JP2007177094A - Cleanser composition - Google Patents

Cleanser composition Download PDF

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JP2007177094A
JP2007177094A JP2005377819A JP2005377819A JP2007177094A JP 2007177094 A JP2007177094 A JP 2007177094A JP 2005377819 A JP2005377819 A JP 2005377819A JP 2005377819 A JP2005377819 A JP 2005377819A JP 2007177094 A JP2007177094 A JP 2007177094A
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alkali metal
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JP4877918B2 (en
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Yoshiyuki Watanabe
義幸 渡辺
Shin Aihara
伸 相原
Kazukuni Tsukuda
一訓 佃
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Kao Corp
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Kao Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a cleanser composition capable of extruding dense and rich foams when extruded with a relevant container having foam-making mechanism, and also excellent in feeling in use, visibility and adhesion persistence onto object's surface. <P>SOLUTION: The cleanser composition comprises (a) a specific compound represented by the general formula (1):X<SP>1</SP>-O(AO)<SB>n</SB>-X<SP>2</SP>, (b) a specific compound represented by the general formula (2):X<SP>2</SP>-O(AO)<SB>n</SB>-X<SP>2</SP>, and (c) a surfactant. This cleanser composition is 5-210 mPa s in the viscosity determined using a Brookfield viscometer under the conditions of 20°C in temperature and 60 rpm in revolutions and 60 s in revolution time. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、造泡機構を有する吐出容器で吐出した際に、緻密で豊富な泡が吐出されることで得られる使い心地や視認性、及び対象面への付着滞留性のどちらにも優れた洗浄剤組成物に関する。   The present invention is superior in both usability and visibility obtained by discharging dense and abundant bubbles, and adhering and staying on the target surface when discharged with a discharge container having a foam-forming mechanism. The present invention relates to a cleaning composition.

従来、住居内における、台所、浴室、浴槽、配水管、トイレ等の硬質表面に付着した汚れの除去を目的として、界面活性剤を主成分とする洗浄剤組成物や、次亜塩素酸アルカリ金属塩を主成分とする漂白洗浄剤組成物が広く使用されている。上記の如き洗浄剤組成物は、適用される硬質表面が水平面に限らず垂直面、傾斜面など、様々であることから、いかなる表面に適用された場合にも優れた洗浄/漂白性能を発揮させるために、対象となる汚れへの付着滞留性が要求されている。このような要求に応えるべく、種々の方法による組成物の付着滞留性の向上が試みられている。例えば、特許文献1には組成物に粘性を付与することで付着滞留性を高めた洗浄剤製品が開示されている。特許文献2にはチキソトロピー性を有する比較的高粘度の洗浄剤をスプレーヤーを用いて適度な粗さの泡状に噴霧することで、対象物が網目構造体であっても網目を通過することなく対象物の表面を均一に覆うように付着し、優れた付着滞留性を発揮することが可能な洗浄剤及び洗浄剤製品が開示されている。また、特許文献3では特定の重合体を含有する貯蔵安定性に優れた漂白剤組成物が開示されている。
特開2003−41300 特開2003−253297 特開平7−305099
Conventionally, in order to remove dirt adhered to hard surfaces such as kitchens, bathrooms, bathtubs, water pipes, and toilets in a residence, a detergent composition mainly composed of a surfactant or an alkali metal hypochlorite Bleach detergent compositions based on salt are widely used. The cleaning composition as described above exhibits excellent cleaning / bleaching performance when applied to any surface, since the hard surface to be applied is not limited to a horizontal plane, but various such as a vertical surface and an inclined surface. For this reason, adherence retention to the target dirt is required. In order to meet such demands, attempts have been made to improve the adhesion and retention of the composition by various methods. For example, Patent Document 1 discloses a detergent product having increased adhesion retention by imparting viscosity to the composition. Patent Document 2 discloses that a relatively high viscosity cleaning agent having thixotropy is sprayed into a foam having an appropriate roughness using a sprayer, so that even if the object is a network structure, it passes through the network. There is disclosed a cleaning agent and a cleaning product that can be attached so as to uniformly cover the surface of an object and exhibit excellent adhesion retention. Patent Document 3 discloses a bleaching composition having a specific polymer and excellent in storage stability.
JP 2003-41300 A JP 2003-253297 A JP 7-305099 A

特許文献1記載の洗浄剤製品は、組成物の付着滞留性は高まるが、トリガー式のスプレーヤーで噴霧しても泡にならず、使い心地や視認性に劣る。特許文献2記載の洗浄剤及び洗浄剤製品は、洗浄剤の付着滞留性は高まるが、粗い泡のため視認性や使い心地に劣る。また、特許文献3記載の漂白剤組成物は、次亜塩素酸アルカリ金属塩の貯蔵安定性には優れるが、トリガー式スプレーヤーで噴霧した際の状態についての記載はなく、特徴的な泡特性についても具体的に示唆されていない。   Although the detergent product described in Patent Document 1 has increased adhesion retention of the composition, it does not form bubbles even when sprayed with a trigger sprayer, and is inferior in comfort and visibility. The cleaning agent and the cleaning product described in Patent Document 2 increase the adhesion retention of the cleaning agent, but are inferior in visibility and comfort due to rough foam. Further, the bleaching composition described in Patent Document 3 is excellent in the storage stability of alkali metal hypochlorite, but there is no description about the state when sprayed with a trigger sprayer, and the characteristic foam characteristics There is no specific suggestion.

すなわち、造泡機構を有する吐出容器で吐出した際に、緻密で豊富な泡が吐出でき、使い心地や視認性及び対象面への付着滞留性にも優れた洗浄剤組成物が求められている。   That is, there is a demand for a detergent composition that is capable of discharging dense and abundant bubbles when discharged with a discharge container having a foam-forming mechanism, and is excellent in usability, visibility, and adhesion retention on the target surface. .

本発明は、(a)下記一般式(1)で表される化合物、(b)下記一般式(2)で表される化合物、及び(c)界面活性剤、を含有し、且つB型粘度計を用いて20℃、回転数60rpm、60sの条件で測定した粘度が5〜210mPa・sである洗浄剤組成物に関する。
1−O(AO)n−X2 (1)
2−O(AO)n−X2 (2)
〔式中、AOは炭素数2〜4のアルキレンオキシ基、nはアルキレンオキシ基の平均付加モル数を示し、5〜1000の数である。また、一般式(1)及び一般式(2)のAOの総モル数に対して50モル%以上がエチレンオキシ基である。X1は水素原子又は炭素数1〜6のアルキル基であり、X2は、−SO3H、−CH2COOH、あるいはこれらのアルカリ金属塩を示す。〕
The present invention contains (a) a compound represented by the following general formula (1), (b) a compound represented by the following general formula (2), and (c) a surfactant, and has a B-type viscosity. The present invention relates to a detergent composition having a viscosity of 5 to 210 mPa · s measured using a meter at 20 ° C., rotation speed 60 rpm, and 60 s.
X 1 -O (AO) n -X 2 (1)
X 2 -O (AO) n -X 2 (2)
[Wherein, AO represents an alkyleneoxy group having 2 to 4 carbon atoms, and n represents an average number of added moles of the alkyleneoxy group, and is a number of 5 to 1000. Moreover, 50 mol% or more is ethyleneoxy group with respect to the total mole number of AO of General formula (1) and General formula (2). X 1 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and X 2 represents —SO 3 H, —CH 2 COOH, or an alkali metal salt thereof. ]

また、本発明は、上記本発明の洗浄剤組成物を収納する容器本体と、その容器本体内に収納された洗浄剤組成物を吐出させる造泡機構を有する吐出装置と、を備える洗浄剤製品に関する。   Further, the present invention provides a cleaning product comprising a container main body that stores the cleaning composition of the present invention, and a discharge device having a foam-forming mechanism that discharges the cleaning composition stored in the container main body. About.

本発明によれば、造泡機構を有する吐出容器で吐出した際に、緻密で豊富な泡が吐出でき、使い心地や視認性及び対象面への付着滞留性にも優れた洗浄剤組成物が得られる。   According to the present invention, when discharged with a discharge container having a foam-forming mechanism, a dense and abundant foam can be discharged, and a cleaning composition that is excellent in usability, visibility, and adhesion retention on a target surface. can get.

本発明の洗浄剤組成物は、粘性を付与した組成物をトリガー等の吐出容器を用いて吐出した際に、造泡させることを目的として、(a)下記一般式(1)〔以下、(a)成分と記載する〕で表される化合物、(b)下記一般式(2)〔以下、(b)成分と記載する〕で表される化合物を含有している。
1−O(AO)n−X2 (1)
2−O(AO)n−X2 (2)
〔式中、AOは炭素数2〜4のアルキレンオキシ基、nはアルキレンオキシ基の平均付加モル数を示し、5〜1000の数である。また、一般式(1)及び一般式(2)のAOの総モル数に対して50モル%以上がエチレンオキシ基である。X1は水素原子又は炭素数1〜6のアルキル基であり、X2は、−SO3H、−CH2COOH、あるいはこれらのアルカリ金属塩を示す。〕
The detergent composition of the present invention has the following general formula (1) [below, (a) for the purpose of foaming when a composition having a viscosity is discharged using a discharge container such as a trigger. a) described as a component], and (b) a compound represented by the following general formula (2) [hereinafter described as a component (b)].
X 1 -O (AO) n -X 2 (1)
X 2 -O (AO) n -X 2 (2)
[Wherein, AO represents an alkyleneoxy group having 2 to 4 carbon atoms, and n represents an average number of added moles of the alkyleneoxy group, and is a number of 5 to 1000. Moreover, 50 mol% or more is ethyleneoxy group with respect to the total mole number of AO of General formula (1) and General formula (2). X 1 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and X 2 represents —SO 3 H, —CH 2 COOH, or an alkali metal salt thereof. ]

上記一般式(1)、及び(2)で表される化合物のAOは炭素数2〜4のアルキレンオキシ基を示し、具体的にはエチレンオキシ基、プロピレンオキシ基等が挙げられるが、一般式(1)及び(2)のAOの総モル数に対して50モル%以上、好ましくは60モル%以上、より好ましくは70モル%以上がエチレンオキシ基である。nはアルキレンオキシ基の平均付加モル数を示し、5〜1000の数であり、10〜100が更に好ましく、10〜40が特に好ましい。アルキレンオキシ基の平均付加モル数が5以上では良好な起泡力と付着滞留性が得られ、また1000以下では組成物の白濁を抑制できる等、良好な組成物の安定性が得られる。X1は水素原子又は炭素数1〜6のアルキル基であり、X2は、−SO3H、−CH2COOH、あるいはこれらのアルカリ金属塩を示す。(a)成分及び(b)成分の比率としては、(a)成分/(b)成分がモル比で1/1〜1/1000が好ましく、2/3〜1/100が更に好ましく、3/7〜1/9が特に好ましい。(a)成分及び(b)成分はそれぞれの単品を用いて、あるいは予め混合した混合品を用いて、製品中の(a)成分と(b)成分の比率が上記比率になるように調整できる。また、(a)成分及び(b)成分は、例えば溶媒中でポリエチレングリコールに無水硫酸を反応させ、水酸化ナトリウムで中和することで得られるが、このような合成をおこなう過程でポリエチレングリコールと無水硫酸のモル比を変化させて得られた(a)成分及び(b)成分の混合品を用いて製品中の(a)成分と(b)成分の比率が上記比率になるように調整することもできる。 AO of the compounds represented by the general formulas (1) and (2) represents an alkyleneoxy group having 2 to 4 carbon atoms, and specific examples include an ethyleneoxy group and a propyleneoxy group. 50 mol% or more, preferably 60 mol% or more, more preferably 70 mol% or more of the total number of moles of AO in (1) and (2) is an ethyleneoxy group. n shows the average addition mole number of an alkyleneoxy group, is a number of 5-1000, 10-100 are still more preferable, and 10-40 are especially preferable. When the average number of added moles of the alkyleneoxy group is 5 or more, good foaming force and adhesion retention can be obtained, and when it is 1000 or less, good composition stability can be obtained. X 1 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and X 2 represents —SO 3 H, —CH 2 COOH, or an alkali metal salt thereof. As a ratio of the component (a) and the component (b), the component (a) / component (b) is preferably 1/1 to 1/1000 in terms of molar ratio, more preferably 2/3 to 1/100, and more preferably 3 / 7 to 1/9 is particularly preferable. The component (a) and the component (b) can be adjusted so that the ratio of the component (a) and the component (b) in the product is the above ratio by using each single product or a premixed product. . In addition, the component (a) and the component (b) can be obtained, for example, by reacting sulfuric acid anhydride with polyethylene glycol in a solvent and neutralizing with sodium hydroxide. Using a mixture of component (a) and component (b) obtained by changing the molar ratio of sulfuric anhydride, adjust the ratio of component (a) and component (b) in the product to the above ratio. You can also

本発明の洗浄剤組成物中における(a)成分及び(b)成分は合計で、0.05〜3.0質量%含有することが好ましく、0.05〜2.0質量%が更に好ましく、0.05〜1.0質量%が特に好ましい。(a)成分及び(b)成分の総含有量が0.05質量%以上では良好な起泡力が得られ、3.0質量%以下では良好な次亜塩素酸アルカリ金属塩の安定性が得られる。   The component (a) and component (b) in the cleaning composition of the present invention is a total, preferably 0.05 to 3.0% by mass, more preferably 0.05 to 2.0% by mass, 0.05-1.0 mass% is especially preferable. When the total content of the component (a) and the component (b) is 0.05% by mass or more, good foaming power is obtained, and when the total content is 3.0% by mass or less, good stability of the alkali metal hypochlorite is obtained. can get.

本発明の洗浄剤組成物に使用される(c)界面活性剤としては特に制限されないが、下記成分(I)〔以下、(I)成分と記載する〕及び(II)〔以下、(II)成分と記載する〕からなる群から選ばれる1種又は2種以上の界面活性剤を使用することが好ましい。また、(I)及び(II)成分を混合して用いた場合は、それらのコンプレックスが形成され低濃度で目的の粘度が得られるため、配合コストや安定性の点で更に好ましい。   The surfactant (c) used in the cleaning composition of the present invention is not particularly limited, but the following components (I) [hereinafter referred to as (I) components] and (II) [hereinafter (II) It is preferable to use one or two or more surfactants selected from the group consisting of [described as components]. In addition, when the components (I) and (II) are mixed and used, their complexes are formed and the desired viscosity can be obtained at a low concentration, which is more preferable in terms of blending cost and stability.

(I)下記一般式(2)、(3)、(4)、(5)及び(6)で表される化合物からなる群から選ばれる1種又は2種以上。
1SO3M (2)
264SO3M (3)
3O(AO)mSO3M (4)
4COOM (5)
5O(AO)n6COOM (6)
(式中、R1、R2、R3、R4及びR5はそれぞれ炭素数6〜22の直鎖又は分岐鎖のアルキル基を示す。Aは炭素数1〜4の直鎖又は分岐鎖のアルキレン基の1種又は2種以上を示し、R6は炭素数1〜4のアルキレン基を示す。m及びnは、平均付加モル数であり、それぞれ0〜100の数を示し、Mは水素原子、アルカリ金属原子又はアルカリ土類金属原子を示す。)
(I) One or more selected from the group consisting of compounds represented by the following general formulas (2), (3), (4), (5) and (6).
R 1 SO 3 M (2)
R 2 C 6 H 4 SO 3 M (3)
R 3 O (AO) m SO 3 M (4)
R 4 COOM (5)
R 5 O (AO) n R 6 COOM (6)
(Wherein R 1 , R 2 , R 3 , R 4 and R 5 each represent a linear or branched alkyl group having 6 to 22 carbon atoms. A is a linear or branched chain having 1 to 4 carbon atoms. And R 6 represents an alkylene group having 1 to 4 carbon atoms, m and n are average added mole numbers, and each represents a number of 0 to 100, and M represents Represents a hydrogen atom, an alkali metal atom or an alkaline earth metal atom.)

(II)下記の一般式(7)で表される第3級アミンオキシド。
789N→O (7)
(式中、R7は炭素数8〜20の直鎖又は分岐のアルキル基を示し、R8、R9は炭素数1〜3の直鎖又は分岐のアルキル基を示す。)
(II) A tertiary amine oxide represented by the following general formula (7).
R 7 R 8 R 9 N → O (7)
(In the formula, R 7 represents a linear or branched alkyl group having 8 to 20 carbon atoms, and R 8 and R 9 represent a linear or branched alkyl group having 1 to 3 carbon atoms.)

上記成分(I)における化合物の具体例を以下に示す。上記一般式(2)で表されるアルカンスルホネート(炭素数6〜22の直鎖又は分岐鎖のアルカンスルホネート)としては、ドデシルスルホン酸ナトリウム等が挙げられるが、通常、安価に入手可能な炭素数10〜14程度のアルキル基を有するアルカンスルホン酸塩(特にナトリウム塩)、又はそれらの混合物が用いられる。   Specific examples of the compound in the component (I) are shown below. Examples of the alkane sulfonate represented by the general formula (2) (linear or branched alkane sulfonate having 6 to 22 carbon atoms) include sodium dodecyl sulfonate and the like. Alkanesulfonic acid salts (especially sodium salts) having about 10 to 14 alkyl groups, or mixtures thereof are used.

上記一般式(3)で表されるアルキルベンゼンスルホン酸又はその塩(炭素数6〜22の直鎖又は分岐鎖のアルキル基を有するもの)としては、ドデシルベンゼンスルホン酸ナトリウム等が挙げられるが、通常、安価に入手可能な炭素数10〜14程度のアルキル基を有するアルキルベンゼンスルホン酸塩(特にナトリウム塩)、又はそれらの混合物が用いられる。   Examples of the alkylbenzenesulfonic acid represented by the general formula (3) or a salt thereof (having a linear or branched alkyl group having 6 to 22 carbon atoms) include sodium dodecylbenzenesulfonate, etc. An alkylbenzene sulfonate (especially sodium salt) having an alkyl group having about 10 to 14 carbon atoms, which can be obtained at low cost, or a mixture thereof is used.

上記一般式(4)で表されるポリオキシアルキレンアルキルエーテル硫酸エステル又はその塩(炭素数6〜22の直鎖又は分岐鎖のアルキル基を有するもの)としては、R3が炭素数6〜22のアルキル基が好ましく、8〜18が更に好ましく、10〜14が特に好ましい。Aはエチレン基、プロピレン基又はブチレン基が好ましく、エチレン基が更に好ましい。mは平均付加モル数を示し、0〜100が好ましく、0〜20が更に好ましく、0〜10が特に好ましい。具体的には、デシル硫酸エステルナトリウム(m=0)、ドデシル硫酸エステルナトリウム(m=0)、ポリオキシエチレン(m=2.5)ラウリルエーテル硫酸ナトリウム、ポリオキシエチレン(m=4.0)ラウリルエーテル硫酸ナトリウム等が挙げられる。 As polyoxyalkylene alkyl ether sulfate represented by the above general formula (4) or a salt thereof (having a linear or branched alkyl group having 6 to 22 carbon atoms), R 3 has 6 to 22 carbon atoms. Alkyl groups are preferred, 8-18 are more preferred, and 10-14 are particularly preferred. A is preferably an ethylene group, a propylene group or a butylene group, more preferably an ethylene group. m shows an average added mole number, 0-100 are preferable, 0-20 are more preferable, and 0-10 are especially preferable. Specifically, sodium decyl sulfate ester (m = 0), sodium dodecyl sulfate ester (m = 0), polyoxyethylene (m = 2.5) sodium lauryl ether sulfate, polyoxyethylene (m = 4.0) Examples include sodium lauryl ether sulfate.

上記一般式(5)で表される脂肪酸又はその塩(炭素数6〜22の直鎖又は分岐鎖のアルキル基を有するもの)としては、R4で示される炭素数6〜22の直鎖のアルキル基を有する脂肪酸のアルカリ金属塩が好ましく、カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸等の直鎖脂肪酸のナトリウム塩、カリウム塩等が挙げられる。また、低温保管時の安定性の面で、アルキル基に分布があると更に好ましく、具体的には、アルキル基の炭素数が10〜16の脂肪酸の混合物であって、炭素数12のものが全脂肪酸の60%以上を占めるものを用いることが最も好ましい。 As the fatty acid represented by the general formula (5) or a salt thereof (having a linear or branched alkyl group having 6 to 22 carbon atoms), a straight chain having 6 to 22 carbon atoms represented by R 4 Alkali metal salts of fatty acids having an alkyl group are preferred, and examples thereof include sodium salts and potassium salts of linear fatty acids such as capric acid, lauric acid, myristic acid, palmitic acid and stearic acid. Further, in terms of stability during low temperature storage, it is more preferable that the alkyl group has a distribution. Specifically, the alkyl group is a mixture of fatty acids having 10 to 16 carbon atoms, and those having 12 carbon atoms. It is most preferable to use those that occupy 60% or more of the total fatty acids.

上記一般式(6)で表されるポリオキシアルキレンアルキルエーテルカルボキシレート(炭素数6〜22の直鎖又は分岐鎖のアルキル基を有するもの)のR5で示される炭素数6〜22の直鎖又は分岐鎖のアルキル基としては、ヘキシル基、オクチル基、デシル基、ドデシル基、テトラデシル基、ヘキサデシル基、オクタデシル基等が挙げられ、特にドデシル基、テトラデシル基が好ましい。また、Aで示される炭素数1〜4の直鎖又は分岐鎖のアルキレン基としては、炭素数2〜4のものが好ましく、例えばエチレン基、プロピレン基、イソプロピレン基、ブチレン基等が挙げられ、特にエチレン基、イソプロピレン基が好ましい。また、R6で示される炭素数1〜4の直鎖又は分岐鎖のアルキレン基としては、メチレン基、プロピレン基、イソプロピレン基、ブチレン基等が挙げられ、特にメチレン基、プロピレン基、イソプロピレン基が好ましい。また、Mで示されるアルカリ金属原子としては、例えばナトリウム原子、カリウム原子等が挙げられ、特にナトリウム原子が好ましく、アルカリ土類金属原子としては、カルシウム、マグネシウム等が挙げられる。また、nは平均付加モル数であり、1〜50、特に1〜20の範囲のものが更に好ましい。 A straight chain having 6 to 22 carbon atoms represented by R 5 of the polyoxyalkylene alkyl ether carboxylate represented by the general formula (6) (having a straight or branched alkyl group having 6 to 22 carbon atoms). Or as a branched alkyl group, a hexyl group, an octyl group, a decyl group, a dodecyl group, a tetradecyl group, a hexadecyl group, an octadecyl group etc. are mentioned, Especially a dodecyl group and a tetradecyl group are preferable. Moreover, as a C1-C4 linear or branched alkylene group shown by A, a C2-C4 thing is preferable, for example, an ethylene group, a propylene group, an isopropylene group, a butylene group etc. are mentioned. In particular, an ethylene group and an isopropylene group are preferable. Moreover, as a C1-C4 linear or branched alkylene group shown by R < 6 >, a methylene group, a propylene group, an isopropylene group, a butylene group etc. are mentioned, Especially a methylene group, a propylene group, isopropylene. Groups are preferred. Further, examples of the alkali metal atom represented by M include a sodium atom and a potassium atom, and a sodium atom is particularly preferable, and examples of the alkaline earth metal atom include calcium and magnesium. Moreover, n is an average added mole number, and the thing of the range of 1-50, especially 1-20 is still more preferable.

また、上記一般式(6)で表される化合物の具体例としては、ヘキシルポリオキシエチレンオキシ酢酸ナトリウム(n=3.8)、オクチルポリオキシエチレンオキシ酢酸ナトリウム(n=4.5)、ドデシルポリオキシエチレンオキシ酢酸ナトリウム(n=10)、ドデシルポリオキシプロピレンオキシ酢酸ナトリウム(n=2)、ドデシルポリオキシエチレンオキシプロピオン酸ナトリウム(n=6.0)等が挙げられ、これらのうち、製造コストの点で特にアルキル(炭素数8〜10の直鎖又は分岐鎖)ポリオキシエチレン(n=1〜20)オキシ酢酸ナトリウムのような混合物として使用することが好ましい。   Specific examples of the compound represented by the general formula (6) include sodium hexyl polyoxyethylene oxyacetate (n = 3.8), sodium octyl polyoxyethylene oxyacetate (n = 4.5), dodecyl. Examples include sodium polyoxyethylene oxyacetate (n = 10), sodium dodecyl polyoxypropylene oxyacetate (n = 2), sodium dodecyl polyoxyethylene oxypropionate (n = 6.0), and among these, production In particular, it is preferable to use it as a mixture such as sodium alkyloxy (linear or branched chain having 8 to 10 carbon atoms) polyoxyethylene (n = 1 to 20) sodium oxyacetate.

(I)成分における上記一般式(2)〜(6)で表される化合物は、単独又は2種以上の混合物として使用できる。   The compounds represented by the general formulas (2) to (6) in the component (I) can be used alone or as a mixture of two or more.

本発明の洗浄剤組成物中における(I)成分の含有量は、0.1〜5.0質量%が好ましく、0.1〜3.0質量%が更に好ましく、0.1〜1.0質量%が特に好ましい。(I)成分の含有量が0.1質量%以上で洗浄力が得られ、5.0質量%以下で目的の粘度が得られる。   The content of the component (I) in the cleaning composition of the present invention is preferably 0.1 to 5.0% by mass, more preferably 0.1 to 3.0% by mass, and 0.1 to 1.0%. Mass% is particularly preferred. Detergency is obtained when the content of component (I) is 0.1% by mass or more, and the desired viscosity is obtained at 5.0% by mass or less.

(II)成分において一般式(7)で表される第3級アミンオキサイドの具体例を以下に示す。R7で示される炭素数8〜20のアルキル基としてはオクチル基、デシル基、ドデシル基、テトラデシル基、ヘキサデシル基、オクタデシル基等が挙げられ、これらのなかでも特にデシル基、ドデシル基、テトラデシル基及びヘキサデシル基が好ましい。また(II)成分は、天然物から誘導された炭素数の異なるアルキル基を有する第3級アミンオキシドの混合物であってもよい。また、R8及びR9で示される炭素数1〜3のアルキル基としては、メチル基、エチル基、プロピル基等が挙げられ、これらのうちメチル基が特に好ましい。 Specific examples of the tertiary amine oxide represented by the general formula (7) in the component (II) are shown below. Examples of the alkyl group having 8 to 20 carbon atoms represented by R 7 include an octyl group, a decyl group, a dodecyl group, a tetradecyl group, a hexadecyl group, and an octadecyl group. And a hexadecyl group is preferred. Further, the component (II) may be a mixture of tertiary amine oxides having alkyl groups having different carbon numbers derived from natural products. Moreover, as a C1-C3 alkyl group shown by R < 8 > and R < 9 >, a methyl group, an ethyl group, a propyl group, etc. are mentioned, A methyl group is especially preferable among these.

本発明の洗浄剤組成物中における(II)成分の含有量は、0.1〜5.0質量%が好ましく、0.1〜3.0質量%が更に好ましく、0.1〜1.0質量%が特に好ましい。(II)成分の含有量が0.1質量%以上で洗浄力が得られ、5.0質量%以下で目的の粘度が得られる。   The content of the component (II) in the cleaning composition of the present invention is preferably 0.1 to 5.0% by mass, more preferably 0.1 to 3.0% by mass, and 0.1 to 1.0%. Mass% is particularly preferred. Detergency is obtained when the content of the component (II) is 0.1% by mass or more, and the desired viscosity is obtained when the content is 5.0% by mass or less.

(c)成分の界面活性剤は、合計で、好ましくは0.1〜10.0質量%、より好ましくは0.3〜5.0質量%、最も好ましくは0.5〜3.0質量%含有される。   Component (c) surfactants in total are preferably 0.1 to 10.0% by mass, more preferably 0.3 to 5.0% by mass, and most preferably 0.5 to 3.0% by mass. Contained.

本発明の洗浄剤組成物は、B型粘度計を用いて20℃、回転数60rpm、60sの条件で測定した粘度が5〜210mPa・sの範囲に調製される。組成物の粘度が5mPa・s以上で付着滞留性を付与でき、210mPa・s以下で緻密で豊富な泡が得られる。   The detergent composition of the present invention has a viscosity measured in the range of 5 to 210 mPa · s using a B-type viscometer at 20 ° C., rotation speed 60 rpm, and 60 s. Adhesion retention can be imparted when the viscosity of the composition is 5 mPa · s or more, and dense and abundant bubbles can be obtained when the viscosity is 210 mPa · s or less.

本発明の洗浄剤組成物には、粘度の調整や、トリガー式のスプレーヤーで噴霧した際の起泡力、及び泡の緻密さを更に向上する成分として、(d)ベンゼン環を有するハイドロトロープ剤〔以下、(d)成分と記載する〕を配合することが出来る。(d)成分としては、例えばキシレンスルホン酸、トルエンスルホン酸、クメンスルホン酸、安息香酸、又はこれらのアルカリ金属塩が挙げられ、これらの中でも特にメタキシレンスルホン酸又はそのアルカリ金属塩が好ましい。   The cleaning composition of the present invention includes (d) a hydrotrope having a benzene ring as a component for further improving the viscosity, foaming power when sprayed with a trigger sprayer, and foam density. An agent [hereinafter referred to as component (d)] can be blended. Examples of the component (d) include xylene sulfonic acid, toluene sulfonic acid, cumene sulfonic acid, benzoic acid, and alkali metal salts thereof. Among these, metaxylene sulfonic acid or alkali metal salts thereof are particularly preferable.

本発明の洗浄剤組成物中における(d)成分の含有量は、0.1〜5.0質量%が好ましく、0.1〜3.0質量%が更に好ましく、0.1〜2.0質量%が特に好ましい。(d)成分の含有量が0.1質量%以上で起泡力が得られ、5.0質量%以下で組成物の粘度を目的の範囲内に調整することができる。   The content of the component (d) in the cleaning composition of the present invention is preferably 0.1 to 5.0% by mass, more preferably 0.1 to 3.0% by mass, and 0.1 to 2.0%. Mass% is particularly preferred. When the content of the component (d) is 0.1% by mass or more, foaming power is obtained, and when the content is 5.0% by mass or less, the viscosity of the composition can be adjusted within the target range.

本発明の洗浄剤組成物には、高い漂白洗浄力を付与することを目的として、(e)次亜塩素酸アルカリ金属塩〔以下、(e)成分と記載する〕を含有することができる。(e)成分の次亜塩素酸アルカリ金属塩としては、次亜塩素酸ナトリウム、次亜塩素酸カリウム等が挙げられ、特に次亜塩素酸ナトリウムが好ましい。次亜塩素酸ナトリウムは、製造上次亜塩素酸ナトリウムと当モルの塩化ナトリウムが混在するが、塩化ナトリウムが多量に存在する次亜塩素酸ナトリウムは貯蔵安定性を損なう場合があるため、予め塩化ナトリウムを低減化したものを用いることが好ましい。具体的には塩化ナトリウムを次亜塩素酸ナトリウムに対して10〜60モル%、好ましくは10〜40モル%のものが好適である。このような塩化ナトリウムを低減化した次亜塩素酸ナトリウムは、低食次亜塩素酸ナトリウムとして市販されている。本発明の洗浄剤組成物中における(e)成分の含有量は、0.1〜5.0質量%が好ましく、0.5〜4.0質量%が更に好ましく、1.0〜3.0質量%が特に好ましい。(e)成分の含有量が0.1質量%以上では充分な漂白力が得られ、5.0質量%以下では次亜塩素酸アルカリ金属塩の良好な安定性が得られる。   The detergent composition of the present invention can contain (e) an alkali metal hypochlorite (hereinafter referred to as component (e)) for the purpose of imparting high bleaching detergency. Examples of the alkali metal hypochlorite of component (e) include sodium hypochlorite and potassium hypochlorite, with sodium hypochlorite being particularly preferred. Sodium hypochlorite is mixed with sodium hypochlorite and equimolar sodium chloride in production, but sodium hypochlorite containing a large amount of sodium chloride may impair storage stability. It is preferable to use one with reduced sodium. Specifically, sodium chloride is 10 to 60 mol%, preferably 10 to 40 mol%, based on sodium hypochlorite. Such sodium hypochlorite with reduced sodium chloride is commercially available as low dietary sodium hypochlorite. The content of the component (e) in the cleaning composition of the present invention is preferably 0.1 to 5.0% by mass, more preferably 0.5 to 4.0% by mass, and 1.0 to 3.0. Mass% is particularly preferred. When the content of the component (e) is 0.1% by mass or more, sufficient bleaching power is obtained, and when it is 5.0% by mass or less, good stability of the alkali metal hypochlorite is obtained.

本発明の洗浄剤組成物には、次亜塩素酸アルカリ金属塩の貯蔵安定性を向上することを目的として、(f)アルカリ金属の水酸化物〔以下、(f)成分と記載する〕を配合することができる。(f)成分のアルカリ金属の水酸化物とは、液体洗浄剤組成物中に存在するアルカリ金属イオンとヒドロキシイオンとの組合せ、すなわち遊離アルカリを示し、他の対イオンとの組合せの場合はカウントされない。例えば別途有機酸を配合する場合は、アルカリ金属水酸化物として配合したとしても、有機酸の対イオンとなるため、アルカリ金属水酸化物としてカウントしない。(f)成分としては、水酸化ナトリウム、水酸化カリウム等が挙げられ、これらのうち水酸化ナトリウムが好ましい。なお、本発明において、組成物中の(f)成分の量はASTM D 2022−89記載の方法により測定される。すなわち、この方法は、漂白剤中の遊離アルカリ量を水酸化ナトリウム(NaOH)として測定するものであり、本発明においてもこの方法で得られた組成物中の遊離アルカリの量を組成物中の(f)成分の量とする。   In the cleaning composition of the present invention, for the purpose of improving the storage stability of alkali metal hypochlorite, (f) an alkali metal hydroxide (hereinafter referred to as component (f)) is added. Can be blended. The component (f) alkali metal hydroxide represents a combination of an alkali metal ion and a hydroxy ion present in the liquid detergent composition, that is, a free alkali, and is counted in the case of a combination with another counter ion. Not. For example, when an organic acid is added separately, even if it is added as an alkali metal hydroxide, it is not counted as an alkali metal hydroxide because it becomes a counter ion of the organic acid. (F) As a component, sodium hydroxide, potassium hydroxide, etc. are mentioned, Among these, sodium hydroxide is preferable. In the present invention, the amount of component (f) in the composition is measured by the method described in ASTM D 2022-89. That is, in this method, the amount of free alkali in the bleaching agent is measured as sodium hydroxide (NaOH). Also in the present invention, the amount of free alkali in the composition obtained by this method is determined in the composition. (F) The amount of component.

本発明の洗浄剤組成物における(f)成分の含有量は、0.1〜1.0質量%が好ましく、0.2〜0.8質量%が更に好ましく、0.3〜0.7質量%が特に好ましい。(f)成分の含有量が0.1質量%以上では良好な次亜塩素酸アルカリ金属塩の安定性が得られ、1.0質量%以下では良好な安定性が得られる。   The content of the component (f) in the cleaning composition of the present invention is preferably 0.1 to 1.0% by mass, more preferably 0.2 to 0.8% by mass, and 0.3 to 0.7% by mass. % Is particularly preferred. When the content of the component (f) is 0.1% by mass or more, good alkali metal hypochlorite stability is obtained, and when 1.0% by mass or less, good stability is obtained.

また、本発明の洗浄剤組成物には、増粘助剤として無機塩を含有することができる。具体的には、塩化ナトリウム、炭酸ナトリウム、硫酸ナトリウム、リン酸三ナトリウム等が挙げられ、含有量としては0.1〜5.0質量%が好ましい。無機塩の含有量が0.1質量%以上では良好な粘度が得られ、5.0質量%以下では良好な起泡性が得られる。   Further, the cleaning composition of the present invention can contain an inorganic salt as a thickening aid. Specific examples include sodium chloride, sodium carbonate, sodium sulfate, and trisodium phosphate, and the content is preferably 0.1 to 5.0% by mass. When the content of the inorganic salt is 0.1% by mass or more, a good viscosity is obtained, and when the content is 5.0% by mass or less, a good foaming property is obtained.

本発明の洗浄剤組成物は、その他の任意成分として、香料成分を含有することができる。香料成分としては特に制限されないが、組成物中に次亜塩素酸アルカリ金属塩を含有させた場合、安定性を損なう恐れがあるので、配合成分と含有量には注意を要する。次亜塩素酸塩系に配合可能な香料成分の例としては、特開昭50−74581号公報及び特開昭62−205200号公報を参考にすることができ、単体香料及びそれらを組合せた配合香料であってもよい。香料は通常、組成物中に0.001〜0.5質量%含有される。   The cleaning composition of the present invention can contain a fragrance component as another optional component. Although it does not restrict | limit especially as a fragrance | flavor component, When an alkali metal hypochlorite is contained in a composition, since there exists a possibility of impairing stability, a caution is required for a compounding component and content. As examples of perfume ingredients that can be blended into hypochlorite systems, reference can be made to JP-A-50-74581 and JP-A-62-205200. Perfume may be used. A fragrance | flavor is normally contained in 0.001-0.5 mass% in a composition.

本発明の洗浄剤組成物の残部は水であり、保存安定性の上で、微量に存在する金属イオンなどを除去したイオン交換水や蒸留水が好ましい。水の含有量は保存安定性の点から、組成物中80〜98質量%、更に90〜98質量%が好ましい。また、洗浄剤組成物のpHは特に制限されないが、組成物中に次亜塩素酸アルカリ金属塩を含有させた場合、保存安定性及び漂白効果の点から20℃における組成物のpHを12.5〜13.5に調整することが好ましい。   The balance of the cleaning composition of the present invention is water, and ion-exchanged water or distilled water from which metal ions and the like that are present in a trace amount are removed is preferable in terms of storage stability. The water content is preferably 80 to 98% by mass, more preferably 90 to 98% by mass in the composition from the viewpoint of storage stability. The pH of the cleaning composition is not particularly limited, but when an alkali metal hypochlorite salt is contained in the composition, the pH of the composition at 20 ° C. is 12. It is preferable to adjust to 5 to 13.5.

本発明の洗浄剤組成物の製品形態としては、造泡機構を備えた吐出容器に充填してなる、容器入り洗浄剤の形態が好ましい。例えば、本発明の洗浄剤組成物を収納する容器本体と、その容器本体内に収納された洗浄剤組成物を吐出させる造泡機構を有する吐出装置と、を備える洗浄剤製品が挙げられる。吐出装置としては、本発明の洗浄剤組成物を泡状にして噴霧することができるトリガー式スプレー、具体的には1回の操作で0.5〜2mLの組成物を吐出し、泡を形成する機構を備えたトリガーが好ましく、さらに具体的には特開2002−68265号公報の図1及び特開2004−261790号公報に示される機構のトリガー式スプレーヤーを使用することが特に好ましい。また、本発明の洗浄剤組成物を使用する際には対象物1m2に対して5〜15gの割合で噴霧することが好ましい。 The product form of the cleaning composition of the present invention is preferably in the form of a container-containing cleaning agent that is filled in a discharge container equipped with a foam-forming mechanism. For example, a detergent product comprising a container main body that stores the cleaning composition of the present invention and a discharge device having a foam-forming mechanism that discharges the cleaning composition stored in the container main body can be mentioned. The discharge device is a trigger type spray that can spray the detergent composition of the present invention in the form of foam. Specifically, 0.5 to 2 mL of the composition is discharged in one operation to form bubbles. A trigger provided with a mechanism is preferable, and more specifically, it is particularly preferable to use a trigger type sprayer having a mechanism shown in FIG. 1 of JP-A-2002-68265 and JP-A-2004-261790. Moreover, when using the cleaning composition of this invention, it is preferable to spray at the ratio of 5-15g with respect to 1 m < 2 > of target objects.

表1〜4に示す液体洗浄剤組成物を調製し、それらの泡の付着滞留性、泡比容、及び粘度を下記の方法で評価した。結果を表1〜4に示す。尚、試料1−1〜1−19及び2−1〜2−8は、アルカリ剤として水酸化ナトリウムを用いることで25℃のpHを12.9に、また試料2−9〜2−19はpH13.0に調整した。 Liquid detergent compositions shown in Tables 1 to 4 were prepared, and the adhesion and retention properties of these bubbles, the foam specific volume, and the viscosity were evaluated by the following methods. The results are shown in Tables 1-4. Samples 1-1 to 1-19 and 2-1 to 2-8 use sodium hydroxide as an alkaline agent, so that the pH at 25 ° C. is 12.9, and samples 2-9 to 2-19 are The pH was adjusted to 13.0.

<泡の付着滞留性評価>
表1〜4に調製した液体洗浄剤組成物を花王(株)製カビとりハイタートリガー(噴霧量1g/回)を用いて、10cm×10cmの陶器タイルが張られた浴室壁のタイル目地に沿って10cm離れたところから、横幅10cmの範囲内に横に4回噴霧し、泡が付着した位置から1分後に泡が垂れ落ちた位置までの面積を算出した。数値が小さい程、付着滞留性が高く良好な効果感が得られる。なお、泡立ちが少なく、付着滞留性の評価を行うことができなかった組成物については表中、「−」として表示した。
<Evaluation of adhesion and retention of foam>
Using the liquid detergent composition prepared in Tables 1 to 4 by Kao Co., Ltd. mold remover Higher trigger (spray amount 1 g / time), along the tile joints of the bathroom wall with 10 cm x 10 cm ceramic tiles. Then, spraying was performed four times horizontally within a range of 10 cm in width, and the area from the position where the bubbles adhered to the position where the bubbles dropped after 1 minute was calculated. The smaller the value, the higher the adhesion retention and the better effect. In addition, in the table | surface, it displayed as "-" about the composition with few foaming and which could not evaluate adhesion residence property.

<泡比容の測定>
表1〜4に調製した液体洗浄剤組成物を花王(株)製カビとりハイタートリガー(噴霧量1g/回)を用いて、200mLのメスシリンダーに10回スプレーした時に出来る泡の容量(mL)を読みとる。また、その時の噴霧量(g)を下2ケタ天秤を用いて測定し、泡比容(mL/g)=泡の容量(mL)/噴霧量(g)の計算式で算出した。数値が大きい程、良好な効果感や視認性が得られる。
<Measurement of foam specific volume>
Foam volume (mL) when the liquid detergent composition prepared in Tables 1 to 4 is sprayed 10 times into a 200 mL graduated cylinder using a mold catcher made by Kao Corporation (spray amount 1 g / time). Is read. Further, the spray amount (g) at that time was measured using a lower two-digit balance, and was calculated by the following formula: foam specific volume (mL / g) = foam volume (mL) / spray amount (g). The larger the value, the better the effect and visibility.

<粘度の測定>
表1〜4に調製した液体洗浄剤組成物を、B型粘度計(TOKIMEC製)を使用して、組成物の温度を20℃、回転数を60rpm、測定時間を60秒の条件で測定した。
<Measurement of viscosity>
The liquid detergent compositions prepared in Tables 1 to 4 were measured using a B-type viscometer (manufactured by TOKIMEC) at a temperature of 20 ° C., a rotation speed of 60 rpm, and a measurement time of 60 seconds. .

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・化合物1:溶媒中でポリエチレングリコール1540(一般式(1)において、AOがエチレンオキシ基、X1、X2がともに水素原子、n=35のもの、三洋化成工業(株)製)と、上記ポリエチレングリコール1540のモル数に対して1.8倍モルの無水硫酸を反応させて、水酸化ナトリウムで中和することで化合物1を得た。〔(a)成分と(b)成分のモル比は理論値で(a)成分/(b)成分が1/4.5になると推測される。〕。
・デシル硫酸エステルナトリウム:カルコール1098(デシルアルコール、花王(株)製)を硫酸化したサンプル、花王(株)製。
・ドデシル硫酸エステルナトリウム:エマール0、花王(株)製。
・カプリン酸塩:ルナック10−98のナトリウム塩、花王(株)製。
・ラウリン酸塩:ルナックL−98のナトリウム塩、花王(株)製。
・脂肪酸塩の混合物:ルナックL−70(カプリン酸10,ラウリン酸76、ミリスチン酸14の組成質量比である脂肪酸の混合物)のナトリウム塩、花王(株)製。
・ラウリルベンゼンスルホン酸ナトリウム:ネオペレックスG−25、花王(株)製。
・デシルジメチルアミンオキサイド:ファーミン DM1098(ジメチルデシルアミン、花王(株)製)と過酸化水素水(日本パーオキサイド社製)から合成したサンプル。
・ドデシルジメチルアミンオキサイド:アンヒトール20N、花王(株)製。
・テトラデシルジメチルアミンオキサイド:ファーミン DM4098(ジメチルミリスチルアミン、花王(株)製)と過酸化水素水(日本パーオキサイド社製)から合成したサンプル。
・ヘキサデシルジメチルアミンオキサイド:ファーミン DM6098(ジメチルパルミチルアミン、花王(株)製)と過酸化水素水(日本パーオキサイド社製)から合成したサンプル。
・次亜塩素酸ナトリウム:次亜塩素酸ナトリウム、南海化学工業(株)製。
・メタキシレンスルホン酸塩:ナトリウム塩、SXA−60、三菱瓦斯化学(株)製。
・水酸化ナトリウム:32%液体苛性ソーダ、南海化学工業(株)製。(表中の数値は、遊離した水酸化ナトリウム量を示す。)
・塩化ナトリウム:シグマアルドリッチジャパン(株)製、試薬1級。
Compound 1: polyethylene glycol 1540 in a solvent (in the general formula (1), AO is an ethyleneoxy group, X 1 and X 2 are both hydrogen atoms, n = 35, manufactured by Sanyo Chemical Industries, Ltd.) Compound 1 was obtained by reacting 1.8 times moles of sulfuric anhydride with respect to the number of moles of polyethylene glycol 1540 and neutralizing with sodium hydroxide. [The molar ratio of the (a) component to the (b) component is a theoretical value, and it is estimated that the (a) component / (b) component is 1 / 4.5. ].
Sodium decyl sulfate ester: A sample obtained by sulfating calcoal 1098 (decyl alcohol, manufactured by Kao Corporation), manufactured by Kao Corporation.
-Sodium dodecyl sulfate ester: Emar 0, manufactured by Kao Corporation.
Caprate: Sodium salt of Lunac 10-98, manufactured by Kao Corporation.
Laurate: Sodium salt of Lunac L-98, manufactured by Kao Corporation.
-Fatty acid salt mixture: Sodium salt of Lunac L-70 (a mixture of fatty acids with a compositional mass ratio of capric acid 10, lauric acid 76, myristic acid 14), manufactured by Kao Corporation.
-Sodium laurylbenzenesulfonate: Neoperex G-25, manufactured by Kao Corporation.
Decyldimethylamine oxide: A sample synthesized from Pharmin DM1098 (dimethyldecylamine, manufactured by Kao Corporation) and hydrogen peroxide (manufactured by Nippon Peroxide).
-Dodecyldimethylamine oxide: Anhithol 20N, manufactured by Kao Corporation.
Tetradecyldimethylamine oxide: A sample synthesized from Farmin DM4098 (dimethylmyristylamine, manufactured by Kao Corporation) and hydrogen peroxide (manufactured by Nippon Peroxide).
Hexadecyldimethylamine oxide: A sample synthesized from Farmin DM6098 (dimethyl palmitylamine, manufactured by Kao Corporation) and hydrogen peroxide (manufactured by Nippon Peroxide).
-Sodium hypochlorite: Sodium hypochlorite, manufactured by Nankai Chemical Industry.
Metaxylene sulfonate: sodium salt, SXA-60, manufactured by Mitsubishi Gas Chemical Company, Inc.
Sodium hydroxide: 32% liquid caustic soda, manufactured by Nankai Chemical Industries, Ltd. (The numbers in the table indicate the amount of free sodium hydroxide.)
Sodium chloride: Sigma-Aldrich Japan Co., Ltd., reagent grade 1.

表1の試験No.1−4、1−6、1−8、1−10、表2の試験No.1−17、1−19、表3の試験No.2−2、2−3、2−6、2−7、2−10、及び表4の試験No.2−13、2−14、2−15、2−16の組成物について、化合物1の代わりに下記化合物2及び化合物3を総配合濃度1%、モル比で化合物2/化合物3が1/1〜1/99となるように配合比率を変化させて配合した組成物でも同等の効果が得られる。
・化合物2:メタノールにエチレンオキサイドを付加させたものに無水硫酸を反応させて、水酸化ナトリウムで中和したサンプル(エチレンオキシ基が平均で23モル、方末端が全て硫酸エステル化されている)。
・化合物3:溶媒中でポリエチレングリコール1540(一般式(1)において、AOがエチレンオキシ基、X1、X2がともに水素原子、n=35のもの、三洋化成工業(株)製)と、上記ポリエチレングリコール1540のモル数に対して2.05倍モルの無水硫酸を反応させて、水酸化ナトリウムで中和したサンプル(ポリエチレングリコールの両末端は全て硫酸エステル化されている)。
Test No. in Table 1 1-4, 1-6, 1-8, 1-10, Test No. in Table 2. 1-17, 1-19, Test No. in Table 3. 2-2, 2-3, 2-6, 2-7, 2-10, and Test No. in Table 4. For the compositions 2-13, 2-14, 2-15, and 2-16, instead of compound 1, the following compound 2 and compound 3 were mixed at a total blending concentration of 1% and molar ratio of compound 2 / compound 3 was 1/1. An equivalent effect can be obtained even with a composition formulated by changing the blending ratio so as to be ˜1 / 99.
Compound 2: Sample obtained by reacting methanol with ethylene oxide and reacting with anhydrous sulfuric acid and neutralizing with sodium hydroxide (average of 23 moles of ethyleneoxy group, all terminals are sulfated) .
Compound 3: Polyethylene glycol 1540 in a solvent (in the general formula (1), AO is an ethyleneoxy group, X 1 and X 2 are both hydrogen atoms, n = 35, manufactured by Sanyo Chemical Industries, Ltd.) A sample obtained by reacting 2.05-fold moles of sulfuric anhydride with respect to the number of moles of polyethylene glycol 1540 and neutralizing with sodium hydroxide (both ends of polyethylene glycol are all sulfated).

Claims (5)

(a)下記一般式(1)で表される化合物、(b)下記一般式(2)で表される化合物、及び(c)界面活性剤、を含有し、且つB型粘度計を用いて20℃、回転数60rpm、60sの条件で測定した粘度が5〜210mPa・sである洗浄剤組成物。
1−O(AO)n−X2 (1)
2−O(AO)n−X2 (2)
〔式中、AOは炭素数2〜4のアルキレンオキシ基、nはアルキレンオキシ基の平均付加モル数を示し、5〜1000の数である。また、一般式(1)及び一般式(2)のAOの総モル数に対して50モル%以上がエチレンオキシ基である。X1は水素原子又は炭素数1〜6のアルキル基であり、X2は、−SO3H、−CH2COOH、あるいはこれらのアルカリ金属塩を示す。〕
(A) a compound represented by the following general formula (1), (b) a compound represented by the following general formula (2), and (c) a surfactant, and using a B-type viscometer A detergent composition having a viscosity of 5 to 210 mPa · s measured under the conditions of 20 ° C., rotation speed 60 rpm, and 60 s.
X 1 -O (AO) n -X 2 (1)
X 2 -O (AO) n -X 2 (2)
[Wherein, AO represents an alkyleneoxy group having 2 to 4 carbon atoms, and n represents an average number of added moles of the alkyleneoxy group, and is a number of 5 to 1000. Moreover, 50 mol% or more is an ethyleneoxy group with respect to the total mole number of AO of General formula (1) and General formula (2). X 1 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and X 2 represents —SO 3 H, —CH 2 COOH, or an alkali metal salt thereof. ]
(a)成分/(b)成分がモル比で1/1〜1/1000である請求項1記載の洗浄剤組成物 The cleaning composition according to claim 1, wherein component (a) / component (b) is 1/1 to 1/1000 in molar ratio. 更に(d)ベンゼン環を有するハイドロトロープ剤を含有する請求項1又は2記載の洗浄剤組成物。 The cleaning composition according to claim 1 or 2, further comprising (d) a hydrotrope having a benzene ring. 更に(e)次亜塩素酸アルカリ金属塩、(f)アルカリ金属の水酸化物を含有する請求項1〜3何れか記載の洗浄剤組成物。 The detergent composition according to any one of claims 1 to 3, further comprising (e) an alkali metal hypochlorite salt and (f) an alkali metal hydroxide. 請求項1〜4何れか記載の洗浄剤組成物を収納する容器本体と、その容器本体内に収納された洗浄剤組成物を吐出させる造泡機構を有する吐出装置と、を備える洗浄剤製品。 A cleaning agent product comprising: a container body that stores the cleaning composition according to any one of claims 1 to 4; and a discharge device that has a foam-forming mechanism that discharges the cleaning composition stored in the container body.
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WO2009001474A1 (en) * 2007-06-26 2008-12-31 Kao Corporation Detergent composition
JP2010235722A (en) * 2009-03-31 2010-10-21 Kao Corp Liquid bleaching agent composition
JP2010280866A (en) * 2009-06-08 2010-12-16 Niitaka:Kk Pretreatment detergent composition and method for washing plastic container
JP2017036346A (en) * 2015-08-06 2017-02-16 花王株式会社 Liquid detergent composition for tableware
WO2017047170A1 (en) * 2015-09-14 2017-03-23 住友電気工業株式会社 Composition for mineral oil cleaning and method for cleaning mineral oil-adhering article using same
WO2018139389A1 (en) * 2017-01-25 2018-08-02 花王株式会社 Liquid detergent composition
JP2019156929A (en) * 2018-03-09 2019-09-19 株式会社ニイタカ Foaming cleaner composition and cleaning method
JP2019199619A (en) * 2019-08-27 2019-11-21 株式会社Adeka Cleaning method of article to be cleaned

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Cited By (10)

* Cited by examiner, † Cited by third party
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WO2009001474A1 (en) * 2007-06-26 2008-12-31 Kao Corporation Detergent composition
JP2010235722A (en) * 2009-03-31 2010-10-21 Kao Corp Liquid bleaching agent composition
JP2010280866A (en) * 2009-06-08 2010-12-16 Niitaka:Kk Pretreatment detergent composition and method for washing plastic container
JP2017036346A (en) * 2015-08-06 2017-02-16 花王株式会社 Liquid detergent composition for tableware
WO2017047170A1 (en) * 2015-09-14 2017-03-23 住友電気工業株式会社 Composition for mineral oil cleaning and method for cleaning mineral oil-adhering article using same
CN107922891A (en) * 2015-09-14 2018-04-17 住友电气工业株式会社 Mineral oil composition for cleaning and using its cleaning be attached with mineral oil article method
JPWO2017047170A1 (en) * 2015-09-14 2018-06-28 住友電気工業株式会社 Composition for cleaning mineral oil and cleaning method for depositing mineral oil using the same
WO2018139389A1 (en) * 2017-01-25 2018-08-02 花王株式会社 Liquid detergent composition
JP2019156929A (en) * 2018-03-09 2019-09-19 株式会社ニイタカ Foaming cleaner composition and cleaning method
JP2019199619A (en) * 2019-08-27 2019-11-21 株式会社Adeka Cleaning method of article to be cleaned

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