JP2021188884A - Pipe cleaning method - Google Patents
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- JP2021188884A JP2021188884A JP2020097867A JP2020097867A JP2021188884A JP 2021188884 A JP2021188884 A JP 2021188884A JP 2020097867 A JP2020097867 A JP 2020097867A JP 2020097867 A JP2020097867 A JP 2020097867A JP 2021188884 A JP2021188884 A JP 2021188884A
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- 238000004140 cleaning Methods 0.000 title claims abstract description 95
- 238000000034 method Methods 0.000 title claims abstract description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 47
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 10
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 claims abstract description 8
- 239000007788 liquid Substances 0.000 claims description 42
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 6
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical group [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 claims description 5
- 229940045872 sodium percarbonate Drugs 0.000 claims description 5
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 4
- 235000010323 ascorbic acid Nutrition 0.000 claims description 4
- 229960005070 ascorbic acid Drugs 0.000 claims description 4
- 239000011668 ascorbic acid Substances 0.000 claims description 4
- 239000012459 cleaning agent Substances 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 4
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 3
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 3
- 229930003268 Vitamin C Natural products 0.000 claims description 3
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 3
- 239000001630 malic acid Substances 0.000 claims description 3
- 235000011090 malic acid Nutrition 0.000 claims description 3
- 239000011975 tartaric acid Substances 0.000 claims description 3
- 235000002906 tartaric acid Nutrition 0.000 claims description 3
- 235000019154 vitamin C Nutrition 0.000 claims description 3
- 239000011718 vitamin C Substances 0.000 claims description 3
- 235000002639 sodium chloride Nutrition 0.000 claims description 2
- 238000005187 foaming Methods 0.000 abstract description 21
- 230000002401 inhibitory effect Effects 0.000 description 13
- 239000000243 solution Substances 0.000 description 11
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 8
- 238000005406 washing Methods 0.000 description 8
- 229910021642 ultra pure water Inorganic materials 0.000 description 6
- 239000012498 ultrapure water Substances 0.000 description 6
- 230000009257 reactivity Effects 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000005708 Sodium hypochlorite Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- -1 percarbonate alkali metal salt Chemical class 0.000 description 3
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- LAQYHRQFABOIFD-UHFFFAOYSA-N 2-methoxyhydroquinone Chemical compound COC1=CC(O)=CC=C1O LAQYHRQFABOIFD-UHFFFAOYSA-N 0.000 description 2
- ALRHLSYJTWAHJZ-UHFFFAOYSA-N 3-hydroxypropionic acid Chemical compound OCCC(O)=O ALRHLSYJTWAHJZ-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 244000052616 bacterial pathogen Species 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- AUFZRCJENRSRLY-UHFFFAOYSA-N 2,3,5-trimethylhydroquinone Chemical compound CC1=CC(O)=C(C)C(C)=C1O AUFZRCJENRSRLY-UHFFFAOYSA-N 0.000 description 1
- RYYXDZDBXNUPOG-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine;dihydrochloride Chemical compound Cl.Cl.C1C(N)CCC2=C1SC(N)=N2 RYYXDZDBXNUPOG-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004155 Chlorine dioxide Substances 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-araboascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 150000000996 L-ascorbic acids Chemical class 0.000 description 1
- 241000589248 Legionella Species 0.000 description 1
- 208000007764 Legionnaires' Disease Diseases 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
- QAFDKYYSTRGTLH-UHFFFAOYSA-L [Na+].[Na+].[O-]Cl=O.[O-]Cl=O Chemical compound [Na+].[Na+].[O-]Cl=O.[O-]Cl=O QAFDKYYSTRGTLH-UHFFFAOYSA-L 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 235000019398 chlorine dioxide Nutrition 0.000 description 1
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 1
- BXJGUBZTZWCMEX-UHFFFAOYSA-N dimethylhydroquinone Natural products CC1=C(C)C(O)=CC=C1O BXJGUBZTZWCMEX-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 239000004318 erythorbic acid Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003673 groundwater Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 229940079826 hydrogen sulfite Drugs 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 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
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 239000008237 rinsing water Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
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- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
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- 229940095064 tartrate Drugs 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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- Cleaning By Liquid Or Steam (AREA)
Abstract
Description
本発明は、配管の洗浄方法に関する。 The present invention relates to a method for cleaning pipes.
病院、入居施設、温泉旅館、銭湯などで使用されている大型の浴槽は、浴槽水(温水)を有効利用するために、一般に、循環浄化処理が行われている。浴槽水の循環は、例えば、浴槽の底面や側面に穿設した2つの通水口を循環配管で接続し循環ポンプを使用して行われている。ポンプや配管などで構成される循環経路には、毛髪、タオル布屑、ゴミなどの異物を除去するフィルタ(ヘアキャッチャー)、濾過器、熱交換器などが設けられる。また、レジオネラ属菌などの病原性細菌の増殖を抑制するために、塩素消毒が行われることもある。 Large bathtubs used in hospitals, occupancy facilities, hot spring inns, public baths, etc. are generally subjected to circulation purification treatment in order to effectively use bathtub water (hot water). The circulation of bathtub water is performed, for example, by connecting two water passages bored in the bottom surface or the side surface of the bathtub with a circulation pipe and using a circulation pump. Filters (hair catchers), filters, heat exchangers, etc. that remove foreign substances such as hair, towel cloth, and dust are provided in the circulation path composed of pumps and pipes. In addition, chlorine disinfection may be performed to suppress the growth of pathogenic bacteria such as Legionella spp.
循環経路に配置された配管は、一般に狭い機械室に設置されており、洗浄がしにくく、また、浴槽のように頻繁に洗浄できないために、配管内に付着したスライムやスケールが成長しやすい。配管内でのスライムやスケールの付着は雑菌の発生につながるため、衛生的な環境を整備するためにも、効率的な洗浄が望まれている。 The pipes arranged in the circulation path are generally installed in a narrow machine room, are difficult to wash, and cannot be washed frequently like a bathtub, so slime and scale adhering to the inside of the pipes tend to grow. Adhesion of slime and scale in the pipe leads to the generation of germs, so efficient cleaning is desired to maintain a hygienic environment.
特許文献1には、用水系の機器、装置、配管などの内面に付着したスケールおよびスライムを無機酸あるいは有機酸の水溶液で処理する工程、および前記工程で使用した液を系から排出することなくこれに過酸化ナトリウム、過炭酸ナトリウムあるいは安定化二酸化塩素水に過炭酸ナトリウムを溶解した溶液を添加混合する工程からなる、スケールおよびスライムの化学的除去方法が開示されている。
特許文献2には、酸または酸性塩と過炭酸塩とからなる風呂釜洗浄剤が開示されている。
特許文献3には、配管内を洗浄する方法において、配管の内側を過硫酸塩又は過硫酸塩と界面活性剤を含有する水溶液に接触させた後、過硫酸塩、界面活性剤及び過炭酸アルカリ塩を含有する水溶液に接触させる配管洗浄方法が開示されている。
特許文献4には、所定の無機過酸化物、カチオン系殺菌剤、炭酸塩もしくは重炭酸塩と固体酸とからなる発泡剤を含有する、殺菌性能を有する硬質表面用固形洗浄剤組成物が開示されている。
In
Patent Document 4 discloses a solid cleaning composition for a hard surface having bactericidal activity, which contains a predetermined inorganic peroxide, a cationic bactericide, a carbonate or a foaming agent composed of a bicarbonate or a solid acid, and has bactericidal performance. Has been done.
本発明は、配管、例えば浴槽などの設備に接続された配管のバイオフィルムに由来する汚れに対して、効率よく、かつ確実に洗浄でき、また、配管の洗浄中やすすぎの際の発泡を抑制することができる配管の洗浄方法を提供する。 INDUSTRIAL APPLICABILITY The present invention can efficiently and reliably clean pipes, for example, stains derived from biofilms of pipes connected to equipment such as bathtubs, and suppress foaming during cleaning and rinsing of pipes. Provide a method of cleaning pipes that can be used.
本発明は、配管内に付着した汚れに(a)過炭酸塩、(b)還元剤及び水を含有する洗浄液〔以下、本発明の洗浄液ともいう〕を所定時間接触させた後、前記配管の総容量の2倍以上の量の水で前記配管内をすすぐ、配管の洗浄方法に関する。 In the present invention, a cleaning liquid containing (a) a percarbonate, (b) a reducing agent and water [hereinafter, also referred to as a cleaning liquid of the present invention] is brought into contact with the dirt adhering to the inside of the pipe for a predetermined time, and then the above-mentioned pipe is used. The present invention relates to a method of cleaning the pipe by rinsing the inside of the pipe with an amount of water more than twice the total capacity.
また、本発明は、(a)過炭酸塩〔以下、(a)成分という〕及び(b)還元剤〔以下、(b)成分という〕を含有し、前記本発明の洗浄方法に用いられる、配管用洗浄剤組成物に関する。 Further, the present invention contains (a) a percarbonate [hereinafter referred to as (a) component] and (b) a reducing agent [hereinafter referred to as (b) component], and is used in the cleaning method of the present invention. Regarding the cleaning agent composition for piping.
本発明によれば、配管、例えば浴槽などの設備に接続された配管のバイオフィルムに由来する汚れに対して、効率よく、かつ確実に洗浄でき、また、配管の洗浄中やすすぎの際の発泡を抑制することができる配管の洗浄方法及びこれに用いる配管用洗浄剤組成物が提供される。
本発明では、配管のバイオフィルムを効率よく洗浄できる上に、配管の洗浄中やすすぎの際の発泡を抑制できるため、過剰な発泡によるバイオフィルムに由来する汚れへの洗浄性の低下や循環装置のエアーロック等の作業性の低下等の不利益が低減され、例えば、すすぎ回数を減らすことが可能となる。
According to the present invention, dirt derived from biofilm of pipes, for example, pipes connected to equipment such as bathtubs, can be efficiently and surely washed, and foaming during washing and rinsing of pipes. A method for cleaning a pipe and a composition for cleaning a pipe used for the method are provided.
In the present invention, the biofilm of the pipe can be efficiently washed, and foaming during cleaning and rinsing of the pipe can be suppressed. Disadvantages such as deterioration of workability such as air lock are reduced, and for example, the number of rinses can be reduced.
(a)成分は、過炭酸塩である。(a)成分は、バイオフィルムに由来する汚れへの洗浄性(以下、洗浄性ともいう)及び作業時の発泡の抑制(以下、発泡抑制性ともいう)の観点から、過炭酸アルカリ金属塩が好ましい。(a)成分は、過炭酸ナトリウムがより好ましい。 The component (a) is a percarbonate. The component (a) is a percarbonate alkali metal salt from the viewpoint of detergency against stains derived from biofilm (hereinafter, also referred to as detergency) and suppression of foaming during work (hereinafter, also referred to as foaming inhibitory property). preferable. As the component (a), sodium percarbonate is more preferable.
本発明の洗浄液中の(a)成分の濃度は、洗浄性及び発泡抑制性の観点から、好ましくは100ppm以上、より好ましくは200ppm以上、更に好ましくは500ppm以上、より更に好ましくは800ppm以上、そして、好ましくは10000ppm以下、より好ましくは8000ppm以下、更に好ましくは6000ppm以下、より更に好ましくは4000ppm以下である。 The concentration of the component (a) in the cleaning liquid of the present invention is preferably 100 ppm or more, more preferably 200 ppm or more, still more preferably 500 ppm or more, still more preferably 800 ppm or more, and from the viewpoint of detergency and foaming inhibitory property. It is preferably 10000 ppm or less, more preferably 8000 ppm or less, still more preferably 6000 ppm or less, still more preferably 4000 ppm or less.
(b)成分は、還元剤である。本発明でいう還元剤は、遷移金属の還元作用を有する化合物であってよい。
(b)成分としては、(b1)エンジオール構造を有する化合物、例えばアスコルビン酸又はその塩、ビタミンC、タンニン酸、エリソルビン酸又はその塩、(b2)ヒドロキシルアミン、例えばN,N−ジエチルヒドロキシルアミン、(b3)フェノール系還元剤、例えば没食子酸、メチルヒドロキノン、ジメチルヒドロキノン、トリメチルヒドロキノン、t−ブチルヒドロキノン、メトキシヒドロキノン、クロロヒドロキノン、及び(b4)その他の還元剤、例えばアスコルビン酸誘導体又はその塩、ハイドロサルファイト、ピロ亜硫酸塩、亜硫酸塩、亜硫酸水素塩、チオ硫酸塩、二酸化チオ尿素、から選ばれる還元剤が挙げられる。
(b)成分は、洗浄性、発泡抑制性及び製品化での適用容易性の観点から、アスコルビン酸及びその塩、並びにビタミンCから選ばれる1種以上の化合物が好ましい。
(B) The component is a reducing agent. The reducing agent referred to in the present invention may be a compound having a reducing action of a transition metal.
The component (b) includes (b1) a compound having an endiol structure, for example, ascorbic acid or a salt thereof, vitamin C, tannic acid, erythorbic acid or a salt thereof, and (b2) a hydroxylamine, for example, N, N-diethylhydroxylamine. , (B3) phenolic reducing agents such as gallic acid, methylhydroquinone, dimethylhydroquinone, trimethylhydroquinone, t-butylhydroquinone, methoxyhydroquinone, chlorohydroquinone, and (b4) other reducing agents such as ascorbic acid derivatives or salts thereof. Examples thereof include a reducing agent selected from hydrosulfite, pyrosulfite, sulfite, hydrogen sulfite, thiosulfate, and thiourea dioxide.
As the component (b), ascorbic acid and a salt thereof, and one or more compounds selected from vitamin C are preferable from the viewpoints of detergency, foaming inhibitory property, and ease of application in commercialization.
本発明の洗浄液中の(b)成分の濃度は、洗浄性及び発泡抑制性の観点から、好ましくは10ppm以上、より好ましくは50ppm以上、更に好ましくは100ppm以上、より更に好ましくは300ppm以上、より更に好ましくは500ppm以上、より更に好ましくは1000ppm以上、より更に好ましくは2500ppm以上、そして、好ましくは100000ppm以下、より好ましくは50000ppm以下、更に好ましくは30000ppm以下、より更に好ましくは10000ppm以下、より更に好ましくは5000ppm以下である。 The concentration of the component (b) in the cleaning liquid of the present invention is preferably 10 ppm or more, more preferably 50 ppm or more, still more preferably 100 ppm or more, still more preferably 300 ppm or more, still more, from the viewpoint of detergency and foaming inhibitory property. It is preferably 500 ppm or more, more preferably 1000 ppm or more, still more preferably 2500 ppm or more, and preferably 100,000 ppm or less, more preferably 50,000 ppm or less, still more preferably 30,000 ppm or less, still more preferably 10,000 ppm or less, still more preferably 5000 ppm. It is as follows.
本発明の洗浄液は、洗浄性及び発泡抑制性の観点から、更に(c)有機酸及びその塩から選ばれる1種以上の化合物〔以下(c)成分という〕を含有することが好ましい。(c)成分としては、マロン酸、リンゴ酸、3−ヒドロキシプロピオン酸、コハク酸、乳酸、酒石酸、グリコール酸、マレイン酸、フマル酸が挙げられる。(c)成分としては、洗浄性及び発泡抑制性の観点から、酒石酸、コハク酸、リンゴ酸及びこれらの塩から選ばれる1種以上の化合物が好ましい。 From the viewpoint of detergency and foaming inhibitory property, the cleaning liquid of the present invention preferably further contains (c) one or more compounds selected from organic acids and salts thereof [hereinafter referred to as (c) component]. Examples of the component (c) include malonic acid, malic acid, 3-hydroxypropionic acid, succinic acid, lactic acid, tartrate acid, glycolic acid, maleic acid, and fumaric acid. As the component (c), one or more compounds selected from tartaric acid, succinic acid, malic acid and salts thereof are preferable from the viewpoint of detergency and foaming inhibitory property.
本発明の洗浄液が(c)成分を含有する場合、該洗浄液中の(c)成分の濃度は、洗浄性の観点から、好ましくは100ppm以上、より好ましくは500ppm以上、更に好ましくは1000ppm以上、より更に好ましくは2500ppm以上、そして、発泡抑制性の観点から、好ましくは10000ppm以下、より好ましくは8000ppm以下、更に好ましくは6000ppm以下、より更に好ましくは4000ppm以下である。 When the cleaning liquid of the present invention contains the component (c), the concentration of the component (c) in the cleaning liquid is preferably 100 ppm or more, more preferably 500 ppm or more, still more preferably 1000 ppm or more, and more, from the viewpoint of cleaning property. It is more preferably 2500 ppm or more, and from the viewpoint of foaming inhibitory property, it is preferably 10000 ppm or less, more preferably 8000 ppm or less, still more preferably 6000 ppm or less, still more preferably 4000 ppm or less.
本発明の洗浄液は、本発明の効果を阻害しない範囲で、(a)成分、(b)成分、(c)成分以外に、例えば、界面活性剤、キレート剤、酵素、消泡剤などの成分を含有することができる。 In addition to the components (a), (b), and (c), the cleaning solution of the present invention contains, for example, components such as a surfactant, a chelating agent, an enzyme, and an antifoaming agent, as long as the effects of the present invention are not impaired. Can be contained.
本発明の洗浄液のpHは、洗浄性及び発泡抑制性の観点から、好ましくは3以上、より好ましくは3.5以上、更に好ましくは3.8以上、そして、好ましくは11以下、より好ましくは6以下、更に好ましくは5以下である。 The pH of the cleaning solution of the present invention is preferably 3 or more, more preferably 3.5 or more, still more preferably 3.8 or more, and preferably 11 or less, more preferably 6 from the viewpoint of detergency and foaming inhibitory property. Below, it is more preferably 5 or less.
本発明の洗浄液の温度は、好ましくは20℃以上、より好ましくは35℃以上、そして、好ましくは60℃以下、より好ましくは45℃以下である。 The temperature of the cleaning liquid of the present invention is preferably 20 ° C. or higher, more preferably 35 ° C. or higher, and preferably 60 ° C. or lower, more preferably 45 ° C. or lower.
本発明の洗浄方法では、配管内に付着した汚れに本発明の洗浄液を所定時間接触させる。汚れはバイオフィルムを含む汚れであってよい。従って、本発明の洗浄方法は、配管内に付着したバイオフィルムを含む汚れに本発明の洗浄液を所定時間接触させる洗浄方法であってよい。前記所定時間、すなわち本発明の洗浄液を汚れに接触させる時間は、洗浄性及び発泡抑制性の観点から、好ましくは5分以上、より好ましくは10分以上、より更に好ましくは20分以上、そして、好ましくは100分以下、より好ましくは60分以下、更に好ましくは45分以下である。 In the cleaning method of the present invention, the cleaning liquid of the present invention is brought into contact with the dirt adhering to the inside of the pipe for a predetermined time. The stain may be a stain containing a biofilm. Therefore, the cleaning method of the present invention may be a cleaning method in which the cleaning liquid of the present invention is brought into contact with the dirt containing the biofilm adhering to the inside of the pipe for a predetermined time. The predetermined time, that is, the time for contacting the cleaning liquid of the present invention with the dirt is preferably 5 minutes or more, more preferably 10 minutes or more, still more preferably 20 minutes or more, and from the viewpoint of detergency and foaming inhibitory property. It is preferably 100 minutes or less, more preferably 60 minutes or less, still more preferably 45 minutes or less.
本発明の洗浄方法では、洗浄後の洗浄液をpH5超、更に6以上、そして、9以下、更に8以下に調整してから配管から排出することが好ましい。
In the cleaning method of the present invention, it is preferable that the cleaning liquid after cleaning is adjusted to
本発明の洗浄方法では、例えば、排液槽や浴槽等に連結された配管の場合、洗浄液のpHを好ましくは3以上6以下、更に好ましくは3以上5以下として配管と接触させた後、配管から流出させて排液槽や浴槽等に貯め、当該洗浄排出液のpHを好ましくは5超9以下、より好ましくは6以上8以下に調整してから排出することが好ましい。この方法では、初期段階で配管内の汚れが洗浄水中に溶解し、次いでpH調整により溶解した汚れが適度な大きさの水不溶物として析出することで、汚れが配管中に残留しにくく、又、配管外に排出されやすくなり、洗浄効率がより向上するうえ、排出液から汚れ部分をスラッジとして分離等の後処理が容易となり、環境への負荷も低減できるものと考えられる。 In the cleaning method of the present invention, for example, in the case of a pipe connected to a drainage tank, a bathtub, or the like, the pH of the cleaning liquid is preferably 3 or more and 6 or less, more preferably 3 or more and 5 or less, and then the pipe is brought into contact with the pipe. It is preferable that the washing drainage liquid is discharged from the water and stored in a drainage tank, a bathtub, or the like, and the pH of the washing drainage liquid is preferably adjusted to 5 or more and 9 or less, more preferably 6 or more and 8 or less, and then discharged. In this method, the dirt in the pipe is dissolved in the washing water at the initial stage, and then the dirt dissolved by adjusting the pH is deposited as a water-insoluble matter of an appropriate size, so that the dirt is less likely to remain in the pipe, and the dirt is less likely to remain in the pipe. It is considered that the waste can be easily discharged to the outside of the pipe, the cleaning efficiency can be further improved, the post-treatment such as separating the dirty portion from the discharged liquid as sludge can be facilitated, and the load on the environment can be reduced.
本発明の洗浄方法では、洗浄対象の配管内に付着した汚れに本発明の洗浄液を所定時間接触させた後、前記配管の総容量の2倍以上の量の水で前記配管内をすすぐ。すすぎは、複数回行うことが好ましい。配管の洗浄後、例えば、循環浴槽では、運転を再開させるにあたって、次亜塩素酸塩等を低濃度で維持して浴槽水を消毒しながら操業する。その際、本発明の洗浄液が過剰に残留したまま運転すると、次亜塩素酸塩の効果を低下させるため、次亜塩素酸塩の効果に影響を及ぼさない程度まですすぎを行う必要がある。本発明の洗浄方法において、洗浄液の発泡が抑えられることは、一定量の水を用いてすすぎを行う場合に生じる過剰な起泡の抑制につながり、すすぎ回数が増えてもすすぎ効率を損なうことがない。
本発明では、すすぎを複数回行い、1回あたりのすすぎに用いる水の量が、発泡抑制性の観点から、配管の総容量の1倍以上、更に2倍以上、更に3倍以上、そして、4倍以下、更に5倍以下であることが好ましい。
すすぎを行う水の温度は、洗浄性及び発泡抑制性の観点から、例えば、5℃以上60℃以下とすることができる。
In the cleaning method of the present invention, the cleaning liquid of the present invention is brought into contact with the dirt adhering to the inside of the pipe to be cleaned for a predetermined time, and then the inside of the pipe is rinsed with water in an amount of at least twice the total capacity of the pipe. Rinsing is preferably performed multiple times. After cleaning the pipes, for example, in a circulating bathtub, when restarting the operation, the operation is performed while maintaining a low concentration of hypochlorite or the like and disinfecting the bathtub water. At that time, if the operation is performed with the cleaning solution of the present invention remaining excessively, the effect of hypochlorite is reduced, so it is necessary to rinse until the effect of hypochlorite is not affected. In the cleaning method of the present invention, suppressing foaming of the cleaning liquid leads to suppression of excessive foaming that occurs when rinsing with a certain amount of water, and even if the number of rinses increases, the rinsing efficiency may be impaired. No.
In the present invention, rinsing is performed a plurality of times, and the amount of water used for each rinsing is 1 times or more, further 2 times or more, further 3 times or more the total capacity of the pipe from the viewpoint of foaming inhibition, and It is preferably 4 times or less, and more preferably 5 times or less.
The temperature of the water to be rinsed can be, for example, 5 ° C. or higher and 60 ° C. or lower from the viewpoint of detergency and foaming inhibitory property.
本発明の洗浄液、すすぎ水に用いる水は、特に限定されるものではないが、水道水、地下水、温泉水、イオン交換水、蒸留水等を用いることができる。 The water used for the cleaning liquid and the rinsing water of the present invention is not particularly limited, but tap water, groundwater, hot spring water, ion-exchanged water, distilled water and the like can be used.
配管は、循環経路の少なくとも一部を形成していてよい。
循環経路は、配管と接続する浴槽を含んでいてよい。
循環経路は、配管と接続する熱交換器を含んでいてよい。
循環経路は、配管と接続する集塵手段及び/又はろ過手段を含んでいてよい。
これら、浴槽、熱交換器、集塵手段、ろ過手段は、それぞれ、給湯システムなどで用いられている公知のものを採用することができる。
The piping may form at least part of the circulation path.
The circulation path may include a bathtub connected to the pipe.
The circulation path may include a heat exchanger connected to the piping.
The circulation path may include dust collecting means and / or filtering means connected to the pipe.
As these bathtubs, heat exchangers, dust collecting means, and filtering means, known ones used in hot water supply systems and the like can be adopted.
本発明の洗浄方法では、配管が循環経路の少なくとも一部を形成し、洗浄液を循環させて接触させることができる。更に、配管が循環経路の少なくとも一部を形成し、洗浄液を循環させて接触させた後、洗浄液を配管から排出してからすすぎを行うことができる。 In the cleaning method of the present invention, the piping forms at least a part of the circulation path, and the cleaning liquid can be circulated and brought into contact with each other. Further, after the pipe forms at least a part of the circulation path and the cleaning liquid is circulated and brought into contact with the pipe, the cleaning liquid can be discharged from the pipe and then rinsed.
図1を参照して本発明を説明する。図1は、本発明の配管の洗浄方法を行う循環風呂システムの一例を示す概略図である。図1中、1は配管、2は浴槽、3は熱交換器、4はろ過器、5はヘアキャチャー、6は封止栓であり、7は必要に応じて設置される分離装置(例えば、ろ過器、遠心分離機等)であり、矢印は洗浄水又はすすぎのための水(以下、すすぎ水ともいう)の進行方向を示している。図1のシステムでは、配管1と浴槽2は接続して循環経路を構成している。循環経路には配管と接続する熱交換器3、ろ過器4、集塵手段であるヘアキャッチャー5が配置されている。図1のシステムでは、図示しないポンプにより、洗浄水やすすぎ水を送り出すように設定されている。図1では、洗浄水は、配管1から浴槽2に搬送され、更に浴槽2から排出されて配管1に搬送されて、循環経路を矢印の方向に移動して配管の洗浄を行う。循環時間を接触時間であってよく、前記の範囲から選択できる。洗浄液のpH、温度は前記の範囲から選択できる。本発明では、循環させる洗浄液のpHは3以上5以下が好ましい。洗浄液は、所定時間接触を終えた後、循環を止めて、必要に応じてpH調整剤を添加してpHを5超9以下に調整した後、封止栓6を解放して、析出する固形分を浴槽2から排出する経路で、例えば、必要に応じて分離装置7で、ろ過等で除いた後、このシステムから排出される。洗浄液が排出された後、配管1の総容量の2倍以上の量のすすぎ水を循環経路に供給して配管1、浴槽2などのすすぎを行う。図1のように配管が循環経路を形成する場合、すすぎ水の供給を開始する地点から、配管1の総容量に相当する量が供給された時点でいったんすすぎ水の供給を停止し、すすぎ水を循環させて所定時間すすぎを行えばよい。この1回の循環すすぎは、配管1の総容量の1倍の量の水ですすぎを行ったものに相当する。所定時間の循環すすぎが終了した後、そのすすぎ水を排出し、同じ要領で、1回以上すすぎを追加で行うことで、配管1の総容量の2倍以上の量の水で配管のすすぎが行われる。すすぎ水は、水道水などを用いることができる。すすぎ水の温度は特に限定されないが、例えば、5℃以上60℃以下とすることができる。図1では、配管1の斜線部分が総容量となる。すすぎ水を循環させる場合は、封止栓6は閉じておく。
The present invention will be described with reference to FIG. FIG. 1 is a schematic view showing an example of a circulation bath system that performs the method for cleaning pipes of the present invention. In FIG. 1, 1 is a pipe, 2 is a bathtub, 3 is a heat exchanger, 4 is a filter, 5 is a hair catcher, 6 is a sealing plug, and 7 is a separating device installed as needed (for example, Filters, centrifuges, etc.), and the arrows indicate the direction of travel of wash water or water for rinsing (hereinafter, also referred to as rinse water). In the system of FIG. 1, the
<実施例1>
(1)洗浄液
洗浄液として、
(a)過炭酸ナトリウム1000ppm
(b)アスコルビン酸 1000ppm
(c)酒石酸 1000ppm
を含有する洗浄液(残部は水、pH4.1)を用いた。
<Example 1>
(1) Cleaning liquid As a cleaning liquid
(A) Sodium percarbonate 1000ppm
(B) Ascorbic acid 1000ppm
(C) Tartaric acid 1000ppm
A cleaning solution containing water (the balance is water, pH 4.1) was used.
(2)バイオフィルム除去試験(配管モデル)
洗浄液又はコントロール(超純水)5mLを入れた6wellプレートにバイオフィルムが形成されたテストピースを浸し、40℃、60rpmで所定の時間振とうした(TAITEC製、BioShaker BR−43FL)。振とう時間を、表1では洗浄時間として示した。振とう後の洗浄液の中和には、炭酸ナトリウムを用い、pH7に調整した。なお、本発明のpHは、ガラス電極を用いたpHメーターによって測定した値である。
洗浄液を1mL残し、超純水を2mL添加後、60rpmで5分間振とうすることですすぎ1回とした。この1回のすすぎは、配管の総容量の1倍の量の水によるすすぎに相当する。この試験は、ここでの全体容量の3/5が配管の総容量、同全体容量の2/5が浴槽容量に相当し、1回の排水で全体容量の1/5の洗浄液又はすすぎ水が系中に残留するような実機設備を想定した配管モデルで実施したものである。
1回のすすぎが終了したごとにすすぎ水を捨てて、新たな超純水を用いて、表1に示す回数まですすぎを繰り返した。2回目以降のすすぎは、すすぎ水を1mLずつ残し、そこに新たな超純水2mLを添加して実施した。所定回数のすすぎを終えた後、各テストピースを0.1%クリスタルバイオレット溶液中に浸し、バイオフィルムを染色した後、過剰となるクリスタルバイオレットをすべて除去するために超純水で洗浄した後、1mLのエタノールでテストピースのバイオフィルムと結合して染色していたクリスタルバイオレット染料を抽出し、吸光度(OD570)を測定し、バイオフィルムの残存量を求めた。
測定したOD570をもとに、下記式に従ってバイオフィルム除去率を測定した。結果を表1に示した。
バイオフィルム除去率(%)={(コントロールOD570−ブランクOD570)−(実施例のOD570−ブランクOD570)}×100/(コントロールOD570−ブランクOD570)
尚、コントロールはバイオフィルムが形成されたテストピースの洗浄操作を行わずにクリスタルバイオレット処理を行ったものであり、ブランクはエタノールのOD570を指す。
(2) Biofilm removal test (piping model)
A test piece on which a biofilm was formed was immersed in a 6-well plate containing 5 mL of a cleaning solution or control (ultrapure water) and shaken at 40 ° C. and 60 rpm for a predetermined time (BioShaker BR-43FL manufactured by TAITEC). The shaking time is shown as the washing time in Table 1. Sodium carbonate was used to neutralize the washing liquid after shaking, and the pH was adjusted to 7. The pH of the present invention is a value measured by a pH meter using a glass electrode.
After leaving 1 mL of the cleaning solution and adding 2 mL of ultrapure water, it was rinsed once by shaking at 60 rpm for 5 minutes. This single rinse corresponds to rinsing with water in an amount of 1 times the total capacity of the pipe. In this test, 3/5 of the total capacity here corresponds to the total capacity of the piping, and 2/5 of the total capacity corresponds to the bathtub capacity. This was carried out using a piping model that assumes actual equipment that remains in the system.
After each rinse, the rinse water was discarded, and fresh ultrapure water was used to repeat the rinse up to the number shown in Table 1. The second and subsequent rinses were carried out by leaving 1 mL of rinse water and adding 2 mL of fresh ultrapure water to it. After a predetermined number of rinses, each test piece is immersed in a 0.1% crystal violet solution, stained with a biofilm, washed with ultrapure water to remove any excess crystal violet, and then washed with ultrapure water. The crystal violet dye that had been stained by binding to the biofilm of the test piece was extracted with 1 mL of ethanol, and the absorbance (OD570) was measured to determine the residual amount of the biofilm.
Based on the measured OD570, the biofilm removal rate was measured according to the following formula. The results are shown in Table 1.
Biofilm removal rate (%) = {(Control OD570-Blank OD570)-(Example OD570-Blank OD570)} x 100 / (Control OD570-Blank OD570)
The control is a crystal violet treatment without cleaning the test piece on which the biofilm is formed, and the blank refers to ethanol OD570.
<実施例2>
実施例1と同様に、ただし処理条件を表2の通りとして、バイオフィルム除去試験を行った。また、表2の洗浄液について、以下の方法で発泡抑制性を評価した。また、バイオフィルム除去試験で行った最後のすすぎのすすぎ水について、次亜塩素酸ナトリウムとの反応性(表では、「次亜塩素酸Naとの反応性」と表示した)を以下の方法で評価した。結果を表2に示した。
<Example 2>
The biofilm removal test was carried out in the same manner as in Example 1, except that the treatment conditions were as shown in Table 2. In addition, the foaming inhibitory properties of the cleaning liquids shown in Table 2 were evaluated by the following methods. In addition, the reactivity with sodium hypochlorite (indicated as "reactivity with Na hypochlorite" in the table) of the rinse water for the final rinse performed in the biofilm removal test was determined by the following method. evaluated. The results are shown in Table 2.
*発泡抑制性評価
50mL遠沈管に洗浄液を30mL加え、20往復激しく振とう後の泡体積を遠沈管の目盛りより算出した。
泡体積(mL)=(泡からなる層の最上部の目盛り)−(液状部分と泡状部分の境界部の目盛り)
* Evaluation of foaming inhibitory property 30 mL of cleaning solution was added to a 50 mL centrifuge tube, and the foam volume after vigorous shaking for 20 reciprocations was calculated from the scale of the centrifuge tube.
Foam volume (mL) = (scale at the top of the layer consisting of bubbles)-(scale at the boundary between the liquid part and the foam part)
*すすぎ水の次亜塩素酸ナトリウムとの反応性評価
最後のすすぎのすすぎ水1mLに、次亜塩素酸ナトリウム水溶液を2ppmとなるように加えた。全塩素濃度をDPD法で測定し、1.9ppm以上であれば次亜塩素酸ナトリウムと反応性がないと判断し、表2には○で示した。前記濃度が1.9ppm未満の場合は反応性があると判断し、表2には×で示した。すなわち、ジ亜塩素酸ナトリウムとの反応性がない場合(評価として〇と表した場合)とは、すすぎが良好に行われていることを示している。
* Evaluation of reactivity of rinse water with sodium hypochlorite To 1 mL of rinse water for the final rinse, an aqueous solution of sodium hypochlorite was added so as to be 2 ppm. The total chlorine concentration was measured by the DPD method, and if it was 1.9 ppm or more, it was judged that there was no reactivity with sodium hypochlorite, and it is indicated by ◯ in Table 2. When the concentration was less than 1.9 ppm, it was judged to be reactive, and is indicated by x in Table 2. That is, when there is no reactivity with sodium dichlorite (when it is expressed as 〇 as an evaluation), it indicates that rinsing is performed well.
<実施例3>
実施例2と同様に、ただし条件を表3の通りとして、バイオフィルム除去試験を行った。その際、洗浄後の中和の有無による汚れの析出の様子を目視観察した。なお、中和を行う場合は、振とう後の洗浄液に、炭酸ナトリウムを添加して、pH7になるように調整して行った。結果を表3に示した。
<Example 3>
A biofilm removal test was performed in the same manner as in Example 2, but with the conditions as shown in Table 3. At that time, the state of precipitation of stains due to the presence or absence of neutralization after cleaning was visually observed. In the case of neutralization, sodium carbonate was added to the washing liquid after shaking to adjust the pH to 7. The results are shown in Table 3.
<実施例4及び比較例4>
表4に示す組成の洗浄液を表4に示す条件で用いて、実施例1と同様にバイオフィルム除去試験を行った。また、表4の洗浄液について、実施例2と同様の方法で発泡抑制性を評価した。結果を表4に示した。
<Example 4 and Comparative Example 4>
A biofilm removal test was carried out in the same manner as in Example 1 using the cleaning solution having the composition shown in Table 4 under the conditions shown in Table 4. Moreover, about the cleaning liquid of Table 4, the foaming inhibitory property was evaluated by the same method as in Example 2. The results are shown in Table 4.
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JPS61207500A (en) * | 1985-03-08 | 1986-09-13 | 大阪瓦斯株式会社 | Bath furnace detergent |
JPH09118993A (en) * | 1995-07-04 | 1997-05-06 | Ebara Kogyo Senjo Kk | Method and device for chemical cleaning of plant |
JPH11262459A (en) * | 1998-03-17 | 1999-09-28 | Toto Ltd | Bathroom washing device |
JP2002003899A (en) * | 2000-06-19 | 2002-01-09 | Kansai Koso Kk | Fume inhibitor for detergent and detergent composition |
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JP2008075976A (en) * | 2006-09-21 | 2008-04-03 | Nippon Soda Co Ltd | Bathtub water circulation pipe washing tool and bathtub water circulation pipe washing method |
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