JPS6222746B2 - - Google Patents

Info

Publication number
JPS6222746B2
JPS6222746B2 JP9550178A JP9550178A JPS6222746B2 JP S6222746 B2 JPS6222746 B2 JP S6222746B2 JP 9550178 A JP9550178 A JP 9550178A JP 9550178 A JP9550178 A JP 9550178A JP S6222746 B2 JPS6222746 B2 JP S6222746B2
Authority
JP
Japan
Prior art keywords
abrasive
mixture
mold
spherical
abrasive grains
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.)
Expired
Application number
JP9550178A
Other languages
Japanese (ja)
Other versions
JPS5524833A (en
Inventor
Nobuo Konnai
Hiroshi Iimori
Yoshinori Kubo
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP9550178A priority Critical patent/JPS5524833A/en
Publication of JPS5524833A publication Critical patent/JPS5524833A/en
Publication of JPS6222746B2 publication Critical patent/JPS6222746B2/ja
Granted legal-status Critical Current

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  • Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は改良された球形の砥料研摩材の製造方
法に関するものである。 砥粒を遊離状態として被加工物の研摩加工に用
いる遊離砥粒研摩材はバレルに被加工物、遊離砥
粒研摩材、水およびコンパウンドを装入し、バレ
ルに回転、遠心、旋回、振動往復運動を与えて遊
離砥粒研摩材と被加工物との相対的な運動差によ
りスケール、バリなどを除去し、コーナーのR付
け、メツキ下地のほか、平滑仕上げ、粗中細仕上
げ、光沢仕上げ、梨地仕上げおよび塗装下地など
の二次加工法として多用されているバレル研摩法
に用いられる。 遊離砥粒研摩材の形状は、従来、角柱、直柱、
角錐、円錐などであり、このような形状のものを
単独あるいは組合せて用いてきた。しかしなが
ら、このような形状の研摩材を用いると、被加工
物の研摩効果が著しく均一性を欠き、被加工物の
角部、凸部が研摩材によつて深傷を受けるなどの
欠陥が生じた。このような欠点を改良するために
球状遊離砥粒研摩材が最適であるが、従来、この
ような研摩材の経済的な製造は、次の理由によつ
て困難であり、実用化されなかつた。 すなわち、従来球状遊離砥粒研摩材の製造方法
は組合せ型の組合せ面端部に注入孔を、型平面に
削孔した半球形状並に液状硬化性高分子化合物と
砥粒の混合物を注入孔より球状部に注入できる注
入用溝を形成する必要があり、混合物を注入硬化
すると注入用溝部に残留する硬化物が球体に接続
しているため除去した球状成形品は高精度の球体
を得ることは困難であり、被研摩材の研摩のさい
被研摩材の均一研摩を欠き、圧痕を与えるため実
用化されなかつた。 本発明は被加工物に過大な衝撃を与えず、傷を
つけず、軟質金属にも打痕をつけないで極上級の
仕上面が短かい研摩時間で得られる球状の遊離砥
粒研摩材の製造方法を提供しようとするものであ
る。 本発明の遊離砥粒研摩材の製造方法は砥粒Aと
液状硬化性高分子結合材Bとからなる混合物を型
を用いて硬化させ球状の遊離砥粒研摩材を製造す
るに当り、Bとして不飽和ポリエステルを用い
A/Bの重量比を(10〜100)/100としチキソ付
与剤を添加してチキソ指数を2〜50に調整した混
合物を、組合せ型の対称面の対称の位置にうがた
れた所定の径の半球形状部に充填し、型を組合せ
て圧締して該半球形状部内の混合物を硬化させる
ことを特徴とするものである。 本発明において、砥粒と液状硬化性高分子化合
物結合材とからなる混合物は、2〜50のチキソ指
数をもつことが必要である。こゝでチキソ指数と
はブルツクフイールド型粘度計を用い6回転と60
回転のローターの標示する粘度比を表わしてい
る。 組合せ型の上下の各型を組合せる場合、上下の
各型をそれぞれ90度回転させる鉛直組合せ法、ま
たは下型を水平に置き、同じく水平に置かれた上
型を180度回転させて下型の上に上型の対称面を
対向させて乗せ、組合せる方法があるが、いずれ
の方法によつても、チキソ指数が2未満の場合
は、型を回転させるときに未硬化の混合物が半球
状部から流出して完全な球体の製造が困難であ
る。 さらに、チキソ指数2未満では、砥粒と液状硬
化性高分子化合物結合材とからなる混合物中の砥
粒は放置硬化前に分離沈降するため硬化成形され
た球形砥粒研摩材は硬度が不均一に分散すること
になり、被研摩材との接触中不均一に該研摩材が
摩耗し、ひつかき、傷、埋込み等を生じるため実
用的ではない。 チキソ指数が50を越えると混合物の型への充填
不良が起る。 砥粒としてはアルミナ、二硫化モリブデン、硅
砂、石英、コランダム、グラフアイト、金属粉末
などが単独で、または二種以上の混合物が用いら
れる。この砥粒のサイズは被研摩材の形状、材質
等により適且決められるが、一般に60メツシユ以
下の粒径が使用されている。 液状硬化性高分子結合材としては、製品の高弾
力性、研摩性などから不飽和ポリエステルが用い
られる。上記不飽和ポリエステルは、たとえば公
知のα,β―不飽和二塩基酸および必要に応じ飽
和二塩基酸と多価アルコールとをアルコール成分
と酸成分のモル比を0.8〜1.3の範囲で、炭酸ガ
ス、窒素ガスのような不活性ガス中で140〜250℃
の範囲の温度で縮合反応せしめて得られる分子量
約600〜5000の範囲、酸価5〜100の範囲にあるも
のである。 なお本発明に用いられる液状硬化性高分子結合
材は上記の性質以外に砥粒との強固な接着性、耐
衝撃性、耐水性、被研摩材へ腐食生成物を付与し
ない硬化物表面が粘着性がない等の性質が好まし
い。 砥粒と液状硬化性高分子結合材との混合物は2
―50のチキソ指数をもつことが必要であるが、混
合物のチキソ指数をこの範囲に調整するには、次
の方法による。 すなわち、上記混合物に粒径10〜20ミリミクロ
ンの無水ケイ酸、短繊維アスベスト、水素化ヒマ
シ油等のチキソ付与剤を単独で、または二種以上
を併用して上記混合物100重量部に対して好まし
くはチキソ付与剤0.5〜5重量部の割合で添加し
てチキソ指数を2〜50に調整する。 砥粒と液状硬化性高分子化合物結合材との混合
比は重量で10―100:100の範囲である。混合比が
10:100よりも砥粒が少ない場合は結合材の比率
が高いので研摩効率が低下し、100:100よりも砥
粒が多い場合は研摩材の弾力性が低下し、研摩作
業中に研摩材が破壊して形状を失う率が多くなる
ので本発明には不適当である。 本発明の球状研摩材の大きさは最小直径1mm、
最大直径50mmの範囲であることが好ましく、特に
2mmから30mmの径が実用的である。 組合せ型はミーハナイト鋳鋼、鋳鋼、炭素工具
鋼、クロムモリブデン鋼などの型材によるのが成
型品精度の点で好ましい。この型の上下の各型の
対称面には、1mm―50mmの範囲から適宜に所定の
径の半球形状部がうがたれる。金型の表面にメツ
キ処理、シリコン樹脂焼付けなどの離型処理をす
ると成型品の離型が容易になる。 本発明方法により得られた遊離砥粒研摩材は球
形であるから被加工物に過大な衝撃を与えず、傷
をつけず、軟質金属にも打痕をつけないで極上級
の仕上面が短かい研摩時間で得られる。また、液
状硬化性高分子化合物の硬化物は弾力性があるか
ら、砥粒切刃高さが不揃いを生じていても被加工
物の加工面に接触した場合、大きい切刃の高さは
一定高さに調節されるため、研摩条痕は均一化し
平滑な仕上面が得られる。さらに、砥粒の粒度も
微細なものを使用することが可能であり、かつ砥
粒の混合比を大きくすることができる。その上
に、結合材の硬化物は適度に摩耗することによつ
て自生発刃作用を生じ、目づまり、目こぼれを生
ずることなく一定の研摩量が得られ、かつ摩耗し
た結合材が、ひつかき、傷、埋込みなどがないた
め焼成研摩材では得られない仕上効果が発揮でき
る。また、研摩材の結合度および弾力性は目的に
応じて自由に調整が可能である。 次に本発明の方法を図面を参照して説明する。 第1図および第2図において、上型1および下
型2とに1―50mmの範囲の所定の径の半球形状部
3を予め削孔形成しておく。いうまでもないがこ
の半球形状部3は上下の各型を組合せたときに上
下の各型の半球形状部が組合わされて完全な球を
形成するように構成されている。液状硬化性高分
子結合材と砥剤との前記適当な混合比の混合物に
樹脂用促進剤および触媒を添加し、チキソ付与剤
の添加によりチキソ指数2〜50の混合物に調整し
て、上下の各型の半球状部に充填する。充填後第
2図に示すように、上型を180゜回転させて下型
の対称面と組合せ、ついでプレス5などの圧締装
置に押入し、0.1Kg/cm2以上の圧力で押圧するこ
とにより上下組合せ型は完全に密着し、球状部以
外の過剰の混合物は漏出除去される。すなわち
0.1Kg/cm2以下の圧力で押圧すると上下型の間に
前記混合物の硬化物が球体と一体化してバリとし
て付着するため好ましくない。圧締時間は前記混
合物の流動性がなくなるまでゞよい。組合せ型に
は混合物を充填した対称面の上下型の半球部の位
置を完全に一致させるためガイドピン6を設ける
ことが好ましい。なお、成型サイクルを向上させ
るため金型内部を蒸気配管または電熱配線等を内
蔵させることも可能である。または金型全体を養
生室に入れ硬化促進してもよい。混合物硬化後脱
型するか、上下組合せ型を脱型するには、組合せ
型にノツクアウトピン7を設置すると容易とな
る。硬化した球状成型物を離型するには、完全硬
化してからよりも、硬度としてシヨアAで50A―
90A程度の多少弾力性をもつている状態が好まし
い。 本発明の製造方法により得られた球状遊離砥粒
研摩材は成型時に組合せ型の半球部以外の過剰の
混合物が漏出除去されるので離型時にはバリが殆
んど付着しない精度の高い成型品が得られる。 本発明の製造方法はバツチ方式または連続方式
のいずれによつても行ない得る。 本発明方法によつて得られた球状遊離砥粒研摩
材は回転バレル研摩法、振動バレル研摩法、遠心
旋回バレル研摩法、ジヤイロフイニツシユ法、レ
シプロフイニツシユ法等いずれにも使用できる。
また、この研摩材は自動車部品、電気および電子
機器部品、機械部品、時計、カメラ部品、プラス
チツクス部品、窯業製品、航空機部品、作業工
員、玩具類、家庭用品、宝石、ガラス製品などの
多くの分野に利用できる。 以下に本発明の実施例を示す。 実施例 1 不飽和ポリエステル樹脂「エスターRG22」(三
井東圧化学製)60重量部に1000メツシユのアルミ
ナ砥粒40重量部、6%ナフテン酸コバルト1重量
部55%メチルエチルケトンパーオキサイド1重量
部の順序で混合撹拌してから、さらに、チキソ付
与剤アエロジル(日本アエロジル社製無水ケイ
酸)を第1表の重量添加混合し、チキソ指数を調
整した混合物を得た。 この混合物を6mmの半球を300mm×300mmの金型
に900個削孔した上下型に充填してから型を組合
せ、2Kg/cm2の圧力で圧締し、常温で硬化させ20
分後に脱型し、室温(23℃)で1週間放置して研
摩材を得た。ついでバレル容量1の遠心研摩機
に上記研摩材と、被研摩材片として50mm×30mm
(厚み2mm)の板状アルミニウムとを第1表の研
摩前重量の欄にそれぞれ示した量で装填して更に
アルミニウムコンパウンド3g/及び水0.4
を添加してから研摩機を公転、自転300r.p.mの
回転速度で30分運転した後被研摩材の減量および
充填状態について第1表の結果を得た。 これらの結果から、混合物のチキソ指数が2〜
50のものを用いるのが、型からの流出、型への充
填不良がなく、かつ得られた研摩材の特性もすぐ
れていることが明らかである。
The present invention relates to an improved method of manufacturing spherical abrasive material. Free abrasive abrasives are used to polish workpieces with abrasive grains in a free state.The workpiece, free abrasive abrasives, water, and compound are charged into a barrel, and the barrel is rotated, centrifuged, swiveled, and vibrated back and forth. It applies motion to remove scale, burrs, etc. using the relative motion difference between the free abrasive abrasive and the workpiece, and can be used for corner radiusing, plating base, smooth finishing, coarse/medium fine finishing, gloss finishing, etc. It is used in the barrel polishing method, which is often used as a secondary processing method for matte finishes and paint bases. The shapes of free abrasive abrasives are conventionally prismatic, straight,
They are pyramids, cones, etc., and these shapes have been used singly or in combination. However, when an abrasive material with such a shape is used, the polishing effect on the workpiece is significantly uneven, and defects such as deep scratches on the corners and convex parts of the workpiece result from the abrasive material. Ta. Spherical free abrasive abrasives are ideal for improving these drawbacks, but until now it has been difficult to economically manufacture such abrasives for the following reasons, and they have not been put to practical use. . In other words, the conventional manufacturing method for spherical free abrasive abrasives involves making an injection hole at the end of the combined surface of a combination mold, drilling a hemispherical hole in the plane of the mold, and injecting a mixture of a liquid hardenable polymer compound and abrasive grains through the injection hole. It is necessary to form an injection groove that can be injected into the spherical part, and when the mixture is injected and hardened, the cured material remaining in the injection groove is connected to the sphere, so it is impossible to obtain a high-precision sphere from the removed spherical molded product. It was difficult to polish, and it was not put to practical use because it lacked uniform polishing of the material to be polished and caused impressions. The present invention is a spherical free abrasive abrasive that can obtain a top-quality surface finish in a short polishing time without giving an excessive impact to the workpiece, without causing scratches, and without making dents on soft metals. The purpose is to provide a manufacturing method. The method for producing a free abrasive abrasive of the present invention involves curing a mixture consisting of abrasive grains A and a liquid curable polymer binder B using a mold to produce a spherical free abrasive abrasive. A mixture made of unsaturated polyester with an A/B weight ratio of (10 to 100)/100 and a thixotropic agent added to adjust the thixotropic index to 2 to 50 is applied to the symmetrical position of the symmetry plane of the combination mold. This method is characterized by filling a sagging hemispherical portion with a predetermined diameter, and then combining molds and pressing together to harden the mixture within the hemispherical portion. In the present invention, the mixture consisting of abrasive grains and liquid curable polymer binder must have a thixotropic index of 2 to 50. Here, the thixotropic index is 6 revolutions and 60 revolutions using a Bruckfield viscometer.
It represents the viscosity ratio indicated by the rotating rotor. When combining the upper and lower molds of a combination mold, use the vertical combination method in which the upper and lower molds are rotated 90 degrees each, or the lower mold is placed horizontally and the upper mold, which is also placed horizontally, is rotated 180 degrees. There is a method of placing the symmetrical surfaces of the upper mold on top of the upper mold and assembling them, but with either method, if the thixotropic index is less than 2, the uncured mixture will form a hemisphere when the mold is rotated. It flows out from the shaped part, making it difficult to manufacture a perfect sphere. Furthermore, if the thixotropic index is less than 2, the abrasive grains in the mixture consisting of the abrasive grains and the liquid hardenable polymer binder will separate and settle before being left to harden, so the hardness of the hardened spherical abrasive material will be uneven. This is not practical because the abrasive material is unevenly worn during contact with the material to be polished, causing scratches, scratches, embedding, etc. If the thixotropic index exceeds 50, failure to fill the mixture into the mold will occur. As the abrasive grains, alumina, molybdenum disulfide, silica sand, quartz, corundum, graphite, metal powder, etc. may be used alone or in a mixture of two or more. The size of the abrasive grains is appropriately determined depending on the shape and material of the material to be polished, but generally a grain size of 60 mesh or less is used. As the liquid curable polymer binder, unsaturated polyester is used because of its high elasticity and abrasiveness of the product. The above-mentioned unsaturated polyester can be prepared using, for example, a known α,β-unsaturated dibasic acid and, if necessary, a saturated dibasic acid and a polyhydric alcohol at a molar ratio of alcohol component to acid component in the range of 0.8 to 1.3, and carbon dioxide gas. , 140-250℃ in an inert gas such as nitrogen gas
It has a molecular weight in the range of about 600 to 5,000 and an acid value in the range of 5 to 100, obtained by condensation reaction at a temperature in the range of . In addition to the above-mentioned properties, the liquid curable polymer binder used in the present invention has strong adhesion to abrasive grains, impact resistance, water resistance, and has an adhesive surface that does not impart corrosion products to the material to be polished. Characteristics such as no gender are preferable. The mixture of abrasive grains and liquid curable polymeric binder is 2
It is necessary to have a thixotropic index of -50, but the following method can be used to adjust the thixotropic index of the mixture to this range. That is, a thixotropic agent such as silicic anhydride, short fiber asbestos, hydrogenated castor oil, etc. with a particle size of 10 to 20 millimicrons is added to the above mixture alone or in combination of two or more, based on 100 parts by weight of the above mixture. Preferably, the thixotropic agent is added in an amount of 0.5 to 5 parts by weight to adjust the thixotropic index to 2 to 50. The mixing ratio of the abrasive grains and the liquid hardenable polymer binder is in the range of 10-100:100 by weight. The mixing ratio
When the abrasive grains are less than 10:100, the ratio of binder is high, which reduces the polishing efficiency, and when the abrasive grains are more than 100:100, the elasticity of the abrasive material decreases, and the abrasive material is It is unsuitable for the present invention because it has a high probability of breaking and losing its shape. The size of the spherical abrasive material of the present invention is a minimum diameter of 1 mm,
A maximum diameter of 50 mm is preferred, and a diameter of 2 mm to 30 mm is particularly practical. The combination mold is preferably made of meehanite cast steel, cast steel, carbon tool steel, chromium molybdenum steel, etc. from the viewpoint of molded product accuracy. On the symmetry plane of each of the upper and lower molds, a hemispherical portion having a predetermined diameter suitably in the range of 1 mm to 50 mm is carved. If the surface of the mold is subjected to mold release treatment such as plating or baking with silicone resin, the molded product can be easily released from the mold. Since the free abrasive abrasive obtained by the method of the present invention is spherical, it does not apply excessive impact to the workpiece, does not cause scratches, and does not leave dents even on soft metals, resulting in a very high-quality finished surface. Obtained in a considerable amount of sanding time. In addition, since the cured product of liquid curable polymer compound is elastic, even if the height of the abrasive cutting edge is uneven, when it comes into contact with the machined surface of the workpiece, the height of the large cutting edge remains constant. Since the height is adjusted, the polishing marks are uniform and a smooth finished surface is obtained. Furthermore, it is possible to use fine abrasive grains, and the mixing ratio of abrasive grains can be increased. In addition, the cured material of the bonding material produces a self-sharpening effect when worn appropriately, and a constant amount of polishing can be obtained without causing clogging or spillage, and the worn bonding material is constantly removed. Since there are no scratches, scratches, or embeddings, it can produce finishing effects that cannot be obtained with fired abrasives. Furthermore, the degree of bonding and elasticity of the abrasive can be freely adjusted depending on the purpose. Next, the method of the present invention will be explained with reference to the drawings. In FIGS. 1 and 2, a hemispherical portion 3 having a predetermined diameter in the range of 1 to 50 mm is previously drilled in the upper mold 1 and the lower mold 2. Needless to say, this hemispherical portion 3 is constructed so that when the upper and lower molds are combined, the hemispherical portions of the upper and lower molds are combined to form a complete sphere. A resin accelerator and a catalyst are added to the mixture of the liquid curable polymer binder and the abrasive at the appropriate mixing ratio, and the mixture is adjusted to have a thixotropic index of 2 to 50 by the addition of a thixotropic agent. Fill the hemisphere of each mold. After filling, as shown in Figure 2, the upper mold is rotated 180° and combined with the symmetrical surface of the lower mold, and then pushed into a pressing device such as a press 5 and pressed with a pressure of 0.1 kg/cm 2 or more. As a result, the upper and lower combination molds are brought into complete contact with each other, and excess mixture other than the spherical part leaks out and is removed. i.e.
Pressing with a pressure of 0.1 Kg/cm 2 or less is not preferable because the cured product of the mixture will be integrated with the spheres and adhere as burrs between the upper and lower dies. The pressing time may be set until the mixture loses its fluidity. It is preferable to provide a guide pin 6 in the combination mold in order to completely match the positions of the hemispherical parts of the upper and lower molds of the symmetrical surface filled with the mixture. In addition, in order to improve the molding cycle, it is also possible to incorporate steam piping, electric heating wiring, etc. inside the mold. Alternatively, the entire mold may be placed in a curing chamber to accelerate curing. In order to remove the mold after the mixture has hardened or to demold the upper and lower combination mold, it is easy to install a knockout pin 7 in the combination mold. To release a cured spherical molded product, the hardness should be 50 A at shore A after it is completely cured.
It is preferable that it has some elasticity of about 90A. In the spherical free abrasive abrasive obtained by the manufacturing method of the present invention, excess mixture other than the hemispherical part of the combination mold is leaked and removed during molding, so a highly accurate molded product with almost no burrs attached during mold release can be obtained. can get. The manufacturing method of the present invention can be carried out either batchwise or continuously. The spherical free abrasive abrasive obtained by the method of the present invention can be used in any of the rotating barrel polishing methods, vibrating barrel polishing methods, centrifugal rotating barrel polishing methods, gyroscope finishing methods, reciprocating finishing methods, etc. .
This abrasive can also be used in many applications such as automobile parts, electrical and electronic equipment parts, mechanical parts, watches, camera parts, plastic parts, ceramic products, aircraft parts, workers, toys, household goods, jewelry, glass products, etc. Can be used in various fields. Examples of the present invention are shown below. Example 1 60 parts by weight of unsaturated polyester resin "Estar RG22" (manufactured by Mitsui Toatsu Chemicals), 40 parts by weight of 1000 mesh alumina abrasive grains, 1 part by weight of 6% cobalt naphthenate, 1 part by weight of 55% methyl ethyl ketone peroxide. After mixing and stirring, a thixotropic agent Aerosil (anhydrous silicic acid manufactured by Nippon Aerosil Co., Ltd.) was further added and mixed by the weight shown in Table 1 to obtain a mixture with an adjusted thixotropic index. This mixture was filled into the upper and lower molds of a 300 mm x 300 mm mold with 900 holes made using a 6 mm hemisphere, then the molds were assembled, compressed with a pressure of 2 kg/cm 2 , and cured at room temperature for 20 minutes.
After a few minutes, the mold was removed and left at room temperature (23°C) for one week to obtain an abrasive. Next, the above abrasive material and a 50 mm x 30 mm piece of material to be polished were placed in a centrifugal polisher with a barrel capacity of 1.
(thickness: 2 mm) plate aluminum in the amounts shown in the weight before polishing column in Table 1, and then added 3 g of aluminum compound and 0.4 g of water.
After adding , the polishing machine was operated for 30 minutes at a rotational speed of 300 rpm, and the results shown in Table 1 were obtained regarding the weight loss of the material to be polished and the filling state. From these results, the thixotropic index of the mixture is 2~
It is clear that the use of abrasives with a diameter of 50% causes no outflow from the mold or poor filling into the mold, and the resulting abrasive has excellent properties.

【表】 実施例 2 三井東圧化学(株)製不飽和ポリエステル「エスタ
ーG20」(B)100重量部に、100メツシユの石英粉末
(A)を、それぞれ10,20,40,60,80,120重量部
添加し、さらにこれら7種の混合物の各々に、6
%ナフテン酸コバルト1重量部および55%メチル
エチルケトンパーオキサイド1重量部を順次加え
て混合撹拌した。これらの混合物の各々に、さら
にチキソ付与剤としてアエロジル(日本アエロジ
ル社製)3重量部を添加して充分混合した。 このようにして得られた7種の混合物を10mmの
半球を300mm×300mmの金型に625個削孔した上下
型に充填し、型を合せ、実施例1と同様に操作し
て研摩材を得た。得られた研摩材を室温にて1週
間放置した。 バレル容量1の遠心研摩機に上記の研摩材の
50gを装入し、被研摩材として40mm×35mm×3mm
の板状アルミニウムを装填し、さらにアルミニウ
ムコンパウンド3g/および水0.4を添加し
て研摩機を300rpmの回転速度で、30分間公転お
よび自転したときの研摩材の破壊状態を調べた結
果は第2表のとおりであつた。
[Table] Example 2 Add 100 mesh of quartz powder to 100 parts by weight of unsaturated polyester "Estar G20" (B) manufactured by Mitsui Toatsu Chemical Co., Ltd.
Add 10, 20, 40, 60, 80, and 120 parts by weight of (A), respectively, and add 6 parts by weight to each of these seven mixtures.
% cobalt naphthenate and 1 part by weight of 55% methyl ethyl ketone peroxide were sequentially added and mixed with stirring. To each of these mixtures, 3 parts by weight of Aerosil (manufactured by Nippon Aerosil Co., Ltd.) as a thixotropic agent was further added and thoroughly mixed. The seven kinds of mixtures thus obtained were filled into upper and lower molds in which 625 holes were drilled using a 10 mm hemisphere in a 300 mm x 300 mm mold. Obtained. The obtained abrasive material was left for one week at room temperature. Add the above abrasive to a centrifugal sander with a barrel capacity of 1.
Charge 50g, and the material to be polished is 40mm x 35mm x 3mm.
Table 2 shows the results of examining the fracture state of the abrasive material when the abrasive machine was loaded with sheet aluminum, added with 3 g of aluminum compound and 0.4 g of water, and rotated and rotated for 30 minutes at a rotation speed of 300 rpm. It was as follows.

【表】 これらの結果から、砥粒添加量が(A)/(B)で(10
〜100)/100の範囲にあるきが、研摩材の破壊率
が著しく小さいことが明らかである。
[Table] From these results, the amount of abrasive grains added is (A)/(B) (10
-100)/100, it is clear that the fracture rate of the abrasive is significantly lower.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の実施に用いられる組合せ型の
上型および下型の一例を示す断面図、第2図は圧
締装置に挿入した組合せ型の一例を示す断面図で
ある。 1……上型、2……下型、3……混合物充填用
半球状部、4……充填混合物、5……圧締プレ
ス、6……ガイドピン、7……ノツクアウトピ
ン。
FIG. 1 is a cross-sectional view showing an example of the upper and lower molds of a combination mold used in carrying out the present invention, and FIG. 2 is a cross-sectional view showing an example of the combination mold inserted into a clamping device. DESCRIPTION OF SYMBOLS 1... Upper die, 2... Lower die, 3... Hemispherical part for filling mixture, 4... Filling mixture, 5... Pressing press, 6... Guide pin, 7... Knockout pin.

Claims (1)

【特許請求の範囲】[Claims] 1 砥粒Aと液状硬化性高分子化合物結合材Bと
からなる混合物を型を用いて硬化させて球状の遊
離砥粒研摩材を製造するに当り、液状硬化性高分
子化合物結合材Bとして不飽和ポリエステルを用
いA/Bの重量比を(10〜100)/100とし、チキ
ソ付与剤を添加してチキソ指数を2〜50に調整し
た混合物を、組合せ型の対称面の対称の位置にう
がたれた所定の径の半球形状部に充填し、型を組
合せて圧締して該半球形状部内の混合物を硬化さ
せることを特徴とする遊離砥粒研摩材の製造方
法。
1. When producing a spherical free abrasive abrasive by curing a mixture consisting of abrasive grains A and liquid curable polymer compound binder B using a mold, a mixture of abrasive grains A and liquid curable polymer compound binder B is used to produce a spherical free abrasive abrasive material. A mixture made of saturated polyester with a weight ratio of A/B of (10 to 100)/100 and a thixotropic index adjusted to 2 to 50 by adding a thixotropic agent is applied to the symmetrical position of the symmetry plane of the combination mold. 1. A method for producing a free abrasive abrasive material, which comprises filling a hemispherical part with a predetermined diameter that has sagged, and hardening the mixture in the hemispherical part by combining and pressing molds.
JP9550178A 1978-08-07 1978-08-07 Method of producing isolated grain abrasive Granted JPS5524833A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9550178A JPS5524833A (en) 1978-08-07 1978-08-07 Method of producing isolated grain abrasive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9550178A JPS5524833A (en) 1978-08-07 1978-08-07 Method of producing isolated grain abrasive

Publications (2)

Publication Number Publication Date
JPS5524833A JPS5524833A (en) 1980-02-22
JPS6222746B2 true JPS6222746B2 (en) 1987-05-19

Family

ID=14139334

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9550178A Granted JPS5524833A (en) 1978-08-07 1978-08-07 Method of producing isolated grain abrasive

Country Status (1)

Country Link
JP (1) JPS5524833A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03102130U (en) * 1989-11-24 1991-10-24

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63127876A (en) * 1986-11-19 1988-05-31 Mitsui Toatsu Chem Inc Abrasive

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03102130U (en) * 1989-11-24 1991-10-24

Also Published As

Publication number Publication date
JPS5524833A (en) 1980-02-22

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