JPS59121117A - Production of low-density sodium carbonate - Google Patents

Production of low-density sodium carbonate

Info

Publication number
JPS59121117A
JPS59121117A JP22748282A JP22748282A JPS59121117A JP S59121117 A JPS59121117 A JP S59121117A JP 22748282 A JP22748282 A JP 22748282A JP 22748282 A JP22748282 A JP 22748282A JP S59121117 A JPS59121117 A JP S59121117A
Authority
JP
Japan
Prior art keywords
sodium carbonate
carbon dioxide
sodium
density
low
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
Application number
JP22748282A
Other languages
Japanese (ja)
Inventor
Keiichi Nakaya
圭一 中矢
Kunio Sato
邦夫 佐藤
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.)
AGC Inc
Original Assignee
Asahi Glass Co Ltd
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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP22748282A priority Critical patent/JPS59121117A/en
Publication of JPS59121117A publication Critical patent/JPS59121117A/en
Pending legal-status Critical Current

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  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Abstract

PURPOSE:To obtain a granular low-density sodium carbonate having excellent solubility and handleable without dusting, by reacting hydrated sodium carbonate or a mixture of sodium bicarbonate and sodium carbonate with carbon dioxide gas in the presence of water. CONSTITUTION:Hydrated sodium carbonate and/or a mixture of sodium bicarbonate and sodium carbonate, e.g. sodium sesquicarbonate, etc. obtained by the carbonation of sodium hydroxide, etc. is made to react with carbon dioxide gas having an arbitrary concentration in the presence of about 0.5-45wt% of water to convert about >=40% of the sodium carbonate to bicarbonate. The product is calcined at about 140-500 deg.C to convert the bicarbonate to sodium carbonate and obtain the objective low-density sodium carbonate. The concentration of the carbon dioxide gas is adjusted by the ratio of air, etc., added to the gas, and a sodium carbonate having desired low density can be obtained by controlling the concentration of carbon dioxide gas.

Description

【発明の詳細な説明】 本発明は低密度炭酸ソーダの製造方法、特に取妙扱いに
際し粉塵が生ずることのない粒状であって且溶解性の良
好な炭酸ソーダの製造方法に係るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing low-density soda carbonate, and particularly to a method for producing soda carbonate that is granular and has good solubility and does not generate dust when handled.

炭酸ソーダは工業的にはツルベイ法、アンモニアソーダ
法等によシ得られた重炭酸ソーダを■焼して軽灰を、又
これを水利後鍜焼して見掛は密度の高い電入として得て
いる。
Industrially, soda carbonate is produced by burning bicarbonate of soda obtained by the Tsurubei method, ammonia soda method, etc. to produce light ash, which is then calcined after water use to obtain what appears to be a dense electric charge. There is.

このうち比較的水に溶解し易い性質が安来される用途に
は、従来軽灰が専ら用いられてきた。
Among these, light ash has conventionally been used exclusively for applications where it is relatively easy to dissolve in water.

しかしながら、軽灰は一般的に発塵性が高いと共に、細
粒状であシ、これが為に団塊状になる性質があシ流動性
が悪い等必ずしも取シ扱い容いものでは力かった。
However, light ash generally has a high dust-generating property, is finely granular, has a tendency to form nodules, has poor fluidity, and is not necessarily difficult to handle.

本発明者は、これらの点に鑑み、発塵性がなく、容易に
溶解し得る粒状の炭酸ソーダを得ることを目的として種
々研究、検討した結果、通常行なわれている重炭酸ソー
ダを経て炭酸ソーダを得る手段をいかに調節しようとも
本発明の目的を達成し得ることは出来ず、態々任意の手
段で一旦炭酸ソーダを得、かかる炭酸ソーダを特定の手
段で処理し、低密度化せしめる−ことによジ、前記目的
を達成し得ることを見出した。
In view of these points, the inventor of the present invention conducted various research and examinations with the aim of obtaining granular soda carbonate that does not generate dust and is easily soluble. No matter how the means for obtaining the carbonate is adjusted, the object of the present invention cannot be achieved, and it is necessary to first obtain the soda carbonate by any means and then process the soda by a specific means to reduce the density. It has been found that the above object can be achieved.

かくして本発明は炭酸ソーダ水和物及び/又は重炭酸ソ
ーダと炭酸ソーダの混合塩を水分の存在下に任意の濃度
の炭酸ガスと反応せしめ、その少なくとも一部を重炭酸
化し、次いで■焼せしめることによシ、炭酸ガス濃度に
応じて低密度化せしめることを特徴とする低密度炭酸ソ
−ダの製造方法を提供するにある。
Thus, the present invention involves reacting sodium carbonate hydrate and/or a mixed salt of sodium bicarbonate and sodium carbonate with carbon dioxide gas at an arbitrary concentration in the presence of water, bicarbonating at least a portion of it, and then baking it. Another object of the present invention is to provide a method for producing low-density soda carbonate, which is characterized in that the density is reduced in accordance with the carbon dioxide concentration.

本発明において、低密度化せしめる炭酸ソーダの原料は
、炭酸ソーダ水和物の他、セスキ炭酸ソーダに代表され
る重炭酸ソーダと炭酸ソーダの混合塩でも同様な結果が
得られることが見出された。
In the present invention, it has been found that similar results can be obtained by using not only sodium carbonate hydrate but also a mixed salt of sodium bicarbonate and soda carbonate, typified by sodium sesquicarbonate, as the raw material for the soda carbonate that lowers the density.

原料として用いられる炭酸ソーダ水和物とI2ては、例
えば1水塩、7水塩であシ、これらの製法に特に制限は
なく、例えば苛性ソーダの炭酸化、ツルベイ法、アンモ
ニアソーダ法等適宜な手段を採用し得る。又、セスキ炭
酸ソーダ等の重曹と炭酸ソーダの混合塩(以下混合塩と
呼ぶ)も公知の手段で適宜製造したものが用いられる。
Sodium carbonate hydrate and I2 used as raw materials may be, for example, monohydrate or heptahydrate, and there are no particular restrictions on their production methods, such as carbonation of caustic soda, Truvay method, ammonia soda method, etc. means may be adopted. Also, mixed salts of baking soda and soda carbonate (hereinafter referred to as mixed salts) such as sodium sesquicarbonate may be appropriately prepared by known means.

又、本発明によって最終的に得られる低密度の炭酸ソー
ダが有する粒径は、通常原料として用いられる上記炭酸
ソーダ水和拘着しくは混合塩の粒径によって決められる
。更に本発明に用いられる炭酸ソーダ水和物や混合塩は
、これが結晶化していてもしていなくても何れでも差し
支えない。
Furthermore, the particle size of the low-density soda carbonate finally obtained according to the present invention is determined by the particle size of the above-mentioned hydrated sodium carbonate salt or mixed salt that is normally used as a raw material. Furthermore, the sodium carbonate hydrate and mixed salt used in the present invention may be crystallized or not.

これら炭酸ソーダ水和物や混合塩は先づ水分の存在下に
炭酸ガスと反応せしめられる。
These sodium carbonate hydrates and mixed salts are first reacted with carbon dioxide gas in the presence of moisture.

、このとき存在せしめられる水分量は、厳密には炭酸ソ
ーダの水利量、混合塩等によって多少異なるが、一般に
α5〜45重量−程度が適当である。水分量が前記範囲
を逸脱する場合には、反応の進行が遅くなったシ、粒子
間の固結現象を起す虞れがあるので好ましくない。
Strictly speaking, the amount of water present at this time varies somewhat depending on the amount of water used for soda carbonate, the mixed salt, etc., but in general, approximately α5 to 45 weight is appropriate. If the water content deviates from the above range, the progress of the reaction may be slowed down and caking between particles may occur, which is not preferable.

そしてこれら範囲のうち、水分量が5〜20重量%程度
を採用すると反応速度も速く、取り扱いも容易なので特
に好ましい。
Among these ranges, it is particularly preferable to adopt a water content of about 5 to 20% by weight because the reaction rate is fast and handling is easy.

又これら水分の存在下に反応せしめられる炭酸ガスの量
は、低密度化せしめる程度や必要とする溶解速度等によ
り決定される。
The amount of carbon dioxide gas reacted in the presence of water is determined by the degree of density reduction, required dissolution rate, etc.

特に炭酸ガス濃度は、低密度化の程度に大きく影響する
ことが見出され、一般に炭酸ガス濃度が低い程最終製品
となる炭酸ソーダの嵩比重は軽くなシ、又溶解速度も速
くなし得ることが見出された。従って炭酸ガス濃度を調
節することによって任意の低密度の炭酸ソーダを得るこ
とが可能となる。この様な具体例は後述する実施例によ
り容易に理解される。
In particular, it has been found that the carbon dioxide concentration greatly affects the degree of density reduction, and in general, the lower the carbon dioxide concentration, the lighter the bulk specific gravity of the final product, sodium carbonate, and the faster the dissolution rate. was discovered. Therefore, by adjusting the carbon dioxide concentration, it is possible to obtain soda carbonate of any desired low density. Such specific examples will be easily understood from the examples described below.

又、炭酸ガスの濃度調節は例えば空気や窒素ガス等のガ
スとの混合割合によって行ない得る。
Further, the concentration of carbon dioxide gas can be adjusted, for example, by adjusting the mixing ratio with gases such as air and nitrogen gas.

重炭酸化における庶度はあまシ低すぎると工業的に装置
が煩雑となシ、逆にあtb高すぎると重炭酸化反応の反
応到達率が低くなる虞れがあるので好ましくなく、この
為一般に0〜80℃を採用するのが適当である。
If the generality in bicarbonation is too low, the industrial equipment will become complicated, and conversely, if the atb is too high, the reaction rate of the bicarbonation reaction may decrease, which is undesirable. Generally, it is appropriate to adopt a temperature of 0 to 80°C.

かくして炭酸ソーダ水和物や混合塩はその少なくとも一
部が重炭酸化される。重炭酸化せしめる程度は\低密度
化せしめる程度や必要とする溶解速度によって決められ
るが、一般に炭酸ソーダ水和物や混合塩中の炭酸ソーダ
に対し、40重量%以上を採用するのが効果的である。
Thus, at least a portion of the sodium carbonate hydrate or mixed salt is bicarbonated. The degree of bicarbonation is determined by the degree of low density and the required dissolution rate, but it is generally effective to use 40% by weight or more of the sodium carbonate in the sodium carbonate hydrate or mixed salt. It is.

かくして得られた重炭酸化物は、次いでこれを履焼して
炭酸ソーダに転化せしめる。このとき採用される腰部条
件としては、140〜500℃程度を採用するのが適当
である。かかる■焼条件を逸脱する場合には、十分な低
密度化や溶解速度が得られなかったシ、強度、特に耐摩
耗強度が低下する等の不都合が生ずる虞れがあるので好
ましくない。
The bicarbonate thus obtained is then converted to soda carbonate by calcining it. As the waist condition to be adopted at this time, it is appropriate to adopt a temperature of about 140 to 500°C. If these firing conditions are deviated from, it is not preferable because there is a risk that problems such as insufficient density reduction and dissolution rate may not be obtained, and strength, especially abrasion resistance, may be reduced.

次に本発明を実施例によシ説明する。Next, the present invention will be explained using examples.

尚、以下の実施例で採用された溶解速度の測定法は、5
ooccのビーカーに50℃の水200筐を入れ、20
0〜300 r、p、mのマグネチツクスターラーで攪
拌した中に試料60fを投入し、完全に溶解する迄の時
間を測定した。又、流動性指数とは、線用粉体工学研究
所のノくウダーテスターによる。
The dissolution rate measurement method adopted in the following examples is 5.
Pour 200 liters of 50°C water into an oocc beaker, and
Sample 60f was placed in a stirrer stirred with a magnetic stirrer at 0 to 300 r, p, m, and the time required for complete dissolution was measured. In addition, the fluidity index is based on the powder tester of the Wire Powder Engineering Research Institute.

Claims (1)

【特許請求の範囲】[Claims] 1、 炭酸ソーダ水和物及び/又は重炭酸ソーダと炭酸
ソーダの混合塩を水1分の存在下に任意の濃度の炭酸ガ
スと反応せしめ、その少なくとも一部を重炭酸化し、次
いで爆焼せしめることによシ、炭酸ガス濃度に応じて低
密度化せしめることを特徴とする低密度炭酸ソーダの製
造方法。
1. Reacting sodium carbonate hydrate and/or a mixed salt of sodium bicarbonate and sodium carbonate with carbon dioxide gas at an arbitrary concentration in the presence of 1 minute of water, bicarbonating at least a portion of it, and then exploding it. A method for producing low-density carbonated soda, which is characterized by lowering the density according to the carbon dioxide concentration.
JP22748282A 1982-12-28 1982-12-28 Production of low-density sodium carbonate Pending JPS59121117A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22748282A JPS59121117A (en) 1982-12-28 1982-12-28 Production of low-density sodium carbonate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22748282A JPS59121117A (en) 1982-12-28 1982-12-28 Production of low-density sodium carbonate

Publications (1)

Publication Number Publication Date
JPS59121117A true JPS59121117A (en) 1984-07-13

Family

ID=16861568

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22748282A Pending JPS59121117A (en) 1982-12-28 1982-12-28 Production of low-density sodium carbonate

Country Status (1)

Country Link
JP (1) JPS59121117A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003192337A (en) * 2001-12-25 2003-07-09 Asahi Glass Co Ltd Porous potassium carbonate and manufacturing method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56149317A (en) * 1980-04-18 1981-11-19 Asahi Glass Co Ltd Manufacture of sodium hydrogencarbonate

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56149317A (en) * 1980-04-18 1981-11-19 Asahi Glass Co Ltd Manufacture of sodium hydrogencarbonate

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003192337A (en) * 2001-12-25 2003-07-09 Asahi Glass Co Ltd Porous potassium carbonate and manufacturing method thereof

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