Patent US4190714A successfully refreshed from Google Patents.
US4190714A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Powder coating resin process containing an aromatic carbonamide condensate
Assignee: Monsanto Co
•
Filing: 1978-03-17
•
Granted: 1980-02-26
•
Expires: 1998-03-17
Abstract
Abstract A process for preparing a free-flowing curable powder resin composition with a sintering temperature above 40 DEG C., comprising the steps of condensing a methylolurea or methylolaminotriazine with an aliphatic alcohol and a reactive compound containing hydroxyl or amide groups; blending the condensate with a polyester or polyacrylate; and grinding the blend to a powder of average particle size in the range of 20 to 150 microns.
Inventors
- 👤 Robert A. Isaksen
- 👤 Frederic J. Locke
- 👤 John L. Smith
- 👤 George T. Spitz
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 09:04
CPC Classifications
C; C09; C09D; C09D133/00; C08; C08G; C08G12/00; C08G12/02; C08G12/04; C08G12/043; C08G12/046; C08G12/26; C08G12/34; C08G12/40; C08G12/42; C09D167/00; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31678; Y10T428/31681
Claims Analysis
Total Claims: 6
Claim 1
Independent Claim
338 words
A process for preparing a curable powder resin composition with a sintering temperature above 40° C. and curable in the temperature range of 120° to 220° C., comprising: (A) Condensing a methylolamino compound with an aliphatic alcohol and an aromatic carbonamide of number average molecular weight less than 500 to produce an aminoplast condensate with a glass transition temperature in the range of -10° C. to 100° C., wherein the methylolamino compound is selected from the group consisting of methylolureas and methylolaminotriazines and contains no more than one unmethylolated N--H bond per molecule, wherein the aliphatic alcohol contains from 1 to 4 carbon atoms, wherein at least about 50 percent of the methylol groups of the methylolamino compound have been condensed with the aliphatic alcohol or the aromatic carbonamide, wherein the molar ratio of the aliphatic alcohol to the methylolamino compound is at least 2, and wherein the molar ratio of the methylolamino compound to the aromatic carbonamide is from about 1:0.5 to about 1.2 when the aromatic carbonamide contains one reactive group per molecule and is from about 1:0.5 to about 1:1.5 when the aromatic carbonamide contains 2 or more reactive groups per molecule, (B) Blending from about 15 to about 30 parts by weight of the aminoplast condensate with from about 85 to 70 parts by weight of a polyester resin or an acrylic resin, wherein the resin has a glass transition temperature in the range of from 60° to 100° C. and a number average molecular weight in the range of 500 to 25,000 and contains alcoholic hydroxyl groups, carboxyl groups or amide groups heat reactive with the aminoplast condensate, wherein the polyester resin has an acid number in the range of 1 to 25 or a hydroxyl number in the range of 11 to 200, and wherein the acrylic resin contains from 0.13 to 18 weight percent of hydroxyl, carboxyl or amide groups, and (C) Crushing the blend to form a powder of average particle size in the range of 20 to 150 microns.
Claim 2
Dependent Claim
338 words
A process for preparing a curable powder resin composition with a sintering temperature above 40° C. and curable in the temperature range of 120° to 220° C., comprising: (A) Condensing a methylolamino compound with an aliphatic alcohol and an aromatic carbonamide of number average molecular weight less than 500 to produce an aminoplast condensate with a glass transition temperature in the range of -10° C. to 100° C., wherein the methylolamino compound is selected from the group consisting of methylolureas and methylolaminotriazines and contains no more than one unmethylolated N--H bond per molecule, wherein the aliphatic alcohol contains from 1 to 4 carbon atoms, wherein at least about 50 percent of the methylol groups of the methylolamino compound have been condensed with the aliphatic alcohol or the aromatic carbonamide, wherein the molar ratio of the aliphatic alcohol to the methylolamino compound is at least 2, and wherein the molar ratio of the methylolamino compound to the aromatic carbonamide is from about 1:0.5 to about 1.2 when the aromatic carbonamide contains one reactive group per molecule and is from about 1:0.5 to about 1:1.5 when the aromatic carbonamide contains 2 or more reactive groups per molecule, (B) Blending from about 15 to about 30 parts by weight of the aminoplast condensate with from about 85 to 70 parts by weight of a polyester resin or an acrylic resin, wherein the resin has a glass transition temperature in the range of from 60° to 100° C. and a number average molecular weight in the range of 500 to 25,000 and contains alcoholic hydroxyl groups, carboxyl groups or amide groups heat reactive with the aminoplast condensate, wherein the polyester resin has an acid number in the range of 1 to 25 or a hydroxyl number in the range of 11 to 200, and wherein the acrylic resin contains from 0.13 to 18 weight percent of hydroxyl, carboxyl or amide groups, and (C) Crushing the blend to form a powder of average particle size in the range of 20 to 150 microns.
Claim 3
Dependent Claim
38 words
The process of claim 1 wherein the methylolamino compound is a methylolmelamine, a methylolurea or a or a methylolbenzoguanamine, and wherein the aromatic carbonamide is selected from the group consisting of benzamide, terephthalamide and o-, m- and p-toluamide.
Claim 4
Dependent Claim
18 words
The process of claim 2 wherein the methylolamino compound is a methylolmelamine and the aliphatic alcohol is methanol.
Claim 5
Dependent Claim
31 words
The process of claim 1 wherein the aminoplast condensate and the polyester resin or acrylic resin are blended at a temperature slightly above the melting point of the higher melting component.
Claim 6
Dependent Claim
54 words
The process of claim 1 wherein the molar ratio of the methylolamino compound to the aromatic carbonamide is from about 1:1 to about 1:2 when the aromatic carbonamide contains one reactive group per molecule and is from about 1:0.5 to about 1:1 when the aromatic carbonamide contains 2 or more reactive groups per molecule.
References Cited (Backward Citations)
GB766819A
Cited
US3303168A
Cited
US3557031A
Cited
US3808167A
Cited
US3806480A
Cited
US3759854A
Cited
US3804920A
Cited
US3919352A
Cited
US3842021A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1983-02-25 | 1983-08-27 | 1984-02-26 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1987-02-25 | 1987-08-27 | 1988-02-26 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1991-02-25 | 1991-08-27 | 1992-02-26 | $7700.00 | Window Closed / Lapsed |