JP5144100B2 - Beast repellent - Google Patents
Beast repellent Download PDFInfo
- Publication number
- JP5144100B2 JP5144100B2 JP2007088048A JP2007088048A JP5144100B2 JP 5144100 B2 JP5144100 B2 JP 5144100B2 JP 2007088048 A JP2007088048 A JP 2007088048A JP 2007088048 A JP2007088048 A JP 2007088048A JP 5144100 B2 JP5144100 B2 JP 5144100B2
- Authority
- JP
- Japan
- Prior art keywords
- animal repellent
- repellent
- resin
- biodegradable
- animal
- 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 - Fee Related
Links
- 239000005871 repellent Substances 0.000 title claims description 82
- 230000002940 repellent Effects 0.000 title claims description 82
- 241001465754 Metazoa Species 0.000 claims description 56
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- 239000011347 resin Substances 0.000 claims description 34
- 239000004014 plasticizer Substances 0.000 claims description 33
- 229920000747 poly(lactic acid) Polymers 0.000 claims description 25
- 239000004626 polylactic acid Substances 0.000 claims description 25
- 239000000126 substance Substances 0.000 claims description 20
- 239000007788 liquid Substances 0.000 claims description 14
- 239000002609 medium Substances 0.000 claims description 12
- 229920000229 biodegradable polyester Polymers 0.000 claims description 11
- 239000004622 biodegradable polyester Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
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- 239000000203 mixture Substances 0.000 claims description 8
- 239000012736 aqueous medium Substances 0.000 claims description 6
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims description 6
- 235000021419 vinegar Nutrition 0.000 claims description 6
- 239000000052 vinegar Substances 0.000 claims description 6
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- 235000017663 capsaicin Nutrition 0.000 claims description 5
- 239000002023 wood Substances 0.000 claims description 4
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 3
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 29
- 238000000576 coating method Methods 0.000 description 22
- 239000011248 coating agent Substances 0.000 description 21
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- 239000011230 binding agent Substances 0.000 description 4
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- 238000002156 mixing Methods 0.000 description 4
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- 239000002245 particle Substances 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
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- 239000002904 solvent Substances 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 3
- 239000013585 weight reducing agent Substances 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
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Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は、山林の樹木を傷つけ、倒すなど有害な獣に対する忌避剤およびその使用方法に関する。 The present invention relates to a repellent against harmful beasts such as damaging and defeating forest trees and a method of using the same.
近年、野生鹿によって枝葉を食べられたり、鹿や熊などにより幹の皮を剥がれて木が枯れるという被害が増え、林業に与える影響は、非常に大きなものとなっている。それだけでなく、鹿が木の実、稚樹、幼樹を食べるために新たな樹木が育たずに森林全体が枯れてしまうという問題に発展し、さらに深刻化している。 In recent years, wild deer has eaten branches and leaves, and deer and bears have peeled off the trunk and the trees have withered, increasing the impact on forestry. Not only that, but the deer has developed a problem that the whole forest will die without growing new trees because it eats nuts, seedlings and young trees, and it is getting more serious.
有害な鳥獣による被害を防ぐ方法として、特許文献1のような動物忌避組成物および動物忌避スプレー、特許文献2のような鳥獣忌避ネット、特許文献3のような食害防御用保護材、特許文献4および特許文献5のような動物忌避塗料が提案されている。 As methods for preventing damage caused by harmful birds and beasts, animal repellent compositions and animal repellent sprays as in Patent Document 1, bird and animal repellent nets as in Patent Document 2, protective materials for food damage protection as in Patent Document 3, and Patent Document 4 In addition, animal repellent paints such as Patent Document 5 have been proposed.
しかし、特許文献1のような動物忌避組成物は、カプサイシンのような動物忌避成分をマイクロカプセルに内包したものを散布あるいはスプレーとして使用しているが、バインダーとなるものを含んでいないため十分に固着することができず、散布された動物忌避組成物が風により飛ばされたり、雨で流される可能性があり、持続的な忌避効果は期待できない。特許文献2のような鳥獣忌避ネットおよび特許文献3のような食害防御用保護材は、ひとつひとつの樹木に対してネットを設置する必要があり、多くの労力を要するため、高齢化の進んだ林業人口にとって作業上の負担が非常に大きいという問題点がある。特許文献4および特許文献5のような動物忌避塗料は、バインダーとして、塩化ビニル系、アクリル系、ウレタン系の重合体を使用することにより、持続的な効果が得られ、作業上の負担を軽減するものであるが、忌避効果が薄れた後も塗工した部分に合成樹脂が残留することで、植物や環境に負担を与えかねないといった欠点があった。
本発明は、上記の問題点を解決し、作業上の負担が小さく簡単に使用でき、獣による被害を防止する効果が持続的に得られ、植物への悪影響や土壌汚染などの問題も回避できる獣忌避剤を提供することを目的とする。 The present invention solves the above-mentioned problems, can be used easily with a small work burden, can continuously obtain the effect of preventing damage caused by beasts, and can also avoid problems such as adverse effects on plants and soil contamination. The aim is to provide a beast repellent.
本発明者らは、上記課題を解決するために鋭意検討した結果、本発明に達した。 The inventors of the present invention have reached the present invention as a result of intensive studies to solve the above problems.
本発明の要旨は、次の通りである。
(1)生分解性ポリエステル樹脂、獣忌避性を有する物質、可塑剤および液状媒体よりなり、液状であることを特徴とする獣忌避剤。
(2)生分解性ポリエステル樹脂がポリ乳酸系樹脂であることを特徴とする(1)記載の獣忌避剤。
(3)可塑剤が生分解性であることを特徴とする(1)または(2)記載の獣忌避剤。
(4)獣忌避性を有する物質がカプサイシン、メンソール、リモネン、木酢液、竹酢液、辛子から選ばれる少なくとも一種類であることを特徴とする(1)から(3)のいずれかに記載の獣忌避剤。
(5)液状媒体が水または水性媒体であることを特徴とする(1)から(4)のいずれかに記載の獣忌避剤。
(6)(1)から(5)のいずれかに記載の獣忌避剤より液状媒体を除去してなる獣忌避組成物。
The gist of the present invention is as follows.
(1) biodegradable polyester resin, a substance having a beast repellency, Ri name from plasticizers and liquid medium, beast repellents, which is a liquid.
(2) The animal repellent according to (1), wherein the biodegradable polyester resin is a polylactic acid resin.
(3) The animal repellent according to (1) or (2 ), wherein the plasticizer is biodegradable .
(4) The substance according to any one of (1) to (3), wherein the substance having animal repellent properties is at least one selected from capsaicin, menthol, limonene, wood vinegar, bamboo vinegar, and hot pepper Beast repellent.
(5) The animal repellent according to any one of (1) to (4), wherein the liquid medium is water or an aqueous medium .
(6) An animal repellent composition obtained by removing a liquid medium from the animal repellent according to any one of (1) to (5) .
本発明の獣忌避剤は、保護しようとする樹木等の周辺に散布、あるいは樹木そのものに直接塗工すればよいため、使用に際して大きな労力を要しない。 The veterinary repellent of the present invention only needs to be sprayed around the trees to be protected, or directly applied to the trees themselves.
本発明の獣忌避剤は、生分解性樹脂をバインダーとして、塗工した箇所に製膜するため、獣忌避性を有する物質が風で飛ばされたり、雨によって流されにくく、長期にわたって忌避効果を得ることができる。また、可塑剤を配合することにより、柔軟性、造膜性および接着性が向上し、さらなる持続性が期待できる。 The animal repellent of the present invention forms a film at a coated site using a biodegradable resin as a binder, so that a substance having animal repellent properties is not easily blown away by wind or rain, and has a long-term repellent effect. Can be obtained. Further, by blending a plasticizer, flexibility, film-forming property and adhesiveness are improved, and further sustainability can be expected.
本発明の獣忌避剤には、生分解性の樹脂および忌避成分が用いられるため、獣忌避剤を散布または塗工後長期間放置しておいたとしても、微生物等により分解されるので地球環境への影響が小さい。 Since the biodegradable resin and the repellent component are used for the animal repellent of the present invention, even if it is left for a long time after spraying or coating the animal repellent, it is decomposed by microorganisms etc. The impact on is small.
以下、本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail.
本発明における生分解性樹脂としては、生分解性ポリエステル樹脂、ポリビニルアルコール、でん粉、キトサン等の多糖類、ゼラチン等のたんぱく質、ポリリンゴ酸、ポリグルタミン酸、ポリアスパラギン酸などが挙げられる。生分解性樹脂の種類は限定されないが、一般的に優れた耐水性を有している生分解性ポリエステル樹脂が好ましい。生分解性ポリエステル樹脂としては、ポリ乳酸(L型、D型)、ポリグリコール酸、ポリ−3−ヒドロキシ酪酸、ポリ−4−ヒドロキシ酪酸、ポリ−4−ヒドロキシ吉草酸、ポリ−5−ヒドロキシ吉草酸、ポリ−ε−カプロラクトン、ポリ−γ−プロピオラクトン等のヒドロキシアルカノエート単位からなる脂肪族ポリエステルや、ポリエチレンサクシネート、ポリブチレンサクシネート、ポリブチレンアジペートなどの炭素4〜12の脂肪族ジカルボン酸成分と炭素数2〜12の脂肪族ジオール成分とからなる脂肪族ポリエステル、又はこれらの共重合体のほか、前記脂肪族ポリエステルに生分解性を損なわない範囲でテレフタル酸などの芳香族ジカルボン酸成分を共重合した、ポリ(エチレンジアジペート/テレフタレート)、ポリ(ブチレンアジペート/テレフタレート)などが挙げられる。上記のポリエステルは単独で用いてもよいし、2種類以上の共重合体または混合物でもよい。中でも、更なる環境への配慮から、石油原料に頼らずしかも廃棄時の環境負荷が小さい植物由来であるポリ乳酸または乳酸と他の化合物とを共重合したコポリマー、もしくはこれらの混合物であるポリ乳酸系樹脂が特に好ましい。 Examples of biodegradable resins in the present invention include biodegradable polyester resins, polysaccharides such as polyvinyl alcohol, starch and chitosan, proteins such as gelatin, polymalic acid, polyglutamic acid, and polyaspartic acid. Although the kind of biodegradable resin is not limited, generally a biodegradable polyester resin having excellent water resistance is preferred. Examples of biodegradable polyester resins include polylactic acid (L-type and D-type), polyglycolic acid, poly-3-hydroxybutyric acid, poly-4-hydroxybutyric acid, poly-4-hydroxyvaleric acid, and poly-5-hydroxyvalid. Aliphatic polyesters composed of hydroxyalkanoate units such as herbic acid, poly- [epsilon] -caprolactone, poly- [gamma] -propiolactone, and aliphatic dicarboxylic acids having 4 to 12 carbon atoms such as polyethylene succinate, polybutylene succinate, polybutylene adipate In addition to an aliphatic polyester comprising an acid component and an aliphatic diol component having 2 to 12 carbon atoms, or a copolymer thereof, an aromatic dicarboxylic acid such as terephthalic acid as long as the biodegradability of the aliphatic polyester is not impaired. Poly (ethylene diadipate / terephthalate), poly (butyrate), copolymerized components Ren adipate / terephthalate) and the like. Said polyester may be used independently and 2 or more types of copolymers or mixtures may be sufficient as it. Above all, for further environmental considerations, polylactic acid derived from plants that does not rely on petroleum raw materials and has a low environmental impact during disposal, or a copolymer obtained by copolymerizing lactic acid and other compounds, or polylactic acid that is a mixture of these. A resin is particularly preferred.
ポリ乳酸系樹脂は、従来公知の方法で合成することができ、合成法は特に限定されないが、例えば、ポリ乳酸の場合、L−乳酸、D−乳酸、DL−乳酸を直接脱水重縮合する方法や、乳酸の環状2量体であるラクチドを開環重合する方法があげられる。また、市販されているものを用いてもよい。 The polylactic acid resin can be synthesized by a conventionally known method, and the synthesis method is not particularly limited. For example, in the case of polylactic acid, L-lactic acid, D-lactic acid, and DL-lactic acid are directly subjected to dehydration polycondensation. And a method of ring-opening polymerization of lactide, which is a cyclic dimer of lactic acid. Moreover, you may use what is marketed.
本発明における獣忌避性を有する物質としては、発する臭いによって獣が刺激を受けたり、獣がくわえたり、かじる際に刺激を与える物質が使用できる。例えば、天然植物由来の物質としては、カプサイシン、メンソール、リモネン、クレオソート、クジン、ウルシ類由来フェノール、ナリンギン、木酢液、竹酢液、辛子など、合成物質としては、グリコールエーテル類、サリチル酸メチル、ナフタレン、含硫テルペン類、ポリブテン、ルバフラン、安息香酸デナトリウム、2−ブトキシメタノールなどが挙げられ、天然植物由来のものが、地球環境への影響が小さく好ましい。なかでも、カプサイシンは辛味が強く、よい忌避効果が期待でき、好ましい。 As the substance having the animal repellent property in the present invention, a substance that gives irritation when the animal is stimulated by the smell it emits, or when the animal is biting or biting can be used. For example, natural plant-derived substances include capsaicin, menthol, limonene, creosote, kudin, urushi-derived phenol, naringin, wood vinegar, bamboo vinegar, and hot pepper, and synthetic substances include glycol ethers, methyl salicylate, Naphthalene, sulfur-containing terpenes, polybutene, rubafuran, desodium benzoate, 2-butoxymethanol and the like can be mentioned, and those derived from natural plants are preferable because they have little influence on the global environment. Among them, capsaicin is preferable because it has a strong pungency and can be expected to have a good repellent effect.
これらの獣忌避性を有する物質は単独で使用してもよく、2種類以上を併用してもよい。 These substances having animal repellent properties may be used alone or in combination of two or more.
これらの獣忌避性を有する物質の配合割合は、特に限定されないが、生分解性樹脂100質量部に対して、0.1〜100質量部、好ましくは1〜30質量部、3〜20質量部であることが、特に好ましい。生分解性樹脂に対する獣忌避性を有する物質の割合が少ない場合、獣忌避効果が不十分であり、逆に多すぎた場合、コストアップとなるだけでなく、塗剤の保存安定性が低下するうえ、形成される塗膜に十分な耐久性がなく、長期的な効果が得られない可能性がある。 The blending ratio of these substances having animal repellent properties is not particularly limited, but is 0.1 to 100 parts by weight, preferably 1 to 30 parts by weight, and 3 to 20 parts by weight with respect to 100 parts by weight of the biodegradable resin. It is particularly preferred that When the ratio of the substance having the animal repellent property to the biodegradable resin is small, the animal repellent effect is insufficient. On the other hand, when it is too much, not only the cost is increased, but also the storage stability of the coating is lowered. In addition, the formed coating film does not have sufficient durability, and long-term effects may not be obtained.
忌避効果の長期持続性の観点から、獣忌避性を有する物質は、マイクロカプセル化されていることが好ましい。獣忌避性を有する物質がマイクロカプセル粒子内に内包されている場合、外力等が加わることにより、マイクロカプセル粒子内の忌避性を有する物質を放出することができる。具体的には、獣の接触、鹿や熊の剥皮行為などにより外力がかかることにより、マイクロカプセル粒子内の忌避成分が放出され、獣忌避効果を発揮し、獣による外力がかからない場合には、忌避性を有する物質の放出が抑制されるので、より効果的かつ持続的な獣忌避効果を得ることができる。 From the viewpoint of long-term persistence of the repellent effect, the substance having beast repellent properties is preferably microencapsulated. When a substance having animal repellent properties is encapsulated in the microcapsule particles, the substance having repellent properties in the microcapsule particles can be released by applying an external force or the like. Specifically, when an external force is applied due to beast contact, deer or bear skinning, etc., the repellent component in the microcapsule particles is released, exerting the beast repellent effect, and when the external force is not applied by the beast, Since the release of substances having repellent properties is suppressed, a more effective and lasting animal repellent effect can be obtained.
獣忌避性を有する物質を内包するマイクロカプセルを作る方法は特に限定されるものではなく、コアソルベーション法、界面重合法、in site法等、従来公知の方法を用いることができる。 A method for producing a microcapsule enclosing a substance having animal repellent properties is not particularly limited, and a conventionally known method such as a core solvation method, an interfacial polymerization method, or an in situ method can be used.
本発明において使用される液状媒体としては特に限定されず、有機溶剤であってもよいし、水または水と親水性溶媒の混合物であってもよい。有機溶剤としては、ジエチルケトン(3−ペンタノン)、メチルプロピルケトン(2−ペンタノン)、メチルイソブチルケトン(4−メチル−2−ペンタノン)、2−ヘキサノン、5−メチル−2−ヘキサノン、2−へプタノン、3−へプタノン、4−へプタノン、シクロペンタノン、シクロヘキサノン等のケトン類、トルエン、キシレン、ベンゼン、ソルベッソ100、ソルベッソ150等の芳香族炭化水素類、ブタン、ペンタン、ヘキサン、シクロヘキサン、ヘプタン、オクタン、ノナン等の脂肪族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素、1,2−ジクロロエタン、1,1,2,2−テトラクロロエタン、クロロベンゼン、o−ジクロロベンゼン、m−ジクロロベンゼン、p−ジクロロベンゼン等の含ハロゲン類、酢酸エチル、酢酸イソプロピル、酢酸−n−ブチル、酢酸イソブチル、酢酸−sec−ブチル、酢酸−3−メトキシブチル、プロピオン酸メチル、プロピオン酸エチル、炭酸ジエチル、γ―ブチロラクトン、イソホロン等のエステル類、加えて後述の親水性の有機溶剤などが挙げられる。 The liquid medium used in the present invention is not particularly limited, and may be an organic solvent or water or a mixture of water and a hydrophilic solvent. Examples of organic solvents include diethyl ketone (3-pentanone), methyl propyl ketone (2-pentanone), methyl isobutyl ketone (4-methyl-2-pentanone), 2-hexanone, 5-methyl-2-hexanone, and 2-to. Ketones such as butanone, 3-heptanone, 4-heptanone, cyclopentanone, cyclohexanone, aromatic hydrocarbons such as toluene, xylene, benzene, Solvesso 100, Solvesso 150, butane, pentane, hexane, cyclohexane, heptane Aliphatic hydrocarbons such as octane and nonane, methylene chloride, chloroform, carbon tetrachloride, 1,2-dichloroethane, 1,1,2,2-tetrachloroethane, chlorobenzene, o-dichlorobenzene, m-dichlorobenzene, Halogen-containing compounds such as p-dichlorobenzene, acetic acid Esters such as chill, isopropyl acetate, n-butyl acetate, isobutyl acetate, sec-butyl acetate, 3-methoxybutyl acetate, methyl propionate, ethyl propionate, diethyl carbonate, γ-butyrolactone, isophorone, etc. Examples include hydrophilic organic solvents described below.
さらに、液状媒体としては、環境保護、省資源、消防法等による危険物規制、職場環境改善等の観点から、水性媒体の使用が好ましい。水性媒体とは水を主成分とする液体からなる媒体である。水以外の溶媒を混合する場合には、親水性の有機溶剤を用いることが好ましい。親水性の有機溶剤の具体例としては、メタノール、エタノール、n−プロパノール、イソプロパノール、n−ブタノール、イソブタノール、sec−ブタノール、tert−ブタノール、n−アミルアルコール、イソアミルアルコール、sec−アミルアルコール、tert−アミルアルコール、1−エチル−1−プロパノール、2−メチル−1−ブタノール、n−ヘキサノール、シクロヘキサノール、エチレングリコールモノメチルエーテル、エチレングリコールモノエチルエーテル、エチレングリコールモノプロピルエーテル、エチレングリコールモノブチルエーテル等のアルコール類、テトラヒドロフラン、1,4−ジオキサン等のエーテル類、アセトン、メチルエチルケトン等のケトン類、酢酸メチル、酢酸−n−プロピル、酢酸イソプロピル、酢酸−tert−ブチル、プロピオン酸メチル、プロピオン酸エチル、炭酸ジメチル等のエステル類、ジメチルホルムアミド、ジメチルアセトアミド、ジアセトンアルコール、アセトニトリル、そのほか、アンモニアを含む、ジエチルアミン、トリエチルアミン、ジエタノールアミン、トリエタノールアミン、N,N−ジメチルエタノールアミン、N,N−ジエチルエタノールアミン、N−ジエタノールアミン、3−メトキシプロピルアミン、3−ジエチルアミノプロピルアミン、ジメチルアミノプロピルアミン等の有機アミン化合物等を挙げることができる。 Furthermore, as the liquid medium, it is preferable to use an aqueous medium from the viewpoints of environmental protection, resource saving, dangerous goods regulations by the Fire Service Act, etc., workplace environment improvement, and the like. An aqueous medium is a medium composed of a liquid mainly composed of water. When a solvent other than water is mixed, it is preferable to use a hydrophilic organic solvent. Specific examples of the hydrophilic organic solvent include methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol, tert-butanol, n-amyl alcohol, isoamyl alcohol, sec-amyl alcohol, tert. -Amyl alcohol, 1-ethyl-1-propanol, 2-methyl-1-butanol, n-hexanol, cyclohexanol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, etc. Alcohols, ethers such as tetrahydrofuran and 1,4-dioxane, ketones such as acetone and methyl ethyl ketone, methyl acetate, acetic acid-n-propyl, ethyl acetate Esters such as propyl, acetic acid-tert-butyl, methyl propionate, ethyl propionate, dimethyl carbonate, dimethylformamide, dimethylacetamide, diacetone alcohol, acetonitrile, other ammonia, diethylamine, triethylamine, diethanolamine, triethanolamine And organic amine compounds such as N, N-dimethylethanolamine, N, N-diethylethanolamine, N-diethanolamine, 3-methoxypropylamine, 3-diethylaminopropylamine, and dimethylaminopropylamine.
液状媒体中に生分解性樹脂が含有された状態としては、生分解性樹脂が液状媒体に溶解している状態、微粒子として液状媒体に分散している状態が挙げられ、生分解性樹脂、液状媒体の組み合わせにより、いずれの状態をとっていてもよいが、保存安定性、取り扱いの容易さ、環境保護などの理由から、特に、生分解性樹脂が水または水性媒体に微粒子として分散した、いわゆる水性分散体の状態が好ましい。 Examples of the state in which the biodegradable resin is contained in the liquid medium include a state in which the biodegradable resin is dissolved in the liquid medium and a state in which the biodegradable resin is dispersed in the liquid medium as fine particles. Depending on the combination of media, any state may be taken, but for reasons of storage stability, ease of handling, environmental protection, etc., the biodegradable resin is dispersed as fine particles in water or an aqueous medium, in particular. An aqueous dispersion state is preferred.
生分解性樹脂を水性媒体に分散させる方法は特に限定されず、転相乳化法、強制乳化法などが挙げられ、例えば、密閉可能な容器に生分解性樹脂、塩基性化合物、親水性の有機溶剤などの原料を投入し、次いで、槽内の温度を45〜200℃、好ましくは60〜150℃、さらに好ましくは80〜120℃の温度に保ちつつ、好ましくは粗大粒子が無くなるまで、5〜120分間程度攪拌を続けることにより生分解性樹脂を十分に分散化させ、その後、好ましくは攪拌下で40℃以下に冷却することにより、分散体を得ることができる。槽内の温度が45℃未満の場合は、生分解性樹脂の分散化が困難になる。槽内の温度が200℃を超える反応は不経済なので好ましくない。 A method for dispersing the biodegradable resin in the aqueous medium is not particularly limited, and examples thereof include a phase inversion emulsification method and a forced emulsification method. Raw materials such as a solvent are charged, and then the temperature in the tank is maintained at 45 to 200 ° C., preferably 60 to 150 ° C., more preferably 80 to 120 ° C., and preferably 5 to 5 until coarse particles disappear. By continuously stirring for about 120 minutes, the biodegradable resin is sufficiently dispersed, and then preferably cooled to 40 ° C. or lower with stirring to obtain a dispersion. When the temperature in the tank is lower than 45 ° C., it becomes difficult to disperse the biodegradable resin. Reaction in which the temperature in the tank exceeds 200 ° C. is not preferable because it is uneconomical.
本発明で用いられる生分解性樹脂分散体としては、市販されているものを使用してもよく、例えば、ユニチカ株式会社製LAEシリーズ、第一工業製薬株式会社製プラセマシリーズやミヨシ油脂株式会社製ランディPLシリーズなどのポリ乳酸系樹脂分散体、昭和高分子株式会社製EMシリーズなどの生分解性脂肪族ポリエステル樹脂分散体があげられる。 As the biodegradable resin dispersion used in the present invention, commercially available products may be used. For example, the LAE series manufactured by Unitika Ltd., the Prasema series manufactured by Daiichi Kogyo Seiyaku Co., Ltd., and Miyoshi Oil & Fat Co., Ltd. Examples thereof include polylactic acid resin dispersions such as Randy PL series manufactured by Biotechnology, and biodegradable aliphatic polyester resin dispersions such as EM series manufactured by Showa Polymer Co., Ltd.
本発明の獣忌避剤には、柔軟性、造膜性および接着性を向上させるために可塑剤を配合することができる。特にポリ乳酸系樹脂を使用した場合には、獣忌避剤の忌避効果が長期持続するため、可塑剤を配合することが望ましい。可塑剤の配合割合は、生分解性樹脂100質量部に対して1〜100質量部の範囲であることが好ましく、3〜50質量部の範囲であることがより好ましく、5〜30質量部の範囲であることが特に好ましい。配合量が1質量部未満であると添加効果が小さく、塗膜が剛直になり、塗膜がもろいため、はがれやすくなってしまう恐れがあり、100質量部を超えると耐ブロッキング性や塗膜の耐水性が低下する傾向にある。 In the animal repellent of the present invention, a plasticizer can be blended in order to improve flexibility, film-forming property and adhesiveness. In particular, when a polylactic acid resin is used, it is desirable to add a plasticizer because the repellent effect of the animal repellent lasts for a long time. The blending ratio of the plasticizer is preferably in the range of 1 to 100 parts by weight, more preferably in the range of 3 to 50 parts by weight, and 5 to 30 parts by weight with respect to 100 parts by weight of the biodegradable resin. A range is particularly preferred. If the blending amount is less than 1 part by mass, the effect of addition is small, the coating film becomes stiff, and the coating film becomes brittle, so that it may be easily peeled off. Water resistance tends to decrease.
可塑剤としては、生分解性を有することが好ましく、エーテルエステル系可塑剤、オキシ酸エステル系可塑剤、グリセリンエステル系可塑剤、多塩基酸エステル系可塑剤、多価アルコールエステル系可塑剤、ロジンエステル系可塑剤、フタル酸誘導体系可塑剤、ポリヒドロキシカルボン酸系可塑剤などが挙げられる。 The plasticizer preferably has biodegradability, and is an ether ester plasticizer, oxyester plasticizer, glycerin ester plasticizer, polybasic acid ester plasticizer, polyhydric alcohol ester plasticizer, rosin Examples include ester plasticizers, phthalic acid derivative plasticizers, and polyhydroxycarboxylic acid plasticizers.
エーテルエステル系可塑剤の具体例としては、ビスメチルジエチレングリコールアジペート、ビスブチルジエチレングリコールアジペート、ビス[2−(2−メトキシエトキシ)エチル]アジペート、トリエチレングリコールジプロピオネートなどが挙げられる。 Specific examples of the ether ester plasticizer include bismethyldiethylene glycol adipate, bisbutyldiethylene glycol adipate, bis [2- (2-methoxyethoxy) ethyl] adipate, and triethylene glycol dipropionate.
オキシ酸エステル系可塑剤の具体例としては、アセチルリシノール酸メチル、アセチルリシノール酸ブチル、アセチルクエン酸トリエチル、アセチルクエン酸トリブチル、アセチルクエン酸トリブチルアセテート、クエン酸トリエチル、クエン酸トリブチルなどが挙げられる。 Specific examples of the oxyester plasticizer include methyl acetyl ricinoleate, butyl acetyl ricinoleate, triethyl acetyl citrate, tributyl acetyl citrate, tributyl acetyl citrate, triethyl citrate, tributyl citrate and the like.
グリセリンエステル系可塑剤の具体例としては、グリセリンモノカプレート、グリセリンモノラウレート、グリセリンモノパルミテート、グリセリンモノステアレート、グリセリンモノオレート、グリセリンジパルミテート、グリセリンジステアレート、グリセリンジオレート、グリセリントリアセテート、グリセリントリプロピオネート、グリセリントリブチレート、グリセリンジアセトモノカプリレート、グリセリンジアセトモノカプレート、グリセリンジアセトモノラウレート、グリセリンジアセトモノミリスチレート、グリセリンジアセトモノパルミテート、グリセリンジアセトモノステアレート、グリセリンジアセトモノオレート、グリセリンジアセトモノリノレネート、グリセリンモノアセトジカプリレート、グリセリンモノアセトジカプレート、グリセリンモノアセトジラウレート、ジグリセリン酢酸エステルなどが挙げられる。 Specific examples of the glycerin ester-based plasticizer include glycerin monocaprate, glycerin monolaurate, glycerin monopalmitate, glycerin monostearate, glycerin monooleate, glycerin dipalmitate, glycerin distearate, glycerin dioleate, glycerin triacetate. , Glycerol tripropionate, glycerol tributyrate, glycerol diacetomonocaprylate, glycerol diacetomonocaprate, glycerol diacetomonolaurate, glycerol diacetomonomyristylate, glycerol diacetomonopalmitate, glycerol diacetomonostearate, glycerol dia Setomonooleate, glycerin diacetomonolinolenate, glycerin monoacetodicaprylate, glycerin monoa Tojikapureto, glycerol mono-acetoacetate dilaurate, etc. diglycerin acetate ester.
多塩基酸エステル系可塑剤の具体例としては、ジメチルアジペート、ジ−2−エチルヘキシルアジペート、ジイソブチルアジペート、ジブチルアジペート、ジイソデシルアジペート、ジブチルジグリコールアジペート、ジブチルセバケート、ジ−2−エチルヘキシルセバケートなどが挙げられる。 Specific examples of the polybasic acid ester plasticizer include dimethyl adipate, di-2-ethylhexyl adipate, diisobutyl adipate, dibutyl adipate, diisodecyl adipate, dibutyl diglycol adipate, dibutyl sebacate, di-2-ethylhexyl sebacate and the like. Can be mentioned.
多価アルコールエステル系可塑剤の具体例としては、ジエチレングリコールジベンゾエート、ジエチレングリコールモノメチルエーテル、ジエチレングリコールジメチルエーテル、ジエチレングリコールモノエチルエーテル、ジエチレングリコールジエチルエーテル、ジエチレングリコールモノブチルエーテル、ジエチレングリコールジブチルエーテル、ジエチレングリコールモノヘキシルエーテル、ジエチレングリコールモノオレイルエーテル、ジエチレングリコールジアセテート、トリエチレングリコールジアセテート、トリエチレングリコールモノエチルエーテル、トリエチレングリコールモノブチルエーテル、トリエチレングリコールモノオレイルエーテルなどが挙げられる。 Specific examples of the polyhydric alcohol ester plasticizer include diethylene glycol dibenzoate, diethylene glycol monomethyl ether, diethylene glycol dimethyl ether, diethylene glycol monoethyl ether, diethylene glycol diethyl ether, diethylene glycol monobutyl ether, diethylene glycol dibutyl ether, diethylene glycol monohexyl ether, diethylene glycol monooleyl ether , Diethylene glycol diacetate, triethylene glycol diacetate, triethylene glycol monoethyl ether, triethylene glycol monobutyl ether, triethylene glycol monooleyl ether, and the like.
ロジンエステル系可塑剤の具体例としては、アビエチン酸メチル、アビエチン酸ジエチルグリコール、2−ヒドロアビエチン酸ジエチレングリコール、2−ヒドロキシアビエチン酸ジエチレングリコール、ロジンのモノエチレングリコールエステル、ロジンのペンタエリトリットエステルなどが挙げられる。 Specific examples of the rosin ester plasticizer include methyl abietate, diethyl glycol abietate, 2-hydroabietic acid diethylene glycol, 2-hydroxyabietic acid diethylene glycol, rosin monoethylene glycol ester, and rosin pentaerythritol ester. It is done.
フタル酸誘導体系可塑剤の具体例としては、エチルフタリルエチルグリコレート、エチルフタリルブチルグリコレート、ブチルフタリルブチルグリコレートなどが挙げられる。 Specific examples of the phthalic acid derivative plasticizer include ethyl phthalyl ethyl glycolate, ethyl phthalyl butyl glycolate, and butyl phthalyl butyl glycolate.
ポリヒドロキシカルボン酸系可塑剤の具体例としては、ポリカプロラクトン、ポリプロピオラクトンなどが挙げられる。 Specific examples of the polyhydroxycarboxylic acid plasticizer include polycaprolactone and polypropiolactone.
これらの可塑剤は単独で使用してもよく、あるいは2種類以上を併用してもよい。 These plasticizers may be used alone or in combination of two or more.
上記した可塑剤の中でも、ポリ乳酸系樹脂に対して相溶し、かつ、不揮発性であり、環境問題などの観点から無毒性で、さらに米国FDA(Food and Drug Administration)に合格しているものが好ましい。具体的には、エーテルエステル系可塑剤、オキシ酸エステル系可塑剤がある。 Among the plasticizers described above, those that are compatible with polylactic acid-based resins, are non-volatile, are non-toxic from the viewpoint of environmental problems, and have passed the US FDA (Food and Drug Administration). Is preferred. Specific examples include ether ester plasticizers and oxyacid ester plasticizers.
また、本発明の獣忌避剤には、その特性が損なわれない範囲内で、耐候剤、湿潤剤、増粘剤、着色剤、安定化剤、滑剤、酸化防止剤、防腐剤、凝固剤などを添加することができる。これらの種類は特に限定されない。 Further, the animal repellent of the present invention includes a weathering agent, a wetting agent, a thickening agent, a coloring agent, a stabilizer, a lubricant, an antioxidant, an antiseptic, a coagulant, and the like as long as the characteristics are not impaired. Can be added. These types are not particularly limited.
本発明の獣忌避剤は、保護しようとする樹木および保護しようとする部分に直接、またはその周辺に塗工、または散布した後、自然乾燥することにより塗膜を形成できる。塗工方法としては、特に限定されず、刷毛やローラーを使用することができる。散布する場合には、じょうろ等の散布器具を用いてもよく、スプレー容器に封入して噴霧することもできる。塗膜の厚さは、特に限定されるものではないが、0.1μm〜5mm、好ましくは5μm〜3mm、さらに好ましくは10μm〜1mmであることが望ましい。塗膜が薄すぎると、長期間にわたっての獣忌避効果が得られない場合があり、逆に塗膜が厚すぎた場合には、コストアップとなるだけでなく乾燥が不十分になり、雨により流されてしまう場合がある。 The animal repellent of the present invention can form a coating film by coating or spraying directly on or around the tree to be protected and the part to be protected and then naturally drying. It does not specifically limit as a coating method, A brush and a roller can be used. In the case of spraying, a spraying device such as a watering can be used, and it can be sprayed by being sealed in a spray container. Although the thickness of a coating film is not specifically limited, It is desirable that they are 0.1 micrometer-5 mm, Preferably they are 5 micrometers-3 mm, More preferably, they are 10 micrometers-1 mm. If the coating film is too thin, it may not be possible to obtain a beast repellent effect over a long period of time. Conversely, if the coating film is too thick, not only will the cost be increased, but drying will be insufficient, It may be washed away.
以下、実施例に基づき本発明を具体的に説明するが、本発明はこれらのみに限定されるものではない。各種の特性については、以下の方法で評価した。 EXAMPLES Hereinafter, although this invention is demonstrated concretely based on an Example, this invention is not limited only to these. Various characteristics were evaluated by the following methods.
(1)塗膜の耐久性
木材に獣忌避剤を塗工した後、屋外に放置し、2週間後および2か月後の塗膜の状態について目視で観察し、塗膜のはがれがないものを耐久性に優れる(○)とし、塗膜の一部にはがれがあるものを耐久性を有するが、不十分である(△)とし、塗膜がはがれたものを耐久性がない(×)と判断した。
(1) Durability of coating film After applying animal repellent to wood, leave it outdoors and visually observe the state of the coating film after 2 weeks and 2 months, and there is no peeling of the coating film Is excellent in durability (○), if the coating film is partly peeled, it has durability, but it is insufficient (△), and the coating film is not durable (×) It was judged.
(2)塗膜の生分解性
JIS K6953の試験手順に従い、コンポスト化8週間後の生分解度が60%を超すものを生分解性がある(○)とし、40%以上60%未満のものを(△)とし、40%を超さないものを生分解性がない(×)と判断した。
(2) Biodegradability of the coating film According to the test procedure of JIS K6953, the biodegradability of more than 60% after composting 8 weeks is considered as biodegradable (○), and 40% or more and less than 60% (△), and those not exceeding 40% were judged as not biodegradable (×).
(3)獣忌避性
未処理および塗工処理を行った2つの容器(サンナップ株式会社製 紙コップ ホワイト 205ml容量を高さ3cmに切断)に飼料(日本クレア製 CLEA Rodent Diet CE−7)を同量入れ、プラスチックケージ(日本クレア製 クリーンS−PC サイズ/282×451×157mm)内の隅に配置し、10匹の1週間馴化飼育したBalb/cマウス(5週齢、日本クレア製)を入れ、2日間経過したときのそれぞれの容器内の飼料の重量減少を比較し、塗工処理を行った容器内の飼料の重量減少が、未処理の容器内の飼料の重量減少に対し、10%未満であるものを獣忌避性に非常に優れる(◎)とし、10%以上30%未満のものを獣忌避性に優れる(○)、30%以上70%未満のものを獣忌避性を有する(△)とし、70%以上のものを獣忌避性がない(×)と判断した。
(3) Beast repellent The feed (CLEA Rodent Diet CE-7 made by CLEA Japan) is fed to two containers (Sanup Co., Ltd., paper cup white, 205 ml capacity cut to a height of 3 cm) that have been untreated and coated. Weighed and placed 10 Balb / c mice (5 weeks old, manufactured by CLEA Japan, Inc.) placed in the corner of a plastic cage (CLEAN S-PC size / 282 × 451 × 157 mm manufactured by CLEA Japan) The weight reduction of the feed in each container when two days have passed is compared, and the weight reduction of the feed in the container subjected to the coating treatment is 10% compared to the weight reduction of the feed in the untreated container. % Is very excellent in animal repellency (◎), 10% or more and less than 30% is excellent in animal repellency (○), and 30% or more and less than 70% has animal repellency. (△), 70% or more The above was judged to have no beast repellent (x).
参考例1
生分解性ポリエステル樹脂水性分散体E−1の調製
エコフレックス(BASF社製 ポリ(ブチレンアジペート/テレフタレート))300gをオートクレーブ中に仕込み、乾燥後、230℃に加熱して溶融した後、1,2,3,4−ブタンテトラカルボン酸(和光純薬株式会社製)13.1gを添加し、3時間加熱撹拌して解重合を行い、払い出し生分解性ポリエステル樹脂Aを得た。ヒーター付きの密閉可能な耐圧1L容ガラス容器を備えた撹拌機を用いて、生分解性ポリエステル樹脂A 50.0g、トリエチルアミン(ナカライテスク株式会社製)3.3g(樹脂中のカルボキシル基に対して1.2倍当量)、イソプロピルアルコール 45.0gおよび151.7gの蒸留水をガラス容器内に仕込み、撹拌翼の回転速度を400rpmとして撹拌し、加熱し、系内の温度が100℃になった状態で30分間温度を維持した後、室温(約25℃)まで冷却した。その後、300メッシュのステンレス製フィルター(線径0.035mm、平織)で加圧濾過(空気圧0.2MPa)し、乳白色の均一な生分解性ポリエステル樹脂水性分散体E−1を得た。水性分散体中に含まれる固形分の割合は20質量%であった。
Reference example 1
Preparation of Biodegradable Polyester Resin Aqueous Dispersion E-1 Ecoflex (BASF Poly (butylene adipate / terephthalate)) 300 g was charged into an autoclave, dried, heated to 230 ° C. and melted, and then 1, 2 3,4-butanetetracarboxylic acid (manufactured by Wako Pure Chemical Industries, Ltd.) 13.1 g was added, heated and stirred for 3 hours for depolymerization, and a biodegradable polyester resin A was obtained. Using a stirrer equipped with a hermetic pressure-resistant 1 L glass container with a heater, 50.0 g of biodegradable polyester resin A, 3.3 g of triethylamine (manufactured by Nacalai Tesque Co., Ltd.) (based on carboxyl groups in the resin) 1.2 times equivalent), 45.0 g of isopropyl alcohol and 151.7 g of distilled water were charged into a glass container, stirred at a rotation speed of the stirring blade of 400 rpm, and heated to reach 100 ° C. After maintaining the temperature in the state for 30 minutes, it was cooled to room temperature (about 25 ° C.). Then, pressure filtration (air pressure 0.2 MPa) was performed with a 300-mesh stainless steel filter (wire diameter 0.035 mm, plain weave) to obtain a milky white uniform biodegradable polyester resin aqueous dispersion E-1. The ratio of the solid content contained in the aqueous dispersion was 20% by mass.
参考例2
ポリ乳酸樹脂溶液S−1の調製
ポリ乳酸樹脂(ネイチャーワークス社製、6300D) 30.0g、トルエン(ナカライテスク株式会社製)270gを密閉可能なガラス容器内に仕込み、撹拌翼の回転速度を500rpmとして撹拌し、ポリ乳酸樹脂がすべて溶解するまで撹拌を続け、ポリ乳酸樹脂溶液S−1を得た。溶液中に含まれる固形分の割合は、10質量%であった。
Reference example 2
Preparation of polylactic acid resin solution S-1 30.0 g of polylactic acid resin (manufactured by Nature Works, 6300D) and 270 g of toluene (manufactured by Nacalai Tesque) were charged in a sealable glass container, and the rotational speed of the stirring blade was 500 rpm. And stirring was continued until all the polylactic acid resin was dissolved to obtain a polylactic acid resin solution S-1. The ratio of the solid content contained in the solution was 10% by mass.
実施例1
ポリ乳酸樹脂分散体(第一工業製薬株式会社製 L−110G、固形分濃度 52質量%、以下L−110Gと略称する)、可塑剤(グリセリンジアセトモノカプレート 理研ビタミン株式会社製 PL−019、以下PL−019と略称する)およびカプサイシン内包マイクロカプセル製剤(日本化薬株式会社製 R−731、以下R−731と略称する)を、L−110G中の固形分であるポリ乳酸樹脂100質量部に対して、PL−019が20質量部、R−731が10質量部となるように混合し、獣忌避剤を調製し、各種特性について評価した。
Example 1
Polylactic acid resin dispersion (D-Daiichi Kogyo Seiyaku Co., Ltd. L-110G, solid content concentration 52 mass%, hereinafter abbreviated as L-110G), plasticizer (glycerin diacetate monocaprate Riken Vitamin Co., Ltd. PL-019, (Hereinafter abbreviated as PL-019) and capsaicin-encapsulated microcapsule preparation (R-731 manufactured by Nippon Kayaku Co., Ltd., hereinafter abbreviated as R-731), 100 parts by mass of a polylactic acid resin as a solid content in L-110G On the other hand, it mixed so that PL-019 might be 20 mass parts and R-731 might be 10 mass parts, the animal repellent was prepared, and various characteristics were evaluated.
実施例2
実施例1の獣忌避剤の調製において、可塑剤(ビス[2−(2−メトキシ)エチル]アジペート 大八化学株式会社製 MXA、以下MXAと略称する)を用いた以外は、同様にして獣忌避剤を調製し、各種特性について評価した。
Example 2
In the preparation of the veterinary repellent of Example 1, the same procedure was followed except that a plasticizer (bis [2- (2-methoxy) ethyl] adipate made by Daihachi Chemical Co., Ltd., MXA, hereinafter abbreviated as MXA) was used. A repellent was prepared and evaluated for various properties.
実施例3
実施例1の獣忌避剤の調製において、カプサイシン内包マイクロカプセル(三木理研工業社製 リケンレジン TO−2、以下TO−2と略称する)を用いた以外は、同様にして獣忌避剤を調製し、各種特性について評価した。
Example 3
In the preparation of the veterinary repellent of Example 1, capsaicin-encapsulated microcapsules (Riken Resin TO-2 manufactured by Miki Riken Kogyo Co., Ltd., hereinafter abbreviated as TO-2) were prepared in the same manner, Various characteristics were evaluated.
参考例1
L−110GおよびR−731を、L−110G中のポリ乳酸樹脂100質量部に対して、R−731が10質量部となるように混合し、獣忌避剤を調製し、各種特性について評価した。
Reference example 1
L-110G and R-731 were mixed with 100 parts by mass of polylactic acid resin in L-110G so that R-731 was 10 parts by mass to prepare a veterinary repellent, and various properties were evaluated. .
実施例4
実施例1の獣忌避剤の調製において、R−731の量をポリ乳酸樹脂100質量部に対して1部とした以外は、同様にして獣忌避剤を調製し、各種特性について評価した。
Example 4
In the preparation of the animal repellent of Example 1, the animal repellent was prepared in the same manner except that the amount of R-731 was 1 part relative to 100 parts by mass of the polylactic acid resin, and various properties were evaluated.
実施例5
実施例1の獣忌避剤の調製において、R−731の量をポリ乳酸樹脂100質量部に対して0.1部とした以外は、同様にして獣忌避剤を調製し、各種特性について評価した。
Example 5
In the preparation of the animal repellent of Example 1, the animal repellent was prepared in the same manner except that the amount of R-731 was 0.1 part with respect to 100 parts by mass of the polylactic acid resin, and various properties were evaluated. .
参考例2
E−1およびR−731を、E−1中のポリ乳酸樹脂100質量部に対して、R−731が10質量部となるように混合し、獣忌避剤を調製し、各種特性について評価した。
Reference example 2
E-1 and R-731 were mixed with 100 parts by mass of polylactic acid resin in E-1 so that R-731 was 10 parts by mass to prepare a veterinary repellent, and various characteristics were evaluated. .
実施例6
S−1、PL−019およびR−731を、S−1中のポリ乳酸樹脂100質量部に対して、PL−019が20質量部、R−731が10質量部となるように混合し、獣忌避剤を調製し、各種特性について評価した。
Example 6
S-1, PL-019 and R-731 are mixed such that PL-019 is 20 parts by mass and R-731 is 10 parts by mass with respect to 100 parts by mass of the polylactic acid resin in S-1. Veterinary repellents were prepared and evaluated for various properties.
参考例3
生分解性脂肪族ポリエステル樹脂分散体(昭和高分子株式会社製 ビオノーレエマルションEM−301、固形分濃度 53.1質量%、以下EM−301と略称する)およびR−731を、EM−301中の生分解性脂肪族ポリエステル樹脂100質量部に対して、R−731が10質量部となるように混合し、獣忌避剤を調製し、各種特性について評価した。
Reference example 3
Biodegradable aliphatic polyester resin dispersion (Bionor Emulsion EM-301, Showa Polymer Co., Ltd., solid content concentration 53.1% by mass, hereinafter abbreviated as EM-301) and R-731 in EM-301 The biodegradable aliphatic polyester resin was mixed with 100 parts by mass of R-731 so as to be 10 parts by mass to prepare a veterinary repellent, and various characteristics were evaluated.
比較例1
L−110Gについて、各種特性を評価した。
Comparative Example 1
Various characteristics were evaluated for L-110G.
比較例2
L−110GおよびPL−019を、L−110G中のポリ乳酸樹脂100質量部に対してPL−019が20質量部となるように混合し、各種特性について評価した。
Comparative Example 2
L-110G and PL-019 were mixed so that PL-019 was 20 parts by mass with respect to 100 parts by mass of the polylactic acid resin in L-110G, and various properties were evaluated.
比較例3
水100質量部に対して、R−731を10質量部となるように混合し、十分に撹拌し、動物忌避剤を調製し、各種特性について評価した。
Comparative Example 3
R-731 was mixed to 10 parts by mass with respect to 100 parts by mass of water, sufficiently stirred to prepare an animal repellent, and various characteristics were evaluated.
比較例4
変性ポリオレフィン樹脂水性分散体(ユニチカ株式会社製 アローベース SB−1010)およびR−731を、SB−1010中の樹脂100質量部に対して、R−731が10質量部となるように混合し、獣忌避剤を調製し、各種特性について評価した。
Comparative Example 4
A modified polyolefin resin aqueous dispersion (Unitika Ltd. Arrow Base SB-1010) and R-731 were mixed with 100 parts by mass of the resin in SB-1010 so that R-731 was 10 parts by mass, Veterinary repellents were prepared and evaluated for various properties.
実施例1〜6、参考例1〜3、比較例1〜4で得られた評価結果をまとめて表1に示す。 Table 1 summarizes the evaluation results obtained in Examples 1 to 6, Reference Examples 1 to 3 , and Comparative Examples 1 to 4.
実施例1〜6、参考例1〜3に示した獣忌避剤は、いずれも塗膜の耐久性、生分解性、獣忌避性を有したものであった。生分解性樹脂としてポリ乳酸樹脂を使用した場合、可塑剤を含むものがより優れた塗膜の耐久性を示した。また、生分解性樹脂としてポリ乳酸を用いた場合に、より生分解性に優れていた。これに対し、比較例1および比較例2では、獣忌避成分を含んでいないため獣忌避性がないものであった。比較例3では、バインダーとなる成分を含んでいないため、塗工した箇所に残存していなかった。比較例4については、生分解性がなかった。
The animal repellents shown in Examples 1 to 6 and Reference Examples 1 to 3 all had durability, biodegradability, and animal repellent properties of the coating film. When a polylactic acid resin was used as the biodegradable resin, the one containing a plasticizer showed better coating film durability. Moreover, when polylactic acid was used as a biodegradable resin, it was more excellent in biodegradability. On the other hand, Comparative Example 1 and Comparative Example 2 did not have animal repellent properties because they did not contain animal repellent components. In Comparative Example 3, since it did not contain a component that becomes a binder, it did not remain in the coated part. Comparative Example 4 was not biodegradable.
このように、生分解性樹脂、獣忌避性を有する物質を含むことにより優れた塗膜の耐久性、生分解性、優れた獣忌避性を有する獣忌避剤が得られる。ポリ乳酸樹脂を用いた場合、可塑剤を含むことによって、より優れた塗膜の耐久性を有する獣忌避剤が得られる。
As described above, by including a biodegradable resin and a substance having animal repellent properties, a veterinary repellent having excellent coating film durability, biodegradability, and excellent animal repellent properties can be obtained. When a polylactic acid resin is used, the animal repellent which has the durability of the more excellent coating film is obtained by including a plasticizer.
Claims (6)
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| CN101433194A (en) * | 2008-12-12 | 2009-05-20 | 青岛美今宠物用品有限公司 | Spray for repelling cat |
| JP5829865B2 (en) * | 2011-08-30 | 2015-12-09 | フマキラー株式会社 | Animal repellent |
| CN102792975B (en) * | 2012-08-14 | 2014-04-09 | 安徽巨地农业科技有限公司 | Taste-type bird and mouse repellent composition |
| AU2016218108B2 (en) * | 2015-02-10 | 2020-03-05 | Basf Se | Composition comprising a pesticide and an alkoxylated ester |
| CN109392953A (en) * | 2017-08-18 | 2019-03-01 | 黑龙江省带岭林业科学研究所 | A kind of biological repellent for preventing and controlling forest rodents and preparation method |
| JP7075106B2 (en) * | 2017-09-05 | 2022-05-25 | 合同会社ツリーワーク | Wood tar and its manufacturing method |
| EP4424166A1 (en) | 2021-10-29 | 2024-09-04 | Sony Group Corporation | Method for producing repellent or attractant for organisms, repellent or attractant for organisms, and method for repelling or attracting organisms |
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| JPH07112908A (en) * | 1993-10-15 | 1995-05-02 | Toyo Ink Mfg Co Ltd | Animal repellent |
| JP2001247866A (en) * | 2000-03-06 | 2001-09-14 | Suzuki Sogyo Co Ltd | Plant growth environment imparting material, method for producing the same, soil composition containing the same, and soil improvement method using the same |
| JP2004026746A (en) * | 2002-06-27 | 2004-01-29 | Ohara:Kk | Spreading liquid for repellent containing glucomannan as main component |
| JP2005143349A (en) * | 2003-11-13 | 2005-06-09 | Unitica Fibers Ltd | Bird and beast-repelling net |
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