CN102993582B - A kind of CPE/SBS/PET blended compound material and preparation method thereof - Google Patents

A kind of CPE/SBS/PET blended compound material and preparation method thereof Download PDF

Info

Publication number
CN102993582B
CN102993582B CN201210399832.6A CN201210399832A CN102993582B CN 102993582 B CN102993582 B CN 102993582B CN 201210399832 A CN201210399832 A CN 201210399832A CN 102993582 B CN102993582 B CN 102993582B
Authority
CN
China
Prior art keywords
cpe
pet
sbs
modified
resistance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201210399832.6A
Other languages
Chinese (zh)
Other versions
CN102993582A (en
Inventor
冯玉柱
宿英迁
叶林
刘平
冯云祥
张朝哲
杨波
郭茂发
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jinzhou Anda Automobile Parts Co., Ltd.
Original Assignee
WUHU XINHAI RUBBER AND PLASTIC PRODUCTS CO Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by WUHU XINHAI RUBBER AND PLASTIC PRODUCTS CO Ltd filed Critical WUHU XINHAI RUBBER AND PLASTIC PRODUCTS CO Ltd
Priority to CN201210399832.6A priority Critical patent/CN102993582B/en
Publication of CN102993582A publication Critical patent/CN102993582A/en
Application granted granted Critical
Publication of CN102993582B publication Critical patent/CN102993582B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

The invention discloses a kind of CPE/SBS/PET blended compound material, be made up of the raw material of following weight portion: CPE 70-80, SBS 20-30, modified PET 10-20, dibutyl phthalate 5-10, semi-reinforcing hydrocarbon black 20-30, activated Calcium carbonate 10-20, attapulgite modified 10-15, cumyl peroxide 5-8, APP 2-4, lead sulfate tribasic 2-3, magnesium oxide 2-3, zinc oxide 1-2, waste oil residue 10-20, Vulcanization accelerator TMTD 0.1-0.3, altax 0.5-1, age resistor ODA 1-2, antioxidant 168 1-2.Compared with pure CPE, CPE/SBS/PET blended compound material has following feature: 1. significantly improve resistance to ozone and the performance such as Weather-resistant, resistant of high or low temperature;2. improve hot strength, stress at definite elongation, tear resistance, thermostability, flame resistance, fatigue resistance and rub resistance;3. improve the performances such as oil resistant, resistance to fuel oil and chemical-resistant resistance;4. improve extrusion, drawability, sizing material not easily autovulcanization, enhances bin stability simultaneously.

Description

A kind of CPE/SBS/PET blended compound material and preparation method thereof
Technical field
The present invention relates to a kind of rubber-plastics material, be specifically related to a kind of CPE/SBS/PET blended compound material and preparation method thereof.
Background technology
CPE(chlorinated polyethylene) it is a kind of new modified materials, it it is the product after the part hydrogen atom on polyethylene molecular chain is substituted by a chlorine atom both, chlorinty is the CPE genus thermoplastic elastomer (TPE) of about 35%, it is characterized in that namely without sulfuration be have higher intensity and dimensional stability, and substantial amounts of inorganic filler can be filled, therefore it is widely used in all kinds of rubber-plastics materials.But, add rubber-plastics material prepared by inorganic filler with CPE merely, though intensity is higher, hardness also tends to relatively big, but this all solves by adding a large amount of plasticizer, due to migration of plasticizer, brings again the decline of this kind of material serviceability.Owing to there is the good compatibility with other macromolecular material, we can pass through CPE and SBS, PET blended, form CPE/SBS/PET co-mixing system, avoid CPE to need to add a large amount of plasticizer to obtain higher-strength and hardness.
Summary of the invention
It is an object of the invention to provide a kind of CPE/SBS/PET blended compound material and preparation method thereof, it is to avoid CPE needs to add a large amount of plasticizer to obtain higher-strength and hardness, thus improving the combination property of CPE material.
For reaching object above, the technical solution used in the present invention is as follows:
A kind of CPE/SBS/PET blended compound material, is made up of the raw material of following weight portion: CPE70-80, SBS20-30, modified PET 10-20, dibutyl phthalate 5-10, semi-reinforcing hydrocarbon black 20-30, activated Calcium carbonate 10-20, attapulgite modified 10-15, cumyl peroxide 5-8, APP 2-4, lead sulfate tribasic 2-3, magnesium oxide 2-3, zinc oxide 1-2, waste oil residue 10-20, Vulcanization accelerator TMTD 0.1-0.3, altax 0.5-1, age resistor ODA1-2, antioxidant 1681-2.
Described CPE chlorinty is 35-38%;Described SBS medium vinyl content is 76-78%;
Described modified PET is prepared by following method: weigh a certain amount of PET, TPU and modified Nano SiO2, in 70-80 DEG C of vacuum drying oven, place 6-8h, dried rear PET, TPU and modified Nano SiO2Putting into mix homogeneously in high-speed mixer by 3-4:1:0.2-0.3 weight ratio, then put into double screw extruder pelletize, extrusion temperature is 190-225 DEG C, and extruded material is at 140-150 DEG C of dry 6-8h, wherein, and described modified Nano SiO2Following method prepares: to Nano-meter SiO_22Amino coupling agent A-1100, the mixed at high speed 1-2h at 80-85 DEG C of middle silane coupler KH-560 and the 1-2% adding 2-3%, dries, pulverizes.??
Described attapulgite modified prepared by following method: attapulgite being placed in 10-15% soak with hydrochloric acid 3-4 hour, deionized water wash is to neutral, then soaks 3-4 hour with 10-12% sodium hydroxide solution, then with deionized water wash to neutral, drying;It is subsequently adding the sodium tripolyphosphate being equivalent to attapulgite weight 2-3%, add the aluminium oxide of the sodium laurylsulfate of attapulgite weight 2-3%, the paregal O of 1-2%, the tributyl citrate of 2-3%, 3-5%, add appropriate deionized water, it is high-speed stirred 2-3h under 1200-1500r/min at rotating speed, obtain dispersion liquid, finally dispersion liquid is dried, pulverized to obtain powder.
The preparation method of described CPE/SBS/PET blended compound material, detailed process is as follows: first SBS, modified PET and age resistor ODA, antioxidant 168 are opened on twin-screw extruder at 50-60 DEG C refining, open refining 20-30min every time, 10-15h is parked after having refined, carry out out refining again, be so repeatedly performed 2-3 time.Then CPE, the surplus stock such as attapulgite modified are put into mixing 10-20min in high-speed mixer, again the material mixed is plasticated 8-10min with the above-mentioned SBS/PET glue refined of opening in twin-roll plastic mixing mill, in double; two roller mills, mixing pulling-on piece is carried out after taking-up, temperature is 160-170 DEG C, sheet thickness 1-2mm, roll on calender after pull-out, carry out sawing by required specification after taking out cooling, pack.
The rotating speed of described high-speed mixer is 1000-1200r/min;The rotating speed of described double; two roller mills is 50-60r/min.
CPE/SBS/PET blended compound material of the present invention has the ageing-resistant performance of CPE, ozone resistance, oil resistivity concurrently, the fatigue resistance of the lower temperature resistance of SBS, high resiliency, breathability and PET, weatherability, rub resistance, compared with pure CPE, CPE/SBS/PET blended compound material has following feature:
1. significantly improve resistance to ozone and the performance such as Weather-resistant, resistant of high or low temperature;
2. improve hot strength, stress at definite elongation, tear resistance, thermostability, flame resistance, fatigue resistance and rub resistance;
3. improve the performances such as oil resistant, resistance to fuel oil and chemical-resistant resistance;
4. improve extrusion, drawability, sizing material not easily autovulcanization, enhances bin stability simultaneously.
Detailed description of the invention
Below in conjunction with embodiment, the present invention is described in further details.
Embodiment.
The preparation method of CPE/SBS/PET blended compound material, detailed process is as follows:
Take off the raw material of row weight portion: CPE70 part, SBS30 part, modified PET 15 parts, dibutyl phthalate 6 parts, semi-reinforcing hydrocarbon black 25 parts, activated Calcium carbonate 20 parts, attapulgite modified 15 parts, cumyl peroxide 6 parts, APP 3 parts, lead sulfate tribasic 2 parts, magnesium oxide 3 parts, zinc oxide 2 parts, waste oil residue 15 parts, Vulcanization accelerator TMTD 0.3 part, altax 0.8 part, age resistor ODA1.5 part, antioxidant 1682 parts.
Wherein, described CPE chlorinty is 35%;Described SBS medium vinyl content is 78%;Described modified PET is prepared by following method: weigh a certain amount of PET, TPU and modified Nano SiO2, in 80 DEG C of vacuum drying ovens, place 8h, dried rear PET, TPU and modified Nano SiO2Putting into mix homogeneously in high-speed mixer by 3:1:0.2 weight ratio, then put into double screw extruder pelletize, extrusion temperature is 205 DEG C, and extruded material is at 150 DEG C of dry 8h, wherein said modified Nano SiO2Following method prepares: to Nano-meter SiO_22Amino coupling agent A-1100, the mixed at high speed 1-2h at 80-85 DEG C of middle silane coupler KH-560 and the 1-2% adding 2-3%, dries, pulverizes;
Described attapulgite modified prepared by following method: attapulgite being placed in 15% soak with hydrochloric acid 4 hours, deionized water wash is to neutral, then soaks 4 hours with 12% sodium hydroxide solution, then with deionized water wash to neutral, drying;It is subsequently adding the sodium tripolyphosphate being equivalent to attapulgite weight 3%, add the sodium laurylsulfate of attapulgite weight 3%, 2% paregal O, 3% tributyl citrate, 5% aluminium oxide, add appropriate deionized water, it is high-speed stirred 3h under 1400r/min at rotating speed, obtain dispersion liquid, finally dispersion liquid is dried, pulverized to obtain powder.
First SBS, modified PET and age resistor ODA, antioxidant 168 are opened refining at 60 DEG C on twin-screw extruder, open refining 30min every time, park 15h after having refined, then carry out out refining, be so repeatedly performed 3 times.Then CPE, the surplus stock such as attapulgite modified are put into mixing 20min in high-speed mixer, again the material mixed is plasticated 10min with the above-mentioned SBS/PET glue refined of opening in twin-roll plastic mixing mill, in double; two roller mills, mixing pulling-on piece is carried out after taking-up, temperature is 170 DEG C, sheet thickness 2mm, roll on calender after pull-out, carry out sawing by required specification after taking out cooling, pack.
The rotating speed of described high-speed mixer is 1200r/min;The rotating speed of described double; two roller mills is 60r/min.
Relevant physics, measuring mechanical property are as follows:
Hardness (shore) is 88 ° (A);Elongation at break is 480%;Hot strength is 1423MPa;Mooney viscosity (ML1+4, 100 DEG C) and it is 92;Tearing strength is 54kN/m.

Claims (1)

1. a CPE/SBS/PET blended compound material, it is characterized in that, be made up of the raw material of following weight portion: CPE70-80, SBS20-30, modified PET 10-20, dibutyl phthalate 5-10, semi-reinforcing hydrocarbon black 20-30, activated Calcium carbonate 10-20, attapulgite modified 10-15, cumyl peroxide 5-8, APP 2-4, lead sulfate tribasic 2-3, magnesium oxide 2-3, zinc oxide 1-2, waste oil residue 10-20, Vulcanization accelerator TMTD 0.1-0.3, altax 0.5-1, age resistor ODA1-2, antioxidant 1681-2;Described CPE chlorinty is 35-38%;Described SBS medium vinyl content is 76-78%;
Described modified PET is prepared by following method: weigh a certain amount of PET, TPU and modified Nano SiO2, in 70-80 DEG C of vacuum drying oven, place 6-8h, dried rear PET, TPU and modified Nano SiO2Putting into mix homogeneously in high-speed mixer by 3-4:1:0.2-0.3 weight ratio, then put into double screw extruder pelletize, extrusion temperature is 190-225 DEG C, and extruded material is at 140-150 DEG C of dry 6-8h, wherein, and described modified Nano SiO2Following method prepares: to Nano-meter SiO_22Amino coupling agent A-1100, the mixed at high speed 1-2h at 80-85 DEG C of middle silane coupler KH-560 and the 1-2% adding 2-3%, dries, pulverizes;
Described attapulgite modified prepared by following method: attapulgite being placed in 10-15% soak with hydrochloric acid 3-4 hour, deionized water wash is to neutral, then soaks 3-4 hour with 10-12% sodium hydroxide solution, then with deionized water wash to neutral, drying;It is subsequently adding the sodium tripolyphosphate being equivalent to attapulgite weight 2-3%, add the aluminium oxide of the sodium laurylsulfate of attapulgite weight 2-3%, the paregal O of 1-2%, the tributyl citrate of 2-3%, 3-5%, add appropriate deionized water, it is high-speed stirred 2-3h under 1200-1500r/min at rotating speed, obtain dispersion liquid, finally dispersion liquid is dried, pulverized to obtain powder;
The detailed process of the preparation method of described CPE/SBS/PET blended compound material is as follows: first SBS, modified PET and age resistor ODA, antioxidant 168 are opened on twin-screw extruder at 50-60 DEG C refining, open refining 20-30min every time, 10-15h is parked after having refined, carry out out refining again, be so repeatedly performed 2-3 time;Then CPE, the surplus stock such as attapulgite modified are put into mixing 10-20min in high-speed mixer, again the material mixed is plasticated 8-10min with the above-mentioned SBS/PET glue refined of opening in twin-roll plastic mixing mill, in double; two roller mills, mixing pulling-on piece is carried out after taking-up, temperature is 160-170 DEG C, sheet thickness 1-2mm, roll on calender after pull-out, carry out sawing by required specification after taking out cooling, pack;
The rotating speed of described high-speed mixer is 1000-1200r/min;The rotating speed of described double; two roller mills is 50-60r/min.
CN201210399832.6A 2012-10-19 2012-10-19 A kind of CPE/SBS/PET blended compound material and preparation method thereof Expired - Fee Related CN102993582B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210399832.6A CN102993582B (en) 2012-10-19 2012-10-19 A kind of CPE/SBS/PET blended compound material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210399832.6A CN102993582B (en) 2012-10-19 2012-10-19 A kind of CPE/SBS/PET blended compound material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN102993582A CN102993582A (en) 2013-03-27
CN102993582B true CN102993582B (en) 2016-06-29

Family

ID=47922728

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210399832.6A Expired - Fee Related CN102993582B (en) 2012-10-19 2012-10-19 A kind of CPE/SBS/PET blended compound material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102993582B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103756164A (en) * 2013-12-16 2014-04-30 芜湖万润机械有限责任公司 High-strength rubber sealing gasket material and preparation method thereof
CN105125057B (en) * 2015-10-10 2018-07-03 杭州好菜网络科技有限公司 A kind of SMART COOKWARE with mobile client interactive function
CN113105685B (en) * 2021-04-16 2022-12-06 潍坊亚星化学股份有限公司 Chlorinated polyethylene blending modified high-density polyethylene material and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101585951A (en) * 2009-04-23 2009-11-25 曹天志 Method for preparing a TZ-SBSEC welding type rubber waterproof sheet
CN102382397A (en) * 2011-09-29 2012-03-21 芜湖海杉型材有限公司 Environment-friendly plastic sectional material and preparation method thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3765174B2 (en) * 1997-12-19 2006-04-12 ダイソー株式会社 Elastomer composition and cross-linked product thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101585951A (en) * 2009-04-23 2009-11-25 曹天志 Method for preparing a TZ-SBSEC welding type rubber waterproof sheet
CN102382397A (en) * 2011-09-29 2012-03-21 芜湖海杉型材有限公司 Environment-friendly plastic sectional material and preparation method thereof

Also Published As

Publication number Publication date
CN102993582A (en) 2013-03-27

Similar Documents

Publication Publication Date Title
Mohamad Aini et al. Lignin as alternative reinforcing filler in the rubber industry: a review
Sae-Oui et al. Roles of silane coupling agents on properties of silica-filled polychloroprene
CN102786743B (en) High and low temperature resistant and oil resistant blending material and preparation method thereof
CN103333406B (en) A kind of modified expanded flame-proof polypropelene composition and preparation method thereof
JP5666824B2 (en) Polypropylene composition and method for producing the same
JP5092216B2 (en) Propylene-based resin composition production method, propylene-based resin composition, and injection-molded body comprising the same
CN106519460A (en) Flame-retardant thermoplastic vulcanized rubber material
Sekharan et al. Utilization of waste expanded polystyrene: Blends with silica-filled natural rubber
JP6352691B2 (en) Truck / Bus Tire
CN101792559B (en) Sizing material for coating rubber of chemical fiber bleaching rubber roll
CN102993582B (en) A kind of CPE/SBS/PET blended compound material and preparation method thereof
CN100365053C (en) Process for preparing ethylene-propylene rubber/montmorillonite nano composite material
CN102604222B (en) Polypropylene material for automobile interior trimming parts and preparation method thereof
CN102352070A (en) Cross-linking agent masterbatch used in dynamic sulfidation preparation of thermoplastic rubber and its prepared thermoplastic rubber
CN106751007B (en) A kind of high-strength low-density thermoplastic vulcanizate material and preparation method thereof
CN102807711B (en) Scratching-resistant polypropylene material and preparation method thereof
CN108102229A (en) A kind of resistance to braking fluid hose recipe
CN107337859A (en) Oil-immersed pump electric power cable oil resistant EP rubbers sheath material and preparation method thereof
Joseph et al. Incorporation of devulcanised rubber in fresh rubber compounds: Impact of filler correction on vulcanisate properties
CN115926344A (en) Modified fluororubber compound and preparation method thereof
CN101585977B (en) Preparation method of polypropylene reinforced plasticized modifier
CN108070115A (en) A kind of weather strip for automobile and preparation method thereof
CN102775683A (en) Scratch-resistant PP/HDPE (polypropylene/high-density polyethylene) plastic for automobile interior decorations and preparation method thereof
CN103012875B (en) Trans-polyisoprene/polypropylene thermoplastic vulcanized rubber
CN105602081B (en) Composite material of illite powder and thermoplastic elastomer POE, and preparation method and application thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20180423

Address after: 052200 total ten Zhuang village, ten Zhuang Town, Jinzhou City, Shijiazhuang, Hebei

Patentee after: Jinzhou Anda Automobile Parts Co., Ltd.

Address before: 241002 No. 35 spark ignition Industrial Park, Yijiang high tech Industrial Development Zone, Wuhu, Anhui

Patentee before: Wuhu Xinhai Rubber and Plastic Products Co., Ltd.

CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20160629

Termination date: 20181019