USRE29954E - Abrasion-resistant mineral-filled thermosetting molding composition - Google Patents
Abrasion-resistant mineral-filled thermosetting molding composition Download PDFInfo
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- USRE29954E USRE29954E US05/722,801 US72280176A USRE29954E US RE29954 E USRE29954 E US RE29954E US 72280176 A US72280176 A US 72280176A US RE29954 E USRE29954 E US RE29954E
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- 238000000465 moulding Methods 0.000 title claims abstract description 73
- 239000000203 mixture Substances 0.000 title claims abstract description 68
- 238000005299 abrasion Methods 0.000 title claims abstract description 47
- 229920001187 thermosetting polymer Polymers 0.000 title claims abstract description 20
- 229910052500 inorganic mineral Inorganic materials 0.000 title abstract description 8
- 239000011707 mineral Substances 0.000 title abstract description 8
- -1 polyethylene Polymers 0.000 claims abstract description 44
- 239000004698 Polyethylene Substances 0.000 claims abstract description 39
- 229920000573 polyethylene Polymers 0.000 claims abstract description 39
- 229920000098 polyolefin Polymers 0.000 claims abstract description 34
- 229920005989 resin Polymers 0.000 claims abstract description 34
- 239000011347 resin Substances 0.000 claims abstract description 34
- 239000012764 mineral filler Substances 0.000 claims abstract description 22
- 229920001225 polyester resin Polymers 0.000 claims abstract description 15
- 239000004645 polyester resin Substances 0.000 claims abstract description 15
- 150000003254 radicals Chemical class 0.000 claims abstract description 15
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- 230000002787 reinforcement Effects 0.000 claims abstract description 5
- 239000005062 Polybutadiene Substances 0.000 claims abstract description 3
- 229920002857 polybutadiene Polymers 0.000 claims abstract description 3
- 239000000945 filler Substances 0.000 claims description 8
- 239000003365 glass fiber Substances 0.000 claims description 8
- 239000002557 mineral fiber Substances 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- 239000004743 Polypropylene Substances 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 6
- 229920001155 polypropylene Polymers 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 229920003002 synthetic resin Polymers 0.000 claims description 2
- 238000010136 thermoset moulding Methods 0.000 claims 5
- 229920005672 polyolefin resin Polymers 0.000 claims 4
- 239000000654 additive Substances 0.000 claims 3
- 230000000996 additive effect Effects 0.000 claims 3
- 229920000728 polyester Polymers 0.000 claims 3
- 229920013716 polyethylene resin Polymers 0.000 claims 2
- 229920006026 co-polymeric resin Polymers 0.000 claims 1
- 239000002952 polymeric resin Substances 0.000 claims 1
- 239000011152 fibreglass Substances 0.000 abstract description 4
- 238000007792 addition Methods 0.000 description 19
- 230000035515 penetration Effects 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 9
- 239000000463 material Substances 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000011953 free-radical catalyst Substances 0.000 description 3
- 238000010137 moulding (plastic) Methods 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 230000007257 malfunction Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000012783 reinforcing fiber Substances 0.000 description 2
- 239000012779 reinforcing material Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- 235000011132 calcium sulphate Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003828 free initiator Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- CABDEMAGSHRORS-UHFFFAOYSA-N oxirane;hydrate Chemical compound O.C1CO1 CABDEMAGSHRORS-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Images
Classifications
-
- 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
- C08L67/06—Unsaturated polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- C08L63/08—Epoxidised polymerised polyenes
-
- 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
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
Definitions
- This invention relates to plastic moldings and particularly to moldings and molding compositions which possess a high degree of abrasion resistance.
- Thermosetting molding compositions containing mineral fillers and reinforced with mineral fibers are widely used to provide electrical and mechanical components having advantageous physical, chemical and electrical characteristics.
- moldings made with mineral fillers such as aluminum hydrate, glass fibers, and polyester or epoxy resins have good dimensional stability, high mechanical strength, good corrosion resistance, and high arc-resistance, arc quenching and non-tracking properties.
- these otherwise advantageous moldings have low abrasion resistance, due both to the abrasive properties of the mineral fillers and fibers, and also to the low abrasion resistance of otherwise desirable resins.
- high abrasion resistance would greatly increase the usefulness and life of such moldings. Abrasive surface wear causes dimensional changes and produces a fine dust.
- the dust not only causes mechanical problems such as binding of close-fitting moving parts, but in electrical equipment can also cause malfunction by settling between electrical contacts and preventing them from closing the electrical circuits. The problem is accentuated by the increased life now required in electrical apparatus. Where previous moldings performed for thousands of cycles, equipment is now designed to operate for millions of cycles, so that previously acceptable abrasion resistance has now become marginal or unsatisfactory.
- the principal object of the present invention is to provide a high degree of abrasion resistance in mineral-filled, thermosetting plastic moldings.
- a further object of the invention is to improve abrasion resistance without appreciably decreasing the physical and electrical properties of the moldings, and in at least some cases to improve such properties. It is a further object of the invention to decrease the wetting characteristics of the surfaces of moldings, and thereby improve their electrical properties. It is a further object of the invention to obtain these improvements by the addition to the molding composition of components which, in the proportions used, are compatible therewith and stable therein, and which in the preferred compositions appear to interact or cross-link with other components of the composition.
- polyolefin in accordance with the invention, these objects are accomplished by incorporating in the mineral-filled thermosetting molding compound a small proportion of a polyolefin which is solid resin at room temperature.
- polyolefin applies to a known group of synthetic resins of which polyethylene and polypropylene are presently the most readily available and preferred polymers.
- the group comprises various classes or types of solid polyethylenes, including the low-density or branched-chain polymers, the high-density or linear polyethylenes, and the medium-density polyethylenes. As a family, these have many common properties and are in general useful and applicable in accordance with the invention.
- the group of polyethylenes also includes polyethylene copolymers produced by copolymerizing the polyethylene with a minor proportion of an alpha-olefin such as propylene or butene-1 or an acrylate for the purpose of modifying certain characteristics of the basic polyethylene, and these may also be used in accordance with the invention.
- an alpha-olefin such as propylene or butene-1 or an acrylate
- the molding composition to which the polyolefin is added may be any of various conventional compositions comprising a thermosetting resin and a mineral filler, which preferably includes a reinforcing mineral fiber, together with small proportions of other conventional components such as parting agents, pigments or coloring agents, weathering agents, etc.
- the character and proportions of these components may be chosen on the usual basis of intercompatability, molding characteristics, intended usage, desired properties, overall economics, etc.
- the invention is applicably generally to mineral-filled thermosetting resin compositions, to improve the abrasion resistance of moldings made therefrom.
- the invention is especially applicable to, and in its preferred embodiment is applied to, compositions in which thermosetting resin is a free radical initiated polymer and which contain a free radical catalyst or initiator, since in the presence of such a catalyst the added polyolefin will chemically react and cross link in the composition, to yield finished moldings which, besides improved abrasion resistance, have substantially the same physical properties as without the addition of polyolefin, and in some cases, have better physical properties.
- the free radical initiated polymers which may constitute the resins in preferred compositions include conventional polyester-type resins, which generally require and contain free radical initiators. They also include epoxy type resins which are modified to be reactive in the presence of a free radical catalyst. They include, for example, epoxidized polybutadiene resins.
- the mineral fillers used may be any of a large number of conventional fillers and mixtures of fillers, and may be selected from the following typical groups: calcium carbonate, clay, silica, talc, alumina, hydrated alumina, calcium sulphate, calcium silicate, antimony trioxide, etc.
- the reinforcing fibers used may be any of the conventional mineral fibers, such as fiberglass, asbestos, etc.
- a conventional method of manufacturing a mineral filled, fiberglass-reinforced polyester resin molding compound is as follows: First, the catalyzed resin, pigments, and parting agents are charged into a mixer and mixed together. Second, the mineral fillers are added, and mixed until there is an even dispersion of the fillers in the resin. Third, the glass reinforcements is added and the mixing is continued only long enough to coat or cover the glass fibers. The compound is then ready to mold, using conventional thermosetting molding practices.
- the polyolefin is preferably incorporated in the molding-composition in the form of a fine powder, desirably 100-mesh or finer, if optimum properties of surface appearance and uniformity of abrasion resistance are to be obtained. Coarser powders may be used, but surface appearance may suffer. The finer the polyolefin powder used the easier it will be to obtain a uniform blending and dispersion in the mix, which is desirable both for purposes of abrasion resistance and to minimize surface blemishing. When the polyolefin is added as a fine powder, I prefer to thoroughly admix it with the resin before adding the mineral filler. The polyolefin may also be added with the mineral fibers, for ease of handling.
- the polyolefin may be prepared by first dissolving it in a volatile solvent, such as carbon tetrachloride, with heat as needed, and mixing the solution with a quantity of mineral filler, and subsequently removing the solvent and grinding the solid mixture to a fine condition.
- a volatile solvent such as carbon tetrachloride
- the exact method or time of adding the polyolefin to the molding composition is not as important as complete dispersion of the polyolefin throughout the compound.
- a uniform blend of resin, filler, and polyolefin powder is desirably obtained before adding the glass or other mineral fiber reinforcing material, in order to minimize the amount of mixing to which the fiber is subjected.
- the amount of polyolefin added will, of course, depend on the desired degree of improvement in abrasion resistance, on the character and proportions of other components present, on the physical properties required, etc. Effective amounts of polyolefin range from about one-half (1/2) percent or less up to about 10% by weight of the total composition. In general, small additions of polyolefin produce proportionately greater improvement in abrasion resistance per increment of polyolefin added than do additional increments of added polyolefin, and an optimal percentage will be reached at which further additions produce little further improvement in abrasion resistance. In the preferred compositions containing free radical initiated polymers and free radical catalysts, the first increments of added polyolefin may improve physical properties, although in at least some cases further additions have an adverse effect on such properties.
- Tests for abrasion resistance of moldings in accordance with the invention have been conducted on various types of equipment, designed to simulate various abrasion conditions encountered in electrical or mechanical devices. Three types of test equipment which I have found appropriate are illustrated in the accompanying drawing.
- FIG. 1 is a diagrammatic side elevation of a test device in which abrasion resistance is indicated by the depth to which a vibrating metal ball penetrates into a test sample in a predetermined time;
- FIG. 2 is a diagrammatic side elevation of a test device in which abrasion resistance is indicated by the depth of penetration of the corner of one test sample into the face of another test sample vibrated against the first;
- FIG. 3 is a diagrammatic side elevation of a test device in which abrasion resistance is indicated by the number of rubbing cycles required to produce a given weight loss in a test sample when reciprocated under load against a stainless steel surface.
- a test sample 10 is fixed on a support 12 and a steel ball 14 is vibrated in contact with the sample, under a predetermined load, by a vibrator 16. Depth of ball penetration in a given time indicates the abrasion resistance of the sample.
- one test sample 20 is fixed on a support 12, and a second sample 22 is mounted on an angle block 24 in contact with the corner of the first sample 20, under a predetermined pressure.
- the angle block 24 and second sample 22 are vibrated by a vibrator 26 for a specified length of time, and the depth of penetration into the surface of the test sample 22 is taken as the indication of abrasion resistance.
- a test sample 30 is reciprocated by a bar 32 against the surface of a stainless steel wear plate 34, under a load 36 which applies a predetermined weight per square inch of rubbing surface of the sample.
- the weight loss in a given number of cycles required indicates the abrasion resistance of the sample.
- the proportions given are by weight.
- a group of five test samples were tested under standardized test conditions and the abrasive penetration results given represent the results on all five samples.
- the numerical values given for abrasive penetration represent depth of penetration measured on a standardized scale.
- Moldings were made from a molding compound containing 19% catalyzed polyester resin, 5% glass fiber, and 76% mineral filler, with and without the addition of 3% polyethylene. Groups of test samples of such moldings were tested on the apparatus of FIGS. 1 and 2, and the following abrasion resistance results were obtained.
- Moldings were made from a molding compound containing 25% catalyzed polyester resin, 15% glass fiber, and 60% mineral filler, with and without the addition of 3% polyethylene. Test samples of such moldings gave the following abrasion resistance results:
- Moldings were made from a molding compound containing 30% catalyzed polyester resin, 30% glass fiber, and 40% mineral filler, with and without the addition of 3% polyethylene. Test samples of such moldings gave the following abrasion resistance results:
- Moldings were made from molding compounds containing 30% modified epoxy resin, 15% glass fiber, and 55% mineral filler, with and without the addition of 3% polyethylene.
- the modified epoxy resin used was that sold as "Oxiron" PC-1 the manufacturer of which identifies it as a stable premix material such as is described in U.S. Pat. No. 2,829,135, with an oxirane content of about 9%, and containing fumaric acid in sufficient amount to react with the oxirane oxygen on heating.
- Test samples of such moldings were tested on the apparatus of FIGS. 1 and 2, and the following abrasion resistance results were obtained:
- the amount of polyolefin to be used in any particular molding composition will vary with the character and proportions of resin, filler and fiber in the composition and with the degree of abrasion resistance and other properties desired. The optimum will vary with the properties required. The amount used may range from an effective small amount sufficient to produce effective improvement in abrasion resistance, up to an optimal percentage at which abrasion resistance is substantially maximum and beyond which additional polyolefin produces little or no improvement in abrasion resistance and may adversely effect other properties, as indicated by the following examples.
- Moldings were made from a molding composition containing 30% catalyzed polyester resin, 30% glass fiber, and 40% mineral filler, by weight, with varying percentages of polyethylene, ranging from none to 10%. Test samples of these moldings were tested on the apparatus of FIG. 2 and the results obtained are tabulated below. In addition, test samples of the same compositions were tested for flexural strength by a standard method. The results of these flexure tests are also tabulated below.
- Moldings were made of compositions containing 24% catalyzed polyester resin, 15% fiberglass, and 61% mineral filler, by weight, with varying percentages of polyethylene. Tests of the moldings on the apparatus of FIG. 1, gave the following results:
- Moldings were prepared from a composition containing 25% catalyzed polyester resin, 15% fiberglass, and 60% mineral filler, with varying amounts of added polyethylene, as in Example II. Test samples were subjected to flexure until failure occurred, and the results obtained were as follows:
- Moldings were made from the molding compositions of Example 2, except that 3% polypropylene was used instead of polyethylene. Samples were tested for abrasion resistance with the following results.
- compositions may be made in which up to 10% of polyolefin is added to other thermosetting resin compositions containing varying proportions of components in accordance with conventional practices in the art.
- the proportion of resin present is preferably at least about 15% and may range up to 60% or more of the basic compositions.
- the top limit on resin is usually a matter of economics.
- the mineral filler may comprise from 40% to 85% of the total basic composition, and such filler may be partially or wholly composed of fibrous reinforcing material in amounts of from 5% to 50% of the basic composition.
- polyolefin in accordance with the invention is especially advantageous in compositions containing free radical initiated resins, such as polyester resins and modified epoxy resins.
- the polyester resin molding compounds have a very high tolerance for polyolefins compared to that for materials such as wax and metallic soaps previously used in attempts to reduce the abrasion resistance of mineral-filled molding compositions.
- the improved abrasion resistance of moldings made in accordance with this invention greatly increases the usefulness of the moldings.
- the designer is no longer required to minimize or avoid rubbing contact at the surfaces of the moldings, and bearing surfaces can often be formed as part of a molding and special bearing elements can be eliminated.
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- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
______________________________________
Abrasive Penetration
Test Method
No Polyethylene
3% Polyethylene
______________________________________
FIG. 1 36 6
FIG. 2 15 3
______________________________________
______________________________________
Abrasive Penetration
Test Method No Polyethylene
3% Polyethylene
______________________________________
FIG. 1 17 6
FIG. 2 15 3
FIG. 3 (20 × 10.sup.4 cycles)
10.6 10.1
______________________________________
.sup.1 Gm. loss
______________________________________
Abrasive Penetration
Test Method
No Polyethylene
3% Polyethylene
______________________________________
FIG. 1 19 7
FIG. 2 17 10
______________________________________
______________________________________
Abrasive Penetration
Test Method
No Polyethylene
3% Polyethylene
______________________________________
FIG. 1 8 41/2
FIG. 2 171/2 31/2
______________________________________
______________________________________
Flexure
Percent Poly- Abrasive Strength
ethylene Penetration Lbs./sq. in.
______________________________________
0 25 32,453
21/2 13 33,542
5 11 25,013
71/2 7 21,467
10 6 20,594
______________________________________
______________________________________
Abrasive
Percent polyethylene: penetration
______________________________________
0 17
1 103/4
11/2 9
2 61/4
21/2 61/4
3 6
______________________________________
______________________________________
Flexure strength,
Percent polyethylene:
Lbs./sq.in
______________________________________
0 23,000
1 23,700
11/2 24,200
2 21,000
3 21,300
______________________________________
______________________________________
Test Method
No Polyolefin 3% Polypropylene
______________________________________
FIG. 1 17 10
FIG. 2 15 8
______________________________________
Claims (8)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US360038A US3397169A (en) | 1964-04-15 | 1964-04-15 | Abrasion-resistant mineral-filled thermosetting molding composition |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US360038A Reissue US3397169A (en) | 1964-04-15 | 1964-04-15 | Abrasion-resistant mineral-filled thermosetting molding composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE29954E true USRE29954E (en) | 1979-04-03 |
Family
ID=23416339
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US360038A Expired - Lifetime US3397169A (en) | 1964-04-15 | 1964-04-15 | Abrasion-resistant mineral-filled thermosetting molding composition |
| US05/722,801 Expired - Lifetime USRE29954E (en) | 1964-04-15 | 1976-09-13 | Abrasion-resistant mineral-filled thermosetting molding composition |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US360038A Expired - Lifetime US3397169A (en) | 1964-04-15 | 1964-04-15 | Abrasion-resistant mineral-filled thermosetting molding composition |
Country Status (1)
| Country | Link |
|---|---|
| US (2) | US3397169A (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3480577A (en) * | 1965-12-27 | 1969-11-25 | Shell Oil Co | Paint compositions comprising epoxy resin ester,pigment and glass fibers or polypropylene powder |
| US3534120A (en) * | 1966-05-11 | 1970-10-13 | Kanebo Ltd | Copolyester filaments containing minor amount of polyolefins |
| US3923726A (en) * | 1969-06-09 | 1975-12-02 | Minnesota Mining & Mfg | Process of making colored high temperature polymers |
| BE789450R (en) * | 1971-09-29 | 1973-01-15 | Siemens Ag | IMPREGNATION MATERIAL FOR FIBER MATS |
| US3988412A (en) * | 1973-04-12 | 1976-10-26 | Youngstown Sheet And Tube Company | Method of making pipe having a liner layer of mixed resins |
| US4134937A (en) * | 1974-06-12 | 1979-01-16 | Monsanto Research Corporation | Polyester resin composition |
| GB1477253A (en) * | 1974-06-29 | 1977-06-22 | Bayer Ag | Polymerisable organic dispersions |
| US4008294A (en) * | 1974-11-27 | 1977-02-15 | W. R. Grace & Co. | Thickened polyester composition containing ultrafine polypropylene fibers |
| US3988291A (en) * | 1975-05-27 | 1976-10-26 | Rostone Corporation | Precision-moldable abrasion-resistant molding composition and moldings |
| US4146586A (en) * | 1977-07-06 | 1979-03-27 | Eastman Kodak Company | Polyester/substantially amorphous polyolefin hot-melt adhesive blends |
| US4271061A (en) * | 1979-03-06 | 1981-06-02 | Nitto Electric Industrial Co., Ltd. | Epoxy resin compositions for sealing semiconductors |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2518462A (en) * | 1946-09-10 | 1950-08-15 | Du Pont | Abrasion resistant finishes containing polyethylene |
| FR1291844A (en) | 1960-04-26 | 1962-04-27 | British Industrial Plastics | Molding composition comprising in particular a polyester resin |
| DE1137209B (en) * | 1960-08-19 | 1962-09-27 | Norddeutsche Kabelwerke Ag | Process for the production of molded parts by thermosetting molding compositions which contain resinous polyepoxides and polymeric organic compounds |
| GB936351A (en) | 1960-04-26 | 1963-09-11 | British Industrial Plastics | Polyester moulding compositions |
| US3256362A (en) * | 1960-10-19 | 1966-06-14 | Roemmler Gmbh H | Process for modifying polyolefines with unsaturated polyesters |
| US3291857A (en) * | 1960-02-17 | 1966-12-13 | William W Howerton | Curable polymers |
| US3328339A (en) * | 1963-08-28 | 1967-06-27 | Monsanto Co | Reinforced plastics containing base treated, calcined particulate fillers and organosilane coupling agents |
-
1964
- 1964-04-15 US US360038A patent/US3397169A/en not_active Expired - Lifetime
-
1976
- 1976-09-13 US US05/722,801 patent/USRE29954E/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2518462A (en) * | 1946-09-10 | 1950-08-15 | Du Pont | Abrasion resistant finishes containing polyethylene |
| US3291857A (en) * | 1960-02-17 | 1966-12-13 | William W Howerton | Curable polymers |
| FR1291844A (en) | 1960-04-26 | 1962-04-27 | British Industrial Plastics | Molding composition comprising in particular a polyester resin |
| GB936351A (en) | 1960-04-26 | 1963-09-11 | British Industrial Plastics | Polyester moulding compositions |
| DE1137209B (en) * | 1960-08-19 | 1962-09-27 | Norddeutsche Kabelwerke Ag | Process for the production of molded parts by thermosetting molding compositions which contain resinous polyepoxides and polymeric organic compounds |
| US3256362A (en) * | 1960-10-19 | 1966-06-14 | Roemmler Gmbh H | Process for modifying polyolefines with unsaturated polyesters |
| US3328339A (en) * | 1963-08-28 | 1967-06-27 | Monsanto Co | Reinforced plastics containing base treated, calcined particulate fillers and organosilane coupling agents |
Non-Patent Citations (2)
| Title |
|---|
| Bjorksten et al., "Polyesters and their Applications", 1956, p. 73. * |
| Skeist, "Epoxy Resins", Plastics Application Series, Reinhold Publishing Co., 1958, pp. 77 & 78. * |
Also Published As
| Publication number | Publication date |
|---|---|
| US3397169A (en) | 1968-08-13 |
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