CN102352063A - Oxygen barrier composite material and preparation method thereof - Google Patents
Oxygen barrier composite material and preparation method thereof Download PDFInfo
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- CN102352063A CN102352063A CN2011102660619A CN201110266061A CN102352063A CN 102352063 A CN102352063 A CN 102352063A CN 2011102660619 A CN2011102660619 A CN 2011102660619A CN 201110266061 A CN201110266061 A CN 201110266061A CN 102352063 A CN102352063 A CN 102352063A
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- resistance
- compoiste material
- compatilizer
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Abstract
The invention relates to an oxygen barrier composite material and a preparation method thereof, and belongs to the technical field of composite materials. The oxygen barrier composite material comprises the following components in part by weight: 0.1 to 50 parts of glass fibers, 40 to 80 parts of polyolefin and 0.01 to 20 parts of aid. The oxygen barrier composite material has the advantages that: a pipe base material and an oxygen barrier composite material layer are not required to be glued by hot melting and can be fused together to be subjected to molecular bonding; meanwhile, the influence of temperature or humidity increase on the barrier property of the oxygen barrier composite material is eliminated.
Description
Technical field
The invention belongs to technical field of composite materials, be specifically related to a kind of resistance O compoiste material and preparation method thereof.
Background technology
Barrier material is exactly to have the material that stops the gas molecule through characteristic, and EVOH numerical value (ethylene-vinyl alcohol copolymer) is a kind of known barrier material at present, is widely used in soft or hard food, sauce, tomato-sauce, meat, tealeaves and cosmetic package field.
Any material all has its suitability, and the EVOH resin is under the lower condition of relative humidity, and barrier is only second to aluminium foil.But owing to contain the polar functional base on the EVOH molecular resin key; Be easy to environment in water molecules; So wet quick property is prone to moisture absorption by force; Barrier property sharply descends after the moisture absorption of EVOH resin; For overcoming the drawback that barrier property lost efficacy after a large amount of moisture absorptions of EVOH resin; At present packaging industry is clipped in multilayer in the middle of wet film at a distance from wet plastic film composite methods food year with the EVOH barrier layer, intercepts validity period to reduce moisture absorption, to prolong.However, also can only prolong packing material about 18 months storage tives.
At present, because limited aspect special-purpose barrier material selection, the plastic pipe industry is generally all transferred to the good barrier properties of EVOH resin the oxidation prevention layer material of hot water or cold water, heating, air-conditioning system resistance oxygen tubing, so that tubing possesses resistance oxygen function.
In addition because the EVOH resinous molecular structure has acute functional group; And the tubing base-material is not with, thus two kinds of materials do not melt mutually, therefore; Must adopt the hot melt adhesive Vilaterm to connect the skill acid anhydrides during use, with surface, internal layer or the centre of EVOH resin bond to tubing as tackiness agent.General oxidation prevention layer and oxidation prevention layer both sides hot melt adhesive total thickness have only 0.015~0.020mm; So precision and processing requirement to equipment when tubing is made are very strict; Production process control difficulty is big; Unavoidably cause EVOH oxidation prevention layer, hot melt adhesive adhesive layer thickness deviation big and uneven thus; And EVOH oxidation prevention layer, hot melt adhesive bonding break material phenomenon; Also can cause resistance oxygen pipe mechanical property and resistance oxygen effect to descend in case lack material, cause tubing can not reach the desired result of permanently effective resistance oxygen.
Summary of the invention
The objective of the invention is provides a kind of new resistance O compoiste material in order to solve the problems referred to above of present resistance O compoiste material.
Technical scheme of the present invention is following:
A kind of resistance O compoiste material comprises following components in part by weight: glass fibre 0.1~50, polyolefine 40~80 and auxiliary agent 0.01~20.
Resistance O compoiste material described in the technique scheme, wherein, said resistance O compoiste material also comprises the mineral filler that weight part is X, wherein 0<X≤100; Wherein said mineral filler is preferably mica or talcum powder.
Resistance O compoiste material described in the technique scheme, wherein, polyolefine is selected from one or more the combination in polypropylene, Vilaterm or the polybutene.
Resistance O compoiste material described in the technique scheme, wherein, auxiliary agent is compatilizer, coupling agent, linking agent or oxidation inhibitor.
Resistance O compoiste material described in the technique scheme, wherein, said compatilizer is a maleic anhydride graft class compatilizer.
The preparation method of the described resistance O compoiste material of arbitrary technical scheme in the technique scheme; Said method is the auxiliary agent that base mateiral adds said weight part for the polyolefine with said weight part; With the glass fibre of said weight part as toughener; The three is mixed in high speed agitator; On twin screw extruder, carry out granulation, obtain hindering O compoiste material behind the granulating and drying.
The described preparation method of technique scheme wherein, also is added with the mineral filler that weight part is X, wherein 0<X≤100 in said preparing method's the raw material.
The described preparation method of technique scheme, wherein, mineral filler is mica or talcum powder; Polyolefine is selected from one or more the combination in polypropylene, Vilaterm or the polybutene; Auxiliary agent is compatilizer, coupling agent, linking agent or oxidation inhibitor.
The described preparation method of technique scheme, wherein, said compatilizer is a maleic anhydride graft class compatilizer.
Adopting polyolefine among the present invention is matrix resin; The auxiliary agent that adds corresponding content; Like compatilizer, coupling agent, linking agent and oxidation inhibitor; Interface binding power between glass fibre and the polyolefine is strengthened; And glass fibre combines with ionic linkage between the polyolefine to strengthen; And make that contained free molecule is cross-linked with each other in the polyolefine, become a reticulated structure system.
The present invention has following beneficial effect: because resistance O compoiste material of the present invention does not have acute functional group; Therefore do not need sticking can the combining together of hot melt adhesive to form the molecular linkage of tubing base-material and resistance O compoiste material interlayer between tubing base-material and the resistance O compoiste material layer, overcome temperature or humidity simultaneously and raise the influence of its barrier property with the tubing base-material.
Embodiment:
For making technical scheme of the present invention be convenient to understand, the present invention is further illustrated below in conjunction with embodiment.
Embodiment 1:The preparation of resistance O compoiste material
Polypropylene with 40 parts of weight parts is base mateiral, uses the maleic anhydride inoculated polypropylene of 0.01 part of weight part to be compatilizer; With the glass fibre of 5 parts of weight parts as toughener; The three is mixed in high speed agitator; On twin screw extruder, carry out granulation, obtain hindering O compoiste material behind the granulating and drying.
Embodiment 2:The preparation of resistance O compoiste material
The step of present embodiment is identical with embodiment one; Difference is: the Vilaterm with 80 parts of weight parts in the present embodiment is a base mateiral; Maleic anhydride grafted polyethylene with 1 part of weight part is a compatilizer, is toughener with the glass fibre of weight part 0.1, preparation resistance O compoiste material.
Embodiment 3:The preparation of resistance O compoiste material
The step of present embodiment is identical with embodiment two with embodiment one; Difference is: the polypropylene with 60 parts of weight parts in the present embodiment is a base mateiral; Maleic anhydride inoculated polypropylene with 20 parts of weight parts is a compatilizer; With the glass fibre of weight part 50 as toughener, preparation resistance O compoiste material.
Embodiment 4:The preparation of resistance O compoiste material
As improvement, added mica or the talcum powder of 50 parts of weight parts in the present embodiment to embodiment 1.
Embodiment 5:The preparation of resistance O compoiste material
As improvement, in the step of embodiment 2, added the mica or the talcum powder of 100 parts of weight parts to embodiment 2.
The technological method that generally adopts through employing this area carries out OTR oxygen transmission rate (m to the product of the embodiment of the invention 1~5
3/ cm
2SPa) and water vapor transmission rate (WVTR) (gcm/cm
2SPa) test, the OTR oxygen transmission rate of the embodiment of the invention 1~4 is 0.61 * 10
-13~1.52 * 10
-13, the water vapour percent of pass is 0.56 * 10
-14~1.66 * 10
-14, matrix material of the present invention effect aspect blocking oxygen and water vapour is remarkable.
The above; It only is preferred embodiment of the present invention; Be not that the present invention is done any formal and substantial restriction; Allly be familiar with the professional and technical personnel; In not breaking away from technical scheme scope of the present invention; When can utilizing the above technology contents that discloses, and a little change of making, modify the equivalent variations with differentiation, be equivalent embodiment of the present invention; Simultaneously, all foundations essence technology of the present invention all still belongs in the scope of technical scheme of the present invention change, modification and the differentiation of any equivalent variations that above embodiment did.
Claims (10)
1. a resistance O compoiste material comprises following components in part by weight: glass fibre 0.1~50, polyolefine 40~80 and auxiliary agent 0.01~20.
2. resistance O compoiste material according to claim 1 is characterized in that: said resistance O compoiste material also comprises the mineral filler that weight part is X, wherein 0<X≤100.
3. resistance O compoiste material according to claim 2 is characterized in that: said mineral filler is mica or talcum powder.
4. according to the described resistance O compoiste material of arbitrary claim in the claim 1~3, it is characterized in that: polyolefine is selected from one or more the combination in polypropylene, Vilaterm or the polybutene.
5. according to the described resistance O compoiste material of arbitrary claim in the claim 1~3, it is characterized in that: auxiliary agent is compatilizer, coupling agent, linking agent or oxidation inhibitor.
6. resistance O compoiste material according to claim 5 is characterized in that: said compatilizer is a maleic anhydride graft class compatilizer.
7. the preparation method of the described resistance O compoiste material of arbitrary claim in the claim 1~6; Said method is the auxiliary agent that base mateiral adds said weight part for the polyolefine with said weight part; With the glass fibre of said weight part as toughener; The three is mixed in high speed agitator; On twin screw extruder, carry out granulation, obtain hindering O compoiste material behind the granulating and drying.
8. preparation method according to claim 7 is characterized in that: also be added with the mineral filler that weight part is X in said preparing method's the raw material, wherein 0<X≤100.
9. according to claim 7 or 8 described preparing methods, it is characterized in that: mineral filler is mica or talcum powder; Polyolefine is selected from one or more the combination in polypropylene, Vilaterm or the polybutene; Auxiliary agent is compatilizer, coupling agent, linking agent or oxidation inhibitor.
10. preparation method according to claim 9 is characterized in that: said compatilizer is a maleic anhydride graft class compatilizer.
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CN2011102660619A CN102352063A (en) | 2011-09-09 | 2011-09-09 | Oxygen barrier composite material and preparation method thereof |
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CN2011102660619A CN102352063A (en) | 2011-09-09 | 2011-09-09 | Oxygen barrier composite material and preparation method thereof |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102617920A (en) * | 2012-04-16 | 2012-08-01 | 上海金发科技发展有限公司 | Glass-fiber reinforced bimodal polyethylene material and preparation process thereof |
CN102643487A (en) * | 2012-04-25 | 2012-08-22 | 金发科技股份有限公司 | Polyolefin composition excellent in scraping resistance and preparation method and application of polyolefin composition |
CN103694563A (en) * | 2013-12-18 | 2014-04-02 | 上海日之升新技术发展有限公司 | Novel high-gloss fiberglass-reinforced polypropylene composite material and preparation method thereof |
CN109535524A (en) * | 2018-11-26 | 2019-03-29 | 铜陵熙成塑料制品有限公司 | A kind of highstrenghtpiston packs inner bag material and preparation method thereof |
CN111040304A (en) * | 2019-12-27 | 2020-04-21 | 上海邦中新材料有限公司 | High-strength high-oxygen-resistance polypropylene bonding resin and preparation method thereof |
CN114921010A (en) * | 2021-07-30 | 2022-08-19 | 集瑞泽管业(江苏)有限公司 | Oxygen-resistant irradiation crosslinked polyethylene material and polyethylene pipe thereof |
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CN1235990A (en) * | 1999-03-04 | 1999-11-24 | 上海杰事杰材料新技术公司 | Extrudable glass fibre reinforced polypropylene composition |
CN1328084A (en) * | 2001-07-03 | 2001-12-26 | 成都市华硕实业有限公司 | Composite of microfibre, superfine powder and polypropylene |
CN1468897A (en) * | 2003-06-10 | 2004-01-21 | 上海英泰塑胶有限公司 | Composite polypropylene material containing potassium titanate whisker and glass fiber |
CN101338051A (en) * | 2008-08-08 | 2009-01-07 | 苏州工业园区和昌电器有限公司 | Long glass fiber reinforced polypropylene material and preparation thereof |
-
2011
- 2011-09-09 CN CN2011102660619A patent/CN102352063A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN1235990A (en) * | 1999-03-04 | 1999-11-24 | 上海杰事杰材料新技术公司 | Extrudable glass fibre reinforced polypropylene composition |
CN1328084A (en) * | 2001-07-03 | 2001-12-26 | 成都市华硕实业有限公司 | Composite of microfibre, superfine powder and polypropylene |
CN1468897A (en) * | 2003-06-10 | 2004-01-21 | 上海英泰塑胶有限公司 | Composite polypropylene material containing potassium titanate whisker and glass fiber |
CN101338051A (en) * | 2008-08-08 | 2009-01-07 | 苏州工业园区和昌电器有限公司 | Long glass fiber reinforced polypropylene material and preparation thereof |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102617920A (en) * | 2012-04-16 | 2012-08-01 | 上海金发科技发展有限公司 | Glass-fiber reinforced bimodal polyethylene material and preparation process thereof |
CN102617920B (en) * | 2012-04-16 | 2014-01-22 | 上海金发科技发展有限公司 | Glass-fiber reinforced bimodal polyethylene material and preparation process thereof |
CN102643487A (en) * | 2012-04-25 | 2012-08-22 | 金发科技股份有限公司 | Polyolefin composition excellent in scraping resistance and preparation method and application of polyolefin composition |
CN103694563A (en) * | 2013-12-18 | 2014-04-02 | 上海日之升新技术发展有限公司 | Novel high-gloss fiberglass-reinforced polypropylene composite material and preparation method thereof |
CN109535524A (en) * | 2018-11-26 | 2019-03-29 | 铜陵熙成塑料制品有限公司 | A kind of highstrenghtpiston packs inner bag material and preparation method thereof |
CN111040304A (en) * | 2019-12-27 | 2020-04-21 | 上海邦中新材料有限公司 | High-strength high-oxygen-resistance polypropylene bonding resin and preparation method thereof |
CN114921010A (en) * | 2021-07-30 | 2022-08-19 | 集瑞泽管业(江苏)有限公司 | Oxygen-resistant irradiation crosslinked polyethylene material and polyethylene pipe thereof |
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Application publication date: 20120215 |