JPS6096614A - Reaction of phenol with tung oil - Google Patents

Reaction of phenol with tung oil

Info

Publication number
JPS6096614A
JPS6096614A JP20648783A JP20648783A JPS6096614A JP S6096614 A JPS6096614 A JP S6096614A JP 20648783 A JP20648783 A JP 20648783A JP 20648783 A JP20648783 A JP 20648783A JP S6096614 A JPS6096614 A JP S6096614A
Authority
JP
Japan
Prior art keywords
phenol
reaction
water
tung oil
toluenesulfonic acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP20648783A
Other languages
Japanese (ja)
Inventor
Atsuhiro Nakamoto
中本 篤宏
Akitsugu Miwa
晃嗣 三輪
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.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works 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 Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP20648783A priority Critical patent/JPS6096614A/en
Publication of JPS6096614A publication Critical patent/JPS6096614A/en
Pending legal-status Critical Current

Links

Landscapes

  • Phenolic Resins Or Amino Resins (AREA)

Abstract

PURPOSE:To improve the electrical properties of a paper-phenol laminated sheet and decrease the amount of triethylamine used in the synthesis of the resin, by reacting a phenol with tung oil in the presence of p-toluenesulfonic acid and water used in a specified ratio. CONSTITUTION:0.1-0.5wt% p-toluenesulfonic acid and 0.7-4wt% water are added to a phenol and tung oil in such amounts that the weight ratio of the water to the p-toluenesulfonic acid is 1:5-20, and the resulting mixture is subjected to the primary reaction. The product of this primary reaction is made slightly alkaline by the addition of triethylamine. After adding formaldehyde, the resulting mixture is subjected to the secondary reaction in the presence of triethylamine as a catalyst.

Description

【発明の詳細な説明】 〔技術分野〕 積層板用樹脂の製造技術の分野に属する。[Detailed description of the invention] 〔Technical field〕 It belongs to the field of manufacturing technology for resin for laminates.

〔背景技術〕[Background technology]

紙、フェノールから構成される積層板において桐油変性
をおこなった樹脂を用いたものは従来、電気性能の点で
要求を満たさない場合があった。
Conventionally, laminates made of paper and phenol using resin modified with tung oil sometimes did not meet the requirements in terms of electrical performance.

またフェノールと桐油を反応させた後に行なうホルムア
ルデヒドを加えCの2次反応で触媒を多く必要とするこ
とからコスト面の問題があった。
Furthermore, the secondary reaction of C with formaldehyde, which is carried out after the reaction of phenol and tung oil, requires a large amount of catalyst, which poses a cost problem.

〔発明の目的〕[Purpose of the invention]

本発明では紙フェノール積層板における電気性能の改善
及び積層板に用いる樹脂の合成過程における触媒のトリ
エチルアミンの使用縫の削ak目的とした。
The present invention aims to improve the electrical performance of paper phenol laminates and to eliminate the use of triethylamine as a catalyst in the process of synthesizing the resin used in the laminates.

〔発明の課示〕[Imposition of invention]

積層板の特性としてa 気性能の良いことが要求される
が、そのためには樹脂中のカルボン酸を少なくすること
か必要であることを見い出した。
The laminate is required to have good aeration properties, and we have discovered that to achieve this, it is necessary to reduce the amount of carboxylic acid in the resin.

カルボン酸を少なくするためにはフェノールと桐油の反
応の際に生成する加水分解物の生成を抑制することか必
要である。そこで加水分解物lit k抑制するために
は、フェノールと桐油との反応(1次反応)で添加する
触媒パラトルエンスルホン酸及び水の量を適度に定める
必要があることを見出した。触媒のパラトルエンスルホ
ン酸は全配合に対して重量比で0.1%から0.5%の
範囲で使用する。この範囲より少ないと反応の目的であ
る桐油へのフェノールの付加がおこりにククする。また
この範囲より多いと加水分解物か多くなりすぎ性能に悪
化子もたらす。水の量は少なすぎるとゲル化がおこり、
多すぎると加水分解物が増加する。
In order to reduce the amount of carboxylic acid, it is necessary to suppress the production of hydrolysates produced during the reaction between phenol and tung oil. Therefore, it has been found that in order to suppress the hydrolyzate lit, it is necessary to appropriately determine the amounts of the catalyst p-toluenesulfonic acid and water added in the reaction between phenol and tung oil (first reaction). The catalyst para-toluenesulfonic acid is used in a weight ratio of 0.1% to 0.5% based on the total formulation. If the amount is less than this range, addition of phenol to tung oil, which is the purpose of the reaction, will occur. Moreover, if the amount exceeds this range, the amount of hydrolyzate increases too much, which deteriorates the performance. If the amount of water is too small, gelation will occur,
If it is too large, the amount of hydrolyzate increases.

反応が進行し、かつ電気性能の向上全もたらすためには
水とパラトルエンスルホン酸の配合の重量比を5〜30
の範囲としかつ、水及びパラトルエンスルホン酸の全配
合に対する配合比率をそれぞrLo、5〜4チ、0.1
〜0.5チとすることが必要であることを見いだした。
In order for the reaction to proceed and to bring about an improvement in electrical performance, the weight ratio of water and para-toluenesulfonic acid should be 5 to 30.
and the blending ratio of water and paratoluenesulfonic acid to the total blend is rLo, 5 to 4, and 0.1, respectively.
It has been found that it is necessary to set the value to 0.5 cm.

また1次反応が終了した後1次生成物とホルムアルデヒ
ドの反応(2次反応)を行なうが、この際に加える触媒
としてトルエチルアミンを用いる。また反応をすすめる
ためVては微アルカリ性でなけnばならないため加水分
解物が多いとその中のカルボン酸の影響で多くのトリエ
チル アミンが必要である。7JD水分解物量’trg
らすことにより、トリエチルアミンの量全削減すること
ができコスト低減に効果がある。
After the primary reaction is completed, the primary product is reacted with formaldehyde (secondary reaction), and toluethylamine is used as a catalyst to be added at this time. Furthermore, in order to promote the reaction, V must be slightly alkaline, so if there is a large amount of hydrolyzate, a large amount of triethylamine is required due to the influence of the carboxylic acid contained therein. 7JD water decomposition product amount'trg
By reducing the amount of triethylamine, the total amount of triethylamine can be reduced, which is effective in reducing costs.

本反応の実施例全以下に示す。All examples of this reaction are shown below.

本反応は1次反応としてフェノール60ii部と桐油4
0重量部に、次表のとおりの水及びパラトルエンスルホ
ン酸を加え80℃にて180分反応させた。反応終了後
トリエタノールアミンにて反応物を中和する。その後2
次反応として1次反応物68重量部と37ホルマリン3
2重量部[25%T7モニア水1.5 数量部とトリエ
チルアミノを下記の量加えて330℃にて180分反応
させた。
This reaction involves 60 ii parts of phenol and 4 parts of tung oil as a primary reaction.
To 0 parts by weight, water and para-toluenesulfonic acid as shown in the following table were added and reacted at 80°C for 180 minutes. After the reaction is completed, the reactant is neutralized with triethanolamine. After that 2
For the next reaction, 68 parts by weight of the primary reactant and 37 parts of formalin
2 parts by weight [1.5 parts of 25% T7 monia water] and the following amounts of triethylamino were added and reacted at 330°C for 180 minutes.

脱水後メタノールで希釈して得らtl、たワニス金紙(
(含浸させ、積層板を作りJISK−6911による煮
沸処理2時間の絶縁抵抗の測定全行なった。
After dehydration, diluted with methanol to obtain tl, varnished gold paper (
(The insulation resistance was measured after 2 hours of boiling according to JISK-6911.)

残存二重結合は赤外吸収スペクトルの990cmでの吸
収ピークより判断した。加水分解物量はGPC,フェノ
ール反応率はガスクロマトグラフィーより算出した。
The residual double bond was determined from the absorption peak at 990 cm in the infrared absorption spectrum. The amount of hydrolyzate was calculated by GPC, and the phenol reaction rate was calculated by gas chromatography.

〔発明の効果〕〔Effect of the invention〕

この発明は、水とパラトルエンスルホン酸の添加量の重
量比を5以上20以下でありかつ全配合にしめる水、パ
ラトルエンスルホン酸の配合の重量比がそれぞれ0.7
%以上4係以下、0.1%以上0.5係以下であること
’t%徴とするので、フェノール類と桐油の反応全好都
合に進行させることができ、よってこnl使用した積j
・5板の電気性能が改善され、さらに樹脂の合成過程に
おけるトリエチルアミンの使用量が削減できた。
This invention provides that the weight ratio of water and para-toluene sulfonic acid added is 5 or more and 20 or less, and the weight ratio of water and para-toluene sulfonic acid in the total formulation is 0.7, respectively.
% or more and 4% or less, and 0.1% or more and 0.5% or less, so the reaction between phenols and tung oil can proceed in a favorable manner, and therefore the product used
・The electrical performance of the 5 plates has been improved, and the amount of triethylamine used in the resin synthesis process has been reduced.

特許出願人 松′)′電工株式会社 代理人弁理士 竹 元 敏 丸 (ほか2名)patent applicant Matsu')'Denkou Co., Ltd. Representative Patent Attorney Toshimaru Takemoto (2 others)

Claims (1)

【特許請求の範囲】[Claims] (1) フェノール類と桐油を反応させる場合に8いて
、パラトルエンスルホン酸及び水を添加して反応させる
こととし、かつその量を、水のパラトルエンスルホン酸
の添加量1に対する重量比を5以上20以下となしかつ
全配合にしめる水、パラトルエンスルホン酸の配合の重
量比をそれぞれ0゜7%以上4%以下、0.1%以上0
.5%以下とすることを特徴とするフェノールと桐油の
反応法。
(1) When reacting phenols with tung oil, para-toluenesulfonic acid and water are added and reacted, and the weight ratio of water to the amount of para-toluenesulfonic acid added is 5. The weight ratio of water and para-toluenesulfonic acid in the total formulation should be 0.7% or more and 4% or less, and 0.1% or more and 0.1% or more and 0.1% or more and 0.1% or more and 0.7% or more and 4% or less, respectively.
.. A method for reacting phenol and tung oil, characterized in that the amount is 5% or less.
JP20648783A 1983-10-31 1983-10-31 Reaction of phenol with tung oil Pending JPS6096614A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20648783A JPS6096614A (en) 1983-10-31 1983-10-31 Reaction of phenol with tung oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20648783A JPS6096614A (en) 1983-10-31 1983-10-31 Reaction of phenol with tung oil

Publications (1)

Publication Number Publication Date
JPS6096614A true JPS6096614A (en) 1985-05-30

Family

ID=16524184

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20648783A Pending JPS6096614A (en) 1983-10-31 1983-10-31 Reaction of phenol with tung oil

Country Status (1)

Country Link
JP (1) JPS6096614A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61145216A (en) * 1984-12-19 1986-07-02 Shin Kobe Electric Mach Co Ltd Production of water-soluble phenolic resin for laminate
JPH03188118A (en) * 1989-12-15 1991-08-16 Matsushita Electric Works Ltd Production of oil-modified phenolic resin

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61145216A (en) * 1984-12-19 1986-07-02 Shin Kobe Electric Mach Co Ltd Production of water-soluble phenolic resin for laminate
JPH03188118A (en) * 1989-12-15 1991-08-16 Matsushita Electric Works Ltd Production of oil-modified phenolic resin

Similar Documents

Publication Publication Date Title
JPS6096614A (en) Reaction of phenol with tung oil
CN108822779A (en) A kind of low-temperature setting lignin-base condensation copolymerization resin adhesive and preparation method
CN115418255A (en) Synthetic method for preparing coal water slurry additive by oxidizing, grafting and modifying papermaking black liquor and using method thereof
CN104877610B (en) A kind of resorcinol dialdehyde starch formaldehyde condensation copolymerization resin adhesive and preparation method thereof
CN114133913A (en) Waste molasses-based high-strength environment-friendly formaldehyde-free adhesive and preparation method and application thereof
US3210309A (en) Curing phenolic resins with alphapolyoxymethylene
NO149694B (en) PROCEDURE FOR REDUCING THE QUANTITY OF FREE FORMALDEHYDE IN AN AMINOFORMALDEHYDE RESIN
JPS5831297B2 (en) Manufacturing method of phenolic resin laminate
JP2002137201A (en) Method for forming plywood
CN116478351B (en) Environment-friendly modified light-color phenolic resin and preparation method thereof
CN114479761B (en) Cottonseed protein-based environment-friendly adhesive for plywood and preparation method and application thereof
JPH03203979A (en) Adhesive for plywood
JPS60199014A (en) Production of tung oil-modified phenolic resin
JP2654958B2 (en) Phenol-modified melamine resin adhesive
JPS5853941A (en) Melamine resin composition
CN113861903A (en) High-stability environment-friendly urea-formaldehyde resin and production process thereof
CN106675445A (en) Esterified starch-modified urea-formaldehyde adhesive and preparation method thereof
JP3252730B2 (en) Method for producing phenolic resin composition
CN106883799A (en) One kind is without aldehyde level wood-based plate adhesive and its production technology
CN116284636A (en) Methyl ether amino resin and synthetic method thereof
US1354154A (en) Potentially-reactive composition and process of making same
JP2005206740A (en) Urea-melamine resin composition, adhesive for woody material using the same, woody laminate, and method for producing urea-melamine resin aqueous solution
CN113789144A (en) Flame-retardant polyurethane adhesive and preparation method thereof
CN117402575A (en) Preparation method of urea-formaldehyde resin adhesive
CN115819198A (en) Propylene glycol monovinyl ether and synthesis method and application thereof