CN106189164A - A kind of preparation method of PC/ carbon nanotube conducting master batch - Google Patents
A kind of preparation method of PC/ carbon nanotube conducting master batch Download PDFInfo
- Publication number
- CN106189164A CN106189164A CN201610528902.1A CN201610528902A CN106189164A CN 106189164 A CN106189164 A CN 106189164A CN 201610528902 A CN201610528902 A CN 201610528902A CN 106189164 A CN106189164 A CN 106189164A
- Authority
- CN
- China
- Prior art keywords
- mass parts
- dispersant
- lubricant
- carbon nanotubes
- activated carbon
- 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
Links
Classifications
-
- 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
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/001—Conductive 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
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/04—Antistatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- 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
Abstract
The invention discloses the preparation method of a kind of PC/ carbon nanotube conducting master batch, described method is: CNT is carried out high-speed stirred, dispersant is dissolved in liquid in the carbon nanotube dust being sprayed in stirring by the way of spraying simultaneously, carbon nano tube surface is activated, the Activated Carbon Nanotubes obtained adds to PC material matrix as conductive filler, thus prepares the PC/ carbon nanotube conducting master batch that electric conductivity is good.PC/ carbon nanotube conducting master batch prepared by the present invention can be used for preparing antistatic article, and antistatic property is excellent.
Description
One, technical field
The present invention relates to the preparation method of a kind of PC/ carbon nanotube conducting master batch.
Two, background technology
Merlon (PC) is a kind of noncrystal engineering material, has and particularly preferred anti-fills hit intensity, heat stability, gloss
Degree, suppression bacteria characteristic, flame-retarding characteristic and resistance tocrocking.
Owing to its electrical insulating property is excellent, therefore its goods are extremely suitable to make industry insulant, this be due to its sheet resistance or
The reason that specific insulation is higher.But in numerous applications, when because of friction, peeling off or sensing process can make PC product surface produce
Raw and accumulation electrostatic charge, these characteristics can cause serious potential danger, such as dust suction, shocks by electricity, discharges and even burn and explode.For
Avoiding this kind of danger, carrying out antistatic modified to it is industrial conventional effective ways, it is intended that reduce frosting
The generation of electrostatic charge and accumulation.
Traditional antistatic PC is material modified generally adds antistatic additive, metal dust or carbon system implant, thus makes
For going out antistatic PC goods, eliminate its surface electrostatic lotus produced during producing, using.
The advantage of antistatic additive filled-type product is that color articles is unrestricted, and wherein low molecule type antistatic additive is to product
Performance impact is little, and its surface resistivity is 1010-1013Ω.But the electrical property of low molecule antistatic additive filled-type product can be with
The passage of time and gradually lose.
Carbon system implant is mainly conductive black, graphite and carbon fiber, and the specific insulation of manufactured goods is 102-109Ω·
cm.The most carbon black filled is main flow, and why carbon black filled type conducting polymer is widely adopted, and the first is because of conductive black
Price is the cheapest;It two is because white carbon black and can have bigger choice according to different electric conductivity demands, its manufactured goods
Resistance value can be 102-109Change in broad range between Ω;Its three be electric conductivity persistently, stable;Therefore it is the most anti-
Electrostatic material.
Metal system conductive agglomerate is roughly divided into and forms the method for conductive layer at frosting and be mixed into by electroconductive stuffing
Plastics are made the method two kinds of conductive plastics.Different screen methods is respectively arranged with its pluses and minuses and the scope of application, and application in the past is relatively
Many is zinc spraying plating and electrically-conducting paint method.
But, use carbon system or metal based material the highest as consumption required during implant, this not only makes to gather
Laminate material characteristic inherently is a greater impact, and the mechanical property of composite and processing characteristics are become
Difference.
CNT relies on the one-dimensional nano structure of its uniqueness and excellent electric property, and extremely low consumption can make polymerization
The electric conductivity of thing material obtains the biggest raising, and can be effectively improved the mechanical property of composite, becomes a kind of excellent
Conductive modified agent.
But, owing to CNT is a kind of high degree of polarization, ganoid inorganic macromolecule compound, surface defect
Less, lack active group, between CNT, there is stronger Van der Waals force and its huge specific surface area, the highest simultaneously
Draw ratio, causes in the ordinary course of things, and CNT is easily wound around reunion bunchy.CNT game performance to be played makes it extensive
Application, the dispersion how solving CNT is critical problem.At present, the method for dispersing Nano carbon tubes have grinding with stirring,
The washing of high-energy ball milling, ultrasonic Treatment, strong acid and strong base, interpolation surfactant, growth in situ synthesis, multiple method integrated treatment
Deng.
Three, summary of the invention
The invention provides the preparation method of a kind of PC/ carbon nanotube conducting master batch, CNT is preprocessed modified,
Add to PC material matrix as conductive filler, thus prepare the PC/ carbon nanotube conducting master batch that electric conductivity is good.
The technical solution used in the present invention is:
The preparation method of a kind of PC/ carbon nanotube conducting master batch, said method comprising the steps of:
(1) dispersant A is dissolved in solvent, obtains dispersant solution, then by dispersant solution by high-pressure spraying method
Spray in the CNT of high-speed stirred, after high-speed stirred mixing, prepare Activated Carbon Nanotubes;
Described CNT, dispersant A, the mass fraction ratio of solvent are 85~95:0.1~5:5~10;
(2) Activated Carbon Nanotubes and PC polymeric matrix material stirring and evenly mixing, then mix with auxiliary agent, through twin-screw extrusion
Machine melt extrudes pelletize and prepares PC/ carbon nanotube conducting master batch;
Described PC polymeric matrix material, Activated Carbon Nanotubes, the mass fraction of auxiliary agent be 70~95 mass parts, 0.01~
30 mass parts, 0.1~20 mass parts;
Described auxiliary agent is one or more the mixing in dispersant B, coupling agent, antioxidant, lubricant;Preferably institute
State auxiliary agent be one or more mixing with dispersant B, more preferably auxiliary agent in coupling agent, antioxidant, lubricant be idol
One or both in connection agent, antioxidant are with dispersant B, the mixing of lubricant.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersant
The mass fraction of B is 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersant
B, the mass fraction of coupling agent are 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~5 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersant
B, the mass fraction of antioxidant are 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~2 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersant
B, the mass fraction of lubricant are 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~10 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersant
B, coupling agent, the mass fraction of antioxidant be 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~5
Mass parts, 0.01~2 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersant
B, coupling agent, the mass fraction of lubricant be 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~5
Mass parts, 0.01~10 mass parts, wherein dispersant B, coupling agent, total mass fraction of lubricant are 0.2~20 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersant
B, antioxidant, the mass fraction of lubricant be 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~2
Mass parts, 0.01~10 mass parts, wherein dispersant B, antioxidant, total mass fraction of lubricant are 0.2~20 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersion
Agent B, coupling agent, antioxidant, the mass fraction of lubricant are 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass
Part, 0.01~5 mass parts, 0.01~2 mass parts, 0.01~10 mass parts, wherein dispersant B, coupling agent, antioxidant, lubrication
Total mass fraction of agent is 0.2~20 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersion
Agent B, coupling agent, antioxidant, the mass fraction of lubricant be 70~95 mass parts, 0.1~30 mass parts, 1~10 mass parts,
0.01~3 mass parts, 0.01~2 mass parts, 0.01~3 mass parts.
Further, in preferred steps (2), the formula of raw material is: PC polymeric matrix material, Activated Carbon Nanotubes, dispersion
Agent B, coupling agent, antioxidant, the mass fraction of lubricant be 70~95 mass parts, 1~30 mass parts, 1~10 mass parts, 0.01
~3 mass parts, 0.01~2 mass parts, 0.01~3 mass parts.
In described method, dispersant A and dispersant B are for distinguishing the dispersant used in different step, and A, B do not have
Chemical sense.
Described dispersant A and dispersant B each stand alone as dodecylbenzene sodium sulfonate, polyvinylpyrrolidone, polyethylene
Alcohol, xanthan gum, sodium lauryl sulphate, Triton X-100, sodium carboxymethyl cellulose, Dihexadecylphosphate, Ah
Draw primary glue, cetyl trimethylammonium bromide, alkyl phenol ethylene oxide condensation substance emulsifying agent, cetyl trimethyl sodium bromide,
One or more mixture in Kynoar.
In described step (1), described solvent is water, DMF, N-Methyl pyrrolidone, n-butyl alcohol, chlorine
One or more mixture in imitative, dehydrated alcohol, acetone, petroleum ether, ethyl acetate, butyl acetate;
In described step (1), described CNT is one or both in multi-walled carbon nano-tubes, SWCN
Mixture, preferably multi-walled carbon nano-tubes.
In described step (2), described PC polymeric matrix material is particle or pulverulent material, and PC polymer powder is preferably used
Shape material, mean diameter be 0.5 μm to the melt index of 5mm, preferably PC polymeric matrix material be 2-100g/10min, preferably
10-30g/10min, the beneficially CNT dispersion in PC matrix.
In described step (2), described coupling agent be in titante coupling agent, silane coupling agent one or both with
On mixture;Described titante coupling agent can be isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, isopropyl
Three (dioctyl phosphoric acid acyloxy) titanate esters, isopropyl two oleic acid acyloxy (dioctyl phosphoric acid acyloxy) titanate esters, single alcoxyl
One or more mixed in base unsaturated fatty acid titanate esters or Di(dioctylpyrophosphato) ethylene titanate
Compound;Described silane coupler can use KH550, one or both in KH560, KH570, KH792, DL602, DL171
Above mixture;
Described antioxidant is preferably 1098,168,1010,1076, DLTP, one or more in MB, 164,264
Mixture.
Described lubricant is fatty acid, aliphatic amide type and ester lubricant, paraffin class lubricant, metallic soap salt profit
One or more mixing in lubrication prescription, low-molecular-weight wax, further, described lubricant is preferably PE wax, montanin wax, silicone
One or more mixture in powder, stearic acid, oleic acid, calcium stearate, ethylene bis stearic acid amide, erucyl amide.
In described step (2), the processing technique of described double screw extruder is screw speed 100~1000r/min, extrusion
Temperature is 260-290 DEG C.
Described double screw extruder melt extrudes pelletize, and pelletize mode has multiple, optional water cooling bracing pelletizing, air-cooled tie rod
Pelletizing, die face are earnestly, cut under water.The method being well known to those skilled in the art.
High-pressure spraying method used when preparing Activated Carbon Nanotubes is that dispersant solution is passed through high-pressure spray device with spray
The form of mist sprays into the CNT of high-speed stirred, and described high-pressure spray device can use high-pressure spraying machine, pass through high-pressure hydraulic pump
Spray form is become to spray in material through high-pressure nozzle dispersant solution.Described high-pressure spraying machine still belongs to for CNT pretreatment
First.Dispersant solution is atomized by high-pressure spraying method, obtains a large amount of fine droplet after atomization, significantly increases solution and carbon nanometer
The contact area of pipe, beneficially carbon nanotube particulate are coated with by auxiliary agent, strengthen its dispersibility.
In described high-pressure spraying method, spray rate is generally 10~100ml/min;
Atomized particle size is 0.1~1um.
When preparing Activated Carbon Nanotubes, the rotating speed of described high-speed stirred is 300~1500 turns/min.
The time of described high-speed stirred mixing is generally 0~1 hour, preferably 5~40 minutes.
The present invention carries out high-speed stirred to CNT, to its surface pretreatment, simultaneously by dispersant, surface activity
The auxiliary agents such as agent are dissolved in liquid in the carbon nanotube dust being sprayed in stirring by the way of spraying so that CNT table
Face activation, simultaneously by the material uniform wet such as dispersant, surfactant, causes to be formed between CNT and repels, and can be same
The bulk density of Shi Tigao CNT, to obtain optimal dispersion effect and good processability.
The present invention, by preprocessed for CNT modified, adds to PC material matrix as conductive filler, thus
Prepare PC/ carbon nanotube conducting master batch.Compared with traditional antistatic modified material of PC, reaching same electric conductivity condition
Under, the Activated Carbon Nanotubes implant consumption that the present invention uses can reduce by more than 5 times, therefore can make PC characteristic inherently
Hardly suffer from impact, and the mechanical property and processing characteristics impact on composite is relatively low, also assures that antistatic simultaneously
The persistency of performance.Therefore, the PC conductive agglomerate that the present invention provides can expand the range of PC antistatic article, improves system
The service life of product.
Four, detailed description of the invention
With specific embodiment, technical scheme is described further below, but the protection content of the present invention is not
It is limited to this.
Embodiment 1~16
According to the form below 1 takes each raw material, is dissolved in solvent by dispersant, obtains dispersant solution, is then led to by dispersant solution
Cross high pressure spray process and spray into the CNT (diameter 1~30nm, length 1~100 μm, bulk density 0.02g/mL) of high-speed stirred
In, technological parameter is as shown in table 1, after high-speed stirred mixing, prepares Activated Carbon Nanotubes;
Table 1
The performance test results such as table 2 below of the Activated Carbon Nanotubes prepared
Table 2
Dispersibility experiment detection by the following method: the Activated Carbon Nanotubes 10mg that embodiment 1~16 prepares is separately added into
10mL prepares in the solvent (seeing table 1) used by this Activated Carbon Nanotubes, and ultrasonic disperse 30 minutes obtains suspension, stands, goes out
When being the most substantially layered, the record time is the holding time, and acquired results refers to table 2.Holding time is the longest, shows that its dispersibility is more
Good.The most pretreated CNT cannot form stable suspension.
Above-mentioned test result indicate that, after pretreatment, the bulk density of CNT improve about 10 times (untreated
The bulk density of CNT is about 0.02g/mL), dispersibility is all significantly increased.
Embodiment 17~32
Activated Carbon Nanotubes prepared by embodiment 1~16 and PC polymer pulverulent material (mean diameter 100 μm~2mm)
Stirring and evenly mixing, consumption is shown in Table 3, and then the auxiliary agent with table 4 mixes, and melt extrudes through double screw extruder, stretches, cooling and dicing system
Obtain PC/ carbon nanotube conducting master batch;The processing technique of double screw extruder is screw speed 200r/min, and extrusion temperature is 280
℃。
The content of carbon nanotubes of the PC/ carbon nanotube conducting master batch prepared is as shown in table 5.
The content of carbon nanotubes of conductive agglomerate of embodiment 17,21,24 preparation more than 10%, the conduction of these high-loads
Master batch is conducive to production and sales.When subsequent production is applied can by the conductive agglomerate of high content of carbon nanotubes again with PC matrix material
Material and the mixing of other auxiliary agent, prepare antistatic article.
Concrete, PC/ carbon nanotube conducting master batch prepared by embodiment 17~32 is mixed with PC base material according to the formula of table 5
Close, and add the auxiliary agents such as flow ability modifying agent, thermal oxidation stabilizer, antifriction liniment, prepare antistatic film through biaxial tension, according to
The sheet resistance of " GB/T1410-2006 solid insulating material specific insulation and surface resistivity test method " testing film
Rate, result is as shown in table 5.
Table 3
Table 4
Table 5
In table 5, thermal oxidation stabilizer is 1098, and flow ability modifying agent is erucyl amide, and antifriction liniment is nano-calcium carbonate.
Embodiment data show, the surface resistivity of antistatic article prepared by conductive agglomerate prepared by the present invention is preferable,
In the case of content of carbon nanotubes 2~4wt.%, surface resistivity is 103~106About Ω, antistatic property is good.
Claims (10)
1. the preparation method of a PC/ carbon nanotube conducting master batch, it is characterised in that said method comprising the steps of:
(1) dispersant A is dissolved in solvent, obtains dispersant solution, then dispersant solution is sprayed into by high-pressure spraying method
In the CNT of high-speed stirred, after high-speed stirred mixing, prepare Activated Carbon Nanotubes;
(2) Activated Carbon Nanotubes and PC polymeric matrix material stirring and evenly mixing, then mix with auxiliary agent, melts through double screw extruder
Melt extruding pelletization and prepare PC/ carbon nanotube conducting master batch
Described PC polymeric matrix material, Activated Carbon Nanotubes, the mass fraction of auxiliary agent are 70~95 mass parts, 0.01~30 matter
Amount part, 0.1~20 mass parts;
Described auxiliary agent is one or more the mixing in dispersant B, coupling agent, antioxidant, lubricant.
2. the method for claim 1, it is characterised in that in described step (1), described CNT, dispersant A, solvent
Mass fraction ratio be 85~95:0.1~5:5~10.
3. the method for claim 1, it is characterised in that described dispersant A and dispersant B each stand alone as dodecyl
Benzene sulfonic acid sodium salt, polyvinylpyrrolidone, polyvinyl alcohol, xanthan gum, sodium lauryl sulphate, Triton X-100, carboxylic
Sodium carboxymethylcellulose pyce, Dihexadecylphosphate, arabic gum, cetyl trimethylammonium bromide, alkyl phenol ethylene oxide are condensed
One or more mixture in thing emulsifying agent, cetyl trimethyl sodium bromide, Kynoar.
4. the method for claim 1, it is characterised in that in described step (1), described solvent is water, N, N-dimethyl methyl
In amide, N-Methyl pyrrolidone, n-butyl alcohol, chloroform, dehydrated alcohol, acetone, petroleum ether, ethyl acetate, butyl acetate one
Kind or two or more mixture.
5. the method for claim 1, it is characterised in that in described step (2), the formula of described raw material is one of following:
Formula (one) PC polymeric matrix material, Activated Carbon Nanotubes, the mass fraction of dispersant B be 70~95 mass parts,
0.01~30 mass parts, 0.1~10 mass parts;
Formula (two) PC polymeric matrix material, Activated Carbon Nanotubes, dispersant B, the mass fraction of coupling agent are 70~95 matter
Amount part, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~5 mass parts;
Formula (three) PC polymeric matrix material, Activated Carbon Nanotubes, dispersant B, the mass fraction of antioxidant are 70~95 matter
Amount part, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~2 mass parts;
Formula (four) PC polymeric matrix material, Activated Carbon Nanotubes, dispersant B, the mass fraction of lubricant are 70~95 matter
Amount part, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~10 mass parts;
Formula (five) PC polymeric matrix material, Activated Carbon Nanotubes, dispersant B, coupling agent, the mass fraction of antioxidant are 70
~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~5 mass parts, 0.01~2 mass parts;
Formula (six) PC polymeric matrix material, Activated Carbon Nanotubes, dispersant B, coupling agent, the mass fraction of lubricant are 70
~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~5 mass parts, 0.01~10 mass parts, wherein disperse
Agent B, coupling agent, total mass fraction of lubricant are 0.2~20 mass parts;
Formula (seven) PC polymeric matrix material, Activated Carbon Nanotubes, dispersant B, antioxidant, the mass fraction of lubricant are 70
~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~2 mass parts, 0.01~10 mass parts, wherein disperse
Agent B, antioxidant, total mass fraction of lubricant are 0.2~20 mass parts;
Formula (eight) PC polymeric matrix material, Activated Carbon Nanotubes, dispersant B, coupling agent, antioxidant, the quality of lubricant
Number be 70~95 mass parts, 0.01~30 mass parts, 0.1~10 mass parts, 0.01~5 mass parts, 0.01~2 mass parts,
0.01~10 mass parts, wherein dispersant B, coupling agent, antioxidant, total mass fraction of lubricant are 0.2~20 mass parts.
6. the method for claim 1, it is characterised in that in described step (2), described coupling agent is titanate ester coupling
One or more mixture in agent, silane coupling agent.
7. the method for claim 1, it is characterised in that in described step (2), described antioxidant is 1098,168,
1010,1076, one or more the mixture in DLTP, MB, 164,264.
8. the method for claim 1, it is characterised in that in described step (2), described lubricant is fatty acid, fat
In race's amide-type and ester lubricant, paraffin class lubricant, metallic soap salt lubricant, low-molecular-weight wax one or more
Mixing.
9. method as claimed in claim 8, it is characterised in that described lubricant be PE wax, montanin wax, silicone powder, stearic acid,
One or more mixture in oleic acid, calcium stearate, ethylene bis stearic acid amide, erucyl amide.
10. the method for claim 1, it is characterised in that in described step (2), the formula of raw material is: PC polymer base
Body material, Activated Carbon Nanotubes, dispersant B, coupling agent, antioxidant, the mass fraction of lubricant be 70~95 mass parts, 1~
30 mass parts, 1~10 mass parts, 0.01~3 mass parts, 0.01~2 mass parts, 0.01~3 mass parts.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610528902.1A CN106189164A (en) | 2016-06-30 | 2016-06-30 | A kind of preparation method of PC/ carbon nanotube conducting master batch |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610528902.1A CN106189164A (en) | 2016-06-30 | 2016-06-30 | A kind of preparation method of PC/ carbon nanotube conducting master batch |
Publications (1)
Publication Number | Publication Date |
---|---|
CN106189164A true CN106189164A (en) | 2016-12-07 |
Family
ID=57466326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610528902.1A Pending CN106189164A (en) | 2016-06-30 | 2016-06-30 | A kind of preparation method of PC/ carbon nanotube conducting master batch |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106189164A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114316558A (en) * | 2021-12-20 | 2022-04-12 | 杨劲光 | Carbon nano tube concentrated composition and preparation method and application thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1410475A (en) * | 2002-03-14 | 2003-04-16 | 四川大学 | Polymer/carbon nano pipe composite powder and its solid phase shear break up preparation method |
WO2005034144A1 (en) * | 2003-09-29 | 2005-04-14 | General Electric Company | Conductive thermoplastic compositions, methods of manufacture and articles derived from such compositions |
CN1760269A (en) * | 2004-10-13 | 2006-04-19 | 上海扬泽纳米新材料有限公司 | Electric polymer and preparation method |
CN104479410A (en) * | 2014-11-03 | 2015-04-01 | 重庆和泰塑胶股份有限公司 | Calcium carbonate surface treatment method |
-
2016
- 2016-06-30 CN CN201610528902.1A patent/CN106189164A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1410475A (en) * | 2002-03-14 | 2003-04-16 | 四川大学 | Polymer/carbon nano pipe composite powder and its solid phase shear break up preparation method |
WO2005034144A1 (en) * | 2003-09-29 | 2005-04-14 | General Electric Company | Conductive thermoplastic compositions, methods of manufacture and articles derived from such compositions |
CN1760269A (en) * | 2004-10-13 | 2006-04-19 | 上海扬泽纳米新材料有限公司 | Electric polymer and preparation method |
CN104479410A (en) * | 2014-11-03 | 2015-04-01 | 重庆和泰塑胶股份有限公司 | Calcium carbonate surface treatment method |
Non-Patent Citations (2)
Title |
---|
卢寿慈: "《粉体技术手册》", 31 July 2004, 化学工业出版社 * |
王荣: "制备工艺对聚合物基多壁碳纳米管复合材料导电性能的影响", 《塑料》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114316558A (en) * | 2021-12-20 | 2022-04-12 | 杨劲光 | Carbon nano tube concentrated composition and preparation method and application thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106046709A (en) | Carbon nanotube modified PET antistatic thin film | |
CN106167554A (en) | A kind of PA/ carbon nanotube conducting master batch | |
KR101666881B1 (en) | Manufacturing method of metal-free CNT Composite materials having excellent chemical resistance and electric resistance, CNT pellet used the same that, product manufactured thereby | |
CN106084738A (en) | A kind of TPU antistatic film of carbon nano-tube modification | |
CN106046707A (en) | PET (polyethylene glycol terephthalate) and carbon nanotube conductive masterbatch | |
CN106084404A (en) | The polyethylene antistatic film that a kind of Activated Carbon Nanotubes is modified | |
CN105504713B (en) | A kind of 3D printing is material modified and preparation method thereof with polylactic acid microsphere | |
CN106117737A (en) | A kind of polyethylene antistatic film of carbon nano-tube modification | |
CN102719065A (en) | Polylactic acid/shear thickening fluid high-toughness material and preparation method | |
CN106046496A (en) | Preparation method of activated carbon nanotube modified polyethylene antistatic thin film | |
CN106189178A (en) | The preparation method of the TPU antistatic film that a kind of Activated Carbon Nanotubes is modified | |
CN106146977A (en) | A kind of PE/ carbon nanotube conducting master batch | |
CN104140672A (en) | Electric conduction nylon composition and preparing method thereof | |
CN106167611A (en) | A kind of PC/ carbon nanotube conducting master batch | |
CN106188828A (en) | The preparation method of the polypropylene antistatic thin film that a kind of Activated Carbon Nanotubes is modified | |
CN106046708A (en) | Preparation method of activated carbon nanotube modified PET antistatic thin film | |
CN106243637A (en) | The PET antistatic film that a kind of Activated Carbon Nanotubes is modified | |
CN106189375A (en) | A kind of Activated Carbon Nanotubes | |
CN106432899A (en) | Activated carbon nanotube modified polypropylene (PP) antistatic film | |
CN106128556A (en) | A kind of preparation method of high dispersive type oil system carbon nanotube conducting slurry | |
CN106084680A (en) | A kind of preparation method of PET/ carbon nanotube conducting master batch | |
CN106189164A (en) | A kind of preparation method of PC/ carbon nanotube conducting master batch | |
CN106188827A (en) | A kind of PP/ carbon nanotube conducting master batch | |
CN103709653A (en) | Antistatic master batch for polyester | |
CN106147200A (en) | The modified TPU antistatic film of a kind of Activated Carbon Nanotubes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20161207 |
|
RJ01 | Rejection of invention patent application after publication |