CN107418045B - A kind of high intensity high rigidity graphene modified polypropene and preparation method thereof - Google Patents

A kind of high intensity high rigidity graphene modified polypropene and preparation method thereof Download PDF

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CN107418045B
CN107418045B CN201710286138.6A CN201710286138A CN107418045B CN 107418045 B CN107418045 B CN 107418045B CN 201710286138 A CN201710286138 A CN 201710286138A CN 107418045 B CN107418045 B CN 107418045B
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high rigidity
graphene modified
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intensitive
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CN107418045A (en
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王宁
鲍海程
高伟
刘池茂
孙菁联
徐红红
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NINGBO HAIYU ADVANCED MATERIALS TECHNOLOGY Co Ltd
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
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    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
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    • CCHEMISTRY; METALLURGY
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Abstract

The present invention relates to a kind of modified polypropenes, and in particular to a kind of high intensity high rigidity graphene modified polypropene belongs to technical field of polymer materials.The modified polypropylene material includes following component according to parts by weight: homopolypropylene: 38~51 parts, graphene: 15~20 parts, alkali-free glass fibre: 28~32 parts, enzymolysis xylogen: 2-4 parts, compatilizer: 5~8 parts, antioxidant: 0.5-2 parts, lubricant: 0.5~1.0 part, coupling agent: 0.1-0.2 parts.The present invention is added high strength glass fiber inorganic matter, is re-introduced into conducting medium bilayer graphene using homopolypropylene as carrier, enzymolysis xylogen is then added, high-intensitive high rigidity graphene modified polypropene is made.For high-intensitive high rigidity graphene modified polypropene of the invention compared with plain polypropylene, tensile strength, bending strength are high, and not easy to break, rigidity is good, corrosion-resistant, anti-aging, and have both conductive characteristic.

Description

A kind of high intensity high rigidity graphene modified polypropene and preparation method thereof
Technical field
The present invention relates to a kind of modified polypropenes, and in particular to a kind of high intensity high rigidity graphene modified polypropene belongs to In technical field of polymer materials.
Technical background
Polypropylene PP is one of five big general-purpose plastics, has that density is small, easy processing, resistant to chemical etching, electrical insulating property is good etc. Good characteristic is suitable for production common mechanical part, corrosion-resistant part and insulating part, and the organic solvents such as common acid, alkali are to it It does not almost work, can be used for tableware.However polypropylene also has that molding shrinkage is big, very sensitive to notch, low temperature is easy to crack The disadvantages of shock resistance is poor limits its use scope.
In order to expand the application range of material, the machinery such as more high tensile property, impact property, bending property are especially obtained The polypropylene material of performance, it will usually some modified measures be made to material, wherein blending and modifying is a kind of simple and effective Method of modifying can improve low-temperature impact resistance, coloring, antistatic property of polymer etc., have the easy to operate, production cycle The advantages that short, suitable for mass production.The reinforcing materials such as glass fibre, glass fiber reinforcement can be generally added in polypropylene material Polypropylene enhances composite material as a kind of general thermoplasticity, because having elasticity modulus height, intensity height, dimensionally stable, thermal deformation The advantages such as temperature height, excellent electrical properties, cheap and paid close attention to by people.But glass fibre and polypropylene are due to itself pole Property difference, both cause interface binding power poor, requirement is not achieved in performance.General glass fiber reinforced polypropylene material Material shows very big defect in impact strength, and only with glass fiber reinforced polypropylene, can not change polypropylene material Isolation material, be also restricted in practical application.
Existing reinforced polypropylene material technology is to use graphene/glass fiber reinforced polypropylene composite material, is obtained Graphene/glass fiber reinforced polypropylene composite material has good mechanical property, processing performance and thermal stability.But due to Polypropylene dimensional stability itself is small, poor rigidity, and the graphene content of addition is less, can receive resistance in use, lead Buckling deformation is caused, rigidity is insufficient, also has very big limitation in practical application area.And since polypropylene material is in product injection molding Degree of orientation and internal stress in the process, product, by torsional forces and damping, reduce its intensity in assembly and use process, contract Its short service life.
Summary of the invention
The purpose of the present invention is being directed to the above-mentioned problems in the prior art, a kind of high-intensitive high rigidity graphite is proposed Alkene modified polypropene.
Object of the invention can be realized by the following technical scheme: a kind of high intensity high rigidity graphene modified poly- third Alkene, including following component according to parts by weight: homopolypropylene: 38~51 parts, graphene: 15~20 parts, alkali-free glass is fine Dimension: 28~32 parts, enzymolysis xylogen: 2-4 parts, compatilizer: 5~8 parts, antioxidant: 0.5-2 parts, lubricant: 0.5~1.0 part, Coupling agent: 0.1-0.2 parts.
High strength glass fiber inorganic matter is added using homopolypropylene as carrier in the present invention, is re-introduced into conducting medium bilayer Then graphene is added enzymolysis xylogen and high-intensitive high rigidity graphene modified polypropene is made.Compared with plain polypropylene, draw It is high to stretch intensity, bending strength, not easy to break, rigidity is good, and bending modulus is corrosion-resistant up to 7200MPa, and it is anti-aging, and have both Conductive characteristic, the conductive order of magnitude (sheet resistance) reach 103Ohms/sq or less and tend towards stability.
In the present invention, by addition alkali-free glass fibre, graphene, enzymolysis xylogen, the compound system of three can be formed, The homopolypropylene material made further enhances in performance, while having better compatibility.
Lignin is that one kind is naturally difficult to the complex compound decomposed, is one of main composition of plant.In nature The decomposition of lignin is completed mainly by fungi, can will wherein cellulose and hemicellulose by the extracellular and intracellular enzyme of fungus secretion It is converted into monosaccharide, and can further be fermented into other high value added products such as alcohol or production protein feed, here remaining enzyme Solving slag is exactly enzymolysis xylogen.Enzymolysis xylogen contains a large amount of phenylpropyl alcohol alkyl structure skeletons, has certain compatibility with polypropylene, And containing a large amount of phenolic hydroxyl group, it can be improved the uvioresistant weatherability of polypropylene material, while the material obtained that meets has There is intensity height, good toughness, environmentally protective.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the molecule of the homopolypropylene Amount is between 4000-6000.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the graphene is double-layer graphite Alkene.Graphene is the two dimensional crystal for the only one layer of atomic thickness for being stripped out from graphite material, being made of carbon atom.Graphite Alkene is both most thin material, and most tough material, and 200 times more taller than best steel of breaking strength.It has again simultaneously Elasticity, stretch range can reach the 20% of own dimensions well.It is that current nature is most thin, the highest material of intensity.? Graphene is added in polypropylene material can make it have the comprehensive performances such as excellent mechanics, calorifics, electricity.And the present invention is using double Layer graphene can not only increase intensity with the parabola shaped band structure of unique class, while as carbon-based nano material Expect that there is excellent adhesiveness and surface tension between bilayer graphene, can guarantee the stability of material.So in the present invention The middle bilayer graphene that is added can increase substantially the intensity and toughness of polypropylene material.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the length of the alkali-free glass fibre For 1.5-3.0mm, diameter is 9-14 μm.The present invention controls the length and diameter of alkali-free glass fibre respectively in above range, Alkali-free glass fibre can be made to be uniformly dispersed in polypropylene material, further increase shear-mixed effect and melt plasticizing effect.? If alkali-free glass fibre diameter is too big in the present invention, the cementability and compatibility with polypropylene material can be reduced;If alkali-free Glass fibre is too thin, easily by screw rod shearing at fine-powder, loses the humidification of itself.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the high intensity high rigidity graphene Also containing 1-3 parts of nucleating agent in modified polypropylene material.Impurity in polymer has a great impact to its crystallization process, has A little impurity will hinder to crystallize, and other impurity can promote to crystallize, these can promote the impurity of crystallization in the crystallization of polymer Play nucleus in the process, nucleating agent is exactly this impurity that can promote crystallization.Nucleating agent is added in polypropylene, it can Accelerate crystallization rate, forms fine and compact spherocrystal particle, making strand at relatively high temperatures has cracking crystallization rate, ball Crystalline substance can more regularly grow up, and there are many number, small-sized.Nucleating agent, which can reach, to be shortened molding cycle, improves product surface The effect of the physical mechanical properties such as gloss, tensile strength, rigidity, heat distortion temperature, impact resistance, creep resistance.
Preferably, the partial size of the nucleating agent is 5-10 μm.Nucleating agent partial size is excessive, then its dispersion in polypropylene Property it is poor, the effective at nuclear concentration of nucleating agent can be reduced, the improvement for influencing Nucleating Agent on Pp Mechanical Properties and crystal property is made With.Nucleating agent partial size is too small, then it is difficult evenly dispersed in polypropylene, and lesser nucleating agent particle is easier to gather, can shadow Ring the performance of its effect.
Further preferably, the nucleating agent is one of mica, talcum powder, white carbon black or a variety of.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the compatilizer is bromination poly- third One or both of alkene, monoethanolamine.Above-mentioned compatilizer can be compatible with polypropylene and graphene respectively, thus make polypropylene with The mixed system of graphene forms stable mixture under the action of the compatilizer.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the antioxidant is by antioxidant 1010, one or both of antioxidant 1076.The oxidant of mentioned kind can significantly improve the ageing properties of composite material, be Composite material provides better aging protection in production and use process, and then improves the service life of the polypropylene material.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the lubricant be calcium stearate, It is one or more of in silicone powder, low-molecular polyethylene wax.It is processed that thermoplastic plastics shaping can be effectively reduced in the addition of lubricant High shear force appeared in journey and high frictional force, improve the mobile performance of PP composite material, avoid polymer high temperature by The decline of thermal decomposition and product quality.
In a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the coupling agent is that amino silane is even Join agent, purity >=98%.By addition coupling agent, the interface binding power between glass fibre and polypropylene material can increase, Increase its intensity.
It is another object of the present invention to provide a kind of above-mentioned high-intensitive high rigidity graphene modified polypropylene materials Preparation method, the preparation method include the following steps:
The component of high-intensitive high rigidity graphene modified polypropylene material is weighed in parts by weight, and will be fine except alkali-free glass Other components outside dimension are added in batch mixer and are uniformly mixed, and material after mixing is poured into double screw extruder and is squeezed out It is granulated, alkali-free glass fibre is added from dual-screw-stem machine side spout using weightless feed method while extruding pelletization, is obtained high-strength Spend high rigidity graphene modified polypropene pellet.
In a kind of preparation method of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the twin-screw is squeezed Machine selects the screw combinations of Strong shear out.
In a kind of preparation method of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the batch mixer Setting speed is 300-600rpm/min.
In a kind of preparation method of above-mentioned high-intensitive high rigidity graphene modified polypropylene material, the twin-screw is squeezed The engine speed 25-35HZ, main feeding 15-20HZ, side feed material 8-12HZ of machine, temperature are set as 230-245 DEG C out.
Compared with prior art, the present invention has the advantage that
1, it in high-intensitive high rigidity graphene modified polypropylene material of the invention, joined in homopolypropylene double Layer graphene, alkali-free glass fibre and enzymolysis xylogen, substantially increase the intensity and rigidity of polypropylene material.
2, it is also added into nucleating agent in high-intensitive high rigidity graphene modified polypropylene material of the invention, can be shortened molding Period improves the performances such as product surface gloss, tensile strength, rigidity.
3, the high-intensitive high rigidity graphene modified polypropylene material ingredient configuration of the present invention is reasonable, while using specific Preparation method, thus obtained modified polypropylene material have tensile strength, bending strength height, and not easy to break, rigidity is good, bending Modulus is corrosion-resistant up to 7200MPa, anti-aging, and has both the characteristics such as conduction.
Specific embodiment
The following is specific embodiments of the present invention, and technical scheme of the present invention will be further described, but the present invention is simultaneously It is not limited to these embodiments.
Table 1: the constituent and its quality of 1-5 high intensity high rigidity graphene modified polypropylene material of the embodiment of the present invention Percentage
Table 2: the constituent and its matter of 6-10 high intensity high rigidity graphene modified polypropylene material of the embodiment of the present invention Measure percentage
Embodiment 1:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 1 in table 1 Point, wherein the molecular weight of homopolypropylene is 5000, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 2.0mm, Diameter is 12 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 4min, the revolving speed of batch mixer is 500rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 25HZ, main feeding 15HZ, side feed material 10HZ, temperature are set as 235 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 2:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight as described in example 2 in table 1 Point, wherein the molecular weight of homopolypropylene is 5200, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 2.1mm, Diameter is 12 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 4min, the revolving speed of batch mixer is 300rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 30HZ, main feeding 17HZ, side feed material 10HZ, temperature are set as 240 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 3:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 3 in table 1 Point, wherein the molecular weight of homopolypropylene is 4700, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 1.8mm, Diameter is 13 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 3min, the revolving speed of batch mixer is 400rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 35HZ, main feeding 18HZ, side feed material 11HZ, temperature are set as 235 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 4:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight as described in example 4 in table 1 Point, wherein the molecular weight of homopolypropylene is 4000-6000, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 2.2mm, diameter are 11 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 5min, the revolving speed of batch mixer is 600rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 28HZ, main feeding 18HZ, side feed material 11HZ, temperature are set as 237 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 5:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 5 in table 1 Point, wherein the molecular weight of homopolypropylene is 5000, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 2.0mm, Diameter is 12 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 4min, the revolving speed of batch mixer is 500rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 30HZ, main feeding 17HZ, side feed material 10HZ, temperature are set as 240 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 6:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 6 in table 2 Point, wherein the molecular weight of homopolypropylene is 5200, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 2.8mm, Diameter is 13 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 3min, the revolving speed of batch mixer is 450rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 30HZ, main feeding 16HZ, side feed material 10HZ, temperature are set as 240 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 7:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 7 in table 2 Point, wherein the molecular weight of homopolypropylene is 5500, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 1.5mm, Diameter is 9 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 3min, the revolving speed of batch mixer is 300rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 30HZ, main feeding 17HZ, side feed material 10HZ, temperature are set as 240 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 8:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 8 in table 2 Point, wherein the molecular weight of homopolypropylene is 4300, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 1.7mm, Diameter is 10 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 5min, the revolving speed of batch mixer is 350rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 30HZ, main feeding 17HZ, side feed material 10HZ, temperature are set as 240 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 9:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 9 in table 2 Point, wherein the molecular weight of homopolypropylene is 5600, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 2.4mm, Diameter is 13 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 4min, the revolving speed of batch mixer is 480rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 30HZ, main feeding 17HZ, side feed material 10HZ, temperature are set as 240 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Embodiment 10:
The group of high-intensitive high rigidity graphene modified polypropylene material is weighed by parts by weight described in embodiment 10 in table 2 Point, wherein the molecular weight of homopolypropylene is 4700, and graphene is bilayer graphene, and the length of alkali-free glass fibre is 3.0mm, Diameter is 14 μm;
Other components in addition to alkali-free glass fibre are added in batch mixer and mix 5min, the revolving speed of batch mixer is 600rpm/min;
Material after mixing is poured into extruding pelletization in double screw extruder, the engine speed of double screw extruder 30HZ, main feeding 17HZ, side feed material 10HZ, temperature are set as 240 DEG C, by alkali-free glass fibre from double spiral shells while extruding pelletization Bar pusher side spout is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
Activeness and quietness modified polyacetal pellet made of above-described embodiment 1-10 is sampled, dumbbell is respectively prepared with injection molding machine Shape iso standard test bars, and properties test is carried out according to mechanical property requirements to batten, test condition is as shown in table 3, Test result is as shown in table 4 and table 5.
Table 3: test condition
Table 4: test result
Table 5: test result
Comparative example 1:
It chooses commercially available plain polypropylene material and dumbbell shaped iso standard test bars is respectively prepared with injection molding machine, and to batten Properties test is carried out according to mechanical property requirements, test condition is shown in Table 3, and test result is as shown in table 6.
Table 6: testing result
Test item Unit Test result
Tensile strength MPa 40
Elongation at break % 2
Notch impact strength KJ/m2 4
Unnotched impact strength KJ/m2 40
Bending strength MPa 65
Bending modulus MPa 3000
Sheet resistance Ohms/sq Insulation, 10E15 or more
Comparative example 2:
It chooses commercially available pure homopolypropylene material and dumbbell shaped iso standard test bars is respectively prepared with injection molding machine, and to sample Item carries out properties test according to mechanical property requirements, and test condition is shown in Table 3, and test result is as shown in table 7.
Table 7: testing result
Comparative example 3:
It chooses commercially available common fiberglass reinforced non-graphite alkene modified polypropylene material and dumbbell shaped ISO mark is respectively prepared with injection molding machine Quasi- test bars, and properties test is carried out according to mechanical property requirements to batten, test condition is shown in Table 3, and test result is such as Shown in table 8.
Table 8: testing result
Test item Unit Test result (range)
Tensile strength MPa 60
Elongation at break % 5
Notch impact strength KJ/m2 8
Unnotched impact strength KJ/m2 53
Bending strength MPa 78
Bending modulus MPa 3800
Sheet resistance Ohms/sq Insulation, 10E14 or more
Comparative example 4:
It chooses commercially available graphene modified polypropylene material and dumbbell shaped iso standard test bars is respectively prepared with injection molding machine, and Properties test is carried out according to mechanical property requirements to batten, test condition is shown in Table 3, and test result is as shown in table 10.
Table 10: testing result
Test item Unit Test result (range)
Tensile strength MPa 55
Elongation at break % 6
Notch impact strength KJ/m2 8
Unnotched impact strength KJ/m2 50
Bending strength MPa 80
Bending modulus MPa 3700
Sheet resistance Ohms/sq Insulation, 10E14 or more
The embodiment and comparative example listed by the present invention is it is found that common fiberglass reinforced non-graphite alkene modified polypropylene material power It is extremely unstable to learn performance, and the strength of materials is clearly lower than high-intensitive high rigidity graphene modified polypropene of the invention, especially In tensile strength, bending strength and bending modulus, high-intensitive high rigidity graphene modified polypropene occupies great advantage.Simultaneously The sheet resistance of high intensity high rigidity graphene modified polypropene of the invention reaches 10E3 hereinafter, solving polypropylene material insulation Technical problem.Therefore, the present invention is an important breakthrough in modified fiber glass reinforced polypropylene field.
In view of the numerous embodiments of the scheme of the present invention, each embodiment experimental data is huge numerous, is not suitable for arranging one by one herein Explanation is lifted, but the content verified required for each embodiment and obtained final conclusion are close, obtained high-intensitive high rigidity For graphene modified polypropene compared with plain polypropylene, tensile strength, bending strength are high, and not easy to break, rigidity is good, corrosion-resistant, It is anti-aging, and have both conductive characteristic.So do not explained one by one to the verifying content of each embodiment, only with reality herein A 1-10 is applied as representative and illustrates the excellent place of the present patent application.
Specific embodiment described herein is only an example for the spirit of the invention.The neck of technology belonging to the present invention The technical staff in domain can do various modifications or supplement or is substituted in a similar manner to described specific embodiment, but simultaneously Spirit or beyond the scope defined by the appended claims of the invention is not deviated by.
It is skilled to this field although present invention has been described in detail and some specific embodiments have been cited For technical staff, as long as it is obvious for can making various changes or correct without departing from the spirit and scope of the present invention.

Claims (7)

1. a kind of high intensity high rigidity graphene modified polypropene, which is characterized in that the high intensity high rigidity graphene is modified Polypropylene material includes following component according to parts by weight:
Homopolypropylene: 38 ~ 51 parts,
Graphene: 15 ~ 20 parts,
Alkali-free glass fibre: 28 ~ 32 parts,
Enzymolysis xylogen: 2-4 parts,
Compatilizer: 5 ~ 8 parts,
Antioxidant: 0.5-2 parts,
Lubricant: 0.5-1.0 parts,
Coupling agent: 0.1-0.2 parts;
The graphene is bilayer graphene;
The length of the alkali-free glass fibre is 1.5-3.0mm, and diameter is 9-14 μm.
2. a kind of high-intensitive high rigidity graphene modified polypropylene material according to claim 1, which is characterized in that described Also containing 1-3 parts of nucleating agent in high-intensitive high rigidity graphene modified polypropylene material, the partial size of the nucleating agent is 5-10 μ m。
3. a kind of high-intensitive high rigidity graphene modified polypropylene material according to claim 2, which is characterized in that it is described at Core agent is one of mica, talcum powder, white carbon black or a variety of.
4. a kind of high-intensitive high rigidity graphene modified polypropylene material according to claim 1, which is characterized in that described Compatilizer is one or both of bromination polypropylene, monoethanolamine.
5. a kind of preparation method of the high-intensitive high rigidity graphene modified polypropene as described in claim 1-4 is any, special Sign is that the method includes the following steps: to weigh high-intensitive high rigidity graphene modified polypropylene material in parts by weight Component, and by the other components in addition to alkali-free glass fibre be added in batch mixer be uniformly mixed, by object after mixing Material pours into extruding pelletization in double screw extruder, by alkali-free glass fibre from double screw extruder side feed material while extruding pelletization Mouth is added using weightless feed method, obtains high-intensitive high rigidity graphene modified polypropene pellet.
6. the preparation method of high intensity high rigidity graphene modified polypropene according to claim 5, which is characterized in that institute The setting speed for stating batch mixer is 300-600rpm.
7. the preparation method of high intensity high rigidity graphene modified polypropene according to claim 5, which is characterized in that institute The engine speed 25-35HZ, main feeding 15-20HZ, side feed material 8-12HZ of double screw extruder are stated, temperature is set as 230-245 ℃。
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105063795A (en) * 2015-09-10 2015-11-18 孟红琳 Preparation method of graphene doped polypropylene conductive fiber
CN105802019A (en) * 2016-05-14 2016-07-27 湖北运来塑胶科技有限公司 Graphene/glass fiber reinforcement polypropylene composite material and preparation method thereof
CN105968570A (en) * 2016-06-12 2016-09-28 安徽双荣电器电缆有限公司 Polypropylene filling rope

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105063795A (en) * 2015-09-10 2015-11-18 孟红琳 Preparation method of graphene doped polypropylene conductive fiber
CN105802019A (en) * 2016-05-14 2016-07-27 湖北运来塑胶科技有限公司 Graphene/glass fiber reinforcement polypropylene composite material and preparation method thereof
CN105968570A (en) * 2016-06-12 2016-09-28 安徽双荣电器电缆有限公司 Polypropylene filling rope

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