CN102634179A - Method for preparing fascia board polylactic acid special material - Google Patents
Method for preparing fascia board polylactic acid special material Download PDFInfo
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- CN102634179A CN102634179A CN2011100357161A CN201110035716A CN102634179A CN 102634179 A CN102634179 A CN 102634179A CN 2011100357161 A CN2011100357161 A CN 2011100357161A CN 201110035716 A CN201110035716 A CN 201110035716A CN 102634179 A CN102634179 A CN 102634179A
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Abstract
The fascia board polylactic acid special material prepared by the method related by the invention solves the following problems: 1. the material has lower total carbon content than traditional fascia board plastic products, is easy to recovery, and meets environmental protection requirements; 2. the material solves the problems of poor aging resistance and poor compatibility among components in the system of fascia board materials by adding additives (ie, a coupling agent: a compound of one or more than one of coupling agents of a silane coupling agent (one of KH550, KH560), a titanate coupling agent (one of NDZ101, NDZ102), an aluminate coupling agent, and a borate coupling agent; an antiaging agent: a compound of one or more than one of antiaging agents of 3114, DSTP, DLTP, 168, 1010); 3. core-shell polymer with stable performance, uniform particle size, and good dispersibility is prepared by special processes such as controlling the conditions of temperature, time, system emulsifier concentration, and the like in the core-shell polymer preparation process, and finally the general shock resistance of the material is improved.
Description
Technical field
The invention belongs to the polymer composite field in the Materials science, relate to a kind of method of utilizing the core-shell polymer polydactyl acid and preparing the fascia PP Pipe Compound.According to the prepared POLYACTIC ACID fascia PP Pipe Compound of the inventive method, solved the orthodox car test board and be difficult for problem degraded, toughness reinforcing component bad dispersibility in material system.Method involved in the present invention is easy and simple to handle, the performance controllability of preparation material is strong, is applicable to prepared in laboratory and enterprise's industrialization production, environmental protection, low-carbon (LC).
Background technology
21 century is the epoch of low-carbon economy, and Sustainable development becomes to be the theme, and environmental protection concept is rooted in the hearts of the people, and the national policy guiding also begins to focus on the environmental protection aspect.Automobile and plastic industry become peak point wave, beginning in 2009, and China becomes the production and consumption first big country of automobile and plastics.Under international environmental protection situation pressure, China is to begin to greatly develop easy degradative plastics-biological plastics, and the POLYACTIC ACID industry has obtained significant progress.No matter in the POLYACTIC ACID compound probability, still processing modified industry, POLYACTIC ACID (PLA) technology reaches its maturity.Yet; POLYACTIC ACID is because its result's singularity; Exist not enough at aspects such as toughness, resistance to deteriorations; And traditional method of modifying is that nano-particles filled or the elastomer-filled guaranteed performance that all is difficult to are stable, has reduced the original thermotolerance of PLA material, high transparent, high rigidity and readily degradable simultaneously significantly.The introducing of nucleocapsid technology becomes the way that solves an above difficult problem.With a kind of and the higher shell monomers of POLYACTIC ACID avidity, coated elastomer or inorganic nano-particle, filling components is guaranteed dispersed the time, improved itself and the avidity of POLYACTIC ACID system greatly, finally make the material monolithic performance reach optimum.
Summary of the invention:
Method involved in the present invention is through in the POLYACTIC ACID system, introducing Core-Shell Polymer Particles, and then when reaching the original mechanical property of maintenance system, thermal property, fluid property and the transparency, increases substantially POLYACTIC ACID system toughness; Simultaneously, in system, add auxiliary agents such as inhibitor, improve the poly-lactic acid material resistance to deterioration.Finally prepare easy degraded, shock resistance and aging-resistant fascia POLYACTIC ACID PP Pipe Compound.The Core-Shell Polymer Particles that present method is introduced, its shell monomers are a kind of in basic methyl acrylate, Jia Jibingxisuanyizhi, the NSC 20956, and this shell monomers and POLYACTIC ACID have good avidity; Nuclear layer monomer is a kind of in Bing Xisuandingzhi, ethyl propenoate, vinylbenzene, the ethene, and its shock resistance and elongation at break aspect have excellent performance.
At the core-shell polymer preparatory phase; Through the control to the temperature in the process, system tension force, reaction times (comprising that nucleation time and shell coat the time), shell and these several kinds of conditions of nuclear layer monomer addition, evenly (size distribution is interval: 80~130nm), dispersed height, shell coat nano level Core-Shell Polymer Particles completely finally to prepare size distribution.
In core-shell polymer preparing carriers process; With the Core-Shell Polymer Particles and the polylactic acid raw material of certain proportion (30~70 parts), add tensio-active agent (0.5~3 part), coupling agent (0.5~5 part), fully mix; Dry 12h; Extrude pelletizing through twin screw extruder then, after water-cooled, air-cooled, pelletizing, drying, obtain the core-shell polymer carrier.
At last, with the polylactic resin more than the prior dry 12h, with the core-shell polymer carrier with certain adding proportion (5~30%), through the high mixer blend, dual-screw-stem machine is extruded, pelletizing, air-dry, finally obtains fascia POLYACTIC ACID PP Pipe Compound.Through the fascia inside gadget that this PP Pipe Compound processes, intensity and toughness are balanced, are prone to degraded, can be applicable to the new-energy automobile field.
Description of drawings:
Accompanying drawing 1 is technological process of production figure.
Embodiment:
One, core-shell polymer preparation
Get the buffered soln of finite concentration (5~20%), feed protection gas (N
2) add 0.5~3 part emulsifying agent, 30~70 nuclear layer monomer, 30 ℃ are stirred 15~30min down, slowly are warming up to 65~80 ℃; Splash into 0.1~3 part initiator potassium persulfate then, drip (can accurately control rate of addition) fully in 30~60min, keep stirring velocity at 100~300r/min through peristaltic pump; Reacted 3 hours; Then be cooled to 40 ℃ of slakings 3 hours, be increased to 65~80 ℃ afterwards, drip shell monomers (30~70 parts), emulsifying agent (0.5~3 part) and initiator (0.1~3 part) simultaneously; Drip in 30~60min fully; Dropwised continued reaction fully 4 hours, and slowly cooled to room temperature, obtain Core-Shell Polymer Particles through filtration, breakdown of emulsion, after air-dry.
Two, core-shell polymer preparing carriers
Core-shell polymer (30~70 parts) and polylactic resin (30~70 parts) after thorough drying dewatered; Add a certain amount of coupling agent (0.5~5 part) and tensio-active agent (0.5~3 part); The high mixer blend; Through twin screw extruder extrude, cooling, pelletizing, drying, obtain the core-shell polymer carrier.Processing parameter is following:
Barrel zone temperature: 40~50 ℃
Extruder temperature: 160~190 ℃
Head temperature: 150~180 ℃
Screw rod revolution: 80~120r/min
Feeding revolution: 3~6r/min
Vacuum exhaust pressure: 0.05~0.1MPa
Coolant water temperature: 40~50 ℃
Dicing machine speed: 150~240r/min
Three, polylactic resin and the blend of core-shell polymer carrier are extruded
With the polylactic resin after the thorough drying (100 parts), core-shell polymer carrier (5~30 parts), through the high mixer blend, twin screw extruder is extruded, water-cooled, air-cooled, pelletizing, drying, finally obtains POLYACTIC ACID fascia PP Pipe Compound.Concrete processing parameter is following:
Barrel zone temperature: 40~50 ℃
Extruder temperature: 160~190 ℃
Head temperature: 150~180 ℃
Screw rod revolution: 100~200r/min
Feeding revolution: 5~8r/min
Vacuum exhaust pressure: 0.05~0.1MPa
Coolant water temperature: 40~50 ℃
Dicing machine speed: 200~360r/min
Four, precaution in the preparation process:
(1) core-shell polymer preparatory phase, rate of addition will be with system endosome type polymkeric substance and diagram of system surface tension situation and corresponding control.
(2) polymerization temperature will be strict controlled in the scope provided by the present invention, otherwise impact polymer particle diameter and productive rate.
(3) preparation core-shell polymer final stage, speed of cooling is unsuitable too fast, otherwise influences productive rate.
(4) extrude the stage, feeding and screw rod revolution are unsuitable too fast, otherwise influence system mixed effect and plasticizing.
(5) extrude the stage, water temperature should not be low excessively, and the pelletizing pulling speed is unsuitable too fast, otherwise cause the material bar frequently to rupture easily.
(6) injection moulding process, die temperature should not be low excessively, otherwise be easy to generate weld mark and cold drawn fracture.
The expressing technique parameter:
Barrel zone temperature: 45 ℃
Extruder temperature: 170 ℃
Head temperature: 160 ℃
Screw rod revolution: 100r/min
Feeding revolution: 4r/min
Vacuum exhaust pressure: 0.05~0.1MPa
Coolant water temperature: 40~50 ℃
Dicing machine speed: 180~200r/min.
Claims (3)
1. a method for preparing fascia POLYACTIC ACID PP Pipe Compound through adding core-shell polymer and relevant auxiliary agent, has solved the difficult problem that conventional instrument plate shock resistance is low, feature of environmental protection difference reaches difficult degraded.
2. core-shell polymer according to claim 1, addition are 5~30% of oeverall quality, and shell monomers is a kind of in TEB 3K, Jia Jibingxisuanyizhi, the NSC 20956, and its quality accounting in core-shell polymer is 30~70%; The core-shell polymer that adds, its nuclear layer monomer are a kind of in Bing Xisuandingzhi, ethyl propenoate, vinylbenzene, the ethene, and its quality accounting in core-shell polymer is 30~70%.
3. relevant auxiliary agent according to claim 1; Comprise coupling agent; Like the compound of one or more coupling agents in silane coupling agent (among KH550, the KH560 a kind of), titanate coupling agent (as among NDZ101, the NDZ102 a kind of), aluminate coupling agent, the boric acid ester coupler, its addition is 0.5~5% of an oeverall quality; Other auxiliary agents such as inhibitor, one or more ageing-resistant compounds as 3114, among the DSTP, DLTP, 168,1010, addition is 0.5~5% of an oeverall quality.
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CN201110035716.1A CN102634179B (en) | 2011-02-10 | 2011-02-10 | Method for preparing fascia board polylactic acid special material |
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CN102634179A true CN102634179A (en) | 2012-08-15 |
CN102634179B CN102634179B (en) | 2015-07-22 |
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CN101665618A (en) * | 2008-09-02 | 2010-03-10 | 第一毛织株式会社 | Environmentally-friendly polylactic acid resin composition |
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CN101665618A (en) * | 2008-09-02 | 2010-03-10 | 第一毛织株式会社 | Environmentally-friendly polylactic acid resin composition |
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Address after: Pingfang District Road 150060 Heilongjiang Hanan city of Harbin Province, No. 9 Applicant after: Heilongjiang Xinda Enterprise Group Co.,Ltd. Address before: Haping Road Development Zone in Harbin City, Heilongjiang province 150060 District Dalian Road No. 9 Applicant before: Heilongjiang Xinda Enterprise Group Co.,Ltd. |
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Granted publication date: 20150722 Termination date: 20190210 |