US20050284029A1

US20050284029A1 - Aluminum and zirconium oxynitride abrasive grains

Info

Publication number: US20050284029A1
Application number: US11/152,783
Authority: US
Inventors: Florent Bourlier; Florence Peillon
Original assignee: PEM Abrasifs Refractaires
Current assignee: PEM Abrasifs Refractaires
Priority date: 2002-12-23
Filing date: 2005-06-15
Publication date: 2005-12-29
Also published as: FR2848889A1; DE60306428D1; EP1576069B1; BRPI0317694B1; ATE331009T1; AU2003299340A1; ES2266912T3; BR0317694A; FR2848889B1; EP1576069A1; WO2004063306A1; PT1576069E; CA2511069C; CA2511069A1; DE60306428T2

Abstract

Corundum-zirconia abrasive grains containing more than 50 wt % of an alumina-zirconia eutectic mixture. The grains contain 0.3 to 3% nitrogen, and more than 75% of the zirconia crystals are cubic in shape. The abrasive grains are of particular use for making grinding wheels, abrasive fabrics and papers, polishing compounds and sprayed abrasives.

Description

BACKGROUND OF THE INVENTION

The invention relates to the domain of abrasive grains, and particularly agglomerated grains intended for grinding wheels, grains applied to fabric and paper type supports, and grains used for spraying or contained in a polishing paste.
Description of Related Art
Alumina-zirconia based electromolten abrasives have been known for more than forty years and in particular have been described in several patents by the Norton company. Patent U.S. Pat. No. 3,181,939, filed in 1962, describes alumina-zirconia type electromolten abrasives with ZrO₂content between 10 and 60%, and a microstructure comprising an alumina-zirconia eutectic and zirconia and α alumina crystals. Patent U.S. Pat. No. 3,891,408 filed in 1971 relates to alumina-zirconia type electromolten abrasives with ZrO₂content of between 35 and 50%. Patent U.S. Pat. No. 3,993,119 published in 1976 describes a molten abrasive oxides casting machine capable of vigorously quenching the molten mass. Patent U.S. Pat. No. 4,457,767, 1984, protects alumina-zirconia type electromolten abrasives with a content of yttrium oxide Y₂O₃between 0.1 and 2%.
More recently, the 3M Innovative Properties Company has deposited patent applications:

- WO 02/08143 that claims an electromolten abrasive grain characterised by a fraction of at least 20% by volume, composed of a eutectic mixture formed between firstly ZrO₂and secondly at least two other constituents, including Al₂O₃and/or defined compounds of the Al₂O₃, Y₂O₃type.
- WO 02/08146 that claims an electromolten abrasive grain with eutectic composition in which eutectic is formed between firstly ZrO₂and secondly at least two constituents including Al₂O₃and/or defined compounds of the Al₂O₃— rare earth oxides type.

The common point between these patent applications is that the abrasive grains always contain either yttrium oxide or at least one rare earth oxide, in one manner or another.
The Inorganic Chemistry Treaty by Paul Pascal, Masson, 1962, already described that ZrO₂had three allotropic varieties. The monoclinical form stable at low temperature is transformed into quadratic zirconia at about 1100° C., and then into cubic zirconia. The cubic form is metastable at ambient temperature and it can be obtained by quenching; some elements, without any further precision, stabilise the cubic form.
The patents mentioned above always indicate that the product is prepared by casting the molten product followed by vigorous quenching, a process that tends to stabilise the metastable cubic form; however, experience shows that the efficiency of this quenching is fairly limited, which is the reason for the interest in patent U.S. Pat. No. 4,457,767 that divulges that yttrium oxide stabilises the cubic phase of ZrO₂. Patent application WO 02/08146 suggests that other stabilising elements exist in the group of rare earth metals.
Furthermore, patent EP 0 509 940 issued by the applicant describes a wide range of electromolten products for abrasive or refractory applications, composed of one or several oxynitrides of metallic elements in the list containing aluminum and zirconium; but there is no example of the case that mentions aluminum and zirconium oxynitrides nor double aluminum and zirconium oxynitrides.

SUMMARY OF THE INVENTION

The purpose of the invention is to provide abrasive grains to be applied onto fabric or paper supports or agglomerated in grinding wheels, or sprayed or contained in a polishing paste, and that have a better tenacity and machining performances than corundum—zirconia abrasives according to prior art with an equivalent content of zirconia.
The subject of the invention is corundum—zirconia abrasive grains containing more than 50% of a eutectic alumina—zirconia mixture, characterised in that they contain more than 0.3% of nitrogen, preferably from 0.3% to 3% of nitrogen, and more preferably from 0.3 to 1% of nitrogen, and in that less than 25% of the zirconia crystals are in monoclinic form. According to the invention, more than 75% of the zirconia crystals are in tetragonal or cubic form. Preferably, more than 75% of the zirconia crystals are in cubic form
The content of metallic aluminum is less than 0.1% and preferably 0.01%, and the content of aluminum nitride is less than 0.1% and preferably less than 0.01%.
Another purpose of the invention is a process for manufacturing this type of abrasive grains by melting in an electric arc furnace with a load composed of alumina and baddeleyite, by adding a nitride material to this load composed of aluminum nitride and/or one or several aluminum oxynitrides.
Another purpose is a process for preparation of abrasive grains including the preparation of a mixture of aluminum nitride and/or oxynitride Al_XO_YN_Z, alumina and zirconia powders, the reactive sintering of this mixture at a temperature between 1500° C. and 1600° C., and fast cooling of the sintered grains between 1100° C. and ambient temperature.

DETAILED DESCRIPTION OF THE INVENTION

Within the very wide range of abrasive compositions described in patent EP 0509940, the applicant has demonstrated that products based on aluminum and zirconium oxynitrides have better performances than products according to prior art of the corundum—zirconia type or the aluminum oxynitride type such as AlON.
Products according to the invention contain oxides, nitrides and oxynitrides of aluminum and zirconium, and it is not always easy to measure the content of each of these compounds. However, it is easy to measure the elementary contents of aluminum, zirconium and nitrogen. This is why the “equivalent content” concept is used by arbitrarily considering the product as being a mixture of Al₂O₃, ZrO₂and AlN. The equivalent content of AlN is the content for which all the nitrogen would be in AlN form, the equivalent content of ZrO₂is the content for which all the zirconium would be in ZrO₂form, and the equivalent content of Al₂O₃is the content for which aluminum would be in Al₂O₃form, except aluminum corresponding to the equivalent content of AlN. Another advantage of this concept of equivalent content is that the product can be compared with corundum—zirconia abrasives according to prior art.
Products according to the invention are of the corundum—zirconia type with an equivalent content of ZrO₂between 21 and 44%, an equivalent content of Al₂O₃between 57 and 80% and a nitrogen content between 0.3 and 3%, and preferably between 0.3 and 1%. For more than 50% of their weight, their structure consists of a eutectic mixture of α alumina and zirconia crystals. More than 75% of the zirconia crystals are in cubic form, the remainder being in monoclinical form. Nitrogen is present essentially in the form of zirconium nitride, more than 90% of the remainder being in the form of aluminum oxynitride.
It has been experimentally observed that the presence of zirconium nitride in the product is accompanied by a large increase in the relative proportion of the cubic form in the zirconia contained. Zirconium nitride is a perfectly stable product in contact with the water and acids, which is not the case for aluminum nitride, which makes it an excellent stabilising agent.
These products may be obtained by melting in an electric arc furnace with a load composed of alumina, zirconia, for example in the form of baddeleyite, and a nitride compound based on aluminum nitride and/or oxynitride. The aluminum nitride and/or oxynitride react with the zirconia during melting to form zirconium nitride.
The molten mass is cast and solidified quickly by any means known to those skilled in the art to cause efficient quenching; during these tests, the applicant used the technique described in patent U.S. Pat. No. 3,993,119, but using fixed casting equipment considering the size of the tests. Casting is done on a cold support, with a mass equal to at least twice the mass of the molten mass, and at a temperature of between 50° C. and 350° C. before casting.
If a product prepared by direct nitriding according to patent EP 0494129 issued by the applicant and containing aluminum nitride and oxynitride is used as the nitride compound, a product is obtained in which the content of free aluminum nitride is small, and typically less than 0.1%. Furthermore, this content can be reduced to less than 0.01% by slight acid etching, with final washing of the grains by a solution with a pH between 2 and 7, without reducing the mechanical strength of the material. The same is true for metallic aluminum.
Abrasive grains according to the invention can also be prepared by reactive sintering starting from a mixture of alumina, zirconia, and aluminum nitride and/or oxynitride powders.
Sintering is done at a temperature between 1500 and 1600° C., followed by fast cooling of the grains starting from 1100° C.
Exceptional mechanical properties are obtained using abrasive grains according to the invention, and particularly a Knoop hardness greater than or equal to 19 GPa, or even 20 GPa, and between 19 and 21 GPa, a tenacity of at least 2.3 MPa.m^1/2, very often more than 2.7 MPa.m^1/2, and performances in the machining test equal to 70% more than is obtained with a conventional corundum—zirconia abrasive with the same content of zirconia.

EXAMPLES

Analysis and Test Methods
The nitrogen content was measured on 5 mg samples weighed to the nearest 0.1 mg, by combustion in a LECO TC 436 gas analyser, and analysis by thermal conductivity of the gas obtained. The result indicated on each sample is the average of five measurements.

Example 1

2500 kg of powder Bayer alumina with a size grading of less than 100 μm was mixed with 1000 kg of powder aluminum with a size grading of less than 1.2 mm. This mixture was placed in a sealed furnace, vacuum degassed and then heated under a nitrogen pressure of 1 atm.
Nitriding began at about 700° C., and the nitrogen pressure was maintained to facilitate the increase in the temperature of the load. The exothermal reaction resulted in a temperature of about 1750° C. at the end of the operation.
After cooling, and at the end of the operation, the mass of porous, homogenous and mechanically unsound aluminum oxynitride recovered was 4010 kg.
The operation was repeated three times and finally a batch of 16 100 kg of product was obtained and was ground to a size grading of less than 10 mm, and then sampled and analysed; the result of the analysis gave an equivalent AlN content equal to 35.6%.

Example 2

400 kg of a mixture composed of 30 kg of the product obtained in example No. 1, 100 kg of baddeleyite with 95% of ZrO₂and 270 kg of Bayer alumina, was prepared.
This load was melted in a 100 kW melting arc furnace; the molten mass was cast on an ingot mould composed of 12 vertical cast iron plates (0.8 m×0.8 m×0.05 m) separated by 0.025 m. The cast mass was 390 kg; the product analysis was:

Equivalent AlN content: 2.3%

Zr content expressed in ZrO₂: 23.6%

Al content expressed in Al₂O₃: 73.7%
An examination of the product structure demonstrated the existence of two majority phases:
α alumina and cubic zirconia, and two minority phases: zirconium nitride and monoclinical zirconia. The chemical analysis also gave a free AlN content of 0.07% in the product.

The hardness and tenacity measurements are shown in Table 1, which also shows the results for similar product:

TABLE 1


Knoop	Vickers
hardness	hardness	Tenacity

Product in	19.9 GPa	18.9	GPa	2.8 MPa · m^1/2
example 2
Corundum -	18.7 GPa	17.9	GPa	2.1 MPa · m^1/2
Zirconia with
25% ZrO₂
according to
prior art
White corundum	20.3 GPa	20	GPa	2.0 MPa · m^1/2

It can be seen that the grains according to the invention are slightly harder and with higher tenacity than grains of corundum—zirconium with the same zirconia content.

Example 3

A batch of F80 abrasive grains (according to the FEPA standard) was prepared starting from the product prepared in Example 2 and tested in grinding according to the following procedure:
A single layer of grains is fixed on the side part of a 160 mm diameter metallic drum using an acrylic thermosetting resin. The grinding test consists of attacking an 18-8 stainless steel bar with section 12 mm×12 mm pushed perpendicular with a force of 85 Newtons, in contact with the side face of the drum driven at 6000 rpm. The duration of the operation is three times one minute.

The mass of the stainless steel bar is tested after one minute, two minutes and three minutes to evaluate the weight loss. The steel mass removed expressed in grams per minute are shown in Table 2, which also shows the results of this test obtained with other products using F80 grains.

	TABLE 2


	Mass removed minute by
	minute

	Product	Supplier	1	2	3

Corundum	The applicant	11.0	7.5	6.8
zirconia with
25% ZrO₂
Corundum	Competitive	10.8	7.9	7.7
zirconia with	product
25% ZrO₂
Product in	The applicant	19.6	16.5	14.9
example 2

It can be seen that the grains according to the invention have significantly better abrasive performances than corundum—zirconia grains with the same zirconia content.

Claims

1. Abrasive grains containing more than 50% of a eutectic alumina—zirconia mixture by weight, containing more than 0.3% of nitrogen, wherein less than 25% of the zirconia crystals are in monoclinic form

2. Abrasive grains according to claim 1 containing from 0.3% to 3% of nitrogen, preferably from 0.3% to 1% of nitrogen.

3. Abrasive grains according to claim 1 wherein more than 75% of the zirconia crystals are in tetragonal or in cubic form.

4. Abrasive grains according to claim 1 wherein more than 75% of the zirconia crystals are in cubic form.

5. Abrasive grains according to claim 1, wherein most of the nitrogen is in zirconium nitride form.

6. Abrasive grains according to claim 1, wherein the content of metallic aluminum is less than 0.1% by weight and the content of free aluminum nitride AlN is less than 0.1%.

7. Abrasive grains according to claim 6, wherein the content of metallic aluminum is less than 0.01% and the content of free aluminum nitride AlN is less than 0.01%.

8. Abrasive grains according to claim 5, wherein more than 90% of the nitrogen not combined in the form of zirconium nitride is combined in the form of aluminum oxynitride.

9. Abrasive grains according to claim 1, wherein the total contents of zirconium and aluminum in the form of oxides, nitrides and oxynitrides expressed in the form of equivalent contents of oxides, are between 21 and 44% for ZrO₂and between 57 and 80% for Al₂O₃.

10. Abrasive grains according to claim 1, characterised in that they have a Knoop hardness equal to or greater than 19 GPa and a tenacity equal to or greater than 2.3 MPa^1/2.

11. Abrasive grains according to claim 1, having a Knoop hardness equal to or greater than 20 GPa and a tenacity equal to or greater than 2.7 MPa.m^1/2.

12. Process of manufacturing abrasive grains according to claim 1, by melting in an electric arc furnace with a load composed of alumina and baddeleyite, characterised in that a nitride material is added to this load composed of aluminum nitride and/or one or several aluminum oxynitrides.

13. Process according to claim 12, wherein the nitride material is prepared by nitriding of a load composed of an alumina and aluminum powder mixture.

14. Process according to claim 12, wherein the nitride and/or the aluminum oxynitrides react with zirconium during melting to form zirconium nitride.

15. Process according to claim 12, wherein the mass melted in the electric furnace is cast and solidified quickly.

16. Process according to claim 15, in which the fast solidification of the molten mass is obtained by pouring it on a cold support, wherein the mass of the cold support is equal to at least twice the mass of the molten mass, and wherein its temperature before casting is between 50° C. and 350° C.

17. Process for preparation of abrasive grains according to claim 1, including the preparation of a mixture of aluminum nitride AlN and/or oxynitride Al_XO_YN_Z, alumina and zirconia powders, the reactive sintering of this mixture at a temperature between 1500° C. and 1600° C., and fast cooling of the sintered grains between 1100° C. and ambient temperature.

18. Process according to claim 17, comprising a final washing of the grains with a solution with a pH between 2 and 7.

19. Grinding wheels designed for grinding metals and metallic alloys or for precision grinding containing abrasive grains according to claim 1.

20. Abrasive fabrics and papers designed for polishing containing abrasive grains according to claim 1.

21. Polishing paste containing abrasive grains according to claim 1.