JPH0881615A - Resinoid wheel - Google Patents
Resinoid wheelInfo
- 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
Links
- 239000011347 resin Substances 0.000 claims abstract description 28
- 229920005989 resin Polymers 0.000 claims abstract description 28
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 claims abstract description 24
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229950011260 betanaphthol Drugs 0.000 claims abstract description 13
- 239000011230 binding agent Substances 0.000 claims abstract description 11
- 150000002989 phenols Chemical class 0.000 claims description 11
- 239000006061 abrasive grain Substances 0.000 claims description 8
- 150000001299 aldehydes Chemical class 0.000 claims description 8
- 239000011342 resin composition Substances 0.000 claims 1
- 239000005011 phenolic resin Substances 0.000 abstract description 13
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 12
- 230000035939 shock Effects 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 6
- 238000000227 grinding Methods 0.000 abstract description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract description 4
- 239000003513 alkali Substances 0.000 abstract description 4
- 239000003054 catalyst Substances 0.000 abstract description 4
- 239000003377 acid catalyst Substances 0.000 abstract description 3
- 238000005520 cutting process Methods 0.000 abstract description 3
- 239000002245 particle Substances 0.000 abstract description 3
- 229920001568 phenolic resin Polymers 0.000 abstract description 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 2
- 238000002156 mixing Methods 0.000 abstract 2
- 238000005299 abrasion Methods 0.000 abstract 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 12
- 238000005452 bending Methods 0.000 description 7
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000009833 condensation Methods 0.000 description 6
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 6
- 239000004312 hexamethylene tetramine Substances 0.000 description 4
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 4
- 235000006408 oxalic acid Nutrition 0.000 description 4
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 3
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 3
- 239000000292 calcium oxide Substances 0.000 description 3
- 235000012255 calcium oxide Nutrition 0.000 description 3
- 229910001610 cryolite Inorganic materials 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000013003 hot bending Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical group O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- JIRHAGAOHOYLNO-UHFFFAOYSA-N (3-cyclopentyloxy-4-methoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC1CCCC1 JIRHAGAOHOYLNO-UHFFFAOYSA-N 0.000 description 1
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 235000006173 Larrea tridentata Nutrition 0.000 description 1
- 244000073231 Larrea tridentata Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
- -1 bisphenol A. Phenols Chemical class 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229960002126 creosote Drugs 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000010680 novolac-type phenolic resin Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 150000003739 xylenols Chemical class 0.000 description 1
Landscapes
- Phenolic Resins Or Amino Resins (AREA)
- Polishing Bodies And Polishing Tools (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【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)
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.
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)
| 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 |
-
1994
- 1994-09-14 JP JP22048294A patent/JPH0881615A/en active Pending
Cited By (6)
| 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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