JPH11209190A - Production of coated granular fertilizer - Google Patents

Production of coated granular fertilizer

Info

Publication number
JPH11209190A
JPH11209190A JP10013846A JP1384698A JPH11209190A JP H11209190 A JPH11209190 A JP H11209190A JP 10013846 A JP10013846 A JP 10013846A JP 1384698 A JP1384698 A JP 1384698A JP H11209190 A JPH11209190 A JP H11209190A
Authority
JP
Japan
Prior art keywords
resin
starch
coating
spray
fertilizer
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.)
Withdrawn
Application number
JP10013846A
Other languages
Japanese (ja)
Inventor
Koichi Adachi
浩一 足立
Yasushi Terada
泰史 寺田
Kengo Zensei
健吾 前正
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical 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 Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp
Priority to JP10013846A priority Critical patent/JPH11209190A/en
Publication of JPH11209190A publication Critical patent/JPH11209190A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G5/00Fertilisers characterised by their form
    • C05G5/30Layered or coated, e.g. dust-preventing coatings
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G5/00Fertilisers characterised by their form
    • C05G5/30Layered or coated, e.g. dust-preventing coatings
    • C05G5/37Layered or coated, e.g. dust-preventing coatings layered or coated with a polymer

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Fertilizers (AREA)

Abstract

PROBLEM TO BE SOLVED: To stably produce a coated granular fertilizer by spray-coating the surface of a granular fertilizer with a liquid containing a sugar polymer o the derivative and a resin and having a specific viscosity by using spray nozzle having a specific aperture. SOLUTION: As the sugar polymer or the derivative, a corn starch, an enzyme denatured starch or a chemically denatured starch each having 1-100 μm particle diameter is preferably used usually by 1-80 wt.% of the resin. As the resin, a polyolefin resin such as thermoplastic PE or PP is desirably used. In addition, if necessary an inorganic material as a filler of the resin, an organic metallic compound accelerating biological decomposition of the resin, a hydrocarbon base or a chlorinated hydrocarbon for dissolving the resin can be used. The viscosity of the liquid is preferably 0.5-100 cP. By using the spray nozzle having 0.9-3.0 mm aperture, the possibility of clogging of a liquid supply pipe line is decreased and the stable production is performed.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は溶解速度を制御した
被覆粒状肥料の製造方法に関する。
The present invention relates to a method for producing a coated granular fertilizer having a controlled dissolution rate.

【0002】[0002]

【従来の技術】従来、農業分野においては様々な種類の
肥料が用いられてきており、形態的には固体粒状のもの
や液状のもの、肥効速度的には速効性のものから緩効性
のものまである。中でも特に、肥料を樹脂等でコーティ
ング(被覆)して効果を持続させたコーティング(被
覆)肥料は肥料成分が長期に渡り徐々に放出される等の
特徴があり、施肥回数が少なくて済む等の理由から、近
年の農業人口の減少に対応する省力型肥料として注目さ
れている。
2. Description of the Related Art Conventionally, various types of fertilizers have been used in the field of agriculture. There are even things. Above all, coating (coating) fertilizers that maintain the effect by coating (coating) the fertilizer with a resin or the like have the characteristic that the fertilizer component is gradually released over a long period of time, and the number of times of fertilization can be reduced. For this reason, it has attracted attention as a labor-saving fertilizer that responds to the recent decline in the agricultural population.

【0003】このようななコーティングには、通常、安
価で非生分解性の汎用樹脂であるポリエチレン、ポリプ
ロピレン等のポリオレフィン系樹脂や、ポリ塩化ビニル
およびそれらの誘導体などが活用されている。特に、土
壌中に施肥された肥料成分の溶出を物理的に制御するた
めに、粒状肥料の表面を溶出速度調節剤を含有した皮膜
で被覆する検討が広く実施され、皮膜材としてポリオレ
フィン系樹脂等を用いた被覆肥料の製造方法(特開昭5
0−99858号公報、特公昭60−3040号公報、
特公昭60−37074号公報等)が実用化までに至っ
ている。
For such coatings, polyolefin resins such as polyethylene and polypropylene which are inexpensive and non-biodegradable general-purpose resins, polyvinyl chloride and derivatives thereof are usually used. In particular, in order to physically control the dissolution of fertilizer components applied in soil, coating of the surface of granular fertilizer with a film containing a dissolution rate regulator has been widely studied. Production method of coated fertilizer using
No. 0-99858, Japanese Patent Publication No. 60-3040,
Japanese Patent Publication No. 60-37074) has been put to practical use.

【0004】一方、上記のような樹脂皮膜は非生分解性
のため、土壌中に中空粒子様の形態を維持して蓄積さ
れ、灌水時に圃場系外へ流亡する等、環境への負荷を懸
念する声が上がっている。このため、皮膜に生分解性樹
脂や材料を用いたコーティング肥料が種々検討されてい
る。なかでも、澱粉を樹脂に混合した生分解性樹脂は、
汎用的な樹脂の成形加工やフィルムの分野で実用化の段
階にあり、コーティング肥料への適用の可能性は高いと
考えられ、すでに、ポリオレフィン系樹脂やポリ塩化ビ
ニル系樹脂に澱粉を加えた皮膜のコーティング肥料が報
告されている(特開平6−87684号公報、特開平8
−333185号公報)。皮膜中の澱粉の効果として
は、澱粉が土壌中の微生物から分泌されるアミラーゼ等
により分解消失し、皮膜にミクロボイドが生成して、皮
膜の機械的強度の低下、土壌との接触面積の増大、水の
吸収などの微生物の生存に好ましい環境を作ること、樹
脂を分解する種々の微生物を誘引するなどが挙げられ
る。このような効果により、従来、難分解性と考えられ
ていたポリエチレンなどの樹脂でも生分解を受けること
が報告されている。
[0004] On the other hand, since the resin film as described above is non-biodegradable, it is accumulated in the soil while maintaining a hollow particle-like morphology, and is likely to run out of the field system during irrigation. A voice is rising. For this reason, various coating fertilizers using a biodegradable resin or material for the film have been studied. Above all, biodegradable resin obtained by mixing starch with resin,
It is in the stage of practical application in the field of molding and processing of general-purpose resins and films, and it is considered that the possibility of application to coating fertilizers is high, and already a film made by adding starch to polyolefin resin or polyvinyl chloride resin. Coating fertilizers have been reported (JP-A-6-87684, JP-A-8-87684).
-333185). The effect of starch in the film is as follows: starch is decomposed and eliminated by amylase secreted from microorganisms in the soil, and microvoids are formed in the film, resulting in a decrease in mechanical strength of the film, an increase in contact area with the soil, Examples of such methods include creating a favorable environment for the survival of microorganisms such as water absorption, and attracting various microorganisms that degrade the resin. Due to such an effect, it has been reported that resins such as polyethylene, which were conventionally considered to be hardly degradable, undergo biodegradation.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、上記の
澱粉添加系樹脂皮膜のコーティング肥料は研究段階であ
り、その工業的製造法については種々の問題が予想され
る。コーティング肥料の工業的製造方法としては、一般
に、溶剤に樹脂を溶解させた溶液、もしくは樹脂の溶融
液を原料肥料粒子にスプレーすることにより皮膜を形成
させるスプレーコ−ティングが用いられる。この方法を
澱粉添加系樹脂に同じように適用した場合、澱粉が樹脂
の溶解に用いられる極性の低い有機溶剤や、樹脂自体と
の相溶性が非常に低く、澱粉をコーティング溶液に懸濁
させた状態でスプレーする必要があり、このため、スプ
レーノズルや液供給配管の閉塞など懸濁液の移送・噴霧
に特有の問題が起こる可能性があり、安定的に生産でき
ないおそれがある。特に、溶剤を用いた場合、溶液が低
粘度であるため澱粉粒子の凝集が問題となることも予想
される。
However, the above-mentioned fertilizer coated with a starch-added resin film is in a research stage, and various problems are expected in its industrial production method. As an industrial production method of a coated fertilizer, generally, a spray coating is used in which a solution in which a resin is dissolved in a solvent or a molten liquid of the resin is sprayed on the raw material fertilizer particles to form a film. When this method was similarly applied to a starch-added resin, the starch was very low in compatibility with the low-polarity organic solvent used for dissolving the resin and the resin itself, and the starch was suspended in the coating solution. It is necessary to spray in a state, and therefore, there is a possibility that a problem peculiar to transfer / spraying of the suspension such as blockage of a spray nozzle or a liquid supply pipe may occur, and stable production may not be performed. In particular, when a solvent is used, aggregation of starch particles is expected to be a problem because the solution has a low viscosity.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上記の課
題の中で、特に安定的にスプレーコーテイングを行う方
法につき検討した結果、特定口径のスプレーノズルを用
いることにより安定的にスプレーできることを見いだ
し、本発明に到った。即ち、本発明は、粒状肥料の表面
に、(ア)糖重合体若しくはその誘導体と(イ)樹脂を
含む液を、口径0.9mmから3.0mmのノズルを用
いてスプレーコーテイングすることを特徴とする被覆粒
状肥料の製造方法に存する。
Means for Solving the Problems The inventors of the present invention have studied a method for performing spray coating in a stable manner, and found that a spray can be stably sprayed by using a spray nozzle having a specific diameter. And arrived at the present invention. That is, the present invention is characterized in that a liquid containing (a) a sugar polymer or a derivative thereof and (a) a resin is spray-coated on the surface of the granular fertilizer using a nozzle having a diameter of 0.9 mm to 3.0 mm. In the method for producing a coated granular fertilizer.

【0007】[0007]

【発明の実施の形態】以下、本発明を詳細に説明する。 (1)被覆する粒状肥料 本発明で使用される肥料は,特に限定されない。尿素、
硫安、塩安、塩化加里、硫酸加里、燐酸アンモニウム等
の粒状の単肥の他に、N、K2O、P25等の多成分を
含む粒状の肥料が本発明品の原肥に使用される。肥料の
粒径、形状は特に限定されないが、好ましくは、平均粒
径が0.5〜4.0mmであり、角張った形態や不規則
な形態のものより、球状または球状に近い形態の粒子の
方が望ましい。 (2)被覆材料 本発明の適用される皮膜材料は、(ア)糖重合体若しく
はその誘導体、(イ)樹脂及び(ウ)その他任意成分に
分けられる。 (ア)糖重合体若しくはその誘導体 糖重合体若しくはその誘導体とは、グルコース、フラク
トールなどの6炭糖及びその誘導体、キシロース、アラ
ビノース、リボースなどの5炭糖及びその誘導体の1種
以上よりなる重合体であり、例えば、澱粉、セルロー
ス、寒天、アルギン酸等の多糖類、キチン、キトサン等
の誘導体であり、好ましくは、澱粉若しくはその誘導体
である。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail. (1) Granular fertilizer to be coated The fertilizer used in the present invention is not particularly limited. urea,
Granular fertilizers containing multiple components such as N, K 2 O and P 2 O 5 in addition to granular monofertilizers such as ammonium sulfate, salt ammonium chloride, potassium sulfate, ammonium phosphate, etc. used. The particle size and shape of the fertilizer are not particularly limited, but preferably, the average particle size is 0.5 to 4.0 mm, and the shape of the particles is more spherical or nearly spherical than that of the angular or irregular shape. Is more desirable. (2) Coating Material The coating material applied to the present invention is classified into (A) a saccharide polymer or a derivative thereof, (A) a resin, and (C) other optional components. (A) Glycopolymer or derivative thereof Glycopolymer or a derivative thereof is a polysaccharide composed of at least one of hexose such as glucose and fructol and its derivatives, and pentose such as xylose, arabinose and ribose and its derivatives. And a derivative such as starch, cellulose, agar, polysaccharides such as alginic acid, chitin, chitosan, etc., preferably starch or a derivative thereof.

【0008】澱粉としては、生澱粉(トウモロコシ澱
粉、馬鈴薯澱粉、甘藷澱粉、コムギ澱粉、キッサバ澱
粉、サゴ澱粉、タピオカ澱粉、モロコシ澱粉、コメ澱
粉、マメ澱粉、クズ澱粉、ワラビ澱粉、ハス澱粉、ヒシ
澱粉)、物理的変性澱粉(α-澱粉、分別アミロース、
湿熱処理澱粉等)、酵素変性澱粉 (加水分解処理澱
粉、酵素分解デキストリン、アミロース等)、化学分解
変性澱粉(酸処理澱粉、酸化澱粉、ジアルデヒド澱粉
等)、化学変性澱粉誘導体(エステル化澱粉、エーテル
化澱粉、カチオン化澱粉、架橋澱粉等)などが用いられ
る。なお、化学変性澱粉誘導体のうちエステル化澱粉と
しては酢酸エステル澱粉、コハク酸エステル化澱粉、硝
酸エステル化澱粉、リン酸エステル化澱粉、尿素リン酸
エステル化澱粉、キサントゲン酸エステル化澱粉、アセ
ト酢酸エステル化澱粉など、エーテル化澱粉としては、
アリルエーテル化澱粉、メチルエーテル化澱粉、カルボ
キシメチルエーテル化澱粉、ヒドロキシエチルエーテル
化澱粉、ヒドロキシプロピルエーテル化澱粉など、カチ
オン化澱粉としては、澱粉と2、3−エポキシプロピル
トリメチルアンモニウムクロライドの反応物など、架橋
澱粉としては、ホルムアルデヒド架橋澱粉、エピクロル
ヒドリン架橋澱粉、リン酸架橋澱粉、アクロレイン架橋
澱粉などが挙げられる。
[0008] As the starch, raw starch (corn starch, potato starch, sweet potato starch, wheat starch, kissava starch, sago starch, tapioca starch, sorghum starch, rice starch, legume starch, kuzu starch, bracken starch, lotus starch, sis starch, Starch), physically modified starch (α-starch, fractionated amylose,
Enzyme-modified starch (hydrolyzed starch, enzyme-degraded dextrin, amylose, etc.), chemically degraded starch (acid-treated starch, oxidized starch, dialdehyde starch, etc.), chemically-modified starch derivative (esterified starch, etc.) Etherified starch, cationized starch, cross-linked starch, etc.). Among the chemically modified starch derivatives, esterified starch includes acetate starch, succinate ester, nitrate ester starch, phosphate ester starch, urea phosphate ester starch, xanthate ester starch, and acetoacetate ester. As etherified starch such as acetylated starch,
Allyl etherified starch, methyl etherified starch, carboxymethyl etherified starch, hydroxyethyl etherified starch, hydroxypropyl etherified starch, and the like. Cationic starches include, for example, a reaction product of starch and 2,3-epoxypropyltrimethylammonium chloride. Examples of the crosslinked starch include formaldehyde crosslinked starch, epichlorohydrin crosslinked starch, phosphate crosslinked starch, and acrolein crosslinked starch.

【0009】このような澱粉の中でも糊化澱粉の粘度が
低いほど溶融成形が容易に行えることや、価格の点から
トウモロコシ澱粉、酵素変性澱粉、化学変性澱粉が好適
に用いられる。澱粉の粒径としては、平均粒径として、
通常0.1〜100μm、好ましくは1〜10μmであ
る。澱粉の高分子化合物への添加方法としては、溶融樹
脂と澱粉の混練や、樹脂を溶剤に溶解した後、澱粉を溶
液に添加し、直接肥料へスプレーする方法などが挙げら
れる。澱粉の樹脂に対する添加量は、皮膜の生分解性と
溶出制御性を両立させる観点から、通常、樹脂の1〜8
0重量%、好ましくは5〜40重量%である。 (イ)樹脂 被覆材料として樹脂を用いるが、その種類は、特に限定
されない。例として、ポリオレフィン、ポリ塩化ビニリ
デン樹脂、ポリ塩化ビニル樹脂、ポリスチレン樹脂、ポ
リカーボネート、ポリアミド、ポリメタクリル酸メチ
ル、ポリウレタン、エチレン−酢酸ビニル等の熱可塑性
樹脂、アルキド樹脂、フェノ−ル樹脂、尿素樹脂、メラ
ミン樹脂等の熱硬化性樹脂、ABS樹脂、エポキシ樹
脂、シリコ−ン樹脂、その他、天然ゴムやSBR,NB
Rなどの合成ゴム、更には、ポリカプロラクトン、ポリ
酪酸、脂肪族ポリエステル、ポリグリコット、ポリビニ
ルアルコ−ル、酸化ポリエチレン、ポリビニルアルコー
ル系樹脂、ポリアクリル酸ソーダ、ポリエチレンオキシ
ド、ポリビニルピロリドン等の分解性ポリマ−が挙げら
れる。中でも、透湿性が低いため少量でも溶出防止効果
の高い熱可塑性樹脂が好ましく、ポリエチレンやポリプ
ロピレン等のポリオレフィン樹脂が特に好ましい。これ
らの樹脂は単独でも、2種以上の混合物として用いるこ
とも可能である。 (ウ)その他 以上の2種類の必須成分の他、被覆する目的を損なわな
ければ、他の無機物や有機物を共存させて被覆しても構
わない。例えば、上記の様な透水性の高い樹脂で被覆し
た場合には、溶出性の調整や樹脂の増量等の目的で、タ
ルク、炭酸カルシウム、クレイ、ケイソウ土、シリカ、
金属酸化物、イオウ等の無機質の他、界面活性剤、ワッ
クス、可塑剤等の有機物質を加えても構わない。また、
澱粉以外の、樹脂の生分解を促進する物質、たとえば
鉄、アルミニウム、ナトリウム、カリウム、カルシウ
ム、マグネシウム、亜鉛、マンガン等の有機金属塩、水
酸化物、酸化オイル等を添加する場合もある。 (3)溶剤 前記の被覆材料をコ−ティングする場合、その材料を溶
融させて直接粒状肥料にスプレーする方法と、溶剤に溶
解させその溶液をスプレーする方法、およびプレポリマ
ーをスプレー後、硬化させる方法などがあり、その方法
は特に限定されない。しかしながら、一般に本発明に適
するような高分子化合物は、融点が高く、またその溶融
粘度も高いため工業的には溶融液の直接スプレーコ−テ
ィングに不適であり、溶剤を用いて溶液とし、スプレー
コ−ティングする方法が好ましい。その際、溶剤種は特
に限定されないが、様様な条件を考慮して適宜選択され
る。その判断材料としては、皮膜材料となる高分子化合
物の溶解力、溶解温度、ハンドリング性、回収の容易
さ、毒性、安全性、価格等が挙げられる。例えば、皮膜
材料としてポリオレフィン系樹脂、特に低密度のポリエ
チレンを用いる場合は、ヘキサン、オクタン、トルエ
ン、キシレン、テトラリン等の炭化水素系溶剤、トリク
ロロエチレン、パークロロエチレン等の塩素化炭化水素
系溶剤が好ましい。また、水溶性ポリマ−やエマルジョ
ン樹脂、ラテックスなどで被覆する際は溶剤として水が
用いられる。なお、本発明で使用する糖重合体若しくは
その誘導体の多くはは、これらの溶剤にほとんど溶解し
ないため、懸濁状態でスプレーすることになる。
Among such starches, corn starch, enzyme-modified starch, and chemically-modified starch are preferably used in view of the fact that the lower the viscosity of the gelatinized starch, the easier the melt-molding can be carried out, and the lower the price. As the particle size of starch, as an average particle size,
It is usually from 0.1 to 100 μm, preferably from 1 to 10 μm. Examples of the method of adding starch to a polymer compound include a method of kneading a molten resin and starch, a method of dissolving a resin in a solvent, adding the starch to a solution, and spraying the solution directly on a fertilizer. The amount of starch added to the resin is usually 1 to 8 of the resin, from the viewpoint of achieving both biodegradability of the film and control of dissolution.
0% by weight, preferably 5 to 40% by weight. (A) Resin A resin is used as the coating material, but the type is not particularly limited. For example, polyolefin, polyvinylidene chloride resin, polyvinyl chloride resin, polystyrene resin, polycarbonate, polyamide, polymethyl methacrylate, polyurethane, thermoplastic resin such as ethylene-vinyl acetate, alkyd resin, phenol resin, urea resin, Thermosetting resin such as melamine resin, ABS resin, epoxy resin, silicone resin, other natural rubber, SBR, NB
Synthetic rubber such as R, further decomposable polymers such as polycaprolactone, polybutyric acid, aliphatic polyester, polyglycot, polyvinyl alcohol, polyethylene oxide, polyvinyl alcohol-based resin, sodium polyacrylate, polyethylene oxide, polyvinylpyrrolidone, etc. Is mentioned. Among them, a thermoplastic resin having a high elution prevention effect even in a small amount due to low moisture permeability is preferable, and a polyolefin resin such as polyethylene and polypropylene is particularly preferable. These resins can be used alone or as a mixture of two or more. (C) Others In addition to the above two kinds of essential components, other inorganic or organic substances may be coexistently coated as long as the purpose of coating is not impaired. For example, when coated with a resin having high water permeability as described above, talc, calcium carbonate, clay, diatomaceous earth, silica,
Organic substances such as surfactants, waxes and plasticizers may be added in addition to inorganic substances such as metal oxides and sulfur. Also,
Substances that promote biodegradation of the resin other than starch, for example, organic metal salts such as iron, aluminum, sodium, potassium, calcium, magnesium, zinc, and manganese, hydroxides, and oxidized oils may be added. (3) Solvent When coating the coating material, a method in which the material is melted and sprayed directly on the granular fertilizer, a method in which the material is dissolved in a solvent and the solution is sprayed, and a prepolymer is sprayed and cured. There is a method, and the method is not particularly limited. However, polymer compounds suitable for the present invention generally have high melting points and high melt viscosities, so they are industrially unsuitable for direct spray coating of melts. Is preferred. At this time, the type of the solvent is not particularly limited, but is appropriately selected in consideration of various conditions. As the judgment material, the dissolving power, dissolving temperature, handleability, ease of recovery, toxicity, safety, price, and the like of the polymer compound serving as the film material can be cited. For example, when a polyolefin resin, particularly low-density polyethylene is used as a coating material, hydrocarbon solvents such as hexane, octane, toluene, xylene, and tetralin, and chlorinated hydrocarbon solvents such as trichloroethylene and perchloroethylene are preferable. . When coating with a water-soluble polymer, emulsion resin, latex, or the like, water is used as a solvent. Most of the saccharide polymers or derivatives thereof used in the present invention hardly dissolve in these solvents, so that they are sprayed in a suspended state.

【0010】溶液の濃度についても特に限定されない。
例えば、濃度を高くすると溶剤の使用量が低減しかつ処
理時間が短くなるので好ましい。また、濃度を低くする
と溶液の粘度が低くなりハンドリング性が良好になる。
ただし、スプレーコーテイングする場合は、使用するス
プレーノズルおよび噴霧圧力に応じ、適当な噴霧状態が
得られる粘度になるよう濃度を調整する必要がある。粘
度としては、通常0.5〜100cP、好ましくは10
〜50cPである。具体的な例を挙げると、皮膜材料と
して低密度ポリエチレンを用い、溶剤としてパークロロ
エチレンを用いる場合、溶液の濃度は通常1〜12重量
%、好ましくは3〜10重量%である。また、一般に高
分子化合物は冷時には、溶剤難溶性のものが多いため、
溶解するには通常加熱攪伴が必要である。 (4)被覆装置 本発明に適用できる被覆装置としては、粒状物質を混合
攪伴し、かつ気流と十分接触せしめる構造、機能を持っ
た装置であれば特に限定されない。混合攪伴方式で分類
すると、攪伴翼を用いて混合攪伴するタイプの装置とし
ては、例えば、ヘンシェルミキサーやナウターミキサー
等が挙げられる。装置自身の運動に付随して粒状物質を
攪伴するものとしては、回転ドラム式コーター(特開昭
52−61216号公報)、回転パン式コーター(特開
平5−85873号公報)、回転落下式コーター(特開
平5−139376号公報,特開平5−185612号
公報,特開平5−342527号公報)などが挙げられ
る。また、振動力で攪伴する振動流動装置(特開平1−
245847)は、大量の粒状物質を激しく攪伴できる
ので好ましい。気力で攪伴するタイプとしては、粒子を
吹き飛ばして循環混合するワースター型または噴流層型
コーター、粒子を浮遊流動させる方式として、流動層型
コーター(特公平4−61840号公報)などが挙げら
れる。被覆溶液の粒状物質への添着は、通常、一流体も
しくは二流体スプレーノズルを用い、攪伴粒子中の適切
な位置に噴霧することによって行う。また溶剤除去は上
述の通り熱気流で行うが、そのガスとしては、空気のほ
かに、安全面から窒素、炭酸ガスなどの不活性気体も使
用できる。 (5)スプレーノズル スプレーノズルの口径は、液を噴霧するノズルの先端部
分の孔の大きさであり、液をガスの噴出力で噴霧化する
二流体ノズルの場合は通常、孔は円形で、この場合口径
はその内側の直径である。一方、液自体の噴出圧力で噴
霧化する形式の一流体ノズルの場合、孔は円形ではな
く、一般的に使われるオリフィス径を口径とする。これ
まで述べたとおり、懸濁液を安定的にスプレーするため
には、このノズル口径を0.9〜3.0mm、好ましく
は1.0〜2.5mmとする。これより口径が細いと、
ノズル先端部分で澱粉等の粒子の閉塞が起こりやすく、
安定、継続的に懸濁液をスプレーすることができない。
本発明者らの観察によると、通常、本発明に用いるよう
なコーティング液に懸濁している澱粉等の1次粒子は、
ノズル口径に比べ1/100以下の大きさであるが、液
の流れる管路がノズル先端部分でしぼられているため、
その直前で液の流速が減少し滞留が起こり、その結果、
澱粉等の粒子が管路内で凝集し、ノズル先端部分で閉塞
を発生すると考えられる。一方、ノズル口径が3.0m
mより大きくなると、スプレー液滴径が大きくなるため
肥料粒子の添着した溶剤の乾燥速度が遅くなり、その結
果、肥料粒子の凝集が発生し、コーティング肥料の品質
が悪化するという問題がある。 (6)製造方法 溶剤に(2)で述べた被覆材料を溶解させ、被覆材溶液
を調製する。一方、原料の粒状肥料を(4)の被覆装置
に仕込み、熱風により品温を通常30〜100℃、好ま
しくは40から80℃に保ちながら、スプレーノズルを
利用して被覆材溶液を噴霧することによりコーティング
を行う。なお、ここでいう品温とは、噴霧されている状
態の肥料粒子集団に直接、温度検出端子を挿入して測定
される温度をいう。この品温の調整、保持は、溶剤を除
去する熱風で行う。熱風の温度は、当然ながら、品温以
上必要であり、通常50〜150℃である。その流速
は、溶剤除去速度、品温および粒子の流動状態などを勘
案して決定される。被覆材料の添着量(被覆率)は、原
料の粒状肥料に対し、通常3〜20重量%、好ましくは
5〜15重量%である。皮膜の厚みでみると、通常10
〜200μm、好ましくは30〜150μmである。ま
た、スプレーコーテイングの時間は、被覆溶液濃度、噴
霧速度、被覆率等により決められるが、通常0.1〜1
0時間、好ましくは0.2〜3時間である。コーティン
グ終了後は、そのままコーティング装置から肥料を抜き
出すことにより被覆肥料を得ることができる。
[0010] The concentration of the solution is not particularly limited.
For example, it is preferable to increase the concentration because the amount of the solvent used is reduced and the processing time is shortened. On the other hand, when the concentration is lowered, the viscosity of the solution is lowered and the handling property is improved.
However, in the case of spray coating, it is necessary to adjust the concentration so as to have a viscosity that allows an appropriate spray state to be obtained according to the spray nozzle and spray pressure used. The viscosity is generally 0.5 to 100 cP, preferably 10 to 100 cP.
5050 cP. As a specific example, when low-density polyethylene is used as the coating material and perchlorethylene is used as the solvent, the concentration of the solution is usually 1 to 12% by weight, preferably 3 to 10% by weight. Also, in general, polymer compounds are often hardly soluble in solvents when cooled,
Heating is usually required for dissolution. (4) Coating device The coating device applicable to the present invention is not particularly limited as long as the device has a structure and a function of mixing and stirring the particulate matter and sufficiently bringing the particulate material into contact with the air flow. When classified according to the mixing and stirring method, examples of the type of mixing and stirring using stirring blades include a Henschel mixer and a Nauter mixer. Examples of the apparatus that accompanies the particulate matter accompanying the movement of the apparatus itself include a rotary drum type coater (Japanese Patent Laid-Open No. 52-61216), a rotary pan type coater (Japanese Patent Laid-Open No. 5-85873), and a rotary drop type coater. Coater (JP-A-5-139376, JP-A-5-185612, JP-A-5-342527) and the like. In addition, a vibrating fluid device that is stirred by a vibrating force (Japanese Unexamined Patent Publication No.
245847) is preferred because it can vigorously entrain large amounts of particulate matter. Examples of the type of agitation with a viscous force include a Wurster-type or spouted-bed type coater for blowing and circulating and mixing particles, and a fluidized-bed type coater (Japanese Patent Publication No. 4-61840) as a method for floating and flowing particles. The application of the coating solution to the particulate material is usually carried out by spraying to a suitable location in the entrained particles using a one-fluid or two-fluid spray nozzle. The solvent is removed by a hot air flow as described above. As the gas, in addition to air, an inert gas such as nitrogen or carbon dioxide can be used for safety. (5) Spray nozzle The diameter of the spray nozzle is the size of the hole at the tip of the nozzle that sprays the liquid. In the case of a two-fluid nozzle that atomizes the liquid with the jet power of the gas, the hole is usually circular, In this case the bore is the inside diameter. On the other hand, in the case of a one-fluid nozzle of a type in which atomization is performed by the ejection pressure of the liquid itself, the hole is not circular but has a generally used orifice diameter. As described above, in order to spray the suspension stably, the nozzle diameter is set to 0.9 to 3.0 mm, preferably 1.0 to 2.5 mm. If the caliber is smaller than this,
Particles such as starch are easily clogged at the nozzle tip,
Stable, unable to spray suspension continuously.
According to observations of the present inventors, primary particles such as starch usually suspended in a coating solution used in the present invention are:
Although the size is 1/100 or less compared to the nozzle diameter, the pipe through which the liquid flows is squeezed at the nozzle tip,
Just before that, the flow velocity of the liquid decreases and stagnation occurs, and as a result,
It is considered that particles such as starch agglomerate in the pipeline and cause clogging at the nozzle tip. On the other hand, the nozzle diameter is 3.0m
When it is larger than m, the spray droplet diameter becomes large, so that the drying speed of the solvent to which the fertilizer particles are attached becomes slow. As a result, there is a problem that the fertilizer particles aggregate and the quality of the coated fertilizer deteriorates. (6) Manufacturing method The coating material described in (2) is dissolved in a solvent to prepare a coating material solution. On the other hand, the raw material granular fertilizer is charged into the coating device of (4), and the coating material solution is sprayed using a spray nozzle while keeping the product temperature at usually 30 to 100 ° C, preferably 40 to 80 ° C by hot air. The coating is performed by Here, the product temperature refers to a temperature measured by inserting a temperature detection terminal directly into the fertilizer particle group in a sprayed state. The adjustment and holding of the product temperature are performed with hot air for removing the solvent. The temperature of the hot air naturally needs to be higher than the product temperature, and is usually 50 to 150 ° C. The flow rate is determined in consideration of the solvent removal rate, the product temperature, the flow state of the particles, and the like. The amount of coating material (coverage) is usually 3 to 20% by weight, preferably 5 to 15% by weight, based on the granular fertilizer as the raw material. In terms of film thickness, it is usually 10
To 200 μm, preferably 30 to 150 μm. The time of the spray coating is determined by the concentration of the coating solution, the spray rate, the coating rate, and the like.
0 hours, preferably 0.2 to 3 hours. After the coating is completed, the coated fertilizer can be obtained by extracting the fertilizer from the coating apparatus as it is.

【0011】[0011]

【実施例】次に、本発明を実施例により具体的に説明す
るが、本発明はその要旨を越えない限り、以下の実施例
に限定されるものではない。 実施例1 (1)コーティング溶液の調整 皮膜材料として低密度ポリエチレン(密度0.919、
メルトフローレート22、融点107℃)90重量部
と、とうもろこし澱粉10重量部を溶融混合して得られ
た樹脂を用いた。これを溶剤のパークロロエチレンに5
重量%の濃度になるように85℃で溶解させ、コーティ
ング溶液とした。この際、澱粉は、溶剤に溶解せず、懸
濁状態となった。 (2)コ−ティング コ−ティング装置として、図1に示す撹拌転動流動層型
のスパイラフローSFC5型(フロイント産業製)を用
いた(内径0.26m)。原料肥料として平均粒径2.
5mmの粒状尿素10kgを装置に仕込み、温度80℃
の空気を500Nm3/hの流量で吹き込んで尿素粒子
を流動させた。次に、流動床面からの高さ40cmの位
置に設置したスプレーノズルから、上記(1)のコーテ
ィング溶液を定量ポンプを用いて30kg/hの流量で
40分間スプレーした。スプレー時間は、下記(4)の
被覆率が10%となる量のコーティング溶液を供給する
時間とした。 (3)スプレーノズル 上記(2)のスプレーノズルとして、口径0.9mmの
外部混合型の2流体ノズルを用いた。2流体ノズルの場
合は、適当な流量のノズルエアを液と同時に供給した。 (4)得られたコーティング肥料の品質評価 コーティング終了後、得られたコーティング肥料を4m
mの篩いでふるい、ふるい下のものにつき、被覆率(原
料尿素に対する皮膜の重量%)と団粒化率(2粒以上が
凝集、接着した形態の団粒粒子の重量%)を測定した。
被覆率は、コーティング肥料10gを粉砕して、中の尿
素のみを水で溶解除去し、残った皮膜の重量を測定する
ことにより算出した。団粒化率は、20g中の団粒を目
視で選別し、その重量を測定することで算出した。スプ
レーは40分間安定的に噴霧でき、得られたコーティン
グ肥料の被覆率は、9.9%、団粒化率は1.2%で良
好であった(表−1参照)。 実施例2〜4 実施例1において、口径1.2、2.2、および2.8
mmの2流体スプレーノズルに置き換え、その他の条件
は同じでコーティングを行った。その結果を表−1にま
とめたが、いずれもスプレー状態は安定しており、良好
なコーティング肥料が得られた。 比較例1 実施例1において、口径0.7mmの2流体ノズルを用
い、その他は同じ条件でコーティングを行ったところ、
スプレー開始10分後に噴霧が停止した。ノズルを外し
て点検したところ、ノズル先端部で澱粉粒子の固まりが
閉塞していることが観察された(表−1参照)。 比較例2、3 実施例1において、口径0.79および0.66mmの
1流体ノズルを用い、その他は同じ条件でコーティング
を行ったところ、それぞれ、スプレー開始25、5分後
に噴霧が停止した。ノズルを外して点検したところ、ノ
ズル先端部で澱粉粒子の固まりが閉塞していることが観
察された(表−1参照)。 比較例4 実施例1において、口径3.5mmの2流体スプレーノ
ズルに置き換え、その他の条件は同じでコーティングを
行った。その結果、スプレー状態は安定しており40分
間噴霧できたが、得られたコーティング肥料のなかに
は、凝集粒子が多数みられ、団粒化率は22%と高かっ
た(表−1参照)。
EXAMPLES Next, the present invention will be described in detail with reference to examples, but the present invention is not limited to the following examples unless it exceeds the gist. Example 1 (1) Preparation of coating solution Low density polyethylene (density 0.919,
A resin obtained by melting and mixing 90 parts by weight of a melt flow rate 22, melting point of 107 ° C.) and 10 parts by weight of corn starch was used. This is added to the solvent perchlorethylene 5
The coating solution was dissolved at 85 ° C. so as to have a concentration of% by weight to obtain a coating solution. At this time, the starch did not dissolve in the solvent but was in a suspended state. (2) Coating As a coating device, a stirring-rolling fluidized bed type spiral flow SFC5 type (manufactured by Freund Corporation) shown in FIG. 1 was used (inner diameter: 0.26 m). Average particle size as raw material fertilizer 2.
10 kg of 5 mm granular urea was charged into the apparatus, and the temperature was 80 ° C.
Was blown at a flow rate of 500 Nm3 / h to flow the urea particles. Next, the coating solution of the above (1) was sprayed at a flow rate of 30 kg / h for 40 minutes using a metering pump from a spray nozzle installed at a position 40 cm above the fluidized bed surface. The spray time was set to a time for supplying the coating solution in an amount such that the coating rate of the following (4) became 10%. (3) Spray nozzle An external mixing type two-fluid nozzle having a diameter of 0.9 mm was used as the spray nozzle of (2). In the case of a two-fluid nozzle, an appropriate flow rate of nozzle air was supplied simultaneously with the liquid. (4) Quality evaluation of the obtained coated fertilizer After coating is completed, the obtained coated fertilizer is 4 m
With respect to the sieves with and under the sieve of m, the covering ratio (% by weight of the film with respect to the raw urea) and the agglomeration ratio (% by weight of aggregated particles in which two or more particles were agglomerated and bonded) were measured.
The coverage was calculated by crushing 10 g of the coated fertilizer, dissolving and removing only urea therein with water, and measuring the weight of the remaining film. The aggregation rate was calculated by visually selecting the aggregates in 20 g and measuring the weight. The spray could be sprayed stably for 40 minutes, and the coverage of the obtained coated fertilizer was 9.9%, and the agglomeration rate was 1.2%, which was good (see Table 1). Examples 2 to 4 In Example 1, calibers 1.2, 2.2, and 2.8.
mm, and the coating was carried out under the same other conditions. The results are summarized in Table 1. The spray state was stable in each case, and good coating fertilizer was obtained. Comparative Example 1 In Example 1, a two-fluid nozzle having a diameter of 0.7 mm was used, and the other coating was performed under the same conditions.
Spraying was stopped 10 minutes after the start of spraying. When the nozzle was removed and inspected, it was observed that the starch particles were blocked at the nozzle tip (see Table 1). Comparative Examples 2 and 3 In Example 1, coating was performed under the same conditions using one fluid nozzle having a diameter of 0.79 and 0.66 mm, and the spraying was stopped 25 and 5 minutes after the start of spraying, respectively. When the nozzle was removed and inspected, it was observed that the starch particles were blocked at the nozzle tip (see Table 1). Comparative Example 4 The coating was performed in the same manner as in Example 1, except that the two-fluid spray nozzle having a diameter of 3.5 mm was used. As a result, the spray state was stable and spraying was possible for 40 minutes. However, many agglomerated particles were observed in the obtained coated fertilizer, and the aggregation rate was as high as 22% (see Table 1).

【0012】[0012]

【表1】 [Table 1]

【0013】[0013]

【発明の効果】本発明によれば、(ア)糖重合体若しく
はその誘導体と(イ)樹脂からなる皮膜を有する被覆粒
状肥料を、安定して製造することができる。
According to the present invention, a coated granular fertilizer having a coating consisting of (a) a saccharide polymer or a derivative thereof and (a) a resin can be stably produced.

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

【図1】 図1は、実施例1の肥料のスプレーコーテイ
ングに用いた撹拌転動流動層型コーテイング装置の概念
図である。
FIG. 1 is a conceptual diagram of a stirred rolling fluidized bed type coating apparatus used for spray coating of fertilizer of Example 1.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 粒状肥料の表面に、(ア)糖重合体若し
くはその誘導体と(イ)樹脂を含む液を、口径0.9m
mから3.0mmのノズルを用いてスプレーコーテイン
グすることを特徴とする被覆粒状肥料の製造方法。
1. A liquid containing (a) a saccharide polymer or a derivative thereof and (a) a resin is coated on a surface of a granular fertilizer with a diameter of 0.9 m.
A method for producing a coated granular fertilizer, comprising spray-coating using a nozzle having a diameter of 3.0 to 3.0 mm.
【請求項2】 糖重合体若しくはその誘導体が、樹脂の
1〜80重量%であることを特徴とする請求項1の被覆
粒状肥料の製造法。
2. The method for producing a coated granular fertilizer according to claim 1, wherein the sugar polymer or a derivative thereof accounts for 1 to 80% by weight of the resin.
【請求項3】 液の粘度が0.5〜100cPであるで
あることを特徴とする請求項1又は2の被覆粒状肥料の
製造法。
3. The method for producing a coated granular fertilizer according to claim 1, wherein the viscosity of the liquid is 0.5 to 100 cP.
【請求項4】 糖重合体若しくはその誘導体が、澱粉若
しくはその誘導体であることを特徴とする請求項1ない
し3のいずれかの被覆粒状肥料の製造法。
4. The method for producing a coated granular fertilizer according to claim 1, wherein the sugar polymer or a derivative thereof is starch or a derivative thereof.
JP10013846A 1998-01-27 1998-01-27 Production of coated granular fertilizer Withdrawn JPH11209190A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10013846A JPH11209190A (en) 1998-01-27 1998-01-27 Production of coated granular fertilizer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10013846A JPH11209190A (en) 1998-01-27 1998-01-27 Production of coated granular fertilizer

Publications (1)

Publication Number Publication Date
JPH11209190A true JPH11209190A (en) 1999-08-03

Family

ID=11844651

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10013846A Withdrawn JPH11209190A (en) 1998-01-27 1998-01-27 Production of coated granular fertilizer

Country Status (1)

Country Link
JP (1) JPH11209190A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002028466A (en) * 2000-05-10 2002-01-29 Mitsubishi Chemicals Corp Granular particles treatment device and producing method for coated fertilizer
EP0976699A4 (en) * 1997-02-19 2009-06-03 Chisso Asahi Fertilizer Granular fertilizer coated with decomposable coating film and process for producing the same
CN103664363A (en) * 2013-11-29 2014-03-26 安徽六国化工股份有限公司 Compound fertilizer anti-caking agent supply device
WO2016007460A1 (en) * 2014-07-07 2016-01-14 The Mosaic Company Incorporation of biological agents in fertilizers
US10487016B2 (en) 2015-08-12 2019-11-26 The Mosaic Company Acid treatment for fertilizers to increase zinc solubility and availability
US10654759B2 (en) 2013-08-19 2020-05-19 The Mosaic Company System and methods for addition of beneficial agricultural, biological, and/or dedusting additives to granular fertilizers
CN113429243A (en) * 2021-07-19 2021-09-24 成都师范学院 Preparation method of multifunctional slow-release fertilizer

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0976699A4 (en) * 1997-02-19 2009-06-03 Chisso Asahi Fertilizer Granular fertilizer coated with decomposable coating film and process for producing the same
JP2002028466A (en) * 2000-05-10 2002-01-29 Mitsubishi Chemicals Corp Granular particles treatment device and producing method for coated fertilizer
US10654759B2 (en) 2013-08-19 2020-05-19 The Mosaic Company System and methods for addition of beneficial agricultural, biological, and/or dedusting additives to granular fertilizers
US11084762B2 (en) 2013-08-19 2021-08-10 The Mosaic Company System and methods for addition of beneficial agricultural, biological, and/or dedusting additives to granular fertilizers
CN103664363A (en) * 2013-11-29 2014-03-26 安徽六国化工股份有限公司 Compound fertilizer anti-caking agent supply device
WO2016007460A1 (en) * 2014-07-07 2016-01-14 The Mosaic Company Incorporation of biological agents in fertilizers
US10487016B2 (en) 2015-08-12 2019-11-26 The Mosaic Company Acid treatment for fertilizers to increase zinc solubility and availability
US11807587B2 (en) 2015-08-12 2023-11-07 The Mosaic Company, Inc. Acid treatment for fertilizers to increase zinc solubility and availability
CN113429243A (en) * 2021-07-19 2021-09-24 成都师范学院 Preparation method of multifunctional slow-release fertilizer

Similar Documents

Publication Publication Date Title
Naz et al. Slow release coating remedy for nitrogen loss from conventional urea: a review
EP1487761B1 (en) Method for producing a particulate urea-formaldehyde polymer as slow release nitrogen fertilizer
EP2170042B1 (en) Superabsorbent polymer suspension for use in agriculture
DE102004021384A1 (en) Process for the production of granules with improved storage stability and abrasion resistance
JPH11209190A (en) Production of coated granular fertilizer
Channab et al. Starch-based controlled release fertilizers: a review
JP2001072484A (en) Polymer-sulfur-polymer-type improved coated fertilizer and its formation
NZ248351A (en) Granular fertiliser having a coating comprising a powdered polysaccharide dispersed in a resin and exhibiting delayed and/or controlled release characteristics
WO2000066515A1 (en) Conditioned fertilizer product containing lactic acid derivative, method of manufacture and use thereof
US20210101848A1 (en) Core-shell composite particles and methods of making same
DE102005028016A1 (en) Coated controlled release fertilizer and process for its production
US20200269204A1 (en) Method and assembly for producing coated prills or granulates, prills obtained therewith, and use thereof
JP3467978B2 (en) Collapse type coated granular fertilizer
JP4050052B2 (en) Coated granular fertilizer
JP2002028466A (en) Granular particles treatment device and producing method for coated fertilizer
JP4804634B2 (en) Coated bioactive granular material subjected to anti-floating treatment and method for producing the same
CN112142525A (en) Slow release fertilizer
JP3399054B2 (en) Improved disintegration membrane-coated granular fertilizer
JP2642874B2 (en) Method for producing coated fertilizer and product thereof
JP2023009027A (en) coated granular fertilizer
JP2004075479A (en) Coated granular fertilizer
JPH09309783A (en) Improved soil collapse type coated granular fertilizer
WO1999018148A1 (en) Composition of powder-coated tacky material and method of making same
JPH11116371A (en) Granular agricultural and horticultural composition comprising degradable coating film
JPH11228272A (en) Production of coated granular fertilizer

Legal Events

Date Code Title Description
A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20040917

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20050208

A761 Written withdrawal of application

Free format text: JAPANESE INTERMEDIATE CODE: A761

Effective date: 20050413