CN106317657A - Stone-wood-plastic material - Google Patents
Stone-wood-plastic material Download PDFInfo
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- CN106317657A CN106317657A CN201610704681.9A CN201610704681A CN106317657A CN 106317657 A CN106317657 A CN 106317657A CN 201610704681 A CN201610704681 A CN 201610704681A CN 106317657 A CN106317657 A CN 106317657A
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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
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
- C08B31/003—Crosslinking of starch
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J103/00—Adhesives based on starch, amylose or amylopectin or on their derivatives or degradation products
- C09J103/04—Starch derivatives
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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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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a stone-wood-plastic material which is prepared from heavy calcium carbonate powder, polyhexylene plastic, poplar powder, an adhesive, fatty acid amide, silica gel, a flame retardant, a smoke inhibitor, an aerosol generator, a titanate coupling agent, a PP-g-MAH (polypropylene graft maleic anhydride) compatilizer, a WINGSTAYL antioxidant, a JINHASS regulator, a reinforcer, polyaluminum ferric chloride, di-n-octyl phthalate, potassium stearate and styrene. The stone-wood-plastic material has the advantages of favorable flame-retardant effect, high impact resistance, high toughness and low water absorptivity, obtains excellent flame retardancy on the premise of keeping favorable mechanical properties of the stone-wood-plastic material, is a stone-wood-plastic material with favorable properties, can be widely used for decorating hotels, restaurants and buildings, and has obvious economic 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 stone Wood-plastic material.
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 stone wood plastic composite, but, due to problems such as interface compatibilities, the mechanical performance of the composite finally given is relatively
Difference.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of stone Wood-plastic material, to solve adding of fire retardant in prior art
Add the mechanical property that can deteriorate wood plastic composite, and introducing stone powder is for molding stone wood plastic composite, owing to interface is compatible
The problems such as property, the problem such as the mechanical performance of the composite finally given is poor.The stone Wood-plastic material good flame retardation effect of the present invention,
Strong shock resistance, toughness is strong, and water absorption rate is little, not only obtains excellent fire resistance but also maintain the preferable power of stone Wood-plastic material
Learn performance, be the excellent stone Wood-plastic material of a kind of performance, can be widely applied to hotel, restaurant, building decoration and fitment, have significant warp
Ji and social benefit.
In order to solve above technical problem, the present invention by the following technical solutions:
A kind of stone Wood-plastic material, in units of weight portion, including following raw material: dicalcium powder 82-98 part, polyhexene plastics 42-58
Part, Poplar Powder 21-29 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 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 stone Wood-plastic material, 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: by step S1 prepare adhesive, dicalcium powder, polyhexene plastics, Poplar Powder, fatty acid amide, silica gel, fire retardant,
Smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS adjust
Joint agent, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
Pressure is HIGH PRESSURE TREATMENT 1-2h under 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 stone Wood-plastic material.
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 stone Wood-plastic material of the present invention has high flame resistance and smoke suppressing effect, at high temperature will not discharge venomous injurant
Matter, it is to avoid the secondary injury to human body；
(2) heat-proof quality of the stone Wood-plastic material of the present invention is the best, it is to avoid the scald to human body, and has well insulation
Property；
(3) the stone Wood-plastic material material of the present invention is fine and close, and mechanical property is good, extremely durable.
(4) the stone Wood-plastic material good flame retardation effect of the present invention, strong shock resistance, toughness is strong, and water absorption rate is little, both obtains
Excellent fire resistance maintains again the preferable mechanical property of stone Wood-plastic material, is the excellent stone Wood-plastic material of a kind of performance, can be wide
General it is 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 stone Wood-plastic material, in units of weight portion, including following raw material: dicalcium powder 82-98 part,
Polyhexene plastics 42-58 part, Poplar Powder 21-29 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 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, strong
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 stone Wood-plastic material, 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: by step S1 prepare adhesive, dicalcium powder, polyhexene plastics, Poplar Powder, fatty acid amide, silica gel, fire retardant,
Smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS adjust
Joint agent, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
Pressure is HIGH PRESSURE TREATMENT 1-2h under 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 stone Wood-plastic material.
Below by more specifically embodiment, the present invention will be described.
Embodiment 1
A kind of stone Wood-plastic material, in units of weight portion, including following raw material: dicalcium powder 90 parts, 50 parts of polyhexene plastics, poplar
25 parts of 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, aerosol are sent out
Raw 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, tristearin
Acid 0.3 part of potassium, 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 stone Wood-plastic material, 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: by step S1 prepare adhesive, dicalcium powder, polyhexene plastics, Poplar Powder, fatty acid amide, silica gel, fire retardant,
Smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS adjust
Joint agent, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
Pressure is HIGH PRESSURE TREATMENT 1.5h under 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 stone Wood-plastic material.
Embodiment 2
A kind of stone Wood-plastic material, in units of weight portion, including following raw material: dicalcium powder 82 parts, 42 parts of polyhexene plastics, poplar
21 parts of 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, aerosol occur
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 stone Wood-plastic material, 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: by step S1 prepare adhesive, dicalcium powder, polyhexene plastics, Poplar Powder, fatty acid amide, silica gel, fire retardant,
Smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS adjust
Joint agent, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
Pressure is HIGH PRESSURE TREATMENT 2h under 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 stone Wood-plastic material.
Embodiment 3
A kind of stone Wood-plastic material, in units of weight portion, including following raw material: dicalcium powder 98 parts, 58 parts of polyhexene plastics, poplar
29 parts of 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, aerosol occur
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 stone Wood-plastic material, 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: by step S1 prepare adhesive, dicalcium powder, polyhexene plastics, Poplar Powder, fatty acid amide, silica gel, fire retardant,
Smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS adjust
Joint agent, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
Pressure is HIGH PRESSURE TREATMENT 1h under 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 stone Wood-plastic material.
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 stone wood
Moulding material carries out oxygen index (OI) and combustibility measures, oxygen index (OI) 37%-41%, and horizontal vertical combustibility is without catching fire, and cigarette is light, fire-retardant
Respond well.
(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 stone
Wood-plastic material carries out stretching and impact test, tensile figure (maximum pull, unit: N) 855.35-923.92, Impact Index
(toughness, non-notch), unit: ki/m2, 6.326-6.569, 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 stone Wood-plastic material good flame retardation effect of the present invention, strong shock resistance, toughness is strong, and water absorption rate is little, both
Obtain excellent fire resistance and maintain again the preferable mechanical property of stone Wood-plastic material, be the excellent stone wood plastic of a kind of performance
Material, 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 stone Wood-plastic material, it is characterised in that in units of weight portion, including following raw material: dicalcium powder 82-98 part, poly-
Hexene plastics 42-58 part, Poplar Powder 21-29 part, adhesive 8-14 part, fatty acid amide 0.6-1.2 part, silica gel 0.6-1 part, resistance
Combustion 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, strengthening
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 stone Wood-plastic material, 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: by step S1 prepare adhesive, dicalcium powder, polyhexene plastics, Poplar Powder, fatty acid amide, silica gel, fire retardant,
Smoke suppressant, aerogel generating agent, titanate coupling agent, PP-g-MAH compatilizer, WINGSTAYL antioxidant, JINHASS adjust
Joint agent, hardening agent, PAFC, dinoctyl phthalate, potassium stearate, styrene are put in pressure cooker,
Pressure is HIGH PRESSURE TREATMENT 1-2h under 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 stone Wood-plastic material.
Stone Wood-plastic material the most according to claim 1, it is characterised in that speed of agitator described in step S6 is 200-
400r/min。
Stone Wood-plastic material the most according to claim 2, it is characterised in that described mixing time is 12-18min.
Stone Wood-plastic material the most according to claim 3, it is characterised in that described speed of agitator is 400r/min, during stirring
Between be 12min.
Stone Wood-plastic material the most according to claim 1, it is characterised in that extrusion temperature described in step S7 is 195-210
℃。
Stone Wood-plastic material the most according to claim 5, it is characterised in that described extrusion temperature is 210 DEG C.
Stone Wood-plastic material the most according to claim 1, it is characterised in that cool down molding described in step 7 and use air-cooled side
Formula cooling molding.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610704681.9A CN106317657A (en) | 2016-08-22 | 2016-08-22 | Stone-wood-plastic material |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610704681.9A CN106317657A (en) | 2016-08-22 | 2016-08-22 | Stone-wood-plastic material |
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| CN106317657A true CN106317657A (en) | 2017-01-11 |
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| Application Number | Title | Priority Date | Filing Date |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106867215A (en) * | 2017-03-12 | 2017-06-20 | 广西丰达三维科技有限公司 | A kind of stone Wood-plastic material strong with toughness and its application |
| CN106867216A (en) * | 2017-03-12 | 2017-06-20 | 广西丰达三维科技有限公司 | A kind of stone Wood-plastic material with high heat distortion temperature |
| CN106893283A (en) * | 2017-03-12 | 2017-06-27 | 广西丰达三维科技有限公司 | A kind of printing consumables with high impact-resistance and preparation method thereof |
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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
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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 (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106867215A (en) * | 2017-03-12 | 2017-06-20 | 广西丰达三维科技有限公司 | A kind of stone Wood-plastic material strong with toughness and its application |
| CN106867216A (en) * | 2017-03-12 | 2017-06-20 | 广西丰达三维科技有限公司 | A kind of stone Wood-plastic material with high heat distortion temperature |
| CN106893283A (en) * | 2017-03-12 | 2017-06-27 | 广西丰达三维科技有限公司 | A kind of printing consumables with high impact-resistance and preparation method thereof |
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Application publication date: 20170111 |