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US4731191A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for protecting carbonyl iron powder and compositions therefrom

Assignee: Dow Silicones Corp
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Filing: 1985-12-31
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Granted: 1988-03-15
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Expires: 2005-12-31
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Abstract

Abstract Carbonyl iron powder (CIP) can be protected from extensive atmospheric oxidation by mixing and heating it with a silicon compound having one or more reactive groups. The resulting CIP is more readily accepted by a silicone binder when preparing mixtures thereof.

Inventors

  • 👤 Terence J. Swihart

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 09:40
CPC Classifications
H; H01; H01F; H01F1/00; H01F1/01; H01F1/03; H01F1/12; H01F1/14; H01F1/20; H01F1/22; H01F1/24; H01F1/26

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 64 words
A method for preparing a composition containing carbonyl iron powder and a silicone binder, said method comprising heating and mixing the carbonyl iron powder with an amount of a silicon compound which contains one or more reactive silicon-bonded radicals, said amount being sufficient to reduce the atmospheric oxidation of the carbonyl iron powder, and then mixing the resulting carbonyl iron powder with the binder.
Claim 2
Independent Claim 64 words
A method for preparing a composition containing carbonyl iron powder and a silicone binder, said method comprising heating and mixing the carbonyl iron powder with an amount of a silicon compound which contains one or more reactive silicon-bonded radicals, said amount being sufficient to reduce the atmospheric oxidation of the carbonyl iron powder, and then mixing the resulting carbonyl iron powder with the binder.
Claim 3
Dependent Claim 142 words
A method according to claim 1 wherein the silicon compound is a liquid copolymeric organopolysiloxane containing SiO 4/2 siloxane units, SiH sites and SiOH sites which has been prepared by (A) forming an acidic homogeneous mixture comprising (a) an organic solvent solution of a resinous copolymeric siloxane containing silicon-bonded hydroxyl radicals and consisting essentially of R 3 SiO 1/2 siloxane units and SiO 4/2 siloxane units wherein the ratio of the former to the latter, on a molar basis, has a value of from 0.6/1 to 0.9/1 and each R denotes, independently, a monovalent hydrocarbon radical; and (b) a liquid organohydrogenpolysiloxane wherein each organic radical is, independently, a monovalent hydrocarbon radical, there being an average of at least one silicon-bonded hydrogen atom per molecule of said organohydrogenpolysiloxane; and, (B) heating the homogenous mixture to remove substantially all of the organic solvent therefrom.
Claim 4
Dependent Claim 149 words
A method according to claim 2 wherein the silicon compound is a liquid copolymeric organopolysiloxane containing SiO 4/2 siloxane units, SiH sites and SiOH sites which has been prepared by (A) forming an acidic homogeneous mixture comprising (a) an organic solvent solution of from 40 to 60 parts by weight of a resinous copolymeric siloxane containing silicon-bonded hydroxyl radicals and consisting essentially of (CH.sub. 3) 3 SiO 1/2 siloxane units and SiO 4/2 siloxane units wherein the ratio of the former to the latter, on a molar basis, has a value of from 0.6/1 to 0.9/1, and (b) 40 to 60 parts by weight of a methylhydrogenpolysiloxane having the formula Me 3 SiO(Me 2 SiO) x SiMe 3 wherein Me denotes the methyl radical and x has a value of from 35 to 70; and (B) heating the homogenous mixture to remove substantially all of the organic solvent therefrom.
Claim 5
Dependent Claim 13 words
A method according to claim 1 wherein the silicon compound is an alkoxysilane.
Claim 6
Dependent Claim 11 words
A method according to claim 4 wherein the alkoxysilane is methyltrimethoxysilane.
Claim 7
Dependent Claim 26 words
A method according to claim 1 wherein the carbonyl iron powder is heated to a temperature of 150° C. in the presence of the silicon compound.
Claim 8
Dependent Claim 145 words
A method according to claim 1 wherein the binder is a silicone binder comprising a liquid copolymeric organopolysiloxane containing SiO 4/2 siloxane units, SiH sites and SiOH sites which has been prepared by (A) forming an acidic homogeneous mixture comprising (a) an organic solvent solution of a resinous copolymeric siloxane containing silicon-bonded hydroxyl radicals and consisting essentially of R 3 SiO 1/2 siloxane units and SiO 4/2 siloxane units wherein the ratio of the former to the latter, on a molar basis, has a value of from 0.6/1 to 0.9/1 and each R denotes, independently, a monovalent hydrocarbon radical; and (b) a liquid organohydrogenpolysiloxane wherein each organic radical is, independently, a monovalent hydrocarbon radical, there being an average of at least one silicon-bonded hydrogen atom per molecule of said organohydrogenpolysiloxane; and, (B) heating the homogenous mixture to remove substantially all of the organic solvent therefrom.
Claim 9
Dependent Claim 153 words
A method according to claim 7 wherein the binder is a silicone binder comprising a liquid copolymeric organopolysiloxane containing SiO 4/2 siloxane units, SiH sites and SiOH sites which has been prepared by (A) forming an acidic homogeneous mixture comprising (a) an organic solvent solution of from 40 to 60 parts by weight of a resinous copolymeric siloxane containing silicon-bonded hydroxyl radicals and consisting essentially of (CH 3 ) 3 SiO 1/2 siloxane units and SiO 4/2 siloxane units wherein the ratio of the former to the latter, on a molar basis, has a value of from 0.6/1 to 0.9/1, and (b) 40 to 60 parts by weight of a methylhydrogenpolysiloxane having the formula Me 3 SiO(Me 2 SiO) x SiMe 3 wherein Me denotes the methyl radical and x has a value of from 35 to 70; and (B) heating the homogenous mixture to remove substantially all of the organic solvent therefrom.
Claim 10
Dependent Claim 9 words
The composition produced by the method of claim 1.

References Cited (Backward Citations)

US3628986A Cited
NL7012276A Cited
US4310678A Cited
US4322518A Cited
US4475946A Cited
JPS59107504A Cited
US4530894A Cited
US4601753A Cited
US4537829A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-03-15 1991-09-14 1992-03-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-03-15 1995-09-14 1996-03-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-03-15 1999-09-14 2000-03-15 $7700.00 Window Closed / Lapsed

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