CN108219251A - Wood plastic composite and preparation method thereof - Google Patents

Wood plastic composite and preparation method thereof Download PDF

Info

Publication number
CN108219251A
CN108219251A CN201810029994.8A CN201810029994A CN108219251A CN 108219251 A CN108219251 A CN 108219251A CN 201810029994 A CN201810029994 A CN 201810029994A CN 108219251 A CN108219251 A CN 108219251A
Authority
CN
China
Prior art keywords
plastic composite
parts
wood plastic
charcoal
coupling agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201810029994.8A
Other languages
Chinese (zh)
Inventor
陈占军
田修营
罗飞
钟洪彬
文瑾
彭秧锡
胡传跃
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hunan University of Humanities Science and Technology
Original Assignee
Hunan University of Humanities Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hunan University of Humanities Science and Technology filed Critical Hunan University of Humanities Science and Technology
Priority to CN201810029994.8A priority Critical patent/CN108219251A/en
Publication of CN108219251A publication Critical patent/CN108219251A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • 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
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • 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
    • B29B7/00Mixing; Kneading
    • B29B7/002Methods
    • 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
    • B29B9/00Making granules
    • B29B9/02Making granules by dividing preformed material
    • B29B9/06Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C43/00Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
    • B29C43/32Component parts, details or accessories; Auxiliary operations
    • B29C43/58Measuring, controlling or regulating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C45/00Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
    • B29C45/17Component parts, details or accessories; Auxiliary operations
    • B29C45/76Measuring, controlling or regulating
    • B29C45/78Measuring, controlling or regulating of temperature
    • CCHEMISTRY; METALLURGY
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L97/00Compositions of lignin-containing materials
    • C08L97/02Lignocellulosic material, e.g. wood, straw or bagasse
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C43/00Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
    • B29C43/32Component parts, details or accessories; Auxiliary operations
    • B29C43/58Measuring, controlling or regulating
    • B29C2043/5816Measuring, controlling or regulating temperature
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2945/00Indexing scheme relating to injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould
    • B29C2945/76Measuring, controlling or regulating
    • B29C2945/76494Controlled parameter
    • B29C2945/76531Temperature
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/08Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/14Polymer mixtures characterised by other features containing polymeric additives characterised by shape
    • C08L2205/16Fibres; Fibrils

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Manufacturing & Machinery (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Dry Formation Of Fiberboard And The Like (AREA)

Abstract

The present invention provides a kind of wood plastic composite, wood plastic composite by weight, including:Thermoplastic resin 30~80%, biomass fiber 10~50%, coupling agent 0.2~4%, activated Calcium carbonate 1~20%, plastic processing additives 1~8%, charcoal 0.5~20%.By introducing charcoal in the formula system of wood plastic composite, improve the interface compatibility and heat dissipation performance of biomass fiber and thermoplastic resin, significantly improve the mechanical property of wood plastic composite at ambient and elevated temperatures.Meanwhile charcoal is derived from the product after biomass waste material Pintsch process, also functions to the effect to turn waste into wealth in this way.The preparation method of wood plastic composite provided by the invention is easy to operate, low for equipment requirements, suitable for industrialized production, has a vast market application prospect.

Description

Wood plastic composite and preparation method thereof
Technical field
The present invention relates to field of compound material, particularly, are related to a kind of wood plastic composite and preparation method thereof.
Background technology
Wood plastic composite (abbreviation WPC) is a kind of using biomass fiber and thermoplastic resin as primary raw material, is added It is process after some auxiliary agents (colorant, coupling agent and lubricant) by modes such as extrusion molding, compression molding, injection moldings Environment friendly composite material.Although wood plastic composite has many advantages, such as that environmental protection, processability are good and recyclable, normal Comprehensive mechanical property under mild high temperature is relatively low to cause application field partially narrow, is current to restrict the main of wood plastic composite development One of factor.The hydrophily of biomass fiber and the hydrophobicity of thermoplastic resin make interface compatibility between the two poor, lead It causes its binding force smaller, is reduced so as to cause mechanical properties such as the tensile strength of product and impact strengths.In addition, thermoplastic resin All it is the non-conductor of heat with biomass fiber, in the case where outdoor solar light is exposed to the sun for a long time, since heat cannot heat loss through conduction meeting in time Component is caused to be decomposed to react and the physical mechanical property of wood plastic composite is made to decline rapidly, simultaneously as heat transfer is not smooth, Wood-plastic profiles surface temperature is higher than body temperature, causes thermal stress inconsistent, causes Wood-plastic profiles face checking.These shortcomings are tight Its further development is limited again.Therefore it needs to be modified the interface of biomass fiber and thermoplastic resin, to improve Compatibility between them, meanwhile, heat transfer improvement is carried out to it, improves the performance and durability of composite material.
Improvement for the interface compatibility of biomass fiber and thermoplastic resin, general there are as below methods:Pass through change The chemical constitution of thermoplastic resin or biomass fiber, crystallite form, surface microscopic topographic, surface energy etc. are compatible to improve its Property, but this method will certainly cause the rising of cost of material.It is answered alternatively, adding in some carbon fiber class reinforcing materials to improve wood moulding The tensile strength and rigidity of condensation material, although improvement is more notable, carbon fiber cost is higher, uneconomical.
Invention content
The present invention provides a kind of wood plastic composite and preparation method thereof, to solve existing wood plastic composite in room temperature With comprehensive mechanical property under high temperature it is relatively low the problem of.
The technical solution adopted by the present invention is as follows:
According to an aspect of the invention, there is provided a kind of wood plastic composite, wood plastic composite by weight, wraps It includes:30~80 parts of thermoplastic resin, 10~50 parts of biomass fiber, 0.2~4 part of coupling agent, 1~20 part of activated Calcium carbonate, modeling Expect 1~8 part of processing aid, 0.5~20 part of charcoal.
Thermoplastic resin is polyolefin polymer and/or polyolefin polymer reclaimed materials.
Biomass fiber is one or more in wood powder, cavings, coconut shell flour, straw powder and cornstalk powder.
Coupling agent is in maleic anhydride grafted polyethylene, silane coupling agent, titante coupling agent and aluminate coupling agent It is one or more.
Plastic processing additives are ethylene bis stearamide, zinc stearate, PE waxes, antioxidant 1010, fatty chloroflo and oxidation It is one or more in polyethylene.
Charcoal is with one or more for raw material system in tea residue, agricultural crop straw, corn ear, bagasse and cavings The product obtained.
Further, wood plastic composite by weight, including:40~60 parts of thermoplastic resin, biomass fiber 10 ~30 parts, 2~4 parts of coupling agent, 4~17 parts of activated Calcium carbonate, 2~6 parts of plastic processing additives, 5~20 parts of charcoal.
Further, wood plastic composite by weight, including:50 parts of thermoplastic resin, 20 parts of biomass fiber are even Join 3 parts of agent, 13 parts of activated Calcium carbonate, 4 parts of plastic processing additives, 10 parts of charcoal.
Further, charcoal is using tea residue product made from raw material.
Further, charcoal is small by 300~500 DEG C of processing 2~10 in an inert atmosphere by raw material of tea residue When after products therefrom, it is preferable that charcoal for by raw material of tea residue in nitrogen atmosphere by 400 DEG C processing 4 hours after institute Obtain product.
Further, polyolefin polymer is polyethylene and/or polypropylene;Polyolefin polymer reclaimed materials is returned for polyethylene Rewinding and/or polypropylene reclaimed material.
Further, biomass fiber is wood powder, and the granularity of wood powder is 70~120 mesh, preferably 100 mesh.
Further, coupling agent is maleic anhydride grafted polyethylene.
Plastic processing additives include PE waxes and zinc stearate, and the mass ratio of PE waxes and zinc stearate is 1:1.
According to another aspect of the present invention, a kind of preparation method of wood plastic composite is provided, is included the following steps;
By thermoplastic resin, biomass fiber, coupling agent, activated Calcium carbonate, plastic processing additives and charcoal by weight After weighing, first stirred 5~10 minutes with 40~60 revs/min of speed at normal temperatures, then again with 80~150 revs/min Speed stir 10~20 minutes, then, stirred 10~20 minutes under conditions of 105~120 DEG C and 60~80 revs/min, Obtain premix.
By premix melt blending extruding pelletization, melt zone temperature controls at 155~200 DEG C, is then molded or is molded into Wood plastic composite is made in type.
Further, the moisture content of biomass fiber 3% hereinafter, by by biomass fiber materials at 100~150 DEG C Lower baking is made for 4~6 hours.
Charcoal is by regarding one or more in tea residue, agricultural crop straw, corn ear, bagasse and cavings as original Material obtains after 300~500 DEG C are handled 2~10 hours in an inert atmosphere.
The invention has the advantages that:
The present invention provides a kind of wood plastic composite, by introducing biology in the formula system of wood plastic composite Charcoal improves the interface compatibility and heat dissipation performance of biomass fiber and thermoplastic resin, significantly improves wood plastic composite normal Mechanical property under mild high temperature.Meanwhile charcoal is derived from the product after biomass waste material Pintsch process, also functions in this way The effect to turn waste into wealth.The preparation method of wood plastic composite provided by the invention is easy to operate, low for equipment requirements, suitable for work Industry metaplasia is produced, and has a vast market application prospect.
Other than objects, features and advantages described above, the present invention also has other objects, features and advantages. Below with reference to accompanying drawings, the present invention is described in further detail.
Description of the drawings
The attached drawing for forming the part of the application is used to provide further understanding of the present invention, schematic reality of the invention Example and its explanation are applied for explaining the present invention, is not constituted improper limitations of the present invention.In the accompanying drawings:
Fig. 1 is the charcoal pictorial diagram of different material and preparation;
Fig. 2 is charcoal XRD diagram prepared by different material;
Fig. 3 is the preparation method flow chart of the wood plastic composite of the preferred embodiment of the present invention;
Fig. 4 is the different wood plastic composite of the tea beverage process residues biology carbon content of the preferred embodiment of the present invention 55 DEG C when bending strength and tensile strength schematic diagram;
Fig. 5 is that the different wood plastic composite of the bagasse biology carbon content of the preferred embodiment of the present invention is curved at 55 DEG C Qu Qiangdu and tensile strength schematic diagram;
Fig. 6 is that the different wood plastic composite of the corn ear biology carbon content of the preferred embodiment of the present invention is curved at 55 DEG C Qu Qiangdu and tensile strength schematic diagram;
Fig. 7 is bending strength of the wood plastic composite of the biological carbon content of difference of the preferred embodiment of the present invention at 25 DEG C With tensile strength schematic diagram;
Fig. 8 is impact strength of the wood plastic composite of the biological carbon content of difference of the preferred embodiment of the present invention at 25 DEG C With bending modulus schematic diagram;
Fig. 9 is the different wood plastic composite of the tea beverage process residues biology carbon content of the preferred embodiment of the present invention 50 DEG C when bending strength and tensile strength schematic diagram;
Figure 10 is that the different wood plastic composite of the tea beverage process residues biology carbon content of the preferred embodiment of the present invention exists Impact strength and bending modulus schematic diagram at 50 DEG C.
Specific embodiment
It should be noted that in the absence of conflict, the feature in embodiment and embodiment in the application can phase Mutually combination.The present invention will be described in detail below with reference to the accompanying drawings and in conjunction with the embodiments.
According to an aspect of the invention, there is provided a kind of wood plastic composite, wood plastic composite by weight, wraps It includes:30~80 parts of thermoplastic resin, 10~50 parts of biomass fiber, 0.2~4 part of coupling agent, 1~20 part of activated Calcium carbonate, modeling Expect 1~8 part of processing aid, 0.5~20 part of charcoal.Thermoplastic resin is returned for polyolefin polymer and/or polyolefin polymer Rewinding.Biomass fiber is one or more in wood powder, cavings, coconut shell flour, straw powder and cornstalk powder.Coupling agent is Malaysia It is one or more in anhydride grafted lldpe, silane coupling agent, titante coupling agent and aluminate coupling agent.Plastic processing Auxiliary agent is ethylene bis stearamide, zinc stearate, PE waxes, antioxidant 1010, fatty chloroflo and one kind in oxidic polyethylene or It is a variety of.It with one or more in tea residue, agricultural crop straw, corn ear, bagasse and cavings is that raw material is made that charcoal, which is, Product.
Thermoplastic resin can be entirely derived from recycled plastic, and recycled plastic is sorted out using preceding without sorting, can be direct Mixing milling uses, and reduces the recycling cost of waste plastic.
Silane coupling agent has RSiX3Structure, R is vinyl, the methacryloxypropyl combined with nonpolar organic matter Base, epoxy group, amido etc., X are the groups such as methoxyl group, ethyoxyl and chlorine that same polarity biomass fiber is combined.Titanate ester Coupling agent is a kind of organic titanic compound that inorganic matter is made to have chemical bonding effect with organic matter and between organic matter, close Organic moiety is usually C12-C18 long chain hydrocarbon groups.Aluminate coupling agent mainly has three benzyl ester of three isopropyl ester of aluminic acid and aluminic acid etc..
Charcoal particle is small, can be filled in the interfacial gap of biomass fiber particle and thermoplastic resin, and superelevation The thermoplastic resin of molecular weight is with good mobility, in the micropore that can penetrate and be filled into biological carbon surface after melting, and Charcoal has larger specific surface and pore characteristics, and therefore, synthesis result is exactly to be formed between charcoal and thermoplastic resin Good mechanical connection, this good mechanical connection are generally evenly distributed in the boundary of biomass fiber particle and thermoplastic resin again In the gap of face, so as to play interface humidification, improve the mechanical property of wood plastic composite.Charcoal be with tea residue, One or more for raw material in agricultural crop straw, corn ear, bagasse and cavings, preparation method can refer to standard biologic charcoal Preparation method.Tea residue is to utilize residue after the progress tea beverage processing such as tea stalks and/or tealeaves.Agricultural crop straw can be water Rice, wheat, sorghum stalk.
In addition, charcoal is the good conductor of heat, Wood-plastic profiles under long-term be exposed to the sun, the temperature difference in surface layer and ontology compared with Small, thermal stress is more uniform, so as to reduce the trend of its crack of surface layer, reaches the mesh for promoting its anti-cracking performance at high temperature 's.
By introducing charcoal in the formula system of wood plastic composite, improve biomass fiber and thermoplastic resin Interface compatibility and heat dissipation performance significantly improve the mechanical property of wood plastic composite at ambient and elevated temperatures.Meanwhile charcoal The product being derived from after biomass waste material Pintsch process also functions to the effect to turn waste into wealth in this way.
Preferably, wood plastic composite by weight, including:40~60 parts of thermoplastic resin, biomass fiber 10~ 30 parts, 2~4 parts of coupling agent, 4~17 parts of activated Calcium carbonate, 2~6 parts of plastic processing additives, 5~20 parts of charcoal.
Preferably, wood plastic composite by weight, including:50 parts of thermoplastic resin, 20 parts of biomass fiber, coupling 3 parts of agent, 13 parts of activated Calcium carbonate, 4 parts of plastic processing additives, 10 parts of charcoal.
Preferably, charcoal is using tea residue product made from raw material.
It when tealeaves or tea stalks prepare tea beverage, needs to impregnate through boiling water, tea residue, that is, tea beverage process residues more.In water After high temperature impregnates, some are soluble, the organic matter of the carbon containing hydrogen-oxygen atom of short chain and soluble inorganic salt are dissolved in water, And often this partial organic substances cannot be carbonized or be carbonized at high temperature that yield is relatively low, and remaining tea residue is all based on cellulose Long-chain carbon organic matter, carbonization yield is very high, and the charcoal yield that is obtained after high-temperature process is high, and micropore is more.And bagasse With corn ear raw material without leaching process, it is impossible to which the material composition for forming charcoal is more, causes its yield relatively low, economic valency Value is not high.
As shown in Figure 1, it is raw material in nitrogen gas to take tea beverage process residues, bagasse and the corn ear of essentially identical volume In atmosphere after 400 DEG C of processing 4 hours the corresponding charcoal of gained.The volume of tea beverage process residues charcoal is about bagasse 6 times of charcoal volume, the volume of tea beverage process residues charcoal are about 2 times of corn ear charcoal volume.
Above-mentioned each charcoal is taken to carry out XRD tests, as described in Figure 2, is all deposited in about 22 ° and 43 ° or so three samples Bao Feng is overflow apparent, corresponding to the characteristic peak of amorphous carbon, it is seen that corresponding charcoal can be made in above-mentioned raw materials.In addition, It is tested by specific surface instrument it is found that with the charcoal that tea beverage process residues are obtained with maximum specific surface area, reached 489m2·g-1, and be respectively 135m by the specific surface area of bagasse and the obtained charcoal of corn ear2·g-1And 102m2·g-1, with many micropores or mesoporous, this feature is conducive to melt to be set the charcoal that this explanation tea beverage process residues is obtained Fat is penetrated and is filled into the micropore of biological carbon surface, makes to form good mechanical connection between charcoal and thermoplastic resin, This good mechanical connection is generally evenly distributed in the interfacial gap of biomass fiber particle and thermoplastic resin again, so as to rise Interface humidification has been arrived, has improved the mechanical property of wood plastic composite.
Preferably, charcoal is to be handled 2~10 hours by 300~500 DEG C in an inert atmosphere using tea residue as raw material Products therefrom afterwards, it is preferable that charcoal be by raw material of tea residue in nitrogen atmosphere by 400 DEG C processing 4 hours after gained Product.
Preferably, polyolefin polymer is polyethylene and/or polypropylene;Polyolefin polymer reclaimed materials is recycled for polyethylene Material and/or polypropylene reclaimed material.
Preferably, biomass fiber is wood powder, and the granularity of wood powder is 70~120 mesh, preferably 100 mesh.
Wood powder is mainly made of three kinds of cellulose, hemicellulose and lignin natural polymers, and content is 90% More than rather than the sugar content of wood powder and the carbohydrate content of various low molecular weights it is higher, the producing high-moleculars such as cellulose close Object content is below 90%.Biomass fiber particle size is smaller, better with the composite effect of thermoplastic resin, but too it is small again Easily occurring to reunite, it is homodisperse in thermoplastic resin to be unfavorable for it.
Preferably, coupling agent is maleic anhydride grafted polyethylene.Maleic anhydride grafted polyethylene price is relatively low.
Plastic processing additives include PE waxes and zinc stearate, and the mass ratio of PE waxes and zinc stearate is 1:1.PE waxes and tristearin Sour zinc can improve lubricating effect, reduce dosage.
According to another aspect of the present invention, a kind of preparation method of wood plastic composite is provided, with reference to Fig. 1, including Following steps;
S100:Thermoplastic resin, biomass fiber, coupling agent, activated Calcium carbonate, plastic processing additives and charcoal are pressed After weight ratio weighs, first stir 5~10 minutes at normal temperatures with 40~60 revs/min of speed, then again with 80~150 turns/ The speed of minute stirs 10~20 minutes, then, 10~20 points is stirred under conditions of 105~120 DEG C and 60~80 revs/min Clock obtains premix.
S200:By premix melt blending extruding pelletization, melt zone temperature is controlled at 155~200 DEG C, then injection or mould Molded obtained wood plastic composite.
Preferably, the moisture content of biomass fiber 3% hereinafter, by by biomass fiber materials at 100~150 DEG C Baking is made for 4~6 hours.
Charcoal is by regarding one or more in tea residue, agricultural crop straw, corn ear, bagasse and cavings as original Material obtains after 300~500 DEG C are handled 2~10 hours in an inert atmosphere.
Charcoal is entirely using biomass waste materials such as tea stalks as raw material, is handled by simple Pintsch process, This method not only solve biomass waste material arbitrarily discard or burn caused by problem of environmental pollution, also opened for charcoal A kind of new application approach.
The preparation method of wood plastic composite provided by the invention is easy to operate, low for equipment requirements, suitable for industrial metaplasia Production, has a vast market application prospect.
Below according to the charcoal additive amount in each embodiment of adjustment of following table charcoal additive amount.
Sample name 1# 2# 3# 4# 5#
Charcoal additive amount (part) 0 0.5 5 10 20
Embodiment one
With reference to Fig. 3, the preparation of wood plastic composite is carried out:
(1) wood powder at 100 DEG C is toasted 6 hours, makes its moisture content below 3%.
(2) using tea residue as raw material, it is obtained into charcoal after 300 DEG C are handled 10 hours in an inert atmosphere.
(3) by weight, 30 parts of thermoplastic resin, 40 parts of biomass fiber of the moisture content below 3%, coupling are weighed 1.5 parts of agent, 20 parts of activated Calcium carbonate, 8 parts of plastic processing additives separately weigh 0 part, 0.5 part, 5 parts, 10 parts and 20 of charcoal respectively Part is mixed with other components, obtains including the raw material of different biological carbon contents.
(4) above-mentioned raw materials are added in high-speed mixer respectively, first stir 10 at normal temperatures with 40 revs/min of speed Minute, it is then stirred 20 minutes with 80 revs/min of speed again, then, 20 is stirred under conditions of 105 DEG C and 60 revs/min Minute, obtain corresponding premix.
(5) corresponding premix is transferred to melt blending extruding pelletization in extruder respectively, melt zone temperature is controlled 155 DEG C, wood plastic composite 1#~5# is made in then injection or compression molding.
Embodiment two
With reference to Fig. 3, the preparation of wood plastic composite is carried out:
(1) cavings at 120 DEG C is toasted 5 hours, makes its moisture content below 3%.
(2) using bagasse as raw material, it is obtained into charcoal after 400 DEG C are handled 8 hours in an inert atmosphere.
(3) by weight, 40 parts of thermoplastic resin, 30 parts of biomass fiber of the moisture content below 3%, coupling are weighed 2 parts of agent, 17 parts of activated Calcium carbonate, 6 parts of plastic processing additives separately weigh 0 part, 0.5 part, 5 parts, 10 parts and 20 parts of charcoal respectively It is mixed with other components, obtains including the raw material of different biological carbon contents.
(4) above-mentioned raw materials are added in high-speed mixer respectively, first stir 9 at normal temperatures with 50 revs/min of speed Minute, it is then stirred 15 minutes with 100 revs/min of speed again, then, 15 is stirred under conditions of 110 DEG C and 70 revs/min Minute, obtain corresponding premix.
(5) corresponding premix is transferred to melt blending extruding pelletization in extruder respectively, melt zone temperature is controlled 170 DEG C, wood plastic composite 1#~5# is made in then injection or compression molding.
Embodiment three
With reference to Fig. 3, the preparation of wood plastic composite is carried out:
(1) coconut shell flour at 135 DEG C is toasted 4 hours, makes its moisture content below 3%.
(2) using corn ear as raw material, it is obtained into charcoal after 500 DEG C are handled 5 hours in an inert atmosphere.
(3) by weight, 50 parts of thermoplastic resin, 20 parts of biomass fiber of the moisture content below 3%, coupling are weighed 3 parts of agent, 13 parts of activated Calcium carbonate, 4 parts of plastic processing additives separately weigh 0 part, 0.5 part, 5 parts, 10 parts and 20 parts of charcoal respectively It is mixed with other components, obtains including the raw material of different biological carbon contents.
(4) above-mentioned raw materials are added in high-speed mixer respectively, first stir 7 at normal temperatures with 60 revs/min of speed Minute, it is then stirred 10 minutes with 125 revs/min of speed again, then, 10 is stirred under conditions of 115 DEG C and 80 revs/min Minute, obtain corresponding premix.
(5) corresponding premix is transferred to melt blending extruding pelletization in extruder respectively, melt zone temperature is controlled 185 DEG C, wood plastic composite 1#~5# is made in then injection or compression molding.
Example IV
With reference to Fig. 3, the preparation of wood plastic composite is carried out:
(1) straw powder at 150 DEG C is toasted 4 hours, makes its moisture content below 3%.
(2) using cavings as raw material, it is obtained into charcoal after 500 DEG C are handled 2 hours in an inert atmosphere.
(3) by weight, 60 parts of thermoplastic resin, 10 parts of biomass fiber of the moisture content below 3%, coupling are weighed 4 parts of agent, 4 parts of activated Calcium carbonate, 2 parts of plastic processing additives, 20 parts of charcoal.
(4) above-mentioned raw materials are added in high-speed mixer, are first stirred 5 minutes with 60 revs/min of speed at normal temperatures, Then it is stirred 10 minutes with 150 revs/min of speed, then, is stirred 10 minutes under conditions of 120 DEG C and 80 revs/min again, Obtain premix.
(5) premix is transferred to melt blending extruding pelletization in extruder, melt zone temperature is controlled at 200 DEG C, then Wood plastic composite is made in injection or compression molding.
The corresponding wood plastic composite 1#~5# being prepared in Example 1~3 respectively, is tested respectively at 55 DEG C Bending strength, tensile strength, as shown in figures 4-6, specific test number is as shown in table 1 for experimental result.It can be seen that tealeaves charcoal system Standby wood plastic composite comprehensive performance is best.And 50 parts of thermoplastic resin of addition, biomass fiber of the moisture content below 3% 20 parts, 3 parts of coupling agent, 13 parts of activated Calcium carbonate, 4 parts of plastic processing additives, sample 4# synthesis mechanics made from 10 parts of charcoal Performance is best.
Table 1, the bending strength of wood plastic composite 1#~5# of each embodiment, tensile strength test results
Corresponding wood plastic composite 1#~5# prepared by Example 1, the bending tested respectively at 20 DEG C, 50 DEG C are strong Degree, tensile strength, impact strength and bending modulus, for experimental result as shown in Fig. 7~10, specific test number is as shown in table 2.It surveys Examination is statistics indicate that sample 4# comprehensive mechanical properties are best made from tealeaves charcoal.
The performance parameter of the wood plastic composite of 2 embodiment 1 of table at different temperatures
The foregoing is only a preferred embodiment of the present invention, is not intended to restrict the invention, for the skill of this field For art personnel, the invention may be variously modified and varied.All within the spirits and principles of the present invention, that is made any repaiies Change, equivalent replacement, improvement etc., should all be included in the protection scope of the present invention.

Claims (10)

1. a kind of wood plastic composite, which is characterized in that the wood plastic composite by weight, including:Thermoplastic resin 30~80 parts, 10~50 parts of biomass fiber, 0.2~4 part of coupling agent, 1~20 part of activated Calcium carbonate, plastic processing additives 1~8 Part, 0.5~20 part of charcoal;
The thermoplastic resin is polyolefin polymer and/or polyolefin polymer reclaimed materials;
The biomass fiber is one or more in wood powder, cavings, coconut shell flour, straw powder and cornstalk powder;
The coupling agent is in maleic anhydride grafted polyethylene, silane coupling agent, titante coupling agent and aluminate coupling agent It is one or more;
The plastic processing additives are ethylene bis stearamide, zinc stearate, PE waxes, antioxidant 1010, fatty chloroflo and oxidation It is one or more in polyethylene;
The charcoal is with one or more for raw material system in tea residue, agricultural crop straw, corn ear, bagasse and cavings The product obtained.
2. wood plastic composite according to claim 1, which is characterized in that the wood plastic composite by weight, Including:40~60 parts of thermoplastic resin, 10~30 parts of biomass fiber, 2~4 parts of coupling agent, 4~17 parts of activated Calcium carbonate, modeling Expect 2~6 parts of processing aid, 5~20 parts of charcoal.
3. wood plastic composite according to claim 2, which is characterized in that the wood plastic composite by weight, Including:50 parts of thermoplastic resin, 20 parts of biomass fiber, 3 parts of coupling agent, 13 parts of activated Calcium carbonate, 4 parts of plastic processing additives, 10 parts of charcoal.
4. wood plastic composite described in any one of claim 1 to 3, which is characterized in that
The charcoal is using tea residue product made from raw material.
5. wood plastic composite according to claim 4, which is characterized in that
The charcoal is that gained produces after 300~500 DEG C are handled 2~10 hours in an inert atmosphere by raw material of tea residue Object, it is preferable that the charcoal be by raw material of tea residue in nitrogen atmosphere by 400 DEG C processing 4 hours after products therefrom.
6. wood plastic composite described in any one of claim 1 to 3, which is characterized in that
The polyolefin polymer is polyethylene and/or polypropylene;The polyolefin polymer reclaimed materials is polyethylene reclaimed materials And/or polypropylene reclaimed material.
7. wood plastic composite described in any one of claim 1 to 3, which is characterized in that
The biomass fiber is wood powder, and the granularity of the wood powder is 70~120 mesh, preferably 100 mesh.
8. wood plastic composite described in any one of claim 1 to 3, which is characterized in that
The coupling agent is maleic anhydride grafted polyethylene;
The plastic processing additives include PE waxes and zinc stearate, and the mass ratio of PE waxes and zinc stearate is 1:1.
9. a kind of preparation method of wood plastic composite according to any one of claims 1 to 8, which is characterized in that including with Lower step:
By thermoplastic resin, biomass fiber, coupling agent, activated Calcium carbonate, plastic processing additives and charcoal by weight title After taking, first stirred 5~10 minutes with 40~60 revs/min of speed at normal temperatures, then again with 80~150 revs/min of speed Degree stirring 10~20 minutes, then, stirs 10~20 minutes under conditions of 105~120 DEG C and 60~80 revs/min, obtains Premix;
By the premix melt blending extruding pelletization, melt zone temperature controls at 155~200 DEG C, is then molded or is molded into The wood plastic composite is made in type.
10. the preparation method of wood plastic composite according to claim 9, which is characterized in that
The moisture content of the biomass fiber 3% hereinafter, by biomass fiber materials toast to 4 at 100~150 DEG C~ It is made within 6 hours;
The charcoal is by regarding one or more in tea residue, agricultural crop straw, corn ear, bagasse and cavings as original Material obtains after 300~500 DEG C are handled 2~10 hours in an inert atmosphere.
CN201810029994.8A 2018-01-12 2018-01-12 Wood plastic composite and preparation method thereof Pending CN108219251A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810029994.8A CN108219251A (en) 2018-01-12 2018-01-12 Wood plastic composite and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810029994.8A CN108219251A (en) 2018-01-12 2018-01-12 Wood plastic composite and preparation method thereof

Publications (1)

Publication Number Publication Date
CN108219251A true CN108219251A (en) 2018-06-29

Family

ID=62640798

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810029994.8A Pending CN108219251A (en) 2018-01-12 2018-01-12 Wood plastic composite and preparation method thereof

Country Status (1)

Country Link
CN (1) CN108219251A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109651732A (en) * 2018-12-26 2019-04-19 山东霞光集团有限公司 A kind of charcoal modified composite material of woods and plastics and preparation method thereof
CN109867974A (en) * 2019-03-21 2019-06-11 天津商业大学 A kind of preparation method of PE composite wood-plastic material and preparation method thereof, pallet
CN110395941A (en) * 2019-08-01 2019-11-01 北京理工大学珠海学院 Charcoal based thermoset applications composite material and preparation method
CN110698807A (en) * 2019-09-12 2020-01-17 泉州龙晟轻工有限公司 Recycled plastic for 3D printing and preparation method thereof
CN111014281A (en) * 2019-12-30 2020-04-17 肇庆市武大环境技术研究院 Multi-biochar combined microorganism composite material for petroleum-polluted soil remediation and preparation method and application thereof
CN112063191A (en) * 2020-08-20 2020-12-11 咖法科技(上海)有限公司 Tea residue wood plastic and preparation method thereof
CN115093716A (en) * 2022-06-28 2022-09-23 安徽爱瑞德新材料有限公司 Bio-based wood-plastic composite material and preparation method thereof
CN115216075A (en) * 2022-08-29 2022-10-21 山西农业大学 Antistatic wood-plastic composite material and preparation method thereof
CN115403865A (en) * 2022-10-15 2022-11-29 温州市梵特日用品有限公司 Antibacterial degradable plastic particle containing nano-silver and preparation method thereof
CN117363046A (en) * 2023-10-31 2024-01-09 恩平市健琪新材料科技有限公司 PP material and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103351514A (en) * 2013-07-09 2013-10-16 杭州亨林科技有限公司 High-strength high-filling degradable wood-plastic composite and manufacturing technique thereof
CN104371748A (en) * 2014-10-24 2015-02-25 东华大学 Preparation method of high-yield biochar
WO2015039237A1 (en) * 2013-09-17 2015-03-26 University Of Guelph Hybrid sustainable composites and methods of making and using thereof
CN104672697A (en) * 2015-01-22 2015-06-03 浙江保森新型材料有限公司 Wood-plastic composite material
CN107199235A (en) * 2017-06-08 2017-09-26 四川农业大学 Based on pyrolytical condition to tealeaf residue charcoal characteristic and cadmium pollution soil restorative procedure
CN107286970A (en) * 2016-04-01 2017-10-24 勐海茶业有限责任公司 A kind of tea grounds smokeless char and preparation method thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103351514A (en) * 2013-07-09 2013-10-16 杭州亨林科技有限公司 High-strength high-filling degradable wood-plastic composite and manufacturing technique thereof
WO2015039237A1 (en) * 2013-09-17 2015-03-26 University Of Guelph Hybrid sustainable composites and methods of making and using thereof
CN104371748A (en) * 2014-10-24 2015-02-25 东华大学 Preparation method of high-yield biochar
CN104672697A (en) * 2015-01-22 2015-06-03 浙江保森新型材料有限公司 Wood-plastic composite material
CN107286970A (en) * 2016-04-01 2017-10-24 勐海茶业有限责任公司 A kind of tea grounds smokeless char and preparation method thereof
CN107199235A (en) * 2017-06-08 2017-09-26 四川农业大学 Based on pyrolytical condition to tealeaf residue charcoal characteristic and cadmium pollution soil restorative procedure

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
常萧楠: "竹炭和壳聚糖对聚氯乙烯基木塑复合材料界面性能的影响", 《复合材料学报》 *
梁月荣: "《茶资源综合利用》", 30 November 2013, 浙江大学出版社 *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109651732A (en) * 2018-12-26 2019-04-19 山东霞光集团有限公司 A kind of charcoal modified composite material of woods and plastics and preparation method thereof
CN109867974A (en) * 2019-03-21 2019-06-11 天津商业大学 A kind of preparation method of PE composite wood-plastic material and preparation method thereof, pallet
CN110395941A (en) * 2019-08-01 2019-11-01 北京理工大学珠海学院 Charcoal based thermoset applications composite material and preparation method
CN110698807A (en) * 2019-09-12 2020-01-17 泉州龙晟轻工有限公司 Recycled plastic for 3D printing and preparation method thereof
CN111014281A (en) * 2019-12-30 2020-04-17 肇庆市武大环境技术研究院 Multi-biochar combined microorganism composite material for petroleum-polluted soil remediation and preparation method and application thereof
CN111014281B (en) * 2019-12-30 2021-06-04 肇庆市武大环境技术研究院 Multi-biochar combined microorganism composite material for petroleum-polluted soil remediation and preparation method and application thereof
CN112063191A (en) * 2020-08-20 2020-12-11 咖法科技(上海)有限公司 Tea residue wood plastic and preparation method thereof
CN112063191B (en) * 2020-08-20 2022-08-02 咖法科技(上海)有限公司 Tea residue wood plastic and preparation method thereof
CN115093716A (en) * 2022-06-28 2022-09-23 安徽爱瑞德新材料有限公司 Bio-based wood-plastic composite material and preparation method thereof
CN115216075A (en) * 2022-08-29 2022-10-21 山西农业大学 Antistatic wood-plastic composite material and preparation method thereof
CN115403865A (en) * 2022-10-15 2022-11-29 温州市梵特日用品有限公司 Antibacterial degradable plastic particle containing nano-silver and preparation method thereof
CN117363046A (en) * 2023-10-31 2024-01-09 恩平市健琪新材料科技有限公司 PP material and preparation method thereof

Similar Documents

Publication Publication Date Title
CN108219251A (en) Wood plastic composite and preparation method thereof
CN102051002B (en) Zymolytic lignin-wood fiber-polyolefin hybrid composite material and preparation method thereof
CN101899181B (en) Wood-plastic composite for walls and preparation method thereof
CN104804331B (en) The reuse method of FRP garbage, PVC base wood-plastic composite material and preparation method thereof
CN1642409A (en) Compositions and composites of cellulosic and lignocellulosic materials and resins, and methods of making the same
CN102775779B (en) Polyamide 11/high-density polyethylene composition prepared by in-situ reaction compatibilization method and preparation method thereof
CN112226053B (en) Biomass-based graphene-reinforced degradable polymer composite material and preparation method thereof
CN115141495A (en) Reinforced and toughened degradable material and preparation method thereof
CN109940929A (en) A kind of summer double-wall corrugated pipe and preparation method thereof
CN108864659A (en) A kind of anti-aging cable cover(ing) and preparation method thereof containing modified straw
CN109401273A (en) A kind of high scorching hot flame-retardant PPO alloy material and preparation method thereof
CN102585431B (en) Preparation method of ABS (Acrylonitrile Butadiene Styrene)-based wood-plastic composite
Ketabchi et al. Effect of oil palm EFB-biochar on properties of PP/EVA composites
CN109838628A (en) A kind of winter double-wall corrugated pipe and preparation method thereof
CN106433067A (en) Formula and preparation method of environment-friendly PC (polycarbonate)/ABS (acrylonitrile-butadiene-styrene) alloy material
CN113667207A (en) Preparation method of Polyethylene (PE) composite material
CN103408949B (en) Ultrahigh hardness rubber unvulcanizate and preparation method thereof
CN104710765B (en) The high-performance heat conductive insulating PC/ABS Alloy And Preparation Method prepared by waste electrical equipment shell
CN101805525A (en) Water absorption master batch for wood-plastic composite material and product and production method thereof
CN112063147A (en) Two-dimensional organic metal framework MOF modified PC material
CN110358258A (en) A method of it is prepared using spent resin and moulds the wooden particle
CN103613842B (en) A kind of high water-resistant wood-plastic composite material
CN109749428A (en) A kind of environment-friendly type plastic rubber new material
CN112679829A (en) Aluminum silicate fiber waste reinforced biomass composite material and preparation method thereof
CN113999460A (en) Thermo-oxidative aging resistant and weather resistant PP material for household appliances and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20180629

RJ01 Rejection of invention patent application after publication