EP1299501A2 - High tracking index liquid crystalline polymers and related applications - Google Patents

High tracking index liquid crystalline polymers and related applications

Info

Publication number
EP1299501A2
EP1299501A2 EP01950885A EP01950885A EP1299501A2 EP 1299501 A2 EP1299501 A2 EP 1299501A2 EP 01950885 A EP01950885 A EP 01950885A EP 01950885 A EP01950885 A EP 01950885A EP 1299501 A2 EP1299501 A2 EP 1299501A2
Authority
EP
European Patent Office
Prior art keywords
electronic
electrical apparatus
liquid crystalline
acid
volts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP01950885A
Other languages
German (de)
French (fr)
Inventor
Steve Gust Cottis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ticona LLC
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of EP1299501A2 publication Critical patent/EP1299501A2/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/38—Polymers
    • 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
    • C08K7/00—Use of ingredients characterised by shape
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00—Fireproofing materials
    • C09K21/14—Macromolecular materials
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
    • C08G63/605—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds the hydroxy and carboxylic groups being bound to aromatic rings
    • 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
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2237—Oxides; Hydroxides of metals of titanium

Definitions

  • thermotropic liquid crystalline polymer compositions having a high tracking index and excellent flame-retarding properties and applications made therefrom.
  • Liquid crystalline polymers have become important items of commerce, being useful as molding resins for general purpose uses, and more specifically in the electrical and electronics industries due to their thermal stability, chemical resistance, and other desirable properties.
  • the molding resins should exhibit good tracking resistance and good flame-retarding properties.
  • Tracking is a phenomenon associated with the formation of permanent and progressive conducting paths on the surface of materials by the combined effects of an electrical field and external surface pollution. Electrical tracking can occur when a damaged energized electrical part becomes wet, e.g., from electrolytes or condensation. This tracking may lead to flash over and arcing that causes further damage in the electrical part, causing a catastrophic cascade failure. Tracking can occur at low voltages, e.g., 100V AC or less but becomes less likely as the voltage is reduced.
  • the comparative tracking index (CTI) rating provides a quantitative indication of a composition's ability to perform as an electrical insulating material under wet and/or contaminated conditions. In determining the CTI rating of a resin composition, two electrodes are placed on a molded test specimen.
  • the CTI rating of the test specimen is the maximum electrode voltage differential at which, in five consecutive tests, more than 50 drops of the solution must be applied to the test specimen in order to cause tracking to occur.
  • the CTI value is the voltage at which a molding is found to exhibit conductivity.
  • the CTI value is expected to be at least 220 volts. Flame-retarding properties are measured according to the Underwriters' Laboratories Bulletin No. 94 test, in which a sample having approximate dimensions of 2.5" by 0.5" by 0.0625" is contacted with a Bunsen burner flame for 10 seconds.
  • the sample is then removed and the amount of time it takes for the flame to be out is recorded.
  • the test also characterizes the material as "dripping" or “non-dripping," since flaming drops of resin which could cause adjacent structures to burn are of concern.
  • a sample is said to "drip” when some molten resin falls off the bar in the test. If the drip is burning, and it burns enough to ignite a cotton ball located beneath the bar, the material fails the test. Even self-extinguishing drips, which technically do not cause the material to fail the test, are considered undesirable in practice.
  • the test is repeated with the same sample placed in contact with a Bunsen burner flame again for 10 seconds.
  • a UL V-0 rating requires a flame-out-time (FOT) of not more than 10 seconds for any one sample in a test of five samples ⁇ each repeated twice, and a cumulative FOT of not more than 50 seconds total for the five samples.
  • FOT flame-out-time
  • a V-1 rating is universally required for electrical applications with V-0 being necessary, although flame retardants having V-1 or V-2 ratings are also suitable for many end uses.
  • a V-0 rating with a maximum cumulative FOT of 35 seconds is often mandated by purchasers.
  • halogen-containing compounds such as decabromodiphenylethane or brominated polystyrene
  • US Patent No. 4,824,723 discloses a flame resistant electrically insulating multilayer material comprising a core of a thermoplastic polymer and blends and an outer layer comprising blends of the polymers with a halogen-containing flame-retardant, with a V-0 rating and an excellent CTI rating of greater than 500 volts.
  • US Patent No. 4,636,544 discloses the use of titanium dioxide (TiO2) to improve the
  • My invention includes compositions consisting essentially of: a) a wholly aromatic polyester which is melt processible and which displays anisotropy in the molten state; b) a non-conductive filler material having a mean particle size of less than about 4 ⁇ m, present in an amount sufficient to increase the comparative tracking index (CTI) rating of said composition to above 220 volts and render the composition non-burning; and optionally c) at least one fluorescent optical brightener in an amount of greater than 0.005 wt. % and having a boiling point of T P > T m -60C, where T m is the melting point of the LCP.
  • Compositions with and without at least one fluorescent optical brightener are included within my invention.
  • My invention also includes a practical method for the production of a resin composition for electrical and electronics application having good tracking index as well as flame-resistant properties by blending a wholly aromatic polyester with a non-conductive filler material having a mean particle size of less than about 4 ⁇ m, preferably a chloride- process rutile-type metal-oxides coated titanium dioxide and preferably in an amount of about 30 to 50 weight percent filler material based on total weight of said aromatic polyester and said filler material.
  • an electronic or electrical apparatus comprising a component formed from a liquid crystalline polymer composition consisting essentially of a) a thermotropic liquid crystalline polymer component which is an aromatic polyester, poly(ester-amide), poly(ester-imide), poly(ester-amide-imide), or mixtures thereof; b) at least one non-conductive filling agent component having a longest dimension of less than about 4 ⁇ m; and optionally c) at least one fluorescent optical brightener in an amount of greater than 0.005 wt.
  • said electronic or electrical apparatus has a comparative tracking index (CTI) rating above 220 volts and a flammability rating of V-0 in test UL-94 at a .0625" thickness, and said apparatus also comprises an electrical conductor carrying a voltage of 200 volts or more.
  • CTI comparative tracking index
  • my invention includes applications made from the foregoing compositions where surface and/or optical quality is/are desired.
  • thermotropic liquid crystalline polymer compositions of my invention are first described.
  • Thermotropic liquid crystalline polymers are known in the art by various terms, including “liquid crystal” and “anisotropic melts.”
  • a polymer is optically anisotropic if, in the melt phase, it transmits light when examined between crossed polarizers using a polarizing microscope.
  • thermotropic is meant that the polymer may be melted and then re-solidified, i.e. is thermoplastic.
  • the LCP polymers useful herein include thermotropic liquid crystalline polyesters and liquid crystalline poly(ester-amides), poly(ester-imide), poly(ester-amide-imide), or mixtures thereof. These terms have their usual meaning, and simply indicate that the repeat units in the polymer are joined by ester and optionally amide and / or imide linkages. Preferred polymers are liquid crystalline polyesters, and it is further preferred that these polyesters be aromatic polyesters.
  • aromatic is meant that, except for the carbon atoms contained in functional groups such as ester, amide or imide, all of the carbon atoms in the main chain of the polymer are present in aromatic rings such as phenylene, naphthylylene, biphenylene, etc. Carbon atoms in other types of groupings such as alkyl may be present as substituents on the aromatic rings, as in a repeat unit derived from methylhydroquinone or 2-t-butyl-4-hydroxybenzoic acid, and or also present at other places in the polymer such as in n-alkyl amides. Other substituent groups such as halogen, ether, and aryl may also be present in the LCP.
  • the components of the wholly aromatic polyester used in the LCP compositions of the present invention there may be used for example: i) hydroquinone; ii) 4,4'- dihydroxybiphenyl(4, 4'-biphenol); iii) isophthalic acid; iv) terephthalic acid; v) p- hydroxybenzoic acid or its derivatives; vi) 4,4'-dihydroxybiphenyl (4,4'-bibenzoic acid) or its derivatives; viii) 2,6-naphthalenedicarboxylic acid; iv) 6-hydroxy-2-naphthoic acid, or combinations thereof.
  • LCP compositions are known to have exceptionally high tensile strength and modulus compared to analogous polymers not having a liquid crystalline character. Applicants have found that an addition of about 30 to 50 percent by weight of a non-conductive filler having a mean particle size of less than 4 ⁇ m to the wholly aromatic polyester surprisingly improves the tracking index and flame-resistant properties of the compositions for meeting material specifications required for electrical apparatuses such as circuit breakers, relays, connectors, etc., without the need for a flame-retardant component commonly required in the prior art.
  • non-conductive filler The precise nature of the operation of the non-conductive filler is unknown in improving both the tracking index and flame-resistant properties of the LCP resin. It is believed that the high concentration of non-conductive particles in the resin and especially at the surface, leads to the formation of insulated regions which hinder the formation of the carbonaceous conducting deposits during the tracking process. However, this is not meant to be a limitation or requirement of the present invention.
  • non-conductive powdery fillers include, but not limited to: diatomaceous earth and wollastonite; metal oxides such as iron oxides, titanium oxides, barium oxides, zinc oxides and alumina; metal carbonates such as calcium carbonate and magnesium carbonate; metal sulfates such as calcium sulfate and barium sulfate; phosphates of aluminum, calcium, magnesium, zinc, cerium and mixed metals; titanates of magnesium, calcium, aluminum and mixed metals; fluorides of magnesium and calcium; silicates of zinc, zirconium, calcium, barium, magnesium, mixed alkaline earths and naturally occurring silicate minerals and the like; aluminosilicates of alkali and alkaline earths, and naturally occurring aluminosilicates and the like; oxalates of calcium, zinc, magnesium, aluminum and mixed metals; aluminates of zinc, calcium, magnesium, and mixed alkaline earth silicon carbide; silicon nitride; and boron nitride.
  • Preferred non-conductive fillers for use in the LCP composition of the present invention include titanium dioxide and modified titanium dioxide pigments. Titanium dioxide generally finds wide application as a white pigment having a large hiding power. The surfaces of the titanium oxide particles may be untreated, or may be coated with an oxide of a metal such as aluminum, silicon or zirconia giving them a coating with high surface area, or may be treated with an organic acid such as stearic acid or lauric acid or an organosiloxane oil.
  • Useful crystal forms of titanium dioxide include anatase and rutile. The former is semi- stable and changes to the stable rutile form at high temperature. The rutile form is preferred.
  • the titanium dioxide particulates may take any discrete form such as particles, flakes, and the like.
  • a preferred non-conductive filler is a rutile-type high solids metal oxides coated titanium dioxide, such as a chloride process rutile type titanium dioxide.
  • a most preferred non-conductive filler is a titanium dioxide pigment with 97% TiO2 and with surface treated with alumina and an organic substance.
  • the size of the non-conductive filler is desirable that the filler particulates be of a size of less than 4 ⁇ m, and preferably less than 1 ⁇ m, and most preferably in the range of 0.10 to 0.30 ⁇ m.
  • Aggregates or agglomerates of non- conductive filler particulates are also useful as long as the average diameter of the aggregate or agglomerate is within the above prescribed size range of the non-conductive filler particles. Aggregates are distinguished from agglomerates in that aggregates are held together by strong bonds such as fusion bonds and cannot be fragmented easily, while agglomerates are weakly bonded and can be broken up by high energy agitation.
  • the amount of non-conductive filler present in the LCP compositions of the present invention is defined as a level sufficient to achieve a UL94 flammability rating of V-0 at .0625" while maintaining a CTI exceeding 220 volts.
  • the level of the non- conductive filler may range from about 30 to about 50 percent by weight of the total weight of the resin.
  • the boiling point of the brightening agent should preferably be as follows: Tb p > T m -60C, where T p is the boiling point of the brightening agent and T m is the melting point of the LCP.
  • Brightness enhancing agents are also commonly known as fluorescent optical brighteners. They include, but are not particularly limited to, 2,2'-(thiophendiyl)-bis-(t-butyl benzoxazole); 2-(stibyl-4")-(naphtho-r,2',4,5)-l,2,3-triazole-2"-sulfonic acid phenyl ester; and 7-(4 , -chloro-6"-diethylamino-r,3',5'-triazine-4'-yl)amino-3-phenyl coumarin.
  • fluorescent optical brighteners which have one or more moieties derived from substituted anthracene, stilbene, triazine, thiazole, benzoxazole, coumarin, xanthene, triazole, oxazole, thiophene or pyrazoline may be utilized in the LCP compositions of the present invention.
  • suitable optical brighteners which can be used in accordance with this invention are Uvitex® OB from the Ciba-Geigy Chemical Company, Ardsley, N.Y.
  • Uvitex® OB is thought to be 2,5-Bis(5-tert-butyl-2-benzoxazoly)thiopene having bis(alkyl-substituted benzoxazolyl)thiophene structure;
  • Leucopure® EGM from Sandoz, East Hanover, N. J. Leucopure.
  • Leucopure® EGM is thought to be 7-(2h-naphthol(l,2-d)-triazol-2yl)-3phenyl- coumarin; Phorwhite® K-20G2 from Mobay Chemical Corporation, Union, N.J. and is thought to be a pyrazoline derivative; Eastobrite® OB-1 from Eastman Chemical Products, Inc.
  • Uvitex® OB is most preferred for use in accordance with this invention.
  • a high-boiling brightness enhancing agent or fluorescent brightener
  • a high-boiling brightness enhancing agent or fluorescent brightener
  • this extraordinarily small amount of fluorescent brightener when used in combination with the non-conductive filler not only substantially enhances the appearance (e.g., surface and optical quality) of the material, but also improves the flame resistance of the composition in general by lowering its burn time.. Consequently, the addition of the fluorescent brightener allows more non-conductive fillers to be used.
  • the fluorescent brighteners extends the range of non-conductive filler in the LCP compositions of the present invention from about 43 to above 45 weight percent.
  • compositions of the invention may also optionally contain various well-known additives that are non-conductive in amounts which do not affect the flame-retardant and electrical insulating properties of the resins.
  • additives include UV stabilizers, lubricants, and colorants such as anthraquinone, direct dyes, para red, and the like.
  • the initial LCP compositions of the present invention maybe prepared from the appropriate monomers, or precursors thereof, by standard polycondensation techniques (which can include either melt, solution, and/or solid phase polymerization), preferably under anhydrous conditions and in an inert atmosphere.
  • polycondensation techniques which can include either melt, solution, and/or solid phase polymerization
  • the requisite amounts of acetic anhydride, the diols, the hydroxybenzoic acid (or optionally the acetate/diacetate derivatives of the diols/hydroxybenzoic acid), and the diacids, and optionally up to 20 percent excess acetic anhydride are combined in a reaction vessel equipped with a stirrer, nitrogen inlet tube, and combination distillation head/condenser (to facilitate by-product removal).
  • the reaction vessel and other equipment are dried and purged with nitrogen prior to use.
  • the vessel and stirred contents, maintained under nitrogen, are heated during which time the ingredients react and any by-product formed (such as, for example, acetic acid) is removed via the distillation head / condenser and is collected.
  • any by-product formed such as, for example, acetic acid
  • the molten mass is placed under reduced pressure (e.g. 10 mm of Hg(abs) or less) and is heated to a higher temperature, to facilitate removal of any remaining by-product and to complete the polymerization.
  • Polymerization conditions maybe varied according to, e.g., the reactants employed and the degree of polymerization desired.
  • the LCP melt may then be removed, cooled, and allowed to solidify prior to purification and / or subsequent processing such as melt compounding the liquid crystalline polyester composition with the non-conductive filler and optionally, the brightness enhancing agent of the present invention.
  • Melt compounding can be accomplished by any device capable of mixing the molten liquid crystalline polyester and filler compositions, such as an extruder, either single or twin screw. It is critical that the components are thoroughly blended together at an effective temperature at which the ingredients flux sufficiently for a uniform and maximum dispersion of the non-conductive particulates in the LCP melt.
  • Twin screw extruders may be either co-rotating or counter-rotating.
  • the compounded compositions may be cut into pellets for melt fabrication into a wide variety of articles by conventional processes such as extrusion and injection molding into such forms molded articles and films.
  • the molten polymer along with the non-conductive filler and the elective brightness enhancing agent may be transferred directly to an appropriate apparatus such as a melt extruder and/or injection molding machine or spinning unit, for the preparation of articles, such as molded and/or shaped electrical apparatuses.
  • the components should be thoroughly blended for maximum dispersions of the particulates.
  • the high CTI/flame-resistant LCP compositions described herein are useful in an electrical apparatus (which also includes an "electronic" apparatus) in which electrical conductors carrying relatively high voltages are present in or part of the apparatus.
  • high voltages herein is meant greater than about 200 volts, more preferably about 220 volts or more, especially preferably about 240 volts or more, and very preferably about 250 volts or more.
  • at least one of the conductors may carry a current of at least 0.5 amp, more preferably at least 1 amp. In a sense one could say the apparatus is exposed to voltages of a certain minimum level. These voltages may also be the "ratings" of the electrical apparatus.
  • the electrical apparatus is rated by an appropriate rating organization (for example Underwriter's Laboratories) to carry (be exposed) to an electrical current at a certain maximum voltage.
  • the high CTI flame-resistant LCP compositions described herein may function as suitable insulators in such an electrical apparatus at these higher voltages because of their high CTI ratings, that is they do not lose their insulating properties (over time) when exposed to such voltages.
  • compositions of this invention may be used in applications where surface and optical quality is desirable, such as reflectors and bezels for automobiles (e.g., headlights, rear lights, brake lights, direction indicators, foglamps and auxiliary lamps); reflectors for strobe lights (e.g., in aircraft, rescue and emergency vehicles, and warning lights of all kinds, e.g.
  • reflectors and bezels for automobiles e.g., headlights, rear lights, brake lights, direction indicators, foglamps and auxiliary lamps
  • reflectors for strobe lights e.g., in aircraft, rescue and emergency vehicles, and warning lights of all kinds, e.g.
  • reflectors for high-intensity lights e.g., in floodlights for sports stadiums, medical operating theater or surgery
  • reflectors for halogen lights e.g., spotlights for interior use in residential, industrial, commercial housing, spotlights for displays
  • general lighting e.g., searchlights for military, marine, police or personal use
  • reflectors for optical and photographic use e.g., in movie projectors, photo flash systems, slide projectors
  • aesthetic, reflective under-the-hood automotive parts e.g., manifold covers, rocker covers, valve covers); other aesthetic, reflective automotive parts (e.g., exhaust tailpipe ends, wheelcovers)
  • thermal (infrared) reflectors e.g., automotive use, such as heat shields around brakes, exhaust systems, or industrial use, such as reflecting heat from glass, metal or other furnaces
  • laser reflectors e.g., in research and industry, audio and electronics (CD players), space technology (satellites)
  • Comparative Tracking Index (CTI) test was in accordance to ASTM UL 746A to determine a specimen's ability to perform as an insulating material under wet and contaminated conditions, as volts of electricity which may be applied before tracking takes place in the polymer sample.
  • the maximum voltage that can be measured in a CTI test is 600 volts.
  • compounding of LCP compositions in the Examples below with the non-conductive filler and optionally in some examples, the brightening agent was done in a 30 or 40 mm ZSK Werner and Pfleiderer twin-screw extruder having a zone with conventional conveying elements, a zone with kneading or mixing elements, and a low pressure zone with venting under vacuum of any volatiles from the polymer melt, and a die.
  • the agent was first mixed with about 1/8 to 1/3 of the required non-conductive filler and this concentrate was introduced to the rear zone of the extruder.
  • the rest of the non-conductive filler (without brightening agent) was added from a different feeder to the rear zone.
  • the LCP pellets were added from a third feeder to the rear zone.
  • only two feeders were used, one for pellets and the other for the fine powdered ingredients.
  • As the compounded compositions exited the die they were quenched with a water spray and cut into pellets with a conventional strand cutter.
  • the extruder barrel and die temperatures were maintained at about 340°C. Prior to molding the pellets, the pellets were dried overnight for approximately 16 hours in a vacuum oven with N2 purge at 100 - 130°C
  • the dried polymer pellets were molded into standard test specimens, 1/16" T-bars, 1/8" T-bars or 2"diameter x 1/8" discs, using a 6 oz HPM molding machine with barrel temperatures of about 340°C and injection pressures of about 4000 psi. Unless indicated otherwise, the samples were injection molded at a high injection speed and a medium boost pressures of between 7000-12000 psi. In the examples denoted as "HIGH SPEED,” the injection molding was done at a high speed ( ⁇ 0.5-sec.) with a low boost pressures of 7000 - 10000 psi.
  • A This LCP polymer has the same composition as that of Example 4 of U.S. Patent 5,110,896 of hydroquinone / 4,4'-biphenol terephthlatic acid / 2,6-naphthalenedicarboxylic acid / 4-hydroxybenzoic acid in molar ratio 50/50/70/30/320.
  • B A LCP polymer with the same composition as that of Example 9 of U.S. Patent 5,110,896, comprising hydroquinone / 4,4'-biphenol / terephthalic acid / 2,6- naphthalenedicarboxylic acid / 4-hydroxybenzoic acid in molar ratio 50/50/85/15/320.
  • C A LCP polymer comprising of hydroquinone/terephthalic acid/isophthalic 'acid/2,6-naphthalenedicarboxylic acid/4-hydroxybenzoic acid in molar ratio 100/33/34/33/300.
  • the non-conductive filler is a chloride process rutile type titanium dioxide available from SMC Corp. of Baltimore, Md. as Tiona® RCL-4, with 97% TiO2 and with surface treated with alumina and an organic substance.
  • the following non-conductive filler materials were used: a titanium dioxide pigment from SMC Corp. as Tiona® RCL-2 with 90% TiO2 and with surface treated with Al/Si and an organic substance; titanium dioxide pigment Tiona® RCL- 3 80% TiO2 and with surface treated with Al/Si; a titanium dioxide pigment TIPURE R102 from E.I. du Pont de Nemours and Company of Wilmington, DE.
  • the brightening agent is from Ciba-Geigy Chemical Company, Ardsley, N.Y. as Uvitex® OB, which is a fine, yellow crystalline powder with a melting point of about 196-230°C. The material vaporizes starting at about 300°C.
  • Jetfil 575 C Talc known under the trade name Jetfil 575 C is obtained commercially from Luzenac America, Inc., Englewood, Colorado.
  • the glass filler is chopped E-glass fiber from Owens -Corning Fiberglas Technology h e, Summit, Illinois, as OC 408BC.
  • injection molding conditions were also found to affect the properties. Samples were prepared from the same compounded material and injection molded under high filling rate and low boost pressure, and then low feeding rate and high boost pressure. The properties including UL 94 rating and CTI were found to vary depending on the feeding method. Injection feeding speed is time in seconds to move the screw ram forward. Typically for the 6 OZ HPM used, a fast speed is less than 0.5 sec (primarily in the range of 0.1 - 0.2 sec) residence time, and a slow speed is greater than 0.5 sec. A high feeding rate is preferred to give a low residence time in the injection molding machine for optimum molding.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Excellent tracking index as well as flame-resistant properties are achieved with other desirable characteristics of LCPs in a resin composition consisting essentially of: a) a wholly aromatic polyester which is melt processible and which displays anisotropy in the molten state; b) a non-conductive filler material having a diameter of less than about 3 µm, with said non-conductive filler material being present in an amount sufficient to increase the comparative tracking index (CTI) rating of said composition to above 220 volts and render the composition non-burning. Optionally, an extraordinarily small amount of non-volatile fluorescent brightener can be added to the resin composition. In combination with the non-conductive filler, the fluorescent brightener is found to surprisingly and significantly improve the flame-retardant property of the resin.

Description

HIGH TRACKING INDEX LIQUID CRYSTALLINE POLYMERS AND RELATED APPLICATIONS
FIELD OF THE INVENTION The field of invention relates to thermotropic liquid crystalline polymer compositions having a high tracking index and excellent flame-retarding properties and applications made therefrom.
BACKGROUND OF THE INVENTION Liquid crystalline polymers (LCPs) have become important items of commerce, being useful as molding resins for general purpose uses, and more specifically in the electrical and electronics industries due to their thermal stability, chemical resistance, and other desirable properties. For many electrical and electronics applications, the molding resins should exhibit good tracking resistance and good flame-retarding properties.
Tracking is a phenomenon associated with the formation of permanent and progressive conducting paths on the surface of materials by the combined effects of an electrical field and external surface pollution. Electrical tracking can occur when a damaged energized electrical part becomes wet, e.g., from electrolytes or condensation. This tracking may lead to flash over and arcing that causes further damage in the electrical part, causing a catastrophic cascade failure. Tracking can occur at low voltages, e.g., 100V AC or less but becomes less likely as the voltage is reduced. The comparative tracking index (CTI) rating provides a quantitative indication of a composition's ability to perform as an electrical insulating material under wet and/or contaminated conditions. In determining the CTI rating of a resin composition, two electrodes are placed on a molded test specimen. A voltage differential is then established between the electrodes while an aqueous ammonium chloride solution is slowly dripped on the test specimen. The CTI rating of the test specimen is the maximum electrode voltage differential at which, in five consecutive tests, more than 50 drops of the solution must be applied to the test specimen in order to cause tracking to occur. Hence, the CTI value is the voltage at which a molding is found to exhibit conductivity. For some applications in the electrical and electronics industry, the CTI value is expected to be at least 220 volts. Flame-retarding properties are measured according to the Underwriters' Laboratories Bulletin No. 94 test, in which a sample having approximate dimensions of 2.5" by 0.5" by 0.0625" is contacted with a Bunsen burner flame for 10 seconds. The sample is then removed and the amount of time it takes for the flame to be out is recorded. The test also characterizes the material as "dripping" or "non-dripping," since flaming drops of resin which could cause adjacent structures to burn are of concern. A sample is said to "drip" when some molten resin falls off the bar in the test. If the drip is burning, and it burns enough to ignite a cotton ball located beneath the bar, the material fails the test. Even self-extinguishing drips, which technically do not cause the material to fail the test, are considered undesirable in practice. The test is repeated with the same sample placed in contact with a Bunsen burner flame again for 10 seconds. A UL V-0 rating requires a flame-out-time (FOT) of not more than 10 seconds for any one sample in a test of five samples ~ each repeated twice, and a cumulative FOT of not more than 50 seconds total for the five samples. When the five test samples have a cumulative FOT of 50 seconds and one or more of the five samples fails the 10-second test, than a V-1 rating is granted. A V-1 rating is universally required for electrical applications with V-0 being necessary, although flame retardants having V-1 or V-2 ratings are also suitable for many end uses. However, as a practical matter, a V-0 rating with a maximum cumulative FOT of 35 seconds is often mandated by purchasers.
It is known that halogen-containing compounds, such as decabromodiphenylethane or brominated polystyrene, can be used to prepare flame-retardant thermoplastics. US Patent No. 4,824,723 discloses a flame resistant electrically insulating multilayer material comprising a core of a thermoplastic polymer and blends and an outer layer comprising blends of the polymers with a halogen-containing flame-retardant, with a V-0 rating and an excellent CTI rating of greater than 500 volts. US Patent No. 4,636,544 discloses the use of titanium dioxide (TiO2) to improve the
CTI of resin molding compositions. However, a flame retardant is still required in the composition. TiO2 is used in a limited amount, preferably in an amount of about 1 to about 10 parts TiO2 for each 85 parts by weight of resin and halogenated poly(l,4-butylene terephthalate) composition. US Patent No. 4,421,888 discloses an article molded from a non- burning, non-dripping filled polyester composition having a high level of tracking resistance, comprising a mixture of polyethylene terephthalate and polybutylene terephthalate, a mixture of fiber glass and talc, and an effective amount of a halogen-containing flame-retardant. The disadvantage of flame-resistant agents, particularly flame- resistant agents based on halogenated hydrocarbons in thermoplastics and particularly in polyesters, is that they cause the electrical properties to deteriorate. Additionally, the use of halogen-containing compounds in thermoplastics is severely restricted in certain countries for the reason that they give off toxic fumes while burning, and the halogenated flame retardants themselves may be toxic. A need presently exists for plastic compositions which possess the thermal stability, chemical resistance, and other desirable characteristics of LCPs as well as excellent flame- resistant property and high CTI rating without the use of halogen-containing compounds as flame-retardants.
SUMMARY OF INVENTION My invention includes compositions consisting essentially of: a) a wholly aromatic polyester which is melt processible and which displays anisotropy in the molten state; b) a non-conductive filler material having a mean particle size of less than about 4 μm, present in an amount sufficient to increase the comparative tracking index (CTI) rating of said composition to above 220 volts and render the composition non-burning; and optionally c) at least one fluorescent optical brightener in an amount of greater than 0.005 wt. % and having a boiling point of T P > Tm-60C, where Tm is the melting point of the LCP. Compositions with and without at least one fluorescent optical brightener are included within my invention.
My invention also includes a practical method for the production of a resin composition for electrical and electronics application having good tracking index as well as flame-resistant properties by blending a wholly aromatic polyester with a non-conductive filler material having a mean particle size of less than about 4μm, preferably a chloride- process rutile-type metal-oxides coated titanium dioxide and preferably in an amount of about 30 to 50 weight percent filler material based on total weight of said aromatic polyester and said filler material.
Also includes in my invention are electrical devices, by fabricating the electrical devices from a resin composition consisting essentially of: a) a wholly aromatic polyester which is melt processible and which displays anisotropy in the molten state; b) a non- conductive filler material having a mean particle size of less than about 4 μm; and optionally c) at least one fluorescent optical brightener in an amount of greater than 0.005 wt. % and having a boiling point of Tt,p > Tm-60C, where Tm is the melting point of the LCP.
Also included in my invention is an electronic or electrical apparatus, comprising a component formed from a liquid crystalline polymer composition consisting essentially of a) a thermotropic liquid crystalline polymer component which is an aromatic polyester, poly(ester-amide), poly(ester-imide), poly(ester-amide-imide), or mixtures thereof; b) at least one non-conductive filling agent component having a longest dimension of less than about 4 μm; and optionally c) at least one fluorescent optical brightener in an amount of greater than 0.005 wt. % and having a boiling point of Tbp > Tm-60C, where Tm is the melting point of the LCP; and wherein said electronic or electrical apparatus has a comparative tracking index (CTI) rating above 220 volts and a flammability rating of V-0 in test UL-94 at a .0625" thickness, and said apparatus also comprises an electrical conductor carrying a voltage of 200 volts or more.
Furthermore, my invention includes applications made from the foregoing compositions where surface and/or optical quality is/are desired.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS Preferred embodiments of thermotropic liquid crystalline polymer compositions of my invention are first described. Thermotropic liquid crystalline polymers (LCPs) are known in the art by various terms, including "liquid crystal" and "anisotropic melts." A polymer is optically anisotropic if, in the melt phase, it transmits light when examined between crossed polarizers using a polarizing microscope. By "thermotropic" is meant that the polymer may be melted and then re-solidified, i.e. is thermoplastic. High CTI / Flame resistant LCP Compositions: The LCP polymers useful herein include thermotropic liquid crystalline polyesters and liquid crystalline poly(ester-amides), poly(ester-imide), poly(ester-amide-imide), or mixtures thereof. These terms have their usual meaning, and simply indicate that the repeat units in the polymer are joined by ester and optionally amide and / or imide linkages. Preferred polymers are liquid crystalline polyesters, and it is further preferred that these polyesters be aromatic polyesters. By "aromatic" is meant that, except for the carbon atoms contained in functional groups such as ester, amide or imide, all of the carbon atoms in the main chain of the polymer are present in aromatic rings such as phenylene, naphthylylene, biphenylene, etc. Carbon atoms in other types of groupings such as alkyl may be present as substituents on the aromatic rings, as in a repeat unit derived from methylhydroquinone or 2-t-butyl-4-hydroxybenzoic acid, and or also present at other places in the polymer such as in n-alkyl amides. Other substituent groups such as halogen, ether, and aryl may also be present in the LCP.
As the components of the wholly aromatic polyester used in the LCP compositions of the present invention, there may be used for example: i) hydroquinone; ii) 4,4'- dihydroxybiphenyl(4, 4'-biphenol); iii) isophthalic acid; iv) terephthalic acid; v) p- hydroxybenzoic acid or its derivatives; vi) 4,4'-dihydroxybiphenyl (4,4'-bibenzoic acid) or its derivatives; viii) 2,6-naphthalenedicarboxylic acid; iv) 6-hydroxy-2-naphthoic acid, or combinations thereof. These components are all known in the art and are commercially available or can be prepared by techniques readily available to those in the art. Of the combinations of these components, a combination of hydroquinone, 4,4'-dihydroxybiphenyl, terephthalic acid, 4-hydroxybenzoic acid, and 2,6-naphthalenedicarboxylic acid, is particularly preferred.
LCP compositions are known to have exceptionally high tensile strength and modulus compared to analogous polymers not having a liquid crystalline character. Applicants have found that an addition of about 30 to 50 percent by weight of a non-conductive filler having a mean particle size of less than 4 μm to the wholly aromatic polyester surprisingly improves the tracking index and flame-resistant properties of the compositions for meeting material specifications required for electrical apparatuses such as circuit breakers, relays, connectors, etc., without the need for a flame-retardant component commonly required in the prior art.
The precise nature of the operation of the non-conductive filler is unknown in improving both the tracking index and flame-resistant properties of the LCP resin. It is believed that the high concentration of non-conductive particles in the resin and especially at the surface, leads to the formation of insulated regions which hinder the formation of the carbonaceous conducting deposits during the tracking process. However, this is not meant to be a limitation or requirement of the present invention.
Examples of non-conductive powdery fillers include, but not limited to: diatomaceous earth and wollastonite; metal oxides such as iron oxides, titanium oxides, barium oxides, zinc oxides and alumina; metal carbonates such as calcium carbonate and magnesium carbonate; metal sulfates such as calcium sulfate and barium sulfate; phosphates of aluminum, calcium, magnesium, zinc, cerium and mixed metals; titanates of magnesium, calcium, aluminum and mixed metals; fluorides of magnesium and calcium; silicates of zinc, zirconium, calcium, barium, magnesium, mixed alkaline earths and naturally occurring silicate minerals and the like; aluminosilicates of alkali and alkaline earths, and naturally occurring aluminosilicates and the like; oxalates of calcium, zinc, magnesium, aluminum and mixed metals; aluminates of zinc, calcium, magnesium, and mixed alkaline earth silicon carbide; silicon nitride; and boron nitride. Preferred non-conductive fillers for use in the LCP composition of the present invention include titanium dioxide and modified titanium dioxide pigments. Titanium dioxide generally finds wide application as a white pigment having a large hiding power. The surfaces of the titanium oxide particles may be untreated, or may be coated with an oxide of a metal such as aluminum, silicon or zirconia giving them a coating with high surface area, or may be treated with an organic acid such as stearic acid or lauric acid or an organosiloxane oil. Useful crystal forms of titanium dioxide include anatase and rutile. The former is semi- stable and changes to the stable rutile form at high temperature. The rutile form is preferred. The titanium dioxide particulates may take any discrete form such as particles, flakes, and the like. A preferred non-conductive filler is a rutile-type high solids metal oxides coated titanium dioxide, such as a chloride process rutile type titanium dioxide. A most preferred non-conductive filler is a titanium dioxide pigment with 97% TiO2 and with surface treated with alumina and an organic substance.
One important aspect of the invention is the size of the non-conductive filler. It is desirable that the filler particulates be of a size of less than 4 μm, and preferably less than 1 μm, and most preferably in the range of 0.10 to 0.30 μm. Aggregates or agglomerates of non- conductive filler particulates are also useful as long as the average diameter of the aggregate or agglomerate is within the above prescribed size range of the non-conductive filler particles. Aggregates are distinguished from agglomerates in that aggregates are held together by strong bonds such as fusion bonds and cannot be fragmented easily, while agglomerates are weakly bonded and can be broken up by high energy agitation.
The amount of non-conductive filler present in the LCP compositions of the present invention is defined as a level sufficient to achieve a UL94 flammability rating of V-0 at .0625" while maintaining a CTI exceeding 220 volts. Typically, the level of the non- conductive filler may range from about 30 to about 50 percent by weight of the total weight of the resin.
High CTI / Flame-resistant LCP Compositions with Optional Brightness Enhancing Agent
It was surprisingly found that when a brightening agent was added to the electrically insulating composition, there was noticeable improvement in the flame-retardant properties of the material. The boiling point of the brightening agent should preferably be as follows: Tbp > Tm-60C, where T p is the boiling point of the brightening agent and Tm is the melting point of the LCP.
Brightness enhancing agents are also commonly known as fluorescent optical brighteners. They include, but are not particularly limited to, 2,2'-(thiophendiyl)-bis-(t-butyl benzoxazole); 2-(stibyl-4")-(naphtho-r,2',4,5)-l,2,3-triazole-2"-sulfonic acid phenyl ester; and 7-(4,-chloro-6"-diethylamino-r,3',5'-triazine-4'-yl)amino-3-phenyl coumarin. Other fluorescent optical brighteners which have one or more moieties derived from substituted anthracene, stilbene, triazine, thiazole, benzoxazole, coumarin, xanthene, triazole, oxazole, thiophene or pyrazoline may be utilized in the LCP compositions of the present invention. Examples of suitable optical brighteners which can be used in accordance with this invention are Uvitex® OB from the Ciba-Geigy Chemical Company, Ardsley, N.Y. Uvitex® OB is thought to be 2,5-Bis(5-tert-butyl-2-benzoxazoly)thiopene having bis(alkyl-substituted benzoxazolyl)thiophene structure; Leucopure® EGM from Sandoz, East Hanover, N. J. Leucopure. Leucopure® EGM is thought to be 7-(2h-naphthol(l,2-d)-triazol-2yl)-3phenyl- coumarin; Phorwhite® K-20G2 from Mobay Chemical Corporation, Union, N.J. and is thought to be a pyrazoline derivative; Eastobrite® OB-1 from Eastman Chemical Products, Inc. Kingsport, Tenn., which is thought to be 4,4-Bis(benzoxazoyι)stilbene. The above- mentioned Uvitex® OB is most preferred for use in accordance with this invention. A concentration of greater than about 0.005 weight percent, and preferably from about
0.005 to about 0.3 weight percent of a high-boiling brightness enhancing agent, or fluorescent brightener, was used in the high CTI flame-resistant LCP composition of the present invention. Surprisingly, this extraordinarily small amount of fluorescent brightener when used in combination with the non-conductive filler, not only substantially enhances the appearance (e.g., surface and optical quality) of the material, but also improves the flame resistance of the composition in general by lowering its burn time.. Consequently, the addition of the fluorescent brightener allows more non-conductive fillers to be used. The fluorescent brighteners extends the range of non-conductive filler in the LCP compositions of the present invention from about 43 to above 45 weight percent. The compositions of the invention may also optionally contain various well-known additives that are non-conductive in amounts which do not affect the flame-retardant and electrical insulating properties of the resins. Such additives include UV stabilizers, lubricants, and colorants such as anthraquinone, direct dyes, para red, and the like. Preparation of the High CTI / Flame-Resistant LCP Compositions
The initial LCP compositions of the present invention maybe prepared from the appropriate monomers, or precursors thereof, by standard polycondensation techniques (which can include either melt, solution, and/or solid phase polymerization), preferably under anhydrous conditions and in an inert atmosphere. For example, the requisite amounts of acetic anhydride, the diols, the hydroxybenzoic acid (or optionally the acetate/diacetate derivatives of the diols/hydroxybenzoic acid), and the diacids, and optionally up to 20 percent excess acetic anhydride, are combined in a reaction vessel equipped with a stirrer, nitrogen inlet tube, and combination distillation head/condenser (to facilitate by-product removal). The reaction vessel and other equipment are dried and purged with nitrogen prior to use. The vessel and stirred contents, maintained under nitrogen, are heated during which time the ingredients react and any by-product formed (such as, for example, acetic acid) is removed via the distillation head / condenser and is collected. When the polymerization appears nearly complete, as indicated by the amount of by-product collected remaining constant, the molten mass is placed under reduced pressure (e.g. 10 mm of Hg(abs) or less) and is heated to a higher temperature, to facilitate removal of any remaining by-product and to complete the polymerization. Polymerization conditions maybe varied according to, e.g., the reactants employed and the degree of polymerization desired.
The LCP melt may then be removed, cooled, and allowed to solidify prior to purification and / or subsequent processing such as melt compounding the liquid crystalline polyester composition with the non-conductive filler and optionally, the brightness enhancing agent of the present invention. Melt compounding can be accomplished by any device capable of mixing the molten liquid crystalline polyester and filler compositions, such as an extruder, either single or twin screw. It is critical that the components are thoroughly blended together at an effective temperature at which the ingredients flux sufficiently for a uniform and maximum dispersion of the non-conductive particulates in the LCP melt. Twin screw extruders may be either co-rotating or counter-rotating. The compounded compositions may be cut into pellets for melt fabrication into a wide variety of articles by conventional processes such as extrusion and injection molding into such forms molded articles and films. Optionally, the molten polymer along with the non-conductive filler and the elective brightness enhancing agent, may be transferred directly to an appropriate apparatus such as a melt extruder and/or injection molding machine or spinning unit, for the preparation of articles, such as molded and/or shaped electrical apparatuses. Again, the components should be thoroughly blended for maximum dispersions of the particulates.
The high CTI/flame-resistant LCP compositions described herein are useful in an electrical apparatus (which also includes an "electronic" apparatus) in which electrical conductors carrying relatively high voltages are present in or part of the apparatus. By high voltages herein is meant greater than about 200 volts, more preferably about 220 volts or more, especially preferably about 240 volts or more, and very preferably about 250 volts or more. Preferably at least one of the conductors may carry a current of at least 0.5 amp, more preferably at least 1 amp. In a sense one could say the apparatus is exposed to voltages of a certain minimum level. These voltages may also be the "ratings" of the electrical apparatus. By this is meant that the electrical apparatus is rated by an appropriate rating organization (for example Underwriter's Laboratories) to carry (be exposed) to an electrical current at a certain maximum voltage. The high CTI flame-resistant LCP compositions described herein may function as suitable insulators in such an electrical apparatus at these higher voltages because of their high CTI ratings, that is they do not lose their insulating properties (over time) when exposed to such voltages. In addition it is required that many if not most of the equipment which is used to conduct or handle electricity have a certain minimum level of flame or burning resistance, and the compositions described herein have this required property. Alternatively, compositions of this invention, particularly those containing optical brightening agent as described above, may be used in applications where surface and optical quality is desirable, such as reflectors and bezels for automobiles (e.g., headlights, rear lights, brake lights, direction indicators, foglamps and auxiliary lamps); reflectors for strobe lights (e.g., in aircraft, rescue and emergency vehicles, and warning lights of all kinds, e.g. road barriers); reflectors for high-intensity lights (e.g., in floodlights for sports stadiums, medical operating theater or surgery); reflectors for halogen lights (e.g., spotlights for interior use in residential, industrial, commercial housing, spotlights for displays); general lighting (e.g., searchlights for military, marine, police or personal use); reflectors for optical and photographic use (e.g., in movie projectors, photo flash systems, slide projectors); aesthetic, reflective under-the-hood automotive parts (e.g., manifold covers, rocker covers, valve covers); other aesthetic, reflective automotive parts (e.g., exhaust tailpipe ends, wheelcovers); thermal (infrared) reflectors (e.g., automotive use, such as heat shields around brakes, exhaust systems, or industrial use, such as reflecting heat from glass, metal or other furnaces); laser reflectors (e.g., in research and industry, audio and electronics (CD players), space technology (satellites)); aesthetic, reflective parts that reach high temperature (e.g., in space heaters, stovetops / oventops, pressing irons, electronic entertainment goods, computer parts, power tools, lit signs with incandescent bulbs; and solar reflectors (e.g., for energy production).
EXAMPLES The following examples illustrate preferred embodiments of my invention. My invention is not limited to these examples.
Tests:
Melt viscosities of dried samples were determined using a GalaxyO V, Model 8052 capillary rheometer made by Kayeness, Inc. The measurements were made at 350°C or 360° C at a shear rate of 1000 1/sec and with a die having an orifice of 30/1000 inch and a L/D of 20. Flammability tests were performed according to UL-94.
The following physical tests described herein were carried out according to procedures established by the American Society for Testing and Materials (ASTM), including: Flexural Modulus and Flexural Strength - ASTM D-790. Elongation to break strain gauges - ASTM D-638. Notched Izod - ASTM D-256.
DTUL (Heat Deflection Temperature) - ASTM D-648.
Comparative Tracking Index (CTI) test was in accordance to ASTM UL 746A to determine a specimen's ability to perform as an insulating material under wet and contaminated conditions, as volts of electricity which may be applied before tracking takes place in the polymer sample. The maximum voltage that can be measured in a CTI test is 600 volts. Preparations
Unless otherwise specified, compounding of LCP compositions in the Examples below with the non-conductive filler and optionally in some examples, the brightening agent, was done in a 30 or 40 mm ZSK Werner and Pfleiderer twin-screw extruder having a zone with conventional conveying elements, a zone with kneading or mixing elements, and a low pressure zone with venting under vacuum of any volatiles from the polymer melt, and a die. In examples utilizing the brightening agent and the 40MM ZSK, the agent was first mixed with about 1/8 to 1/3 of the required non-conductive filler and this concentrate was introduced to the rear zone of the extruder. The rest of the non-conductive filler (without brightening agent) was added from a different feeder to the rear zone. The LCP pellets were added from a third feeder to the rear zone. In examples utilizing the 30MM ZSK, only two feeders were used, one for pellets and the other for the fine powdered ingredients. As the compounded compositions exited the die, they were quenched with a water spray and cut into pellets with a conventional strand cutter. The extruder barrel and die temperatures were maintained at about 340°C. Prior to molding the pellets, the pellets were dried overnight for approximately 16 hours in a vacuum oven with N2 purge at 100 - 130°C
The dried polymer pellets were molded into standard test specimens, 1/16" T-bars, 1/8" T-bars or 2"diameter x 1/8" discs, using a 6 oz HPM molding machine with barrel temperatures of about 340°C and injection pressures of about 4000 psi. Unless indicated otherwise, the samples were injection molded at a high injection speed and a medium boost pressures of between 7000-12000 psi. In the examples denoted as "HIGH SPEED," the injection molding was done at a high speed (< 0.5-sec.) with a low boost pressures of 7000 - 10000 psi. In the samples denoted as "LO SPEED," the molding was done at a low speed of >0.5 sec, but with a high boost pressure of > 10000 psi. to facilitate the filling of the mold. Components: The compositions of LCP resins, the non-conductive filler, the brightening agent, and other fillers used in the examples are as follows:
A: This LCP polymer has the same composition as that of Example 4 of U.S. Patent 5,110,896 of hydroquinone / 4,4'-biphenol terephthlatic acid / 2,6-naphthalenedicarboxylic acid / 4-hydroxybenzoic acid in molar ratio 50/50/70/30/320. B: A LCP polymer with the same composition as that of Example 9 of U.S. Patent 5,110,896, comprising hydroquinone / 4,4'-biphenol / terephthalic acid / 2,6- naphthalenedicarboxylic acid / 4-hydroxybenzoic acid in molar ratio 50/50/85/15/320. C: A LCP polymer comprising of hydroquinone/terephthalic acid/isophthalic 'acid/2,6-naphthalenedicarboxylic acid/4-hydroxybenzoic acid in molar ratio 100/33/34/33/300.
Unless indicated otherwise, the non-conductive filler is a chloride process rutile type titanium dioxide available from SMC Corp. of Baltimore, Md. as Tiona® RCL-4, with 97% TiO2 and with surface treated with alumina and an organic substance. In some of the examples, the following non-conductive filler materials were used: a titanium dioxide pigment from SMC Corp. as Tiona® RCL-2 with 90% TiO2 and with surface treated with Al/Si and an organic substance; titanium dioxide pigment Tiona® RCL- 3 80% TiO2 and with surface treated with Al/Si; a titanium dioxide pigment TIPURE R102 from E.I. du Pont de Nemours and Company of Wilmington, DE.
The brightening agent is from Ciba-Geigy Chemical Company, Ardsley, N.Y. as Uvitex® OB, which is a fine, yellow crystalline powder with a melting point of about 196-230°C. The material vaporizes starting at about 300°C.
Talc known under the trade name Jetfil 575 C is obtained commercially from Luzenac America, Inc., Englewood, Colorado.
The glass filler is chopped E-glass fiber from Owens -Corning Fiberglas Technology h e, Summit, Illinois, as OC 408BC.
It should be noted that the compounding conditions and the screw design affect the properties of the molded parts. Samples were prepared from the same composition and compounded using different screw designs. The properties of the samples, including burn time and CTI rating, were found to vary depending on the screw design with a large screw design being preferred for optimum blending to assure that the components are thoroughly blended .
The injection molding conditions were also found to affect the properties. Samples were prepared from the same compounded material and injection molded under high filling rate and low boost pressure, and then low feeding rate and high boost pressure. The properties including UL 94 rating and CTI were found to vary depending on the feeding method. Injection feeding speed is time in seconds to move the screw ram forward. Typically for the 6 OZ HPM used, a fast speed is less than 0.5 sec (primarily in the range of 0.1 - 0.2 sec) residence time, and a slow speed is greater than 0.5 sec. A high feeding rate is preferred to give a low residence time in the injection molding machine for optimum molding.
Under the compounding and injection molding conditions tested, it was found that a titanium dioxide pigment available from SMC Corp. as Tiona® RCL-4, with 97% TiO2 and surface treated with alumina and an organic substance to be best. It was also found that certain LCP starting materials were better than others under certain conditions. Results are shown in Table 1. Table 1
Additional tests were conducted using RCL-4 as the non-conductive filler material. The test results in Table 2 shows that the mere presence of filler material in the compositions provides a resin that has a high track index performance and flame-retardant property as well as excellent mechanical properties.
Table 2
As shown in the following Table 3, the presence of a very small amount of a brightening agent such as Uvitex OB substantially and unexpectedly improves the composition's comparative tracking index and flame-resistance performance.
Table 3
As is apparent from the foregoing description, the materials prepared and procedures followed relate only to specific embodiments of the broad invention. While forms of the invention have been illustrated and described, modifications can be made without departing from the spirit and scope of the invention. Accordingly, it is not intended that the invention be limited thereby.

Claims

WHAT IS CLAIMED IS:
1. A electronic or electrical apparatus, comprising a component formed from a liquid crystalline polymer composition consisting essentially of: a) a thermotropic liquid crystalline polymer component which is an aromatic polyester, poly(ester-amide), poly(ester-imide), poly(ester-amide-imide), or mixtures thereof, b) at least one non-conductive filling agent filling agent component having a longest dimension of less than about 4 μm; and wherein said electronic or electrical apparatus has a comparative tracking index (CTI) rating above 220 volts and a flammability rating of V-0 in test UL-94 at a .0625" thickness.
2. The electronic or electrical apparatus of claim 1, wherein said liquid crystalline polymer (LCP) composition further comprises at least one fluorescent optical brightener: having a boiling point of Tbp > Tm-60C, where Tm is the melting point of the LCP; having one or more moieties derived from substituted anthracene, stilbene, triazine, thiazole, benzoxazole, coumarin, xanthene, triazole, oxazole, thiophene or pyrazoline; and in an amount of greater than 0.005 wt. % based on the total weight percents of a) and b).
3. The electronic or electrical apparatus of claim 1, wherein said non-conductive filling agent is a chloride process rutile type titanium dioxide having a diameter of about 0.1 to 0.3 μm.
4. The electronic or electrical apparatus of claim 1, wherein said non-conductive filling agent is a titanium dioxide pigment with 97% TiO2 and with surface treated with alumina and an organic substance and having a diameter of about 0.1 to about 0.3 μm.
5. The electronic or electrical apparatus of claim 1, wherein said thermotropic liquid crystalline polymer is a wholly aromatic polyester comprises repeating units derived from the group consisting of: i) hydroquinone; ii) 4,4'-dihydroxybiphenyl (4, 4'-biphenol); iii) isophthalic acid; iv) terephthalic acid; v) p-hydroxybenzoic acid; vi) 4,4'-dicarboxybiphenyl (4,4'bibenzoic acid); viii) 2,6-naphthalenedicarboxylic acid; iv) 6-hydroxy-2-naphthoic acid, or combinations thereof.
6. An electronic or electrical apparatus, comprising a component formed from a liquid crystalline polymer composition consisting essentially of: a) a thermotropic liquid crystalline polymer component which is an aromatic polyester, poly(ester-amide), poly(ester-imide), poly(ester-amide-imide), or mixtures thereof, b) at least one non-conductive filling agent filling agent component having a longest dimension of less than about 4 μm; and wherein said electronic or electrical apparatus has a comparative tracking index (CTI) rating above 220 volts and a flammability rating of V-0 in test UL-94 at a .0625" thickness, and said apparatus also comprises an electrical conductor carrying a voltage of 200 volts or more.
7. The electronic or electrical apparatus of claim 6, wherein said liquid crystalline polymer (LCP) composition further comprises at least one fluorescent optical brightener: having a boiling point of T p > Tm-60C, where Tm is the melting point of the LCP; having one or more moieties derived from substituted anthracene, stilbene, triazine, thiazole, benzoxazole, coumarin, xanthene, triazole, oxazole, thiophene or pyrazoline; and in an amount of greater than 0.005 wt. % based on the total weight percents of a) and b),
8. The electronic or electrical apparatus of claim 6, wherein said non-conductive filling agent is a chloride process rutile type titanium dioxide having a diameter of about 0.1 to 0.3 μm.
9. The electronic or electrical apparatus of claim 6, wherein said non-conductive filling agent is a titanium dioxide pigment with 97% TiO2 and with surface treated with alumina and an organic substance and having a diameter of about 0.1 to about 0.3 μm.
10. The electronic or electrical apparatus of claim 6, wherein said thermotropic liquid crystalline polymer is a wholly aromatic polyester comprises repeating units derived from the δ group consisting of: i) hydroquinone; ii) 4,4'-dihydroxybiphenyl (4, 4'-biphenol); iii) isophthalic acid; iv) terephthalic acid; v) p-hydroxybenzoic acid; vi) 4,4'-dicarboxybiphenyl (4,4'bibenzoic acid); viii) 2,6-naphthalenedicarboxylic acid; iv) 6-hydroxy-2-naphthoic acid, or combinations thereof.
11. The electronic or electrical apparatus of claim 6, wherein said voltage is about 250 volts or more.
12. The apparatus as recited in claim 6 which is rated to carry 200 volts or more.
13. The apparatus as recited in claim 6 which is rated to carry about 250 volts or more.
EP01950885A 2000-07-05 2001-07-05 High tracking index liquid crystalline polymers and related applications Withdrawn EP1299501A2 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US21581300P 2000-07-05 2000-07-05
US21581400P 2000-07-05 2000-07-05
US215814P 2000-07-05
US215813P 2000-07-05
PCT/US2001/021267 WO2002002717A2 (en) 2000-07-05 2001-07-05 High tracking index liquid crystalline polymers and related applications

Publications (1)

Publication Number Publication Date
EP1299501A2 true EP1299501A2 (en) 2003-04-09

Family

ID=26910414

Family Applications (1)

Application Number Title Priority Date Filing Date
EP01950885A Withdrawn EP1299501A2 (en) 2000-07-05 2001-07-05 High tracking index liquid crystalline polymers and related applications

Country Status (7)

Country Link
EP (1) EP1299501A2 (en)
JP (1) JP5349724B2 (en)
KR (1) KR20030019953A (en)
CN (1) CN100489029C (en)
AU (1) AU2001271837A1 (en)
CA (1) CA2410570A1 (en)
WO (1) WO2002002717A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11901499B2 (en) 2019-04-22 2024-02-13 Samsung Electronics Co., Ltd. Battery case and battery

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040235998A1 (en) * 2003-05-08 2004-11-25 Kirchner Olaf Norbert Liquid crystalline polymer composition
JP4758079B2 (en) 2004-07-14 2011-08-24 上野製薬株式会社 Liquid crystal polyester resin and method for producing the same
US8692272B2 (en) 2008-10-28 2014-04-08 Sumitomo Chemical Company, Limited Resin composition, reflective board and light-emitting apparatus
TW201030087A (en) * 2008-10-30 2010-08-16 Solvay Advanced Polymers Llc Power LED device with a reflector made of aromatic polyester and/or wholly aromatic polyester
JP2011157533A (en) * 2010-02-04 2011-08-18 Sumitomo Chemical Co Ltd Liquid crystalline polyester composition and film of the same
US8906259B2 (en) 2011-11-15 2014-12-09 Ticona Llc Naphthenic-rich liquid crystalline polymer composition with improved flammability performance
KR101947215B1 (en) 2011-11-15 2019-02-12 티코나 엘엘씨 Fine pitch electrical connector and a thermoplastic composition for use therein
US8932483B2 (en) 2011-11-15 2015-01-13 Ticona Llc Low naphthenic liquid crystalline polymer composition
WO2013074467A1 (en) 2011-11-15 2013-05-23 Ticona Llc Low naphthenic liquid crystalline polymer composition for use in molded parts of a small dimensional tolerance
JP6131638B2 (en) * 2013-03-07 2017-05-24 東レ株式会社 Liquid crystal polyester and method for producing the same
JP6324701B2 (en) * 2013-10-31 2018-05-16 住友化学株式会社 Liquid crystalline polyester composition
JP6689606B2 (en) * 2013-11-01 2020-04-28 住友化学株式会社 Resin composition
WO2016137876A1 (en) * 2015-02-23 2016-09-01 Sabic Global Technologies B.V. Electrical tracking resistance compositions, articles formed therefrom, and methods of manufacture thereof

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61316A (en) * 1984-06-13 1986-01-06 住友化学工業株式会社 Oven wear
US4636544A (en) * 1985-02-25 1987-01-13 General Electric Company Flame retarded polyester molding composition with improved electrical performance
JP2560752B2 (en) * 1987-11-19 1996-12-04 東ソー株式会社 Wholly aromatic polyester resin composition
JPH01165667A (en) * 1987-12-23 1989-06-29 Tosoh Corp Thermotropic liquid crystal molding material
JPH083034B2 (en) * 1990-03-14 1996-01-17 住友化学工業株式会社 Wholly aromatic polyester resin composition and ovenware
JP3156863B2 (en) * 1991-12-26 2001-04-16 日本ジーイープラスチックス株式会社 Reinforced flame retardant polyester resin composition
JPH05271465A (en) * 1992-01-29 1993-10-19 Ebara Corp Themotropic liquid crystalline polymer composition and insulating material
JP3568699B2 (en) * 1996-07-30 2004-09-22 富士写真フイルム株式会社 Method for producing silver halide photographic light-sensitive material
JP4033520B2 (en) * 1996-08-12 2008-01-16 ゼネラル・エレクトリック・カンパニイ Flame retardant polyester composition
JPH11116817A (en) * 1997-10-09 1999-04-27 Daihachi Chemical Industry Co Ltd Flame-retardant resin composition
JP4055258B2 (en) * 1998-08-28 2008-03-05 大日本インキ化学工業株式会社 Thermoplastic polyester resin composition
WO2000040655A1 (en) * 1999-01-08 2000-07-13 E.I. Du Pont De Nemours And Company High arc tracking-index poly(phenylene oxide)-liquid crystalline polymer blend compositions

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0202717A3 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11901499B2 (en) 2019-04-22 2024-02-13 Samsung Electronics Co., Ltd. Battery case and battery

Also Published As

Publication number Publication date
CA2410570A1 (en) 2002-01-10
JP5349724B2 (en) 2013-11-20
CN1451033A (en) 2003-10-22
WO2002002717A3 (en) 2002-04-25
AU2001271837A1 (en) 2002-01-14
KR20030019953A (en) 2003-03-07
CN100489029C (en) 2009-05-20
WO2002002717A2 (en) 2002-01-10
JP2004502828A (en) 2004-01-29

Similar Documents

Publication Publication Date Title
US6833405B1 (en) Compositions containing liquid crystalline polymers
EP0167009B1 (en) Ovenwares
CN101821336B (en) Flame-retardant polyamide composition
WO2002002717A2 (en) High tracking index liquid crystalline polymers and related applications
JP2019094465A (en) Liquid crystal polyester resin composition, and molded article
EP0653460B1 (en) Synthetic resin composition and product of molding thereof
JP2003519707A (en) Liquid crystal polymer composition containing small particle size filler
JP5332081B2 (en) Resin composition and molded article comprising the same
JP2019094489A (en) Liquid crystal polyester resin composition, and molded article
WO2008007529A1 (en) Flame-retardant polybutylene terephthalate resin composition
JP2531307B2 (en) Wholly aromatic polyester resin composition and oven wear
JP2019094497A (en) Liquid-crystal polyester resin composition and molded body
KR920009392B1 (en) Liquid crystal polyester resin composition
EP1405879A1 (en) Flame retardant polyethylene terephthalate resin composition
CA2008864A1 (en) Liquid-crystal polyester resin composition
EP0540289B1 (en) Electrical and electronic parts formed of polybutylene naphthalenedicarboxylate
WO1997015631A1 (en) Synthetic resin composition and molded article thereof
KR102215676B1 (en) Liquid crystal polyester composition
JP2002534550A (en) High arc tracking index poly (phenylene oxide) liquid crystal polymer blend composition
EP3064550B1 (en) Resin composition
JPH11140283A (en) Liquid crystalline polyester molded products
CA2021893A1 (en) Highly heat-resistant resin composition
JP2000080290A (en) Liquid crystalline resin composition and molded article
JP2000239503A (en) Flame retardant liquid crystalline resin composition
EP0781810A2 (en) Liquid crystal polyester resin composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20021216

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

RBV Designated contracting states (corrected)

Designated state(s): AT BE CH CY DE FR GB IT LI

17Q First examination report despatched

Effective date: 20080624

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: TICONA LLC

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20130724