JPS5945039B2 - cleaning composition - Google Patents
cleaning compositionInfo
- Publication number
- JPS5945039B2 JPS5945039B2 JP1561378A JP1561378A JPS5945039B2 JP S5945039 B2 JPS5945039 B2 JP S5945039B2 JP 1561378 A JP1561378 A JP 1561378A JP 1561378 A JP1561378 A JP 1561378A JP S5945039 B2 JPS5945039 B2 JP S5945039B2
- Authority
- JP
- Japan
- Prior art keywords
- present
- carbon atoms
- weight
- foaming power
- detergency
- 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
Links
- 239000000203 mixture Substances 0.000 title claims description 14
- 238000004140 cleaning Methods 0.000 title claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 159000000003 magnesium salts Chemical group 0.000 claims description 10
- 239000004711 α-olefin Substances 0.000 claims description 10
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003599 detergent Substances 0.000 description 15
- 238000005187 foaming Methods 0.000 description 14
- -1 alkylbenzene sulfonates Chemical class 0.000 description 8
- 238000000034 method Methods 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 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
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- ZZXDRXVIRVJQBT-UHFFFAOYSA-M Xylenesulfonate Chemical compound CC1=CC=CC(S([O-])(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-M 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 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
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 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
- 235000019794 sodium silicate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- XGMYMWYPSYIPQB-UHFFFAOYSA-J tetrasodium;2-(1,2-dicarboxylatoethoxy)butanedioate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CC(C([O-])=O)OC(C([O-])=O)CC([O-])=O XGMYMWYPSYIPQB-UHFFFAOYSA-J 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229940071104 xylenesulfonate Drugs 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Description
【発明の詳細な説明】
本発明は洗浄剤組成物、さらに詳しくは洗浄力、起泡力
などの性能の優れた洗浄剤組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a detergent composition, and more particularly to a detergent composition with excellent performance such as detergency and foaming power.
従来から使用されている界面活性剤で最も一般的なもの
としては、アルキルベンゼンスルホン酸塩がある。The most common conventionally used surfactants are alkylbenzene sulfonates.
しかしアルキルベンゼンスルホン酸塩は、台所用洗剤に
使用した場合、洗浄力、泡立ちなどがかなり劣るという
欠点があり、衣類用洗剤に使用した場合、洗浄力が水の
硬度に大きく影響され、縮合リン酸塩を多量配合しなけ
ればならないという欠点があつた。また近年、環境保全
に関連して、生分解性が問題にされるようになつてきた
が、ベンゼン環を有しているアルキルペンチッスルホン
酸塩は、生分解性の点からも満足できるものではなかつ
た。本発明者らは、上記の、従来の洗剤の欠点を克服し
、時代の要望に沿つた洗浄剤を開発するため鋭意研究を
重ねた結果、生分解性が優れているα−オレフィンスル
ホン酸(AOS)と第二級アルカンスルホン酸塩(SA
S)とを特定比率で配合し、これらのアニオン界面活性
剤の一定割合以上をマグネシウム塩とした場合、洗浄剤
組成物の洗浄性能が相乗効果的に向上することを見出し
、本発明を完成するに至つた。However, when alkylbenzene sulfonates are used in kitchen detergents, they have the disadvantage of considerably inferior detergency and foaming, and when used in clothing detergents, the detergency is greatly affected by the hardness of the water, and condensed phosphoric acid The drawback was that a large amount of salt had to be added. In addition, in recent years, biodegradability has become an issue in connection with environmental conservation, but alkylpentylsulfonates that have a benzene ring are also satisfactory in terms of biodegradability. It wasn't. The inventors of the present invention have conducted extensive research to overcome the drawbacks of conventional detergents and develop detergents that meet the needs of the times. AOS) and secondary alkanesulfonate (SA
The present invention has been completed based on the discovery that the cleaning performance of the cleaning composition is synergistically improved when magnesium salt is added to S) in a specific ratio and a certain proportion or more of these anionic surfactants are magnesium salts. It came to this.
すなわち本発明は、炭素数10〜20個のα−オレフィ
ンスルホン酸塩と炭素数10〜18個の第二級アルカン
スルホン酸塩とを重量比で95■5〜40:60の範囲
で含有し、この両アニオン界面活性剤の少なくとも40
重量%がマグネシウム塩であることを特徴とする洗浄剤
組成物を提供するものである。That is, the present invention contains an α-olefin sulfonate having 10 to 20 carbon atoms and a secondary alkanesulfonate having 10 to 18 carbon atoms in a weight ratio of 95:5 to 40:60. , at least 40% of this both anionic surfactant
The present invention provides a cleaning composition characterized in that % by weight is a magnesium salt.
本発明のα−オレフィンスルホン酸塩は炭素数10〜2
0個のものが適当であり、平均炭素数13.5〜16.
0個で、炭素数14個のものが25%以上のものが好ま
しい。The α-olefin sulfonate of the present invention has 10 to 2 carbon atoms.
0 carbon atoms is suitable, and the average carbon number is 13.5 to 16.
It is preferable that the number of carbon atoms is 0 and that the number of carbon atoms is 14 or more than 25%.
通常、α−オレフィンスルホン酸塩は、アルケニルスル
ホン酸塩、ヒドロキシアルカンスルホン酸塩を主とし、
若干のジスルホン酸塩が含まれるが、アルケニルスルホ
ン酸塩とヒドロキシアルカンスルホン酸塩との比率は重
量比で、40:60〜90:10が好ましく、50:5
0〜80■20がより好ましい。Usually, α-olefin sulfonates mainly include alkenyl sulfonates and hydroxyalkanesulfonates,
Although some disulfonate is included, the ratio of alkenyl sulfonate to hydroxyalkane sulfonate is preferably 40:60 to 90:10, and 50:5 by weight.
0 to 80×20 is more preferable.
またジスルホン酸塩は3〜13重量%が好ましい。本発
明のα−オレフィンスルホン酸塩は、公知の方法により
、α−オレフィンをスルホン化反応後、アルカリ金属又
はアルカリ土類金属で中和し、次いで加水分解して得ら
れる。Further, the amount of the disulfonate is preferably 3 to 13% by weight. The α-olefin sulfonate of the present invention can be obtained by sulfonating an α-olefin, neutralizing it with an alkali metal or alkaline earth metal, and then hydrolyzing it by a known method.
原料のα−オレフィンとしては、たとえばワックス・ク
ラツキング法、チーグラ一触媒によるエチレン重合法又
はそれらの改良法で得られたものが用いられる。本発明
の第二級アルカンスルホン酸塩は、炭素数10〜18個
のものが適当である。このアルカンスルホン酸塩は例え
ば、炭素数10〜18個のn−パラフインをいわゆるス
ルフオキシデーシヨンしてアルカンスルホン酸とした後
中和して得ることができる。本発明のα−オレフインス
ルホン酸塩と第二級アルカンスルホン酸塩の配合比率は
重量比で95:5〜40:60であり、この範囲を外れ
ると洗浄力、起泡力のいずれも不十分となる。As the raw material α-olefin, those obtained by, for example, a wax cracking method, an ethylene polymerization method using a Ziegler catalyst, or an improved method thereof are used. The secondary alkanesulfonate of the present invention preferably has 10 to 18 carbon atoms. This alkanesulfonic acid salt can be obtained, for example, by subjecting n-paraffin having 10 to 18 carbon atoms to so-called sulfoxidation to form an alkanesulfonic acid, followed by neutralization. The blending ratio of α-olefin sulfonate and secondary alkanesulfonate of the present invention is 95:5 to 40:60 by weight, and outside this range, both detergency and foaming power are insufficient. becomes.
また、これらのアニオン界面活性剤において、マグネシ
ウム塩が40重量%以上であることが必要である。マグ
ネシウム塩がこれより少ないと洗浄力、起泡力共著しく
低下する。本発明の洗浄剤組成物には、上記各成分以外
に例えば、粒状洗剤の場合、ケイ酸ナトリウム、炭酸ナ
トリウム、トリポリリン酸ナトリウム、ピロリン酸ナト
リウム、オルソリン酸ナトリウム、アルミノシリケート
などの無機ビルダ一、ポリカルボン酸(例えば無水マレ
イン酸、アクリル酸の重合体もしくはオレフインとの共
重合体)、オキシジコハク酸ナトリウム、NTAなどの
有機ビルダ一、EDTAなどの有機キレート剤、アンチ
ケーキング剤、螢光増白剤、香料など、また液体洗剤の
場合、エタノール、尿素、ポリエチレングリコール、脂
肪酸のモノ、ジ、トリエタノールアミド、ベンゼンスル
ホン酸塩、パラトルエンスルホン酸塩、キシレンスルホ
ン酸塩、安息香酸塩、クエン酸塩、モノ、ジ、トリエタ
ノールアミン、EDTAなどの慣用成分を加えることが
できる。Further, in these anionic surfactants, it is necessary that the magnesium salt content is 40% by weight or more. If the amount of magnesium salt is less than this, both the detergency and foaming power will be significantly reduced. In addition to the above-mentioned components, the cleaning composition of the present invention may also contain, for example, in the case of granular detergents, inorganic builders such as sodium silicate, sodium carbonate, sodium tripolyphosphate, sodium pyrophosphate, sodium orthophosphate, and aluminosilicate; Carboxylic acids (e.g. maleic anhydride, polymers of acrylic acid or copolymers with olefins), sodium oxydisuccinate, organic builders such as NTA, organic chelating agents such as EDTA, anticaking agents, fluorescent brighteners, Fragrances, etc., and in the case of liquid detergents, ethanol, urea, polyethylene glycol, mono-, di-, and triethanolamide of fatty acids, benzenesulfonate, paratoluenesulfonate, xylene sulfonate, benzoate, citrate, Conventional ingredients such as mono-, di-, triethanolamine, EDTA, etc. can be added.
また、この組成物の洗浄性、起泡力、生分解性をそこな
わない範囲で、適宜、直鎖アルキルベンゼンスルホン酸
塩、アルコール硫酸エステル塩、アルコールエトキシ硫
酸エステル塩などのアニオン活性剤、アルコールエトキ
シレート、アルキルフエノールエトキシレートなどのノ
ニオン活性剤、アルキルベタイン、アルキルスルホベタ
インなどの両性活性剤を配合できることはもちろんであ
る。本発明の洗浄剤組成物は生分解性が優れ、縮合リン
酸塩を配合しなくとも、高い洗浄力と起泡力を示す。In addition, anionic surfactants such as linear alkylbenzene sulfonates, alcohol sulfate ester salts, alcohol ethoxy sulfate ester salts, alcohol ethoxy Of course, nonionic surfactants such as esters, alkyl phenol ethoxylates, and amphoteric surfactants such as alkyl betaines and alkyl sulfobetaines can be incorporated. The detergent composition of the present invention has excellent biodegradability and exhibits high detergency and foaming power even without the addition of condensed phosphate.
さらに、この組成物は環境保全の観点からも優れている
。本発明の組成物は台所用洗剤、衣類用洗剤などの汎用
洗浄剤などとして好適である。Furthermore, this composition is excellent from the viewpoint of environmental conservation. The composition of the present invention is suitable as a general-purpose cleaning agent such as a kitchen detergent and a laundry detergent.
次に、本発明を実施例に基づき詳細に説明する。Next, the present invention will be explained in detail based on examples.
なお、洗浄力及び起泡力は次のようにして測定した。洗
浄力:局方大豆油、局方牛脂それぞれ10yをクロロホ
ルムに溶解した後、この液に76mm×2611×1.
371tmのガラスプレートを浸漬し、次いで、クロロ
ホルムを風乾して汚染プレートを作成する。Note that the detergency and foaming power were measured as follows. Cleaning power: After dissolving 10 y of each of Japanese soybean oil and beef tallow in chloroform, a 76 mm x 2611 x 1.
A 371tm glass plate is immersed and then the chloroform is air dried to create a contaminated plate.
汚染プレート6枚1組を洗剤溶液(濃度0.15%)中
で、3分間攪拌洗浄し、洗浄前後の汚垢量から汚垢除去
率を算出する。尚、温度は25℃、撹拌速度は250r
.p.m.とした。A set of six contaminated plates is washed in a detergent solution (concentration 0.15%) for 3 minutes with stirring, and the dirt removal rate is calculated from the amount of dirt before and after washing. The temperature was 25℃ and the stirring speed was 250r.
.. p. m. And so.
起泡力:容量31、濃度0.15%、液温25℃の洗剤
溶液を入れた直径30CTn、高さ12儂のバツト中で
、バターで汚染した皿(0.5y/皿)の表面を5回、
裏面を3回、スポンジでこすり洗いし、洗液の泡高が1
m7!Lになるまでの皿洗い枚数を起泡力とした。Foaming power: In a vat with a diameter of 30CTn and a height of 12F containing a detergent solution with a volume of 31, a concentration of 0.15%, and a liquid temperature of 25°C, the surface of a dish (0.5y/dish) contaminated with butter was 5 times,
Scrub the back side three times with a sponge until the foam height of the washing liquid is 1.
m7! The number of dishes washed until L was reached was defined as the foaming power.
実施例 1
下記洗浄剤組成で、α−オレフインスルホン酸のマグネ
シウム塩(AOS−Mgl/2、Cl4/Cl6=1/
1)及び炭素数14〜18個の第二級アルカンスルホン
酸のナトリウム塩(SAS一Na)の配合比率を第1表
に示したように変え、その洗浄力と起泡力を測定した。Example 1 The following cleaning agent composition was prepared using magnesium salt of α-olefin sulfonic acid (AOS-Mgl/2, Cl4/Cl6=1/
1) and the sodium salt of a secondary alkanesulfonic acid having 14 to 18 carbon atoms (SAS-Na) were varied as shown in Table 1, and the detergency and foaming power thereof were measured.
この結果を第1表に示した。この表の結果より明らかな
ように、本発明の洗浄剤組成物(実験滝1〜3)は、洗
浄力、起泡力共、本発明の範囲を外れる比較例のもの(
実験應4、5)より優れている。The results are shown in Table 1. As is clear from the results in this table, the detergent compositions of the present invention (Experimental Waterfalls 1 to 3) are different from those of the comparative examples (Experimental Waterfalls 1 to 3), which are outside the scope of the present invention in both detergency and foaming power.
This is better than experimental results 4 and 5).
実施例 2
実施例1と同様の方法により、α−オレフインスルホン
酸塩(Cl4/Cl6=1/1)と第二級アルカンスル
ホン酸塩の配合比率を重量比で75:25としそのマグ
ネシウム塩含量を種々変えた場合の洗浄力、起泡力を測
定した。Example 2 By the same method as in Example 1, the blending ratio of α-olefin sulfonate (Cl4/Cl6 = 1/1) and secondary alkanesulfonate was set to 75:25 by weight, and the magnesium salt content was The cleaning power and foaming power were measured with various changes.
この結果を第2表に示した。この表の結果よりマグネシ
ウム塩含量40重量%以上の本発明の洗浄剤組成物(実
験滝6〜8)は、洗浄力、起泡力共マグネシウム塩含量
が40重量%未満の比較例(実験S).9、10)より
はるかに優れることがわかる。The results are shown in Table 2. From the results in this table, the cleaning compositions of the present invention (Experiment Taki 6 to 8) with a magnesium salt content of 40% by weight or more have both cleaning power and foaming power, and the comparative examples (Experiment S) with a magnesium salt content of less than 40% by weight. ). 9, 10).
実施例 3
第3表に示した各種の配合組成の洗浄剤を調製し、その
洗浄力?よび起泡力を測定した結果を示した。Example 3 Detergents with various formulations shown in Table 3 were prepared, and their cleaning power was evaluated. The results of measuring foaming power and foaming power are shown below.
Claims (1)
と炭素数10〜18個の第二級アルカンスルホン酸塩と
を重量比で95:5〜40:60の範囲で含有し、前記
界面活性剤の少なくとも40重量%がマグネシウム塩で
あることを特徴とする洗浄剤組成物。1 Contains an α-olefin sulfonate having 10 to 20 carbon atoms and a secondary alkanesulfonate having 10 to 18 carbon atoms in a weight ratio of 95:5 to 40:60, and has the above-mentioned surface activity. A cleaning composition characterized in that at least 40% by weight of the agent is a magnesium salt.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1561378A JPS5945039B2 (en) | 1978-02-14 | 1978-02-14 | cleaning composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1561378A JPS5945039B2 (en) | 1978-02-14 | 1978-02-14 | cleaning composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54107909A JPS54107909A (en) | 1979-08-24 |
| JPS5945039B2 true JPS5945039B2 (en) | 1984-11-02 |
Family
ID=11893547
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1561378A Expired JPS5945039B2 (en) | 1978-02-14 | 1978-02-14 | cleaning composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5945039B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3370164D1 (en) * | 1982-10-28 | 1987-04-16 | Procter & Gamble | Liquid detergent compositions |
-
1978
- 1978-02-14 JP JP1561378A patent/JPS5945039B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54107909A (en) | 1979-08-24 |
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