JPS5813700A - Detergent composition - Google Patents
Detergent compositionInfo
- Publication number
- JPS5813700A JPS5813700A JP11169381A JP11169381A JPS5813700A JP S5813700 A JPS5813700 A JP S5813700A JP 11169381 A JP11169381 A JP 11169381A JP 11169381 A JP11169381 A JP 11169381A JP S5813700 A JPS5813700 A JP S5813700A
- Authority
- JP
- Japan
- Prior art keywords
- detergent
- acid
- amphoteric
- cleaning
- water
- 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0084—Antioxidants; Free-radical scavengers
-
- 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
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
-
- 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
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3773—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
-
- 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
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3796—Amphoteric polymers or zwitterionic polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biochemistry (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Detergent Compositions (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は特定の両性ポリマーを含有する洗浄#1lIl
成物に閤する。更に詳しくは、カチオン性ビニルモノ!
−とアニオン性ビニルモノマーを共重合して得た、特定
の両性ポリマーを含有せしめるととKよって、洗浄性能
が大幅に向上した洗浄剤組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention provides cleaning solutions containing specific amphoteric polymers.
Sprinkle on finished product. For more details, see cationic vinyl mono!
The present invention relates to a detergent composition whose cleaning performance is significantly improved by containing a specific amphoteric polymer obtained by copolymerizing K and an anionic vinyl monomer.
従来、ポリマーは種々の目的で洗浄剤系の添加剤として
用いられてきた。たとえば、増粘剤、安定化剤、保li
コロイド剤、ビルグー、柔軟艦カプセル化剤、濁り剤、
パール化剤、皮膚及び唱髪保膜剤等として、洗浄剤に添
加した系は知られている。併しながらそれらの用い方は
、高分子の特性として一般Kil識されてきた性質な単
に利用したものにすぎなかった。Traditionally, polymers have been used as additives in detergent systems for a variety of purposes. For example, thickeners, stabilizers,
Colloidal agent, bilgoo, flexible carrier encapsulating agent, clouding agent,
Systems added to detergents as pearlizing agents, skin and hair retention agents, etc. are known. However, their use was merely to take advantage of the generally recognized properties of polymers.
ところが、本発明者らは洗浄剤系へのポリマーめ新規な
応用に関し検討するうちに、驚くぺ會ことに、特定のポ
リ!−が、41に界面活性剤と共存するととにより、洗
浄剤組成物の洗浄性能等を大幅に向上せしめ得る事実を
見出し、本発明を完成するに至った。However, as the present inventors investigated new applications for polymers in detergent systems, they were surprised to find that a specific polyester! The present inventors have discovered the fact that the cleaning performance of a cleaning composition can be significantly improved by coexisting 41 with a surfactant, and have completed the present invention.
すなわち、本発明はカチオン1ビニルモノマーとアニオ
ン性ビニルモノマーの共重合により得られる、特定の両
性ポリマーを洗浄剤組成物中に含有せしめてなるもので
あるが、その洗浄効果からみて、本発明における両性ポ
リ!−の効果は、分散効果等の従来知られている洗浄と
は直接関係のない高分子界面活性剤の効果とは。That is, in the present invention, a specific amphoteric polymer obtained by copolymerizing a cationic vinyl monomer and an anionic vinyl monomer is contained in a cleaning composition. Bisexual! - The effects of polymer surfactants, such as dispersion effects, are not directly related to conventional cleaning.
全く異質のものである。It is completely different.
即ち本発F14に使用される両性共重金ポリ!−は重合
性不飽和基を有するアニオン性ビニルモノマーと重合性
不飽和基を有するカチオン性ビニルモノマーとを1〜?
9:??〜1、好ましくは20〜80:80〜20のモ
ル比で共重合してなるものであるが、かかる共重合両性
ポリマーは次の一般式(1)であられすことが出来る。In other words, the amphoteric heavy metal polyester used in the original F14! - represents an anionic vinyl monomer having a polymerizable unsaturated group and a cationic vinyl monomer having a polymerizable unsaturated group from 1 to ?
9:? ? -1, preferably 20-80:80-20, and such a copolymerized amphoteric polymer can be represented by the following general formula (1).
式中
X : −H−又は−aooir
Y : ”Hs −OH2+−OH@0OOH−又は−
〇HaIf。In the formula, X: -H- or -aooir Y: "Hs -OH2+-OH@0OOH- or -
〇HaIf.
■ 叉は−001210−011,80,II 。■ Or -001210-011,80,II.
011゜
1+
ム : −OH,−誠−1゜
訊* (X−)
(Je Rye Rsはo、〜a、の7にキル基、X″
″はハロゲン又はジエチル硫酸等の陰イオン以下同じ)
町
−OR,−N
!
1
(−I B、はC1〜C3のアルキル基)(R4はC1
〜C3のアルキル基)
(14m l@ s Reはcl〜O易のアルキル基、
y、tt2〜4のll数)
町
(R4,Ill、はOI〜O8のアルキル基、p、は2
〜4の整数)
Rテ R,8口
(R@ * Ry * ’R@ s *@はH又はC−
1R16s RH+翼lはC3〜C1のアルキル基)
11
薗
(!IHe R84e都はC1〜C1のアルキル基、P
、は2〜4の整数)
R1畠
冒
1日114
(IIts*鳳、はC1〜osのアルキル基、P、は2
″II)
RIV Le R,、Ru (x−)(”I@〜
都は■又は011g 、Ig e mg m−は’O,
〜o1)7 ルa? ルi!tI)尚罷は0.01〜0
.99の任意の数、pは5〜10000f)ll数でX
e Y * Zは7にカリ金属あることも出来る
上記一般式(I)で表わされる本発IKかかる両□性ポ
リ!−は、カチオン性ビニルモノ!−とアより得られる
。これらの両性ポリl−は全知の方法で調造され得る。011゜1+mu: -OH, -Makoto-1゜Question* (X-) (Je Rye Rs is a kill group at 7 of o, ~a, and X''
'' is a halogen or an anion such as diethyl sulfate, the same applies below) Machi -OR, -N! 1 (-I B is a C1 to C3 alkyl group) (R4 is C1
~C3 alkyl group) (14ml@s Re is an alkyl group of Cl~O,
y, tt2-4 ll number) town (R4, Ill is an alkyl group of OI-O8, p is 2
~4 integer) Rte R, 8 mouths (R@ * Ry * 'R@ s *@ is H or C-
1R16s RH + wing l is a C3-C1 alkyl group) 11 Sono (!IHe R84e is a C1-C1 alkyl group, P
, is an integer of 2 to 4) R1 Hatanobu 1 day 114 (IIts*Otori is an alkyl group of C1 to os, P is 2
"II) RIV Le R,, Ru (x-) ("I@〜
Capital is ■ or 011g, Ige mg m- is 'O,
~o1)7 Rua? Le i! tI) Scratch is 0.01~0
.. 99 arbitrary number, p is 5 to 10000f)ll number
e Y * Z is an amphoteric polyamide expressed by the above general formula (I), in which potash metal can be present at 7. - is a cationic vinyl mono! It is obtained from − and a. These amphoteric polyl- may be prepared by known methods.
即ち溶媒として水が一般的に使用され、屍始削としては
ベルオキソニ硫酸カリクムやベルオキソニ硫酸カリクム
ー皿硫酸水素ナトリクム、過酸化水素−ν・2+系等が
用(〜られ得る。得られた共重合体はそのままか、精製
して使用される。精側方法としては、透斬法や再沈層流
がある。That is, water is generally used as a solvent, and potassium beroxonisulfate, potassium potassium hydrogensulfate, hydrogen peroxide-v. It is used either as it is or after being purified.Processing methods include the permeation method and the reprecipitation laminar flow method.
即ち本発#4の共重金両性ボy−q−はノミー構造単位
モノマー構造単位
とが1〜??:99〜1、好ましくは20〜mossO
〜2oのモル比で線状で不規則に配列した分子量t、o
o o〜31000.000の両性ポリ!−であρて
、上記アニオン性ビニルモノマーとカチオン性ビニル七
ノi−との所定の割合の混合物を水中で重合開始剤を用
い通常窒素気流下で重合せしめて得られる。重合温度+
1一般に富温〜?O’Cで、2〜2パ′□1・4時間反
応を行ない、好ましくはHe0OO”−1,QOOeO
OQの分子量の共重合体が得られる。重合は溶液重合で
も塊状重合でもよい、又得られた重合体はアルー身ア々
ンを反応させて塩とすることも出来る。That is, the coheavy metal amphoteric boy-q- of the present invention #4 has a nomie structural unit and a monomer structural unit of 1 to 1? ? :99-1, preferably 20-mossO
Linear and irregularly arranged molecular weights t, o with a molar ratio of ~2o
o o~31000.000 amphoteric poly! - and is obtained by polymerizing a mixture of the above-mentioned anionic vinyl monomer and cationic vinyl monomer in a predetermined ratio in water using a polymerization initiator, usually under a nitrogen stream. Polymerization temperature +
1. Tomi-on in general? The reaction is carried out for 2 to 2 days at O'C for 1.4 hours, preferably He0OO''-1,QOOeO
A copolymer with a molecular weight of OQ is obtained. The polymerization may be carried out by solution polymerization or bulk polymerization, and the obtained polymer can also be made into a salt by reacting with Aru-mi Aman.
使用するアニオン性モノ!−としては、重合性不飽1g
基を有するアニオン性モノマーの全てが適用され得る0
例えばアクリル酸、メタアタリル酸、イタコン酸、アコ
ニット酸、ヒドロキシアクリル酸、無水iレイン酸、7
マ〜ル酸、ビニルスルホン酸、アリルスルホン酸、メタ
アリルスルホン酸、スチレンスルホン酸、2−アクリ・
ルアオド−2メチルプロパンスルホン酸等fが挙げられ
る・
使用するカチオン性七ツマ−も、重合性不飽和基を有す
るものであればよく、2−ビニルピリジン、4−ビニル
ピリジン、ジメチルアミノエチルメタアクリレート、ジ
ェチルアミノエチルメタアタリレー□ト、ジブ駄ビルア
建ノエチル・11
)#ア19レート、□、、ジメチルアンノブ菅ピルメタ
アク゛リルア建ド、アリルジメチルアミン、アリルジエ
チルアきン、アリルジブ■ピルア建ン、メタアリルジメ
チルアセン、メタアリルジエチルアミン、メタアリルジ
プロピルアミン及びこれらのメチル、エチル又はプロピ
ル化物等が挙げられる。Anionic things to use! - is 1 g of polymerizable unsaturated
All anionic monomers with groups 0 can be applied.
For example, acrylic acid, metatallylic acid, itaconic acid, aconitic acid, hydroxyacrylic acid, oleic anhydride, 7
Maric acid, vinyl sulfonic acid, allyl sulfonic acid, methalylsulfonic acid, styrene sulfonic acid, 2-acrylic acid,
2-methylpropanesulfonic acid, etc. The cationic seven-mer used may also be one having a polymerizable unsaturated group, such as 2-vinylpyridine, 4-vinylpyridine, dimethylaminoethyl methacrylate. , diethylaminoethyl meta-alylate □, dibutavil-based noethyl 11) #a19-late, □, , dimethylaminoethyl meta-alylate, allyl dimethylamine, allyl diethyl aquine, allyl dib■ Examples include pyruacene, methalyldimethylacene, methalyldiethylamine, methalyldipropylamine, and methyl, ethyl, or propylated products thereof.
本発明の洗浄剤履成物は上記両性ポリマーを一般KO,
01〜10重量%、好ましくは0.05〜5%含有する
。The detergent footwear of the present invention uses the above amphoteric polymer as general KO,
01 to 10% by weight, preferably 0.05 to 5%.
又洗浄鋼組成物中には洗滲成分として界面活性剤を含有
するが、本発明で用いることのできる界面活性剤は通常
のアニオン性、非イオン性、カチオン性、両性界面活性
剤が、その使用目的に応じて使用される。かかる界面活
性剤としてはアルキル硫酸塩、アル中ルベンゼンスルホ
ン酸塩、アルキルポリオキシエチレン硫酸塩、アルファ
オレフィンスルホン酸塩、アルカンスルホン酸塩、アル
キルグリセリルエーテルスルホン酸塩、アルキル又はア
ルケニルカルボン酸塩、アルケニルコハクll塩、M−
yシルずル;シネート、アルキルポリオキシエチレン★
ルぽキシメチル化物の塩、アルキルリン酸エステル塩等
のアニオン性界面活性剤、脂肪酸ジエタノールア建ド、
ジメチルアルキルアセンオキシド、アルキルポリオキシ
エチレン、アル中ルアリールポリ矛命ジエチレン等の非
イオン性界両活性札アル中ルトリメチルアンモニウム塩
、シアル中ルシメチルアンモニウム塩、アルキル−(N
−ヒトW午ジエチル)ジメチルアンモニウム塩等のカチ
オン性界面活性剤、アルキルイミダゾール誘導体、ジメ
チルアルキルベメイン、ジメチルアルキルスルホベタイ
ン等の両性界面活性剤等が挙げられるが、本発@に係る
両性ポリマーはこれらの界面活性剤に対し0.02〜5
0重量%、好ましくは0.2S〜25重量%の割合で使
用される。尚界面活性剤量は洗浄剤の使用目的に応じて
適尚量が使用出来、本発明の実施に轟っては界面活性剤
を使用しないこともあり得る。In addition, the cleaning steel composition contains a surfactant as a cleaning component, and the surfactants that can be used in the present invention include ordinary anionic, nonionic, cationic, and amphoteric surfactants. It is used depending on the purpose of use. Such surfactants include alkyl sulfates, alkylbenzene sulfonates, alkyl polyoxyethylene sulfates, alpha olefin sulfonates, alkanesulfonates, alkyl glyceryl ether sulfonates, alkyl or alkenyl carboxylates, alkenyl Amber ll salt, M-
y Silzul; Cinate, alkyl polyoxyethylene★
Anionic surfactants such as lupoxymethylated salts, alkyl phosphate ester salts, fatty acid diethanolate,
Dimethylalkyl acene oxide, alkylpolyoxyethylene, arylpolydiethylene in alkali, etc.
Examples include cationic surfactants such as dimethylammonium salt, amphoteric surfactants such as alkylimidazole derivatives, dimethylalkylbemaine, and dimethylalkylsulfobetaine, but the amphoteric polymer according to the present invention 0.02-5 for these surfactants
It is used in a proportion of 0% by weight, preferably 0.2S to 25% by weight. Note that an appropriate amount of surfactant can be used depending on the intended use of the cleaning agent, and if the present invention is carried out, no surfactant may be used.
尚本発明の洗浄Mal成物のその他の成分としてはモノ
アルコール、ジアルコール、グリ竜リン、エチレングリ
コール峰ノブチルエーテル、ジエチレ7/9コール場ツ
メチルエーテル等の溶剤、ベンゼンスルホン酸塩、パラ
ドルエンスルホン酸塩、メタキシレンスルホン酸塩、尿
素等のヒドロトロープ剤、キレート剤、紡腐削、色素、
香料、紫外線吸収削、酸化安定剤、濁り剤、増粘剤等が
使用される。又本発、明の洗浄剤組成物の形態は水を加
えて液体洗剤とするのが一般的であるが、固体洗浄剤と
することも出来る。Other components of the cleaning Mal composition of the present invention include monoalcohols, dialcohols, glycol phosphorus, solvents such as ethylene glycol butyl ether, diethyl 7/9 methyl ether, benzenesulfonates, and paradolenesulfone. Hydrotropes such as acid salts, metaxylene sulfonates, urea, chelating agents, spinning corrosion, pigments,
Fragrances, UV absorbers, oxidation stabilizers, clouding agents, thickeners, etc. are used. Further, although the detergent composition of the present invention is generally in the form of a liquid detergent by adding water, it can also be made into a solid detergent.
本発明の洗浄剤組成物は、金属、機械、船舶、織物、ガ
ラス器具、食品、食器、繊維、家庭用品等の洗浄剤及び
シャンプー基材として使用出来る。かかる洗浄剤に畳−
求される性能としては洗浄力、増泡性、すすぎ性(泡ぎ
れ性、手の感触等)等があげられるが、本発@に於ては
両性ポリ!−の添加量が増す穆洗浄力等の性能が原着に
向上する。併しながら余り大量に添加すると安電性、粘
度等の製品―性に悪影響を及ぼす恐れがある。The cleaning composition of the present invention can be used as a cleaning agent for metals, machines, ships, textiles, glassware, foods, tableware, textiles, household goods, etc., and as a shampoo base material. Tatami-
Required performance includes cleaning power, foam increasing ability, rinsing performance (foaming properties, hand feel, etc.), but in this development @, amphoteric poly! - Performance such as detergency improves when the amount of addition increases. However, if too large a quantity is added, there is a risk of adversely affecting product properties such as electrical stability and viscosity.
以下本発明を両性ポリ!−の合成例及び実施例について
説明するが、本発明はこれらにより限定されるものでは
ない。Hereinafter, the present invention will be described as an amphoteric poly! Synthesis examples and examples of - will be described, but the present invention is not limited thereto.
合成例1
攪拌機、温度針、環流冷却器及び窒素ガス導入管をつけ
た1Jのフラスコに、イオン交換水600 It、ジメ
チルアミノエチルメタアクリレ)5S#r、メタアクリ
ル酸goJ’rsベルオキソニ硫酸カリウム0.51r
を加え、窒素気流下70℃において6時間反応(重
合)させる、つづいて反応混液を室温まで冷却し、30
00jr のアセトン中に注いで、沈殿してくる両性ポ
リ!−をろ別する。減圧乾燥後の重量は83It であ
り、重合率は98%であった。Synthesis Example 1 In a 1J flask equipped with a stirrer, a temperature needle, a reflux condenser, and a nitrogen gas inlet tube, add ion-exchanged water 600 It, dimethylaminoethyl methacrylate) 5S#r, methacrylic acid goJ'rs potassium peroxonisulfate. 0.51r
was added and reacted (polymerized) for 6 hours at 70°C under a nitrogen stream, then the reaction mixture was cooled to room temperature and heated for 30
Pour it into 00jr of acetone and precipitate out the amphoteric poly! − is filtered out. The weight after drying under reduced pressure was 83 It, and the polymerization rate was 98%.
合成例2
合成例1と同様にして第1表に示すアニオン性モノマー
とカチオン性モノ!−とを1モル対1モルの割合で共重
合させた。脅威条件は次の如くであった。:
イオン妥・換水 400−
モノ!″′−″ 0.5M
温度 70℃
反応時間 6時間
一始剤 区、S、0・
第1表
合成ム アニオン性モノマ−カチオン性モノマーI
AA DMAI!
Mム2 AA 丁MA罵Mム5
ムム 罵DMA罵Mム4
MA テ賛ム罵Mム5
MA ICDMA凰Mムロ
8B TMAIMム7
518 TMAPMAム8
ムムMPa XDMOMム! ムム
MP8 冨VPY10 ムムMP5
1 テMAPMムム11 ムLI
lDMA罵MA12 V8
KDMAI1Mム13 V
8 DMAPMAA第1表中の略号の
説明
■
A A H,0=C−0001! 7クリル
酸M A II、0=O−00011メタア
クリル酸Oll。Synthesis Example 2 Anionic monomers and cationic monomers shown in Table 1 were prepared in the same manner as Synthesis Example 1! - and were copolymerized at a ratio of 1 mole to 1 mole. The threat conditions were as follows. : Ion replacement/water change 400-thing! ″′-″ 0.5M Temperature 70℃ Reaction time 6 hours Starting agent Ward, S, 0 Table 1 Synthesis Anionic monomer - Cationic monomer I
AADMAI!
Mmu 2 AA Ding MA abuse Mmu 5
Mmu abuse DMA abuse Mmu 4
MA praise and abuse Mmu 5
MA ICDMA 凰MMURO
8B TMAIM7
518 TMAPMA 8
Mumu MPa XDMOMmu! Mumu MP8 Tomi VPY10 Mumu MP5
1 TE MAPM MMU 11 MLI
lDMA Abuse MA12 V8
KDMAI1M 13V
8 Explanation of abbreviations in DMAPMAA Table 1■ A A H,0=C-0001! 7 Acrylic acid M A II, 0=O-00011 Methacrylic acid Oll.
C−ホン酸
ムL II H,O= OH−Ci!、80.
H7すにスA/ yjt 7酸V 11 11
sO=O)!−80.Hビニルスルホン酸メタアクリル
アンド
C11180M。C-phonic acid L II H, O= OH-Ci! , 80.
H7 Sunis A/yjt 7 acid V 11 11
sO=O)! -80. H vinyl sulfonic acid methacrylic and C11180M.
Oll、 ON。Oll, ON.
OH,OH。OH, OH.
以下、第1表に示した合成11〜13のポリマーを洗浄
剤組成物中に用いた実施例を示すが、夷llll1w中
の洗浄剤の諸性能の試験法は次の如(である0、・・2
1
〈試験法〉 −
イ)洗浄力
牛脂に指示薬としてスダン■(赤色色素)を0.1%添
加し、この5JFを磁性の皿(直径215m)K塗布し
たものを洗1iJ1ON、水201をしみ込ませたスポ
ンジでこすり洗いし、もはや皿より牛脂が清浄WC@れ
なくなる迄の洗浄された皿の枚数をもって示す。Examples in which the polymers of Synthesis 11 to 13 shown in Table 1 were used in a cleaning composition are shown below.・・2
1 <Test method> - A) Detergent power Add 0.1% Sudan ■ (red pigment) as an indicator to beef tallow, and wash the dish coated with 5JF on a magnetic dish (diameter 215 m) and soak it with 1iJ1ON and 201ml water. The number of plates that have been cleaned is indicated by the number of plates that have been scrubbed with a damp sponge until the tallow is no longer clean from the plates.
口)起泡力
汚れ成分として重版のバターを洗剤濃度O,S%の洗剤
溶液KO11%添加した時の起泡力を測定する。測定法
は直径551のガラス円筒にパターを添加した上記洗M
溶液40Jを入れ、10分間回転攪拌を行ない、停止直
後の溝高を測定する。Mouth) Foaming power The foaming power is measured when reprinted butter is added as a stain component in a detergent solution KO 11% with a detergent concentration of O, S%. The measurement method was to add putter to a glass cylinder with a diameter of 551 mm.
Add 40 J of solution, rotate and stir for 10 minutes, and measure the groove height immediately after stopping.
→ 水はじき
市販の20011jのガラスコツプをクレンザ−等で良
く洗い、水がはじかない事を確認した後、イオン交−水
ですすぎ乾燥させる。こ::1
のコツプに1%水濱液150−を入れ、50″′。→Wash a commercially available 20011j glass tip with a cleanser, etc., make sure it does not repel water, then rinse with ionized water and dry. Pour 150ml of 1% aqueous solution into a 1-inch cup and boil for 50''.
分間回転攪拌を行なった後、水溶液を流す。After rotating and stirring for a minute, the aqueous solution is poured.
次に′3ツブに水道水200−を入れ50秒静置後水を
流す。、これを1回繰返す、4@目に水を流した時の水
はじき臭合及び1日放置後のコツプの仕上り状態を観察
する。Next, pour 200 liters of tap water into the tube and let it stand for 50 seconds, then drain the water. , Repeat this once. 4. Observe the water repellent odor when water is poured on the eye, and the finished state of the pot after leaving it for one day.
工)すすぎ
洗剤濃度0.25%(温度20℃)の水溶液100CC
を500a分濱ロートに採り、一定回数振とうすも液を
流し出し泡量な測定する。 、次にすすぎ水soag(
温度20℃)を流し込み、分液−一トをゆつ(910回
転させる。Engineering) 100 cc of rinsing detergent concentration 0.25% aqueous solution (temperature 20°C)
Pour 500 micrometers of water into a funnel, shake it a certain number of times, pour out the liquid, and measure the amount of foam. , then rinse water soap (
Pour in the liquid (temperature: 20°C), and rotate the liquid at 910 rpm.
これを繰返し、泡が消滅するまでの回数を求めすすぎ回
数とする。Repeat this and find the number of times until the bubbles disappear and use it as the number of rinses.
実施例1
の配合で液体洗剤をつくり、その洗浄力、起泡力を測定
した結果を第2表に示す・
第2表
第2表よりポリマーを添加する事により洗浄力、起泡力
が大幅に増大する事が分る。A liquid detergent was made with the formulation in Example 1, and its detergent power and foaming power were measured. The results are shown in Table 2. From Table 2, the detergent power and foaming power were significantly increased by adding polymer. It can be seen that it increases.
実施例2
の配合で液体洗剤をつくり、その水はじ1テストを行な
った結果を第5表に示す。A liquid detergent was prepared using the formulation of Example 2, and the results of a water splash test are shown in Table 5.
jlli表
実施例5
〈泡の嗜好性の試験方法〉
女性io名により、洗浄力試験方法と同様の方法で洗浄
した際の泡の嗜好性をム、12種の洗浄剤親戚物の一対
比較法で調査した。jlli Table Example 5 <Test method for foam palatability> The palatability of foam when washed using the same method as the detergency test method was determined by female io name, and a pairwise comparison method of 12 kinds of detergent relatives was conducted. I investigated.
親戚物の配合を第4表に、又試験結果を第5□ 表に示す。The composition of relatives is shown in Table 4, and the test results are shown in Table 5□ Shown in the table.
、・・、:1・:・、。,...,:1...:...
評価法 +2 ムが好き
+1 ムがや\好ぎ
Oどちらとも言えない
−1mがや一好t
#15表
(註)畳平均炭素鎖長12、エチレンオキシド5(ル付
加
夷輪例4
本発明の組成物及びポリマーを含まない比i親戚物のす
すぎ試験を行なった。組成物の配合を第6表に、又試験
結果なN7表に示す。Evaluation method +2 I like it +1 I like it, I can't say -1m I like it. Rinse tests of the composition and its polymer-free relatives were conducted.The formulation of the composition is shown in Table 6 and the test results are shown in Table N7.
Claims (1)
と重合性不飽和基を有するカチオン性ビニルモノマーと
を1〜??!?f〜10毫ル比で共重合してなる両性共
重合ポリマーを含有することを響黴とする洗浄剤組成物
2 洗浄成分として一種以上の界面活性剤を含有する特
許請求の範囲第1項記載の洗浄剤組成物t an anionic vinyl monomer having a polymerizable unsaturated group and a cationic vinyl monomer having a polymerizable unsaturated group from 1 to ? ? ! ? Cleaning composition 2 containing an amphoteric copolymer copolymerized at a ratio of f to 10.Claim 2, which contains one or more surfactants as a cleaning component. cleaning composition
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11169381A JPS5813700A (en) | 1981-07-17 | 1981-07-17 | Detergent composition |
GB08217326A GB2104091B (en) | 1981-07-17 | 1982-06-15 | Detergent composition |
SG63187A SG63187G (en) | 1981-07-17 | 1987-08-07 | Detergent composition |
MY8700549A MY8700549A (en) | 1981-07-17 | 1987-12-30 | Detergent composition |
HK46788A HK46788A (en) | 1981-07-17 | 1988-06-23 | Detergent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11169381A JPS5813700A (en) | 1981-07-17 | 1981-07-17 | Detergent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5813700A true JPS5813700A (en) | 1983-01-26 |
JPH0155320B2 JPH0155320B2 (en) | 1989-11-24 |
Family
ID=14567767
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11169381A Granted JPS5813700A (en) | 1981-07-17 | 1981-07-17 | Detergent composition |
Country Status (5)
Country | Link |
---|---|
JP (1) | JPS5813700A (en) |
GB (1) | GB2104091B (en) |
HK (1) | HK46788A (en) |
MY (1) | MY8700549A (en) |
SG (1) | SG63187G (en) |
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US11441002B2 (en) | 2017-05-31 | 2022-09-13 | Rohm And Haas Company | Free standing dispersant film |
BR112020000981A2 (en) | 2017-07-24 | 2020-07-14 | Union Carbide Corporation | method for producing a cationic polymer, and, cationic polymer. |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5748335A (en) * | 1980-09-08 | 1982-03-19 | Mitsubishi Petrochem Co Ltd | Dispersion stabilizer of pearl gloss agent |
JPS57198800A (en) * | 1981-05-08 | 1982-12-06 | Oreal | Composition for keratin fiber treatment and treating process |
-
1981
- 1981-07-17 JP JP11169381A patent/JPS5813700A/en active Granted
-
1982
- 1982-06-15 GB GB08217326A patent/GB2104091B/en not_active Expired
-
1987
- 1987-08-07 SG SG63187A patent/SG63187G/en unknown
- 1987-12-30 MY MY8700549A patent/MY8700549A/en unknown
-
1988
- 1988-06-23 HK HK46788A patent/HK46788A/en unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5748335A (en) * | 1980-09-08 | 1982-03-19 | Mitsubishi Petrochem Co Ltd | Dispersion stabilizer of pearl gloss agent |
JPS57198800A (en) * | 1981-05-08 | 1982-12-06 | Oreal | Composition for keratin fiber treatment and treating process |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11323390A (en) * | 1998-05-15 | 1999-11-26 | Kao Corp | Detergent composition |
US7241729B2 (en) * | 1999-05-26 | 2007-07-10 | Rhodia Inc. | Compositions and methods for using polymeric suds enhancers |
US8907033B2 (en) | 1999-05-26 | 2014-12-09 | Solvay Usa Inc. | Polymers, compositions and methods of use for foams, laundry detergents, shower rinses and coagulants |
US6306815B1 (en) * | 1999-09-10 | 2001-10-23 | National Starch And Chemical Investment Holding Corporation | Quaternary polyvinylpyrridinium derivatives as anti-dye transfer agents |
JP2006241460A (en) * | 2005-03-04 | 2006-09-14 | Rohm & Haas Co | Laundry composition and use thereof |
JP2009503161A (en) * | 2005-07-25 | 2009-01-29 | ロディア・シミ | Method for removing dirt and makeup from the surface |
WO2007037448A1 (en) * | 2005-09-30 | 2007-04-05 | Kao Corporation | Detergent composition for automatic dishwashing machine |
US8044012B2 (en) | 2005-09-30 | 2011-10-25 | Kao Corporation | Detergent composition for automatic dishwashing machines |
JP2008223022A (en) * | 2007-03-09 | 2008-09-25 | Rohm & Haas Co | Cationic polymer latex |
Also Published As
Publication number | Publication date |
---|---|
MY8700549A (en) | 1987-12-31 |
HK46788A (en) | 1988-07-01 |
GB2104091A (en) | 1983-03-02 |
SG63187G (en) | 1988-02-19 |
GB2104091B (en) | 1986-05-29 |
JPH0155320B2 (en) | 1989-11-24 |
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