US3936582A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Differential release coated articles
Assignee: HP SMITH Inc A Corp OF
•
Filing: 1974-06-03
•
Granted: 1976-02-03
•
Expires: 1994-06-03
Abstract
Abstract This invention relates to low release value polyorganosiloxane coatings comprising a mixture of (a) polyorganosiloxanes having silicon-bonded hydroxyl groups on the ends of the molecule, and (b) polymethylhydrogensiloxanes having an average of at least 3 SiH groups per molecule, and high release value polyorganosiloxane coatings comprising a mixture of (a) and (b) together with polyorganosiloxanes containing triorganosiloxy end groups. The use of the improved high release value coating for coating one side of a differential release paper or laminate where the paper or laminate is stacked or rolled for storage so that there is contact with the opposite side of the differential release paper which is coated with the lower release value coating reduces the migration of high release value coating to the low value coating in contact thereby improving shelf life of the differential release paper.
Inventors
- 👤 LeRoy H. Keiser
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 20:41
CPC Classifications
C; C09; C09D; C09D183/00; C09D183/04; C08; C08J; C08J7/00; C08J7/04; C08J7/0427; C08J7/043; C08K; C08K5/00; C08K5/04; C08K5/09; C08K5/14; C08L; C08L83/00; C08L83/04; C09J; C09J7/00; C09J7/40; C09J7/401; D; D21; D21H; D21H19/00; D21H19/10; D21H19/14; D21H19/24; D21H19/32; D21H19/80; D21H19/82; D21H19/824; D21H19/84; D21H27/00; D21H27/001; C08J2323/00; C08J2323/02; C08J2323/04; C08J2323/06; C08J2483/00; C09J2400/00; C09J2400/20; C09J2400/26; C09J2400/263; C09J2423/00; C09J2423/006; C09J2483/00; C09J2483/005; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31652; Y10T428/31663; Y10T428/31971; Y10T428/31993
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
193 words
A differential release coated article comprising a substrate coated on one side with I. a low release value cured polyorganosiloxane coating comprising a mixture of a. a polyorganosiloxane having silicon-bonded hydroxyl groups on the ends of the molecule, b. a polymethylhydrogensiloxane having an average of at least three SiH groups per molecule and c. a functional amount sufficient to effect curing of said polyorganosiloxane of a carboxylic acid salt of an organic metallic compound selected from lead, zinc, iron or tin; and coated on the opposite side with Ii. a high release cured polyorganosiloxane coating comprising a mixture of d. a polyorganosiloxane having silicon-bonded hydroxyl groups on the ends of the molecule, e. a polymethylhydrogensiloxane having an average of at least three SiH groups per molecule, f. a three-dimensional highly cross-linked polyorganosiloxane containing triorganosiloxy end groups in which the ratio of the monovalent hydrocarbon radicals to SiO 2 units ranges from about 1.5:1 to about 3:1, and g. a curing catalyst mixture comprising a functional amount sufficient to effect curing of said polyorganosiloxane of a carboxylic acid salt of an organometallic compound selected from lead, zinc, iron or tin and an organic peroxide.
Claim 2
Dependent Claim
193 words
A differential release coated article comprising a substrate coated on one side with I. a low release value cured polyorganosiloxane coating comprising a mixture of a. a polyorganosiloxane having silicon-bonded hydroxyl groups on the ends of the molecule, b. a polymethylhydrogensiloxane having an average of at least three SiH groups per molecule and c. a functional amount sufficient to effect curing of said polyorganosiloxane of a carboxylic acid salt of an organic metallic compound selected from lead, zinc, iron or tin; and coated on the opposite side with Ii. a high release cured polyorganosiloxane coating comprising a mixture of d. a polyorganosiloxane having silicon-bonded hydroxyl groups on the ends of the molecule, e. a polymethylhydrogensiloxane having an average of at least three SiH groups per molecule, f. a three-dimensional highly cross-linked polyorganosiloxane containing triorganosiloxy end groups in which the ratio of the monovalent hydrocarbon radicals to SiO 2 units ranges from about 1.5:1 to about 3:1, and g. a curing catalyst mixture comprising a functional amount sufficient to effect curing of said polyorganosiloxane of a carboxylic acid salt of an organometallic compound selected from lead, zinc, iron or tin and an organic peroxide.
Claim 3
Dependent Claim
110 words
A coated article according to claim 1 wherein said low release value polyorganosiloxane coating comprises a mixture of a. 90 to 99 weight percent of a polyorganosiloxane having siliconbonded hydroxyl groups on the ends of the molecule, said polymer having a viscosity of at least about 2,000 centistokes (cs) at 25°C and said polymer being composed of polymer units of the formula R n SiO 4 -n/2 in which each R is selected from the group consisting of monovalent hydrocarbon radicals and n has an average value of 2, and b. 1 to 10 weight percent of a polymethylhydrogensiloxane having an average of at least three SiH groups per molecule.
Claim 4
Dependent Claim
169 words
A coated article according to claim 1 wherein the high release value polyorganosiloxane coating comprises a mixture of d. 90 to 99 weight percent of a polyorganosiloxane having silicon-bonded hydroxyl groups on the ends of the molecule, said polymer having a viscosity of at least about 2,000 centistokes (cs) at 25°C and said polymer being composed of polymer units of the formula R n SiO 4 -n/2 in which each R is selected from the group consisting of monovalent hydrocarbon radicals and n has an average value of 2, e. 1 to 10 weight percent of a polymethylhydrogensiloxane having an average of at least three SiH groups per molecule, and f. a polyorganosiloxane which contains triorganosiloxy end groups and which has a molecular weight in the range of about 2,000 to about 40,000 and is resinous in nature due to its three-dimensional, highly cross-linked structure, the ratio of (f) to the mixture of (d) and (e) ranging from about 0.01 to 1 to about 0.2 to 1 by weight.
Claim 5
Dependent Claim
70 words
A coated article according to claim 1 wherein the low release value polyorganosiloxane coating contains a functional curing amount of a carboxylic acid salt of an organometallic compound selected from lead, zinc, iron and tin, and the high release polyorganosiloxane coating contains as a curing agent a mixture of a carboxylic acid salt of an organometallic compound selected from lead, zinc, iron or tin in combination with an organic peroxide.
Claim 6
Dependent Claim
23 words
A differential release coated article according to claim 1 wherein at least one of coating (I) or coating (II) contains a filler material.
Claim 7
Dependent Claim
25 words
A differential release coated article according to claim 1 wherein the substrate is a fibrous material coated on at least one side with a polyolefin.
Claim 8
Dependent Claim
31 words
A differential release coated article according to claim 6 wherein said polyolefin has been subjected to a surface treatment to activate said polyolefin coating prior to application of the polyorganosiloxane coatings.
Claim 9
Dependent Claim
38 words
A coated article according to claim 1 in which the low release value polyorganosiloxane coating (I) contains organotin as the curing agent and the high release value polyorganosiloxane coating (II) contains organotin and a peroxide as curing agent.
Claim 10
Dependent Claim
38 words
A coated article according to claim 8 wherein the organotin used as the curing agent in each of the coatings (I) and (II) is dibutyltin di(2-ethylhexoate) and the peroxide in the high release coating (II) is 2,4-dichlorobenzoyl peroxide.
Claim 11
Dependent Claim
135 words
A coated article according to claim 3 wherein the low release value polyorganosiloxane coating comprises a mixture of a. 90 to 99 weight percent of a polyorganosiloxane having silicon-bonded hydroxyl groups on the ends of the molecule, said polymer having a viscosity of at least about 2,000 centistokes (cs) at 25°C and said polymer being composed of polymer units of the formula R.sub.n SiO.sub.4.sub.-n/2 in which each R is selected from the group consisting of monovalent hydrocarbon radicals and n has an average value of 2, b. 1 to 10 weight percent of a polymethylhydrogensiloxane having an average of at least three SiH groups per molecule, and c. a functional amount sufficient to effect curing of said polyorganosiloxane of a carboxylic acid salt of an organic metallic compound selected from lead, zinc, iron, or tin.
References Cited (Backward Citations)
US3419508A
Cited
US3432333A
Cited
US3403045A
Cited
US3503782A
Cited
US3628996A
Cited
US3749593A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1979-02-02 | 1979-08-04 | 1980-02-03 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-02-02 | 1983-08-04 | 1984-02-03 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-02-02 | 1987-08-04 | 1988-02-03 | $7700.00 | Window Closed / Lapsed |