JPS6049124B2 - Method for drying aluminosilicate slurry - Google Patents
Method for drying aluminosilicate slurryInfo
- Publication number
- JPS6049124B2 JPS6049124B2 JP7323978A JP7323978A JPS6049124B2 JP S6049124 B2 JPS6049124 B2 JP S6049124B2 JP 7323978 A JP7323978 A JP 7323978A JP 7323978 A JP7323978 A JP 7323978A JP S6049124 B2 JPS6049124 B2 JP S6049124B2
- Authority
- JP
- Japan
- Prior art keywords
- aluminosilicate
- drying
- slurry
- particles
- detergent
- 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
Links
Landscapes
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Detergent Compositions (AREA)
Description
【発明の詳細な説明】
本発明はアルミノ珪酸塩を含む衣類用粒状洗剤に使用す
るアルミノ珪酸塩スラリーの乾燥方法に関するもので、
さらに詳しくは微細アルミノ珪酸塩粒子を含むアルミノ
珪酸塩懸濁スラリーを乾燥するに当り、乾燥工程で微細
アルミノ珪酸塩粒子が2次凝集等により粗大粒子を形成
することを極めて少なくする乾燥方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for drying an aluminosilicate slurry used in a granular laundry detergent containing an aluminosilicate.
More specifically, the present invention relates to a method for drying an aluminosilicate suspension slurry containing fine aluminosilicate particles, which greatly reduces the formation of coarse particles due to secondary aggregation of the fine aluminosilicate particles during the drying process.
従来、衣類用の洗剤ビルダーとしてトリポリ燐酸塩等の
燐酸塩が多く使用されてきたが、近年燐分は湖沼の高栄
養化、赤潮等の環境問題を引き起す一因であることが指
摘されており、洗剤中の燐酸塩の配合量が規制されるよ
うになつてきた。Traditionally, phosphates such as tripolyphosphate have been widely used as laundry detergent builders, but in recent years it has been pointed out that phosphorus is a contributing factor to environmental problems such as high nutrient content in lakes and red tide. As a result, the amount of phosphates contained in detergents has come to be regulated.
このようなことから、燐酸塩に代替するビルダーとして
、珪酸塩、炭酸塩、重炭酸塩等のアルカリビルダーやク
エン酸塩等の有機ビルダーが提案されているが、これら
は水の硬度が比較的低い場合はある程度効果を有するも
のの、硬度が高い場合は必らずしも十分でない。水の硬
度が高い場合も十分な効果を発揮するビルダーとして硬
水中のCaイオンを捕捉する性質を有するゼオライトの
使用が提案されている(特開昭50−12381、特開
昭50−100378、特開昭50−53404)。For this reason, alkali builders such as silicates, carbonates, and bicarbonates, and organic builders such as citrates have been proposed as builders to replace phosphates, but these builders have relatively low water hardness. Although it has some effect when the hardness is low, it is not necessarily sufficient when the hardness is high. The use of zeolite, which has the property of capturing Ca ions in hard water, has been proposed as a builder that is sufficiently effective even when water hardness is high (Japanese Patent Application Laid-open No. 50-12381, JP-A No. 50-100378, JP-A-50-100378, (1976-53404).
しかしア?レミノ珪酸塩は水不溶性であり、洗剤ビルダ
ーとして使用するには極めて微細な粒子とする必要があ
る。粒径10μ以下、好ましくは数μ以下の微細な粒子
として使用することにより、洗濯中でのCaイオン捕促
能も高まるし、又被洗物に付着するのを防止することが
でき、あるいはたとえ付着しても目立たなくすることが
できる。アルミノ珪酸塩は粉体あるいは水懸濁スラリー
として入手することができる。But a? Reminosilicates are water-insoluble and must be made into extremely fine particles for use as detergent builders. By using fine particles with a particle size of 10 μm or less, preferably several μm or less, the ability to capture Ca ions during washing can be increased, and it is possible to prevent them from adhering to the laundry. Even if it sticks, it can be made inconspicuous. Aluminosilicates are available as powders or slurries in water suspension.
しかし粉体のアルミノ珪酸塩は粒径0.1μ〜数μ程度
の1次粒子が・凝集して、殆んどが粒径50〜400μ
の2次粒子(粗大粒子)を形成しており、このまま洗剤
に配合しても、Caイオンを捕捉する効果も十分でなく
、被洗物にも付着することから好ましくない。一方、水
懸濁スラリーではアルミノ珪酸塩粒子はフ殆んど1次粒
子として存在しており、流動性もあり取扱い易いもので
はあるが、その固形分は30〜40Wt%が普通であり
、これ以上固形分を増大させると、その固有の性質から
ダイラタンシーな粘性が強まり、実際的な取扱いが不可
能な状態にな5る。ところで、噴霧乾燥用洗剤スラリー
は固形分が60wt%程度以上が多いが固形分30〜4
0wt%のアルミノ珪酸塩懸濁スラリーを界面活性剤や
その他ビルダーを含む洗剤スラリーに配合する楊合、ア
ルミノ珪酸塩の配合量が少なければともかく、配合量を
多くしようとすると、調製された洗剤スラリーの固形分
はかなり低下することになり、このようなスラリーを噴
霧乾燥すると、乾燥塔の負荷が著しく、乾燥効率の低下
ばかりでなく、乾燥洗剤粒子の嵩密度や粉体物性にも影
響を及ぼし好ましくない。However, in powdered aluminosilicate, primary particles with a particle size of about 0.1 μm to several μm aggregate, and most of them have a particle size of 50 to 400 μm.
Ca ions form secondary particles (coarse particles), and even if they are blended into detergents as they are, the effect of capturing Ca ions will not be sufficient and they will also adhere to the items being washed, which is not preferable. On the other hand, in an aqueous suspension slurry, aluminosilicate particles exist mostly as primary particles, and although they are fluid and easy to handle, the solid content is usually 30 to 40 wt%, which is If the solid content is increased above, the dilatant viscosity increases due to its inherent properties, making it impossible to handle it practically. By the way, most detergent slurries for spray drying have a solid content of about 60 wt% or more, but the solid content is 30 to 4 wt%.
When blending 0wt% aluminosilicate suspension slurry into a detergent slurry containing surfactants and other builders, even if the amount of aluminosilicate is small, if the amount is increased, the detergent slurry prepared The solid content of the slurry will be considerably reduced, and spray drying such a slurry will place a significant load on the drying tower, which will not only reduce drying efficiency but also affect the bulk density and powder properties of the dried detergent particles. Undesirable.
洗剤スラリーの固形分を低下させずにアルミノ珪酸塩を
配合する方法として、アルミノ珪酸塩懸濁スラリーのみ
をあらかじめ噴霧乾燥により半乾きないし乾燥状態とす
ることも考えられるが、この方法では乾燥工程中で凝集
が起り、2次粒子(粗大粒子)が生ずるため、洗剤配合
に適したアルミノ珪酸塩を得ることができない。又、ア
ルミノ珪酸塩スラリーと洗剤スラリーを別々に同一乾燥
空間内に噴霧乾燥する方法(特開昭53−39307号
、特開昭53−51212号)、が提案されているが、
物体物性及び粉塵の点で使用量が限定される。本発明者
等はアルミノ珪酸塩懸濁スラリーの乾燥工程におけるア
ルミノ珪酸塩粒子の凝集機構について鋭意研究を重ねた
結果、アルミノ珪酸塩懸濁液液滴は外部加熱により、そ
の表面層のみが急速に乾燥し、強固な殼を形成し、この
殻に囲まれ2た状態で凝集体一粗大粒子−が生成するこ
とを見出し、さらにこのような凝集を防止するには液滴
の内外部をより均一に乾燥することが有効であることを
見出し、この知見に基づいて本発明を完成するに至つた
。As a method of blending aluminosilicate without reducing the solid content of the detergent slurry, it is possible to spray dry only the aluminosilicate suspension slurry in advance to a semi-dry or dry state, but this method Since agglomeration occurs and secondary particles (coarse particles) are produced, it is not possible to obtain aluminosilicate suitable for detergent formulation. Furthermore, a method has been proposed in which an aluminosilicate slurry and a detergent slurry are spray-dried separately in the same drying space (Japanese Patent Application Laid-open Nos. 53-39307 and 53-51212).
The amount used is limited due to physical properties and dust. As a result of extensive research into the agglomeration mechanism of aluminosilicate particles during the drying process of aluminosilicate suspension slurry, the present inventors found that when aluminosilicate suspension droplets are heated externally, only their surface layer rapidly It was discovered that when the droplet dries, it forms a strong shell, and when it is surrounded by this shell, aggregates (coarse particles) are formed.In order to prevent such aggregation, the inside and outside of the droplet should be made more uniform. We have found that drying is effective, and based on this knowledge, we have completed the present invention.
3即ち本発明は、アル
ミノ珪酸塩10〜50重量%、水分50〜9呼量%を含
有するアルミノ珪酸塩スラリーを乾燥するに当り、該ア
ルミノ珪酸塩スラリーを5k9/CTl以上に加圧下1
00℃以上に加熱し、温度50℃以下、大気圧中に噴霧
乾燥することを特3徴とするアルミノ珪酸塩スラリーの
乾燥方法を要旨とし、これによつて洗剤配合に適したア
ルミノ珪酸塩粒子を得んとするものである。本発明で使
用可能なアルミノ珪酸塩としては、天然及び合成ゼオラ
イトが挙げられ、具体的には41天然ゼオライトであれ
ばモルデナイト、クリノブチロライトなどが、合成ゼオ
ライトであればA型、X型、Y型などが使用できるが、
なかでも同一重量当りのイオン交換容量が高く、かつ立
方体に近い粒子であるA型が好ましい。本発明のアルミ
ノ珪酸塩スラリーは、これに分散するアルミノ珪酸塩粒
子径が0.1〜10μ、好ましくは0.5〜5μの範囲
にあり、アルミノ珪酸塩を10〜50重量%、水分を5
0〜9鍾量%含有する。アルミノ珪酸塩量が10%未満
では効率的な乾燥ができない。逆に50%以上になると
スラリーのダイラタンシー粘性が高く、噴霧できず、さ
らに高くなると乾燥の必要がない。本発明で採用される
噴霧条件は次の通りである。3 That is, in the present invention, when drying an aluminosilicate slurry containing 10 to 50% by weight of aluminosilicate and 50 to 9% by weight of water, the aluminosilicate slurry is dried under pressure of 5k9/CTl or more.
A method for drying aluminosilicate slurry characterized by heating above 00°C and spray drying at a temperature below 50°C under atmospheric pressure, thereby producing aluminosilicate particles suitable for formulation in detergents. The aim is to obtain the following. Examples of the aluminosilicate that can be used in the present invention include natural and synthetic zeolites.Specifically, 41 natural zeolites include mordenite and clinobutyrolite, and synthetic zeolites include A-type, X-type, Y type etc. can be used, but
Among these, type A, which has a high ion exchange capacity per weight and has nearly cubic particles, is preferred. The aluminosilicate slurry of the present invention has aluminosilicate particles dispersed therein in a diameter of 0.1 to 10 μm, preferably 0.5 to 5 μm, contains 10 to 50% by weight of aluminosilicate, and has a water content of 5% by weight.
Contains 0-9% by weight. If the amount of aluminosilicate is less than 10%, efficient drying cannot be achieved. On the other hand, if it exceeds 50%, the dilatancy viscosity of the slurry is so high that it cannot be sprayed, and if it becomes even higher, there is no need for drying. The spraying conditions employed in the present invention are as follows.
スラリー圧力;5k9/d以上、好ましくは10k9/
C!i〜20k9/Dl5k9/dよ りも
低いと、粒子凝集を十分防 止できない。Slurry pressure: 5k9/d or more, preferably 10k9/d
C! If it is lower than i~20k9/Dl5k9/d, particle aggregation cannot be sufficiently prevented.
20k9/C!iを越える と特別な耐圧装
置が必要とな る。20k9/C! If it exceeds i, special pressure-resistant equipment is required.
スラリー温度;100耐C以上、好ましくは100〜
200℃、100゜Cよりも低いと、粒子凝集
を十分防止できない。Slurry temperature: 100C or more, preferably 100~
200℃, lower than 100℃, particle aggregation
cannot be adequately prevented.
噴霧雰囲気温度・圧力;50゜C以下、大気圧下、温度
;80%RH以下、好ましくは60%RH以 下、
噴霧ノズル;使用可能のノズルのタイプは渦巻 室
型、遠心噴射型のいずれでも良い。Spraying atmosphere temperature/pressure: 50°C or less, atmospheric pressure, temperature: 80%RH or less, preferably 60%RH or less,
Spray nozzle: The type of nozzle that can be used is either a swirl chamber type or a centrifugal spray type.
2流体ノズルの使用も可能である。既述した通り、
アルミノ珪酸塩懸濁スラリーを通常の噴霧乾燥(200
〜300゜C気流中への噴霧)に上り乾燥すると凝集が
著しい。The use of two-fluid nozzles is also possible. As already mentioned,
The aluminosilicate suspension slurry was subjected to conventional spray drying (200
When the temperature rises to ~300°C (spraying into an air stream) and dries, significant agglomeration occurs.
これは多数の微細rルミノ珪酸塩を含む液滴が200〜
300℃の高温気頓こ接触すると、まず液滴の表層部が
急激に乾燥rるが、その時表層部に存在するアルミノ珪
酸塩立子が凝集して強固な殼を形成し、この殼に囲まt
た形で全体が乾燥することにより凝集粗大粒子バ形成す
る。これに対して本発明方法では高温高(ミ状態から低
温・低圧状態に液滴を噴霧すること=より、液滴表層部
からの乾燥が行なわれると同1に液滴内部水分の表層部
への急速な移動、蒸発く起るため、粒子凝集が抑制され
るものと考えらLる。従つて、本発明方法で得られたア
ルミノ珪乏塩は凝集粗大粒子(粒径50〜400μ)が
少な、殆んどが微細1次粒子(粒径0.1〜10μ)の
=態にある。この乾燥アルミノ珪酸塩は洗剤スラーに配
合しても良いし、あるいは別途調製した粒状洗剤と粉体
混合しても良い。実施例
平均粒径0.7μのアルミノ珪酸ソーダ(商シルトンD
BK、水沢化学工業(株)製)を40Wtむ水懸濁液を
表−1の条件で噴霧乾燥し、凝大粒子(粒径50μ以上
)の割合を測定した。This means that there are 200 to 200 droplets containing a large number of fine r-luminosilicate.
When the droplet comes into contact with high temperature air at 300°C, the surface layer of the droplet dries rapidly, but at that time, the aluminosilicate particles present on the surface agglomerate to form a strong shell, and the droplets are surrounded by this shell.
By drying the entire product in this state, agglomerated coarse particles are formed. On the other hand, in the method of the present invention, the droplets are sprayed from a high temperature state to a low temperature and low pressure state, so that when the droplets are dried from the surface layer, the moisture inside the droplets is transferred to the surface layer. It is thought that particle aggregation is suppressed due to the rapid movement and evaporation of Most of them are in the form of fine primary particles (particle size 0.1 to 10μ).This dry aluminosilicate can be blended into detergent slurry, or it can be mixed with separately prepared granular detergent and powder. They may be mixed.Example Sodium aluminosilicate (Shon Silton D) with an average particle size of 0.7μ
A water suspension containing 40 Wt of BK (manufactured by Mizusawa Chemical Industry Co., Ltd.) was spray-dried under the conditions shown in Table 1, and the proportion of coagulated particles (particle size of 50 μm or more) was measured.
実施例2−平均粒径4.3μのアルミノ珪酸ソーダ(水
沢化学工業(株)製シルトンDBK)を40W′t%、
ポリエチレングリコールー(ライオン油脂(株)製PE
G#400)をふ■%含む水懸濁液を表−2に示す条件
で噴霧乾燥し、凝集粗大粒子(粒径50μ以上)の割合
を測定した。Example 2 - 40W't% of sodium aluminosilicate (Silton DBK, manufactured by Mizusawa Chemical Industry Co., Ltd.) with an average particle size of 4.3μ,
Polyethylene glycol (PE manufactured by Lion Yushi Co., Ltd.)
An aqueous suspension containing 5% of G#400) was spray-dried under the conditions shown in Table 2, and the proportion of aggregated coarse particles (particle size of 50 μm or more) was measured.
Claims (1)
重量%を含有するアルミノ珪酸塩スラリーを乾燥するに
当り、該アルミノ珪酸塩スラリーを5kg/cm^2以
上に加圧下100℃以上に加熱し、温度50℃以下、大
気圧中に噴霧乾燥することを特徴とするアルミノ珪酸塩
スラリーの乾燥工方法。1 Aluminosilicate 10-50% by weight, moisture 50-90%
In drying the aluminosilicate slurry containing % by weight, the aluminosilicate slurry is heated to 100°C or more under pressure of 5 kg/cm^2 or more, and spray-dried at a temperature of 50°C or less at atmospheric pressure. A method for drying aluminosilicate slurry characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7323978A JPS6049124B2 (en) | 1978-06-19 | 1978-06-19 | Method for drying aluminosilicate slurry |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7323978A JPS6049124B2 (en) | 1978-06-19 | 1978-06-19 | Method for drying aluminosilicate slurry |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS553319A JPS553319A (en) | 1980-01-11 |
JPS6049124B2 true JPS6049124B2 (en) | 1985-10-31 |
Family
ID=13512425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7323978A Expired JPS6049124B2 (en) | 1978-06-19 | 1978-06-19 | Method for drying aluminosilicate slurry |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6049124B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01125334U (en) * | 1988-02-18 | 1989-08-25 | ||
JPH01153341U (en) * | 1988-04-14 | 1989-10-23 | ||
JP3025231U (en) * | 1995-07-19 | 1996-06-11 | ギュン−ゴン キム | Rescue band |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0818880B2 (en) * | 1987-10-13 | 1996-02-28 | 旭硝子株式会社 | High zirconia heat melting refractory |
JP2926966B2 (en) * | 1989-11-28 | 1999-07-28 | 旭硝子株式会社 | High zirconia hot-melt cast refractories |
US5344801A (en) * | 1992-06-26 | 1994-09-06 | Asahi Glass Company Ltd. | High zirconia fused cast refractory |
JP6030953B2 (en) | 2012-12-28 | 2016-11-24 | Agcセラミックス株式会社 | High zirconia electroformed refractory |
EP3453689B1 (en) | 2017-09-08 | 2020-08-26 | AGC Ceramics Co., Ltd. | High-zirconia electrocast refractory and method for manufacturing the same |
JP7099898B2 (en) | 2017-09-08 | 2022-07-12 | Agcセラミックス株式会社 | High zirconia electroformed refractory and its manufacturing method |
US20230406775A1 (en) | 2020-11-24 | 2023-12-21 | Saint-Gobain Tm K.K. | High-zirconia electro-fused cast refractory material |
-
1978
- 1978-06-19 JP JP7323978A patent/JPS6049124B2/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01125334U (en) * | 1988-02-18 | 1989-08-25 | ||
JPH01153341U (en) * | 1988-04-14 | 1989-10-23 | ||
JP3025231U (en) * | 1995-07-19 | 1996-06-11 | ギュン−ゴン キム | Rescue band |
Also Published As
Publication number | Publication date |
---|---|
JPS553319A (en) | 1980-01-11 |
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