JPH013093A - slow release coated fertilizer - Google Patents
slow release coated fertilizerInfo
- Publication number
- JPH013093A JPH013093A JP63-36523A JP3652388A JPH013093A JP H013093 A JPH013093 A JP H013093A JP 3652388 A JP3652388 A JP 3652388A JP H013093 A JPH013093 A JP H013093A
- Authority
- JP
- Japan
- Prior art keywords
- fertilizer
- coated
- resin
- film
- 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.)
- Pending
Links
- 239000003337 fertilizer Substances 0.000 title claims description 46
- 229920005989 resin Polymers 0.000 claims description 28
- 239000011347 resin Substances 0.000 claims description 28
- 230000009477 glass transition Effects 0.000 claims description 14
- 239000011248 coating agent Substances 0.000 description 28
- 238000000576 coating method Methods 0.000 description 28
- 239000000839 emulsion Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 10
- -1 Aliphatic diene Chemical class 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 239000003995 emulsifying agent Substances 0.000 description 8
- 238000013268 sustained release Methods 0.000 description 6
- 239000012730 sustained-release form Substances 0.000 description 6
- 238000010828 elution Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- GTELLNMUWNJXMQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCC(CO)(CO)CO GTELLNMUWNJXMQ-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008360 acrylonitriles Chemical class 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical class [H]C([*])=C([H])[H] 0.000 description 1
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
産業上の利用分野
本発明は緩効性被覆肥料を提供するものであり、肥料産
業の分野において有用である。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention provides a slow-release coated fertilizer, which is useful in the field of fertilizer industry.
従来技術
一般に化学肥料は速効性であり、長期にわたって肥効を
持続させることは困難である。また−度に大量の施肥を
行うと、農作物の塩類濃度障害および肥料の溶脱による
河川の汚染などのおそれがある。以上の点を改善する手
段として従来より種々の樹脂などで被覆した緩効性肥料
が提案されている。BACKGROUND OF THE INVENTION Chemical fertilizers are generally fast-acting, and it is difficult to maintain their effectiveness over a long period of time. Furthermore, if a large amount of fertilizer is applied at once, there is a risk of damage to the salt concentration of agricultural crops and pollution of rivers due to fertilizer leaching. As a means to improve the above points, slow-release fertilizers coated with various resins have been proposed.
緩効性被覆肥料を噴霧式による被覆方法で製造しようと
した場合、一般に次の被覆樹脂系が考えられる。When attempting to produce a slow-release coated fertilizer using a spray coating method, the following coating resin systems are generally considered.
(+) 有機溶剤で溶解した樹脂溶液(2)水溶性樹
脂の水溶液
(3) 1を脂の水性エマルション
発明が解決しようとする問題点
上記の樹脂系を用いて被覆肥料を製造する場合、種々の
問題点が存在している。(+) Resin solution dissolved in organic solvent (2) Aqueous solution of water-soluble resin (3) 1. Aqueous emulsion of fat Problems to be solved by the invention When producing coated fertilizer using the above resin system, there are various problems. There are problems with this.
(1)の場合は、有機溶剤を用いるため、[4費が高く
なる。また大気汚染や製造時における火災の−おそれも
ある。溶剤回収を行う場合には、その設備が必要となり
、設備費が大幅に増大する。In the case of (1), since an organic solvent is used, [4] costs increase. There is also the risk of air pollution and fire during manufacturing. In the case of solvent recovery, equipment is required, which significantly increases equipment costs.
(2)の場合は、樹脂が水溶性であるため、本質的に肥
効成分の溶出速度を緩め、遅効化するための保護膜とし
ての能力に限界がある。In the case of (2), since the resin is water-soluble, there is a limit to its ability as a protective film to essentially slow down the elution rate of the fertilizing ingredients and slow the effect.
(3)の場合は、(1)、(2)の問題点はないが、水
性エマルション系の被覆材料には次のような問題点が挙
げられる。In the case of (3), there are no problems like (1) and (2), but the following problems can be raised with aqueous emulsion-based coating materials.
■ 連続被膜の形成
樹脂の水性エマルションは水中に微細デ;樹、指の粒子
が分散状態で存在している。肥効成分の徐放性をつける
には、均一な膜で肥料を被覆することが必要である。こ
のため個々のエマルション粒子が融着し、連続被膜をう
まく作らなければなるない。■ Formation of a continuous film In the aqueous emulsion of resin, fine particles of resin exist in a dispersed state in water. In order to achieve sustained release of fertilizer components, it is necessary to cover the fertilizer with a uniform film. For this purpose, individual emulsion particles must be fused together to form a continuous coating.
■ 被覆肥料の固結
被覆膜のガラス転移温度が低いと温度や荷重がかかった
場合、たとえば夏場に肥料が袋積みされた状態などでは
、被覆肥料同志が被覆膜表面で融着を起こし、固結する
。■ If the glass transition temperature of the solidified coating film of the coated fertilizer is low, when temperature or load is applied, for example when fertilizers are piled up in bags in the summer, the coated fertilizers will fuse together on the surface of the coating film. , solidify.
問題点を解決するための手段
以上2つの問題点を解決すべく鋭意検討をした結果、樹
脂の水性エマルションを主成分とする被覆材より得られ
る樹脂膜が60℃以上のガラス転移温度を有すれば、そ
の樹脂膜で被覆された被覆肥料は、優れた肥効成分の徐
放性と肥料同志の耐固結性を示すことが明らかとなり、
本発明を完成するに至った。Means for Solving the Problems As a result of intensive studies to solve the above two problems, we found that the resin film obtained from the coating material whose main component is an aqueous emulsion of resin has a glass transition temperature of 60°C or higher. For example, it has been revealed that coated fertilizers coated with the resin film exhibit excellent sustained release of fertilizer components and anti-caking properties among fertilizers.
The present invention has now been completed.
ここで樹脂膜のガラス転移温度とは、実際に肥料に被覆
した場合に得られる被覆膜のガラス転移温度で、使用し
た(封脂自体の場合または樹脂と成膜助剤や可塑剤を含
んだ場合などを含む。Here, the glass transition temperature of the resin film is the glass transition temperature of the coating film obtained when it is actually coated on fertilizer. This includes cases where
以下本発明について詳細に説明する。The present invention will be explained in detail below.
本発明は樹脂の水性エマルションを主成分とした被覆材
料で被覆することによって得られる、60℃以上のガラ
ス転移温度を有する樹脂膜で被覆されてなる緩効性被覆
肥料を提供する。The present invention provides a slow-release coated fertilizer coated with a resin film having a glass transition temperature of 60° C. or higher, which is obtained by coating with a coating material containing an aqueous resin emulsion as a main component.
本発明の緩効性被覆肥料は一般に用いられる流動層式コ
ーティング装置、ドラム回転式コーティング装置などを
用い、固体肥料に被覆材料を噴霧することによって得ら
れる。The slow-release coated fertilizer of the present invention can be obtained by spraying the coating material onto a solid fertilizer using a commonly used fluidized bed coating device, rotary drum coating device, or the like.
本発明における樹脂のエマルションとしては、以下のよ
うなモノマーの1種または2種以上を重合させて得られ
る単独または共重合体の水性エマルション、さらには2
種以上の水性エマルションの混合物が用いられ、それに
よって得られる樹脂膜が、60℃以上のガラス転移温度
を有するものを用いることができる。The resin emulsion in the present invention includes an aqueous emulsion of a single or copolymer obtained by polymerizing one or more of the following monomers, and furthermore,
A mixture of more than one aqueous emulsion can be used, and the resulting resin film can have a glass transition temperature of 60° C. or higher.
1)スチレンで代表される芳香族ビニル化合物2)アク
リル酸、メタクリル酸、クロトン酸、フマール酸、イタ
コン酸などの不飽和カルボン酸、その塩中和物及びその
エステル。1) Aromatic vinyl compounds represented by styrene 2) Unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, fumaric acid, itaconic acid, neutralized salts thereof, and esters thereof.
3)グリンノルメタクリレート、2−ヒドロキシエチル
アクリレート及び2−ヒドロキシプロピルアクリレート
のような官能基をさらに含むアルコールの不飽和カルボ
ン酸エステル。3) Unsaturated carboxylic esters of alcohols further containing functional groups such as grinnor methacrylate, 2-hydroxyethyl acrylate and 2-hydroxypropyl acrylate.
4)酢酸ビニルで代表されるビニルカルボン酸エステル
。4) Vinyl carboxylic acid ester represented by vinyl acetate.
5)アクリロニトリルで代表されるビニルシアン化合物
。5) Vinyl cyanide compounds represented by acrylonitrile.
6)アクリルアミド、メタクリルアミドで代表されるビ
ニルアミド化合物。6) Vinylamide compounds represented by acrylamide and methacrylamide.
7)ブタジェンで代表される脂肪族ジエン。7) Aliphatic diene represented by butadiene.
8)エチレン、プロピレン、イソブチレンなどのオレフ
ィン化合物。8) Olefin compounds such as ethylene, propylene, and isobutylene.
9)塩化ビニル、塩化ビニリデンで代表されるハロゲン
置換ビニル化合物。9) Halogen-substituted vinyl compounds represented by vinyl chloride and vinylidene chloride.
10)ジビニルベンゼン、1.4−ブタンジオールジア
クリレート、トリメチロール、プロパントリアクリレー
トのようなジ及びトリビニル化合物。10) Di- and trivinyl compounds such as divinylbenzene, 1,4-butanediol diacrylate, trimethylol, propane triacrylate.
水性エマルションの製造に際し、重合開始剤としては過
硫酸塩などの熱分解開始剤、過硫酸塩−第一鉄系、過酸
化水素−第一鉄系のFenton試薬、過硫酸塩−チオ
硫酸ソーダ系、過硫酸塩−酸性亜硫酸ソーダ系、過酸化
水素−オキシカルボン酸系などのレドックス系開始剤な
どが使用できる。また乳化剤としては通常の高分子乳化
剤、低分子乳化剤を用いることができるが、とくに併用
した場合に良好な性能を示す。高分子乳化剤としては水
溶性アルキド樹脂などが、低分子乳化剤としては脂肪酸
塩類、高級アルコール硫酸エステル類、アルキルアリル
スルホン酸塩などのアニオン系乳化剤ポリオキシエチレ
ンアルキルエーテル類、ポリオキシエチレンアルキルフ
ェノールエーテル類、ポリオキシエチレンアルキルエス
テル頚などの7ニオン系乳化剤などを用いることができ
る。When producing an aqueous emulsion, polymerization initiators include thermal decomposition initiators such as persulfates, persulfate-ferrous, hydrogen peroxide-ferrous Fenton reagents, persulfate-sodium thiosulfate, etc. , persulfate-acidic sodium sulfite type, hydrogen peroxide-oxycarboxylic acid type, and other redox type initiators can be used. Further, as the emulsifier, ordinary polymer emulsifiers and low-molecular emulsifiers can be used, but they exhibit particularly good performance when used in combination. Polymer emulsifiers include water-soluble alkyd resins, low-molecular emulsifiers include fatty acid salts, higher alcohol sulfuric esters, anionic emulsifiers such as alkylaryl sulfonates, polyoxyethylene alkyl ethers, polyoxyethylene alkylphenol ethers, A 7-ion emulsifier such as polyoxyethylene alkyl ester can be used.
ガラス転移温度が60℃よりも低い樹脂膜で被覆された
肥料は固結しやすくなる。40℃以下のガラス転移温度
のものではさらに明確となり、室温で放置した場合でも
被覆肥料が固結するようになる。Fertilizer coated with a resin film with a glass transition temperature lower than 60°C tends to solidify. This becomes even clearer when the glass transition temperature is 40°C or lower, and the coated fertilizer becomes solidified even when left at room temperature.
被覆樹脂量は、肥料に対し、2〜15重量%が好ましい
。これよりも少ないと、十分な被覆効果が得られず、徐
放性は良くない。これよりも多すぎると、価格的に高(
なりまた被覆肥料中の被覆材の割合が多くなって実用的
ではない。The amount of coating resin is preferably 2 to 15% by weight based on the fertilizer. When the amount is less than this, sufficient coating effect cannot be obtained and sustained release properties are not good. If the amount is too high, the price will be high (
Also, the ratio of the coating material in the coated fertilizer increases, making it impractical.
なお、肥効成分の溶出率は、被覆率を変化させることに
よって調節することが可能である。また、樹脂の水性エ
マルションを構成するモノマーの種類を変えたり、2種
以上の樹脂の水性エマルンヨンの混合物の組合せを選択
することによって、肥効成分の溶出率を調整することが
可能である。Note that the elution rate of the fertilizing ingredients can be adjusted by changing the coverage rate. Furthermore, it is possible to adjust the elution rate of the fertilizing component by changing the type of monomer constituting the aqueous resin emulsion or by selecting a combination of a mixture of two or more resin aqueous emulsions.
被覆成膜過程において、必要に応じてエマルション粒子
の成膜性を向上させるために、成膜助材または可塑剤を
併用することもできる。In the coating film forming process, a film forming aid or a plasticizer may be used in combination, if necessary, in order to improve the film forming properties of the emulsion particles.
成膜助材または可塑剤としては、一般に用いられる成膜
助剤または可塑剤を用いることができるが、具体的には
、プチルカルビトーノペブチルセロソルブ、フェニルセ
ロソルブ、ジブチルフタレート、ジオクチルフタレート
、ブチルカルピトールアセテート、キ/レン、ペンジル
アルコーノペヘキシレンクリコーノペへキンルセロソル
ブ、2−エチルへキンルセロソルフ、オクチルセロソル
ブなどが挙げられる。As the film-forming aid or plasticizer, commonly used film-forming aids or plasticizers can be used, and specifically, butyl carbitonopebutyl cellosolve, phenyl cellosolve, dibutyl phthalate, dioctyl phthalate, butyl carpitol. Examples include acetate, xy/lene, pendylalconopehexylene criconopequinlucerosolve, 2-ethylhexylcellosolve, octylcellosolve, and the like.
成膜助剤および可塑剤の使用量については、用いる樹脂
の水性エマルションのガラス転移温度によって異なるが
、−船釣には(工(脂固形分に対し、2〜30重量%が
好ましい。少なすぎると成膜性の悪い樹脂では十分な連
続被膜の形成を促進できず、徐放性は改良されない。多
すぎると被着処理温度を下げ、被覆処理性が悪くなり、
できた被覆肥料は固結しやすくなる。さらに価格的にも
高くなり一般的ではない。The amount of film-forming aid and plasticizer used varies depending on the glass transition temperature of the aqueous emulsion of the resin used. A resin with poor film-forming properties will not be able to promote the formation of a continuous film and will not improve the sustained release properties.
The resulting coated fertilizer will solidify more easily. Furthermore, it is expensive and not common.
耐固結性の弱い被覆系については、アエロジル、タルク
などを用いてできた被覆肥料に粉まぶしをほどこすこと
によってかなりの固結防止を行うことができ、耐固結性
の弱い樹脂エマルションを用いる場合には効果的である
。For coating systems with low caking resistance, significant caking prevention can be achieved by dusting coated fertilizers made with Aerosil, talc, etc., and using resin emulsions with low caking resistance. It is effective when used.
実施例および比較例で具体的に用いる樹脂の水性エマル
ションの組成を第1表に例示する。Table 1 illustrates the composition of the aqueous resin emulsion specifically used in the Examples and Comparative Examples.
第 1 表 水性エマルンヨンの調製は下記のとおり行う。Chapter 1 Table The aqueous emulsion is prepared as follows.
乳化剤と水を反応器に仕込み、撹拌する。80℃まで昇
温し、初めにモノマーの10%量を添加する。次に、重
合開始剤の水溶液の90%量を添加する。しばらくして
残りのモノマーの滴下を始める。約3時間で滴下を終了
し残りの重合開始剤を加えて熟成を1時間行う。反応温
度は約80℃で一定に保つ。反応終了後冷却しアンモニ
ア水で中和し、−布で濾過を行う。Charge the emulsifier and water into a reactor and stir. The temperature is raised to 80° C. and 10% of the monomer is initially added. Next, 90% of the aqueous solution of polymerization initiator is added. After a while, start dropping the remaining monomer. The dropwise addition was completed in about 3 hours, the remaining polymerization initiator was added, and the mixture was aged for 1 hour. The reaction temperature is kept constant at about 80°C. After the reaction is completed, the mixture is cooled, neutralized with aqueous ammonia, and filtered through cloth.
なお、樹脂膜のガラス転移温度は、実施例で製造した被
覆肥料からけずりとった被覆膜をDSC測定装置:セイ
コー電子■製を用いて昇温速度lO℃/分の条件で測定
し求めたものである。The glass transition temperature of the resin film was determined by measuring the coating film scraped from the coated fertilizer produced in the example using a DSC measurement device: Seiko Electronics at a temperature increase rate of 10°C/min. It is something.
ガラス転移点は第3図のチャートの矢印で示す部位の値
を採用した。For the glass transition point, the value at the location indicated by the arrow in the chart in FIG. 3 was adopted.
本発明方法は、粉状、粒状、頚粒状など種々の固型肥料
に利用することができるが、粒状の肥料にとくに好適に
利用できる。粒状肥料としては燐硝安加里1号〈旭化成
工業社製)、塩加燐安1号、高度化成肥料777号(日
本化学社製)、KH12−8−10(協和発酵工業社製
)などが例示される。The method of the present invention can be used for various solid fertilizers such as powder, granules, and granular fertilizers, but is particularly suitable for granular fertilizers. Examples of granular fertilizers include Phosphorous Ankari No. 1 (manufactured by Asahi Kasei Kogyo Co., Ltd.), Shioka Rinyan No. 1, Advanced Chemical Fertilizer No. 777 (manufactured by Nippon Kagaku Co., Ltd.), and KH12-8-10 (manufactured by Kyowa Hakko Kogyo Co., Ltd.). be done.
実施例においてはKHII−8−10を用いた。In the examples, KHII-8-10 was used.
実施例において第1図に示すコーティング装置を用い、
被覆肥料を製造した。In the examples, a coating apparatus shown in FIG. 1 was used,
A coated fertilizer was produced.
以下に本発明の実施例および比較例を示す。Examples and comparative examples of the present invention are shown below.
実施例1
成膜助剤;オクチルセロソルブ 14重量部水
28重量部の被
覆材を粒状肥料500重量部に約80℃で被覆した。Example 1 Film-forming aid; octyl cellosolve 14 parts by weight water
28 parts by weight of the coating material was applied to 500 parts by weight of granular fertilizer at about 80°C.
実施例2
成膜助剤:へキンルセロソルブ 7 tflfm水
35重
量部の被覆材を粒状肥料500重量部に約75℃で被覆
した。Example 2 Film-forming aid: Hekinlucerosolve 7 tflfm water 35 parts by weight of the coating material was coated on 500 parts by weight of granular fertilizer at about 75°C.
実施例3
成膜助剤ニブチルカルピトール 14重量部水
28重量部の被覆材を粒状肥
料500重量部に約80℃で被覆した。Example 3 Film-forming aid Nibutylcarpitol 14 parts by weight Water
28 parts by weight of the coating material was applied to 500 parts by weight of granular fertilizer at about 80°C.
比較例1
水 42重量部の被覆材
を粒状肥料500重量部に約43℃で被1した。Comparative Example 1 500 parts by weight of granular fertilizer was coated with 42 parts by weight of water at about 43°C.
比較例2
水 42
重N部の被覆材を粒状肥料500重量部に約35℃で被
覆した。Comparative example 2 water 42
500 parts by weight of the granular fertilizer was coated with the heavy nitrogen coating material at about 35°C.
実施例1〜3のものは40℃で荷重250g/c11の
条件でも被覆肥料に変化はなかったが、比較例のもので
は条件で激しい固結を生じた。In Examples 1 to 3, there was no change in the coated fertilizer even under the conditions of 40°C and a load of 250 g/c11, but in the comparative example, severe caking occurred under the conditions.
徐放性について第2図に示す。第2図は実施例により得
られた被覆肥料Logを水温30℃の水20 Qmlへ
浸漬した時のアンモニア窒素の溶出率である。The sustained release properties are shown in Figure 2. FIG. 2 shows the elution rate of ammonia nitrogen when the coated fertilizer Log obtained in the example was immersed in 20 Qml of water at a water temperature of 30°C.
発明の効果
本発明により樹脂皮膜が60℃以上のガラス転 1移
温度を有する、各種樹脂の水性エマル/コンを主成分と
する被覆材料で固体肥料を被覆することで、水性エマル
ンヨン系にて優れた徐放性と耐固結性を有する緩効性被
覆肥料を得ることができる。Effects of the Invention According to the present invention, by coating a solid fertilizer with a coating material whose main component is an aqueous emul/con of various resins, the resin film has a glass transition temperature of 60°C or higher, and is excellent in aqueous emulsion systems. A slow-release coated fertilizer having sustained release properties and caking resistance can be obtained.
また被覆処理は特別な方法を必要とせず製造が非常に簡
単であり、溶剤類をほとんど使用しないので災害、公害
の心配性もない。さらに被覆肥料の外観にはつやがあり
、見た目も非常に美しく商品価値は高い。In addition, the coating treatment does not require any special method and is very easy to manufacture, and almost no solvents are used, so there is no risk of disaster or pollution. Furthermore, the coated fertilizer has a glossy appearance and is very beautiful and has high commercial value.
第1図は実施例、比較例において用いた流動層式コーテ
ィング装置の略図である。
第2図は実施例、比較例において作製した被覆肥料の溶
出率を示す。図中実−1〜3、比−1゜2は実施例1〜
3、比較例1および2をそれぞれ示す。
第3図は被覆膜のガラス転移温度の変化を示すチャート
である。
与許出願人 (102)協和醗酵工業株式会社第1図
第2図
擾濱日数(θ)FIG. 1 is a schematic diagram of a fluidized bed coating apparatus used in Examples and Comparative Examples. FIG. 2 shows the elution rate of coated fertilizers produced in Examples and Comparative Examples. Figures -1 to 3, ratio -1゜2 are examples 1 to 3.
3, Comparative Examples 1 and 2 are shown, respectively. FIG. 3 is a chart showing changes in the glass transition temperature of the coating film. Grant applicant (102) Kyowa Hakko Kogyo Co., Ltd. Figure 1 Figure 2 Number of days at sea (θ)
Claims (1)
てなる緩効性被覆肥料。A slow-release coated fertilizer coated with a resin film having a glass transition temperature of 60°C or higher.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63036523A JPS643093A (en) | 1987-02-19 | 1988-02-19 | Controlled release coated fertilizer |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3680787 | 1987-02-19 | ||
| JP62-36807 | 1987-02-19 | ||
| JP63036523A JPS643093A (en) | 1987-02-19 | 1988-02-19 | Controlled release coated fertilizer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH013093A true JPH013093A (en) | 1989-01-06 |
| JPS643093A JPS643093A (en) | 1989-01-06 |
Family
ID=26375578
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63036523A Pending JPS643093A (en) | 1987-02-19 | 1988-02-19 | Controlled release coated fertilizer |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS643093A (en) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS528795B2 (en) * | 1971-12-30 | 1977-03-11 | ||
| US3816331A (en) * | 1972-07-05 | 1974-06-11 | Ncr | Continuous encapsulation and device therefor |
| JPS54109078A (en) * | 1978-02-15 | 1979-08-27 | Norio Tanaka | Photoocollapsible microcapsule |
-
1988
- 1988-02-19 JP JP63036523A patent/JPS643093A/en active Pending
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