of neutralized polyalkyleneiminate with stirring.
R1 is hydrogen or a methyl group, R2 and R3 are alkyl groups having 1 to 3 carbon atoms, alkoxy groups or benzyl groups, R4 is hydrogen, an alkyl group having 1 to 3 carbon atoms, alkoxy groups or benzyl groups. But it ’s okay. A represents oxygen or NH, B represents an alkylene group or alkoxylene group having 2 to 4 carbon atoms, and X1 represents an anion.
R5 represents hydrogen or a methyl group, R6 and R7 each represents an alkyl group having 1 to 3 carbon atoms, an alkoxy group or a benzyl group, and X2 represents an anion.
R8 is hydrogen, methyl group or carboxymethyl group, Q is SO3, C6H4SO3, CONHC (CH3) 2CH2SO3, C6H4COO or COO, R9 is hydrogen or COOY2, Y1 or Y2 is hydrogen or cation.
請求項3の発明は、前記粒径100μm以下の微粒子からなる水溶性重合体の構成成分が、下記一般式(1)及び/又は(2)で表わされるカチオン性水溶性単量体をaモル%、下記一般式(3)で表わされるアニオン性水溶性単量体をbモル%とする時、aとbが10≧a/b≧0.7の条件を満たす範囲に存在する両性水溶性重合体であることを特徴とする請求項1あるいは2に記載の活性汚泥流出防止方法である。
R1は水素又はメチル基、R2、R3は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、R4は水素、炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基であり、同種でも異種でも良い。Aは酸素またはNH、Bは炭素数2〜4のアルキレン基またはアルコキシレン基、X1は陰イオンをそれぞれ表わす。
R5は水素又はメチル基、R6、R7は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、X2は陰イオンをそれぞれ表わす。
R8は水素、メチル基またはカルボキシメチル基、QはSO3、C6H4SO3、CONHC(CH3)2CH2SO3、C6H4COOあるいはCOO、R9は水素またはCOOY2、Y1あるいはY2は水素または陽イオンをそれぞれ表す。
In the invention of claim 3, the constituent of the water-soluble polymer composed of fine particles having a particle diameter of 100 μm or less is a mole of the cationic water-soluble monomer represented by the following general formula (1) and / or (2). %, When the anionic water-soluble monomer represented by the following general formula (3) is b mol%, a and b are in the range satisfying the condition of 10 ≧ a / b ≧ 0.7. It is a polymer, The activated sludge outflow prevention method of Claim 1 or 2 characterized by the above-mentioned.
R1 is hydrogen or a methyl group, R2 and R3 are alkyl groups having 1 to 3 carbon atoms, alkoxy groups or benzyl groups, R4 is hydrogen, an alkyl group having 1 to 3 carbon atoms, alkoxy groups or benzyl groups. But it ’s okay. A represents oxygen or NH, B represents an alkylene group or alkoxylene group having 2 to 4 carbon atoms, and X1 represents an anion.
R5 represents hydrogen or a methyl group, R6 and R7 each represents an alkyl group having 1 to 3 carbon atoms, an alkoxy group or a benzyl group, and X2 represents an anion.
R8 represents hydrogen, a methyl group or a carboxymethyl group, Q represents SO3, C6H4SO3, CONHC (CH3) 2CH2SO3, C6H4COO or COO, R9 represents hydrogen or COOY2, Y1 or Y2 represents hydrogen or a cation, respectively.
本発明で使用するカチオン性あるいは両性からなる粒径100μm以下の水溶性重合体微粒子とポリアルキレンイミン酸中和物とが共存する水溶性重合体分散液は、以下の操作によって製造することができる。すなわちポリアルキレンイミンの20〜50重量%水溶液を用意し、有機又は無機酸によりアミン当量の50〜100%を中和する。この時の水溶液pHは、2〜12に調整した後、この水溶液に単量体を加え混合する。単量体濃度としては、10〜40重量%であり、好ましくは15〜30重量%である。ポリアルキレンイミンの単量体に対する添加量は、20〜200重量%であるが、好ましくは20〜150重量%、さらに好ましくは40〜150重量%である。 The water-soluble polymer dispersion in which the water-soluble polymer fine particles having a particle diameter of 100 μm or less and the neutralized polyalkyleneiminate used in the present invention coexist can be produced by the following operation. . That is, a 20 to 50% by weight aqueous solution of polyalkylenimine is prepared, and 50 to 100% of the amine equivalent is neutralized with an organic or inorganic acid. The aqueous solution pH at this time is adjusted to 2 to 12, and then the monomer is added to the aqueous solution and mixed. The monomer concentration is 10 to 40% by weight, preferably 15 to 30% by weight. The amount of polyalkyleneimine added to the monomer is 20 to 200% by weight, preferably 20 to 150% by weight, and more preferably 40 to 150% by weight.
その後、窒素雰囲気下にて、重合開始剤、例えば2、2’−アゾビス(アミジノプロパン)二塩化水素化物または2、2’−ビス〔2−(5−メチル−2−イミダゾリン−2−イル)プロパン〕二
塩化水素化物のような水溶性アゾ系重合開始剤、あるいは過硫酸アンモニウムおよび亜硫酸水素ナトリウム併用のような水溶性レドックス系重合開始剤を添加し、撹拌下ラジカル重合を行う。重合の反応温度は0〜100℃の範囲で重合開始剤の性質に応じて任意に選ぶ事ができるが、好ましくは10〜60℃であり、更に好ましくは20〜50℃である。
Then, under a nitrogen atmosphere, a polymerization initiator such as 2,2′-azobis (amidinopropane) dichloride or 2,2′-bis [2- (5-methyl-2-imidazolin-2-yl) Propane] A water-soluble azo polymerization initiator such as dihydrochloride or a water-soluble redox polymerization initiator such as ammonium persulfate and sodium bisulfite in combination is added, and radical polymerization is carried out with stirring. The polymerization reaction temperature can be arbitrarily selected in the range of 0 to 100 ° C. according to the properties of the polymerization initiator, but is preferably 10 to 60 ° C., more preferably 20 to 50 ° C.
本発明で使用するポリアルキレンイミンは、ポリエチレンイミンあるいはポリプロピレンイミンなどであるが、実用的にはポリエチレンイミンである。分子量は、5000以上あれば本発明の分散重合に使用できるが、あまり重合度が高いと分散液の粘性が高くなり好ましくない。従って好ましくは5,000以上、500,000以下であり、更に好ましくは5,000以上、200,000以下である。 The polyalkyleneimine used in the present invention is polyethyleneimine or polypropyleneimine, but is practically polyethyleneimine. If the molecular weight is 5000 or more, it can be used for the dispersion polymerization of the present invention, but if the degree of polymerization is too high, the viscosity of the dispersion becomes high, which is not preferable. Therefore, it is preferably 5,000 or more and 500,000 or less, more preferably 5,000 or more and 200,000 or less.
重合は一般的には中性〜酸性で行うのが、単量体も安定であり、反応性も良好であり、重合度や重合率も向上するので、ポリアルキレンイミンは、中和して弱アルカリ〜酸性の水溶液とすることが好ましい。pHとしては12〜2であり、好ましくは10〜3であり、更好ましくは6〜3である。中和する酸は、有機あるいは無機の酸を使用する。有機酸としては、蟻酸、酢酸、アジピン酸などであり、無機酸としては塩酸、硫酸、スルファミン酸などであるが、硫酸が特に好ましい。中和度としては、分子中のアミノ基に対して50〜100当量%である。 Polymerization is generally carried out from neutral to acidic, but the monomer is stable, the reactivity is good, the degree of polymerization and the polymerization rate are improved, so the polyalkyleneimine is neutralized and weakened. An alkaline to acidic aqueous solution is preferred. As pH, it is 12-2, Preferably it is 10-3, More preferably, it is 6-3. As the acid to be neutralized, an organic or inorganic acid is used. Examples of the organic acid include formic acid, acetic acid, and adipic acid, and examples of the inorganic acid include hydrochloric acid, sulfuric acid, sulfamic acid, and the like, and sulfuric acid is particularly preferable. As a neutralization degree, it is 50-100 equivalent% with respect to the amino group in a molecule | numerator.
分子量調節のため通常のラジカル重合に用いられるようなイソプロピルアルコールやメルカプタン等の連鎖移動剤の添加が任意に選択できる。重合体微細粒子の分散安定化のため、撹拌を行う必要がり、撹拌速度の上限は無く、任意の撹拌条件を選ぶことができる。 Addition of a chain transfer agent such as isopropyl alcohol or mercaptan, which is used for ordinary radical polymerization for molecular weight control, can be arbitrarily selected. In order to stabilize the dispersion of the polymer fine particles, it is necessary to perform stirring, and there is no upper limit of the stirring speed, and arbitrary stirring conditions can be selected.
次に水溶性重合体を製造する場合に使用する単量体について説明する。カチオン性水溶性重合体を製造する場合には、カチオン性単量体の一種以上を使用し、また非イオン性単量体との共重合をすることもできる。カチオン性水溶性単量体の例としては、一般式(1)で表される(メタ)アクリル酸ジメチルアミノエチルやジメチルアミノプロピル(メタ)アクリルアミド、メチルジアリルアミンなどの重合体や共重合体が上げられ、四級アンモニウム基含重合体の例は、前記三級アミノ含有単量体の塩化メチルや塩化ベンジルによる四級化物である(メタ)アクリロイルオキシエチルトリメチルアンモニウム塩化物、(メタ)アクリロイルオキシ2−ヒドロキシプロピルトリメチルアンモニウム塩化物、(メタ)アクリロイルアミノプロピルトリメチルアンモニウム塩化物、(メタ)アクリロイルオキシエチルジメチルベンジルアンモニウム塩化物、(メタ)アクリロイルオキシ2−ヒドロキシプロピルジメチルベンジルアンモニウム塩化物、(メタ)アクリロイルアミノプロピルジメチルベンジルアンモニウム塩化物などである。また、一般式(2)で表されるジメチルジアリルアンモニウム系単量体も使用可能であり、その例としてジメチルジアリルアンモニウム塩化物、ジアリルメチルベンジルアンモニウム塩化物などである。 Next, the monomer used when manufacturing a water-soluble polymer is demonstrated. In the case of producing a cationic water-soluble polymer, one or more cationic monomers can be used, and copolymerization with a nonionic monomer can also be performed. Examples of cationic water-soluble monomers include polymers and copolymers such as dimethylaminoethyl (meth) acrylate, dimethylaminopropyl (meth) acrylamide, and methyldiallylamine represented by the general formula (1). Examples of the quaternary ammonium group-containing polymer are (meth) acryloyloxyethyltrimethylammonium chloride and (meth) acryloyloxy 2 which are quaternized products of the above-mentioned tertiary amino-containing monomers with methyl chloride or benzyl chloride. -Hydroxypropyltrimethylammonium chloride, (meth) acryloylaminopropyltrimethylammonium chloride, (meth) acryloyloxyethyldimethylbenzylammonium chloride, (meth) acryloyloxy 2-hydroxypropyldimethylbenzylammonium chloride, (meth) Acryloyl aminopropyl dimethyl benzyl ammonium chloride, and the like. Moreover, the dimethyl diallyl ammonium-type monomer represented by General formula (2) can also be used, for example, dimethyl diallyl ammonium chloride, diallyl methyl benzyl ammonium chloride, etc.
非イオン性水溶性単量体の例としては、(メタ)アクリルアミド、N,N−ジメチルアクリルアミド、酢酸ビニル、アクリロニトリル、アクリル酸メチル、(メタ)アクリル酸2−ヒドロキシエチル、ジアセトンアクリルアミド、N−ビニルピロリドン、N−ビニルホルムアミド、N−ビニルアセトアミド、アクリロイルモルホリン、アクリロイルピペラジンなどがあげられる。 Examples of nonionic water-soluble monomers include (meth) acrylamide, N, N-dimethylacrylamide, vinyl acetate, acrylonitrile, methyl acrylate, 2-hydroxyethyl (meth) acrylate, diacetone acrylamide, N- Examples include vinylpyrrolidone, N-vinylformamide, N-vinylacetamide, acryloylmorpholine, acryloylpiperazine and the like.
両性水溶性重合体を製造する場合には、前記カチオン性と非イオン性水溶性単量体に加えて、さらに一般式(3)で表されるアニオン性水溶性単量体を共重合する。その例としては、スルホン基でもカルボキシル基でもさしつかいなく、両方を併用しても良い。スルホン基含有単量体の例は、ビニルスルホン酸、ビニルベンゼンスルホン酸あるいは2−アクリルアミド2−メチルプロパンスルホン酸などである。またカルボキシル基含有単量体の例は、メタクリル酸、アクリル酸、イタコン酸、マレイン酸あるいはp−カルボキシスチレンなどである。 When the amphoteric water-soluble polymer is produced, in addition to the cationic and nonionic water-soluble monomers, an anionic water-soluble monomer represented by the general formula (3) is further copolymerized. For example, either a sulfone group or a carboxyl group may be used, and both may be used in combination. Examples of the sulfone group-containing monomer are vinyl sulfonic acid, vinyl benzene sulfonic acid, 2-acrylamido 2-methylpropane sulfonic acid, and the like. Examples of the carboxyl group-containing monomer include methacrylic acid, acrylic acid, itaconic acid, maleic acid, and p-carboxystyrene.
重合開始は、ラジカル重合開始剤を用いる。そのような開始剤は油溶性あるいは水溶性のどちらでも良く、アゾ系,過酸化物系、レドックス系いずれでも重合することが可能である。油溶性アゾ系開始剤の例としては、2、2’−アゾビスイソブチロニトリル、1、1’−アゾビス(シクロヘキサンカルボニトリル)、2、2’−アゾビス(2−メチルブチロニトリル)、2、2’−アゾビス(2−メチルプロピオネ−ト)、4、4−アゾビス(4−メトキシ−2、4ジメチル)バレロニトリルなどがあげられ、水混溶性溶剤に溶解し添加する。 For initiation of polymerization, a radical polymerization initiator is used. Such an initiator may be either oil-soluble or water-soluble, and can be polymerized by any of azo, peroxide and redox systems. Examples of oil-soluble azo initiators are 2,2′-azobisisobutyronitrile, 1,1′-azobis (cyclohexanecarbonitrile), 2,2′-azobis (2-methylbutyronitrile), 2,2′-azobis (2-methylpropionate), 4,4-azobis (4-methoxy-2,4dimethyl) valeronitrile and the like are mentioned and dissolved in a water-miscible solvent and added.
水溶性アゾ系開始剤の例としては、2、2’−アゾビス(アミジノプロパン)二塩化水素化物、2、2’−アゾビス〔2−(5−メチル−2−イミダゾリン−2−イル)プロパン〕二塩化水素化物、4、4’−アゾビス(4−シアノ吉草酸)などがあげられる。またレドックス系の例としては、ペルオクソ二硫酸アンモニウムと亜硫酸ナトリウム、亜硫酸水素ナトリウム、トリメチルアミン、テトラメチルエチレンジアミンなどとの組み合わせがあげられる。さらに過酸化物の例としては、ペルオクソ二硫酸アンモニウムあるいはカリウム、過酸化水素、ベンゾイルペルオキサイド、ラウロイルペルオキサイド、オクタノイルペルオキサイド、サクシニックペルオキサイド、t-ブチルペルオキシ2−エチルヘキサノエ−トなどをあげることができる。 Examples of water-soluble azo initiators include 2,2′-azobis (amidinopropane) dichloride, 2,2′-azobis [2- (5-methyl-2-imidazolin-2-yl) propane] And dihydrochloride, 4,4′-azobis (4-cyanovaleric acid), and the like. Examples of redox systems include a combination of ammonium peroxodisulfate and sodium sulfite, sodium hydrogen sulfite, trimethylamine, tetramethylethylenediamine, and the like. Further examples of peroxides include ammonium or potassium peroxodisulfate, hydrogen peroxide, benzoyl peroxide, lauroyl peroxide, octanoyl peroxide, succinic peroxide, t-butylperoxy 2-ethylhexanoate, and the like. I can give you.
本発明のイオン性水溶性重合体分散液は、単量体を重合する際、ポリアルキレンイミンを共存させるので、ポリアルキレンイミンの一部に一般式(1)〜(3)で表される単量体がグラフト重合していると推定される。さらにポリアルキレンイミンは、非常に枝分かれした構造をしているため、それだけグラフト重合も起こりやすいと考えられ、分散液の安定化にも大いに寄与すると推定され、重合の分散媒としては非常に適した材料である。 In the ionic water-soluble polymer dispersion of the present invention, since a polyalkyleneimine is allowed to coexist when the monomer is polymerized, a single unit represented by the general formulas (1) to (3) is included in a part of the polyalkyleneimine. It is presumed that the monomer is graft polymerized. Furthermore, since polyalkyleneimine has a very branched structure, it is considered that graft polymerization is likely to occur as much, and it is estimated that it will greatly contribute to the stabilization of the dispersion, and is very suitable as a dispersion medium for polymerization. Material.
また、本発明のイオン性水溶性重合体分散液は、ポリアルキレンイミンの他、分子量の比較的低い他のカチオン性水溶性重合体を併用することも好ましい。そのようなカチオン性水溶性重合体としては、前記一般式(1)及び/又は前記一般式(2)で表されるカチオン性単量体一種以上の重合体あるいは共重合体である。あるいは前記カチオン性単量体一種以上と水溶性非イオン性単量体との共重合体も使用できる。これらカチオン性水溶性重合体は、重合時、あるいは重合後添加する。分子量は、1,000〜3,000,000であり、好ましくは10,000〜2,000,000である。 The ionic water-soluble polymer dispersion of the present invention is preferably used in combination with another cationic water-soluble polymer having a relatively low molecular weight in addition to the polyalkyleneimine. Such a cationic water-soluble polymer is a polymer or copolymer of one or more cationic monomers represented by the general formula (1) and / or the general formula (2). Alternatively, a copolymer of at least one cationic monomer and a water-soluble nonionic monomer can also be used. These cationic water-soluble polymers are added during polymerization or after polymerization. The molecular weight is 1,000 to 3,000,000, preferably 10,000 to 2,000,000.
重合は10〜50℃で実施することが好ましく、15〜40℃で実施することが更に好ましい。単量体濃度は15質量%から40質量%で実施することが好ましく、15質量%から30質量%で実施することが更に好ましい。また水溶性重合体の分子量は100万〜1500万であるが、好ましくは100万〜700万である。 The polymerization is preferably carried out at 10 to 50 ° C, more preferably 15 to 40 ° C. The monomer concentration is preferably 15 to 40% by mass, more preferably 15 to 30% by mass. The molecular weight of the water-soluble polymer is 1 million to 15 million, but preferably 1 million to 7 million.
本発明で使用するカチオン性あるいは両性からなる粒径100μm以下の水溶性重合体微粒子とポリアルキレンイミン酸中和物とが共存する水溶性重合体分散液は水で任意の割合で容易に希釈または溶解され、かつ添加後すぐに効果を発揮するので、排液処理における被処理液の急激な増加や汚泥沈降不良などに対して迅速に対応することができ、処理水への活性汚泥の流出を迅速に防止できる。また形成されるフロックは緻密で沈降性および圧密性に優れているので、固液分離を容易に行うことができ、このため処理水への活性汚泥の流出を簡単な操作で効率よく防止することができる。さらに少量の薬剤添加量で優れた沈降性改善効果を発揮するので、薬剤の使用量を少なくして低コストで処理することができる。 The water-soluble polymer dispersion in which the water-soluble polymer fine particles having a particle size of 100 μm or less and the neutralized polyalkyleneiminate used in the present invention coexist is easily diluted with water at an arbitrary ratio or Since it is dissolved and exerts its effect immediately after addition, it can respond quickly to sudden increase in liquid to be treated and sludge sedimentation failure in drainage treatment, and it can prevent activated sludge from flowing into the treated water. It can be prevented quickly. In addition, the flocs that are formed are dense and have excellent sedimentation and compaction properties, so that solid-liquid separation can be easily performed. Therefore, it is possible to efficiently prevent the activated sludge from flowing into the treated water with a simple operation. Can do. Furthermore, since an excellent effect of improving the sedimentation property is exhibited with a small amount of drug added, the amount of drug used can be reduced and processing can be performed at low cost.
水溶性カチオン性あるいは両性水溶性重合体の添加位置は曝気槽から沈殿槽に至る系路であれば特に限定されず、例えば曝気槽;曝気槽から沈殿槽までの間の連絡路;沈殿槽のセンターコア部などで添加することができる。また、曝気槽から沈殿槽までの間に凝集槽を設けて添加することができる。曝気槽に添加する場合は曝気により撹拌されるので特別な撹拌を行う必要はなく、また曝気槽から沈殿槽までの間の連絡路に添加する場合も水が移送される際の撹拌で十分であるので特別な撹拌は必要ない。 The addition position of the water-soluble cationic or amphoteric water-soluble polymer is not particularly limited as long as it is a system route from the aeration tank to the precipitation tank. For example, the aeration tank; the communication path from the aeration tank to the precipitation tank; It can be added at the center core portion or the like. Moreover, a coagulation tank can be provided and added between an aeration tank and a precipitation tank. When adding to the aeration tank, it is agitated by aeration, so there is no need to perform special agitation. Also when adding to the communication path from the aeration tank to the precipitation tank, the agitation when water is transferred is sufficient. There is no need for special stirring.
水溶性カチオン性あるいは両性重合体の添加は連続的に行うこともできるし、間欠的に行うこともできる。また、活性汚泥の沈降性が悪化した場合、または悪化が予想される場合に添加することができる。 The addition of the water-soluble cationic or amphoteric polymer can be performed continuously or intermittently. Moreover, when the sedimentation property of activated sludge deteriorates, or when deterioration is anticipated, it can add.
水溶性カチオン性あるいは両性水溶性重合体は、分散液の状態で添加することもできるし、水で希釈して添加することもでき、水に溶解して添加することもできる。本発明では水に溶解した溶液状態で添加すると直ちに汚泥と反応するため、新たに撹拌装置などを設けることなく、そのまま液の流動する系路に添加しても十分な沈降促進効果が得られるので好ましい。 The water-soluble cationic or amphoteric water-soluble polymer can be added in the form of a dispersion, diluted with water, or dissolved in water. In the present invention, when it is added in a solution dissolved in water, it immediately reacts with sludge. Therefore, a sufficient settling promoting effect can be obtained even if it is added as it is to a system in which the liquid flows without newly providing a stirring device or the like. preferable.
添加時の水溶液濃度は、0.05〜1.0質量%、好ましくは0.1〜0.5質量%である。添加量は、被処理液のSS濃度などにより異なるが、被処理液に対して通常1〜50mg/L、好ましくは2〜20mg/Lとするのが望ましい。 The aqueous solution density | concentration at the time of addition is 0.05-1.0 mass%, Preferably it is 0.1-0.5 mass%. The addition amount varies depending on the SS concentration of the liquid to be treated, but is usually 1 to 50 mg / L, preferably 2 to 20 mg / L with respect to the liquid to be treated.
(実施例)以下、実施例および比較例によって本発明をさらに詳しく説明するが、本発明はその要旨を超えない限り、以下の実施例に制約されるものではない。 (Examples) Hereinafter, the present invention will be described in more detail with reference to examples and comparative examples. However, the present invention is not limited to the following examples unless it exceeds the gist.
(合成例1)攪拌機および温度制御装置を備えた反応器に50重量%ポリエチレンイミン水溶液(重量平均分子量;50,000)50部をイオン交換水21.5部に溶解し、75重量%硫酸28.5部を冷却攪拌下添加し、pHを4.8〜5.5に調整した。攪拌機、窒素曝気管および温度制御装置を備えた反応器に前記操作により中和したポリエチレンイミン水溶液78.0gを仕込み、メタクロイルオキシエチルトリメチルアンモニウムクロリド80%水溶液48.8g、イオン交換水63.2gを仕込み混合した。窒素で置換しながら10重量%の2,2アゾビス(N,N−ジメチレンイソブチルアミジン)ジハイドロクロライド水溶液を重合開始剤として対モノマーあたり重量で500ppm添加し、撹拌下36℃で18時間重合した。その結果、粒径10〜100μmの微粒子の重合体分散液が得られた(試料−1)。生成したポリマ―分散液をB型粘度計により測定した分散液の粘度、及び静的光散乱法による分子量測定器(大塚電子製DLS−7000)によって重量平均分子量を測定した。結果を表1に示す。 (Synthesis Example 1) In a reactor equipped with a stirrer and a temperature controller, 50 parts by weight of a 50% by weight aqueous polyethyleneimine solution (weight average molecular weight; 50,000) was dissolved in 21.5 parts of ion-exchanged water, and 75% by weight sulfuric acid 28 0.5 part was added under cooling and stirring, and the pH was adjusted to 4.8 to 5.5. A reactor equipped with a stirrer, a nitrogen aeration tube and a temperature controller was charged with 78.0 g of the aqueous solution of polyethylenimine neutralized by the above-mentioned operation, 48.8 g of 80% aqueous solution of methacryloyloxyethyltrimethylammonium chloride, 63.2 g of ion-exchanged water. Were mixed. While substituting with nitrogen, 500 ppm by weight of a 2,2 azobis (N, N-dimethyleneisobutylamidine) dihydrochloride aqueous solution as a polymerization initiator was added by weight per monomer and polymerized at 36 ° C. for 18 hours with stirring. . As a result, a polymer dispersion of fine particles having a particle size of 10 to 100 μm was obtained (Sample-1). The resulting polymer dispersion was measured for the viscosity of the dispersion measured with a B-type viscometer, and the weight average molecular weight was measured using a molecular weight measuring device (DLS-7000, manufactured by Otsuka Electronics Co., Ltd.) by the static light scattering method. The results are shown in Table 1.
また上記操作と同様に表ー1記載の組成のモノマーを表1記載の単量体濃度になるように仕込み、重合操作を行い水溶性重合体分散液を得た(試料−2〜試料−5)。結果を表1に示す。
Similarly to the above operation, monomers having the composition shown in Table-1 were charged so as to have the monomer concentration shown in Table 1, and polymerization operation was performed to obtain water-soluble polymer dispersions (Sample-2 to Sample-5). ). The results are shown in Table 1.
(表1)
DMQ:アクロルオキシエチルトリメチルアンモニウムクロリド、
DMC:メタクロルオキシエチルトリメチルアンモニウムクロリド、
AAC:アクリル酸、AAM:アクリルアミド、
PEI比;ポリエチレンイミンの対単量体質量%、製品粘度:mPa・s
a/b;カチオン性単量体とアニオン性単量体とのモル比
水溶液(1);ポリアミン系凝結剤(濃度50質量%)
(Table 1)
DMQ: chlorooxyethyltrimethylammonium chloride,
DMC: methachlorooxyethyltrimethylammonium chloride,
AAC: acrylic acid, AAM: acrylamide,
PEI ratio:% by weight of monomer of polyethyleneimine, product viscosity: mPa · s
a / b: molar ratio aqueous solution of cationic monomer and anionic monomer (1); polyamine coagulant (concentration: 50 mass%)
沈殿槽において沈降性が悪く流出トラブルが発生している活性汚泥、MLSS濃度2800mg/L、SVIが220(mL/g)を曝気槽から1000mLメスシリンダーに1000mL採取し、表1の試料1〜試料5を対活性汚泥分散液5mg/L添加後転倒攪拌5回を行い静置し、対活性汚泥分散液の沈降性を比較するため5分後の沈降界面容積を測定した。その結果を表2に示す。 Collect 1000 mL of activated sludge with poor sedimentation in the sedimentation tank, MLSS concentration of 2800 mg / L, SVI of 220 (mL / g) from the aeration tank into a 1000 mL graduated cylinder. 5 was added after 5 mg / L of the activated sludge dispersion, and the mixture was allowed to stand by inversion 5 times. The sedimentation interface volume after 5 minutes was measured in order to compare the sedimentation properties of the activated sludge dispersion. The results are shown in Table 2.
(比較試験)比較試験として実施例1と同様の操作により表1の比較1〜比較3のポリアミン系凝結剤、および粉末形態の重合系高分子凝集剤を対活性汚泥分散液5mg/L添加し、対活性汚泥分散液の沈降性を比較するため5分後の沈降界面容積を測定した。なおポリアミン系凝結剤は製品のまま添加、粉末高分子凝集剤は0.2質量%で添加した。その結果を表2に示す。 (Comparative test) As a comparative test, 5 mg / L of the activated sludge dispersion liquid was added to the polyamine-based coagulant of Comparative 1 to Comparative 3 in Table 1 and the polymerized polymer flocculant in powder form by the same operation as in Example 1. In order to compare the sedimentation properties of the activated sludge dispersion liquid, the sedimentation interface volume after 5 minutes was measured. The polyamine coagulant was added as it was, and the powder polymer flocculant was added at 0.2% by mass. The results are shown in Table 2.
(表2)
添加量;対汚泥分散液(mg/L)、沈降界面容積(mL)
(Table 2)
Amount added; sludge dispersion (mg / L), sedimentation interface volume (mL)
本発明の活性汚泥の流出防止方法は、活性汚泥を保持する曝気槽に排液を導入して生物処理する活性汚泥法において、混合液を沈殿槽に導いて沈殿分離し、分離汚泥の一部を曝気槽に返送する排液処理方法において、曝気槽から沈殿槽に至る系路に沈降剤としてカチオン性あるいは両性からなる粒径100μm以下の水溶性重合体微粒子とポリアルキレンイミン酸中和物とが共存する水溶性重合体分散液を添加することからなる。この活性汚泥の流出防止方法は水処理分野において種々の適用が可能であり、産業上の利用価値は高い。
The activated sludge spill prevention method of the present invention is an activated sludge method in which waste liquid is introduced into an aeration tank holding activated sludge and biologically treated. In the drainage treatment method for returning the water to the aeration tank, a water-soluble polymer fine particle having a particle size of 100 μm or less having a particle size of 100 μm or less as a precipitating agent and a neutralized polyalkyleneimine acid as a precipitating agent in the system from the aeration tank to the precipitation tank It consists of adding a water-soluble polymer dispersion in which coexist. This activated sludge spill prevention method can be applied in various ways in the field of water treatment and has high industrial utility value.
Claims (3)
R1は水素又はメチル基、R2、R3は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、R4は水素、炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基であり、同種でも異種でも良い。Aは酸素またはNH、Bは炭素数2〜4のアルキレン基またはアルコキシレン基、X1は陰イオンをそれぞれ表わす。
R5は水素又はメチル基、R6、R7は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、X2は陰イオンをそれぞれ表わす。
R8は水素、メチル基またはカルボキシメチル基、QはSO3、C6H4SO3、CONHC(CH3)2CH2SO3、C6H4COOあるいはCOO、R9は水素またはCOOY2、Y1あるいはY2は水素または陽イオンをそれぞれ表す。 The water-soluble polymer dispersion in which the water-soluble polymer fine particles and the polyalkyleneiminate neutralized substance coexist is a cationic water-soluble monomer 5 represented by the following general formula (1) and / or (2): A monomer (mixture) composed of 100 mol%, 0 to 50 mol% of an anionic water-soluble monomer represented by the following general formula (3), and 0 to 95 mol% of a nonionic water-soluble monomer is stirred. The method of preventing activated sludge outflow according to claim 1, wherein the activated sludge is produced by dispersion polymerization in an aqueous solution of a neutralized polyalkylenimine acid.
R1 is hydrogen or a methyl group, R2 and R3 are alkyl groups having 1 to 3 carbon atoms, alkoxy groups or benzyl groups, R4 is hydrogen, an alkyl group having 1 to 3 carbon atoms, alkoxy groups or benzyl groups. But it ’s okay. A represents oxygen or NH, B represents an alkylene group or alkoxylene group having 2 to 4 carbon atoms, and X1 represents an anion.
R5 represents hydrogen or a methyl group, R6 and R7 each represents an alkyl group having 1 to 3 carbon atoms, an alkoxy group or a benzyl group, and X2 represents an anion.
R8 represents hydrogen, a methyl group or a carboxymethyl group, Q represents SO3, C6H4SO3, CONHC (CH3) 2CH2SO3, C6H4COO or COO, R9 represents hydrogen or COOY2, Y1 or Y2 represents hydrogen or a cation, respectively.
R1は水素又はメチル基、R2、R3は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、R4は水素、炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基であり、同種でも異種でも良い。Aは酸素またはNH、Bは炭素数2〜4のアルキレン基またはアルコキシレン基、X1は陰イオンをそれぞれ表わす。
R5は水素又はメチル基、R6、R7は炭素数1〜3のアルキル基、アルコキシ基あるいはベンジル基、X2は陰イオンをそれぞれ表わす。
R8は水素、メチル基またはカルボキシメチル基、QはSO3、C6H4SO3、CONHC(CH3)2CH2SO3、C6H4COOあるいはCOO、R9は水素またはCOOY2、Y1あるいはY2は水素または陽イオンをそれぞれ表す。
The component of the water-soluble polymer comprising fine particles having a particle size of 100 μm or less is a mol% of a cationic water-soluble monomer represented by the following general formula (1) and / or (2), and the following general formula (3 ) Is an amphoteric water-soluble polymer existing in a range where a and b satisfy the condition of 10 ≧ a / b ≧ 0.7 when the anionic water-soluble monomer represented by b) is b mol%. The activated sludge outflow prevention method according to claim 1 or 2.
R1 is hydrogen or a methyl group, R2 and R3 are alkyl groups having 1 to 3 carbon atoms, alkoxy groups or benzyl groups, R4 is hydrogen, an alkyl group having 1 to 3 carbon atoms, alkoxy groups or benzyl groups. But it ’s okay. A represents oxygen or NH, B represents an alkylene group or alkoxylene group having 2 to 4 carbon atoms, and X1 represents an anion.
R5 represents hydrogen or a methyl group, R6 and R7 each represents an alkyl group having 1 to 3 carbon atoms, an alkoxy group or a benzyl group, and X2 represents an anion.
R8 represents hydrogen, a methyl group or a carboxymethyl group, Q represents SO3, C6H4SO3, CONHC (CH3) 2CH2SO3, C6H4COO or COO, R9 represents hydrogen or COOY2, Y1 or Y2 represents hydrogen or a cation, respectively.
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JP2009119310A (en) * | 2007-11-12 | 2009-06-04 | Hymo Corp | Activated sludge settling method |
JP2017154033A (en) * | 2016-02-29 | 2017-09-07 | ハイモ株式会社 | Active sludge settling method |
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JPH09141006A (en) * | 1995-11-21 | 1997-06-03 | Kurita Water Ind Ltd | Flocculating and settling device |
JP2001276873A (en) * | 2000-03-29 | 2001-10-09 | Kurita Water Ind Ltd | Waste liquor treating method |
JP2004057927A (en) * | 2002-07-29 | 2004-02-26 | Hymo Corp | Using method of water-soluble polymer dispersion |
JP2004344741A (en) * | 2003-05-21 | 2004-12-09 | Nippon Soda Co Ltd | Sewage treatment method |
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JPH09141006A (en) * | 1995-11-21 | 1997-06-03 | Kurita Water Ind Ltd | Flocculating and settling device |
JP2001276873A (en) * | 2000-03-29 | 2001-10-09 | Kurita Water Ind Ltd | Waste liquor treating method |
JP2004057927A (en) * | 2002-07-29 | 2004-02-26 | Hymo Corp | Using method of water-soluble polymer dispersion |
JP2004344741A (en) * | 2003-05-21 | 2004-12-09 | Nippon Soda Co Ltd | Sewage treatment method |
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JP2009119310A (en) * | 2007-11-12 | 2009-06-04 | Hymo Corp | Activated sludge settling method |
JP2017154033A (en) * | 2016-02-29 | 2017-09-07 | ハイモ株式会社 | Active sludge settling method |
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