CN105542402B - A kind of PBT permanent types anti-static material and its preparation method and application - Google Patents
A kind of PBT permanent types anti-static material and its preparation method and application Download PDFInfo
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- CN105542402B CN105542402B CN201510957367.7A CN201510957367A CN105542402B CN 105542402 B CN105542402 B CN 105542402B CN 201510957367 A CN201510957367 A CN 201510957367A CN 105542402 B CN105542402 B CN 105542402B
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- 239000002216 antistatic agent Substances 0.000 title claims abstract description 64
- 238000002360 preparation method Methods 0.000 title claims abstract description 31
- 239000003063 flame retardant Substances 0.000 claims abstract description 53
- 239000004594 Masterbatch (MB) Substances 0.000 claims abstract description 52
- 239000000463 material Substances 0.000 claims abstract description 43
- 238000002156 mixing Methods 0.000 claims abstract description 41
- 230000003068 static effect Effects 0.000 claims abstract description 8
- 238000001125 extrusion Methods 0.000 claims abstract description 6
- 239000002994 raw material Substances 0.000 claims description 24
- 238000003756 stirring Methods 0.000 claims description 17
- -1 polyethylene Polymers 0.000 claims description 13
- 239000004020 conductor Substances 0.000 claims description 11
- 239000004698 Polyethylene Substances 0.000 claims description 10
- 229920000573 polyethylene Polymers 0.000 claims description 10
- 229920000767 polyaniline Polymers 0.000 claims description 9
- 229920000123 polythiophene Polymers 0.000 claims description 9
- 238000010348 incorporation Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229910000410 antimony oxide Inorganic materials 0.000 claims description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000012876 carrier material Substances 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 239000004115 Sodium Silicate Substances 0.000 claims description 2
- 239000003990 capacitor Substances 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- 239000004519 grease Substances 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 235000019795 sodium metasilicate Nutrition 0.000 claims description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 claims description 2
- 239000001488 sodium phosphate Substances 0.000 claims description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims description 2
- 238000002485 combustion reaction Methods 0.000 claims 1
- 238000009413 insulation Methods 0.000 abstract description 6
- 239000007789 gas Substances 0.000 abstract description 4
- 230000015556 catabolic process Effects 0.000 abstract description 3
- 238000004377 microelectronic Methods 0.000 abstract description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 2
- 230000005611 electricity Effects 0.000 abstract description 2
- 229910052760 oxygen Inorganic materials 0.000 abstract description 2
- 239000001301 oxygen Substances 0.000 abstract description 2
- 230000005622 photoelectricity Effects 0.000 abstract description 2
- 239000004753 textile Substances 0.000 abstract description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 64
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 238000005453 pelletization Methods 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 3
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- 238000010998 test method Methods 0.000 description 2
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- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 229910021389 graphene Inorganic materials 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- 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
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- 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
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/9258—Velocity
- B29C2948/9259—Angular velocity
-
- 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
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2465/00—Characterised by the use of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Derivatives of such polymers
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2479/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2461/00 - C08J2477/00
- C08J2479/02—Polyamines
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- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
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- C08L2201/00—Properties
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- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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Abstract
The present invention provides a kind of PBT permanent types anti-static material and its preparation method and application, and PBT anti-static materials of the invention are prepared by 5 25% fire-retardant, electrostatic-conducting dissipative type master batch and 75 95% PBT.In the present invention by the way that fire-retardant, electrostatic-conducting dissipative type master batch and PBT blendings, extrusion are obtained into the PBT anti-static materials, the PBT anti-static materials reach high oxygen index (OI) flame-retardant V 0-stage, and specific insulation is 106‑8Ω, surface resistivity is 106‑9Ω, static decay time > 10s, so as to solve each field product because electrostatic causes breakdown and serious harm, to temperature humidity without dependence, it is widely used in intelligent microelectronic, electrical equipment, electrostatic sheet-material package, electric wire, photoelectricity photovoltaic solar, machinery, medical equipment, electrostatic textile and takes the fields such as footwear, fire-fighting, military project electrostatic equipment, the explosion-proof industry of electrostatic, gas electrostatic protection safety, fireworks and firecrackers protection electrostatic safety, petrochemical industry energy protection electrostatic, Static Electricity at Gas Stations protection.
Description
Technical field
The invention belongs to fire-retardant, electrostatic-conducting field of material preparation, be related to a kind of PBT anti-static materials and preparation method thereof and
Using, more particularly to a kind of PBT permanent types anti-static material and its preparation method and application.
Background technology
Polybutylene terephthalate (PBT) (PBT) is a kind of thermoplastic engineering plastic, be widely used in electronic apparatus,
The fields such as household electrical appliances, auto industry, but due to its low-temperature impact toughness is poor and notch sensitivity is big at room temperature, non-antiflaming effect and
Antistatic resistance rate is up to 10-15-20The shortcomings of Ω high insulating materials, there is greatly limitation for applying electronic product, and it is serious difficult
To control the harm of electrostatic:Heavy losses may be caused to the product of human body discharge or each industry during use and are ignited
The disaster such as quick-fried, but Chinese every profession and trade electrostatic art preceding in nearly 20-30 is all produced from traditional (carbon system) static conductive at present
Product application, such as acetylene carbon black of (carbon system), graphene, carbon fiber intermingling material in use and product transported in turnover
Cheng Zhong, rubbed collision scratch the carbon system dust micron order for making surface:Moment takes off in powered entrance microelectronic component, caused
Product in electron system because electrostatic breakdown it is easily breaking the defects of, as electronic technology constantly brings forth new ideas, electrostatic new material day crescent
Different, carbon system (black) material is substituted by true qualities electrostatic material, a kind of PBT electrostatic materials of this project development and preparation method thereof and
Using (true qualities) adjustable color, performances such as (physics, the mechanics) of material, outward appearance clean aesthetic and volume resistance and table are not influenceed
Simple and traditional (carbon series) electrostatic material of surface resistance permanent stabilization, moderate cost, technique carries out quality and contrasted and nothing with cleaning
Method is compared, and has been relied on import white electrostatic material and high price and monopoly product since having broken the several years, is related to this area from chief creating
New PBT Combined Electrostatic materials are the important key points of urgent need to resolve.
The content of the invention
For the deficiency of currently available technology, it is an object of the invention to provide a kind of PBT permanent types anti-static material and
Its preparation method and application.
To use following technical scheme up to this purpose, the present invention:
On the one hand, the present invention provides a kind of PBT anti-static materials, the fire-retardant, electrostatic-conducting dissipative type master batch of the 5-25% and
PBT anti-static materials are prepared by 75-95% PBT.
In the raw material of the PBT anti-static materials of the present invention, PBT dosage is 75-95%, for example, 76%, 77%,
78%th, 79%, 80%, 82%, 84%, 86%, 88%, 90%, 92%, 93% or 94%.
In the raw material of the PBT anti-static materials of the present invention, the dosage of fire-retardant, electrostatic-conducting dissipative type master batch is 5-25%, example
Such as 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23% or 24%.
Preferably, the PBT anti-static materials are prepared by 20% fire-retardant, electrostatic-conducting dissipative type master batch and 80% PBT
Obtain.
In the present invention, the fire-retardant, electrostatic-conducting dissipative type master batch is prepared by the following raw material of mass percent:
In the preparing raw material of the fire-retardant, electrostatic-conducting dissipative type master batch of the present invention, the dosage of polyaniline is 5-15%, such as
5.5%th, 6%, 6.5%, 7%, 7.5%, 8%, 8.5%, 9%, 9.5%, 10%, 10.5%, 11%, 11.5%, 12%,
12.5%th, 13%, 13.5%, 14% or 14.5%.
In the preparing raw material of the fire-retardant, electrostatic-conducting dissipative type master batch of the present invention, the dosage of polythiophene is 5-15%, such as
5.5%th, 6%, 6.5%, 7%, 7.5%, 8%, 8.5%, 9%, 9.5%, 10%, 10.5%, 11%, 11.5%, 12%,
12.5%th, 13%, 13.5%, 14% or 14.5%.
In the preparing raw material of the fire-retardant, electrostatic-conducting dissipative type master batch of the present invention, the dosage of organosilicon is 2-8%, such as
2.3%th, 2.5%, 2.8%, 3%, 3.2%, 3.5%, 3.8%, 4%, 4.3%, 4.5%, 4.8%, 5%, 5.3%,
5.5%th, 5.8%, 6%, 6.5%, 6.8%, 7%, 7.3%, 7.5% or 7.8%.
In the preparing raw material of the fire-retardant, electrostatic-conducting dissipative type master batch of the present invention, the dosage of antimony oxide is 4-10%,
Such as 4.2%, 4.5%, 4.8%, 5%, 5.3%, 5.5%, 5.8%, 6%, 6.3%, 6.5%, 6.8%, 7%, 7.5%,
7.8%th, 8%, 8.5%, 8.8%, 9%, 9.5% or 9.8%.
In the preparing raw material of the fire-retardant, electrostatic-conducting dissipative type master batch of the present invention, the dosage of conductor material is 22-63%, example
Such as 23%, 25%, 28%, 30%, 32%, 35%, 38%, 40%, 42%, 44%, 46%, 48%, 50%, 53%, 55%,
58%th, 60%, 61% or 62%.
In the preparing raw material of the fire-retardant, electrostatic-conducting dissipative type master batch of the present invention, the dosage of carrier material is 25-40%, example
Such as 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38% or 39%.
Preferably, fire-retardant, electrostatic-conducting dissipative type master batch of the present invention is prepared by the following raw material of mass percent:
In the present invention, the organosilicon is any in silicone grease, silicon emulsion, silicon rubber, sulphurated siliastic or silicones
It is a kind of or at least two combination.
Preferably, the conductor material is any one in sodium chloride, sodium phosphate or sodium metasilicate or at least two group
Close.
Preferably, the carrier material is any one in polyethylene, PBT or polypropylene or at least two combination.
In the present invention, the preparation method of described fire-retardant, electrostatic-conducting dissipative type master batch comprises the following steps:
(1) polyaniline, polythiophene, conductor material and polyethylene are added in batch mixer and carries out blending doping, mixed
Material;
(2) antimony oxide and organosilicon are added into mixed material obtained by step (1), mixing, then utilizes extruder
Middle extruding pelletization, obtain the fire-retardant, electrostatic-conducting dissipative type master batch.
In the preparation method of fire-retardant, electrostatic-conducting dissipative type master batch of the present invention, stirring when step (1) blending is adulterated
Speed is 20-90r/min, for example, 23r/min, 25r/min, 28r/min, 30r/min, 35r/min, 38r/min, 40r/min,
43r/min、45r/min、48r/min、50r/min、55r/min、58r/min、60r/min、65r/min、68r/min、70r/
Min, 73r/min, 75r/min, 78r/min, 80r/min, 83r/min, 85r/min or 88r/min.
Preferably, the incorporation time of step (1) the blending doping is 10-30min, for example, 11min, 12min, 13min,
14min、15min、16min、17min、18min、19min、20min、21min、22min、23min、24min、25min、
26min, 27min, 28min or 29min.
In preparation method of the present invention, step (2) described extruder is double screw extruder.
Preferably, the preheating temperature in step (2) the extruder screw region be 180-250 DEG C, such as 180 DEG C, 185
DEG C, 190 DEG C, 195 DEG C, 200 DEG C, 205 DEG C, 210 DEG C, 215 DEG C, 220 DEG C, 225 DEG C, 230 DEG C, 235 DEG C, 240 DEG C, 245 DEG C or
248 DEG C, preferably 200-220 DEG C.
Preferably, the screw speed of step (2) described extruder is 190r/min-320r/min, such as 193r/min,
195r/min、198r/min、200r/min、210r/min、220r/min、230r/min、240r/min、250r/min、260r/
Min, 270r/min, 280r/min, 290r/min, 300r/min, 310r/min or 315r/min, preferably 220-300r/min.
Preferably, the preparation method of fire-retardant, electrostatic-conducting dissipative type master batch of the present invention comprises the following steps:
(1) polyaniline, polythiophene, conductor material and polyethylene are added in batch mixer and carries out blending doping, stir speed (S.S.)
For 20-90r/min, blending doping 10-30min, mixed material is obtained;
(2) antimony oxide and organosilicon are added into mixed material obtained by step (1), mixing, adds to twin-screw and squeezes
Go out extruding pelletization in machine, the preheating temperature in the extruder screw region is 180-250 DEG C, screw speed 190r/min-
320r/min, obtain the fire-retardant, electrostatic-conducting dissipative type master batch.
On the other hand, the invention provides the preparation method of PBT anti-static materials as described in relation to the first aspect, methods described
For:PBT and fire-retardant, electrostatic-conducting dissipative type master batch blending doping, extrusion are obtained into the PBT anti-static materials.
In the preparation method of PBT anti-static materials of the present invention, the stir speed (S.S.) when blending is adulterated is 100-
200r/min, for example, 110r/min, 120r/min, 130r/min, 140r/min, 150r/min, 170r/min, 180r/min or
190r/min。
Preferably, the incorporation time of the blending doping is 15-30min, for example, 16min, 17min, 18min, 19min,
20min、21min、22min、23min、24min、25min、26min、27min、28min、29min。
Preferably, the extrusion is completed using double screw extruder.
Preferably, the preheating temperature in the screw rod region of the double screw extruder be 260-350 DEG C, such as 270 DEG C, 280
DEG C, 290 DEG C, 300 DEG C, 310 DEG C, 320 DEG C, 330 DEG C or 340 DEG C.
Preferably, the screw speed of the double screw extruder is 200-300r/min, such as 210r/min, 220r/
Min, 230r/min, 240r/min, 250r/min, 260r/min, 270r/min, 280r/min or 290r/min.
As the preferred technical solution of the present invention, the preparation method of PBT anti-static materials of the present invention is:By PBT and
Fire-retardant, electrostatic-conducting dissipative type master batch is blended, and stir speed (S.S.) during blending is 100-200r/min, and the incorporation time of blending is 15-
30min, then extruded using double screw extruder, the preheating temperature in the screw rod region of the double screw extruder is 260-350
DEG C, the screw speed of double screw extruder is 200-300r/min, obtains the PBT anti-static materials.
The technical scheme further preferred as the present invention, the preparation method of PBT anti-static materials of the present invention include
Following steps:
A, polyaniline, polythiophene, conductor material and polyethylene are added in batch mixer and carries out blending doping, stir speed (S.S.) is
20-90r/min, blending doping 10-30min, obtains mixed material;Antimony oxide and organosilicon are added into mixed material,
Mixing, extruding pelletization is added into double screw extruder, the preheating temperature in the extruder screw region is 180-250 DEG C, spiral shell
Bar rotating speed is 190r/min-320r/min, obtains fire-retardant, electrostatic-conducting dissipative type master batch;
B, PBT and fire-retardant, electrostatic-conducting dissipative type master batch are blended, stir speed (S.S.) during blending be 100-200r/min, is blended
Incorporation time be 15-30min, then extruded using double screw extruder, the screw rod region of the double screw extruder it is pre-
Hot temperature is 260-350 DEG C, and the screw speed of double screw extruder is 200-300r/min, obtains the PBT anti-static materials.
On the other hand, the invention provides PBT anti-static materials as described in relation to the first aspect electronic apparatus, capacitor or
Application in antistatic film material.
Relative to prior art, the invention has the advantages that:
The PBT anti-static materials of the present invention are prepared by 5-25% fire-retardant, electrostatic-conducting dissipative type master batch and 75-95% PBT
Obtain.In the present invention by the way that fire-retardant, electrostatic-conducting dissipative type master batch and PBT blendings, extrusion are obtained into the antistatic materials of the PBT
Material, the PBT anti-static materials reach high oxygen index (OI) flame-retardant V 0-stage, and specific insulation is 106-8Ω, surface resistivity is 106-9Ω,
Static decay time > 10s, so as to solve each field product because electrostatic causes breakdown and serious harm, to temperature humidity without
Rely on, be widely used in intelligent microelectronic, electrical equipment, electrostatic sheet-material package, electric wire, photoelectricity photovoltaic solar, machinery, medical treatment
Equipment, electrostatic textile take footwear, fire-fighting, military project electrostatic equipment, the explosion-proof industry of electrostatic, gas electrostatic protection safety, fireworks and firecrackers
Protect the fields such as electrostatic safety, petrochemical industry energy protection electrostatic, Static Electricity at Gas Stations protection.
Embodiment
Technical scheme is further illustrated below by embodiment.Those skilled in the art should be bright
, the embodiment be only to aid in understand the present invention, be not construed as to the present invention concrete restriction.
Embodiment 1
In the present embodiment, PBT anti-static materials are prepared by following raw material:
PBT 80%
Fire-retardant, electrostatic-conducting dissipative type master batch 20%
Wherein, fire-retardant, electrostatic-conducting dissipative type master batch is prepared by following raw material:
The preparation method of PBT anti-static materials is as follows:
A, polyaniline, polythiophene, organosilicon, conductor material and polyethylene are added in batch mixer, stir speed (S.S.) 20r/
Min, blending doping 30min, obtains mixed material;Mixed material is added into double screw extruder extruding pelletization, it is described to squeeze
The preheating temperature for going out machine screw rod region is 180 DEG C, screw speed 320r/min, obtains fire-retardant, electrostatic-conducting dissipative type master batch;
B, PBT and fire-retardant, electrostatic-conducting dissipative type master batch are blended, stir speed (S.S.) during blending be 150r/min, and blending mixes
The conjunction time is 20min, is then extruded using double screw extruder, and the preheating temperature in the screw rod region of the double screw extruder is
300 DEG C, the screw speed of double screw extruder is 200r/min, obtains PBT anti-static materials.
Embodiment 2
In the present embodiment, PBT anti-static materials are prepared by following raw material:
PBT 75%
Fire-retardant, electrostatic-conducting dissipative type master batch 25%
Wherein, fire-retardant, electrostatic-conducting dissipative type master batch is prepared by following raw material:
The preparation method of PBT anti-static materials is as follows:
A, polyaniline, polythiophene, organosilicon, conductor material and polyethylene are added in batch mixer, stir speed (S.S.) 90r/
Min, blending doping 10min, obtains mixed material;Mixed material is added into double screw extruder extruding pelletization, it is described to squeeze
The preheating temperature for going out machine screw rod region is 250 DEG C, screw speed 190r/min, obtains fire-retardant, electrostatic-conducting dissipative type master batch;
B, PBT and fire-retardant, electrostatic-conducting dissipative type master batch are blended, stir speed (S.S.) during blending be 200r/min, and blending mixes
The conjunction time is 15min, is then extruded using double screw extruder, and the preheating temperature in the screw rod region of the double screw extruder is
260 DEG C, the screw speed of double screw extruder is 300r/min, obtains PBT anti-static materials.
Embodiment 3
In the present embodiment, PBT anti-static materials are prepared by following raw material:
PBT 95%
Fire-retardant, electrostatic-conducting dissipative type master batch 5%;
Wherein, fire-retardant, electrostatic-conducting dissipative type master batch is prepared by following raw material:
The preparation method of PBT anti-static materials is as follows:
A, polyaniline, polythiophene, organosilicon, conductor material and polyethylene are added in batch mixer, stir speed (S.S.) 50r/
Min, blending doping 15min, obtains mixed material;Mixed material is added into double screw extruder extruding pelletization, it is described to squeeze
The preheating temperature for going out machine screw rod region is 200 DEG C, screw speed 220r/min, obtains fire-retardant, electrostatic-conducting dissipative type master batch;
B, PBT and fire-retardant, electrostatic-conducting dissipative type master batch are blended, stir speed (S.S.) during blending be 100r/min, and blending mixes
The conjunction time is 30min, is then extruded using double screw extruder, and the preheating temperature in the screw rod region of the double screw extruder is
350 DEG C, the screw speed of double screw extruder is 200r/min, obtains PBT anti-static materials.
Embodiment 4
In the present embodiment, PBT anti-static materials are prepared by following raw material:
PBT 85%
Fire-retardant, electrostatic-conducting dissipative type master batch 15%
Wherein, fire-retardant, electrostatic-conducting dissipative type master batch is prepared by following raw material:
The preparation method of PBT anti-static materials is as follows:
A, polyaniline, polythiophene, organosilicon, conductor material and polyethylene are added in batch mixer, stir speed (S.S.) 70r/
Min, blending doping 20min, obtains mixed material;Mixed material is added into double screw extruder extruding pelletization, it is described to squeeze
The preheating temperature for going out machine screw rod region is 230 DEG C, screw speed 250r/min, obtains fire-retardant, electrostatic-conducting dissipative type master batch.
B, PBT and fire-retardant, electrostatic-conducting dissipative type master batch are blended, stir speed (S.S.) during blending be 200r/min, and blending mixes
The conjunction time is 20min, is then extruded using double screw extruder, and the preheating temperature in the screw rod region of the double screw extruder is
300 DEG C, the screw speed of double screw extruder is 300r/min, obtains PBT anti-static materials.
Comparative example 1
The difference of this comparative example and embodiment 1 is that PBT anti-static materials are prepared by following raw material:
PBT 97%
Fire-retardant, electrostatic-conducting dissipative type master batch 3%
In addition, the raw material components of fire-retardant, electrostatic-conducting dissipative type master batch and its content and the system of PBT anti-static materials
Preparation Method is same as Example 1.
Comparative example 2
The difference of this comparative example and embodiment 1 is that PBT anti-static materials are prepared by following raw material:
PBT 70%
Fire-retardant, electrostatic-conducting dissipative type master batch 30%
In addition, the raw material components of fire-retardant, electrostatic-conducting dissipative type master batch and its content and the system of PBT anti-static materials
Preparation Method is same as Example 1.
Performance test
PBT anti-static materials prepared by embodiment 1-4 and comparative example 1-3 are carried out anti-flammability and specific insulation and
Electrostatic is permanently tested, and is permanently contrasted with PBT anti-flammability and specific insulation and electrostatic.Electrostatic prevention plastic
Expect specific insulation method of testing GB/T1566, Flame Retardancy test is carried out according to UL94 method of testings, and electrostatic is permanent
Test is according to GB/T14447-93《Plastic sheeting antistatic performance test method-half-life period method》Carry out, test result is shown in Table 1.
Table 1
As can be seen from Table 1, the specific insulation as little as 10 of PBT anti-static materials of the invention6Ω, fire resistance reach
To V0 levels, and its static decay time > 200s, there is good permanent antistatic performance.
Applicant state, the present invention by above-described embodiment come illustrate the present invention PBT permanent types anti-static material and its
Preparation method and application, but the invention is not limited in above-described embodiment, that is, do not mean that the present invention has to rely on above-mentioned implementation
Example could be implemented.Person of ordinary skill in the field is it will be clearly understood that any improvement in the present invention, to each original of product of the present invention
The equivalence replacement of material and the addition of auxiliary element, the selection of concrete mode etc., all fall within protection scope of the present invention and open model
Within enclosing.
Claims (22)
1. a kind of PBT anti-static materials, it is characterised in that the PBT anti-static materials are dissipated by 5-25% fire-retardant, electrostatic-conducting
Type master batch and 75-95% PBT are prepared;
The fire-retardant, electrostatic-conducting dissipative type master batch is prepared by the following raw material of mass percent:
2. PBT anti-static materials according to claim 1, it is characterised in that the PBT anti-static materials by 20% resistance
Combustion static conductive dissipative type master batch and 80% PBT are prepared.
3. PBT anti-static materials according to claim 1, it is characterised in that the fire-retardant, electrostatic-conducting dissipative type master batch by
The following raw material of mass percent is prepared:
4. PBT anti-static materials according to claim 1, it is characterised in that the organosilicon is silicone grease, silicon emulsion, silicon
In rubber, sulphurated siliastic or silicones any one or at least two combination.
5. PBT anti-static materials according to claim 1, it is characterised in that the conductor material is sodium chloride, sodium phosphate
With any one in sodium metasilicate or at least two combination.
6. PBT anti-static materials according to claim 1, it is characterised in that the carrier material be polyethylene, PBT or
In polypropylene any one or at least two combination.
7. the PBT anti-static materials according to any one of claim 1-6, it is characterised in that the fire-retardant, electrostatic-conducting consumption
The preparation method for dissipating type master batch comprises the following steps:
(1) polyaniline, polythiophene, conductor material and polyethylene are added in batch mixer and carries out blending doping, obtain mixed material;
(2) antimony oxide and organosilicon are added into mixed material obtained by step (1), mixing, is then squeezed using in extruder
Go out to be granulated, obtain the fire-retardant, electrostatic-conducting dissipative type master batch.
8. PBT anti-static materials according to claim 7, it is characterised in that stirring when step (1) blending is adulterated
Speed is 20-90r/min.
9. PBT anti-static materials according to claim 7, it is characterised in that during the mixing of step (1) the blending doping
Between be 10-30min.
10. PBT anti-static materials according to claim 7, it is characterised in that step (2) described extruder is twin-screw
Extruder.
11. PBT anti-static materials according to claim 7, it is characterised in that step (2) the extruder screw region
Preheating temperature be 180-250 DEG C.
12. PBT anti-static materials according to claim 11, it is characterised in that step (2) the extruder screw region
Preheating temperature be 200-220 DEG C.
13. PBT anti-static materials according to claim 7, it is characterised in that the screw rod of step (2) described extruder turns
Speed is 190r/min-320r/min.
14. PBT anti-static materials according to claim 13, it is characterised in that the screw rod of step (2) described extruder turns
Speed is 220-300r/min.
15. the preparation method of the PBT anti-static materials according to any one of claim 1-14, it is characterised in that described
Method is:PBT and the blending of fire-retardant, electrostatic-conducting dissipative type master batch, extrusion are obtained into the PBT anti-static materials.
16. preparation method according to claim 15, it is characterised in that the stir speed (S.S.) during blending is 100-
200r/min。
17. preparation method according to claim 16, it is characterised in that the incorporation time of the blending is 15-30min.
18. preparation method according to claim 15, it is characterised in that the extrusion is completed using double screw extruder.
19. preparation method according to claim 18, it is characterised in that the screw rod region of the double screw extruder it is pre-
Hot temperature is 260-350 DEG C.
20. preparation method according to claim 18, it is characterised in that the screw speed of the double screw extruder is
200-300r/min。
21. according to the preparation method any one of claim 15-20, it is characterised in that methods described is:By PBT, resistance
Fire the blending of static conductive dissipative type master batch, stir speed (S.S.) during blending is 100-200r/min, and the incorporation time of blending is 15-
30min, then extruded using double screw extruder, the preheating temperature in the screw rod region of the double screw extruder is 260-350
DEG C, the screw speed of double screw extruder is 200-300r/min, obtains the PBT anti-static materials.
22. the PBT anti-static materials according to any one of claim 1-14 are in electronic apparatus, capacitor or antistatic film
Application in material.
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