JPS6340404B2 - - Google Patents
Info
- Publication number
- JPS6340404B2 JPS6340404B2 JP12435382A JP12435382A JPS6340404B2 JP S6340404 B2 JPS6340404 B2 JP S6340404B2 JP 12435382 A JP12435382 A JP 12435382A JP 12435382 A JP12435382 A JP 12435382A JP S6340404 B2 JPS6340404 B2 JP S6340404B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- mildew
- diphenylmethane diisocyanate
- terminal hydroxyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、防黴性材料に関し、さらに詳しくは
防黴剤を別途配合しなくても自体が防黴性を有し
ている材料に関する。
紙、木、ゴム、プラスチツク、金属などほとん
どの材料は特定の環境下ではカビの侵食から免れ
ることができない。このため、フエノール類また
はその塩素化合物、ナフテン酸などの有機酸の金
属塩、第四アンモニウム化合物などの防黴剤をこ
れら材料に配合したり、あるいは防黴剤を含む物
質で当該材料を被覆することによつて防黴対策を
構じている。さらには、防黴力の強い抗生物質を
使用して防黴性を保つことも行なわれている。
しかしながら、上記材料の使用目的などによつ
ては上記の如き防黴対策では十分な効果が得難い
ことがあり、たとえば水道用の地中埋設鋼管、電
気・電子機器の絶縁材、プリント配線板の封止材
等についてはカビの発生によるトラブルの防止が
緊急課題とされている。
そこで、本発明者らは前記したような防黴剤、
抗性物質などを配合しなくても材料自体が防黴性
を有するものを開発すべく検討を重ねた結果、特
定の組成からなる材料がすぐれた防黴性を有して
いることを見出し、かかる知見に基いて本発明を
完成したのである。
本発明は、末端水酸基含有液状ジエン系重合
体、4、4′―ジフエニルメタンジイソシアネート
のカルボジイミド変性体および下記の式で表わさ
れるアニリン系ポリオール
(ここでRは低級アルキレン基を示す。)からな
る防黴性材料に関する。
本発明に用いる末端水酸基含有ジエン系重合体
としては炭素数4〜12個のジオレフインの重合
体、共重合体のほか炭素数4〜12個のジオレフイ
ンと炭素数2〜22個のα―オレフイン性付加重合
性モノマー(好ましくは75重量%以下)の共重合
体などがある。具体的に例示するとポリブタジエ
ン、ポリイソプレン、ポリクロロプレン、ブタジ
エン―イソプレンコポリマー、ブタジエン―アク
リロニトリルコポリマー、ブタジエン―スチレン
コポリマー、ブタジエン―2―エチルヘキシルア
クリレートコポリマー、ブタジエン―n―オクタ
デシルアクリレートコポリマーなどがある。これ
らは既知の方法で得ることができ、ジエンモノマ
ーを過酸化水素と反応させる方法もその1つであ
る。この末端水酸基含有ジエン系重合体は数平均
分子量が500〜10000のものが好ましい。
また、アニリン系ポリオールとしては下記の式
(ここでRは低級アルキレン基を示す。)で表わ
される化合物がある。具体的な化合物としては、
たとえば次のようなものをあげることができる。
The present invention relates to an anti-mildew material, and more particularly to a material which itself has anti-mildew properties without the need for separately incorporating an anti-mildew agent. Most materials such as paper, wood, rubber, plastic, and metal are susceptible to mold attack under certain environments. For this reason, fungicides such as phenols or their chlorine compounds, metal salts of organic acids such as naphthenic acid, and quaternary ammonium compounds are added to these materials, or the materials are coated with substances containing fungicides. In particular, anti-mildew measures are taken. Furthermore, anti-mildew properties are maintained by using antibiotics with strong anti-mildew properties. However, depending on the purpose of use of the materials, it may be difficult to achieve sufficient effects with the above-mentioned anti-mold measures, such as underground steel pipes for water supply, insulating materials for electrical and electronic equipment, and sealing of printed wiring boards. Preventing problems caused by the growth of mold is an urgent issue when it comes to retaining materials and the like. Therefore, the present inventors used the above-mentioned fungicide,
As a result of repeated studies to develop a material that itself has anti-mildew properties without adding anti-fungal substances, we discovered that a material with a specific composition has excellent anti-mildew properties. The present invention was completed based on this knowledge. The present invention relates to a liquid diene polymer containing a terminal hydroxyl group, a carbodiimide modified product of 4,4'-diphenylmethane diisocyanate, and an aniline polyol represented by the following formula. (wherein R represents a lower alkylene group). The diene polymers containing terminal hydroxyl groups used in the present invention include polymers and copolymers of diolefins having 4 to 12 carbon atoms, as well as diolefins having 4 to 12 carbon atoms and α-olefins having 2 to 22 carbon atoms. Examples include copolymers of addition-polymerizable monomers (preferably 75% by weight or less). Specific examples include polybutadiene, polyisoprene, polychloroprene, butadiene-isoprene copolymer, butadiene-acrylonitrile copolymer, butadiene-styrene copolymer, butadiene-2-ethylhexyl acrylate copolymer, and butadiene-n-octadecyl acrylate copolymer. These can be obtained by known methods, including reacting diene monomers with hydrogen peroxide. This terminal hydroxyl group-containing diene polymer preferably has a number average molecular weight of 500 to 10,000. In addition, as an aniline polyol, the following formula (Here, R represents a lower alkylene group.) There is a compound represented by the following. As a specific compound,
For example, the following can be given:
【式】【formula】
【式】
本発明の防黴性材料における各成分の配合割合
については末端水酸基含有液状ジエン系重合体
100重量部あたり4、4′―ジフエニルメタンジイ
ソシアネートのカルボジイミド変性体10〜60重量
部、アニリン系ポリオール5〜30重量部が適当で
ある。ここで4、4′―ジフエニルメタンジイソシ
アネートのカルボジイミド変性体が10重量部以下
であると十分な強度が得られず、一方60重量部以
上になると硬化しなくなる。また、アニリン系ポ
リオールが5重量部以下であると十分な強度が得
られず、30重量部以上になると硬くなりすぎ好ま
しくない。本発明の防黴性材料には必要に応じて
他の成分、たとえば老化防止剤、可塑剤、充填
材、着色剤、強化材などを適宜配合することがで
きる。
本発明の防黴性材料は硬化成形体として電気・
電子機器の絶縁材、プリント配線板の封止材等と
して用いられるほか鋼管、樹脂管などのコーテイ
ング材として用いたり、可塑剤、防水剤、塗装剤
等として使用することができ、すぐれた防黴作用
を発揮する。
次に、下記の組成を有する本発明の防黴性材料
よりJIS Z2911×1976およびASTM G21−75に
規定されている試験片を作成し、各試験法に従い
カビ胞子を試験片に接種して3ケ月間培養し、カ
ビに対する抵抗性を評価した。結果を第1表に示
す。
試料A:
末端水酸基含有液状ポリブタジエン(数平均分
子量2800) 100重量部
4、4′―ジフエニルメタンジイソシアネートの
カルボジイミド変性体 38重量部
アニリン系ポリオール(式の化合物)
17重量部
試料B:
末端水酸基含有液状ポリブタジエン(数平均分
子量2800) 100重量部
4、4′―ジフエニルメタンジイソシアネートの
カルボジイミド変性体 12重量部
試料C:
オキシカルボニルペンタメチレン重合体(数平
均分子量850) 100重量部
4、4′―ジフエニルメタンジイソシアネートの
カルボジイミド変性体 54重量部[Formula] Regarding the blending ratio of each component in the anti-mildew material of the present invention, the liquid diene polymer containing terminal hydroxyl groups
Appropriate amounts per 100 parts by weight are 10 to 60 parts by weight of the carbodiimide-modified 4,4'-diphenylmethane diisocyanate and 5 to 30 parts by weight of the aniline polyol. Here, if the amount of the carbodiimide modified product of 4,4'-diphenylmethane diisocyanate is less than 10 parts by weight, sufficient strength cannot be obtained, while if it is more than 60 parts by weight, it will not harden. Furthermore, if the amount of aniline polyol is less than 5 parts by weight, sufficient strength cannot be obtained, and if it is more than 30 parts by weight, it becomes too hard, which is not preferable. Other components, such as anti-aging agents, plasticizers, fillers, colorants, reinforcing materials, etc., can be appropriately blended into the anti-mildew material of the present invention, if necessary. The anti-mildew material of the present invention can be used as a cured molded product for electrical and
It is used as an insulating material for electronic equipment, a sealing material for printed wiring boards, etc. It can also be used as a coating material for steel pipes, resin pipes, etc., and can be used as a plasticizer, waterproofing agent, coating agent, etc., and has excellent mildew resistance. exerts its effect. Next, a test piece specified in JIS Z2911×1976 and ASTM G21-75 was prepared from the anti-mold material of the present invention having the following composition, and mold spores were inoculated into the test piece according to each test method. The cells were cultured for several months and their resistance to mold was evaluated. The results are shown in Table 1. Sample A: Liquid polybutadiene containing terminal hydroxyl groups (number average molecular weight 2800) 100 parts by weight 4,4'-diphenylmethane diisocyanate modified with carbodiimide 38 parts by weight Aniline polyol (compound of formula)
17 parts by weight Sample B: Liquid polybutadiene containing terminal hydroxyl groups (number average molecular weight 2800) 100 parts by weight 4,4'-diphenylmethane diisocyanate modified with carbodiimide 12 parts by weight Sample C: Oxycarbonylpentamethylene polymer (number average molecular weight 850) ) 100 parts by weight Carbodiimide modified product of 4,4'-diphenylmethane diisocyanate 54 parts by weight
【表】【table】
【表】
表から明らかなように、本発明の防黴性材料よ
り作成した試験片Aにはカビが発育せずカビに対
する抵抗性が大きいことが確かめられた。[Table] As is clear from the table, mold did not grow on test piece A prepared from the anti-mold material of the present invention, and it was confirmed that the test piece A had high resistance to mold.
Claims (1)
4′―ジフエニルメタンジイソシアネートのカルボ
ジイミド変性体および下記の式で表わされるアニ
リン系ポリオール (ここでRは低級アルキレン基を示す。)からな
る防黴性材料。 2 末端水酸基含有液状ジエン系重合体100重量
部に対し、4、4′―ジフエニルメタンジイソシア
ネートのカルボジイミド変性体10〜60重量部、ア
ニリン系ポリオール5〜30重量部を配合してなる
特許請求の範囲第1項記載の防黴性材料。[Scope of Claims] 1. Liquid diene polymer containing terminal hydroxyl group, 4.
Carbodiimide modified product of 4′-diphenylmethane diisocyanate and aniline polyol represented by the following formula (wherein R represents a lower alkylene group). 2. A patent claim consisting of 10 to 60 parts by weight of a carbodiimide modified 4,4'-diphenylmethane diisocyanate and 5 to 30 parts by weight of an aniline polyol to 100 parts by weight of a liquid diene polymer containing a terminal hydroxyl group. The anti-mildew material according to scope 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12435382A JPS5916809A (en) | 1982-07-19 | 1982-07-19 | Antifungal material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12435382A JPS5916809A (en) | 1982-07-19 | 1982-07-19 | Antifungal material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5916809A JPS5916809A (en) | 1984-01-28 |
| JPS6340404B2 true JPS6340404B2 (en) | 1988-08-11 |
Family
ID=14883280
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12435382A Granted JPS5916809A (en) | 1982-07-19 | 1982-07-19 | Antifungal material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5916809A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02115817U (en) * | 1989-03-07 | 1990-09-17 |
-
1982
- 1982-07-19 JP JP12435382A patent/JPS5916809A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02115817U (en) * | 1989-03-07 | 1990-09-17 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5916809A (en) | 1984-01-28 |
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