JPS61197164A - Synthetic grindstone and its production method - Google Patents

Synthetic grindstone and its production method

Info

Publication number
JPS61197164A
JPS61197164A JP3465785A JP3465785A JPS61197164A JP S61197164 A JPS61197164 A JP S61197164A JP 3465785 A JP3465785 A JP 3465785A JP 3465785 A JP3465785 A JP 3465785A JP S61197164 A JPS61197164 A JP S61197164A
Authority
JP
Japan
Prior art keywords
resin
synthetic
grindstone
liquid
melamine
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.)
Granted
Application number
JP3465785A
Other languages
Japanese (ja)
Other versions
JPH0583343B2 (en
Inventor
Yoji Tomita
富田 洋司
Kan Sato
佐藤 敢
Mitsuru Maruya
丸屋 充
Masaru Nakamura
勝 中村
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.)
Kanebo Ltd
Original Assignee
Kanebo 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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP3465785A priority Critical patent/JPS61197164A/en
Publication of JPS61197164A publication Critical patent/JPS61197164A/en
Publication of JPH0583343B2 publication Critical patent/JPH0583343B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a resinoid synthetic grindstone having excellent smoothness and a high void ratio by adding grindstone particles, a pore formation promoter and a catalyzer to the mixed liquid of a liquid type phenolic resin and a melamine resin the then hardening it through equal churning, drying and heating. CONSTITUTION:Phenolic and melamine liquid resins are used for materials. And grindstone particles, a pore formation promoter as well as a catalyzer are added to the material which is hardened by equal churning, drying and heating. A synthetic grindstone produced by the above method is an excellent semi-elastic grindstone and various grindstones are obtainable by changing properly mixing rate, between both resins, void ratio and heat treatment conditions. Furthermore, this synthetic grindstone has a good autogenous formation due to its proper fragility and capability to discharge smoothly grinding scraps and dropped grindstone particles from the surface of metarials to be abraded through voids and further the production of high count grindstones is possible, whereby the high precision abrasion of comparatively hard metals is feasible.

Description

【発明の詳細な説明】 〈産業との利用分野) 本発明は1合成樹脂を結合材とした固形砥石。[Detailed description of the invention] (Applications with industry) The present invention provides a solid grindstone using synthetic resin as a binding material.

所謂レジメイド系砥石で、比較的精密研磨に適したもの
およびその製造方法に関するものである。
This article relates to a so-called remade grindstone that is suitable for relatively precision polishing, and a method for manufacturing the same.

(従来の技術〉 従来、研磨用の固形砥石としては、砥粒の微細粒子を何
らかの結合材を用いて把持し固定化したものか−・般的
であり、その結合材にセラミックスを用いたビトリファ
イド系砥石、フェノール系熱硬化性樹脂を用いたレジノ
イド系砥石、あるいはポリビニルアセタール樹脂を用い
たPVA系弾性砥石等が挙げられ、各々その特性に応じ
て使用分IIIも異なるものであった・ 就中、し/ノイド系砥石は、樹脂の種:n、製ごキ件、
使用砥粒の粒径等に応じて多様化がTI7 j屯、屯研
削から仕上げ研磨の分野まで広い範囲のネ11用分野が
あり、特にその位置付けとしては、ビトリファイド系砥
石に代表される剛性砥石と、ポリビニルアセタール系弾
性砥石との中間にあり。
(Conventional technology) Conventionally, solid grindstones for polishing have generally been made by holding and fixing fine particles of abrasive grains using some kind of binding material. Examples include a resin-based grindstone using a phenolic thermosetting resin, a PVA-based elastic grindstone using a polyvinyl acetal resin, etc., and the amount III used for each differs depending on its characteristics. 、Shi/noid type grindstone has resin type: n、manufacturing condition、
There are a wide range of applications for TI7, from grinding to final polishing, which vary depending on the particle size of the abrasive grains used. and polyvinyl acetal-based elastic grinding wheels.

セミ弾性砥石と称せられ、研削力および磨き力を、せも
つ高性能砥石として高い評価を受けていた。レジノイド
系砥石の結合材として用いられる熱硬化性樹脂はフェノ
ール系の樹脂が一般的で。
It was called a semi-elastic whetstone and was highly praised as a high-performance whetstone with excellent grinding and polishing power. The thermosetting resin used as the binding material for resinoid grinding wheels is generally phenolic resin.

その製法は通常、砥粒粉末とフェノール系樹脂粉末とを
混合し、液状フェノール系樹脂粉末をもって混練して粘
稠ペーストとなし、これを所定の型に入れプレス成形し
た後、熱プレス固化し更にキユアリングを行ない硬化せ
しめるという方法がとられていた。
The manufacturing method is usually to mix abrasive grain powder and phenolic resin powder, knead with liquid phenolic resin powder to make a viscous paste, put this into a predetermined mold, press mold, heat press solidify, and then The method used was to perform curing to harden the material.

(本発明が解決しようとする問題点) 前述の如き方法にて製造されるレジノイド系砥石は、砥
石の重要要素である空隙率が比較的低く嵩比重が高いた
めに重くて使用しにくい上、粉末樹脂と砥粒とを機械的
に混合するという手段を用いるため、微細な砥粒を均一
に分散することが極めて難しく、製造の限界が高々10
004手(砥粒平均粒径約leg■)程度で、それ以上
の高番手のものは頗る得にくいという欠点があった。し
かも空隙率が低いということは、研磨屑の逃げ、研磨熱
の放散という点で著しく不利であり、従って広い面積で
・被研磨体と接触し、研磨すること、すなわち平面研磨
という方式には梢々不向きな点があった。また比較的硬
質の金属1例えばクロム、ニッケル等で鍍金された面の
精密研■に対しても適用には難があり、それら高精度を
要求される研磨は依然として非能率、高コストにして作
業環境上問題の多い、遊離砥粒によるうシピング方式や
、パフ仕上げ方式に依存していた。
(Problems to be Solved by the Present Invention) Resinoid grindstones manufactured by the method described above have a relatively low porosity, which is an important element of a grindstone, and a high bulk specific gravity, making them heavy and difficult to use. Since a method of mechanically mixing powdered resin and abrasive grains is used, it is extremely difficult to uniformly disperse fine abrasive grains, and the manufacturing limit is at most 10%.
The abrasive grain size is about 0.004 (average grain size of approximately leg ■), and it has the disadvantage that it is very difficult to obtain one with a higher grit. Moreover, the low porosity is extremely disadvantageous in terms of escape of polishing debris and dissipation of polishing heat. There were some disadvantages. It is also difficult to apply precision polishing to surfaces plated with relatively hard metals such as chromium, nickel, etc., and polishing that requires high precision remains inefficient and costly. It relied on the sipping method using loose abrasive grains and the puff finishing method, which had many environmental problems.

本発明者等は、従来のレジノイド系砥石に見られる上述
の欠点および現状の問題点に鑑み、鋭意研究を行ない本
発明を完成するに至ったものであり、その目的とすると
ころは、優れた平滑度と高い面精度とを几えた金属表面
、特に比較的硬質の金属表面を、経済的有利にしかも1
33境汚染問題を伴なわずに取得するにある。他の目的
は、比較的空隙率が高く研磨性能にすぐれたレジノイド
蓄舎  □成砥石を提供するにある。
In view of the above-mentioned drawbacks and current problems of conventional resinoid grinding wheels, the present inventors conducted intensive research and completed the present invention. Metal surfaces with excellent smoothness and high surface precision, especially relatively hard metal surfaces, can be economically advantageously and
33 to be obtained without environmental pollution problems. Another purpose is to provide a resinoid grindstone with a relatively high porosity and excellent polishing performance.

(問題点を解決するための手段〉 上述の目的は、空隙率が30〜80容量%の三次元別状
組織をなす構造体であって、該組織が、フェノール系樹
脂(P)とメラミン系樹脂(M)との2成分系熱硬化性
樹脂硬化体を主成分とするマトリックスと、該マトリッ
クス中に緻密に内在し固定化された砥粒とからなること
を特徴とする合成研石によって達成される。
(Means for Solving the Problems) The above object is to provide a structure having a three-dimensional separate structure with a porosity of 30 to 80% by volume, the structure consisting of a phenolic resin (P) and a melamine resin. This is achieved by a synthetic abrasive stone characterized by consisting of a matrix whose main component is a two-component thermosetting resin cured product of (M) and abrasive grains that are densely embedded and fixed in the matrix. Ru.

か−る合成砥石を取得するための本発明方法は、液状フ
ェノール果樹11ti(P)と液状メラミン系樹脂(M
)とから主としてなる混合液に砥粒。
The method of the present invention for obtaining such a synthetic grindstone is based on liquid phenolic fruit tree 11ti (P) and liquid melamine resin (M
) and abrasive grains to the mixture mainly consisting of.

′“【花生成剤および触媒を加え均一に攪拌したスラリ
ー状原液を反応固化せしめた中間体を、乾燥して水分お
よび/または溶剤を除去した後、熱処理上流して硬化す
ることを特徴とするものである。
``[It is characterized in that the intermediate is made by reacting and solidifying a slurry-like stock solution in which a flower-forming agent and a catalyst are added and uniformly stirred, and after drying to remove moisture and/or solvent, the intermediate is cured by heat treatment. It is something.

すなわち1、従来のレジノイド系砥石の結合材がほとん
どフェノール系樹脂の硬化体を主体とするものであるの
に対し1本発明は、その靭性を抑え脆性(もろさ)を与
えるために、メラミン系樹脂の硬化体を併用したもので
あり、更にその空隙率を高くし研磨性能の持続性を向上
し、特に、精密研磨に適した物性をレジノイド系砥石に
賦与することを主眼点とするものである。
In other words, 1. While the bonding material of conventional resinoid grinding wheels is mostly composed of hardened phenolic resin, the present invention uses melamine resin to suppress the toughness and give brittleness. The main aim is to further increase the porosity and improve the sustainability of polishing performance, and in particular to give resinoid-based grindstones physical properties suitable for precision polishing. .

本発明者等は、精密研磨に適した性能、換言すれば切刃
の自生作用に優れた性能は、砥石のマトリックスの主成
分としてフェノール系樹脂とメラミン系樹脂との2成分
系硬化体を適用し、結合材としてのフェノール系樹脂硬
化体の靭性(ねばり)を抑制し、適度な脆性(もろさ)
をマトリックスに付与することによって得られることを
知見した。つまり、フェノール系樹脂の硬化体は比較的
靭性が高いため、従来のレジノイド系砥石は。
The present inventors have found that performance suitable for precision polishing, in other words, excellent performance for self-sharpening of the cutting edge, is achieved by applying a two-component hardened product of phenolic resin and melamine resin as the main components of the grinding wheel matrix. This suppresses the toughness (stickiness) of the cured phenolic resin as a binder and maintains appropriate brittleness.
It was discovered that this can be obtained by adding . In other words, the hardened phenolic resin has relatively high toughness, so conventional resinoid grinding wheels.

高い圧力で圧着しつつ研磨を行なわなければその性能を
充分に発揮し得ないが、マトリックスにメラミン系樹脂
の硬化体を併用することにより、低重゛でその性能を充
分に発揮し得ることを見出したのである。
Although it is not possible to fully demonstrate its performance unless it is crimped with high pressure and polished, it is possible to fully demonstrate its performance with a low weight by using a hardened melamine resin in the matrix. I found it.

フェノール系樹脂 (P)とメラミン系樹脂(M)との
組成比率は1mμ基亭にてP/M・1/2〜3/lに設
定することが好ましい、これを上回ると、メラミン系樹
脂併用の効果は薄く、従来のレジノイド系合成砥石とほ
とんど変わらず、また。
The composition ratio of phenolic resin (P) and melamine resin (M) is preferably set to P/M 1/2 to 3/l at 1 mμ base; if it exceeds this, melamine resin is used in combination. The effect is weak and almost the same as that of conventional resinoid-based synthetic whetstones.

これを下回ると脆すざて、レジノイド系砥石としての性
能を発揮し難くなるので何れにしても好ましくない、更
に、マトリックスの空隙率は30〜30容量%の範囲内
に設定することが必要である。
If it is less than this, it will become brittle and it will be difficult to demonstrate its performance as a resinoid-based grinding wheel, so it is undesirable in any case.Furthermore, the porosity of the matrix needs to be set within the range of 30 to 30% by volume. be.

すなわち30容量%を下回ると研磨屑、脱落砥粒の)h
促能力に欠け、目詰まり現象等を惹起し易い。
In other words, if it is less than 30% by volume, polishing debris and falling abrasive grains)
It lacks accelerating ability and tends to cause clogging phenomena.

また、90容掻%を超えるものは、その構造的強度に欠
け、砥石としての性能を果たし難い、特に好ましい範囲
は40〜80容量%である。
Moreover, if the volume exceeds 90%, it lacks structural strength and is difficult to perform as a grindstone.A particularly preferable range is 40 to 80% by volume.

次に該合成砥石の製法について詳述する。Next, the method for manufacturing the synthetic grindstone will be described in detail.

従来のレジノイド系砥石の製法は、砥粒とフェノール系
ノボラック樹脂の硬化体の粉末とを所定の比率にて混合
し、これに液状フェノール系樹脂を加えて混練しペース
ト状の原液を調製し、該ペースト状の原液を所定の型で
成形後、熱プレスにて硬化せしめるという方法が一般的
であった。
The conventional manufacturing method for resinoid grinding wheels is to mix abrasive grains and hardened phenolic novolac resin powder at a predetermined ratio, add liquid phenolic resin to this, and knead to prepare a paste-like stock solution. A common method has been to mold the paste-like stock solution in a predetermined mold and then harden it using a hot press.

かかる方法では、高い空隙率のものは望むべくもなく、
高々30容量%のものが限度である上、粉末状原料の混
合という手法を経るため、微細粒子の場合均一混合が困
難で、偏在した塊粒、所謂「ママコ」や不均一層を形成
し易く、砥粒々度の限界は高々tooo番手であって、
それ以上の高岳手のものは得られなかった。
With this method, high porosity is undesirable;
The limit is 30% by volume at most, and since the method involves mixing powdered raw materials, it is difficult to mix fine particles uniformly, and unevenly distributed lumps, so-called "mamako", and uneven layers are likely to form. , the limit of abrasive grain size is too much,
I couldn't get anything better than that.

本発明者等は、樹脂の原料を粉末に求めず。The inventors did not seek powder as the raw material for the resin.

フェノール系およびメラミン系の液状樹脂、すなわち樹
脂原液または樹脂、あるいはその七ツマ−、オリゴマー
、低重合体等、前駆体の水溶液、溶液、エマルジョンを
その原料となし、該液中に砥粒々−Fを投入、均一攪拌
をすることにより、如何なる粒度の砥粒をも極めて容易
且つ均一に原液中に分散し得ることを見出したのである
The raw material is an aqueous solution, solution, or emulsion of phenol-based and melamine-based liquid resins, that is, resin stock solutions or resins, or their precursors such as polymers, oligomers, and low polymers, and abrasive particles -F are added to the liquid. It was discovered that abrasive grains of any particle size can be dispersed extremely easily and uniformly in the stock solution by adding and stirring uniformly.

加うるに、フェノール系樹脂、メラミン系樹脂の各液状
体を用いることにより樹脂液相互の混合も2全であり、
例えば、一方の樹脂のみが塊状、縞状あるいは層状に偏
在するという弊害をも回避し得るのである。更に好まし
くは1両樹脂液の粘度 □をほぼ同レベルにして用いる
ことで、上述の弊害を完全に回避し得るのである。
In addition, by using each liquid of phenolic resin and melamine resin, mutual mixing of resin liquids is possible.
For example, it is possible to avoid the disadvantage that only one resin is unevenly distributed in the form of lumps, stripes, or layers. More preferably, the above-mentioned disadvantages can be completely avoided by using the two resin liquids with substantially the same viscosity □.

次に本発明方法において、気孔生成剤を用いたことも@
要な特長である。すなわち、従来のレジノイド系砥石は
前述の如き方法にて製造されるため、その空隙は、樹脂
粉末と砥粒粉末との混合時において生ずる粒子間の間隙
によって形成曙れるものであり、その混合方法によって
空隙率、セロ変動し、同時に不安定なものであった。そ
れに村、シ本発明方法に、おいては気孔生成剤を用いる
ことによりその空隙率、気孔径を規制しうるため、極め
て安定に所期の構造のものが得られる。
Next, in the method of the present invention, a pore-forming agent was also used.
This is an important feature. That is, since conventional resinoid grindstones are manufactured by the method described above, the voids are formed by the gaps between particles that occur when resin powder and abrasive powder are mixed, and the mixing method The porosity varied depending on the temperature and was unstable at the same time. In addition, in the method of the present invention, the porosity and pore diameter can be controlled by using a pore-forming agent, so that the desired structure can be obtained extremely stably.

すなわち、液状の樹脂液は、触媒存在下に比較η低温で
縮合架橋反応を起こしてゲル化ル固化してゆくものであ
って、固化に伴い媒体である水あ5いは溶媒と分離して
体積の収縮を起こし易いのであるが、かかる固化反応過
程における体積の収縮を防ぎ安定な気孔を形成するため
に、未発明方法においては気孔生成剤を用いるものであ
る。
In other words, the liquid resin liquid undergoes a condensation cross-linking reaction at a relatively low temperature in the presence of a catalyst to solidify into a gel, and as it solidifies, it separates from the medium water or solvent. However, in order to prevent the volume shrinkage during the solidification reaction process and form stable pores, a pore forming agent is used in the uninvented method.

気孔生成剤としては水に分散し易いものが適用され、具
体的には澱粉、C粉変性体、セルロース変性体、界面活
性剤、水溶性高分子物質等が挙げられる。澱粉類、セル
ロース変性体等、水に分散型の気孔生成剤は、そのもの
の存在していた部位が気孔となるため、気孔生成剤のね
度を種々変化させることにより、気孔径を適宜制御し得
る。これ等の気孔生成剤の使用量は0.5〜5.0’/
、%程度が好ましい、少な過ぎると効果が薄く、多iざ
ると混練が難しく、均一・な組織体を形成し得なくなる
。また、界面活性剤やポリエチレングリコール、ポリプ
ロピレングリコールあるいはその誘導体等の水溶性高分
子は、前記澱粉類等よりも微細な気孔を均一に形成させ
るのに好適であり、特に平均気孔径0.1〜 le#L
s程度のものを安定に形成する性質を有する。
As the pore-forming agent, one that is easily dispersible in water is used, and specific examples thereof include starch, C powder modified product, cellulose modified product, surfactant, water-soluble polymeric substance, and the like. Pore-generating agents that are dispersed in water, such as starches and modified cellulose, form pores where they existed, so the pore size can be controlled appropriately by varying the consistency of the pore-generating agent. obtain. The amount of these pore forming agents used is 0.5 to 5.0'/
% is preferable; if it is too small, the effect will be weak, and if it is too large, it will be difficult to knead and it will be impossible to form a uniform structure. Furthermore, water-soluble polymers such as surfactants, polyethylene glycol, polypropylene glycol, or their derivatives are more suitable for uniformly forming fine pores than the starches, and in particular, the average pore diameter is 0.1 to le#L
It has the property of stably forming a substance of about s.

本発明に用いる液状フェノール系樹脂とは樹脂原液また
はモノマー、オリゴマー、重合体等からぅ・る前駆体の
水溶液エマルジ、ン、適当な溶媒に浩解した溶′NI等
で、酸類等の触媒の存在下に架橋i化し得るもの、すな
わちフェノール類をアルデヒド類と塩基性触媒の存在下
で反応することによって生ずるレゾール系樹脂の初期生
成物の水溶液が特に好適である。
The liquid phenolic resin used in the present invention is a resin stock solution, an aqueous emulsion of a precursor of monomers, oligomers, polymers, etc., a solution of NI etc. dissolved in an appropriate solvent, and a catalyst such as an acid. Particularly suitable are aqueous solutions of initial products of resol resins that can be crosslinked in the presence of a basic catalyst, that is, phenols, and aldehydes, which are produced by reacting them with aldehydes in the presence of a basic catalyst.

また、液状メラミン系樹脂とは、樹脂またはそのモノマ
ー、オリゴマー、重合体等からなる前駆体の水溶液エマ
ルジョン、適当な溶媒に溶解した溶液等で、酸類等の触
媒の存在下に分子間縮合すなわち架橋硬化し得るもの、
特にその水溶液を用いることが本発明方法を実施するに
好適である。
Liquid melamine resin is an aqueous emulsion of a resin or a precursor made of its monomers, oligomers, polymers, etc., or a solution dissolved in an appropriate solvent, which undergoes intermolecular condensation or crosslinking in the presence of a catalyst such as an acid. that can be hardened,
In particular, it is suitable to use an aqueous solution thereof to carry out the method of the present invention.

ξ ここに述べたフェノール系樹脂およびメラミン樹脂は、
触媒存在下であれば比較的低温(30〜100℃)にお
いても縮合、固化反応を行ない、固  □形化するもの
であるが、この段階では軟弱で硬度が足りず、砥石とし
ての性能はta’%されていない、いわば中間体である
ξ The phenolic resins and melamine resins mentioned here are
In the presence of a catalyst, condensation and solidification reactions occur even at relatively low temperatures (30 to 100°C), resulting in a solid form, but at this stage it is soft and not hard enough, and its performance as a grindstone is poor. It is an intermediate, so to speak.

この中間体を乾燥し水分あるいは溶剤を除去した後、熱
処理キユアリングを行なうことで前述の縮合による架橋
反応を促進し硬化せしめ、所期の砥石として必要な物性
を得ることができるが。
After drying this intermediate to remove moisture or solvent, heat treatment curing is performed to accelerate the crosslinking reaction caused by the aforementioned condensation and harden it, thereby making it possible to obtain the physical properties required for the desired grindstone.

キユアリングに好適な温度は100〜200℃1時間は
3〜50時間程度である。
The temperature suitable for curing is 100 to 200° C. for 1 hour for about 3 to 50 hours.

ここで用いられる触媒とは、酸類をさすもので、具体的
には1M酸、硫酸、硝鮪等の鉱酸類、酢醜、シュウ酸、
酪酸、マレイン酸、アジピン酸。
The catalyst used here refers to acids, specifically 1M acid, sulfuric acid, mineral acids such as salted tuna, vinegar, oxalic acid,
Butyric acid, maleic acid, adipic acid.

乳酸、ベンゼンスルホン酸、パラトルエンスルホン酸等
の有機酸類、あるいは強醸と弱塩基とよりなる墳類すな
わち水溶液中で酸性を示すもの、更には有機アミンの塩
酸塩等、加温により酸を発生するもの等が挙げられる。
Organic acids such as lactic acid, benzenesulfonic acid, and paratoluenesulfonic acid, or those that are acidic in aqueous solution, such as those made of strong acid and weak base, and hydrochlorides of organic amines, which generate acids when heated. Examples include things to do.

本発明方法においては、前述の如く前工程では比較的低
温で固化を進め、後工程では、やや高温で熱硬化を進め
るため1例えば鉱S類版等、強い触媒性能を有するもの
は、添加量を低いレベルにおさえることがよい0強酸と
弱塩基とよりなる金属塩等マイルドな触媒を用いること
が、均一な反応を進めるためには好適である。
In the method of the present invention, as mentioned above, solidification proceeds at a relatively low temperature in the front step, and heat curing proceeds at a slightly high temperature in the subsequent step. It is preferable to use a mild catalyst, such as a metal salt made of a strong acid and a weak base, which can keep the chemical reaction to a low level, in order to proceed with the homogeneous reaction.

砥粒の原液中における分散を向上し、マトリ7クスの砥
粒保持力を増して砥石としての性能を更に高める為に、
少量のポリビニルアルコールを添加することも有効であ
る。ここでいうポリビニルアルコールとは、平均重合度
300〜2000.1度のポリビニルアルコールおよび
その誘導体をさし1本発明方法においては、メラミン樹
脂あるいはフェノール樹脂の縮合反応で発生するアルデ
ヒド類と反応し、ポリビニルアセタール樹脂となるもの
である。
In order to improve the dispersion of abrasive grains in the stock solution and increase the abrasive retention power of Matrix 7, further enhancing its performance as a whetstone,
It is also effective to add small amounts of polyvinyl alcohol. Polyvinyl alcohol here refers to polyvinyl alcohol with an average degree of polymerization of 300 to 2000.1 degrees and its derivatives. In the method of the present invention, the polyvinyl alcohol reacts with aldehydes generated in the condensation reaction of melamine resin or phenol resin, This is polyvinyl acetal resin.

添加量は、本発明砥石の性能を変化させない程度、具体
的には全体に対し0,1〜5重量%程度を加えるのが好
ましい、ポリビニルアルコールを添加することにより、
特に高岳手のもの(粒度の細かい砥粒を用いたもの)の
砥粒保持力および均一分散性が向上するものであり、具
体的には2000番以上のものに適用することが好適で
ある。
By adding polyvinyl alcohol, it is preferable to add the amount to an extent that does not change the performance of the grindstone of the present invention, specifically, about 0.1 to 5% by weight based on the total weight.
In particular, it improves the abrasive retention and uniform dispersibility of Takatake's abrasives (those using fine abrasive grains), and specifically, it is suitable to apply to abrasives of No. 2000 or higher.

本発明になる合成砥石は1以上の如き方法にて製造され
、セミ弾性砥石として極めて優れた性能を有するもので
あり、その性能も1両樹脂の混合1.1.空隙率、更に
は熱処理(キユアリング)条件を適宜変更することで多
様な製品を(りることが可能である。
The synthetic whetstone of the present invention is manufactured by one or more of the following methods, and has extremely excellent performance as a semi-elastic whetstone, and its performance is also achieved by mixing 1.1. By appropriately changing the porosity and heat treatment (curing) conditions, it is possible to create a wide variety of products.

また、砥粒の種類も特に限定を受けず、ダイヤモ/ド、
窒化ホウ素、炭化珪素、熔融アルミナ。
In addition, the type of abrasive grains is not particularly limited; diamond/de,
Boron nitride, silicon carbide, fused alumina.

酸化クロム、酸化セリウム等の微粉末が使用可能である
が、特に炭化珪素、熔融アルミナ、S化クロム、酸化セ
リウムからなる群より選ばれた少なくも一つの研磨材料
よりなるものが好適である。
Although fine powders of chromium oxide, cerium oxide, etc. can be used, those made of at least one abrasive material selected from the group consisting of silicon carbide, fused alumina, chromium sulfide, and cerium oxide are particularly preferred.

(作用) 一般に固形砥石による研磨作用は大路次の如く説明され
る。
(Function) Generally, the polishing action of a solid grindstone can be explained as follows.

被研磨体と接する砥石面にある砥粒は、相対的に摺動ま
たは回動、擦過されることにより切刃の役割を果たし、
被研磨体表面を研削するとともにその摩擦力により脱落
する。同時に新しい砥粒が表面に現われ、同様の作用、
所謂自生作用を繰り返すもので、全体的に研削および磨
き作用が並行して行なわれるものである。すなわち、砥
石は自身を摩滅させつつ相手を研磨していくもので、結
合材であるマトリックスは砥粒を適度に保持し、11Q
 iNさせ、また自身も摩滅していくものでなければな
らない、すなわち、マトリックスは被研賎材の材質に応
じた硬度、靭性、脆性を有することが必要である。更に
加えて大切なことは、研磨作用に起因する研削屑、脱落
砥粒が研磨面よりスムースに排出されることである。こ
の作用が不充分であると、砥面の目詰まり現象が起こり
研磨性能が経時的に極端に低下し、更に研磨斑1条痕等
好ましからざる結果を惹き起こす。
The abrasive grains on the surface of the whetstone in contact with the object to be polished play the role of a cutting edge by sliding, rotating, or being rubbed relative to each other.
As it grinds the surface of the object to be polished, it falls off due to the frictional force. At the same time, new abrasive grains appear on the surface and have the same effect,
The so-called self-growth process is repeated, and the overall grinding and polishing operations are performed in parallel. In other words, the whetstone polishes the other object while abrading itself, and the matrix, which is the binding material, holds the abrasive grains appropriately, and the 11Q
In other words, the matrix must have hardness, toughness, and brittleness depending on the material of the material to be polished. What is also important is that grinding debris and fallen abrasive grains caused by the polishing action are smoothly discharged from the polishing surface. If this effect is insufficient, the abrasive surface will become clogged, the polishing performance will be extremely degraded over time, and undesirable results such as a single polishing spot will occur.

本発明になる合成砥石は、上述の研磨作用に極めて適し
たものであり、適度な脆性を有するため自生作用に優れ
、またその空隙により研磨屑、脱藩砥粒を捕捉し得る能
力を有するものである。また、従来のレジノイド系砥石
では困難な高番手品つ製造も可能である為、従来M超砥
粒を用いたラッピング研磨方式あるいはパフ研磨方式で
しか遂行し得なっかた。比較的硬質の金属の精密研磨(
仕上げ研磨)も本発明合成砥石によって可能になった。
The synthetic whetstone of the present invention is extremely suitable for the above-mentioned polishing action, has appropriate brittleness, has excellent self-growth action, and has the ability to trap polishing debris and de-abrasive grains through its voids. be. In addition, since it is possible to manufacture high-grip products that are difficult to produce with conventional resinoid grindstones, this has conventionally been possible only with a lapping polishing method or a puff polishing method using M superabrasive grains. Precision polishing of relatively hard metals (
Final polishing) has also become possible with the synthetic grindstone of the present invention.

以下、実施例をあげて本発明を具体的に詳述す □(実
施例 1) 水溶性フェノール系樹脂として住友ベークライト■製P
R−981Aの66%水溶液2501を、水溶性メラミ
ン樹脂として住友化学■製に−3の60%水溶液150
g1lを互いに混合し、触媒として硝酸亜鉛および塩化
第!■鉄鉄量量加え、更にコーンスターチ40gを25
01の水に分散させた液および砥粒として炭化珪素15
00番の微粉1kgを加えて均一攪拌し、所定の型枠に
注型し、50℃にて50時間水浴中で反応固化し中間体
を得た。これを乾燥後。
Hereinafter, the present invention will be specifically explained in detail by giving examples.
66% aqueous solution 2501 of R-981A was made into a 60% aqueous solution 150 of Sumitomo Chemical -3 as a water-soluble melamine resin.
g 1 l mixed with each other, zinc nitrate and chloride as catalyst! ■Add the amount of iron and add 40g of cornstarch to 25g.
Silicon carbide 15 as a liquid dispersed in water of 01 and abrasive grains
1 kg of No. 00 fine powder was added, stirred uniformly, cast into a predetermined mold, and reacted and solidified in a water bath at 50° C. for 50 hours to obtain an intermediate. After drying this.

145℃にて20時間キュ7りングを行ない合成砥石を
得た。 ここで得られた砥石は、フェノール分15.2
%、メラミン分8.3%、P/)I−1,871、砥粒
率7G、5vt%、空隙率43マ01%、ロックウェル
硬度計スーパーフィシャルl5−Yスケールで測定した
硬度が55であった。
Curing was performed at 145° C. for 20 hours to obtain a synthetic grindstone. The grindstone obtained here has a phenol content of 15.2
%, melamine content 8.3%, P/) I-1,871, abrasive grain rate 7G, 5vt%, porosity 43mm 01%, hardness measured with Rockwell hardness meter Superficial l5-Y scale is 55. there were.

これを成形し円盤状となし、クロム鍍金を施した円筒の
研削に供した所、良好な表面精度を得、また目詰まり等
の現象も起こらなかった。
When this was molded into a disk shape and subjected to grinding of a chrome-plated cylinder, good surface accuracy was obtained, and phenomena such as clogging did not occur.

(実施例2〉 実施例1で用いたフェノール系樹脂水溶液2001とメ
ラミン系樹脂水溶液1201を混合し。
(Example 2) The phenolic resin aqueous solution 2001 used in Example 1 and the melamine resin aqueous solution 1201 were mixed.

□ それに触媒として有機アミン塩酸塩少量を加え、  ′
コーンスターチ40gを 2501の水に分散させた液
、ポリビニルアルコール10%水溶液1001及びホワ
イトアルミナ(熔融アルミナ) 4000番砥粒微粉9
00gをそれぞれ加えて均一攪拌して得たスラII−状
原液を、所定の型枠に注型し40℃にて40時間水浴中
で反応固化し中間体を得た。これを乾燥後170℃にて
24時間キユアリングを行ない所期の合成砥石を得た。
□ Add a small amount of organic amine hydrochloride as a catalyst,
A liquid in which 40 g of corn starch was dispersed in 2501 water, a 10% polyvinyl alcohol aqueous solution 1001, and white alumina (fused alumina) No. 4000 abrasive fine powder 9
The slurry II-like stock solution obtained by adding 00 g of each and stirring uniformly was cast into a predetermined mold, and reacted and solidified in a water bath at 40° C. for 40 hours to obtain an intermediate. After drying this, curing was performed at 170° C. for 24 hours to obtain the desired synthetic grindstone.

この砥石は、フェノール分10.1vt$、メラミン分
 5.6wt$、P/M = 1.8/1.砥粒率84
.4wt$、空隙$ 57 v o I Z *ロック
ウェル硬度計。
This whetstone has a phenol content of 10.1vt$, a melamine content of 5.6wt$, and a P/M = 1.8/1. Abrasive grain rate 84
.. 4wt$, void $57 v o I Z *Rockwell hardness tester.

スーパーフィシヤシ15Yスケールで測定した硬度が−
28,平均気孔径2OIL■のものであった。この合成
砥石をリング状に成形し、ニッケル鍍金を施した金属板
の平面研磨に供したところ1表面積度R4=0.02#
L■の仕上げ面が得られた。
The hardness measured with the Super Fishiyashi 15Y scale is -
28, with an average pore diameter of 2 OIL. When this synthetic whetstone was formed into a ring shape and used for surface polishing of a nickel-plated metal plate, the degree of surface area R4 = 0.02 #
A finished surface of L■ was obtained.

(比較例〉 Jib例1 テ用いたフェノール系樹脂水溶液およびメ
ラミン系樹脂水溶液を樹脂原料とし、触媒として硝阿亜
鉛および塩化第11鉄を、砥粒として炭化珪素1500
番の微粉末を、気孔生成剤としてコー7スターチを用い
、実施例1に示す方法に準じて次の組成の合成砥石を得
た。
(Comparative example) Jib Example 1 The phenolic resin aqueous solution and melamine resin aqueous solution used in Te were used as resin raw materials, zinc nitrate and ferrous chloride were used as catalysts, and silicon carbide 1500 was used as abrasive grains.
A synthetic whetstone having the following composition was obtained according to the method shown in Example 1 using Co7 starch as a pore-forming agent.

砥粒率    75.OwtX 砥粒率    ?2.5 wtX 空隙率    43.8vo1% 砥粒率   53.9 wtX 空隙率   23.0マ01駕 メラミン%   lZ、awt為 砥粒率   65.1 wtX 空隙率   30.11o1% これらを実施例1と同様にクロム鍍金を施した円筒研削
に供した所、下記の如き結果を得た。
Abrasive grain rate 75. OwtX abrasive rate? 2.5 wtX porosity 43.8vo1% abrasive grain rate 53.9 wtX porosity 23.0mm01 melamine% lZ, awt abrasive grain rate 65.1 wtX porosity 30.11o1% These are Example 1 Similarly, when a chromium-plated cylinder was subjected to grinding, the following results were obtained.

(イ)やや硬すぎて、クロム鍍金面に適合せず。(a) It is a little too hard and does not fit the chrome plated surface.

研磨ができなかった。I couldn't polish it.

(a)脆弱すぎて、砥石の摩耗激しく、また高速回転に
耐え得なかった。
(a) It was too brittle, causing severe wear on the grindstone, and could not withstand high-speed rotation.

(ハ)目詰まり現象激しく、頻繁なドレッシング作業が
必要であった。
(c) The clogging phenomenon was severe and frequent dressing operations were required.

(ニ)砥石の摩耗激しく2機械精度に追随し得ず研磨用
が著しかった。
(d) The grinding wheel was severely worn and could not keep up with the accuracy of the 2nd machine for polishing.

(発明の効果) 従来のレジノイド砥石の欠点とされていた。空隙率の低
いことに起因する目詰まり現象は1本発明合成砥石の出
現によって大幅に減少するとともに、今迄比較的困難と
されていた平面精密研磨分野のレジノイド砥石の適用も
可能となった。また、軽量でハンドリングが容易な製品
が得られるようになった点も特筆されよう。
(Effect of the invention) This was considered to be a drawback of conventional resinoid grindstones. The clogging phenomenon caused by low porosity has been significantly reduced with the advent of the synthetic grindstone of the present invention, and it has also become possible to apply resinoid grindstones in the field of flat precision polishing, which has been relatively difficult until now. Also noteworthy is the fact that it has become possible to obtain products that are lightweight and easy to handle.

更に1本発明方法により、従来困難であった高番手品の
製造が可能となり、*離砥粒を用いたラッピング方式、
あるいはパフ仕上げ方式の分野までカバーし得るものが
得られるようになった。
Furthermore, the method of the present invention makes it possible to manufacture high-count products, which was previously difficult. *A lapping method using abrasive grains,
In addition, it has become possible to obtain products that can cover the field of puff finishing methods.

また更に本発明方法では、原液の製造に量的な困難を伴
なわず、型枠への注型方法を採るため、かなり大形のも
のまで製造可能であり、@状も、板状0円盤状1円筒状
、ブロック状等となすことができ、特に中間体の段階で
加工を行なえば、どのような複雑な形状にでも成型し得
る。すなわち性能上も、また形状面でも多様化が可能と
なり、従来のレジノイド系砥石の応用[1mを遥かに超
えるものとなり得るものであ3る。
Furthermore, in the method of the present invention, there is no quantitative difficulty in producing the stock solution, and the method of casting into a mold is adopted, so it is possible to produce even quite large products, including @-shaped and plate-shaped zero discs. It can be formed into a cylindrical shape, a block shape, etc., and can be molded into any complicated shape, especially if it is processed at the intermediate stage. In other words, it becomes possible to diversify in terms of performance and shape, and the application of conventional resinoid grindstones [which can be far beyond 1 m]3.

このように1本発明になる合成砥石の効果は極めて大き
く、従来合成砥石では困難であり、 am砥粒によるラ
ッピング方式、パフ仕上げ方式に依存していた硬質金属
1例えば、クロム、ニッケル等で鍍金された面の精密研
磨が、高精度品の適用により充分に可能になった。この
ため高価な砥粒の消費が格段に減り、経済的効果をもた
らすと共−二、環境0作業者の汚染問題も少なくなるの
みならず、また高濃度廃液の処理という面での負担h(
軽減され、その及ぼす影響は極めて大である。加うるに
、従来番手のものであっても、空隙率が高くなり、研磨
性能の持続性が向上し、具体的にはドレッシング(表面
更新)作業なしに研磨作業が続けられること、および比
重の低下により交換作業、i!!!搬作業等の労力が極
めて軽減されること等々、作業性の向上に資する所も頗
る大である。
In this way, the effects of the synthetic whetstone of the present invention are extremely large, and it has been difficult to use conventional synthetic whetstones for hard metals, for example, plating with chromium, nickel, etc., which relied on lapping and puff finishing methods using AM abrasive grains. Precise polishing of polished surfaces has become possible with the use of high-precision products. As a result, the consumption of expensive abrasive grains is significantly reduced, which brings about economic effects.It also reduces the problem of contamination of workers and the environment, and also reduces the burden of processing high-concentration waste liquid.
The impact is extremely large. In addition, even with conventional grits, the porosity is higher and the sustainability of polishing performance is improved, specifically, the polishing work can be continued without dressing (surface renewal) work, and the specific gravity is lower. Replacement work due to decline, i! ! ! It also significantly contributes to improving work efficiency, such as by significantly reducing the labor involved in transport work.

Claims (1)

【特許請求の範囲】 1)空隙率が30〜90容量%の三次元網状組織をなす
構造体であって、該組織が、フェノール系樹脂(P)と
メラミン系樹脂(M)との 2成分系熱硬化性樹脂硬化体を主成分とするマトリック
スと、該マトリックス中に緻密に内在し固定化された砥
粒とからなることを特徴とする合成砥石。 2)フェノール系樹脂(P)とメラミン系樹脂(M)と
が重量基準で1/2〜3/1の組成比率を有する特許請
求の範囲第1項記載の合成砥石。 3)砥粒が、炭化珪素、熔融アルミナ、酸化セリウムお
よび酸化クロムよりなる群から選ばれた少なくとも一つ
の研磨材料からなる特許請求の範囲第1項または第2項
記載の合成砥石。 4)液状フェノール系樹脂(P)と液状メラミン系樹脂
(M)とから主としてなる混合液に砥粒、気孔生成剤お
よび触媒を加え均一に攪拌したスラリー状原液を反応固
化せしめた中間体を、乾燥して水分および/または溶剤
を除去した後、熱処理を施して硬化することを特徴とす
る合成砥石の製造方法。 5)液状フェノール樹脂(P)と液状メラミン樹脂(M
)とが固形分換算重量基準で、 P/M=1/2〜3/1の組成比率を有する特許請求の
範囲第4項記載の合成砥石の製造方法。 6)液状フェノール系樹脂が水溶性レゾール樹脂の水溶
液である特許請求の範囲第4項または第5項記載の合成
砥石の製造方法。 7)液状メラミン系樹脂が水溶性メラミン樹脂の水溶液
である特許請求の範囲第4項乃至第6項の何れかに記載
の合成砥石の製造方法。 8)気孔生成剤が澱粉またはその変性体である特許請求
の範囲第4項乃至第7項の何れかに記載の合成砥石の製
造方法。 9)触媒が強酸と弱塩基とよりなる塩類である特許請求
の範囲第4項乃至第8項の何れかに記載の合成砥石の製
造方法。 10)スラリー状原液にポリビニルアルコールを全量に
対し、0.1〜5重量%添加する特許請求の範囲第4項
乃至第9項の何れかに記載の合成砥石の製造方法。
[Scope of Claims] 1) A structure having a three-dimensional network structure with a porosity of 30 to 90% by volume, wherein the structure is composed of two components of a phenolic resin (P) and a melamine resin (M). A synthetic whetstone characterized by comprising a matrix whose main component is a cured thermosetting resin, and abrasive grains that are densely embedded and fixed in the matrix. 2) The synthetic whetstone according to claim 1, wherein the phenolic resin (P) and the melamine resin (M) have a composition ratio of 1/2 to 3/1 on a weight basis. 3) The synthetic whetstone according to claim 1 or 2, wherein the abrasive grains are made of at least one abrasive material selected from the group consisting of silicon carbide, fused alumina, cerium oxide, and chromium oxide. 4) An intermediate obtained by reacting and solidifying a slurry-like stock solution obtained by adding abrasive grains, a pore-forming agent, and a catalyst to a mixed liquid mainly consisting of a liquid phenolic resin (P) and a liquid melamine-based resin (M) and stirring uniformly, A method for producing a synthetic whetstone, which comprises drying to remove moisture and/or solvent, and then subjecting it to heat treatment to harden it. 5) Liquid phenolic resin (P) and liquid melamine resin (M
) and has a composition ratio of P/M=1/2 to 3/1 on a solid content basis. 6) The method for producing a synthetic grindstone according to claim 4 or 5, wherein the liquid phenolic resin is an aqueous solution of a water-soluble resol resin. 7) The method for manufacturing a synthetic grindstone according to any one of claims 4 to 6, wherein the liquid melamine resin is an aqueous solution of a water-soluble melamine resin. 8) The method for producing a synthetic grindstone according to any one of claims 4 to 7, wherein the pore-forming agent is starch or a modified product thereof. 9) The method for producing a synthetic grindstone according to any one of claims 4 to 8, wherein the catalyst is a salt consisting of a strong acid and a weak base. 10) The method for producing a synthetic grindstone according to any one of claims 4 to 9, wherein 0.1 to 5% by weight of polyvinyl alcohol is added to the slurry stock solution based on the total amount.
JP3465785A 1985-02-25 1985-02-25 Synthetic grindstone and its production method Granted JPS61197164A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3465785A JPS61197164A (en) 1985-02-25 1985-02-25 Synthetic grindstone and its production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3465785A JPS61197164A (en) 1985-02-25 1985-02-25 Synthetic grindstone and its production method

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP4318892A Division JPH07106546B2 (en) 1992-11-27 1992-11-27 Method for manufacturing synthetic whetstone

Publications (2)

Publication Number Publication Date
JPS61197164A true JPS61197164A (en) 1986-09-01
JPH0583343B2 JPH0583343B2 (en) 1993-11-25

Family

ID=12420510

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3465785A Granted JPS61197164A (en) 1985-02-25 1985-02-25 Synthetic grindstone and its production method

Country Status (1)

Country Link
JP (1) JPS61197164A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63150162A (en) * 1986-12-15 1988-06-22 Kanebo Ltd Grindstone for polishing semiconductive wafer
JPH01171746A (en) * 1987-12-24 1989-07-06 Taiho Ind Co Ltd Method for precision polishing
JP2020131352A (en) * 2019-02-19 2020-08-31 信濃電気製錬株式会社 Grind stone and production method therefor

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5540386A (en) * 1979-08-22 1980-03-21 Kayaba Ind Co Ltd Shock absorber
JPS5642431A (en) * 1979-09-14 1981-04-20 Matsushita Electric Works Ltd Timer circuit

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5540386A (en) * 1979-08-22 1980-03-21 Kayaba Ind Co Ltd Shock absorber
JPS5642431A (en) * 1979-09-14 1981-04-20 Matsushita Electric Works Ltd Timer circuit

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63150162A (en) * 1986-12-15 1988-06-22 Kanebo Ltd Grindstone for polishing semiconductive wafer
JPH01171746A (en) * 1987-12-24 1989-07-06 Taiho Ind Co Ltd Method for precision polishing
JP2020131352A (en) * 2019-02-19 2020-08-31 信濃電気製錬株式会社 Grind stone and production method therefor

Also Published As

Publication number Publication date
JPH0583343B2 (en) 1993-11-25

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