Patent US4782008A successfully refreshed from Google Patents.
US4782008A
Expired / Lapsed
US
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Plasma-resistant polymeric material, preparation thereof, and use thereof
Assignee: International Business Machines Corp
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Filing: 1985-03-19
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Granted: 1988-11-01
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Expires: 2005-03-19
Abstract
Abstract Plasma-resistant polymeric materials are prepared by reacting a polymeric material containing reactive hydrogen functional groups with a multifunctional organometallic material containing at least two functional groups which are reactive with the reactive hydrogen functional groups of the polymeric material, such as hexamethylcyclotrisilazane.
Inventors
- 👤 Edward D. Babich
- 👤 Michael Hatzakis
- 👤 Scott L. Jacobs
- 👤 Juri R. Parasczcak
- 👤 Jane M. Shaw
- 👤 David F. Witman
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-25 22:27
CPC Classifications
G; G03; G03F; G03F7/00; G03F7/004; G03F7/038; G03F7/26; G03F7/265
Claims Analysis
Total Claims: 28
Claim 1
Independent Claim
128 words
A process which comprises: a. providing a layer of polymeric material wherein said polymeric material contains at least reactive hydrogen functional groups or reactive hydrogen functional precursor groups and when said polymeric material contains said precursor groups, converting said precursor groups to reactive hydrogen functional groups; b. then reacting at least a portion of said layer of polymeric material with a multifunctional organometallic material containing at least two functional groups which are reactive with the reactive groups of said polymeric material to thereby render the said at least portion of said layer resistant to oxygen plasma which is at least about 20 times greater than is the polymeric material before it is reacted with said organometallic material and; c. then subjecting said layer to a gas plasma atmosphere.
Claim 2
Dependent Claim
128 words
A process which comprises: a. providing a layer of polymeric material wherein said polymeric material contains at least reactive hydrogen functional groups or reactive hydrogen functional precursor groups and when said polymeric material contains said precursor groups, converting said precursor groups to reactive hydrogen functional groups; b. then reacting at least a portion of said layer of polymeric material with a multifunctional organometallic material containing at least two functional groups which are reactive with the reactive groups of said polymeric material to thereby render the said at least portion of said layer resistant to oxygen plasma which is at least about 20 times greater than is the polymeric material before it is reacted with said organometallic material and; c. then subjecting said layer to a gas plasma atmosphere.
Claim 3
Dependent Claim
15 words
The process of claim 1 wherein said gas plasma atmosphere is an oxygen-containing plasma atmosphere.
Claim 4
Dependent Claim
32 words
The process of claim 1 wherein the resistance to oxygen plasma is increased at least about 50 times, as compared to the polymeric material before it is reacted with the organometallic material.
Claim 5
Dependent Claim
32 words
The process of claim 1 wherein the increase in resistance to oxygen plasma is at least about 100 times that of the polymeric material before it is reacted with the organometallic material.
Claim 6
Dependent Claim
25 words
The process of claim 1 wherein at least about 25% of the thickness of the layer of polymeric material is reacted with the organometallic material.
Claim 7
Dependent Claim
25 words
The process of claim 1 wherein at least about 50% of the thickness of the layer of polymeric material is reacted with the organometallic material.
Claim 8
Dependent Claim
24 words
The process of claim 1 wherein at least substantially, the entire thickness of the layer of polymeric material is reacted with the organometallic material.
Claim 9
Dependent Claim
32 words
The process of claim 1 wherein said multifunctional organometallic material is provided as a liquid composition in a solvent for the organometallic material wherein the solvent is nonreactive with the organometallic material.
Claim 10
Dependent Claim
36 words
The process of claim 1 wherein that portion of the layer which is reacted contains at least about 1 part by weight of the metallic component of the organometallic material per 20 parts of polymeric material.
Claim 11
Dependent Claim
38 words
The process of claim 9 wherein that portion of the layer which is reacted contains up to 1 part by weight of the metallic component of the organometallic material per 2 parts by weight of the polymeric material.
Claim 12
Dependent Claim
35 words
The process of claim 1 wherein that portion of the layer which is reacted contains a ratio of a metallic component of the organometallic material to the polymeric material of about 1:15 to about 1:4.
Claim 13
Dependent Claim
13 words
The process of claim 1 wherein said organometallic material is an organosilicon material.
Claim 14
Dependent Claim
14 words
The process of claim 1 wherein said organometallic material is a cyclic organosilicon compound.
Claim 15
Dependent Claim
11 words
The process of claim 1 wherein said organometallic material is hexamethylcyclotrisilazane.
Claim 16
Dependent Claim
16 words
The process of claim 1 wherein said layer is about 0.4 to about 10 microns thick.
Claim 17
Dependent Claim
169 words
A process for rendering a polymeric material resistant to oxygen plasma which comprises: providing a polymeric material containing at least reactive hydrogen functional groups or reactive hydrogen functional precursor groups, and when said polymeric material contains said precursor groups, converting said precursor groups to reactive hydrogen functional groups and wherein said polymeric material is a phenolic-formaldehyde polymer; providing a liquid composition containing a multifunctional organosilicon material containing at least two functional groups which are reactive with the reactive functional groups of said phenolic-formaldehyde polymeric material, a solvent for said multifunctional organosilicon material wherein said solvent is nonreactive with said organosilicon material, and a solvent for said polymeric material in an amount effective to decrease the reaction time between said multifunctional organosilicon material and said polymeric material, and not sufficient to dissolve said polymeric material, and wherein said solvent for said polymeric material is not reactive with said multifunctional organosilicon material; and contacting said liquid composition with said polymeric material to thereby render said polymeric material resistant to oxygen plasma.
Claim 18
Dependent Claim
169 words
A process for rendering a polymeric material resistant to oxygen plasma which comprises: providing a polymeric material containing at least reactive hydrogen functional groups or reactive hydrogen functional precursor groups, and when said polymeric material contains said precursor groups, converting said precursor groups to reactive hydrogen functional groups and wherein said polymeric material is a phenolic-formaldehyde polymer; providing a liquid composition containing a multifunctional organosilicon material containing at least two functional groups which are reactive with the reactive functional groups of said phenolic-formaldehyde polymeric material, a solvent for said multifunctional organosilicon material wherein said solvent is nonreactive with said organosilicon material, and a solvent for said polymeric material in an amount effective to decrease the reaction time between said multifunctional organosilicon material and said polymeric material, and not sufficient to dissolve said polymeric material, and wherein said solvent for said polymeric material is not reactive with said multifunctional organosilicon material; and contacting said liquid composition with said polymeric material to thereby render said polymeric material resistant to oxygen plasma.
Claim 19
Dependent Claim
11 words
The process of claim 16 wherein said organosilicon material is hexamethylcyclotrisilazane.
Claim 20
Dependent Claim
19 words
The process of claim 17 wherein said reacting is carried out at about room temperature to about 75° C.
Claim 21
Dependent Claim
15 words
The process of claim 17 wherein said reacting is carried out at about 40° C.
Claim 22
Dependent Claim
168 words
A process for rendering a polymeric material resistant to oxygen plasma which comprises: providing a polymeric material containing at least reactive hydrogen functional groups or reactive hydrogen functional precursor groups, and when said polymeric material contains said precursor groups, converting said precursor groups to reactive hydrogen functional groups; providing a liquid composition containing a multifunctional organosilicon material containing at least two functional groups which are reactive with the reactive functional groups of said polymeric material, a solvent for said multifunctional organosilicon material wherein said solvent is nonreactive with said organosilicon material and is an aromatic hydrocarbon or substituted aromatic hydrocarbon, and a solvent for said polymeric material in an amount effective to decrease the reaction time between said multifunctional organosilicon material and said polymeric material, and not sufficient to dissolve said polymeric material, and wherein said solvent for said polymeric material is not reactive with said multifunctional organosilicon material; and contacting said liquid composition with said polymeric material to thereby render said polymeric material resistant to oxygen plasma.
Claim 23
Dependent Claim
168 words
A process for rendering a polymeric material resistant to oxygen plasma which comprises: providing a polymeric material containing at least reactive hydrogen functional groups or reactive hydrogen functional precursor groups, and when said polymeric material contains said precursor groups, converting said precursor groups to reactive hydrogen functional groups; providing a liquid composition containing a multifunctional organosilicon material containing at least two functional groups which are reactive with the reactive functional groups of said polymeric material, a solvent for said multifunctional organosilicon material wherein said solvent is nonreactive with said organosilicon material and is an aromatic hydrocarbon or substituted aromatic hydrocarbon, and a solvent for said polymeric material in an amount effective to decrease the reaction time between said multifunctional organosilicon material and said polymeric material, and not sufficient to dissolve said polymeric material, and wherein said solvent for said polymeric material is not reactive with said multifunctional organosilicon material; and contacting said liquid composition with said polymeric material to thereby render said polymeric material resistant to oxygen plasma.
Claim 24
Dependent Claim
34 words
The process of claim 20 wherein said organic solvent for the polymeric material is present in an amount of about 0.01 to about 25% by volume based on the total amount of organic solvent.
Claim 25
Dependent Claim
37 words
The process of claim 20 wherein said organic solvent for the polymeric material is present in an amount of about 0.25 to about 5% by volume based upon the total amount of organic solvent in the composition.
Claim 26
Dependent Claim
16 words
The process of claim 20 wherein said polymeric material is in the form of a layer.
Claim 27
Dependent Claim
31 words
The process of claim 20 wherein said organosilicon composition is a solution of hexamethylcyclotrisilazane in xylene containing a solvent for the polymeric material selected from the group of N-methylpyrrolidone and γ-butyrolactone.
Claim 28
Dependent Claim
13 words
The process of claim 24 wherein said polymeric material is a phenolic-formaldehyde polymer.
References Cited (Backward Citations)
US3652274A
Cited
GB1246704A
Cited
GB1367830A
Cited
US4007047A
Cited
GB1520466A
Cited
JPS527719A
Cited
US4125650A
Cited
US4289473A
Cited
US4307178A
Cited
US4373043A
Cited
US4426247A
Cited
US4493855A
Cited
US4489200A
Cited
US4502916A
Cited
US4430153A
Cited
US4507331A
Cited
GB2154330A
Cited
US4552833A
Cited
US4521274A
Cited
JPS6129214A
Cited
US4551418A
Cited
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| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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