US1638579A - Coating compositions - Google Patents
Coating compositions Download PDFInfo
- Publication number
- US1638579A US1638579A US680343A US68034323A US1638579A US 1638579 A US1638579 A US 1638579A US 680343 A US680343 A US 680343A US 68034323 A US68034323 A US 68034323A US 1638579 A US1638579 A US 1638579A
- Authority
- US
- United States
- Prior art keywords
- oil
- resin
- glycerol
- mixture
- copal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000008199 coating composition Substances 0.000 title description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 50
- 239000003921 oil Substances 0.000 description 27
- 235000019198 oils Nutrition 0.000 description 27
- 239000000203 mixture Substances 0.000 description 24
- 239000011347 resin Substances 0.000 description 23
- 229920005989 resin Polymers 0.000 description 23
- 239000002383 tung oil Substances 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 11
- 235000015112 vegetable and seed oil Nutrition 0.000 description 11
- 239000008158 vegetable oil Substances 0.000 description 11
- 239000007788 liquid Substances 0.000 description 10
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 9
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 9
- 125000005456 glyceride group Chemical group 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
- 241000350151 Guibourtia demeusei Species 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 210000003298 dental enamel Anatomy 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004859 Copal Substances 0.000 description 4
- 241000782205 Guibourtia conjugata Species 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 229920001800 Shellac Polymers 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 235000013874 shellac Nutrition 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- 240000000972 Agathis dammara Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- -1 glycerol ester Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D191/00—Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
- C09D191/005—Drying oils
Definitions
- This invention relates to coating compositions, and its object is to produce a li uidcoating composition which may be rea ily applied toan article and baked thereon to 5 form a hard, tough, flexible and durable coating.
- liquid coating composition which is of such nature that itmay be rapidly baked one metallic article.
- an eleetricalconductor to form a hard enamel which *is" flexible and inert to solvents, and whichhas' good insulating properties v r
- polymerized vegetable oil' is used as the basis of a liquid coatlng composition.
- the vegetable oils which have been found most suitable are those such as tung oil and castor oil whichhavetheprop' 0 erties of polymerizing and thereafter gelatinizing when heated.
- Such oils give the best results when polymerizedto a state ust short of gelatinization.
- the oil maybe heated in the presence of some: 'embstanc'e, such g as,
- rosin oil which will delay or prevent its gelatinization as set forth in my copendin'g' application,' erial No. 633,322, filed April 19, 1923.
- a liquid coating composition prepared from vegetable oils alone is slow baking the polymerized oil is mixed with certain substances which will decrease the time required to bake it on a metallic article, and which will for this reason considerably reduce the cost which have been found most satisfactory for this purpose are certainresin glycerides.
- a ,resin such as Congo copalmight be used; but it has been found preferable to 4 use the glyceride of such a resin, both be:
- the substances cause it may be transformed by heat into' verts the acid bodies ofthe resin into 'sub-' WYQ K -F @Q H N or s s me q v v etable Oils" gelatinize,.l*it. is; deslrabl'eto ad during he e r fi io of.
- he resin a substance such as rosin oil which- '55 will maintain the glyceride's in :an unge producing a liquid coating composition which contains a minimum amount of acid bodies likely to attack'the to, form inetallic'soa s; f w ese soaps tends-toma fe' the] coating less flexible, whenj'hea'ted "to '-'a” degree at which it has the nee inert.
- composition' then spread on the metallic
- Tun oil (Chinese wood oil) is treated in any 0 the following ways:
- a glyceride of Congo copal is formed 1n any of the following ways:
- the tung oil prepared as in (a), above is then mixed with the resin glyceride as in one of the foregoing examples in approximately the following proportions:
- Castor oil, corn oil, soya bean oil, rapeseed oil, sesame oil, cottonseed oil and peanut oil may be used in place of either the tung oil or the linseed oil and either of these two oils may replace the other.
- Other resin oils may be used in place of the rosin oil.
- Manila copal and shellac are examples of other resins which will form gelatinizable esters with glycerol and are best adapted for use in this invention.
- gelatinization as used herein is intended to describe the sudden thickening that occurs when vegetable oils or resin glycerides are polymerized beyond a certain degree by heat, as contrasted with the very gradual thickening which occurs during the precedin polymerization.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Description
Patented j. e,t192
em 1). nocxnn; or Ener cannon, isnw'e nnsnghssrcnon 'ro wnsrnnn comm, mconrona'rnnzor 80 Drawing,
This invention relates to coating compositions, and its object is to produce a li uidcoating composition which may be rea ily applied toan article and baked thereon to 5 form a hard, tough, flexible and durable coating. v
In particular it is desired-to produce a liquid coating composition which is of such nature that itmay be rapidly baked one metallic article. such as an eleetricalconductor to form a hard enamel which *is" flexible and inert to solvents, and whichhas' good insulating properties v r In accordance with the general features of the invention, polymerized vegetable oil' is used as the basis of a liquid coatlng composition. The vegetable oils which have been found most suitable are those such as tung oil and castor oil whichhavetheprop' 0 erties of polymerizing and thereafter gelatinizing when heated. Such oils give the best results when polymerizedto a state ust short of gelatinization. To realize this state of polymerization, the oil maybe heated in the presence of some: 'embstanc'e, such g as,
rosin oil, which will delay or prevent its gelatinization as set forth in my copendin'g' application,' erial No. 633,322, filed April 19, 1923. Vegetable oils prepared in this; way may be spread upon a metallic article and baked thereon to form a hard, flexible insulating enamel. Inasmuch 'as a liquid coating composition prepared from vegetable oils alone is slow baking the polymerized oil is mixed with certain substances which will decrease the time required to bake it on a metallic article, and which will for this reason considerably reduce the cost which have been found most satisfactory for this purpose are certainresin glycerides. A ,resin such as Congo copalmight be used; but it has been found preferable to 4 use the glyceride of such a resin, both be:
a hard substance at a. temperature similar to that at :which vegetable oils are thus transformed, and because the glycerol constances which are'more inert chemically. As
s is; k
.such' gasses; as 1.
' that "certain to zized, liquid condition; One feature of the inventionficons'ists' during the bakin T e presence oft and baked" o article and baked.
of coating 'such' articles. The substances cause it may be transformed by heat into' verts the acid bodies ofthe resin into 'sub-' WYQ K -F @Q H N or s s me q v v etable Oils" gelatinize,.l*it. is; deslrabl'eto ad during he e r fi io of. he resin a substance such as rosin oil which- '55 will maintain the glyceride's in :an unge producing a liquid coating composition which contains a minimum amount of acid bodies likely to attack'the to, form inetallic'soa s; f w ese soaps tends-toma fe' the] coating less flexible, whenj'hea'ted "to '-'a" degree at which it has the nee inert.
'ness to solvents, p V Afterthe add'tion of the glycerid, thv mixture should be" heated over a period of tlme, and, solvents, added, if,necessary,'.iin. order that the resulting composition will" produceasmooth coating whe reapplied.to?-
the metallic article. The
composition'is then spread on the metallic Such 'a' composition ba esrapi y-..--at .a temperature similar to that at which vege-' table oil hardens', which is hard enough to withstand thejtreatment to which electricalconductors are normally subjected, which. 'has a tou hness greater than that of an enamel forme 'from' vegetable oil alone, which-is soflexible that V a wire coated therewith may besha 1y bent without cracking the.' enamel, an d which has good. insulating fproperties. .Furthermore, this enamelis very resistant to the solvent actionoffthe benzol or carbon tetrav chloride contained in cleaning fluids commonly used upon; enameled conductors of v the linseedoil in certain varnishes with which enameled conductors are often coated of the denatured alcohol used in shellacs, of the resin-rosin oil combinations or the parafin used in the melted moistnre-proofin compositions with which coils of enamele wireare often impregnated, or of the gase line or: benzene contained in various liquids me allic article H and forms-Y'anenamel processes are given below to enable thein-Q vention to be more readily practiced. When proportions are given they are by weight" unless otherwise stated.
Tun oil (Chinese wood oil) is treated in any 0 the following ways:
(a) Equal parts of-tung oil and IOSlIl 011 are mixed and the mixture heated at a temperature between 210 C. and 220 C. for about two hours.
A glyceride of Congo copal is formed 1n any of the following ways:
(a) Two or more parts of ros1n 011 (preferably having a high boiling point) are added to one part of Congo copal and the mixture heated at between 275 C. and 300 C. for two hours or until the copal is entirely fused. One gallon of glycerol for each fourteen pounds of Congo copal is then added to the mixture and the temperature maintained at between 280 C. and 300 C. for about one hour. At the completion of this heating, the mass will still contain a considerable amount of uncombined copal and the above treatment with glycerol is reeated until the acid number of the mixture is reduced to about 10. If apparatus is used which will prevent to a certain extent the volatilization of the glycerol, all the glycerol may be added at once. During the treatment with glycerol the proportions of rosin oil to the copal should be maintained at not less than two to one.
(6') Congo copal is fused until it has lost twenty percent to thirty-five percent of its weight. To one part of this fused copal is added two parts of rosin oil. Glycerol is then added, and the process continued in either of the ways indicated in (a') above.
(0) Congo copal is fused with an e ual proportion of rosin, the resultant pro uct heated with glycerol, preferably in the presence of rosin oil and the process continued as in (a') above.
((2') Three parts of Congo copal are fused as described in my Patent 1,422,861 of July 18, 1922, with two parts of those fatty acids derived from tung oil by saponification. Sufficient glycerol to neutralize both the resin and the fatty acid is then added and the mixture heated, preferably in the presence of rosin oil, in the manner described in (a) above. A certain amount of tung oil is formed from the glycerol and the tung oil fatty-acids and is polymerized by the heating. 1,
The tung oil prepared as in (a), above is then mixed with the resin glyceride as in one of the foregoing examples in approximately the following proportions:
Four parts of treated tung oil to one part of resin glyceride prepared as in (a), (b'),
or Sf) T ree parts of treated tung oil to one part of the mixture o'f resin glyceride and six hours, when a suitable proportion of volatile solvent such as benzine or Hi-flashnaphtha is added. This composition is applied to the article to be coated and is baked thereon at or about a temperature of about300 C. to drive off the benzene or naphtha, any excess of lycerol, and the rosin oil, and to harden t e coating. If a thicker coating is desired, the application and baking of the composition may .be repeated as manytimes as necessary.
Any substance which will erform a like function should be considere as the equivalent of any of the substances mentioned in the specific examples described above.
Castor oil, corn oil, soya bean oil, rapeseed oil, sesame oil, cottonseed oil and peanut oil, for instance, may be used in place of either the tung oil or the linseed oil and either of these two oils may replace the other. Other resin oils may be used in place of the rosin oil.
Manila copal and shellac are examples of other resins which will form gelatinizable esters with glycerol and are best adapted for use in this invention.
The term gelatinization as used herein is intended to describe the sudden thickening that occurs when vegetable oils or resin glycerides are polymerized beyond a certain degree by heat, as contrasted with the very gradual thickening which occurs during the precedin polymerization.
What 1s claimed is:
1. The process of forming an insulating enamel which comprises heating gelatinizable vegetable oil inthe presence of a substance which will delay the gelatinization thereof, heatin together a resin, resin oil and lycerol mlxing the products so formed, heatmg the resulting mass and diluting the mass with a volatile material.
- 2. The process of forming a liquid coating composition which com rises heating tung oil with a mixture 0 glycerol and resin oil, heatin glycerol with a mixture of Congo copal and resin oil, mixing the products so formed and heating the mixture.
3. The process of producing a 1i uid coating composition which comprises eating a mixture of tung oil and resin oil with a quantity of glycerol less than said tung oil and mixing therewith a resin glyceride.
4. The process of forming a liquid coating composition which comprises heating a mixture of resin oil and gelatinizable vegetable oil, mixing therewith a substance to give a quick baking quality to said coating composition, and heatmg the mixture.
5. The process of forming a liquid coating composition which comprises neutralizing the acid bodies of a substance having a quick baking quality with glycerol, heating a mixture 0 gelatinizable vegetable oil and resin oil, mixing the product so formed, and
heating the resulting mixture.
6. The process of producing a liquid coating composition which comprises heating resin and resin oil, adding thereto sufficient glycerol to produce a glycerol ester of said resin having a loW acid number, and heat- 10 in the resulting mixture, heating gelatinizab e vegetable oil in the presence of resin oil, mixing the product so formed, and heating the resulting mass.
In witness whereof, I hereunto subscribe my name this 11 day of December, A. D. 1923.
CARL D. HOCKER.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US680343A US1638579A (en) | 1923-12-13 | 1923-12-13 | Coating compositions |
| US41880A US1634359A (en) | 1923-12-13 | 1925-07-06 | Coating composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US680343A US1638579A (en) | 1923-12-13 | 1923-12-13 | Coating compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1638579A true US1638579A (en) | 1927-08-09 |
Family
ID=24730706
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US680343A Expired - Lifetime US1638579A (en) | 1923-12-13 | 1923-12-13 | Coating compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1638579A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070199483A1 (en) * | 2006-02-09 | 2007-08-30 | Wendell Peery | Table |
-
1923
- 1923-12-13 US US680343A patent/US1638579A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070199483A1 (en) * | 2006-02-09 | 2007-08-30 | Wendell Peery | Table |
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