JPS5935874B2 - Method for producing slow-release granular fertilizer - Google Patents
Method for producing slow-release granular fertilizerInfo
- Publication number
- JPS5935874B2 JPS5935874B2 JP51072728A JP7272876A JPS5935874B2 JP S5935874 B2 JPS5935874 B2 JP S5935874B2 JP 51072728 A JP51072728 A JP 51072728A JP 7272876 A JP7272876 A JP 7272876A JP S5935874 B2 JPS5935874 B2 JP S5935874B2
- Authority
- JP
- Japan
- Prior art keywords
- magnesium
- fertilizer
- product
- ammonium
- coating
- 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
- 239000003337 fertilizer Substances 0.000 title claims description 28
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 22
- 238000000576 coating method Methods 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 14
- 239000008187 granular material Substances 0.000 claims description 14
- 239000002002 slurry Substances 0.000 claims description 13
- 229910021529 ammonia Inorganic materials 0.000 claims description 10
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 claims description 10
- 239000004137 magnesium phosphate Substances 0.000 claims description 10
- 229960002261 magnesium phosphate Drugs 0.000 claims description 10
- 229910000157 magnesium phosphate Inorganic materials 0.000 claims description 10
- 235000010994 magnesium phosphates Nutrition 0.000 claims description 10
- MXZRMHIULZDAKC-UHFFFAOYSA-L ammonium magnesium phosphate Chemical compound [NH4+].[Mg+2].[O-]P([O-])([O-])=O MXZRMHIULZDAKC-UHFFFAOYSA-L 0.000 claims description 7
- 229910052567 struvite Inorganic materials 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 238000004176 ammonification Methods 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 30
- 238000000034 method Methods 0.000 description 17
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 12
- 239000000347 magnesium hydroxide Substances 0.000 description 12
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 12
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 10
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 10
- 238000010828 elution Methods 0.000 description 9
- 235000013339 cereals Nutrition 0.000 description 8
- 239000000395 magnesium oxide Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 7
- 229910052749 magnesium Inorganic materials 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 238000000354 decomposition reaction Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 235000019270 ammonium chloride Nutrition 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 4
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 3
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 3
- 235000011130 ammonium sulphate Nutrition 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 238000005469 granulation Methods 0.000 description 3
- 230000003179 granulation Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Natural products C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 150000002681 magnesium compounds Chemical class 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- LQXZLHKVIRVBTC-UHFFFAOYSA-O [N+](=O)([O-])[O-].[NH4+].[P] Chemical compound [N+](=O)([O-])[O-].[NH4+].[P] LQXZLHKVIRVBTC-UHFFFAOYSA-O 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- ZNEDPPLXCAFZOU-UHFFFAOYSA-N azane phosphane urea Chemical compound NC(N)=O.N.P ZNEDPPLXCAFZOU-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 239000006012 monoammonium phosphate Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000000618 nitrogen fertilizer Substances 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
Landscapes
- Glanulating (AREA)
- Fertilizers (AREA)
Description
【発明の詳細な説明】
本発明は粒状化成肥料の被覆方法に関し、さらに詳しく
は粒状肥料表面にリン酸マグネシウムアンモニウム(M
gNH4PO4・H2O)を主成分とした被膜をアンモ
ニアガス雰囲気中で形成させ肥料の緩効化を図ることに
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for coating granular chemical fertilizers, and more specifically, the present invention relates to a method for coating granular chemical fertilizers, and more specifically, coating magnesium ammonium phosphate (M
The purpose of this method is to form a film containing gNH4PO4.H2O as the main component in an ammonia gas atmosphere to slow the release of fertilizer.
近時省力農業の一環として緩効性窒素肥料が注目され該
肥料に関する研究も数多(報告されている。Slow-release nitrogen fertilizers have recently attracted attention as part of labor-saving agriculture, and many studies have been reported regarding these fertilizers.
従来、硫安、尿素、塩安、硝安などの代表的窒素肥料の
すべては水によ(溶けるため土壌中で植物に吸収される
まえに流出する場合が多く、とくに温暖な気候、起伏の
多い耗地、降雨量の多い条件下では硝化後雨水により流
出する窒素肥料の損失は著しく長期間の肥効を持続させ
ることができず、そのため追肥量および回数を一層多く
する必要が生じる。Traditionally, typical nitrogen fertilizers such as ammonium sulfate, urea, ammonium chloride, and ammonium nitrate are all soluble in water, so they often run off before they can be absorbed by plants in the soil, especially in warm climates and areas with high undulations. Under conditions of high soil and rainfall, the loss of nitrogen fertilizer due to rainwater runoff after nitrification is significant, making it impossible to maintain the fertilizer's effectiveness over a long period of time, and therefore it becomes necessary to increase the amount and frequency of topdressing.
したがってこのような水溶性肥料の欠点を除きかつ作物
の生育に合せて肥効酸物を供給する目的で粒状化を始め
被覆法、硝化抑制剤添加法、など各種方法が提案され、
特に肥効成分をも加味した苦土成分の併用による方法が
提案されている。Therefore, various methods such as granulation, coating methods, and adding nitrification inhibitors have been proposed in order to eliminate these drawbacks of water-soluble fertilizers and supply fertilizing acids in accordance with the growth of crops.
In particular, a method has been proposed that uses a combination of magnesia ingredients that also include fertilizing ingredients.
例えばNPK肥効成分と共に造粒機内にリン酸アンモニ
ウム系スラリーと水酸化マグネシウム粉末を添加造粒す
る方法、あるいは造粒肥料表面にリン酸と水酸化マグネ
シウム粉末を交互に反覆添加したのち未反応の水酸化マ
グネシウムのアルカリ性成分を粒子表面に残すため水を
噴霧する方法(特公昭49−17826号公報)、ある
いはジシアンジアミドの如き硝酸化成抑制剤を含有する
粒状肥料に酸化マグネシウム又は水酸化マグネシウムを
含むリン酸マグネシウム系難溶性塩類で表面を被覆する
方法(特開昭48−90850号公報)等がある。For example, ammonium phosphate slurry and magnesium hydroxide powder are added to the granulator together with NPK fertilizer ingredients for granulation, or phosphoric acid and magnesium hydroxide powder are alternately added to the surface of the granulated fertilizer and then the unreacted A method of spraying water to leave the alkaline component of magnesium hydroxide on the particle surface (Japanese Patent Publication No. 17826/1982), or a method of spraying water to leave the alkaline component of magnesium hydroxide on the particle surface, or a method of spraying water containing magnesium oxide or magnesium hydroxide to a granular fertilizer containing a nitrification inhibitor such as dicyandiamide. There is a method of coating the surface with a poorly soluble magnesium acid salt (Japanese Unexamined Patent Publication No. 48-90850).
しかしながら前者はリン酸マグネシウムの被膜形成を数
回の反覆添加により行うものであるため処理能力に問題
があり、また後者は溶出するアンモニウム塩、リン酸塩
が拡散により被覆表面に流出せんとするとき、表面のリ
ン酸マグネシウムと反応し難溶性のリン酸マグネシウム
アンモニウムを生成させるため土壌中におけるこれら反
応速度が問題である。However, the former method has a problem with processing capacity because it forms a coating of magnesium phosphate by repeating the addition several times, and the latter method has problems in processing capacity because the eluted ammonium salts and phosphates do not flow out onto the coated surface due to diffusion. , reacts with magnesium phosphate on the surface to produce sparingly soluble magnesium ammonium phosphate, so the rate of these reactions in soil is a problem.
本発明者らはこれら従来法の種々の問題点を解決するた
め研究した結果、化成肥料造粒物の表面に直接リン酸マ
グネシウムアンモニウムを生成させながら被覆する方法
が極めて優れた効果をもたらす事実を発見し本発明に到
達した。As a result of research to solve various problems of these conventional methods, the present inventors found that a method of coating the surface of chemical fertilizer granules while directly producing magnesium ammonium phosphate has an extremely excellent effect. This discovery led to the present invention.
すなわち、本発明は化成肥料造粒物の表面をリン酸マグ
ネシウムスラリーで被覆しながらアンモニア化造粒機内
でアンモニアと反応させて該表面にリン酸マグネシウム
アンモニウムの被覆を形成することを特徴とする緩効性
粒状肥料の製造方法に関する。That is, the present invention is a slow-removal method characterized in that the surface of a chemical fertilizer granule is coated with a magnesium phosphate slurry and reacted with ammonia in an ammonification granulator to form a coating of magnesium ammonium phosphate on the surface. This invention relates to a method for producing effective granular fertilizer.
こ又において用いられるリン酸マグネシウムスラリーは
通常P20.として20〜45%のリン酸と水酸化マグ
ネシウム、酸化マグネシウム、蛇紋岩、カンラン岩等の
適宜のマグネシウム化合物もしくは苦土含有鉱物との反
応により生成される。The magnesium phosphate slurry used in Komata is usually P20. It is produced by the reaction of 20 to 45% phosphoric acid with a suitable magnesium compound or magnesium-containing mineral such as magnesium hydroxide, magnesium oxide, serpentine, and peridotite.
使用されるリン酸の濃度は、原料によっても相違するが
、あまり低いと分解に時間を要し高いと膠化し分解が困
難となる。The concentration of phosphoric acid used varies depending on the raw material, but if it is too low, it will take time to decompose, and if it is too high, it will become agglomerated and difficult to decompose.
そこで適正な分解と被覆に適当な流動性を有するスラリ
ーを得るためには20〜45%の濃度が好ましい。Therefore, a concentration of 20 to 45% is preferred in order to obtain a slurry with adequate fluidity for proper decomposition and coating.
分解温度は60〜100°Cとし、スラリー濃度は30
〜60%(固形分)に調整するのが好ましい。The decomposition temperature is 60-100°C, and the slurry concentration is 30°C.
It is preferable to adjust the solid content to ~60% (solid content).
なおリン酸マグネシウムスラリーによる被覆は、別工程
で調製したリン酸マグネシウムスラリーを用いて行なっ
てもよいが、肥料造粒物の存在下にこのスラリーの生成
反応を行ない被覆を同時に行なうこともできる。Note that the coating with the magnesium phosphate slurry may be performed using a magnesium phosphate slurry prepared in a separate step, but it is also possible to carry out the formation reaction of this slurry in the presence of the fertilizer granules and perform the coating at the same time.
本発明において使用される肥料造粒物は、特にその成分
は限定される必要はな(、水溶性の肥効成分を含む任意
の化成肥料に適用して優れた緩効性を賦与することがで
きる。The fertilizer granules used in the present invention do not need to be particularly limited in their ingredients (they can be applied to any chemical fertilizer containing water-soluble fertilizer ingredients to impart excellent slow-release properties). can.
このような化成肥料としては、例えば硫すン安、尿素リ
ン安、塩加すン安、リン硝安系複合肥料が挙げられる。Examples of such chemical fertilizers include ammonium sulfate, ammonium urea phosphorus, ammonium chloride, and ammonium phosphorus nitrate complex fertilizers.
以下本発明な塩加燐安系肥料について添付の図面に沿っ
て具体的に説明する。The ammonium chloride fertilizer of the present invention will be specifically described below with reference to the accompanying drawings.
P2O520〜45%のリン酸2およびマグネシウム源
3は分解反応槽5において分解反応を行なう。Phosphoric acid 2 and magnesium source 3 containing 20-45% P2O undergo a decomposition reaction in a decomposition reaction tank 5.
この分解反応において蛇紋岩のような苦土含有鉱物を使
用する場合は60メツシユ以下に粉砕し約60〜100
℃で分解を行なうのが好ましい。When using magnesium-containing minerals such as serpentine in this decomposition reaction, they must be crushed to 60 mesh or less.
Preferably, the decomposition is carried out at °C.
このようにして得られたリン酸マグネシウムスラリーは
その濃度30〜60%で、予め別工程で公知の方法で製
造された塩加燐安乾燥造粒物1に対し、1:0.05〜
0.5(重量)の範囲内でアンモニア化造粒機6におい
て造粒物表面に被覆する。The magnesium phosphate slurry thus obtained has a concentration of 30 to 60%, and is 1:0.05 to 1:0.05 to 1:1 of the salted and phosphorous ammonium dry granules prepared in advance in a separate step by a known method.
The surface of the granulated product is coated in the ammonification granulator 6 within a range of 0.5 (weight).
その間アンモニア化造粒機6にはアンモニア4が供給さ
れてアンモニア濃度5〜20%のアンモニア雰囲気が保
たれ、造粒物の表面に被覆されたリン酸マグネシウムは
アンモニア化によってリン酸マグネシウムアンモニウム
を生成する。During this time, ammonia 4 is supplied to the ammonia granulator 6 to maintain an ammonia atmosphere with an ammonia concentration of 5 to 20%, and the magnesium phosphate coated on the surface of the granules produces magnesium ammonium phosphate by ammonification. do.
このアンモニア化はリン酸マグネシウムアンモニウムの
生成に必要な量より10〜50%過剰のアンモニアの存
在下で行なうことが好適である。This ammonification is preferably carried out in the presence of 10 to 50% excess ammonia over the amount required to produce magnesium ammonium phosphate.
得られた造粒物は、乾燥機7において温度100〜12
0℃で乾燥し製品8とする。The obtained granules are dried in the dryer 7 at a temperature of 100 to 12
Dry at 0°C to obtain product 8.
本発明の方法に使用されるマグネシウム化合物は純粋で
ある必要はなくマグネシウムの使用量は所望の被覆ある
いは銘柄によって適宜調節することができる。The magnesium compound used in the method of the present invention does not need to be pure, and the amount of magnesium used can be adjusted as appropriate depending on the desired coating or brand.
また窒素源としては塩安ど共に尿素、硫酸アンモニウム
、硝酸アンモニウム等が、カリ源としては塩化加里とと
もに硫酸カリウム、硝酸カリウム等が挙げられ、これら
の肥料成分については所望の銘柄に応じてその種類およ
び量を適宜選択することができるが、マグネシウム源と
してこれを分解するために使用したリン酸分、つまりリ
ン酸マグネシウムから介入するリン酸分はこれを減じた
量を塩加燐安乾燥物の製造時に使用するものである。In addition, nitrogen sources include urea, ammonium sulfate, ammonium nitrate, etc. as well as ammonium chloride, and potassium sources include potassium chloride, potassium sulfate, potassium nitrate, etc. The types and amounts of these fertilizer components are determined according to the desired brand. It can be selected as appropriate, but the phosphoric acid content used to decompose this as a magnesium source, that is, the phosphoric acid content that intervenes from magnesium phosphate, is used in the production of the salted and phosphorous ammonium dry product. It is something to do.
このように本発明はリン酸液を2段に分割して供給する
ので中和、混合、造粒機は縮少され従来面を被覆するた
め均一かつ緻密な被膜が得られ、硬度が高くなる等の効
果がある。In this way, the present invention divides the phosphoric acid solution into two stages and supplies it, reducing the need for neutralization, mixing, and granulation machines.As it covers conventional surfaces, a uniform and dense coating can be obtained, resulting in higher hardness. There are other effects.
以下本発明の実施例を示す。Examples of the present invention will be shown below.
実施例 l
P2O5275%リン酸液1471kg、塩化アンモニ
ウム1827kgを70℃にて30分混合溶解しアンモ
ニアガス0.111kgを吹込みながら110℃に昇温
中和する。Example 1 1471 kg of P2O5275% phosphoric acid solution and 1827 kg of ammonium chloride were mixed and dissolved at 70°C for 30 minutes, and the mixture was heated and neutralized at 110°C while blowing 0.111 kg of ammonia gas.
このスラリー液に塩化カリウム1205kgおよび戻し
粉4.0kgを添加し径80CrrL深さ20CrrL
の皿型造粒機で造粒し、この間下部よりバーナーで50
〜70°Cに加熱保温した。1205 kg of potassium chloride and 4.0 kg of reconstituted powder were added to this slurry liquid, and the diameter was 80 CrrL and the depth was 20 CrrL.
Pelletize with a dish-type granulator, and during this time, use a burner from the bottom to
It was heated and kept at ~70°C.
この造粒・乾燥物(種籾)にP2O5275%リン酸液
1.55kgと水酸化マグネシウム0.35kgを混合
し70℃で10分間反応させて生成したMgHPO,・
3H20スラリー1.90kgとアンモニア0.11k
gをドラム型造粒機(アンモニア化造粒機)に添加、噴
霧させて種粒表面に
MgNH4PO4・H2Oを被覆生成させた。This granulated and dried product (seed rice) was mixed with 1.55 kg of P2O5275% phosphoric acid solution and 0.35 kg of magnesium hydroxide, and reacted at 70°C for 10 minutes to produce MgHPO,
3H20 slurry 1.90kg and ammonia 0.11k
g was added to a drum-type granulator (ammonification granulator) and sprayed to coat the surface of the seed grains with MgNH4PO4.H2O.
しかるのちこれを110℃で2時間乾燥させ粒度4T−
8メツシユの製品3.70kgを得た。Then, this was dried at 110℃ for 2 hours to obtain a particle size of 4T-
3.70 kg of 8 mesh product was obtained.
製品粒の成分組成、硬度および該製品12.5gr
を30℃の水500m1に24時間浸漬させた後の溶出
率は下記の通りであった。Product grain composition, hardness and product 12.5gr
The elution rate after immersing the sample in 500 ml of water at 30°C for 24 hours was as follows.
A−N 、C−P2O5W−に20 C−MgO製
品粒成分組成(%) 12.42 16.85
14.45 4.63硬度(kg) 1
5.5
溶出率(NH,−N%) 4’3.5
また未被覆品の溶出率は98.5%、硬度8.0kgで
あった。A-N, C-P2O5W-20 C-MgO product grain composition (%) 12.42 16.85
14.45 4.63 Hardness (kg) 1
5.5 Elution rate (NH, -N%) 4'3.5 The elution rate of the uncoated product was 98.5% and the hardness was 8.0 kg.
実施例 2
塩尻燐安656(16−5−16)3.00kgを種粒
として実施例1と同様な方法でP2O527,5%リン
酸液1.55kgと水酸化マグネシウム0.35kgを
混合し、70℃で10分間反応させて生成したMgHP
O4・3H20スラリーとアンモニア0、101<9を
同時に添加、噴霧し、種粒表面にMgNH4PO4・H
2Oを被覆生成させた。Example 2 1.55 kg of P2O527, 5% phosphoric acid solution and 0.35 kg of magnesium hydroxide were mixed in the same manner as in Example 1 using 3.00 kg of Shiojiri Rin'an 656 (16-5-16) as seed grains, MgHP produced by reacting at 70°C for 10 minutes
O4.3H20 slurry and ammonia 0, 101<9 were added and sprayed at the same time, and MgNH4PO4.H was added to the surface of the seed grains.
A coating of 2O was produced.
しかるのちこれを110℃で2時間乾燥させ粒度4〜8
メツシユの製品1.62kgを得た。Then, this was dried at 110℃ for 2 hours to obtain a particle size of 4 to 8.
1.62 kg of mesh product was obtained.
この製品につき実施例1と同様の解析をした値を下記に
示す。The values obtained by analyzing this product in the same manner as in Example 1 are shown below.
A−N C−P2O,、W−に20 C−MgO
製品粒成分組成(%) 12.90 13.80
11.6’0 5.30硬度(Kg)
140
溶出率(NH4−N%)36.3
また未被覆品の溶出率は97.8%、硬度6.8kgで
あった。A-N C-P2O,, W- to 20 C-MgO
Product grain composition (%) 12.90 13.80
11.6'0 5.30 Hardness (Kg)
140 Elution rate (NH4-N%) 36.3 The elution rate of the uncoated product was 97.8% and the hardness was 6.8 kg.
実施例 3
実施例2と同様な方法、同一の配合条件により、ただし
マグネシウム源を工業用酸化マグネシウム(C−Mg0
70%)O,’30kyに代え以下同様の処理をおこな
った。Example 3 A method similar to Example 2 and the same compounding conditions were used, except that the magnesium source was industrial magnesium oxide (C-Mg0
70%)O, '30ky, and the same treatment was performed below.
A−N C−P2O5W−に20 C−MgO製品粒
成分組成(%) 12.81 13.72 11
.92 5.70硬度(kg) 15・
2
溶出率(NH4−N%) 46.5
比較例 1
塩尻燐安656(16−5−16)粉砕物3.0kgに
P2O527,5%リン酸液1.55kgと水酸化マグ
ネシウム0.35kgを混合し、80〜90℃で15分
間反応させ、濃縮後粒度4〜8メツシユの製品1.62
kgを得た。A-N C-P2O5W-20 C-MgO product grain composition (%) 12.81 13.72 11
.. 92 5.70 Hardness (kg) 15・
2 Elution rate (NH4-N%) 46.5 Comparative example 1 1.55 kg of P2O527, 5% phosphoric acid solution and 0.35 kg of magnesium hydroxide were added to 3.0 kg of Shiojiri Rin'an 656 (16-5-16) pulverized material. Mix and react at 80-90°C for 15 minutes to obtain a product with a particle size of 4-8 mesh after concentration 1.62
I got kg.
この製品につき硬度および窒素の溶出速度を実施例1と
同様に測定した結果は下記の通りであった。The hardness and nitrogen dissolution rate of this product were measured in the same manner as in Example 1, and the results were as follows.
硬度(k!9) 12.2溶出率
(卆) 985
(NH4−N24時間後)
比較例 2
塩尻燐安656(16−5−16)3、Okgを種肥料
として径80(J、深さ20礪のロツシエ造粒機に入れ
、下部よりバーナーで加熱し、100℃に造粒物を加熱
した。Hardness (k!9) 12.2 Elution rate (volume) 985 (after 24 hours of NH4-N) Comparative example 2 Shiojiri Rin'an 656 (16-5-16) 3, Okg was used as a seed fertilizer and the diameter was 80 (J, depth) The granules were placed in a 20-tub Rossier granulator and heated with a burner from the bottom to 100°C.
これにP2O527,5%のリン酸液と水酸化マグネシ
ウムを交互(3回)に分別添加しくリン酸液添加合計1
.55kg、水酸化マグネシウム添加合計0.35kg
)L粒表面にMgHPO3・3H20を被覆生成させた
。To this, add P2O527.5% phosphoric acid solution and magnesium hydroxide alternately (3 times) separately, totaling 1 phosphoric acid solution addition.
.. 55kg, total addition of magnesium hydroxide 0.35kg
) The surface of the L grains was coated with MgHPO3.3H20.
ついでこの粒状物を105℃で2時間乾燥させ、粒度4
〜8メツシユの製品1..55kgを得た。The granules were then dried at 105°C for 2 hours to obtain a particle size of 4.
~8 mesh products 1. .. Obtained 55 kg.
この製品につき硬度および窒素の溶出速度を同様に測定
した結果は下記の通りであった。The hardness and nitrogen dissolution rate of this product were similarly measured and the results were as follows.
硬度(kg) 11.8溶出率(
卆) 52.0(NH,−N
24時間後)
比較例 3
塩尻燐安656(16−5−16)造粒物の表面にP2
O527,5%のリン酸液1.55kgおよび水酸化マ
グネシウム0.35kgおよびアンモニア0.1kgを
同時に噴霧し、種肥料面に
MgNH4PO4・H2Oの膜を形成させた、ついでこ
の粒状物を105℃で2時乾燥させ、粒度4〜8メツシ
ユの製品1.35kgを得た。Hardness (kg) 11.8 Elution rate (
卆) 52.0 (NH, -N
24 hours later) Comparative Example 3 P2 on the surface of Shiojiri Rin'an 656 (16-5-16) granules
1.55 kg of O527.5% phosphoric acid solution, 0.35 kg of magnesium hydroxide, and 0.1 kg of ammonia were simultaneously sprayed to form a film of MgNH4PO4.H2O on the seed fertilizer surface.Then, the granules were heated at 105°C. After drying for 2 hours, 1.35 kg of a product with a particle size of 4 to 8 mesh was obtained.
この製品につき、硬度および窒素の溶出速度を同様に測
定した結果は下記の通りであった。The hardness and nitrogen dissolution rate of this product were similarly measured and the results were as follows.
比較例 4
塩尻燐安656(16−5−16)造粒物の表面にP2
O,555%のリン酸液0.7 kgおよび酸化マグネ
シウム0.24kgおよびリン酸1アンモニウム0.6
8 kgを種肥料表面に噴霧し、MgNH4PO4・H
2Oの膜を形成させた。Comparative Example 4 P2 on the surface of Shiojiri Rin'an 656 (16-5-16) granules
O, 555% phosphoric acid solution 0.7 kg and magnesium oxide 0.24 kg and monoammonium phosphate 0.6
Spray 8 kg onto the surface of the seed fertilizer and add MgNH4PO4.H.
A film of 2O was formed.
ついでこの粒状物を105°Cで2時間乾燥させ、粒度
4〜8メツシユの製品14.2kgを得た。The granules were then dried at 105°C for 2 hours to obtain 14.2 kg of a product with a particle size of 4 to 8 mesh.
この製品につき硬度および窒素の溶出速度を測定した結
果は下記の通りであった。The hardness and nitrogen elution rate of this product were measured and the results were as follows.
添付の図面は本発明方法を実施する工程の一例を示した
フローシートである。The accompanying drawing is a flow sheet showing an example of steps for carrying out the method of the present invention.
Claims (1)
ーで被覆しながらアンモニア化造粒機内でアンモニアと
反応させて該表面にリン酸マグネシウムアンモニウムの
被覆を形成することを特徴とする緩効性粒状肥料の製造
方法。1. A slow-release granular fertilizer characterized in that the surface of a chemical fertilizer granule is coated with a magnesium phosphate slurry and reacted with ammonia in an ammonification granulator to form a coating of magnesium ammonium phosphate on the surface. manufacturing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51072728A JPS5935874B2 (en) | 1976-06-22 | 1976-06-22 | Method for producing slow-release granular fertilizer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51072728A JPS5935874B2 (en) | 1976-06-22 | 1976-06-22 | Method for producing slow-release granular fertilizer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS532271A JPS532271A (en) | 1978-01-11 |
| JPS5935874B2 true JPS5935874B2 (en) | 1984-08-31 |
Family
ID=13497695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP51072728A Expired JPS5935874B2 (en) | 1976-06-22 | 1976-06-22 | Method for producing slow-release granular fertilizer |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5935874B2 (en) |
-
1976
- 1976-06-22 JP JP51072728A patent/JPS5935874B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS532271A (en) | 1978-01-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2091891B1 (en) | Production of npk or np material containing polyphosphates | |
| JP2002539067A (en) | Method for formulating the components of a granular composite fertilizer and the product produced by the method | |
| AU2019397602B2 (en) | Acidified NP, PK, NPK fertilizer granules for fertigation | |
| JPH0254315B2 (en) | ||
| US3423199A (en) | Fertilizers containing microand macronutrients | |
| US3425819A (en) | Method of preparing a complex fertilizer comprising urea coated with ammonium phosphate | |
| US3617239A (en) | Method for producing micronutrient coated urea prills and products | |
| WO2024003865A1 (en) | Production of nitrogen, potassium, sulfur nutrient through de-carbonization and utilization of calcium sulfate | |
| US3520651A (en) | Fertilizers containing microand macronutrients | |
| WO2001042172A1 (en) | Process for the preparation of urea superphosphate fertilizers | |
| JP2005272218A (en) | Method for producing granular composite fertilizer | |
| CN85101008B (en) | Coated fertilizer and its production method | |
| US20260035313A1 (en) | Complex fertilizer comprising nitrogen, phosphorous, and sulfur encapsulated within secondary calcium and magnesium nutrients | |
| JPS5935874B2 (en) | Method for producing slow-release granular fertilizer | |
| CN1062846C (en) | Technology for production of modified calcium superphosphate compounded fertilizer | |
| JP4337534B2 (en) | Granular composite fertilizer composition and method for producing the same | |
| JPH0243708B2 (en) | ||
| EP4317118A1 (en) | Fertilizer comprising immediate- and slow-release agents in soil complex nutrients | |
| EP4613726A1 (en) | Production of nitrogen, potassium, sulfur nutrient through de-carbonization and utilization of calcium sulfate | |
| WO2025243232A1 (en) | A method for the production of a fertilizer granule | |
| EP4619361A1 (en) | Method for multi-phase preparation of complex mineral fertilizer from phosphate rock and nitric acid | |
| EP4619363A1 (en) | Fertiliser composition from nitric acid metal slag | |
| EP4416120A1 (en) | Method for producing a potassium-containing fertilizer with a low content of water-insoluble material | |
| WO2025141411A1 (en) | Sustainable slow-release complex calcium, nitrogen, potassium, and sulfur fertilizer | |
| JPH0132199B2 (en) |