JPH01121400A - Production of high bulk density detergent and detergent composition - Google Patents

Production of high bulk density detergent and detergent composition

Info

Publication number
JPH01121400A
JPH01121400A JP27798787A JP27798787A JPH01121400A JP H01121400 A JPH01121400 A JP H01121400A JP 27798787 A JP27798787 A JP 27798787A JP 27798787 A JP27798787 A JP 27798787A JP H01121400 A JPH01121400 A JP H01121400A
Authority
JP
Japan
Prior art keywords
detergent
powder
zeolite
bulk density
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP27798787A
Other languages
Japanese (ja)
Inventor
Ken Takiyama
瀧山 謙
Atsushi Sato
淳 佐藤
Shozo Naito
内藤 省三
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NIPPON GOSEI SENZAI KK
Original Assignee
NIPPON GOSEI SENZAI KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by NIPPON GOSEI SENZAI KK filed Critical NIPPON GOSEI SENZAI KK
Priority to JP27798787A priority Critical patent/JPH01121400A/en
Publication of JPH01121400A publication Critical patent/JPH01121400A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/10Carbonates ; Bicarbonates

Abstract

PURPOSE:To obtain the title detergent with excellent combination of good fluidity of a powder with increased solubility, by neutralizing an alkylbenzenesulfonic acid with a mixture of sodium carbonate and zeolite in an amount more than the equimolar one to form sodium bicarbonate without liberation of carbon dioxide. CONSTITUTION:An alkylbenzenesulfonic acid is neutralized by combining it gradually with more than equimolar amount, preferably more than 2 fold molar amount of sodium carbonate and the same amount of zeolite under stirring at a high speed. Then, the mixture is crushed by high-speed agitation and sieved to give the subject detergent. The powdery bulk detergent is mixed with an anionic or nonionic surface active agent, an inorganic or organic builder, an anti-reblocking agent, an anticaking agent, a bleaching agent, enzymes and perfumes to give the subject detergent composition.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は従来の噴霧乾燥法によって得られる粉末洗浄剤
よりも高い嵩密度の洗浄剤をアルキルベンゼンスルフォ
ン酸より直接に製造する方法並びに!4該方法によって
得られた洗浄剤組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention provides a method for directly producing a detergent from alkylbenzenesulfonic acid that has a higher bulk density than powder detergents obtained by conventional spray drying methods, and! 4. The present invention relates to a cleaning composition obtained by the method.

〔従来の技術〕[Conventional technology]

従来粉末洗浄剤は一般に界面活性剤と無機ビルダーの水
性スラリーを噴震乾燥することによって製造され嵩比重
0.2乃至0.4の粉末として商品化されている。最近
省エネル・ギー、包装並びに輸送コストの低減、消費者
の使い易さなどを目的として高嵩密度の粉末洗浄剤が内
外で脚光を浴びて来ている。公知の方法としてはアルキ
ルベンゼンスルフォン酸を高濃度のアルカリとニーダ−
のような混練機で中和し、更にビルダーを混合し粉砕す
る方法、スルフォン酸をソーダ灰、トリポリ燐酸ソーダ
、ぼう硝等の無機ビルダーの混合物で粉体中和する方法
、噴霧乾燥によって得られた低嵩密度の洗剤粉末を粉砕
した後に造粒する方法等がある。
Conventional powder detergents are generally manufactured by spray drying an aqueous slurry of a surfactant and an inorganic builder, and are commercialized as a powder with a bulk specific gravity of 0.2 to 0.4. Recently, powder cleaning agents with high bulk density have been attracting attention at home and abroad for the purpose of saving energy, reducing packaging and transportation costs, and making it easier for consumers to use. A known method is to mix alkylbenzenesulfonic acid with a highly concentrated alkali in a kneader.
A method of neutralizing the sulfonic acid with a kneader such as a kneader, followed by mixing and pulverizing a builder, a method of neutralizing the sulfonic acid as a powder with a mixture of inorganic builders such as soda ash, sodium tripolyphosphate, and sulfur sulfate, and a method of spray drying. There is a method in which detergent powder with a low bulk density is pulverized and then granulated.

〔発明が解決しようとする間迎点〕[The point where the invention is trying to solve the problem]

アルキルベンゼンスルフォン酸の直接中和方法による製
品は使用に際し水に対する溶解速度が遅く、家庭用の電
気洗濯機には適当でない。
Products produced by direct neutralization of alkylbenzene sulfonic acids have a slow dissolution rate in water during use, and are not suitable for household electric washing machines.

又噴霧乾燥によって得られた低嵩密度の洗剤を粉砕造粒
し高嵩密度化した製品は水に対する溶解性は優れている
が、省エネルギーの目的からは逸脱しており、コスト高
となることは逃れ得ない現状である。
In addition, products made by pulverizing and granulating detergents with low bulk density obtained by spray drying to have high bulk density have excellent solubility in water, but they deviate from the purpose of energy conservation and are expensive. This is a situation that cannot be escaped.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者らはこれらの公知の方法の是点を解決すべく鋭
意研究を重ねた結果、乾燥のエネルギーを必要としない
、簡単な装置で実施出来る、溶解性の優れた高嵩密度洗
浄剤の製造方法を確立する事が出来た1本発明の方法は
次式で示されるアルキルベンゼンスルフォン酸と炭酸ア
ルカリの等モル反応を原理としている。
The inventors of the present invention have conducted extensive research to resolve the merits of these known methods, and have developed a high-density cleaning agent with excellent solubility that does not require drying energy and can be carried out using simple equipment. The method of the present invention, in which a manufacturing method has been established, is based on the equimolar reaction of an alkylbenzenesulfonic acid and an alkali carbonate represented by the following formula.

C工2I(25C61(4S03H+Na2CO3□C
121(2%61i4SO3Na+NafrCO3Rは
平均炭素数12−13の直鎖状又は側鎖を有するアルキ
ル基であり、ドデシルベンゼン又はトリデシルベンゼン
で代表されるアルキルベンゼンである。
C engineering 2I (25C61 (4S03H+Na2CO3□C
121 (2%61i4SO3Na+NafrCO3R is an alkyl group having an average carbon number of 12-13 and having a linear or side chain, and is an alkylbenzene represented by dodecylbenzene or tridecylbenzene.

アルキルベンゼンスルフォン酸はアルキルベンゼンを無
水硫酸でスルフォン化し生成したアルキルベンゼンスル
フォン酸に1−2%の水を添加しスルフォン酸無水物を
分解したスルフォン酸、又は更に10%の水を添加し過
酸化水素で漂白したスルフォン酸、ケーキング防止を目
的にトルエン又はベンゼンスルフォン酸を配合したアル
キルベンゼンスルフォン酸などを用いる事ができる。
Alkylbenzene sulfonic acid is produced by sulfonating alkylbenzene with sulfuric anhydride and adding 1-2% water to the alkylbenzene sulfonic acid to decompose the sulfonic acid anhydride, or by adding 10% water and bleaching with hydrogen peroxide. For the purpose of preventing caking, alkylbenzenesulfonic acid mixed with toluene or benzenesulfonic acid can be used.

炭酸ナトリウムは軽質又は重質のソーダ灰を用いること
が出来る。
Light or heavy soda ash can be used as the sodium carbonate.

両者の反応は等モル以上好ましくはアルキルベンゼンス
ルフオン酸1モルに対し2モル以上のソーダ灰を同量の
ゼオライトと混合して中和するのが反応過程における粉
体の流動性の保持に好ましい0反応により発生する反応
熱は低、く冷却の必要は認められない。
In order to maintain the fluidity of the powder during the reaction process, it is preferable to neutralize both reactions by mixing equal moles or more, preferably 2 moles or more of soda ash per mole of alkylbenzenesulfonic acid with the same amount of zeolite. The reaction heat generated by the reaction is low and there is no need for cooling.

反応に使用する装置としてはリボンミキサー、レデイゲ
ミキサー(松阪貿易)等を用いることが出来るが本発明
の方法の実施に際しては特定の装置を限定することなく
種々の粉体混合装置を使用することが可能である。
As the apparatus used for the reaction, a ribbon mixer, a Ledeige mixer (Matsusaka Trading), etc. can be used, but when carrying out the method of the present invention, various powder mixing apparatuses can be used without being limited to a specific apparatus. is possible.

中和反応によって製造された次の組成物アルキルベンゼ
ンスルフオン酸ソーダ34−43%ソーダ灰     
         24−17%炭酸水素ナトリウム 
       8−10%ゼオライト        
    34−30%を基剤として更に種々の原料を配
合することにより洗浄剤組成物を誘導することが出来る
The following composition sodium alkylbenzene sulfonate 34-43% soda ash produced by neutralization reaction
24-17% sodium bicarbonate
8-10% zeolite
Detergent compositions can be derived by further blending various raw materials with 34-30% as a base.

アニオン系界面活性剤としては天然又は合成高級アルコ
ール硫酸塩、高級アルコールエトオキシレート硫酸塩、
アルファーオレフィンスルフォン酸塩、Na−アルカン
スルフオネ−1−。
Examples of anionic surfactants include natural or synthetic higher alcohol sulfates, higher alcohol ethoxylate sulfates,
Alpha olefin sulfonate, Na-alkanesulfone-1-.

アルファースルフオ脂肪酸塩脂肪酸石鹸類等を任意に選
択することが出来るが、これらは何れも実質的に水分を
含有しない乾燥品であることが好ましい。
Although alpha sulfur fatty acid salt fatty acid soaps and the like can be arbitrarily selected, it is preferable that all of these are dry products containing substantially no water.

非イオン系としては天然又は合成高級アルコールエトオ
キシレート、高級脂肪酸アルキロールアミド、エチレン
−プロピレンオキサイドブロックポリマー、無機ビルダ
ーとしてはけい酸ソーダ、メタけい酸ソーダ、ぼう硝。
Examples of nonionic builders include natural or synthetic higher alcohol ethoxylates, higher fatty acid alkylolamides, and ethylene-propylene oxide block polymers; examples of inorganic builders include sodium silicate, sodium metasilicate, and sulfate.

トリポリ燐酸ソーダ、有機ビルダーとしてはポリアクリ
ル酸塩、クエン酸ソーダ、グルコン酸ソーダ等が用いら
れ再汚染防止剤としてCMC、ポリエチレングリコール
等、漂白剤として過炭酸ソーダ、過炭酸ソーダ、亜塩素
酸ソーダ等ケーキング防止剤としてトルエンスルフオン
酸ソーダ、ほかに蛍光染料、酵素、香料等を任意に配合
することが出来る。
Sodium tripolyphosphate, organic builders such as polyacrylate, sodium citrate, and sodium gluconate are used; CMC and polyethylene glycol are used as anti-recontamination agents; and sodium percarbonate, sodium percarbonate, and sodium chlorite are used as bleaching agents. In addition to sodium toluene sulfonate as an anti-caking agent, fluorescent dyes, enzymes, fragrances, etc. can be optionally added.

本発明の方法の実施に際しては従来の噴霧乾燥法のごと
く大量の熱エネルギーを必要としないが、原料より混入
する水分により粉体の流動性が低下する場合は少量の熱
量で流動又は静置乾燥により付着水分を低下させ粉体の
流動性を向上することが出来る。
The method of the present invention does not require a large amount of thermal energy unlike the conventional spray drying method, but if the fluidity of the powder decreases due to moisture mixed in from the raw materials, it can be fluidized or left to dry with a small amount of heat. This makes it possible to reduce adhering moisture and improve the fluidity of the powder.

実施例1゜ ソーダ灰    0.75 K、、(7,1モル)ゼオ
ライ1〜 0.75 Kg LAS()1202漂白) 1.0 Kg(2,7モル
)LAS/ソーダ灰モル比=1:2.6 屯上型小型リボンミキサー(toe、)にソーダ灰とゼ
オライトを装入し均一に混合した後、過酸化水素で漂白
した生分解型のアルキルベンゼンスルフォン酸(以下L
AS 、 N22塩をLAS−Naと略称する)をかく
はんしつつ徐々に添加した。得られた粉末状の基剤に対
し更に次の原料を添加しかくはん混合した。
Example 1 Soda ash 0.75 K, (7,1 mol) Zeolite 1-0.75 Kg LAS ()1202 bleaching) 1.0 Kg (2,7 mol) LAS/soda ash molar ratio = 1: 2.6 After charging soda ash and zeolite into a small ribbon mixer (TOE) and mixing them uniformly, add biodegradable alkylbenzenesulfonic acid (hereinafter referred to as L) bleached with hydrogen peroxide.
AS, N22 salt (abbreviated as LAS-Na) was gradually added with stirring. The following raw materials were further added to the obtained powder base and mixed by stirring.

高級アルコール硫酸塩 噴霧乾燥品(AT=/10%)0.4にG非イオン活性
剤N5A (三洋化成工業)    0.2K。
Higher alcohol sulfate spray-dried product (AT=/10%) 0.4 and G nonionic activator N5A (Sanyo Chemical Industries) 0.2K.

石鹸粉       0.1 Kg 得られた混合物3.2K[をヘンシェルタイプの小型ミ
キサーに装入し20秒高速かくはん粉砕した後]2メツ
シュのふるいにかけて3.1Kgの洗浄剤粉末を得た。
Soap powder 0.1 Kg The resulting mixture (3.2K) was charged into a Henschel type small mixer and pulverized with high speed stirring for 20 seconds, and then passed through a 2-mesh sieve to obtain 3.1Kg of detergent powder.

嵩密度の測定結果は0.76であった。The bulk density measurement result was 0.76.

更にタンパク分解酵素エスペラーゼ(ノボ社)を3%、
蛍光染料を0.5%香料を0.2%を配合して得られた
洗浄剤組成物の性能試験結果を第−表並びに第二衣に示
す。
Furthermore, 3% of the proteolytic enzyme esperase (Novo),
The performance test results of the detergent composition obtained by blending 0.5% of fluorescent dye and 0.2% of fragrance are shown in Table 1 and the second column.

実施例2゜ ソーダ灰    1.OKg(9,4モル)ゼオライト
  1.2にg LAS(+1202漂白) I Kg(2,7モル)L
AS/ソーダ灰モル比=l:3.5 卓上型小型リボンミキサー(JOL)にソーダ灰とゼオ
ライトを装入し均一に混合した後、過酸化水素で漂白し
た1、、A Sをかくはんしつつ徐々に添加した。
Example 2゜Soda ash 1. OKg (9,4 mol) Zeolite 1.2g LAS (+1202 bleached) I Kg (2,7 mol) L
AS/soda ash molar ratio = l: 3.5 After charging soda ash and zeolite into a tabletop small ribbon mixer (JOL) and mixing them uniformly, while stirring the AS bleached with hydrogen peroxide, Added gradually.

得られた粉末状の基剤に対し更に次の原料を添加しかく
はん混合した。
The following raw materials were further added to the obtained powder base and mixed by stirring.

高級アルコール硫酸塩 噴震乾燥品(AI=40%)0.6Kg非イオン活性剤
N5A (三洋化成工業)    0.8Kg 石鹸粉       0.2 KK メタけい酸ソーダ  0.2 K。
Higher alcohol sulfate spray dried product (AI=40%) 0.6Kg Nonionic activator N5A (Sanyo Chemical Industries) 0.8Kg Soap powder 0.2 KK Sodium metasilicate 0.2K.

得られた混合物5 Kgを粉砕し12メツシユのふるい
にかけ4.9 Kgの洗浄剤粉末を得た。
5 kg of the resulting mixture was ground and sifted through a 12 mesh sieve to obtain 4.9 kg of detergent powder.

嵩密度の測定結果は0.74であった。更にタンパク分
解酵素3%、蛍光染料0.5%、香料0.2%を配合し
て得られた洗浄剤組成物の性能試験結果を第−表並びに
第二衣に示す。
The bulk density measurement result was 0.74. Furthermore, the performance test results of a cleaning composition obtained by blending 3% of proteolytic enzyme, 0.5% of fluorescent dye, and 0.2% of fragrance are shown in Table 1 and 2.

実施例3゜ ソーダ灰    0.85 Kg(8モル)ゼオライl
−0,85Kg LAS(+1202漂白) I Kg(2,7モル)P
TS      O,I Kg LAS/ソーダ灰モル比=1=3 卓上型小型リボンミキサー(IOL)にソーダ灰とゼオ
ライト、PTS (パラトルエンスルフオン酸ソーダ)
を装入し均一に混合した後、過酸化水素で漂白したLA
Sをかくはんしつつ徐々に添加した。
Example 3゜Soda ash 0.85 Kg (8 mol) Zeolite l
-0,85Kg LAS (+1202 bleaching) I Kg (2,7 mol) P
TSO, I Kg LAS/soda ash molar ratio = 1 = 3 Soda ash, zeolite, PTS (para-toluenesulfonate soda) in a small tabletop ribbon mixer (IOL)
After charging and mixing uniformly, LA was bleached with hydrogen peroxide.
S was added gradually while stirring.

得られた粉末状の基剤に対し次の原料を添加しかくはん
混合した。
The following raw materials were added to the obtained powder base and mixed by stirring.

α−オレフィンスルフォン酸塩 (ライオン、デタージェント!+5 ) 0 、4 K
 IK非イオン活性剤N5A (三洋化成工業)        0.2Kg石鹸粉 
          0.1K。
α-Olefin sulfonate (Lion, Detergent!+5) 0, 4 K
IK nonionic activator N5A (Sanyo Chemical Industries) 0.2Kg soap powder
0.1K.

メタけい酸ソーダ       0.2K[得られた混
合物3.7Kgを粉砕し12メツシユのふるいにかけ1
.6 Kgの洗浄剤粉末をt:)た。
Sodium metasilicate 0.2K [3.7Kg of the resulting mixture was ground and sieved through a 12-mesh 1
.. 6 Kg of detergent powder was collected.

嵩密度の測定結果は0.72であった。The bulk density measurement result was 0.72.

更にタンパク分解酵素3%、蛍光染料0.5%、香料0
.2%を配合して得られた洗浄剤組成物の性能試験結果
を第−表並びに第二衣に示す。
Additionally, 3% proteolytic enzymes, 0.5% fluorescent dyes, and 0 fragrances.
.. The performance test results of the detergent composition obtained by blending 2% are shown in Table 1 and the second layer.

比較例 ソーダ灰       0.15にg(1,4モル)ゼ
オライト     0.75Kg LAS(11202漂白)     1.0Kg(2,
7モル)LAS/ソーダ灰モル比=1:0.52卓上型
リボンミキサー(101,)にソーダ灰とゼオライトを
装入し均一に混合した後、過酸化水素で漂白したLAS
をかくはんしつつ徐々に添加した。
Comparative example Soda ash 0.15g (1.4 mol) Zeolite 0.75Kg LAS (11202 bleached) 1.0Kg (2,
7 mol) LAS/soda ash molar ratio = 1:0.52 After charging soda ash and zeolite into a tabletop ribbon mixer (101,) and mixing them uniformly, LAS was bleached with hydrogen peroxide.
was added gradually while stirring.

反応物は炭酸ガスを発生し生成したペーストは団子状と
なり粉末化は困難であった。
The reactants generated carbon dioxide gas, and the resulting paste was lump-like and difficult to powder.

〔効果〕〔effect〕

本発明により乾燥のエネルギーを必要とすることなく高
嵩密度の粉末洗剤が得られ懸念される溶解性の問題も解
決された。
According to the present invention, a powder detergent with a high bulk density can be obtained without requiring energy for drying, and the problem of solubility, which was a concern, has been solved.

従来の噴霧乾燥法に基く粉末洗剤製品より生産コストが
安く、排ガス公害の心配の無い無公害プロセスとして実
施可能であり、尚製品の輸送、貯蔵の経費が節約され省
エネルギーの目的を達成することが出来た。
The production cost is lower than that of powder detergent products based on the conventional spray drying method, and it can be implemented as a pollution-free process without worrying about exhaust gas pollution.It also saves on product transportation and storage costs and can achieve the goal of energy conservation. done.

第−表 実施番号/組成(%) 成分     1   2   3    対比傘LA
S−Na     27.5  17.2  23.3
  24.0^S       4.7  4.5  
−    7.4非イオ’/    5.9  14.
8  5,0  5.0AO59,5− 石鹸     2.9  3.7  2.5  4.8
PTS               2.5  −ソ
ーダ灰    13.9  15.2  14.2  
15.0重炭酸ソーダ  6.7  4.1  5.6
  −ゼオライト  22.2  22.1  21.
4  25.5ぼう硝    8.0  7.4  1
.5  4.5けい酸ソーダ −3,75,05,2 酵素     3.0  3.0  3.0  3.0
蛍光染料   0.5  0.5  0.5  0.5
香料      0.2  0.2   α、2  0
.2水分     4.5  3.6  5.8  4
.9串対比噴霧乾燥粉末洗剤を粉砕造粒した製品。
Table - Implementation number/composition (%) Component 1 2 3 Comparative umbrella LA
S-Na 27.5 17.2 23.3
24.0^S 4.7 4.5
- 7.4 non-io'/5.9 14.
8 5,0 5.0AO59,5- Soap 2.9 3.7 2.5 4.8
PTS 2.5 - Soda ash 13.9 15.2 14.2
15.0 Soda bicarbonate 6.7 4.1 5.6
-Zeolite 22.2 22.1 21.
4 25.5 8.0 7.4 1
.. 5 4.5 Sodium silicate -3,75,05,2 Enzyme 3.0 3.0 3.0 3.0
Fluorescent dye 0.5 0.5 0.5 0.5
Fragrance 0.2 0.2 α, 2 0
.. 2 Moisture 4.5 3.6 5.8 4
.. A product made by crushing and granulating nine skewers of spray-dried powder detergent.

第二表 1嵐に簾■盟 実施番号 試験項目   1  2  3   対比傘1嵩比重 
   0.76  0,74  0,72  0.72
溶解性”2   0   0   0   0洗浄カー
3   79.4  78.1  80.2  79.
6−1対比 噴霧乾燥粉末洗剤を粉砕造粒した製品。
Table 2 1 Arashi ni Blind ■Mei Implementation Number Test Item 1 2 3 Comparative Umbrella 1 Bulk Specific Gravity
0.76 0.74 0.72 0.72
Solubility”2 0 0 0 0 Washing car 3 79.4 78.1 80.2 79.
Comparison with 6-1 A product obtained by crushing and granulating a spray-dried powder detergent.

惺llI虹友迭 傘2溶解性 8’Cの冷水2000m1を一定の速度でかくはんしつ
つ洗浄剤1.7gを添加し10分後かくはんを止めて静
置し不溶Mの洗剤の存在が認められないものを合格O印
とした。
惺llI Rainbow Friendship Umbrella 2 2000ml of cold water with a solubility of 8'C was stirred at a constant speed and 1.7g of detergent was added. After 10 minutes, the stirring was stopped and the mixture was allowed to stand, and the presence of insoluble M detergent was confirmed. Those that did not have a passing mark were marked O.

傘3洗浄力 人口汚染布 牛乳1000+alに墨汁6mlを混合し超音波浴で木
綿布(糊抜きした)を浸し自然乾燥したものを用いた。
Umbrella 3 Cleaning Power Artificially Contaminated Cloth A cotton cloth (desized) was mixed with 1000+al of milk and 6 ml of Indian ink, and then soaked in an ultrasonic bath and dried naturally.

試験機  ターボ1−メーター 使用水  八尾市水道水 水温   30’ C 洗浄条件 予備浸種   20分 洗浄     10分 水洗     5分 使用濃度 OJ5g/1000mlTest machine Turbo 1-meter Water used: Yao city tap water Water temperature 30’C Cleaning conditions Pre-soaking 20 minutes Cleaning 10 minutes Wash with water 5 minutes Usage concentration OJ5g/1000ml

Claims (2)

【特許請求の範囲】[Claims] (1)アルキルベンゼンスルフォン酸を等モル以上の炭
酸ソーダとゼオライトの混合物で中和し、炭酸ガスを発
生させることなく炭酸水素ナトリウムを生成せしめ粉末
の流動性を保持すると共に溶解性を向上させることを特
徴とする高嵩密度粉末洗浄剤の製造方法。
(1) Neutralize alkylbenzenesulfonic acid with a mixture of at least the same mole of soda carbonate and zeolite to generate sodium hydrogen carbonate without generating carbon dioxide gas, maintain fluidity of the powder, and improve solubility. A method for producing a characteristic high bulk density powder cleaning agent.
(2)アルキルベンゼンスルフォン酸を等モル以上の炭
酸ソーダとゼオライトの混合物で中和することにより得
られた粉末基剤に更にアニオン系、非イオン系の活性剤
、無機ビルダー、有機ビルダー、再付着防止剤、ケーキ
ング防止剤、漂白剤、蛍光染料、酵素、香料などを配合
して得られる高嵩密度粉末洗浄剤組成物。
(2) A powder base obtained by neutralizing alkylbenzenesulfonic acid with a mixture of at least the same mole of sodium carbonate and zeolite, and anionic and nonionic activators, inorganic builders, organic builders, and redeposition prevention. A high bulk density powder detergent composition obtained by blending agents, anti-caking agents, bleaching agents, fluorescent dyes, enzymes, fragrances, etc.
JP27798787A 1987-11-04 1987-11-04 Production of high bulk density detergent and detergent composition Pending JPH01121400A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27798787A JPH01121400A (en) 1987-11-04 1987-11-04 Production of high bulk density detergent and detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27798787A JPH01121400A (en) 1987-11-04 1987-11-04 Production of high bulk density detergent and detergent composition

Publications (1)

Publication Number Publication Date
JPH01121400A true JPH01121400A (en) 1989-05-15

Family

ID=17591048

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27798787A Pending JPH01121400A (en) 1987-11-04 1987-11-04 Production of high bulk density detergent and detergent composition

Country Status (1)

Country Link
JP (1) JPH01121400A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0345090A2 (en) * 1988-06-03 1989-12-06 Colgate-Palmolive Company Process for manufacturing particulate detergent composition directly from in situ produced anionic detergent salt
JPH0333199A (en) * 1988-07-21 1991-02-13 Unilever Nv Detergent compound and its manufacture
US5527489A (en) * 1990-10-03 1996-06-18 The Procter & Gamble Company Process for preparing high density detergent compositions containing particulate pH sensitive surfactant
KR100394762B1 (en) * 1996-02-13 2003-11-20 주식회사 엘지생활건강 Concentrated powdery detergent composition with excellent long period storage stability
WO2004053046A1 (en) * 2002-12-12 2004-06-24 Henkel Kommanditgesellschaft Auf Aktien Dry neutralisation method

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0345090A2 (en) * 1988-06-03 1989-12-06 Colgate-Palmolive Company Process for manufacturing particulate detergent composition directly from in situ produced anionic detergent salt
JPH0333199A (en) * 1988-07-21 1991-02-13 Unilever Nv Detergent compound and its manufacture
US5527489A (en) * 1990-10-03 1996-06-18 The Procter & Gamble Company Process for preparing high density detergent compositions containing particulate pH sensitive surfactant
CN1035626C (en) * 1990-10-03 1997-08-13 普罗格特-甘布尔公司 Process for preparing high density detergent compositions containing particulate pH sensitive surfactant
KR100394762B1 (en) * 1996-02-13 2003-11-20 주식회사 엘지생활건강 Concentrated powdery detergent composition with excellent long period storage stability
WO2004053046A1 (en) * 2002-12-12 2004-06-24 Henkel Kommanditgesellschaft Auf Aktien Dry neutralisation method

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