JPH01229100A - Detergent composition - Google Patents
Detergent compositionInfo
- Publication number
- JPH01229100A JPH01229100A JP5493088A JP5493088A JPH01229100A JP H01229100 A JPH01229100 A JP H01229100A JP 5493088 A JP5493088 A JP 5493088A JP 5493088 A JP5493088 A JP 5493088A JP H01229100 A JPH01229100 A JP H01229100A
- Authority
- JP
- Japan
- Prior art keywords
- water
- weight
- alkanesulfonate
- parts
- sodium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003599 detergent Substances 0.000 title claims abstract description 17
- 239000000203 mixture Substances 0.000 title claims abstract description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 14
- 238000002156 mixing Methods 0.000 claims abstract description 10
- 229920005989 resin Polymers 0.000 claims abstract description 10
- 239000011347 resin Substances 0.000 claims abstract description 10
- 239000000843 powder Substances 0.000 claims description 15
- 239000008187 granular material Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 24
- -1 alkane sulfonate Chemical class 0.000 abstract description 15
- 230000005484 gravity Effects 0.000 abstract description 6
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 abstract description 4
- 238000000227 grinding Methods 0.000 abstract description 2
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- 239000004744 fabric Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 9
- 238000004140 cleaning Methods 0.000 description 7
- 238000003756 stirring Methods 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 239000003513 alkali Substances 0.000 description 4
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229910002012 Aerosil® Inorganic materials 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 108010010803 Gelatin Proteins 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
- 239000004372 Polyvinyl alcohol Substances 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
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 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
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229940045872 sodium percarbonate Drugs 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical compound C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 0.000 description 1
- HIJFENKJMYXCST-IHWYPQMZSA-N (z)-4-acetyloxy-4-oxobut-2-enoic acid Chemical compound CC(=O)OC(=O)\C=C/C(O)=O HIJFENKJMYXCST-IHWYPQMZSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920000858 Cyclodextrin Polymers 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
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GEHGBIHYCUWRPO-UHFFFAOYSA-M [Na+].[Cl-].OO Chemical compound [Na+].[Cl-].OO GEHGBIHYCUWRPO-UHFFFAOYSA-M 0.000 description 1
- HJGMKWIPJMNGKW-UHFFFAOYSA-L [Na+].[Na+].OO.[O-]S([O-])(=O)=O Chemical compound [Na+].[Na+].OO.[O-]S([O-])(=O)=O HJGMKWIPJMNGKW-UHFFFAOYSA-L 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000012851 eutrophication Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical class OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 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
- 239000002689 soil Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229940117986 sulfobetaine Drugs 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、界面活性剤としてアルカンスルホン酸塩を含
む、流動性を有する粒状又は粉末状の洗剤組成物に関す
る。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a fluid granular or powder detergent composition containing an alkanesulfonate as a surfactant.
[従来の技術〕
アルカンスルホン酸塩は、アルキルベンゼンスルホン酸
塩やα−オレフィンスルホン酸塩に比べて、優れた洗浄
力を有するにもかかわらず、粉末洗剤としてはほとんど
使用されておらず、もっばら液状或いはフレーク状で用
いられている。これは、アルカンスルホン酸塩が、粉末
にすると粘着性の塊を形成し、粉末洗剤として要求され
る流動性の良い乾燥粉末が得られないことに起因してい
る。[Prior Art] Although alkanesulfonates have superior detergency compared to alkylbenzene sulfonates and α-olefin sulfonates, they are rarely used as powder detergents and are widely used. It is used in liquid or flake form. This is because the alkanesulfonate forms a sticky lump when powdered, making it impossible to obtain a dry powder with good fluidity required for a powder detergent.
このため、アルカンスルホン酸塩に珪酸アルカリ及び燐
酸アルカリを配合して粉末化する方法が提案されている
(特開昭50−155506号公報)。For this reason, a method has been proposed in which an alkanesulfonate is blended with an alkali silicate and an alkali phosphate to form a powder (Japanese Unexamined Patent Publication No. 155506/1983).
し発明が解決しようとする問題点]
上記珪酸アルカリ及び燐酸アルカリを配合して粉末化す
る方法は、アルカンスルホン酸塩5〜35重量部に対し
て珪酸アルカリを2〜10重量部、燐酸アルカリを5〜
75重量部配置部せる必要があり、大量の水離溶性の無
機物を含むため、アルカンスルホン酸塩の溶解性が多少
落ちるとともに、水1!溶性の無機物及びリンの大量配
合は、河川、湖沼等の汚濁、富栄養化などの公害上から
の問題と、保存安定性の優れた弱アルカリ性洗剤ができ
にくいという問題とがあった。また、珪酸アルカリや燐
酸アルカリは比較的価格が高く、洗剤の製造コストを押
し上げる要因ともなっていた。[Problems to be Solved by the Invention] The method of blending and powdering the alkali silicate and alkali phosphate is as follows: 2 to 10 parts by weight of the alkali silicate and the alkali phosphate to 5 to 35 parts by weight of the alkanesulfonate. 5~
Since it contains a large amount of water-dissolvable inorganic substances, the solubility of the alkanesulfonate is somewhat reduced, and the amount of water is 1! The combination of large amounts of soluble inorganic substances and phosphorus poses problems in terms of pollution such as contamination of rivers, lakes, and marshes, eutrophication, and the problem that it is difficult to produce weakly alkaline detergents with excellent storage stability. Furthermore, alkali silicates and alkali phosphates are relatively expensive, which is a factor that increases the manufacturing cost of detergents.
本発明は、かかる問題点を解決しようとするもので、本
発明の目的は、水不溶性の無機物を極めて僅かしか配合
せず、アルカンスルホン酸塩の水への溶解度が高く、公
害上の問題を低下させ、しかも、比較的安価に粒状又は
粉末化したアルカンスルホン酸塩含有洗剤組成物を提供
することにある。The present invention is intended to solve such problems, and an object of the present invention is to incorporate only a very small amount of water-insoluble inorganic substances, to increase the solubility of alkanesulfonate in water, and to avoid pollution problems. It is an object of the present invention to provide a detergent composition containing an alkanesulfonate which is granular or powdered and which reduces the amount of alcohol used.
[問題点を解決するための手段]
本発明は、アルカンスルホン酸塩100重量部に対し、
微粉末シリカを0.5〜15重量部、さらにこれに所望
により吸水性樹脂を0.1〜10重量部配合して粒状又
は粉末化したことから成るものである。[Means for solving the problems] The present invention provides that, for 100 parts by weight of alkanesulfonate,
It consists of 0.5 to 15 parts by weight of finely powdered silica, and further 0.1 to 10 parts by weight of a water-absorbing resin, if desired, and granulated or powdered.
本発明においてアルカンスルホン酸塩は、水分を少なく
とも50%以下、特には10〜30%含むものが好まし
い。水分を多量に含む場合は、そのままでは粉末化が困
難であったり、又は吸水性樹脂を多量に必要とし経済的
でない。In the present invention, the alkanesulfonate preferably contains at least 50% water, particularly 10 to 30% water. If it contains a large amount of water, it may be difficult to powder it as it is, or it may require a large amount of water-absorbing resin, which is not economical.
従って、水分の多いアルカンスルホン酸塩を用いる場合
は、あらかじめ脱水して水分を減らしておくことが良い
、又、水分が10%以下になると微粉末シリカ等、他の
配合剤の分散、混合が悪くなり、また水への溶解性も低
下するのであまり好ましくない。Therefore, when using an alkanesulfonate with a high water content, it is better to dehydrate it in advance to reduce the water content.Also, if the water content is less than 10%, dispersion and mixing of other ingredients such as finely powdered silica will be difficult. This is not very preferable since it deteriorates and the solubility in water also decreases.
アルカンスルホン酸塩は、一般にはオキシスルホネーシ
ョン又はクロルスルホネーション等の方法で製造される
が、これらのいずれの方法で製造されたものを用いても
何ら支障はないが、特には、アルキル基が直鎖で炭素数
15以上のものを40%以上含み、又、モノスルホネー
トが80%以上含むものが、洗浄性及び水溶解性の面で
好ましい。Alkanesulfonates are generally produced by methods such as oxysulfonation or chlorosulfonation, and there is no problem in using products produced by either of these methods, but in particular, alkanesulfonates with an alkyl group Those containing 40% or more of straight chain carbon atoms with 15 or more carbon atoms and 80% or more of monosulfonate are preferred in terms of detergency and water solubility.
本発明では、このアルカンスルホン酸塩100重量部に
対し微粉末シリカを0.5〜15重量部配置部るもので
あるが、微粉末シリカの配合が0.5重量部以下の場合
は、アルカンスルホン酸塩の粘着性が改善されず、粒状
又は粉状化しても流動性が得られない。又、微粉末シリ
カの配合量は、多くすればするほど、乾燥性のある流動
性に優れた粒状又は粉状の洗剤組成物が得られるが、配
合量が、アルカンスルホン酸塩100重量部に対し15
重量部を越えると配合量の増加の割合に比し、効果の顕
著な向上は認められず、又、公害上の見地等から望まし
いものではない。In the present invention, 0.5 to 15 parts by weight of finely powdered silica is arranged with respect to 100 parts by weight of this alkanesulfonate. However, if the amount of finely powdered silica is 0.5 parts by weight or less, The tackiness of the sulfonate is not improved, and fluidity cannot be obtained even if it is granulated or powdered. In addition, the larger the amount of finely powdered silica is, the more a granular or powdery detergent composition with excellent drying properties and fluidity can be obtained. Against 15
If the amount exceeds 1 part by weight, no significant improvement in effectiveness will be observed compared to the proportion of increase in the amount blended, and this is not desirable from the standpoint of pollution.
本発明に云う微粉末シリカは平均粒径が5μ以下で嵩比
重が0.05〜0.2のものであり、アエロジル200
(日本アエロジル社製)、レオロシールQS−102(
徳山曹達社11.) 、カープレックスFPS−1、F
PS−3、FPS−4(ジオツギ製薬社製)、ニップシ
ールNS・T(日本シリカニ業社製)等の商品名により
市販されているものを用いることができる。これらの微
粉末シリカは、水不溶性ではあるが、水分散性に優れて
おり、洗濯の際に繊維に残ることはほとんどない。The fine powder silica referred to in the present invention has an average particle size of 5 μm or less and a bulk specific gravity of 0.05 to 0.2, and Aerosil 200
(manufactured by Nippon Aerosil Co., Ltd.), Rheosil QS-102 (
Tokuyama Sodasha 11. ), Carplex FPS-1, F
Those commercially available under trade names such as PS-3, FPS-4 (manufactured by Geotsugi Pharmaceutical Co., Ltd.), and Nip Seal NS-T (manufactured by Nippon Silikani Gyo Co., Ltd.) can be used. Although these finely powdered silicas are water-insoluble, they have excellent water dispersibility and hardly remain on fibers during washing.
また、本発明においては、所望により吸水性の樹脂を配
合する。この吸水性樹脂は、アルカンスルホン酸塩中の
水分の含量が多い場合に配合すると特に効果がある。こ
の吸水性樹脂の配合は、アルカンスルホン酸塩中の水分
の量にもよるが、水分が10〜50重量%含有する場合
は、アルカンスルホン酸塩100重量部に対し0.1〜
5重量部の範囲で適宜調整する。Further, in the present invention, a water-absorbing resin is blended if desired. This water-absorbing resin is particularly effective when added when the alkanesulfonate has a high water content. The composition of this water-absorbing resin depends on the amount of water in the alkanesulfonate, but if the water content is 10 to 50% by weight, the content is 0.1 to 0.1 to 100 parts by weight per 100 parts by weight of the alkanesulfonate.
Adjust as appropriate within the range of 5 parts by weight.
勿論、必ずしも配合しなければならないものではない、
この吸水性樹脂としては、フィルム形成能を有し、水不
溶性でないものが好ましく、ポリアクリル酸、ポリマレ
イン酸、カルボキシメチルセルロース、アルギン酸、ビ
ニールメチルエーテルと無水マレイン酸のコポリマー、
ポリビニールピロリドン、酢酸−無水マレイン酸のコポ
リマー、ジアセトンアクリルアミドとアクリル酸のコポ
リマー、ウレタン化ポリビニールアルコール、ポリビニ
ールアミド、シクロデキストリン、セルロースグラフト
化ポリアクリル酸アマイド、ゼラチングラフト化ポリア
クリル酸アマイド、ウレタン化変性シクロデキストリン
、ポリビニールブチラール、及びこわらの塩等を用いる
ことが・できるが、特には、ポリアクリル酸ソーダ、ポ
リマレイン酸ソーダ、カルボキシメチルセルロースナト
リウム塩、アルギン酸ナトリウム等を用いることが好ま
しい。Of course, it is not necessarily necessary to combine them.
The water-absorbing resin preferably has a film-forming ability and is not water-insoluble, such as polyacrylic acid, polymaleic acid, carboxymethyl cellulose, alginic acid, a copolymer of vinyl methyl ether and maleic anhydride,
Polyvinyl pyrrolidone, copolymer of acetic acid-maleic anhydride, copolymer of diacetone acrylamide and acrylic acid, urethanized polyvinyl alcohol, polyvinylamide, cyclodextrin, cellulose grafted polyacrylamide, gelatin grafted polyacrylamide, Urethane-modified cyclodextrin, polyvinyl butyral, Kowara's salt, etc. can be used, but it is particularly preferable to use sodium polyacrylate, sodium polymaleate, sodium carboxymethylcellulose, sodium alginate, etc.
尚、本発明においては、上記成分以外にも、アルキルベ
ンゼンスルホン酸塩、α−オレフィンスルフォン酸塩、
アルキル又はアルケニル硫酸塩、エーテル硫酸塩、脂肪
酸塩、エーテルカルボン酸塩、α−スルホ脂肪酸塩又は
そのエステル、カルボキシ又はスルホベタイン型界面活
性剤、ポリオキシアルキレンアルキル又はアルケニルエ
ーテル、ポリオキシエチレンアルキルフェニルエーテル
等の陰イオン性、両性又は非イオン性の界面活性剤や、
リン酸塩、ポリリン酸塩、ホスホノカルボン酸塩、アミ
ノ酸塩、アミノポリ酢酸塩等の二価金属イオン捕捉剤や
、珪酸ソーダ、硫酸ソーダ等のアルカリ剤や、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、カルボキシメチルセルロース等の再汚染防止
剤や、過炭酸ソーダ、過炭酸ソーダ、硫酸ナトリウム過
酸化水素付加体、塩化ナトリウム過酸化水素付加体等の
漂白剤や、螢光塗料や、香料や、酵素等を配合しても良
いことは云うまでもない。この場合、アルカンスルホン
酸塩の配合は15重量%以上とすることが好ましい。1
5重量%未満であれば、アルカンスルホン酸塩を配合す
ることにより生じる良好な洗浄効果を得ることが困難と
なるためである。In addition, in the present invention, in addition to the above components, alkylbenzene sulfonate, α-olefin sulfonate,
Alkyl or alkenyl sulfate, ether sulfate, fatty acid salt, ether carboxylate, α-sulfo fatty acid salt or its ester, carboxy or sulfobetaine type surfactant, polyoxyalkylene alkyl or alkenyl ether, polyoxyethylene alkylphenyl ether Anionic, amphoteric or nonionic surfactants such as
Divalent metal ion scavengers such as phosphates, polyphosphates, phosphonocarboxylates, amino acid salts, and aminopolyacetates, alkaline agents such as sodium silicate and sodium sulfate, polyethylene glycol, polyvinyl alcohol, polyvinylpyrrolidone, Do not use recontamination preventive agents such as carboxymethyl cellulose, bleaching agents such as sodium percarbonate, sodium percarbonate, sodium sulfate hydrogen peroxide adduct, sodium chloride hydrogen peroxide adduct, fluorescent paints, fragrances, enzymes, etc. Needless to say, they may be combined. In this case, the content of alkanesulfonate is preferably 15% by weight or more. 1
This is because if the amount is less than 5% by weight, it will be difficult to obtain a good cleaning effect produced by incorporating the alkanesulfonate.
このようしこ配合された組成物は、良く混合した後に粒
状又は粉状化するが、アルカンスルホン酸塩と微粉末シ
リカ及び所望により配合される吸水性樹脂を配合、混合
した後に粒状又は粉状化し、他のものは、別途配合混合
して、粒状、粉状化した後で配合する方法でも、最初か
ら全ての配合剤を混合して1粒状、粉状化する方法のい
ずれで行なっても良いことは云うまでもない。A composition blended in this way is granulated or powdered after being thoroughly mixed, but after blending and mixing the alkanesulfonate, finely powdered silica, and a water-absorbing resin that is optionally blended, it is granulated or powdered. For other ingredients, it can be done either by mixing them separately and blending them into granules or powders, or by mixing all the ingredients from the beginning and making them into granules or powders. Needless to say, it's a good thing.
粒状、又は粉状化は、一般に知られている方法、例えば
転動造粒機、押出造粒機、ハンマーミル、■−ブレンダ
ー、リボンミキサー、凍結解凍粉砕機等を用いて造粒、
解砕等により容易に行なうことができる。Granulation or pulverization is carried out by generally known methods, such as granulation using a rolling granulator, extrusion granulator, hammer mill, ■-blender, ribbon mixer, freeze-thaw pulverizer, etc.
This can be easily done by crushing or the like.
[実施例コ
第1表に記載した配合組成の粒状の洗剤組成物を次の方
法で製造した。[Example 2] A granular detergent composition having the formulation shown in Table 1 was produced by the following method.
5AS−60とポリアクリル酸ソーダとアエロジル20
0を■−ブレンダーに入れ、回転数30Orpmで高速
回転させ、次に、硫酸ソーダの全使用量の半分をAEと
共に上から一定量で10分間散布し、撹拌をしながら、
さらに残りの成分を順次配合していった。5AS-60, sodium polyacrylate and Aerosil 20
0 into a blender, rotate at a high speed of 30 rpm, then sprinkle half of the total amount of sodium sulfate together with AE from above at a constant rate for 10 minutes, while stirring.
The remaining ingredients were then sequentially added.
その後、粒径が1 m = 0 、1 unのふるいに
かけて粒度を調整し、見掛は比重0.75の粉末製品を
得た。Thereafter, the particle size was adjusted by passing through a sieve with a particle size of 1 m = 0 and 1 un, to obtain a powder product with an apparent specific gravity of 0.75.
なお、見掛は比重を大きくしたい場合は、さらに撹拌を
続行すればよいことが分かった。In addition, it was found that if it is desired to increase the apparent specific gravity, stirring may be continued further.
JIS−に−3362に規定した方法により確認だ結果
、P)Iは1%濃度で10.3、みがけ比重は0.75
、有効成分は27%であった。Confirmed using the method specified in JIS-3362, the P)I is 10.3 at 1% concentration and the polished specific gravity is 0.75.
, the active ingredient was 27%.
EO二9)
尚、アルカンスルホン酸塩は、炭素数15のものが50
%、モノスルホン酸ソーダが90%のもので、60重量
%の水溶液のものを用い、微粉末シリカとしては、市販
のアエロジル200(粒径0.5μ嵩比重0.05:日
本アエロジル社製)を、又吸水性樹脂としてポリアクリ
ル酸ソーダ(平均分子量6000)をそれぞれ用いた。EO29) In addition, the alkanesulfonate having 15 carbon atoms is 50
%, 90% sodium monosulfonate, 60% by weight aqueous solution was used, and the fine powder silica was commercially available Aerosil 200 (particle size 0.5μ bulk specific gravity 0.05: manufactured by Nippon Aerosil Co., Ltd.) and sodium polyacrylate (average molecular weight 6000) were used as the water-absorbing resin.
得られた粒状物について、目視による流動性及び次に記
載した方法によるアンチケーキングテスト、洗浄力テス
ト及び分散溶解性試験を行なった。これらの結果を第2
表に示した。The resulting granules were subjected to a visual fluidity test, an anti-caking test, a detergency test, and a dispersion solubility test using the methods described below. These results are the second
Shown in the table.
(アンチケーキングテスト法)
100gの秤量びんに、サンプルを充てんし、サンプル
を75℃の相対湿度、35℃の温度での恒温恒湿状態に
て3力月放置した後、かたまり状況を観察し、目視で判
定した0判定基準は、全く問題なしをOlかたまりを生
じたものを△、固結物がかなり多いものを×とした。(Anti-Caking Test Method) Fill a 100g weighing bottle with a sample, leave the sample in a constant temperature and humidity condition at a relative humidity of 75°C and a temperature of 35°C for 3 months, and then observe the clumps. The 0 criteria for visual judgment was as follows: No problem at all, △ when Ol clumps were formed, and × when there was a considerable amount of solidified matter.
(洗浄力テスト法)
T erg−0−T ometerを使用し、150r
pmの回転数で、汚染布10枚、添加布3枚(各布当り
油性汚垢成分60■付着)及び清浄メリヤス布を加えて
、浴比1:30に調整して、洗浄時間10分、洗浄温度
25℃、使用水として純水を用いて、洗浄力テストを行
った。(Cleaning power test method) Using Terg-0-Tometer, 150r
At a rotation speed of pm, add 10 contaminated cloths, 3 additive cloths (60 μm of oily dirt attached to each cloth), and clean knitted cloth, adjust the bath ratio to 1:30, and wash for 10 minutes. A detergency test was conducted at a cleaning temperature of 25° C. and using pure water as the water used.
洗浄率(D)は、次の式を用いて算出した。The cleaning rate (D) was calculated using the following formula.
D=(Rw−Rs/Ro−Rs)X 100 (%)
ここで、Ro:清浄布の反射率
R8:汚染布の洗浄前の反射率
Rす:汚染布の洗浄後の反射率
尚、清浄布の反射率は85%、汚染布の反射率を35%
として評価した。D=(Rw-Rs/Ro-Rs)X 100 (%)
Here, Ro: Reflectance of clean cloth R8: Reflectance of contaminated cloth before cleaning R: Reflectance of contaminated cloth after cleaning Note that the reflectance of clean cloth is 85%, and the reflectance of contaminated cloth is 35%.
It was evaluated as
また、汚染布は、次の方法で作成した。In addition, the contaminated cloth was prepared by the following method.
■標準布として1日本油化学会指定の綿布(たて、よこ
60番手、糸密度たて、よこ39本/asの未漂白布)
を糊抜き、精錬、漂白し105℃で3時間乾燥したもの
を用いた。■As a standard cloth 1 Cotton cloth specified by the Japan Oil Chemists' Society (warp and width 60 count, thread density warp and width 39 threads/as unbleached cloth)
The material was desensitized, refined, bleached, and dried at 105°C for 3 hours.
■カーボンブラックは、圧縮6級カーボンブラックを1
05℃で3時間乾燥したものを用いた。■Carbon black is compressed grade 6 carbon black.
The sample was dried at 05°C for 3 hours.
■泥汚垢成分として、土泥、洪積台地、赤黄色土を水に
懸濁し、74μmのふるいを通過させ、風乾した後、2
00℃で24時間乾燥して微粉砕機で平均1μmまで解
砕して用いた。■ As mud sludge components, mud, diluvial plateau, and red-yellow soil are suspended in water, passed through a 74 μm sieve, and air-dried.
It was dried at 00° C. for 24 hours and crushed to an average size of 1 μm using a pulverizer.
先ず、40℃の水950raQに、たん白質(ゼラチン
)3.5g(乾量基準)を溶解し、カーボンブラック0
.5gを添加して乳化機を用いて分散させる。そこへ、
更に上記泥汚垢成分を15.0gを加えてひきつづき分
散させ、さらにたん白質以外の有機汚垢成分31.5g
を加えて乳化して汚染浴を調製する。First, 3.5 g (dry weight basis) of protein (gelatin) was dissolved in 950 raQ of water at 40°C, and carbon black 0
.. Add 5g and disperse using an emulsifier. There,
Furthermore, 15.0 g of the above mud sludge components were added and continuously dispersed, and further 31.5 g of organic sludge components other than protein were added.
Add and emulsify to prepare a pollution bath.
次に、汚染浴中に、上記標準布の10 cs X20a
lを浸漬し、汚垢分散液が沈殿しないようにかきまぜな
がら、当該布に汚垢を十分付着させた後、この布をゴム
製の2本ロールにて絞った。これを30分〜1時間風乾
して、布の2.0〜2.3倍の水が残っている状態にし
て、汚染布として供した。Next, in the pollution bath, 10 cs X 20a of the above standard cloth
After soaking the cloth and stirring to prevent the dirt dispersion from settling, the cloth was sufficiently covered with dirt, and then the cloth was squeezed using two rubber rolls. This was air-dried for 30 minutes to 1 hour, leaving 2.0 to 2.3 times as much water as the cloth, and used as a contaminated cloth.
(分散溶解性試験法)
全自動洗濯機を用い、洗濯機底部に上記で調整した洗剤
40gを一箇所にまとめて置き、衣料2kgを当該洗剤
の上に乗せ、水道水を毎分8Qの流速で洗剤に直接に水
が当らないようにして、40Qになるまで5分間かけて
ゆっくり注水した。その後撹拌を開始し、撹拌3分後と
5分後に撹拌を止め、排水し3分間脱水後、洗剤の残留
散在を目視で判定した0判定基準は残留がないものを○
、僅かに残留があるものをΔ、残留がかなりあるものを
×とした。(Dispersion solubility test method) Using a fully automatic washing machine, place 40g of the detergent prepared above in one place at the bottom of the washing machine, place 2kg of clothing on top of the detergent, and pour tap water at a flow rate of 8Q/min. I poured water slowly over 5 minutes until the detergent reached 40Q, making sure not to let the water hit the detergent directly. After that, stirring was started, and after 3 minutes and 5 minutes of stirring, the stirring was stopped, the water was drained, and after 3 minutes of dehydration, the presence of residual detergent was visually judged.
, those with a slight amount of residue were rated Δ, and those with a large amount of residue were rated ×.
以上の結果から、アルカンスルホン酸塩に微粉末シリカ
を配合することにより、良好な流動性を有する粒状又は
粉状物を得ることができ、又、これらは、洗浄力1分散
溶解性等に優れていることが分かる。From the above results, by blending finely powdered silica with alkanesulfonate, granules or powders with good fluidity can be obtained, and these have excellent detergency, dispersion solubility, etc. I can see that
[発明の効果]
以上のように本発明は、アルカンスルホン酸塩に微粉末
シリカを配合したことにより、流動性の良い、乾燥粒状
又は粉状とすることができ、洗浄力の優れた、又公害上
の問題の低減された洗浄組成物とすることができる等、
格別な効果を奏するものである。[Effects of the Invention] As described above, the present invention blends alkanesulfonate with finely powdered silica, so that it can be made into a dry granule or powder form with good fluidity, and has excellent detergency. It can be a cleaning composition with reduced pollution problems, etc.
It has a special effect.
Claims (2)
末シリカを0.5〜15重量部配合して粒状又は粉末化
したことからなる洗剤組成物。(1) A detergent composition comprising 0.5 to 15 parts by weight of finely powdered silica mixed with 100 parts by weight of an alkanesulfonate salt and granulated or powdered.
シリカ0.5〜15重量部及び吸水性樹脂0.1〜10
重量部配合して粒状又は粉末化したことからなる洗剤組
成物。(2) 0.5 to 15 parts by weight of fine powder silica and 0.1 to 10 parts by weight of water-absorbing resin per 100 parts by weight of alkanesulfonate
A detergent composition formed by blending parts by weight into granules or powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63054930A JPH0726120B2 (en) | 1988-03-10 | 1988-03-10 | Detergent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63054930A JPH0726120B2 (en) | 1988-03-10 | 1988-03-10 | Detergent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01229100A true JPH01229100A (en) | 1989-09-12 |
JPH0726120B2 JPH0726120B2 (en) | 1995-03-22 |
Family
ID=12984343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63054930A Expired - Lifetime JPH0726120B2 (en) | 1988-03-10 | 1988-03-10 | Detergent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0726120B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998031775A1 (en) * | 1997-01-21 | 1998-07-23 | Clariant Gmbh | Granular secondary alkane sulphonate |
EP0894850A1 (en) * | 1997-08-01 | 1999-02-03 | Martini S.p.A. | Detergent composition and means which comprises it |
EP0863968A4 (en) * | 1995-09-12 | 2000-06-21 | Procter & Gamble | Compositions comprising hydrophilic silica particulates |
KR100346812B1 (en) * | 1999-08-28 | 2002-08-03 | 주식회사 엘지씨아이 | Composition for Tablet Detergent |
-
1988
- 1988-03-10 JP JP63054930A patent/JPH0726120B2/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0863968A4 (en) * | 1995-09-12 | 2000-06-21 | Procter & Gamble | Compositions comprising hydrophilic silica particulates |
WO1998031775A1 (en) * | 1997-01-21 | 1998-07-23 | Clariant Gmbh | Granular secondary alkane sulphonate |
JP2008285683A (en) * | 1997-01-21 | 2008-11-27 | Clariant Produkte (Deutschland) Gmbh | Granular secondary alkane sulfonate |
EP0894850A1 (en) * | 1997-08-01 | 1999-02-03 | Martini S.p.A. | Detergent composition and means which comprises it |
KR100346812B1 (en) * | 1999-08-28 | 2002-08-03 | 주식회사 엘지씨아이 | Composition for Tablet Detergent |
Also Published As
Publication number | Publication date |
---|---|
JPH0726120B2 (en) | 1995-03-22 |
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