JPS6022644B2 - aqueous zeolite suspension - Google Patents

aqueous zeolite suspension

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Publication number
JPS6022644B2
JPS6022644B2 JP13613580A JP13613580A JPS6022644B2 JP S6022644 B2 JPS6022644 B2 JP S6022644B2 JP 13613580 A JP13613580 A JP 13613580A JP 13613580 A JP13613580 A JP 13613580A JP S6022644 B2 JPS6022644 B2 JP S6022644B2
Authority
JP
Japan
Prior art keywords
zeolite
water
suspension
viscosity
sodium
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP13613580A
Other languages
Japanese (ja)
Other versions
JPS5761615A (en
Inventor
輝夫 鈎
誠治 阿部
昌允 中村
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP13613580A priority Critical patent/JPS6022644B2/en
Publication of JPS5761615A publication Critical patent/JPS5761615A/en
Publication of JPS6022644B2 publication Critical patent/JPS6022644B2/en
Expired legal-status Critical Current

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  • Detergent Compositions (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Description

【発明の詳細な説明】 本発明は洗浄剤原料用のゼオラィト懸濁液に関するもの
であり、さらに詳しくは環境温度で流動性を保ち、長時
間の貯蔵においても層分離することのない安定なゼオラ
ィトスラリーに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a zeolite suspension for use as a raw material for cleaning agents, and more specifically to a stable zeolite suspension that maintains fluidity at ambient temperatures and does not undergo phase separation even during long-term storage. Regarding the title slurry.

衣類用洗剤のビルダ−として従来の燐酸塩の代りに水不
溶性のアルミノ珪酸塩(ゼオラィト)の使用が提案され
ている(持開昭50−12斑1)。ゼオラィトを含む粉
粒状洗剤を製造する方法としてはゼオラィトを除く洗剤
スラリーに微粉末ゼオラィトを分散させ、それを頃霧乾
燥する方法があるが、微粉末ゼオラィトを洗剤スラリー
に分散するのは(1}洗剤スラリーの粘性が高いことも
あり均一に分散するのはむずかしい、{21粉塵が発生
し易いなどの問題があり、これを解決する方法としてゼ
オラィトを水に分散させ、ゼオラィト含有量30〜50
%程度のゼオラィト懸濁液をあらかじめ調製し、このゼ
オラィト懸濁液を洗剤スラIJ一に混合する方法が良好
と思われる。しかし、ゼオラィト−水懸濁液は水とゼオ
ラィトの比重差があることもあり不安定で、静贋貯蔵し
た場合にゼオラィトが沈降分離して好ましくない。
The use of a water-insoluble aluminosilicate (zeolite) in place of the conventional phosphate as a builder for laundry detergents has been proposed (1977-12, 1993). As a method for producing powdery detergent containing zeolite, there is a method of dispersing finely powdered zeolite in a detergent slurry excluding zeolite and then spray-drying it. Due to the high viscosity of the detergent slurry, there are problems such as it is difficult to disperse uniformly and dust is easily generated.As a way to solve this problem, zeolite is dispersed in water and the zeolite content is 30 to 50%.
% of zeolite suspension is prepared in advance and this zeolite suspension is mixed into the detergent slurry IJ. However, zeolite-water suspensions are unstable due to the difference in specific gravity between water and zeolite, and when stored statically, the zeolite will settle and separate, which is not preferred.

ゼオラィト水懸濁液の安定化方法としては水灘溶性非イ
オン活性剤の添加(特関昭51−91898)あるいは
水溶性非イオン活性剤と可溶性塩の併用(椿開昭54−
155200)や珪酸ナトリウム溶液への分散(特開昭
54一64504)などが提案されているが、水難溶性
非イオン活性剤の場合は安定化に十分な量添加すると懸
濁液の粘度、特に低温での粘度が高くなり、常温では流
動性を失なってしまうため、懸濁液の貯蔵、ポンプ移送
は加熱保温状態で行う必要があり、実際の操作や装作や
装置上問題がある。水溶性非イオン活性剤と可溶性塩と
の併用の場合は非イオン活性剤が水落性であるため懸濁
液の粘度に対する影響はあまりないが、安定化効果が不
十分であり、しかもかなり多量の非イオン活性剤を必要
とするので、その後の粉粒状洗剤の製造工程のうち熱風
燈霧乾燥工程中で非イオン活性剤の一部飛散が起り、環
境汚染防止面で特別の装置を必要とするなどもあって良
好な方法ではない。
Methods for stabilizing zeolite aqueous suspensions include adding a water-soluble nonionic activator (Tokusei 1989-91898) or using a combination of a water-soluble nonionic activator and a soluble salt (Tsubaki 1977-91898).
155200) or dispersion in a sodium silicate solution (Japanese Patent Application Laid-Open No. 54-164504). However, in the case of poorly water-soluble nonionic surfactants, adding a sufficient amount to stabilize the viscosity of the suspension, especially at low temperatures, has been proposed. Since the viscosity increases and the suspension loses its fluidity at room temperature, the suspension needs to be stored and pumped while being heated and kept warm, which poses problems in actual operation, equipment, and equipment. When a water-soluble nonionic surfactant and a soluble salt are used together, the nonionic surfactant is water-soluble, so it does not have much effect on the viscosity of the suspension, but the stabilizing effect is insufficient, and a considerably large amount Since a non-ionic activator is required, some of the non-ionic activator will be scattered during the hot air lamp fog drying process of the subsequent manufacturing process of powdered detergent, and special equipment is required to prevent environmental pollution. This is not a good method due to other reasons.

また珪酸ナトリウム水溶液への微細ゼオラィトの分散方
法は珪酸ナトリウムが洗剤原料の1つであり、操作面で
も簡便な方法であるが、長時間貯蔵すると下層に粘着性
ゲル状物が徐々に沈積し、この汝積ゲル状物は再分散が
困難であるので、貯蔵する場合には常に十分な損拝を必
要として、実際の操作面で問題がある。本願発明者等は
長時間の貯蔵においても安定で、低温においても流動性
良好で取り扱い易い水性ゼオラィト懸濁液を得るため鋭
意研究を重ねた結果、分散安定化剤として水難潟性非イ
オン活性剤と特定の水溶性塩を併用することにより、熱
風乾燥において飛散する非イオン活性剤の量も非常に少
なくして、しかも安定で流動性のあるゼオラィト懸濁液
が得られることを見出し、この知見に基づいて本発明を
完成するに至った。
In addition, the method of dispersing fine zeolite in an aqueous sodium silicate solution uses sodium silicate as one of the detergent raw materials, and is a simple method in terms of operation, but when stored for a long time, a sticky gel-like substance gradually deposits in the lower layer. This gelatinous material is difficult to redisperse, and therefore requires sufficient storage whenever stored, which poses a problem in practical operation. The inventors of the present application have conducted intensive research to obtain an aqueous zeolite suspension that is stable even during long-term storage, has good fluidity even at low temperatures, and is easy to handle. We discovered that by using a specific water-soluble salt in combination with a specific water-soluble salt, the amount of non-ionic active agent scattered during hot air drying could be extremely reduced, and a stable and fluid zeolite suspension could be obtained. Based on this, the present invention was completed.

即ち本発明の水性ゼオラィト懸濁液は、【a}無水物と
して35〜50重量%の微細ゼオラィト、{b’0.2
〜0.4重量%の水鱗熔性非イオン界面活性剤および{
c}0.3〜3.の重量%の硫酸ナトリウム、炭酸ナト
リウム、塩化ナトリウムおよびクエン酸ナトリウムの群
から選ばれる1種以上の水溶性塩を含有することを特徴
とする。
That is, the aqueous zeolite suspension of the present invention contains [a] 35 to 50% by weight of fine zeolite as anhydride, {b'0.2
~0.4% by weight of a scale-melting nonionic surfactant and {
c}0.3-3. % by weight of one or more water-soluble salts selected from the group of sodium sulfate, sodium carbonate, sodium chloride and sodium citrate.

以下、本発明についてさらに詳細に説明する。The present invention will be explained in more detail below.

【a)ゼオラィトとしては、天然及び合成ゼオラィトが
使用できる。合成ゼオライトとしてはA型、X型、Y型
などがあるが、A型ゼオラィトがもっとも好ましい。ゼ
オラィトの平均粒径は0.5〜10仏、好ましくは1〜
5Aが良い。ゼオラィト量は無水物として35〜5仇九
%好ましくは40〜45M%である。35%未満では通
常の洗剤スラリーの固形分は35%以上であるので、ゼ
オラィトスラリーを洗剤スラリーに添加すると、洗剤ス
ラリー中の水分量が増加し、(曙霧)乾燥における負荷
が大きくなって好ましくない。
(a) As the zeolite, natural and synthetic zeolites can be used. Synthetic zeolites include A-type, X-type, Y-type, etc., but A-type zeolite is most preferred. The average particle size of zeolite is 0.5-10 French, preferably 1-10
5A is good. The amount of zeolite is 35-5.9% as anhydride, preferably 40-45M%. If it is less than 35%, the solid content of normal detergent slurry is more than 35%, so when zeolite slurry is added to the detergent slurry, the water content in the detergent slurry increases and the load during drying (Akebono fog) increases. Undesirable.

50%を越えるとゼオラィトスラリーの粘度が高くなり
取扱いが困難となる。
If it exceeds 50%, the viscosity of the zeolite slurry becomes high and handling becomes difficult.

肋 非イオン活性剤としては、水難綾性で、1%水溶液
の雲点が室温以下のものが用いられる。
As the nonionic activator, one that is water-resistant and has a cloud point of a 1% aqueous solution below room temperature is used.

その代表例としては、炭素数9〜2帆旨肪族アルコール
エチレンオキシドおよび/またはプロピレンオキシド付
加物、例えばャシアルコールェトキシレート(EO P
=1〜3)、牛脂アルコールヱトキシレート(EO P
=2〜7)、オレイルアルコールエトキシレート(EO
P=2〜7)など、アルキル炭素数6〜12アルキル
フエノールエチレンオキシドおよび/またはプロピレン
オキシド付加物、例えばノニルフェノールエトキシレー
ト(EO P=2〜6)などが挙げられる。ここで「E
O P」はエチレンオキシドの平均付加モル数を表わす
。非イオン活性剤の添加量は0.2〜0.4M%である
Typical examples thereof include ethylene oxide and/or propylene oxide adducts of aliphatic alcohols with 9 to 2 carbon atoms, such as chasal alcohol ethoxylates (EOPs).
= 1 to 3), beef tallow alcohol ethoxylate (EO P
= 2-7), oleyl alcohol ethoxylate (EO
P=2-7), alkylphenol having 6-12 carbon atoms, ethylene oxide and/or propylene oxide adducts, such as nonylphenol ethoxylate (EO P=2-6), and the like. Here, “E
"OP" represents the average number of added moles of ethylene oxide. The amount of nonionic activator added is 0.2 to 0.4 M%.

0.2%未満では静層安定性が劣り層分離を起こし、0
.4%を越えると長期保存によりスラリーの粘度が高く
なり流動性を失なって取扱い困難となる。‘cー 水落
性塩としては硫酸ナトリウム、炭酸ナトリウム、塩化ナ
トリウム、クエン酸ナトリウムの1種以上が使用され、
好ましくはクエン酸ナトリウムである。
If it is less than 0.2%, static layer stability will be poor and layer separation will occur.
.. If it exceeds 4%, the viscosity of the slurry increases due to long-term storage, and it loses fluidity, making it difficult to handle. 'c- One or more of sodium sulfate, sodium carbonate, sodium chloride, and sodium citrate is used as the water-dropping salt,
Preferred is sodium citrate.

水溶性塩の量は0.3〜3.0%であり、0.3%未満
では安定性が劣り、3%を越えると粘度が高くなり、流
動性を失なって取扱いが困難となる。
The amount of water-soluble salt is 0.3 to 3.0%, and if it is less than 0.3%, the stability will be poor, and if it exceeds 3%, the viscosity will be high and the fluidity will be lost, making it difficult to handle.

上記非イオン活性剤と水溶性塩は単独で使用しても十分
な効果が得られない。実施例 【bー非イオン活性剤および‘c}水溶性塩の種類およ
び量を表−1に示すように変化させて下記の処方で水性
ゼオラィト懸濁液No.1〜No.15を調製した。
Even if the above-mentioned nonionic activator and water-soluble salt are used alone, sufficient effects cannot be obtained. Example [b - Nonionic active agent and 'c] Aqueous zeolite suspension No. 1 was prepared with the following formulation by changing the type and amount of the water-soluble salt as shown in Table 1. 1~No. 15 was prepared.

A型ゼオラィト 4肌t%(水沢化学
シルトン、平均流蓬1.4〃)非イオン活性剤
所定量%水溶性塩 所定
量%水 残量これらに
ついて、保存試験を行ない保存後の分離安定性及び粘度
変化を測定し、その結果を表−1に示した。
A-type zeolite 4 skin t% (Mizusawa Chemical Silton, average flow rate 1.4) Nonionic active agent
Predetermined amount % water-soluble salt Predetermined amount % water Remaining amount These were subjected to a storage test to measure separation stability and viscosity change after storage, and the results are shown in Table 1.

粘度および保存安定性について次のように測定し、検定
した。【11 粘 度 B型粘度計を用いて、回転数2仇pm,2500で測定
した。
The viscosity and storage stability were measured and verified as follows. [11. Viscosity Measured using a B-type viscometer at a rotational speed of 2 pm and 2500 rpm.

粘度が10肥を越えると流動性が小さくなり実際のハン
ドリングが困難になり好ましくない。■ 保存安定性 懸濁液をガラスビンにとり密封して25qoで静贋保存
した。
If the viscosity exceeds 10 ml, the fluidity becomes low and actual handling becomes difficult, which is not preferable. (2) Storage stability The suspension was placed in a glass bottle, sealed and stored statically at 25 qo.

経日により分離安定性及び粘度を測定した。分離安定性
は上層の透明層は肉眼で判定し、下層の沈着ゲル状物は
直径5側のガラス榛をガラスビンの上から垂直に静かに
差しこみ、ゲル状物に当って止まった時の長さを測定し
全量に対する容積%で表わす。分離安定性は9日間静暦
保存して上層は30%以下、下層は1%以下のものが良
好である。
Separation stability and viscosity were measured over time. Separation stability is determined by visually inspecting the upper transparent layer, and determining the gel-like substance deposited in the lower layer by gently inserting a diameter 5 glass rod vertically from the top of the glass bottle and measuring the length of time when it hits the gel-like substance and stops. The density is measured and expressed as volume % based on the total amount. Separation stability is good if the upper layer is 30% or less and the lower layer is 1% or less after static storage for 9 days.

表−1 (1)*は本発明の水性ゼオラィト懸濁液である。Table-1 (1) * is the aqueous zeolite suspension of the present invention.

Claims (1)

【特許請求の範囲】[Claims] 1 (a)無水物として35〜50重量%の微細ゼオラ
イト、(b)0.2〜0.4重量%の水難溶性非イオン
界面活性剤および(c)0.3〜3.0重量%の硫酸ナ
トリウム、炭酸ナトリウム、塩化ナトリウムおよびクエ
ン酸ナトリウムの群から選ばれる1種以上の水溶性塩を
含有することを特徴とする水性ゼオライト懸濁液。
1 (a) 35-50% by weight of fine zeolite as anhydride, (b) 0.2-0.4% by weight of poorly water-soluble nonionic surfactant, and (c) 0.3-3.0% by weight. An aqueous zeolite suspension characterized by containing one or more water-soluble salts selected from the group of sodium sulfate, sodium carbonate, sodium chloride and sodium citrate.
JP13613580A 1980-09-30 1980-09-30 aqueous zeolite suspension Expired JPS6022644B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13613580A JPS6022644B2 (en) 1980-09-30 1980-09-30 aqueous zeolite suspension

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13613580A JPS6022644B2 (en) 1980-09-30 1980-09-30 aqueous zeolite suspension

Publications (2)

Publication Number Publication Date
JPS5761615A JPS5761615A (en) 1982-04-14
JPS6022644B2 true JPS6022644B2 (en) 1985-06-03

Family

ID=15168117

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13613580A Expired JPS6022644B2 (en) 1980-09-30 1980-09-30 aqueous zeolite suspension

Country Status (1)

Country Link
JP (1) JPS6022644B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH055328U (en) * 1991-07-11 1993-01-26 コベルコ建機エンジニアリング株式会社 Steel plate cutting machine

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5866496A (en) * 1989-03-10 1999-02-02 Thiele Kaolin Company Cracking catalyst and process for preparing same
US5330943A (en) * 1989-03-10 1994-07-19 Thiele Kaolin Company Process for improving the physical and catalytic properties of a fluid cracking catalyst
US5711930A (en) * 1989-03-10 1998-01-27 Thiele Kaolin Company Process for improving the phyiscal properties of formed particles
US5476610A (en) * 1991-07-22 1995-12-19 Henkel Kommanditgesellschaft Auf Aktien Process for stabilizing aqueous zeolite suspensions
DE4203789A1 (en) * 1992-02-10 1993-08-12 Henkel Kgaa METHOD FOR STABILIZING AQUEOUS ZEOLITE SUSPENSIONS

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH055328U (en) * 1991-07-11 1993-01-26 コベルコ建機エンジニアリング株式会社 Steel plate cutting machine

Also Published As

Publication number Publication date
JPS5761615A (en) 1982-04-14

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