JPH0525246B2 - - Google Patents
Info
- Publication number
- JPH0525246B2 JPH0525246B2 JP15228285A JP15228285A JPH0525246B2 JP H0525246 B2 JPH0525246 B2 JP H0525246B2 JP 15228285 A JP15228285 A JP 15228285A JP 15228285 A JP15228285 A JP 15228285A JP H0525246 B2 JPH0525246 B2 JP H0525246B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- resistance
- present
- polyester resin
- 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 - Lifetime
Links
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 229920001225 polyester resin Polymers 0.000 claims description 15
- 239000004645 polyester resin Substances 0.000 claims description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 239000011342 resin composition Substances 0.000 claims description 9
- 239000004744 fabric Substances 0.000 claims description 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 5
- 239000002904 solvent Substances 0.000 description 11
- 239000002966 varnish Substances 0.000 description 11
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 8
- 239000003822 epoxy resin Substances 0.000 description 7
- 229920000647 polyepoxide Polymers 0.000 description 7
- 230000000694 effects Effects 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- -1 aliphatic glycols Chemical class 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- INSRQEMEVAMETL-UHFFFAOYSA-N decane-1,1-diol Chemical compound CCCCCCCCCC(O)O INSRQEMEVAMETL-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Description
[発明の技術分野]
本発明は、柔軟性、耐溶剤性、耐ベアリング発
錆性等を改良した布管用柔軟性樹脂組成物に関す
る。
[発明の技術的背景とその問題点]
従来、布管用ワニスとして、油性系樹脂、油変
性アルキツド樹脂等が使用されてきた。しかしこ
れらの樹脂は樹脂中にいずれも脂肪酸を含んでい
るため本質的な欠点として
1 加熱乾燥時の着色と変化が大きいこと
2 柔軟性の経時変化が大きいこと
3 耐溶剤性に劣ること
4 ベアリング発錆性が大きいこと
5 油臭がすること
等がある。これまでこれらの欠点を改良しようと
様々の検討が行われてきたが満足すべく結果は得
られていなかつた。
[発明の目的]
本発明の目的は、従来の欠点を解消するために
なされたもので、柔軟性、耐溶剤性、耐ベアリン
グ発錆性に優れるとともに、着色変化が少なく、
また油臭のしない布管用柔軟性樹脂組成物を提供
しようとするものである。
[発明の概要]
本発明者は、上記の目的を達成しようとする鋭
意検討を重ねた結果、脂肪酸を使用しないで分子
内可塑化作用をもたせるメチレン長鎖結合を分子
内に導入した、オイルフリーのポリエステル樹脂
を使用し、その硬化剤としてアミノアルデヒド樹
脂を用い、同時にカプロラクトン変性エポキシ樹
脂を組み合わせることによつて、従来の欠点を解
消し、柔軟性、耐溶剤性、耐ベアリング発錆等に
優れることを見いだし、本発明を完成するに至つ
たものである。即ち本発明は、
(A) 脂肪族二塩基酸および脂肪族グリコールを10
〜40重量%含むポリエステル樹脂と、
(B) 一般式
(但し、1〜6、nは1〜9の整数を表す)
で示されるカプロラクトン変性エポキシ樹脂
と、
(C) アミノアルデヒド樹脂とを含み、カプロラク
トン変性エポキシ樹脂をポリエステル樹脂に対
して5〜20重量%、アミノアルデヒド樹脂を全
樹脂量[(A)+(B)+(C)]に対して5〜25重量%そ
れぞれ含有することを特徴とする布管用柔軟性
樹脂組成物である。
本発明に用いる(A)ポリエステル樹脂としては、
一般式
HOOC(−−CH2)x――
(但しxは4〜10の整数)で示される脂肪族二
塩基酸と、一般式
HO(−−CH2)y――
(但しyは4〜10の整数)で示される脂肪族グ
リコールとを10〜40重量%含むポリエステル樹脂
である。脂肪族二塩基酸としては、アジピン酸、
セバチン酸、ドデカンニ酸等が挙げられ、これら
は単独もしくは2種以上混合して用いる。また脂
肪族二塩基酸の他に、イソフタル酸、テトラヒド
ロフタル酸、フマール酸、無水マイレン酸等の酸
成分も使用される。脂肪族グリコールとしては、
1,4−ブチレングリコール、1,5−ペンタン
ジオール、1,6−ヘキサンジオール、1,10−
デカンジオール等が挙げられ、これらは単独もし
くは2種以上混合して用いる。更に前記の脂肪族
グリコールの他に、例えばエチレングリコール、
プロピレングリコール、ジエチレングリコール、
ネオペングリコール、グリセリン、トリメチロー
ルプロパン、ペンタエリスリトール、ジグリセリ
ン、ジペンタエリスリトール、ソルビトール等の
アルコール成分を使用することができる。(A)ポリ
エステル樹脂中に占める脂肪族二塩基酸および脂
肪族グリコールは、ポリエステル樹脂固形分に対
し、10〜40重量%の範囲とすることが望ましい。
10重量%未満では柔軟性が著しく低下して好まし
くない。また40重量%を超えると耐溶剤性や皮膜
強度が低下し実用に耐えない。
本発明に用いる(B)カプロラクトン変性エポキシ
樹脂としては、エポキシ樹脂にε−カプロラクト
ンを付加反応させたもので、具体的な化合物とし
ては、プラクセルG103、プラクセルG104、プラ
クセルG105(いずれもダイセル社製、商品名)等
が挙げられ、これらは単独もしくは2種以上混合
して用いる。カプロラクトン変性エポキシ樹脂の
配合割合はポリエステル樹脂固形分に対して5〜
20重量%の範囲が望ましい。その配合量が5重量
%未満では柔軟性、耐ベアリング発錆効果が低下
し、また20重量%を超えると乾燥性が低下して好
ましくない。
本発明に用いる(C)アミノアルデヒド樹脂として
は、メラミン樹脂、尿素樹脂、ベンゾグアナミン
樹脂等が含まれ、これらは樹脂組成物の硬化剤と
して作用する。具体的なものとしては、例えばメ
ラミン樹脂では、スーパーベツカミンJ−820(大
日本インキ化学工業社製、商品名)、ユーバン
20SE−60、ユーバン220(三井東圧化学社製、商
品名)、バンセミン125−60(播磨化成工業社製、
商品名)等が挙げられ、これらは単独もしくは2
種以上混合して用いる。アミノアルデヒド樹脂の
配合割合は、全樹脂固形分の5〜25重量%の範囲
にすることが望ましい。配合量が5重量%未満の
場合では乾燥性、耐溶剤性が低下し、また25重量
%を超えると樹脂が硬質化して、いずれも好まし
くない。従つて上記範囲に限定される。
本発明の布管用柔軟性樹脂組成物は、ポリエス
テル樹脂、カプロラクトン変性エポキシ樹脂、ア
ミノアルデヒド樹脂を配合して極めて容易に製造
することができる。そして通常はこの樹脂組成物
を溶剤に溶解してワニスとして使用する。また本
発明の効果を阻害しない範囲において、必要に応
じ他の添加剤を加えることもできる。こうして得
られる布管用柔軟性樹脂組成物は電気機器等に使
用されるワニスチユーブ管に含浸に用いれらる。
[発明の実施例]
次に本発明を実施例によつて説明するが、本発
明はこれらの実施例によつて限定されるものでは
ない。
実施例 1〜2
第1表に示したポリエステル樹脂成分をフラス
コに仕込み、窒素ガスの存在下まで撹拌しながら
徐々に昇温する。160℃から230℃まで1時間当り
約15℃の昇温割合である。230℃に達したならば、
キシレンを少量加えて230℃の一定温度に保ちな
がらキシレン還流を行いエステル化反応をさせ、
生成された縮合水を系外に除去する。酸価が3以
下になつたら加熱をやめて冷却して反応を終了さ
せ、ポリエステル樹脂を得た。このポリエステル
樹脂に溶剤を加えて溶解した後、カプロラクトン
変性エポキシ樹脂およびアミノアルデヒド樹脂の
所定量を加えて、実施例1、2のワニスをそれぞ
れ調製した。
比較例 1〜2
第1表に示した組成により、実施例と同様にし
てポリエステル樹脂を得た。このポリエステル樹
脂に溶剤を加えて溶解し、次いでアミノアルデヒ
ド樹脂を加えて、比較例1、2のワニスをそれぞ
れ調製した。
こうして実施例1〜2および比較例1〜2で得
られたワニスを用いて、3φのポリエステルスリ
ーブ処理をし、140℃で20分間の加熱乾燥を4回
繰り返し行つてワニスチユーブを製作し、このワ
ニスチユーブについて耐曲げ性、耐油性、耐湿熱
性、絶縁破壊電圧、耐溶剤性、柔軟性、ベアリン
グ発錆性について試験を行つた。その結果を第2
表に示したが、どの特性においても本発明の顕著
な効果が認められた。
各試験は次のような方法で行つた。
耐曲げ性、耐油性、耐湿熱性および絶縁破壊電
圧はJIS−C−2347による。
耐スチレン性および耐キシレン性は、スチレン
又はキシレン中にワニスチユーブを浸漬し、外観
の変化を判定した。柔軟性は、20cmのワニスチユ
ーブの端部5cmを固定し、他端に5gの荷重をつ
りさげ固定部位からのたわみ量を、加熱前、およ
び150℃で24時間処理の加熱後について測定した。
ベアリング発錆性は、日本精工社製NS−7グリ
ースが使用されているベアリングとワニスチユー
ブを、温度70℃相対湿度70%に調湿されるビーカ
ーに入れて密閉後、70℃に恒温槽中に入れ2ヶ月
経過後のベアリング表面の錆発生状態を、表面の
錆発面積比率(%)で示した。
[Technical Field of the Invention] The present invention relates to a flexible resin composition for cloth pipes that has improved flexibility, solvent resistance, bearing rust resistance, and the like. [Technical background of the invention and its problems] Conventionally, oil-based resins, oil-modified alkyd resins, and the like have been used as varnishes for cloth pipes. However, since all of these resins contain fatty acids, they have essential drawbacks: 1. Large coloration and change during heat drying 2. Large change in flexibility over time 3. Poor solvent resistance 4. Bearings High rust potential 5. May have an oily odor, etc. Up to now, various studies have been carried out to improve these drawbacks, but no satisfactory results have been obtained. [Object of the Invention] The object of the present invention was to eliminate the drawbacks of the conventional technology, and it has excellent flexibility, solvent resistance, and bearing rust resistance, and has little discoloration.
Another object of the present invention is to provide a flexible resin composition for cloth pipes that does not have an oily odor. [Summary of the Invention] As a result of extensive studies aimed at achieving the above object, the present inventor has developed an oil-free product in which a methylene long chain bond is introduced into the molecule to have an intramolecular plasticizing effect without using fatty acids. By using polyester resin, aminoaldehyde resin as a hardening agent, and caprolactone-modified epoxy resin at the same time, the disadvantages of conventional products are overcome, and the product has excellent flexibility, solvent resistance, bearing rust resistance, etc. This discovery led to the completion of the present invention. That is, the present invention provides (A) an aliphatic dibasic acid and an aliphatic glycol with 10
~40% by weight of polyester resin and (B) General formula (However, 1 to 6, n represents an integer of 1 to 9)
(C) an aminoaldehyde resin, the caprolactone-modified epoxy resin is 5 to 20% by weight based on the polyester resin, and the aminoaldehyde resin is the total resin amount [(A) + (B) +(C)], the flexible resin composition for cloth pipes is characterized by containing 5 to 25% by weight, respectively. The (A) polyester resin used in the present invention includes:
An aliphatic dibasic acid represented by the general formula HOOC(--CH 2 ) x -- (where x is an integer of 4 to 10) and a general formula HO(--CH 2 ) y -- (where y is 4 to 10) It is a polyester resin containing 10 to 40% by weight of aliphatic glycol (an integer of 10). Examples of aliphatic dibasic acids include adipic acid,
Examples include sebacic acid and dodecanniic acid, which may be used alone or in combination of two or more. In addition to aliphatic dibasic acids, acid components such as isophthalic acid, tetrahydrophthalic acid, fumaric acid, and maleic anhydride are also used. As aliphatic glycols,
1,4-butylene glycol, 1,5-pentanediol, 1,6-hexanediol, 1,10-
Examples include decanediol, which may be used alone or in combination of two or more. Furthermore, in addition to the aliphatic glycols mentioned above, for example, ethylene glycol,
propylene glycol, diethylene glycol,
Alcohol components such as neopene glycol, glycerin, trimethylolpropane, pentaerythritol, diglycerin, dipentaerythritol, sorbitol, etc. can be used. (A) The aliphatic dibasic acid and aliphatic glycol occupying the polyester resin are desirably in the range of 10 to 40% by weight based on the solid content of the polyester resin.
If it is less than 10% by weight, the flexibility will be significantly reduced, which is not preferable. Moreover, if it exceeds 40% by weight, the solvent resistance and film strength will decrease and it will not be suitable for practical use. The caprolactone-modified epoxy resin (B) used in the present invention is one obtained by addition-reacting ε-caprolactone to an epoxy resin. Specific compounds include Plaxel G103, Plaxel G104, and Plaxel G105 (all manufactured by Daicel, (trade name), and these may be used alone or in combination of two or more. The blending ratio of caprolactone-modified epoxy resin is 5 to 5 to the solid content of polyester resin.
A range of 20% by weight is desirable. If the amount is less than 5% by weight, the flexibility and anti-corrosion effect of the bearing will decrease, and if it exceeds 20% by weight, the drying properties will be decreased, which is not preferable. The aminoaldehyde resin (C) used in the present invention includes melamine resins, urea resins, benzoguanamine resins, etc., and these act as curing agents for the resin composition. Specifically, for example, melamine resins include Supervetsucomin J-820 (manufactured by Dainippon Ink & Chemicals Co., Ltd., trade name), Yuvan
20SE-60, Yuban 220 (manufactured by Mitsui Toatsu Chemical Co., Ltd., trade name), Vansemin 125-60 (manufactured by Harima Kasei Kogyo Co., Ltd.,
product name), etc., and these can be used singly or in combination.
Use by mixing more than one species. The blending ratio of the aminoaldehyde resin is preferably in the range of 5 to 25% by weight of the total resin solid content. If the amount is less than 5% by weight, drying properties and solvent resistance will decrease, and if it exceeds 25% by weight, the resin will become hard, both of which are undesirable. Therefore, it is limited to the above range. The flexible resin composition for cloth pipes of the present invention can be produced extremely easily by blending a polyester resin, a caprolactone-modified epoxy resin, and an aminoaldehyde resin. Usually, this resin composition is dissolved in a solvent and used as a varnish. Further, other additives may be added as necessary within a range that does not impede the effects of the present invention. The flexible resin composition for cloth pipes thus obtained is used to impregnate tubes with varnish used in electrical equipment and the like. [Examples of the Invention] Next, the present invention will be explained using Examples, but the present invention is not limited to these Examples. Examples 1-2 The polyester resin components shown in Table 1 are placed in a flask, and the temperature is gradually raised while stirring in the presence of nitrogen gas. The temperature rise rate is approximately 15°C per hour from 160°C to 230°C. If the temperature reaches 230℃,
Add a small amount of xylene and reflux the xylene while keeping it at a constant temperature of 230°C to cause an esterification reaction.
The generated condensation water is removed from the system. When the acid value became 3 or less, heating was stopped and the reaction was completed by cooling to complete a polyester resin. After adding a solvent to this polyester resin and dissolving it, predetermined amounts of caprolactone-modified epoxy resin and aminoaldehyde resin were added to prepare the varnishes of Examples 1 and 2, respectively. Comparative Examples 1-2 Polyester resins were obtained using the compositions shown in Table 1 in the same manner as in Examples. A solvent was added to this polyester resin to dissolve it, and then an aminoaldehyde resin was added to prepare the varnishes of Comparative Examples 1 and 2, respectively. In this way, using the varnishes obtained in Examples 1 and 2 and Comparative Examples 1 and 2, a 3φ polyester sleeve was treated and heat-dried for 20 minutes at 140°C four times to produce a varnish tube. Tests were conducted on bending resistance, oil resistance, heat and humidity resistance, dielectric breakdown voltage, solvent resistance, flexibility, and bearing rust resistance. The result is the second
As shown in the table, remarkable effects of the present invention were observed in all properties. Each test was conducted in the following manner. Bending resistance, oil resistance, heat and humidity resistance, and dielectric breakdown voltage are based on JIS-C-2347. Styrene resistance and xylene resistance were determined by immersing a varnish tube in styrene or xylene and determining changes in appearance. Flexibility was determined by fixing 5 cm of one end of a 20 cm varnish tube and suspending a 5 g load from the other end, and measuring the amount of deflection from the fixed part before heating and after heating at 150° C. for 24 hours.
Bearing rusting was determined by placing a bearing and varnish tube using NSK NS-7 grease in a beaker that was kept at a temperature of 70°C and relative humidity of 70%, and then placing it in a sealed beaker and placing it in a constant temperature bath at 70°C. The state of rust on the bearing surface after 2 months of installation is shown in terms of the surface rust area ratio (%).
【表】【table】
【表】【table】
【表】
[発明の効果]
以上の説明および第2表から明らかなように、
本発明の布管用柔軟性樹脂組成物は、経時変化に
おいても柔軟性を失わずに、耐溶剤性、耐ベアリ
ング発錆性に優れている。そして脂肪酸を使用し
ていないため着色変化がなく、また油臭すること
なもない。従つて、ワニスチユーブ用として好適
なものである。[Table] [Effects of the invention] As is clear from the above explanation and Table 2,
The flexible resin composition for cloth pipes of the present invention does not lose its flexibility even over time and has excellent solvent resistance and bearing rust resistance. Since no fatty acids are used, there is no color change and no oily odor. Therefore, it is suitable for use in varnish tubes.
Claims (1)
を10〜40重量%含むポリエステル樹脂と、 (B) 一般式 (但しmは1〜6、nは1〜9の整数を表
す)で示されるカプロラクトン変性エポキシ樹
脂と、 (C) アミノアルデヒド樹脂とを含み、カプロラク
トン変性エポキシ樹脂をポリエステル樹脂に対
して5〜20重量%、アミノアルデヒド樹脂を全
樹脂量[(A)+(B)+(C)]に対して5〜25重量%そ
れぞれ含有することを特徴とする布管用柔軟性
樹脂組成物。[Scope of Claims] 1 (A) a polyester resin containing 10 to 40% by weight of an aliphatic dibasic acid and an aliphatic glycol; (B) a general formula (where m is an integer of 1 to 6 and n is an integer of 1 to 9); (C) an aminoaldehyde resin; 1. A flexible resin composition for cloth pipes, comprising 5 to 25% by weight of aminoaldehyde resin based on the total resin amount [(A)+(B)+(C)].
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15228285A JPS6213431A (en) | 1985-07-12 | 1985-07-12 | Flexible resin composition for fabric pipe |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15228285A JPS6213431A (en) | 1985-07-12 | 1985-07-12 | Flexible resin composition for fabric pipe |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6213431A JPS6213431A (en) | 1987-01-22 |
| JPH0525246B2 true JPH0525246B2 (en) | 1993-04-12 |
Family
ID=15537107
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15228285A Granted JPS6213431A (en) | 1985-07-12 | 1985-07-12 | Flexible resin composition for fabric pipe |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6213431A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2788131B2 (en) * | 1991-01-29 | 1998-08-20 | 日本パーカライジング株式会社 | Method for forming composite film on aluminum or aluminum alloy surface |
| US7323521B2 (en) | 2004-03-19 | 2008-01-29 | Pp6 Industries Ohio, Inc. | Epoxy polymer additives for powder coatings |
-
1985
- 1985-07-12 JP JP15228285A patent/JPS6213431A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6213431A (en) | 1987-01-22 |
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