JPH10204500A - Effervescent tablet detergent - Google Patents
Effervescent tablet detergentInfo
- Publication number
- JPH10204500A JPH10204500A JP9041364A JP4136497A JPH10204500A JP H10204500 A JPH10204500 A JP H10204500A JP 9041364 A JP9041364 A JP 9041364A JP 4136497 A JP4136497 A JP 4136497A JP H10204500 A JPH10204500 A JP H10204500A
- Authority
- JP
- Japan
- Prior art keywords
- phosphate
- anhydrous
- sodium
- component
- carbonate
- 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
Links
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は保存安定性が改良された
発泡錠剤洗浄剤に関する。The present invention relates to a foamed tablet detergent having improved storage stability.
【0002】[0002]
【従来の技術及び発明が解決しようとする課題】通常使
用されている発泡錠剤洗浄剤には水に可溶な固体アルカ
リと酸が使用されている。アルカリとして一般には炭酸
水素ナトリウムが、酸として有機酸では酒石酸、クエン
酸、コハク酸、リンゴ酸、スルファミン酸が、また無機
酸ではホウ酸等の酸が使用されている。2. Description of the Related Art Water-soluble solid alkalis and acids are used in commonly used effervescent tablet detergents. In general, sodium bicarbonate is used as an alkali, tartaric acid, citric acid, succinic acid, malic acid, and sulfamic acid are used as organic acids and acids such as boric acid are used as inorganic acids.
【0003】これらの成分の他に洗浄成分としてイオン
系、非イオン系の界面活性剤が、また錠剤の形を作る為
の結合剤として多糖類やグリコール類などが用いられる
他に、添加剤として酵素、香料等が一般に使用されてい
る。[0003] In addition to these components, ionic and nonionic surfactants are used as detergent components, and polysaccharides and glycols are used as binders for forming tablets. Enzymes, fragrances and the like are commonly used.
【0004】発泡反応は炭酸水素ナトリウムのような炭
酸塩と酸の反応により炭酸ガスが発生するものである
が、この反応には水分の介在が必要となる。水分として
は非常に微量でも反応を起し炭酸ガスが発生してしまう
為、原料には通常無水物が使用され、製造環境も通常、
温度20℃、湿度20±10%の環境下でプレスを行う
必要がある。In the foaming reaction, carbon dioxide gas is generated by a reaction between a carbonate such as sodium hydrogen carbonate and an acid, and this reaction requires the presence of moisture. Since even a very small amount of water causes a reaction and carbon dioxide gas is generated, anhydrous is usually used as a raw material, and the production environment is usually
Pressing must be performed in an environment of a temperature of 20 ° C. and a humidity of 20 ± 10%.
【0005】水分を含む原料の使用や、湿度の高い環境
下で製造を行うと、徐々にではあるが反応による炭酸ガ
スの発生に伴い、製品が崩壊すると共に製品の個別包装
がふくらみ破裂を起し、発泡洗浄性が失われ商品として
の価値を無くすという問題があった。[0005] When a raw material containing water is used or production is performed in an environment with high humidity, the product gradually collapses due to the generation of carbon dioxide due to the reaction, and the individual packaging of the product bulges and ruptures. However, there is a problem in that foam cleaning properties are lost and the value as a product is lost.
【0006】また発泡錠剤入浴剤には錠剤内部の脱水剤
として無水アルミン酸ナトリウムを添加してることが公
知の事実として知られている(特開昭59−70610
号)。しかし、アルミン酸ナトリウムは洗浄剤としての
アニオン系界面活性剤と反応を起し、アルミニウム塩を
生成し水に不溶になってしまう為、発泡錠剤洗浄剤に添
加すると、その効力が発揮出来なくなってしまう。It is also known as a known fact that an anhydrous sodium aluminate is added as a dehydrating agent inside a tablet to a foaming tablet bath agent (Japanese Patent Laid-Open No. 59-70610).
issue). However, sodium aluminate reacts with an anionic surfactant as a detergent, generates an aluminum salt, and becomes insoluble in water. I will.
【0007】そこで、本発明では室温30℃、湿度60
%の環境下で製造しても良好な洗浄能力を有し、長期間
高温の環境下に於いても従来品のような変質を起さない
安定な発泡錠剤洗浄剤を提供しようとするものである。Therefore, in the present invention, a room temperature of 30.degree.
%, Which has a good cleaning ability even when manufactured in an environment of high%, and aims to provide a stable foaming tablet detergent that does not cause deterioration like conventional products even in a high temperature environment for a long time. is there.
【0008】[0008]
【課題を解決するための手段及び作用】前記課題を解決
するために発明者が鋭意研究の結果本発明に到達したも
ので、本発明は界面活性剤、炭酸塩、固体の有機酸又は
無機酸、結合剤及び安定剤として無水リン酸塩を0.0
1〜10.0重量%含有することを特徴とする発泡錠剤
洗浄剤である。Means for Solving the Problems and Actions In order to solve the above problems, the present inventors have made intensive studies and arrived at the present invention. The present invention relates to surfactants, carbonates, solid organic acids or inorganic acids. , Anhydrous phosphate as a binder and stabilizer
An effervescent tablet detergent containing 1 to 10.0% by weight.
【0009】本発明においては炭酸塩は10.0〜8
0.0重量%であることが好ましく、炭酸塩としては炭
酸水素ナトリウム、炭酸ナトリウム、炭酸アンモニウム
等があげられ、固体の有機酸又は無機酸は5.0〜60
重量%であることが好ましく、かかるものとしては前述
の公知の酸があげられ、結合剤は0.1〜20重量%で
あることが好ましく、界面活性剤は0.01〜10.0
重量%であることが好ましい。In the present invention, the carbonate is 10.0 to 8%.
It is preferably 0.0% by weight, and examples of the carbonate include sodium hydrogencarbonate, sodium carbonate, ammonium carbonate and the like.
% By weight, such as the above-mentioned known acids. The binder is preferably 0.1 to 20% by weight, and the surfactant is 0.01 to 10.0% by weight.
% By weight.
【0010】前記結合剤としては平均分子量が4,00
0〜10,000以下のポリエチレングリコール等や庶
糖、乳糖等が用いられ、界面活性剤には脂肪酸石鹸やア
ルキルサルフェート等を含有しても良い。しかし結合
剤、界面活性剤はこれらに限定されるものではない。ま
た、その他の添加剤として酵素や香料などを添加するこ
とも出来るが、添加剤としてはこれらに限定されるもの
ではない。The binder has an average molecular weight of 4,000.
0 to 10,000 or less polyethylene glycol or the like, sucrose, lactose, or the like is used, and the surfactant may contain a fatty acid soap, an alkyl sulfate, or the like. However, the binder and the surfactant are not limited to these. In addition, enzymes and fragrances can be added as other additives, but the additives are not limited to these.
【0011】[0011]
【実施例、比較例】以下に本発明の発泡錠剤洗浄剤、お
よびその製造方法を実施例、比較例を挙げて説明する
が、本発明はこれら実施例に限定されるものではない。
尚、実施例、比較例の数値は重量%である。EXAMPLES AND COMPARATIVE EXAMPLES The foaming tablet detergent of the present invention and the method for producing the same are described below with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.
The numerical values of the examples and comparative examples are% by weight.
【0012】実施例1 炭酸水素ナトリウム 52.5 無水コハク酸 25.0 庶糖 15.5 ラウリン酸ナトリウム 4.5 無水リン酸二ナトリウム 2.5Example 1 Sodium hydrogen carbonate 52.5 Succinic anhydride 25.0 Sucrose 15.5 Sodium laurate 4.5 Disodium phosphate anhydrous 2.5
【0013】室温20℃、湿度60%の環境下にて、粉
末状の上記組成物を均一に混合し、3.0gを計量し直
径2cmの金型に入れ200kgでプレスし発泡錠剤洗
浄剤を調製した。この錠剤を厚さ50μm、大きさ5.
0cm四方のアルミでラミネートされたヒートシールフ
ィルム2枚で挾み4辺をヒートシールしサンプルを作製
した。以下の実施例、比較例においても同様にしてサン
プルを作製した。Under an environment of room temperature of 20 ° C. and humidity of 60%, the above powdery composition is uniformly mixed, 3.0 g is weighed, placed in a mold having a diameter of 2 cm, and pressed with 200 kg to prepare a foamed tablet detergent. Prepared. This tablet is 50 μm thick and 5.
A sample was prepared by sandwiching two heat sealing films laminated with 0 cm square aluminum and heat sealing the four sides. Samples were prepared in the same manner in the following Examples and Comparative Examples.
【0014】実施例2 炭酸水素ナトリウム 60.0 無水リンゴ酸 23.0 庶糖 10.0 ドデシルベンゼンスルホン酸ナトリウム 6.5 無水ピロリン酸カリウム 0.5Example 2 Sodium hydrogen carbonate 60.0 Malic anhydride 23.0 Sucrose 10.0 Sodium dodecylbenzenesulfonate 6.5 Anhydrous potassium pyrophosphate 0.5
【0015】実施例3 炭酸水素ナトリウム 61.5 無水クエン酸 20.0 乳糖 12.0 α−オレフィンスルホン酸ナトリウム 3.0 無水ヘキサメタリン酸ナトリウム 3.5Example 3 Sodium bicarbonate 61.5 Citric anhydride 20.0 Lactose 12.0 Sodium α-olefin sulfonate 3.0 Anhydrous sodium hexametaphosphate 3.5
【0016】実施例4 炭酸水素ナトリウム 52.5 無水酒石酸 25.0 乳糖 14.5 ラウリル硫酸ナトリウム 5.5 無水ピロリン酸カリウム 2.0 アルカラーゼ(酵素) 0.5Example 4 Sodium bicarbonate 52.5 Tartaric anhydride 25.0 Lactose 14.5 Sodium lauryl sulfate 5.5 Anhydrous potassium pyrophosphate 2.0 Alcalase (enzyme) 0.5
【0017】実施例5 炭酸水素ナトリウム 65.5 無水クエン酸 20.0 ポリエチレングリコール(平均分子量8000) 6.0 ラウロイルメチルタウリンナトリウム 7.0 無水トリポリリン酸カリウム 1.5Example 5 Sodium hydrogen carbonate 65.5 Anhydrous citric acid 20.0 Polyethylene glycol (average molecular weight 8000) 6.0 Sodium lauroylmethyltaurine 7.0 Anhydrous potassium tripolyphosphate 1.5
【0018】実施例6 炭酸水素ナトリウム 54.0 スルファミン酸 25.0 乳糖 13.0 ラウリル硫酸ナトリウム 4.0 無水リン酸二カリウム 1.5 無水リン酸二ナトリウム 2.5Example 6 Sodium bicarbonate 54.0 Sulfamic acid 25.0 Lactose 13.0 Sodium lauryl sulfate 4.0 Dipotassium phosphate anhydrous 1.5 Disodium phosphate anhydrous 2.5
【0019】実施例7 炭酸水素ナトリウム 54.3 無水クエン酸 25.0 ホウ酸 5.0 ポリエチレングリコール(平均分子量4000) 7.5 ラウロイルサルコシン 5.0 無水メタリン酸カリウム 3.0 メントール油(香料) 0.2Example 7 Sodium hydrogen carbonate 54.3 Anhydrous citric acid 25.0 Boric acid 5.0 Polyethylene glycol (average molecular weight 4000) 7.5 Lauroyl sarcosine 5.0 Anhydrous potassium metaphosphate 3.0 Menthol oil (perfume) 0.2
【0020】比較例1 炭酸水素ナトリウム 56.0 無水リンゴ酸 25.0 庶糖 15.0 ラウリン酸ナトリウム 4.0Comparative Example 1 Sodium bicarbonate 56.0 Malic anhydride 25.0 Sucrose 15.0 Sodium laurate 4.0
【0021】比較例2 炭酸水素ナトリウム 64.0 無水クエン酸 20.0 乳糖 12.5 ラウリル硫酸ナトリウム 3.5Comparative Example 2 Sodium bicarbonate 64.0 Citric anhydride 20.0 Lactose 12.5 Sodium lauryl sulfate 3.5
【0022】比較例3 炭酸水素ナトリウム 54.5 無水リンゴ酸 25.0 乳糖 12.0 ラウロイルメチルタウリンナトリウム 5.5 アルミン酸ナトリウム 3.0Comparative Example 3 Sodium bicarbonate 54.5 Malic anhydride 25.0 Lactose 12.0 Sodium lauroylmethyltaurine 5.5 Sodium aluminate 3.0
【0023】総合評価 次に、発泡時間、洗浄性、溶解性、経時安定性の各項目
に関する実施例、比較例の評価結果を表1に示す。Comprehensive Evaluation Next, Table 1 shows the evaluation results of Examples and Comparative Examples for each item of foaming time, detergency, solubility, and stability over time.
【0024】[0024]
【表1】 [Table 1]
【0025】300mlのビーカーに2.0×6.0c
mのスライドガラスならびに2.0×6.0cmのステ
ンレス板に人の皮脂を綿棒で均一に付着させたものをセ
ットし水温20℃、250mlの水を注入した後、各錠
剤を1錠いれ発泡終了までの時間ならびに10分後の汚
れの残存量ならびに液の状態を観察した。また、経時安
定性については50℃で100時間保存したものの状態
ならびに前記試験を同様に行った。2.0 × 6.0 c in a 300 ml beaker
After placing the human sebum uniformly on a 2.0 x 6.0 cm stainless steel plate with a cotton swab on a glass slide and a 2.0 x 6.0 cm stainless steel plate, injecting 250 ml of water at a water temperature of 20 ° C, add 1 tablet of each tablet and foam. The time until completion, the remaining amount of soil after 10 minutes, and the state of the liquid were observed. In addition, the stability with the lapse of time was measured in the same manner as in the case of storage at 50 ° C. for 100 hours, and the above-mentioned test was performed.
【0026】洗浄性 ○ 皮脂の残存は認められない。 △ 一部皮脂の残存が認められる。 × 殆ど皮脂が残存している。Detergency: No sebum remains. △ Some sebum remains. × Almost sebum remains.
【0027】溶解性 ○ 溶け残りはなく無色透明。 △ 底部に溶け残りあり。 × 懸濁もしくは水面に浮遊物あり。Solubility ○ Colorless and transparent with no undissolved residue. △ Undissolved at bottom. × Suspended or floating on the water surface.
【0028】経時安定性については包装材の変化につい
て評価した。 ○ 変化がなかった。 △ 包材がやや膨潤していた。 × 包材が破裂し錠剤が崩壊した。With respect to the stability over time, changes in the packaging material were evaluated. ○ There was no change. △ The packaging material was slightly swollen. × The packaging material burst and the tablet disintegrated.
【0029】[0029]
【発明の効果】本発明は上述のような構成を有するもの
であり、長期間高温の環境下に於いても従来品のような
変質を起さない安定な発泡錠剤洗浄剤を提供することが
出来る。According to the present invention, which has the above-mentioned structure, it is possible to provide a stable foaming tablet detergent which does not cause deterioration unlike conventional products even under a high temperature environment for a long time. I can do it.
フロントページの続き (51)Int.Cl.6 識別記号 FI //(C11D 3/60 3:06 3:10 3:20 3:22) (C11D 9/60 9:12 9:26) Continued on the front page (51) Int.Cl. 6 Identification symbol FI // (C11D 3/60 3:06 3:10 3:20 3:22) (C11D 9/60 9:12 9:26)
Claims (2)
無機酸、結合剤及び安定剤として無水リン酸塩を0.0
1〜10.0重量%含有することを特徴とする発泡錠剤
洗浄剤。1. Anhydrous phosphate as a surfactant, carbonate, solid organic or inorganic acid, binder and stabilizer in an amount of 0.0
An effervescent tablet detergent containing 1 to 10.0% by weight.
二ナトリウム、リン酸三ナトリウム、ピロリン酸ナトリ
ウム、トリポリリン酸ナトリウム、テトラリン酸ナトリ
ウム、ヘキサメタリン酸ナトリウム、リン酸一カリウ
ム、リン酸二カリウム、リン酸三カリウム、ピロリン酸
カリウム、トリポリリン酸カリウム、テトラリン酸カリ
ウム、ヘキサメタリン酸カリウムから選ばれる1種又は
2種以上の無水リン酸塩である請求項1記載の発泡錠剤
洗浄剤。2. The phosphate salt is monosodium phosphate, disodium phosphate, trisodium phosphate, sodium pyrophosphate, sodium tripolyphosphate, sodium tetraphosphate, sodium hexametaphosphate, monopotassium phosphate, dipotassium phosphate, 2. The foamed tablet detergent according to claim 1, wherein the detergent is one or more anhydrous phosphates selected from tripotassium phosphate, potassium pyrophosphate, potassium tripolyphosphate, potassium tetraphosphate, and potassium hexametaphosphate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9041364A JPH10204500A (en) | 1997-01-20 | 1997-01-20 | Effervescent tablet detergent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9041364A JPH10204500A (en) | 1997-01-20 | 1997-01-20 | Effervescent tablet detergent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10204500A true JPH10204500A (en) | 1998-08-04 |
Family
ID=12606416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9041364A Pending JPH10204500A (en) | 1997-01-20 | 1997-01-20 | Effervescent tablet detergent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10204500A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000027986A1 (en) * | 1998-11-09 | 2000-05-18 | Henkel Kommanditgesellschaft Auf Aktien | Moulded detergent and cleaning agent bodies with additives |
WO2000039260A1 (en) * | 1998-12-23 | 2000-07-06 | Henkel Kommanditgesellschaft Auf Aktien | Phosphate compounds |
WO2000077150A1 (en) * | 1999-06-10 | 2000-12-21 | Henkel Kommanditgesellschaft Auf Aktien | Effervescent tablets with a long shelf-life |
GB2345916B (en) * | 1997-12-30 | 2002-07-24 | Ecolab Inc | Alkaline solid block composition |
JP2018083763A (en) * | 2016-11-21 | 2018-05-31 | 花王株式会社 | Intraoral foaming formulation and production method thereof |
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JPS4858006A (en) * | 1971-11-11 | 1973-08-15 | ||
JPS51144743A (en) * | 1975-06-06 | 1976-12-13 | Blendax Werke Schneider Co | Compound for artificial tooth washing |
JPS5748712A (en) * | 1980-09-08 | 1982-03-20 | Hoya Corp | Contact lens washing agent |
JPS61228100A (en) * | 1985-04-01 | 1986-10-11 | 株式会社ソフト九九コーポレーション | Foamable detergent composition |
JPS6250400A (en) * | 1985-08-30 | 1987-03-05 | 三金工業株式会社 | Method for preparing washing solution of tray for impressionmaterial |
JPS6386799A (en) * | 1986-07-15 | 1988-04-18 | ワ−ナ−−ランバ−ト・コンパニ− | Denture purifying and/or cleaning composition containing bleaching activator |
JPH03284604A (en) * | 1990-03-30 | 1991-12-16 | Hoya Corp | Agent composition for contact lens |
JPH07109499A (en) * | 1993-10-08 | 1995-04-25 | Osaka Seiyaku:Kk | Foaming detergent |
JPH07278598A (en) * | 1994-04-05 | 1995-10-24 | Pias Arise Kk | Deodorizing and washing agent for water closet |
WO1996028558A1 (en) * | 1995-03-09 | 1996-09-19 | The Procter & Gamble Company | Thermitase variants having decreased adsorption and increased hydrolysis |
WO1996028557A2 (en) * | 1995-03-09 | 1996-09-19 | The Procter & Gamble Company | Subtilisin dy variants having decreased adsorption and increased hydrolysis |
WO1996028556A2 (en) * | 1995-03-09 | 1996-09-19 | The Procter & Gamble Company | Proteinase k variants having decreased adsorption and increased hydrolysis |
WO1996028566A2 (en) * | 1995-03-08 | 1996-09-19 | The Procter & Gamble Company | Subtilisin carlsberg variants having decreased adsorption and increased hydrolysis |
-
1997
- 1997-01-20 JP JP9041364A patent/JPH10204500A/en active Pending
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4858006A (en) * | 1971-11-11 | 1973-08-15 | ||
JPS51144743A (en) * | 1975-06-06 | 1976-12-13 | Blendax Werke Schneider Co | Compound for artificial tooth washing |
JPS5748712A (en) * | 1980-09-08 | 1982-03-20 | Hoya Corp | Contact lens washing agent |
JPS61228100A (en) * | 1985-04-01 | 1986-10-11 | 株式会社ソフト九九コーポレーション | Foamable detergent composition |
JPS6250400A (en) * | 1985-08-30 | 1987-03-05 | 三金工業株式会社 | Method for preparing washing solution of tray for impressionmaterial |
JPS6386799A (en) * | 1986-07-15 | 1988-04-18 | ワ−ナ−−ランバ−ト・コンパニ− | Denture purifying and/or cleaning composition containing bleaching activator |
JPH03284604A (en) * | 1990-03-30 | 1991-12-16 | Hoya Corp | Agent composition for contact lens |
JPH07109499A (en) * | 1993-10-08 | 1995-04-25 | Osaka Seiyaku:Kk | Foaming detergent |
JPH07278598A (en) * | 1994-04-05 | 1995-10-24 | Pias Arise Kk | Deodorizing and washing agent for water closet |
WO1996028566A2 (en) * | 1995-03-08 | 1996-09-19 | The Procter & Gamble Company | Subtilisin carlsberg variants having decreased adsorption and increased hydrolysis |
WO1996028558A1 (en) * | 1995-03-09 | 1996-09-19 | The Procter & Gamble Company | Thermitase variants having decreased adsorption and increased hydrolysis |
WO1996028557A2 (en) * | 1995-03-09 | 1996-09-19 | The Procter & Gamble Company | Subtilisin dy variants having decreased adsorption and increased hydrolysis |
WO1996028556A2 (en) * | 1995-03-09 | 1996-09-19 | The Procter & Gamble Company | Proteinase k variants having decreased adsorption and increased hydrolysis |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2345916B (en) * | 1997-12-30 | 2002-07-24 | Ecolab Inc | Alkaline solid block composition |
WO2000027986A1 (en) * | 1998-11-09 | 2000-05-18 | Henkel Kommanditgesellschaft Auf Aktien | Moulded detergent and cleaning agent bodies with additives |
WO2000039260A1 (en) * | 1998-12-23 | 2000-07-06 | Henkel Kommanditgesellschaft Auf Aktien | Phosphate compounds |
WO2000077150A1 (en) * | 1999-06-10 | 2000-12-21 | Henkel Kommanditgesellschaft Auf Aktien | Effervescent tablets with a long shelf-life |
JP2018083763A (en) * | 2016-11-21 | 2018-05-31 | 花王株式会社 | Intraoral foaming formulation and production method thereof |
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