CN109354755A - A kind of sole of shoe material and preparation method thereof - Google Patents
A kind of sole of shoe material and preparation method thereof Download PDFInfo
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- CN109354755A CN109354755A CN201811080653.XA CN201811080653A CN109354755A CN 109354755 A CN109354755 A CN 109354755A CN 201811080653 A CN201811080653 A CN 201811080653A CN 109354755 A CN109354755 A CN 109354755A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
-
- A—HUMAN NECESSITIES
- A43—FOOTWEAR
- A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
- A43B13/00—Soles; Sole-and-heel integral units
- A43B13/02—Soles; Sole-and-heel integral units characterised by the material
- A43B13/04—Plastics, rubber or vulcanised fibre
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0023—Use of organic additives containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0066—Use of inorganic compounding ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0095—Mixtures of at least two compounding ingredients belonging to different one-dot groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2400/00—Characterised by the use of unspecified polymers
- C08J2400/30—Polymeric waste or recycled polymer
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2423/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2423/16—Ethene-propene or ethene-propene-diene copolymers
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
The invention discloses a kind of sole of shoe materials, belong to shoes field, the raw material including following parts by weight meter: 30-40 parts of polyethylene vinegar ethylene, 5-15 parts of EVA particles, 6-12 parts of rubber, 15-25 parts of elastomer, EPDM5-15 parts of EPDM, 20-30 parts of recycled plastic modified materials, 2-5 parts of anti-wear agent, 2-4 parts of filler, 1-2 parts of stearic acid, 1-2 parts of bridge formation agent aid, 1-2 parts of zinc oxide, 2-4 parts of Masterbatch, 1-2 parts of bridging agent, 1-2 parts of foaming agent.There is good mechanical performance using sole made of material of the present invention, wearability is good, anti-skidding, deodorization and sole is softer, and waste and old plastics can be recycled by the present invention, environmental protection and reduces production cost.
Description
Technical field
The invention belongs to shoes field, it is related to a kind of sole of shoe material and preparation method thereof.
Background technique
Existing sole generally uses SBS main materials, is equipped with the auxiliary materials such as polystyrene, naphthenic oil, using this material
The sole of production is at high cost and performance is more general.In addition, generally existing in production plastics, Rubber & Rubber Products industry
The pernicious gas of association during ultimate product is formed when problem, useless defective goods cause serious pollution to the environment on periphery, mould
The phenomenon that service life of glue product abandons everywhere when reaching the limit of is on the rise, and the processing of especially plastic products causes not in time
Public hazards.
Summary of the invention
The needle above problem, the present invention provides a kind of sole of shoe materials and preparation method thereof.The purpose of the present invention is logical
The product being mixed using waste plastic, polybag and rubber etc. is crossed, with waste plastic is main former by different products
Material, configuration, production, preparation links in do not generate environmentally harmful substance, faced with the image of environment-friendly products
Consumer, and the defect ware Litter for being included in waste plastic classification field can be passed through by these methods and be recycled, most
The excellent product of lifelong output.
In order to solve the above technical problems, the technical scheme adopted by the invention is that: a kind of sole of shoe material, feature exist
In: the raw material including following parts by weight meter: 30-40 parts of polyethylene vinegar ethylene, 5-15 parts of EVA particles, 6-12 parts of rubber, bullet
15-25 parts of body of property, EPDM5-15 parts of EPDM, 20-30 parts of recycled plastic modified materials, 2-5 parts of anti-wear agent, 2-4 parts of filler,
1-2 parts of stearic acid, 1-2 parts of bridge formation agent aid, 1-2 parts of zinc oxide, 2-4 parts of Masterbatch, 1-2 parts of bridging agent, 1-2 parts of foaming agent.
Preferably, the raw material including following parts by weight meter: 35 parts of polyethylene vinegar ethylene, 10 parts of EVA particles, rubber 6
Part, it is 20 parts of elastomer, EPDM10 parts of EPDM, 25 parts of recycled plastic modified materials, 5 parts of anti-wear agent, 3.3 parts of filler, stearic
1.6 parts, 1.0 parts of bridge formation agent aid, 1.0 parts of zinc oxide, 3.0 parts of Masterbatch, 1.5 parts of bridging agent, 1.0 parts of foaming agent of acid.
It further, further include rubber pange reclaimed materials.
Further, the mass fraction of the rubber pange reclaimed materials is 80-150.
Further, the mass fraction of the rubber pange reclaimed materials is 100.
A kind of preparation method of sole of shoe material, step include:
(1) it develops: being set and be formulated by physical property, confirmation color, physical property, multiplying power, hardness and the journey of contraction after setting
Degree;
(2) foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid, titanium dioxide ingredient: are prepared according to formula
Weighting error value is 5g, and Masterbatch weighting error value is 0.1g, and foaming agent, bridge formation foaming agent, bridge formation agent aid separately pack son,
It convenient for multiple title, examines grammes per square metre whether accurate, the auxiliary material prepared is indicated into color, type body, number, date;
(3) mixing: EVA particles, filler, anti-wear agent are prepared according to formula, weighting error value ± 0.1kg moulds EVA
Micelle and configured foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid pour into mixing slot together, carry out
Pressurization production;Opening time 7-8 hours, setting air pressure reached 190-250 pa, and 92-98 DEG C of temperature, progress first time stirring simultaneously will
The dust on pressurization lid periphery is removed;Air pressure reaches 290-350 pa, and at 102-108 DEG C of temperature, carrying out second of stirring simultaneously will pressurization
The dust on lid periphery is removed;Air pressure reaches 390-450 pa, at 109-115 DEG C of temperature, carries out third time stirring simultaneously for pressurization lid week
The dust on side is removed, while being put into bridge formation foaming agent, and at this moment pressurization lid cannot be fully pressurized the bottom of to, because foaming agent is preheated to liquid
Know from experience and sprays and must dally 30 degree and can pressurize in right to the left;Stirring is primary at machine pressurization operating 60 seconds, when pressurization operates 120 seconds
Carry out second of stirring, when pressurization runs to 180 seconds, temperature is at 117-123 DEG C at this time, examine material whether beating, the rear OK
It can discharge.
(4) mill is granulated: first open mill is cleaned out first, sets 65-75 DEG C of open mill temperature, be granulated in trough,
Air hose, cooling bucket, the full sieve of vibration are cleaned out, and sets that pelletizer, die head, expects pipe, temperature as 85-95 DEG C, debug by open mill in slot
Material, is finally involved in pelletizer slot by good thin and thick, thickness setting: 5-8m/m, thin: 0.8-1m/m, by material extruding pelletization, setting
Grain length is 2m/m, opens cooling water, cooling wind, fan shaking screen, particle is finally sent into agitator.
(5) be put in storage: agitator, which is cleaned up, to enter bucket for particle, finished writing designation card, weight, pack, accomplished fluently sample
Test, is finally put in storage.
By the above-mentioned description of this invention it is found that compared to the prior art, the present invention has the advantage that
1, there is good mechanical performance using sole made of material of the present invention, wearability is good, anti-skidding, deodorization and sole
It is softer.
2, waste and old plastics can be recycled by the present invention, environmental protection and reduction production cost.
3, the present invention will not generate pernicious gas during the manufacturing, pollute environment.
Specific embodiment
In order to make the objectives, technical solutions, and advantages of the present invention clearer, by the following examples to the present invention
It is further elaborated.It should be appreciated that the specific embodiments described herein are merely illustrative of the present invention, it is not used to
Limit the present invention.
Embodiment 1
A kind of sole of shoe material, the raw material including following parts by weight meter: 35 parts of polyethylene vinegar ethylene, EVA particles 10
Part, 20 parts of elastomer, 6 parts of rubber, EPDM10 parts of EPDM, 25 parts of recycled plastic modified materials, 5 parts of anti-wear agent, filler 3.3
Part, 1.6 parts of stearic acid, 1.0 parts of bridge formation agent aid, 1.0 parts of zinc oxide, 3.0 parts of Masterbatch, 1.5 parts of bridging agent, foaming agent 1.0
Part, the mass fraction of rubber pange reclaimed materials is 100.
A kind of preparation method of sole of shoe material, step include:
(1) it develops: being set and be formulated by physical property, confirmation color, physical property, multiplying power, hardness and the journey of contraction after setting
Degree;
(2) foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid, titanium dioxide ingredient: are prepared according to formula
Electronic scale weighting error value is 5g, and Masterbatch electronic scale weighting error value is 0.1g, and foaming agent, is built bridge at bridge formation foaming agent
Whether agent aid separately packs son, claim convenient for multiple, examine grammes per square metre accurate, and the auxiliary material prepared is indicated color, type body, part
Number, date;
(3) mixing: EVA particles, filler, anti-wear agent are prepared according to formula, electronic scale weighting error value is
0.1kg falls EVA particles and configured foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid together
Enter mixing slot, carries out pressurization production;Opening time 7 hours, setting air pressure reached 220 pas, 95 DEG C of temperature, carried out first time stirring
And the dust on pressurization lid periphery is removed;Air pressure reaches 320 pas, at 105 DEG C of temperature, carries out second of stirring simultaneously for pressurization lid week
The dust on side is removed;Air pressure reaches 420 pas, and at 112 DEG C of temperature, it is simultaneously that the dust on pressurization lid periphery is clear to carry out third time stirring
It removes, while being put into bridge formation foaming agent, at this moment pressurization lid cannot be fully pressurized the bottom of to, because foaming agent is preheated to liquid and can spray palpus
Right dallies 30 degree and can pressurize to the left;Stirring is primary at machine pressurization operating 60 seconds, and pressurization carries out second when operating 120 seconds
Secondary stirring, pressurization is when running to 180 seconds, and temperature is at 117-123 DEG C at this time, examine material whether beating, can discharge after OK.
(4) mill is granulated: first first being cleaned out open mill, is set open mill temperature 70 C, is granulated in trough, wind
Pipe, cooling bucket, the full sieve of vibration are cleaned out, and set that pelletizer, die head, expects pipe, temperature as 90 DEG C, debugged thin by open mill in slot
Thickness, time thickness of standard, three times thin, one time material is finally involved in pelletizer slot by thickness, thickness setting: 5-8m/m, thin: 0.8-1m/
Material extruding pelletization is set grain length as 2m/m by m, is opened cooling water, cooling wind, fan shaking screen, is finally sent into particle and stirs
Bucket.
(5) be put in storage: agitator, which is cleaned up, to enter bucket for particle, finished writing designation card, weight, packed by 25kg, beat
Good sample test, last plate stack storage by 40 colors.
Embodiment 2
A kind of sole of shoe material, the raw material including following parts by weight meter: 30 parts of polyethylene vinegar ethylene, EVA particles 5
Part, 8 parts of rubber, 15 parts of elastomer, EPDM5 parts of EPDM, 20 parts of recycled plastic modified materials, 2 parts of anti-wear agent, 2 parts of filler,
1 part of stearic acid, 1.2 parts of bridge formation agent aid, 1.2 parts of zinc oxide, 2 parts of Masterbatch, 1 part of bridging agent, 1.2 parts of foaming agent, rubber hair
The mass fraction for steeping reclaimed materials is 80.
A kind of preparation method of sole of shoe material, step include:
(1) it develops: being set and be formulated by physical property, confirmation color, physical property, multiplying power, hardness and the journey of contraction after setting
Degree;
(2) foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid, titanium dioxide ingredient: are prepared according to formula
Electronic scale weighting error value is 5g, and Masterbatch electronic scale weighting error value is 0.1g, and foaming agent, is built bridge at bridge formation foaming agent
Whether agent aid separately packs son, claim convenient for multiple, examine grammes per square metre accurate, and the auxiliary material prepared is indicated color, type body, part
Number, date;
(3) mixing: EVA particles, filler, anti-wear agent are prepared according to formula, electronic scale weighting error value is
0.1kg falls EVA particles and configured foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid together
Enter mixing slot, carries out pressurization production;Opening time 7 hours, setting air pressure reached 220 pas, 95 DEG C of temperature, carried out first time stirring
And the dust on pressurization lid periphery is removed;Air pressure reaches 320 pas, at 105 DEG C of temperature, carries out second of stirring simultaneously for pressurization lid week
The dust on side is removed;Air pressure reaches 420 pas, and at 112 DEG C of temperature, it is simultaneously that the dust on pressurization lid periphery is clear to carry out third time stirring
It removes, while being put into bridge formation foaming agent, at this moment pressurization lid cannot be fully pressurized the bottom of to, because foaming agent is preheated to liquid and can spray palpus
Right dallies 30 degree and can pressurize to the left;Stirring is primary at machine pressurization operating 60 seconds, and pressurization carries out second when operating 120 seconds
Secondary stirring, pressurization is when running to 180 seconds, and temperature is at 117-123 DEG C at this time, examine material whether beating, can discharge after OK.
(4) mill is granulated: first first being cleaned out open mill, is set open mill temperature 70 C, is granulated in trough, wind
Pipe, cooling bucket, the full sieve of vibration are cleaned out, and set that pelletizer, die head, expects pipe, temperature as 90 DEG C, debugged thin by open mill in slot
Thickness, time thickness of standard, three times thin, one time material is finally involved in pelletizer slot by thickness, thickness setting: 5-8m/m, thin: 0.8-1m/
Material extruding pelletization is set grain length as 2m/m by m, is opened cooling water, cooling wind, fan shaking screen, is finally sent into particle and stirs
Bucket.
(5) be put in storage: agitator, which is cleaned up, to enter bucket for particle, finished writing designation card, weight, packed by 25kg, beat
Good sample test, last plate stack storage by 40 colors.
Embodiment 3
A kind of sole of shoe material, the raw material including following parts by weight meter: 40 parts of polyethylene vinegar ethylene, EVA particles 15
Part, 12 parts of rubber, 25 parts of elastomer, EPDM15 parts of EPDM, 30 parts of recycled plastic modified materials, 2.5 parts of anti-wear agent, filler
4 parts, 2 parts of stearic acid, 2 parts of bridge formation agent aid, 2 parts of zinc oxide, 4 parts of Masterbatch, 2 parts of bridging agent, 2 parts of foaming agent, rubber pange
The mass fraction of reclaimed materials is 150.
A kind of preparation method of sole of shoe material, step include:
(1) it develops: being set and be formulated by physical property, confirmation color, physical property, multiplying power, hardness and the journey of contraction after setting
Degree;
(2) foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid, titanium dioxide ingredient: are prepared according to formula
Electronic scale weighting error value is 5g, and Masterbatch electronic scale weighting error value is 0.1g, and foaming agent, is built bridge at bridge formation foaming agent
Whether agent aid separately packs son, claim convenient for multiple, examine grammes per square metre accurate, and the auxiliary material prepared is indicated color, type body, part
Number, date;
(3) mixing: EVA particles, filler, anti-wear agent are prepared according to formula, electronic scale weighting error value is
0.1kg falls EVA particles and configured foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid together
Enter mixing slot, carries out pressurization production;Opening time 7 hours, setting air pressure reached 220 pas, 95 DEG C of temperature, carried out first time stirring
And the dust on pressurization lid periphery is removed;Air pressure reaches 320 pas, at 105 DEG C of temperature, carries out second of stirring simultaneously for pressurization lid week
The dust on side is removed;Air pressure reaches 420 pas, and at 112 DEG C of temperature, it is simultaneously that the dust on pressurization lid periphery is clear to carry out third time stirring
It removes, while being put into bridge formation foaming agent, at this moment pressurization lid cannot be fully pressurized the bottom of to, because foaming agent is preheated to liquid and can spray palpus
Right dallies 30 degree and can pressurize to the left;Stirring is primary at machine pressurization operating 60 seconds, and pressurization carries out second when operating 120 seconds
Secondary stirring, pressurization is when running to 180 seconds, and temperature is at 117-123 DEG C at this time, examine material whether beating, can discharge after OK.
(4) mill is granulated: first first being cleaned out open mill, is set open mill temperature 70 C, is granulated in trough, wind
Pipe, cooling bucket, the full sieve of vibration are cleaned out, and set that pelletizer, die head, expects pipe, temperature as 90 DEG C, debugged thin by open mill in slot
Thickness, time thickness of standard, three times thin, one time material is finally involved in pelletizer slot by thickness, thickness setting: 5-8m/m, thin: 0.8-1m/
Material extruding pelletization is set grain length as 2m/m by m, is opened cooling water, cooling wind, fan shaking screen, is finally sent into particle and stirs
Bucket.
(5) be put in storage: agitator, which is cleaned up, to enter bucket for particle, finished writing designation card, weight, packed by 25kgg, beat
Good sample test, last plate stack storage by 40 colors.
The sole material of 1-3 of embodiment of the present invention preparation is tested for the property below, test result is shown in Table 1:
Project | To contrasting | Embodiment 1 | Embodiment 2 | Embodiment 3 |
Hardness | 50 | 40 | 42 | 43 |
Wearability/mm3 | 140 | 153 | 148 | 150 |
Rebound degree/% | 35 | 50 | 46 | 48 |
The foregoing is merely illustrative of the preferred embodiments of the present invention, is not intended to limit the invention, all in essence of the invention
Made any modifications, equivalent replacements, and improvements etc., should all be included in the protection scope of the present invention within mind and principle.
Claims (6)
1. a kind of sole of shoe material, it is characterised in that: the raw material including following parts by weight meter: 30-40 parts of polyethylene vinegar ethylene,
5-15 parts of EVA particles, 6-12 parts of rubber, 15-25 parts of elastomer, EPDM5-15 parts of EPDM, recycled plastic modified materials 20-
30 parts, 2-5 parts of anti-wear agent, 2-4 parts of filler, 1-2 parts of stearic acid, 1-2 parts of bridge formation agent aid, 1-2 parts of zinc oxide, Masterbatch 2-
4 parts, 1-2 parts of bridging agent, 1-2 parts of foaming agent.
2. a kind of sole of shoe material according to claim 1, it is characterised in that: the raw material including following parts by weight meter:
35 parts of polyethylene vinegar ethylene, 10 parts of EVA particles, 6 parts of rubber, 20 parts of elastomer, EPDM10 parts of EPDM, recycled plastic changes
25 parts of material of property, 5 parts of anti-wear agent, 3.3 parts of filler, 1.6 parts of stearic acid, 1.0 parts of bridge formation agent aid, 1.0 parts of zinc oxide, Masterbatch
3.0 parts, 1.5 parts of bridging agent, 1.0 parts of foaming agent.
3. a kind of sole of shoe material according to claim 1, it is characterised in that: further include rubber pange reclaimed materials.
4. a kind of sole of shoe material according to claim 4, it is characterised in that: the quality of the rubber pange reclaimed materials
Number is 80-150.
5. the shoes that a kind of sole according to claim 4 and vamp can be freely combined, it is characterised in that: the rubber hair
The mass fraction for steeping reclaimed materials is 100.
6. a kind of preparation method of sole of shoe material according to claim 1, it is characterised in that: step includes:
(1) it develops: being set and be formulated by physical property, confirmation color, physical property, multiplying power, hardness and the degree of contraction after setting;
(2) foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid, foaming agent, frame ingredient: are prepared according to formula
Whether bridge foaming agent, bridge formation agent aid separately pack son, claim convenient for multiple, examine grammes per square metre accurate, the auxiliary material prepared is indicated
Color, type body, number, date;
(3) EVA particles, filler, anti-wear agent, weighting error value ± 0.1kg, by EVA particles mixing: are prepared according to formula
And configured foaming agent, bridge formation foaming agent, titanium dioxide, Masterbatch, bridge formation agent aid pour into mixing slot together, pressurize
Production;Opening time 7-8 hours, setting air pressure reached 190-250 pa, 92-98 DEG C of temperature, carries out first time stirring and will pressurize
The dust on lid periphery is removed;Air pressure reaches 290-350 pa, at 102-108 DEG C of temperature, carries out second of stirring simultaneously for pressurization lid week
The dust on side is removed;Air pressure reaches 390-450 pa, at 109-115 DEG C of temperature, carries out third time stirring and by pressurization lid periphery
Dust is removed, while being put into bridge formation foaming agent, and at this moment pressurization lid cannot be fully pressurized the bottom of to, because foaming agent is preheated to liquid meeting
Spraying to dally 30 degree and can pressurize in right to the left;Stirring is primary at machine pressurization operating 60 seconds, and pressurization carries out when operating 120 seconds
Second of stirring, pressurization is when running to 180 seconds, and temperature is at 117-123 DEG C at this time, examine material whether beating, can go out after OK
Material.
(4) mill be granulated: first open mill is cleaned out first, set 65-75 DEG C of open mill temperature, be granulated trough in, air hose,
Cooling bucket, the full sieve of vibration are cleaned out, and set that pelletizer, die head, expects pipe, temperature as 85-95 DEG C, debugged thin by open mill in slot
Material is finally involved in pelletizer slot by thickness, thickness setting: 5-8m/m, thin: material extruding pelletization is set grain length by 0.8-1m/m
For 2m/m, cooling water, cooling wind, fan shaking screen are opened, particle is finally sent into agitator.
(5) be put in storage: agitator, which is cleaned up, to enter bucket for particle, finish writing designation card, weight, pack, accomplish fluently sample test,
Finally it is put in storage.
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CN201811080653.XA CN109354755A (en) | 2018-09-17 | 2018-09-17 | A kind of sole of shoe material and preparation method thereof |
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CN201811080653.XA CN109354755A (en) | 2018-09-17 | 2018-09-17 | A kind of sole of shoe material and preparation method thereof |
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CN109354755A true CN109354755A (en) | 2019-02-19 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115141425A (en) * | 2022-08-09 | 2022-10-04 | 杭州朴西生活家居有限公司 | High-elasticity EVA sole material and preparation method thereof |
Citations (4)
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CN102993546A (en) * | 2012-08-13 | 2013-03-27 | 茂泰(福建)鞋材有限公司 | High-elasticity light-weight rubber-plastic foam material with good wear resistance and preparation method of foam material |
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