JPS6065716A - Treatment of bittern by ionic salt preparation wherein device preparing potassium sulfate from mixed potassium salt containing magnesium chloride is combined with multiple effect evaporator and operated - Google Patents

Treatment of bittern by ionic salt preparation wherein device preparing potassium sulfate from mixed potassium salt containing magnesium chloride is combined with multiple effect evaporator and operated

Info

Publication number
JPS6065716A
JPS6065716A JP17175483A JP17175483A JPS6065716A JP S6065716 A JPS6065716 A JP S6065716A JP 17175483 A JP17175483 A JP 17175483A JP 17175483 A JP17175483 A JP 17175483A JP S6065716 A JPS6065716 A JP S6065716A
Authority
JP
Japan
Prior art keywords
potassium
bittern
potassium sulfate
sulfate
product
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
JP17175483A
Other languages
Japanese (ja)
Inventor
Yoshiroku Sakamoto
坂本 佳六
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.)
NIO KOSAN KK
Original Assignee
NIO KOSAN KK
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 NIO KOSAN KK filed Critical NIO KOSAN KK
Priority to JP17175483A priority Critical patent/JPS6065716A/en
Publication of JPS6065716A publication Critical patent/JPS6065716A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F11/00Compounds of calcium, strontium, or barium
    • C01F11/46Sulfates

Abstract

PURPOSE:To convert potassium chloride into potassium sulfate more effective as a fertilizer and to utilize it more efficiently, by combining a production apparatus for potassium sulfate from a potassium salt containing magnesium chloride with a multiple effect evaporator, operating them. CONSTITUTION:A magnesium sulfate solution and a potassium salt containing magnesium chloride formed separately are added to the first reaction tank 5 of potassium sulfate, and reacted to give the bittern of potassium sulfate 9. The separated solution is stored in the mother liquor tank 10. The intermediate product 9 of first potassium sulfate and the regenerated potassium chloride obtained by the device 1 for regenerating potassium chloride are added to the reaction tank 5' of secondary potassium sulfate, water is further added to it, and they are stirred, potassium sulfate is formed, and sent to the centrifugal separator 6 to give the product 11 of potassium sulfate. The separated mother liquor having prepared the gypsum product 14 is stored in the tank 15 for bittern from which calcium is removed, the bittern freed from calcium is sent to the triple effect vacuum evaporator 18 in parallel by the pump 16, evaporated under reduced pressure, a mixed solution containing potassium is collected, and dehydrated by the centrifugal separator 21, to give a product.

Description

【発明の詳細な説明】 イオン製塩法苦汁の組成は、従来の蝮日法苦汁に比べる
と大いに、その組成成分が異なっている。
DETAILED DESCRIPTION OF THE INVENTION The composition of bittern produced by the ionic salt production method is significantly different from that of the conventional bittern produced by the ion salt production method.

従来の苦汁組成の主要成分であったところの、硝酸苦土
、Mg80.がなくなり、その代わりに、塩イ七カルシ
ウム、0aOL2が相当か含まれてψる。良弊Br と
、塩化加l、 KO,Lが茗しく増加してきた。y素に
ありては、従来苦汁の約3.3倍、塩(?J里qありて
は、約2倍の含有瓜である。
Magnesium nitrate, Mg80. In its place, a considerable amount of 7-calcium salt, 0aOL2, is contained. Br, chloride, KO, and L have been increasing rapidly. It contains about 3.3 times as much salt as conventional bittern, and about twice as much salt as bittern.

イオン製塩法苦汁の化学組成は、大体状の如きものであ
る0 Mg0I、2It 、 !r%、KQX、11..2%
、 Na0L 2 、1% 、0aOL25%、 Mg
Br20.9%。
The chemical composition of ionic salt production bittern is roughly as follows: 0 Mg0I, 2It, ! r%, KQX, 11. .. 2%
, Na0L2, 1%, 0aOL25%, Mg
Br20.9%.

この原料苦汁から、有効成力を強次無靭なく、合理的に
、V済的にjyり出し、氾2、・・化する斯粂(Cあり
て、先ずOa OL 2成分を、外界からめたところの
MgSO4成分を使用して、Mg5O,+ 0aOIa
2 =MgOL2 +0a304の化学反応に依り、石
壷Oa 804AH,0に転化する。いわゆる、脱カル
工程が必ず選録、採用される化学的手法である。
From this raw material bittern, the active ingredients are forcefully, rationally, and economically extracted, and the two ingredients are extracted from the outside world. Mg5O, + 0aOIa using the MgSO4 component found in
2=MgOL2+0a304 is converted into stone pot Oa 804AH,0 by a chemical reaction. The so-called decaling process is a chemical method that is always selected and adopted.

この脱カル苦汁に、蒸発工程か加えられ、濃縮して塩化
ソーダ、加里塩類の混塩が、採取される。
An evaporation step is added to this decalcified bittern to concentrate and collect a mixed salt of sodium chloride and potassium salts.

、加里塩類を採取した残シの液が、濃厚苦汁と称される
。液体マグネシウムの主成分である。この主要成分Mg
0L、が各種重要苦土製品製造の原料母体である。以上
が斯楯の一般的工程の権道である。
The liquid from which potassium salts are collected is called thick bittern. It is the main component of liquid magnesium. This main component Mg
0L is the raw material base for manufacturing various important magnesia products. The above is the principle of the general process of the shield.

1 脱カル苦汁を濃縮して、加里塩を採取する際、先:
 ず最初に採取されるものは、Na0I+を含む塩化加
工の混塩である。次に苦汁の濃度が進むに従ってカーナ
ライトと称するMg0L、KOL6H20なる複塩が採
取される。この複塩の母液が、上記液体マグネシラふと
称さる濃厚苦汁である。
1. When concentrating decalcified bittern and collecting potassium salt, first:
The first thing to be collected is a chlorinated mixed salt containing Na0I+. Next, as the concentration of bittern increases, a double salt called carnallite called Mg0L and KOL6H20 is collected. The mother liquor of this double salt is the thick bittern called liquid magnesilla fu.

この二種類の加里塩の内、Na0Lを含む加圧混塩の化
学組成はおよそ、0a804/ 、j%、 Mg0I+
27 、0%、KOL’lu、0%、 Na0L 4’
コ%である。
Among these two types of potassium salt, the chemical composition of the pressurized mixed salt containing Na0L is approximately 0a804/, j%, Mg0I+
27, 0%, KOL'lu, 0%, Na0L 4'
%.

加里狛料としては、用速か少く、専ら、皮革製造業方面
に広い販路をもつものである。故に、ことさら問題はな
い。然るに、二次析出加里塩であるところの、カーナラ
イトにつ−ては、その用途が限定されている。従来はこ
の塩に、約重量ダO%程度の加水か施され、加水分解反
応Mg0L2KOL6H20+ ’7.8H20−→0
.84KOL + Mg0L20.16KOL+ 13
.8H20f)通シ、粗製の塩化加里KOL#J41r
%程度のものが原カーナライト71当り、約230Kg
が採取され、KOI+の収率は約70%であるがこの工
程けあまシ、経済的に有利でな−。今日ではKOL製造
面でははとんど顧りみられない。然しRMg0L2の回
収のためには、その意義は失なわれていないのである〇 本発明は以上工程に、改良発明を施したものである。塩
化物の加里塩を肥料として、より有効な硫酸体の&酸加
里に2SO4に転化し、尚展化をはかるのである。2K
OIL +Mg5O4= K2Bo4+Mg0L2O化
学反応に従い硫酸加圧をW造する。一方この研酸加里を
採取したところの後の世酸、−次硫酸加里母液と、二次
母液とを、その生産公比で混4合し°C得られるところ
の母液の組成は約Mg0L2り、1%Mg5O,3,Q
−%、Na0LJ 、 17%、MOL 1.3%、で
ある。
It is used sparingly and has a wide sales channel exclusively in the leather manufacturing industry. Therefore, there is no particular problem. However, the uses of carnallite, which is a secondary precipitated potassium salt, are limited. Conventionally, this salt was subjected to hydration of about 0% by weight, resulting in a hydrolysis reaction Mg0L2KOL6H20+ '7.8H20-→0
.. 84KOL + Mg0L20.16KOL+ 13
.. 8H20f) General, crude potassium chloride KOL#J41r
% of raw carnallite 71, approximately 230 kg
The yield of KOI+ is about 70%, but this process is not economically advantageous. Today, KOL production is hardly neglected. However, for the recovery of RMg0L2, its significance is not lost. The present invention is an improvement to the above process. Potassium chloride is used as fertilizer and converted to more effective sulfate and acid potassium, 2SO4, in order to promote further development. 2K
OIL + Mg5O4 = K2Bo4 + Mg0L2O According to the chemical reaction, sulfuric acid pressurization is made using W. On the other hand, the composition of the mother liquor that is obtained by mixing the secondary mother liquor with the sodium chloride acid, -subsulfuric acid potassium mother liquor from which the polished potassium was collected and the secondary mother liquor is obtained at 4°C is about Mg0L2. , 1%Mg5O,3,Q
-%, Na0LJ 17%, MOL 1.3%.

この砧酸加里分離母液が、重要なる役割を北ずのである
。このものが、原七Fl19臭苦汁のOa OL2除去
石井に転化する反応、0aOL、、 +Mg5O,=(
!aso4+Mg0L2、脱カル反応の好適の、睨カル
反応用の辱料源となるのである。この反応に用いていた
、従来の単なる&麻液MgSO4汐と興なり、有効成分
KOL、 MgSO4、Mg0L2、N&OLを含も。
This potassium minutate separation mother liquor plays an important role in Kitazuno. This is the reaction that converts Haranachi Fl19 odor bittern into Oa OL2 removal Ishii, 0aOL,, +Mg5O, = (
! aso4+Mg0L2 is suitable for the decaling reaction and serves as a source of oxidizing agent for the calcification reaction. In addition to the conventional liquid MgSO4 used in this reaction, it also contains active ingredients KOL, MgSO4, Mg0L2, and N&OL.

上記石膏製造、脱カル反応に与かるMg5O,のほかに
Mg0L2を含み、Oa S O4生成時に生ずるMg
0L2と合波して、脱カル苦汁中のMg0L20私展上
昇を確保するのみならず、Na0L、 KOLの有効成
分が随伴するという利点がある。従来の単なるvl、麻
峨のみ使用時の苦汁の説カル反応の鳩舎Mg5O,の濃
度社約/7.!;%、 2709/A なるに比し、本
母液は、Mg804!、’i%、tlr、t9/J)で
ある。
In addition to Mg5O, which participates in the above-mentioned gypsum production and decaling reaction, it also contains Mg0L2, and Mg generated during Oa SO4 production.
Not only does it combine with 0L2 to ensure an increase in the Mg0L20 concentration in the decalcifying bittern, but it also has the advantage of being accompanied by the active ingredients of Na0L and KOL. Conventional simple VL, the concentration of bittern theory cal reaction when only hemp is used, Mg5O, concentration company approx./7. ! ;%, 2709/A, compared to this mother liquor, Mg804! , 'i%, tlr, t9/J).

そのため従来法にお−て、原脱臭苦汁・との脱カル反応
において、原脱臭苦汁中のOa(lLg A 0.9 
g/71/のものixlに対しては、所要碓府液は1,
0.9Kgg80 ×−−にλ70==(J−J/KJ!/である。これに
比べ0aOL2 ’ て本液硫酸加里分離母液を使用する場合は、60.9K
gX7e/i14 =1.0ttKLを必要とする。
Therefore, in the conventional method, Oa (lLg A 0.9
For g/71/ ixl, the required Usufu liquid is 1,
0.9Kgg80 ×−−,λ70==(J−J/KJ!/
Requires gX7e/i14 = 1.0ttKL.

Mg8O この事は生成膜カル苦汁を基本に考えると、単なる硫麻
液を使用すると原脱臭苦汁/KA当り ハ3ixAの脱
カル苦汁が得られるのに比し、2.041HAの脱カル
苦汁生成量となる。
Mg8O Considering this based on the produced membrane cal bittern, compared to the use of simple sulfuric hemp liquid, a decalcified bittern of HA3ixA per original deodorized bittern/KA is obtained, whereas a decalcified bittern of 2.041 HA is produced. becomes.

この様に脱カル苦汁量の増加は約ハロ倍となる。In this way, the amount of decalcified bittern increases by approximately half the amount of bittern.

従来の脱カル苦汁成分が、Mg0L2112.!;9/
込xol+ J4.99/LNaOI+ 23.39p
Be J4(、j(/j’o)であったものが、本発明
上記脱カル苦汁の組成は、ugOI+2/13 、09
/Z 、1IaoI+ J7.69/A * KOL 
77−79、々、、 n630.2(1!00)となる
。溶液の比重の増加、塩類の総#度が著しく上昇してい
る。従って蒸発缶の消費溶料を約20%節減することが
可能である。別図に依り工程順に、硫酪加片を製造して
行く枦作方法について、詳述すると次の通りである。操
作は回分法である。Sなる飢酸加里−次反応檜に別途生
成した硫麻漬Be211 、 Mg5o、/7.3%の
もの約IKI−と、自家製塩化マグネシウム含有加里塩
り、その化学組成はMg0L222.3%、 KOLt
to、s%、に20表示コs、s%、 Na0I+ 5
.1%、約uoooKgを投入、S時間励井反応を行う
。ざなるミキサーを鮭て6なる遠心分1i1Aにて遠心
脱水を行って、9なる(iii酸加回加l苦土る。分離
母液け10なる母液槽に貯溜する。9は砺@加用の中間
製品である。このものの収量は約3000にりである。
The conventional decalcifying bittern component is Mg0L2112. ! ;9/
Including xol+ J4.99/LNaOI+ 23.39p
Be J4(,j(/j'o), the composition of the decalcified bittern of the present invention is ugOI+2/13,09
/Z, 1IaoI+ J7.69/A *KOL
77-79, etc., n630.2 (1!00). The specific gravity of the solution increases, and the total number of salts increases significantly. Therefore, it is possible to reduce the consumption of solvent in the evaporator by about 20%. A detailed description of the method for producing sulfurized butyric pieces in the order of steps as shown in the separate drawings is as follows. The operation is batchwise. A sulfur-marinated Be211, Mg5o, /7.3% product separately produced in the starved potassium cypress called S, and a homemade potassium salt containing magnesium chloride, the chemical composition of which is Mg0L222.3%, KOLt.
20 displayed in to, s%, s, s%, Na0I+ 5
.. 1%, approximately uooo kg was added, and the reaction was carried out for S hours. Using a mixer, perform centrifugal dehydration at 6 centrifugal fractions 1 and 1A, and remove 9 (iii) acid. It is an intermediate product.The yield of this product is about 3000 ni.

結合化学組成は、約に2So、 31−1%、 Mg8
0.23.lI%KOL ?、!;%、 1iaOL 
O,4%、に20表示22.弗であムに20の収率は約
、IG4’、7%である。母液量は約tKAテアル。比
fiB= 3 /″(/!;oO) 母11cD組1f
、KoLA、/%、NaffL 、2.9LMg0I、
21113%、Mg80,3.32%である。5′は二
次髄酸加里反応槽である。容量けSと同様、同じ構造内
容であり、q、5yxL入りの容器であシ、イttK 
翼を設えている。その回転数2S回/分である。この二
次勧酸加里反応檜へ、9なる一次碓酸加里中間製品約j
tと、lなる再生坂化加里装置にて得られた再製塩化加
里を、約、2 tを投入コなる淡水槽より、淡水的7K
Lを加えりt忙することS時間にして、硫酸加里を生成
させ、lrなるミキサー、tなる分N機を紗て、llな
る製品硫酸加用を得る。再製塩化加里の組成は、IOL
約rr、o%、1iaoI+ 6%のものであシ、0a
SO4の含有量は、コ%以下のものである。製品硫酸加
用の組成は、約KOL 5.9%、0a802.0%j
1g80 /、2%4280゜番 4 rt、o%、に、O表示30.1%である。1回分、収
fi、2.,2を分−熱母液約7にムB5.2j’(/
j’0 )を得る。母液(・組成はKOI+/J、4[
%、MaOL 1.J%1Mg0I+21.5%、Mg
5O4j、5%である。この砒酸加里分断母渣が10な
る母液槽に、前記−次f#:#加y分訃母治と混合して
貯溜され、苦汁処理の本工程の石井生成反応槽13に送
られ、/、2なる脱臭苦汁の、脱カル原料沼源材料とし
て、石膏製造、脱カル芳汁生成という、重要な役割を、
演するのである。即ちllなる石膏製品を製造する。そ
の分離母液が、脱カル苦汁15に貯溜さる。この脱カル
苦汁の組成は、MgO稲/IJ9h JOL 77.7
/、4.Na0L 37.6φ、B530.2(100
)前述の通りである。lSに貯溜された脱カル苦汁は、
llなるポンプによシ、三重効用真空蒸発缶に、並列に
給液され、17なる蒸気溜の蒸気を、smとして、減圧
下にて、蒸発され、濃縮されて、加圧混塩が採取され、
21なる遠心分離機にて、脱水、製品とされる。その分
離母液が23なる濃厚苦汁檜に集められ、貯溜される。
The bond chemistry is approximately 2So, 31-1%, Mg8
0.23. lI%KOL? ,! ;%, 1iaOL
O, 4%, 20 display 22. The yield of IG4'20 is approximately 7%. The amount of mother liquor is approximately tKAteal. Ratio fiB= 3 /''(/!; oO) Mother 11cD group 1f
,KoLA,/%,NaffL,2.9LMg0I,
21113%, Mg80, 3.32%. 5' is a secondary marrow acid potassium reaction tank. It has the same structure as the capacity container S, and it is a container with q, 5yxL, itttK.
It has wings. The number of rotations is 2S times/minute. To this secondary potassium sulfuric acid reaction hinoki, about 9 primary potassium silicic acid intermediate products
Approximately 2 tons of recycled potassium chloride obtained from the regenerated potassium sulfurization device are added to a freshwater tank of 7K.
Add L for t time to produce potassium sulfate, mix with lr mixer and t for N machine to obtain ll product sulfuric acid. The composition of recycled potassium chloride is
Approximately rr, o%, 1iaoI + 6%, 0a
The content of SO4 is less than 1%. The composition of the product with sulfuric acid added is approximately KOL 5.9%, 0a802.0%j
1g80/, 2% 4280° No. 4 rt, o%, O display is 30.1%. 1 serving, yield, 2. , 2 minutes - heat the mother liquor to about 7 minutes B5.2j' (/
j'0). Mother liquor (・Composition is KOI+/J, 4 [
%, MaOL 1. J%1Mg0I+21.5%, Mg
5O4j, 5%. This potassium arsenate separated mother residue is mixed with the above-mentioned -next f#:#additional mother liquor and stored in a mother liquor tank 10, and sent to the Ishii production reaction tank 13 of the main step of bittern processing, / Second, deodorized bittern plays an important role in producing gypsum and producing decalcifying aromatic juice as a decalcifying raw material.
It is to perform. That is, 11 gypsum products are manufactured. The separated mother liquor is stored in the decalcified bittern 15. The composition of this decalcified bittern is MgO rice/IJ9h JOL 77.7
/, 4. Na0L 37.6φ, B530.2 (100
) As mentioned above. The decalcified bittern stored in the IS is
The liquid was supplied in parallel to a triple-effect vacuum evaporator by a pump named 1, and the steam from a vapor reservoir named 17 was evaporated and concentrated under reduced pressure as sm, and a pressurized mixed salt was collected. ,
It is dehydrated and made into a product in a centrifugal separator 21. The separated mother liquor is collected and stored in a thick bittern cypress 23.

ltのポンプ以下廚工程は、おおむね、h紗辻転である
The process below the pump of lt is generally a gauze rotation.

1日当り、原イオン苦汁換眞の処理Mは、約73−にノ
である。これよシ、哲取埴造される製品としれ、E<+
m加里3./l、品位’g2o so%、加圧混塩1t
tK、02t、0%、ah苦汁得意、約3j、jKi、
B6J J −j (/ j”0 ) 9M E OL
 g J 1%である。従来の方法単に、硫酸苦土Mg
5O,溶液を使用して、同じ処理賢1、同じ脱臭苦汁を
使用した貌合の、1日当りの製品、生産生を示すと、次
の通りである。従来の方法は鯖E醗加里は得られず、加
止渉塩はに2021r%のもの/、2tS濃庁苦汁の収
量、3.2.sKAである。
Per day, the treatment M of the original ion bittern is about 73-days. This is a product made from Tetsutori clay, E<+
mkari3. /l, quality 'g2o so%, pressurized mixed salt 1t
tK, 02t, 0%, ah bittern good, about 3j, jKi,
B6J J -j (/j”0) 9M E OL
g J 1%. The conventional method simply involves adding magnesium sulfate to Mg
The products and production volume per day using the same treatment method and the same deodorized bittern using 5O, solution are as follows. With the conventional method, it is not possible to obtain mackerel, and the yield of 2021r%/2tS bittern is obtained.3.2. It is sKA.

本発明方式にありては、従来の方式よりも副原料の硫酸
と水麻の使用量がそれぞれ約20%使用増″伽である。
In the method of the present invention, the amount of sulfuric acid and water hemp used as auxiliary raw materials is increased by about 20% compared to the conventional method.

又別に粗製塩化加圧の新規使用があシ1日当約、4tを
消費する◇硫酸の使用量は、直接硫酸加里の硫酸に、転
化するものであり、水麻の使用量iは新規使用の塩化加
里と結合して、MgOLg製品に転化して行くのである
。又未反応のそれ等の化合物鉱、全部加里混塩として製
品化されるのである。従来の製造方式に比べ本発明の方
式が製品の生産性、品質において、はるかに優位にある
ことが明瞭である〇 以上は、イオン製塩苦汁の総合利用処理方式において、
硫酸加里を製造する装置と蒸発缶による、濃縮工程を、
組合せ連係して、運転する方式について、述べたのであ
るが、本発明方式が従来の方法に比べ、工場の原料苦汁
消化能力の増進、省エネルギー、製品の高度化、生産性
の向上、に大きく寄与するものである。
In addition, new use of pressurized crude chloride consumes approximately 4 tons per day.◇The amount of sulfuric acid used is directly converted into sulfuric acid from potassium sulfate, and the amount of water hemp used is the amount used for new use. It combines with potassium chloride and is converted into MgOLg products. In addition, all unreacted compound ores are turned into products as potassium mixed salt. It is clear that the method of the present invention is far superior to the conventional production method in terms of product productivity and quality.
The concentration process is carried out using a device that produces potassium sulfate and an evaporator.
As mentioned above, the method of combining and linking operations has been described, and compared to the conventional method, the method of the present invention greatly contributes to improving the factory's ability to digest raw bittern, saving energy, improving the sophistication of products, and improving productivity. It is something to do.

苦汁から単にf4.a加里を製造する事自体他の企業で
は実施、工業化して−な一現状にありて、その製造方法
の実施を更に進めて、多重効用蒸発缶との連係を緊密に
して省エネルギー、生産性の向上をはかったところに、
本発明の特徴、独創性プ・;あノ る。特に餅酸加里分原fit液の白眉の古使用利用Gで
鋭意、注目して、原料加里塩の選抜に当シて、Mg0L
2を含む加圧混塩の使用を強調しているのである。この
方式は出願人の工場に2いて、現笑に・依動中のもので
あることを附記する。
Just f4 from bittern. Currently, the production of a-potassium itself has not been implemented or industrialized by other companies, but we are working to further advance the implementation of the production method and improve energy savings and productivity by closely linking it with multi-effect evaporators. While trying to improve,
Characteristics of the present invention, originality. In particular, we are paying close attention to the old use of mochi acid potassium fillet liquid, and are focusing on the selection of raw material potassium salt, Mg0L.
It emphasizes the use of pressurized mixed salts containing 2. It should be noted that this method is currently in use at the applicant's factory.

【図面の簡単な説明】[Brief explanation of drawings]

lは塩化加里書生装愼 2は淡水槽 3け硫麻液檜 弘は自家製加里塩 5は一次硫酸加■1反応槽 Sは二次砕酸加里反応檜 乙は遠心分離機 7tf再製塩化加里 jはミキサー タは硫酸加工中間製品 10は硫酸加里母液槽 llは硫酸加里製品 12は脱臭苦汁槽 13は石膏反応槽 llは石膏製品 isは脱カル苦汁槽 16は輸送ポンプ 17祉蒸気溜 II祉真空蒸発缶 19社復水器 20は真空ポンプ 21は遠心分離機 2コは加里、カーナライト、混墳 23祉濃厚苦汁槽 特rf用願人 塩 1)雄 − 手続神正書 2v〜グネシウムをζ′む茄i M”ffl’Th b
 % ’fi; U;贅をV景するiを蟹懺督背i菖i
tと、1容わせて、事件との関係 特許出願人 住Wl 17.、箋呈す首e騎升仁爪1−ft4 1囁
バm ダ代理人 な し S補正命令の日付 昭和59年181184図面の簡単
な説明
1 is for potassium chloride. 2 is for freshwater tank. 3 is for sulfurized hemp liquid. 5 is for homemade potassium salt. 5 is for primary sulfuric acid. The mixer is the sulfuric acid processing intermediate product 10 is the potassium sulfate mother liquor tank 12 is the sulfuric acid potassium product 12 is the deodorizing bittern tank 13 is the gypsum reaction tank 1 is the gypsum product Can 19 Condenser 20 Vacuum pump 21 Centrifugal separator 2 Cali, Carnalite, Mixed tomb 23 Healthy concentrated bittern tank Special RF user Salt 1) Male - Procedural Shinshosho 2v ~ Gnesium ζ'M'ffl'Th b
% 'fi;
Relationship between t and 1 and the incident Patent applicant residence Wl 17. , 1-ft 4 1-ft 4 1-ft 4 1 whisper bad agent None Date of S amendment order 1984 181184 Brief explanation of the drawings

Claims (1)

【特許請求の範囲】[Claims] 塩化マグネシウムを呑む加里涙廖から、を酸加里を製造
する装置を、多重効用蒸発irJ装置と組合わせて、構
成する苦汁処理方法。
A bittern treatment method comprising a device for producing acid potassium from potassium lachrymal fluid containing magnesium chloride in combination with a multi-effect evaporation IRJ device.
JP17175483A 1983-09-16 1983-09-16 Treatment of bittern by ionic salt preparation wherein device preparing potassium sulfate from mixed potassium salt containing magnesium chloride is combined with multiple effect evaporator and operated Pending JPS6065716A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17175483A JPS6065716A (en) 1983-09-16 1983-09-16 Treatment of bittern by ionic salt preparation wherein device preparing potassium sulfate from mixed potassium salt containing magnesium chloride is combined with multiple effect evaporator and operated

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17175483A JPS6065716A (en) 1983-09-16 1983-09-16 Treatment of bittern by ionic salt preparation wherein device preparing potassium sulfate from mixed potassium salt containing magnesium chloride is combined with multiple effect evaporator and operated

Publications (1)

Publication Number Publication Date
JPS6065716A true JPS6065716A (en) 1985-04-15

Family

ID=15929064

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17175483A Pending JPS6065716A (en) 1983-09-16 1983-09-16 Treatment of bittern by ionic salt preparation wherein device preparing potassium sulfate from mixed potassium salt containing magnesium chloride is combined with multiple effect evaporator and operated

Country Status (1)

Country Link
JP (1) JPS6065716A (en)

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CN105271308A (en) * 2015-11-20 2016-01-27 湖南省湘衡盐化有限责任公司 Vapor recovery method and device for salt and sodium sulfate co-production
CN108726763A (en) * 2017-04-21 2018-11-02 中国石油化工股份有限公司 A kind of processing method of catalyst production waste water
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