Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
  • C08G63/54—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation the acids or hydroxy compounds containing carbocyclic rings
  • C08G63/553—Acids or hydroxy compounds containing cycloaliphatic rings, e.g. Diels-Alder adducts
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/16—Dicarboxylic acids and dihydroxy compounds
  • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
  • C08G63/199—Acids or hydroxy compounds containing cycloaliphatic rings
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/16—Dicarboxylic acids and dihydroxy compounds
  • C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/46—Polyesters chemically modified by esterification
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
  • C08L67/08—Polyesters modified with higher fatty oils or their acids, or with resins or resin acids

Definitions

• An alkyd resin composition comprising the esterification reaction product of a phthalic acid, a polyhydric alcohol and a dimer of an ethylenically unsaturated aliphatic monocarboxylic acid having beeween 14 and 22 carbon atoms, wherein said polyhydric alcohol is present at least in part as a glycol in an amount sufficient to constitute at least 65 by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between and 32% by weight based on the total weight of the aforesaid reactants in the composition, said alkyd resin being soluble in an inert organic solvent at room temperature.
• This invention relates to a novel alkyd resin composition and to the process of preparing the same. More particularly, this invention relates to a novel alkyd .resin composition comprising the reaction of a phthalic acid and a polyhydric alcohol compirsing at least 65% by weight of a glycol based on the total weight of polyhydric alcohol present and a dimer of an unsaturated aliphatic monocarboxylic acid having between 14 and 22 carbon atoms. Still further, this invention relates to blends of the novel alkyd resin composition with aminoplast resins.
• One of the objects of the present invention is to produce a novel alkyd resin having utility primarily in the field of coating resins.
• a further object of the present invention is to produce a novel alkyd resin from a phthalic acid, a polyhydric alcohol.and a dimer of an unsaturated aliphatic monocarboxylic acid having between 14 and 22 carbon atoms.
• a phthalic acid In the preparation of the alkyd resin compositions of the present invention, one will use a phthalic acid.
• phthalic acids which may be used in the practice of the process of the present invention are: phthalic acid per se, isophthalic acid, terephthalic acid, endomethylene-tetrahydrophthalic acid and halo substituted phthalic acids such as the hexachlorophthalic acid and the like.
• the anhydrides of these acids may be utilized. Obviously, these acids and/or their anhydrides may be used either singly or in combination with one another.
• the amount of the phthalic acid to be used will be discussed in greater detail hereinbelow with reference to the amount of dimer acid utilized in light of the amount of polyhydric alcohol utilized.
• the second essential component used in the preparation of the novel alkyd resins of the present invention is a polyhydric alcohol. It is essential that the polyhydric alcohol used be a glycol in an amount suflicient to con- 'ice stitute at least 65 by Weight based on the total weight of the polyhydric alcohols present in the ultimate alkyd resin produced. One may utilize as much as 100% of a glycol if desired. Preferably one would use between 75% and 80% of a glycol based on the total weight of polyhydric alcohols used in the preparation of the alkyd resins of the present invention.
• glycols which may be used in the compositions of the present invention are: ethylene glycol, propylene glycol, butylene glycol and the diols such as pentane diol-1,5; hexane diol-1,6; and the like. Additionally one may use diethylene glycol, dipropylene glycol and the like. Obviously, these glycols may be used either singly or in combination with one another or in combination with higher functional polyhydric alcohols such as the trihyric alcohols, tetrahydric alcohols, hexahyric alcohols and the like.
• glycols are used singly or in combination with other glycols the requirement of 65 of a glycol used in the composition of the present invention will be calibrated to the total of glycol or glycols when contrasted with the higher functional polyhydric alcohols utilized.
• the higher functional polyhydric alcohols that may be used in combination with I the glycols such as those set forth hereinabove are: glycerol, pentaerythritol, dipentaerythritol, sorbitol, trimethylol ethane, trimethylol propane, hexanetriol-l,2,6 and the like.
• These higher functional polyhydric alcohols may be used singly or in combination with one another when used in combination with glycols such as those set forth hereinabove, but never to an extent greater than about 35% by weight based on the total weight of polyhydric alcohol used. If desired, these higher functional polyhydric alcohols can be eliminated from the composition entirely such as in a case when the glycol or glycols are used exclusively to the exclusion of higher functional polyhydric alcohols.
• the amount of polyhydric alcohol used in the system will depend upon the amount of the phthalic acid and the dimer acid used in the system.
• the amount of the polyhydric alcohol used will be that amount which is stiochiometrically calculated to esterify completely or substantially completely esterify all of the carboxyl groups present in the reaction system; whether derived from the phthalic acid component or the dimer acid component.
• the amount of polyhydric alcohol utilized will be in excess by about 10% or 20% of the amount stiochiornetrically calculated to esterify or substantially completely esterify the carboxyl components present in the system.
• the third essential component used in the practice of the process of the present invention is one or more dimers of an unsaturated aliphatic monocarboxylic acid having between 14 and 22 carbon atoms.
• dimer acids are Well known in the art and a plurality of these dimers are available commercially. 'It will be apparent that these dimer acids are dicarboxylic acids.
• dimer acids are derived by conventional procedures by dimerizing such aliphatic monocarboxylic acids as myristoleic, palmitoleic, oleic, linoleic, linolenic, elaeosteric, licanic, ricinoleic, erucic, and the like.
• dimers may be used either singly or in combination with one another.
• the preferred dimer acid is the dimer of linoleic acid.
• the amount of the dimer acid used in the composition of the present invention is fairly critical and should be present in an amount varying between about 10% and 32% and preferably between about 20% and 22% by weight, based on the total weight of the reactants in the composition. It has been mentioned hereinabove that the amount of phthalic acid used in the composition would be discussed in greater detail in the delineation of the amount of dimer acid used in the composition.
• the phthalic acid and the Jolyhydric alcohol composition may be introduced into a suitable reaction ressel and esterify the reactants in part prior to the ad iition of the dimer acid.
• the alkyd resins of the present invention make ex- :ellent coating resins which may be used alone or in :ombination with aminoplast resins which will be dis- :ussed in greater detail hereinbelow or with nitrocellulose acquers.
• he novel alkyd resins of the present invention may be :ut with an appropriate solvent such as an inert organic IOlVBl'lt.
• an inert organic solvents that may be ised as solvent medium for the novel resins of the present nvention are: benzene, toluene, xylene, or Solvesso No. 100 or No.
• he novel resins of the present invention are not critical and proportions conventionally used in the art may be )bserved depending upon the ultimate mode of use of he coating compositions of the present invention. These :ompositions may be applied by brushing, roller coating, :praying, knife coating, hot melt and the like. For certain tpplications no diluting solvent medium is necessary such is in the case of hot melt adhesives. Quite obviously, f one wants a clear coating, no additives such as dyes )r pigments will be added. On the other hand, if one vishes a colored coating composition the selected dye ind/OI pigment may be added according to choice in :onventional quantities.
• alkyd resins of the present invention when blended vith aminoplast resins in certain proportions, produce :oating compositions which are capable of producing ilms that possess a combination of properties not preiously known in any coating composition. These out- .tanding properties are to be noted particularly in the trea of impact resistance and hardness.
• the impact reistance of the films produced by the blend of the alkyd esins of the present invention with aminoplast resins or esin forming compositions, particularly the polymethyl :thers of polymethylol melamines, is so surprisingly ex- :ellent that it is possible through the use of this novel :oating composition to coat sheet steel with these coatngs and upon drying, such as by baking, the coated steel heet can then be fabricated into desired contours with- :ut any display of cracking or peeling which would iormally be experienced even with conventional comnercially available alkyd coating compositions currently in the market.
• Whei'i such a dent were to be sulfered, on an automotive body part, such as a fender, the same couldvbe hammered out to substantially original form without need for a recoating except possibly in extreme cases when the damage was so great as to render such an approach not possible.
• aminoplast resins used with the alkyd resins of the present invention are well known in the art as is the term used to identify them.
• aminoplast resins which may be utilized in combination with the novel alkyd resins of the present invention are those resinous materials prepared by reacting an aldehyde such as form aldehyde with a compound such as urea, thiourea, dicyandiamide or the aminotriazines such as melamine, benzoguanamine, acetoguanamine, formoguanamine, and the like,
• the mol ratios of the aldehyde to the amino compound are all well known in the art depending on the particular amine selected and it is not deemed necessary therefore to elaborate further on details that are well known in the art.
• amine-aldehyde resins or po. tentially resin forming materials may be alkylated or unalkylated.
• the alkylated aminoplast resins are those which have been reacted with a monohydric aliphatic alcohol such as methanol, ethanol, propanol, butanol and the like.
• the degree of alkylation may also be varied significantly as is well known in the art and further elaboration of this concept is also deemed to be unnecessary.
• the preferred aminoplast materials used in the composition of the present invention are the polymethyl ethers of polymethylol melamines including the dimethyl ether of dimethylol melamine, tetramethyl ether or tetramethylol melamine and particularly preferred is the hexamethyl ether of hexamethylol melamine. It should be noted that these polymethyl ethers of polymethylol melamine may be resinous or nonresinous as used in the coating compositions of the present invention.
• the amount of aminoplast material used in the composition of the present invention may be varied to some extent but not over a very substantial range.
• the amount of aminoplast material should be limited within the range of about 5% to 30% by weight based on the total weight of aminoplast material and alkyd resin.
• the aminoplast material should be varied between about 15% and 25% by weight based on the total weight of the aminoplast material and the alkyd resin.
• the compositions of the present invention can be modified further by the addition to the alkyd resinaminoplast composition, varying proportions of nitrocellulose lacquers, epoxy resins, polyvinyl chloride resins and the like.
• Example 1 Into a suitble reaction vessel equipped with thermometer, stirrer, reflux condenser and inert gas inlet and outlet tubes, there is introduced 129 parts of phthalic anhydride, 284 parts of isophthalic acid, 124 parts of ethylene glycol, 152 parts of propylene glycol and 113 parts of the dimer of linoleic acid.
• the charge is heated with constant stirring to a temperature of about 220225 C. and held at about that temperature while removing the water of esterification by a stream of nitrogen gas bubbling through the reactants in the reaction vessel. The heating is continued until an acid number 2.2 is reached. Thereupon the resin is cut with enough Xylene to provide a 75% solids solution which has a viscosity of 15 poises at 25 C.; the alkyd resin solution thus produced is clear and sparkling.
• Example 2 Example 1 is repeated in all details with respect to processing steps except that the reactants charged to the vessel are as follows: 388 parts of phthalic anhydride, 124 parts ethylene glycol, 114 parts propylene glycol, 40 parts of trimethylol ethane and 113 parts of the dimer of linoleic acid. The reaction is continued until an acid number of 3.0 is reached. The alkyd resin produced is cut in xylene to give a 75% solids solution having a viscosity of 17 poises at 25 C.
• the reactants charged to the vessel are as follows: 388 parts of phthalic anhydride, 124 parts ethylene glycol, 114 parts propylene glycol, 40 parts of trimethylol ethane and 113 parts of the dimer of linoleic acid. The reaction is continued until an acid number of 3.0 is reached. The alkyd resin produced is cut in xylene to give a 75% solids solution having a viscosity of 17 poises at 25 C.
• Example 3 Example 1 is repeated in every detail with respect to the processing steps except that the reactants charged to the vessel are as follows: 185 parts of phthalic anhydride, 228 parts of isophthalic acid, 186 parts of ethylene glycol, 80 parts of trimethylol ethane and 113 parts of the dimer of linoleic acid. The reaction is continued until an acid number of 5.0 is reached. Thereupon the resin is cut with xylene to give a 70% solids solution having a viscosity of 23 poises at 25 C.
• the reactants charged to the vessel are as follows: 185 parts of phthalic anhydride, 228 parts of isophthalic acid, 186 parts of ethylene glycol, 80 parts of trimethylol ethane and 113 parts of the dimer of linoleic acid.
• the reaction is continued until an acid number of 5.0 is reached. Thereupon the resin is cut with xylene to give a 70% solids solution having a viscosity of 23 poises at
• Example 4 Example l is repeated in all details with respect to the processing steps except that the following reactants are used: 185 parts of phthalic anhydride, 288 parts of isophthalic acid, 109 parts of ethylene glycol, 114 parts of propylene glycol, 40 parts of trimethylol ethane and 113 parts of the dimer of linoleic acid. The reaction is continued until an acid number of 1.0 is reached. The alkyd resin is then cut with xylene to give a 75% solids solution having a viscosity of 36 poises at 25 C.
• Example 1 is again repeated in all details with respect to the processing steps except that the following reactants were utilized: 388 parts of phthalic anhydride, 265 parts of glycerin and 265 parts of lauric acid. The charge is heated until an acid number of 5 is reached. A viscous material results which when out with xylene to a 60% solids solution still displays a viscosity of 46 poises at 25 C.
• Each of the alkyd resins of Examples 1-5 inclusive were mixed with a xylene solution of the hexamethyl ether of hexamethylol melamine so as to produce a composition which has, on a nonvolatile basis, the proportion of 80% solids of alkyd resin to 20% solids of the melamine compound.
• White baking enamels were prepared from each of these samples by grinding titanium dioxide into the solution so as to have equal weights of titanium dioxide and total resin solids (including the melamine compound). To the resultant coating composition there is added 1% of para toluene sulfonic acid by weight based on the total weight of the melamine compound present.
• Example 1 Each of the five enamels thus prepared were reduced to spray consistency by adding xylene and in each instance the coatings were applied to 30 gauge tinned-steel panels. After baking each panel for 30 minutes in an oven at a temperature of 300 F., all of the panels are smooth and glossy. Each of the baked film panels were then subjected Into a suitable reaction vessel equipped as in Example 1, there is introduced 185 parts of phthalic anhydride, 197 parts of isophthalic acid, 171 parts of ethylene glycol, 32 parts of glycerin and 187 parts of the dimer of linoleic acid. The procedure of Example 1 is followed until the alkyd resin has an acid number of 6. Thereupon the resin is cut with xylene to yield a solution having a 70% resin solids. The viscosity of the solution is 64 poises at 25 C.
• Example 7 Into a suitable reaction vessel equipped as in Example 1, there is introduced 185 parts of phthalic anhydride, 196 parts of isophthalic acid, 8 parts of fumaric acid, 109 parts of ethylene glycol, parts of butanediol-1,3,32 parts of glycerin and 150 parts of the dimer of linoleic acid. The procedure of Example 1 is followed until the resin has an acid number of 5. The resin is then cut with xylene to a resin solids solution of 70% which has a viscosity of 98 poises at 25 C.
• Example 8 Example 1 is followed in all details except that the ingredients charged are as follows: 148 parts of phthalic anhydride, 67 parts of ethylene glycol, 35 parts of pentaerythritol and parts of the dimer of linoleic acid. The
• Example 1 Procedure of Example 1 is followed until the resin has an acid number of 15. The resin is then cut with xylene to a solids content of 60%. The viscosity of the resin solution is 64 poises at 25 C.
• Example 9 The procedure of Example 1 is repeated using the following ingredients: 355 parts of phthalic anhydride, 11 parts of fumaric acid, 210 parts of propylene glycol-1,2, 32. parts glycerin and 150 parts of the dimer of linoleic acid. The procedure of Example 1 is continued until the resin has an acid number of 6. The resin is cut with xylene to a 70% solids solution. The viscosity of the resin solution is 95 poises at 25 C. p
• a portion of each of the resins prepared according to Examples 69 inclusive is blended with a xylene solution of hexamethyl ether of hexamethylol melamine in pro portions sufficient to provide 80% alkyd resin solids to 20% hexamethyl ether of hexamethylol melamine solids.
• White baking enamels are prepared, as in the earlier examples, by grinding titanium dioxide into the resin solutions so as to have equal weights of titanium dioxide to the total of the alkyd resin and the melamine compound. One percent of para toluene sulfonic acid by weight based on the weight of the melamine compound is added.
• the enamels are reduced by further dilution with xylene to spray consistency and applied as before to 30 gauge tinned-steel panels. These enamels were baked at 300350 F. for 30 minutes in order to give hard, tough, glossy films having impact values greater than 28 in./pounds and possessing high resistance to attack by aliphatic solvents, acetic acid and dilute sodium hydroxide. After the baked coatings of Examples 6-9 inclusive had aged for several months, adhesion to the steel panel was still excellent whereas the enamel made from Example 5 exhibited very poor adhesion as determined by a conventional scratch test.
• dimer acid compositions of the class described iereinabove which contain impurities in the nature of mall percentages of monomers of these same acids or rimers of these same acids.
• the monomer content in :ommercially avail-able dimer acid compositions is gen- :rally quite small, such as in the order of magnitude of 1% to 4% by Weight based on the total weight of the limer acid composition.
• the trimer acid content, in the :ommercially available dimer acid compositions, is gen- :rally more sizeable such as in the order of magnitude )f 20% to 25% by weight based on the total weight of the limer acid composition.
• the dimer acid per se in the dimer LCld composition is present in preponderant amounts such [8 about 73% to about 76% by weight based on the total weight of the dimer acid composition.
• the trimer acid is considered to )e a polyfunctional acid, as is the dimer acid, and when )roportions are calculated for use in the compositions of be present invention, the amount of dimer acid comiosition used should be calculated as though the dimer :omposition was in fact pure dimer acid.
• Example 10 Into a suitable reaction vessel equipped as in Exam- )le 1, there is introduced 185 parts of phthalic anhydride, .97 parts of isophthalic acid, 133 parts of propylene gly- :ol, 62 parts of ethylene glycol, 40 parts of trimethylol :thane and 187 parts of the dimer of linoleic acid.
• the irocedure of Example 1 is followed until the acid number if the alkyd resin reaches 4.0.
• the resin is then cut with :ylene to a solids content of 70%.
• the viscosity is 98 )oises at 25 C.
• Example 11 Into a suitable reaction vessel equipped as in Exam- 11B 1, there is introduced 370 parts of phthalic anhydride, '7 parts of propylene glycol, 108 parts of ethylene glycol, 10 parts of trimethylol ethane and 150 parts of the dimer if linoleic acid. The procedure is continued, as before, intil an acid number of is reached. The alkyd resin is hen cut with xylene to a 70% solids solution. The vis- :osity is 64 poises at 25 C.
• Each of the resins in Examples and 11 is blended vith of the hexamethyl ether of hexamethylol meltrnine by weight based on the total alkyd resin solids and nelarnine compound.
• the composition is catalyzed with 1% para toluene sulfonic acid based on melamine com- )ound solids.
• Comparative Example 12 A commercially available alkyd resin is prepared ac- :ording to the process of Example 1 except that the folowing reactants are charged to the vessel: 360 parts of )hthalic anhydride, 7.4 parts of fumaric acid, 252 parts f glycerine and 304 parts soya oil fatty acids. The retctants are heated according to the process of Example 1 mtil an acid number of 5 is reached. The alkyd resin is hen cut with xylene to a 55% solids solution having a 'iscosity of 35 poises at C.
• the alkyd resins of the present invention may be used with or without benefit of any catalyst as may be the combination of the alkyd resin of the present invention and the aminoplast material.
• a catalytic material such as an acid catalyst of which a greater plurality are known in the art.
• the acidic catalysts are preferred and may be used in combination with amines such as those disclosed in the US. Pat. No. 2,750,355 particularly if a latent catalyst is desired.
• the acidic catalyst may be used alone.
• the preferred acidic catalyst is para toluene sulfonic acid.
• An alkyd resin composition comprising the esterification reaction product of a phthalic acid, a polyhydric alcohol and a dimer of an ethylenically unsaturated aliphatic monocarboxylic acid having between 14 and 22 carbon atoms, wherein said polyhydric alcohol is present at least in part as a glycol in an amount sufiicient to constitute at least 65% by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition, said alkyd resin being soluble in an inert organic solvent at 25 C.
• An alkyd resin composition comprising the esterification reaction product of phthalic anhydride, a polyhydric alcohol and a dimer of an ethylenically unsaturated aliphatic monocarboxylic acid having between 14 and 22 carbon atoms, wherein said polyhydric alcohol is present at least in part as ethylene glycol in an amount suflicient to constitute at least 65 by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition.
• An alkyd resin composition comprising the esterification reaction product of phthalic anhydride, a polyhydric alcohol and a dimer of an ethylenically unsaturated aliphatic monocanboxylic acid having between 14 and 22 carbon atoms, wherein said polyhydric alcohol is present at least in part as propylene glycol in an amount sufiicient to constitute at least 65 by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition.
• An alkyd resin composition comprising the esterification reaction product of phthalic anhydride, a polyhydric alcohol and a dimer of an ethylenically unsaturated aliphatic monocarboxylic acid having between 14 and 22 carbon atoms, wherein said polyhydric alcohol is present at least in part as butylene glycol in an amount sufficient to constitute at least 65% by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition.
• An alkyd resin composition comprising the esterification reaction product of phthalic anhydride, a polyhydric alcohol and a dimer of linoleic acid, wherein said polyhydric alcohol is present at least in part as ethylene glycol in an amount sufficient to constitute at least 65% by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about and 32% by weight based on the total weight of the aforesaid reactants in the compositions.
• An alkyd resin composition comprising the esterification reaction product of phthalic anhydride, a polyhydric alcohol and a dimer of linoleic acid, wherein said polyhydric alcohol is present at least in part as propylene glycol in an amount suflicient to constitute at least 65% by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition.
• An alkyd resin composition comprising the esterification reaction product of phthalic anhydride, a polyhydric alcohol and a dimer of linoleic acid, wherein said polyhydric alcohol is present at least in part as butylene glycol in an amount sufiicient to constitute at least 65 by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition.
• a process for the preparation of an alkyd resin composition comprising esterifying a phthalic acid, a polyhydric alcohol and a dimer of an ethylenically unsaturated aliphatic monocarboxylic acid having between 14 and 22 canbon atoms, wherein said polyhydric alcohol is present at least in part as a glycol in an amount sulficient to constitute at least 65 by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition, said alkyd resin being soluble in an inert Organic solvent at 25 C.
• a process for the preparation of an alkyd resin composition comprising esterifying a phthalic acid, a polyhydric alcohol and a dimer of linoleic acid, wherein said polyhydric alcohol is present at least in part as ethylene glycol in an amount snflicient to constitute at least 65 by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% 'by weight based on the total weight of the aforesaid reactants in the composition, said alkyd resin bein soluble in an inert organic solvent at 25 C.
• a process for the preparation of an alkyd resin composition comprising esterifying a phthalic acid, a polyhydric alcohol and a dimer of linoleic acid, wherein said polyhydric alcohol is present at least in part as propylene glycol in an amount suflicient to constitute at least by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer is present in an amount varying between about 10% and 32% by weight based on the total weight of the aforesaid reactants in the composition, said alkyd r sin being soluble in an inert Organic solvent at 25 C.
• a process for the preparation of an alkyd resin composition comprising esterifying a phthalic acid, a polyhydric alcohol and a dimer of linoleic acid, wherein said polyhydric alcohol is present at least in part as butylene glycol in an amount sufiicient to constitute at least 65 by weight based on the total weight of polyhydric alcohols present in said reaction product and wherein said dimer acid is present in an amount varying between about 10% and 32% by weight 'based on the total weight of the aforesaid reactants in the composition, said alkyd resin being soluble in an inert rganic solvent at 25 C.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• General Chemical & Material Sciences (AREA)
• Polyesters Or Polycarbonates (AREA)

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Cited By (2)

• 0
  • NL NL272020D patent/NL272020A/xx unknown
• 1970
  • 1970-07-10 US US27279D patent/USRE27279E/en not_active Expired

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