US 5,218,045 AGrant

Coating Binders Comprising Liquid Crystalline Enhanced Polymers

Issue Date:1993-06-08

•18 Claims

•10 Drawing Sheets

Abstract

Coating compositions comprising liquid crystalline binders are provided by a combination of mesogenic groups and amorphous resins. The mesogenic groups are either covalently bonded or cross-linked to the amorphous resins to provide coatings of exceptional hardness and toughness. Also provided is an economical process suitable for commercial manufacture of mesogenic compounds and more particularly for the production of liquid-crystalline oligoester polyols.

Metadata

Assignee

North Dakota State University

Inventors

Frank N. Jones
Der-Shyang Chen
Adel F. Dimian
Daozhang Wang

Application Information

Application Number:US 6791743

Filing Date:1991-03-26

Priority Date:1987-03-27

Art Unit:152

Classifications

IPC:

C09K 1938C06G 8100C08L 6704

Field of Search:

52569;118;119;123;131;132;162;163;328.8;330.1;384;386;437;438;440;443

Patent Drawings (10 sheets)

Description

Background of Invention

Liquid-crystal (L-C) polymers are known to form mesophases having one- and two-dimensional order as disclosed by Flory, P. J., Advances in Polymer Science, Liquid Crystal Polymers I; Springer-Verlag: New York (1984) Volume 59; Schwarz, J. Mackromol, Chem. Rapid Commun. (1986) 7, 21. Further, mesophases are well known to impart strength, toughness and thermal stability to plastics and fibers as described by Kwolek et al in Macromolecules (1977) 10, 1390; and by Dobb et al, Advances in Polymer Science, Liquid Crystal Polymers II/III (1986) 255(4), 179.

While L-C polymers have been widely studied, their potential utility as coatings binders seems to have been overlooked. Japanese patents claiming that p-hydroxybenzoic acid (PHBA), a monomer commonly used in L-C polymers, enhances the properties of polyester powder coatings are among the very few reports that may describe L-C polymers in coatings; Japanese Kokai 75/40,629 (1975) to Maruyama et al; Japanese Kokai 76/56,839 (1976) to Nakamura et al; Japanese Kokai 76/44,130 (1976) to Nogami et al; and Japanese Kokai 77/73,929 (1977) to Nogami et al.

Further, coatings binders with lower viscosities which provide harder coatings and less drying times through combinations of amorphous polymers with mesogenic groups are not disclosed in the prior art and are to be desired.

An object of this invention is to provide improved coatings binders comprising amorphous polymers in combination with mesogenic groups.

A further object of this invention is the provision of improved coatings binders comprising low Tg amorphous polymers in combination with mesogenic groups.

A more particular object of this invention is to provide cross-linked and uncross-linked enamels of improved hardness and impact resistance.

Other important objects are to provide high solids/low viscosity coatings formulations with fast drying coatings which provide harder resultant coatings.

Still further objects and advantages of the invention will be found by reference to the following description.

Brief Description of the Figures

FIG. 1 outlines the synthesis of L-C alkyds.

FIG. 2 provides a thermogram of an L-C alkyd.

FIG. 3 shows the effect PHBA content in alkyd resins has on viscosity.

FIG. 4 shows the effect solution solid content has on viscosity for alkyd resins.

FIG. 5 outlines the sythesis of L-C acrylic copolymers.

FIG. 6 outlines the snythesis of L-C acrylic copolymers with spacers.

FIGS. 7 and 8 show the effect solution solid content has on viscosity for acrylic resins.

FIG. 9 shows phase diagrams for L-C acrylic copolymers.

FIG. 10 shows thermograms of L-C diols.

Description of the Invention

Hardness and impact resistance are two desirable characteristics of coatings. However, because hardness is associated with higher T.sub.g s (glass transition temperatures), and good impact resistance with lower T.sub.g s, there is usually a trade-off between hardness and impact resistance. This invention provides for using low T.sub.g binders while enjoying hardness and toughness.

We have found that liquid crystalline domains in an amorphous polymer binder can substantially harden the binder without substantially raising its T.sub.g. Thus, it is possible to prepare very hard coatings while retaining the elasticity and adhesion associated with a low T.sub.g. Amorphous polymer binders with T.sub.g s in a range from -50.degree. C. to +10.degree. C. are generally too soft to be useful in most coatings applications. It is, therefore, beneficial to impart L-C characteristics to coating polymers with lower T.sub.g s to avoid the problems of higher T.sub.g polymers, i.e., high viscosity requiring large amounts of solvent for application and reduced elasticity and impact resistance. The use of increased amounts of solvent results in drying problems including increased drying times and costs, as well as environmental problems.

Among the groups that tend to form liquid crystals and provide the L-C binders of the invention are molecules containing a sequence of two or more aromatic rings connected in the para position by rigid or semi-rigid linkages. Such groups are called "mesogenic", and the L-C materials including such groups are called "mesomorphous". The amorphous binders of our invention have mesogenic groups between 5 percent and 50 percent by weight of the binder to provide the desired liquid crystal behavior.

Although it is especially important that mesogenic groups substantially harden low T.sub.g amorphous polymer binders, the mesogenic groups improve binders in at least two other ways. Addition of mesogenic groups to binders effectively lowers the viscosity of amorphous polymer binder solutions because non-aqueous dispersions are formed. Thus, less solvent is required. Furthermore, the mesogenic groups greatly reduce the time necessary for the binder to harden, referred to as the "dry-to-touch" time.

Because of these further enhancements, binders with T.sub.g s sufficiently high (although low in value) to form acceptably hard coatings can therefore be improved by having their solution viscosities and dry-to-touch times lowered. We have found that mesogenic groups can improve coating binders having a T.sub.g as low as -50.degree. C. or as high as +10.degree. C. while providing improved hardness and impact resistance.

In accord with this invention, mesogenic groups in various forms are used to modify amorphous polymers. Some polymers call for modification with L-C oligomers while others are modified by direct grafting of compounds which will impart L-C characteristics to the amorphous polymers. The former modification is generally referred to as cross-linked because the polymer resin cross-links with the L-C oligomer to provide a cross-linked binder. The latter modification is generally referred to as uncross-linked because the polymer resin itself is provided with L-C characteristics and needs no cross-linking to achieve the desired L-C effect.

P-hydroxybenzoic acid, PHBA, is a commonly used monomer in L-C polymers. One method of imparting liquid crystalline behavior to polymers is by the DCC-p-TSA process described by Chen and Jones, J. Polym. Sci., Polym. Chem. Ed., in press, (1987). It can be generally depicted as follows: ##STR1##

It can be seen that the mesogenic groups which impart the L-C characteristics to the polymer binder are oligomeric PHBA having the general formula: ##STR2## where n=2 to 12.

These mesogenic groups are grafted or covalently bonded to the polymer backbone and should comprise between 5 percent and 50 percent by weight of the reaction product.

Typical amorphous polymers that can be modified in this way are acrylic resins and alkyd resins. The mesogenic groups described above do not covalently bond randomly but require reactive sites on the polymer to bond. These reactive sites can be either OH or C00H terminal groups. PHBA, however, bonds more efficiently to C00H terminal groups, and alkyds or acrylics having OH terminal groups can be modified with a residue of a dicarboxylic acid to obtain the more favorable reactive sites.

A second method of imparting L-C characteristics to coating binders is to combine the binder resins with a mesogenic compound and cross-linking them below the clearing temperature, T.sub.cl (T.sub.cl is the temperature at which a compound loses its L-C characteristics).

Typical mesogenic compounds for this method are oligoester polyols, mesomorphous acrylic resins and mesomorphous alkyd resins. These mesogenic oligoester polyols and mesomorphous resins can be created by the first method or a similar method using PHBA.

One procedure which is particularly successful is the production of oligoester polyols. This procedure involves production of a non-L-C linear oligoester polyol by reacting an aliphatic dicarboxylic acid having a carbon chain length of from 4 to 36, an aliphatic primary or secondary diol or polyol having a carbon chain length of from 2 to 12, and a residue of a dicarboxylic acid. PHBA is then covalently bonded to this non-L-C oligoester polyol as generally depicted above; thereby providing the L-C oligoester polyol for cross-linking. The reasons that this procedure is considered particularly successful and preferred are: (1.) it can be used in large scale production; and (2.) the use of p-TSA reduces the yield of by-product phenol to a barely detectable trace insuring product purity.

Typical amorphous resins which can be modified in this cross-linking method are melamine resins, polyisocyanate resins and epoxy resins. Here, again, the weight percent of mesogenic groups in this composition should be between 5% and 50% and the T.sub.g of the amorphous resin can be between -50.degree. C. and +10.degree. C.

This second method is effective for baked or non-baked coatings. If the coating is to be baked, the oligoester polyol or mesormorphous resin and the particular amorphous resin or mixture of resins can be combined and handled in this way until baked. The cross-linking does not occur until raised to the baking temperature, which will be below the corresponding Thd cl. At this point, the mesogenic groups will covalently bond to the coating resins yielding the desired coating of this invention.

The following examples suggest methods of imparting L-C characteristics to coatings and binders. These L-C binders are also compared to amorphous resins and the comparisons will demonstrate the improvements of this invention: 1) a lowered solution viscosity, 2) a toughened and hardened coating while maintaining good impact resistance and 3) a greatly reduced dry-to-touch time.

Example 1

This example concerns model alkyd resins made by a synthetic procedure. Here the objective is to demonstrate the usefulness of L-C alkyds.

Linoleic acid (Emersol 315, Emery Ind. Inc., equivalent weight 288) was dried with anhydrous Na.sub.2 SO.sub.4. Pyridine (Aldrich) was distilled and dried with anhydrous Na.sub.2 SO.sub.4. All other materials (Aldrich) were used as received.

Synthesis of PHBA-modified alkyds is outlined in FIG. 1.

A low molecular weight model alkyd, U1, with 55% oil length and 22% OH excess was prepared from 25.00 g (0.0868 mol) of linoleic acid, 10.70 g (0.0722 mol) of phthalic anhydride, and 12.61 g (0.094 mol) of trimethylolpropane using the DCC-p-TSA process described by Kangas, S. and Jones, F. N., "Model alkyd resins for higher-solids coatings, I", J. Coat. Technol., 59(744), 89 (1987). Yield was 85%. The OH value was 56 mg-KOH/g determined by the phthalic anhydride/pyridine method.

Alkyd U1 was heated with succinic anhydride (one mol per equiv OH) in pyridine at 80.degree. C. for 12 hr. The solution was concentrated; the residue was dissolved in CH.sub.2 Cl.sub.2 and washed with 10% aq. HCl. The CH.sub.2 Cl.sub.2 layer was concentrated and the residue was vacuum dried at 80.degree. C. Yield of resin was above 90%; acid number was 64 mg-KOH/g.

A solution of 10.0 g (0.010 equiv) of alkyd U1, 8.51 g (0.050 mol) of terephthalic acid, TPA, 2.27 g (0.011 mol) of DCC and 0.11 g of p-TSA in 150 ml of pyridine was stirred at 25.degree. C. for 12 hr. The mixture was filtered to remove DCU and excess TPA. The filtrate was concentrated, dissolved in CH.sub.2 Cl.sub.2, washed with 10% aq. HCl and concentrated as above. Traces of crystalline material were removed by dissolving the residue in 1/1 pentane/ethyl acetate, cooling in a freezer, filtering, reconcentrating and vacuum drying at 80.degree. C. Yield was 9.62 g of resin; acid number was 62 mg-KOH/g.

The intermediate step of modifying alkyd U1 with succinic anhydride or with TPA is desirable to improve grafting efficiency. This step converts --OH groups of U1 to --COOH groups; grafting to --COOH groups is more efficient. The succinic anhydride modified alkyd was grafted or covalently bonded with PHBA using the DCC-p-TSA/pyridine process. Weight ratios (PHBA/alkyd) of 0.1, 0.2, 0.3 and 0.5 gave alkyds G1-G4 respectively. For example, the synthesis on alkyd G2 is described:

A solution of 10.0 g (0.0114 equiv) of carboxyl-terminated model alkyd 2.0 g (0.0145 mol) of PHBA, 3.14 g (0.0152 mol) of DCC, and 0.16 g of p-TSA in 120 ml of pyridine was stirred at 25.degree. C. for 12 hrs. The product (10.2 g, 85% yield) was isolated essentially as described immediately above in the TPA modification.

TPA modified alkyd was covalently bonded by a similar process using a weight ratio (PHBA/alkyd) of 0.5 to give alkyd G5. Modification with TPA has the additional advantage of putting half the structure needed for liquid crystal formation into place.

A series of random model alkyds R1, R2 and R3 containing 15%, 22% and 27% by weight in the feed were prepared from linoleic acid, phthalic anhydride, trimethylolpropane, and PHBA in a single step by the DCC-p-TSA process. These wt % s correspond roughly to the wt % s of PHBA actually incorporated in alkyds G2, G3 and G4, respectively. For example, preparation of R3 is described:

A solution of 5.50 g (0.0190 mol) of linoleic acid, 2.54 g (0.017 mol) of phthalic anhydride, 2.91 g (0.022 mol) of trimethylolpropane, 4 g (0.029 mol) of PHBA, 12.24 g (0.060 mol) of DCC, and 0.612 g of p-TSA in 200 ml of anhydrous pyridine were mixed in a 250 ml flask for 12 hrs. at 25.degree. C. Alkyd R3 was isolated essentially as described above in the TPA modification. Structure Characterization and Testing. .sup.1 H-NMR spectra were determined at 34.degree. C. using a Varian Associates EM 390 NMR spectrometer with Me.sub.4 Si as internal standard. IR spectra were recorded on a Perkin-Elmer 137 spectrophotometer using a 20 wt-% solution in CH.sub.2 Cl.sub.2.

Differential scanning calorimetry (DSC) was effected with a du Pont model 990 thermal analyzer at a heating rate of 20.degree. C./min using samples that had been vacuum dried at 80.degree. C. to constant weight. T.sub.g was assigned as the onset of the endothermic inflection. Clearing points (T.sub.cl) of L-C phases were assigned as the maxima of the endothermic peaks.

Equivalent weight per carboxyl group was determined by titration of pyridine solution with KOH/CH.sub.3 OH to the phenolphthalein end point.

Number average molecular weight (M.sub.n), weight average molecular weight (M.sub.w), and polydispersity index (PDI=M.sub.w /M.sub.n) were measured by gel permeation chromatography (GPC) in tetrahydrofuran using a Waters model 510 pump, a R401 refractive index detector and a model M730 data module; columns were Ultrastyragel 100 A, 500 A, 10.sup.3 A, and 10.sup.4 A. Monodisperse polystyrene calibration standards were used.

Optical textures were examined with a Leitz D-6330 polarizing microscope equipped with a Reichert hot stage.

Grafting efficiency (GE %) and average number of PHBA units per COOH were estimated from equivalent weight difference as described in Chen, D. S. and Jones, F. N., "Graft-copolymers of p-hydroxylbenzoic acid, Part I, A general method for grafting mesogenic groups to oligomers", J. Polym. Sci., Polym. Chem. Ed., in press, (1987).

Solution viscosity was measured in xylene using an ICI cone and plate viscometer at 25.degree. C. Films were prepared by dissolving or dispersing resins and driers in xylene and casting films on untreated rolled steel panels by a casting bar to give the dry thickness of 0.5 ml.

Dry-to-touch time was measured according to ASTM D1640. Film properties were measured after 7 days of drying at ambient temperature. Reverse impact resistance and pencil hardness were measured according to ASTM D2794 and D3363 respectively; resistance to acetone was measured by the number of double rubs to remove trace of film with paper tissue after the dropping of acetone on the dry film. Extractability was measured by subjecting cured films to 8 hr. in a Soxhlet extractor using tetrahydrofuran.

The equivalent weight per carboxyl, M.sub.n, M.sub.w, PDI, and number average PHBA units per carboxyl of the control alkyd and the PHBA-grafted alkyds are shown in Table 1. As PHBA content increases equivalent weight, M.sub.n, and M.sub.w increase in proportion to the mass of PHBA grafted but no more; PDI remains nearly constant. These results indicate that little or no coupling of molecules occurs during grafting. Data for "random" alkyds R1-R3 are shown in Table 2.

IR spectra of the PHBA grafted alkyds are characterized by two sharp peaks at 1610 and 1510 cm.sup.-1. .sup.1 H-NMR spectra show complex peaks in the range of 7.0-8.0 ppm. These spectral features are characteristic of PHBA grafted polymers. IR of random alkyds R1-R3 also showed two sharp peaks at 1610 and 1510 cm.sup.-1.

Onset T.sub.g (by DSC) of the unmodified alkyd U1was -29.degree. C.; PHBA-grafted alkyds G1-G5 had onset T.sub.g s at -24.degree., -20.degree., -15.degree., -10.degree., and +17.degree. C., respectively. DSC traces of the alkyd U1 and grafted alkyds G1-G3 were featureless except for the inflection assigned to T.sub.g and the broad exothermic peaks due to thermal cross-linking. DSCs of alkyds G4 and G5 had sharp endothermic peaks at 190.degree. and 225.degree. C., respectively; these peaks are attributable to the clearing temperature (T.sub.cl) of the L-C phases. The DSC thermogram of alkyd G4 is shown in FIG. 2. DSC thermograms of random alkyds R1-R3 are similar to those of alkyds U1, G1, G2, and G3, no endothermic peaks appeared. T.sub.g s of R1, R2, and R3 were -23.degree., -18.degree., and -12.degree. C., respectively.

Optical textures of the dried films were examined under a polarizing microscope with a hot stage. Films of alkyds U1, G1-G3 and R1-R3 had no visible L-C phases. However, L-C (mesomorphous) phases were clearly visible in films of alkyds G4 and G5. The L-C phase in films of alkyd G4 disappeared when the specimen was heated above 190.degree. C. and reappeared quickly as it was cooled to around 190.degree. C.

Alkyds U1, G1-G3 and R1-R3 appeared soluble in commercial xylene at all concentrations. In contrast, alkyds G4 and G5 formed stable, opaque dispersions in xylene at concentrations of 5 wt % or higher.

The relationship between viscosity and PHBA content of 70/30 (w/w) mixtures of alkyds G1-G4 and R1-R3 in xylene are shown in FIG. 3. Viscosity increases with increasing PHBA content for alkyds G1-G3, but it drops sharply for alkyd G4. This drop is presumably associated with the tendency of alkyd G4 to form non-aqueous dispersions. On the other hand, "random" alkyd R3, whose overall composition is similar to that of G4, has the highest viscosity in the series. The solids/viscosity relationship of alkyd G4 is shown in FIG. 4.

As shown in Table 3, all PHBA-grafted alkyds dried faster than unmodified alkyd U1, and drying speed increased with PHBA content. Acceleration of drying is by far the greatest for L-C alkyds G4 and G5. The latter dried very rapidly (in 5 minutes). As shown in Table 4, the drying speed of "random" alkyds R1-R3 also increased with the PHBA content, but the effect was much smaller than observed for their grafted counterparts G2-G4.

Coatings made from all alkyds had good adhesion. Films made from alkyds U1, G1G3 and R1-R3 were glossy and transparent, while film from alkyds G4 and G5 were glossy and translucent.

As shown in Table 3, seven-day old films of PHBA-grafted alkyds G1-G5 had better reverse impact resistance, were harder, and had slightly better acetone resistance than alkyd U1. All these film properties are favored by higher PHBA content. Alkyd G4 had the best balance of properties, while alkyd G5 was the hardest.

Hardness and solvent resistance of films made from "random" alkyds R1-R3 improved with increasing PHBA content (Table 4). On the other hand, impact strength decreased with increasing PHBA content.

The data of the above example indicates the vast improvements made in an alkyd coating and resin when mesogenic groups are covalently bonded to the alkyd binder.

Example 2

This example reports use of mesogenic groups to modify acrylic polymers. The experimental approach was to prepare several series of --COOH functional acrylic copolymers in which molecular weight, Tg, and functionality were varied and then to graft oligo-p-hydroxybenzoic acid (oligo-PHBA) to the --COOH groups. The oligo-PHBA groups were the mesogenic groups which imparted the desired L-C characteristics.

Two types of L-C acrylic polymers were synthesized. In type A the oligo-PHBA was grafted to --COOH groups attached directly to MMA/BA/(M)AA acrylic copolymer backbones (FIG. 5). In type B an 8-unit flexible spacer was placed between the copolymer backbone and the oligo-PHBA (FIG. 6). The behavior of these copolymers as film formers was investigated. Materials. Monomers were distilled before use. Pyridine was distilled and then dried by stirring with anhydrous Na.sub.2 SO.sub.4. All other reagents (Aldrich) were used as received.

COOH-functional acrylic polymers were prepared as substrates for grafting by radical copolymerization in toluene at 90.degree.-100.degree. C. under monomer starved conditions as described by R. A. Gray, J. Coat. Technol., 57, 83 (1985), using azobisisobutyronitrile (AIBN) as initiator. Substrates for Type A copolymers (FIG. 5) were composed of methyl methacrylate (MMA), butyl acrylate (BA), and acrylic acid (AA) or methacrylic acid (MAA). Substrates for Type B copolymers (FIG. 6) were composed of MMA, BA, and 2-hydroxyethyl methacrylate (HEMA); they were modified to become COOH-functional by treatment with stoichiometrically equivalent amount of succinic anhydride in pyridine at 80.degree. C.

The following is an example for the preparation of a COOH-functional acrylic polymer of Type B:

(a). Polymerization: Toluene (57 g) was placed in a 250-ml, 3-neck flask, heated in an oil bath and stirred mechanically. A solution of 32.68 g (0.255 mol) of BA, 22.03 g (0.22 mol) of MMA, 3.25 g (0.025 mol) of HEMA, and 0.57 g of AIBN was added dropwise during 3 hr with continuous stirring. Temperature was maintained at 95.degree. to 100.degree. C. during addition and for 2 hr. thereafter. A solution of 0.2 g of AIBN in 10 g of toluene was added during 10 min, and the temperature was maintained for 1 hr. The solution was concentrated on a rotary evaporator and was vacuum dried at 80.degree. C. The residue (polymer B6) had 5 mol % OH functionality (calcd), a Tg of 10.degree. C. (calcd) and Mn of 15,400 (measured by GPC). Acrylic copolymers of type A were prepared similarly.

b). Modification with succinic anhydride: A solution of 11.45 g (0.005 eq OH) of the above polymer and 0.50 g (0.005 mol) of succinic anhydride in 50 g of pyridine was stirred and heated at 80.degree. C. for 12 hr. The solution was concentrated; the residue was dissolved in CH.sub.2 Cl.sub.2 and washed with 10% aq. HCl. The CH.sub.2 Cl.sub.2 layer was concentrated and the residue was vacuum dried at 80.degree. C. Yield was 92%. Acid number was 24.

Both types of COOH-functional acrylic copolymers were grafted with PHBA in pyridine at 100.degree. C. for 36 hr by the DCC-p-TSA process. Ratios of mol of PHBA to equiv of --COOH ("equivalent ratios") were 3.5, 5.5, and 7.0 in order to vary the length of the grafted oligo-PHBA segments. The PHBA-grafted products of Types A and B were designated GA and GB respectively. The procedure is exemplified by the grafting of succinic anhydride-modified polymer B6 at equivalent ratio of 7.0.

A solution of 11.80 g (0.005 eq COOH) of polymer B6, 4.84 g (0.035 mol) of PHBA, 7.94 g (0.0385 mol) of dicyclohexycarbodiimide (DCC), and 0.40 g of p-toluenesulfonic acid (p-TSA) in 150 g of pyridine was stirred at 100.degree. C. for 36 hr. The mixture was filtered to remove urea of DCC (DCU) and PHBA oligomers. The filtrate was concentrated, dissolved in CH.sub.2 Cl.sub.2, washed with 10% aq. HCl, and concentrated. Traces of crystalline contaminates were removed by dissolving the residue in 1:1 pentane-ethyl acetate, cooling in a freezer, filtering, reconcentrating, and vacuum drying at 80.degree. C. Yield was 85%. The combined crystalline by-products weighed 9.40 g after vacuum drying at 80.degree. C. to constant weight. Grafting efficiency (GE %) was estimated to be 70% indicating an average length of oligo-PHBA grafts (#PHBA/COOH) of 4.9 PHBA units.

Grafting was effected to give L-C copolymers of Types GA and GB. These types differ in that the mesogenic PHBA-grafts are attached directly to the polymer backbone of Type GA copolymers while Type GB copolymers have eight-atom flexible spacers between the polymer backbone and the mesogenic grafts. Individual copolymers were numbered as shown in Tables 5 to 11. Grafting efficiency (GE %) was determined gravimetrically. It ranged from about 85% to about 70%. As expected, GE % decreased as the COOH equivalent ratio of PHBA/acrylic increased.

Average #PHBA/COOH ratios were calculated from GE %. In order to achieve #PHBA/COOH ratios of 3.+-.0.2, 4 .+-.0.2, and 5.+-.0.3 it proved necessary to feed PHBA monomer in the ratio of 3.5, 5.5 and 7.0 moles, respectively, to the grafting reaction.

Structure Characterization and Testing--.sup.1 H-NMR spectra, IR spectra, differential scanning calorimetry (DSC), optical textures under polarizing microscope, M.sub.n, M.sub.w, polydispersity index, and average #PHBA/COOH ratio were determined as described in Chen and Jones. The term "#PHBA/COOH ratio" refers to the number average degree of polymerization of oligo-PHBA graft segments actually incorporated in the graft copolymer.

X-ray spectra were recorded with a Philip wide angle diffractometer at 25.degree. C. Samples for X-ray diffraction studies were dissolved or dispersed in acetone, cast on glass slides, and vacuum dried at 80.degree. C. for 12 hr.

Viscosity was measured using an ICI cone and plate viscometer (shear rate 10.sup.4 s.sup.-1) at 25.degree. C. Samples were dissolved or thoroughly dispersed in methylisobutylketone (MIBK) before measuring.

Samples were dissolved or dispersed thoroughly in MIBK and then put in test tubes. Appearance was observed when the test tubes were immersed in an oil bath and equilibrated at different temperatures. Optical textures of some L-C polymer dispersions were examined under polarizing microscope at 25.degree. C.

Samples were dissolved or dispersed in MIBK and cast on untreated cold rolled steel panels by a casting bar to give the dry film thickness of 1.0 ml. Reverse impact strength and pencil hardness were measured according to ASTM D2794 and D3363, respectively.

The IR spectra of the oligo-PHBA grafted acrylics have sharp peaks at 1610 cm.sup.-1 and 1510 cm.sup.-1 assignable to the para aromatic C-H stretching. These two peaks are characteristic of oligo-PHBA grafted polymers. They are absent in the ungrafted acrylics.

.sup.1 H-NMR spectra of the PHBA-grafted acrylics show multiple peaks in the range of 7.0-7.3 ppm and 8.0-8.3 ppm, assignable to the aromatic protons ortho to the OH group and to the COOH group, respectively. They are absent in the ungrafted acrylics.

Polarizing microscopy, differential scanning calorimetry (DSC), and wide angle X-ray diffraction (WAXS) were used to further characterize the microstructures of the graft copolymers in the bulk phase. Results (Tables 5 and 6) were consistent with assignment of L-C microstructure to all polymers except GA21a-c.

FIG. 7 shows shear viscosities (shear rate 10.sup.4 s.sup.-1) of MIBK solutions of three ungrafted acrylic copolymers and of a dispersion of an L-C graft copolymer derived from one of them as a function of concentration. The ungrafted copolymers (B1, B2, and B6) differ only in T.sub.g (-10.degree., 0.degree., +10.degree. C., respectively); all three have M.sub.n of about 15,000 and functionality of 5 mol %. L-C copolymer GB1 was prepared by grafting B1 with an average #PHBA/COOH ratio of 5.0. As expected, solution viscosities of ungrafted copolymers increase moderately as T.sub.g increases. However, viscosity of GB1, an anisotropic dispersion throughout most of the concentration range studied, was substantially lower than that of the copolymer from which it was made. The viscosity range 0.1 to 0.2 Pa.s (a viscosity suitable for spray application of coatings) was attained at about 40 to 45 wt. % with the ungrafted polymers and at about 45 to 50 wt. % with L-C copolymer GB1.

The effect of #PHBA/COOH ratio on viscosity was studied; results are shown in FIG. 8. B2 is an ungrafted acrylic copolymer with M.sub.n of about 15,000, T.sub.g of 0.degree. C., and functionality of 5 mol %. GB2a and GB2b are L-C graft copolymers prepared from B2 with actual #PHBA/COOH ratios of 4.8 and 3.2, respectively. Again, viscosities of anisotropic dispersions of the grafted copolymers were significantly lower than solutions of the copolymers from which they were made. It appears that increasing #PHBA/COOH ratio slightly reduces viscosity of the dispersions. Viscosity of dispersions of a third L-C copolymer in this series, GB2c (#PHBA/COOH ratio=4.1) was intermediate between GB2a and GB2b.

The behavior of L-C copolymer/MIBK mixtures depended on temperature, concentration and #PHBA/COOH ratio. The phase diagrams in FIG. 9 are typical. Behavior of two copolymers, GB2b (#PHBA/COOH=3.2, dashed line) and GB2a (#PHBA/COOH=4.8, solid line) is shown. These graft copolymers are from the same acrylic copolymer substrate; they differ only in #PHBA/COOH ratio. Both copolymers formed transparent isotropic "solutions" (A) at low concentrations and/or at elevated temperatures. At lower temperatures both copolymers formed biphasic states (B) and anisotropic states (C) at high concentrations. This sort of behavior is typical of lyotropic L-C polymers. Increasing #PHBA/COOH ratio from 3 to 5 decreases solubility, shifting the phase diagram by about 10 wt % as shown.

#PHBA/COOH ratio strongly affected the concentrations at phase boundries. As #PHBA/COOH ratio increases the phase boundaries shift to lower concentrations. Temperature also affect the phase boundaries. For example, as shown in FIG. 9, both the biphasic state and the anisotropic state become isotropic (i.e., they "clear") when heated. The clearing temperatures increased as the #PHBA/COOH ratios increased.

Properties of cast films of selected L-C acrylic copolymers were compared with those of a series of ungrafted, amorphous acrylic copolymers (A1-A10). Three empirical indicators of film properties were used: crosshatch adhesion, reverse impact resistance and pencil hardness. Adhesion was good in every case; other results are shown in Table 7.

Film properties of the amorphous copolymers were poor. When calculated T.sub.g was below 25.degree. C., the films were very soft, and when it was higher they were very brittle. When M.sub.n was below 30,000 impact resistance was negligible regardless of T.sub.g. Copolymer A10 (M.sub.n =39,500 and T.sub.g =+10.degree. C.) had the best properties in the series, although films are too soft for practical use.

Film properties of representative L-C copolymers were substantially better than those of amorphous counterparts (Table 7). Reverse impact resistance of 65 to >80 in-lb is attainable with backbone M.sub.n as low as 15,000, and pencil hardness of H to 3H is attainable with T.sub.g as low as -10.degree. C.

It is evident from the above results that films made from L-C acrylic copolymers can have substantially better hardness and impact resistance than those made from comparable amorphous copolymers.

Preliminary Guidelines for LC Copolymer Design--Having established that liquid crystallinity can dramatically improve film properties, a second objective was addressed to develop preliminary guidelines for copolymer design to optimize film properties of non-cross-linked acrylic coatings. Variables studied included M.sub.n, T.sub.g, functionality (number of graft segments), flexible spacer effects, and #PHBA/COOH ratio (length of graft segments). Results are shown in Tables 8 through 12.

Effects of M.sub.n of ungrafted and grafted acrylic copolymer backbones are shown in Table 8. T.sub.g, T.sub.cl, and adhesion were essentially independent of M.sub.n regardless of the presence or absence of flexible spacer. However, reverse impact resistance and hardness increased greatly with M.sub.n. L-C copolymers with backbone M.sub.n of 15,000 and 28,000 had excellent reverse impact resistance (>70 in-lb) and good hardness (H - 2H) when T.sub.g, functionality, and #PHBA/COOH ratio were optimal.

In Table 10, L-C copolymers having different functionalities are compared. While the reported data were obtained for L-C copolymers with backbone Mns of about 5,000, similar trends were observed for higher M.sub.n s. It can be seen that increasing functionality increased T.sub.g and T.sub.cl. Increasing functionality increased hardness but had an adverse effect on reverse impact resistance. In general, films with functionality above 7.5 mol % had poor reverse impact resistance.

The effects of the presence of flexible spacer between the acrylic backbone and the oligo-PHBA segments are exemplified in Table 11. The flexible spacer reduces the effect of grafting on T.sub.g. Impact resistance improved when flexible spacer was present. However, the effect of flexible spacer on reverse impact resistance appeared less substantial when the backbone T.sub.g was decreased to about -10.degree. C. Films with flexible spacer were slightly softer than those without one.

Effects of #PHBA/COOH ratio are exemplified in Table 12. As this ratio increased, T.sub.g (after grafting) increased slightly, T.sub.cl of L-C phase increased significantly, reverse impact resistance increased greatly, and hardness increased slightly.

Appearance of films were also greatly influenced by the PHBA/COOH ratio. At functionality of 5 mol %, films were translucent when this ratio was about 3, but they were opaque when it was 4 or above.

To summarize the observations in this example, it appears that the following guidelines may be useful in designing L-C acrylic copolymers for coatings binders:

(1) T.sub.g of the amorphous part of the copolymer may be low; the optimum for a given end use may be in the range of -20.degree. to 0.degree. C. Amorphous copolymers of such low T.sub.g are normally far too soft to be usable as coatings. Acrylic lacquers are usually formulated with T.sub.g near or slightly above the highest service temperature. Apparently the presence of L-C domains can harden low T.sub.g films, yet the elasticity associated with low T.sub.g is at least partly retained.

(2) The best combination of hardness and elasticity is attained when functionality is low but PHBA/COOH ratio is high.

(3) Flexible spacer improves impact resistance when backbone T.sub.g is 0.degree. C. or higher but has relatively little effect when T.sub.g is -10.degree. C. Introduction of flexible spacer by the method used in this study has the disadvantage of placing relatively unhindered ester groups between the acrylic backbone and the mesogenic group; these ester groups are relatively vulnerable to hydrolysis in water and weather. Other potential routes for introducing flexible spacers are costly. Thus for practical purposes it may be preferable to use low T.sub.g backbones and dispense with flexible spacer.

Example 3

In this example it will be demonstrated that the L-C acrylic copolymers of Example 2 can be cross-linked with a melamine resin to provide hard, tough enamels.

Amorphous acrylic copolymers composed of MMA, BA, and acrylic acid having calculated T.sub.g of -30.degree., -10.degree., and +10.degree. C. and M.sub.n of 4,700.+-.200 and functionality of 5 mol percent acrylic acid were synthesized as described in Example 2. Each was grafted with PHBA, as described, to provide L-C graft copolymers having PHBA-COOH ratios of 4.+-.0.2. Liquid crystallinity was confirmed by polarizing miscroscopy.

Each of the above copolymers was dissolved or dispersed in a methyl isobutyl ketone solution containing HMMM crosslinking resin and p-toluene sulfonic acid (p-TSA) catalyst. The weight ratio was 70.6/28.6/0.7 L-C copolymer/HMMM/p-TSA. The mixture was exposed to ultrasonic energy to promote mixing. It was cast on untreated cold, rolled steel panels and baked in a forced air oven for 30 minutes at 150.degree. C. to give a cured film.

Knoop hardness and reverse impact resistance of the 6 enamels were tested as described in Example 2. Results are shown in Table 13.

Thus, it is evident that the presence of mesogenic groups improved both hardness and impact resistance for enamels made from copolymers having T.sub.g s of -30.degree. and -10.degree.. When T.sub.g is +10.degree., the impact resistance of the L-C film is inferior but the finish is extraordinarily hard. For comparison, the hardness of current auto topcoat enamels is about about 12 Kn.

In other experiments it was determined that the optimum M.sub.n for HMMM crosslinked L-C copolymers for high-solids enamels is about 5,000. As shown in Example 2, higher molecular weights are desirable for uncrosslinked enamels.

Example 4

L-C telechelic oligoester diols are prepared and cross-linked with a resin, preferably a melamine resin, to provide the coatings of this example. After baking, the coatings retained their L-C character which provided the improved characteristics to the coatings. The properties of the coatings were tested on cold-rolled steel panels.

The ratio of L-C telechelic oligoester diols to resin should be in the range of 95:5 to 50:50, and is preferably about 70:30. The L-C oligoester diols were prepared by reacting 4,4'-terephthaloyldioxydibenzoyl (TOBC) with molar equivalents of aliphatic diols. The general formula is as follows: ##STR3## Where R" and R"" are residues of aliphatic or cycloaliphatic radicals having carbon chain lengths up to 12 and R'" is a residue of aromatic (up to 10 carbons) or cycloaliphatics (up to 12 carbons) or aliphatics (up to 36 carbons) radicals

n=5 to 16; m=2 to 4; p=2 to 100;

q=1 to 20.

The value of n, sometimes referred to as spacer length, should preferably be in the range of 5 to 12. When n=5 or less, there is poor miscibility in forming enamels and at higher n values mixing becomes increasingly difficult.

Coatings were prepared by mixing the L-C oligoester diols or polyols after solubilization with melamine or polyisocyante resin in the presence of an accelerator. The coatings were cast on panels and baked at cross-linking temperatures for testing. L-C oligoester polyols may be prepared by replacing part of the aliphatic diol with a triol or tetrol.

Testing.

Proton NMR spectra were recorded at 34.degree. C. on a Varian Associates EM-390 90 MHz NMR spectrometer, using Me.sub.4 Si as internal standard. IR spectra were recorded at 25.degree. C. on a Mattson Cygnus FT-IR using films cast on NaCl plates with polystyrene as standard. A DuPont model 990 thermal analyzer was used for differential scanning calorimetry (DSC) at heating rates of 10.degree./min. After the crystalline-mesophase transition temperature (T.sub.m) was reached, the temperature was held for 1 min. before the scan was resumed. Capillary melting points were used to confirm the thermal data. M.sub.n and M.sub.w were determined by gel-permeation chromatography (GPC) with a Waters model 520 pump equipped with a model R401 refractive index detector, a model M730 data analyzer, and Ultrastragel 100 A, 500 A, 1000 A, and 10000 A columns. Mass analysis was performed. A Leitz Labolux microscope equipped with a polarizing filter was used for optical micrographs at 500x magnification; diols were observed immediately after heating to T.sub.m, enamels were observed at room temperature.

Seven samples of the L-C oligoester diols were prepared and designated 1a to 1g, inclusive and, for comparison, seven samples of non L-C oligoester diols were prepared and designated 2a to 2g, inclusive, having corresponding n values and made into amorphous coatings. These corresponding n values are indicated, as follows: ##EQU1##

In the preparation of the products, reagent materials were used and the steel panels which were coated were commercially available cold-rolled steel panels sold under the trademark Bonderite 1000 and having a size of 3 inches by 9 inches by 24 GA.

Preparation of 1a-g. TOBC was prepared from terephthaloyl chloride and p-hydroxybenzoic acid (PHBA) as described by Bilibin et al at Polymer Science USSR (1984) 26, 2882. TOBC (0.005 mol), diol (0.025 mol), and diphenyl oxide (10 mL) were placed in a 100 mL single-necked round-bottomed flask equipped with a magnetic stirring bar, a distillation adapter, and a septum. The flask was flushed with argon for 15 min., and was stirred and heated in an oil bath at 190.degree.-200.degree. C. under slow argon flow. The reaction mixture became homogeneous after 5 minutes and the evolution of HCl was observed. The reaction was continued until the evolution of HCl was no longer detectable by moistened litmus paper (4-5 hr.). The hot reaction mixture was poured cautiously into 100 mL of toluene and cooled. The oily residue that separated was dissolved in CH.sub.2 Cl.sub.2, washed 3 times with water, and dried over anhydrous MgSO.sub.4. The solution was filtered and concentrated using a rotary evaporator. The residue was precipitated from methanol. Yields were 87-92% based on TOBC .sup.1 H NMR for 1c in CDCl.sub.3 ; 1.4 (broad), 3.6 (triplet), 4.2 (multiplet), 6.8 (doublet), 8.1 ppm (multiplet). FT-IR for 1c: 3420, 2960, 2938, 1720, 1606, 1512 cm.sup.-1. L-C diols 1a-g had similar spectra.

For comparison to the L-C oligoester diols of this example, non-L-C oligoester diols were prepared from diols in which R=(CH.sub.2).sub.4 and made into amorphous coating.

Preparation of 2a-g. The diacid chloride precursor was prepared by substituting adipoyl chloride for terepthaloyl chloride in Bilibin's procedure. Reaction of this precursor with diols was carried out as described for 1a-g except that the products were not poured into toluene. Diols 2a-g were resinous solids which solidified on standing.

Enamel formation. Oligoester diols 1b-g and 2a-g, HMMM (hexakis (methyloxy-methyl) melamine resin), methyl isobutyl ketone (MIBK), as a solvent and p-toluenesulfonic acid (p-TSA) as a catalyst were thoroughly mixed in a 70/30/30/0.3 wt. ratio. The solution was cast on cold rolled steel panels and baked at 150.degree. C. for 30 minutes. Less soluble L-C diols 1e-g were melted, dispersed in solvent, mixed with HMMM and immediately cast as films.

Oligoester Diols. The physical properties of 1a-g obtained by GPC, DSC and polarizing optical microscopy are summarized in Table 14.

.sup.1 H NMR and 1R spectra were consistent with structures 1a-g and 2a-g assuming that partial chain extension occurred as indicated by GPC. Low M.sub.n values and slightly high H analyses suggest that small amounts of unreacted HO(CH.sub.2).sub.n OH were present in the product.

The L-C nature of 1a-g was demonstrated by DSC (FIG. 10) in which two first order transitions were observed; the crystalline-mesophase transition temperature (T.sub.m), and the mesophase-isotropic transition temperature (T.sub.i). The thermal data revealed an odd-even spacer effect for T.sub.m. Smectic-nematic transitions were not evident in the DSC.

In contrast, diols 2a-g were apparently not L-C materials. Only one first order transition was observed by DSC.

The mesophases of 1a-g were observed in polarized optical micrographs taken immediately after melting the sample. Textures were identified by comparing appearance with published micrographs. See: Noel, Polymeric Liquid Crystals, Plenum Press, New York, (1984). A nematic texture is observed for 1f, while more highly ordered smectic textures are observed for 1b-e and 1g. Crystals were observed by microscopy for diols 2a-g.

Cross-linked Enamels. Diols 1b-g and 2a-g were cross-linked with HMMM at 150.degree. C., which falls within the temperature range at which 1b-g are liquid crystalline. Enamel formation of 1a was nearly impossible because of its poor miscibility. The properties of the cross-linked enamels are summarized in Table 15.

As shown in Table 15, all enamels had excellent adhesion, solvent resistance, and flexibility. The L-C enamels were far superior to control enamels in both hardness (5H-6H vs. H-2H) and impact resistance (50 to 80 in-lb vs. 8 to 15 in-lb). The odd spacers 1b and 1d afforded the best properties. Spacer variations did not measurably affect enamel properties in the control oligoesters.

DSC thermograms of the cross-linked enamels revealed onset of glass transitions (T.sub.g) ranging from T.sub.g 15.degree. to 35.degree. for L-C enamels 1b-g and amorphous enamels 2a-g. An odd-even pattern was not observed in either type.

Polarized optical micrographs revealed L-C regions in the cross-linked enamels of 1b-g. Enamels of 2a-g appeared amorphous. IR spectra of the baked L-C and amorphous enamels had peaks attributable to unreacted OH groups at 3420 cm.sup.-1 (OH stretch) and at 1271 cm.sup.-1 (OH bend).

In summary, the method used to make oligoester diols 1a-g was adapted from Bilibin's method for making chain L-C high polymers by using a five-fold excess of HO(CH.sub.2).sub.n OH. Spectral, chromatographic and mass analytical evidence all indicated that the expected products were obtained from the adapted process.

GPC and analytical data suggested that the structures with x=0 and x=1 predominate; smaller amounts of structures with x=1 and of HO(CH.sub.2).sub.n OH are probably present in 1a-g and 2a-g.

The thermal behavior of 1a-g observed by DSC (FIG. 10) confirms the presence of mesophases and is typical of low molecular weight liquid crystals. The odd-even effect is of interest because of its direct affect on the physical properties of the L-C diols. The lower T.sub.m for 1b and 1d is consistent with the higher entropy of activation for crystallization of odd-n spacers, demonstrated in several main chain L-C polymers, Ober et al, Advances in Polymer Science, Liquid Crystal Polymers I, Springer-Verlag (1984), Vol. 59. The apparent absence of nematic-smetic transitions in the DSC suggests the observed morphology exists for the entire mesophase.

The nematic texture of oligomeric L-C diol 1f is the same as reported for the homologous main chain L-C high polymer, Lenz, Journal Polymer Science, Polymer Symposium (1985) 72, 1-8.

Oligomeric diols lb-d were soluble in MIBK and were miscible with the HMMM cross-linker; films were readily cast. Higher melting diols 1e-g were less miscible, but the consistently good film properties indicate that adequate mixing was achieved. Mixing of diol 1a with HMMM was inadequate to produce uniform films.

Enamels made from odd-n L-C diols 1b and 1d had better impact resistance than those made from even-n diols. This effect may be attributed to an odd-even effect, although other variables may be involved.

The enhanced properties of the L-C diol enamels are not simply explainable by the monomer raising the T.sub.g of the coating. In fact, T.sub.g s of the cross-linked enamels of 1b-g are abnormally low for hard coatings, and are similar to the much softer control enamels.

Example 5

A non-L-C linear oligoester diol was prepared by heating a mixture of:

a) phthalic acid (PA), isophthalic acid, terephthalic acid hexahydrophthalic anhydride;

b) an aliphatic dicarboxylic acid having a carbon chain length of from 4 to 36, such as adipic acid (AA); and

c) aliphatic primary or secondary diols or polyols, the aliphatic chain having from 2 to 12 carbons, such as neopentyl glycol (NPG).

The reaction of the mixture is effected under N.sub.2 at 230.degree. C. with removal of H.sub.2 O until the acid number was less than 10 mg KOH/g. The sum of the mols of acids should be less than the mols of diols and the ratio should be in the range of 1:2 to 1:1.1. A particular example of a mixture of PA, AA and NPG at a mol ratio of 1:1:3 was highly satisfactory.

A mixture of the diol or polyol, PHBA, an acid catalyst and particularly p-TSA and solvent was heated under N.sub.2 in a 3-neck flask equipped with stirrer, Dean-Stark trap, condenser and thermometer. The PHBA/diol or PHBA/polyol weight ratio varied from 20/80 to 60/40, but the preferred ratio is about 40/60; 0.2 weight % of p-TSA was used as an acid catalyst to provide a predominantly phenolic L-C oligoester diol or polyol. About 10 weight % of solvent was used; the amount was adjusted to maintain the temperature in the range of 210.degree. C. to 250.degree. C., and preferably in the range of 227.degree. to 233.degree. C. In an actual preparation the temperature was held at 230.degree. +/-3.degree. C. Distillate (cloudy H.sub.2 O) was collected in the Dean-Stark trap during 9 to 11 hr. The reaction mass was cooled to 115.degree. C., and MIBK was added to yield a solution (20/80 PHBA/diol ratio) or suspension (other PHBA/diol ratios) of the crude L-C polyol. A preferred solvent is Aromatic 150" sold by Exxon.

It is important that the acid catalyst be used and that the temperature be controlled to provide the L-C predominately phenolic oligoesters of the invention. Likewise, it is important that the PHBA be used in the weight ratio range specified to give the L-C diols desired.

The linear oligoester diol was heated with salycilic acid and with MHBA using a similar procedure to yield modified polyols. 60% to 80% of theoretical distillation was obtained.

Purification. The crude L-C polyols made from 20/80 and 30/70 PHBA/diol ratios were concentrated and dissolved in CH.sub.2 Cl.sub.2. The solution was washed 5 times with H.sub.2 O, dried with Na.sub.2 SO.sub.4, and concentrated on a rotary evaporator. The residues were heated at 120.degree. C. to constant weight. The crude L-C polyols made from 40/60 to 60/40 ratios were purified similarly but were not washed with water. They were heated at about 80.degree. C. under vacuum on a rotary evaporator to remove small amounts of volatile, crystalline material.

Enamel preparation. Solutions or mixtures of L-C polyol, HMMM and p-TSA in a 75/25/0.25 weight ratio were cast on cold-rolled panels and baked at 175.degree. C. for the specified time. Dry film thicknesses were 20 to 25 um.

Characterization and testing. lR spectra were recorded using a Perkin-Elmer 137 NaCl-prism spectrophotometer. A DuPont model 990 thermal analyzer was used for differential scanning calorimetry (DSC) at heating rates of 10.degree./min. After the crystalline-mesophase transition temperature (T.sub.m) was reached, the temperature was held for 1 min. before the scan was resumed. Capillary melting points were used to confirm the thermal data. M.sub.n and M.sub.w were determined by gel-permeation chromatography (GPC) with a Waters model 520 pump equipped with a model R401 refractive index detector, a model M730 data analyzer, and Ultrastragel 100 A, 500 A, 1000 A and 10000 A columns. Mass analysis was performed. A Leitz Labolux microscope equipped with a polarizing filter was used for optical micrographs at 500x magnification; L-C polyols were cast on glass slides and were dried and observed at 25.degree. C., and enamels were baked at 175.degree. C. for 20 minutes on the glass slides.

Hydroxyl numbers were determined by the pyromellitic dianhydride/imidazole method. See: Demarest, B. O.; Harper, L. E. Journal of Coating Technology 1983, 55(701), 65-77. Impact resistance and pencil hardness were tested according to ASTM-D 2793 and ASTM-D 3363, respectively. Solvent resistance was tested by spotting films with methyl ethyl ketone. Potentiometric titration in DMF indicated that a substantial fraction of phenolic groups are present in the oligomers, but it has not yet been feasible to reproducibly obtain quantitative results because precipitate formed during titration.

This preparation yields PHBA-modified oligomers, apparently with side reactions. The odor of phenol was barely detectable in the products, indicating that little phenol had been formed. p-TSA catalyst plays a crucial role. When p-TSA was not used in the 30/70 PHBA/diol reaction only 75% of theoretical distillate was collected, and the product smelled strongly of phenol. Solvent also plays an important role by helping control temperature and by facilitating removal of water. If desired, the products can be purified as described to remove small amounts of unreacted PHBA and possibly of phenol.

Modification of the PA/AA/NPG diol with salicylic and m-hydroxybenzoic acids apparently did not proceed as smoothly as the modification with PHBA. No liquid crystals could be detected in the products by polarizing microscopy.

Potentiometric titration and infrared spectra (peak at 3400 cm.sup.-1) indicate that phenolic end groups predominate in the product oligomers. Quantitative methods for end group analysis are being developed.

Molecular weights determined by GPC are provided in Table 16. Also provided are rough estimates of the average number of PHBA units per number average molecule. These estimates were obtained by multiplying product M.sub.n by the weight fraction of PHBA charged and dividing the result by 120, the molar mass of PHBA minus water.

The L-C character of PHBA-containing oligomers was demonstrated by polarizing microscopy as indicated in Table 16.

DSC data in Table 17 indicate that T.sub.g increases with increasing PHBA/diol ratios except for the 60/40 PHBA/diol ratio.

Enamel Coatings Properties. Clear coatings were formed by cross-linking the PHBA-modified oligomers with a standard melamine resin. Baking at 175.degree. C. was necessary to obtain optimal properties. The cured films were nearly transparent and glossy except for films made from 60/40 PHBA ratio L-C polyol. Adhesion was excellent.

The outstanding feature of enamels made from 40/60 to 50/50 PHBA/diol ratio L-C polyols is that they are both very hard and very impact resistant as shown in Table 18.

The enamels described in Table 18 with pencil hardness of 3H to 6H had excellent solvent (methyl ethyl ketone) resistance.

The salycilic acid modified oligomers did not cure at 175.degree. C. The MHBA modified oligomers cured at 175.degree. C. to give hard films, but all failed the 80 in-lb impact resistance test.

Polarizing micrographs showed clear evidence of the presence of liquid crystals in enamel films made from polyols modified by 30 percent or more of PHBA. L-C regions were not visible in cured films made from the PA/AA/NPG polyol or from the MPHA-modified enamels.

The results of the above experiments indicate that L-C regions substantially enhance a polymer resin's coating quality. Grafting oligomeric segments derived from PHBA or TPA/PHBA onto coating resins yields resins that contain liquid crystalline (L-C) phases. These phases impart at least three benefits: "solution" viscosity is reduced by the formation of non-aqueous dispersions, dry-to-touch times are sharply reduced, and films are both hardened and toughened. Imparting L-C characteristics to a resin minimizes the hardness/impact resistance tradeoff necessary with non-modified coating resins.

Although the invention has been described with regard to its preferred embodiments, it should be understood that various changes and modifications as would be obvious to one having the ordinary skill in this art may be made without departing from the scope of the invention which is set forth in the claims appended hereto.

The various features of this invention which are believed new are set forth in the following claims:

Claims

We claim:

1. A coating composition comprising a polymer composition which provides a coating binder having a T.sub.g between -50.degree. C. and +10.degree. C., the polymer composition having mesogenic groups in an amount between about 5 to about 50 percent by weight, the mesogenic groups comprising oligomeric p-hydroxybenzoic acid having the general formula: ##STR4## wherein n=2 to 12 and the mesogenic groups being covalently bound with an amorphous resin selected from the group consisting of 1. an acrylic resin; 2. a hydroxyl functional acrylic resin reacted with an acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride; 3. an alkyd resin; and 4. a hydroxyl functional alkyd resin reacted with an acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

2. A coating composition in accord with claim 1 which further comprises a cross-linking resin selected from the group consisting of (a) a melamine resin, (b) an epoxy resin and (c) a polyisocyante.

3. A coating composition as recited in claim 2 wherein the amorphous resin is the alkyd resin or the hydroxyl functional alkyd resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

4. A coating composition as recited in claim 2 wherein the amorphous resin is the acrylic resin or the hydroxyl functional acrylic resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

5. A coating composition as recited in claim 2 wherein the amorphous resin is the alkyd resin.

6. A coating composition as recited in claim 2 wherein the amorphous resin is the acrylic resin.

7. A coating composition in accord with claim 1 wherein the the acid is selected from the group consisting of succinic acid and succinic anhydride.

8. A coating composition as recited in claim 7 wherein the amorphous resin is the alkyd resin or the hydroxyl functional alkyd resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

9. A coating composition as recited in claim 7 wherein the amorphous resin is the acrylic resin or the hydroxyl functional acrylic resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

10. A coating composition as recited in claim 1 wherein the amorphous resin is the acrylic resin.

11. A coating composition as recited in claim 1 wherein the amorphous resin is the alkyd resin.

12. A coating composition as recited in claim 1 wherein the amorphous resin is the alkyd resin or the hydroxyl functional alkyd resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

13. A coating composition as recited in claim 12 wherein the alkyd resin is a reaction product of phthalic acid or the anhydride thereof, trimethylolpropane and linoleic acid.

14. A coating composition as recited in claim 1 wherein the amorphous resin is the acrylic resin or the hydroxyl functional acrylic resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

15. A composition in accord with claim 14 wherein the acrylic resin is the reaction product of methyl methacrylate, butyl acrylate and an acrylate selected from the group consisting of acrylic acid, methacrylic acid, 2-hydroxyethyl methacrylate or mixtures thereof.

16. A coating composition in accord with claim 1 wherein the acid is terephthalic acid.

17. A coating composition as recited in claim 16 wherein the amorphous resin is the alkyd resin or the hydroxyl functional alkyd resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

18. A coating composition as recited in claim 16 wherein the amorphous resin is the acrylic resin or the hydroxyl functional acrylic resin reacted with the acid selected from the group consisting of a dicarboxylic acid and dicarboxylic acid anhydride.

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