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US4467081A Expired / Lapsed US ⏱️ 0.0 years remaining

Gelable, silicate rich resins from hydrophobic polyols and volatile and/or incompatible organosilicates

Assignee: PPG Industries Inc
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Filing: 1983-01-31
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Granted: 1984-08-21
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Expires: 2003-01-31
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Abstract

Abstract Disclosed is a resin comprising a reaction product prepared by partially reacting to homogeneity a hydrophobic polyol and an organosilicon-containing material comprising an organosilicon-containing substance. The organosilicon-containing substance has atoms bonded directly to silicon, all of which atoms are selected from oxygen, nitrogen, and/or chlorine, and additionally has moieties directly bonded to silicon which are easily displaceable by reaction with water and/or alcohol. At least a part of the organosilicon-containing substance is hydrolyzed. The reaction product is homogeneous and contains residual hydroxyl moieties from the hydrophobic polyol and residual moieties bonded directly to silicon which are easily displaceable. the reaction product is capable of self-curing, optionally with a catalyst, by reaction with moisture and/or with the residual hydroxyl moieties, of the residual moieties directly bonded to silicon which are easily displaceable.

Inventors

  • 👤 Wen-Hsuan Chang
  • 👤 David T. McKeough
  • 👤 John R. Peffer

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 04:08
CPC Classifications
C; C09; C09D; C09D183/00; C09D183/14; C08; C08G; C08G77/00; C08G77/42; C08G77/48; C08G77/50; C09D183/10

Claims Analysis

Total Claims: 20
Claim 1
Independent Claim 253 words
A liquid composition comprising a reaction product prepared by partially reacting to homogeneity: (A) at least one hydrophobic polyol essentially free of modification by fatty acid; and (B) an organosilicon-containing material comprising (1) at least one organosilicon-containing substance free of functional groups attached directly to carbon and essentially free of alkali metal ions, having atoms bonded directly to Si, all of said atoms being selected from the group consisting of O, N and/or Cl, said organosilicon-containing substance additionally having moieties directly bonded to Si which are easily displaceable by reaction with water and/or alcohol, wherein at least a part of said organosilicon-containing substance is hydrolyzed to a compound or mixture of compounds, said compound or mixture of compounds containing a residual amount of the moieties directly bonded to Si which are easily displaceable by reaction with water and/or alcohol; (2) optionally a nonfunctional organosilane, a hydrolyzed nonfunctional organosilane, or a mixture thereof; and (3) optionally a functional organosilane, a hydrolyzed functional organosilane, or a mixture thereof; wherein said reaction product is homogeneous and contains (i) residual moieties from the organosilicon-containing material which are directly bonded to Si and are easily displaceable by reaction with water and/or alcohol and (ii) residual hydroxyl moieties from the hydrophobic polyol; and said reaction product is capable of self curing to a continuous film by reaction of (i) said residual moieties from the organosilicon-containing material which are directly bonded to Si and are easily displaceable, with moisture and/or with (ii) said residual hydroxyl moieties from the hydrophobic polyol.
Claim 2
Dependent Claim 253 words
A liquid composition comprising a reaction product prepared by partially reacting to homogeneity: (A) at least one hydrophobic polyol essentially free of modification by fatty acid; and (B) an organosilicon-containing material comprising (1) at least one organosilicon-containing substance free of functional groups attached directly to carbon and essentially free of alkali metal ions, having atoms bonded directly to Si, all of said atoms being selected from the group consisting of O, N and/or Cl, said organosilicon-containing substance additionally having moieties directly bonded to Si which are easily displaceable by reaction with water and/or alcohol, wherein at least a part of said organosilicon-containing substance is hydrolyzed to a compound or mixture of compounds, said compound or mixture of compounds containing a residual amount of the moieties directly bonded to Si which are easily displaceable by reaction with water and/or alcohol; (2) optionally a nonfunctional organosilane, a hydrolyzed nonfunctional organosilane, or a mixture thereof; and (3) optionally a functional organosilane, a hydrolyzed functional organosilane, or a mixture thereof; wherein said reaction product is homogeneous and contains (i) residual moieties from the organosilicon-containing material which are directly bonded to Si and are easily displaceable by reaction with water and/or alcohol and (ii) residual hydroxyl moieties from the hydrophobic polyol; and said reaction product is capable of self curing to a continuous film by reaction of (i) said residual moieties from the organosilicon-containing material which are directly bonded to Si and are easily displaceable, with moisture and/or with (ii) said residual hydroxyl moieties from the hydrophobic polyol.
Claim 3
Dependent Claim 96 words
The liquid composition of claim 1 wherein said moieties directly bonded to Si which are easily displaceable by reaction with water and/or alcohol are selected from the group consisting of ##STR16## and the C 2 to C 3 residue of a 1,2- or 1,3-glycol, wherein R 1 represents C 1 -C 3 alkyl, R 2 represents H or C 1 -C 4 alkyl, R 3 and R 4 independently represent H, C 1 -C 4 alkyl, C 6 -C 8 cycloalkyl or C 6 -C 8 aryl, and R 5 represents C 4 -C 7 alkylene.
Claim 4
Dependent Claim 20 words
The liquid composition of claim 1 wherein all atoms directly bonded to Si of said organosilicon-containing substance are oxygen atoms.
Claim 5
Dependent Claim 37 words
The liquid composition of claim 1 wherein said moieties directly bonded to Si which are easily displaceable by reaction with water and/or alcohol are lower alkoxy moieties selected from the group consisting of methoxy, ethoxy and propoxy.
Claim 6
Dependent Claim 17 words
The liquid composition of claim 1 wherein said hydrophobic polyol is essentially free of phenolic hydroxyl moieties.
Claim 7
Dependent Claim 16 words
The liquid composition of claim 1 wherein said hydrophobic polyol is essentially free of 1,2-epoxy moieties.
Claim 8
Dependent Claim 19 words
The liquid composition of claim 1 wherein at least a part of said hydrophobic polyol contains novicinal hydroxyl groups.
Claim 9
Dependent Claim 14 words
The liquid composition of claim 4 wherein said lower alkoxy moieties are ethoxy moieties.
Claim 10
Dependent Claim 20 words
The liquid composition of claim 1 wherein said hydrophobic polyol has a hydroxyl equivalent weight of from 45 to 1000.
Claim 11
Dependent Claim 39 words
The liquid composition of claim 1 wherein said organosilicon-containing material comprises from 50 to 100 percent by weight, based on the total weight of said organosilicon-containing material, of said organosilicon-containing substance at least a portion of which is hydrolyzed.
Claim 12
Dependent Claim 13 words
The liquid composition of claim 1 wherein said hydrophobic polyol comprises a diol.
Claim 13
Dependent Claim 20 words
The liquid composition of claim 1 wherein said hydrophobic polyol has a hydroxyl equivalent weight of from 59 to 600.
Claim 14
Dependent Claim 34 words
The liquid composition of claim 1 wherein said hydrophobic polyol is selected from the group consisting of simple diols, triols, and higher hydric alcohols; polyester polyols; polyether polyols; amide containing polyols; and polyurethane polyols.
Claim 15
Dependent Claim 77 words
The liquid composition of claim 1 wherein said organosilicon-containing material comprises from greater than 2 to less than 80 percent by weight based on the total weight of said organosilicon-containing material of a nonfunctional organosilane, a hydrolyzed nonfunctional organosilane, or a mixture thereof, and optionally from greater than 2 to less than 50 percent by weight based on the total weight of said organosilicon-containing material of a functional organosilane, a hydrolyzed functional organosilane, or a mixture thereof.
Claim 16
Dependent Claim 53 words
The liquid composition of claim 14 wherein said organosilicon-containing material comprises a hydrolyzed mixture of at least a part of said organosilicon-containing substance; at least a part of said nonfunctional organosilane, hydrolyzed nonfunctional organosilane, or mixture thereof; and optionally, at least a part of said functional organosilane, hydrolyzed functional organosilane, or mixture thereof.
Claim 17
Dependent Claim 31 words
The liquid composition of claim 4 wherein said reaction product has a content of lower alkoxy moieties ranging from 20 milliequivalents per gram to 0.5 milliequivalents per gram of reaction product.
Claim 18
Dependent Claim 30 words
The liquid composition of claim 16 wherein said reaction product has a content of hydroxyl moieties ranging from 0.5 milliequivalents per gram to 20 milliequivalents per gram of reaction product.
Claim 19
Dependent Claim 39 words
The liquid composition of claim 1 additionally comprising an organic solvent, said composition having a percent by weight solids content of at least 50 percent by weight based on the total weight of resin solids present in said composition.
Claim 20
Dependent Claim 108 words
The liquid composition of claim 1 which gels when subjected to a three-step gel test consisting of (1) heating a 10 gram sample of said reaction product in a glass jar covered with a cap at 149° C. for 120 minutes, followed by (2) heating said sample at 149° C. for 120 minutes in the presence of 0.5 grams of stannous octoate in said glass jar with a vent hole covered by a piece of masking tape in said cap, followed by (3) repeating step 2 except that no additional stannous octoate is introduced into said sample and said heating is conducted at a temperature of 204° C.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-08-21 1988-02-20 1988-08-21 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-08-21 1992-02-20 1992-08-21 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-08-21 1996-02-20 1996-08-21 $7700.00 Window Closed / Lapsed

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