JP2001252630A - Cleaning method - Google Patents
Cleaning methodInfo
- Publication number
- JP2001252630A JP2001252630A JP2000065917A JP2000065917A JP2001252630A JP 2001252630 A JP2001252630 A JP 2001252630A JP 2000065917 A JP2000065917 A JP 2000065917A JP 2000065917 A JP2000065917 A JP 2000065917A JP 2001252630 A JP2001252630 A JP 2001252630A
- Authority
- JP
- Japan
- Prior art keywords
- cleaning
- buffer
- cleaning method
- solution
- washing
- 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.)
- Pending
Links
- 238000004140 cleaning Methods 0.000 title claims abstract description 59
- 238000000034 method Methods 0.000 title claims abstract description 28
- 239000000872 buffer Substances 0.000 claims abstract description 31
- 238000005406 washing Methods 0.000 claims description 22
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 14
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 7
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- 229910021538 borax Inorganic materials 0.000 claims description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
- 239000004328 sodium tetraborate Substances 0.000 claims description 4
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004327 boric acid Substances 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 2
- 235000011181 potassium carbonates Nutrition 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- 235000017550 sodium carbonate Nutrition 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims 1
- 235000015497 potassium bicarbonate Nutrition 0.000 claims 1
- 239000011736 potassium bicarbonate Substances 0.000 claims 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 abstract description 8
- 230000000694 effects Effects 0.000 abstract description 7
- 239000007788 liquid Substances 0.000 abstract description 7
- 230000007613 environmental effect Effects 0.000 abstract description 4
- 238000012851 eutrophication Methods 0.000 abstract description 4
- 239000002351 wastewater Substances 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract 2
- 239000000725 suspension Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 239000000243 solution Substances 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 16
- 239000007853 buffer solution Substances 0.000 description 7
- 239000000356 contaminant Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000008399 tap water Substances 0.000 description 3
- 235000020679 tap water Nutrition 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 150000001768 cations Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000271 synthetic detergent Substances 0.000 description 2
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- FHNINJWBTRXEBC-UHFFFAOYSA-N Sudan III Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC(C=C1)=CC=C1N=NC1=CC=CC=C1 FHNINJWBTRXEBC-UHFFFAOYSA-N 0.000 description 1
- FZQSLXQPHPOTHG-UHFFFAOYSA-N [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 Chemical compound [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 FZQSLXQPHPOTHG-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- -1 alkali metal salt Chemical class 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- LLSDKQJKOVVTOJ-UHFFFAOYSA-L calcium chloride dihydrate Chemical compound O.O.[Cl-].[Cl-].[Ca+2] LLSDKQJKOVVTOJ-UHFFFAOYSA-L 0.000 description 1
- 229940052299 calcium chloride dihydrate Drugs 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- UPWGQKDVAURUGE-UHFFFAOYSA-N glycerine monooleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC(CO)CO UPWGQKDVAURUGE-UHFFFAOYSA-N 0.000 description 1
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- XLSMFKSTNGKWQX-UHFFFAOYSA-N hydroxyacetone Chemical compound CC(=O)CO XLSMFKSTNGKWQX-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229940050906 magnesium chloride hexahydrate Drugs 0.000 description 1
- DHRRIBDTHFBPNG-UHFFFAOYSA-L magnesium dichloride hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-] DHRRIBDTHFBPNG-UHFFFAOYSA-L 0.000 description 1
- 235000013310 margarine Nutrition 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 229940074096 monoolein Drugs 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229940099373 sudan iii Drugs 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000003911 water pollution Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47L—DOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
- A47L15/00—Washing or rinsing machines for crockery or tableware
- A47L15/42—Details
- A47L15/4236—Arrangements to sterilize or disinfect dishes or washing liquids
- A47L15/4238—Arrangements to sterilize or disinfect dishes or washing liquids by using electrolytic cells
Landscapes
- Cleaning By Liquid Or Steam (AREA)
- Detergent Compositions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、洗浄方法に関し、
特に、洗浄液中に界面活性剤を含まない状態であって
も、十分な洗浄力が得られるとともに、洗浄後の排水に
よる環境汚染を引き起こすことの少ない洗浄方法に関す
る。TECHNICAL FIELD The present invention relates to a cleaning method,
In particular, the present invention relates to a cleaning method capable of obtaining a sufficient detergency even in a state where a surfactant is not contained in a cleaning solution and causing less environmental pollution by wastewater after cleaning.
【0002】[0002]
【従来の技術】食品製造業においては、製造工程のさま
ざまな場所で洗浄が繰り返し実施される。このような洗
浄には、従来は、種々の界面活性剤を用いた合成洗剤が
使用されてきた。更に一般家庭においても同様な洗浄方
法が行われている。2. Description of the Related Art In the food manufacturing industry, washing is repeatedly performed at various places in a manufacturing process. Conventionally, synthetic detergents using various surfactants have been used for such washing. Further, a similar cleaning method is performed in general households.
【0003】また、電子工業界においても、有機系の油
汚れや、金属粉や鉱物等の無機系の汚れが表面に付着し
たプリント基板やガラス基板の洗浄工程が必要となる。
このような洗浄には、従来は、フロン系の溶剤やアセト
ン・アルコール系の有機溶剤や界面活性剤を用いた洗浄
が行われてきている。[0003] In the electronics industry as well, it is necessary to carry out a step of cleaning a printed board or a glass substrate having organic oil stains or inorganic stains such as metal powders and minerals adhered to the surface.
Conventionally, such cleaning has been performed using a CFC-based solvent, an acetone-alcohol-based organic solvent, or a surfactant.
【0004】しかし、上記の界面活性剤を使用した洗浄
方法では、洗浄排水に界面活性剤が大量に残存し、河川
や、海洋の富栄養化といった問題、つまり、水質汚染の
原因となっていた。また、フロン系、有機溶剤系の有機
溶剤を使用した洗浄方法ではこれら有機溶剤による地球
環境、更には環境ホルモンを筆頭に、人体への悪影響等
の問題を引き起こしてきている。[0004] However, in the above-mentioned cleaning method using a surfactant, a large amount of the surfactant remains in the cleaning wastewater, causing a problem of eutrophication of rivers and the ocean, that is, a cause of water pollution. . Further, a cleaning method using a chlorofluorocarbon-based or organic solvent-based organic solvent has caused problems such as adverse effects on the human environment, such as the global environment and environmental hormones caused by these organic solvents.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記の問題
の解決を図ったもので、環境負荷が小さく、人体に対す
る洗浄液自身の安全性が高く、且つ、安全で衛生的な洗
浄が可能で、洗浄後の排水の汚染や富栄養化といったこ
との生じない洗浄方法を提供することを目的としてい
る。DISCLOSURE OF THE INVENTION The present invention has been made to solve the above-mentioned problems, and has a small environmental load, a high safety of the cleaning solution itself to a human body, and a safe and hygienic cleaning. It is another object of the present invention to provide a cleaning method that does not cause pollution of wastewater after cleaning and eutrophication.
【0006】[0006]
【課題を解決するための手段】これらのことに鑑み本発
明はなされたものであり、具体的にはアルカリ性緩衝液
を用いて洗浄対象物の汚れを膨潤・解離させ、液中に油
成分を主とした汚れ成分を浮遊させることにある。ここ
で言う緩衝液とは、外部からの温度やpHを変化させる
因子による影響を緩和する作用を有する、更には、液の
希釈、濃縮によっても安定なpHを有する溶液の総称で
ある。特に、アルカリ性緩衝液の場合、汚れ物質との反
応が活発であるため、洗浄槽内に載置した被洗浄物に付
着する汚れを積極的に除去することができる上、緩衝液
の特徴として、アルカリ度が洗浄の進行に伴い、汚れ成
分の液中への溶解によるpHの変化作用を受けたとして
も、その変化の影響を緩和でき、安定な条件下で洗浄が
行われる。SUMMARY OF THE INVENTION In view of the above, the present invention has been made. Specifically, an alkaline buffer solution is used to swell and dissociate stains on an object to be washed, and an oil component is contained in the solution. The main purpose is to float dirt components. The term “buffer solution” as used herein is a generic term for a solution that has an action of alleviating the influence of an external factor that changes the temperature or the pH, and has a stable pH even when the solution is diluted or concentrated. In particular, in the case of an alkaline buffer, since the reaction with the contaminant is active, it is possible to positively remove the dirt attached to the object to be cleaned placed in the cleaning tank, and as a feature of the buffer, Even if the alkalinity is affected by a change in pH due to dissolution of the dirt component in the liquid as the washing proceeds, the influence of the change can be reduced and washing is performed under stable conditions.
【0007】これらアルカリ性緩衝液としては、種々の
タイプのものを例挙可能であるが、これらアルカリ緩衝
液に関しては、NBS(National Bureau of Standards)
に記載されているものに準じている。または、丸善刊化
学便覧基礎編II355ページに記載されている配合比を
用いて種々のpHの緩衝溶液が得られる。[0007] Various types of alkaline buffers can be exemplified. With respect to these alkaline buffers, NBS (National Bureau of Standards) is used.
According to those described in. Alternatively, buffer solutions of various pHs can be obtained by using the compounding ratio described in Maruzen Kagaku Binran Handbook, Basic Edition, page II355.
【0008】この中でも、環境への対応、洗浄効果の大
きさ、更にはコスト面等により、弱酸の塩(特にナトリ
ウム、カリウム等のアルカリ金属塩)を主成分とした緩
衝液が好適に用いられる。更に、弱酸としては炭酸、ホ
ウ酸、りん酸等が挙げられる。但し、りん酸及びその塩
は前述の富栄養化と大きく係わっており、この面から好
ましくない。Among them, a buffer solution containing a salt of a weak acid (particularly an alkali metal salt such as sodium or potassium) as a main component is preferably used in view of environmental friendliness, a large washing effect, and cost. . Further, examples of the weak acid include carbonic acid, boric acid, and phosphoric acid. However, phosphoric acid and its salts are greatly involved in the above-mentioned eutrophication, and are not preferred from this aspect.
【0009】本発明で用いられる、安全面、洗浄作用、
環境面、コスト等がより好ましい具体的な緩衝剤として
は、炭酸水素ナトリウム、炭酸ナトリウム、炭酸カリウ
ム、四ホウ酸ナトリウム、四ホウ酸カリウムの単独若し
くはこれらの複合塩が挙げられる。また、酢酸ナトリウ
ム等の有機系の緩衝剤も場合によっては、この無機系緩
衝剤の助剤として、たとえば30重量%以下といった少
量添加してもよい。[0009] The safety aspect, cleaning action,
Specific buffers more preferable in terms of environment, cost and the like include sodium hydrogen carbonate, sodium carbonate, potassium carbonate, sodium tetraborate, potassium tetraborate alone or a complex salt thereof. In addition, an organic buffer such as sodium acetate may be optionally added in a small amount, for example, 30% by weight or less, as an auxiliary for the inorganic buffer.
【0010】これらのアルカリ性緩衝液の濃度は別に規
定されていないが、一般的に、濃度が高いほど緩衝作用
が大きく、また、一定の濃度を超えると緩衝剤の析出と
いった問題が生じ、この点から比較的高濃度の10重量
%程度で行うことが好ましいが、コスト面も考慮すれ
ば、数重量%でもよい。また、洗浄温度は冷水(15℃
以下)でない常温以上の温度であれば特に問題はない。[0010] The concentration of these alkaline buffers is not specified separately, but in general, the higher the concentration, the greater the buffering effect. If the concentration exceeds a certain concentration, problems such as precipitation of the buffer occur. For this reason, it is preferable to carry out the treatment at a relatively high concentration of about 10% by weight. The washing temperature is cold water (15 ° C).
There is no particular problem as long as the temperature is not lower than normal temperature and not below.
【0011】場合によっては、少量の界面活性剤(特に
ノニオン系)を本発明のアルカリ性緩衝液に添加するこ
とにより、相乗的な洗浄効果が得られる。In some cases, a synergistic washing effect can be obtained by adding a small amount of a surfactant (particularly, a nonionic surfactant) to the alkaline buffer of the present invention.
【0012】また、更に被洗浄物から洗浄により遊離さ
れた物質が再付着することを防止する効果を有する物質
(再付着防止剤)を添加することにより、被洗浄物に対
する洗浄効果がより向上する。これら再付着防止剤とし
ては、一般にカルボキシメチルセルロース(CMC)、
メチルセルロース(MC)、ヒドロキシエチルセルロー
スといったセルロース誘導体や、ポリエチレングリコー
ル、ポリビニルアルコール、ポリビニルピロリドン、サ
ポニン等が用いられる。これらの界面活性剤及び再付着
防止剤を添加する割合は緩衝剤の30重量%以下であれ
ばよい。Further, by adding a substance having an effect of preventing a substance released by washing from the object to be washed from re-adhering (anti-adhesion agent), the effect of washing the object to be washed is further improved. . These anti-redeposition agents generally include carboxymethyl cellulose (CMC),
Cellulose derivatives such as methylcellulose (MC) and hydroxyethylcellulose, polyethylene glycol, polyvinyl alcohol, polyvinylpyrrolidone, saponin and the like are used. The ratio of adding these surfactants and anti-redeposition agent may be 30% by weight or less of the buffer.
【0013】[0013]
【発明の実施の形態】以下に本発明の実施例及び比較例
を、図面を用いて説明する。Embodiments of the present invention and comparative examples will be described below with reference to the drawings.
【0014】図1に洗浄力の比較を行うための試験器具
の一例としてJISで規定されている、リーナツ型試験
器を元に試作した洗浄試験器具を図示する。FIG. 1 shows a cleaning test device prototyped on the basis of a linac type test device specified by JIS as an example of a test device for comparing cleaning power.
【0015】ビーカー1に洗浄液2を、試料固定具3に
て固定した被洗浄物4に付着した汚染部分5が浸漬する
ように適量満たす。被洗浄物4は攪拌具6にて洗浄液2
を攪拌した際にも落下しないように試料固定具3にて固
定されている。また、攪拌によりビーカー1との位置関
係は変化しないように固定されている。A beaker 1 is filled with an appropriate amount of a washing liquid 2 so that a contaminated portion 5 adhered to an object 4 to be washed fixed by a sample fixture 3 is immersed. The object 4 to be cleaned is washed with the cleaning liquid 2 by the stirrer 6.
Is fixed by the sample fixture 3 so that it does not drop even when it is stirred. Further, it is fixed so that the positional relationship with the beaker 1 does not change due to the stirring.
【0016】攪拌具6による攪拌はJIS K 336
2に基づいて10分間実施し、被洗浄物4に付着させて
おいた汚染の保持量をもって洗浄率の評価を行う。The stirring by the stirrer 6 is performed according to JIS K 336.
The cleaning rate is evaluated based on the amount of the contaminants retained on the object 4 to be cleaned 4 for 10 minutes.
【0017】図2に比較例1及び比較例3で用いるアル
カリイオン水を生成させる装置の概念図を示す。FIG. 2 is a conceptual diagram of an apparatus for producing alkaline ionized water used in Comparative Examples 1 and 3.
【0018】水槽7に電解質を含む溶液8を満たし、陽
極9と陰極10の間に陽イオン透過膜11を介して電解
電圧を印加する。こうして陰極10側に得られる水がア
ルカリイオン水と呼ばれ、排出口12より取り出して比
較例1及び比較例3に用いた。一般には水道水にも電気
分解に十分な電解質が含まれているため、水道水を用い
る場合は、あえて電解質の溶解操作は行わない。A water tank 7 is filled with a solution 8 containing an electrolyte, and an electrolytic voltage is applied between an anode 9 and a cathode 10 via a cation permeable membrane 11. The water thus obtained on the cathode 10 side is called alkaline ionized water, taken out from the outlet 12 and used in Comparative Examples 1 and 3. Generally, tap water contains an electrolyte sufficient for electrolysis. Therefore, when tap water is used, the operation of dissolving the electrolyte is not performed.
【0019】<実施例1>被洗浄物に付着させる汚染は
次のようにして調製する。<Example 1> Contamination to be adhered to an object to be cleaned is prepared as follows.
【0020】使用水は、塩化カルシウム二水和物59.
0mg及び塩化マグネシウム六水和物27.2mgを量
り取り、水に溶かして1000mlとする。この使用水
を1100ml調製する。汚こう浴は、牛脂(日本薬局
方)と大豆油(日本薬局方)の代用としてサラダ油を各
10gずつ用いて混合した油脂20g、市販のマーガリ
ン10g、モノオレイン(化粧品原料基準の親油型モノ
オレイン酸グリセリンに規定するもの)0.25g及び
オイルレッド(スダンIII カラー・インデックス26
100に規定)(汚れの付着・脱着状況が目視確認でき
るように汚れを着色させるために添加する)0.1gを
同時にクロロホルム60mlに溶かして調製する。The water used was calcium chloride dihydrate.
Weigh 0 mg and 27.2 mg of magnesium chloride hexahydrate and dissolve in water to make 1000 ml. Prepare 1100 ml of this working water. As a substitute for beef tallow (Japanese Pharmacopoeia) and soybean oil (Japanese Pharmacopoeia), 20 g of fat mixed with 10 g each of salad oil, 10 g of commercially available margarine, and monoolein (a lipophilic product based on cosmetic raw materials) 0.25 g of glycerin oleate and oil red (Sudan III Color Index 26)
It is prepared by dissolving 0.1 g simultaneously in 60 ml of chloroform (added to color the stain so that the adhesion and desorption of the stain can be visually checked).
【0021】汚こう浴に浸すスライドグラスはJIS
R 3703に規定した標準型のものを使用し、清浄な
状態に洗浄・乾燥し、1mgまで重量測定しておく。こ
の値をスライドガラスの初期重量(ag)とする。The slide glass immersed in the dirty bath is JIS
Use a standard type specified in R 3703, wash and dry in a clean state, and measure the weight up to 1 mg. This value is defined as the initial weight (ag) of the slide glass.
【0022】重量測定後、汚こう液にスライドガラスを
浸し、汚こうを付着させた後、1時間風乾し重量を測定
する。この値を汚れ付着乾燥後の重量(bg)とする。After the weight is measured, the slide glass is immersed in a fouling solution, and the fouling is allowed to adhere. This value is defined as the weight (bg) after the adhesion and drying of the stain.
【0023】こうして準備した、被洗浄物に対して、台
所用合成洗剤の洗浄力評価方法であるJIS K 33
62に基づいて洗浄試験を施した。洗浄終了後のガラス
片は、室温で1時間風乾後重量を測定する。この値を洗
浄終了乾燥後の重量(cg)とする。洗浄力はJIS
K 3362に規定した洗浄力評価と異なり、これらの
値を用いて得られる、重量変化を元に(1)式を用いて
判定することとした。JIS K33, which is a method for evaluating the detergency of the synthetic detergent for kitchen, on the object to be cleaned thus prepared.
A cleaning test was performed based on No. 62. After the washing, the glass pieces are air-dried at room temperature for 1 hour and then weighed. This value is defined as the weight (cg) after the washing and drying. Detergency is JIS
Unlike the detergency evaluation defined in K 3362, the determination was made using the equation (1) based on the change in weight obtained using these values.
【0024】一方、アルカリ性緩衝液は次の方法により
調整する。On the other hand, the alkaline buffer is prepared by the following method.
【0025】たとえば、一般に重曹として市販されてい
る炭酸水素ナトリウムと水酸化ナトリウムとを混合す
る。具体的に実例を示すと、0.05mol/lの炭酸
水素ナトリウム溶液50mlに0.1mol/lの水酸
化ナトリウム溶液17.8mlを加え水で薄めて100
mlとする。簡便には、0.05モル(0.48g)の
重曹と0.037モル(0.15g)の水酸化ナトリウ
ムとを1000mlの水に溶解・混合し、pH10.5
のアルカリ性緩衝液を得る。For example, sodium hydrogen carbonate and sodium hydroxide, which are generally sold as baking soda, are mixed. To give a concrete example, 17.8 ml of a 0.1 mol / l sodium hydroxide solution was added to 50 ml of a 0.05 mol / l sodium hydrogen carbonate solution, diluted with water and diluted with 100 ml.
ml. For convenience, 0.05 mol (0.48 g) of sodium bicarbonate and 0.037 mol (0.15 g) of sodium hydroxide are dissolved and mixed in 1000 ml of water, and the pH is adjusted to 10.5.
To obtain an alkaline buffer solution.
【0026】これを用いて、図1に示すリーナツ型洗浄
試験槽に投入し、被洗浄物を設置して洗浄力試験を実施
した。洗浄率をそれぞれに試験片に対して計算し、他の
試験片との間で比較できる数値を算出した。Using this, it was put into a lnut-type cleaning test tank shown in FIG. 1 and an object to be cleaned was installed to perform a cleaning power test. The cleaning rate was calculated for each test piece, and a value that can be compared with other test pieces was calculated.
【0027】 洗浄率(%)=(b−c)/(b−a)×100 (1)式 洗浄率は、同時に洗浄槽内に設置し洗浄試験に供した3
サンプルの平均洗浄度で評価する。その結果を表1に示
す。Cleaning rate (%) = (bc) / (ba) × 100 Formula (1) The cleaning rate was simultaneously set in a cleaning tank and subjected to a cleaning test.
Evaluate the average degree of washing of the sample. Table 1 shows the results.
【0028】[0028]
【表1】 [Table 1]
【0029】<実施例2>一方、pH10.6のアルカ
リ性緩衝液は次の方法によって調整できる。たとえば、
一般に4ホウ酸ナトリウム(ホウ砂)と水酸化ナトリウ
ムとを混合する。具体的に実例を示すと、0.025m
ol/lの溶液50mlに、0.1mol/lの水酸化
ナトリウム溶液23.3mlを加え水で薄めて100m
lとする。Example 2 On the other hand, an alkaline buffer having a pH of 10.6 can be adjusted by the following method. For example,
Generally, sodium tetraborate (borax) and sodium hydroxide are mixed. To show a concrete example, 0.025m
ol / l solution (50 ml), 0.1 mol / l sodium hydroxide solution (23.3 ml) was added and diluted with water to 100 m
l.
【0030】この割合で作製したアルカリ性緩衝水を、
実施例1で用いた緩衝液の代わりに用いるだけで、被洗
浄物の作製方法も含めて、他は実施例1と同様に洗浄試
験を実施した。その結果を表1に示す。The alkaline buffer water prepared at this ratio is
A washing test was carried out in the same manner as in Example 1, except for the method of preparing an object to be washed, except that the buffer was used in place of the buffer used in Example 1. Table 1 shows the results.
【0031】<実施例3>一方、pH8.0の弱アルカ
リ性緩衝液は次の方法によって調整できる。Example 3 On the other hand, a weak alkaline buffer having a pH of 8.0 can be adjusted by the following method.
【0032】たとえば、一般にリン酸水素カリウムKH
2PO3と水酸化ナトリウムとを混合する。具体的に実例
を示すと、0.1mol/lの炭酸水素ナトリウム溶液
50mlに、0.1mol/lの水酸化ナトリウム溶液
46.1mlを加え水で薄めて100mlとする。For example, generally, potassium hydrogen phosphate KH
2 Mix PO 3 and sodium hydroxide. More specifically, 46.1 ml of a 0.1 mol / l sodium hydroxide solution is added to 50 ml of a 0.1 mol / l sodium bicarbonate solution, and diluted with water to 100 ml.
【0033】このようにして得たアルカリ性緩衝液を、
実施例1で用いた緩衝液の代わりに用いるだけで、被洗
浄物の作製方法も含めて、他は実施例1と同様に洗浄試
験を実施した。その結果を表1に示す。The alkaline buffer thus obtained is
A washing test was carried out in the same manner as in Example 1, except for the method of preparing an object to be washed, except that the buffer was used in place of the buffer used in Example 1. Table 1 shows the results.
【0034】<比較例1>図2に示す市販のイオン水生
成器で電解によって作ったアルカリイオン水による洗浄
の場合を詳述する。<Comparative Example 1> The case of washing with alkaline ionized water produced by electrolysis using a commercially available ionized water generator shown in FIG. 2 will be described in detail.
【0035】アルカリイオン水生成器として、コロナ社
製アルカリイオン水生成器CI−2000を用いた。水
道水(pH6.8)の蛇口に接続し、生成器の内部タン
クにて電気分解を応用したイオン分離を行う。通電時間
は1分で生成したアルカリ水のpHは9.5であった。
このようにして得たアルカリイオン水を、実施例1で用
いた緩衝液の代わりに用いるだけで、被洗浄物の作製方
法も含めて、他は実施例1と同様に洗浄試験を実施し
た。その結果を表1に示す。An alkaline ionized water generator CI-2000 manufactured by Corona was used as the alkaline ionized water generator. It is connected to a tap of tap water (pH 6.8), and performs ion separation applying electrolysis in the internal tank of the generator. The energization time was 1 minute, and the pH of the generated alkaline water was 9.5.
A washing test was carried out in the same manner as in Example 1, except for the method of preparing the object to be washed, except that the alkaline ionized water thus obtained was used instead of the buffer used in Example 1. Table 1 shows the results.
【0036】<比較例2>実施例1で用いた緩衝液の代
わりにイオン交換水を用いるだけで、被洗浄物の作製方
法も含めて、他は同様に洗浄試験を実施した。その結果
を表1に示す。<Comparative Example 2> A washing test was carried out in the same manner as in Example 1, except that ion-exchanged water was used instead of the buffer solution. Table 1 shows the results.
【0037】以上の結果より、実施例1の洗浄方法は、
比較例1及び比較例2の洗浄率と比較して、汚染物の除
去の点で優れていることがわかった。From the above results, the cleaning method of Example 1 was
Compared with the cleaning rates of Comparative Example 1 and Comparative Example 2, it was found that the cleaning rate was superior in removing contaminants.
【0038】<実施例4>4ホウ酸ナトリウム10g
(市販のpH標準液用粉末)を500mlのイオン交換
水に溶かし、洗浄試験用洗浄液を作成した。この時の洗
浄液のpHは9.22(20℃)であった。洗浄試験に
ついては実施例1で用いた緩衝液の代わりに用いるだけ
で、被洗浄物の作製方法も含めて、他は実施例1と同様
に洗浄試験を実施した。その結果を表1に示す。Example 4 10 g of sodium 4-borate
(Powder for a commercially available pH standard solution) was dissolved in 500 ml of ion-exchanged water to prepare a cleaning solution for a cleaning test. At this time, the pH of the cleaning solution was 9.22 (20 ° C.). The washing test was carried out in the same manner as in Example 1 except that the buffer used in Example 1 was used in place of the buffer used in Example 1, except for the method of preparing the object to be washed. Table 1 shows the results.
【0039】実施例1と同様に実施例2の洗浄方法によ
れば、比較例1及び比較例2の洗浄率と比較して、汚染
物の除去の点で優れていることがわかった。According to the cleaning method of Example 2 as in Example 1, it was found that the cleaning rate of Comparative Example 1 and Comparative Example 2 was excellent in removing contaminants.
【0040】また、市販の緩衝錠剤を用いることなく、
緩衝錠剤から自作する場合は、実施例1記載の薬品を所
定の混合比にて、乳鉢やすり鉢にて充分混合し、必要量
を分取して使用することにより可能となる。Further, without using a commercially available buffer tablet,
In the case of self-manufacturing from a buffer tablet, the medicine described in Example 1 can be sufficiently mixed at a predetermined mixing ratio in a mortar or mortar, and a necessary amount thereof is fractionated and used.
【0041】<実施例5>再付着防止剤を実施例1で用
いたアルカリ性緩衝液に添加した場合について詳述す
る。<Example 5> The case where the anti-redeposition agent was added to the alkaline buffer used in Example 1 will be described in detail.
【0042】カルボキシメチルセルロース(CMC)を
10mg量り取り、実施例1で用いたアルカリ性緩衝液
500mlに添加して洗浄液とする以外は、被洗浄物の
作製方法も含めて、他は実施例1と同様に洗浄試験を実
施した。その結果を表2に示す。The same procedures as in Example 1 were carried out, except for the method of preparing the object to be cleaned, except that 10 mg of carboxymethylcellulose (CMC) was weighed and added to 500 ml of the alkaline buffer used in Example 1 to prepare a cleaning solution. A cleaning test was performed. Table 2 shows the results.
【0043】<比較例3>カルボキシメチルセルロース
(CMC)を10mg量り取り、比較例1で用いたアル
カリイオン水500mlに添加して洗浄液とする以外
は、被洗浄物の作製方法も含めて、他は実施例1と同様
に洗浄試験を実施した。その結果を表2に示す。<Comparative Example 3> Except for the preparation method of the object to be cleaned, except that 10 mg of carboxymethylcellulose (CMC) was weighed and added to 500 ml of the alkaline ionized water used in Comparative Example 1 to prepare a cleaning solution. A cleaning test was performed in the same manner as in Example 1. Table 2 shows the results.
【0044】<比較例4>カルボキシメチルセルロース
(CMC)を10mg量り取り、比較例2で用いたイオ
ン交換水500mlに添加して洗浄液とする以外は、被
洗浄物の作製方法も含めて、他は実施例1と同様に洗浄
試験を実施した。その結果を表2に示す。<Comparative Example 4> Except for weighing 10 mg of carboxymethylcellulose (CMC) and adding it to 500 ml of the ion-exchanged water used in Comparative Example 2 to prepare a washing liquid, the method of preparing an object to be washed was the same. A cleaning test was performed in the same manner as in Example 1. Table 2 shows the results.
【0045】再付着防止剤を添加することにより、洗浄
率の向上は見られるが、実施例5の洗浄方法が比較例3
及び比較例4の洗浄率と比較して、汚染物の除去の点で
優れていることがわかった。Although the cleaning rate is improved by adding the anti-redeposition agent, the cleaning method of Example 5 is applied to Comparative Example 3
And it was found that the cleaning rate of Comparative Example 4 was excellent in removing contaminants.
【0046】[0046]
【表2】 [Table 2]
【0047】[0047]
【発明の効果】電解槽が不用であるため、電気工事とい
った設置のための面倒な作業が不用となる。一般家庭で
も容易に混合によって緩衝液を形成でき、これを利用す
ることにより、より効率的な洗浄が可能となる。Since the electrolytic cell is unnecessary, troublesome installation work such as electric work is not required. Even in ordinary households, a buffer solution can be easily formed by mixing, and by using this, more efficient washing can be performed.
【図1】本発明の洗浄試験に用いる洗浄試験テスト冶具
を示す概念図である。FIG. 1 is a conceptual diagram showing a cleaning test test jig used for a cleaning test of the present invention.
【図2】本発明の比較例に用いるアルカリイオン水を生
成させる装置の概念図である。FIG. 2 is a conceptual diagram of an apparatus for generating alkaline ionized water used in a comparative example of the present invention.
1 ビーカー 2 洗浄液 3 試料固定具 4 被洗浄物 5 汚染部分 6 攪拌翼 6’ 攪拌モーター 7 水槽 8 電解質を含む溶液 9 陽極 10 陰極 11 陽イオン透過膜 12 排出口 DESCRIPTION OF SYMBOLS 1 Beaker 2 Cleaning liquid 3 Sample fixture 4 Object to be cleaned 5 Contaminated part 6 Stirring blade 6 'Stirring motor 7 Water tank 8 Solution containing electrolyte 9 Anode 10 Cathode 11 Cation permeable membrane 12 Discharge port
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C11D 7/26 C11D 7/26 (72)発明者 榎本 和弘 大阪府大阪市阿倍野区長池町22番22号 シ ャープ株式会社内 (72)発明者 隅田 憲武 大阪府大阪市阿倍野区長池町22番22号 シ ャープ株式会社内 Fターム(参考) 3B201 BB92 BB96 CC21 4H003 BA12 DA15 DA17 EA16 EA18 EA21 ED02 FA01 FA03 FA06──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI theme coat ゛ (Reference) C11D 7/26 C11D 7/26 (72) Inventor Kazuhiro Enomoto 22-22 Nagaikecho, Abeno-ku, Osaka-shi, Osaka (72) Inventor Noritake Sumida 22-22 Nagaikecho, Abeno-ku, Osaka City, Osaka Prefecture F-term (reference) 3B201 BB92 BB96 CC21 4H003 BA12 DA15 DA17 EA16 EA18 EA21 ED02 FA01 FA03 FA06
Claims (5)
ることを特徴とする洗浄方法。1. A cleaning method, comprising washing an object to be washed with an alkaline buffer.
を含有する弱酸の塩を含むことを特徴とする請求項1に
記載の洗浄方法。2. The method according to claim 1, wherein the alkaline buffer contains a salt of a weak acid containing an alkali metal.
れかからなることを特徴とする請求項2に記載の洗浄方
法。3. The cleaning method according to claim 2, wherein the weak acid comprises one of carbonic acid, phosphoric acid, and boric acid.
カリウム、炭酸水素ナトリウム、炭酸水素カリウム、四
ホウ酸ナトリウムの単独若しくはこれらの複合体を用い
ることを特徴とする請求項2又は3に記載の洗浄方法。4. The salt according to claim 2, wherein the salt of the weak acid is sodium carbonate, potassium carbonate, sodium hydrogencarbonate, potassium hydrogencarbonate, sodium tetraborate alone or a complex thereof. Cleaning method.
あらかじめ添加していることを特徴とする請求項1乃至
4のいずれかに記載の洗浄方法。5. The cleaning method according to claim 1, wherein an anti-redeposition agent is added to the alkaline buffer in advance.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000065917A JP2001252630A (en) | 2000-03-10 | 2000-03-10 | Cleaning method |
PCT/JP2001/001664 WO2001066682A1 (en) | 2000-03-10 | 2001-03-02 | Cleaning solution, and method and apparatus for cleaning using the same |
US10/221,224 US7015184B2 (en) | 2000-03-10 | 2001-03-02 | Cleaning solution, and method and apparatus for cleaning using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000065917A JP2001252630A (en) | 2000-03-10 | 2000-03-10 | Cleaning method |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2001252630A true JP2001252630A (en) | 2001-09-18 |
Family
ID=18585365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000065917A Pending JP2001252630A (en) | 2000-03-10 | 2000-03-10 | Cleaning method |
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Country | Link |
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JP (1) | JP2001252630A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004286797A (en) * | 2003-03-19 | 2004-10-14 | Fuji Xerox Co Ltd | Method for washing electrophotographic member |
WO2011107561A1 (en) * | 2010-03-04 | 2011-09-09 | Industrie De Nora S.P.A. | Electrochlorination method for above-ground swimming pools |
JP2012094852A (en) * | 2010-10-01 | 2012-05-17 | Mitsubishi Chemicals Corp | Substrate cleaning liquid and cleaning method for semiconductor device |
-
2000
- 2000-03-10 JP JP2000065917A patent/JP2001252630A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004286797A (en) * | 2003-03-19 | 2004-10-14 | Fuji Xerox Co Ltd | Method for washing electrophotographic member |
WO2011107561A1 (en) * | 2010-03-04 | 2011-09-09 | Industrie De Nora S.P.A. | Electrochlorination method for above-ground swimming pools |
JP2012094852A (en) * | 2010-10-01 | 2012-05-17 | Mitsubishi Chemicals Corp | Substrate cleaning liquid and cleaning method for semiconductor device |
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