JP4748773B2 - Disinfectant algicide having ability to prevent discoloration and discoloration prevention method - Google Patents
Disinfectant algicide having ability to prevent discoloration and discoloration prevention method Download PDFInfo
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- JP4748773B2 JP4748773B2 JP2005144878A JP2005144878A JP4748773B2 JP 4748773 B2 JP4748773 B2 JP 4748773B2 JP 2005144878 A JP2005144878 A JP 2005144878A JP 2005144878 A JP2005144878 A JP 2005144878A JP 4748773 B2 JP4748773 B2 JP 4748773B2
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- discoloration
- bactericidal
- mbcp
- benzophenones
- algicidal
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- 238000002845 discoloration Methods 0.000 title claims description 25
- 238000000034 method Methods 0.000 title claims description 12
- 239000003619 algicide Substances 0.000 title description 12
- 238000004649 discoloration prevention Methods 0.000 title description 4
- 239000000645 desinfectant Substances 0.000 title 1
- 230000000844 anti-bacterial effect Effects 0.000 claims description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 31
- 230000002353 algacidal effect Effects 0.000 claims description 26
- 239000012965 benzophenone Substances 0.000 claims description 23
- 239000003795 chemical substances by application Substances 0.000 claims description 23
- 150000008366 benzophenones Chemical class 0.000 claims description 19
- 230000003405 preventing effect Effects 0.000 claims description 14
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 claims description 10
- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical group C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 9
- 230000007797 corrosion Effects 0.000 claims description 5
- 238000005260 corrosion Methods 0.000 claims description 5
- 239000003112 inhibitor Substances 0.000 claims description 5
- 239000002455 scale inhibitor Substances 0.000 claims description 5
- 230000001954 sterilising effect Effects 0.000 claims description 5
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 claims description 4
- 239000002738 chelating agent Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 238000004659 sterilization and disinfection Methods 0.000 claims description 4
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 230000000855 fungicidal effect Effects 0.000 claims description 2
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 claims 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 claims 1
- 230000003641 microbiacidal effect Effects 0.000 claims 1
- CVRALZAYCYJELZ-UHFFFAOYSA-N O-(4-bromo-2,5-dichlorophenyl) O-methyl phenylphosphonothioate Chemical compound C=1C=CC=CC=1P(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl CVRALZAYCYJELZ-UHFFFAOYSA-N 0.000 description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 21
- 239000000203 mixture Substances 0.000 description 14
- 238000009472 formulation Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- -1 MBCP alkali metal salt Chemical class 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 241000195493 Cryptophyta Species 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 241000589248 Legionella Species 0.000 description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- 208000007764 Legionnaires' Disease Diseases 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 3
- 239000012964 benzotriazole 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
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000498 cooling water Substances 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- OKJFKPFBSPZTAH-UHFFFAOYSA-N (2,4-dihydroxyphenyl)-(4-hydroxyphenyl)methanone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O OKJFKPFBSPZTAH-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 239000007995 HEPES buffer Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 239000008235 industrial water Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000013055 pulp slurry Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- ZRDYULMDEGRWRC-UHFFFAOYSA-N (4-hydroxyphenyl)-(2,3,4-trihydroxyphenyl)methanone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C(O)=C1O ZRDYULMDEGRWRC-UHFFFAOYSA-N 0.000 description 1
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical class O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 description 1
- MXYOPVWZZKEAGX-UHFFFAOYSA-N 1-phosphonoethylphosphonic acid Chemical compound OP(=O)(O)C(C)P(O)(O)=O MXYOPVWZZKEAGX-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 description 1
- 208000019901 Anxiety disease Diseases 0.000 description 1
- 241000192700 Cyanobacteria Species 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-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
- 241000589242 Legionella pneumophila Species 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-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
- 206010040880 Skin irritation Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- WXNRYSGJLQFHBR-UHFFFAOYSA-N bis(2,4-dihydroxyphenyl)methanone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O WXNRYSGJLQFHBR-UHFFFAOYSA-N 0.000 description 1
- OCWYEMOEOGEQAN-UHFFFAOYSA-N bumetrizole Chemical compound CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O OCWYEMOEOGEQAN-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229940115932 legionella pneumophila Drugs 0.000 description 1
- 239000007788 liquid Substances 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
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QJQAMHYHNCADNR-UHFFFAOYSA-N n-methylpropanamide Chemical compound CCC(=O)NC QJQAMHYHNCADNR-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- LYKRPDCJKSXAHS-UHFFFAOYSA-N phenyl-(2,3,4,5-tetrahydroxyphenyl)methanone Chemical compound OC1=C(O)C(O)=CC(C(=O)C=2C=CC=CC=2)=C1O LYKRPDCJKSXAHS-UHFFFAOYSA-N 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 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
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
本発明は、変色防止効果能を有する殺菌殺藻剤及びそれを使用する変色防止方法に関するものである。
更に詳しくは、紙・パルプ工場における抄紙工程水やパルプスラリー、各種工業用の冷却水や工程水、洗浄水、コーティングカラー、切削油、ラテックス、合成樹脂エマルジョン、デンプンスラリー、炭酸カルシウムスラリー、繊維油剤等の微生物による被害を防止するのに有用な殺菌殺藻剤及び変色防止方法に関するものである。
The present invention relates to a bactericidal algicidal agent having a discoloration preventing effect and a discoloration preventing method using the same.
More specifically, papermaking process water and pulp slurry in paper and pulp mills, various industrial cooling water and process water, washing water, coating color, cutting oil, latex, synthetic resin emulsion, starch slurry, calcium carbonate slurry, fiber oil agent The present invention relates to a bactericidal algicide and a method for preventing discoloration that are useful for preventing damage caused by microorganisms such as the above.
近年、各種工業用水のスライムによる障害が多発し、種々の弊害をもたらしている。スライムは、主として微生物の繁殖によって生じる粘性塊状〜泥状の物質であり、例えば、工場の冷却水系統の熱交換器や配管などにこのスライムが発生すると、冷却効率を低下させたり、あるいは増殖により配管を閉塞させるトラブルを引起す原因となる。また、紙・パルプ工場の抄紙工程水やパルプスラリーにスライムが発生すると、これが剥離して、紙・パルプに混入して紙切れの原因になったり、紙やパルプ製品自体に斑点、着色を生じさせ、製品品質の低下につながる。この微生物に起因するスライム障害を防止するためにこれまで各種の微生物防除剤が開発されている。2,2’−メチレンビス(4−クロロフェノール)(以下、MBCPという)は、古くから殺菌剤として知られており、その改良が広く行われている。例えばMBCPにエチレンジアミンを配合するもの(特許文献1)やグリコール類又はアミン類を配合するもの(特許文献2)等が提案されている。また、本発明で使用するベンゾフェノン類、例えば2,4−ジヒドロキシベンゾフェノン、4,4’−ジヒドロキシベンゾフェノン、2,2’,4,4’−テトラヒドロキシベンゾフェノンは、イソチアゾロン系化合物の皮膚刺激性を低減する化合物として知られている。 In recent years, various obstacles caused by slimes of various industrial waters have occurred, causing various adverse effects. Slime is a viscous mass to mud that is mainly produced by the growth of microorganisms. For example, when this slime is generated in a heat exchanger or piping of a cooling water system in a factory, it reduces cooling efficiency or This may cause troubles that block the piping. In addition, when slime is generated in the papermaking process water and pulp slurry of a paper / pulp factory, it may be peeled off and mixed into the paper / pulp, causing paper breakage, and causing spots and coloring in the paper and pulp products themselves. , Leading to product quality degradation. Various microorganism control agents have been developed so far to prevent slime damage caused by these microorganisms. 2,2'-methylenebis (4-chlorophenol) (hereinafter referred to as MBCP) has long been known as a bactericidal agent, and has been widely improved. For example, an MBCP blended with ethylenediamine (Patent Document 1) and a blend of glycols or amines (Patent Document 2) have been proposed. The benzophenones used in the present invention, such as 2,4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone, and 2,2 ′, 4,4′-tetrahydroxybenzophenone, reduce the skin irritation of isothiazolone compounds. It is known as a compound.
このようにMBCPは、殺菌剤、殺藻剤として知られており、その改良製剤も提案されているが、MBCP製剤を工業用水系等に添加した場合、有効成分濃度として数mg/1〜数十mg/lという低濃度でも、時間が経つと添加した水系が褐色に変色することがある。これは、水系の品質低下となり、また金属腐食を起しているとの不安を、作業者や使用者等にいだかせる。そして、この変色現象は、特に太陽光や紫外線照射条件下で加速される傾向がある。 Thus, MBCP is known as a bactericidal agent and an algicidal agent, and an improved preparation thereof has been proposed. However, when the MBCP preparation is added to an industrial water system or the like, the active ingredient concentration is several mg / 1 to several. Even at a low concentration of 10 mg / l, the added aqueous system may turn brown over time. This causes deterioration of the quality of the water system and gives anxiety to workers and users that metal corrosion has occurred. And this discoloration phenomenon tends to be accelerated especially under sunlight or ultraviolet irradiation conditions.
本発明は、これらの課題を解決しようとするものであり、MBCPを添加した殺菌殺藻処理対象水系の変色を防止すると共に、優れた殺菌殺藻効果を有する殺菌殺藻剤を提供することにある。更に、本発明は、MBCPを添加した殺菌殺藻処理対象水系の変色防止方法を提供するものである。 The present invention is intended to solve these problems, and provides a bactericidal algicidal agent having an excellent bactericidal and algicidal effect while preventing discoloration of the target water system for bactericidal and algae treatment to which MBCP has been added. is there. Furthermore, this invention provides the discoloration prevention method of the sterilization algae processing target water system which added MBCP.
本発明を概説すれば、本発明は、MBCPと特定のベンゾフェノン類とを含むことを特徴とする変色防止効果能を有する殺菌殺藻剤及びそれを使用する変色防止方法に関する。 Briefly, the present invention relates to a bactericidal algicidal agent having an anti-discoloration effect, characterized by containing MBCP and specific benzophenones, and a discoloration preventing method using the same.
前記の課題を解決するため、本発明者らは、鋭意研究を進めた結果、MBCPに特定のベンゾフェノン類を配合して使用した結果、MBCPによる殺菌殺藻処理対象水系の変色を防止する効果があることを見出し、この知見に基づき本発明を完成した。 In order to solve the above-mentioned problems, the present inventors have conducted extensive research, and as a result of using specific benzophenones in MBCP, the effect of preventing discoloration of the target water system for sterilization by MBCP is effective. Based on this finding, the present invention was completed.
すなわち、本発明は、
(1)MBCPと、下記一般式(1)
(式中、R1、R2、R3、R4及びR5は、同一又は異なり、水素、ヒドロキシル基又は炭素数1〜8を有するアルコキシ基を示す)で表されるベンゾフェノン類の1種又は2種以上とを含むことを特徴とする変色防止効果能を有する殺菌殺藻剤、
(2)ベンゾフェノン類が、4−ヒドロキシベンゾフェノン、2,4−ジヒドロキシベンゾフェノン、4,4’−ジヒドロキシベンゾフェノン及び2,4,4’−トリヒドロキシベンゾフェノンから選択される化合物である(1)項記載の殺菌殺藻剤、
(3)MBCPとベンゾフェノン類とを質量比で1:0.01〜1:0.5の割合で含む(1)項又は(2)項に記載の殺菌殺藻剤、
(4)水、有機溶媒並びにキレート剤、スケール防止剤及び腐食防止剤の少なくとも1種を含有する(1)項〜(3)項のいずれか1項に記載の殺菌殺藻剤。
(5)殺菌殺藻処理対象水系に対し、MBCPと、(1)項記載の一般式(I)で表されるベンゾフェノン類とを1:0・01〜1:0.5(質量比)の割合で使用することを特徴とする当該処理対象水系の変色防止方法。
That is, the present invention
(1) and MBCP, under following general formula (1)
(Wherein R 1 , R 2 , R 3 , R 4 and R 5 are the same or different and each represents hydrogen, a hydroxyl group or an alkoxy group having 1 to 8 carbon atoms), one kind of benzophenones Or bactericidal algicidal agent having anti-discoloration effect, characterized by containing two or more types ,
( 2 ) The benzophenone is a compound selected from 4-hydroxybenzophenone, 2,4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone and 2,4,4′-trihydroxybenzophenone according to item (1 ) Bactericidal algicide,
( 3 ) The bactericidal algicidal agent according to (1) or (2) , comprising MBCP and benzophenones at a mass ratio of 1: 0.01 to 1: 0.5,
( 4 ) The bactericidal algicidal agent according to any one of (1) to ( 3 ), which contains at least one of water, an organic solvent, a chelating agent, a scale inhibitor, and a corrosion inhibitor.
( 5 ) MBCP and the benzophenone represented by the general formula (I) described in the item (1) with respect to the water system subject to sterilization and algae treatment: A method for preventing discoloration of the water system to be treated, characterized by being used in a proportion.
木発明によれば、MBCPを含有する殺菌殺藻剤を添加した水系の変色を防止することができると共に、藻類や藍藻類を効果的に殺滅することができること、特にレジオネラ属細菌を始めとする各種細菌に対して優れた殺菌効果を示すこと、また、金属腐食性がないという設備面でのメリットも有するものである。 According to the present invention, it is possible to prevent discoloration of an aqueous system to which a bactericidal algicidal agent containing MBCP is added, and to effectively kill algae and cyanobacteria, particularly including Legionella bacteria. The present invention has an excellent sterilizing effect against various bacteria, and also has a merit in terms of equipment that is not corrosive to metals.
以下、本発明を具体的に説明する。
本発明の変色防止効果能を有する殺菌殺藻剤は、MBCPとベンゾフェノン類とを含有してなり、MBCPは、そのまま溶剤に溶かして配合するか、又は水酸化ナトリウムや水酸化カリウム等と溶剤を加えてMBCPアルカリ金属塩として配合することができる。
また、木発明のベンゾフェノン類としては、前記一般式(I)で示される化合物を使用するのが好適である。
Hereinafter, the present invention will be specifically described.
The bactericidal algicidal agent having the effect of preventing discoloration of the present invention contains MBCP and benzophenones, and MBCP is dissolved in a solvent as it is, or mixed with sodium hydroxide, potassium hydroxide or the like and a solvent. In addition, it can be formulated as an MBCP alkali metal salt.
As the benzophenones of the present invention, it is preferable to use the compound represented by the general formula (I).
ベンゾフェノン類としては、具体的に、4−ヒドロキシベンゾフェノン、2,4−ジヒドロキシベンゾフェノン、4,4’−ジヒドロキシベンゾフェノン、2,4,4’−トリヒドロキシベンゾフェノン、2,2’,4,4’−テトラヒドロキシベンゾフェノン、2,3,4,4’−テトラヒドロキシベンゾフェノン等が挙げられる。これらのベンゾフェノン類は、単独で用いても良く、また2種以上併用することもできる。 Specific examples of benzophenones include 4-hydroxybenzophenone, 2,4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone, 2,4,4′-trihydroxybenzophenone, 2,2 ′, 4,4′- Examples thereof include tetrahydroxybenzophenone and 2,3,4,4′-tetrahydroxybenzophenone. These benzophenones may be used alone or in combination of two or more.
このベンゾフェノン類は、予めMBCPに配合して殺菌殺藻剤として製剤しなくとも、MBCPを添加した殺菌殺藻処理対象水系に、ベンゾフェノン類を添加しても変色を防止することもできる。すなわち本発明は、MBCP及びベンゾフェノン類を別個に製剤して使用し、水系においてMBCPとベンゾフェノン類が同時に存在する状態を形成することで変色防止効果を得ることができる。 Even if this benzophenone is not previously blended with MBCP and formulated as a bactericidal algicide, discoloration can also be prevented by adding a benzophenone to a bactericidal algae treatment target water system to which MBCP has been added. That is, according to the present invention, MBCP and benzophenones are separately formulated and used, and an effect of preventing discoloration can be obtained by forming a state in which MBCP and benzophenones are simultaneously present in an aqueous system.
本発明の殺菌殺藻剤は、MBCPとベンゾフェノン類を質量比で1:0.01〜0.5の割合で含有することが好ましい。上記範囲よりもベンゾフェノン類の割合が低い場合には、充分な変色防止効果は得られず、逆に上記範囲よりもベンゾフェノン類の割合が高い場合には、変色防止効果は得られるものの、コストが高くなり経済性の点で好ましくない。
本発明の殺菌殺藻剤の使用方法は、特に限定されるものではなく、殺菌殺藻処理対象水系に対し、MBCP及びベンゾフェノン類をあらかじめ所定の割合で殺菌殺藻剤に配合して殺菌殺藻処理対象水系に添加してもよく、また各々別個に添加して、系内で質量比が1:0.01〜1:0.5の割合になるようにすることが必要である。
The bactericidal algicidal agent of the present invention preferably contains MBCP and benzophenones at a mass ratio of 1: 0.01 to 0.5. When the proportion of benzophenones is lower than the above range, a sufficient discoloration preventing effect cannot be obtained. Conversely, when the proportion of benzophenones is higher than the above range, the discoloration preventing effect can be obtained, but the cost is low. It becomes high and is not preferable in terms of economy.
The method of using the bactericidal algicidal agent of the present invention is not particularly limited, and MBCP and benzophenones are preliminarily mixed with the bactericidal algicidal agent in a predetermined ratio with respect to the water system subject to the bactericidal algicidal treatment. It may be added to the water system to be treated, or added separately so that the mass ratio is 1: 0.01 to 1: 0.5 in the system.
溶媒を用いて本発明の殺菌殺藻剤を製剤する場合、溶剤として、水や次のような有機溶媒を適用することができる。例えば、(1)グリコール類として、エチレングリコール、ジエチレングリコール、トリエチレングリコール、テトラエチレングリコール、プロピレングリコール、ジプロピレングリコール、ポリエチレングリコール、ポリプロピレングリコール等、(2)グリコールエーテル類として、ジエチレングリコールモノメチルエーテル、ジエチレングリコールモノエチルエーテル、ジエチレングリコールモノブチルエーテル、エチレングリコールモノメチルエーテル、トリエチレングリコールモノメチルエーテル、ポリエチレングリコールモノメチルエーテル等、(3)アミド類として、ジメチルホルムアミド、ジメチルアセトアミド、N−メチルプロピオンアミド、2−ピロリドン、N−メチルピロリドン等、(4)アミン類として、モノメチルアミン、ジメチルアミン、トリメチルアミン、モノエチルアミン、ジエチルアミン、トリエチルアミン、プロピルアミン、ジプロピルアミン、ジイソプロピルアミン、ブチルアミン、3−アミノプロピルメチルエーテル等を挙げることができる。これらの溶媒は、単独で又は2種以上を併用することもできる。 When formulating the bactericidal algicidal agent of the present invention using a solvent, water or the following organic solvent can be applied as the solvent. For example, (1) glycols include ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, etc. (2) glycol ethers include diethylene glycol monomethyl ether, diethylene glycol mono Ethyl ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether, triethylene glycol monomethyl ether, polyethylene glycol monomethyl ether, etc. (3) As amides, dimethylformamide, dimethylacetamide, N-methylpropionamide, 2-pyrrolidone, N-methyl Pyrrolidone, etc. (4) Monomethyl as amines Amine, dimethylamine, trimethylamine, monoethylamine, diethylamine, triethylamine, propylamine, can be given dipropylamine, diisopropylamine, butylamine, 3-aminopropyl methyl ether. These solvents may be used alone or in combination of two or more.
また、本発明の殺菌殺藻剤には、キレート剤、スケール防止剤、腐食防止剤を配合することができる。キレート剤としては、エチレンジアミン四酢酸、及びそのアルカリ金属塩、クエン酸、等を挙げることができる。スケール防止剤としては、従来から知られているスケール防止剤を用いることができ、例えば、アクリル酸系ポリマー、マレイン酸系ポリマー等を挙げることができる。腐食防止剤としては、従来から公知の防錆剤を用いることができ、例えば、トリルトリアゾール、ベンゾトリアゾール、メチルベンゾトリアゾール、2−ホスホノブタン−1,2,4−トリカルボン酸、及びそのナトリウム塩、ヒドロキシエチリデンジホスホン酸、及びそのナトリウム塩等を挙げることができる。 Moreover, a chelating agent, a scale inhibitor, and a corrosion inhibitor can be mix | blended with the bactericidal algicide of this invention. Examples of chelating agents include ethylenediaminetetraacetic acid, alkali metal salts thereof, citric acid, and the like. As the scale inhibitor, conventionally known scale inhibitors can be used, and examples thereof include acrylic acid-based polymers and maleic acid-based polymers. As the corrosion inhibitor, conventionally known rust inhibitors can be used. For example, tolyltriazole, benzotriazole, methylbenzotriazole, 2-phosphonobutane-1,2,4-tricarboxylic acid, and a sodium salt thereof, hydroxy Examples thereof include ethylidene diphosphonic acid and its sodium salt.
次に、製剤例を挙げて本発明を説明するが、本発明はこの製剤例のみに限定されるものではない。なお、以下の製剤例において部は、質量部を意味する。 Next, the present invention will be described with reference to formulation examples, but the present invention is not limited to this formulation example. In the following formulation examples, “part” means “part by mass”.
製剤例1
MBCP 10部、水酸化ナトリウム 3部、4−ヒドロキシベンゾフェノン類 1部、ジエチレングリコール 39部、水 47部を混合撹拌して殺菌殺藻剤を得た。
製剤例2
MBCP 10部、水酸化ナトリウム 3部、4−ヒドロキシベンゾフェノン
0.5部、4,4’−ジヒドロキシベンゾフェノン 0.5部、ジエチレングリコール 39部、水 47部を混合撹拌して殺菌殺藻剤を得た。
製剤例3
MBCP 5部、水酸化ナトリウム 2部、4,4’−ジヒドロキシベンゾフェノン 0.5部、ポリマレイン酸ナトリウム 10部、ベンゾトリアゾール 1.5部、ジエチレングリコール 10部、水 71部を混合撹拌して殺菌殺薬剤を得た。
Formulation Example 1
MBCP (10 parts), sodium hydroxide (3 parts), 4-hydroxybenzophenone (1 part), diethylene glycol (39 parts) and water (47 parts) were mixed and stirred to obtain a bactericidal algicidal agent.
Formulation Example 2
MBCP 10 parts, sodium hydroxide 3 parts, 4-hydroxybenzophenone
0.5 parts, 0.5 part of 4,4′-dihydroxybenzophenone, 39 parts of diethylene glycol and 47 parts of water were mixed and stirred to obtain a bactericidal algicidal agent.
Formulation Example 3
MBCP 5 parts, sodium hydroxide 2 parts, 4,4'-dihydroxybenzophenone 0.5 part, sodium polymaleate 10 parts, benzotriazole 1.5 parts, diethylene glycol 10 parts, water 71 parts Got.
比較例1
MBCP 10部、水酸化ナトリウム 3部、ジエチレングリコール 39部、水 48部を混合撹拌して比較薬剤を得た。
比較例2
MBCP 10部、水酸化ナトリウム 3部、2−(3−ターシャリブチル−2−ヒドロキシ−5−メチルフェニル)−5−クロロ−2H−ベンゾトリアゾール(紫外線吸収剤)1部、ジエチレングリコール 39部、水 47部を混合撹拌して比較薬剤を得た。
Comparative Example 1
MBCP (10 parts), sodium hydroxide (3 parts), diethylene glycol (39 parts) and water (48 parts) were mixed and stirred to obtain a comparative drug.
Comparative Example 2
MBCP 10 parts, sodium hydroxide 3 parts, 2- (3-tert-butyl-2-hydroxy-5-methylphenyl) -5-chloro-2H-benzotriazole (ultraviolet absorber) 1 part, diethylene glycol 39 parts, water A comparative drug was obtained by mixing and stirring 47 parts.
次に、試験例を挙げて本発明の殺菌殺藻剤としての有用性を説明する。
試験例1 殺菌殺藻剤希釈液のUV−A照射による変色試験(1)
100ml容ポリプロピレン製容器に、製剤例1、2、比較例1、2に従って得た殺菌殺藻剤を水道水で希釈した薬剤希釈液(MBCP濃度100ppm)を100ml入れ、この容器をブラックライトブルー蛍光ランプ(15W、2本)下に置き、室温で照射した。2週間照射後、希釈液の色調の変化を観察した。外観は、下記の判定基準により判定した。結果を表1に示す。
Next, the usefulness as a bactericidal algicidal agent of the present invention will be described with reference to test examples.
Test Example 1 Discoloration test by UV-A irradiation of diluted fungicidal algicide (1)
In a 100 ml polypropylene container, 100 ml of a drug dilution solution (MBCP concentration of 100 ppm) obtained by diluting the bactericidal algicide obtained according to Formulation Examples 1 and 2 and Comparative Examples 1 and 2 with tap water was placed. Placed under a lamp (15W, 2) and irradiated at room temperature. After 2 weeks of irradiation, changes in the color of the diluted solution were observed. The appearance was determined according to the following criteria. The results are shown in Table 1.
判定基準
− :変色なし。
± :わずかに変色。水で更に10倍に希釈すれば、ほとんど変色が気になら
ない程度になる。
+ :やや変色。
++:かなり変色。
Criteria-: No discoloration.
±: Slightly discolored. If diluted further 10 times with water, the discoloration is hardly noticed.
+: Slightly discolored.
++: Very discoloration.
表1より、MBCPの実際の殺菌殺藻剤として使用される濃度よりも、約10倍高い濃度で試験しても変色防止効果が得られることが分る。また、比較例2に示すようにベンゾトリァゾール系紫外線吸収剤を使用しても希釈液の変色を抑えることができない。 From Table 1, it can be seen that the discoloration prevention effect can be obtained even when tested at a concentration about 10 times higher than the concentration of MBCP used as an actual bactericidal algicidal agent. Further, as shown in Comparative Example 2, even if a benzotriazole-based ultraviolet absorber is used, the color change of the diluted solution cannot be suppressed.
試験例2 殺菌殺藻剤緬釈液のUV−A照射による変色試験(2)
まず、次の組成のMBCP又は4,4’−ジヒドロキシベンゾフェノンを含有する製剤A(MBCP 20部、水酸化ナトリウム 6部、水 74部)、及び製剤B(4,4’−ジヒドロキシベンゾフェノン 0.2部、ジエチレングリコール 99.8部)を得る。
100ml容ポリプロピレン製容器に、この製剤Aを0.05g、製剤Bを0.05g〜2.5g及び水道水100gを入れて希釈液を調製した。この容器をブラックライトブルー蛍光ランプ(15W、2本)下に、室温で2週間放置した後、色調の変化を観察した。結果を表2に示す。表中の記号は、試験例1と同じである.
Test Example 2 Discoloration test of bactericidal algicidal solution by UV-A irradiation (2)
First, Formulation A (MBCP 20 parts, sodium hydroxide 6 parts, water 74 parts) containing MBCP or 4,4′-dihydroxybenzophenone having the following composition, and Formulation B (4,4′-dihydroxybenzophenone 0.2 Part, 99.8 parts diethylene glycol).
In a 100 ml polypropylene container, 0.05 g of this preparation A, 0.05 g to 2.5 g of preparation B, and 100 g of tap water were added to prepare a diluted solution. The container was allowed to stand at room temperature for 2 weeks under a black light blue fluorescent lamp (15 W, 2 tubes), and the change in color tone was observed. The results are shown in Table 2. The symbols in the table are the same as in Test Example 1.
表2に示すように、MBCPとベンゾフェノンの比率が1:0.01〜1:0.5の範囲で変色防止効果が認められる。 As shown in Table 2, the effect of preventing discoloration is observed when the ratio of MBCP to benzophenone is in the range of 1: 0.01 to 1: 0.5.
試験例3 冷却塔における変色防止試験
製剤例2に従って得た殺菌殺藻剤を屋外に設置された30冷凍トンの冷却塔の補給水に200mg/l濃度で30日間連続添加を行った。その結果、太陽光が当る冷却塔に30日間にわたり使用しても、冷却水はほとんど着色が認められなかった。一方、上記の殺菌殺藻剤で4,4’−ジヒドロキシベンゾフェノンの代りに水を配合した殺菌殺藻剤を同じ冷却塔補給水に200mg/l濃度で連続添加し、30日間続けたところ、冷却水は褐色に着色した。
Test Example 3 Discoloration Prevention Test in Cooling Tower The bactericidal algicide obtained according to Formulation Example 2 was continuously added at a concentration of 200 mg / l for 30 days to make-up water in a cooling tower of 30 refrigeration tons installed outdoors. As a result, even when used for 30 days in a cooling tower where sunlight hits, the cooling water was hardly colored. On the other hand, when the bactericidal algicide containing water in place of 4,4′-dihydroxybenzophenone in the above bactericidal algicide was continuously added to the same cooling tower make-up water at a concentration of 200 mg / l and continued for 30 days, The water was colored brown.
試験例4 レジオネラ菌に対する殺菌効果
(1)試験菌液の調製:
レジオネラ菌〔レジオネラ/ニューモフィラ(Legione11a pneumophila)ATCC 33153〕をB−CYEα寒天培地で35℃で48時間培養したものを、滅菌蒸留水に懸濁させ、1ml当りの菌数が106となるように試験菌液を調製する。
(2)試験操作:
滅菌蒸留水で、製剤例3に従って得た殺菌殺藻剤の2000、1000、500mg/l薬剤希釈液を調製する。これらの薬剤希釈液1mlをHEPES緩衝液(pH8.5)8mlに添加・混合して試験液とする。また、比較例1の殺菌殺藻剤についても同様に操作し試験液を調製する。なお、HEPES緩衝液(pH8.5)9m1を薬剤無添加の試験液とする。
試験液に試験菌液1mlを加え30℃で振とうして、初期、3時間後、24時間後に生菌数を測定する。(B−CYEα寒天培地を使用)
結果を表3に示す。
Test Example 4 Bactericidal effect against Legionella (1) Preparation of test bacterial solution:
Legionella [Legionella 11pneumophila ATCC 33153] cultured in B-CYEα agar medium at 35 ° C. for 48 hours is suspended in sterilized distilled water so that the number of bacteria per ml is 10 6. Prepare a test bacterial solution.
(2) Test operation:
Prepare a 2000, 1000, 500 mg / l drug dilution of the bactericidal algicide obtained according to Formulation Example 3 with sterile distilled water. Add 1 ml of these drug dilutions to 8 ml of HEPES buffer (pH 8.5) to prepare a test solution. Moreover, it operates similarly about the bactericidal algicide of the comparative example 1, and prepares a test liquid. In addition, 9 ml of HEPES buffer (pH 8.5) is used as a test solution to which no drug is added.
Add 1 ml of the test bacterial solution to the test solution, shake at 30 ° C., and measure the number of viable bacteria initially, 3 hours later and 24 hours later. (Uses B-CYEα agar medium)
The results are shown in Table 3.
表3から、本発明の殺菌殺藻剤は、レジオネラ・ニューモフィラに対して優れた殺菌効果を示すことが分る。 From Table 3, it can be seen that the bactericidal algicidal agent of the present invention exhibits an excellent bactericidal effect against Legionella pneumophila.
Claims (5)
(式中、R1、R2、R3、R4及びR5は、同一又は異なり、水素、ヒドロキシル基又は炭素数1〜8を有するアルコキシ基を示す)
で表されるベンゾフェノン類の1種又は2種以上とを含むことを特徴とする変色防止効果能を有する殺菌殺藻剤。 2,2'-methylenebis (the 4-chlorophenol), under following general formula (I):
(Wherein R 1 , R 2 , R 3 , R 4 and R 5 are the same or different and represent hydrogen, a hydroxyl group or an alkoxy group having 1 to 8 carbon atoms)
A fungicidal algicidal agent having anti-discoloration effect, characterized in that it comprises one or more benzophenones represented by the formula:
(式中、R1、R2、R3、R4及びR5は、同一又は異なり、水素、ヒドロキシル基又は炭素数1〜8を有するアルコキシ基を示す)
で表されるベンゾフェノン類とを1:0.01〜1:0.5(質量比)の割合で使用することを特徴とする当該処理対象水系の変色防止方法。 Against sterilization algicidal process target water system, and 2,2'-methylenebis (4-chlorophenol), under following general formula (I):
(Wherein R 1 , R 2 , R 3 , R 4 and R 5 are the same or different and represent hydrogen, a hydroxyl group or an alkoxy group having 1 to 8 carbon atoms)
The method for preventing discoloration of the water system to be treated is characterized in that it is used in a ratio of 1: 0.01 to 1: 0.5 (mass ratio) .
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