JPH0694411B2 - Insect repellent fiber - Google Patents

Insect repellent fiber

Info

Publication number
JPH0694411B2
JPH0694411B2 JP23117592A JP23117592A JPH0694411B2 JP H0694411 B2 JPH0694411 B2 JP H0694411B2 JP 23117592 A JP23117592 A JP 23117592A JP 23117592 A JP23117592 A JP 23117592A JP H0694411 B2 JPH0694411 B2 JP H0694411B2
Authority
JP
Japan
Prior art keywords
test
mites
sample
mol
insect repellent
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
Application number
JP23117592A
Other languages
Japanese (ja)
Other versions
JPH05262613A (en
Inventor
道夫 河合
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.)
Ishizuka Glass Co Ltd
Original Assignee
Ishizuka Glass Co Ltd
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 Ishizuka Glass Co Ltd filed Critical Ishizuka Glass Co Ltd
Publication of JPH05262613A publication Critical patent/JPH05262613A/en
Publication of JPH0694411B2 publication Critical patent/JPH0694411B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Carpets (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はB2O3を含有する硝子質物
質を利用した、ダニ等に対する防虫効果に優れた防虫繊
維に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an insect repellent fiber using a vitreous substance containing B 2 O 3 and having an excellent insect repellent effect against mites and the like.

【0002】[0002]

【従来の技術】従来、ダニの駆除のためには、有機リン
酸、ピレスロイド系物質、カーバメイト系物質、ダイア
ジノン系物質等の有機物質や、オルト硼酸、硼酸ソー
ダ、8硼酸ナトリウム4水和物等の無機系の硼素化合物
が使用されている。またこれらの物質を繊維に担持させ
た防虫繊維も、例えば特開平1-148206号公報等によって
知られている。ところが、上記したような防ダニ効果の
ある有機物質は毒性が強いため、大量に使用すると人体
に対する影響が懸念される。一方、無機系の硼素化合物
は毒性の問題はないが、水溶性であるために短期間で薬
効が失われるという問題があった。
2. Description of the Related Art Conventionally, for the control of mites, organic substances such as organic phosphoric acid, pyrethroid type substances, carbamate type substances, diazinon type substances, orthoboric acid, sodium borate, sodium octaborate tetrahydrate, etc. Inorganic boron compounds are used. Insect-proof fibers in which these substances are carried on fibers are also known, for example, from Japanese Patent Application Laid-Open No. 1-148206. However, since the above-mentioned organic substance having a tick-proofing effect is highly toxic, there is a concern that it may affect the human body when used in a large amount. On the other hand, the inorganic boron compound has no problem of toxicity, but has a problem that the drug effect is lost in a short period of time because it is water-soluble.

【0003】[0003]

【発明が解決しようとする課題】本発明は上記した従来
の問題点を解決して、毒性がほとんどなく、しかも長期
間にわたり薬効を維持することができる防虫繊維を提供
するために完成されたものである。
The present invention has been completed to solve the above-mentioned conventional problems and provide an insect-repellent fiber having little toxicity and capable of maintaining a medicinal effect for a long period of time. Is.

【0004】[0004]

【課題を解決するための手段】上記の課題を解決するた
めになされた本発明は、B2O3を20℃、1時間の条件で1
mg/g〜300 mg/g の速度で溶出する硝子質物質による防
虫処理が施されていることを特徴とする防虫繊維を要旨
とするものである。
The present invention, which has been made to solve the above-mentioned problems, provides a method in which B 2 O 3 is added at a temperature of 20 ° C. for 1 hour.
The gist is insect-repellent fiber, which is characterized by being treated with a vitreous substance that elutes at a rate of mg / g to 300 mg / g.

【0005】上記のように、本発明ではB2O3を溶出する
ことができる硝子質物質が使用される。このような機能
を持つ硝子としては、B2O3−SiO2−Na2O系、B2O3−Na2O
−RO系、B2O3−Na2O−Al2O3 系のものがある。ここでRO
はCaO 、MgO のようなアルカリ土類金属の酸化物を意味
する。これらの硝子質物質はダニが繁殖し易い高温多湿
の条件下でダニの駆除に有効なB2O3を溶出するが、ダニ
の繁殖に適しない低温乾燥の条件下ではB2O3をあまり溶
出させないため、ダニの駆除にきわめて適したものであ
る。
As described above, the present invention uses a vitreous substance capable of eluting B 2 O 3 . As a glass having such a function, B 2 O 3 --SiO 2 --Na 2 O system, B 2 O 3 --Na 2 O system
-RO based, there is a B 2 O 3 -Na 2 O- Al 2 O 3 system. Where RO
Means an oxide of an alkaline earth metal such as CaO or MgO. These vitreous substances elute B 2 O 3 which is effective in controlling mites under high temperature and high humidity conditions where mites easily proliferate, but B 2 O 3 is not so much produced under low temperature drying conditions that are not suitable for mites breeding. Since it does not elute, it is extremely suitable for controlling ticks.

【0006】B2O3の溶出速度は、20℃の蒸留水中に粒径
を例えば420 〜600 μm とした硝子質物質を1時間浸漬
し、硝子質物質1g当りのB2O3重量として算出される。
ただし本発明においては粒径はこれに限定されるもので
はない。本発明においてB2O3の溶出速度を1mg/g〜300
mg/gとしたのは、溶出速度がこれより低いと防虫効果が
なく、逆にこれより高くても防虫効果に変化がなくて無
駄となり、しかも短期間に溶出が完了してしまうからで
ある。
[0006] dissolution rate of B 2 O 3 is a vitreous material and a particle size in distilled water at 20 ° C. for example 420 to 600 [mu] m was immersed for 1 hour, calculated as B 2 O 3 by weight per vitreous material 1g To be done.
However, in the present invention, the particle size is not limited to this. In the present invention, the dissolution rate of B 2 O 3 is 1 mg / g to 300
The reason why the mg / g is set is that if the dissolution rate is lower than this, there is no insect repellent effect, and conversely, if it is higher than this, there is no change in the insect repellent effect, which is wasted, and the dissolution is completed in a short period of time. .

【0007】上記の硝子質物質を繊維に含有させるには
種々の方法が考えられるが、例えば硝子質物質を微粉末
として例えばアクリル系バインダーと混合し、スプレ
ー、ディッピング等の方法で繊維表面に付着させたり、
合成繊維の場合には繊維中に最初から練り込んでおく等
の方法がある。
Various methods can be considered for incorporating the above-mentioned vitreous substance into the fiber. For example, the vitreous substance is mixed as a fine powder with, for example, an acrylic binder and attached to the fiber surface by a method such as spraying or dipping. Or
In the case of synthetic fiber, there is a method of kneading it into the fiber from the beginning.

【0008】[0008]

【実施例】以下に本発明を実施例により更に詳細に説明
する。まず本発明で使用する硝子質物質の毒性試験を行
った。その内容は次の通りである。 〔毒性試験〕 試験に使用した物質 (1) B2O3 80モル%、SiO2 10 モル%、Na2O 10 モル
%の硝子質物質を粒径20μm 以下に粉砕した微粉末。 (2) B2O3 45モル%、SiO2 40 モル%、Na2O 15 モル
%の硝子質物質を粒径20μm 以下に粉砕した微粉末。 試験方法 マウス使用の急性毒性試験であり、5000mg/kg を上限と
して、3段階の用量を雌雄マウスに経口単回投与し、マ
ウスの異常を観察する方法で行った。 試験実施場所 財団法人 日本食品分析センター大阪支所 試験結果 (1) LD50マウス 3250mg/kg (2) LD50マウス 5000mg/kg 以上 考察 この結果は、H3BO3(硼酸) のLD50マウスが3450mg/kg
(文献値:米国国立労働安全衛生研究所編、化学物質毒
性データー総覧)と比較してほとんど差のない値であ
り、本発明で使用する硝子質物質の哺乳類に対する毒性
は極めて弱いことが確認された。
EXAMPLES The present invention will be described in more detail below with reference to examples. First, the toxicity test of the vitreous substance used in the present invention was conducted. The contents are as follows. [Toxicity test] Substances used in the test (1) Fine powder obtained by grinding a glassy substance of 80 mol% B 2 O 3 , 10 mol% SiO 2 and 10 mol% Na 2 O to a particle size of 20 μm or less. (2) Fine powder obtained by pulverizing a glassy substance of B 2 O 3 45 mol%, SiO 2 40 mol% and Na 2 O 15 mol% to a particle size of 20 μm or less. Test method This is an acute toxicity test using mice. It was carried out by a method of observing abnormalities in mice by single oral administration to male and female mice in three steps with an upper limit of 5000 mg / kg. Test location Japanese Food Analysis Center Osaka Branch Test results (1) LD 50 mouse 3250mg / kg (2) LD 50 mouse 5000mg / kg or more Discussion This result shows that LD 50 mouse of H 3 BO 3 (boric acid) is 3450mg /kg
(Reference value: Comprehensive data on toxicity data of chemical substances, edited by National Institute of Occupational Safety and Health, Comprehensive list), it was confirmed that the toxicity of the vitreous substance used in the present invention to mammals is extremely weak. It was

【0009】〔殺ダニ試験1〕 試験に使用した試料 B2O3 60 モル%、SiO2 20 モル%、Na2O 10 モル%、Ca
O 10モル%の硝子質物質を、粒径20μm 以下に粉砕した
微粉末(但し20℃、1時間の条件下におけるB2O3の溶出
速度は2mg/g)をウレタン系バインダー中に混合し、そ
の中に綿布をディッピングすることにより、硝子質物質
を綿布の繊維の表面に0.05g/m2と5g/m2の割合でそれぞ
れ付着させた。このようにして得られた綿布の一部を切
断し、試料とした。 試験方法 厚生省指定の医薬部外品認定基準の方法を準用した大阪
府立公衆衛生研究所の試験方法(培地接触方法)で実施
した。即ち、プラスチックシャーレ(面積28cm2 )の底
面に上記試料を密着するように敷き込み、その表面にコ
ナヒョウダニを含む培地0.025gを一様に拡げた。培地中
の生存ダニ数は予め試験開始直前に0.1gを飽和食塩水浮
遊法により計数しておく。このようにしたプラスチック
シャーレを各処理区毎に飽和食塩水を入れて湿度を75%
に保った食品保存用のプラスチック容器に収納し、温度
25±1℃の恒温器中で飼育した。同様に試料を敷き込ま
ないものを対照区として飼育し、14日後にシャーレ内の
生存ダニ数を全数調査し、対照区の生存ダニ数との比較
により殺虫率を次式により算出した。 殺虫率(%)=〔(対照区のダニ数−処理区のダニ数)
/対照区のダニ数〕 なお、試験は3連1区にて行った。 試験結果 各試料の殺虫率は、硝子質物質の付着量が0.05g/m2の試
料では10%、硝子質物質の付着量が5g/m2の試料では99
%であった。
[Acaricidal test 1] Samples used in the test B 2 O 3 60 mol%, SiO 2 20 mol%, Na 2 O 10 mol%, Ca
A fine powder of 10 mol% O 2 pulverized to a particle size of 20 μm or less (however, the elution rate of B 2 O 3 at 20 ° C. for 1 hour is 2 mg / g) is mixed with a urethane binder. by dipping the cotton therein were attached respectively vitreous material on the surface of the cotton fabric fibers at a rate of 0.05 g / m 2 and 5 g / m 2. A part of the cotton cloth thus obtained was cut and used as a sample. Test method The test method was carried out by the test method (medium contact method) of the Osaka Prefectural Institute of Public Health, which mutatis mutandis applies the method of Quasi-drug Qualification Standard designated by the Ministry of Health and Welfare. That is, the above sample was laid on the bottom of a plastic petri dish (area: 28 cm 2 ) so as to be in close contact, and 0.025 g of a medium containing Dermatophagoides farinae was uniformly spread on the surface. The number of surviving mites in the medium is previously counted by 0.1 g by the saturated saline suspension method immediately before the start of the test. Put a saturated saline solution into each treated area of the plastic petri dish to keep the humidity at 75%.
Store in a plastic container for food storage kept at
The animals were kept in an incubator at 25 ± 1 ° C. Similarly, the animals without the sample spread were bred as a control group, and after 14 days, the total number of living mites in the petri dish was investigated, and the insecticidal rate was calculated by the following formula by comparison with the number of living mites in the control group. Insect killing rate (%) = [(number of mites in control plot-number of mites in treatment plot))
/ Number of mites in control group] The test was carried out in three groups and one group. Test results The insecticidal rate of each sample is 10% for the sample with 0.05g / m 2 of vitreous material and 99% for the sample with 5g / m 2 of vitreous material.
%Met.

【0010】〔殺ダニ試験2〕 試験に使用した試料 B2O3 80 モル%、SiO2 10 モル%、Na2O 10 モル%の硝
子質物質の微粉末(但し20℃、1時間の条件下における
B2O3の溶出速度は300 mg/g)を表1の通りの条件で繊維
原料中に3%練り込んで繊維化し、目付量が60g/m2の不
織布を製造した。番号1〜6は本発明の実施例に相当
し、番号7は硝子を含有しない比較例である。これらの
布の一部を切断して試料とした。
[Acaricide Test 2] Sample used for the test B 2 O 3 80 mol%, SiO 2 10 mol%, Na 2 O 10 mol% fine powder of vitreous substance (however, condition of 20 ° C. for 1 hour) Below
A B 2 O 3 elution rate of 300 mg / g) was kneaded into a fiber raw material at a rate of 3% under the conditions shown in Table 1 to form fibers, and a non-woven fabric having a basis weight of 60 g / m 2 was produced. Numbers 1 to 6 correspond to the examples of the present invention, and number 7 is a comparative example containing no glass. Some of these cloths were cut into samples.

【0011】[0011]

【表1】 [Table 1]

【0012】 試験方法 厚生省指定の医薬部外品認定基準の方法を準用した大阪
府立公衆衛生研究所の試験方法(培地接触方法)で実施
した。即ち、プラスチックシャーレ(面積28cm2 )の底
面に上記試料を密着するように敷き込み、その表面にケ
ナガコナダニを含む培地0.025gを一様に拡げた。培地中
の生存ダニ数は予め試験開始直前に0.1gを飽和食塩水浮
遊法により計数しておく。このようにしたプラスチック
シャーレを各処理区毎に飽和食塩水を入れて湿度を75%
に保った食品保存用のプラスチック容器に収納し、温度
25±1℃の恒温器中で飼育した。7日後にシャーレ内の
生存ダニ数を全数調査し、比較例の生存ダニ数との比較
により殺虫率を次式により算出した。 殺虫率(%)=〔(対照区のダニ数−処理区のダニ数)
/対照区のダニ数〕 なお、試験は3連1区にて行った。 試験結果 各試料の殺虫率は、次の通りである。 試料1 21% 試料2 95% 試料3 45% 試料4 96% 試料5 98% 試料6 92% 試料7 0%
Test method The test method (medium contact method) of the Osaka Prefectural Institute of Public Health, which mutatis mutandis applies the method of quasi-drug approval standard designated by the Ministry of Health and Welfare. That is, the above sample was laid on the bottom surface of a plastic petri dish (area: 28 cm 2 ) so as to be in close contact, and 0.025 g of a medium containing a mite mite was spread evenly on the surface. The number of surviving mites in the medium is previously counted by 0.1 g by the saturated saline suspension method immediately before the start of the test. Put a saturated saline solution into each treated area of the plastic petri dish to keep the humidity at 75%.
Store in a plastic container for food storage kept at
The animals were kept in an incubator at 25 ± 1 ° C. Seven days later, the total number of living mites in the petri dish was examined, and the insecticidal rate was calculated by the following formula by comparison with the number of living mites in Comparative Example. Insect killing rate (%) = [(number of mites in control plot-number of mites in treatment plot))
/ Number of mites in control group] The test was carried out in three groups and one group. Test results The insecticidal rate of each sample is as follows. Sample 1 21% Sample 2 95% Sample 3 45% Sample 4 96% Sample 5 98% Sample 6 92% Sample 70%

【0013】[0013]

【発明の効果】以上に説明したように、本発明の防虫繊
維はB2O3を20℃、1時間の条件で1mg/g〜300 mg/g の
速度で溶出する硝子質物質を繊維表面に付着させたり、
繊維の内部に練り込むことにより、優れた防虫効果を発
揮させることができたものである。しかも従来の有機物
質を使用したものに比較して毒性がほとんどなく、また
従来の無機系の硼素化合物を使用したものに比較してし
かも長期間にわたり薬効を維持することができる利点が
ある。
INDUSTRIAL APPLICABILITY As described above, the insect repellent fiber of the present invention has a glass surface containing a vitreous substance capable of eluting B 2 O 3 at a rate of 1 mg / g to 300 mg / g at 20 ° C. for 1 hour. Attached to
By kneading it into the inside of the fiber, it was possible to exhibit an excellent insect repellent effect. Moreover, it has almost no toxicity as compared with the one using the conventional organic substance, and has an advantage that the drug effect can be maintained for a long period of time as compared with the one using the conventional inorganic boron compound.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 D06M 23/08 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location D06M 23/08

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 B2O3を20℃、1時間の条件で1mg/g〜30
0 mg/g の速度で溶出する硝子質物質による防虫処理が
施されていることを特徴とする防虫繊維。
1. B 2 O 3 is 1 mg / g to 30 at 20 ° C. for 1 hour.
An insect-repellent fiber characterized by being treated with a vitreous substance that elutes at a rate of 0 mg / g.
JP23117592A 1990-02-21 1992-08-31 Insect repellent fiber Expired - Fee Related JPH0694411B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2-40030 1990-02-21
JP4003090 1990-02-21

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2187574A Division JPH0645522B2 (en) 1990-02-21 1990-07-16 Composition having insect repellent effect

Publications (2)

Publication Number Publication Date
JPH05262613A JPH05262613A (en) 1993-10-12
JPH0694411B2 true JPH0694411B2 (en) 1994-11-24

Family

ID=12569511

Family Applications (4)

Application Number Title Priority Date Filing Date
JP23117792A Expired - Fee Related JPH0694413B2 (en) 1990-02-21 1992-08-31 Insect paper
JP23117692A Expired - Fee Related JPH0694412B2 (en) 1990-02-21 1992-08-31 Insect repellent film
JP23117492A Expired - Fee Related JPH0694410B2 (en) 1990-02-21 1992-08-31 Insect repellent carpet
JP23117592A Expired - Fee Related JPH0694411B2 (en) 1990-02-21 1992-08-31 Insect repellent fiber

Family Applications Before (3)

Application Number Title Priority Date Filing Date
JP23117792A Expired - Fee Related JPH0694413B2 (en) 1990-02-21 1992-08-31 Insect paper
JP23117692A Expired - Fee Related JPH0694412B2 (en) 1990-02-21 1992-08-31 Insect repellent film
JP23117492A Expired - Fee Related JPH0694410B2 (en) 1990-02-21 1992-08-31 Insect repellent carpet

Country Status (1)

Country Link
JP (4) JPH0694413B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005029451A (en) * 2003-07-11 2005-02-03 Ishizuka Glass Co Ltd Glass composition for imparting antibacterial and antitick properties, and antibacterial and antitick resin composition and fiber composition using the same
AU2015300820A1 (en) * 2014-08-08 2017-03-02 Invista Textiles (U.K.) Limited Composition and application method for surface treatment of carpets

Also Published As

Publication number Publication date
JPH05246812A (en) 1993-09-24
JPH05271023A (en) 1993-10-19
JPH0694410B2 (en) 1994-11-24
JPH0694413B2 (en) 1994-11-24
JPH05262613A (en) 1993-10-12
JPH05246811A (en) 1993-09-24
JPH0694412B2 (en) 1994-11-24

Similar Documents

Publication Publication Date Title
CN102665404B (en) Durable pest repellent and pest-repellent resin composition
CN107780210A (en) A kind of mould proof, mosquito fiber/fabric/paper dressing liquid and its application method and product
Flaherty et al. Biological control of Pacific mites and Willamette mites in San Joaquin Valley vineyards: part III. Role of tydeid mites
JPS61500500A (en) microbicidal material
DD146236A5 (en) IN THE FORM OF SOLID PARTICLES AVAILABLE MEANS
Hall Pest control in herbaria
Georghiou et al. Carbamate insecticides: comparative insect toxicity of Sevin, Zectran, and other new materials
CA1334273C (en) Microbiocidal composition and method of preparation thereof
JPH05321444A (en) Insect-proof tatami mat
JPH0694411B2 (en) Insect repellent fiber
GB2139497A (en) Controlling parasitic mites on honeybees
DE60104578T2 (en) Process for denaturing allergens
US5314699A (en) Method for flea and insect control
JPH0645522B2 (en) Composition having insect repellent effect
Meyer Deuterium oxide and Aspergillus
US5133933A (en) Microbiocidal preservative
EP4245131A1 (en) Liquid dispersion for environment improvement use, and method for improving environment
McMurtry et al. Studies on predator-prey interactions between Amblyseius hibisci and Oligonychus punicae: Effects of host-plant conditioning and limited quantities of an alternate food
JPH0694408B2 (en) Insect bedding
Hopkins et al. Field tests with Thimet and Bayer 19639 for cotton-insect control
AU2002329881A1 (en) Insect control device for prolonged treatment of animals containing coumaphos and diazinon
JPH0625971A (en) Method for imparting textile product with house dust mite killing property resistant to light and cleaning
Harris et al. Control of Farm Flies in Malta—II. Residual effectiveness of insecticide formulations on various surfaces to Musca domestica and Stomoxys calcitrans
Musau et al. Comparison of the potential of organophosphorous insecticides and soaps in conifer aphid control
Hadaway et al. Evaluation of the toxicity to adult Anopheles stephensi List, and the residual action of various chlorinated hydrocarbons, organophosphorus compounds and carbamates.

Legal Events

Date Code Title Description
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 19950516

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081124

Year of fee payment: 14

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081124

Year of fee payment: 14

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091124

Year of fee payment: 15

LAPS Cancellation because of no payment of annual fees