WO2005097409A1 - Porous vitrified grinding wheel and method for production thereof - Google Patents

Porous vitrified grinding wheel and method for production thereof Download PDF

Info

Publication number
WO2005097409A1
WO2005097409A1 PCT/JP2005/006595 JP2005006595W WO2005097409A1 WO 2005097409 A1 WO2005097409 A1 WO 2005097409A1 JP 2005006595 W JP2005006595 W JP 2005006595W WO 2005097409 A1 WO2005097409 A1 WO 2005097409A1
Authority
WO
WIPO (PCT)
Prior art keywords
abrasive grains
based abrasive
pore
glass frit
grindstone
Prior art date
Application number
PCT/JP2005/006595
Other languages
French (fr)
Japanese (ja)
Inventor
Kazuyuki Ishioka
Takenori Kanda
Original Assignee
Kure-Norton Co., 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 Kure-Norton Co., Ltd. filed Critical Kure-Norton Co., Ltd.
Priority to JP2006512066A priority Critical patent/JP4769186B2/en
Priority to CN2005800102663A priority patent/CN1938129B/en
Publication of WO2005097409A1 publication Critical patent/WO2005097409A1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
    • B24D3/04Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic
    • B24D3/14Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic ceramic, i.e. vitrified bondings
    • B24D3/18Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic ceramic, i.e. vitrified bondings for porous or cellular structure

Definitions

  • the present invention relates to a porous vitrified grinding wheel and a method for producing the same.
  • the main types of grinding and polishing whetstones include, by binder, vitrified whetstones, resinoid whetstones, metal whetstones, and electrodeposition whetstones.
  • vitrified whetstones are widely used because of their sharpness, high durability and good dressability.
  • a vitrified grindstone selects one or more kinds of inorganic powders such as clay, feldspar, and glass frit as raw materials of an abrasive and a vitrified binder, mixes the powder with a primary binder, and molds the mixture into a mold. Fill and mold. After the drying process, it is manufactured by firing at a high temperature of 600-1300 ° C.
  • Patent Document 1 a technique for manufacturing a grindstone using an inorganic adhesive that cures at a temperature lower than the firing temperature described above is disclosed.
  • paragraph "0005" states that the abrasive layer can be formed by directly baking the abrasive grain layer on a grindstone base at a low sintering temperature of about 150 to 300 ° C.
  • Patent Document 2 Also disclosed is a technique in which 50 to 30 parts by weight of boron carbide and 50 to 10 parts by weight of a ceramic material are added and mixed with 1 to 10 parts by weight of an aqueous solution of water glass, and then dried and fired at 800 to 1200 ° C.
  • Patent Document 1 JP 2001-71268 A
  • Patent Document 2 JP-A-52-26094
  • the present invention relates to a porous vitrified whetstone produced by using an inorganic adhesive and a foamable pore-forming agent, particularly a porosity of 60% by volume or more and / or abrasive grains.
  • An object of the present invention is to provide a grindstone having a uniform grindstone structure, good sharpness, sufficient durability and strength, and a method for producing the same, even with a fine grindstone having a diameter of less than 100 ⁇ m.
  • the porous and inorganic vitrified whetstone of the present invention that solves the above problems is a whetstone having a structure composed of abrasive grains, a binder, and pores, and is a bond formed by an inorganic adhesive and a glass frit. And natural pores and pores formed by a pore-forming agent.
  • the glass frit has a softening point of 300 to 900 ° C, preferably 400 to 900 ° C.
  • the grindstone of the present invention includes fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina zirconium-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, and CBN-based abrasive grains. It is preferable to have one or more abrasive grains selected from the group consisting of grains and diamond-based abrasive grains.
  • a liquid mixture obtained by dissolving an abrasive, an inorganic adhesive, a glass frit, and a pore-forming agent in water is poured into a mold, and the mixture in the mold is washed. It is characterized by drying and solidifying at room temperature to 300 ° C. and foaming the pore-forming agent at the same time, and baking the dried and solidified mixture at 600 to 1000 ° C. to obtain a vitrified whetstone.
  • a liquid foamable pore-forming agent may be used, or a solid foamable pore-forming agent may be used. Further, it is preferable to use a glass frit having a softening point of 300 to 900 ° C, preferably 400 to 900 ° C.
  • the abrasive grains used are fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina zirconia-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, and CBN-based abrasive grains.
  • One or more types can be selected from the group consisting of grains and diamond-based abrasive grains.
  • the present invention can provide a porous vitrified grindstone having a binder formed of an inorganic adhesive and a glass frit and having substantially uniform pores formed of natural pores and a pore-forming agent.
  • a fine grinding stone with a ratio of 60% by volume or more and / or a grain diameter of less than 100 ⁇ m, having a uniform grinding stone structure, excellent sharpness, high durability and strength, and a method for producing the same. can do.
  • FIG. 1 is an electron micrograph of the grindstone structure of the test grindstone prepared in Example 1.
  • FIG. 2 is a cross-sectional view illustrating a schematic configuration of cup-type grindstones of Examples 3 and 4.
  • FIG. 3 is a photograph of a cup-shaped grindstone produced as Examples 3 and 4 taken from the front.
  • FIG. 4 is an enlarged photograph of the vicinity of a grinding wheel piece of the cup-type grinding wheel of FIG. 3 taken from the side.
  • the grindstone of the present invention is a porous vitrified grindstone manufactured by casting a mixture containing an abrasive, an inorganic adhesive, a glass frit, and a pore-forming agent.
  • the "porous vitrified grinding wheel" referred to in the specification of the present application does not include an organic primary binder, uses an inorganic adhesive as a substantial primary binder, and further uses a glass frit together with the inorganic adhesive. It means a grindstone that is sintered using and contains pores formed by a foaming agent and natural pores. According to the present invention, good pore formation is performed at the time of drying and solidifying the grindstone raw material mixture, and then vitrification proceeds through a glass frit, so that the grindstone has a uniform grindstone structure, particularly a fine and uniform pore structure, and A porous vitrified whetstone having sufficient strength can be manufactured.
  • the inorganic adhesive is an inorganic substance which cures at a relatively low temperature and mainly serves to maintain the shape of a grinding wheel from molding to firing.
  • Such an inorganic adhesive is mainly composed of one or more of silica, alumina, alumina, silica, zirconia 'silica, zirconia, sodium silicate, aluminum phosphate, magnesium phosphate, and the like.
  • a binder such as silica sol, aluminum phosphate, magnesium phosphate and the like, and a binder using silicate ion and the like as a curing agent.
  • alkali silicate for example, water glass as a binder, silicate ions are polymerized and cured by heating and dehydration.
  • Preferred inorganic adhesives are those using sodium silicate as a main component and alkali silicate as a binder.
  • any of an organic pore-forming agent and an inorganic pore-forming agent such as an inorganic hollow body may be used, or they may be used together.
  • a foamed pore-forming agent is preferred, and for example, spherical styrene foam is preferably used.
  • the foamable pore-forming agent used in the present invention either a solid foaming agent or a liquid foaming agent may be used, or both may be used in an appropriate ratio.
  • a liquid foaming agent is used.
  • Zodicarboxylate A more preferred dialkylazodicarboxylate is diisopropylpropylazodicarboxylate.
  • other dialkyl azodicarboxylates that can be used in the present invention include dimethyl azodicarboxylate, getyl azodicanoleboxylate, dipropyl azodicarboxylate, ditert-butyl azodicarboxylate. And mixtures thereof.
  • dialkylazodicarboxylates are thermally decomposed by heating to foam and form many foamed pores in the grindstone structure.
  • its pyrolysis temperature is around 250 ° C and at room temperature it is non-volatile and safe.
  • the bubbling starts at around 50 ° C.
  • a liquid foaming agent represented by the above-mentioned dialkylazodicarboxylate foams at room temperature in an acidic solution, an alkaline solution, or when a phenol resin, a sulfonic acid, a butyl chloride, and a metal salt of a fatty acid are added. Occur. Since the inorganic adhesive solution used in the present invention is an alkaline solution, foaming occurs even at room temperature, and the water content of the cast product evaporates due to the heat at that time, and the cast product is solidified.
  • the foaming of the liquid foaming agent and the solidification of the inorganic adhesive can be started at room temperature without performing heating or cooling treatment.
  • room temperature refers to an ambient temperature at which foaming of the liquid foaming agent and solidification of the inorganic adhesive can proceed without heating or cooling the grindstone raw material. Can be defined as 0-30 ° C.
  • an inorganic adhesive which is an alkaline solution
  • pore formation and grinding stone solidification due to foaming at room temperature occur.
  • Glass frit is an inorganic binder necessary for vitrifying a grindstone structure and sintering the grindstone.
  • a glass frit whose chemical component is mainly borosilicate glass is used. it can.
  • soda coal glass, various types of crystallized glass, and the like may be used, but are not limited thereto.
  • the ratio between the glass frit and the solid content of the inorganic adhesive can be changed as appropriate within the range of 3: 1 to 1: 7, but preferably 2.5: 1 to 1: 6.
  • the softening point of the glass frit is preferably such that the temperature at which the glass frit starts melting at a temperature lower than the predetermined firing temperature is preferably 100 ° C higher than the firing temperature so that the glass frit is sufficiently softened and melted during firing. It is preferable that C is lower.
  • firing temperature If the temperature difference between the temperature and the softening point is too large, problems such as cracks will occur during the manufacture of the grinding wheel. Therefore, the temperature difference is desirably 300 ° C or less.
  • the abrasive grains include fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina-zirconia-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, and CBN or Super-abrasive grains such as diamond-based abrasive grains can be suitably used.
  • One or more types of abrasive grains to be used are selected from those described above according to the grinding conditions.
  • the abrasive particle size can be from F4 (according to the particle size indicated in “Type of coarse particles” described in “JIS R6001 Grain size of abrasive for grinding wheel”) to an average particle size of 0.1 ⁇ m Can be used.
  • F4 (according to the particle size indication shown in “Type of coarse particles” described in “JIS R6001 Abrasive material for grinding wheel”) to average particle size of 0.2 ⁇ m it can.
  • # 1000 the particle size is described in ⁇ JIS R6001 Grain size of abrasive for grinding wheel ''
  • ⁇ Electric resistance test method '' the particle size distribution at the cumulative height of 50% point can be used at the average particle size of 0.5 / im.
  • the above-mentioned grinding wheel raw material is mixed and dispersed in an aqueous solution, and this is poured into a grinding wheel molding die.
  • the poured liquid mixture is cooled to room temperature (0 to 30 ° C). It includes a step of drying and solidifying at ⁇ 300 ° C and foaming, and a step of firing the dried and solidified product at a temperature not lower than the melting temperature of the glass frit, specifically, at 600 to 1000 ° C.
  • the casting method is aimed at increasing the dispersibility of each raw material to be mixed and forming a good and uniform grindstone structure.
  • the inorganic adhesive hardens at room temperature to 300 ° C after pouring, and at the same time, the foamable pore-forming agent foams. Artificial pores are formed. The merit of this is that it prevents defects in the production of cast wheels. In other words, at the time of curing, the moisture contained in the mixture evaporates and the molded product dries. At the time of this drying, cracks are generated on the molded product. According to the production method of the present invention, as the solidification proceeds, pores are formed in the liquid mixture by the foaming action of the pore-forming agent, so that the voids in the liquid mixture to escape to the outside are removed.
  • the pore-forming agent forms uniform pores in the liquid mixture and also functions to prevent cracking during production. This effect is particularly advantageous in a method using a liquid foaming agent having a higher dispersibility than a solid foaming agent.
  • the mixed molded product is fired at 600 to 1000 ° C.
  • the glass frit causes a chemical reaction with the inorganic adhesive to improve the strength. That is, according to the grinding wheel manufacturing method using a glass frit according to the present invention, after the inorganic adhesive is cured, the glass frit is further baked at 600 to 1000 ° C. to soften and melt the glass frit. As a result, the binding force between the compound and the compound is improved, and a chemical reaction occurs with the inorganic adhesive, whereby vitrification can be performed.
  • the vitrified grinding wheel manufactured by the conventional method using only the inorganic adhesive has a lower bending strength as compared with the present invention, so the abrasive holding power is insufficient, and the life of the grinding wheel is shortened. .
  • the steps of drying and solidification (curing) and baking are sequentially performed so that the properties of the inorganic adhesive, the glass frit, and the cell forming agent are sufficiently activated. This enables the production of desirable porous vitrified grinding wheels.
  • the production can be carried out with an abrasive grain ratio of 5 to 50% by volume and a porosity of 30 to 90% by volume.
  • a vitrified grindstone having a porosity of 60 to 90% by volume which is generally difficult to produce, can be easily produced.
  • the binder ratio that is, the volume ratio of inorganic adhesive + glass frit, is the value obtained by subtracting the abrasive grain ratio and porosity from 100%. It is.
  • the present invention can provide a porous vitrified whetstone having characteristics of low grinding resistance and good finished surface roughness.
  • the grindstone of the present invention can be favorably used in general grinding conditions, cylindrical grinding, flat grinding, internal grinding, die shaping and the like.
  • the grindstone of the present invention can be favorably used for polishing IJ 'polishing using an iron-based material as a work material, and furthermore, a non-ferrous-based material such as silicon wafer, carbide, alumina, sapphire, quartz, carbide material, and nitrided material. It can be used well for grinding and polishing hard and brittle materials such as material materials, various glasses, and ceramic materials.
  • Example 1 The bending strength of the grindstone to which the present invention was applied (Example 1) and the grindstone using only an inorganic adhesive as a binder (Comparative Example 1) were compared.
  • Tables 1 and 2 show the raw materials and mixing ratios of each test wheel.
  • the slurry mixture was poured into a 120 ⁇ 30 mm mold.
  • each test whetstone was subjected to a three-point bending strength at a span distance of 100 mm and a load drop speed of 1. Omm / min. Three test wheels were manufactured, and the average value of the three test wheels was used as comparison data.
  • Table 3 shows the results of the bending strength test.
  • Example 3 As shown in Table 3, the test grindstone of Example 1 had three times the bending strength of that of Comparative Example 1. This is the effect of adding the glass frit according to the present invention and firing at a high temperature of 900 ° C.
  • FIG. 1 is an electron micrograph of the test grindstone prepared in Example 1. Looking at the microstructure, it can be seen that pores having a uniform pore diameter are formed by the liquid foaming agent together with fine natural pores.
  • a grinding test was performed using a test grindstone (Example 2) to which the present invention was applied, and the finished surface roughness (Ra, Rz) was measured.
  • the slurry mixture was poured into a mold having an outer diameter of 205 mm and a hole diameter of 50 mm.
  • Table 4 shows grinding test conditions.
  • the surface roughness of the finished surface of the grindstone to be tested is measured as the ten-point average roughness Rz.
  • the ten-point average roughness Rz is extracted from the roughness curve by the reference length in the direction of the average line, measured in the vertical magnification direction from the average line of the extracted part, and the elevation of the highest peak to the fifth peak is measured. It is calculated as the sum of the average of the absolute values of ⁇ and the average of the absolute values of the elevations ⁇ from the lowest to the fifth valley bottom.
  • Rz was in the range of more than 0.50 xm and 10.0 zm or less, and the classification of the reference length of 0.8 mm and the evaluation length of 4 mm was followed.
  • the finished surface roughness (Ra, Rz) of the test whetstone of this example was as follows.
  • the test grindstone of this example had good surface roughness. This indicates that the grindstone manufactured according to the present invention can perform good grinding for the processing required according to the surface roughness of the work material.
  • a grinding test was performed using a silicon wafer as a work material, and the finished surface roughness, grinding power, whetstone consumption, and work material removal amount were evaluated.
  • Tables 5 and 6 show the raw materials and mixing ratios of the test grindstones of Examples 3 and 4.
  • Blowing agent disopropylazodicarbo 35 wt% solvent; water 2 1 t%
  • the slurry mixture was poured into a 90 mm long, 70 mm wide mold.
  • the composition of the grindstone after firing was the same as the grindstone of Example 3, with the abrasive grain volume ratio of 20.3%, the binder volume ratio of 18.9%, and the porosity of 60.8%.
  • the volume ratio of abrasive grains was 18.6%
  • the volume ratio of binder was 11.3%
  • the porosity was 70.1%.
  • each grinding wheel piece (1) was pasted at equal intervals on the ring-shaped peripheral part of the cup-shaped base (2), and finished to produce a cup-shaped grinding wheel of ⁇ 200 X t35 Xh40mm ( See photos in Figures 3 and 4).
  • Dressing condition Dresser: WA # 3 0 0 0 0
  • Grinding method Grinding method: Wet in-feed grinding
  • the method of obtaining each evaluation item is as follows.
  • the finish surface roughness Ra was determined by the same calculation procedure as in the above-described grinding test 1. Grinding power (kW):
  • the power consumption of the grinding wheel motor is W, and it can be obtained by the formula: 612XW / peripheral speed (60/100)
  • the said peripheral speed of a grindstone was used as peripheral speed.
  • Example 3 the wafer removal amount showed a removal amount close to the target removal amount of 40 zm.
  • the target removal amount 40 zm.
  • no abnormal wear or stagnation of wear amount was observed, indicating that wafer removal was performed normally and grinding work was performed smoothly.
  • Abnormal values were not found in the characteristics of finished surface roughness (Ra) and grinding power (Ft). From the above results, it was shown that the grindstone of the example can perform proper and good grinding even in a grinding operation for a silicon wafer.

Abstract

A porous vitrified wheel having a structure composed of abrasive grains, a binder and pores, characterized in that it comprises a binder comprising an inorganic adhesive and a glass frit, and natural pores and pores formed by a pore-forming agent; and a method for producing the porous vitrified wheel. The porous vitrified wheel is produced by the use of an inorganic adhesive and a blowing agent for forming pores and has a uniform wheel structure, exhibits good cutting quality and satisfactory durability and strength, even when it is a fine wheel such as the one having a porosity of 60 vol % or more and/or having a particle diameter of an abrasive grain of less than 100 μm.

Description

明 細 書  Specification
多孔質なビトリフアイド砥石及びその製造方法  Porous vitrified grinding wheel and method for producing the same
技術分野  Technical field
[0001] 本発明は、多孔質なビトリフアイド砥石及びその製造方法に関する。  The present invention relates to a porous vitrified grinding wheel and a method for producing the same.
背景技術  Background art
[0002] 研削及び研磨用砥石の主たる種類として結合剤別に列挙するとビトリフアイド砥石、 レジノイド砥石、メタル砥石及び電着砥石が挙げられる。その中でも、ビトリフアイド砥 石は、切れ味がよぐ耐久性が高くかつドレス性がよいため広く利用されている。  [0002] The main types of grinding and polishing whetstones include, by binder, vitrified whetstones, resinoid whetstones, metal whetstones, and electrodeposition whetstones. Among them, vitrified whetstones are widely used because of their sharpness, high durability and good dressability.
[0003] 一般的にビトリフアイド砥石は、砥材とビトリフアイド結合剤の原材料として粘土、長 石、ガラスフリット等の無機質粉体を 1種類以上選択し、一次結合剤とともに混合し、 該混合物を金型に充填し成型する。乾燥工程を経た後 600〜1300°Cの高温で焼 成して製造される。  [0003] In general, a vitrified grindstone selects one or more kinds of inorganic powders such as clay, feldspar, and glass frit as raw materials of an abrasive and a vitrified binder, mixes the powder with a primary binder, and molds the mixture into a mold. Fill and mold. After the drying process, it is manufactured by firing at a high temperature of 600-1300 ° C.
[0004] 一方、前記の焼成温度より低い温度で硬化する無機接着剤を使用して砥石を製造 する技術が開示されている(特許文献 1)。具体的には段落「0005」に焼結温度が 15 0〜300°C前後の低温で砥粒層を砥石台金に直接焼き付けて形成することができる 旨記載されている。  [0004] On the other hand, a technique for manufacturing a grindstone using an inorganic adhesive that cures at a temperature lower than the firing temperature described above is disclosed (Patent Document 1). Specifically, paragraph "0005" states that the abrasive layer can be formed by directly baking the abrasive grain layer on a grindstone base at a low sintering temperature of about 150 to 300 ° C.
[0005] また、炭化ホウ素 50〜30重量部とセラミック材 50〜: 10重量部に対し水ガラス水溶 液 1〜 10重量部%添加混合し、乾燥後 800〜 1200°Cで焼成する技術も開示されて いる (特許文献 2)。  [0005] Also disclosed is a technique in which 50 to 30 parts by weight of boron carbide and 50 to 10 parts by weight of a ceramic material are added and mixed with 1 to 10 parts by weight of an aqueous solution of water glass, and then dried and fired at 800 to 1200 ° C. (Patent Document 2).
特許文献 1:特開 2001— 71268号公報  Patent Document 1: JP 2001-71268 A
特許文献 2 :特開昭 52— 26094号公報  Patent Document 2: JP-A-52-26094
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0006] 特開 2001— 71268号公報に記載されているように無機接着剤を使用しての低温 で焼結した砥石は、曲げ強度が一般的な方法で製造されたビトリフアイド砥石と比較 して低いので砥粒保持力が不足し、砥石寿命に問題がある。また特開昭 52— 2609 4号公報に記載の製法では、添加される無機物質の量が少ないことから見て、それ は高温焼結で作用する主たるビトリフアイド結合剤ではないと考えられるので、十分な 強度等を期待できない。 [0006] As described in JP-A-2001-71268, a grindstone sintered at a low temperature using an inorganic adhesive is compared with a vitrified grindstone having a bending strength manufactured by a general method. Since it is low, the holding power of the abrasive grains is insufficient, and there is a problem in the life of the grinding wheel. In addition, in the production method described in Japanese Patent Application Laid-Open No. 52-26094, the amount of the added inorganic substance is small. Is not considered to be the main vitrisulfide binder that works in high-temperature sintering, so it cannot be expected to have sufficient strength.
[0007] 上記のような無機質砥石の製造は種々の面から検討されてレ、るが、要求される砥 石特性を引き出すために、無機質結合剤等の利用法や製造条件に関して検討すベ き事項が多々残されている。  [0007] The production of the above-mentioned inorganic grindstone has been studied from various aspects. However, in order to bring out the required grindstone characteristics, it is necessary to consider the use of inorganic binder and the like and the production conditions. Much remains to be done.
[0008] 特に多孔質なビトリフアイド砥石を製造する場合、切れ味の良さや耐久性の高さに カロえて、砥石組織の均一性や砥石の強度を考慮しなければならなレ、。従来のビトリフ アイド製造工程において有機質の気孔形成剤を使用すると、焼成中形状保持が維持 されない、また焼成収縮率が大きい等の問題があるため、気孔率の大きい砥石、特 に気孔率 60体積%以上の砥石の製造が制限されている。また、無機質中空体を使 用して多孔質な砥石を製造することも考えられるが、焼成後も砥石中に無機質中空 体の膜壁が残存するため、この作用により研削時の研削抵抗が増大するという問題 力 sある。 [0008] In particular, when manufacturing a porous vitrified grindstone, it is necessary to consider the uniformity of the grindstone structure and the strength of the grindstone in consideration of sharpness and high durability. If an organic pore-forming agent is used in the conventional vitrified eye manufacturing process, there is a problem in that shape retention is not maintained during firing, and firing shrinkage is large. Therefore, whetstones with high porosity, especially 60% by volume porosity The production of the above grindstones is limited. It is also conceivable to manufacture a porous grindstone using an inorganic hollow body, but since the film wall of the inorganic hollow body remains in the grindstone after firing, this action increases the grinding resistance during grinding. problems force s that.
[0009] 一方、従来のビトリフアイド砥石の製造においては砥石組織が均一化しにくいという 問題もある。特に砥粒粒径 100 μ m未満の細目の砥石においては気孔の分散が非 均一となりやすい。  [0009] On the other hand, in the production of conventional vitrified grinding wheels, there is also a problem that it is difficult to make the grinding wheel structure uniform. In particular, pores are likely to be non-uniform in a fine grinding stone having an abrasive grain diameter of less than 100 μm.
[0010] 上記の各問題点に鑑み、本発明は、無機接着剤と発泡性気孔形成剤を使用して 製造される多孔質なビトリフアイド砥石、特に気孔率 60体積%以上且つ/又は砥粒 粒径 100 μ m未満のような細目の砥石においても、均一な砥石組織を持ち、切れ味 が良く且つ十分な耐久性と強度のある砥石、並びにその製造方法を提供することを 課題とする。  [0010] In view of the above problems, the present invention relates to a porous vitrified whetstone produced by using an inorganic adhesive and a foamable pore-forming agent, particularly a porosity of 60% by volume or more and / or abrasive grains. An object of the present invention is to provide a grindstone having a uniform grindstone structure, good sharpness, sufficient durability and strength, and a method for producing the same, even with a fine grindstone having a diameter of less than 100 μm.
課題を解決するための手段  Means for solving the problem
[0011] 上記の課題を解決する本発明の多孔質で無機質なビトリフアイド砥石は、砥粒、結 合剤及び気孔からなる組織を有する砥石であって、無機接着剤とガラスフリットにより 形成された結合剤、及び自然気孔と気孔形成剤により形成された気孔を有すること を特徴とする。 [0011] The porous and inorganic vitrified whetstone of the present invention that solves the above problems is a whetstone having a structure composed of abrasive grains, a binder, and pores, and is a bond formed by an inorganic adhesive and a glass frit. And natural pores and pores formed by a pore-forming agent.
[0012] 本発明の多孔質なビトリフアイド砥石は、前記ガラスフリットの軟化点が 300〜900 °C、好ましくは 400〜900°Cであるとよレヽ。 [0013] また本発明の砥石は、溶融アルミナ系砥粒、ゾルゲルアルミナ質砥粒、炭化珪素系 砥粒、アルミナ ジルコ二ァ系砥粒、酸化セリウム系砥粒、シリカ系砥粒、 CBN系砥 粒、及びダイヤモンド系砥粒よりなる群から一種以上選択される砥粒を有するとよい。 [0012] In the porous vitrified whetstone of the present invention, the glass frit has a softening point of 300 to 900 ° C, preferably 400 to 900 ° C. [0013] Further, the grindstone of the present invention includes fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina zirconium-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, and CBN-based abrasive grains. It is preferable to have one or more abrasive grains selected from the group consisting of grains and diamond-based abrasive grains.
[0014] 本発明による多孔質なビトリフアイド砥石の製造方法は、砥材、無機接着剤、ガラ スフリット及び気孔形成剤を水に溶解して得られる液状混合物を型に流し込み、該型 内の混合物を常温〜 300°Cで乾燥固化させると同時に前記気孔形成剤を発泡させ 、乾燥固化した混合物をさらに 600〜: 1000°Cで焼成してビトリフアイド砥石を得ること を特徴とする。  [0014] In the method for producing a porous vitrified grinding wheel according to the present invention, a liquid mixture obtained by dissolving an abrasive, an inorganic adhesive, a glass frit, and a pore-forming agent in water is poured into a mold, and the mixture in the mold is washed. It is characterized by drying and solidifying at room temperature to 300 ° C. and foaming the pore-forming agent at the same time, and baking the dried and solidified mixture at 600 to 1000 ° C. to obtain a vitrified whetstone.
[0015] 本発明の製造方法では、前記気孔形成剤として、液状の発泡性気孔形成剤を使 用してもよいし、固形の発泡性気孔形成剤を使用してもよい。また、軟化点が 300〜 900°C、好ましくは 400〜900°Cであるガラスフリットを使用するとよレ、。また、使用さ れる砥粒は、溶融アルミナ系砥粒、ゾルゲルアルミナ質砥粒、炭化珪素系砥粒、アル ミナ ジルコ二ァ系砥粒、酸化セリウム系砥粒、シリカ系砥粒、 CBN系砥粒、及びダ ィャモンド系砥粒よりなる群から一種以上選択することができる。  [0015] In the production method of the present invention, as the pore-forming agent, a liquid foamable pore-forming agent may be used, or a solid foamable pore-forming agent may be used. Further, it is preferable to use a glass frit having a softening point of 300 to 900 ° C, preferably 400 to 900 ° C. The abrasive grains used are fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina zirconia-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, and CBN-based abrasive grains. One or more types can be selected from the group consisting of grains and diamond-based abrasive grains.
発明の効果  The invention's effect
[0016] 本発明は、無機接着剤とガラスフリットにより形成された結合剤、及び自然気孔と気 孔形成剤により形成されたほぼ均一な気孔を有する多孔質なビトリフアイド砥石を提 供でき、特に気孔率 60体積%以上且つ/又は砥粒粒径 100 μ m未満の細目の砥 石において、均一な砥石組織を持ち、切れ味が良ぐ且つ耐久性及び強度が高い砥 石、及びその製造方法を提供することができる。  The present invention can provide a porous vitrified grindstone having a binder formed of an inorganic adhesive and a glass frit and having substantially uniform pores formed of natural pores and a pore-forming agent. A fine grinding stone with a ratio of 60% by volume or more and / or a grain diameter of less than 100 μm, having a uniform grinding stone structure, excellent sharpness, high durability and strength, and a method for producing the same. can do.
図面の簡単な説明  Brief Description of Drawings
[0017] [図 1]実施例 1で作製したテスト砥石の砥石組織の電子顕微鏡写真である。  FIG. 1 is an electron micrograph of the grindstone structure of the test grindstone prepared in Example 1.
[図 2]実施例 3, 4のカップ型砥石の概略構成を示す断面図である。  FIG. 2 is a cross-sectional view illustrating a schematic configuration of cup-type grindstones of Examples 3 and 4.
[図 3]実施例 3, 4として作製したカップ型砥石を正面から撮影した写真である。  FIG. 3 is a photograph of a cup-shaped grindstone produced as Examples 3 and 4 taken from the front.
[図 4]図 3のカップ型砥石の砥石片周辺を側面から撮影した拡大写真である。  FIG. 4 is an enlarged photograph of the vicinity of a grinding wheel piece of the cup-type grinding wheel of FIG. 3 taken from the side.
符号の簡単な説明  Brief description of the sign
[0018] 1 砥石片 [0018] 1 Whetstone pieces
2 カップ型金属台金 3 砥石研磨面 2 cup-shaped metal base 3 Grinding stone polishing surface
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0019] 本発明の砥石は、砥材、無機接着剤、ガラスフリット及び気孔形成剤を含んでなる 混合物を流し込み成型することにより製造される、多孔質なビトリフアイド砥石である。  The grindstone of the present invention is a porous vitrified grindstone manufactured by casting a mixture containing an abrasive, an inorganic adhesive, a glass frit, and a pore-forming agent.
[0020] 本願明細書にいう「多孔質なビトリフアイド砥石」とは、有機系の一次結合剤を含ま ず、実質的な一次結合剤として無機接着剤を使用し、さらに無機接着剤と共にガラス フリットを使用して焼結され、発泡剤により形成された気孔と自然気孔を含んだ砥石 を意味する。本発明によれば、砥石原料混合物の乾燥固化時に良好な気孔形成が 行われ、その後、ガラスフリットを介したビトリフアイド化が進むので、均一な砥石組織 、特に微細且つ均一な気孔組織を持ち、且つ十分な強度を有する多孔質ビトリフアイ ド砥石を製造することができる。  [0020] The "porous vitrified grinding wheel" referred to in the specification of the present application does not include an organic primary binder, uses an inorganic adhesive as a substantial primary binder, and further uses a glass frit together with the inorganic adhesive. It means a grindstone that is sintered using and contains pores formed by a foaming agent and natural pores. According to the present invention, good pore formation is performed at the time of drying and solidifying the grindstone raw material mixture, and then vitrification proceeds through a glass frit, so that the grindstone has a uniform grindstone structure, particularly a fine and uniform pore structure, and A porous vitrified whetstone having sufficient strength can be manufactured.
[0021] 先ず、本発明の砥石の製造に使用される各材料について説明する。  First, each material used for manufacturing the grindstone of the present invention will be described.
[0022] 無機接着剤は、比較的低温で硬化し、主として成型から焼成まで砥石形状を維持 するのに役立つ無機物質である。このような無機接着剤は、シリカ ·アルミナ、アルミ ナ、シリカ、ジルコニァ'シリカ、ジルコニァ、珪酸ソーダ、リン酸アルミニウム、リン酸マ グネシゥム等のうち 1種又は 2種以上を主成分とし、水ガラス、シリカゾル、リン酸アル ミニゥム、リン酸マグネシウム等のバインダー、ケィ酸イオン等を硬化剤とするものから 適宜選択することができる。ケィ酸アルカリ系、例えば水ガラスをバインダーとするも のは、加熱脱水によりケィ酸イオンが重合して硬化する。好ましい無機接着剤は、珪 酸ソーダを主成分としてケィ酸アルカリ系をバインダーとして使用したものである。  [0022] The inorganic adhesive is an inorganic substance which cures at a relatively low temperature and mainly serves to maintain the shape of a grinding wheel from molding to firing. Such an inorganic adhesive is mainly composed of one or more of silica, alumina, alumina, silica, zirconia 'silica, zirconia, sodium silicate, aluminum phosphate, magnesium phosphate, and the like. , A binder such as silica sol, aluminum phosphate, magnesium phosphate and the like, and a binder using silicate ion and the like as a curing agent. In the case of using alkali silicate, for example, water glass as a binder, silicate ions are polymerized and cured by heating and dehydration. Preferred inorganic adhesives are those using sodium silicate as a main component and alkali silicate as a binder.
[0023] 気孔形成剤には、有機性気孔形成剤、及び無機中空体などの無機性気孔形成剤 のいずれを使用していもよいし、それらを一緒に使用してもよい。特に発泡性の気孔 形成剤が好ましぐ例えば、球状の発泡スチロール等が好適に使用される。また本発 明に使用される発泡性気孔形成剤は、固形発泡剤又は液状発泡剤のいずれを使用 してもょレ、し、両方を適度な割合で使用してもよい。好ましくは、液状発泡剤を使用す る。  As the pore-forming agent, any of an organic pore-forming agent and an inorganic pore-forming agent such as an inorganic hollow body may be used, or they may be used together. In particular, a foamed pore-forming agent is preferred, and for example, spherical styrene foam is preferably used. As the foamable pore-forming agent used in the present invention, either a solid foaming agent or a liquid foaming agent may be used, or both may be used in an appropriate ratio. Preferably, a liquid foaming agent is used.
[0024] 好ましい液状発泡剤は、一般式 ROOC— N = N— COOR (この式中、それぞれの Rは直鎖でも分岐でもよい 1〜4の低級アルキル基を示す)で表されるジアルキルァ ゾジカルボキシレートである。より好ましいジアルキルァゾジカルボキシレートは、ジィ ソプロピルァゾジカルボキシレートである。また、本発明に使用できる他のジアルキル ァゾジカルボキシレートには、ジメチルァゾジカルボキシレート、ジェチルァゾジカノレ ボキシレート、ジプロピルァゾジカルボキシレート、ジ tert—ブチルァゾジカルボキシレ ート、及びそれらの混合物が含まれる。これらジアルキルァゾジカルボキシレートは、 加熱により熱分解されて発泡し、砥石組織内に多くの発泡気孔を形成する。典型的 にはその熱分解温度が 250°C前後で、また常温で揮発性はなく安全である。その発 泡は 50°C付近から始まる力 好ましい気孔を得るには、 60〜200°Cまで加熱するの がよレ、。前記のジアルキルァゾジカルボキシレートに代表される液状発泡剤は、酸性 溶液下、アルカリ性溶液下、又はフヱノール樹脂、スルホン酸、塩化ビュル、及び脂 肪酸金属塩を添加した場合は常温で発泡が起こる。本発明に使用される無機接着 剤溶液はアルカリ性溶液なので常温でも発泡が起こり、また流し込み成型物の水分 はその時の熱で蒸発し成型物が固化する。 [0024] A preferred liquid foaming agent is a dialkyl group represented by the general formula ROOC-N = N-COOR (wherein each R represents a lower alkyl group of 1 to 4 which may be linear or branched). Zodicarboxylate. A more preferred dialkylazodicarboxylate is diisopropylpropylazodicarboxylate. Further, other dialkyl azodicarboxylates that can be used in the present invention include dimethyl azodicarboxylate, getyl azodicanoleboxylate, dipropyl azodicarboxylate, ditert-butyl azodicarboxylate. And mixtures thereof. These dialkylazodicarboxylates are thermally decomposed by heating to foam and form many foamed pores in the grindstone structure. Typically, its pyrolysis temperature is around 250 ° C and at room temperature it is non-volatile and safe. The bubbling starts at around 50 ° C. To obtain favorable pores, it is better to heat to 60-200 ° C. A liquid foaming agent represented by the above-mentioned dialkylazodicarboxylate foams at room temperature in an acidic solution, an alkaline solution, or when a phenol resin, a sulfonic acid, a butyl chloride, and a metal salt of a fatty acid are added. Occur. Since the inorganic adhesive solution used in the present invention is an alkaline solution, foaming occurs even at room temperature, and the water content of the cast product evaporates due to the heat at that time, and the cast product is solidified.
[0025] 上記のように本発明では、加熱や冷却処理を施すことなく常温下で液状発泡剤の 発泡および無機接着剤の固化を開始することができる。本願明細書に使用される常 温という用語は、砥石原材料の加熱や冷却処理を行わなくとも液状発泡剤の発泡お よび無機接着剤の固化が進行し得る周囲温度を意味し、具体的には 0〜30°Cと定 義し得る。 [0025] As described above, in the present invention, the foaming of the liquid foaming agent and the solidification of the inorganic adhesive can be started at room temperature without performing heating or cooling treatment. As used herein, the term room temperature refers to an ambient temperature at which foaming of the liquid foaming agent and solidification of the inorganic adhesive can proceed without heating or cooling the grindstone raw material. Can be defined as 0-30 ° C.
[0026] 上述の通り、本発明では、アルカリ性溶液である無機接着剤を使用することにより常 温での発泡による気孔形成と砥石固化が起こるので好ましい。  [0026] As described above, in the present invention, the use of an inorganic adhesive, which is an alkaline solution, is preferable since pore formation and grinding stone solidification due to foaming at room temperature occur.
[0027] ガラスフリットは、砥石組織をビトリフアイド化して砥石を焼結させるのに必要な無機 結合剤であり、典型的にはその化学成分が主としてホウケィ酸ガラスであるものを使 用すること力 Sできる。その他、ソーダ石炭ガラス、各種結晶化ガラスなどを使用しても よいが、これらに限定されない。  [0027] Glass frit is an inorganic binder necessary for vitrifying a grindstone structure and sintering the grindstone. Typically, a glass frit whose chemical component is mainly borosilicate glass is used. it can. In addition, soda coal glass, various types of crystallized glass, and the like may be used, but are not limited thereto.
[0028] ガラスフリットと無機接着剤固形分との割合は 3 : 1〜: 1 : 7の範囲で適宜変化させ得 るが、 2. 5 : 1〜: 1 : 6が好ましい。ガラスフリットの軟ィ匕点は、焼成時にガラスフリットが 十分に軟化溶融するように、所定の焼成温度もよりも低い温度で溶融を開始する温 度が好ましぐ例えば、焼成温度よりも 100°Cほど低いことが好ましい。但し、焼成温 度と軟化点との温度差が大きすぎると砥石製造中にクラック等の不具合が発生する ので、その温度差は 300°C以下であることが望ましレ、。 [0028] The ratio between the glass frit and the solid content of the inorganic adhesive can be changed as appropriate within the range of 3: 1 to 1: 7, but preferably 2.5: 1 to 1: 6. The softening point of the glass frit is preferably such that the temperature at which the glass frit starts melting at a temperature lower than the predetermined firing temperature is preferably 100 ° C higher than the firing temperature so that the glass frit is sufficiently softened and melted during firing. It is preferable that C is lower. However, firing temperature If the temperature difference between the temperature and the softening point is too large, problems such as cracks will occur during the manufacture of the grinding wheel. Therefore, the temperature difference is desirably 300 ° C or less.
[0029] 砥粒には、溶融アルミナ系砥粒、ゾルゲルアルミナ質砥粒、炭化珪素系砥粒、アル ミナ—ジルコ二ァ系砥粒、酸化セリウム系砥粒、シリカ系砥粒、及び CBN又はダイヤ モンド系砥粒などの超砥粒などを好適に使用することができる。使用すべき砥粒は、 研削条件に応じて前記のものから 1種類以上が選択される。  [0029] The abrasive grains include fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina-zirconia-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, and CBN or Super-abrasive grains such as diamond-based abrasive grains can be suitably used. One or more types of abrasive grains to be used are selected from those described above according to the grinding conditions.
[0030] 砥粒粒度は、 F4 (「JIS R6001 研削砥石用研磨材の粒度」に記載されている「粗 粒の種類」に示された粒度表示に従う)〜平均粒子径 0. 1 μ mまで使用することがで きる。好適には、 F4 (「JIS R6001 研削砥石用研磨材の粒度」に記載されている「 粗粒の種類」に示された粒度表示に従う)〜平均粒子径 0. 2 μ mで使用することが できる。特に好適には、 # 1000 (「JIS R6001 研削砥石用研磨材の粒度」に記載 されてレ、る粒度表示であって、「精密研磨用微粉の種類」中の「電気抵抗試験方法」 により示された粒度表示に従レ、、累積高さ 50%点の粒度分布 11. 5 ± 1. 0 /i m)〜 平均粒子径 0. 5 /i mで使用すること力 Sできる。  [0030] The abrasive particle size can be from F4 (according to the particle size indicated in "Type of coarse particles" described in "JIS R6001 Grain size of abrasive for grinding wheel") to an average particle size of 0.1 µm Can be used. Preferably, F4 (according to the particle size indication shown in “Type of coarse particles” described in “JIS R6001 Abrasive material for grinding wheel”) to average particle size of 0.2 μm it can. It is particularly preferable to use # 1000 (the particle size is described in `` JIS R6001 Grain size of abrasive for grinding wheel '') and is indicated by `` Electric resistance test method '' in `` Types of fine powder for precision polishing '' According to the given particle size display, the particle size distribution at the cumulative height of 50% point can be used at the average particle size of 0.5 / im.
[0031] 次に、本発明の砥石の製造方法を説明する。  Next, a method for manufacturing a grindstone of the present invention will be described.
[0032] 本発明の砥石の製造工程は、上述の砥石原材料を水溶液中に混合分散し、これ を砥石成型用の型内に流し込む工程、流し込まれた液状混合物を常温 (0〜30°C) 〜300°Cで乾燥固化させると共に発泡させる工程、及びその乾燥固化物をガラスフリ ットの溶融温度以上、具体的には 600〜: 1000°Cで焼成する工程を含む。本法にお いて、流し込み成型を行うのは、混合される各原材料の分散性を高め、よい均一な砥 石組織を形成する狙レ、がある。  [0032] In the manufacturing process of the grinding wheel of the present invention, the above-mentioned grinding wheel raw material is mixed and dispersed in an aqueous solution, and this is poured into a grinding wheel molding die. The poured liquid mixture is cooled to room temperature (0 to 30 ° C). It includes a step of drying and solidifying at ~ 300 ° C and foaming, and a step of firing the dried and solidified product at a temperature not lower than the melting temperature of the glass frit, specifically, at 600 to 1000 ° C. In this method, the casting method is aimed at increasing the dispersibility of each raw material to be mixed and forming a good and uniform grindstone structure.
[0033] 上記の原材料を使用する本発明の製造方法では、乾燥固化工程において、流し 込み後に常温〜 300°Cで無機接着剤が硬化するが、これと同時に発泡性気孔形成 剤が発泡して人工気孔が形成される。このメリットとして、流し込み成型される砥石の 製造上の不具合を防止する働きがある。すなわち、硬化時、混合物に含まれる水分 が蒸発して成型物が乾燥していくが、この乾燥時に成型物上にヒビ割れが発生する こと力 Sある。本発明の製法によると、固化が進む際に液状混合物に気孔形成剤の発 泡作用により気孔が形成されるので、液状混合物内の水分を外部に逃がすための空 洞を形成することになる。こうして気孔形成剤は、液状混合物内で均一な気孔を形成 するとともに製造時にはヒビ割れの発生を防止する働きもする。この効果は、固形発 泡剤より分散性が大きい液状発泡剤を使用する方法において特に有利である。 [0033] In the production method of the present invention using the above-mentioned raw materials, in the drying and solidification step, the inorganic adhesive hardens at room temperature to 300 ° C after pouring, and at the same time, the foamable pore-forming agent foams. Artificial pores are formed. The merit of this is that it prevents defects in the production of cast wheels. In other words, at the time of curing, the moisture contained in the mixture evaporates and the molded product dries. At the time of this drying, cracks are generated on the molded product. According to the production method of the present invention, as the solidification proceeds, pores are formed in the liquid mixture by the foaming action of the pore-forming agent, so that the voids in the liquid mixture to escape to the outside are removed. A sinus will be formed. In this way, the pore-forming agent forms uniform pores in the liquid mixture and also functions to prevent cracking during production. This effect is particularly advantageous in a method using a liquid foaming agent having a higher dispersibility than a solid foaming agent.
[0034] 本発明に従って流し込み成型より製造される砥石の内部には、液状の原料を調製 する時に混入した気泡および水が抜けた跡と思われる部分に由来する自然気孔と添 カロした発泡剤に由来する人工気孔とが形成され、発泡剤による気孔は自然気孔と比 ベて大きな気孔となる。これら双方の気孔が砥石内部に均一に分散することができる ので、製造される砥石は、高い気孔率を持つ均一な砥石組織を有することができる。  [0034] Inside the grindstone manufactured by casting according to the present invention, natural pores originating from a portion thought to be traces of water and bubbles mixed in when preparing a liquid raw material, and a blowing agent added with The resulting artificial pores are formed, and the pores formed by the foaming agent are larger than the natural pores. Since both of these pores can be uniformly dispersed inside the grindstone, the produced grindstone can have a uniform grindstone structure with high porosity.
[0035] また、上記のように先に低温で乾燥固化処理することにより、その後の高温焼成時 に生じおそれのある砥石焼成物のクラック又は変形を防止する効果もある。また原料 に有機系の一次結合剤が含まれていないので、焼成中の異臭及び一次結合剤が原 因とあるクラック等が防止され、さらに砥石中の水分が完全に乾燥されるので残留水 分による焼成中の不具合も防止される。  [0035] In addition, by performing the drying and solidifying treatment at a low temperature first as described above, there is also an effect of preventing cracks or deformation of a burnt stone product which may occur during subsequent high-temperature firing. In addition, since the raw material does not contain an organic primary binder, an unpleasant odor during firing and cracks due to the primary binder are prevented, and since the water in the grinding wheel is completely dried, the residual water content is reduced. The trouble during firing due to the above is also prevented.
[0036] 上記の固化工程に続いて、混合成型物は 600〜: 1000°Cで焼成される。ここで、ガ ラスフリットが無機接着剤と化学反応を起こし強度が向上する。すなわち、本発明に 従ってガラスフリットを使用する砥石製造によれば、無機接着剤の硬化後、さらに 60 0〜: 1000°Cで焼成されてガラスフリットが軟化溶融するので、ガラスフリットは、砥粒と の結合力が向上すると共に無機接着剤とも化学反応を起こしてビトリフアイドィヒするこ とができる。これに対して、無機接着剤のみを使用する従来の方法で製造されたビト リファイド砥石は、本発明と比較して曲げ強度が低いので、砥粒保持力が不足し、砥 石寿命が短くなる。  [0036] Following the solidification step, the mixed molded product is fired at 600 to 1000 ° C. Here, the glass frit causes a chemical reaction with the inorganic adhesive to improve the strength. That is, according to the grinding wheel manufacturing method using a glass frit according to the present invention, after the inorganic adhesive is cured, the glass frit is further baked at 600 to 1000 ° C. to soften and melt the glass frit. As a result, the binding force between the compound and the compound is improved, and a chemical reaction occurs with the inorganic adhesive, whereby vitrification can be performed. On the other hand, the vitrified grinding wheel manufactured by the conventional method using only the inorganic adhesive has a lower bending strength as compared with the present invention, so the abrasive holding power is insufficient, and the life of the grinding wheel is shortened. .
[0037] 上記のように本法は、無機接着剤、ガラスフリット及び気泡形成剤の各特性が十分 に活力^れるように乾燥固化 (硬化)と焼成の各工程を順次分けて行うことにより、望 ましい多孔質なビトリフアイド砥石の製造を可能にしたものである。  [0037] As described above, in the present method, the steps of drying and solidification (curing) and baking are sequentially performed so that the properties of the inorganic adhesive, the glass frit, and the cell forming agent are sufficiently activated. This enables the production of desirable porous vitrified grinding wheels.
[0038] 砥石組成としては、砥粒率は 5〜50体積%、気孔率は 30〜90体積%の範囲で製 造を行うことできる。特に本発明によれば、一般には製造が難しいとされる気孔率 60 〜90体積%のビトリフアイド砥石を容易に製造することができる。なお結合剤率、つま り無機接着剤 +ガラスフリットの体積率は 100%から砥粒率及び気孔率を引いた値 である。 [0038] With regard to the composition of the grindstone, the production can be carried out with an abrasive grain ratio of 5 to 50% by volume and a porosity of 30 to 90% by volume. In particular, according to the present invention, a vitrified grindstone having a porosity of 60 to 90% by volume, which is generally difficult to produce, can be easily produced. The binder ratio, that is, the volume ratio of inorganic adhesive + glass frit, is the value obtained by subtracting the abrasive grain ratio and porosity from 100%. It is.
[0039] 本発明は、低い研削抵抗と良好な仕上げ面粗度の特性を有する多孔質ビトリフアイ ド砥石を提供することができる。本発明の砥石は、一般的な研削条件、円筒研削、平 面研削、内面研削、総型研削等において良好に使用できる。特に本発明の砥石は、 鉄系材料を被削材とする研肖 IJ '研磨に良好に使用でき、さらに非鉄系材料であるシリ コンウェハー、超硬、アルミナ、サフアイャ、石英、炭化物材料、窒化物材料、各種ガ ラス、セラミック材料などの硬脆性材料の研削 ·研磨にも良好に使用できる。  [0039] The present invention can provide a porous vitrified whetstone having characteristics of low grinding resistance and good finished surface roughness. The grindstone of the present invention can be favorably used in general grinding conditions, cylindrical grinding, flat grinding, internal grinding, die shaping and the like. In particular, the grindstone of the present invention can be favorably used for polishing IJ 'polishing using an iron-based material as a work material, and furthermore, a non-ferrous-based material such as silicon wafer, carbide, alumina, sapphire, quartz, carbide material, and nitrided material. It can be used well for grinding and polishing hard and brittle materials such as material materials, various glasses, and ceramic materials.
[0040] 以下、本発明の実施例を比較例とともに説明するが、これらは本発明の実施可能 性及び有用性を例証するものであり、本発明の構成を何ら限定する意図はない。 実施例  Hereinafter, examples of the present invention will be described together with comparative examples, but these exemplify the feasibility and usefulness of the present invention, and do not intend to limit the configuration of the present invention in any way. Example
[0041] [曲げ強度テスト] [0041] [Bending strength test]
本発明を適用した砥石(実施例 1)と、無機接着剤のみを結合剤として使用した砥 石(比較例 1)についての曲げ強度を比較した。  The bending strength of the grindstone to which the present invention was applied (Example 1) and the grindstone using only an inorganic adhesive as a binder (Comparative Example 1) were compared.
[0042] 表 1及び表 2に各テスト砥石の原材料と混合比を示す。 [0042] Tables 1 and 2 show the raw materials and mixing ratios of each test wheel.
[0043] [表 1] 実施例 1の原料混合比 [Table 1] Raw material mixing ratio of Example 1
砥粒; WA # 1 5 ϋ 0 3 7 . 3 w t % 無機接着剤; F J — 5 2 1 3 0 . 1 t %  Abrasive grains; WA # 15 ϋ 0 37.3 wt% Inorganic adhesive; F J — 5 2 130.1 t%
(常盤電機株式会社製)  (Manufactured by Tokiwa Electric Co., Ltd.)
ガラスフリ ッ ト (軟化点 6 5 0 °C) 2 . 9 t %  Glass frit (softening point 650 ° C) 2.9 t%
(化学組成: S i 0 2 3 7 w t % (Chemical composition: S i 0 2 3 7 wt %
A " O 8 w t %  A "O 8 w t%
C a O 3 w t %  C a O 3 w t%
N a 20 1 4 w t % N a 2 0 1 4 wt%
B , 0 ;t 3 8 w t %) B, 0 ; t 38 wt%)
発泡剤; ジィソプロ ト 2 . 3 w t %  Blowing agent: Gisoprot 2.3 wt%
溶媒;水 2 7 . 4 w t %  Solvent; water 27.4 wt%
[0044] [表 2] 比齩例 1の原料混合比 [Table 2] Material ratio of Example 1
砥粒; W A # 1 5◦ 0  Abrasive; W A # 15 5 0
無機接着剤; F J— 5 2 1  Inorganic adhesive; F J— 5 2 1
(常盤電機株式会社製)  (Manufactured by Tokiwa Electric Co., Ltd.)
発泡剤; ジイソプロピルァゾジカルポキシレ  Blowing agent; diisopropylazodicarboxyle
溶媒;水  Solvent; water
[0045] (実施例 1) (Example 1)
実施例 1のテスト砥石の作製丰 I隱:  Preparation of Test Wheel of Example 1
1. 上記に記載した原料を均一に混合した。  1. The raw materials described above were uniformly mixed.
2. スラリー状の混合物を 120 X 30mmの金型に流し込んだ。  2. The slurry mixture was poured into a 120 × 30 mm mold.
3. 60°Cで 72時間加熱した。  3. Heated at 60 ° C for 72 hours.
4. 加熱して得られた固形物を型から取り出した。  4. The solid obtained by heating was removed from the mold.
7. 900°Cで 7時間で焼成した。  7. Baking at 900 ° C for 7 hours.
8. 焼成後、厚み方向を削って 120 X 30 X 40mmの直方体の角型砥石を作製した (比較例 1)  8. After firing, the thickness direction was shaved to produce a 120 x 30 x 40 mm rectangular parallelepiped grinding wheel (Comparative Example 1)
比較例 1のテスト砥石の作製手順:  Preparation procedure of the test wheel of Comparative Example 1:
1. 上記に記載した原料を均一に混合した。  1. The raw materials described above were uniformly mixed.
2. スラリー状の混合物を 120 X 30mmの金型に流し込む。  2. Pour the slurry mixture into a 120 x 30 mm mold.
3. 60°Cで 72時間加熱した。  3. Heated at 60 ° C for 72 hours.
4. 加熱後、厚み方向を削って 120 X 30 X 40mmの直方体の角型砥石を作製した  4. After heating, the thickness direction was shaved to produce a 120 x 30 x 40 mm rectangular parallelepiped square whetstone
言平翻,: Transliteration,
JIS規格 (ファインセラミックスの曲げ強さ試験方法 R1601、 2004)に従い、各テスト 砥石をスパン間距離 100mm、荷重降下速度 1. Omm/minにて 3点曲げ強度を行 つた。テスト砥石は各 3個製造し、 3個の平均値を比較データとした。  In accordance with the JIS standard (Bending strength test method for fine ceramics R1601, 2004), each test whetstone was subjected to a three-point bending strength at a span distance of 100 mm and a load drop speed of 1. Omm / min. Three test wheels were manufactured, and the average value of the three test wheels was used as comparison data.
[0046] 表 3に曲げ強度試験の結果を示す。  Table 3 shows the results of the bending strength test.
[0047] [表 3] 強度値 (M P a ) [Table 3] Strength value (MPa)
実施例 1 3 0  Example 1 3 0
比較例 1 1 0  Comparative Example 1 1 0
[0048] 表 3に示されるように、実施例 1のテスト砥石は比較例 1のものと比べて 3倍の曲げ 強度があった。これは、本発明に従ってガラスフリットを添カ卩し 900°Cの高温で焼成し た効果である。 [0048] As shown in Table 3, the test grindstone of Example 1 had three times the bending strength of that of Comparative Example 1. This is the effect of adding the glass frit according to the present invention and firing at a high temperature of 900 ° C.
[0049] 図 1は、実施例 1で作製したテスト砥石の電子顕微鏡写真である。その組織状態を 見ると微細な自然気孔と共に液状発泡剤により、気孔径の均一な気孔が形成されて レ、ることが分かる。  FIG. 1 is an electron micrograph of the test grindstone prepared in Example 1. Looking at the microstructure, it can be seen that pores having a uniform pore diameter are formed by the liquid foaming agent together with fine natural pores.
[0050] [研削テスト 1] [0050] [Grinding test 1]
本発明を適用したテスト砥石(実施例 2)を使用して研削テストを行レ、、仕上げ面粗 さ(Ra、Rz)を測定した。  A grinding test was performed using a test grindstone (Example 2) to which the present invention was applied, and the finished surface roughness (Ra, Rz) was measured.
(実施例 2)  (Example 2)
実施例 2のテスト石氏石の作製丰順:  Preparation of Test Stone Stone of Example 2
1. 実施例 1に記載したのと同じ原料を均一に混合した。  1. The same ingredients as described in Example 1 were uniformly mixed.
2. スラリー状の混合物を外周 205mm、穴径 50mmの金型に流し込んだ。  2. The slurry mixture was poured into a mold having an outer diameter of 205 mm and a hole diameter of 50 mm.
3. 60°Cで 72時間加熱した。  3. Heated at 60 ° C for 72 hours.
4. 加熱して得られた固形物を型から取り出した。  4. The solid obtained by heating was removed from the mold.
7. 900°Cで 7時間で焼成した。  7. Baking at 900 ° C for 7 hours.
8. 焼成後、仕上げ加工を行い、 205 10 1150111111の1八砥石を作製した。  8. After sintering, finishing was performed to produce 1810 whetstone 205 10 1150111111.
[0051] 表 4に研削テスト条件を示す。 Table 4 shows grinding test conditions.
[0052] [表 4] 研削テスト条件 [Table 4] Grinding test conditions
砥石寸法 2 5 O X t l O X h 5 O. 8 1 Λ砥石  Whetstone dimensions 25 O X t l O X h 5 O. 8 1 Λ Whetstone
被削材 材質 S 5 5 C (焼き入れ材 5 8 H R C )  Work material Material S 5 5 C (Hardened material 58 HRC)
寸法 1 0 0mm (長さ) X 5 mm (Ψ畐)  Dimension 100 mm (length) X 5 mm (Ψ 畐)
研削液 名称 クレカツ 卜 N S 2 0 1  Grinding fluid Name Crecut N S 2 0 1
濃度 2%  Concentration 2%
流量 1 5リツ トル Z分  Flow 15 liters Z min
研削盤 種類 岡木工作製作所製 横軸平面研削盤  Grinding machine type Horizontal surface grinding machine manufactured by Okaki Machine Works
型式 CNC- 5 2 B ( 7. 5 k w)  Model CNC-5 2 B (7.5 kw)
ドレッシング条件 ドレッサ:ニプドレッサ  Dressing conditions Dresser: Nip dresser
砥石周速度: 3 3 mZ s  Wheel speed: 33 mZ s
ドレスリード : 0. 0 5 mm/ r e v  Dress lead: 0.0 5 mm / r e v
ドレス切り込み: 0. 0 0 1 mmノ a s s  Dress notch: 0.0 0 1 mm no a s s
研削方法 平面トラバース研削  Grinding method Surface traverse grinding
砥石周速度: 3 3 mZ s  Wheel peripheral speed: 3 3 mZ s
テープル速度: 1 6 7 m/ s  Table speed: 1 6 7 m / s
クロスフィード: 2 mm/ a s s (往復)  Cross feed: 2 mm / a s s (round trip)
研削切込み: 0. 0 0 l mm/p a s s  Grinding depth: 0.00 l mm / p a s s
取り代: 0. 2mm  Allowance: 0.2mm
スパークアウト : l p a s s 什 hげ面 ffl.さ(Ra Rz)算出手順:  Spark-out: l p a s s 什 h f fl. Sa (Ra Rz) Calculation procedure:
[Ra]  [Ra]
中心線平均粗さ(Ra)は、粗さの曲線からその中心線の方向に測定長さ 1の部分を 抜取り、この抜取り部分の中心線を X軸、縦倍率の方向を Y軸、粗さ曲線 y=f )で 表したとき、次の式によって求められる価をマイクロメートル(μΐη)で表したものをいう  The center line average roughness (Ra) is obtained by extracting a portion of measurement length 1 from the roughness curve in the direction of the center line, the X-axis is the center line of this extracted portion, the Y-axis is the vertical magnification direction, and the roughness is Curve y = f) means the value calculated by the following formula in micrometer (μΐη)
[0054] [数 1] [0054] [Number 1]
Figure imgf000013_0001
Figure imgf000013_0001
[0055] [Rz] テストする砥石の仕上げ面における面粗度は、十点平均粗さ Rzとして測定される。 十点平均粗さ Rzは、粗さ曲線からその平均線の方向に基準長さだけ抜き取り、この 抜き取り部分の平均線から縦倍率方向に測定し、最も高い山頂から 5番目までの山 頂の標高 Υρの絶対値の平均値と、最も低い谷底から 5番目までの谷底の標高 Υνの 絶対値の平均値との和として求められる。本実施例では、 Rzが 0.50 xmを越え 10. O zm以下で、基準長さ 0.8mm及び評価長さ 4mmの区分に従った。 [0055] [Rz] The surface roughness of the finished surface of the grindstone to be tested is measured as the ten-point average roughness Rz. The ten-point average roughness Rz is extracted from the roughness curve by the reference length in the direction of the average line, measured in the vertical magnification direction from the average line of the extracted part, and the elevation of the highest peak to the fifth peak is measured. It is calculated as the sum of the average of the absolute values of Υρ and the average of the absolute values of the elevations Υν from the lowest to the fifth valley bottom. In the present example, Rz was in the range of more than 0.50 xm and 10.0 zm or less, and the classification of the reference length of 0.8 mm and the evaluation length of 4 mm was followed.
¾ff削テス 結 :  ¾ff shaving test
本実施例のテスト砥石の仕上げ面粗さ(Ra、 Rz)は下記の通りであった。  The finished surface roughness (Ra, Rz) of the test whetstone of this example was as follows.
[0056] Ra 0.014 xm  [0056] Ra 0.014 xm
Rz 0.102 zm  Rz 0.102 zm
研削テスト結果で示されるように本実施例のテスト砥石は良好な面粗度となった。こ のことは、本発明に従って製造された砥石は、被削材の表面粗度に応じて要求され る加工に対し、良好な研削が可能であることを示す。  As shown by the grinding test results, the test grindstone of this example had good surface roughness. This indicates that the grindstone manufactured according to the present invention can perform good grinding for the processing required according to the surface roughness of the work material.
[0057] [研削テスト 2]  [0057] [Grinding test 2]
本発明を適用したテスト砥石を使用して、シリコンウェハーを被削材とする研削テス トを行い、仕上げ面粗さ、研削動力、砥石消耗、被削材除去量について評価した。  Using a test grindstone to which the present invention was applied, a grinding test was performed using a silicon wafer as a work material, and the finished surface roughness, grinding power, whetstone consumption, and work material removal amount were evaluated.
[0058] 表 5および表 6に実施例 3および 4の各テスト砥石の原材料と混合比を示す。  [0058] Tables 5 and 6 show the raw materials and mixing ratios of the test grindstones of Examples 3 and 4.
[0059] 実施例 3の原料混合比 [0059] Raw Material Mixing Ratio of Example 3
砥粒; D I A# 3000 (3〜6 m) 1 2 w t %  Abrasive; DIA # 3000 (3-6 m) 1 2 w t%
無機接着剤; F J— 52 1 78 w t %  Inorganic adhesive; F J— 52 1 78 w t%
(常盤電機株式会社製)  (Manufactured by Tokiwa Electric Co., Ltd.)
ガラスフリッ ト (軟化点 650°C) 69 w t %  Glass frit (softening point 650 ° C) 69 w t%
(化学組成: S i Ο 2 37 w t % (Chemical composition: S i Ο 2 37 wt%
A O 8 w t %  A O 8 w t%
C a O 3 w t %  C a O 3 w t%
N a ,0 1 4 w t %  N a, 0 1 4 w t%
B ,0;i 38 w t % B, 0 ; i 38 wt%
発泡剤; ジィソプロピルァゾジカルボキシレ 41 w t %  Blowing agent; diisopropylpropylazodicarboxyle 41 wt%
溶媒;水 50 w t % [0060] [表 6] 実施例 4の原料混合比 Solvent; water 50 wt% [Table 6] Raw material mixing ratio of Example 4
砥粒; D I A# 3 (J 00 (3〜6 im) 3 9. 9 1 w t % 無機接着剤; F J 5 2 1 1 7. 99 w t %  Abrasive grains; DIA # 3 (J00 (3 to 6 im) 39.91 wt% Inorganic adhesive; FJ5 2 1 1 7.99 wt%
(常盤電機株式会社製)  (Manufactured by Tokiwa Electric Co., Ltd.)
ガラスフリット (軟化点 6 50。C) 9. 05 w t % (化学組成: S i O 2 3 7 w t %  Glass frit (softening point 650.C) 9.05 wt% (Chemical composition: SiO 2 37 wt%)
A 1 ,Ο 8 w t %  A 1, Ο 8 w t%
C a O 3 w t %  C a O 3 w t%
N a 0 1 4 w t %  N a 0 1 4 w t%
B 20:J 3 8 w t % B 2 0 : J 3 8 wt%
発泡剤; ジィソプロピルァゾジカルボ 35 w t % 溶媒;水
Figure imgf000015_0001
2 1 t %
Blowing agent; disopropylazodicarbo 35 wt% solvent; water
Figure imgf000015_0001
2 1 t%
[0061] (実施例 3および 4) (Examples 3 and 4)
実施例 3および 4のテスト砥石の作製手順:  Preparation procedure of test wheels of Examples 3 and 4:
1. 上記に記載した原料を均一に混合し、スラリー状にした。  1. The raw materials described above were uniformly mixed to form a slurry.
2. スラリー状の混合物を縦 90mm、横 70mmの金型に流し込んだ。  2. The slurry mixture was poured into a 90 mm long, 70 mm wide mold.
3. 60°Cで 24時間加熱した。  3. Heated at 60 ° C for 24 hours.
4. 前記までで作製した固形物を型から取り出した。  4. The solid prepared above was removed from the mold.
5. 空気雰囲気中、 850°Cで 7時間で焼成した。  5. Firing at 850 ° C for 7 hours in air atmosphere.
6. 焼成後の砥石組成は、実施例 3の砥石で、砥粒体積率 20.3%、結合剤体積率 18.9%、気孔率 60.8%となった。実施例 4の砥石で、砥粒体積率 18.6%、結合 剤体積率 11.3%、気孔率 70.1%となった。  6. The composition of the grindstone after firing was the same as the grindstone of Example 3, with the abrasive grain volume ratio of 20.3%, the binder volume ratio of 18.9%, and the porosity of 60.8%. With the grindstone of Example 4, the volume ratio of abrasive grains was 18.6%, the volume ratio of binder was 11.3%, and the porosity was 70.1%.
7. 図 2に示す形状のカップ型砥石を作製するために、前記した作製手順に従い、 長さ 20mm、幅 3mm、高さ 5mmのセグメント砥石片を各 28個作製した。各砥石片( 1)を、硬化後、カップ型台金(2)のリング状周縁部の上に等間隔に貼り付け、仕上げ 加工を行って φ 200 X t35 Xh40mmのカップ型砥石を作製した(図 3, 4の写真を 参照)。  7. In order to produce a cup-shaped grindstone having the shape shown in FIG. 2, 28 segment grindstone pieces each having a length of 20 mm, a width of 3 mm, and a height of 5 mm were produced in accordance with the above-mentioned production procedure. After hardening, each grinding wheel piece (1) was pasted at equal intervals on the ring-shaped peripheral part of the cup-shaped base (2), and finished to produce a cup-shaped grinding wheel of φ200 X t35 Xh40mm ( See photos in Figures 3 and 4).
[0062] [表 7] 研削テスト条件: [Table 7] Grinding test conditions:
砥石寸法 φ 2 0 0 X t 3 5 X h 4 Omm カツプ型砥石  Whetstone dimensions φ 2 0 0 X t 3 5 X h 4 Omm Cup type whetstone
被削材 材質: シリコンウェハー  Work material Material: Silicon wafer
寸法 : 2 0 O mm (直径) X O. 9mm (厚み)  Dimensions: 20 O mm (diameter) X O. 9 mm (thickness)
研削液 名称:蒸留水  Grinding fluid Name: distilled water
: 1 2 リ ツ トル Zm i n.  : 1 2 liter Zm i n.
研削盤 :東芝機械社製 縦軸平面研削盤  Grinding machine: Vertical surface grinding machine manufactured by Toshiba Machine Co., Ltd.
型式: UVG- 3 8 0 B  Model: UVG-380B
ドレッシング条件: ドレッサ : WA# 3 0 0 0  Dressing condition: Dresser: WA # 3 0 0 0
砥石周速度: 1 9 1 O m i n - 1  Wheel peripheral speed: 1 9 1 O min-1
テーブル回転数 5 0 m 1 n - 1  Table rotation speed 50 m 1 n-1
ドレス切り込み 2 0 μ / m i n X l O p a s s スパークァゥ ト 3 0 s e c .  Dress cut 20 μ / min X l Op a s s Spark ゥ at 30 s e c.
研削方法: 研削方式:湿式インフィ一ド研削  Grinding method: Grinding method: Wet in-feed grinding
砥石周速度: 1 9 1 Om i n- 1  Wheel peripheral speed: 1 9 1 Om i n-1
テープル回転周速度: 5 Om i n- 砥石切込み: 2 0 i m/m i n  Table rotation speed: 5 Om i n- Grinding wheel depth: 20 i m / m i n
取り代: 4 0 m  Allowance: 40 m
スパークァゥト : 1 0 s e c .  Sparkart: 10 sec.
研削枚数: 1 0枚  Number of grinding: 10
[0063] 各評価項目の求め方は、以下の通りである。 The method of obtaining each evaluation item is as follows.
什 hげ面 fflさ Ra ( u m)算出手順:  Calculate the height of the ffl Ra (u m):
仕上げ面粗さ Raは、上記の研削テスト 1と同様の算出手順により求めた。 研削動力(kW):  The finish surface roughness Ra was determined by the same calculation procedure as in the above-described grinding test 1. Grinding power (kW):
砥石軸モーターの消費電力を Wとし、式: 612XW /周速(60/100)により求め られる。なお、周速として前記砥石周速度を使用した。  The power consumption of the grinding wheel motor is W, and it can be obtained by the formula: 612XW / peripheral speed (60/100) In addition, the said peripheral speed of a grindstone was used as peripheral speed.
砥石消耗(um):  Whetstone wear (um):
研削盤の研削寸法自動測定機能を使用して求めた。  It was determined using the automatic measurement function of the grinding dimensions of the grinder.
被削材除去量(um) :  Workpiece removal (um):
研削盤の研削寸法自動測定機能を使用して求めた。  It was determined using the automatic measurement function of the grinding dimensions of the grinder.
テスト結果:  test results:
[0064] [表 8] ウェハー研削枚数 Ra ( n m) 研削動力 (k w) [Table 8] Wafer grinding number Ra (nm) Grinding power (kw)
実施例 3 実施例 4 実施例 3 実施例 4  Example 3 Example 4 Example 3 Example 4
1 2 8 3 2 2. 4 2. 3 1 2 8 3 2 2.4 2.3
2 2 9 2 9 2. 7 2. 52 2 9 2 9 2.7 2.5
5 2 5 2 4 3. 0 8. 35 2 5 2 4 3.0 8.3
1 0 2 3 2 3 3. 4 3. 6 [表' 9] ウェハ一研削枚数 砥石消耗量 ( μ m) ウェハ一除去量 (ji m) 1 0 2 3 2 3 3.4 3.6 Table '9] wafer one grinding number grindstone consumption (mu m) wafers one removal amount (ji m)
実施例 3 実施例 4 実施例 3 実施例 4  Example 3 Example 4 Example 3 Example 4
1 (). 4 0. 4 3 9 4 0 1 (). 4 0. 4 3 9 4 0
2 0. 6 0. 4 3 7 4 02 0.6 0.6 0.4 3 7 4 0
5 0. 7 0. 9 3 6 3 95 0.7 0.7 0.9 3 6 3 9
1 0 1. 3 1. 2 3 7 3 8 1 0 1.3 1.2 3 7 3 8
実施例 3および実施例 4の双方ともウェハー除去量については、 目標の除去量 40 zmに近い除去量を示した。砥石消耗については、異常な消耗及び消耗量の停滞 が認められず、ウェハー除去が正常に行われ、順調に研削作業が行われていたこと を示す。仕上げ面粗さ(Ra)及び研削動力(Ft)の各特性においても異常値は認めら れな力、つた。以上の結果より、実施例の砥石は、シリコンウェハーを対象とする研削 作業においても適正かつ良好な研削が可能であることが示された。 In both Example 3 and Example 4, the wafer removal amount showed a removal amount close to the target removal amount of 40 zm. With regard to grinding wheel wear, no abnormal wear or stagnation of wear amount was observed, indicating that wafer removal was performed normally and grinding work was performed smoothly. Abnormal values were not found in the characteristics of finished surface roughness (Ra) and grinding power (Ft). From the above results, it was shown that the grindstone of the example can perform proper and good grinding even in a grinding operation for a silicon wafer.

Claims

請求の範囲 The scope of the claims
[1] 砥粒、結合剤及び気孔からなる組織を有する砥石であって、無機接着剤とガラスフ リットにより形成された結合剤、及び自然気孔と気孔形成剤により形成された気孔を 有する、多孔質なビトリフアイド砥石。  [1] A grindstone having a structure composed of abrasive grains, a binder, and pores, having a binder formed by an inorganic adhesive and a glass frit, and having pores formed by natural pores and a pore-forming agent. Vitrifide whetstone.
[2] 前記ガラスフリットの軟化点が 300〜900°Cであることを特徴とする、請求項 1に記 載の多孔質なビトリフアイド砥石。 [2] The porous vitrified stone according to claim 1, wherein the glass frit has a softening point of 300 to 900 ° C.
[3] 前記ガラスフリットの軟化点が 400〜900°Cであることを特徴とする、請求項 2に記 載の多孔質なビトリフアイド砥石。 [3] The porous vitrified whetstone according to claim 2, wherein the softening point of the glass frit is 400 to 900 ° C.
[4] 前記砥粒が、溶融アルミナ系砥粒、ゾルゲルアルミナ質砥粒、炭化珪素系砥粒、ァ ルミナージルコニァ系砥粒、酸化セリウム系砥粒、シリカ系砥粒、 CBN系砥粒、及び ダイヤモンド系砥粒よりなる群から一種以上選択されることを特徴とする、請求項 1〜[4] The abrasive grains are fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina zirconia-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, CBN-based abrasive grains, And at least one selected from the group consisting of diamond-based abrasive grains,
3のいずれ力 1項に記載の多孔質なビトリフアイド砥石。 3. The porous vitrified whetstone according to item 1 above.
[5] 砥材、無機接着剤、ガラスフリット及び気孔形成剤を水に分散して得られる液状混 合物を型に流し込み、該型内の混合物を常温〜 300°Cで乾燥固化させると同時に 前記気孔形成剤を発泡させ、乾燥固化したものをさらに 600〜1000°Cで焼成してビ トリファイド砥石を得ることを特徴とする、多孔質なビトリフアイド砥石の製造方法。 [5] A liquid mixture obtained by dispersing an abrasive, an inorganic adhesive, a glass frit, and a pore-forming agent in water is poured into a mold, and the mixture in the mold is dried and solidified at room temperature to 300 ° C. A method for producing a porous vitrified grinding wheel, characterized in that the pore forming agent is foamed, dried and solidified, and further fired at 600 to 1000 ° C to obtain a vitrified grinding wheel.
[6] 前記気孔形成剤として、液状の発泡性気孔形成剤を使用することを特徴とする、請 求項 5に記載の製造方法。 [6] The production method according to claim 5, wherein a liquid foamable pore-forming agent is used as the pore-forming agent.
[7] 前記気孔形成剤として、固形の発泡性気孔形成剤を使用することを特徴とする、請 求項 5又は 6に記載の製造方法。 7. The production method according to claim 5, wherein a solid foamable pore-forming agent is used as the pore-forming agent.
[8] 軟化点が 300〜900°Cであるガラスフリットを使用することを特徴とする、請求項 5[8] The glass frit having a softening point of 300 to 900 ° C. is used.
〜7のいずれ力、 1項に記載の製造方法。 The manufacturing method according to any one of claims 1 to 7, wherein
[9] 軟化点が 400〜900°Cであるガラスフリットを使用することを特徴とする、請求項 8に 記載の製造方法。 [9] The production method according to claim 8, wherein a glass frit having a softening point of 400 to 900 ° C is used.
[10] 使用される砥粒が、溶融アルミナ系砥粒、ゾルゲルアルミナ質砥粒、炭化珪素系砥 粒、アルミナ ジルコ二ァ系砥粒、酸化セリウム系砥粒、シリカ系砥粒、 CBN系砥粒 、及びダイヤモンド系砥粒よりなる群から一種以上選択されることを特徴とする、請求 項 5〜9のいずれか 1項に記載の製造方法。  [10] The abrasive grains used are fused alumina-based abrasive grains, sol-gel alumina-based abrasive grains, silicon carbide-based abrasive grains, alumina zirconium-based abrasive grains, cerium oxide-based abrasive grains, silica-based abrasive grains, and CBN-based abrasive grains. The method according to any one of claims 5 to 9, wherein one or more kinds are selected from the group consisting of grains and diamond-based abrasive grains.
PCT/JP2005/006595 2004-04-06 2005-04-04 Porous vitrified grinding wheel and method for production thereof WO2005097409A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2006512066A JP4769186B2 (en) 2004-04-06 2005-04-04 Porous vitrified grinding wheel and method for producing the same
CN2005800102663A CN1938129B (en) 2004-04-06 2005-04-04 Porous vitrified grinding wheel and method for production thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2004-112028 2004-04-06
JP2004112028 2004-04-06

Publications (1)

Publication Number Publication Date
WO2005097409A1 true WO2005097409A1 (en) 2005-10-20

Family

ID=35124909

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2005/006595 WO2005097409A1 (en) 2004-04-06 2005-04-04 Porous vitrified grinding wheel and method for production thereof

Country Status (4)

Country Link
JP (1) JP4769186B2 (en)
CN (1) CN1938129B (en)
TW (1) TW200538237A (en)
WO (1) WO2005097409A1 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007136559A (en) * 2005-11-15 2007-06-07 Kurenooton Kk Vitrified grinding stone, and its manufacturing method
JP2007290101A (en) * 2006-04-27 2007-11-08 Disco Abrasive Syst Ltd Vitrified bond grindstone and its manufacturing method
JP2009073940A (en) * 2007-09-20 2009-04-09 Toyota Motor Corp Abrasive and method for producing abrasive
ITVI20080194A1 (en) * 2008-08-08 2010-02-09 Lino Fasolato METHOD FOR THE PRODUCTION OF A TOOL AND TOOL PRODUCED ACCORDING TO THIS METHOD
CN102092010A (en) * 2010-12-09 2011-06-15 郭兵健 Method for preparing high-porosity ceramic cement grinding wheel for polishing silicon single crystal rods
JP2012152881A (en) * 2011-01-28 2012-08-16 Allied Material Corp Superabrasive wheel, and grinding processing method using the same
JP2014508661A (en) * 2011-03-31 2014-04-10 サンーゴバン アブレイシブズ,インコーポレイティド Abrasive articles for high-speed grinding operations
US9144885B2 (en) 2011-03-31 2015-09-29 Saint-Gobain Abrasives, Inc. Abrasive article for high-speed grinding operations
US11691247B2 (en) 2017-12-28 2023-07-04 Saint-Gobain Abrasives, Inc. Bonded abrasive articles

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5636144B2 (en) * 2012-01-18 2014-12-03 株式会社ノリタケカンパニーリミテド Vitrified super abrasive wheel
EP2834040B1 (en) * 2012-04-04 2021-04-21 3M Innovative Properties Company Abrasive particles, method of making abrasive particles, and abrasive articles
CN103223643B (en) * 2013-05-03 2015-10-28 鲁启华 A kind of Ultrathin blade
PL3089850T3 (en) * 2013-12-30 2022-03-21 Saint-Gobain Abrasives, Inc. Composite bodies and methods of forming the same
CN103770023A (en) * 2014-01-10 2014-05-07 当涂县南方红月磨具磨料有限公司 Composite binding agent type cubic boron nitride grinding wheel
CN104149041A (en) * 2014-07-30 2014-11-19 浙江中晶科技股份有限公司 Method for manufacturing ceramic grinding wheel for silicon rod polishing by means of organic matter sponge in shaping mode
CN106112838B (en) * 2016-06-25 2018-02-23 佛山市新思维机电研发有限公司 A kind of preparation method of resistance to grinding composite wheel
CN108247553B (en) * 2017-12-30 2020-11-17 义乌市安航科技有限公司 Preparation method of wear-resistant artificial oilstone
JP7034547B2 (en) * 2018-02-02 2022-03-14 株式会社ディスコ An annular grindstone and a method for manufacturing an annular grindstone
JP2019181613A (en) * 2018-04-06 2019-10-24 株式会社ノリタケカンパニーリミテド Vitrified grindstone of coarse-composition homogeneous structure
JP6578036B1 (en) * 2018-04-06 2019-09-18 株式会社ノリタケカンパニーリミテド High porosity CBN vitrified grinding wheel with homogeneous structure
CN110238765B (en) * 2019-06-21 2021-05-18 郑州磨料磨具磨削研究所有限公司 Ceramic bond for super-finishing grinding wheel and application thereof
CN111421477B (en) * 2020-04-12 2021-10-22 江苏赛扬精工科技有限责任公司 Large-porosity ceramic cBN grinding wheel and preparation method and application thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003181763A (en) * 2001-12-19 2003-07-02 Noritake Co Ltd Method for manufacturing porous vitrified grinding stone and method for recycling pore forming agent
JP2003527974A (en) * 2000-03-23 2003-09-24 サンーゴバン アブレイシブズ,インコーポレイティド Abrasive tools bonded with vitrified binder
JP2004009164A (en) * 2002-06-04 2004-01-15 Musashi Seimitsu Ind Co Ltd Grindstone member and its manufacturing method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003527974A (en) * 2000-03-23 2003-09-24 サンーゴバン アブレイシブズ,インコーポレイティド Abrasive tools bonded with vitrified binder
JP2003181763A (en) * 2001-12-19 2003-07-02 Noritake Co Ltd Method for manufacturing porous vitrified grinding stone and method for recycling pore forming agent
JP2004009164A (en) * 2002-06-04 2004-01-15 Musashi Seimitsu Ind Co Ltd Grindstone member and its manufacturing method

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007136559A (en) * 2005-11-15 2007-06-07 Kurenooton Kk Vitrified grinding stone, and its manufacturing method
JP2007290101A (en) * 2006-04-27 2007-11-08 Disco Abrasive Syst Ltd Vitrified bond grindstone and its manufacturing method
JP2009073940A (en) * 2007-09-20 2009-04-09 Toyota Motor Corp Abrasive and method for producing abrasive
ITVI20080194A1 (en) * 2008-08-08 2010-02-09 Lino Fasolato METHOD FOR THE PRODUCTION OF A TOOL AND TOOL PRODUCED ACCORDING TO THIS METHOD
WO2010015923A3 (en) * 2008-08-08 2010-04-01 Lino Fasolato Method for producing a tool and tool produced according to said method
CN102092010A (en) * 2010-12-09 2011-06-15 郭兵健 Method for preparing high-porosity ceramic cement grinding wheel for polishing silicon single crystal rods
CN102092010B (en) * 2010-12-09 2012-04-25 郭兵健 Method for preparing high-porosity ceramic cement grinding wheel for polishing silicon single crystal rods
JP2012152881A (en) * 2011-01-28 2012-08-16 Allied Material Corp Superabrasive wheel, and grinding processing method using the same
JP2014508661A (en) * 2011-03-31 2014-04-10 サンーゴバン アブレイシブズ,インコーポレイティド Abrasive articles for high-speed grinding operations
US9144885B2 (en) 2011-03-31 2015-09-29 Saint-Gobain Abrasives, Inc. Abrasive article for high-speed grinding operations
US9539701B2 (en) 2011-03-31 2017-01-10 Saint-Gobain Abrasives, Inc. Abrasive article for high-speed grinding operations
US11691247B2 (en) 2017-12-28 2023-07-04 Saint-Gobain Abrasives, Inc. Bonded abrasive articles

Also Published As

Publication number Publication date
JPWO2005097409A1 (en) 2008-02-28
CN1938129A (en) 2007-03-28
CN1938129B (en) 2010-11-24
JP4769186B2 (en) 2011-09-07
TW200538237A (en) 2005-12-01

Similar Documents

Publication Publication Date Title
WO2005097409A1 (en) Porous vitrified grinding wheel and method for production thereof
US6702650B2 (en) Porous abrasive article having ceramic abrasive composites, methods of making, and methods of use
JP4854269B2 (en) Resinoid grinding wheel manufacturing method
EP1393859B1 (en) Microabrasive tool with a vitreous binder
JP3336015B2 (en) Manufacturing method of highly permeable whetstone
TWI257340B (en) Method of roll grinding
US6066189A (en) Abrasive article bonded using a hybrid bond
JP2000508249A (en) Silicon carbide polishing wheel
US10589401B2 (en) Sintered vitrified superfinishing grindstone
CN102066055B (en) Self-bonded foamed abrasive articles and machining with such articles
KR20180134025A (en) Vitrified super abrasive grain wheel
JP2007136559A (en) Vitrified grinding stone, and its manufacturing method
US6214069B1 (en) Process for the manufacture of a sintered, ceramic abrasive and grinding tools with this abrasive
JP2007111827A (en) DIAMOND OR cBN GRINDING STONE, AND ITS MANUFACTURING METHOD
KR20070022028A (en) Porous vitrified grinding wheel and method for production thereof
JPH09267263A (en) Coated abrasive grain for vitrified bond cubic boron nitride grinding wheel excellent in press formability
CN115135622B (en) Mold for glass forming and method of forming glass using the same
CN113400209B (en) Sintered grinding wheel pore-forming method
JP2004249459A (en) Glassy binder raw material liquid for vitrified grinding wheel and its manufacturing method
JP2004160646A (en) Porous resinoid grinding wheel and producing method therefor

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2006512066

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 200580010266.3

Country of ref document: CN

WWE Wipo information: entry into national phase

Ref document number: 1020067020870

Country of ref document: KR

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

WWP Wipo information: published in national office

Ref document number: 1020067020870

Country of ref document: KR

122 Ep: pct application non-entry in european phase