JPS6323159B2 - - Google Patents
Info
- Publication number
- JPS6323159B2 JPS6323159B2 JP54161939A JP16193979A JPS6323159B2 JP S6323159 B2 JPS6323159 B2 JP S6323159B2 JP 54161939 A JP54161939 A JP 54161939A JP 16193979 A JP16193979 A JP 16193979A JP S6323159 B2 JPS6323159 B2 JP S6323159B2
- Authority
- JP
- Japan
- Prior art keywords
- urea
- dicyandiamide
- nitrogen
- fertilizer
- coated
- 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
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 60
- 239000004202 carbamide Substances 0.000 claims description 60
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 49
- 239000003337 fertilizer Substances 0.000 claims description 30
- 239000008187 granular material Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 235000013877 carbamide Nutrition 0.000 description 59
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 57
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 38
- 239000002689 soil Substances 0.000 description 30
- 229910052757 nitrogen Inorganic materials 0.000 description 28
- 229910021529 ammonia Inorganic materials 0.000 description 19
- 239000000843 powder Substances 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 12
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 12
- 229910017604 nitric acid Inorganic materials 0.000 description 12
- 238000004090 dissolution Methods 0.000 description 11
- 238000005469 granulation Methods 0.000 description 11
- 230000003179 granulation Effects 0.000 description 11
- 238000010828 elution Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000000155 melt Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000618 nitrogen fertilizer Substances 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 230000004720 fertilization Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- -1 melt Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 238000007909 melt granulation Methods 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 239000012768 molten material Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 239000005033 polyvinylidene chloride Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 208000035240 Disease Resistance Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 240000004296 Lolium perenne Species 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 108010046334 Urease Proteins 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000004660 morphological change Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 230000037039 plant physiology Effects 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 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
- 238000002360 preparation method Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- ZJHHPAUQMCHPRB-UHFFFAOYSA-N urea urea Chemical compound NC(N)=O.NC(N)=O ZJHHPAUQMCHPRB-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Landscapes
- Fertilizers (AREA)
Description
【発明の詳細な説明】
本発明は被覆尿素肥料に関するもので、さらに
詳しくはジシアンジアミドを混合する尿素の粒状
物を被覆し肥料成分等の溶解速度を調節した肥料
に係わるものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coated urea fertilizer, and more particularly to a fertilizer coated with urea particles mixed with dicyandiamide to control the dissolution rate of fertilizer components.
農園芸において作物の生育に用いられる肥料の
主たる成分は窒素、リン酸、カリウムであり、窒
素成分に関しては植物が根から吸収する場合に通
常アンモニアおよび硝酸の形態で利用される。土
壌中の窒素成分は化学的に種々の形態の変化を受
けやすくまたリン酸やカリウム等の他の成分より
も土壌に保持され難い。例えば窒素成分をアンモ
ニア、アンモニウム塩、尿素の形態で施肥しても
その大部分が数週間で硝酸態に変つて溶脱等によ
り消失したりまたは還元されて窒素ガスになつて
空気中に揮散する割合が大きい。さらにまた窒素
成分をアンモニア、アンモニウム塩、尿素の形態
で一度に多量を施肥する場合には他の肥料成分よ
り濃度障害を与え易いので窒素肥料の施肥管理は
施肥回数、施肥量等の面で手間を必要とする。 The main components of fertilizers used for growing crops in agriculture and horticulture are nitrogen, phosphoric acid, and potassium, and nitrogen components are usually utilized in the form of ammonia and nitric acid when plants absorb them through their roots. Nitrogen components in soil are chemically susceptible to various changes in form and are more difficult to retain in soil than other components such as phosphoric acid and potassium. For example, even if nitrogen components are fertilized in the form of ammonia, ammonium salts, or urea, the majority of them will change to nitrate within a few weeks and disappear through leaching, or will be reduced and become nitrogen gas and volatilize into the air. is large. Furthermore, when large amounts of nitrogen components are applied at once in the form of ammonia, ammonium salts, or urea, they tend to cause concentration problems more easily than other fertilizer components, so managing the application of nitrogen fertilizers is time-consuming in terms of the number of times of application, the amount of fertilizer applied, etc. Requires.
窒素肥料単肥として多量に用いられている尿素
について濃度障害の発生を防ぎ施肥を簡易に行な
うため、尿素を鉱油、ワツクス、イオウ、合成樹
脂、鉱物性粉末等で被覆する技術が開発されてい
る。これらの被覆された尿素を作物が吸収利用す
る過程では水が被覆皮膜を通り水が内部の尿素
を溶解し尿素が被覆皮膜の外に溶出し、土壌中
のウレアーゼ等が尿素を分解してアンモニアと
し、土壌中の微生物がアンモニアを亜硝酸を経
て硝酸に変える過程がある。これらの過程のうち
およびは土壌中の微生物の作用が関与するた
め土壌の条件によつて形態変化の速度が異なり、
畑の状態にあつては作物の生育に好ましい環境で
は被覆された尿素から溶出した尿素は速やかに硝
酸に変化しアンモニアは殆んど存在しない。従つ
て尿素の形態の変化を考えると多くの圃場におい
ては被覆された尿素を施肥することは硝酸を除々
に供給していることと同様の効果を植物に与えて
いることになる。 Urea, which is used in large quantities as a simple nitrogen fertilizer, has been developed to coat urea with mineral oil, wax, sulfur, synthetic resin, mineral powder, etc. in order to prevent concentration disturbances and make fertilization easier. . In the process of absorption and utilization of these coated ureas by crops, water passes through the coating film and dissolves the urea inside, urea is eluted out of the coating film, and urease, etc. in the soil decomposes the urea and turns it into ammonia. There is a process in which microorganisms in the soil convert ammonia to nitrite and then to nitric acid. Among these processes, the rate of morphological change differs depending on soil conditions because the action of microorganisms in the soil is involved.
When the field conditions are favorable for crop growth, the urea eluted from the coated urea quickly changes to nitric acid and almost no ammonia is present. Therefore, considering the changes in the form of urea, in many fields, applying coated urea as fertilizer has the same effect on plants as gradually supplying nitric acid.
窒素肥料源としてアンモニアと硝酸とではどち
らが植物にとつて好ましいかという問題は農業技
術者や農業に直接関与している者にとつて重大な
関心事であり、種々の観点、例えば作物の収量、
品質、耐病害性、栽培環境、肥料利用率等との観
点より土壌肥料学的、作物栽培学的、植物生理学
的、作物病理学的な研究ならびに試験が行なわれ
てきた。これらの研究結果から判断するとアンモ
ニアと硝酸との優劣の評価は前提条件によつて変
わるが、肥料としての汎用性を考えると土壌中に
アンモニアと硝酸の両者の共存することが望まし
い。 The question of whether ammonia or nitric acid is preferable for plants as a nitrogen fertilizer source is of great concern to agricultural engineers and those directly involved in agriculture, and it is a matter of great concern to agricultural engineers and those directly involved in agriculture, and it is important to consider the question of whether ammonia or nitric acid is better for plants as a source of nitrogen fertilizer.
From the viewpoints of quality, disease resistance, cultivation environment, fertilizer utilization rate, etc., research and tests have been conducted on soil fertilization, crop cultivation, plant physiology, and crop pathology. Judging from the results of these studies, the evaluation of the superiority of ammonia and nitric acid varies depending on the preconditions, but considering its versatility as a fertilizer, it is desirable for both ammonia and nitric acid to coexist in the soil.
窒素肥料の使用時に窒素肥料と共にジシアンジ
アミド等の硝酸化成抑制剤を使用すると土壌中の
アンモニアの硝酸化を制御できることが知られて
いる。ここで長期間にわたつて土壌中のアンモニ
アと硝酸の存在量を保つように制御しようとすれ
ば適当量のアンモニアおよび/またはアンモニア
源と硝酸化成抑制剤が土壌中に存在していること
が要望され、さらにまた肥料からのアンモニアお
よび/またはアンモニア源と硝酸化成抑制剤との
水への溶解速度(溶出率)の相違を補償できるこ
とが望まれる。本発明は以上のような問題を解決
することを目的としてなされたものである。 It is known that nitrification of ammonia in soil can be controlled by using a nitrification inhibitor such as dicyandiamide together with nitrogen fertilizer. In order to control the amount of ammonia and nitric acid present in the soil over a long period of time, it is necessary that an appropriate amount of ammonia and/or an ammonia source and a nitrate formation inhibitor be present in the soil. Furthermore, it is desired to be able to compensate for the difference in dissolution rate (elution rate) in water between ammonia from fertilizer and/or the ammonia source and the nitrification inhibitor. The present invention has been made to solve the above problems.
本発明の主たる目的は作物に長期間にわたつて
窒素肥料成分としてアンモニアと硝酸の両者に制
御された量と割合で供給できる肥料を供給するこ
とである。本発明の他の目的は降雨等によつても
成分が流亡し難い尿素系肥料を提供することであ
る。本発明のさらに別な目的は濃度障害を作物に
与えない尿素系肥料を提供することである。本発
明のその他の目的は以下の説明により明らかにな
る。 The primary objective of the present invention is to provide a fertilizer that can supply both ammonia and nitric acid as nitrogen fertilizer components in controlled amounts and proportions to crops over an extended period of time. Another object of the present invention is to provide a urea-based fertilizer whose components are unlikely to be washed away even by rain or the like. Still another object of the present invention is to provide a urea-based fertilizer that does not cause concentration problems to crops. Other objects of the invention will become apparent from the following description.
本発明による肥料はジシアンジアミドを混合し
た尿素による粒状物の表面を水で崩壌し難い被膜
で覆い肥料成分等の溶解速度を調節してアンモニ
アと硝酸をバランスよく植物体に供給できるよう
にした肥料である。 The fertilizer according to the present invention is a fertilizer in which the surface of granules made of urea mixed with dicyandiamide is coated with a film that is difficult to disintegrate with water, and the dissolution rate of fertilizer components is adjusted so that ammonia and nitric acid can be supplied to plants in a well-balanced manner. It is.
本発明における該尿素粒状物は次のようにして
作ることができる。ジシアンジアミドを含有ない
し包蔵する溶融物を冷却しながらまたは濃厚溶液
ないしスラリー、バインダーを使用した粉末を溶
剤を蒸発させながら粒状化を行なうことができ
る。溶融物を冷却しながら粒状化する方法は使用
熱量の点で有利である。該溶融物を作る方法とし
ては例えば尿素の粉末(化されたもの)および
ジシアンジアミドの粉末を混合し加熱溶融する方
法(混合装置としては例えば混合槽、回転ドラム
型混合機、リボンブレンダー、V型ブレンダー等
を用いることができる。加熱溶融には例えば撹拌
羽根および加圧蒸気等の熱媒によるジヤケツトま
たはコイル等を有する槽を用いることができ
る。)、粉末の尿素を溶融し次いでジシアンジア
ミドを添加する方法(尿素の融点は132℃で加熱
溶融に用いた水蒸気は140〜150℃であり融点が
207〜209℃のジシアンジアミドは溶融尿素に溶解
し、50分程度溶融状態にあつたものを分析したと
ころ尿素およびジシアンジアミドの分解はわずか
しか生じなかつた。)、ジシアンジアミドの粉末
を溶融し、次いで尿素の粉末を加え溶融する方
法、ジシアンジアミドの粉末と尿素の粉末を
別々に溶融し、次いで両者を混合する方法等を採
用でき、使用する装置および工程が複雑化しない
点でおよびの方法を用いるのが有利である。
またジシアンジアミドを含有ないし包蔵する濃度
溶液ないしスラリーの溶剤として水、低級アルコ
ール等を用いることができる。 The urea granules in the present invention can be produced as follows. Granulation can be carried out while cooling a melt containing or encapsulating dicyandiamide, or by evaporating the solvent from a concentrated solution or slurry or powder using a binder. The method of granulating the melt while cooling it is advantageous in terms of the amount of heat used. The method for producing the melt is, for example, a method of mixing urea powder (formed) and dicyandiamide powder and heating and melting the mixture (mixing equipment includes, for example, a mixing tank, a rotating drum type mixer, a ribbon blender, a V-type blender). For heating and melting, for example, a tank having a jacket or coil using a stirring blade and a heat medium such as pressurized steam can be used.) A method of melting powdered urea and then adding dicyandiamide. (The melting point of urea is 132℃, and the steam used for heating and melting is 140-150℃, so the melting point is 132℃.
Dicyandiamide at 207-209°C was dissolved in molten urea, and analysis of the solution after it remained in the molten state for about 50 minutes revealed that only slight decomposition of urea and dicyandiamide occurred. ), a method in which dicyandiamide powder is melted and then urea powder is added and melted, a method in which dicyandiamide powder and urea powder are melted separately and then the two are mixed, etc., which requires complicated equipment and processes. It is advantageous to use the method of and in that it does not cause
Further, water, lower alcohol, etc. can be used as a solvent for a concentrated solution or slurry containing or encapsulating dicyandiamide.
ジシアンジアミドを含有ないし包蔵する溶融物
または濃度溶液ないしスラリー、バインダーを併
用する粉末を粒状化するには次のような方法を用
いることができる。溶融物の粒状化にあたつては
例えば縦型塔の上部から回転円盤、加圧ノズル等
を用いて溶融物を噴射し下方から冷風を送り塔内
で固化させる方法、回転パンや回転ドラム内で粒
状化する方法、流動層で粒状化する方法、噴流層
で粒状化する方法等を挙げることができ、就中得
られる粒状品の形状、大きさの分布の揃つている
こと等の点で噴流層を用いることが好ましい。濃
厚溶液ないしスラリーの粒状化にあたつても溶融
物の粒状化における場合と同様に噴流層で粒状化
すると良好な結果が得られる。粉末を粒状化する
場合は回転パン等を用いることができる。迅速に
粒状化が行なわれること、粒状化装置における熱
移動量の少ないこと、溶媒の処理が不要であるこ
と等の点で溶融物を粒状化することが工業的に有
利である。 The following method can be used to granulate a melt containing or encapsulating dicyandiamide, a concentrated solution or slurry, and a powder used in combination with a binder. For granulating the molten material, for example, the molten material can be injected from the top of a vertical tower using a rotating disk, pressurized nozzle, etc., and cooled air can be sent from below to solidify it within the tower. Examples include granulation methods such as granulation in a fluidized bed, granulation in a fluidized bed, and granulation in a spouted bed. Preferably, a spouted bed is used. Good results can be obtained when granulating concentrated solutions or slurries using a spouted bed, as in the case of granulating melts. When granulating the powder, a rotary pan or the like can be used. It is industrially advantageous to granulate a melt because granulation can be carried out quickly, the amount of heat transferred in a granulation device is small, and no treatment of a solvent is required.
肥料粒状物を被覆する材料としては合成樹脂系
のもの、イオウ−ワツクス、アスフアルト等があ
り、例えばポリオレフイン樹脂を主成分とする
被覆組成物(例えば特公昭54−3104)、ポリ塩
化ビニリデンまたはエチレン共重合体を含む被覆
組成物(例えば特開昭51−75674)、ポリオレフ
イン樹脂、エチレン−酢酸ビニル共重合体樹脂ま
たはポリ塩化ビニリデン樹脂を含む樹脂組成物に
タルクおよびイオウを均一に分散してなる組成
物、アルキツド樹脂を含む組成物(例えば特公
昭49−46748)、例えば分子量10000以下のポリ
アルキレンとパラフインろうを含む組成物(例え
ば特公昭45−922)、例えば酢酸ビニル樹脂ラテ
ツクスのような乳化重合体を含む組成物(例えば
特公昭37−15832)、イオウで第1層を被覆しそ
の上の第2層にワツクス状物質を被覆したもの
(例えば米国特許3295950)等を挙げることができ
る。被覆を施す方法は被覆用材料を溶液、溶融
体、乳化状物等の液状流動物や粉体となして流動
層、噴流層、回転パン、回転ドラム等で転動、吹
き付け等の方法により粒状体と接触、付着させて
必要に応じて加熱、冷却、溶媒除去等を施し被覆
を行なう。肥料成分の溶解速度の調節が容易であ
る点で前記の、、で示された被覆材料を使
用することが望ましい。 Materials for coating fertilizer granules include synthetic resins, sulfur wax, asphalt, etc. For example, coating compositions containing polyolefin resin as a main component (for example, Japanese Patent Publication No. 3104/1983), polyvinylidene chloride, or ethylene copolymer. A composition obtained by uniformly dispersing talc and sulfur in a coating composition containing a polymer (for example, JP-A-51-75674), a resin composition containing a polyolefin resin, an ethylene-vinyl acetate copolymer resin, or a polyvinylidene chloride resin. Compositions containing alkyd resins (for example, Japanese Patent Publication No. 49-46748), compositions containing polyalkylene with a molecular weight of 10,000 or less and paraffin wax (for example, Japanese Patent Publication No. 45-922), emulsified polymers such as vinyl acetate resin latex, etc. Examples include compositions containing coalescence (for example, Japanese Patent Publication No. 37-15832), and compositions in which a first layer is coated with sulfur and a second layer thereon is coated with a wax-like substance (for example, U.S. Pat. No. 3,295,950). The coating is applied by turning the coating material into a liquid fluid such as a solution, melt, emulsion, or powder, and rolling it in a fluidized bed, spouted bed, rotating pan, rotating drum, etc., or spraying it into particles. The material is brought into contact with and adhered to the body, and then heated, cooled, and solvent removed as necessary to form a coating. It is desirable to use the coating material shown in (2) above because it is easy to control the dissolution rate of fertilizer components.
本発明で得られるジシアンジアミドと共に造粒
された尿素を被覆した肥料の特徴は、該肥料が土
壌中で水に溶解し肥効を呈する際に、ジシアンジ
アミドの水に対する溶解速度が上昇して尿素に近
い割合の溶出率を示すことである。従つて尿素が
硝酸化することを長期間にわたり有効に抑制する
ことができる。これらの効果はジシアンジアミド
を混合した溶融尿素またはジシアンジアミドを混
合した尿素の濃厚溶液ないしスラリーから作られ
た粒状物のいずれにも観察される。被覆皮膜の中
にあるジシアンジアミドは降雨によつて容易に流
失せずまた土壌中で短期間に分解せず硝酸化成抑
制効果を保持する。 The characteristic of the fertilizer coated with urea granulated together with dicyandiamide obtained in the present invention is that when the fertilizer dissolves in water in soil and exhibits a fertilizing effect, the dissolution rate of dicyandiamide in water increases and becomes similar to that of urea. It is to show the percentage dissolution rate. Therefore, nitrification of urea can be effectively suppressed for a long period of time. These effects are observed in either granules made from molten urea mixed with dicyandiamide or concentrated solutions or slurries of urea mixed with dicyandiamide. The dicyandiamide in the coating film is not easily washed away by rain, nor does it decompose in the soil in a short period of time, maintaining its nitrification inhibiting effect.
本発明を次に例により説明する。 The invention will now be illustrated by way of example.
粒状体を作成
(1) 造粒
(A) ジシアンジアミド入粒状尿素
尿素粉末とジシアンジアミドをV型混合器
で均一に混合し、蒸気で加熱できるジヤケツ
トを有する槽で4Kg/cm2・Gの水蒸気を用い
て溶融し、噴流塔で10〜14メツシユのプリル
尿素に吹き付けて付着粒状化後、冷却し5〜
7メツシユの粒を得た。Preparation of granules (1) Granulation (A) Granular urea containing dicyandiamide Urea powder and dicyandiamide were mixed uniformly in a V-type mixer, and then heated using steam at 4 kg/cm 2 G in a tank equipped with a jacket that can be heated with steam. It is melted and sprayed onto 10 to 14 meshes of prill urea in a jet tower to adhere to it and granulate it, then cooled and
7 mesh grains were obtained.
(B) 粒状尿素
尿素粉末を前述のように溶融し粒状化した
5〜7メツシユの粒を得た。 (B) Granular Urea Urea powder was melted and granulated as described above to obtain 5 to 7 mesh granules.
(C) 粒状ジシアンジアミド
微細粉末のジシアンジアミドに0.5重量%
ポリビニルアルコール水溶液を雰霧しパン型
造粒機で造粒し乾燥して5〜7メツシユの粒
を得た。 (C) Granular dicyandiamide 0.5% by weight in finely powdered dicyandiamide
An aqueous polyvinyl alcohol solution was sprayed onto the mixture, and the mixture was granulated using a pan-type granulator and dried to obtain granules of 5 to 7 meshes.
(2) 粒状体を被覆
タルク60重量部、低密度ポリエチレン20重量
部、エチレン−酢酸ビニル共重合体20重量部、
界面活性剤(ポリオキシエチレンノニルフエニ
ルエーテル系)0.5重量部をテトラクロルエチ
レンに7重量%になるように溶解した熱溶液を
粒状体に噴流塔で吹き付けてから乾燥し5重量
%の被覆皮膜を有する粒を作つた。(2) Coating the granules: 60 parts by weight of talc, 20 parts by weight of low-density polyethylene, 20 parts by weight of ethylene-vinyl acetate copolymer,
A hot solution of 0.5 parts by weight of a surfactant (polyoxyethylene nonyl phenyl ether) dissolved in tetrachlorethylene to give a concentration of 7% by weight is sprayed onto the granules using a jet tower and then dried to form a 5% by weight coating film. We made grains with
例 1
本例の試験はジシアンジアミドと共に尿素を溶
融し被覆した肥料の溶出速度が被覆尿素の溶解速
度に近いことを示している。EXAMPLE 1 The tests in this example show that the dissolution rate of the urea coated fertilizer with dicyandiamide is close to the dissolution rate of the coated urea.
2mmパスの風乾土壌(腐植質火山灰・沖積土壌
による耕土・静岡県富士市五味島)による乾土
500gに前述した方法で得た試料を全窒素で200mg
相当量加え、水を最大容水量(85g水/100g乾
土)の60%加え容器の上縁をポリエチレンフイル
ムで覆い25℃の恒温室に静置した。所定の期間の
経過後に試料を全て回収し粉砕して被覆皮膜の殻
の内部に残存する成分を分析し溶出率を算出し
た。試験は全て3反復制とした。結果を第1図A
およびBに示す。 Dry soil with 2mm pass air-dried soil (cultivated soil with humic volcanic ash and alluvial soil, Gomi Island, Fuji City, Shizuoka Prefecture)
Add 200 mg of total nitrogen to 500 g of the sample obtained by the method described above.
A considerable amount of water was added, 60% of the maximum water capacity (85g water/100g dry soil) was added, and the upper edge of the container was covered with polyethylene film and left in a thermostatic chamber at 25°C. After a predetermined period had elapsed, all the samples were collected and crushed, and the components remaining inside the shell of the coating film were analyzed to calculate the elution rate. All tests were conducted in triplicate. The results are shown in Figure 1A.
and shown in B.
第1図−Aはジシアンジアミド態の窒素が全窒
素の7重量%になるように尿素と共に溶融し粒状
化後に被覆を施したものの溶出率を示し、は尿
素の溶出率はジシアンジアミドの溶出率を示
す。第1図Bにおいては尿素単独の溶融粒状化
後に被覆を施したものの尿素の溶出率はジシア
ンジアミド単独の粒状化物に被覆を施したものの
ジシアンジアミドの溶出を示す。 Figure 1-A shows the elution rate of a product in which dicyandiamide nitrogen is melted with urea and coated after granulation so that it accounts for 7% by weight of the total nitrogen, and the elution rate of urea shows the elution rate of dicyandiamide. . In FIG. 1B, the elution rate of urea is obtained when a coating is applied after melt granulation of urea alone, and the elution rate of dicyandiamide is obtained when a coating is applied to a granulation of dicyandiamide alone.
本例の試験により第1図−Bに示されるように
被覆されたジシアンジアミド粒の溶出率(溶解速
度)は被覆された尿素粒の溶出量よりはるかに小
さいことが観察されるが、第1図−Aに示される
ようにジシアンジアミドを尿素と共に溶融粒状化
し被覆したものについてはジシアンジアミドの溶
出率は尿素の溶出率と殆んど同じになることが示
されている。これは尿素の溶出に対応して硝酸化
成抑制剤たるジシアンジアミドが土壌中に溶出し
て作用を及ぼすことを間接的に示すものである。 From the test of this example, it is observed that the dissolution rate (dissolution rate) of the coated dicyandiamide grains is much smaller than the dissolution amount of the coated urea grains, as shown in Figure 1-B. As shown in -A, it has been shown that when dicyandiamide is melted and granulated together with urea and coated, the elution rate of dicyandiamide is almost the same as the elution rate of urea. This indirectly indicates that dicyandiamide, a nitrification inhibitor, is eluted into the soil and exerts its effect in response to the leaching of urea.
例 2
本例の試験は本発明による被覆尿素肥料が長期
間にわたり土壌中でアンモニアと硝酸のバランス
のとれた存在を可能にすることを示す。Example 2 The tests in this example show that the coated urea fertilizer according to the invention allows a balanced presence of ammonia and nitric acid in the soil over a long period of time.
例1に準じた条件で肥料を土壌と混合し水を注
ぎ、所定の期間の経過後に乾燥土壌の5倍の重量
の10重量%塩化カリウム水溶液に肥料と土壌の混
合物の全量を入れ室温で30分間振盪し、次いで
過した液のアンモニア態窒素および硝酸態窒素を
分析した。結果を第2図A,BおよびCに示す。 Mix fertilizer with soil under conditions similar to Example 1, pour in water, and after a predetermined period of time, add the entire amount of the fertilizer and soil mixture to a 10% potassium chloride aqueous solution that is 5 times the weight of the dry soil and leave for 30 minutes at room temperature. The solution was shaken for a minute and then the filtrate was analyzed for ammonia nitrogen and nitrate nitrogen. The results are shown in Figures 2A, B and C.
第2図−Aはジシアンジアミド態の窒素が全窒
素の7重量%になるように尿素と共に溶融し粒状
化後に被覆を施したものを全窒素で200mg加えた
場合の結果を示し、は回収アンモニア態窒素、
は回収硝酸態窒素である。 Figure 2-A shows the results when 200 mg of dicyandiamide nitrogen was melted together with urea and coated after granulation to make it 7% by weight of the total nitrogen; nitrogen,
is recovered nitrate nitrogen.
第2図−Bは尿素単独の溶融粒状化被覆品とジ
シアンジアミドの単独粒状化被覆品による結果を
示したものである。尿素単独の粒を被覆したもの
を全窒素で200mg加えた場合においては回収ア
ンモニア態窒素、は回収硝酸態窒素を示す。尿
素単独の粒を被覆したものを全窒素で186mgおよ
びジシアンジアミドの単独粒状化被覆品をジシア
ンジアミド態窒素で14mg加えた場合(ジシアンジ
アミド態窒素7重量%に相当)については全回
収アンモニア態窒素、は回収硝酸態窒素を示
す。 FIG. 2-B shows the results of a product coated with urea alone and granulated with dicyandiamide alone. When 200 mg of total nitrogen is added to particles coated with urea alone, recovered ammonia nitrogen indicates recovered nitrate nitrogen. When 186 mg of total nitrogen was added to the granules coated with urea alone and 14 mg of dicyandiamide nitrogen was added to the granules coated with dicyandiamide alone (equivalent to 7% by weight of dicyandiamide nitrogen), the total recovered ammonia nitrogen was recovered. Indicates nitrate nitrogen.
第2図−Cは尿素単独の溶融粒状化後に被覆を
施したものを全窒素分で186mg、ジシアンジアミ
ド微粉末をジシアンジアミド態窒素で14mg加えた
ものについては全回収アンモニア態窒素、は
回収硝酸態窒素を示す。 Figure 2-C shows the total nitrogen content of 186 mg of urea alone coated after melt granulation, and 14 mg of dicyandiamide fine powder added with dicyandiamide nitrogen, total recovered ammonia nitrogen, and recovered nitrate nitrogen. shows.
本例の試験により尿素単独の溶融粒状化後に被
覆を施したものが土壌中でアンモニア態窒素およ
び硝酸態窒素の両者を同時に存在する状態はジシ
アンジアミドと尿素を同じ粒として粒状化後に被
覆を施したものが長期間保持できることが分る。
尿素単独の粒状化後に被覆を施したものとは別に
ジシアンジアミドの粒状化後に被覆を施したもの
を併用した場合には土壌中の硝酸態窒素にくらべ
てアンモニア態窒素の存在量ははるかに少なく、
ジシアンジアミド粉末を併用した場合には約1ケ
月を経過した後には硝酸態窒素にくらべてアンモ
ニア態窒素の量が少なくなつていることを観察す
ることができる。 According to the test in this example, when urea alone was fused into granules and then coated, both ammonia nitrogen and nitrate nitrogen were present in the soil at the same time. It turns out that things can be kept for a long time.
When urea alone is granulated and coated, and dicyandiamide is granulated and then coated, the amount of ammonia nitrogen present is much lower than that of nitrate nitrogen in the soil.
When dicyandiamide powder is used in combination, it can be observed that the amount of ammonia nitrogen becomes smaller than that of nitrate nitrogen after about one month.
例 3
本例の試験はジシアンジアミドの含有量を変化
させた場合の尿素を粒状化し被覆したものの硝酸
化成抑制の効果を示すものである。Example 3 The test of this example shows the effect of granulated and coated urea on inhibiting nitrification when the content of dicyandiamide is varied.
例1の方法に準じてジシアンジアミド態窒素が
全窒素の3重量%、5重量%および15重量%のジ
シアンジアミド入り粒状被覆尿素を全窒素分で
200mg用いて所定期間経過後に土壌中に溶出した
アンモニア態窒素および硝酸態窒素を測定した。
結果を第3図A,BおよびCに示す。図中,
,はアンモニア態窒素を示し、,,は
硝酸態窒素を示す。 According to the method of Example 1, granular coated urea containing dicyandiamide containing 3%, 5%, and 15% by weight of dicyandiamide nitrogen was prepared based on the total nitrogen content.
Ammonia nitrogen and nitrate nitrogen eluted into the soil after a predetermined period of time using 200 mg were measured.
The results are shown in Figures 3A, B and C. In the figure,
, indicates ammonia nitrogen, and , indicates nitrate nitrogen.
本例の結果から粒状被覆尿素に含まれるジシア
ンジアミドの量が増加するにつれて、例えば70日
経過後に土壌中にアンモニア態窒素の量が多く硝
酸化成が抑制されていることを観察できる。 From the results of this example, it can be observed that as the amount of dicyandiamide contained in the granular coated urea increases, the amount of ammonia nitrogen increases in the soil after 70 days, for example, and nitrification is suppressed.
例 4
本例の試験は施肥による障害を示すものであ
る。Example 4 The test in this example shows damage caused by fertilization.
風乾土壌(例1で用いたものと同じ土壌)を
3.5Kgおよび供試肥料にて全窒素1.0g、過リン酸
右灰にてP2O50.5g、硫酸カリウムにてK2O0.5g
になるように混合して1/5000アールのポツトに詰
めイタリアンライグラス(牧草)の種を1g播種
し30日間栽培した。窒素源としてジシアンジア
ミド態窒素10重量%を含有する尿素を溶融粒状化
し被覆を施したもの、ジシアンジアミド態窒素
10重量%を含有する尿素を溶融粒状化したもの、
非被覆溶融粒状化尿素、ジシアンジアミド態
窒素を施肥した全窒素の10重量%(0.1gに相当)
するように粉末のジシアンジアミドと被覆溶融粒
状化尿素を用いたものについて試験を行なつた。 Air-dried soil (same soil used in Example 1)
3.5Kg and total nitrogen 1.0g in test fertilizer, P 2 O 5 0.5g in superphosphate right ash, K 2 O 0.5g in potassium sulfate
The mixture was mixed and packed in 1/5000 are pots, and 1 g of Italian ryegrass seeds were sown and cultivated for 30 days. Urea containing 10% by weight of dicyandiamide nitrogen as a nitrogen source is fused and granulated and coated, dicyandiamide nitrogen
Melt granulated urea containing 10% by weight,
Uncoated fused granulated urea, 10% by weight of total nitrogen (equivalent to 0.1g) fertilized with dicyandiamide nitrogen
Tests were conducted using powdered dicyandiamide and coated melt-granulated urea.
およびを窒素源に用いたものについては牧
草が正常に生育したが、およびを窒素源に用
いたものについては牧草の先端部が黄化する障害
が認められた。 Pasture grass grew normally when and was used as the nitrogen source, but when and was used as the nitrogen source, problems such as yellowing of the tips of the grass were observed.
第1図−Aは本発明による肥料の、第1図−B
は比較品の尿素(と)およびジシアンジアミ
ド(と)の溶出率、第2図−Aは本発明によ
る肥料の、第2図−BおよびCは回収アンモニア
態窒素(,と)および回収硝酸態窒素
(,と)第3図−A,B,Cは本発明によ
る肥料の土壌中に溶出したアンモニア態窒素
(,と)および硝酸態窒素(,と)
および硝酸態窒素(,と)を示す。
Figure 1-A shows the fertilizer according to the invention in Figure 1-B.
Figure 2-A is the elution rate of urea (and) and dicyandiamide (and) of the comparison product, Figure 2-B and C are the recovered ammonia nitrogen (, and) and recovered nitrate nitrogen of the fertilizer according to the present invention. (, and) Figure 3-A, B, and C are ammonia nitrogen (, and) and nitrate nitrogen (, and) leached into the soil of the fertilizer according to the present invention.
and nitrate nitrogen (, and).
Claims (1)
得られる粒状物に水で崩壊し難い皮膜を被覆させ
た構造を有することを特徴とする尿素系被覆肥
料。1. A urea-based coated fertilizer characterized by having a structure in which granules obtained from a mixture of urea and dicyandiamide are coated with a film that is difficult to disintegrate with water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16193979A JPS5684394A (en) | 1979-12-13 | 1979-12-13 | Ureaaclad fertilizer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16193979A JPS5684394A (en) | 1979-12-13 | 1979-12-13 | Ureaaclad fertilizer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5684394A JPS5684394A (en) | 1981-07-09 |
JPS6323159B2 true JPS6323159B2 (en) | 1988-05-14 |
Family
ID=15744903
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16193979A Granted JPS5684394A (en) | 1979-12-13 | 1979-12-13 | Ureaaclad fertilizer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5684394A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002104893A (en) * | 2000-09-27 | 2002-04-10 | Chisso Corp | Coated granular material and method of cultivating crop using it |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2002344156A1 (en) * | 2001-05-25 | 2002-12-09 | Henkel Kommanditgesellschaft Auf Aktien | Granules containing one or more highly active substances and method for producing the same |
CN104488430A (en) * | 2014-12-10 | 2015-04-08 | 浙江工商大学 | Application method of nitrogen fertilizer suitable for plantation of vegetable crops in cadmium contaminated field |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2531962A1 (en) * | 1975-07-17 | 1977-01-20 | Sueddeutsche Kalkstickstoff | Slow acting nitrogen fertilisers - with a coating of finely divided dicyandiamide |
-
1979
- 1979-12-13 JP JP16193979A patent/JPS5684394A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2531962A1 (en) * | 1975-07-17 | 1977-01-20 | Sueddeutsche Kalkstickstoff | Slow acting nitrogen fertilisers - with a coating of finely divided dicyandiamide |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002104893A (en) * | 2000-09-27 | 2002-04-10 | Chisso Corp | Coated granular material and method of cultivating crop using it |
Also Published As
Publication number | Publication date |
---|---|
JPS5684394A (en) | 1981-07-09 |
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