JPH0229118B2 - HATSUHOSEIKO HYOMENSENJOZAISOSEIBUTSU - Google Patents
HATSUHOSEIKO HYOMENSENJOZAISOSEIBUTSUInfo
- Publication number
- JPH0229118B2 JPH0229118B2 JP13438582A JP13438582A JPH0229118B2 JP H0229118 B2 JPH0229118 B2 JP H0229118B2 JP 13438582 A JP13438582 A JP 13438582A JP 13438582 A JP13438582 A JP 13438582A JP H0229118 B2 JPH0229118 B2 JP H0229118B2
- Authority
- JP
- Japan
- Prior art keywords
- agent
- cleaning
- amount
- dirt
- foaming
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003795 chemical substances by application Substances 0.000 claims description 45
- 239000000203 mixture Substances 0.000 claims description 24
- 238000005187 foaming Methods 0.000 claims description 21
- 238000004140 cleaning Methods 0.000 claims description 20
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims description 20
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 239000000460 chlorine Substances 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 239000004094 surface-active agent Substances 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 150000002978 peroxides Chemical class 0.000 claims description 7
- 239000007800 oxidant agent Substances 0.000 claims description 3
- 239000007788 liquid Substances 0.000 description 16
- 239000000843 powder Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- -1 Fatty acid salts Chemical class 0.000 description 14
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 13
- 238000011156 evaluation Methods 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 239000012459 cleaning agent Substances 0.000 description 9
- 239000003599 detergent Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 239000003945 anionic surfactant Substances 0.000 description 5
- 239000005708 Sodium hypochlorite Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 4
- 229940045872 sodium percarbonate Drugs 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 150000008051 alkyl sulfates Chemical class 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 210000002700 urine Anatomy 0.000 description 3
- 238000009423 ventilation Methods 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 239000008233 hard water Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- GSGDTSDELPUTKU-UHFFFAOYSA-N nonoxybenzene Chemical compound CCCCCCCCCOC1=CC=CC=C1 GSGDTSDELPUTKU-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 150000003839 salts Chemical group 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000006694 eating habits Nutrition 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000010794 food waste Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910001959 inorganic nitrate Inorganic materials 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000010446 mirabilite 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
- 150000002823 nitrates Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- SATVIFGJTRRDQU-UHFFFAOYSA-N potassium hypochlorite Chemical compound [K+].Cl[O-] SATVIFGJTRRDQU-UHFFFAOYSA-N 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Description
本発明はプラスチツク、陶器、タイル、目地、
排水管内部などの硬表面の汚れを効果的に除去す
ることのできる、2剤型の発泡性硬表面洗浄剤組
成物に関する。
従来、家庭用のプラスチツク、陶器、タイル用
の洗剤としては、酸またはアルカリを主成分とす
る液体洗剤が知られており、また、目地用の洗剤
としては研磨剤を含む粉状または液体洗剤が知ら
れている。しかしながら、これら洗剤はいずれも
未だ洗浄力が不十分であつた。
近年、一般住宅の洋式化あるいは高層集合住宅
の出現および食生活の洋風化に伴ない、台所、浴
室、便所などの排水管、トラツプおよび過管の
内部に、食品廃棄物、排泄物、毛髪、泥、浴室汚
垢などの汚垢が詰まつたり、管内壁面に付着した
りして、管内の水の流れが妨げられる現象が多く
認められる。このような排水管内部の汚れは、汚
れ部に手の届きにくいこともあつて、家庭におけ
る硬表面汚れの中でも最も除去しにくいものの一
つであつた。
従来、排水管、トラツプ、過管などの汚れを
除去する方法としては、塩素化炭化水素と活性剤
を用いて溶解、乳化する方法(米国特許第
3553145号明細書)、酵素および微生物で汚れを分
解す方法(特公昭38−26465号公報)、過炭酸ソー
ダと活性剤による方法(特開昭52−152406)、酸
剤とアルカリ性炭酸塩を用いる方法(特開昭53−
50207号公報)、酸剤、アルカリ性炭酸塩および過
炭酸ソーダなどの酸化剤を用いる方法(特開昭53
−50208号公報)などが報告されているが、これ
らはいずれも洗浄力が未だ十分ではなかつた。
米国特許明細書第3471407号明細書には、苛性
ソーダなどの強アルカリ、アルミニウムおよび無
機硝酸塩を投入する方法が報告されているが、こ
れは極めて危険である。また、米国特許明細書第
3538008号明細書には、H2SO4、HCl、HNO3、
オルトリン酸、スルフアミン酸などの強酸とシリ
カゾルとを投入する方法が開示されているが、こ
の方法も極めて危険であり、且つ、腐食性が大き
い。
一方、エアーゾールの噴射圧を利用して完全に
詰まつた排管を導通せしめることも知られている
が、この方法は壁に堆積した汚れに対しては殆ど
効果がない。排管内の汚れを物理的に行なうこと
も考えられるが、これは手間がかかり家庭で手軽
に行なうのは困難である。
本発明は、上記のような従来技術の問題点を解
決するためになされたものであり、プラスチツ
ク、陶器、タイル、目地、風呂釜、排水管内部等
の硬表面の汚れを容易に且つ効果的に除去しうる
ことのできる2剤型の発泡性硬表面洗浄剤組成物
を提供することを目的とする。
すなわち、本発明の2剤型の発泡性硬表面洗浄
剤組成物は以下のA剤およびB剤を有することを
特徴とする。両者は使用に際して接触ないし混合
され、また、必要により水が添加される。
(1) A剤:無機過酸化物を含み有効酸素量が0.25
〜25%の酸素系酸化物組成物またはこの組成物
の水溶液。
(2) B剤:次亜塩素酸塩を含み有効酸素量が0.25
〜60%の塩素系酸化物組成物またはこの組成物
の水溶液。
以下に本発明をさらに詳細に説明する。
A剤は無機過酸化物を含む酸素系酸化物組成物
またはその水溶液であり、A剤中の無機過酸化物
の量は液体の場合は0.5〜50重量%、固体の場合
は10〜100重量%であることが好ましく、さらに
好ましくはそれぞれ1〜3wt%および30〜90wt%
である。そして、A剤中の有効酸素量は0.25〜25
%であり、好ましくは0.5〜20%である。有効酸
素量が0.25%に満たないと十分な洗浄力が得られ
ず、一方25%を越えると保存安定性が劣化し、ま
た、家庭での取扱い上危険でもあり好ましくな
い。
ここで、有効酸素量とは、A剤中に含まれる漂
白等に有効な酸素量(O)のA剤全体に対する割
合(重量%)である。これは、過マンガン酸カリ
ウム等を用いて常法により測定できる。
A剤の無機過酸化物としては、次亜塩素酸塩と
反応して分解するものであればいずれもが使用可
能であるが、好ましくは過酸化水素および過炭酸
ナトリウム(Na2CO3・nH2O2、典型的にはn=
3/2)で代表される、過酸化水素付加物である。
その他の具体例としては、過ホウ酸ナトリウム、
硫酸ナトリウムの過酸化水素付加物、ケイ酸ナト
リウムの過酸化水素付加物、オルトリン酸ナトリ
ウムの過酸化水素付加物である。上記の中でも特
に好ましいのは過酸化水素および過炭酸ナトリウ
ムである。
B剤は次亜塩素酸塩を含む塩素系酸化物組成物
またはその水溶液であつて、B剤中の次亜塩素酸
塩の量は液体の場合は0.25〜40重量%、粉体の場
合は1〜100重量%であることが好ましく、さら
に好ましくはそれぞれ1〜15wt%および10〜
90wt%である。そして、B剤中の有効塩素量は
0.25〜60%であり、好ましくは1〜15%である。
有効塩素量が0.25%に満たないと十分な洗浄力が
得られず、一方25%を越えると保存安定性が著し
く劣化し、また、家庭での取扱い上危険でもあり
好ましくない。
ここで有効塩素量とは、B剤中に含まれる漂白
等に有効な塩素量(Cl2)のB剤全体に対する割
合である。
B剤の次亜塩素酸塩としては次亜塩素酸ナトリ
ウム、次亜塩素酸カリウム、高度サラシ粉が例示
でき、特に好ましいのは次亜塩素酸塩である。
A剤およびB剤の性状は液体(溶液)でも固体
通常(粉粒状)でもよい。A剤とB剤との組合せ
の中で特に好ましいものを例示すれば次のように
なる。
(1) 液体/液体タイプ
A剤:1.0〜35wt%の過酸化水素水溶液
B剤:1.0〜15wt%の次亜塩素酸ナトリウム水
溶液
(2) 粉体/液体タイプ
A剤:過炭酸ナトリウムを10〜100wt%含む粉
状組成物
B剤:0.5〜15wt%の次亜塩素酸ナトリウム水
溶液
(3) 液体/粉体タイプ
A剤:1.0〜35wt%の過酸化水素水溶液
B剤:さらし粉を2.0〜100wt%含む粉状組成物
(4) 粉体/粉体タイプ
A剤:過炭酸ソーダを10〜100wt%含む粉状組
成物
B剤:さらし粉を2.0〜100wt%含む粉状組成物
本発明の発泡性洗浄剤組成物は、さらにA剤お
よびB剤のいずれの一方にも、また双方にも界面
活性剤を添加することができる。界面活性剤は後
に詳述するように主として発泡の安定性に寄与す
るものである。したがつて、このような効果を有
するものであればいずれも使用でき、A剤成分あ
るいはB剤成分と安定に保存しうるものが好まし
い。界面活性剤としては、陰イオン界面活性剤、
非イオン界面活性剤、陽イオン界面活性剤、両性
界面活性剤のいずれもが使用可能であるが、特に
好ましいのは陰イオン界面活性剤および非イオン
界面活性剤である。このような界面活性剤の具体
例としては以下のものが挙げられる。
(1) 陰イオン界面活性剤
炭素数10〜20の脂肪酸塩
炭素数10〜18のアルキルサルフエート
炭素数10〜18のアルキルベンゼンスルホネー
ト
炭素数8〜18のα−オレフインスルホネート
炭素数8〜18でエチレンオキシド(EO)の
平均付加モル数EOが1〜10モルのポリオキ
シエチレンアルキルエーテルスルホネート
炭素数6〜12でEO=6〜20のポリオキシ
エチレンアルキルフエニルエーテルスルホネー
ト
(2) 非イオン界面活性剤
炭素数10〜20のアルコールEO付加物(EO
=6〜20)
アルキル基の炭素数が6〜12のアルキルフエ
ノールEO付加物(EO=6〜20)
アルキル基の炭素数が12〜18のソルビタンア
ルキルエーテルEO付加物(EO=3〜30)
炭素数12〜18の脂肪酸EO付加物(EO=5
〜50)
(3) 陽イオン界面活性剤
4級アンモニウム塩
イミダゾリニウム4級塩
(4) 両性界面活性剤
ベタイン
アミノ塩
イミダゾリン
上記界面活性剤の中でも、起泡性の点で特に勝
れているものは、平均炭素数が12のアルキルサル
フエート、アルキル基の平均炭素数が12のアルキ
ルベンゼンスルホネート、炭素数12〜18のα−オ
レフインスルホネート、ポリオキシエチレンノニ
ルフエニルエーテル(EO=8〜10)などの陰
イオン界面活性剤、ラウリルアルコールEO付加
物(EO=8〜10)、ノニルフエニルエーテル
EO付加物(EO=8〜10)などの非イオン界面
活性剤などが例示できる。また、保存時の安定性
では、平均炭素数が12のアルキルサルフエート、
ポリオキシエチレンノニルフエニルエーテル
(EO=8〜10)、ラウリルアルコールEO付加物
(EO=8〜10)、ノニルフエニルエーテルEO付
加物(EO=8〜10)などが勝れている。さら
に汚垢に対する浸透作用を助長する効果の勝れて
いるものとしては、平均炭素数が12のアルキルサ
ルフエート、アルキル基の平均炭素数が12のアル
キルベンゼンスルホネート、炭素数12〜18のα−
オレフインスルホネート、ポリオキシエチレンノ
ニルフエニルエーテル(EO=8〜10)などの
陰イオン界面活性剤などが例示できる。
界面活性剤はA剤またはB剤に0.1〜20重量%
含まれるように添加されることが好ましく、さら
に好ましくは0.5〜10重量%である。この量が0.1
%に満たないと十分な起泡力ないし泡安定性が得
られず、20%を越えると保存的における安定性が
著しく劣化すると共に、有効成分の低下に伴う洗
浄効果の低下をきたす。
次に本発明の硬表面洗浄剤組成物の使用方法な
いし洗浄機構について説明する。
A剤およびB剤は別々に保存され、使用に際し
て硬表面汚垢上にそれぞれ別個に適用される。適
用の順序はいずれが先でも構わないし、同時でも
よい。液体/粉体タイプおよび粉体/液体タイプ
の場合は、先ず粉体の方を散布し、ついで液体を
注ぐ方が実際的である。また、粉体/粉体タイプ
では双方を散布した後に適量の水を加える。液
体/液体タイプが取扱いも簡単であり、また、所
望量を任意の硬表面、特に手の届きにくい場所や
垂直面などの硬表面に適用するのに便利である。
この点からは液体でも安定に保存しうる過酸化水
素および次亜塩素酸ナトリウムが好都合である。
A剤とB剤とが硬表面汚垢上で接触して反応す
ると、発生する酸素の酸化力により汚垢の分解が
行なわれる。酸素は無機過酸化物の分解と、次亜
塩素酸塩の分解との双方により発生し、汚垢に対
して相乗的に働いて分解せしめる。特に、次亜塩
素酸塩は強力な殺菌力を有するので、殺菌剤、殊
にカビ取り剤としても働く。
また、反応により多量に生ずる気泡は、汚垢を
物理的な力によつて除去する。したがつて、手の
届きにくい箇所でも有効に除去でき、また外表面
の場合もこする等の作業をしなくても除去が行な
える。さらに、気泡が発生することにより、凹部
などの洗浄剤の行きわたりにくい場所にも、気泡
の充満力によつて洗浄剤が行きわたり、洗浄を効
率的に行なうことができる。また、発泡すること
によつて洗浄剤が硬表面に付着しやすくなり、傾
斜面や垂直面にも洗浄に必要な十分な時間とどま
ることが可能となる。
さらに、A剤とB剤との反応熱により汚垢の付
着力を低下させることができる。
以上のように、本発明の洗浄剤組成物では、過
酸化物および次亜塩素酸塩の分解による。
(1) 酸化力さらには殺菌力
(2) 発泡に伴なう汚垢への物理的外力、洗浄剤の
充満および洗浄剤の付着ないし停滞
(3) 反応熱
が相乗的に働き、従来の洗浄剤では想像できなか
つたような優れた洗浄力が得られる。
洗浄すべき硬表面に傾斜面があつたり、凹部や
隅部のように洗浄しにくい面があるのは極めて普
通のことである。したがつて、発泡力あるいは泡
の安定性は重要な要素である。たとえば家庭用の
流し台の排水管を例に考えてみる。この排水管は
ほぼまつすぐに下降しており、また側壁には蛇腹
構造を有するものが多い。そして管内には所定の
流水路が形成されており、水を流した場合、水は
管内を均一に流れるのではなく、その流水路に沿
つて流れる。このような排水管に洗浄剤を流し込
んでも、洗浄剤は特定部にしか接触せず、また、
すぐに流れ落してしまい効率的に洗浄することが
できない。すでに示した特開昭52−152406号公
報、同53−50207号公報、同53−50208号公報にも
粉状の発泡性組成物が報告されているが、これら
は発泡量、発泡力共に不十分であつて、上記の排
水管に適用した場合は発泡しながら速やかに流れ
落ちる。
これに対して、本発明のA剤とB剤とを用いた
場合は、発泡量、発泡力共に強大であつて、排水
管の内部全体に充満して汚垢に物理的な力を作用
せしめ、しかも、排水管内をゆつくりと下降して
汚垢と十分な時間に亘つて接触する。特に、A剤
またはB剤の少なくとも一方に界面活性剤が含ま
れている場合は、発泡力が増すと共に生成する気
泡が安定となり、上記の発泡効果がさらに増進さ
れる。
以上の説明からも明らかなように、本発明の2
剤型発泡性洗浄剤組成物は硬表面全般に有効であ
つて、カビの生えた面や、傾斜面、垂直面などの
洗浄剤の流れやすい部位や、あるいは、凹部、隅
部、管内部などの洗浄したくい部位に特に有効で
ある。具体的には、トイレ用洗浄剤、カビ除去
剤、換気扇汚れ除去剤、排水管クリーナーとして
特に有効である。
本発明の洗浄剤組成物中には、さらにA剤およ
び/またはB剤中に、芒硝、炭酸ソーダ、食塩、
三リン酸ソーダ、二リン酸ソーダ、トリポリホス
フエート、ピロカリホスフエートなどの増量剤、
着色剤、香料、殺菌剤、キレート剤、活性化剤、
アルカリ剤、あるいはその他の洗浄剤に通常添加
される添加剤を添加することができる。これら添
加剤は、A剤およびB剤の安定性や機能を損なわ
ないように添加されることが好ましく、たとえば
キレート剤や活性化剤はA剤中に添加することが
好ましい。
実施例 1
第1表に示した各試料を作成し、尿垢の除去力
を評価した。なお、数値は重量%を表わす。
評価方法
10cm□のタイルおよび塩化ビニルを人尿中に浸
漬−取り出し−乾燥を繰り返して付着させた尿垢
(0.5g100cm2)を評価汚垢として用いた。
本発明の試料No.1〜4(2液型)はA剤および
B剤を20gづつ使用時に混合して尿垢(2.5×6
cm)を処理し、水ですすいだ後、汚垢の除去率を
目視判定により評価した。また、比較例(1液
型)は40gを使用する他は同様に評価した。
評価基準:◎…95%以上除去
〇…80〜95%除去
△…50%程度除去
The present invention is applicable to plastics, ceramics, tiles, joints,
The present invention relates to a two-component foaming hard surface cleaning composition that can effectively remove dirt from hard surfaces such as the inside of drain pipes. Traditionally, household detergents for plastics, ceramics, and tiles have been known as liquid detergents containing acids or alkalis as their main ingredients, and as detergents for joints, powdered or liquid detergents containing abrasives have been used. Are known. However, all of these detergents still had insufficient cleaning power. In recent years, with the emergence of Western-style general housing or high-rise apartment complexes and the Westernization of eating habits, food waste, excrement, hair, Dirt, bathroom grime, and other dirt clogs or adheres to the inner walls of pipes, which often obstructs the flow of water within the pipes. Such stains inside drain pipes are one of the most difficult to remove among hard surface stains in the home, partly because the dirty parts are difficult to reach. Conventionally, the method for removing dirt from drain pipes, traps, pipes, etc. is to dissolve and emulsify it using chlorinated hydrocarbons and an activator (U.S. Patent No.
3553145 specification), a method of decomposing dirt with enzymes and microorganisms (Japanese Patent Publication No. 38-26465), a method using soda percarbonate and an activator (Japanese Patent Application Laid-open No. 152406/1982), a method using an acid agent and an alkaline carbonate. Method (Unexamined Japanese Patent Publication 1973-
50207), a method using an oxidizing agent such as an acid agent, an alkaline carbonate, and sodium percarbonate (Japanese Unexamined Patent Publication No. 53
-50208 Publication), but none of these have sufficient cleaning power. US Pat. No. 3,471,407 reports a method of adding strong alkalis such as caustic soda, aluminum, and inorganic nitrates, but this is extremely dangerous. Also, U.S. Patent Specification No.
3538008 specifies H 2 SO 4 , HCl, HNO 3 ,
A method of adding a strong acid such as orthophosphoric acid or sulfamic acid and silica sol has been disclosed, but this method is also extremely dangerous and highly corrosive. On the other hand, it is also known to use aerosol injection pressure to open a completely clogged drain pipe, but this method has little effect on dirt deposited on the walls. It is possible to physically clean the inside of the drain pipe, but this is time-consuming and difficult to do easily at home. The present invention was made to solve the problems of the prior art as described above, and can easily and effectively remove stains from hard surfaces such as plastics, ceramics, tiles, joints, bathtubs, and inside drain pipes. It is an object of the present invention to provide a two-part foaming hard surface cleaning composition that can be used to clean surfaces. That is, the two-part foaming hard surface cleaning composition of the present invention is characterized by having the following parts A and B. The two are brought into contact or mixed during use, and water is added if necessary. (1) Agent A: Contains inorganic peroxide and has an effective oxygen amount of 0.25
~25% oxygen-based oxide composition or an aqueous solution of this composition. (2) Agent B: Contains hypochlorite and has an effective oxygen amount of 0.25
~60% chlorine-based oxide composition or an aqueous solution of this composition. The present invention will be explained in more detail below. Part A is an oxygen-based oxide composition containing an inorganic peroxide or an aqueous solution thereof, and the amount of inorganic peroxide in Part A is 0.5 to 50% by weight in the case of a liquid, and 10 to 100% by weight in the case of a solid. %, more preferably 1 to 3 wt% and 30 to 90 wt%, respectively.
It is. And the amount of effective oxygen in agent A is 0.25 to 25
%, preferably 0.5 to 20%. If the amount of effective oxygen is less than 0.25%, sufficient cleaning power cannot be obtained, while if it exceeds 25%, storage stability deteriorates and it is also dangerous to handle at home, which is not desirable. Here, the effective oxygen amount is the ratio (% by weight) of the amount of oxygen (O) contained in the A agent that is effective for bleaching etc. to the entire A agent. This can be measured by a conventional method using potassium permanganate or the like. Any inorganic peroxide that can be used as agent A can be used as long as it reacts with hypochlorite and decomposes, but hydrogen peroxide and sodium percarbonate (Na 2 CO 3 .nH 2 O 2 , typically n=
3/2) is a hydrogen peroxide adduct. Other specific examples include sodium perborate,
These are hydrogen peroxide adducts of sodium sulfate, hydrogen peroxide adducts of sodium silicate, and hydrogen peroxide adducts of sodium orthophosphate. Among the above, particularly preferred are hydrogen peroxide and sodium percarbonate. Agent B is a chlorine-based oxide composition containing hypochlorite or its aqueous solution, and the amount of hypochlorite in Agent B is 0.25 to 40% by weight in the case of a liquid, and 0.25 to 40% by weight in the case of a powder. It is preferably 1 to 100 wt%, more preferably 1 to 15 wt% and 10 to 100 wt%, respectively.
It is 90wt%. And the amount of available chlorine in agent B is
It is 0.25 to 60%, preferably 1 to 15%.
If the amount of available chlorine is less than 0.25%, sufficient cleaning power cannot be obtained, while if it exceeds 25%, storage stability will be significantly deteriorated and it is also dangerous to handle at home, which is not desirable. Here, the effective chlorine amount is the ratio of the amount of chlorine (Cl 2 ) contained in the B agent that is effective for bleaching, etc. to the entire B agent. Examples of the hypochlorite of agent B include sodium hypochlorite, potassium hypochlorite, and highly refined white powder, with hypochlorite being particularly preferred. The properties of the A agent and the B agent may be liquid (solution), solid or normal (powder-like). Particularly preferable combinations of agent A and agent B are as follows. (1) Liquid/liquid type Part A: 1.0-35wt% hydrogen peroxide solution Part B: 1.0-15wt% sodium hypochlorite aqueous solution (2) Powder/liquid type Part A: 10 to 10% of sodium percarbonate Powder composition containing 100wt% Part B: 0.5-15wt% sodium hypochlorite aqueous solution (3) Liquid/powder type Part A: 1.0-35wt% hydrogen peroxide solution Part B: 2.0-100wt% bleaching powder Powder composition containing (4) Powder/powder type Part A: Powder composition containing 10 to 100 wt% of soda percarbonate Part B: Powder composition containing 2.0 to 100 wt% of bleaching powder Foaming cleaning of the present invention In the agent composition, a surfactant may be further added to either or both of the A agent and the B agent. The surfactant mainly contributes to the stability of foaming, as will be explained in detail later. Therefore, any material having such an effect can be used, and it is preferable to use a material that can be stably stored with the A component or the B component. As surfactants, anionic surfactants,
Any of nonionic surfactants, cationic surfactants, and amphoteric surfactants can be used, but anionic surfactants and nonionic surfactants are particularly preferred. Specific examples of such surfactants include the following. (1) Anionic surfactants Fatty acid salts with 10 to 20 carbon atoms Alkyl sulfates with 10 to 18 carbon atoms Alkylbenzene sulfonates with 10 to 18 carbon atoms α-olefin sulfonates with 8 to 18 carbon atoms Ethylene oxide with 8 to 18 carbon atoms Polyoxyethylene alkyl ether sulfonate with an average added mole number of (EO) EO of 1 to 10 moles Polyoxyethylene alkyl phenyl ether sulfonate with 6 to 12 carbon atoms and EO = 6 to 20 (2) Nonionic surfactant Carbon Several 10 to 20 alcohol EO adducts (EO
= 6 to 20) Alkylphenol EO adduct with alkyl group having 6 to 12 carbon atoms (EO = 6 to 20) Sorbitan alkyl ether EO adduct with alkyl group having 12 to 18 carbon atoms (EO = 3 to 30) Fatty acid EO adducts with 12 to 18 carbon atoms (EO=5
~50) (3) Cationic surfactant Quaternary ammonium salt Imidazolinium quaternary salt (4) Ampholytic surfactant Betaine Amino salt Imidazoline Among the above surfactants, it is particularly superior in terms of foaming properties. These include alkyl sulfates with an average number of carbon atoms of 12, alkylbenzene sulfonates with an average number of carbon atoms in the alkyl group of 12, α-olefin sulfonates with 12 to 18 carbon atoms, and polyoxyethylene nonyl phenyl ether (EO = 8 to 10). Anionic surfactants such as lauryl alcohol EO adducts (EO=8-10), nonyl phenyl ether
Examples include nonionic surfactants such as EO adducts (EO=8 to 10). In addition, in terms of stability during storage, alkyl sulfates with an average carbon number of 12,
Polyoxyethylene nonylphenyl ether (EO = 8 to 10), lauryl alcohol EO adduct (EO = 8 to 10), nonylphenyl ether EO adduct (EO = 8 to 10), etc. are superior. In addition, alkyl sulfates with an average number of carbon atoms of 12, alkylbenzene sulfonates with an average number of carbon atoms in the alkyl group of 12, and α-
Examples include anionic surfactants such as olefin sulfonate and polyoxyethylene nonyl phenyl ether (EO=8 to 10). Surfactant is 0.1 to 20% by weight in Part A or Part B.
It is preferable that the amount is added such that it is included, and more preferably 0.5 to 10% by weight. This amount is 0.1
If it is less than 20%, sufficient foaming power or foam stability cannot be obtained, and if it exceeds 20%, the stability during storage will be significantly deteriorated and the cleaning effect will be reduced due to the reduction in the amount of active ingredients. Next, a method for using the hard surface cleaning composition of the present invention and a cleaning mechanism will be explained. Parts A and B are stored separately and each is applied separately onto the hard surface soil at the time of use. The order of application may be either first or simultaneously. For liquid/powder and powder/liquid types, it is more practical to spread the powder first and then pour the liquid. Also, for the powder/powder type, add an appropriate amount of water after spraying both. The liquid/liquid type is also easy to handle and convenient for applying the desired amount to any hard surface, especially hard surfaces such as hard to reach places or vertical surfaces.
From this point of view, hydrogen peroxide and sodium hypochlorite, which can be stably stored even in liquid form, are advantageous. When Agent A and Agent B come into contact with each other on hard surface dirt and react, the dirt is decomposed by the oxidizing power of the generated oxygen. Oxygen is generated by both the decomposition of inorganic peroxide and the decomposition of hypochlorite, and acts synergistically on dirt to decompose it. In particular, since hypochlorite has a strong disinfecting power, it also acts as a disinfectant, especially as a mold remover. In addition, a large amount of air bubbles generated by the reaction is used to remove dirt by physical force. Therefore, it can be effectively removed even in hard-to-reach places, and even on the outer surface, it can be removed without scrubbing or the like. Furthermore, due to the generation of air bubbles, the cleaning agent can be spread even to places where the cleaning agent is difficult to reach, such as recesses, due to the filling power of the air bubbles, making it possible to perform cleaning efficiently. Foaming also makes it easier for the cleaning agent to adhere to hard surfaces, allowing it to remain on inclined and vertical surfaces for a sufficient period of time necessary for cleaning. Furthermore, the adhesion of dirt can be reduced by the heat of reaction between Agent A and Agent B. As described above, in the cleaning composition of the present invention, peroxide and hypochlorite are decomposed. (1) Oxidizing power and sterilizing power (2) Physical external force on dirt due to foaming, filling of cleaning agent, and adhesion or stagnation of cleaning agent (3) Reaction heat works synergistically to prevent conventional cleaning. It provides excellent cleaning power that could not be imagined with detergents. It is very common for the hard surfaces to be cleaned to have slopes or surfaces that are difficult to clean, such as recesses or corners. Therefore, foaming power or foam stability is an important factor. For example, consider the drain pipe of a household sink. These drain pipes descend almost straight down, and many have bellows structures on their side walls. A predetermined flow channel is formed within the pipe, and when water is allowed to flow, the water does not flow uniformly within the pipe, but flows along the flow channel. Even if a cleaning agent is poured into such a drain pipe, the cleaning agent only comes into contact with specific areas, and
It washes off quickly and cannot be cleaned efficiently. Powdered foaming compositions have also been reported in JP-A-52-152406, JP-A-53-50207, and JP-A-53-50208, which have already been mentioned, but these have poor foaming amount and foaming power. It is sufficient and when applied to the above-mentioned drain pipe, it quickly flows down while foaming. On the other hand, when Agents A and B of the present invention are used, both the amount of foaming and the foaming power are strong, and the entire inside of the drain pipe is filled and a physical force is applied to the dirt. Moreover, it slowly descends inside the drain pipe and comes into contact with the dirt for a sufficient period of time. In particular, when at least one of the A agent and the B agent contains a surfactant, the foaming power increases and the generated bubbles become stable, further enhancing the foaming effect described above. As is clear from the above explanation, the second aspect of the present invention
The foaming detergent composition is effective on all hard surfaces, such as moldy surfaces, inclined surfaces, vertical surfaces, and other areas where the cleaning agent easily flows, as well as recesses, corners, and inside pipes. It is particularly effective for areas that need to be cleaned. Specifically, it is particularly effective as a toilet cleaner, mold remover, ventilation fan stain remover, and drain pipe cleaner. The cleaning composition of the present invention further contains mirabilite, soda carbonate, salt,
Bulking agents such as sodium triphosphate, sodium diphosphate, tripolyphosphate, pylocaliphosphate,
Colorants, fragrances, fungicides, chelating agents, activators,
Alkaline agents or other additives commonly added to cleaning agents can be added. It is preferable that these additives are added so as not to impair the stability or function of the A agent and the B agent. For example, it is preferable that a chelating agent or an activator be added to the A agent. Example 1 Each sample shown in Table 1 was prepared and evaluated for its ability to remove urine scale. In addition, the numerical value represents weight %. Evaluation method: Urine plaque (0.5 g, 100 cm 2 ), which was adhered to a 10 cm square tile and vinyl chloride by repeatedly soaking it in human urine, taking it out, and drying it, was used as the evaluation stain. Samples Nos. 1 to 4 (two-component type) of the present invention are prepared by mixing 20 g of agent A and agent B at the time of use.
cm) and rinsed with water, the stain removal rate was evaluated by visual judgment. In addition, a comparative example (one-liquid type) was evaluated in the same manner except that 40 g was used. Evaluation criteria: ◎…95% or more removed 〇…80-95% removed △…approximately 50% removed
【表】
実施例 2
第2表に示した各試料を作成し、カビの除去効
果を評価した。
評価方法
予め目地板(10×10cm)を作成し、その上に一
般の浴室に多く認められるカビ(Cladsporium、
Aureobasidum等)を培養し表面が一様に黒く汚
染されたもの評価汚垢として用いた。
本発明の試料No.8〜11はA剤およびB剤を4g
づつ使用時に混合し、目地カビ(1×10cm)を10
分間処理し、除去率を目視判定により評価した。
比較例は8gを使用する他は同様に行なつた。
評価基準:◎…95%以上除去
〇…80〜95%除去
△…50%程度除去[Table] Example 2 Each sample shown in Table 2 was prepared and the mold removal effect was evaluated. Evaluation method A joint board (10 x 10 cm) is prepared in advance, and mold (Cladsporium,
Aureobasidum, etc.) were cultured and the surface was uniformly contaminated with black and was used as an evaluation stain. Samples No. 8 to 11 of the present invention contain 4g of agent A and agent B.
Mix at the time of use and add 10 pieces of joint mold (1 x 10cm)
The removal rate was evaluated by visual judgment.
A comparative example was carried out in the same manner except that 8 g was used. Evaluation criteria: ◎…95% or more removed 〇…80-95% removed △…approximately 50% removed
【表】
実施例 3
第3表に示した各試料を作成し、排水管汚垢の
除去効果を評価した。
評価方法
以下のようにして評価汚垢を作成した。
(1) 台所汚垢
50゜DHの硬水20Kgに粉石けん200g、天ぷら
油100g、可溶性でんぷん50g、ゼラチン20g
および無機汚垢(粘土鉱物)40gを添加してよ
く混合したものを、循環ポンプを用いて内径2
cmの透明な塩化ビニールホース内を循環させ
た。20〜24時間循環させると塩化ビニール内壁
全面にモデル汚垢が堆積し、これはもはや水洗
だけでは殆ど除くことができない。このホース
を適当な長さに切り、評価汚垢として用いた。
(2) 浴室汚垢
50゜DHの硬水20Kgに粉石けん200g、脂肪酸
(オレイン酸/ステアリン酸=60/40)100g、
ゼラチン50gおよび無機汚垢(関東ローム層表
土)50gを添加、混合する他は台所汚垢と同様
にしてホースを調製した。上記のホースを家庭
用流し台の排水口に取りつけて洗浄効果を試験
した。
No.14〜16はA剤、B剤を別々に排水口に注入し
て混合し2時間放置後に水を流した。
No.17はA剤50gを排水口の周りにまわるく散布
し、B剤50gをA剤の囲りに注ぎ、少量の水でホ
ース内に流しこみ、2時間放置後に水を流した。
No.18、19は、A剤およびB剤50gづつを排水口
の囲りに散布し、水100mlをまわりから流しこみ、
2時間放置後に水を流した。
No.20、21は100gを排水口に注ぎこみ、2時間
放置後に水を流した。
No.22、23は排水口の囲りにまわるく散布し、水
100mlを流し、2時間放置後、再度水を流した。
除去率は目視判定により評価した。
評価基準:◎…60〜100%除去
〇…30〜60%除去
△…10〜30%除去
×…10%以下[Table] Example 3 Each sample shown in Table 3 was prepared, and the effectiveness of removing dirt from drain pipes was evaluated. Evaluation method Evaluation stains were created as follows. (1) Kitchen grime 20kg of 50゜DH hard water, 200g of powdered soap, 100g of tempura oil, 50g of soluble starch, 20g of gelatin
Add 40g of inorganic dirt (clay minerals) and mix well, using a circulation pump to
It was circulated through a transparent vinyl chloride hose. After 20 to 24 hours of circulation, model dirt accumulates on the entire inner wall of the vinyl chloride, which can hardly be removed by washing with water alone. This hose was cut to an appropriate length and used as an evaluation stain. (2) Bathroom stains: 20kg of hard water at 50°DH, 200g of powdered soap, 100g of fatty acids (oleic acid/stearic acid = 60/40),
A hose was prepared in the same manner as for kitchen dirt, except that 50 g of gelatin and 50 g of inorganic dirt (Kanto loam layer topsoil) were added and mixed. The above hose was attached to the drain of a household sink and its cleaning effectiveness was tested. For Nos. 14 to 16, Parts A and B were separately injected into the drain, mixed, and left for 2 hours before being flushed with water. For No. 17, 50 g of agent A was spread around the drain, 50 g of agent B was poured around agent A, and a small amount of water was poured into the hose, and the water was flushed after leaving it for 2 hours. For Nos. 18 and 19, spray 50g of Part A and Part B around the drain, pour in 100ml of water from around the drain,
After leaving it for 2 hours, water was poured off. For Nos. 20 and 21, 100g was poured into the drain, left for 2 hours, and then water was flushed away. Spray Nos. 22 and 23 around the drain, and
After pouring 100 ml of water and leaving it for 2 hours, the water was poured again. The removal rate was evaluated by visual judgment. Evaluation criteria: ◎...60-100% removal 〇...30-60% removal △...10-30% removal ×...10% or less
【表】【table】
【表】
実施例 4
第4表に示した各試料を作成し、換気扇クリー
ナーの汚れの除去効果を評価した。
評価方法
油汚れの付着した換気扇を評価汚垢として用
い、本発明品はA剤およびB剤5gづつを汚垢上
(40cm2)にて混合し、10分間放置後、乾いたタオ
ルで軽く拭きとり汚垢の除去率を目視判定した。
比較例は10gを同様に処理して評価した。
評価基準:◎…90〜100%除去
〇…80〜90%除去
〇〜△…50〜80%程度除去[Table] Example 4 Each sample shown in Table 4 was prepared and the stain removal effect of the ventilation fan cleaner was evaluated. Evaluation method Using a ventilation fan with oil stains as the evaluation stain, the product of the present invention was prepared by mixing 5 g each of Agent A and Agent B on the stain (40 cm 2 ), leaving it for 10 minutes, and then wiping it gently with a dry towel. The removal rate of dirt was visually judged.
As a comparative example, 10 g was treated in the same manner and evaluated. Evaluation criteria: ◎…90-100% removal 〇…80-90% removal 〇-△…50-80% removal
【表】【table】
Claims (1)
の酸素系酸化剤組成物またはその水溶液をA剤と
し、次亜塩素酸塩を含み有効塩素量が0.25〜60%
の塩素系酸化剤組成物またはその水溶液をB剤と
した2剤型の発泡性硬表面洗浄剤組成物。 2 上記A剤およびB剤の少なくともいずれか一
方に界面活性剤が含まれる特許請求の範囲第1項
記載の発泡性硬表面洗浄剤組成物。[Claims] 1 Contains inorganic peroxide and has an effective oxygen amount of 0.25 to 25%
An oxygen-based oxidizing agent composition or an aqueous solution thereof is used as agent A, and contains hypochlorite and has an effective chlorine amount of 0.25 to 60%.
A two-component foaming hard surface cleaning composition in which the chlorine-based oxidizing agent composition or its aqueous solution is used as agent B. 2. The foaming hard surface cleaning composition according to claim 1, wherein at least one of the A agent and the B agent contains a surfactant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13438582A JPH0229118B2 (en) | 1982-07-31 | 1982-07-31 | HATSUHOSEIKO HYOMENSENJOZAISOSEIBUTSU |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13438582A JPH0229118B2 (en) | 1982-07-31 | 1982-07-31 | HATSUHOSEIKO HYOMENSENJOZAISOSEIBUTSU |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5924798A JPS5924798A (en) | 1984-02-08 |
JPH0229118B2 true JPH0229118B2 (en) | 1990-06-27 |
Family
ID=15127154
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13438582A Expired - Lifetime JPH0229118B2 (en) | 1982-07-31 | 1982-07-31 | HATSUHOSEIKO HYOMENSENJOZAISOSEIBUTSU |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0229118B2 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6153396A (en) * | 1984-08-22 | 1986-03-17 | 花王株式会社 | Foamable detergent composition |
JPS6153397A (en) * | 1984-08-22 | 1986-03-17 | 花王株式会社 | Foamable detergent composition |
AU6256098A (en) * | 1997-02-05 | 1998-08-25 | S.C. Johnson & Son, Inc. | Bleaching cleaner that foams |
CA2342248C (en) * | 1998-08-31 | 2005-10-25 | The Clorox Company | Foaming drain cleaner |
US6479444B1 (en) | 1999-07-08 | 2002-11-12 | The Clorox Company | Foaming drain cleaner |
US6660702B2 (en) | 2000-12-08 | 2003-12-09 | The Clorox Company | Binary foaming drain cleaner |
US6638900B2 (en) * | 2001-10-18 | 2003-10-28 | The Clorox Company | Ternary foaming cleaner |
JP4794844B2 (en) * | 2004-10-18 | 2011-10-19 | 四国化成工業株式会社 | Pipe cleaning method |
CN111793530A (en) * | 2020-08-14 | 2020-10-20 | 苏州卫生职业技术学院 | High-performance, safe and environment-friendly foam cleaning agent for bracket-free invisible appliance and preparation method thereof |
-
1982
- 1982-07-31 JP JP13438582A patent/JPH0229118B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS5924798A (en) | 1984-02-08 |
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