JPH0138629B2 - - Google Patents
Info
- Publication number
- JPH0138629B2 JPH0138629B2 JP4256084A JP4256084A JPH0138629B2 JP H0138629 B2 JPH0138629 B2 JP H0138629B2 JP 4256084 A JP4256084 A JP 4256084A JP 4256084 A JP4256084 A JP 4256084A JP H0138629 B2 JPH0138629 B2 JP H0138629B2
- Authority
- JP
- Japan
- Prior art keywords
- abrasive
- abrasive grains
- protective layer
- grinding
- alumina
- 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
Links
- 239000006061 abrasive grain Substances 0.000 claims description 49
- 239000011241 protective layer Substances 0.000 claims description 28
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 25
- 239000012790 adhesive layer Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- 239000011256 inorganic filler Substances 0.000 claims description 11
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 229920003002 synthetic resin Polymers 0.000 claims description 9
- 239000000057 synthetic resin Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 4
- 238000000227 grinding Methods 0.000 description 29
- 239000004744 fabric Substances 0.000 description 23
- 239000000123 paper Substances 0.000 description 17
- 229910000975 Carbon steel Inorganic materials 0.000 description 8
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 239000010962 carbon steel Substances 0.000 description 8
- 239000003082 abrasive agent Substances 0.000 description 7
- 102200082816 rs34868397 Human genes 0.000 description 7
- 230000000694 effects Effects 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000010419 fine particle Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 208000013201 Stress fracture Diseases 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000007499 fusion processing Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
Landscapes
- Polishing Bodies And Polishing Tools (AREA)
Description
この発明は研摩布紙の改良構造に関するもので
ある。
一般に、α―アルミナの焼結砥粒(砥材)はα
―アルミナの微小粒が集合してなるものでありα
アルミナまたは、αアルミナ前駆物質を加熱焼結
して得られる砥粒で、砥粒が研削過程で微小破砕
しながら新しい切れ刃を発刃する自生作用が期待
されるものである。しかしながら、研摩布紙にお
けるα―アルミナの焼結砥粒は研削の際、特に大
きな研削荷重が加わる重研削において、研摩布紙
の使用の初期に砥粒自体が脱落したり、あるいは
本来の微小破砕せずに欠落するため、砥粒が有効
に作用せず、早期に研摩布紙寿命を来たす欠点が
あつた。
本発明の目的は、前述した従来欠点を解消しよ
うとしたものであつて、研削時におけるアルミナ
砥粒の脱落を防ぎ、かつ微小破砕による切れ刃が
有効に自生されるようにした研削性能の高い、研
摩布紙を提供することにある。
また本発明の他の目的は、アルミナ砥粒の研削
初期の脱粒を防ぐ保護層が表面に被着され、研削
持続性の高い、研摩布紙を提供することにある。
本発明は、基材上に接着剤層を介して砥粒が接
着されてなる研摩布紙において、前記砥粒がα―
アルミナを主成分とした焼結砥粒であり、かつ前
記接着剤層が公知の“レジンボンド”研摩布紙に
使用される熱硬化性の合成樹脂を主成分とする接
着剤と無機質充填材との混合物よりなるものであ
り、かつ前記砥粒及び接着剤層上には保護層が被
着されている研摩布紙の構造である。前記基材と
しては紙、布、バルカナイズドフアイバー、およ
び布と紙の複合体など、通常の研摩布紙用の基材
が使用される。前記接着剤層をなす混合物は無機
質充填材/合成樹脂の比率(重量比)が公知の研
摩布紙において、一般的に1.5未満の値である。
混合物の組成は塗布性、接着性、耐熱性などに関
与するものであり、無機質充填材が多い場合は混
合物の接着性は低くなるが圧縮強度及び耐熱性が
高くなり、接着剤層はこれらの関係よりみて前記
範囲で行なわれる。前記アルミナ焼結砥粒はα―
アルミナの微粒子(α―アルミナを主成分とする
微粒子、またはα―アルミナ前駆物質よりなる微
粒子)を圧縮成形し、たとえば1800℃15時間焼成
して焼結させ、冷却し、これを粉砕し、平均粒径
約100〜600μ(JISの砥粒規格の#24〜#120に相
当)に分級したものである。本発明はアルミナ焼
結砥粒の保持性を保護層にて補うようにするため
に、砥粒径が小さい場合は保護層の効果が得られ
ず、実用的よりみて砥粒平均粒径は約100〜600μ
程度のものが選定される。前記保護層は合成樹脂
と無機質充填材との混合物よりなる。この合成樹
脂は、フエノール―ホルムアルデヒド樹脂、ポリ
エステル樹脂、ポリウレタン樹脂、メラミン樹
脂、ユリア樹脂、エポキシ樹脂などの通常の熱硬
化性の樹脂が有効であるが、これらの硬化性樹脂
とポリビニルアルコール(PVA)、エチルセルロ
ース、ポリアクリルアミド、酢酸ビニル、塩化ビ
ニル、ラテツクス等の熱可塑性樹脂とを併用する
こともできる。そして無機質充填材は炭酸カルシ
ウム、氷晶石、クレー、グラフアイト、シリカ、
フツ化カルシウム、ホウフツ化カリなどの研摩布
紙用に使用される通常の無機質材料が用いられ、
研摩布紙の用途に応じて、可塑剤、潤滑材を添加
することもできる。なお保護層の中に空隙を含む
場合もある。無機質充填材は研摩布紙を形成する
際のコーテイング性および本発明で使用される砥
粒の平均粒径からみて、平均粒径が約80μ以下の
ものが好ましい。
前記保護層となす混合物の比率は約1.5〜32.3
の範囲が好ましい。保護層の混合物の比率が前記
範囲より小さくなると研削の際に保護層が摩耗し
にくくなり焼結α―アルミナ砥粒が十分に作用す
ることなく研摩布紙寿命となり、かつ前記範囲よ
り大きくなると砥粒の減りに同調せず、研削初期
に保護層が剥離、脱落する不都合がある。接着剤
層及び保護層は乾燥され熟成(例えば135℃)さ
れて硬化されていて、焼結砥粒はこれらの層によ
り基材に固着されている。
次に本発明の試験例を説明する。
試験
平均粒径2.0μのα―アルミナ微粉末を1800℃で
15時間焼結した後、冷却し、粉砕して、JIS―R
―6001粒度規格の60番に分級したアルミナ砥粒1
〜1を用意した。そして、研摩布用基材、本例で
は樹脂加工されたドリル布2の上に、液状フエノ
ール―ホルムアルデヒド樹脂(昭和ユニオン合成
KK製造、固形分約75%の「レゾール樹脂BRL―
2867」使用)と炭酸カルシウム粉末を重量比1:
1の比率で混合した接着剤を湿潤重量で150g/
m2塗布して一次接着剤層3を形成した。次いで用
意したアルミナ砥粒1〜1を一次接着剤層3上に
静電気的に480g/m2塗り、70〜80℃の乾燥器中
で約2時間乾燥した。そしてアルミナ砥粒1〜1
及び一次接着剤層3上に、一次接着剤と同じ接着
剤を、二次接着剤として湿潤重量で200g/m2塗
布した後、70〜80℃の乾燥器中で2時間予備乾燥
して二次接着剤層4を形成し、次いで、二次接着
剤層4上には、次の第1表に示す配合の保護層5
を乾燥後重量で150g/m2塗布した。
This invention relates to an improved structure for a coated abrasive paper. Generally, α-alumina sintered abrasive grains (abrasive material) are α
-It is made up of a collection of microscopic particles of alumina, α
This is an abrasive grain obtained by heating and sintering alumina or an α-alumina precursor, and is expected to have a self-generating effect in which the abrasive grain breaks into small pieces during the grinding process and generates new cutting edges. However, during grinding, the α-alumina sintered abrasive grains in coated abrasive paper may fall off in the early stages of use, or the abrasive grains themselves may fall off due to the original micro-fractures, especially in heavy grinding where a large grinding load is applied. Since the abrasive grains do not work properly and are missing, the abrasive grains do not work effectively and the abrasive cloth paper has the disadvantage of prematurely ending its life. The purpose of the present invention is to eliminate the above-mentioned conventional drawbacks, and to provide high grinding performance that prevents alumina abrasive grains from falling off during grinding and effectively generates cutting edges by micro-fracture. , to provide abrasive cloth paper. Another object of the present invention is to provide a coated abrasive paper which has a protective layer on its surface that prevents alumina abrasive grains from falling off during the initial stage of grinding, and which has high durability in grinding. The present invention provides an abrasive coated paper in which abrasive grains are bonded to a base material via an adhesive layer, in which the abrasive grains are α-
It is a sintered abrasive grain mainly composed of alumina, and the adhesive layer is composed of an adhesive mainly composed of a thermosetting synthetic resin used in the well-known "resin bond" coated abrasive paper and an inorganic filler. The structure of the coated abrasive paper is made of a mixture of the above-mentioned abrasive grains and a protective layer is deposited on the abrasive grains and the adhesive layer. The substrates used are conventional coated abrasive substrates such as paper, cloth, vulcanized fiber, and cloth-paper composites. The mixture constituting the adhesive layer has an inorganic filler/synthetic resin ratio (weight ratio) of generally less than 1.5 in a known abrasive coated paper.
The composition of the mixture is related to coating properties, adhesion, heat resistance, etc. If there is a large amount of inorganic filler, the adhesion of the mixture will be low, but the compressive strength and heat resistance will be high. Considering the relationship, this will be done within the above range. The alumina sintered abrasive grains are α-
Fine particles of alumina (fine particles mainly composed of α-alumina or fine particles made of α-alumina precursor) are compression molded, fired at 1800°C for 15 hours to sinter, cooled, crushed, and averaged. It is classified into particle sizes of approximately 100 to 600μ (equivalent to #24 to #120 of the JIS abrasive grain standard). In the present invention, in order to compensate for the retention of alumina sintered abrasive grains with a protective layer, if the abrasive grain size is small, the effect of the protective layer cannot be obtained, so from a practical standpoint, the average grain size of the abrasive grains is approximately 100~600μ
The degree is selected. The protective layer is made of a mixture of synthetic resin and inorganic filler. Common thermosetting resins such as phenol-formaldehyde resin, polyester resin, polyurethane resin, melamine resin, urea resin, and epoxy resin are effective for this synthetic resin, but these curable resins and polyvinyl alcohol (PVA) , ethyl cellulose, polyacrylamide, vinyl acetate, vinyl chloride, latex, and other thermoplastic resins can also be used in combination. Inorganic fillers include calcium carbonate, cryolite, clay, graphite, silica,
Common inorganic materials used for coated abrasive paper such as calcium fluoride and potassium fluoride are used.
Depending on the use of the coated abrasive paper, plasticizers and lubricants may also be added. Note that the protective layer may contain voids. The inorganic filler preferably has an average particle size of about 80 μm or less in view of coating properties when forming coated abrasive paper and the average particle size of the abrasive grains used in the present invention. The ratio of the mixture to the protective layer is about 1.5 to 32.3.
A range of is preferred. If the ratio of the mixture in the protective layer is smaller than the above range, the protective layer will be difficult to wear during grinding, and the sintered α-alumina abrasive grains will not work sufficiently and the abrasive paper will last a long time. There is an inconvenience that the protective layer peels off and falls off at the beginning of grinding because it does not synchronize with the reduction of grains. The adhesive layer and the protective layer are dried and cured by aging (for example, at 135° C.), and the sintered abrasive grains are fixed to the base material by these layers. Next, test examples of the present invention will be explained. Test α-alumina fine powder with an average particle size of 2.0μ was heated at 1800℃.
After sintering for 15 hours, it is cooled, crushed, and JIS-R
- Alumina abrasive grains 1 classified into No. 60 according to the 6001 grain size standard
~1 was prepared. Then, liquid phenol-formaldehyde resin (Showa Union Synthetic
Manufactured by KK, "Resole resin BRL" with a solid content of approximately 75%
2867) and calcium carbonate powder in a weight ratio of 1:
150g wet weight of adhesive mixed in a ratio of 1
m 2 was applied to form the primary adhesive layer 3. Next, 480 g/m 2 of the prepared alumina abrasive grains 1 to 1 were applied electrostatically onto the primary adhesive layer 3 and dried in a dryer at 70 to 80° C. for about 2 hours. And alumina abrasive grain 1~1
On the primary adhesive layer 3, the same adhesive as the primary adhesive was applied as a secondary adhesive at a wet weight of 200 g/ m2 , and then pre-dried for 2 hours in a dryer at 70 to 80°C. A secondary adhesive layer 4 is formed, and then a protective layer 5 having a composition shown in Table 1 below is formed on the secondary adhesive layer 4.
After drying, it was applied at a weight of 150 g/m 2 .
【表】
なお、第1表の配合において無機質充填材/合
成樹脂接着剤の固形分重量比は3.3である。そし
て135℃のオーブン中で10時間本乾燥して、保護
層5が被着された試験品の研摩布6となした。
かくして形成された研摩布6は幅50mm、周長
2300mmの無端ベルトに加工した。炭素鋼S45Cの
角棒(断面25×25mmのもの)を被削材として、研
削荷重8Kg重、ベルト周速1600m/分、ゴム硬度
70゜、ランド比1:1のコンタクトホイールを有
する一定荷重研削機を使用してこの無端ベルト状
研摩布の研削性を調べた。その結果、炭素鋼
S45C角棒5分間の研削量は320gであつた。使用
後におけるこの試験品の研摩布6は研摩面の損
傷が少なく、砥粒に摩耗面が生じていなかつたの
で、更に5分間研削を行なつたところ、160gの
研削量が得られ、被削材の炭素鋼には焼けが生じ
なかつた。
次に試験品の研摩布6の対照として、試験品
と同様構造でかつ保護層を設けない研摩布7を
形成し対照品と比較する(第2図参照。なお、
試験品の研摩布6と同一部材は同一番号にて示
す)。この対照品の研摩布7は前記した研摩布
6と同様に無端状ベルトに加工し、試験品と同
条件にて研削性を調べたところ、炭素鋼S45C角
棒の5分間の研削量は212gであつた。使用後の
ベルトは部分的に砥材の欠損が認められたが、被
削材の被削面には焼けは生じなかつた。試験品
のものは対照品に比べ保護層の形成により、研
摩布の研削力、持続力が著しく向上したことが認
められる。
試験
米国ケネコツト社製造の焼結砥粒(SG砥材)
粒度規格36番のものを使用し、保護層を有する試
験品の研摩布(図示しない)を作つた。保護層
は第2表に示す配合のものを乾燥後の重量で300
g/m2塗布し、40℃の乾燥器で3時間乾燥せしめ
た後、25℃、65%相対湿度の部屋へ48時間放置し
ウレタン樹脂を湿気硬化させて形成した。[Table] In the formulation shown in Table 1, the solid content weight ratio of the inorganic filler/synthetic resin adhesive is 3.3. Then, it was dried in an oven at 135° C. for 10 hours to obtain a test article abrasive cloth 6 having a protective layer 5 adhered thereto. The polishing cloth 6 thus formed has a width of 50 mm and a circumference of
Processed into a 2300mm endless belt. A square bar of carbon steel S45C (cross section 25 x 25 mm) was used as the work material, grinding load 8 kg, belt circumferential speed 1600 m/min, rubber hardness.
The grindability of this endless belt-like abrasive cloth was investigated using a constant load grinder with a 70° contact wheel and a land ratio of 1:1. As a result, carbon steel
The amount of grinding for 5 minutes on the S45C square bar was 320g. After use, the abrasive cloth 6 of this test product had little damage to the abrasive surface and no abrasive surfaces were formed on the abrasive grains, so when grinding was continued for an additional 5 minutes, a grinding amount of 160 g was obtained, and the workpiece No burn occurred on the carbon steel material. Next, as a control for the test product abrasive cloth 6, an abrasive cloth 7 having the same structure as the test product but without a protective layer was formed and compared with the control product (see Fig. 2.
Components that are the same as the abrasive cloth 6 of the test product are indicated by the same numbers). This control product, abrasive cloth 7, was processed into an endless belt in the same manner as the abrasive cloth 6 described above, and its grindability was examined under the same conditions as the test product, and the amount of grinding of a carbon steel S45C square bar in 5 minutes was 212 g. It was hot. After use, the belt showed some damage to the abrasive material, but no burning occurred on the surface of the work material. It was observed that the abrasive cloth's abrasive power and durability were significantly improved in the test product compared to the control product due to the formation of the protective layer. Test Sintered abrasive grains (SG abrasive material) manufactured by Kennekotsu Co., Ltd. in the United States
A test abrasive cloth (not shown) with a protective layer was made using a particle size standard No. 36. The protective layer has the composition shown in Table 2 and has a dry weight of 300%.
g/m 2 was applied, dried for 3 hours in a dryer at 40°C, and then left in a room at 25°C and 65% relative humidity for 48 hours to cure the urethane resin with moisture.
【表】
なお第2表の配合において無機質充填材/合成
樹脂接着剤の固形分重量比は1.5である。この研
摩布は無端状ベルトに加工し、試験品の場合と
同条件にて炭素鋼S45Cの角棒を研削試験したと
ころ、5分間の研削量が1180gとなつた。使用後
のベルトの砥材の欠落、脱粒はほとんど認められ
ず、保護層は砥材の主生作用とともに良好に再生
していた。
つぎに試験品の研摩布の対照として、試験品
と同様構造でかつ保護層を設けない研摩布(対
照品)を形成し、これを無端状ベルトに加工
し、試験品の場合と同条件にて研削性を調べた
ところ炭素鋼S45C角棒の5分間の研削量は820g
であつた。対照品の使用後のベルトの砥粒は欠
落したものが多かつたが、砥粒先端部の摩耗面は
生じなかつた。
試験
前記試験品の新たな研摩ベルトにてステンレ
ススチールSUS304の角棒(断面25×25mmのも
の)を被削材として20Kg重の研削荷重で研削し
た。なお、使用した研削機は試験の場合と同じ
ものである。ステンレススチール角棒の5分間の
研削量は1100gであり、使用後の研摩ベルトの砥
粒は良好な自生作用を示しており、保護層の摩耗
状態も順調であつた。
一方、対照品の新たな研摩ベルトにてステン
レススチールSUS304の角棒を20Kg重の研削荷重
で同様に研削したところ、ステンレススチール角
棒の5分間の研削量は730gであり、使用後の研
摩ベルトは砥粒の破損が著しかつた。
試験
溶融法で製造されたアルミナ砥粒(α―アルミ
ナ微粒子を溶融して冷却、粉砕分級したもの)の
60番を使用して前記試験と同様に処理し、表面
に保護層を有する試験品の研摩布(図示せず。)
を作つた。次いでこの研摩布を無端状の研摩ベル
トに加工し試験と同様に炭素鋼S45Cの25×25
mmの被削材に対して試験と同条件にて研削試験
したところ、5分間の研削量は197gであつた。
砥粒の先端部分には摩耗面が生じ、被削材にも焼
けが生じた。
次に試験品の対照品として試験品と同様
構造でかつ保護層を設けない研摩布(図示せず。)
を形成し、これを無端状の研摩ベルトに加工し、
試験と同条件にて炭素鋼S45Cの角棒の研削性
を調べたところ、5分間の研削量は185gであつ
た。
使用後のベルトは砥粒の一部が脱粒(脱落)し
ていたが接着剤と強固に密着している砥粒の先端
部分には摩耗面(台地状に砥材のすりへつた部
分)が形成され被削材の被削面には焼けが生じて
いた。
この試験品及び対照品において溶融法のア
ルミナ砥粒からは焼結砥粒の様な自生作用が観察
されず、保護層の効果もほとんど認められなかつ
た。
しかして、本発明の研摩布紙は基材に接着した
砥粒上に保護層を設けたため、研削時におけるア
ルミナ砥粒の脱落が防止される。すなわち、保護
層は無機質充填材/熱硬化性合成樹脂の比が適切
に定められていて、研摩の際には順次減つていく
ため、研摩を妨害することはなく、かつ砥粒の保
持を良好になす作用を奏する。したがつて、本発
明の研摩布紙によれば、砥材の保持性が良好であ
り、研削中の砥粒は脱落したり、微小破砕せずに
欠落することがなく、砥粒の研削性が高められ
る。また、本発明の砥粒はα―アルミナを主成分
とした焼結砥粒であるため、研削過程において微
小破砕しながら新しい切れ刃が発刃され研削性が
接続される。[Table] In the formulation shown in Table 2, the solid content weight ratio of the inorganic filler/synthetic resin adhesive is 1.5. This abrasive cloth was processed into an endless belt, and when a square bar of carbon steel S45C was subjected to a grinding test under the same conditions as the test product, the amount of grinding in 5 minutes was 1180 g. After use, there was hardly any loss or shedding of the abrasive material on the belt, and the protective layer was well regenerated along with the main action of the abrasive material. Next, as a control for the abrasive cloth of the test product, an abrasive cloth (control product) with the same structure as the test product but without a protective layer was formed, and this was processed into an endless belt and subjected to the same conditions as the test product. When examining the grindability, the amount of grinding of a carbon steel S45C square bar in 5 minutes was 820g.
It was hot. Many of the abrasive grains on the belt after use of the control product were missing, but no worn surfaces were formed at the tips of the abrasive grains. Test A square bar of stainless steel SUS304 (with a cross section of 25 x 25 mm) was ground with a grinding load of 20 kg using the new abrasive belt of the test product. The grinding machine used was the same as in the test. The amount of grinding of the stainless steel square rod in 5 minutes was 1100 g, and the abrasive grains of the abrasive belt after use showed good self-growth, and the wear of the protective layer was also good. On the other hand, when a square bar made of stainless steel SUS304 was similarly ground with a grinding load of 20 kg using a new abrasive belt as a control product, the amount of grinding of the square bar of stainless steel in 5 minutes was 730 g. The abrasive grains were severely damaged. Test Alumina abrasive grains manufactured by the melting method (melted α-alumina fine particles, cooled, crushed and classified)
An abrasive cloth of the test article treated in the same manner as in the above test using No. 60 and having a protective layer on the surface (not shown)
I made it. Next, this abrasive cloth was processed into an endless abrasive belt made of carbon steel S45C 25×25
When a grinding test was carried out on a work material of mm in diameter under the same conditions as the test, the amount of grinding for 5 minutes was 197 g.
A worn surface was formed at the tip of the abrasive grain, and the work material was also burnt. Next, as a control product for the test product, an abrasive cloth (not shown) with the same structure as the test product but without a protective layer.
is formed and processed into an endless abrasive belt,
When the grindability of a square bar made of carbon steel S45C was examined under the same conditions as in the test, the amount of grinding in 5 minutes was 185 g. After use, some of the abrasive grains on the belt were shedding (falling off), but there was a worn surface (a plateau-shaped part where the abrasive material had worn down) at the tip of the abrasive grains, which were in strong contact with the adhesive. The cut surface of the work material was burnt. In this test product and the control product, no self-growth effect like that of sintered abrasive grains was observed from the alumina abrasive grains produced by the fusion process, and almost no effect of the protective layer was observed. Since the coated abrasive paper of the present invention provides a protective layer on the abrasive grains adhered to the base material, the alumina abrasive grains are prevented from falling off during grinding. In other words, the protective layer has an appropriately determined ratio of inorganic filler/thermosetting synthetic resin, and is gradually reduced during polishing, so it does not interfere with polishing and retains abrasive grains well. It has the effect of making something happen. Therefore, according to the coated abrasive paper of the present invention, the retention of the abrasive material is good, and the abrasive grains during grinding do not fall off or become chipped without being micro-fractured, and the grindability of the abrasive grains is improved. is enhanced. Furthermore, since the abrasive grains of the present invention are sintered abrasive grains containing α-alumina as a main component, new cutting edges are generated while being micro-fractured during the grinding process, thereby improving the grindability.
図面は本発明試験例の研摩布を示すものであ
り、第1図は試験品の構造を示す拡大した断面
図、第2図は対照品の構造を示す拡大した断面
図である。
1…アルミナ砥粒、2…ドリル布、3…一次接
着剤層、4…二次接着剤層、5…保護層、6…研
摩布。
The drawings show an abrasive cloth of a test example of the present invention; FIG. 1 is an enlarged sectional view showing the structure of the test product, and FIG. 2 is an enlarged sectional view showing the structure of a control product. DESCRIPTION OF SYMBOLS 1... Alumina abrasive grain, 2... Drill cloth, 3... Primary adhesive layer, 4... Secondary adhesive layer, 5... Protective layer, 6... Abrasive cloth.
Claims (1)
なる研摩布紙において、前記砥粒がα―アルミナ
を主成分とした平均粒径約100〜600μの焼結砥粒
であり、かつ前記砥粒及び接着剤層上には保護層
が被着され該保護層が合成樹脂と平均粒径約80μ
以下の無機質充填材の混合物よりなり無機質充填
材/合成樹脂の固形分重量比が約1.5〜32.3であ
ることを特徴とした研摩布紙の構造。1. A coated abrasive paper in which abrasive grains are adhered to a base material via an adhesive layer, wherein the abrasive grains are sintered abrasive grains containing α-alumina as a main component and having an average particle diameter of about 100 to 600 μm, A protective layer is applied on the abrasive grains and the adhesive layer, and the protective layer is made of synthetic resin and has an average particle size of about 80 μm.
A structure of a coated abrasive paper comprising a mixture of the following inorganic fillers and having an inorganic filler/synthetic resin solid content weight ratio of about 1.5 to 32.3.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4256084A JPS60186377A (en) | 1984-03-05 | 1984-03-05 | Abrasive cloth sheet structure |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4256084A JPS60186377A (en) | 1984-03-05 | 1984-03-05 | Abrasive cloth sheet structure |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60186377A JPS60186377A (en) | 1985-09-21 |
| JPH0138629B2 true JPH0138629B2 (en) | 1989-08-15 |
Family
ID=12639424
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4256084A Granted JPS60186377A (en) | 1984-03-05 | 1984-03-05 | Abrasive cloth sheet structure |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60186377A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014123153A1 (en) * | 2013-02-08 | 2014-08-14 | 昭和電工株式会社 | Alumina sintered body, abrasive grains, grindstone, polishing cloth, and method for manufacturing alumina sintered body |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1298980C (en) * | 1988-02-26 | 1992-04-21 | Clyde D. Calhoun | Abrasive sheeting having individually positioned abrasive granules |
| CN115383637B (en) * | 2022-09-22 | 2024-03-29 | 韶关辰锐研磨材料有限公司 | Production device and production method for abrasive cloth wheel with handle |
| CN117798838A (en) * | 2024-01-24 | 2024-04-02 | 韶关威鸣研磨材料有限公司 | A kind of soft cloth hardware water grinding automatic machine special abrasive cloth and preparation method thereof |
-
1984
- 1984-03-05 JP JP4256084A patent/JPS60186377A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014123153A1 (en) * | 2013-02-08 | 2014-08-14 | 昭和電工株式会社 | Alumina sintered body, abrasive grains, grindstone, polishing cloth, and method for manufacturing alumina sintered body |
| JPWO2014123153A1 (en) * | 2013-02-08 | 2017-02-02 | 昭和電工株式会社 | Alumina sintered body, abrasive grains, grindstone, polishing cloth, and method for producing alumina sintered body |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60186377A (en) | 1985-09-21 |
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