CN102051036A - Flame-resistant polycarbonate moulding compounds for extrusion applications - Google Patents

Flame-resistant polycarbonate moulding compounds for extrusion applications Download PDF

Info

Publication number
CN102051036A
CN102051036A CN2010105475579A CN201010547557A CN102051036A CN 102051036 A CN102051036 A CN 102051036A CN 2010105475579 A CN2010105475579 A CN 2010105475579A CN 201010547557 A CN201010547557 A CN 201010547557A CN 102051036 A CN102051036 A CN 102051036A
Authority
CN
China
Prior art keywords
moulding compound
weight
preferred
compound
contain
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.)
Pending
Application number
CN2010105475579A
Other languages
Chinese (zh)
Inventor
A·赛德尔
T·埃克尔
B·凯勒
D·维特曼
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of CN102051036A publication Critical patent/CN102051036A/en
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] 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
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0066—Flame-proofing or flame-retarding additives
    • 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
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds
    • C08K5/51—Phosphorus bound to oxygen
    • C08K5/52—Phosphorus bound to oxygen only
    • C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
    • C08K5/523—Esters of phosphoric acids, e.g. of H3PO4 with hydroxyaryl compounds
    • 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
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds
    • C08K5/51—Phosphorus bound to oxygen
    • C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
    • C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
    • C08K5/5333—Esters of phosphonic acids
    • C08K5/5357—Esters of phosphonic acids cyclic
    • 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
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds
    • C08K5/5399—Phosphorus bound to nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07—Flat, e.g. panels
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/09—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/12—Articles with an irregular circumference when viewed in cross-section, e.g. window profiles
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L85/00—Compositions of macromolecular compounds obtained by reactions forming a linkage in the main chain of the macromolecule containing atoms other than silicon, sulfur, nitrogen, oxygen and carbon; Compositions of derivatives of such polymers
    • C08L85/02—Compositions of macromolecular compounds obtained by reactions forming a linkage in the main chain of the macromolecule containing atoms other than silicon, sulfur, nitrogen, oxygen and carbon; Compositions of derivatives of such polymers containing phosphorus

Abstract

The invention relates to chlorine and bromine-free, flame-resistant polycarbonate moulding compounds which are characterized by excellent flame resistance combined with good mechanical and thermal properties, good ESC characteristics and a sufficiently good melt stability for extrusion. The invention also relates to moulded parts, profiles, panels, tubes and channels which are produced from the moulding compounds.

Description

Be used to extrude the flame-resistant polycarbonate moulding compounds of application
The application is that international filing date is February 21 calendar year 2001, international application no the dividing an application for the application of " being used to extrude the flame-resistant polycarbonate moulding compounds of application " that be PCT/EP01/01924 (national applications number be 01805912.0), denomination of invention.
Technical field
The present invention relates to polycarbonate compositions not chloride and bromine, that improve shock strength, described composition has high melt viscosity and melts stability, therefore be applicable in expressing technique and process, and have good flame retardant resistance, good ESC-behavior and mechanical property and high hot shape invariance simultaneously.
Background technology
The flame retardant resistance of not chloride and bromine, the polycarbonate molding compositions that improves shock strength are known.
EP-A 0 345 522 (US-A 5 061 745) has for example described by aromatic polycarbonate, ABS-graftomer and/or has contained the polymeric blends of cinnamic multipolymer, and described mixture is given its flame retardant resistance with phosplate.
US-A 5 204 394 and 5 672 645 has described the PC/ABS-moulding compound, and described mixture is given its flame retardant resistance by the mixture of low polyphosphate or low polyphosphate and phosplate.
According to containing of above-mentioned prior art single-be to compare with the characteristics of the PC/ABS-blend of low polyphosphate and greatly reduce hot shape invariance with the comparable blend of non-flame retardant resistance, and at first greatly reduce the viscosity of melts.The latter can process under lower temperature because this makes, and can shorten cycling time thus the benefit that is processed with in the Shooting Technique that is mainly used in this class moulding compound at present.Proved that low melt viscosity can be brought problem and make the corresponding melts stability that obtains be not enough to be arrested in the too early destruction of profile under the conventional processing conditions for process moulding compound in expressing technique.The moulding compound (need use a large amount of plasticity fire retardants) that also needs excellent flame retardancy when this is particluarly suitable for thin-walled to this.The improvement of flame retardant resistance generally causes the reduction of melts stability.Particularly proved and be difficult to realize that good flame-retardance and high melts stability combine with high-intensity, because the latter need add a large amount of shock strength modifying agents, SAN-grafting polybutadiene rubber for example is because its high combustibility makes it to be difficult to provide flame retardant resistance for blend.
JP-A 111 997 68 has described the PC/ABS-blend that flame retardant resistance is provided with monomeric and oligomeric phosphoric acid ester, has wherein obviously improved flame retardant resistance by adding mineral filler such as talcum.But the minimizing of attainable phosphate ester content is not enough to reach be used to extrude and uses required melt viscosity under the situation that does not change flame retardant resistance thus.In addition, mineral filler is to mechanical property in the ordinary course of things, and particularly the intensity to blend polymer has disadvantageous effect.
US-A 5 849 827 and WO 99/07782 have described to use based on Resorcinol or based on the low polyphosphate of dihydroxyphenyl propane provides the PC/ABS-moulding compound of flame retardant resistance, and wherein, the reignition time obviously reduces behind the nano grade inorganic material that adds lower concentration.But moulding compound described herein is used melts stability deficiency for extruding.
The low polyphosphate that WO 99/57198 has described with resorcinol derived provides flame retardant resistance PC/ABS-moulding compound, is characterized in that teflon (Teflon) content is very low, and it is 0.076% with respect to fluorine content that 0.1 weight %-is only arranged.In this moulding compound, use straight chain and side chain have high molecular (31,000 or 32, polycarbonate 000g/mol).The rheological of described moulding compound (MVR) is allowed in expressing technique and is processed.But to be the ESC-behavior weak and hot shape invariance is poor for the characteristics of this moulding compound, particularly under the thin-walled situation when reaching enough flame retardant resistances and use enough fire retardants.
Summary of the invention
Therefore, the purpose of this invention is to provide not chloride and moulding compound bromine, it also has enough flame retardant resistances, favorable mechanical performance and improved ESC-behavior under the situation of thin-walled, and it can be processed at expressing technique owing to high melts stability.
Have now found that, thisly contain high molecular straight or branched polycarbonate, provide flame retardant resistance and the polycarbonate compositions that preferably also contains based on the polyolefinic improvement shock strength of fluoro of whole compositions 〉=0.15 weight % satisfies the performance spectrum of wishing, have good hot shape invariance in addition with not halogen-containing phosphorus compound.
Therefore, the invention provides this class polycarbonate-moulding compound, it passes through the UL94V-combustion test with scoring V-0 under wall thickness≤1.5mm situation, it is 〉=600 with cutting speed for 100s-1 records melt viscosity at 260 ℃, preferably 〉=800, especially preferably 〉=1000Pa.s, and it comprises
A) aromatic polycarbonate at least a high-molecular weight straight chain or side chain or polyestercarbonate,
B) at least a shock strength modifying agent and
C) at least a not halogen-containing phosphorus compound.
Described composition can comprise in addition
D) the fluoro polyene belongs to compound,
E) inorganic materials,
F) other polymeric constituent and
G) conventional polymer additive, for example anti-drops, lubricant and releasing agent, nucleator, static inhibitor, stablizer, dyestuff and pigment.
Preferred moulding compound comprises
A) 60-98 weight part, preferred 70-95 weight part, at least a straight chain of preferred especially 75-90 weight part or the aromatic polycarbonate of straight chain, preferred relative solution viscosity 〉=1.30 (s' in methylene dichloride and under the concentration at 0.5g/100ml, measuring under 25 ℃) aromatic polycarbonate
B) 0.5-30, preferred 1-15, at least a graftomer that contains rubber matrix of preferred especially 2-10 weight part,
C) 1-20 weight part, a kind of oligomeric phosphoric acid ester of preferred 2-15 weight part, especially 3-12 weight part,
D) 0.15-1 weight part, a kind of fluoro polyolefine of especially preferred 0.2-0.5 weight part and
E) 0-5 weight part, a kind of fine particle, sheet or the fibrous inorganic materials of preferred 0-3 weight part, especially 0-1.5 weight part,
Wherein the parts by weight of all components (A-E and other optional component) are 100.
Component A
Being suitable for aromatic polycarbonate of the present invention and/or aromatic polyestercarbonates by component A is that document is known maybe can be by the known method preparation of document (for the preparation of aromatic polycarbonate referring to for example Schnell, " Chemistry and Physics of Ploycarbonates ", Interscience Publishers, 1964 and DE-A 1 495 626, DE-A 2 232 877, DE-A 2 703376, DE-AOS 2 714 544, DE-A 3 000 610, DE-A 3 832 396; For the preparation of aromatic polyestercarbonates referring to (for example DE-A 30 77 934).
The preparation example of aromatic polycarbonate is as by diphenol and carbonyl halide, preferred phosgene and/or with aromatics two acyl dihalo-s, preferred benzene two carboxylic acid halides are undertaken by the phase interface method, for example single phenol of optional use chain terminator and optional use trifunctional or more than the branching agent of trifunctional, for example triphenol or four phenol.
Be used to prepare the diphenol of the diphenol preferred formula (I) of aromatic polycarbonate and/or aromatic polyestercarbonates
Wherein
A represents a singly-bound, C 1-C 5-alkylidene group, C 2-C 5-alkylidene (Aylkyliden), C 5-C 6-ring alkylidene ,-O-,-SO-,-CO-,-S-,-SO 2-, C 6-C 12-arylidene, other is optional contain heteroatomic aromatic ring can with described C 6-C 12-arylidene condenses,
Or expression (II) or group (III)
Figure BSA00000350926200041
B respectively is C 1-C 12-alkyl, preferable methyl,
X independently is respectively 0,1 or 2 separately,
P be 1 or 0 and
R 5And R 6For each X 1Can select separately, independent separately is hydrogen or C 1-C 6-alkyl, preferred hydrogen, methyl or ethyl,
X 1For carbon and
M is the integer of a 4-7, preferred 4 or 5, and condition is, at least one atom X 1Last R 5And R 6Be alkyl simultaneously.
Preferred diphenol is quinhydrones, Resorcinol, dihydroxybiphenyl phenol, two-(hydroxy phenyl)-C 1-C 5-alkane, two-(hydroxy phenyl)-C 5-C 6-naphthenic hydrocarbon, two-(hydroxy phenyl)-ether, two-(hydroxy phenyl)-sulfoxide, two-(hydroxy phenyl)-ketone, two-(hydroxy phenyl)-sulfone and α, α-two-(hydroxy phenyl)-diisopropyl benzene.
Particularly preferred diphenol is 4,4 '-dihydroxybiphenyl, bisphenol-A, 2,4-two (4-hydroxy phenyl)-2-methylbutane, 1,1-two-(4-hydroxy phenyl)-hexanaphthene, 1,1-two-(4-hydroxy phenyl)-3,3,5-trimethyl-cyclohexane, 4,4 '-dihydroxyl diphenylsulfide, 4,4 '-dihydroxyl phenylbenzene-sulfone.
Especially preferred is 2,2-two-(4-hydroxy phenyl)-propane (bisphenol-A).
Can use these diphenol or mixture arbitrarily separately.
To be that document is known maybe can obtain by the known method of document these diphenol.
For the thermoplastic aromatic polycarbonate of preparation, suitable chain terminator is for example phenol and p-tert-butylphenol, but also can be the alkylbenzene phenols of long-chain, as press the 4-(1 of DE-A 2 842 005, the 3-tetramethyl butyl)-phenol or in alkyl substituent, have the monoalkyl phenol or the dialkyl group phenol of 8-20 C-atom altogether, as 3,5-two-tert.-butyl phenol, to isooctyl phenol, to tert-octyl phenol, to dodecyl phenol and 2-(3,5-dimethyl heptyl)-phenol and 4-(3,5-dimethyl heptyl)-phenol.The amount of used chain terminator is generally 0.5 mole of %-10 mole %, based on the total moles meter of used each diphenol.
Thermoplastic aromatic polycarbonate can be by known way branching, and preferred by adding based on the 0.05-2.0 mole % trifunctional of the total moles of used diphenol or more than the compound of trifunctional, for example has those of three or more phenolic group group.
Suitable is homo-polycarbonate and Copolycarbonate.In order to prepare being suitable for Copolycarbonate of the present invention and also can using 1-25 weight %, the polydiorganosiloxane of preferred 2.5-25 weight % (based on the total amount of used diphenol) by component A with bis (hydroxy-aromatic) oxygen cardinal extremity base.This is known, and (referring to for example US-A 3 419 634) maybe can be by the known method preparation of document.The preparation example of Copolycarbonate that contains polydiorganosiloxane is as being described among the DE-A 3 334 782.
Except that bisphenol-A-homo-polycarbonate, preferred polycarbonate be bisphenol-A with 15 moles of % at the most based on the conduct of the total mole number of diphenol preferably or other the Copolycarbonate of especially preferably mentioning of diphenol.
Be used to prepare the preferred m-phthalic acid of aromatics two carboxylic acid halides, terephthalic acid, diphenyl ether-4,4 of aromatic polyestercarbonates '-dioctyl phthalate and naphthalene-2, the diacid chloride of 6-dioctyl phthalate.
The diacid chloride of preferred especially m-phthalic acid and terephthalic acid is with 1: 20-20: 1 mixture.
In addition, use carbonyl halide simultaneously in the preparation polyestercarbonate, preferred phosgene is as difunctional acid derivative.
As the chain terminator of preparation aromatic polyestercarbonates, except already mentioned single phenol, also have their chloro-formic ester and aromatic monocarboxylate's acyl chlorides, it can be chosen wantonly by C 1-C 22-alkyl replaces, and aliphatic C 2-C 22-single acyl chlorides.
The consumption of chain terminator respectively is 0.1-10 mole %, under the situation of phenols chain terminator based on the mole number of diphenol, under the situation of single acyl chlorides based on the mole number of diacid chloride.
Described aromatic polyestercarbonates also can comprise the aromatic hydroxycarboxylic acids that gathers into wherein.
Described aromatic polyestercarbonates both can be a straight chain, also can be by known way branching (to this equally referring to DE-A 2 940 024 and DE-A 3 007 934).
But as the branching agent application examples as three-or more polyfunctional acyl chlorides, as 1,3,5-benzene three acyl chlorides, cyanuric acid three acyl chlorides, 3,3 '-, 4,4 '-benzophenone four acyl chlorides, 1,4,5,8-naphthalene four acyl chlorides or 1,2,4,5-benzene four acyl chlorides, its amount is 0.01-1.0 mole % (based on used diacid chloride meter) or three-or more polyfunctional phenols, for example Phloroglucinol, 4,6-dimethyl-2,4,6-three-(4-hydroxy phenyl)-heptene-2,4,4-dimethyl-2,4,6-three-(4-hydroxy phenyl)-heptane, 1,3,5-three-(4-hydroxy phenyl)-benzene, 1,1,1-three-(4-hydroxy phenyl)-ethane, three-(4-hydroxy phenyl)-phenylmethane, 2,2-two [4,4-two (4-hydroxy phenyl)-cyclohexyl]-propane, 2,4-two (4-hydroxy phenyl-sec.-propyl)-phenol, four-(4-hydroxy phenyl)-methane, 2,6-two (2-hydroxy-5-methyl base-benzyl)-4-methylphenol, 2-(4-hydroxy phenyl)-2-(2, the 4-dihydroxy phenyl)-propane, four-(4-[4-hydroxy phenyl-sec.-propyl]-phenoxy group)-methane, 1,4-two [4,4 '-dihydroxyl three-phenyl)-methyl]-benzene, its amount is 0.01-1.0 mole % (based on used diphenol).The phenols branching agent can add when beginning with diphenol, and the acyl chlorides branching agent can add with diacid chloride.
The content of carbonate structural unit can change arbitrarily in thermoplastic aromatic polyestercarbonates, and the content of preferred carbonic ether is 100 moles of % at the most, 80 moles of % especially at the most, and especially preferred 50 moles of % at the most are based on the total amount meter of ester group and carbonate group.The ester component of aromatic polyestercarbonates and carbonate component both can blocks, also can form at random be present in the polycondensate.
Relative solution viscosity (the η of aromatic polycarbonate and polyestercarbonate Rel) be 1.18-1.4 (the 100ml dichloromethane solution of 0.5g polycarbonate or polyestercarbonate is in 25 ℃ of mensuration).Those polycarbonate and the polyestercarbonate of advantageous applications relative solution viscosity 〉=1.30 in moulding compound of the present invention.
Described thermoplastic aromatic polycarbonate and polyestercarbonate can be used separately or use with the form of the mixture of mutual arbitrary proportion.
B component
B component comprises one or more by the following graftomer that makes
B.15-95, at least a vinyl monomer-grafted of preferred 30-90 weight % in
B.295-5, preferred 70-10 weight % has second-order transition temperature＜10 ℃, preferred＜0 ℃, preferred especially＜one or more graft bases of-20 ℃.
Described graft bases is average particle diameter (d B.2 50Value) be 0.05-10 μ m, preferred 0.1-5 μ m, preferred especially 0.2-1 μ m.
Monomers B .1 is preferably by the following mixture that makes
B.1.150-99 parts by weight of ethylene base aromatic substance and/or cyclosubstituted vinyl aromatic compounds (for example and optimization styrene, alpha-methyl styrene, p-methylstyrene) and/or methacrylic acid-(C 1-C 8)-alkyl ester (for example and preferable methyl methyl acrylate, Jia Jibingxisuanyizhi) and
B.1.21-50 parts by weight of ethylene base prussiate (unsaturated nitrile, for example and preferred vinyl cyanide and methacrylonitrile) and/or (methyl) vinylformic acid (C 1-C 8)-alkyl ester (for example and preferable methyl methyl acrylate, n-butyl acrylate, tert-butyl acrylate) and/or olefinically unsaturated carboxylic acid derivatives (for example and preferred acid anhydride and imide) (for example and preferred maleic anhydride and/or N-phenyl-maleimide).
Preferred monomers B .1.1 is selected from least a of monomer styrene, alpha-methyl styrene and methyl methacrylate, and preferred monomers B .1.2 is selected from least a of monomer vinyl cyanide, maleic anhydride and methyl methacrylate.
Particularly preferred monomers B .1.1 is vinylbenzene and B.1.2 is vinyl cyanide.
B.2, for the suitable graft bases of graftomer B is for example elastoprene, EP (D) M-rubber, promptly based on those rubber of ethylene/propene and optional diene, and acrylic elastomer, urethanes, silicone rubber and Ethylene/vinyl acetate rubber.
B.2, preferred graft bases is the multipolymer of the mixture of elastoprene (for example based on divinyl, isoprene etc.) or elastoprene or elastoprene or the mixture of itself and other copolymerisable monomer (for example according to B.1.1 and B.1.2), condition is, the second-order transition temperature of B component .2＜10 ℃, preferred＜0 ℃; Preferred especially＜-10 ℃.
Preferred especially pure polybutadiene rubber.
Particularly preferred polymer B be the ABS-polymkeric substance (emulsion-, body-and suspension-ABS), as at for example DE-A 2 035 390 (=US-A 3 644 574) or at DE-A 2 248242 (=GB-A 1 409 275) or at Ullmann,
Figure BSA00000350926200071
DerTechnischen Chemie, the 19th volume (1980), the 280th page is worked those that describe.Graft bases gel content B.2 is at least 30 weight %, preferably at least 40 weight % (measuring in toluene).
Graft copolymer B is by radical polymerization, for example by emulsion-, suspension-, solution-and mass polymerization, preferably by emulsion-or mass polymerization preparation.
Special preferred emulsion-ABS is as B component.
The initiator system of being made up of organic hydroperoxide and xitix by US-A 4 937 285 also is specially suitable graft rubber by those ABS-polymkeric substance that redox initiation prepares.
By the B.2 suitable acrylic elastomer of the polymer B polymkeric substance of alkyl acrylate preferably, optional other the polymerisable ethylenically unsaturated monomer of 40 weight % (based on B.2) at the most that contains.Belonging to preferred polymerizable acrylate is C 1-C 8-alkyl ester, for example methyl-, ethyl-, butyl-, n-octyl-and 2-(ethyl hexyl) ester and these monomeric mixtures.
For but crosslinked copolymerization has monomer more than a polymerizable double bond.The preferred embodiment of cross-linking monomer be unsaturated monocarboxylic with 3-8 C atom and unsaturated monohydroxy-alcohol with 3-12 C atom or with the ester of saturated polyol, for example Ethylene glycol dimethacrylate, allyl methacrylate with basic and 2-20 the C atom of 2-4 OH; Heterogeneous ring compound with a plurality of degrees of unsaturation, for example trivinyl-and triallyl cyanurate; Polyfunctional vinyl compound, as two-and trivinylbenzene; And triallyl phosphoric acid ester and phthalic acid diallyl ester.
Preferred cross-linking monomer is allyl methacrylate, Ethylene glycol dimethacrylate, phthalic acid diallyl ester and the heterogeneous ring compound with at least 3 ethylenically unsaturated groups.
Particularly preferred cross-linking monomer is cyclic monomer triallyl cyanurate, triallyl isocyanurate, three acryloyls, six hydrogen-s-triazine, triallyl benzene.The amount of cross-linking monomer is preferably 0.02-5, and especially B.2 0.05-2 weight % counts based on graft bases.
Under the situation of cyclic cross-linking monomer, advantageously its amount should be limited in less than graft bases 1 weight % B.2 with at least 3 ethylenically unsaturated groups.
Can choose except that acrylate that to be used to prepare graft bases preferred " other " polymerisable ethylenically unsaturated monomer B.2 be for example vinyl cyanide, vinylbenzene, alpha-methyl styrene, acrylamide, vinyl-C wantonly 1-C 6-alkyl oxide, methyl methacrylate, divinyl.Be emulsion polymer preferably with gel content at least 60 weight % as graft bases acrylic elastomer B.2.
Other suitable graft bases B.2 is the silicone rubber with grafting active site, and for example at DE-A 3 704 657, DE-A 3 704 655, those described in DE-A 3 631 540 and the DE-A 3 631539.
Graft bases gel content is B.2 measured (M.Hoffmann, H. at 25 ℃ in suitable solvent R.Kuhn, Polymeranalytik I und II, Georg Thieme-Verlag, Stuttgart 1977).
Median size d 50Being a diameter, respectively is the particle of 50 weight % above and below this value.This value can through super centrifugal assay method (W.Scholtan, H.Lange, Kolloid, Z.und Z.Polymere 250 (1972), 782-1796) record.
Component C
Moulding compound of the present invention comprises general formula (IV) phosphorus compound as fire retardant (C)
Figure BSA00000350926200092
Wherein
R 1, R 2, R 3And R 4Independently be respectively C separately 1-C 8-alkyl is for choosing by alkyl preferred C wantonly 1-C 4The C that-alkyl replaces 5-C 6-cycloalkyl, C 6-C 20-aryl or C 7-C 12-aralkyl,
N independently is 0 or 1 separately
N is the number of 0.1-30,
X is the aliphatic group that has the monocycle or the polyaromatic of 6-30 C atom or have the straight or branched of 2-30 C atom, and it can be that OH-replaces and can comprise 8 ehter bonds at the most,
Preferred R 1, R 2, R 3And R 4Independent separately is C 1-C 4-alkyl, phenyl, naphthyl or phenyl-C 1-C 4-alkyl.Aromatic group R 1, R 2, R 3And R 4Itself can be by alkyl, preferred C 1-C 4-alkyl replaces.Particularly preferred aryl is tolyl, phenyl, xylyl (Xylenyl), propyl group phenyl or butyl phenyl.
X in the formula (IV) preferably represents to have the monocycle or the polyaromatic of 6-30 C atom.These aryl preferably come from the diphenol of formula (I).
N in the formula (IV) is preferably 1.
N can be the value of 0.1-30, the value of value, the especially 0.7-5 of preferred 0.5-10.As the mixture that also can use various phosphoric acid ester by formula (IV) by component C of the present invention.In this case, the desirable above-mentioned value of N is as mean value.In described mixture, also can comprise single phosphorus compound (N=0).
Single phosphorus compound of formula (IV) is tributyl phosphate, triphenylphosphate, Tritolyl Phosphate, diphenyl tolyl phosphate, di(2-ethylhexyl)phosphate phenyl octyl group ester, di(2-ethylhexyl)phosphate phenyl-2-ethyltoluene base ester, tricresyl phosphate-(isopropyl phenyl) ester, methyl-phosphorous acid dimethyl esters, methyl-phosphorous acid diphenyl, phenyl-phosphonic acid diethyl ester, triphenyl phosphine oxygen or trimethylphenyl phosphine oxygen especially.Particularly preferred single phosphorus compound is a triphenylphosphate.
Mean value N can be by following mensuration: measure the composition (molecular weight distribution) of phosphate mixture and calculate the mean value of N thus by appropriate means (chromatography of gases (GC), high-pressure liquid phase (HPLC), gel permeation chromatography (GPC)).
X especially preferably represents
Proved the phosphorus compound particularly advantageous that adds logical formula V
Figure BSA00000350926200102
Wherein
R 1, R 2, R 3And R 4Independently be respectively C separately 1-C 8-alkyl and/or optional replaced by alkyl
C 5-C 6-cycloalkyl, C 6-C 10-aryl or C 7-C 12-aralkyl,
N independently is 0 or 1 separately, and is preferred 1,
Q independently is 0,1,2,3 or 4 separately, and is preferred 0,1 or 2,
N is the number between 0.1 and 30, the number between preferred 0.5 and 10, the especially number between 0.7 and 5,
R 5And R 6Independent separately is C 1-C 4-alkyl, preferable methyl and
Y represents C 1-C 7-alkylidene, C 1-C 7-alkylidene group, C 5-C 12-ring alkylidene group, C 5-C 12-ring alkylidene ,-O-,-S-,-SO-, SO 2Or-CO-.
Especially preferably come from those logical formula V compounds of bisphenol-A or its methyl substituted derivative.
By component C, the phosphorus compound of formula (IV) is that known (referring to for example EP-A 363 608, EP-A 640 655) maybe can make (Ullmanns for example similarly by known method
Figure BSA00000350926200111
Der technischen Chemie, the 18th volume, the 301st .1979; Houben-Weyl, Methoden der organischen Chemie, the 12/1st volume, the 43rd volume; Beilstein the 6th volume, the 177th page).
Also can use other not halogen-containing phosphorus compound as flame retardance element C, and both can be separately, also can be with any mixture form of general formula (IV) compound.As the suitable especially phosphazo class (Phosphazene) of this not halogen-containing phosphorus compound and the compound of phosphonic acid ester amine (Phosphonatamine).
Phosphonic acid ester amine is formula (VI) compound
A 3-y-NB 1 y (VI)
Wherein
A expression (VIa)
Or (VIb)
Figure BSA00000350926200113
Group,
R 11And R 12Independent separately expression C 1-C 10-alkyl or represent C unsubstituted or that replace 6-C 10-aryl,
R 13And R 14Independent separately expression C 1-C 10-alkyl or C unsubstituted or that replace 6-C 10-aryl,
Y represent 0,1 or 2 and
B 1Independent expression hydrogen, C 2-C 8-alkyl, the unsubstituted or C that replaces 6-C 10-aryl,
B 1Preferred independent expression hydrogen, ethyl, just-or sec.-propyl, unsubstituted or by C 1-C 4The C that-alkyl replaces 6-C 10-aryl, especially phenyl or naphthyl.
R 11, R 12, R 13And R 14In alkyl preferably represent independently methyl, ethyl, n-propyl, sec.-propyl, just-, different-, secondary-or the tertiary butyl, amyl group or hexyl.
R 11, R 12, R 13And R 14In C 6-C 10-aryl is preferably represented phenyl, naphthyl or dinaphthalene independently.
For example and preferably mention 5,5,5 of formula (VIa-1) ', 5 ', 5 ", 5 " hexamethyl three (1,3,2-two oxa-phosphas oneself ring-methane) amino-2,2 ', 2 " trioxides
Figure BSA00000350926200121
(Solutia Inc. company, St.Louis, the test products of USA).
The preparation example of phosphonic acid ester amine is as described in the US-patent specification 5 844 028.
Phosphazo is formula (VIIa) and (VIIb) compound
Figure BSA00000350926200122
Figure BSA00000350926200131
Wherein
Each identical or different and expression C of R 1-C 8-alkyl or C 1-C 8-alkoxyl group, optional by alkyl, preferred C 1-C 4The C that-alkyl replaces 5-C 6-cycloalkyl, C 6-C 20-aryl, preferred phenyl or naphthyl, C 6-C 20-aryloxy, preferred phenoxy group, naphthyloxy or C 7-C 12-aralkyl, preferred phenyl-C 1-C 4-alkyl,
K represents 0 or the number of 1-15, preferably represents the number of 1-10.
Exemplary mentioning:
Propoxy-phosphazo, phenoxy group phosphazo and methylphenoxy phosphazo.
Preferred phenoxy group phosphazo.
Phosphazo compounds and preparation example thereof are as being described among EP-A 728 811, DE-A 1 961668 and the WO 97/40092.
Component D
The present composition can comprise the fluoro polyolefine as component D.Use the fluoro polyolefine, especially its amount is favourable for 0.15-0.5 weight %, because need relatively large fire retardant when content＜0.15 weight %, to reach the V-0-level in the UL94V-test.But high flame retardant agent content is unfavorable to melt stability, hot shape invariance and notched Izod impact strength.
The fluoro polyolefine generally is known (referring to for example EP-A 640 655).Commercially available product is DuPont company for example
Figure BSA00000350926200132
TM 30 N.
The fluoro polyolefine also can the fluoro polyolefin emulsion and the emulsion of graftomer (B) or use with the agglomerative form of mixtures of the emulsion of the multipolymer that is preferably based on styrene/acrylonitrile, and wherein said fluoro polyolefine mixes with graftomer or copolymer emulsion also as emulsion and condenses subsequently.
In addition, the fluoro polyolefine can be used as with graftomer (B) or a kind of pre-composition that is preferably based on the multipolymer of styrene/acrylonitrile and uses.With the powder of powdery fluoro polyolefine and graftomer or multipolymer or particle mixes and generally under 200-330 ℃ of temperature at conventional equipment, as melt compounded in interior kneader, forcing machine or the twin-spiral mixer.
The fluoro polyolefine also can master batch form use, this master batch belongs to unsaturated monomer by at least a monoene and pass through emulsion polymerization prepared in the presence of the polyolefinic aqueous dispersion of fluoro.The preferred monomers component is vinylbenzene, vinyl cyanide and its mixture.This polymkeric substance is used as the powder that can flow at Acid precipitation and dry back subsequently.
It is 5-95 weight % that described coagulum, pre-composition and master batch generally have solid content, the fluoro polyolefine of preferred 7-60 weight %.
Component E
In addition, can in polycarbonate compositions, add inorganic materials, especially since thixotropic effect improved the stability of melts and/or improved the inorganic materials of the flame retardant resistance of moulding compound.The consumption of described inorganic materials is as far as possible little but effectively, and its mechanical property to material is useful or do not have harmful effect at least.Institute's organic and/or inorganic materials is all suitable in principle, preferably with the thin state of powder.For example described inorganic materials is particle, sheet or fibrous.
Can mention chalk, silica powder, titanium dioxide, silicate/pure aluminium silicate as an example at this, as talcum, wollastonite, mica/multi-layer type clay minerals, polynite, especially the close organic substance form of modifying by ion-exchange, kaolin, zeolite, vermiculite and aluminum oxide, silica, magnesium hydroxide, aluminium hydroxide and glass fibre/sheet glass.Also can use the mixture of various inorganic materials.
Described inorganic materials can be by surface-treated, and silanization for example is to guarantee better polymerization thing consistency.
Described inorganic materials can 0-5 weight %, and preferred 0-3 weight %, the especially concentration of 0-1.5 weight % are used, based on total composition meter.
The inorganic materials of advantageous applications sheet characteristic, for example talcum, mica/layered clay mineral, polynite, the especially close organic substance form of modifying by ion-exchange, kaolin and vermiculite.
Special preferably talc.
Talcum is meant the talcum of naturally occurring or synthetic preparation.
The chemical constitution of pure talc is 3MgO4SiO 2H 2O, so MgO content is 31.9 weight %, SiO 2Content is that 63.4 weight % and chemically combined water-content are 4.8 weight %.It is the silicate of laminate structure.
Naturally occurring talcum mineral generally do not have above-mentioned desirable the composition, and this is because magnesium is partly exchanged by other element, silicon by for example aluminum portions exchange and/or since with other mineral, for example rhombspar, magnesite and the symbiosis of green Buddhist nun's stone and impure.This impure natural talcum powder also can be used in the moulding compound of the present invention, but preferred highly purified talcum type.It is characterized in that MgO content is 28-35 weight %, preferred 30-33 weight %, preferred especially 30.5-32 weight % and SiO 2Content is 55-65 weight %, preferred 58-64 weight %, preferred especially 60-62.5 weight %.In addition, the preferably talc type has Al 2O 3Content is less than 5 weight %, especially preferably less than 1 weight %, especially less than 0.7 weight %.
Especially advantageously use and have median size d 50＜20 μ m, preferred＜10 μ m, especially preferably＜and 5 μ m, most preferably≤2.5 μ m is to grind to form the talcum of fine particulate form.
In addition, what can mention as preferred inorganic component is to come from the 1st to the 5th main group and the 1st to the 8th subgroup metal in one or more periodic table of elements, preferably come from the 2nd to the 5th main group and the 4th to the 8th subgroup, especially preferably come from finely divided (nano level) mineral compound of 3 to the 5th main groups and the 4th to the 8th subgroup metal and elemental oxygen, sulphur, boron, phosphorus, carbon, nitrogen, hydrogen and/or silicon.
Preferred compound is for example oxide compound, oxyhydroxide, hydration/basic oxide, vitriol, sulphite, sulfide, carbonate, carbide, nitrate, nitrite, nitride, borate, silicate, phosphoric acid salt and hydride.
Particularly preferred finely divided mineral compound is for example TiN, TiO 2, SnO 2, WC, ZnO, Al 2O 3, AlO (OH), ZrO 2, SiO 2, ferric oxide, BaSO 4, vanadium oxide, zinc borate, silicate, as pure aluminium silicate, Magnesium Silicate q-agent.But same application mix thing and/or adulterated compound.Described nano-scale particle can carry out finishing with organic molecule.
Especially preferred nano level A1O (OH).
Median size≤the 200nm of nano inorganic material, preferred≤150nm, especially 1-100nm.
Granularity and particle diameter always are meant median size d 50, be that Kolloid-Z.und Z.Polymere 250 (1972) according to W.Scholtan etc., the 782-796 page or leaf is described to be obtained by super centrifugal measurement.
Nm inorganic compound can powder, pasty state, colloidal sol, dispersion or suspensoid form exist.By obtaining powder by dispersion, colloidal sol or suspensoid precipitation.
Component F
The present composition also can comprise other polymkeric substance as component F.
Suitable preferably at least a vinyl aromatic compounds, vinyl cyanide (unsaturated nitrile), (methyl) vinylformic acid-(C of being selected from 1-C 8Monomeric vinyl (being total to) polymkeric substance (F.1) of)-alkyl ester, unsaturated carboxylic acid and olefinically unsaturated carboxylic acid derivatives (as acid anhydride and imide).Especially (being total to) polymkeric substance of Shi Heing is made by following
F.1.150-99, the vinyl aromatic compounds of preferred 60-90 weight part and/or ring are gone up substituted vinyl aromatic compounds, for example and optimization styrene, alpha-methyl styrene, p-methylstyrene) and/or methacrylic acid-(C 1-C 8)-alkyl ester, for example and preferable methyl methyl acrylate, Jia Jibingxisuanyizhi) and
F.1.21-50, preferred 10-40 parts by weight of ethylene base prussiate (unsaturated nitrile), for example and preferred vinyl cyanide and methacrylonitrile and/or (methyl) vinylformic acid-(C 1-C 8)-alkyl ester (for example and preferable methyl methyl acrylate, n-butyl acrylate, tert-butyl acrylate) and/or unsaturated carboxylic acid (for example and preferred toxilic acid) and/or olefinically unsaturated carboxylic acid derivatives (for example and preferred acid anhydride and imide) (for example and preferred maleic anhydride and N-phenylmaleimide).
Described (being total to) polymkeric substance F.1 be resene, thermoplasticity and do not contain rubber.
Preferred especially by F.1.1 being vinylbenzene and F.1.2 being the multipolymer of vinyl cyanide.
(being total to) polymkeric substance of pressing F.1 is known and can especially prepares by letex polymerization, suspension polymerization, solution polymerization or mass polymerization by radical polymerization.Preferably having molecular weight Mw (weight average obtains by scattering of light or analysis by sedimentation) by component (being total to) polymkeric substance F.1 is 15000-200000.
In addition, what be fit to is polyalkylene terephthalates (F.2), as described in the EP-A-841 187.
The preferably polyalkylene terephthalates that makes by terephthalic acid and/or its reactive derivatives (for example its dialkyl) and ethylene glycol and/or butyleneglycol-1,4 and the mixture of these polyalkylene terephthalates.
Component G
Moulding compound of the present invention can comprise other conventional additives of effective concentration, for example dripping inhibitor, lubricant and releasing agent, nucleator, static inhibitor, stablizer, dyestuff and pigment.
The moulding compound of the present invention that comprises component A-G and optional other additive be by by known way at conventional equipment, as mix in interior kneader, forcing machine or the twin-spiral mixer each component and under 200-300 ℃ of temperature melt compounded or melt extrude preparation.
The mixing of each component can be carried out successively or simultaneously by known way, and both can also can at high temperature carry out in about 20 ℃ (room temperatures).
Because its good flame retardant resistance, favorable mechanical performance and chemical reagent resistance and because its high melts stability, thermoplastic composition of the present invention especially are suitable for extruding, preparing sheet material, section bar (Profilen) and molding in extrusion-blown modling and the deep processing technology.
The example of the molding that can prepare is: the cable guide of cover plate, window/door section bar and electronics passage/pipe, electric wire and installation duct, omnibus bar lid and the moulded piece, extrusion profile or the sheet material that are used for automobile/track vehicle/aircraft field (for example interior trim) and building field.
The present invention provides the preparation method of described moulding compound, described moulding compound to be used to prepare the purposes and described molding, sheet material and the section bar itself of molding, sheet material and section bar equally.
Embodiment
Embodiment
Component A
Based on the branched polycarbonate of dihydroxyphenyl propane, in methylene dichloride in 25 ℃ down and the relative solution viscosity that records during for 0.5g/100ml of concentration be 1.34.
B component
Ratio by 45 weight parts is 72: 28 the vinylbenzene and crosslinked polybutadiene rubber (the median size d of graininess of vinyl cyanide and 55 weight parts 50=0.3-0.4 μ m) graftomer that makes by letex polymerization.
Component C.1
Low polyphosphate based on bisphenol-A
Figure BSA00000350926200171
Component C.2
Low polyphosphate based on Resorcinol
Figure BSA00000350926200181
C.1 and number average N value C.2, at first measure the content of oligomeric phosphoric acid ester with the HPLC method of masurement in order to measure given component:
Pillar type: LiChrosorp RP-8
Eluent in the gradient elution: acetonitrile/water 50: 50-100: 0
Concentration: 5mg/ml
Then by the assay weight average N mean value of known method from each component (single-and low polyphosphate).
Component D
Used polytetrafluoroethylproducts products (D) is by the mixture prepared by co-precipitation of the water miscible liquid of the water miscible liquid of graftomer (B) and tetrafluoro ethylene polymer.The weight ratio of graftomer in coagulum (B) and tetrafluoro ethylene polymer is 90 weight %:10 weight %.The solids content that the tetrafluoro ethylene polymer emulsion has is 60 weight %, and mean P TFE-particle diameter is 0.05-0.5 μ m.The solids content that the graftomer emulsion has is 34 weight %, and the average latex particle diameter is 0.3-0.4 μ m.
The emulsion (the Teflon 30N of DuPont company) of tetrafluoro ethylene polymer is mixed with the emulsion of graftomer (B) and with the phenols antiager stabilization of 1.8 weight % (based on polymer solids) in order to prepare (D).At 85-95 ℃ with described mixture MgSO 4The aggegation under pH 4-5 of (Epsom salts) and acetic acid water solution, filtration and washing are removed most water and be dried to powder under 100 ℃ by centrifugal then to not containing ionogen substantially.
Component E
The nano level A1O (OH) with Baume stone structure of Pural 200:Condea Chemie company (Hamburg, Germany).
Component G
Pentaerythritol tetrastearate
Preparation and test by moulding compound of the present invention
Being blended in 3 liters the interior kneader of component A-G carried out.Go up in 260 ℃ of preparation moldings at injector (Arburg270E type).
The fatigue crack performance is measured with the test strip of 80x10x4mm.As tested media, with the mixture of the Virahol of the toluene of 60 volume % and 40 volume %.Specimen is expanded (preliminary draft 0.2-2.4%) in advance by circle curve template and at room temperature be placed in the tested media 5 minutes.(Randfaserdehnung) estimates the fatigue crack performance with the edge elongate fiber, and this edge elongate fiber is necessary at least, so that test strip ruptures in exposure duration of 5 minutes in tested media.
At room temperature measure notched Izod impact strength (a by ISO 180-1A k).
Vicat B 120-temperature is measured with the heating rate of 120K/h and the mould load of 50N by ISO 306.
In the UL94V-combustion testing, on the test strip of 1.5mm thickness, measure flame retardant resistance.
Extruding under the processing situation as the measuring of melts stability, (shearing rate is 100s in low shearing scope in 260 ℃ by DIN 54 811 -1) measure the viscosity of melts.
MVR (melts volume ratio) measures in 260 ℃ of mould load with 5kg by ISO 1133.
Figure BSA00000350926200201
Embodiment 1-3 in the table 1 meets desired following performance fully
A) good flame retardant resistance (UL94V-0-grade when the 1.5mm wall thickness),
B) good notched Izod impact strength,
C) Gai Liang hot shape invariance, and especially,
D) the significantly ESC-behavior of improvement.
Because its good melts stability (high melt viscosity, low MVR) is so be suitable for processing in the expressing technique most.
Table 1 shows to contain based on the low polyphosphate of bisphenol-A ESC-behavior, notched Izod impact strength, hot shape invariance performance and melts rheology aspect to have significant performance advantage (comparing embodiment 2 and 3) by product of the present invention with containing to compare based on the comparable product of the low polyphosphate of Resorcinol as fire retardant.
Embodiment 1-3 and comparative example V1-V7 comparison shows that, the Teflon that adds concentration＞0.15 weight % (based on total composition) has positive effect to total performance.For example, embodiment 2 and 3 and comparison shows that of comparative example V1-V3 because the lower Teflon content of comparative example, has only by the amount that reduces graftomer, the amount that increases fire retardant and adds inorganic materials as retardant synergist, just can reach fire-retardant fully.But improving these fire-retardant measures has adverse influence to ESC-behavior, notched Izod impact strength, hot shape invariance performance and melts rheology.If the amount that increases graftomer is to reach the high rigidity of breaking (comparative example V5), so because lower Teflon content can not reach sufficient flame retardant resistance.Comparative example V3 and V4 comparison shows that, although can improve melts rheology and flame retardant resistance by adding inorganic materials, can not bring up to desired level to notched Izod impact strength and antifatigue crack performance.

Claims (17)

1. moulding compound, form by following component:
A) 75-90 weight % at least a in 25 ℃ in methylene dichloride, be the aromatic polycarbonate of the straight or branched of relative solution viscosity 〉=1.30 measured under the 0.5g/100ml in concentration,
B) at least a graftomer by emulsion polymerization prepared of 2-10 weight % is as the shock strength modifying agent,
C) at least a not halogen-containing phosphonium flame retardant of 3-12 weight %, it has following general formula:
Figure FSA00000350926100011
Wherein
R 1, R 2, R 3And R 4Independent separately is C 1-C 8-alkyl or the optional C that is replaced by alkyl 5-C 6-cycloalkyl, C 6-C 20-aryl or C 7-C 12-aralkyl,
N independently is 0 or 1 separately,
N is the number between the 0.1-30,
X has the monocycle or the polyaromatic of 6-30 C atom or has the straight chain of 2-30 C atom or the aliphatic group of straight chain, and it can be that OH-replaces and can comprise 8 ehter bonds at the most;
D) the fluoro polyolefine of 0.2-0.5 weight % and
Optional be selected from following additive: dripping inhibitor, lubricant, releasing agent, nucleator, static inhibitor, stablizer, dyestuff and pigment,
Wherein the weight % summation of the above component is 100,
It is characterized in that the specific moulding compound of the present invention has excellent flame-retardant performance, promptly in the UL94V-combustion testing during wall thickness≤1.5mm grade be V-0 and be 100s 260 ℃ and shearing rate -1The combination of the performance of the melt viscosity 〉=600Pa.s that records down.
2. according to the moulding compound of claim 1, wherein said composition does not contain AlO (OH).
3. according to the moulding compound of claim 1, contain phosphazo class or phosphonic acid ester amine as fire retardant.
4. according to each moulding compound among the claim 1-3, it contains the fire retardant that to have average low polymerization degree N be 0.5-10.
5. according to each moulding compound among the claim 1-3, it contains the fire retardant that to have average low polymerization degree N be 0.7-5.
6. according to the moulding compound of claim 1, one or more graftomer of the graft bases of its at least a vinyl monomer-grafted that contains 5-95 weight % at least a second-order transition temperature＜10 of 95-5 weight % ℃ are as the shock strength modifying agent.
7. according to the moulding compound of claim 6, contain the graftomer that grafts on elastoprene, EP (D) M rubber, acrylic elastomer or silicone rubber.
8. according to the moulding compound of claim 6, comprise latex A BS as the shock strength modifying agent.
9. according to the moulding compound of claim 1, contain particle, thin slice or fibrous inorganic materials.
10. according to the moulding compound of claim 9, the finely divided powder that contains median size≤100nm is as inorganic materials.
11., contain talcum or other sheet silicate or pure aluminium silicate as inorganic materials according to the moulding compound of claim 9.
12., contain the polycarbonate of branching according to the moulding compound of claim 1.
13. according to each moulding compound of claim 1-12, described composition is an extrusion compositions.
14. each the method for moulding compound of preparation claim 1-13 is wherein mixed each component and compounding at high temperature.
15. be used to prepare the purposes of various moldings, section bar, sheet material, tubing and conduit according to each moulding compound of claim 1-13.
16. be used for the purposes for preparing molding, section bar, sheet material, tubing and be used for the conduit of electronics at expressing technique according to each moulding compound of claim 1-13.
17. the molding or moulded piece and section bar, sheet material, the tubing that make by each moulding compound of claim 1-13 and the conduit that is used for electronics.
CN2010105475579A 2000-03-06 2001-02-21 Flame-resistant polycarbonate moulding compounds for extrusion applications Pending CN102051036A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE10010943 2000-03-06
DE10010943.8 2000-03-06
DE10014608A DE10014608A1 (en) 2000-03-06 2000-03-24 Polycarbonate molding compositions containing an impact modifier and a halogen-free phosphorus-containing flame retardant, useful for making molded products with high stress cracking resistance
DE10014608.2 2000-03-24

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CN01805912A Division CN1408007A (en) 2000-03-06 2001-02-21 Flame-resistant polycarbonate moulding compounds for extrusion applications

Publications (1)

Publication Number Publication Date
CN102051036A true CN102051036A (en) 2011-05-11

Family

ID=7633746

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010105475579A Pending CN102051036A (en) 2000-03-06 2001-02-21 Flame-resistant polycarbonate moulding compounds for extrusion applications

Country Status (5)

Country Link
JP (1) JP4776135B2 (en)
KR (1) KR100730674B1 (en)
CN (1) CN102051036A (en)
DE (1) DE10014608A1 (en)
ES (1) ES2305070T3 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103649224A (en) * 2011-07-14 2014-03-19 普立万公司 Non-halogenated flame retardant polycarbonate compounds
CN103881347A (en) * 2012-12-22 2014-06-25 奇美实业股份有限公司 Polycarbonate composition and application thereof

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10152318A1 (en) 2001-10-26 2003-05-08 Bayer Ag Impact-resistant modified flame-retardant polycarbonate molding compounds
WO2003080728A1 (en) * 2002-03-27 2003-10-02 Teijin Chemicals, Ltd. Flame-retardant aromatic polycarbonate resin composition
US7446144B2 (en) * 2005-09-14 2008-11-04 Bayer Materialscience Llc Thermoplastic molding composition and articles thermoformed therefrom
KR100877291B1 (en) * 2007-11-19 2009-01-07 제일모직주식회사 Non-halogen flameproof polycarbonate resin composition
KR100974015B1 (en) * 2008-12-12 2010-08-05 제일모직주식회사 Non-halogen Flameproof Polycarbonate Resin Composition and Plastic Article

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4443164A1 (en) 1994-12-05 1996-06-13 Bayer Ag Flame retardant, thermoplastic polycarbonate molding compounds
DE19538892A1 (en) 1995-10-19 1997-04-24 Bayer Ag Flame retardant, stress crack resistant polycarbonate / ABS blends
DE19714003A1 (en) * 1997-04-04 1998-10-08 Basf Ag Flame-retardant thermoplastic molding compounds with good flow properties
JPH10298423A (en) * 1997-04-30 1998-11-10 Toray Ind Inc Thermoplastic resin composition for basket
DE19734659A1 (en) * 1997-08-11 1999-02-18 Bayer Ag Flame-retardant polycarbonate ABS molding compounds
DE19734667A1 (en) * 1997-08-11 1999-02-18 Bayer Ag Flame-retardant, reinforced polycarbonate ABS molding compounds
DE19734661A1 (en) * 1997-08-11 1999-02-18 Bayer Ag Flame retardant, stress crack resistant polycarbonate ABS molding compounds
DE19742868A1 (en) * 1997-09-29 1999-04-01 Bayer Ag Polycarbonate ABS molding compounds
EP0933396A3 (en) * 1998-01-28 1999-12-15 General Electric Company Flame retardant polycarbonate resin/abs graft copolymer blends

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103649224A (en) * 2011-07-14 2014-03-19 普立万公司 Non-halogenated flame retardant polycarbonate compounds
CN103649224B (en) * 2011-07-14 2016-02-10 普立万公司 Non-halogenated fire retardant polycarbonate compound
CN103881347A (en) * 2012-12-22 2014-06-25 奇美实业股份有限公司 Polycarbonate composition and application thereof
CN103881347B (en) * 2012-12-22 2015-12-02 奇美实业股份有限公司 Polycarbonate composition and application thereof

Also Published As

Publication number Publication date
KR100730674B1 (en) 2007-06-21
KR20020079943A (en) 2002-10-19
ES2305070T3 (en) 2008-11-01
JP2003526717A (en) 2003-09-09
DE10014608A1 (en) 2001-09-13
JP4776135B2 (en) 2011-09-21

Similar Documents

Publication Publication Date Title
CN101117434B (en) Flame-resistant polycarbonate moulding compounds
CN100415813C (en) Flame-resistant polycarbonate ABS blends
CN101405344B (en) Flame-resistant impact-modified polycarbonate compositions
TWI487743B (en) Flame resistant, impact-modified polycarbonate compositions
CA2410943C (en) Non-inflammable, anti-electrostatic polycarbonate molding materials
CN101263199B (en) Thermoplastic molding composition and thermoformed articles thereof
DE19828536A1 (en) Fire-resistant polycarbonate-graft copolymer molding material, useful for the production of molded products, e.g. housings for monitors, printers, copiers etc.
JP2001512767A (en) Flame retardant polycarbonate-ABS molding composition
EP1802696A1 (en) Glass fiber-reinforced polymer compositions
DE10103238A1 (en) Flame-retardant, mineral-reinforced polycarbonate compositions with high weld line strength
DE10152318A1 (en) Impact-resistant modified flame-retardant polycarbonate molding compounds
CN1408007A (en) Flame-resistant polycarbonate moulding compounds for extrusion applications
DE19962929A1 (en) Polycarbonate compositions useful for making molded articles include an impact modifier and a high-purity talc with a low alumina content for increased toughness
DE10061080A1 (en) Polycarbonate compositions
CN102361923A (en) Flame-resistant impact-modified polycarbonate compositions
CN102051036A (en) Flame-resistant polycarbonate moulding compounds for extrusion applications
CN103189448A (en) Impact-modified polyester/polycarbonate compositions having improved elongation at rupture
CN100434460C (en) Flame-resistant polycarbonate moulding materials
DE10224616A1 (en) Polycarbonate or polyester carbonate composition, useful for the production of molded articles having modified impact resistance, contains at least one oxalate compound

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20110511