US3881910A - Chromium-chromium carbide powder - Google Patents

Chromium-chromium carbide powder Download PDF

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US3881910A
US3881910A US388434A US38843473A US3881910A US 3881910 A US3881910 A US 3881910A US 388434 A US388434 A US 388434A US 38843473 A US38843473 A US 38843473A US 3881910 A US3881910 A US 3881910A
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chromium
wear
coating
carbide
mixture
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US388434A
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John Franklin Pelton
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Praxair ST Technology Inc
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Union Carbide Corp
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Priority to US388434A priority Critical patent/US3881910A/en
Priority to AU71305/74A priority patent/AU7130574A/en
Priority to CA206,051A priority patent/CA1036391A/en
Priority to BR6685/74A priority patent/BR7406685D0/en
Priority to IL45474A priority patent/IL45474A0/en
Priority to SE7410372A priority patent/SE7410372L/xx
Priority to JP49092459A priority patent/JPS5044932A/ja
Priority to DE2438997A priority patent/DE2438997A1/en
Priority to FR7428282A priority patent/FR2245778A1/fr
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Assigned to MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MORGAN BANK ( DELAWARE ) AS COLLATERAL ( AGENTS ) SEE RECORD FOR THE REMAINING ASSIGNEES. reassignment MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MORGAN BANK ( DELAWARE ) AS COLLATERAL ( AGENTS ) SEE RECORD FOR THE REMAINING ASSIGNEES. MORTGAGE (SEE DOCUMENT FOR DETAILS). Assignors: STP CORPORATION, A CORP. OF DE.,, UNION CARBIDE AGRICULTURAL PRODUCTS CO., INC., A CORP. OF PA.,, UNION CARBIDE CORPORATION, A CORP.,, UNION CARBIDE EUROPE S.A., A SWISS CORP.
Assigned to UNION CARBIDE CORPORATION, reassignment UNION CARBIDE CORPORATION, RELEASED BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: MORGAN BANK (DELAWARE) AS COLLATERAL AGENT
Assigned to UNION CARBIDE COATINGS SERVICE TECHNOLOGY CORPORATION reassignment UNION CARBIDE COATINGS SERVICE TECHNOLOGY CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: UNION CARBIDE COATINGS SERVICE CORPORATION
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/06Metallic material

Definitions

  • ABSTRACT A reinforced chromium coating produced by plasma spraying or detonation-gun deposition of powder consisting essentially of a mixture of chromium and at least one chromium carbide taken from the class consisting of Cr C Cr, C, and Cr C wherein said chromium carbides are present in the range of from 3 to 30 volume percent of saidmixture.
  • This invention relates to a novel coating and article produced by plasma spraying or detonation gun deposition of a chromium and chromium carbide powder. More particularly this invention relates to a coating or article having unique wear and frictional characteristics produced from a mechanical mixture of chromium and chromium carbide powders.
  • Chromium metal has been used as an electroplated coating (i.e., hard chromium plating") for many years to restore worn or damaged parts to their original dirnensions, to increase wear resistance, reduce friction, and provide corrosion resistance. Chromium's excellent wear and frictional characteristics have been attributed to its low ratio of energy of adhesion to hardness when mated against a number of materials that are commonly used in engineering applications. Hard chromium electroplate, however, has a number of limitations. The electroplating of chromium is economically feasible when the configuration of the part is relatively simple and the number of parts and/or their size is relatively small. When the configuration of the part becomes complex, obtaining a uniform coating thickness by electrodeposition is difficult and requires precise placement of electrodes and thieves.
  • An alternative method of depositing chromium metal is by metal spraying, such as plasma or detonation gun coating processes. These methods offer a number of processing advantages. Surface preparation is relatively simple and inexpensive. The coatings can be applied to almost any metallic substrate without using undercoats. The rate of deposition is very high so that a large volume of parts can be coated with a minimal capital investment. The coating thickness can be controlled very closely so that any subsequent finishing can be kept to a minimum. The overspray can be easily contained and recovered making pollution control a simple matter.
  • plasma-deposited chromium is not as wear-resistant at ambient temperature as hard electroplated chromium. This is because the wear resistance of chromium electroplate is not an inherent property of elemental chromium but is believed to arise largely from impurities and stresses incorporated in the coating during plating. Plasma deposited chromium, being a purer form of chromium, thus lacks the wear resistance of hard chromium electroplate while retaining the corrosion resistance characteristics of chromium.
  • Cermet-type materials consist of a relatively high-volume fraction of hard phase particles, such as chromium carbide or tungsten carbide, bonded together by a relatively low-volume fraction of a ductile, soft matrix such as cobalt, nickel or nichrome. While these cermets exhibit outstanding wear characteristics, they lack the usual frictional and compatibility characteristics that electrolytic chromium plate exhibits and hence, although a relatively hard coating may be obtained, many of the other advantages exhibited by electroplated chromium metal are lost.
  • Chromium has been used as a binder in some cermets but these are intended for. high-temperature use where chromium is a ductile metal.
  • Another object is to provide a coating which is equivalent to electrolytic chrome plate in resistance to wear and which can be finished with the same type of tooling used for finishing chrome plate to final dimensions.
  • Yet another object is to provide a powder for making such coatings or articles.
  • a further object is to provide a mechanical mixture of chromium powder and chromium carbide powder to provide the coating of this invention.
  • FIG. 1 is a pictorial representation of the structure obtained by depositing the powder of this invention.
  • FIG. 2 shows the variation of wear scar volumes with carbide content of the powder used to produce the coating tested and compared to coatings of hard chrome electroplate.
  • FIG. 1 illustrates the structure of a coating or article of this invention achieved by depositing the powder of about l80rpm; MIL-5606A hydraulic fluid was used as lubricant.
  • mium carbide it has been found that volume fractions of 3 to 30 percent chromium carbide are the most desirable. Above about 30 volume percent the coating becomes harder, more brittle and more difficult to grind. In addition, the powder becomes more difficult to plate.
  • the wear resistance of plasma-deposited coatings prepared from mixtures of chromium and chromium carbide was measured using a Dow-Coming LEW-l Friction and Wear Test Machine according to ASTM Standard Method D-27l4-64. Coatings deposited 12 mils thick on the wear surface of mild steel wear blocks were ground to a final thickness of 6 mils and tested against carburized AlSl 4620 steel rings (surface hardness 58-63 Rockwell C") for 5400 rings revolution at lt is evident that at 450 lb. load, there was little significant difference in wear characteristics of the coating as a function of volume fraction of carbide additions of 18 percent or greater, but the wear scar volumes were significantly lower than hard electroplated chromium. Equally good results were obtained with Cr C additions and with Cr; C additions. Plasma-deposited chromium without chromium carbide additions tends to fail structurally at 450 lb. loads early in the test cycle.
  • class consisting of plasma and detonation-gun type processes consisting essentially of a mixture of chromium and at least one chromium carbide taken from the class consisting of Cr C Cr C and Cr c wherein said chromium carbides are present in the range of from 3 to 30 volume percent of said mixture.

Abstract

A reinforced chromium coating produced by plasma spraying or detonation-gun deposition of powder consisting essentially of a mixture of chromium and at least one chromium carbide taken from the class consisting of Cr23 C6; Cr7 C3 and Cr3 C2 wherein said chromium carbides are present in the range of from 3 to 30 volume percent of said mixture.

Description

United States Patent [191 Pelton May 6,1975
[ CHROMlUM-CHROMIUM CARBIDE POWDER [75] Inventor: John Franklin Pelton, Yorktown Heights, NY.
[73] Assignee: Union Carbide Corporation, New
York, NY.
[22] Filed: Aug. 15, 1973 [2]] Appl. No.: 388,434
[52] US. Cl. 75/.5 R; 75/0.5 B; 117/105 [51] Int. Cl B221 1/00 [58] Field of Search 75/0.5 AC, 0.5 BC, 0.5 R, 75/0.5 B;117/105,105.2, 105.1, 93.1
PFzlOO M;'29/192 CD, 191.2
[56] References Cited UNITED STATES PATENTS 3,150,938 9/1964 Pelton et a1 29/194 carbides chromium Primary Examiner-L. Dewayne Rutledge Assistant Examiner-O. F. Crutchfield Attorney, Agent, or FirmDominic .1. Terminello [57] ABSTRACT A reinforced chromium coating produced by plasma spraying or detonation-gun deposition of powder consisting essentially of a mixture of chromium and at least one chromium carbide taken from the class consisting of Cr C Cr, C, and Cr C wherein said chromium carbides are present in the range of from 3 to 30 volume percent of saidmixture.
2 Claims, 2 Drawing Figures CHROMIUM-CHROMIUM CARBIDE POWDER This invention relates to a novel coating and article produced by plasma spraying or detonation gun deposition of a chromium and chromium carbide powder. More particularly this invention relates to a coating or article having unique wear and frictional characteristics produced from a mechanical mixture of chromium and chromium carbide powders.
Chromium metal has been used as an electroplated coating (i.e., hard chromium plating") for many years to restore worn or damaged parts to their original dirnensions, to increase wear resistance, reduce friction, and provide corrosion resistance. Chromium's excellent wear and frictional characteristics have been attributed to its low ratio of energy of adhesion to hardness when mated against a number of materials that are commonly used in engineering applications. Hard chromium electroplate, however, has a number of limitations. The electroplating of chromium is economically feasible when the configuration of the part is relatively simple and the number of parts and/or their size is relatively small. When the configuration of the part becomes complex, obtaining a uniform coating thickness by electrodeposition is difficult and requires precise placement of electrodes and thieves. Without a uniform coating thickness, grinding to a finished surface configuration becomes necessary, and it is both difficult and expensive with electroplated chromium because of its inherent brittleness and hardness. The rate of deposition by electroplating is relatively low, and thus for a large number of parts and/or large areas and- /or thick coatings a very substantial capital investment in plating tanks and power supplies is required. In chromium electroplating it is often necessary to use expensive surface cleaning and etching procedures to prepare substrates. Further, with many substrate materials it is not possible to directly apply chromium electroplating and one or more undercoats of other metals must be used. Spent plating baths present a disposal problem because they are a serious pollution source, and hence handling them adds significantly to the cost of the process.
An alternative method of depositing chromium metal is by metal spraying, such as plasma or detonation gun coating processes. These methods offer a number of processing advantages. Surface preparation is relatively simple and inexpensive. The coatings can be applied to almost any metallic substrate without using undercoats. The rate of deposition is very high so that a large volume of parts can be coated with a minimal capital investment. The coating thickness can be controlled very closely so that any subsequent finishing can be kept to a minimum. The overspray can be easily contained and recovered making pollution control a simple matter.
Unfortunately, plasma-deposited chromium is not as wear-resistant at ambient temperature as hard electroplated chromium. This is because the wear resistance of chromium electroplate is not an inherent property of elemental chromium but is believed to arise largely from impurities and stresses incorporated in the coating during plating. Plasma deposited chromium, being a purer form of chromium, thus lacks the wear resistance of hard chromium electroplate while retaining the corrosion resistance characteristics of chromium.
in seeking an alternative method of depositing a coating equivalent to that of hard electroplated chromium,
and recognizing that plasma deposition of chromium metal by itself is not successful, it would be normal engineering practice to evaluate materials such as the well-known plasma-deposited cermets; e.g., tungsten carbide-cobalt. Cermet-type materials consist of a relatively high-volume fraction of hard phase particles, such as chromium carbide or tungsten carbide, bonded together by a relatively low-volume fraction of a ductile, soft matrix such as cobalt, nickel or nichrome. While these cermets exhibit outstanding wear characteristics, they lack the usual frictional and compatibility characteristics that electrolytic chromium plate exhibits and hence, although a relatively hard coating may be obtained, many of the other advantages exhibited by electroplated chromium metal are lost. An inherently brittle material, such as chromium, would not normally be chosen as the matrix however, because it would not provide sufficient toughness or impact resistance. Chromium has been used as a binder in some cermets but these are intended for. high-temperature use where chromium is a ductile metal.
Attempts to improve the plasma-deposited chromium coating by intentionally spraying with oxidizing or nitriding conditions to introduce a dispersion of hard precipitates that might strengthen the deposits and improve their wear resistance was unsuccessful. Both plasma and detonation gun deposition result in a multilayer structure of thin, overlapping, lenticular particles or splat." Oxidation or nitridation of the chromium particles during spraying results in weakened splat-tosplat bonding and a friable coating with low strength in which particles tend to pull-out" during wear. Nitriding the chromium powder prior to deposition also created a very friable coating and increased the tendency of particles to pull out during grinding.
It has not been unexpectedly discovered that the compatibility, frictional characteristics, and corrosionresistance normally associated with hard chrome electroplate can be obtained in plasma or detonation-gun coatings and superior wear resistance and finishability obtained as well by incorporating a low-volume dispersion of chromium carbide particles, which are brittle in a chromium matrix, which is brittle. One method of dispersing the carbide phase in the chromium matrix is by mechanically mixing particles of chromium carbide and chromium and co-depositing the mixture.
Accordingly, it is the main object of this invention to provide a coating which is predominantly chromium reinforced with chromium carbides.
Another object is to provide a coating which is equivalent to electrolytic chrome plate in resistance to wear and which can be finished with the same type of tooling used for finishing chrome plate to final dimensions.
Yet another object is to provide a powder for making such coatings or articles.
A further object is to provide a mechanical mixture of chromium powder and chromium carbide powder to provide the coating of this invention.
These and other objects will either be pointed out or become apparent from the following description and drawings where:
FIG. 1 is a pictorial representation of the structure obtained by depositing the powder of this invention; and
FIG. 2 shows the variation of wear scar volumes with carbide content of the powder used to produce the coating tested and compared to coatings of hard chrome electroplate.
FIG. 1 illustrates the structure of a coating or article of this invention achieved by depositing the powder of about l80rpm; MIL-5606A hydraulic fluid was used as lubricant.
Wear tests conducted at 450 lbs. load on coatings of this invention, which were made with mixtures of -325 the invention by the plasma or detonation-gun process. 5 mesh chromium and chromium carbide, resulted in the The structure is characterized by inhomogeneity, that data of Table l and band curves of FIG. 2. The range is, regardless of how fine the powder particles are, of values observed for commercial hard chromium some of the lenticular particles or splats will be comlectroplate is also shown on FIG. 2 by the crosspletely chromium metal and some completely chrohatched area adjacent to the vertical axis.
TABLE I WEAR TESTS OF COATINGS AT 450 LB. LOAD Coating Coating Wear Scar Mating Hardness Vol%ume Volume Ring Weight VPNM Coating Type Carbide cm Change, mg
Mixture,
Cr-l-Cr C, 24 26 to 32 -05 to -2.0 301 I l 13 100 141017 l.3 0-1.9 9001125 Mixture,
Cr+Cr,C 27 to 37 0.9 m l.6 374 I 84 3s 20 m 21 0 m 1.1 50 20 to 1.0 to 3.9 465 i 40 Electroplated Cr 43 to 53 0.6 to +2.9
mium carbide. it has been found that volume fractions of 3 to 30 percent chromium carbide are the most desirable. Above about 30 volume percent the coating becomes harder, more brittle and more difficult to grind. In addition, the powder becomes more difficult to plate.
The wear resistance of plasma-deposited coatings prepared from mixtures of chromium and chromium carbide was measured using a Dow-Coming LEW-l Friction and Wear Test Machine according to ASTM Standard Method D-27l4-64. Coatings deposited 12 mils thick on the wear surface of mild steel wear blocks were ground to a final thickness of 6 mils and tested against carburized AlSl 4620 steel rings (surface hardness 58-63 Rockwell C") for 5400 rings revolution at lt is evident that at 450 lb. load, there was little significant difference in wear characteristics of the coating as a function of volume fraction of carbide additions of 18 percent or greater, but the wear scar volumes were significantly lower than hard electroplated chromium. Equally good results were obtained with Cr C additions and with Cr; C additions. Plasma-deposited chromium without chromium carbide additions tends to fail structurally at 450 lb. loads early in the test cycle.
Differences in wear behavior for different compositions were observed when a 600 lb. load was used. Referring to Table ll below, it is evident that as the Cr C volume fraction increases, the wear of the mating surface (Ring Weight Change Column) increases significantly. A similar increase occurs when a larger Cr C particle size is used, as also shown in Table II, by comparing the wear of 230/+325 mesh Cr C particle additions to 325 mesh additions. Even at a very lowvolume fraction, -l 20/+230 Cr C caused significantly greater mating surface wear in one test, with coating failure probably limiting the mating surface wear in another test. These test data demonstrate that carbide particle size and volume fraction should be kept relatively low to minimize mating surface wear. The lowvolume fraction of carbide also tends to improve finishability since the hardness is minimized.
TABLE ll WEAR TESTS OF COATINGS AT 600 LB. LOAD Some cracking was observed around the indentations. "C implies chipping of the coating occurred and an accurate scar volume could not be measured.
class consisting of plasma and detonation-gun type processes consisting essentially of a mixture of chromium and at least one chromium carbide taken from the class consisting of Cr C Cr C and Cr c wherein said chromium carbides are present in the range of from 3 to 30 volume percent of said mixture.
2. A powder according to claim 1 wherein said chromium carbides are present in the range of about 15 volume percent to 30 volume percent of said mixture.

Claims (2)

1. A POWDER FOR DEPOSITION BY A PROCESS TAKEN FROM CLASS CONSISTING OF PLASMA AND DETONATION-GUN TYPE PROCESSES CONSISTING ESSENTIALLY OF A MIXTURE OF CHROMIUM AND AT LEAST ONE CHROMIUM CARBIDE TAKEN FROM THE CLASS CONSISTING OF CR23C6; CR7C3 AND CR3C2 WHEREIN SAID CHROMIUM BARDIDES ARE PRESENT IN THE RANGE OF FROM 3 TO 30 VOLUME PERCENT OF SAID MIXTURE.
2. A powder according to claim 1 wherein said chromium carbides are present in the range of about 15 volume percent to 30 volume percent of said mixture.
US388434A 1973-08-15 1973-08-15 Chromium-chromium carbide powder Expired - Lifetime US3881910A (en)

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Application Number Priority Date Filing Date Title
US388434A US3881910A (en) 1973-08-15 1973-08-15 Chromium-chromium carbide powder
AU71305/74A AU7130574A (en) 1973-08-15 1974-07-17 Chromium coating
CA206,051A CA1036391A (en) 1973-08-15 1974-07-31 Reinforced chromium coating and powder for making same
IL45474A IL45474A0 (en) 1973-08-15 1974-08-14 A reinforced chromium coating and powder for making same
SE7410372A SE7410372L (en) 1973-08-15 1974-08-14
JP49092459A JPS5044932A (en) 1973-08-15 1974-08-14
BR6685/74A BR7406685D0 (en) 1973-08-15 1974-08-14 ESSENTIALLY COATING OF CHROME AND CHROME CARBURETES METAL SUBSTRATE AND POINT FOR DEPOSITION
DE2438997A DE2438997A1 (en) 1973-08-15 1974-08-14 COVER AND ITEMS COVERED WITH IT
FR7428282A FR2245778A1 (en) 1973-08-15 1974-08-14

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JP (1) JPS5044932A (en)
AU (1) AU7130574A (en)
BR (1) BR7406685D0 (en)
CA (1) CA1036391A (en)
DE (1) DE2438997A1 (en)
FR (1) FR2245778A1 (en)
IL (1) IL45474A0 (en)
SE (1) SE7410372L (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6071324A (en) * 1998-05-28 2000-06-06 Sulzer Metco (Us) Inc. Powder of chromium carbide and nickel chromium
US20070062762A1 (en) * 2005-09-20 2007-03-22 Ernst Ach Elevator installation with drivebelt pulley and flat-beltlike suspension means
US20130230792A1 (en) * 2012-03-01 2013-09-05 Bloom Energy Corporation Coatings for Metal Interconnects to Reduce SOFC Degradation
CN103420373A (en) * 2013-08-01 2013-12-04 西安交通大学 Preparation method for high temperature corrosion resistant Cr23C6 cermet
CN103468991A (en) * 2013-08-01 2013-12-25 西安交通大学 Method for increasing oxidation resistance and high-temperature mechanical performance of Cr23C6 compound

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3150938A (en) * 1958-05-28 1964-09-29 Union Carbide Corp Coating composition, method of application, and product thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3150938A (en) * 1958-05-28 1964-09-29 Union Carbide Corp Coating composition, method of application, and product thereof

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6071324A (en) * 1998-05-28 2000-06-06 Sulzer Metco (Us) Inc. Powder of chromium carbide and nickel chromium
US6254704B1 (en) * 1998-05-28 2001-07-03 Sulzer Metco (Us) Inc. Method for preparing a thermal spray powder of chromium carbide and nickel chromium
US20070062762A1 (en) * 2005-09-20 2007-03-22 Ernst Ach Elevator installation with drivebelt pulley and flat-beltlike suspension means
US20130230792A1 (en) * 2012-03-01 2013-09-05 Bloom Energy Corporation Coatings for Metal Interconnects to Reduce SOFC Degradation
US20160020471A1 (en) * 2012-03-01 2016-01-21 Bloom Energy Corporation Coatings for metal interconnects to reduce sofc degradation
US10431833B2 (en) * 2012-03-01 2019-10-01 Bloom Energy Corporation Coatings for metal interconnects to reduce SOFC degradation
US10446854B2 (en) * 2012-03-01 2019-10-15 Bloom Energy Corporation Coatings for metal interconnects to reduce SOFC degradation
CN103420373A (en) * 2013-08-01 2013-12-04 西安交通大学 Preparation method for high temperature corrosion resistant Cr23C6 cermet
CN103468991A (en) * 2013-08-01 2013-12-25 西安交通大学 Method for increasing oxidation resistance and high-temperature mechanical performance of Cr23C6 compound
CN103468991B (en) * 2013-08-01 2015-07-01 西安交通大学 Method for increasing oxidation resistance and high-temperature mechanical performance of Cr23C6 compound

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IL45474A0 (en) 1974-11-29
AU7130574A (en) 1976-01-22
CA1036391A (en) 1978-08-15
BR7406685D0 (en) 1975-06-10
DE2438997A1 (en) 1975-03-13
SE7410372L (en) 1975-02-17
FR2245778A1 (en) 1975-04-25
JPS5044932A (en) 1975-04-22

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