JPS593404B2 - Method for producing alkali silicate - Google Patents
Method for producing alkali silicateInfo
- Publication number
- JPS593404B2 JPS593404B2 JP18379080A JP18379080A JPS593404B2 JP S593404 B2 JPS593404 B2 JP S593404B2 JP 18379080 A JP18379080 A JP 18379080A JP 18379080 A JP18379080 A JP 18379080A JP S593404 B2 JPS593404 B2 JP S593404B2
- Authority
- JP
- Japan
- Prior art keywords
- silica
- silica stone
- alkali
- caustic alkali
- alkali silicate
- 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
- 229910052910 alkali metal silicate Inorganic materials 0.000 title claims description 11
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 67
- 239000000377 silicon dioxide Substances 0.000 claims description 29
- 239000004575 stone Substances 0.000 claims description 22
- 239000003513 alkali Substances 0.000 claims description 19
- 239000003518 caustics Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000010298 pulverizing process Methods 0.000 description 5
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 238000010411 cooking Methods 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 229910002026 crystalline silica Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910021489 α-quartz Inorganic materials 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910021493 α-cristobalite Inorganic materials 0.000 description 1
Landscapes
- Silicates, Zeolites, And Molecular Sieves (AREA)
Description
【発明の詳細な説明】
本発明は珪酸アルカリを製造する方法、特に珪石と苛性
アルカリとを湿式法はより反応せしめて珪酸アルカリを
製造する場合、珪曹比(Si02/Na20)を高くせ
しめる方法に係るものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an alkali silicate, particularly a method for increasing the silica ratio (Si02/Na20) when producing an alkali silicate by reacting silica stone with a caustic alkali more than the wet method. This is related to.
珪酸ソーダ等の珪酸アルカリは、その製造方法として乾
式法と湿式法に大別される。The production methods for alkali silicates such as sodium silicate are roughly divided into dry methods and wet methods.
そして何れの場合においても原料として珪石及び苛性ア
ルカリが用いられるが、乾式法においてはこれら原料に
直接火焔を吹きつけて原料を溶融反応せしめる手段が採
られており、この方法は湿式法に比較して反応性も高く
、又珪曹比を高くし易い利点がある反面、大量の熱量を
要し、近年各方面の重大関心事となっている省エネルギ
ーの観点からは好ましい方法とは言い難い。In both cases, silica stone and caustic alkali are used as raw materials, but in the dry method, a flame is directly blown onto these raw materials to cause them to melt and react, and this method is superior to the wet method. Although this method has the advantage of having high reactivity and making it easy to increase the silica ratio, it requires a large amount of heat and is not a desirable method from the viewpoint of energy conservation, which has become a major concern in various fields in recent years.
これに対し、湿式法は乾式法より少ないエネルギーで珪
酸ア′ルカリを得ることが出来るが、乾式法に比して1
段の反応では珪曹比がいく分低い傾向にある。On the other hand, the wet method can obtain alkali silicate with less energy than the dry method;
In stage reactions, the silica ratio tends to be somewhat lower.
本発明者はかかる点に鑑み、珪石と苛性アルカリとの反
応率を向上せしめ、以って珪曹比を高くし得る手段を見
出すことを目的として種々研究、検討した結果、反応に
供される珪石を、反応性を向上せしめる為に所定粒径に
粉砕せしめるに当り、苛性アルカリの存在下に粉砕を実
施せしめることにより、前記目的を達成し得ることを見
出した。In view of this, the present inventor conducted various studies and examinations with the aim of improving the reaction rate between silica stone and caustic alkali, thereby increasing the silica ratio. It has been found that the above object can be achieved by pulverizing silica stone to a predetermined particle size in order to improve reactivity, by performing the pulverization in the presence of caustic alkali.
かくして本発明は、珪石と苛性アルカリとをオートクレ
ーブにより蒸解せしめて珪酸アルカリを得るに当り、原
料となる珪石を加熱することなく予め苛性アルカリ水溶
液の存在下に粒径1〜500μに粉砕せしめておくこと
を特徴とする珪酸アルカリの製造方法を提供するにある
。Thus, in the present invention, when obtaining an alkali silicate by digesting silica stone and a caustic alkali in an autoclave, the silica stone serving as a raw material is ground in advance to a particle size of 1 to 500 μ in the presence of an aqueous caustic alkali solution without heating. An object of the present invention is to provide a method for producing an alkali silicate.
本発明において、用いられる珪石に特に制限はないが、
例えばα−石石英中α−クリストバライト晶等の本来反
応しにくい結晶質の珪石が特に適している。In the present invention, there are no particular restrictions on the silica stone used, but
For example, crystalline silica stone that is inherently difficult to react, such as α-cristobalite crystal in α-quartz, is particularly suitable.
又、珪石を粉砕するに当って用いられる苛性アルカリは
、後にオートクレーブ中で反応せしめるに必要な量を用
いてもよく、又それより少なく用いることも出来るか、
粉砕効率及び反応性の向上の為には反応に必要な量の全
量を用いる方が効果的である。Also, the amount of caustic alkali used to crush silica stone can be used in the amount required for the reaction in the autoclave later, or can it be used in a smaller amount?
In order to improve milling efficiency and reactivity, it is more effective to use the entire amount required for the reaction.
珪石が粉砕される粒径としては、オートクレーブ中での
反応率及び珪曹比を有効に向上せしめる為、はぼ1〜5
00μ程度、好ましくは1〜80μ程度に粉砕せしめる
のが適当である。The particle size of the silica stone to be crushed is approximately 1 to 5 in order to effectively improve the reaction rate and silica ratio in the autoclave.
It is appropriate to crush the powder to about 00μ, preferably about 1 to 80μ.
かかる粉砕を実施せしめるには、例えはボールミ、振動
ミル、コロイドミル等の粉砕機を用いることが出来る。To carry out such pulverization, a pulverizer such as a ball mill, a vibration mill, or a colloid mill can be used.
又、粉砕に供される苛性アルカリの濃度は、あまり濃す
ぎたり、固体状であると、珪石全体に苛性アルカリが行
きわたらず、本発明の所期の目的が達成し得なくなる。Furthermore, if the concentration of the caustic alkali used for pulverization is too high or if it is in a solid state, the caustic alkali will not be distributed throughout the silica stone, making it impossible to achieve the intended purpose of the present invention.
この為、濃度は通常5〜50重量係程度の水溶液を用い
るのが適当である。For this reason, it is appropriate to use an aqueous solution whose concentration is usually about 5 to 50% by weight.
本発明方法を採用すると何故に反応率が向上するかにつ
いての理由は必ずしも明確でないが、予め粉砕された珪
石に対し、苛性アルカリをまぶしつけたものに比較する
と本発明方法の方が反応率の向上が見られる処からする
と、粉砕品中に存在する珪石微粉と苛性アルカリとが粉
砕過程で混合し、かかる混合物が粒状珪石の表面に十分
貼着し、これがオートクレーブ中での蒸解反応に際し、
珪石と苛性アルカリとの反応を促進するものと思われる
。The reason why the reaction rate improves when the method of the present invention is adopted is not necessarily clear, but the reaction rate of the method of the present invention is higher than that of a method in which pre-pulverized silica stone is sprinkled with caustic alkali. From the areas where improvement is seen, the silica fine powder and caustic alkali present in the pulverized product are mixed during the pulverization process, and this mixture sufficiently adheres to the surface of the granular silica stone, which causes the silica to react during the cooking reaction in the autoclave.
It seems to promote the reaction between silica stone and caustic alkali.
かくして本発明において所定粒径に粉砕された珪石は、
苛性アルカリと共に、更には必要に応じて苛性アルカリ
を追加せしめてオートクレーブに導入され、蒸解される
。Thus, in the present invention, the silica stone crushed to a predetermined particle size is
The mixture is introduced into an autoclave together with caustic alkali, and additional caustic alkali is added as required, and then digested.
蒸解は、圧力3〜30kFi/cr/l、温度130〜
240℃にて1〜10時間程度を採用するのが適当であ
る。Cooking is carried out at a pressure of 3 to 30 kFi/cr/l and a temperature of 130 to
Appropriately, the heating time is 1 to 10 hours at 240°C.
かかる条件を逸脱する場合には、十分な反応率が得られ
なかったり、最早やそれ以上の効果を期待し得す、単に
エネルギーの浪費となるのみなので好ましくない。If these conditions are deviated from, it is not preferable because a sufficient reaction rate may not be obtained, a greater effect may no longer be expected, or energy will simply be wasted.
そしてこれら範囲のうち、圧力8〜20kg/cm、温
度170〜220℃にて1〜5時間を採用する場合には
、最も効率的に最も高い反応率を期待し得るので特に好
ましい。Among these ranges, it is particularly preferable to use a reaction time of 1 to 5 hours at a pressure of 8 to 20 kg/cm and a temperature of 170 to 220° C., since the highest reaction rate can be expected most efficiently.
本発明方法を採用すると、原料として用いられる珪石と
苛性アルカリ(Na20換算)の使用割合は珪石のSi
O2分10分車00重量部Na2010から最大33.
2重量部が採用され、かくして得られる珪酸アルカリの
珪曹比は2.8の高きに及び又反応率も93係と高(す
ることが可能となる。When the method of the present invention is adopted, the ratio of silica stone and caustic alkali (calculated as Na20) used as raw materials is
O2 minutes 10 minutes car 00 parts by weight Na2010 to maximum 33.
2 parts by weight is employed, and the silicate ratio of the alkali silicate thus obtained can be as high as 2.8, and the reaction rate can also be as high as 93 factors.
勿論、前記より更に高い珪曹比を有する珪酸アルカリを
得たい場合には、例えは副生シリカ、シリカゲル等無定
形ケイ酸、クリストバル石、オパール石等の反応性の珪
酸原料を更に所定量用い、常法に従って反応せしめれば
よい。Of course, if it is desired to obtain an alkali silicate having a higher silicate ratio than the above, a predetermined amount of a reactive silicic acid raw material such as by-product silica, amorphous silicic acid such as silica gel, cristobalite, opalite, etc. may be used. , the reaction may be carried out according to a conventional method.
本発明に用いられる苛性アルカリとしては、通常苛性ソ
ーダであるが、その他苛性カリ等のアルカリ金属の水酸
化物である。The caustic alkali used in the present invention is usually caustic soda, but also alkali metal hydroxides such as caustic potash.
次に本発明を実施例により説明する。Next, the present invention will be explained by examples.
平均粒径80〜100叫のα−石英晶を有する結晶珪石
2.4 kgを、488重量部苛性ソーダ2.07kg
と共に容積14.6Aのボールミルに導入し、回転数5
Or−p、m、温度30〜50℃で5時間粉砕を行ない
、平均粒径40〜100μの珪石を得た。488 parts by weight of 2.07 kg of caustic soda were added to 2.4 kg of crystalline silica having α-quartz crystals with an average particle size of 80 to 100 mm.
It was introduced into a ball mill with a capacity of 14.6A, and the number of revolutions was 5.
Grinding was carried out at Or-p, m and a temperature of 30 to 50°C for 5 hours to obtain silica stone with an average particle size of 40 to 100 μm.
これを前記苛性ソーダと共にオートクレーブに入れ、圧
力18kg/cnt、温度206℃にて3時間蒸解せし
めた。This was placed in an autoclave together with the above caustic soda and digested at a pressure of 18 kg/cnt and a temperature of 206° C. for 3 hours.
反応生成物をJISK−1408の分析法に従って分析
した処、S i02 / N a 20−2.8の珪酸
ソーダが得られ、その反応率は原料珪石に対し、93%
であった。When the reaction product was analyzed according to the analysis method of JISK-1408, sodium silicate with S i02 / Na 20-2.8 was obtained, and the reaction rate was 93% with respect to the raw material silica stone.
Met.
尚、比較の為、同じ珪石を乾式粉砕し、前記と同様な粒
径のみを取り出し、前記と同量の苛性ソーダを用い、同
様に反応せしめた処、その珪曹比は2.4と低く、又反
応率も80%と低かった。For comparison, the same silica stone was dry crushed, only the same particle size as above was taken out, and the same amount of caustic soda was used to react in the same manner as above, and the silica ratio was as low as 2.4. Moreover, the reaction rate was as low as 80%.
Claims (1)
せしめて珪酸アルカリを得るに当り、原料となる珪石を
加熱することなく予め苛性アルカリ水溶液の存在下に粒
径1〜500μに粉砕せしめておくことを特徴とする珪
酸アルカリを製造する方法。 2 粉砕に用いられる苛性アルカリの量は、珪石の5i
02分100重量部に対しNa2010〜33.2重量
部である特許請求の範囲1の方法。[Scope of Claims] 1. In obtaining an alkali silicate by digesting silica stone and a caustic alkali in an autoclave, the silica stone serving as a raw material is ground in advance to a particle size of 1 to 500 μ in the presence of an aqueous caustic alkali solution without heating. A method for producing an alkali silicate, which comprises: 2 The amount of caustic alkali used for crushing is 5i of silica stone.
2. The method according to claim 1, wherein the amount of Na is 2010 to 33.2 parts by weight per 100 parts by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18379080A JPS593404B2 (en) | 1980-12-26 | 1980-12-26 | Method for producing alkali silicate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18379080A JPS593404B2 (en) | 1980-12-26 | 1980-12-26 | Method for producing alkali silicate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57111230A JPS57111230A (en) | 1982-07-10 |
| JPS593404B2 true JPS593404B2 (en) | 1984-01-24 |
Family
ID=16141968
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18379080A Expired JPS593404B2 (en) | 1980-12-26 | 1980-12-26 | Method for producing alkali silicate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS593404B2 (en) |
-
1980
- 1980-12-26 JP JP18379080A patent/JPS593404B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57111230A (en) | 1982-07-10 |
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