JPS60137981A - Binder for grinding whetstone - Google Patents

Binder for grinding whetstone

Info

Publication number
JPS60137981A
JPS60137981A JP24463383A JP24463383A JPS60137981A JP S60137981 A JPS60137981 A JP S60137981A JP 24463383 A JP24463383 A JP 24463383A JP 24463383 A JP24463383 A JP 24463383A JP S60137981 A JPS60137981 A JP S60137981A
Authority
JP
Japan
Prior art keywords
resin
binder
epoxy resin
component
novolak
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
JP24463383A
Other languages
Japanese (ja)
Inventor
Kazuo Morishita
森下 和郎
Hideo Inoue
秀雄 井上
Kenji Yoshida
賢治 吉田
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.)
DIC Corp
Original Assignee
Dainippon Ink and Chemicals 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 Dainippon Ink and Chemicals Co Ltd filed Critical Dainippon Ink and Chemicals Co Ltd
Priority to JP24463383A priority Critical patent/JPS60137981A/en
Publication of JPS60137981A publication Critical patent/JPS60137981A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:To obtain a binder for precision grinding whestone, of high water, alkali and heat resistance, rigidity and whetstone powder sticking power, by imcorporating epoxy resin, novolak-type phenolic resin as curing agent and reaction promotor in whetstone powder. CONSTITUTION:The objective binder can be obtained by incorporating whetstone powder with (A) epoxy resin (e.g. epichlorohydrin bisphenol A-type epoxy resin), (B) novolak-type phenolic resin as curing agent for the component (A) and (C) a reaction promotor (e.g. hexamethylenetetramine) followed by forming, calcination and curing. Preferably, the equivalent ratio of the epoxy group of the component (A) to the active hydrogen in the component (B) is 1/0.8-1/1.1, and the amount of the component (C) is 0.1-1pt.wt. per 100pts.wt. of the components (A) plus (B).

Description

【発明の詳細な説明】 本発明は、耐水性、耐アルカリ性に優れる研削砥石用結
合剤、主に精密研削砥石用結合剤に関わるものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a binder for grinding wheels having excellent water resistance and alkali resistance, and mainly to a binder for precision grinding wheels.

研削砥石は、多数の鈍角を持つ砥粒を結合剤で固着し、
同転研削により目的とする研削、研磨加工を行なうもの
である。一般に要求される結合剤の特性としてU:、 
rAlll性が高いこと、砥粒固着力が強いこと、切削
加工時の衝9gに耐えること、研削熱により変型または
被削材面に融着しないこと、?ill削液により劣化し
々いことq番が挙げられる、従来の結合剤としては、ビ
トリファイド、マグネシアセメント等の蕪機系結合剤の
他、ゴム、フェノール樹脂、ポリビニルアルコール等の
有機系結合剤が公知であり、なかでもフェノール17目
脂系結合剤は作業性、耐熱性が良いために多く使われて
きたが、耐水性、耐アルカリ性に劣るという欠点がある
、 本発明者等は、上記の如き欠点のない有機系結合剤を得
るべく鋭意研究した結果、エポキシ樹脂とノボラック型
フェノール樹脂とを架橋させることによシ、耐熱性、剛
性及び砥粒固着力に優れ、かつ耐水性、耐アルカリ性に
も優れた研削砥石が得られることを見い出し1本発明を
完成するに至った。
Grinding wheels are made by fixing a large number of obtuse-angled abrasive grains with a bonding agent.
The desired grinding and polishing process is performed by simultaneous grinding. Generally required properties of binder are U:,
It has high rAll properties, strong abrasive grain adhesion, withstands 9g of impact during cutting, and does not deform or fuse to the workpiece surface due to grinding heat. Conventional binders that are susceptible to deterioration due to ill removal include vitrified binders, magnesia cement, and other binders, as well as organic binders such as rubber, phenolic resin, and polyvinyl alcohol. Among these, phenol-17 sebum-based binders have been widely used due to their good workability and heat resistance, but they have the disadvantage of poor water resistance and alkali resistance. As a result of intensive research in order to obtain an organic binder that does not have such drawbacks, we found that by crosslinking epoxy resin and novolac type phenolic resin, we have developed a material that has excellent heat resistance, rigidity, and abrasive adhesion, as well as water resistance and alkali resistance. The present invention was completed based on the discovery that an excellent grinding wheel could be obtained.

すなわち本発明は、エポキシ樹脂と7ボラツク型フエノ
ール樹脂と反応促進剤とを含有してなることを特徴とす
る研削砥石用結合剤を提供するものである。
That is, the present invention provides a bonding agent for a grinding wheel, which is characterized by containing an epoxy resin, a 7-borac type phenolic resin, and a reaction accelerator.

従来、本用途のフェノール(I54脂系結合削は、フェ
ノールのオルソ、バラ位にホルムアルデヒドを反応させ
て高分子化させることが看も一般的であり、酸性下で得
られたノボラック型フェノール(a(脂は架橋剤として
ヘキサメチレンテトラミンを用いることにより、又アル
カリ性下で得られたレゾール型フェノール樹脂tよ残存
するメチロール基により、それぞれ加熱硬化が行なわれ
てきた。これに対して本発明は、ノボラック型フェノー
ル(σ(脂をヘキサメチレンテトラミンで硬化させる代
9K、エポキシ樹脂と微量の反応促進剤とを用いること
によって、ノボラック型フェノール樹脂の加熱架橋を行
なわせるものであり、ノボラック構造による耐熱性、1
lIll性とエポキシ樹脂による耐水性、耐アルカリ性
を併せ持たせるものである、さらには、従来のノボラッ
ク型フェノール樹脂とへキサメチレンテトラミンの混合
粉末を用いる場合よりも、低温で完全硬化するという利
点も本発明に使用されるエポキシ樹脂としては、一般に
知られているエポキシ樹脂、例えばエピクロルヒドリン
とビスフェノールAを反応させて得られるエピクロルヒ
ドリン−ビスフェノールA型エポキシ樹脂、ノボラック
型フェノール樹脂またはクレゾール樹脂とエピクロルヒ
ドリンを反応させて得られるエポキシ樹脂、さらにはグ
リコール類トエピクロルヒドリンを反応させて得られる
液状エポキシ樹脂等の多官能エポキシ樹脂が挙げられる
。これらの多官能エポキシ樹脂にはモノグリシジルエー
テル類等の1宮前のエポキシ化合物を併用することもで
きる。
Conventionally, for phenol (I54) fat-based bonding for this purpose, it has been common to react formaldehyde at the ortho and distal positions of phenol to polymerize it, and novolac-type phenol (a (The fat has been thermally cured by using hexamethylenetetramine as a crosslinking agent, or by the methylol groups remaining in the resol type phenolic resin t obtained under alkaline conditions.In contrast, the present invention Novolac-type phenol (σ) is a product in which the novolak-type phenol resin is thermally crosslinked by using an epoxy resin and a small amount of reaction accelerator, and the heat resistance due to the novolak structure is ,1
It has both the water resistance and alkali resistance of epoxy resin, and it also has the advantage of being completely cured at a lower temperature than the conventional mixed powder of novolak type phenol resin and hexamethylenetetramine. The epoxy resin used in the present invention is a generally known epoxy resin, such as an epichlorohydrin-bisphenol A type epoxy resin obtained by reacting epichlorohydrin with bisphenol A, a novolac type phenol resin, or a cresol resin obtained by reacting epichlorohydrin. and polyfunctional epoxy resins such as liquid epoxy resins obtained by reacting glycols toepichlorohydrin. These polyfunctional epoxy resins can also be used in combination with primary epoxy compounds such as monoglycidyl ethers.

またエポキシ樹脂の硬化剤として使用されるノボラック
型フェノール樹脂としては、フェノール、パラターシャ
リ−ブチルフェノール、セカンダリ−ブチルフェノール
、パラオクチルフェノール等のフェノール類、オルソク
レゾール、メタクレゾール、パラクレゾール等のクレゾ
ール類の1種または2種以上とホルムアルデヒドとを反
応させて得られるノボラック型フェノール樹脂で、フェ
ノール性水酸基を有するものが挙げられる。
In addition, the novolac type phenolic resin used as a curing agent for epoxy resins includes phenols such as phenol, paratertiary butylphenol, secondary butylphenol, paraoctylphenol, and cresols such as orthocresol, metacresol, and paracresol. Novolac type phenolic resins obtained by reacting two or more types with formaldehyde, and those having phenolic hydroxyl groups, are mentioned.

さらにまた5反応促進剤としては、2−メチルイミダゾ
ール、2−エチル−4−メチルイミダゾール等のイミダ
ゾール類、ジメチルベンジルアミン、トリエチルアミン
、トリエタノールアミン等のアミン類が使用できる。尚
、ノボラック型フェノール樹脂の架橋剤として使用され
ているヘキサメチレンテトラミンは、硬化反応時に分解
生成するアミン誘導体がエポキシ樹脂とノボラック型フ
ェノール樹脂の硬化を促進させるため、反応促進剤とし
て使用できる。
Furthermore, as the reaction promoter, imidazoles such as 2-methylimidazole and 2-ethyl-4-methylimidazole, and amines such as dimethylbenzylamine, triethylamine, and triethanolamine can be used. Hexamethylenetetramine, which is used as a crosslinking agent for novolac-type phenolic resin, can be used as a reaction accelerator because the amine derivative decomposed and produced during the curing reaction accelerates the curing of the epoxy resin and novolak-type phenolic resin.

本発明で用いるエポキシ樹脂とノボラック型フェノール
樹脂の使用割合は、エポキシ樹脂のエポキシ当量とノボ
ラック型フェノール樹脂の活性水素当量の比がに07〜
1:15、好オしくは1:08〜1:11となる割合で
ある。
The ratio of the epoxy resin and novolac type phenol resin used in the present invention is such that the ratio of the epoxy equivalent of the epoxy resin to the active hydrogen equivalent of the novolak type phenol resin is 07 to
The ratio is 1:15, preferably 1:08 to 1:11.

寸だ1反応促進剤の添加量は、エポキシ樹脂とノボラッ
ク型フェノール樹脂の金言1情100重量部に対して、
通常0.05〜4重量部、好ましくは0.1〜1重量部
の範囲である。
The amount of reaction accelerator added is 100 parts by weight of the epoxy resin and novolak type phenol resin.
The amount is usually 0.05 to 4 parts by weight, preferably 0.1 to 1 part by weight.

本発明の結合剤を用いて研削砥石を製造するには、通常
の方法が適用できる。つまシ、砥粒100重量部に対し
て反応促進剤を含む結合剤を通常10〜60重量部、好
ましくは15〜30重清部の割合で混合して樹脂混合砥
粒とし、次いでこれを金型内に充填し、金型温度10〜
100℃、圧力0.5〜50 kg/m’の条件で成形
した後、140〜200℃まで段階的、あるいは連続的
に外需1して焼成し、十分に結合剤を硬化させることに
より、研削砥石が得られる。
Conventional methods can be applied to produce a grinding wheel using the binder of the present invention. A binder containing a reaction accelerator is mixed with 100 parts by weight of the abrasive grains at a ratio of usually 10 to 60 parts by weight, preferably 15 to 30 parts by weight, to form resin-mixed abrasive grains, which are then mixed with gold. Fill into the mold and set the mold temperature to 10~
After molding at 100℃ and a pressure of 0.5 to 50 kg/m', it is baked stepwise or continuously to 140 to 200℃ to fully harden the binder, and then ground. A whetstone is obtained.

以下に実施例を示す。ただし、いずれも本発明を何ら限
定するものでは々い。尚、例中の%は重量%である。
Examples are shown below. However, none of these limits the present invention in any way. In addition, % in an example is weight %.

実施例1 ノボラック型フェノール樹脂 商品名バーカムTD−2
090[軟化点95℃大日本インキ化学工業(4’lW
J ’)と多官能エポキシ41′Tl脂 商品名エピク
ロン4050 〔軟化点100℃大日本インキ化学工業
0勾製とを、それぞれの活性水素当量とエポキシ当量の
比が1対1となる割合で混合、粉砕し、粉末樹脂を得た
Example 1 Novolac type phenolic resin Product name: Barcam TD-2
090 [Softening point 95℃ Dainippon Ink and Chemicals (4'lW
J') and polyfunctional epoxy 41'Tl resin (trade name: Epiclon 4050 [softening point: 100°C, manufactured by Dainippon Ink & Chemicals, Ltd.) in a ratio of active hydrogen equivalent to epoxy equivalent of 1:1. , and pulverized to obtain powdered resin.

を加えて均一に混合した。さらに、上記で得られた粉末
樹脂を160g加えて均一に混合し、樹脂混合砥粒を得
た。
was added and mixed uniformly. Furthermore, 160 g of the powdered resin obtained above was added and mixed uniformly to obtain resin-mixed abrasive grains.

この混合砥粒を金型内に充填t/%温度60℃、圧力2
0kg/′cIn2の条件で成形した後、80℃で4時
間、120℃で4時間、180℃で2時間焼成して45
0HyJ、厚さ3朋の切断砥石及び試験片を得た。この
砥石は耐熱性、剛性、砥粒固着力、耐水性、耐アルカリ
性に優れるものであった。
This mixed abrasive grain is filled in the mold t/% temperature 60℃, pressure 2
After molding under the conditions of 0 kg/'cIn2, it was baked at 80°C for 4 hours, 120°C for 4 hours, and 180°C for 2 hours.
A cutting wheel and a test piece having a thickness of 0HyJ and a thickness of 3 mm were obtained. This grindstone was excellent in heat resistance, rigidity, abrasive grain adhesion, water resistance, and alkali resistance.

実施例2 ノボラック型フェノール樹脂 商品名パーカムTD−2
090と多官能性エポキシ樹脂 商品名エビクロンN−
775〔軟化点75℃、大日本インキ化学工業(4fJ
?、’! 1とを、それぞれの活性水素当量とエポキシ
肖叶の比がト対09となる割合で混合、粉砕し、粉末樹
脂を得た。
Example 2 Novolac type phenolic resin Product name Percam TD-2
090 and polyfunctional epoxy resin Product name Evicron N-
775 [Softening point 75°C, Dainippon Ink and Chemicals (4fJ
? ,'! 1 and 1 were mixed and pulverized in such a ratio that the ratio of active hydrogen equivalent to epoxy resin was 0:09 to obtain a powdered resin.

砥粒 商品名サフランダムA430 1.000gに1
%2−メチルイミダゾールの水−メタノール混合溶液8
gを加えて均一に混合した。さらに、上記で得られた粉
末樹脂を160g加えて均一に混合し、樹脂混合砥粒を
得た。この混合砥粒を用いて実施例1と同様に成型、焼
成して405朋〆、厚さ3朋の切断砥石及び試験片を得
た。この41に石は耐熱性、剛性、砥粒固着力、耐水性
、耐アルカリ性に優れるものであった。
Abrasive grain Product name Safrandom A430 1 per 1.000g
% 2-methylimidazole water-methanol mixed solution 8
g was added and mixed uniformly. Furthermore, 160 g of the powdered resin obtained above was added and mixed uniformly to obtain resin-mixed abrasive grains. This mixed abrasive grain was molded and fired in the same manner as in Example 1 to obtain a cutting wheel and test piece with a 405mm diameter and 3mm thickness. This stone No. 41 was excellent in heat resistance, rigidity, abrasive grain adhesion, water resistance, and alkali resistance.

比較例1 砥粒 商品名ザクランダム130 1.000gにレゾ
ール型フェノール樹脂 商品名プライオーフェンTD−
2361〔大日本インキ化学工業!4’HW 140.
9を加え、均一に混合した後、ヘキサメチレンテトラミ
ン含有粉末ノボラック型フェノール樹脂 商品名プライ
オーフェンTD−2112(同上社製)120gを加え
、均一に混合して樹脂混合砥粒を得た。この混合砥粒を
用いて実施例1と同様如成型、焼成して405m1Gへ
厚さ3朋の切断砥石及び試験片を得た。この砥石は耐水
性、耐アルカリ性に劣るものであった。
Comparative Example 1 Abrasive grains: Product name: Zakurandom 130 1.000g Resol type phenolic resin: Product name: Pryophen TD-
2361 [Dainippon Ink Chemical Industry! 4'HW 140.
9 was added and mixed uniformly, 120 g of hexamethylenetetramine-containing powdered novolac type phenol resin, trade name Pryophen TD-2112 (manufactured by the same company) was added and mixed uniformly to obtain resin-mixed abrasive grains. Using this mixed abrasive grain, it was molded and fired in the same manner as in Example 1 to obtain a cutting whetstone of 405 ml and a thickness of 3 mm and a test piece. This whetstone had poor water resistance and alkali resistance.

試験例1 実施例1〜2および比較例1で得られた試験片について
曲げ強度を比較し、表1のような結果を得た。
Test Example 1 The bending strengths of the test pieces obtained in Examples 1 to 2 and Comparative Example 1 were compared, and the results shown in Table 1 were obtained.

表 1 註) 1)試験片を沸騰水中で2時間煮沸処理2)試験
片を5%カセイソーダ水溶液中に2時間浸漬抜水洗処理 また、得られた切断砥石の研削性餅を比較し、表2のよ
表 2 被削材 50朋グの5S−41丸棒 註)1)切断砥石を20℃の水中に24時間浸漬。
Table 1 Note) 1) Boiling the test piece in boiling water for 2 hours 2) Immersing the test piece in a 5% caustic soda aqueous solution for 2 hours and washing with water Also, the grindability of the obtained cutting wheels was compared. Noyo Table 2 Work material 50mm 5S-41 round bar Note) 1) Soak the cutting wheel in water at 20°C for 24 hours.

2)上記の被剛材を5回切断した時に要した1回当シの
平均時間。
2) Average time required for each cut when the above rigid material was cut 5 times.

3)上記の被剛材を5回切断した時の砥石の摩耗量。3) Amount of wear on the grindstone when cutting the above rigid material 5 times.

代理人 弁理士 高 橋 勝 利Agent: Patent Attorney Katsutoshi Takahashi

Claims (1)

【特許請求の範囲】[Claims] エポキシ樹脂とノボラック型フェノール樹脂と反応促進
剤とを含有してなることを特徴とする研削砥石用結合剤
A bonding agent for grinding wheels characterized by containing an epoxy resin, a novolac type phenolic resin, and a reaction accelerator.
JP24463383A 1983-12-27 1983-12-27 Binder for grinding whetstone Pending JPS60137981A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24463383A JPS60137981A (en) 1983-12-27 1983-12-27 Binder for grinding whetstone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24463383A JPS60137981A (en) 1983-12-27 1983-12-27 Binder for grinding whetstone

Publications (1)

Publication Number Publication Date
JPS60137981A true JPS60137981A (en) 1985-07-22

Family

ID=17121653

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24463383A Pending JPS60137981A (en) 1983-12-27 1983-12-27 Binder for grinding whetstone

Country Status (1)

Country Link
JP (1) JPS60137981A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6166776A (en) * 1984-09-10 1986-04-05 Nok Corp Vulcanizable adhesive between nbr and metal
JP2786287B2 (en) * 1989-09-01 1998-08-13 トータル、ラフィナージュ、ディストリビュシオン、ソシエテ、アノニム Method and apparatus for steam cracking hydrocarbons in the fluid phase

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6166776A (en) * 1984-09-10 1986-04-05 Nok Corp Vulcanizable adhesive between nbr and metal
JP2786287B2 (en) * 1989-09-01 1998-08-13 トータル、ラフィナージュ、ディストリビュシオン、ソシエテ、アノニム Method and apparatus for steam cracking hydrocarbons in the fluid phase

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