JPS6038338B2 - Method for producing granular ammonium sulfate - Google Patents

Method for producing granular ammonium sulfate

Info

Publication number
JPS6038338B2
JPS6038338B2 JP55011712A JP1171280A JPS6038338B2 JP S6038338 B2 JPS6038338 B2 JP S6038338B2 JP 55011712 A JP55011712 A JP 55011712A JP 1171280 A JP1171280 A JP 1171280A JP S6038338 B2 JPS6038338 B2 JP S6038338B2
Authority
JP
Japan
Prior art keywords
ammonium sulfate
ammonium
mother liquor
added
producing granular
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
Application number
JP55011712A
Other languages
Japanese (ja)
Other versions
JPS56109816A (en
Inventor
義雄 畠山
貞男 辻
一弘 坂野
久明 久保
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP55011712A priority Critical patent/JPS6038338B2/en
Publication of JPS56109816A publication Critical patent/JPS56109816A/en
Publication of JPS6038338B2 publication Critical patent/JPS6038338B2/en
Expired legal-status Critical Current

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  • Fertilizers (AREA)

Description

【発明の詳細な説明】 本発明は粒状硫安の製造方法に関するものである。[Detailed description of the invention] The present invention relates to a method for producing granular ammonium sulfate.

硫安は吸湿性があるため長期間保存した際固結するため
粉砕が必要となり、又近年は窒素、隣、加里成分を任意
且つ迅速に製造配合するため数種類の粒状原料を混合し
、バラ状のまま輸送し施肥することによりコストを安く
するような手段がとられている。
Since ammonium sulfate is hygroscopic, it solidifies when stored for a long period of time, requiring pulverization.In recent years, in order to quickly and arbitrarily produce and blend nitrogen, chloride, and potassium components, several types of granular raw materials have been mixed together, and a bulk material has been developed. Measures are being taken to reduce costs by transporting and fertilizing raw materials.

このような状況にあるため硫安の結晶粒の形状は大きく
且つ丸味を帯びたものが要求されている。
Under these circumstances, ammonium sulfate crystal grains are required to have a large and round shape.

従来の粒状硫安の製造は、飽和器にて遊離硫酸を含む母
液とアンモニアから硫安を生成させ、飽和度、遊離酸濃
度及び温度を一定にした母液を造粒装置に供給してここ
で水分を蒸発させることにより母液の濃縮及び過飽和度
を上げて硫安結晶を発生させると共に結晶の成長を回り
且つ分級を行い造粒装置底部から粒状の硫安を取り出し
、又造粒装置で水分及び結晶を抜きとった後の母液は飽
和器に循環させているが、このようにして製造した硫安
結晶はその形状がいずれも六角柱や四角柱又は板状であ
って、どうしても大形で丸味を帯びた形状の粒状硫安は
製造することはできなかった。
Conventional production of granular ammonium sulfate involves producing ammonium sulfate from a mother liquor containing free sulfuric acid and ammonia in a saturator, and supplying the mother liquor with a constant degree of saturation, free acid concentration, and temperature to a granulation machine, where water is removed. By evaporating, the mother liquor is concentrated and the degree of supersaturation is increased to generate ammonium sulfate crystals, and the crystals are grown and classified to take out granular ammonium sulfate from the bottom of the granulator, and water and crystals are removed in the granulator. The mother liquor after washing is circulated in a saturator, but the ammonium sulfate crystals produced in this way are all hexagonal prisms, square prisms, or plates, and are inevitably large and rounded. Granular ammonium sulfate could not be produced.

本発明はこのような状況に鑑みてなされたものであり、
硫安母液から晶析装置を経て、粒状硫安を製造する工程
において、硫安母液に煤晶剤として硝酸、スルフアミン
酸またはそのアンモニウム塩を同時にそれぞれアンモニ
ウム塩換算値で硝酸は1〜10%、スルフアミン酸は0
.5〜5%添加し晶折する粒状硫安の製造方法である。
The present invention was made in view of this situation,
In the process of producing granular ammonium sulfate from an ammonium sulfate mother liquor through a crystallizer, nitric acid, sulfamic acid, or its ammonium salt is simultaneously added to the ammonium sulfate mother liquor as a soot crystallizing agent, and nitric acid is 1 to 10%, and sulfamic acid is 1 to 10% in terms of ammonium salt. 0
.. This is a method for producing granular ammonium sulfate in which 5 to 5% of ammonium sulfate is added and crystallized.

以下実施例に基づいて図面と共に本発明を詳細に説明す
る。図面は本発明の実施例を示す説明図である。
Hereinafter, the present invention will be described in detail based on embodiments and in conjunction with the drawings. The drawings are explanatory diagrams showing embodiments of the present invention.

飽和器に相当する内容積1あの母液槽1に50qoに加
熱された硫安の飽和母液2を入れて縄杵器3で軽く縄拝
しつつこの母液槽1に媒晶剤4として硝酸アンモニウム
及びスルフアミン酸アンモニウムを該飽和母液2に対し
て硝酸アンモニウムを5%及びスルファミン酸ァンモニ
ゥムを2凝添力oし、硫安結晶を含まない上燈母液を造
粒装置に相当する0.3あの結晶槽5が供給した。結晶
槽5内の飽和母液2Aは擁伴器3Aで櫨拝しながら45
q0に維持し、硫安過飽和度を上げ晶折を行った。この
結果硫安の結晶6が析出し、結晶濃度が上昇してくるた
め結晶分が25%となるように逐次その結晶6を矢印6
Aで示すように抜きとった。結晶槽5内の硫安結晶を含
まない母液はポンプ7により50〜100Z/minだ
母液槽1内へ循環させた。なお結晶槽を蝿拝することに
より硫安結晶が更に良好な丸味を帯びる効果を生ずる。
この時得られた硫安の性状を媒晶剤を添加しない従来法
によるものと比較して第1表に示す。
A saturated mother liquor 2 of ammonium sulfate heated to 50 qo was put into the mother liquor tank 1, which had an internal volume equivalent to a saturator, and while being lightly stirred with a rope pestle 3, ammonium nitrate and sulfamic acid were added to the mother liquor tank 1 as a crystallizing agent 4. Ammonium was added to the saturated mother liquor 2 by 5% ammonium nitrate and ammonium sulfamate at a coagulation force of 2, and the top mother liquor containing no ammonium sulfate crystals was supplied by a crystallization tank 5 corresponding to a granulator. . The saturated mother liquor 2A in the crystallization tank 5 is 45
Crystallization was performed while maintaining the temperature at q0 and increasing the supersaturation degree of ammonium sulfate. As a result, ammonium sulfate crystals 6 are precipitated, and as the crystal concentration increases, the crystals 6 are successively separated by the arrow 6 so that the crystal content becomes 25%.
It was extracted as shown in A. The mother liquor containing no ammonium sulfate crystals in the crystallization tank 5 was circulated into the mother liquor tank 1 at a rate of 50 to 100 Z/min by a pump 7. Note that by rotating the crystal tank, the ammonium sulfate crystals have the effect of giving a better roundness.
The properties of the ammonium sulfate obtained at this time are shown in Table 1 in comparison with those obtained by the conventional method in which no crystal modifier was added.

第1表第1表に示すように煤晶剤として硝酸アンモニウ
ム5%、スルフアミン酸アンモニウムを2%を同時に添
加した本発明方法によれば、媒晶剤を添加しない従来法
に比較し硫安の粒度が大きく、結晶の形状は丸味を帯び
た球状となり、硫安の品質もアンモニア性窒素含有率は
従来のものと殆んど変らず、硝酸性窒素及びスルフアミ
ン酸の増加も微少であり、良効であった。
Table 1 As shown in Table 1, according to the method of the present invention in which 5% ammonium nitrate and 2% ammonium sulfamate were simultaneously added as soot crystallizing agents, the particle size of ammonium sulfate was reduced compared to the conventional method in which no crystallizing agent was added. The crystals are large and have a rounded spherical shape, the quality of the ammonium sulfate, the ammonia nitrogen content is almost the same as the conventional one, and the increase in nitrate nitrogen and sulfamic acid is small, so it is highly effective. Ta.

本発明に係る硝酸アンモニウムの添加量は1%以上で硫
安の結晶粒を丸味を帯びたものにすることができ、10
%を越えると、結晶粒の形状は良好となるがアンモニア
性窒素含有率の低減が著しくなるため、硝酸アンモニウ
ムの添加量は1〜10%の範囲とする。
When the amount of ammonium nitrate added according to the present invention is 1% or more, it is possible to make ammonium sulfate crystal grains round.
%, the shape of the crystal grains will be good, but the ammonia nitrogen content will be significantly reduced, so the amount of ammonium nitrate added should be in the range of 1 to 10%.

特に5%程度の添加が硫安の形状及び品質上から望まし
い。またスルフアミン酸アンモニウムの添加量は0.5
%でも硫安結晶の形状は大きくでき、5%を越えると硫
安品質上からスルフアミン酸が多くなるため、スルフア
ミン酸アンモニウムの添加量は0.5〜5%の範囲とす
る。特に2%程度の添加が硫安の形状及び品質から望し
し、。なお本発明に係る煤晶剤の例を硝酸ァンモニウム
及びスルフアミン酸アンモニウムとして説明したが、こ
れを硝酸及びスルフアミン酸とすることが可能であり、
硝酸及びスルフアミン酸を母液中に添加するとガス状等
のアンモニウムと化合して硝酸アンモニウム及びスルフ
アミン酸アンモニウムとなり、媒晶剤として機能する。
In particular, addition of about 5% is desirable from the viewpoint of the shape and quality of ammonium sulfate. Also, the amount of ammonium sulfamate added is 0.5
%, the shape of the ammonium sulfate crystals can become large, and if it exceeds 5%, the amount of sulfamic acid increases from the viewpoint of quality of ammonium sulfate. Therefore, the amount of ammonium sulfamate added should be in the range of 0.5 to 5%. In particular, addition of about 2% is desirable from the shape and quality of ammonium sulfate. Although examples of the soot crystallizing agent according to the present invention have been described as ammonium nitrate and ammonium sulfamate, it is also possible to use nitric acid and sulfamate.
When nitric acid and sulfamic acid are added to the mother liquor, they combine with gaseous ammonium to form ammonium nitrate and ammonium sulfamate, which function as crystal modifiers.

この場合硝酸及びスルフアミン酸の添加割合は硝酸アン
モニウム及びスルファミン酸アンモニウムに換算した値
で前記範囲内で添加しなければならない。また、硝酸ア
ンモニウム及びスルフアミン酸アンモニウムは第1表に
示すように硫安結晶に混入する量が少いため補給量は徴
量でよい。以上述べたように本発明によれば硫安の結晶
粒の形状を丸味を帯びた球状でかつ粒度を大にすること
ができ、従って硫安の固結を防止でき、数種類の粒状肥
料を混合して使用する市場に対応できるという効果を奏
する。
In this case, the ratio of nitric acid and sulfamic acid added must be within the above range in terms of ammonium nitrate and ammonium sulfamate. Further, as shown in Table 1, the amount of ammonium nitrate and ammonium sulfamate mixed into ammonium sulfate crystals is small, so the amount of replenishment may be sufficient. As described above, according to the present invention, the shape of ammonium sulfate crystal grains can be made round and spherical, and the particle size can be increased, so that caking of ammonium sulfate can be prevented, and several types of granular fertilizers can be mixed together. This has the effect of being able to respond to the market in which it is used.

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

第1図は本発明の実施例を示す説明図である。 1:母液槽、2,2A:飽和母液、3,3A:蝿杵器、
4:煤晶剤、5:結晶槽、6,6A:結晶、7:ポンプ
。 オー図
FIG. 1 is an explanatory diagram showing an embodiment of the present invention. 1: mother liquor tank, 2, 2A: saturated mother liquor, 3, 3A: fly pestle,
4: Soot crystallizing agent, 5: Crystallization tank, 6, 6A: Crystal, 7: Pump. O diagram

Claims (1)

【特許請求の範囲】[Claims] 1 硫安母液から晶析装置を経て粒状硫安を製造する工
程において、硫安母液に媒晶剤として硝酸または硝酸ア
ンモニウムを硝酸アンモニウムの形で1〜10%及びス
ルフアミン酸またはスルフアミン酸アンモニウムをスル
フアミン酸アンモニウムの形で0.5〜5%の範囲で添
加し晶析することを特徴とする粒状硫安の製造方法。
1. In the process of producing granular ammonium sulfate from an ammonium sulfate mother liquor through a crystallizer, 1 to 10% of nitric acid or ammonium nitrate in the form of ammonium nitrate and sulfamic acid or ammonium sulfamate in the form of ammonium sulfamate are added to the ammonium sulfate mother liquor as a crystallizing agent. A method for producing granular ammonium sulfate, which comprises adding and crystallizing 0.5 to 5% of ammonium sulfate.
JP55011712A 1980-02-02 1980-02-02 Method for producing granular ammonium sulfate Expired JPS6038338B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55011712A JPS6038338B2 (en) 1980-02-02 1980-02-02 Method for producing granular ammonium sulfate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55011712A JPS6038338B2 (en) 1980-02-02 1980-02-02 Method for producing granular ammonium sulfate

Publications (2)

Publication Number Publication Date
JPS56109816A JPS56109816A (en) 1981-08-31
JPS6038338B2 true JPS6038338B2 (en) 1985-08-31

Family

ID=11785647

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55011712A Expired JPS6038338B2 (en) 1980-02-02 1980-02-02 Method for producing granular ammonium sulfate

Country Status (1)

Country Link
JP (1) JPS6038338B2 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6038338A (en) * 1983-07-12 1985-02-27 チバ―ガイギ アクチエンゲゼルシヤフト Manufacture of benzanthrone

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6038338A (en) * 1983-07-12 1985-02-27 チバ―ガイギ アクチエンゲゼルシヤフト Manufacture of benzanthrone

Also Published As

Publication number Publication date
JPS56109816A (en) 1981-08-31

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