JPH01289899A - Aqueous zeolite slurry composition - Google Patents
Aqueous zeolite slurry compositionInfo
- Publication number
- JPH01289899A JPH01289899A JP11894388A JP11894388A JPH01289899A JP H01289899 A JPH01289899 A JP H01289899A JP 11894388 A JP11894388 A JP 11894388A JP 11894388 A JP11894388 A JP 11894388A JP H01289899 A JPH01289899 A JP H01289899A
- Authority
- JP
- Japan
- Prior art keywords
- zeolite
- slurry
- fluidity
- aqueous
- slurry composition
- 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
- 239000002002 slurry Substances 0.000 title claims abstract description 49
- 239000010457 zeolite Substances 0.000 title claims abstract description 41
- 229910021536 Zeolite Inorganic materials 0.000 title claims abstract description 37
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 title claims abstract description 37
- 239000000203 mixture Substances 0.000 title claims description 15
- 239000002245 particle Substances 0.000 claims abstract description 12
- 229920002472 Starch Polymers 0.000 claims abstract description 11
- 239000008107 starch Substances 0.000 claims abstract description 11
- 235000019698 starch Nutrition 0.000 claims abstract description 11
- CXHHBNMLPJOKQD-UHFFFAOYSA-N methyl hydrogen carbonate Chemical class COC(O)=O CXHHBNMLPJOKQD-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000000725 suspension Substances 0.000 claims abstract description 4
- 235000012054 meals Nutrition 0.000 claims description 8
- 244000017020 Ipomoea batatas Species 0.000 abstract description 4
- 235000002678 Ipomoea batatas Nutrition 0.000 abstract description 4
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- 244000061456 Solanum tuberosum Species 0.000 abstract description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 abstract description 2
- 239000003513 alkali Substances 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000007788 liquid Substances 0.000 description 11
- 239000013049 sediment Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000003599 detergent Substances 0.000 description 5
- 238000006266 etherification reaction Methods 0.000 description 5
- 239000006228 supernatant Substances 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- GNBYZUQCDMNXML-UHFFFAOYSA-M sodium;2-chlorobutanoate Chemical compound [Na+].CCC(Cl)C([O-])=O GNBYZUQCDMNXML-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/128—Aluminium silicates, e.g. zeolites
- C11D3/1286—Stabilised aqueous aluminosilicate suspensions
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Detergent Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、懸濁安定性および流動性の優れたゼオライト
水性スラリー組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to an aqueous zeolite slurry composition with excellent suspension stability and fluidity.
[従来の技術]
従来、洗剤の原料としてトリポリリン酸塩が用いられて
いたが、洗剤使用後の排水が河川、湖沼及び閉塞海水を
富栄養化する問題が発生し、このため現在では大部分の
洗剤製造においてトリポリリン酸塩のかわりにゼオライ
トが用いられている。[Prior Art] Traditionally, tripolyphosphate has been used as a raw material for detergents, but the problem has arisen that the wastewater after using detergents can eutrophicate rivers, lakes, and blocked seawater. Zeolites are used in place of tripolyphosphate in detergent manufacturing.
洗剤製造において、ゼオライトを粉体のまま用いると配
合添加の際に種々の障害の原因となるため、40〜50
ffi量%の水性スラリーとして用いることが多い。In the manufacture of detergents, if zeolite is used as a powder, it will cause various problems when adding it to the formulation.
It is often used as an aqueous slurry with a ffi amount of %.
「発明が解決しようとする問題点]
しかし、ゼオライトの比重は2.3〜2.4であり、単
独で水中に分散しても短時間で沈澱し。"Problems to be Solved by the Invention" However, the specific gravity of zeolite is 2.3 to 2.4, and even if it is dispersed alone in water, it will precipitate in a short period of time.
安定なゼオライトスラリーが得られない、水性ゼオライ
トスラリーの安定剤としては、従来、CMC1カルボキ
シメチルデンプン、ポリビニルアルコール、ポリアクリ
ルアミド等の水溶性高分子が分散剤として用いられてき
た0本発明者らは、常法で得られた粒子径2〜4pmの
4A型ゼオライトを用いて上記各分散剤の効果を調べる
実験を行なった。Conventionally, water-soluble polymers such as CMC1 carboxymethyl starch, polyvinyl alcohol, and polyacrylamide have been used as dispersants as stabilizers for aqueous zeolite slurries where stable zeolite slurries cannot be obtained. An experiment was conducted to examine the effects of each of the above-mentioned dispersants using 4A type zeolite with a particle size of 2 to 4 pm obtained by a conventional method.
このゼオライトのうち、4#Lm以上の粒子径を有する
ゼオライトを用いて得られた各水性スラリーは1週間以
上静置するとスラリー上部に透明な水溶液が形成されス
ラリー底部にゼオライトの比較的大きい粒子が沈澱して
濃厚なスラリーまたはゲル状ケーキが形成された。従っ
て、このようなスラリーは、製造設備を一週間以上体止
するような場合に、送液管の立ち上りの底部または弁座
等に濃厚スラリーまたはゲル状ケーキを形成して以後の
送液を不可能にする恐れがあることが判明した。Among these zeolites, each aqueous slurry obtained using a zeolite having a particle size of 4#Lm or more will form a transparent aqueous solution at the top of the slurry when left to stand for more than a week, and relatively large particles of zeolite will form at the bottom of the slurry. A thick slurry or gel cake formed upon precipitation. Therefore, when manufacturing equipment is shut down for more than a week, such slurry may form a thick slurry or gel cake at the bottom of the rising edge of the liquid transfer pipe or at the valve seat, preventing subsequent liquid transfer. It has been found that this may be possible.
[問題点を解決するための手段]
本発明者らは、前述の問題点を解消すべく鋭意研究の結
果、通常の製法で得られる粒子径2〜lOpmを有する
ゼオライトを40重量%以上の高濃度で含有し、長時間
少なくとも2週間の貯蔵後も安定であって、送液を支障
なく行える流動性の優れたゼオライトスラリー組成物を
見い出し本発明に到達したものである。すなわち、本発
明は、粒子径2〜lOpmを有するゼオライトに対して
乾燥量基準で、0.05〜5重量%の澱粉粕類のカルボ
キシメチルエーテル塩を含有し、ゼオライト濃度が40
〜55重量%であるFJ濁安定性および流動性の優れた
水性ゼオライトスラリー組成物を提供するものである。[Means for Solving the Problems] As a result of intensive research in order to solve the above-mentioned problems, the present inventors have found that 40% by weight or more of zeolite having a particle size of 2 to 1 Opm, which is obtained by a conventional manufacturing method, is The present invention was achieved by discovering a zeolite slurry composition containing a high concentration of zeolite, which is stable even after storage for a long time of at least two weeks, and has excellent fluidity that allows the liquid to be transferred without any trouble. That is, the present invention contains carboxymethyl ether salt of starch meal in an amount of 0.05 to 5% by weight on a dry basis with respect to zeolite having a particle size of 2 to 1 Opm, and the zeolite concentration is 40% by weight.
The present invention provides an aqueous zeolite slurry composition with excellent FJ turbidity stability and fluidity of up to 55% by weight.
本発明に用いられるゼオライトは、比重が2゜3〜2.
41粒子径が2〜10ルmの4Aまたは3Aタイプのゼ
オライトが好ましい、尚、本発明においては粒子径が1
0#Lmを越えるゼオライトを用いても、安定なスラリ
ーを形成することができるが、洗剤用ビルグーとしては
、l Opm以下の粒子径を有するものが好ましく用い
られており、これはゼオライト製造工程の品質管理を厳
しく行なうことによりlOルm以上の粒子径を有するゼ
オライトを排除することができる。The zeolite used in the present invention has a specific gravity of 2.3 to 2.
4A or 3A type zeolite with a particle size of 2 to 10 lm is preferred;
Although it is possible to form a stable slurry using zeolite exceeding 0 #Lm, it is preferable to use a bilge for detergents with a particle size of 1 Opm or less, which is a problem in the zeolite manufacturing process. By carrying out strict quality control, it is possible to exclude zeolites having a particle size of 10 ml or more.
本発明による水性ゼオライトスラリー中のゼオライトの
量は40ffi量%未満では不経済であり。The amount of zeolite in the aqueous zeolite slurry according to the present invention is uneconomical if it is less than 40% by weight.
55%を越えるとスラリーの粘度が急上昇し、その取扱
、特に送液が困難となる。When it exceeds 55%, the viscosity of the slurry increases rapidly, making it difficult to handle, especially to feed.
本発明において、使用する澱粉粕類のカルボキシメチル
エーテル塩は、サツマイモ、バレイショ等の澱粉粕類を
アルカリの存在下、モノクロル酢酸、モノクロル酪酸ナ
トリウム等のエーテル化剤でエーテル化して得られる。In the present invention, the carboxymethyl ether salt of starch meal used is obtained by etherifying starch meal, such as sweet potato or potato, with an etherification agent such as monochloroacetic acid or sodium monochlorobutyrate in the presence of an alkali.
本発明による水性ゼオライトスラリー中の澱粉粕類のカ
ルボキシメチルエーテル塩の量は0.05正量%未満で
は安定なスラリーとしての寿命が短縮され、5%を越え
るとスラリーの粘度が急上昇し、その取扱、特に送液が
困難となる。また不経済である。If the amount of carboxymethyl ether salt of starch meal in the aqueous zeolite slurry according to the present invention is less than 0.05% by weight, the life as a stable slurry will be shortened, and if it exceeds 5%, the viscosity of the slurry will sharply increase. Handling, especially liquid delivery, becomes difficult. It is also uneconomical.
尚、本発明の実施に際し、澱粉粕類のカルボキシメチル
エーテル塩と分散剤、水溶性高分子等の増粘剤を併用す
ることは、なんら差し支えない。In carrying out the present invention, there is no problem in using the carboxymethyl ether salt of starch meal together with a thickener such as a dispersant or a water-soluble polymer.
次に本発明を実施例により具体的に説明するが1本発明
は、これら実施例に限定されるものでない。EXAMPLES Next, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to these Examples.
実施例
本実施例で用いたゼオライト(平均粒子径4μm)の水
分は20重量%であった。Example The water content of the zeolite (average particle size: 4 μm) used in this example was 20% by weight.
又、澱粉粕類のカルボキシメチルエーテル塩は以下の方
法により製造したものを用いた。In addition, the carboxymethyl ether salt of starch lees produced by the following method was used.
発明品A
−軸の5!Lブレンダーに乾燥サツマイモ粕(多動類含
量81%)500g及び50%メタノール1000gに
水酸化ナトリウム210gを溶かした溶液を加え、30
℃で60分間攪拌混合した。Invention A - Axis 5! Add 500 g of dried sweet potato meal (hyperactive content 81%) and a solution of 210 g of sodium hydroxide in 1000 g of 50% methanol to a L blender, and mix for 30 minutes.
The mixture was stirred and mixed at ℃ for 60 minutes.
次いで、これにモノクロール酢酸224gを90%メタ
ノール224gに溶かした溶液を60分間かけて滴下し
、さらに40℃で10分間混合後、65℃まで昇温させ
、同温度で2時間エーテル化反応させた。Next, a solution of 224 g of monochloroacetic acid dissolved in 224 g of 90% methanol was added dropwise to this over 60 minutes, and after further mixing at 40°C for 10 minutes, the temperature was raised to 65°C and an etherification reaction was carried out at the same temperature for 2 hours. Ta.
エーテル化終了後1反応液を冷却し酢酸で中和した。、
この中和液に70%メタノール2500gを加え、30
分間攪拌後、遠心分離して固液分離に付し、固体部を乾
燥、粉砕した。After the etherification was completed, one reaction solution was cooled and neutralized with acetic acid. ,
Add 2500g of 70% methanol to this neutralized solution and
After stirring for a minute, the mixture was centrifuged and subjected to solid-liquid separation, and the solid portion was dried and pulverized.
得られた製品の性状は、乾燥域i8.42%、2%水溶
液粘度(B型粘度計使用)353cP、PH7,8であ
った。The properties of the obtained product were as follows: dry area i: 8.42%, 2% aqueous solution viscosity (using a B-type viscometer): 353 cP, and pH: 7.8.
発明品B
−軸の5!lブレンダーに乾燥サツマイモ粕(多糖類合
冊82%)500g及び40%メタノール400gに水
酸化ナトリウム150gを溶かした溶液を加え、30”
0で60分間攪拌混合した。Invention B - Axis 5! 1 Add a solution of 150 g of sodium hydroxide dissolved in 500 g of dried sweet potato meal (82% polysaccharide) and 400 g of 40% methanol to a blender.
The mixture was stirred and mixed at 0 for 60 minutes.
次いで、これにモノクロール酸M165gを90%メタ
ノール165gに溶かした溶液を60分間かけて滴下し
、さらに40℃で10分間混合後、72℃まで昇温させ
、同温度で2時間エーテル化反応させた。Next, a solution of 165 g of monochloric acid M dissolved in 165 g of 90% methanol was added dropwise to this over 60 minutes, and after further mixing at 40°C for 10 minutes, the temperature was raised to 72°C and an etherification reaction was carried out at the same temperature for 2 hours. Ta.
エーテル化終了後、反応液を冷却し酢酸で中和した。、
この中和液に70%メタノール3000gを加え、30
分間攪拌後、遠心分離して固液分離に付し、固体部を乾
燥、粉砕した。After the etherification was completed, the reaction solution was cooled and neutralized with acetic acid. ,
Add 3000g of 70% methanol to this neutralized solution,
After stirring for a minute, the mixture was centrifuged and subjected to solid-liquid separation, and the solid portion was dried and pulverized.
得られた製品の性状は、乾燥減量7.39%、2%水溶
液粘度(B型粘度計使用)600cP。The properties of the obtained product were a loss on drying of 7.39% and a 2% aqueous solution viscosity (using a B-type viscometer) of 600 cP.
pH7,5であった。The pH was 7.5.
本実施例においてft51表に示す配合で以下の方法に
より各水性ゼオライトスラリーを得た。In this example, each aqueous zeolite slurry was obtained by the following method using the formulation shown in Table ft51.
水100重夛部に対してゼオライ)100重量部を加え
、家庭■ジュースミキサーを用いて撹拌分散し、さらに
分散剤を加え撹拌溶解して、ゼオライトスラリーを調製
した。A zeolite slurry was prepared by adding 100 parts by weight of zeolite to 100 parts by weight of water, stirring and dispersing using a domestic juice mixer, and then adding a dispersant and dissolving with stirring.
このゼオライトスラリーの粘度及び安定性を以下の方法
により評価した。The viscosity and stability of this zeolite slurry were evaluated by the following method.
■粘度
被試験スラリーを500m1を500m1容トールビー
カーに移しブルックフィールドRVTD型粘度計(東京
針W)使用25℃にて測定した。(2) Viscosity 500 ml of the slurry to be tested was transferred to a 500 ml tall beaker and measured at 25°C using a Brookfield RVTD viscometer (Tokyo Needle W).
■ゼオライトスラリーの9%安定性の評価粘度測定後の
被試験スラリーを30日間静置して、トールビーカー内
のスラリーの状態を観察し、■スラリーに上澄部分が生
じているか否か、■スラリーの底部に沈降物が生じてい
るか否か、を以下のように評価した。■ Evaluation of 9% stability of zeolite slurry After measuring the viscosity, let the slurry under test stand still for 30 days, observe the state of the slurry in the tall beaker, ■ check whether a supernatant portion has formed in the slurry, ■ The presence or absence of sediment at the bottom of the slurry was evaluated as follows.
O印・・・スラリーに上澄液部分が生じておらず且つス
ラリーの底部に沈降物が生じて
いない場合
O印・・・スラリーに上澄液部分がわずかに生じている
がスラリーの底部に沈降物が生
じていない場合
Δ印・・・スラリーに上澄液部分が生じ、スラリーの底
部に沈降物が生じているが流動
性を保っている場合
×印・・・スラリーに上澄液部分が生じ、スラリーの底
部に固く沈降物が生じた場合
■スラリーの流動性評価
スラリーの流動性については、前記懸濁安定性試験が終
了したものについて、ビーカー内のスラリーを各ビーカ
ーを170〜1759傾けた状態で流出させ、流出時の
スラリー粘性、流出時にスラリーに固化物が存在するか
否かを判定し流動性について以下のように評価した。O mark: There is no supernatant liquid in the slurry, and no sediment is formed at the bottom of the slurry. O mark: A slight supernatant liquid part is formed in the slurry, but at the bottom of the slurry. If no sediment has formed, mark Δ... A supernatant liquid portion has formed in the slurry, and if sediment has formed at the bottom of the slurry, but the fluidity has been maintained, mark x... Supernatant liquid portion has formed in the slurry. If this occurs and solid sediment is formed at the bottom of the slurry ■Evaluation of slurry fluidity Regarding the fluidity of the slurry, the slurry in each beaker was heated to 170 to 1759 The slurry was flowed out in an inclined state, and the viscosity of the slurry at the time of flow out was determined, and the presence or absence of solidified matter in the slurry at the time of flow was determined, and the fluidity was evaluated as follows.
0印・・・安定な懸濁状態を示し流動性に富み全量がビ
ーカーから流出する場合。Mark 0: When the suspension is stable and has good fluidity, the entire amount flows out from the beaker.
O印・・・ビーカーから流出するが若干沈降物が生じて
おり沈降物の流動性が劣る場合
Δ印・・・沈降物が生じ流動性のない部分が存在する場
合、
×印・・−上澄液のみが流出し、沈降物が全く流動しな
い場合、
また、スラリー取り出し後のビーカー内に沈降物(固化
物)存在する場合、その固化物について下記の通り観察
し、評価した。O mark: When some sediment flows out of the beaker and the fluidity of the sediment is poor, Δ mark: When there is sediment and there are areas with no fluidity, × mark: -Top When only clear liquid flowed out and no sediment flowed, or when sediment (solidified material) was present in the beaker after the slurry was taken out, the solidified material was observed and evaluated as follows.
@印1111−固化物をスパチュラでかきまわした時に
流動性が認められビーカーを傾けれ
ば流出する場合、
0印・・・固イビ物をスパチュラでかきまわした時に流
動性が認められビーカーを傾けれ
ば流出しない場合、
Δ印・争・固化物をスパチュラでかきまわしても流動性
が認められない場合、
×印・ゆψ固化物をスパチュラでかきまわすことが不可
能なほどかたい場合、
これらのスラリー組成物の各特性について試験し、得ら
れた結果を第1表に示した。第1表から明らかな通り、
本発明により得られたゼオライトスラリー組成物は比較
量に比べて沈降安定性が著しく優れていることが確認で
きた。@ mark 1111 - When a solidified substance is stirred with a spatula, fluidity is observed and it flows out when the beaker is tilted, 0 mark... When a solidified substance is stirred with a spatula, fluidity is observed and the beaker is tilted. If the slurry does not flow out, if the solidified material is so hard that it is impossible to stir it with a spatula, if the solidified material is so hard that it is impossible to stir it with a spatula. The products were tested for each property, and the results are shown in Table 1. As is clear from Table 1,
It was confirmed that the zeolite slurry composition obtained according to the present invention had significantly better sedimentation stability than a comparative amount.
[発明の効果]
本発明水性ゼオライトスラリー組成物は1通常の製法で
得られる粒子径2〜10μmを有するゼオライトを40
〜55正量%の高濃度で含有し、長時間、少なくとも2
i1J間の貯蔵後も安定であって、送液を支障なく行な
えるj’47F+安定性および流動性の優れたゼオライ
トスラリー組成物を提供することができる。[Effects of the Invention] The aqueous zeolite slurry composition of the present invention contains 40 zeolites having a particle size of 2 to 10 μm obtained by a conventional manufacturing method.
Contains at a high concentration of ~55 wt% and for a long period of time at least 2
It is possible to provide a zeolite slurry composition that is stable even after storage for i1J and has excellent j'47F+ stability and fluidity and can be transferred without any trouble.
Claims (1)
基準で、0.05〜5重量%の澱粉粕類のカルボキシメ
チルエーテル塩を含有し、ゼオライト濃度が40〜55
重量%である懸濁安定性および流動性の優れた水性ゼオ
ライトスラリー組成物。Contains carboxymethyl ether salt of starch meal in an amount of 0.05 to 5% by weight on a dry basis with respect to zeolite having a particle size of 2 to 10 μm, and the zeolite concentration is 40 to 55%.
Aqueous zeolite slurry composition with excellent suspension stability and fluidity in weight percent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11894388A JPH01289899A (en) | 1988-05-16 | 1988-05-16 | Aqueous zeolite slurry composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11894388A JPH01289899A (en) | 1988-05-16 | 1988-05-16 | Aqueous zeolite slurry composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01289899A true JPH01289899A (en) | 1989-11-21 |
Family
ID=14749077
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11894388A Pending JPH01289899A (en) | 1988-05-16 | 1988-05-16 | Aqueous zeolite slurry composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01289899A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1037105C (en) * | 1994-08-04 | 1998-01-21 | 安徽省生物研究所 | Phase transfer synthetic process for high substitution value sodium carboxymethyl amyloether |
-
1988
- 1988-05-16 JP JP11894388A patent/JPH01289899A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1037105C (en) * | 1994-08-04 | 1998-01-21 | 安徽省生物研究所 | Phase transfer synthetic process for high substitution value sodium carboxymethyl amyloether |
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