CN106046575A - Novel stone wood-plastic composite material - Google Patents
Novel stone wood-plastic composite material Download PDFInfo
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- CN106046575A CN106046575A CN201610704682.3A CN201610704682A CN106046575A CN 106046575 A CN106046575 A CN 106046575A CN 201610704682 A CN201610704682 A CN 201610704682A CN 106046575 A CN106046575 A CN 106046575A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions 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
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
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- 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
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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- 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
- C08L2205/14—Polymer mixtures characterised by other features containing polymeric additives characterised by shape
- C08L2205/16—Fibres; Fibrils
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Abstract
The invention discloses a novel stone wood-plastic composite material, which comprises the following raw materials: maifanite powder, a polybutene plastic, eucalyptus powder, an adhesive, fatty acid amide, a silica gel, a flame retardant agent, a smoke suppressant, an aerosol generation agent, a titanate coupling agent, a PP-g-MAH compatibilizer, a WINGSTAYL antioxidant, a JINHASS regulator, a strengthening agent, polyaluminum ferric chloride, di-n-octyl phthalate, potassium stearate, and styrene. According to the present invention, the novel stone wood-plastic composite material has characteristics of good flame retardant effect, strong impact resistance, strong toughness and low water absorption, obtains the excellent flame-retardant property and maintains the good mechanical property of the novel stone wood-plastic composite material, is the excellent performance novel stone wood-plastic composite material, can be widely used in decorations of hotels, restaurants, and architectural decorations, and has significant economic benefits and social benefits.
Description
Technical field
The invention belongs to Wood-plastic material technology of preparing and field of Environment Protection, be specifically related to a kind of novel stone wood plastic composite.
Background technology
Wood plastic composite (WPC), is a kind of main by answering that material and plastics based on timber or cellulose are made
Condensation material, it is simply that by a certain proportion of wood fiber (such as wood powder, powder of straw, cotton stalk powder, bamboo powder, shell powder etc.) through pre-place
Reason is allowed to a kind of new material being combined into thermoplastic polymer resin or other materials；The both environmental protections of this new material
There is again good mechanical stability, but the two big raw material wood fiber of composition wood plastic composite and polyolefin are all inflammabilities
Material, is also combustible material for this this composite, and the fire resistance giving wood plastic composite good is that this materials application is sent out
The needs of exhibition；Individually the fire-retardant research to timber and the wood fiber has a lot, typically has phosphorus-nitrogenated flame retardant；Boron flame retardant；Contain
Halogen fire retardant；Other inorganic salts etc.；But main based on phosphorus-nitrogenated flame retardant it is considered to be optimum wood fire retardant,
Phosphorus, two kinds of elements of nitrogen play synergism in wood fire retardant and improve flame retardant effect；But these fire retardants almost have one
Common feature, it is simply that reduce the thermal degradation temperature of the wood fiber significantly, this may result in and cannot be carried out adding of composite
Work；Research for polyolefin flame-retardant is also a lot, and its flame resistant method is frequently with halogen containing flame-retardant and antimony oxide (Sb2O3) join
Close and use；Metal hydroxides (Al (OH)3、Mg(OH)2) fire retardant；Expansibility flame-proof agent；Ammonium polyphosphate flame retardant etc.；Halogen
Fire-retardant is the focus of polyolefin flame-retardant research, expanding fire retardant polyolefin/Wood Fiber Composites is carried out dual fire-retardant be this
The focus of the fire-retardant research of composite；But the interpolation of fire retardant often deteriorates the mechanical property of composite, therefore to resistance
The research of the research flame-proof composite material of retardant composite material to study interface compatibility, heat stability and anti-flammability, to obtain simultaneously
Obtain preferable flame-proof composite material.
Wood plastic composite has preferable machinability, the most anticorrosive, beautiful, generous, but, being in of its defect
Not good enough in its mechanical property, to this end, people seek solution route, once there is people to be re-introduced into stone powder in wood plastic composite, used
In molding novel stone wood plastic composite, but, due to the problems such as interface compatibility, the mechanicalness of the composite finally given
Can be poor.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of novel stone wood plastic composite, to solve to hinder in prior art
The interpolation of combustion agent can deteriorate the mechanical property of wood plastic composite, and introducing stone powder is used for molding stone wood plastic composite, due to
The problems such as interface compatibility, the problem such as the mechanical performance of the composite finally given is poor.The novel stone wood of the present invention is moulded multiple
Condensation material good flame retardation effect, strong shock resistance, toughness is strong, and water absorption rate is little, not only obtains excellent fire resistance but also maintain
The novel preferable mechanical property of stone wood plastic composite, is the excellent novel stone wood plastic composite of a kind of performance, can extensively apply
In hotel, restaurant, building decoration and fitment, have significant economic and social benefit.
In order to solve above technical problem, the present invention by the following technical solutions:
A kind of novel stone wood plastic composite, in units of weight portion, including following raw material: medical stone powder 82-100 part, poly-fourth
Alkene plastics 42-60 part, Eucalyptus powder 21-30 part, adhesive 8-14 part, fatty acid amide 0.6-1.2 part, silica gel 0.6-1 part, fire-retardant
Agent 0.6-0.8 part, smoke suppressant 0.5-0.8 part, aerogel generating agent 0.4-0.5 part, titanate coupling agent 0.6-0.7 part, PP-g-
MAH compatilizer 0.3-0.6 part, WINGSTAYL antioxidant 0.2-0.6 part, JINHASS regulator 0.3-0.7 part, hardening agent
0.3-0.8 part, PAFC 0.6-0.9 part, dinoctyl phthalate 0.5-0.8 part, potassium stearate 0.2-0.4
Part, styrene 0.2-0.3 part；
Described fire retardant is in units of weight portion, including following raw material: antimony oxide 5-8 part, VTES
3-5 part, triethyl phosphate 3-4 part, magnesium chloride 5-7 part, phenolic resin 2-4 part, bentonite 0.6-1 part；
Described smoke suppressant is in units of weight portion, including following raw material: zinc molybdate 8-14 part, aluminium hydroxide 6-10 part, dolomite
Powder 2-3 part, copper oxide 1-2 part；
Described hardening agent is in units of weight portion, including following raw material: ethyl butenoic acid ethyl 10-20 part, phosphoric acid vinyl acetate 8-
15 parts, cobalt naphthenate 3-6 part, aluminum chloride 2-4 part；
The preparation method of described novel stone wood plastic composite, comprises the following steps:
S1: prepare adhesive, its preparation method, comprise the following steps:
S11: compound concentration be 20-30Be ', pH value be para arrowroot slurry A of 3.4-3.7；
S12: in para arrowroot slurry A of step S11 add concentration be the triglyceride of 2%-4%, percarbamide, 2,5-diformazan
Base-2,5-double (benzoyl peroxide)-hexane, Raney nickel, then it is 50-58 DEG C in temperature, speed of agitator is 100-150r/
Carry out cross-linked graft reaction 2-2.5h under min, prepare slurry B；
S13: in the slurry B of step S12 add potassium hydroxide, regulation pH value be 9.3-9.7, be subsequently added into epoxychloropropane,
Carbamide, azo two isopropylformic acid. (acrylic acid ethylene glycol) ester, citrate, poly-propylene diene rubber, propyl trimethoxy silicane, then
Being 60-64 DEG C in temperature, speed of agitator is to carry out cross-linking reaction 1-1.2h under 100-160r/min, prepares slurry C；
S14: will add organic tin stabilizer in the slurry C of step S13, regulation pH value is 8-8.4, is warming up to 80-82 DEG C, gelatinizing
45-50min, gelatinizing is down to 32-36 DEG C after terminating, is added polyoxyethylene polyoxypropylene tetramethylolmethane ether, be 120-at rotating speed
Stir 8-12min under 150r/min, prepare adhesive；
S2: adhesive that step S1 is prepared, medical stone powder, polybutene plastics, Eucalyptus powder, fatty acid amide, silica gel, fire-retardant
Agent, smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS
Regulator, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
HIGH PRESSURE TREATMENT 1-2h under pressure is 9-11MPa, prepares raw material A；
S4: the raw material A that step S3 prepares is put into freezing 3-5h at temperature≤-20 DEG C, prepares raw material B；
S5: put in dehydrator by the raw material B that step S4 prepares, dries to water content≤4%, system at temperature is 82-85 DEG C
Obtain raw material C；
S6: raw material C step S5 prepared puts in blender, agitated rear prepared particle；
S7: put in extruder by the particle that step S6 prepares, extrudes at temperature is 195-210 DEG C, passes through air cooling way
Cooling molding, prepares novel stone wood plastic composite.
Further, speed of agitator described in step S6 is 200-400r/min.
Further, described mixing time is 12-18min.
Further, described speed of agitator is 400r/min, and mixing time is 12min.
Further, extrusion temperature described in step S7 is 195-210 DEG C.
Further, described extrusion temperature is 210 DEG C.
Further, cool down molding described in step 7 and use air cooling way cooling molding.
The method have the advantages that
(1) the novel stone wood plastic composite of the present invention has high flame resistance and smoke suppressing effect, at high temperature will not discharge and have
Poison harmful substance, it is to avoid the secondary injury to human body；
(2) heat-proof quality of the novel stone wood plastic composite of the present invention is the best, it is to avoid the scald to human body, and has very well
Insulating properties；
(3) the novel stone wood plastic composite material of the present invention is fine and close, and mechanical property is good, extremely durable.
(4) the novel stone wood plastic composite good flame retardation effect of the present invention, strong shock resistance, toughness is strong, and water absorption rate is little,
Not only obtain excellent fire resistance but also maintain the novel preferable mechanical property of stone wood plastic composite, be that a kind of performance is excellent
Novel stone wood plastic composite, can be widely applied to hotel, restaurant, building decoration and fitment, has significant economic and social benefit.
Detailed description of the invention
For ease of being more fully understood that the present invention, being illustrated by following example, these embodiments belong to the present invention's
Protection domain, but it is not intended to protection scope of the present invention.
In an embodiment, described novel stone wood plastic composite, in units of weight portion, including following raw material: Maifanitum
Powder 82-100 part, polybutene plastics 42-60 part, Eucalyptus powder 21-30 part, adhesive 8-14 part, fatty acid amide 0.6-1.2 part,
Silica gel 0.6-1 part, fire retardant 0.6-0.8 part, smoke suppressant 0.5-0.8 part, aerogel generating agent 0.4-0.5 part, titanate esters coupling
Agent 0.6-0.7 part, PP-g-MAH compatilizer 0.3-0.6 part, WINGSTAYL antioxidant 0.2-0.6 part, JINHASS regulator
0.3-0.7 part, hardening agent 0.3-0.8 part, PAFC 0.6-0.9 part, dinoctyl phthalate 0.5-0.8 part,
Potassium stearate 0.2-0.4 part, styrene 0.2-0.3 part；
Described fire retardant is in units of weight portion, including following raw material: antimony oxide 5-8 part, VTES
3-5 part, triethyl phosphate 3-4 part, magnesium chloride 5-7 part, phenolic resin 2-4 part, bentonite 0.6-1 part；
Described smoke suppressant is in units of weight portion, including following raw material: zinc molybdate 8-14 part, aluminium hydroxide 6-10 part, dolomite
Powder 2-3 part, copper oxide 1-2 part；
Described hardening agent is in units of weight portion, including following raw material: ethyl butenoic acid ethyl 10-20 part, phosphoric acid vinyl acetate 8-
15 parts, cobalt naphthenate 3-6 part, aluminum chloride 2-4 part；
The preparation method of described novel stone wood plastic composite, comprises the following steps:
S1: prepare adhesive, its preparation method, comprise the following steps:
S11: compound concentration be 20-30Be ', pH value be para arrowroot slurry A of 3.4-3.7；
S12: in para arrowroot slurry A of step S11 add concentration be the triglyceride of 2%-4%, percarbamide, 2,5-diformazan
Base-2,5-double (benzoyl peroxide)-hexane, Raney nickel, then it is 50-58 DEG C in temperature, speed of agitator is 100-150r/
Carry out cross-linked graft reaction 2-2.5h under min, prepare slurry B；
S13: in the slurry B of step S12 add potassium hydroxide, regulation pH value be 9.3-9.7, be subsequently added into epoxychloropropane,
Carbamide, azo two isopropylformic acid. (acrylic acid ethylene glycol) ester, citrate, poly-propylene diene rubber, propyl trimethoxy silicane, then
Being 60-64 DEG C in temperature, speed of agitator is to carry out cross-linking reaction 1-1.2h under 100-160r/min, prepares slurry C；
S14: will add organic tin stabilizer in the slurry C of step S13, regulation pH value is 8-8.4, is warming up to 80-82 DEG C, gelatinizing
45-50min, gelatinizing is down to 32-36 DEG C after terminating, is added polyoxyethylene polyoxypropylene tetramethylolmethane ether, be 120-at rotating speed
Stir 8-12min under 150r/min, prepare adhesive；
S2: adhesive that step S1 is prepared, medical stone powder, polybutene plastics, Eucalyptus powder, fatty acid amide, silica gel, fire-retardant
Agent, smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS
Regulator, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
HIGH PRESSURE TREATMENT 1-2h under pressure is 9-11MPa, prepares raw material A；
S4: the raw material A that step S3 prepares is put into freezing 3-5h at temperature≤-20 DEG C, prepares raw material B；
S5: put in dehydrator by the raw material B that step S4 prepares, dries to water content≤4%, system at temperature is 82-85 DEG C
Obtain raw material C；
S6: raw material C step S5 prepared puts in blender, stirs 12-18min, system under rotating speed is 200-400r/min
Obtain particle；
S7: put in extruder by the particle that step S6 prepares, extrudes at temperature is 195-210 DEG C, passes through air cooling way
Cooling molding, prepares novel stone wood plastic composite.
Below by more specifically embodiment, the present invention will be described.
Embodiment 1
A kind of novel stone wood plastic composite, in units of weight portion, including following raw material: medical stone powder 90 parts, polybutene are moulded
Expect 50 parts, 25 parts of Eucalyptus powder, adhesive 12 parts, fatty acid amide 0.9 part, 0.8 part of silica gel, fire retardant 0.7 part, smoke suppressant 0.7
Part, aerogel generating agent 0.4 part, titanate coupling agent 0.6 part, PP-g-MAH compatilizer 0.5 part, WINGSTAYL antioxidant
0.4 part, JINHASS regulator 0.5 part, hardening agent 0.6 part, PAFC 0.8 part, dinoctyl phthalate 0.7
Part, potassium stearate 0.3 part, styrene 0.2 part；
Described fire retardant is in units of weight portion, including following raw material: antimony oxide 7 parts, VTES 4
Part, triethyl phosphate 3.5 parts, 6 parts of magnesium chloride, 3 parts of phenolic resin, bentonite 0.8 part；
Described smoke suppressant is in units of weight portion, including following raw material: zinc molybdate 12 parts, aluminium hydroxide 8 parts, dolomite dust 2.5
Part, copper oxide 1.5 parts；
Described hardening agent is in units of weight portion, including following raw material: ethyl butenoic acid ethyl 15 parts, phosphoric acid vinyl acetate 12 parts,
Cobalt naphthenate 5 parts, 3 parts of aluminum chloride；
The preparation method of described novel stone wood plastic composite, comprises the following steps:
S1: prepare adhesive, its preparation method, comprise the following steps:
S11: compound concentration be 25Be ', pH value be para arrowroot slurry A of 3.6；
S12: in para arrowroot slurry A of step S11 add concentration be 3% triglyceride, percarbamide, 2,5-dimethyl-2,
5-double (benzoyl peroxide)-hexane, Raney nickel, be then 55 DEG C in temperature, and speed of agitator is to cross-link under 130r/min
Graft reaction 2.2h, prepares slurry B；
S13: adding potassium hydroxide in the slurry B of step S12, regulation pH value is 9.5, is subsequently added into epoxychloropropane, urine
Element, azo two isopropylformic acid. (acrylic acid ethylene glycol) ester, citrate, poly-propylene diene rubber, propyl trimethoxy silicane, then exist
Temperature is 62 DEG C, and speed of agitator is to carry out cross-linking reaction 1.1h under 130r/min, prepares slurry C；
S14: will add organic tin stabilizer in the slurry C of step S13, regulation pH value is 8.2, is warming up to 81 DEG C, gelatinizing
48min, gelatinizing is down to 34 DEG C, is added polyoxyethylene polyoxypropylene tetramethylolmethane ether, stir under rotating speed is 140r/min after terminating
Mix 10min, prepare adhesive；
S2: adhesive that step S1 is prepared, medical stone powder, polybutene plastics, Eucalyptus powder, fatty acid amide, silica gel, fire-retardant
Agent, smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS
Regulator, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
HIGH PRESSURE TREATMENT 1.5h under pressure is 10MPa, prepares raw material A；
S4: the raw material A that step S3 prepares is put into freezing 5h at temperature is-20 DEG C, prepares raw material B；
S5: put in dehydrator by the raw material B that step S4 prepares, drying at temperature is 83 DEG C to water content is 4%, prepares
Raw material C；
S6: raw material C step S5 prepared puts in blender, stirs 15min under rotating speed is 300r/min, prepares particle；
S7: put in extruder by the particle that step S6 prepares, is extruded at temperature is 200 DEG C, is cooled down by air cooling way
Molding, prepares novel stone wood plastic composite.
Embodiment 2
A kind of novel stone wood plastic composite, in units of weight portion, including following raw material: medical stone powder 82 parts, polybutene are moulded
Expect 42 parts, 21 parts of Eucalyptus powder, adhesive 8 parts, fatty acid amide 0.6 part, 0.6 part of silica gel, fire retardant 0.6 part, smoke suppressant 0.5
Part, aerogel generating agent 0.4 part, titanate coupling agent 0.6 part, PP-g-MAH compatilizer 0.3 part, WINGSTAYL antioxidant
0.2 part, JINHASS regulator 0.3 part, hardening agent 0.3 part, PAFC 0.6 part, dinoctyl phthalate 0.5
Part, potassium stearate 0.2 part, styrene 0.2 part；
Described fire retardant is in units of weight portion, including following raw material: antimony oxide 5 parts, VTES 3
Part, triethyl phosphate 3 parts, 5 parts of magnesium chloride, 2 parts of phenolic resin, bentonite 0.6 part；
Described smoke suppressant is in units of weight portion, including following raw material: zinc molybdate 8 parts, aluminium hydroxide 6 parts, dolomite dust 2 parts,
Copper oxide 1 part；
Described hardening agent is in units of weight portion, including following raw material: ethyl butenoic acid ethyl 10 parts, phosphoric acid vinyl acetate 8 parts, ring
Alkanoic acid cobalt 3 parts, 2 parts of aluminum chloride；
The preparation method of described novel stone wood plastic composite, comprises the following steps:
S1: prepare adhesive, its preparation method, comprise the following steps:
S11: compound concentration be 20Be ', pH value be para arrowroot slurry A of 3.4；
S12: in para arrowroot slurry A of step S11 add concentration be 2% triglyceride, percarbamide, 2,5-dimethyl-2,
5-double (benzoyl peroxide)-hexane, Raney nickel, be then 50 DEG C in temperature, and speed of agitator is to cross-link under 100r/min
Graft reaction 2.5h, prepares slurry B；
S13: adding potassium hydroxide in the slurry B of step S12, regulation pH value is 9.3, is subsequently added into epoxychloropropane, urine
Element, azo two isopropylformic acid. (acrylic acid ethylene glycol) ester, citrate, poly-propylene diene rubber, propyl trimethoxy silicane, then exist
Temperature is 60 DEG C, and speed of agitator is to carry out cross-linking reaction 1.2h under 100r/min, prepares slurry C；
S14: will add organic tin stabilizer in the slurry C of step S13, regulation pH value is 8, is warming up to 80 DEG C, gelatinizing 45min,
Gelatinizing is down to 32 DEG C after terminating, add polyoxyethylene polyoxypropylene tetramethylolmethane ether, stirs under rotating speed is 120r/min
12min, prepares adhesive；
S2: adhesive that step S1 is prepared, medical stone powder, polybutene plastics, Eucalyptus powder, fatty acid amide, silica gel, fire-retardant
Agent, smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS
Regulator, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
HIGH PRESSURE TREATMENT 2h under pressure is 9MPa, prepares raw material A；
S4: the raw material A that step S3 prepares is put into freezing 4h at temperature is-18 DEG C, prepares raw material B；
S5: put in dehydrator by the raw material B that step S4 prepares, drying at temperature is 82 DEG C to water content is 3%, prepares
Raw material C；
S6: raw material C step S5 prepared puts in blender, stirs 18min under rotating speed is 200r/min, prepares particle；
S7: put in extruder by the particle that step S6 prepares, is extruded at temperature is 195 DEG C, is cooled down by air cooling way
Molding, prepares novel stone wood plastic composite.
Embodiment 3
A kind of novel stone wood plastic composite, in units of weight portion, including following raw material: medical stone powder 100 parts, polybutene are moulded
Expect 60 parts, 30 parts of Eucalyptus powder, adhesive 14 parts, fatty acid amide 1.2 parts, 1 part of silica gel, fire retardant 0.8 part, smoke suppressant 0.8 part,
Aerogel generating agent 0.5 part, titanate coupling agent 0.7 part, PP-g-MAH compatilizer 0.6 part, WINGSTAYL antioxidant 0.6
Part, JINHASS regulator 0.7 part, hardening agent 0.8 part, PAFC 0.9 part, dinoctyl phthalate 0.8 part,
Potassium stearate 0.4 part, styrene 0.3 part；
Described fire retardant is in units of weight portion, including following raw material: antimony oxide 8 parts, VTES 5
Part, triethyl phosphate 4 parts, 7 parts of magnesium chloride, 4 parts of phenolic resin, bentonite 1 part；
Described smoke suppressant is in units of weight portion, including following raw material: zinc molybdate 14 parts, aluminium hydroxide 10 parts, dolomite dust 3
Part, copper oxide 2 parts；
Described hardening agent is in units of weight portion, including following raw material: ethyl butenoic acid ethyl 20 parts, phosphoric acid vinyl acetate 15 parts,
Cobalt naphthenate 6 parts, 4 parts of aluminum chloride；
The preparation method of described novel stone wood plastic composite, comprises the following steps:
S1: prepare adhesive, its preparation method, comprise the following steps:
S11: compound concentration be 30Be ', pH value be para arrowroot slurry A of 3.7；
S12: in para arrowroot slurry A of step S11 add concentration be 4% triglyceride, percarbamide, 2,5-dimethyl-2,
5-double (benzoyl peroxide)-hexane, Raney nickel, be then 58 DEG C in temperature, and speed of agitator is to cross-link under 150r/min
Graft reaction 2h, prepares slurry B；
S13: adding potassium hydroxide in the slurry B of step S12, regulation pH value is 9.7, is subsequently added into epoxychloropropane, urine
Element, azo two isopropylformic acid. (acrylic acid ethylene glycol) ester, citrate, poly-propylene diene rubber, propyl trimethoxy silicane, then exist
Temperature is 64 DEG C, and speed of agitator is to carry out cross-linking reaction 1h under 160r/min, prepares slurry C；
S14: will add organic tin stabilizer in the slurry C of step S13, regulation pH value is 8.4, is warming up to 82 DEG C, gelatinizing
50min, gelatinizing is down to 36 DEG C, is added polyoxyethylene polyoxypropylene tetramethylolmethane ether, stir under rotating speed is 150r/min after terminating
Mix 8min, prepare adhesive；
S2: adhesive that step S1 is prepared, medical stone powder, polybutene plastics, Eucalyptus powder, fatty acid amide, silica gel, fire-retardant
Agent, smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS
Regulator, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
HIGH PRESSURE TREATMENT 1h under pressure is 11MPa, prepares raw material A；
S4: the raw material A that step S3 prepares is put into freezing 3h at temperature is-15 DEG C, prepares raw material B；
S5: put in dehydrator by the raw material B that step S4 prepares, drying at temperature is 85 DEG C to water content is 2%, prepares
Raw material C；
S6: raw material C step S5 prepared puts in blender, stirs 12min under rotating speed is 400r/min, prepares particle；
S7: put in extruder by the particle that step S6 prepares, is extruded at temperature is 210 DEG C, is cooled down by air cooling way
Molding, prepares novel stone wood plastic composite.
The composite can be widely applied to hotel, restaurant, building decoration and fitment, good flame retardation effect, it is impossible to burn and form fire
Flame, stable and reliable for performance, its performance indications are tested by following fire resistance test experiments and Mechanics Performance Testing and are given:
(1) fire resistance test experiments
Sample prepared by above-described embodiment 1-3 is tailored into the platelet of standard, then uses oxygen index measurer HC-2(Nanjing
Jiangning District analytical tool factory) and analytical tool factory of horizontal vertical burning analyzer CZF-3(Jiangning county) respectively to novel
Stone wood plastic composite carries out oxygen index (OI) and combustibility and measures, oxygen index (OI) 37%-40%, horizontal vertical combustibility without catching fire,
Cigarette is light, and flame retardant effect is good.
(2) Mechanics Performance Testing experiment
Sample prepared by above-described embodiment 1-3 tailors growth 115mm, wide 10mm, the standard platelet of thick 2.5mm, then uses
Tester for elongation 5585(American I NSTRON) and impact specimen machine ZBC1251-B(Mei Tesi industrial system company) respectively to newly
Type stone wood plastic composite carries out stretching and impact test, tensile figure (maximum pull, unit: N) 855.45-923.98, punching
Hit index (toughness, non-notch), unit: ki/m2, 6.312-6.578, note: draw speed is 2mm/min.
(3) other performance indications
Sample prepared by above-described embodiment 1-3 tailors growth 115mm, wide 10mm, the standard platelet of thick 2.5mm, detection bending
Intensity, bending modulus, shore hardness, water absorption rate, result is as shown in the table.
In sum, the novel stone wood plastic composite good flame retardation effect of the present invention, strong shock resistance, toughness is strong, water absorption rate
Little, not only obtain excellent fire resistance but also maintain the novel preferable mechanical property of stone wood plastic composite, be a kind of performance
Excellent novel stone wood plastic composite, can be applicable, have significant economic and social benefit.
Above content it cannot be assumed that the present invention be embodied as be confined to these explanation, technology belonging to the present invention is led
For the those of ordinary skill in territory, without departing from the inventive concept of the premise, it is also possible to make some simple deduction or replace,
All should be considered as belonging to the scope of patent protection that the present invention is determined by the claims submitted to.
Claims (7)
1. a novel stone wood plastic composite, it is characterised in that in units of weight portion, including following raw material: medical stone powder
82-100 part, polybutene plastics 42-60 part, Eucalyptus powder 21-30 part, adhesive 8-14 part, fatty acid amide 0.6-1.2 part, silicon
Glue 0.6-1 part, fire retardant 0.6-0.8 part, smoke suppressant 0.5-0.8 part, aerogel generating agent 0.4-0.5 part, titanate coupling agent
0.6-0.7 part, PP-g-MAH compatilizer 0.3-0.6 part, WINGSTAYL antioxidant 0.2-0.6 part, JINHASS regulator
0.3-0.7 part, hardening agent 0.3-0.8 part, PAFC 0.6-0.9 part, dinoctyl phthalate 0.5-0.8 part,
Potassium stearate 0.2-0.4 part, styrene 0.2-0.3 part；
Described fire retardant is in units of weight portion, including following raw material: antimony oxide 5-8 part, VTES
3-5 part, triethyl phosphate 3-4 part, magnesium chloride 5-7 part, phenolic resin 2-4 part, bentonite 0.6-1 part；
Described smoke suppressant is in units of weight portion, including following raw material: zinc molybdate 8-14 part, aluminium hydroxide 6-10 part, dolomite
Powder 2-3 part, copper oxide 1-2 part；
Described hardening agent is in units of weight portion, including following raw material: ethyl butenoic acid ethyl 10-20 part, phosphoric acid vinyl acetate 8-
15 parts, cobalt naphthenate 3-6 part, aluminum chloride 2-4 part；
The preparation method of described novel stone wood plastic composite, comprises the following steps:
S1: prepare adhesive, its preparation method, comprise the following steps:
S11: compound concentration be 20-30Be ', pH value be para arrowroot slurry A of 3.4-3.7；
S12: in para arrowroot slurry A of step S11 add concentration be the triglyceride of 2%-4%, percarbamide, 2,5-diformazan
Base-2,5-double (benzoyl peroxide)-hexane, Raney nickel, then it is 50-58 DEG C in temperature, speed of agitator is 100-150r/
Carry out cross-linked graft reaction 2-2.5h under min, prepare slurry B；
S13: in the slurry B of step S12 add potassium hydroxide, regulation pH value be 9.3-9.7, be subsequently added into epoxychloropropane,
Carbamide, azo two isopropylformic acid. (acrylic acid ethylene glycol) ester, citrate, poly-propylene diene rubber, propyl trimethoxy silicane, then
Being 60-64 DEG C in temperature, speed of agitator is to carry out cross-linking reaction 1-1.2h under 100-160r/min, prepares slurry C；
S14: will add organic tin stabilizer in the slurry C of step S13, regulation pH value is 8-8.4, is warming up to 80-82 DEG C, gelatinizing
45-50min, gelatinizing is down to 32-36 DEG C after terminating, is added polyoxyethylene polyoxypropylene tetramethylolmethane ether, be 120-at rotating speed
Stir 8-12min under 150r/min, prepare adhesive；
S2: adhesive that step S1 is prepared, medical stone powder, polybutene plastics, Eucalyptus powder, fatty acid amide, silica gel, fire-retardant
Agent, smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS
Regulator, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
HIGH PRESSURE TREATMENT 1-2h under pressure is 9-11MPa, prepares raw material A；
S4: the raw material A that step S3 prepares is put into freezing 3-5h at temperature≤-20 DEG C, prepares raw material B；
S5: put in dehydrator by the raw material B that step S4 prepares, dries to water content≤4%, system at temperature is 82-85 DEG C
Obtain raw material C；
S6: raw material C step S5 prepared puts in blender, agitated rear prepared particle；
S7: put in extruder by the particle that step S6 prepares, extrudes at temperature is 195-210 DEG C, passes through air cooling way
Cooling molding, prepares novel stone wood plastic composite.
Novel stone wood plastic composite the most according to claim 1, it is characterised in that speed of agitator described in step S6 is
200-400r/min。
Novel stone wood plastic composite the most according to claim 2, it is characterised in that described mixing time is 12-
18min。
Novel stone wood plastic composite the most according to claim 3, it is characterised in that described speed of agitator is 400r/
Min, mixing time is 12min.
Novel stone wood plastic composite the most according to claim 1, it is characterised in that extrusion temperature described in step S7 is
195-210℃。
Novel stone wood plastic composite the most according to claim 5, it is characterised in that described extrusion temperature is 210 DEG C.
Novel stone wood plastic composite the most according to claim 1, it is characterised in that cool down molding described in step 7 and adopt
Molding is cooled down with air cooling way.
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| CN201610704682.3A CN106046575A (en) | 2016-08-22 | 2016-08-22 | Novel stone wood-plastic composite material |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610704682.3A CN106046575A (en) | 2016-08-22 | 2016-08-22 | Novel stone wood-plastic composite material |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106833000A (en) * | 2017-03-12 | 2017-06-13 | 广西丰达三维科技有限公司 | A kind of flame retardant type stone wood plastic composite, preparation method and applications |
| CN106832594A (en) * | 2017-03-12 | 2017-06-13 | 广西丰达三维科技有限公司 | A kind of new technology for producing stone wood plastic sectional printed material |
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|---|---|---|---|---|
| CN1420139A (en) * | 2001-11-15 | 2003-05-28 | 晓威国际有限公司 | Ecological environment material nd mfg. method thereof |
| CN102352068A (en) * | 2011-08-01 | 2012-02-15 | 广东晨宝复合材料有限公司 | Wood stone plastic composite material |
| CN102558894A (en) * | 2012-02-21 | 2012-07-11 | 常熟市方塔涂料化工有限公司 | Method for preparing wood-like mould composite material |
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- 2016-08-22 CN CN201610704682.3A patent/CN106046575A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1420139A (en) * | 2001-11-15 | 2003-05-28 | 晓威国际有限公司 | Ecological environment material nd mfg. method thereof |
| CN102352068A (en) * | 2011-08-01 | 2012-02-15 | 广东晨宝复合材料有限公司 | Wood stone plastic composite material |
| CN102558894A (en) * | 2012-02-21 | 2012-07-11 | 常熟市方塔涂料化工有限公司 | Method for preparing wood-like mould composite material |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106833000A (en) * | 2017-03-12 | 2017-06-13 | 广西丰达三维科技有限公司 | A kind of flame retardant type stone wood plastic composite, preparation method and applications |
| CN106832594A (en) * | 2017-03-12 | 2017-06-13 | 广西丰达三维科技有限公司 | A kind of new technology for producing stone wood plastic sectional printed material |
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