CN106893226A - A kind of high resiliency high temperature resistant elastomeric material and preparation method - Google Patents
A kind of high resiliency high temperature resistant elastomeric material and preparation method Download PDFInfo
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- CN106893226A CN106893226A CN201710131884.8A CN201710131884A CN106893226A CN 106893226 A CN106893226 A CN 106893226A CN 201710131884 A CN201710131884 A CN 201710131884A CN 106893226 A CN106893226 A CN 106893226A
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- sbs
- powder
- high temperature
- temperature resistant
- elastomeric material
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- 239000013536 elastomeric material Substances 0.000 title claims abstract description 16
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 26
- 239000000843 powder Substances 0.000 claims abstract description 26
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 17
- 239000011347 resin Substances 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 238000002156 mixing Methods 0.000 claims abstract description 10
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 9
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 9
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims abstract description 9
- 235000013539 calcium stearate Nutrition 0.000 claims abstract description 9
- 239000008116 calcium stearate Substances 0.000 claims abstract description 9
- 239000006229 carbon black Substances 0.000 claims abstract description 9
- BJAJDJDODCWPNS-UHFFFAOYSA-N dotp Chemical compound O=C1N2CCOC2=NC2=C1SC=C2 BJAJDJDODCWPNS-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000003112 inhibitor Substances 0.000 claims abstract description 9
- SZINCDDYCOIOJQ-UHFFFAOYSA-L manganese(2+);octadecanoate Chemical compound [Mn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O SZINCDDYCOIOJQ-UHFFFAOYSA-L 0.000 claims abstract description 9
- 239000004332 silver Substances 0.000 claims abstract description 9
- 229910052709 silver Inorganic materials 0.000 claims abstract description 9
- 239000002002 slurry Substances 0.000 claims abstract description 9
- 235000012424 soybean oil Nutrition 0.000 claims abstract description 9
- 239000003549 soybean oil Substances 0.000 claims abstract description 9
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 4
- 238000005469 granulation Methods 0.000 claims abstract description 4
- 230000003179 granulation Effects 0.000 claims abstract description 4
- 230000001404 mediated effect Effects 0.000 claims abstract description 4
- 239000008188 pellet Substances 0.000 claims abstract description 4
- 238000005453 pelletization Methods 0.000 claims abstract description 4
- 238000007670 refining Methods 0.000 claims abstract description 4
- 229920001971 elastomer Polymers 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 11
- 239000005060 rubber Substances 0.000 claims description 9
- 238000001994 activation Methods 0.000 claims description 5
- 230000001070 adhesive effect Effects 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 5
- 239000000853 adhesive Substances 0.000 claims description 4
- 239000004568 cement Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 4
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 4
- 238000001694 spray drying Methods 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- 239000002861 polymer material Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 description 17
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 235000010216 calcium carbonate Nutrition 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000032683 aging Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000003139 buffering effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- XZVDPRFYVGLYNO-UHFFFAOYSA-N C=CC1=CC=CC=C1.C=CC=C.C=C.C1=CC=CC=C1 Chemical compound C=CC1=CC=CC=C1.C=CC=C.C=C.C1=CC=CC=C1 XZVDPRFYVGLYNO-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012567 medical material Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920006112 polar polymer Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/04—Thermoplastic elastomer
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
A kind of high resiliency high temperature resistant elastomeric material, it is made up of following component and weight percent proportioning:The resins 50% of PVC 1300, UN488(DOTP)5%, ESO soybean oil 1%, PDOP 0.1%, GF78 0.05%, Has fam silver system antibacterial mildew inhibitor 0.6%, PP.PA modifying agent 0.1%, TPU102 powder 10%, carbon black slurry 0.1%, manganese stearate 0.01%, calcium stearate 0.15%, SBS superfines 2%, activated calcium carbonate 2%, the proportioning of above-mentioned component is defined by a hundred per cent;Described preparation method includes:The resins of PVC 1300 and activated calcium carbonate and SBS superfines and TPU powder are mixed in proportion, and various auxiliary agents are proportionally added into mixing are mediated, by beginning to pratise, after banburying and open refining modeling, then by pelletizing, finished product will be made after pellet feeding extruder granulation.
Description
Technical field
The present invention relates to a kind of high resiliency high temperature resistant elastomeric material and preparation method, belong to macromolecular elastomer material
Material and preparing technical field.
Background technology
Flexible foamed material is, with raw material such as plastics (PE, EVA etc.), rubber (SBR, CR etc.), to be subject to catalyst, bubble
The auxiliary materials such as foam stabilizers, foaming agent, by physical blowing or crosslinked foaming, make a large amount of trickle foams occur in plastics and rubber,
Volume increases, and density is reduced, and flexible foamed quality of materials is light, pliability is good, possesses buffering, sound-absorbing, shock-absorbing, insulation, filtering etc.
Function, is widely used in the industries such as electronics, household electrical appliances, automobile, Leisure Sport.
The poor performances such as current some conventional elastomeric material generally existing high temperature resistant, ageing-resistant, wearabilities, and do not have
High resiliency, thus more special application places cannot be met, with constantly widening for high resiliency application field, it is badly in need of some property
Can be excellent, application field is wide, low cost, meets the highly elastic material of national and international nontoxic standard requirement.
The content of the invention
It is an object of the invention to overcome the shortcomings of that prior art is present, and provide a kind of high temperature resistant, ageing-resistant, wearability
Good etc. performance, generation efficiency is high, low cost, function admirable, high resiliency high temperature resistant elastomeric material applied widely and preparation
Method.
The purpose of the present invention is completed by following technical solution, a kind of high resiliency high temperature resistant elastomeric material, its
It is characterised by:It is made up of following component and weight percent proportioning:
PVC-1300 resins 50-70%
UN488(DOTP) 5-15%
ESO soybean oils 1-5%
PDOP 0.1-0.3%
KY-405 0.05-0.15%
Has-fam silver system antibacterial mildew inhibitor 0.6-1.0%
PP.PA modifying agent 0.1-1.0%
TPU102 powder 10-20%
Carbon black slurry 0.1-1.0%
Manganese stearate 0.05-0.1%
Calcium stearate 0.1-0.6%
SBS superfines 2-8%
Activated calcium carbonate 2-7%
The proportioning of above-mentioned component is defined by a hundred per cent.
Preferably, it is made up of following component and weight percent proportioning:
PVC-1300 resins 60%
UN488(DOTP) 10%
ESO soybean oils 3%
PDOP 0.2%
KY-405 0.1%
Has-fam silver system antibacterial mildew inhibitor 0.5%
PP.PA modifying agent 0.5%
TPU102 powder 15%
Carbon black slurry 0.5%
Manganese stearate 0.05%
Calcium stearate 0.5%
SBS superfines 5%
Activated calcium carbonate 4.35%
A kind of preparation method of high resiliency high temperature resistant elastomeric material as described above, described preparation method includes:By PVC-
1300 resins and activated calcium carbonate and SBS superfines and TPU powder mix in proportion, and are proportionally added into mixing various
Auxiliary agent is mediated, by beginning to pratise, after banburying and open refining modeling, then by pelletizing, after pellet feeding extruder granulation
It is made finished product;
Described activated calcium carbonate is first to carry out following activation process before raw material proportioning addition:First by the carbon of 1500 mesh
Sour calcium is added in homogenizer, and then bridging agent is configured to 25% neat solvent, with mixer high-speed rotation, uniformly
Be added in pearl filler, stirring 20 minutes after, use low rate mixing instead 30 minutes, dynamic dry after i.e. can be used.
As preferred:Described SBS superfines is by following treatment:1 part of CPE is added in 30 parts of SBS powder systems;
It is solvent with 60 parts of hexamethylenes, adds adhesive to make diluent in a solvent, using 6 parts of unsaturated, vulcanizable liquid high scores
Sub- material and 0.5 part of vulcanizing agent and 0.35 part of catalyst blending, the SBS rubber cements to being blended are heated to 60 degree and are stirred continuously uniformly,
SBS powder is obtained using high temperature spray-drying legal system.
The method can be widely used in inner tube extruded material heat-barrier materials, encapsulant, insulation material, buffering spacer, sound absorption
The fields such as sheet material, medical material utensil, Aero-Space, good with the performance such as high temperature resistant, ageing-resistant, wearability, generation efficiency is high,
Low cost, function admirable, the features such as applied widely.
Specific embodiment
Below in conjunction with specific embodiment, the present invention will be described in detail:A kind of high resiliency high temperature resistant of the present invention
Elastomeric material, it is characterised in that:It is made up of following component and weight percent proportioning:
PVC-1300 resins 50-70%
UN488(DOTP) 5-15%
ESO soybean oils 1-5%
PDOP 0.1-0.3%
KY-405 0.05-0.15%
Has-fam silver system antibacterial mildew inhibitor 0.6-1.0%
PP.PA modifying agent 0.1-1.0%
TPU102 powder 10-20%
Carbon black slurry 0.1-1.0%
Manganese stearate 0.01-0.1%
Calcium stearate 0.1-0.6%
SBS superfines 2-8%
Activated calcium carbonate 2-7%
The proportioning of above-mentioned component is defined by a hundred per cent.
Preparation method of the present invention includes:By PVC-1300 resins and activated calcium carbonate and SBS superfines and TPU
Powder mixes in proportion, and various auxiliary agents are proportionally added into mixing are mediated, by beginning to pratise, banburying and open refining
After modeling, then by pelletizing, finished product will be made after pellet feeding extruder granulation;
Described activated calcium carbonate is first to carry out following activation process before raw material proportioning addition:First by the carbon of 1500 mesh
Sour calcium is added in homogenizer, and then bridging agent is configured to 25% neat solvent, with mixer high-speed rotation, uniformly
Be added in pearl filler, stirring 20 minutes after, use low rate mixing instead 30 minutes, dynamic dry after i.e. can be used.
SBS superfines of the present invention is by following treatment:1 part of CPE is added in 30 parts of SBS powder systems;With
60 parts of hexamethylenes are solvent, add adhesive to make diluent in a solvent, using 6 parts of unsaturated, vulcanizable Liquid polymerics
Material and 0.5 part of vulcanizing agent and 0.35 part of catalyst blending, the SBS rubber cements to being blended are heated to 60 degree and are stirred continuously uniformly, adopt
SBS powder is obtained with high temperature spray-drying legal system.
Embodiments of the invention can obtain countless by carrying out in number range disclosed above replacement simply
Individual embodiment, and including following three embodiment.
Embodiment 1:High resiliency high temperature resistant elastomeric material of the present invention, it is matched by following component and weight percent
Composition:
PVC-1300 resins 60%
UN488(DOTP) 10%
ESO soybean oils 3%
PDOP 0.2%
KY-405 0.1%
Has-fam silver system antibacterial mildew inhibitor 0.5%
PP.PA modifying agent 0.5%
TPU102 powder 15%
Carbon black slurry 0.5%
Manganese stearate 0.05%
Calcium stearate 0.5%
SBS superfines 5%
Activated calcium carbonate 4.35%
Embodiment 2:A kind of high resiliency high temperature resistant elastomeric material of the present invention, it is matched by following component and weight percent
Composition:
PVC-1300 resins 50%
UN488(DOTP) 15%
ESO soybean oils 5%
PDOP 0.3%
KY-405 0.15%
Has-fam silver system antibacterial mildew inhibitor 1.0%
PP.PA modifying agent 1.0%
TPU102 powder 20%
Carbon black slurry 1.0%
Manganese stearate 0.1%
Calcium stearate 0.25%
SBS superfines 4.2%
Activated calcium carbonate 2%
Embodiment 3:A kind of high resiliency high temperature resistant elastomeric material of the present invention, it is matched by following component and weight percent
Composition:
PVC-1300 resins 70%
UN488(DOTP) 5%
ESO soybean oils 1%
PDOP 0.1%
KY-405 0.05%
Has-fam silver system antibacterial mildew inhibitor 0.6%
PP.PA modifying agent 0.1%
TPU102 powder 10%
Carbon black slurry 0.1%
Manganese stearate 0.01%
Calcium stearate 0.15%
SBS superfines 6.11%
The % of activated calcium carbonate 6
Flexible chain is alternately connected into macromolecular by the present invention using the method for block copolymerization with rigid chain, is in the small soft silk of normal temperature
Rubbery state, hard section is gathered together in glassy state or crystalline state, forms physics crosslinking points, and material has the numerous characteristics of rubber,
Elastomer product is at -50 DEG C -- there is good toughness, tear-proof and Flex-Fatigue within the temperature range of 140 DEG C.
Most of it is a kind of thermoplastic heat molten type superfines present invention adds TPU powder, i.e. polyurethane powder, with
Material has good cohesive force, and temperature range while have initial stage peel strength and heat resistance high and wider is with suitable
Different processing are answered to want, high rigidity, high resiliency, low temperature laminating, bonding is rapid, and production efficiency is high, bonding scope extensively, can be bonded many
Kind of material, can be heated repeatedly, repeatedly bonding, and TPU powder is added in polyvinyl chloride resin, and both are well mixed, good penetrability, can be with
Improve the elasticity and heat-resisting quantity of material.
The present invention is by CaCO3(Calcium carbonate)Inserts carries out following special activation process, directly adds with general inserts
Enter different, activation process is carried out before composition of raw materials, the technique and flow for the treatment of have particularity, first 1500 purposes
CaCO3 is added in mixer high, then bridging agent(Can make by oneself)25% pure solution is configured to, with mixer at a high speed
Rotate, be homogeneously added into CaCO3 inserts, after stirring 20 minutes, use low rate mixing instead 30 minutes, after dynamic is dried, i.e.,
Can be used;CaCO3 dispersivenesses after treatment increase, and increase with polyvinyl chloride resin binding ability, and being added to can reduces cost in being formulated
Enhancing and dispersion effect can be played again.
Also using the SBS superfines of specially treated, SBS is the block copolymer of styrene and butadiene to the present invention.Tool
There is two phase structure:Polybutadiene phase-continuous phase, polystyrene phase-dispersed phase.It is similar to butadiene-styrene rubber, SBS can with water,
Weak acid, alkali etc. are contacted, with excellent tensile strength, big surface friction coefficient, low temperature performance well, excellent electrical properties, processability
The thermoplastic elastomer (TPE) of characteristic can well be waited.Ultra-fine SBS powder is processed by special processing and special modified technique, with non-
Often good mobility, is greatly improved its performance.Do not lump at normal temperatures, thoroughly widened the range of application of SBS.And benzene
Ethene-butadiene-styrene (SBS) triblock polymer is one of maximum thermoplastic elastomer (TPE) of current yield in the world,
The elasticity with rubber, is melt into the material of plasticity under normal temperature under high temperature.Because it has excellent tensile property, good resistance to
The skid resistance of low temperature properties, gas permeability, dissolubility and uniqueness and be widely used in the fields such as shoemaking, modifying plastics, asphalt modification.
Because SBS polarity is small and oil resistivity is poor, use it and be restricted.Polar group can be introduced on SBS chains by functionalization
Group, drastically increases the heat-resisting of SBS, resistance to oxidation, adhesive property and water absorbing properties.1 part is added in 30 parts of SBS powder systems
CPE improves compatibilities of the SBS to polar polymer first, improves SBS polarity.It is solvent with 60 parts of hexamethylenes, adds in a solvent
Enter adhesive and make diluent, using 6 parts of undersaturated vulcanizable liquid polymer materials(Liquid NBR)With 0.5 part of vulcanizing agent
And 0.35 part of catalyst is blended, the SBS rubber cements to being blended are heated to 60 degree and are stirred continuously uniformly, using high temperature spray-drying legal system
Specially treated SBS powder, the rubber powder of system can be such that it is crosslinked well with other materials, and can be the oil resistant of elastomer
Property, cold resistance and the ozone aging resistance of the diaphragm, elasticity and wearability greatly strengthen.
The present invention produces product and reaches following technical indicator:
1)Shore hardness A:70—85
2)Tensile strength:15—20 MPa
3)Stretching strength retentivity:95%
4)Elongation at break:More than 250%
5)Extension at break conservation rate:90%
6)Permanent deformation:5—8%
7)100% stretching strength:4.2—4.6 MPa
8)Tearing strength(Right angle):50—55 KN/m
9)Elastic viscous force(1200/sec)80 Pa—sec
10)Elastic recovery rate 95%
11)Ozone resistance O3test23 DEG C of 100ppm, 72h, flawless.
12)Compressive deformation(ASTM, D395,22H/70 DEG C):30-35%
13)Material product can be used -150 DEG C of temperature range -50 DEG C.
Claims (4)
1. a kind of high resiliency high temperature resistant elastomeric material, it is characterised in that:It is made up of following component and weight percent proportioning:
PVC-1300 resins 50-70%
UN488(DOTP) 5-15%
ESO soybean oils 1-5%
PDOP 0.1-0.3%
KY-405 0.05-0.15%
Has-fam silver system antibacterial mildew inhibitor 0.6-1.0%
PP.PA modifying agent 0.1-1.0%
TPU102 powder 10-20%
Carbon black slurry 0.1-1.0%
Manganese stearate 0.01-0.1%
Calcium stearate 0.10-0.6%
SBS superfines 2-8%
Activated calcium carbonate 2-7%
The proportioning of above-mentioned component is defined by a hundred per cent.
2. high resiliency high temperature resistant elastomeric material according to claim 1, it is characterised in that:It is by following component and weight
Per distribution ratio is constituted:
PVC-1300 resins 60%
UN488(DOTP) 10%
ESO soybean oils 3%
PDOP 0.2%
KY-405 0.1%
Has-fam silver system antibacterial mildew inhibitor 0.8%
PP.PA modifying agent 0.5%
TPU102 powder 15%
Carbon black slurry 0.5%
Manganese stearate 0.05%
Calcium stearate 0.5%
SBS superfines 5%
Activated calcium carbonate 4.35%.
3. a kind of preparation method of high resiliency high temperature resistant elastomeric material as claimed in claim 1 or 2, it is characterised in that described
Preparation method includes:PVC-1300 resins and activated calcium carbonate and SBS superfines and TPU powder are mixed in proportion, and
Various auxiliary agents are proportionally added into mixing to be mediated, by beginning to pratise, after banburying and open refining modeling, then by pelletizing, will
Finished product is made after pellet feeding extruder granulation;
Described activated calcium carbonate is first to carry out following activation process before raw material proportioning addition:First by the carbon of 1500 mesh
Sour calcium is added in homogenizer, and then bridging agent is configured to 25% neat solvent, with mixer high-speed rotation, uniformly
Be added in pearl filler, stirring 20 minutes after, use low rate mixing instead 30 minutes, dynamic dry after i.e. can be used.
4. the preparation method of high resiliency high temperature resistant elastomeric material according to claim 3, it is characterised in that described SBS surpasses
Fine powder is by following treatment:1 part of CPE is added in 30 parts of SBS powder systems;It is solvent with 60 parts of hexamethylenes, in a solvent
Adhesive is added to make diluent, using 6 parts of unsaturated, vulcanizable liquid polymer materials and 0.5 part of vulcanizing agent and 0.35 part
Catalyst is blended, and the SBS rubber cements to being blended are heated to 60 degree and are stirred continuously uniformly, and SBS powder is obtained using high temperature spray-drying legal system
End.
Priority Applications (1)
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110066482A (en) * | 2019-05-17 | 2019-07-30 | 莱恩佳辰(苏州)纳米科技有限公司 | A kind of medical flame-proof PVC rubber mat of long acting antibiotic, formula and preparation method thereof |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006265373A (en) * | 2005-03-24 | 2006-10-05 | Denki Kagaku Kogyo Kk | Vinyl chloride resin composition having maleimide copolymer and vinyl chloride polymer |
| CN101538393A (en) * | 2009-04-23 | 2009-09-23 | 福建思嘉环保材料科技有限公司 | High-elastic wearproof athletic floor material and preparation method thereof |
| CN103628652A (en) * | 2013-11-06 | 2014-03-12 | 安徽圣源橡塑科技有限公司 | Functional co-extrusion composite alloy material floor-heating floor and manufacturing method thereof |
| CN104861359A (en) * | 2014-12-30 | 2015-08-26 | 殷培花 | Carbon fiber filled and modified polyvinyl chloride plastic and preparation method thereof |
| CN104861354A (en) * | 2014-12-30 | 2015-08-26 | 殷培花 | Strengthened polyvinyl chloride composite plastic and preparation method thereof |
-
2017
- 2017-03-07 CN CN201710131884.8A patent/CN106893226A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006265373A (en) * | 2005-03-24 | 2006-10-05 | Denki Kagaku Kogyo Kk | Vinyl chloride resin composition having maleimide copolymer and vinyl chloride polymer |
| CN101538393A (en) * | 2009-04-23 | 2009-09-23 | 福建思嘉环保材料科技有限公司 | High-elastic wearproof athletic floor material and preparation method thereof |
| CN103628652A (en) * | 2013-11-06 | 2014-03-12 | 安徽圣源橡塑科技有限公司 | Functional co-extrusion composite alloy material floor-heating floor and manufacturing method thereof |
| CN104861359A (en) * | 2014-12-30 | 2015-08-26 | 殷培花 | Carbon fiber filled and modified polyvinyl chloride plastic and preparation method thereof |
| CN104861354A (en) * | 2014-12-30 | 2015-08-26 | 殷培花 | Strengthened polyvinyl chloride composite plastic and preparation method thereof |
Non-Patent Citations (1)
| Title |
|---|
| 王宏: "《染整技术(第三册)》", 31 July 2008, 中国纺织出版社 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110066482A (en) * | 2019-05-17 | 2019-07-30 | 莱恩佳辰(苏州)纳米科技有限公司 | A kind of medical flame-proof PVC rubber mat of long acting antibiotic, formula and preparation method thereof |
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Application publication date: 20170627 |