Background technology
Halide-containings such as SE (PVC), X 050 have good flame retardant property and are widely used in the electric wire industry; But when fire or burning disposal, can produce a large amount of toxic gases; Human body is produced harm greatly to environment; In recent years; Some non-government environmental protection organizations appeal that actively each big electronic apparatus manufacturing enterprise removes the material of PVC material and halogen containing flame-retardant in its product, and the non-halogen material that substitutes PVC is also just actively sought by each large enterprises, makes that the exploitation of halogen-free flameproof soft material is urgent day by day.
The matrix material that has occurred at present much aiming at halogen-free flame-retardant wire and developed is main with systems such as polyolefine/inorganic combustion inhibitor, polyolefine or elastomerics/expansion type flame retardant, Noryl/phosphorus-nitrogen containing flame retardant, urethane/phosphorus-nitrogen containing flame retardants.But polyolefine/inorganic combustion inhibitor system just can reach flame retardant effect preferably under the very big situation of fire retardant addition, damaged the mechanical property of material greatly; Though polyolefine or elastomerics/expansion type flame retardant, urethane/phosphorus-nitrogen containing flame retardant system can keep mechanical property preferably reaching under the condition of flame retardant properties, material easily suction to cause that goods produce that electrical property descends, separate out on the surface etc. bad; Noryl/phosphorus-nitrogen containing flame retardant is the good performance of balance each side then, thereby becomes halogen-free flame-retardant wire investigation of materials focus.
Ppe is to be succeeded in developing in 1964 by GE, and formally puts into production in nineteen sixty-five.There are shortcomings such as processing difficulties, goods easy of crack and cost height in polyphenylene oxide resin, mostly is the blend of ppe and high-impact polystyrene in the practical application now.
Noryl itself has certain flame retardant resistance; And mechanical property, electrical property, resistance toheat are all good; Interpolation through a small amount of compound flame retardant makes each item excellent performance of material; Be applied to have leading superiority in the halogen-free flame-retardant wire material; Up to the present, being applied to Noryl the most successful in the halogen-free flame-retardant wire material is SABIC company (purchase GE plastics), and the system that they adopt is ppe/styrene-butadiene-styrene block copolymer/polyolefine/composite flame-retardant agent (phosphoric acid salt, metallic hydrogen Natural manganese dioxide, SULPHOSUCCINIC ACID ESTER is composite).
In the practical application; Usually need stamp literal and sign on the electric wire surface; And the ppe/styrene-butadiene-styrene block copolymer that in current technology, adopts/polyolefine system is the more weak polymkeric substance of polarity, and this has brought certain difficulty for the electric wire surface printing.
Summary of the invention
The objective of the invention is provides a kind of and has better surface printing performance in order to overcome the problem that existing electric wire surface printing has difficulties, and the fire-retardant polyphenyl ether compound of mechanical property, electrical property, resistance toheat excellent combination property.
Another object of the present invention provides a kind of preparation method of above-mentioned fire-retardant polyphenyl ether compound.
Another object of the present invention provides the application of above-mentioned fire-retardant polyphenyl ether compound in the preparation electric wire.
The general following technical scheme of purpose according to the invention is achieved:
A kind of fire-retardant polyphenyl ether compound is made up of the component that following percentage ratio by weight calculates: polyphenylene oxide resin 18~28%, acrylonitritrile-styrene resin 5~30%; Elastomerics 20~35%; Fire retardant 20~35%, softening agent 5~18%, oxidation inhibitor 0.1~1.5%.
Aforesaid propylene nitrile-styrol copolymer is all acrylonitritrile-styrene resins of 7~11 weight % for the weight acrylamide nitrile content based on multipolymer.With current compared with techniques, system of the present invention has been introduced vinyl cyanide, and vinyl cyanide has stronger polarity, better chemical resistance and oil-proofness than vinylbenzene, and just so, system of the present invention has better surface printing performance.When it should be noted that in the selected multipolymer that weight acrylamide nitrile content based on multipolymer is less than 7 weight %, the mixture that the surface printing performance of mixture and present technology are made is approaching; And when in the selected multipolymer based on the weight acrylamide nitrile content of multipolymer during greater than 11 weight %, the consistency of acrylonitritrile-styrene resin and other components can variation, mixture is easy to generate serious phenomenon of phase separation.
As a kind of most preferably scheme, aforesaid propylene nitrile-styrol copolymer is all acrylonitritrile-styrene resins of 9 weight % for the weight acrylamide nitrile content based on multipolymer.
Wherein polyphenylene oxide resin comprises all known polyphenylene oxide resins.Said polyphenylene oxide resin is the resin of limiting viscosity between 0.20~0.60dl/g of measuring in 25 ℃ of chloroforms.Can use a kind of polyphenylene oxide resin of independent limiting viscosity, also can select several kinds of different qualities viscosity polyphenylene oxide resin mixtures for use.The outward appearance of ppe can be Powdered also can be particulate state.
Above-mentioned elastomerics is preferably one or more the mixture in ethylene-propylene rubber(EPR), paracril, cis-1,4-polybutadiene rubber, ethylene vinyl acetate, polyolefin elastomer, styrene-butadiene-styrene block copolymer, styrene-ethylene/butylene-styrene block copolymer, the styrene-ethylene/propylene-styrene segmented copolymer.
As a kind of most preferably scheme, above-mentioned elastomerics most preferably is styrene-ethylene/butylene-styrene block copolymer.
Above-mentioned fire retardant is that to state fire retardant be one or more the mixture in phosphate compound, phosphoric acid salt and the metal hydroxides.Wherein phosphate compound is trimethyl phosphite 99, triethyl phosphate, tricresyl phosphate propyl ester, tributyl phosphate, TNPP tri n pentyl phosphate, tri hexyl phosphate, tricyelohexyl phosphate, triphenylphosphate, tritolyl phosphate, trixylyl phosphate, phosphoric acid cresyl diphenyl ester, di(2-ethylhexyl)phosphate cresyl phenyl ester, di(2-ethylhexyl)phosphate methyl ethyl ester, phosphoric acid methyl dibutylester, phosphoric acid ethyl dipropyl, phosphoric acid phenylor diphenyl ester, tetraphenyl (bisphenol-A) bisphosphate or tetraphenyl resorcinol diphosphate; Phosphoric acid salt is monophosphate monophosphate hydrogen two ammoniums, primary ammonium phosphate, trimeric cyanamide, melamine pyrophosphate, ortho-phosphoric acid trimeric cyanamide, phosphoamide, polyphosphoric acid melamine, ammonium polyphosphate, polyphosphoric acid acid amides; Metal hydroxides is Marinco H, white lake.
Said softening agent is the softening agent that has excellent compatibility with ppe; Said softening agent is preferably one or more the mixture in fatty acid amide, fatty acid mixture, paraffin, organic silicone oil, white mineral oil, NO, the alpha-methyl styrene; Add the dispersiveness that effectively to improve each component man-hour; Reduce plastic melt and the bonding strength of metallic surface and the internal friction of plastic melt; Help improving the melt flow rate(MFR) of mixture, regulate the functions such as pliability of mixture.
As a kind of most preferably scheme, said softening agent most preferably is white mineral oil.
Above-mentioned oxidation inhibitor is phenols, phosphorous acid esters, contain one or more the mixture in thioesters class, the metal passivator; The phenolic antioxidant that wherein is suitable for body series is 2; 4; 6-tri-butyl-phenol, 2,2 methylene-biss (4-methyl-6-tert butyl phenol) or four [β-(3, the 5-di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol ester (antioxidant 1010); Phosphite ester kind antioxidant is tricresyl phosphite (nonyl phenyl) or tricresyl phosphite (2, the 4-di-tert-butyl-phenyl) fat (oxidation inhibitor 168); Containing the thioesters kind antioxidant is thio-2 acid two lauric fats or thio-2 acid two (18) fat; The metal passivator kind antioxidant is N, N-diacetyl adipyl two hydrazides, N-salicylidene-N-salicyl hydrazides or salicil hydrazine.The purpose one that adds oxidation inhibitor is to improve the thermostability of matrix material, prevents that composite materials from degrading in extruding pelletization or Injection moulded part process; Another purpose is to improve the long-term aging performance of mixture.
The preparation method of polyphenyl ether composite of the present invention; The steps include: earlier polyphenylene oxide resin, acrylonitritrile-styrene resin, elastomerics, fire retardant, softening agent and oxidation inhibitor after the high-speed mixer dispersing and mixing, through the twin screw extruder fusion, mix, extrude, cool off, dry, pelletizing and packing.Screw rod is respectively distinguished temperature and should be remained between 200~280 ℃, and the length-to-diameter ratio of twin screw extruder is 36~48, and screw speed is 260~500 rev/mins.
Compared with prior art; The present invention has following beneficial effect: fire-retardant polyphenyl ether compound of the present invention; Halogen-free flameproof, mechanical property, electrical property, thermotolerance are good, and owing to introduced vinyl cyanide, and vinyl cyanide has stronger polarity, better chemical resistance and oil-proofness than vinylbenzene; Make easily the obtained flame-retardant polyphenyl ether composite is carried out surface printing, be suitable for very much preparing supply lead, data transmission line of electronic apparatus etc.
Embodiment
Come further to explain the present invention below in conjunction with embodiment, but embodiment does not do any type of qualification to the present invention.
The preparation method of fire-retardant polyphenyl ether compound of the present invention; The steps include: earlier polyphenylene oxide resin, acrylonitritrile-styrene resin, elastomerics, fire retardant, softening agent and oxidation inhibitor after the high-speed mixer dispersing and mixing, through the twin screw extruder fusion, mix, extrude, cool off, dry, pelletizing and packing.Screw rod is respectively distinguished temperature and should be remained between 260 ℃, and the length-to-diameter ratio of twin screw extruder is 40, and screw speed is 350 rev/mins.
According to above-mentioned preparation method, the ppe that present embodiment adopts is that limiting viscosity is at 0.40dl/g (2,6-dimethyl--1,4-phenylene) ether; Based on multipolymer weight acrylamide nitrile content is the acrylonitritrile-styrene resin (be designated as AS-H, it tests the flow rate 90g/10min of melt at 220 ℃ under 10KG load) of 9 weight %; Based on multipolymer weight acrylamide nitrile content is the acrylonitritrile-styrene resin (be designated as AS-D, it tests the flow rate 60g/10min of melt at 220 ℃ under 10KG load) of 5 weight %; Based on multipolymer weight acrylamide nitrile content is the acrylonitritrile-styrene resin (be designated as AS-G, it tests the flow rate 95g/10min of melt at 220 ℃ under 10KG load) of 13 weight %; Elastomerics is a styrene-ethylene/butylene-styrene block copolymer, and fire retardant is the blend of tetraphenyl (bisphenol-A) bisphosphate (BDP) and polyphosphoric acid melamine, and softening agent is a white mineral oil, and oxidation inhibitor is antioxidant 1010 and oxidation inhibitor 168.Its The performance test results that specifically reaches the gained mixture is seen table 1.
Each test is undertaken by following standard:
Tensile strength: test according to GB1040-2006;
Elongation at break: test according to GB1040-2006;
Combustionproperty:, adopt the sample of 4.0mm to test according to UL94;
Colorfastness to rubbing:, sample surfaces spraying printed in white printing ink is tested according to GB/T 3920;
Dielectric strength: test according to GB1409;
Temperature grade: it is the 2.0mm electric wire of 0.12mm copper conductor that material prepn becomes conductor, tests according to 105 ℃ of level estimate conditions in the UL1581 standard then, and test condition is 136 ℃, 168 hours.
The formula table of table 1 embodiment and the The performance test results of mixture
Component |
Embodiment 1 |
Comparative Examples 1 |
Comparative Examples 2 |
Comparative Examples 3 |
Embodiment 2 |
Comparative Examples 4 |
Comparative Examples 5 |
Ppe |
20 |
20 |
20 |
20 |
25 |
25 |
25 |
AS-H |
20 |
? |
? |
? |
10 |
? |
? |
AS-D |
? |
20 |
? |
? |
? |
? |
? |
AS-G |
? |
? |
20 |
? |
? |
10 |
? |
Styrene-ethylene/butylene-styrene block copolymer |
25 |
25 |
25 |
45 |
21 |
30 |
40 |
BDP |
16 |
16 |
16 |
16 |
16 |
16 |
16 |
Polyphosphoric acid melamine |
12 |
12 |
12 |
12 |
12 |
12 |
12 |
White mineral oil |
6 |
6 |
6 |
6 |
15 |
6 |
6 |
Antioxidant 1010 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
Oxidation inhibitor 168 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
Add up to |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
Performance test |
? |
? |
? |
? |
? |
? |
? |
Tensile strength (MPa) |
12 |
13 |
8 |
14 |
15 |
9 |
19 |
Elongation at break (%) |
120 |
125 |
20 |
130 |
130 |
25 |
120 |
Combustionproperty |
V-0 |
V-0 |
V-0 |
V-0 |
V-0 |
V-0 |
V-0 |
Colorfastness to rubbing (staining progression) |
4 grades |
2 grades |
4 grades |
2 grades |
4 grades |
4 grades |
2 grades |
Dielectric strength (MV/m) |
26 |
26 |
26 |
26 |
26 |
26 |
26 |
UL temperature grade |
105℃ |
105℃ |
- |
105℃ |
105℃ |
- |
105℃ |
Can see from the data of table 1; The mixture good mechanical properties of embodiment 1, embodiment 2; Be suitable for preparing electric wire; And colorfastness to rubbing is 4 grades behind their spray printed in white oil, and being superior to adding based on multipolymer weight acrylamide nitrile content is Comparative Examples 1 and Comparative Examples 3, the Comparative Examples 5 of not adding acrylonitritrile-styrene resin of the acrylonitritrile-styrene resin of 5 weight %, and mixture that can illustrative embodiment carries out surface printing more easily.
It is the acrylonitritrile-styrene resin AS-G of 13 weight % that Comparative Examples 2 has been added based on multipolymer weight acrylamide nitrile content with Comparative Examples 4; Though its colorfastness to rubbing is 4 grades; But because the consistency of system is bad; Be easy to generate layering in the moulding process, and their tensile strength and elongation are all on the low side, can't be prepared into electric wire with it.