JPH0457676A - Tool for grinding - Google Patents
Tool for grindingInfo
- Publication number
- JPH0457676A JPH0457676A JP16431290A JP16431290A JPH0457676A JP H0457676 A JPH0457676 A JP H0457676A JP 16431290 A JP16431290 A JP 16431290A JP 16431290 A JP16431290 A JP 16431290A JP H0457676 A JPH0457676 A JP H0457676A
- Authority
- JP
- Japan
- Prior art keywords
- grinding
- resin
- layer
- abrasive grains
- abrasive grain
- 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
Links
- 238000000227 grinding Methods 0.000 title claims abstract description 70
- 229920005989 resin Polymers 0.000 claims abstract description 60
- 239000011347 resin Substances 0.000 claims abstract description 60
- 239000006061 abrasive grain Substances 0.000 claims abstract description 36
- 239000000463 material Substances 0.000 claims abstract description 29
- 229920002050 silicone resin Polymers 0.000 claims description 11
- 229920001187 thermosetting polymer Polymers 0.000 claims description 11
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 239000011737 fluorine Substances 0.000 claims description 5
- 239000003365 glass fiber Substances 0.000 claims description 4
- 238000005498 polishing Methods 0.000 abstract description 11
- 239000000853 adhesive Substances 0.000 abstract description 8
- 230000001070 adhesive effect Effects 0.000 abstract description 8
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 3
- 238000011049 filling Methods 0.000 abstract description 3
- 229910052710 silicon Inorganic materials 0.000 abstract description 3
- 239000010703 silicon Substances 0.000 abstract description 3
- 230000003578 releasing effect Effects 0.000 abstract 4
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 20
- 239000007788 liquid Substances 0.000 description 16
- 239000000843 powder Substances 0.000 description 16
- 239000000047 product Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 238000000576 coating method Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000012779 reinforcing material Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000001723 curing Methods 0.000 description 3
- 235000012489 doughnuts Nutrition 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 229910052755 nonmetal Inorganic materials 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000002023 wood Substances 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
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 108010039491 Ricin Proteins 0.000 description 2
- 239000003082 abrasive agent Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002843 nonmetals Chemical class 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000005488 sandblasting Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- -1 Alkyl vinyl ether Chemical compound 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- GEIAQOFPUVMAGM-UHFFFAOYSA-N ZrO Inorganic materials [Zr]=O GEIAQOFPUVMAGM-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 238000010422 painting Methods 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
- 239000010453 quartz Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000010081 sangu Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Polishing Bodies And Polishing Tools (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、研削用具に関し、更に詳しくは、粘着性を有
する材料の表面の研磨/研削もしくは粘着性を有する材
料の剥離に用いる研削用具に関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a grinding tool, and more particularly, to a grinding tool used for polishing/grinding the surface of an adhesive material or peeling off an adhesive material. .
[従来の技術]
化学プラント、タンク類、橋梁、車両、船舶及び建物の
塗装やタイル貼り構造物の目地/下地(リシン)は、施
工後ある年数が経過すると劣化する。従って、それらの
基材が健全であるかぎり、再塗装や再貼着を行ない対象
物の延命を計るのを常とする。その際、該塗膜や該リシ
ンの除去/剥離が必須作業となるわけであるが、従来、
この作業は、高圧空気に同伴させた砂粒を該除去対象物
に衝突させて剥離せしめるサンドブラスト法や研磨布紙
のような研削用具の研削面を該除去対象物表面に圧接し
て剥離せしめる方法もしくはタガネ様のもので該除去対
象物を直接ハッル方法等にて行なわれきた。[Prior Art] The joints/substrates (ricin) of painted and tiled structures in chemical plants, tanks, bridges, vehicles, ships, and buildings deteriorate after a certain number of years have passed after construction. Therefore, as long as those base materials are healthy, it is customary to repaint or reapply them to extend the life of the object. At that time, removal/peeling of the coating film and the ricin is essential work, but conventionally,
This work can be carried out using a sandblasting method in which sand grains entrained in high-pressure air collide with the object to be removed, or a method in which the ground surface of a grinding tool such as abrasive paper is pressed against the surface of the object to be removed, or The object to be removed has been directly removed using a chisel-like method such as the Hull method.
又、木工材料やある種の合成樹脂材料例えば合成木材及
び低硬度金属/非金属等の表面研磨/研削においては、
ヤスリやサンドペーパー及び研削砥石等が用いられてき
た。In addition, in surface polishing/grinding of wood materials and certain synthetic resin materials such as synthetic wood and low hardness metals/non-metals,
Files, sandpaper, grinding wheels, etc. have been used.
[発明が解決しようとする課題〕
しかしながら、サンドブラスト法では、該作業に付随し
て発生する粉塵の処置が面倒であり、そのこともあって
タンク等の内面処理に限定され、直接ハツル方法では、
人力に頼る作業数その作業効率に難があり、研磨布紙を
用いる方法やヤスリ、サンドペーパーを用いる方法(こ
れらの研削用具の構造を第4図に示す)及び研削砥石を
用いる方法では、該除去対象物や被研M/研削物がそれ
ら材料本来の性質として有する粘着性や研磨/研削用具
の圧接時発生する熱による粘着性の発現によって、研磨
/研削材の粒間に目詰りを引き起こし、ひいては、研磨
/研削用具が被研磨/研削物表面を滑るだけで該作業の
継続が不能になるいわゆるスベリ現象を起こさしむる。[Problems to be Solved by the Invention] However, in the sandblasting method, it is troublesome to deal with the dust generated along with the work, and for this reason, it is limited to the inner surface treatment of tanks, etc., and in the direct blasting method,
The number of operations that rely on human power and the efficiency of the work are difficult, and methods using coated abrasive paper, files and sandpaper (the structure of these grinding tools are shown in Figure 4), and methods using grinding wheels do not meet the criteria. Clogging occurs between the grains of the polishing/abrasive material due to the inherent tackiness of the object to be removed or the object to be ground/grinded, or due to the heat generated during pressure contact with the polishing/grinding tool. Furthermore, simply slipping the polishing/grinding tool on the surface of the object to be polished/grinded causes a so-called slipping phenomenon, which makes it impossible to continue the work.
塗膜の除去/剥離作業を例に取ると、除去/剥離対象物
が施工後3〜4年と比較的新しいものである場合にその
傾向が著しく、作業開始後数秒で該現象を起こすことが
ある。このスベリ現象が発生すると、直ちに該用具を交
換しなければならず、作業効率の低下及び消耗品コスト
の上昇ひいては作業全体のコスト・アップ要因となるた
め、その改善が切望されていた。しかしながら、未だそ
の要望に応え得る製品が8現しなかったのである。Taking paint film removal/stripping work as an example, if the object to be removed/stripped is relatively new (3 to 4 years after construction), this tendency is most noticeable, and this phenomenon can occur within a few seconds after starting work. be. When this slipping phenomenon occurs, the tool must be replaced immediately, resulting in a decrease in work efficiency, an increase in the cost of consumables, and an increase in the cost of the entire work.Therefore, there has been a strong desire to improve this phenomenon. However, no product has yet appeared that can meet this demand.
[課題を解決するための手段]
本発明の研削用具は、基材と、該基材の上に形成されか
つ研削砥粒を熱硬化性樹脂で結着せしめてなる研削層の
少なくとも研削砥粒間及び/又はその表面にフッ素系樹
脂又はシリコン樹脂を存在せしめた層からなることを特
徴とする(その構造の例を第1図及び第2図に示す)。[Means for Solving the Problems] The grinding tool of the present invention comprises a base material, and at least the grinding abrasive grains of the abrasive layer formed on the base material and having the abrasive grains bound with a thermosetting resin. It is characterized by being composed of a layer in which a fluororesin or silicone resin is present between and/or on its surface (an example of its structure is shown in FIGS. 1 and 2).
基材としては、該研削用具の用途に応じて適宜選択すれ
ばよく、適度の強度1重量を有するもの、例えば、布1
紙、金属、非金属及びプラスチック又はそれらの複合材
等から選択される。勿論、特開昭61−25776号公
報に開示されたバルカナイズドファイバ板であってもよ
い。又、その形状及び厚みも、該研削用具の用途に応じ
て適宜選択すればよく、例えば、シート、ロール、ベル
トディスク、板及び棒が挙げられる。The base material may be selected as appropriate depending on the use of the grinding tool, and may have appropriate strength and weight, such as cloth 1
Selected from paper, metal, non-metal, plastic, composite material thereof, etc. Of course, the vulcanized fiber plate disclosed in Japanese Unexamined Patent Publication No. 61-25776 may also be used. Further, the shape and thickness of the grinding tool may be appropriately selected depending on the use of the grinding tool, and examples thereof include a sheet, a roll, a belt disk, a plate, and a rod.
研削層は、この基材の上に形成された研削砥粒の層であ
って、該基材と熱硬化性樹脂を介してその砥粒の一方の
端部が該樹脂層から首を出すように結着せしめられてい
る。研削砥粒としては、高硬度のものがよく、具体的に
はJIS R6011に規定する人造研削材やZrOの
外に、石英、ダイアモンドやそれらの混合物のようなも
のであってもよい。ここで用いる熱硬化性樹脂としては
、完全硬化したときその機械的強度が大で、しかも、研
削砥粒を強固に結着し得る樹脂であれば何であってもよ
いが、例えば、レゾール型フェノール樹脂。The abrasive layer is a layer of abrasive grains formed on this base material, and is formed through the base material and a thermosetting resin so that one end of the abrasive grains protrudes from the resin layer. It is tied to The grinding abrasive grains preferably have high hardness, and specifically, in addition to artificial abrasives specified in JIS R6011 and ZrO, quartz, diamond, and mixtures thereof may also be used. The thermosetting resin used here may be any resin as long as it has high mechanical strength when completely cured and can firmly bind grinding abrasive grains. For example, resol type phenol may be used. resin.
エポキシ樹脂、尿素樹脂のそれぞれ単独又はこれら2種
以上を適宜に混合したものをあげることができる。Examples include epoxy resins and urea resins, each alone or a mixture of two or more thereof.
フッ素系樹脂又はシリコン樹脂を存在せしめた層(以下
、離型層という)は、該研削層の少なくとも研削砥粒間
(前記熱硬化性樹脂の層が露出している)及び/又はそ
の表面を被覆するように存在する。ここで用いるフッ素
系樹脂としては、四フッ化エチレン樹脂(通称テフロン
)が好ましいが、三フッ化塩化エチレン樹脂、フッ化ビ
ニリデン樹脂、フッ素化エチレン・プロピレン共重合樹
脂、四フッ化エチレン・パーフルオロアルキルビニルエ
ーテル共重合樹脂及び四フッ化エチレン・エチレン共重
合樹脂等を用いてもよい。又、フッ素系樹脂に代えて用
いるシリコン樹脂としては、離型材として市販されてい
るものでよく、例えば、溶剤型剥離紙用シリコンやシリ
コン樹脂微粒子等が挙げられる。The layer in which the fluororesin or silicone resin is present (hereinafter referred to as the release layer) coats at least the space between the abrasive grains of the grinding layer (where the thermosetting resin layer is exposed) and/or the surface thereof. It exists as if it were covered. As the fluororesin used here, tetrafluoroethylene resin (commonly known as Teflon) is preferred, but trifluorochloroethylene resin, vinylidene fluoride resin, fluorinated ethylene/propylene copolymer resin, tetrafluoroethylene/perfluoroethylene resin, etc. Alkyl vinyl ether copolymer resins, tetrafluoroethylene/ethylene copolymer resins, etc. may also be used. Furthermore, the silicone resin used in place of the fluororesin may be one that is commercially available as a mold release material, such as silicone for solvent-based release paper, silicone resin fine particles, and the like.
上記構造を有する本発明の研削用具は、次のようにして
製造することができる。The grinding tool of the present invention having the above structure can be manufactured as follows.
先ず、所定形状及び厚みの基材を用意する。この基材表
面に、所定粘度の熱硬化性樹脂液を適量(後で散布する
研削砥粒が該樹脂より首を出した状態になるよう)注加
した後、この状態のまま、又は、必要に応じて60°C
程度の温度で若干加熱して樹脂を少し硬化させた後、研
削砥粒をその上に散布する。樹脂が未だ柔らかであれば
、この研削砥粒は自重で樹脂内に沈み込み基材と研削砥
粒が相互に密接させられる。樹脂液の粘度があまり高い
と基材及び研削砥粒との濡れの均質性が低下し、又、逆
にあまり低いと結着材としての樹脂の量が少なくなるた
め研削砥粒の脱落が早(なるという問題を生ずる。通常
10.0〜13.oポイズ(25℃)が好ましい。尚、
このときにフィラーとして炭カルを樹脂に対し20〜1
00重量%添加してもよい。First, a base material of a predetermined shape and thickness is prepared. After pouring an appropriate amount of thermosetting resin liquid of a predetermined viscosity onto the surface of this base material (so that the abrasive grains to be sprayed later stick out from the resin), leave it in this state or use it as needed. 60°C depending on
After the resin is slightly cured by heating at a moderate temperature, abrasive grains are sprinkled on it. If the resin is still soft, the abrasive grains sink into the resin under their own weight, bringing the base material and the abrasive grains into close contact with each other. If the viscosity of the resin liquid is too high, the homogeneity of wetting with the base material and the abrasive grains will decrease, and if the viscosity is too low, the amount of resin as a binder will be reduced, causing the abrasive grains to fall off quickly. (This causes the problem of
At this time, as a filler, add charcoal to the resin at a ratio of 20 to 1
00% by weight may be added.
次いで、この状態のまま、60〜100℃程度の温度で
加熱・乾燥して樹脂を少し硬化する。Next, in this state, the resin is heated and dried at a temperature of about 60 to 100°C to slightly harden the resin.
その後、該研削砥粒の上から、該熱硬化性樹脂液にフッ
素系樹脂粉末又はシリコン樹脂粉末を該樹脂液に分散せ
しめた液を更に注加して少し硬化した樹脂の表面より首
を出した研削砥粒の間及びその表面を該樹脂で被覆する
。フッ素系樹脂粉末又はシリコン樹脂粉末の添加量(離
型効果の支配因子)としては、被覆表面積基準で1〜1
00%、好ましくは、5〜100%、更に好ましくは、
50%以上、一方、粒径(該樹脂液中での分散性ひいて
は離型効果を支配する)としては、0.ODm〜0.5
mm、好ましくは、0.1jrln−0,1mm 、更
に好ましくは、 0.l!1n〜1−である。After that, a liquid in which fluorine resin powder or silicone resin powder is dispersed in the thermosetting resin liquid is further poured onto the grinding abrasive grains, so that the necks are exposed from the surface of the slightly hardened resin. The resin is coated between the ground abrasive grains and on their surfaces. The amount of fluororesin powder or silicone resin powder added (controlling factor for mold release effect) is 1 to 1 on the basis of the covered surface area.
00%, preferably 5-100%, more preferably,
50% or more, on the other hand, the particle size (which governs the dispersibility in the resin liquid and hence the mold release effect) is 0. ODm~0.5
mm, preferably 0.1 jrln-0.1 mm, more preferably 0.1 mm. l! 1n to 1-.
次いで、これら全体を所定温度の加熱炉に導入し熱硬化
性樹脂を完全に硬化する。このときの温度は、あまり高
くすると樹脂の発泡が起り、またあまり低いと硬化が進
行しないので、通常は60〜180℃であることが好ま
しく、しかも徐々に昇温して加熱することが好ましい。Next, the whole is introduced into a heating furnace at a predetermined temperature to completely cure the thermosetting resin. If the temperature at this time is too high, foaming of the resin will occur, and if it is too low, curing will not proceed, so it is usually preferably 60 to 180°C, and it is preferable to heat the resin by gradually increasing the temperature.
尚、フッ素系樹脂粉末又はシリコン樹脂粉末を樹脂液と
共に用いる上記方法に代え、研削砥粒間及びその表面に
フッ素系樹脂又はシリコン樹脂による離型層を形成させ
ずに完全に硬化せしめた製品の表面に常温硬化型樹脂、
例えばウレタン系。In addition, instead of the above method of using fluorine-based resin powder or silicone resin powder together with resin liquid, a product that is completely cured without forming a release layer of fluorine-based resin or silicone resin between the abrasive grains and on its surface. Room temperature curing resin on the surface,
For example, urethane.
ナイロン系、アクリル系等の樹脂系接着材又は糊料等を
用いて該粉末を付着せしめたり、もしくは、溶剤タイプ
のフッ素系樹脂又はシリコン樹脂を塗布してもよい。又
、完全硬化を行なわしむる前にまだ流動性を多少残した
該製品の表面に粉末タイプのそれを散布したり、やや乾
燥した該製品の表面に溶剤タイプのそれを塗布してもよ
い。The powder may be attached using a resin-based adhesive or paste such as nylon-based or acrylic-based, or a solvent-type fluororesin or silicone resin may be applied. Also, before complete curing, a powder type of the product may be sprinkled on the surface of the product that still has some fluidity, or a solvent type of the product may be applied to the slightly dry surface of the product.
又、本発明の研削用具において、基材とその上に存在す
る研削砥粒を含む研削層との間に、更に、特開昭61−
25776号公報に開示されたガラスファイバーメツシ
ュを補強材として介在せしめた構造(第3図参照)のも
のも利用できる。表層が粘着質でその下層が硬質な複合
材料である被研磨/研削物の場合には、研磨/研削の進
行につれて硬質面が露出するため、該スベリ現象の防止
と共に研削用具自体の強度が要求されるからである。Furthermore, in the grinding tool of the present invention, between the base material and the grinding layer containing grinding abrasive particles present thereon, JP-A-61-
The structure disclosed in Japanese Patent No. 25776 in which a glass fiber mesh is interposed as a reinforcing material (see FIG. 3) can also be used. In the case of objects to be polished/ground that have a sticky surface layer and a hard composite material underneath, the hard surface is exposed as the polishing/grinding progresses, so the grinding tool itself must be strong to prevent slippage. This is because it will be done.
該補強材の形状は、網状体であることが好適であり、し
かもその材質は 注加する熱硬化性樹脂とよくなじんで
接着性を高めるものが好ましい。The shape of the reinforcing material is preferably a net-like body, and the material thereof is preferably one that is compatible with the thermosetting resin to be added and improves adhesiveness.
網状体としては、例えばメツシュ、不織布、マットのよ
うな形体を適用でき、いずれも空隙部分に樹脂が含浸し
て該網状体を強固に結着する。とりわけ、メツシュは好
適である。また、用いる樹脂との接着性が悪いと、これ
ら網状体は樹脂によって強固に結着されないので補強材
としての有用な機能を喪失し、しかも樹脂と濡れていな
い部分が使用時の発生トルクに基づく破壊点になってし
まうにれら補強材としては、例えばガラスファイバーの
メツシュ、マット、不縁布;鉄の金網、マット、鉄線線
の不織布;ウレタン樹脂又はポリエステル樹脂などのフ
ァイバーメツシュ、マット、不縁布:などをあげること
ができる0例えば、ガラスファイバーのメツシュの場合
、そのファイバー線径が0.1〜1.5mm、網の目の
大きさが1.5mmX 1.5mm 〜5mmX 5m
mのものは補強効果が大きく有効である。特に網の目の
大きさは用いる研削砥粒の粒径との関係から適宜に選定
されるべきであるが、一般に用いられるNo、12〜N
o、24の研削砥粒にあっては上記の網の目が好適であ
る。As the net-like body, shapes such as a mesh, a non-woven fabric, and a mat can be used, and in any case, the voids are impregnated with resin to firmly bind the net-like body. In particular, mesh is preferred. In addition, if the adhesiveness with the resin used is poor, these net-like bodies will not be firmly bound by the resin and will lose their useful function as a reinforcing material. Examples of reinforcing materials that can become breaking points include glass fiber mesh, mats, and non-woven fabrics; iron wire mesh, mats, and non-woven fabrics made of iron wire; fiber mesh, mats, and urethane resin or polyester resin. For example, in the case of a glass fiber mesh, the fiber wire diameter is 0.1 to 1.5 mm, and the mesh size is 1.5 mm x 1.5 mm to 5 mm x 5 m.
The reinforcing effect of m is large and effective. In particular, the mesh size should be appropriately selected in relation to the particle size of the grinding abrasive grains used, but generally used No. 12 to N
For the grinding abrasive grains No. 24, the above-mentioned mesh size is suitable.
該補強材は、基材表面への最初の樹脂液注加に先立ち、
該基材上に載置しおくことによって該構造内に取り入れ
られる。The reinforcing material is made of
It is incorporated into the structure by placing it on the substrate.
[作用]
本発明の研削用具は、製造直後には該離型材の層が研削
砥粒間及びその表面を被覆しているが、該研削用具を使
用することによって該表面被覆部分は除去対象物もしく
は被研磨/研削物との接触によって剥げ落ち、該研削砥
粒が露出する。[Function] Immediately after the grinding tool of the present invention is manufactured, the layer of the mold release material covers the space between the grinding abrasive grains and the surface thereof, but by using the grinding tool, the surface covered portion is removed from the object to be removed. Alternatively, it peels off due to contact with the object to be polished/grinded, and the abrasive grains are exposed.
方、該研削砥粒間に存在する離型材の層/膜は、除去対
象物もしくは被研磨/研削物と接触しないためそのまま
保持されている。従って、該研削砥粒によって剥ぎ取ら
れた粘着物質は、該離型材の離型効果によって該研削砥
粒の間隙を埋めることなく除去もしくは研磨/研削作業
部位がら排除され、除去もしくは研磨/研削作業を継続
せしむるのである
[実施例]
以下に、研削円板を例として、本発明の詳細な説明する
。On the other hand, the layer/film of the release material existing between the grinding abrasive grains is retained as it is because it does not come into contact with the object to be removed or the object to be polished/ground. Therefore, the adhesive substance peeled off by the grinding abrasive grains is removed or removed from the polishing/grinding work area by the mold release effect of the mold release material without filling the gaps between the grinding grains, and the adhesive substance is removed or removed from the polishing/grinding work area. [Example] The present invention will be described in detail below using a grinding disk as an example.
(実施例−1)
JIS C2315で規定する1種バルヵナイズドファ
イバー板(東洋ファイバー■製)から外径150mm、
内径22.3mmのドーナツ板(以下、ドーナツ基板と
いう)を切り出した。厚みは、1.2mmであった。(Example-1) Outer diameter 150 mm from a type 1 vulcanized fiber board (manufactured by Toyo Fiber ■) specified in JIS C2315,
A donut plate (hereinafter referred to as donut substrate) having an inner diameter of 22.3 mm was cut out. The thickness was 1.2 mm.
一方、不揮発分68%、比重(4℃の水1gに対する2
5℃の重量、以下、同様)1.193.粘度(25℃。On the other hand, the non-volatile content is 68%, the specific gravity (2
Weight at 5°C (the same applies hereinafter) 1.193. Viscosity (25℃.
以下、同様) 12.0ボイス、ゲル化時間4.5分7
150℃、水混和性3.’5倍/25℃、 pH9,2
のフェノール樹脂100重量部と炭カル100重量部と
50%メタノール水溶液30重量部とから成る樹脂液(
以下、樹脂液−1という)を用意した。Same hereafter) 12.0 voice, gel time 4.5 minutes 7
150°C, water miscible3. '5x/25℃, pH9.2
A resin liquid (
A resin liquid (hereinafter referred to as resin liquid-1) was prepared.
更に、前記フェノール樹脂100重量部と炭カル20重
量部と水20重量部とから成る樹脂液(以下、樹脂液−
2という)を用意した6
前記ドーナツ基板の上に、前記樹脂液−1を11g1g
注加後、No、16の2rO砥粒38gを散布し、次い
で、全体を100℃の乾燥炉中に90分間放置し、フェ
ノール樹脂を熱硬化せしめた(以下、下塗工程という)
。更にこの上にフッ素樹脂粉末(ダイキン工業(株)製
:商品名ルブロンし−5)14重量部を含む前記樹脂液
−2を7g注加した後、再び、全体を120℃の乾燥炉
中に3時間放置し、フェノール樹脂全体を完全に熱硬化
せしめ(以下、上塗工程という)製品(第1図にその構
造を示す)とした。該製品では、該フッ素樹脂の粒子が
、当然のことながら該樹脂液−2が硬化した層中と該研
削砥粒間及びその表面に存在することになる。Further, a resin liquid (hereinafter referred to as "resin liquid") consisting of 100 parts by weight of the phenolic resin, 20 parts by weight of charcoal, and 20 parts by weight of water was added.
2) was prepared 6. 11 g 1 g of the resin liquid-1 was placed on the donut substrate.
After pouring, 38 g of No. 16 2rO abrasive grains were sprinkled, and then the whole was left in a drying oven at 100° C. for 90 minutes to heat cure the phenol resin (hereinafter referred to as the undercoating step).
. Furthermore, after pouring 7 g of the resin liquid 2 containing 14 parts by weight of fluororesin powder (manufactured by Daikin Industries, Ltd., trade name: Lubron Shi-5) onto this, the whole was placed in a drying oven at 120°C again. The product was left to stand for 3 hours to completely heat cure the entire phenolic resin (hereinafter referred to as the top coating step), resulting in a product (the structure of which is shown in FIG. 1). In this product, particles of the fluororesin naturally exist in the layer where the resin liquid-2 is cured, between the grinding grains, and on the surface thereof.
(実施例−2)
上塗工程において、該樹脂液−2の中にフッ素樹脂粉末
を加えなかったこと以外実施例−1と同様にして完全硬
化した研削円板を作製した。更にこの上に付着剤(帝国
化学産業(株)製:商品名ティサンウレタン310)I
gをメチルエチルケトン4gに溶解せしめたものを塗布
し、しかる後、実施例−1で用いたフッ素樹脂粉末0.
7gを散布することによってフッ素樹脂を存在せしめ最
終製品とした(第2図にその構造を示す)。該製品では
、該フッ素樹脂の粒子が、当然のことながら該研削砥粒
間及びその表面にのみ存在することになる。(Example 2) A completely cured grinding disk was produced in the same manner as in Example 1 except that fluororesin powder was not added to the resin liquid 2 in the top coating step. Furthermore, an adhesive (manufactured by Teikoku Kagaku Sangyo Co., Ltd.: trade name TISSAN URETHANE 310) I
g dissolved in 4 g of methyl ethyl ketone was applied, and then 0.0 g of the fluororesin powder used in Example-1 was applied.
By spraying 7 g of the resin, the fluororesin was made to exist and a final product was obtained (the structure is shown in FIG. 2). In this product, the fluororesin particles naturally exist only between the abrasive grains and on the surface thereof.
(実施例−3)
上塗工程において、該樹脂液−2の中にフッ素樹脂粉末
を加えなかったこと以外実施例−1と同様にして完全硬
化した研削円板を作製した。更にこの上に比重1.51
.希釈倍率1〜5の溶剤タイプのフッ素系離型剤(ダイ
キン工業(株)製:商品名グイフリーM S −743
) 100重量部と99%イソプロピルアルコール2
00重量部とからなる液3gを塗布してフッ素樹脂皮膜
を該研削砥粒間及びその表面に形成せしめた。(Example 3) A completely cured grinding disk was produced in the same manner as in Example 1 except that the fluororesin powder was not added to the resin liquid 2 in the top coating step. Furthermore, on top of this, the specific gravity is 1.51
.. Solvent-type fluorinated mold release agent with a dilution ratio of 1 to 5 (manufactured by Daikin Industries, Ltd.: product name Guifuri MS-743)
) 100 parts by weight and 99% isopropyl alcohol 2
00 parts by weight was applied to form a fluororesin film between and on the surface of the abrasive grains.
(実施例−4)
上塗工程において、該樹脂液−2の中にフッ素樹脂粉末
を加えなかったこと及び熱硬化処理に先立ち、実施例−
1で用いたフッ素樹脂粉末0.7gを前期樹脂液−2の
層の上に該層がまだ濡れている状態の時に散布したこと
以外実施例−1と同様にして研削円板を作製した。(Example-4) In the top coating process, no fluororesin powder was added to the resin liquid-2, and prior to the thermosetting treatment, Example-
A grinding disk was produced in the same manner as in Example 1, except that 0.7 g of the fluororesin powder used in Example 1 was sprinkled onto the layer of resin liquid 2 while the layer was still wet.
(実施例−5)
上塗工程において、該樹脂液−2の中にフッ素樹脂粉末
を加えなかったこと及び熱硬化処理に先立ち、比重0.
92.粘度40〜60ポアズ、シリコン分30%のシリ
コン系剥離剤(信越化学工業(株)製剥離紙用シリコン
K S −841) 100重量部と触媒(信越化学
工業(株)製:商品名CAT PL−7)1重量部と
メチルエチルケトン200重量部からなる液4gを前期
樹脂液−2の層の上に該層がやや乾燥した時塗布したこ
と以外実施例−1と同様にして研削円板を作製した。(Example 5) In the top coating process, no fluororesin powder was added to the resin liquid 2, and prior to the thermosetting treatment, the specific gravity was 0.
92. 100 parts by weight of a silicone release agent with a viscosity of 40 to 60 poise and a silicon content of 30% (Silicone K S-841 for release paper manufactured by Shin-Etsu Chemical Co., Ltd.) and a catalyst (manufactured by Shin-Etsu Chemical Co., Ltd.: trade name CAT PL) -7) A grinding disk was prepared in the same manner as in Example-1, except that 4 g of a liquid consisting of 1 part by weight and 200 parts by weight of methyl ethyl ketone was applied onto the layer of resin liquid-2 when the layer was slightly dry. did.
(比較例−1)
上塗工程において、フッ素樹脂粉末を使用しなかったこ
と以外実施例−1と同様にして研削円板を作製した。(Comparative Example-1) A grinding disk was produced in the same manner as in Example-1 except that fluororesin powder was not used in the top coating process.
上記例で得られたそれぞれの研削円板を電気サングーに
取りつけ、5万klの備蓄用重油タンクの塗膜(厚み:
400 mm、塗装面積: 6,000m2.但し、
外部のみ)の剥離作業に供し、剥離塗料が研削砥粒面に
目詰りを起こさせずに作業し得た面積を測定した。その
結果は、表の通りであった。Each of the grinding discs obtained in the above example was attached to an electric Sangu, and a coating film (thickness:
400 mm, painting area: 6,000 m2. however,
The area on which the peeling paint could be removed without clogging the abrasive grain surface was measured. The results were as shown in the table.
[発明の効果1
以上の説明で明らかなように、本発明の研削用具によれ
ば、従来のものでは、研削用具の頻繁な交換を余儀なく
された粘着質物質の除去/剥離作業を長時間継続して行
なうことができるので、該作業の効率を向上し得る。又
、交換頻度が少ない分、当然のことながら、該研削用具
コスト(消耗品補充コスト)を大幅に低減できる。[Effect of the invention 1 As is clear from the above explanation, the grinding tool of the present invention allows the removal/peeling work of sticky substances to continue for a long time, which required frequent replacement of the grinding tool with the conventional grinding tool. Therefore, the efficiency of the work can be improved. Furthermore, since the frequency of replacement is low, the cost of the grinding tool (cost of replenishing consumables) can be significantly reduced.
尚、本発明の研削用具は、粘着質物質(排除されるべき
物質が微粉数、静電気力等で凝集・付着するものを含む
)が研削砥粒の間隙を埋めることを防止することにその
目的があるため、本発明の用途は、粘着質物質の除去/
剥離作業に限定されるものではなく、例えば、木工材料
やプラスチック及び低硬度金属/非金属のような粘着性
を有する/発現する材料の表面研磨にも使用可能なこと
が上記の説明から容易に解るであろう。The purpose of the grinding tool of the present invention is to prevent sticky substances (including substances to be removed that aggregate and adhere due to fine particles, electrostatic force, etc.) from filling the gaps between grinding abrasive grains. Therefore, the application of the present invention is to remove sticky substances/
It is easy to understand from the above explanation that it is not limited to peeling work, but can also be used for surface polishing of materials that have/exhibit adhesiveness, such as wood materials, plastics, and low-hardness metals/non-metals. You will understand.
第1図は、本発明の研削用具の一実施例の構造を模式的
に示した断面図、第2図は、本発明の研削用具の他の実
施例の構造を模式的に示した断面図、第3図は、従来の
研削用具の構造を模式的に示した断面図である。
1:基材 2:研削砥粒
3:合成樹脂層(結着材層)
4:フッ素系樹脂又はシリコン樹脂の粒子5:付着剤層
6:補強材
[備考コ 実施例−1,−2及び−4の研削円板は、未
だ目詰りを起こしていなかっ
たが、時間の関係で、試験を打ち切っ
たので、その時点までの研削面積で表
示したものである。
第
図
手
続
補
正
書
(方式)
事件の表示
平成2年特許願第1643
12号
2、発明の名称
研削用具
3゜
補正をする者
事件との関係 特許出願人
名称 ミスミ化学株式会社
名称 山 口 景 章
4゜
代
理
人
9月27
第
図
5゜
補正命令の日付
平成2年9月25日
6、補正の対象
明細書の図面の簡単な説明の欄
μ ′
囃〕
補正する。
(1)明細書第18頁第5行目に記載の「第3図は、」
と「従来の」との間に「本発明の研削用具のさらに別の
実施例の構造を模式的に示した断面図、第4図は、」を
挿入する。FIG. 1 is a cross-sectional view schematically showing the structure of one embodiment of the grinding tool of the present invention, and FIG. 2 is a cross-sectional view schematically showing the structure of another embodiment of the grinding tool of the present invention. , FIG. 3 is a sectional view schematically showing the structure of a conventional grinding tool. 1: Base material 2: Grinding grains 3: Synthetic resin layer (binder layer) 4: Fluorine resin or silicone resin particles 5: Adhesive layer 6: Reinforcing material [Remarks Examples -1, -2 and The grinding disk No.-4 had not yet become clogged, but due to time constraints, the test was discontinued, so the grinding area up to that point is shown. Diagram procedural amendment (method) Display of the case 1990 Patent Application No. 1643 No. 12 2, Name of the invention Grinding tool 3゜Relationship with the case Name of patent applicant Misumi Chemical Co., Ltd. Name Keiaki Yamaguchi 4゜Agent September 27 Fig. 5゜Date of amendment order September 25, 1990 6. Column for brief explanation of drawings of the specification subject to amendment μ' Music] Amended. (1) “Figure 3 is” written on page 18, line 5 of the specification.
``A sectional view schematically showing the structure of yet another embodiment of the grinding tool of the present invention, FIG. 4'' is inserted between ``Conventional'' and ``Conventional''.
Claims (2)
硬化性樹脂で結着せしめてなる研削層の少なくとも研削
砥粒間及び/又はその表面にフッ素系樹脂又はシリコン
樹脂を存在せしめた層からなる研削用具。(1) A base material and a fluorine-based resin or silicone resin at least between the abrasive grains and/or on the surface of the abrasive layer formed on the base material and made by bonding the abrasive grains with a thermosetting resin. A grinding tool consisting of a layer of
シュを介在せしめた請求項1に記載の研削用具。(2) The grinding tool according to claim 1, wherein a glass fiber mesh is interposed between the base material and the grinding layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2164312A JP3043371B2 (en) | 1990-06-25 | 1990-06-25 | Grinding tools |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2164312A JP3043371B2 (en) | 1990-06-25 | 1990-06-25 | Grinding tools |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0457676A true JPH0457676A (en) | 1992-02-25 |
JP3043371B2 JP3043371B2 (en) | 2000-05-22 |
Family
ID=15790751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2164312A Expired - Lifetime JP3043371B2 (en) | 1990-06-25 | 1990-06-25 | Grinding tools |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3043371B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003071730A (en) * | 2001-09-03 | 2003-03-12 | Cci Corp | Abrasive material sheet |
-
1990
- 1990-06-25 JP JP2164312A patent/JP3043371B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003071730A (en) * | 2001-09-03 | 2003-03-12 | Cci Corp | Abrasive material sheet |
Also Published As
Publication number | Publication date |
---|---|
JP3043371B2 (en) | 2000-05-22 |
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