Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Processes of preparing a desired or intentional composition...
Reexamination Certificate
2001-10-09
2002-11-05
Szekely, Peter (Department: 1714)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Processes of preparing a desired or intentional composition...
C524S100000, C524S101000, C524S102000, C524S103000, C524S104000, C524S105000, C524S106000, C524S127000
Reexamination Certificate
active
06476105
ABSTRACT:
BACKGROUND OF THE INVENTION
Field of the Invention
The present invention relates to a polyamide resin composition having excellent weather resistance and coating adhesion property and more particularly, to the polyamide resin composition capable of direct painting without pretreatment of primer and maintaining excellent weather resistance for a long period of exposure outside by adding an appropriate amount of a weathering stabilizer and a coating adhesion improver.
Polyamide resins have been widely used in automotive interior and exterior parts, electrical parts, sport goods, and industrial parts because of their excellent physical properties such as mechanical strength, heat resistance, chemical resistance, scratch resistance, insulating property, arc resistance and the like. However, the use of these polyamide resins requiring weather resistance for a long period of time has been restricted since when polyamide resins are exposed outside for a long period of time, color can be deteriorated and physical properties become inferior for photodecomposition.
There have been studied to eliminate such problems by adding antioxidant or weathering stabilizer to polyamide resins (U.S. Pat. Nos. 5,945,469, 5,851,238, and 5,814,107). However, there is a drawback associated with adding such antioxidant or weathering stabilizer in that mechanical properties are remarkably reduced.
As another method to improve weather resistance, surface is coated to maintain its physical properties. However, it requires pretreatment of the surface or primer such as flame treatment, ozone treatment, and plasma treatment since polyamide resins are non-polar polymers having poor adhesion property to paints. And further, this method requires additional devices for surface treatment and primer treatment, thus increase in cost and use of environmental hazard materials.
SUMMARY OF THE INVENTION
In an effort to solve these problems, the inventors of the present invention figured out that the polyamide resin composition can be capable of direct painting without pretreatment of primer and maintaining excellent weather resistance for a long period of exposure outside by adding an appropriate amount of a weathering stabilizer and a coating adhesion improver.
Therefore, an object of the present invention is to provide polyamide resin composition satisfying color for a long period of exposure and manufacturing cost and processability due to simplified preparing method.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is characterized in that polyamide resin composition comprises:
(A) 30-99 parts by weight of polyamide resin;
(B) 1-65 parts by weight of a reinforcing filler;
(C) 0.1-5 parts by weight of a hindered amine based weathering stabilizer having 3000-4000 of molecular weight; and
(D) 0.1-5 parts by weight of a coating adhesion improver selected from the group consisting of phosphorous-containing anti-oxidant, phosphorous-containing anti-oxidant heat stabilizer, phosphorous-containing anti-oxidant anti-static agent and phosphorous-containing anti-oxidant flame retardant.
The present invention is described in detail as set forth hereunder.
(A) Polyamide Resin
The polyamide resin of the present invention is prepared by polycondensation of cyclolactam having higher than 3-membered ring, &ohgr;-amino acid, or a mixture thereof or polycondensation of at least one of dicarboxylic acids and at least one of diamines. Examples of monomers for polycondensation include &egr;-caprolactam, aminocapronic acid, enantholactam, 7-aminoheptanoic acid, 11-aminoundecanoic acid, 9-aminononanoic acid, and &agr;-piperidone. Examples of diamines for polycondensation include tetramethylenediamine, hexamethylenediamine, nonamethylenediamine, decamethylenediamine, undecamethylenediamine, dodecamethylenediamine, p-aminoaniline, and m-xylenediamine. Examples of dicarboxylic acids include adipic acid, sebacic acid, dodecanedicarboxylic acid, glutaric acid, terephthalic acid, 2-methylterephthalic acid, isophthalic acid, and naphthalenedicarboxylic acid. Polyfunctional compounds can be added within less than 5 mol % in addition to dicarboxylic acids or diamines and examples are trimellitic acid and pyromellitic acid. Particular examples of the polyamide resin are nylon 6, nylon 7, nylon 8, nylon 11, nylon 12, nylon 2, nylon 66, nylon 69, nylon 610, nylon 611, nylon 612, nylon 6T, nylon 6/66, nylon 6/12, nylon 6/6T. These nylons can be blended at any desired ratio.
The polyamide resin may be prepared by any polymerization method such as anionic polymerization, mass polymerization, solution polymerization, melt polymerization using salts, interfacial polymerization. Any polymerization can be applied for polyamide copolymers polymerized by using two or three kinds of monomers.
Moreover, polyimide (PI), polysulfone (PSU), polyethersulfone (PES), polyphenylene sulfide (PPS), polyphenylene ether (PPE), high impact polystyrene (HIPS), acrylonitrile-butadiene-styrene copolymer (ABS copolymer), acrylonitrile-ethylenepropylene-styrene copolymer (AES copolymer), acrylonitrile-styrene-arylacrylate (ASA), arylmetacrylate-butadiene-styrene (MBS), styrene-butadiene-styrene triblock copolymer, maleic anhydride grafted SBS block copolymer (SBS-gMA), maleic anhydride grafted SEBS block copolymer (SEBS-g-MA), polycarbonate, polyethyleneterephthalate (PET), polybutyleneterephthalate (PBT), all-acrylic, core-shell rubber, ethylenevinylacetate rubber (EVA), ethyleneethylacrylate (EEA), polyolefin resin, EPR rubber (EPR), EPDM rubber (EPDR), styrene butadiene rubber (SBR), ethylene vinylalcohol (EVOH), thermoplastic elastomer, plastomer, or a mixture thereof can be blended or polymerized to reinforce molecular weight, heat resistance and impact strength. Polystyrene grafted with oxazolines, polyolefin grafted with maleic anhydrides or a compatibilizer can be added to improve properties of these blends. Polyamide resin may be alloyed with one selected from acrylonitrile-butadiene copolymer, polyolefin resin, polycarbonate, polyethylene terephthalate, polybutyene terephthalate, polysulfone, polyethersulfone, polyphenylene sulfide, polyphenylene ether, oxide, high impact strength polystyrene and a mixture thereof. The polyamide resin (A) should be added in the amount of 30-99 parts by weight, preferably 40-99 parts by weight. If the amount of polyamide resin (A) is less than 30 parts by weight, it looses its nylon properties. If it is more than 99 parts by weight, coating adhesion is inferior.
(B) Reinforcing Filler
The polyamide resin composition of the present invention contains a reinforcing filler to reinforce mechanical strength and heat resistance. Particular examples of the filler are glass fiber, glass beads, glass flakes, mica, talc, carbon fibers, kaolin, wollastonite, molybdenum disulfate, potassium titanate, barium sulfate, conductive carbon black, aramide fibers, whisker and a mixture thereof. The filler (B) should be added in the amount of 1-65 parts by weight, preferably 5-60 parts by weight. If the amount is less than 1 part by weight, the physical properties are deteriorated. If the amount is more than 65 parts by weight, appearance of the molded product and processability become deteriorated.
(C) Weathering Stabilizer
Especially, the polyamide resin of the present invention contains a weathering stabilizer at an appropriate amount to reinforce weather resistance for a long period of exposure outside. Examples of weathering stabilizer are hindered amine light stabilizer (HALS), radical hals, phosphorous or phenol based anti-oxidant (AOs), benzotiazoles, hydrobenzophenones or a mixture thereof. When hindered amines are used, its volatile component or dissociated component during extrusion process should be within 10%. It is prefer not to react with other components except the main polymer and more preferably to have 3000-4000 of molecular weight. The weathering stabilizer can be used in the range of from 0.1 to 5 parts by weight, preferably 0.1 to 1 parts by weight. If the amount is less than 0.1 parts by weight, it is insufficient as a stab
Jeong Kie-Youn
Lee Sang-Rok
Seo Hee-Won
Hyundai Motor Company
Szekely Peter
LandOfFree
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