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JPH0881615A - Resinoid wheel - Google Patents

Resinoid wheel

Info

Publication number
JPH0881615A
JPH0881615A JP22048294A JP22048294A JPH0881615A JP H0881615 A JPH0881615 A JP H0881615A JP 22048294 A JP22048294 A JP 22048294A JP 22048294 A JP22048294 A JP 22048294A JP H0881615 A JPH0881615 A JP H0881615A
Authority
JP
Japan
Prior art keywords
resin
naphthol
phenol
parts
condensing
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
JP22048294A
Other languages
Japanese (ja)
Inventor
Masakatsu Asami
昌克 浅見
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.)
Sumitomo Durez Co Ltd
Original Assignee
Sumitomo Durez 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 Sumitomo Durez Co Ltd filed Critical Sumitomo Durez Co Ltd
Priority to JP22048294A priority Critical patent/JPH0881615A/en
Publication of JPH0881615A publication Critical patent/JPH0881615A/en
Pending legal-status Critical Current

Links

Landscapes

  • Phenolic Resins Or Amino Resins (AREA)
  • Polishing Bodies And Polishing Tools (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE: To obtain a resinoid wheel useful for grinding, abrasion and cutting under high load, having improved hot flexing strength, normal-temperature flexing strength after a heat cycle test and excellent thermal shock resistance, containing grinding particles and a binder composed of a specific phenolic resin. CONSTITUTION: This resinoid wheel contains (A) grinding particles and (B) a binder composed of a resin prepared by co-condensing 1 naphthol or 2-naphthol and a phenol resin with an aldehyde. The resin of the component B is a resin obtained by co-condensing 100 pts.wt. of a phenol and 5-300 pts.wt., especially 10-50 pts.wt. of a naphthol with an aldehyde in an amount of 0.5-2.5mol based on 1mol of the phenol by using an acid catalyst or an alkali catalyst. A resin containing the naphthol in the ratio obtained by blending the phenol resin or the naphthol resin with the co-condensed resin may be used. Or a resin obtained by mixing the phenol resin with the naphthol resin and co-condensing the mixture in curing may be used.

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、レジノイド砥石に関す
るものであり、特に耐熱性、耐熱衝撃性が要求される高
荷重用途の研削、研磨及び切断レジノイド砥石に関する
ものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resinoid grindstone, and more particularly to a grinding, polishing and cutting resinoid grindstone for high load applications where heat resistance and thermal shock resistance are required.

【0002】[0002]

【従来の技術】鋳鉄等の高硬度物質を高荷重で、研削、
研磨及び切断レジノイド砥石は、砥粒として主に比較的
粒度の粗い酸化アルミナが用いられ、結合剤には一般に
フェノール樹脂が用いられ、これらから加熱成形して製
造される。近年、割れ防止、高研削性のため耐熱性、耐
熱衝撃性がレジノイド砥石に求められてきた。そこで、
結合剤として、硼酸、マレイミド系樹脂等による変性フ
ェノール樹脂、あるいはマレイミド系樹脂が試みられ
た。しかし、変性フェノール樹脂を結合剤として用いた
レジノイド砥石は、耐熱性は向上するが、耐熱衝撃性が
効果的に向上せず、マレイミド系樹脂を用いたレジノイ
ド砥石は、硬化温度の高いことと砥粒との接着性が劣る
ことにより、結果的に耐熱性が低下する欠点があった。
2. Description of the Related Art Grinding high hardness materials such as cast iron under high load,
Abrasive and cutting resinoid grindstones are mainly made of alumina oxide having a relatively coarse grain size as abrasive grains, and generally a phenol resin is used as a binder, and are manufactured by heat molding from these. In recent years, resinoid grindstones have been required to have heat resistance and thermal shock resistance due to crack prevention and high grindability. Therefore,
As a binder, a modified phenol resin such as boric acid or a maleimide resin, or a maleimide resin has been tried. However, the resinoid grindstone using the modified phenolic resin as the binder improves the heat resistance, but the thermal shock resistance does not effectively improve, and the resinoid grindstone using the maleimide-based resin has a high curing temperature and Due to the poor adhesiveness with the particles, there is a drawback that the heat resistance is consequently lowered.

【0003】[0003]

【本発明が解決しようとする課題】本発明は、主に高荷
重用途での耐熱性、耐熱衝撃性が向上するレジノイド砥
石を鋭意研究した結果、結合剤として1−ナフトール及
び/又は2−ナフトールとフェノール類とをアルデヒド
類により共縮合させた樹脂を用いる事により上記特性を
向上させる知見を得、更にこの知見に基づき種々研究を
進め完成するに至ったのものである。
DISCLOSURE OF INVENTION Problems to be Solved by the Invention The present invention has been earnestly studied for resinoid grindstones having improved heat resistance and thermal shock resistance in high load applications, and as a result, 1-naphthol and / or 2-naphthol as a binder has been obtained. By using a resin in which aldehydes and phenols were co-condensed with aldehydes, we obtained the knowledge that the above characteristics were improved, and based on this knowledge, we proceeded with various researches and completed them.

【0004】[0004]

【課題を解決するための手段】本発明でいう、1−ナフ
トール及び/又は2−ナフトールとフェノール類とをア
ルデヒド類により共縮合させた樹脂は、通常フェノール
類100重量部に対してナフトール5〜300重量部、
好ましくは10〜50重量部とナフトールとフェノール
類に対して0.5〜2.5モルのアルデヒド類とを、酸
触媒あるいはアルカリ触媒によって、共縮合した樹脂で
ある。ナフトール5重量部以下では変性による効果が現
れない。300重量部以上では耐熱性、耐熱衝撃性は同
等かやや向上するが、基材との密着性が低下するように
なる。また、フェノール樹脂あるいはナフトール樹脂と
共縮合樹脂を混合しナフトールの割合を上記割合とした
樹脂、あるいは、フェノール樹脂とナフトール樹脂を混
合し、硬化時に共縮合する樹脂であってもよく、本発明
に含まれる。
In the present invention, a resin obtained by co-condensing 1-naphthol and / or 2-naphthol and a phenol with an aldehyde is usually used in an amount of 5 to 100 parts by weight of a phenol. 300 parts by weight,
A resin obtained by co-condensing 10 to 50 parts by weight of naphthol and 0.5 to 2.5 mol of aldehyde with respect to phenols with an acid catalyst or an alkali catalyst is preferable. If the amount of naphthol is 5 parts by weight or less, the effect due to modification does not appear. When the amount is 300 parts by weight or more, the heat resistance and the thermal shock resistance are the same or slightly improved, but the adhesion to the base material is lowered. Further, it may be a resin in which a phenol resin or a naphthol resin and a co-condensation resin are mixed so that the ratio of naphthol is the above ratio, or a resin in which a phenol resin and a naphthol resin are mixed and co-condensed at the time of curing. included.

【0005】本発明に用いられるフェノール類として
は、フェノール、オルソクレゾール、メタクレゾール、
パラクレゾール、キシレノール、パラターシャリーブチ
ルフェノール、パラオクチルフェノール、パラフェニル
フェノール、ビスフェノールAなどのフェノール類から
選ばれた少なくとも1種以上のフェノール類であり、立
体障害の少ないフェノール類が好ましいが、特に限定は
しない。アルデヒド類としては、ホルムアルデヒド、ア
セトアルデヒド、ブチルアルデヒド、アクロレインやこ
れらの混合物であり、これらのアルデヒド類の発生源と
なる物質あるいはこれらのアルデヒド類の溶液を使用す
ることも可能である。
The phenols used in the present invention include phenol, orthocresol, metacresol,
It is at least one or more phenols selected from phenols such as para-cresol, xylenol, para-tertiary-butylphenol, para-octylphenol, para-phenylphenol, and bisphenol A. Phenols with less steric hindrance are preferable, but the limitation is not particularly limited. do not do. The aldehyde is formaldehyde, acetaldehyde, butyraldehyde, acrolein, or a mixture thereof, and it is also possible to use a substance which is a source of generation of these aldehydes or a solution of these aldehydes.

【0006】アルカリ触媒としては、リチウム、ナトリ
ウム、カリウム等のアルカリ金属水酸化物やマグネシウ
ム、カルシウム、バリウム等のアルカリ土類金属水酸化
物及びこれらと同様の作用効果を示す炭酸塩等の塩類及
び酸化物が使用でき、アミン、アンモニア、さらに他の
アルカリ触媒を併用使用する事ができる。酸触媒として
は、蓚酸、パラトルエンスルホン酸、キシレンスルホン
酸、フェノールスルホン酸等の有機酸や塩酸、硫酸とい
った無機酸が使用できる。また、硬化剤として、ヘキサ
メチレンテトラミン、パラホルムアルデヒド、トリオキ
サン等を含有することができる。
Examples of the alkali catalyst include alkali metal hydroxides such as lithium, sodium and potassium, alkaline earth metal hydroxides such as magnesium, calcium and barium, and salts such as carbonates having the same action and effect. Oxides can be used, and amines, ammonia, and other alkali catalysts can be used together. As the acid catalyst, organic acids such as oxalic acid, p-toluenesulfonic acid, xylenesulfonic acid and phenolsulfonic acid, and inorganic acids such as hydrochloric acid and sulfuric acid can be used. Hexamethylenetetramine, paraformaldehyde, trioxane and the like can be contained as a curing agent.

【0007】本発明に用いられる砥粒は、酸化アルミ
ナ、炭化珪素、ダイヤモンド等があるが、特に限定はし
ない。その他の充填材として、氷晶石、硫化鉄、酸化
鉄、硫酸バリウム、生石灰等の無機フィラー、熱硬化性
樹脂硬化粉末、籾殻、木粉などの有機フィラーを用いる
ことができる。また、砥粒との接着性を向上させる為、
砥粒表面をシランカップリング剤等により処理する事
や、あるいは、フルフラール、フルフリルアルコール、
クレオソート油、その他の有機溶剤、又は液状樹脂であ
るフェノール樹脂などによって予め湿らせることが可能
である。
The abrasive grains used in the present invention include alumina oxide, silicon carbide, diamond and the like, but are not particularly limited. Other fillers that can be used include inorganic fillers such as cryolite, iron sulfide, iron oxide, barium sulfate, quicklime, and organic fillers such as thermosetting resin-cured powder, rice husk, and wood powder. Also, in order to improve the adhesiveness with the abrasive grains,
Treating the abrasive grain surface with a silane coupling agent, or furfural, furfuryl alcohol,
It is possible to pre-moisten it with creosote oil, other organic solvent, or phenol resin which is a liquid resin.

【0008】[0008]

【作用】本発明のレジノイド砥石は、ナフトールとフェ
ノール類との共縮合樹脂であるので、架橋密度が高く、
砥粒保持力が十分であり、高温時においてはナフトール
の耐熱性により強度劣化が極めて小さい特長を有する。
[Function] Since the resinoid grindstone of the present invention is a co-condensation resin of naphthol and phenols, it has a high crosslinking density,
It has sufficient characteristics to retain abrasive grains, and its strength is extremely small due to the heat resistance of naphthol at high temperatures.

【0009】[0009]

【実施例】以下、本発明を実施例により詳細に説明す
る。ここで記載されている「部」及び「%」は、全て
「重量部」及び「重量%」を示す。
EXAMPLES The present invention will be described in detail below with reference to examples. All "parts" and "%" described herein indicate "parts by weight" and "% by weight".

【0010】(製造例1)4つ口フラスコに、フェノー
ル800部と2−ナフトール200部、次いで蓚酸10
部を仕込んで除々に昇温し、温度が96℃に達してから
37%ホルムアルデヒド575部を60分かけて逐添反
応させ、120分間還流反応後、真空脱水反応を行い常
温で固形のフェノールと2−ナフトール重縮合物850
部を得た。得られたフェノールと2−ナフトールとの重
縮合物100部とヘキサメチレンテトラミン14部を予
備混練し、これを粉砕して、粉末状のフェノール類・2
−ナフトール共縮合樹脂A110部を得た。
(Production Example 1) 800 parts of phenol, 200 parts of 2-naphthol, and 10 parts of oxalic acid were placed in a four-necked flask.
After the temperature of the mixture reaches 90 ° C., 575 parts of 37% formaldehyde is added thereto for 60 minutes to carry out an addition reaction. After refluxing for 120 minutes, a vacuum dehydration reaction is performed to form a solid phenol at room temperature. 2-naphthol polycondensate 850
I got a part. 100 parts of the obtained polycondensate of phenol and 2-naphthol and 14 parts of hexamethylenetetramine were pre-kneaded and pulverized to obtain powdered phenols.
-110 parts of naphthol co-condensation resin A were obtained.

【0011】(製造例2)4つ口フラスコに、フェノー
ル600部と2−ナフトール400部、次いで蓚酸10
部を仕込んで除々に昇温し、温度が96℃に達してから
37%ホルムアルデヒド530部を60分かけて逐添反
応させ、120分間還流反応後、真空脱水反応を行い常
温で固形のフェノール・2−ナフトール重縮合物830
部を得た。得られたフェノール・2−ナフトール重縮合
物100部とヘキサメチレンテトラミン14部を予備混
練し、これを粉砕して、粉末状のフェノール類と2−ナ
フトールの共縮合樹脂B110部を得た。
(Production Example 2) In a four-necked flask, 600 parts of phenol and 400 parts of 2-naphthol were added, and then 10 parts of oxalic acid.
After the temperature of the mixture reaches 96 ° C., 530 parts of 37% formaldehyde is added thereto for 60 minutes to carry out a side-by-side reaction. After refluxing for 120 minutes, a vacuum dehydration reaction is carried out to conduct solid phenol reaction at room temperature. 2-naphthol polycondensate 830
I got a part. 100 parts of the obtained phenol-2-naphthol polycondensate and 14 parts of hexamethylenetetramine were pre-kneaded and pulverized to obtain 110 parts of powdery phenols and 2-naphthol co-condensation resin B.

【0012】(製造例3)4つ口フラスコに、フェノー
ル1000部と37%ホルムアルデヒド650部、次い
で蓚酸1部を仕込んで徐々に昇温し、温度が96℃に達
してから120分間還流反応後、真空下で脱水反応を行
い釜出しした。常温で固形のノボラック型フェノール樹
脂960部を得た。得られたノボラック型フェノール樹
脂100部に対してヘキサミン14部を予備混合し、こ
れを粉砕し、粉末状フェノール樹脂C110部を得た。
(Production Example 3) 1000 parts of phenol, 650 parts of 37% formaldehyde, and then 1 part of oxalic acid were charged into a four-necked flask, and the temperature was gradually raised. After the temperature reached 96 ° C., the mixture was refluxed for 120 minutes. Then, the dehydration reaction was carried out under vacuum, and the container was removed from the kettle. 960 parts of a solid novolac type phenolic resin was obtained at room temperature. 14 parts of hexamine was premixed with 100 parts of the obtained novolac type phenol resin, and this was pulverized to obtain 110 parts of powdery phenol resin C.

【0013】(砥石試験片の製造)砥石試験片を作製
し、抗折強度試験を行った。なお、砥石試験片の配合条
件と作成手順は以下の通りである。 砥粒(A# 12) :100.0部 樹脂 : 15.0 硫化鉄 : 10.0 氷晶石 : 10.0 生石灰 : 1.5 フルフラール : 1.0 砥粒とフルフラールを実験用ミキサーで常温で5分間混
練し、その後、樹脂、硫化鉄、氷晶石及び生石灰の混合
粉末を混合し、3分間混練する。上記配合物を15×2
5×100mmの金型に入れ、温度160℃、圧力50
0kg/cm2にて15分間成形した。これを常温から
170℃まで10時間、次いで170℃で5時間、計1
5時間焼成して、砥石カサ比重3.05の砥石試験片を
得た。
(Production of Grindstone Test Piece) A grindstone test piece was prepared and subjected to a bending strength test. In addition, the compounding conditions of the grindstone test piece and the preparation procedure are as follows. Abrasive grains (A # 12): 100.0 parts Resin: 15.0 Iron sulfide: 10.0 Cryolite: 10.0 Quick lime: 1.5 Furfural: 1.0 Abrasive grains and furfural are mixed in a laboratory mixer at room temperature For 5 minutes, and then mixed powder of resin, iron sulfide, cryolite and quicklime is mixed and kneaded for 3 minutes. 15 × 2 of the above mixture
Put in a mold of 5 × 100mm, temperature 160 ℃, pressure 50
It was molded at 0 kg / cm 2 for 15 minutes. From room temperature to 170 ℃ for 10 hours, then 170 ℃ for 5 hours, total 1
Firing was carried out for 5 hours to obtain a whetstone test piece having a whetstone bulk specific gravity of 3.05.

【0014】《実施例1》バインダーとして粉末状のフ
ェノール類・2−ナフトール共縮合樹脂Aを用い、上記
(砥石試験片の製造)に従い、レジノイド砥石試験片を
作製した。 《実施例2》バインダーとして粉末状のフェノール類・
2−ナフトール共縮合樹脂Bを用い、上記(砥石試験片
の製造)に従い、レジノイド砥石試験片を作製した。 《比較例1》バインダーとして粉末状フェノール樹脂C
を用い、上記(砥石試験片の製造)に従い、レジノイド
砥石試験片を作製した。
Example 1 A resinoid grindstone test piece was prepared in accordance with the above (Production of grindstone test piece) using a powdery phenol / 2-naphthol co-condensation resin A as a binder. << Example 2 >> Powdered phenols as a binder
Using the 2-naphthol co-condensation resin B, a resinoid grindstone test piece was prepared according to the above (Production of grindstone test piece). << Comparative Example 1 >> Phenolic resin C in powder form as a binder
Using the above, a resinoid grindstone test piece was prepared according to the above (manufacture of grindstone test piece).

【0015】この試験片により、常温及び熱間(250
℃)でのそれぞれ抗折強度を測定評価した。また、空気
中において、300℃雰囲気下30分と25℃雰囲気下
30分とを交互に10回繰り返して暴露するヒートサイ
クル試験を行い、常温にて抗折強度を測定した。これら
の結果を表1に示す。
With this test piece, at room temperature and hot (250
The bending strength at each temperature was measured and evaluated. Further, in air, a heat cycle test was performed in which exposure was repeated 10 times under a 300 ° C. atmosphere for 30 minutes and a 25 ° C. atmosphere for 30 minutes, and the bending strength was measured at room temperature. Table 1 shows the results.

【0016】 表 1 抗折強度 ───────────────────────────────── 実施例1 実施例2 比較例1 ───────────────────────────────── 用いたフェノール樹脂 A B C 常温抗折強度 (kg/cm2) 436 425 443 熱間抗折強度 (kg/cm2) 248 245 221 ヒートサイクル試験後の抗折強度(kg/cm2) 83 121 41 ─────────────────────────────────Table 1 Bending strength ───────────────────────────────── Example 1 Example 2 Comparative example 1 ───────────────────────────────── Phenolic resin used A B C Normal temperature bending strength (kg / cm 2 ) 436 425 443 Hot bending strength (kg / cm 2 ) 248 245 221 bending strength after heat cycle test (kg / cm 2 ) 83 121 41 41 ───────────────── ─────────────────

【0017】[0017]

【発明の効果】本発明のレジノイド砥石は、上記結果が
示す通り熱間抗折強度、ヒートサイクル試験後の常温抗
折強度が上がっており、耐熱性、耐熱衝撃性に優れてい
ることが認められる。
EFFECTS OF THE INVENTION The resinoid grindstone of the present invention has improved hot bending strength and room temperature bending strength after a heat cycle test as shown by the above results, and is recognized to have excellent heat resistance and thermal shock resistance. To be

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 砥粒と樹脂組成物からなる結合剤等を含
有するレジノイド砥石において、結合剤が1−ナフトー
ル及び/又は2−ナフトールとフェノール類とをアルデ
ヒド類により共縮合させた樹脂であることを特徴とする
レジノイド砥石。
1. A resinoid grindstone containing a binder and the like composed of abrasive grains and a resin composition, wherein the binder is a resin in which 1-naphthol and / or 2-naphthol and phenols are co-condensed with aldehydes. Resinoid grindstone characterized by that.
JP22048294A 1994-09-14 1994-09-14 Resinoid wheel Pending JPH0881615A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22048294A JPH0881615A (en) 1994-09-14 1994-09-14 Resinoid wheel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22048294A JPH0881615A (en) 1994-09-14 1994-09-14 Resinoid wheel

Publications (1)

Publication Number Publication Date
JPH0881615A true JPH0881615A (en) 1996-03-26

Family

ID=16751782

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22048294A Pending JPH0881615A (en) 1994-09-14 1994-09-14 Resinoid wheel

Country Status (1)

Country Link
JP (1) JPH0881615A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012111806A (en) * 2010-11-22 2012-06-14 Sumitomo Bakelite Co Ltd Phenol resin composition for friction material, method for producing phenol resin for friction material and friction material
JP2013194207A (en) * 2012-03-22 2013-09-30 Dic Corp Resol-type phenolic resin composition
CN107336146A (en) * 2017-09-03 2017-11-10 东莞市金利威磨料磨具有限公司 A kind of formula and processing method of antidamping resin thin slice grinding wheel
CN107363743A (en) * 2017-09-03 2017-11-21 东莞市金利威磨料磨具有限公司 A kind of formula and processing method of cutting-grinding dual-purpose resin wheel

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012111806A (en) * 2010-11-22 2012-06-14 Sumitomo Bakelite Co Ltd Phenol resin composition for friction material, method for producing phenol resin for friction material and friction material
JP2013194207A (en) * 2012-03-22 2013-09-30 Dic Corp Resol-type phenolic resin composition
CN107336146A (en) * 2017-09-03 2017-11-10 东莞市金利威磨料磨具有限公司 A kind of formula and processing method of antidamping resin thin slice grinding wheel
CN107363743A (en) * 2017-09-03 2017-11-21 东莞市金利威磨料磨具有限公司 A kind of formula and processing method of cutting-grinding dual-purpose resin wheel
CN107363743B (en) * 2017-09-03 2019-03-15 东莞市金利威磨料磨具有限公司 A kind of formula and processing method of cutting-grinding dual-purpose resin wheel
CN107336146B (en) * 2017-09-03 2019-04-30 东莞市金利威磨料磨具有限公司 A kind of formula and processing method of anti-attenuation resin thin slice grinding wheel

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