CN108314820A - Stretched film and preparation method thereof - Google Patents

Stretched film and preparation method thereof Download PDF

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CN108314820A
CN108314820A CN201810130490.5A CN201810130490A CN108314820A CN 108314820 A CN108314820 A CN 108314820A CN 201810130490 A CN201810130490 A CN 201810130490A CN 108314820 A CN108314820 A CN 108314820A
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parts
density polyethylene
stretched film
low density
10min
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CN108314820B (en
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李昂
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Qingdao Soft Plastic Industry Co Ltd
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Qingdao Soft Plastic Industry Co Ltd
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised 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
    • C08J2323/04Homopolymers or copolymers of ethene
    • C08J2323/06Polyethene
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2423/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2423/02Characterised 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
    • C08J2423/04Homopolymers or copolymers of ethene
    • C08J2423/06Polyethene
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2423/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2423/02Characterised 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
    • C08J2423/10Homopolymers or copolymers of propene
    • C08J2423/12Polypropene
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2423/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2423/26Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers modified by chemical after-treatment
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/02Organic and inorganic ingredients
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/32Phosphorus-containing compounds
    • C08K2003/321Phosphates
    • C08K2003/322Ammonium phosphate
    • C08K2003/323Ammonium polyphosphate
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/346Clay
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
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    • C08K5/05Alcohols; Metal alcoholates
    • C08K5/053Polyhydroxylic alcohols
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/12Esters; Ether-esters of cyclic polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477Six-membered rings
    • C08K5/3492Triazines
    • C08K5/34922Melamine; Derivatives thereof

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  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)

Abstract

The invention discloses a kind of stretched films and preparation method thereof, belong to field of packaging material, its key points of the technical solution are that a kind of stretched film, by the material composition of following parts by weight:15 25 parts of low density polyethylene (LDPE), 58 parts of polypropylene, 49 parts of very low density polyethylene, 25 parts of high density polyethylene (HDPE), 1.1 1.5 parts of toluene di-isocyanate(TDI), 0.2 0.5 parts of polybutadiene, 5 7.5 parts of metallocene, 1.2 1.7 parts of halogen-free flame retardants, 0.3 0.8 parts of plasticizer, modified 0.6 1.1 parts of polyisobutene, the melting means of the low density polyethylene (LDPE) is 3.5g/10min, density 0.926g/cm3, the melting means of the very low density polyethylene is 2g/10min, density 0.891g/cm3, the melting means of high density polyethylene (HDPE) is 6.3g/10min, density 0.953g/cm3;The preparation method of the stretched film includes the following steps:(1) mold is cleared up;(2) it feeds;(3) it squeezes out;(4) it is cast:(5) it winds.Stretched film prepared by the present invention has higher tensile strength and tearing toughness.

Description

Stretched film and preparation method thereof
Technical field
The present invention relates to field of packaging material, more specifically, it is related to a kind of stretched film and preparation method thereof.
Background technology
The packaged form of product is varied, and it is also one of them more commonly used packaged form to stretch membrane material.It can Protection is formed with the periphery in product, can make that product is moisture-proof, dust-proof, waterproof.Membrane material is stretched to pack compared to traditional papery Its cost is more cheap, has very high application value.Stretched film commonly used material is low density polyethylene (LDPE), through overcurrent Prolong or stretched film that film-blowing process is prepared.Stretched film packing method is simple, especially suitable in logistic industry, stretching at present The speedup in film market is very fast, and annual growth rate has boundless market 20% or more.
But conventional stretching membrane material stretches the tensile strength and tear-proof of membrane material due to the unicity of its ingredient Intensity is relatively low, is easily broken when encountering sharppointed article, cannot preferably be applied in packaging product, it is therefore desirable to prepare a kind of Stretched film with good stretch-proof and tear resistance.
Invention content
In view of the deficiencies of the prior art, the present invention intends to provide a kind of stretched film, with good anti- Stretching and tear resistance.
To achieve the above object, the present invention provides following technical solutions:A kind of stretched film, by the substance of following parts by weight Composition:15-25 parts of low density polyethylene (LDPE), 5-8 parts of polypropylene, 4-9 parts of very low density polyethylene, 2-5 parts of high density polyethylene (HDPE), first 1.1-1.5 parts of phenylene diisocyanate, 5-7.5 parts of metallocene, 1.2-1.7 parts of halogen-free flame retardants, increases 0.2-0.5 parts of polybutadiene 0.3-0.8 parts of agent, modified 0.6-1.1 parts of polyisobutene are moulded, the melting means of the low density polyethylene (LDPE) is 3.5g/10min, and density is 0.926g/cm3, the melting means of the very low density polyethylene is 2g/10min, density 0.891g/cm3, high density polyethylene (HDPE) Melting means is 6.3g/10min, density 0.953g/cm3
By using above-mentioned technical proposal, it is blended using very low density polyethylene and polypropylene, high density polyethylene (HDPE), it can The tearing strength for improving stretched film improves its toughness, environmental stress crack resistance and flexibility, and toluene di-isocyanate(TDI) is added, The shock resistance degree, penetration-resistant, anti-weight that stretched film can be improved pound falling property and flexibility, modified polyisobutene are added, as increasing Viscous master batch, can make stretched film have preferable extensibility and good resilience, and it is good that stretched film can be made to have Mechanical strength.
The present invention is further arranged to:The modified polyisobutene is prepared by following methods:It is 3 to weigh mass ratio: 1:1:2:1 isobutene, bis- (2- chloro isopropyls) benzene of Isosorbide-5-Nitrae-, vanadium tetrachloride, 2- picolines and triphenyl allyl silicane, will Bis- (2- chloro isopropyls) benzene of isobutene, Isosorbide-5-Nitrae-, vanadium tetrachloride and 2- picolines be placed in blender stirring bring it about it is poly- Reaction is closed, modified polyisobutene is made triphenyl allyl silicane is added into blender.
By using above-mentioned technical proposal, bis- (2- chloro isopropyls) benzene of isobutene, Isosorbide-5-Nitrae-, vanadium tetrachloride and 2- methyl are utilized Pyridine polymerization generates polyisobutene, is modified polyisobutene end-allyl group is made using triphenyl allyl silicane, can improve The activity of polyisobutene, convenient for polyisobutene and other substance reactions.
The present invention is further arranged to:By the material composition of following parts by weight:20 parts of low density polyethylene (LDPE), polypropylene 6.5 Part, 6.5 parts of very low density polyethylene, 3.5 parts of high density polyethylene (HDPE), 1.3 parts of toluene di-isocyanate(TDI), 0.35 part of polybutadiene, 6 parts of metallocene, 1.55 parts of halogen-free flame retardants, 0.55 part of plasticizer, modified 0.85 part of polyisobutene, the low density polyethylene (LDPE) Melting means is 3.5g/10min, density 0.926g/cm3, the melting means of the very low density polyethylene is 2g/10min, and density is 0.891g/cm3, the melting means of high density polyethylene (HDPE) is 6.3g/10min, density 0.953g/cm3
By using above-mentioned technical proposal, using the proportioning of the parts by weight, stretched film obtained has preferable stretch-proof Performance and tear resistance.
The present invention is further arranged to:Plasticizer refers to dioctyl phthalate, repefral, adjacent benzene two One or more of formic acid dicyclohexyl maleate.
It can enhance the flexibility of stretched film using plasticizer by using above-mentioned technical proposal, stretched film is made to encounter When sharp object, there is preferable degree of drawing, be not easy to be pierced through by sharp object.
The present invention is further arranged to:The halogen-free flame retardants is by melamine, ammonium polyphosphate, pentaerythrite and organic Montmorillonite is 3 in mass ratio:1:1:2 compositions.
By using above-mentioned technical proposal, melamine releases CO when heated2、NH3、N2Gas and H2O reduces sky The concentration of the fuel gas generated when oxygen and high polymer are thermally decomposed in gas, and the non-flammable gases generated, have taken away a part Heat reduces the temperature of polymer surfaces, the N of generation2Free radical can be captured, the chain reaction of high polymer is inhibited, to hinder It only burns, but melamine is used alone that effect is not so good and polyphosphoric acid amine, pentaerythrite and organo montmorillonite is compound makes With effect is more preferable.
In view of the deficienciess of the prior art, it is another object of the present invention to provide a kind of preparation sides of stretched film Method, the stretched film prepared have good stretch-proof and tear resistance, include the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replaces strainer, reaction temperature is set in 80 DEG C, 2-5 parts of 5-8 parts of polypropylene, 4-9 parts of very low density polyethylene and high density polyethylene (HDPE) are weighed according to weight ratio, is sufficiently stirred Uniformly and keep the temperature 20 minutes at 80 DEG C;
(2) it feeds:Reaction temperature is risen to 95 DEG C, sequentially added into the raw material stirred evenly 15-25 parts of low density polyethylene (LDPE), 1.1-1.5 parts of toluene di-isocyanate(TDI), 0.2-0.5 parts of polybutadiene, 5-7.5 parts of metallocene, 1.2-1.7 parts of halogen-free flame retardants, 0.3-0.8 parts of plasticizer, modified 0.6-1.1 parts of polyisobutene, are sufficiently stirred, and keep the temperature 2 hours at 95 DEG C;
(3) it squeezes out:Raw material in step (2) is subjected to Couble screw rod high-temp extruding;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
By using above-mentioned technical proposal, mold is first cleared up, can prevent drop point caused by material lagging from scratching and stretch Film surface influences product quality;First low density polyethylene (LDPE), polypropylene, very low density polyethylene and high density polyethylene (HDPE) are stirred Uniformly, other dispensings are added, are again stirring for uniformly, stirring using gradation, can be convenient for stirring evenly raw material;Utilize strainer Impurity in raw material can be removed, ensure that the stretched film prepared has higher transparency and flatness, without black material residue;It will Casting temperature is set as 220 DEG C, can ensure that stretched film uniformly flows out, and consistency of thickness, prepares the higher stretched film of mass.
The present invention is further arranged to:The mesh number of strainer is 100 mesh in the step (1), and is arranged two layers.
By using above-mentioned technical proposal, the impurity that the strainer for being 100 using mesh number can be in filter stock makes to have prepared At stretched film there is preferable transparency and flatness, quality is higher.
The present invention is further arranged to:The screw diameter of double screw extruder is 55mm in the step (3), and draw ratio is 15:1。
By using above-mentioned technical proposal, screw diameter 55mm, draw ratio 15:1, the length of screw rod is then 8.25m, Longer spiro rod plasticizing effect is good.
The present invention is further arranged to:Step (3) the high temperature extruding is divided into 4 stages, first stage temperature range It it is 154-166 DEG C, second stage temperature range is 174-181 DEG C, and phase III temperature range is 186-198 DEG C, fourth stage Temperature range is 200-210 DEG C.
It by using above-mentioned technical proposal, is squeezed stage by stage during high temperature extrusion, because of the surface of particle Product is little, although viscous dissipation heat is very big, receives the restriction of heat transfer area, the practical energy for coming in and going out solid particle is limited , so that temperature is increased at staged, particle surface and particle inner homogeneous can be made heated, the material quality of extrusion can be made more It is good.
The present invention is further arranged to:Stir speed (S.S.) is 900-1200 revs/min in the step (1) and step (2), Mixing time is 30-50min.
Can be uniform by material stirring using 900-1200 revs/min of rotating speed by using above-mentioned technical proposal, and Mixing time is long, it is ensured that is mixed between each component abundant.
In conclusion the invention has the advantages that:
(1) present invention is blended by using very low density polyethylene and polypropylene, high density polyethylene (HDPE) and is used as raw material, can improve The tearing strength of stretched film improves its toughness, environmental stress crack resistance and flexibility;
(2) present invention can improve the shock resistance degree, penetration-resistant, anti-weight of stretched film by the way that toluene di-isocyanate(TDI) is added Pound falling property and flexibility;
(3) present invention is by the modified polyisobutene of addition, as thickening master batch, can make stretched film have preferable extensibility and Good resilience, and can make stretched film that there is good mechanical strength;
(4) present invention makes temperature rise at staged using being squeezed stage by stage during high temperature extrusion, can make Grain surface and particle inner homogeneous are heated, and the material quality of extrusion can be made more preferable.
Specific implementation mode
With reference to embodiment, invention is further described in detail.
Embodiment 1:A kind of stretched film, by the material composition of following parts by weight:15 parts of low density polyethylene (LDPE), 5 parts of polypropylene, 4 parts of very low density polyethylene, 2 parts of high density polyethylene (HDPE), 1.1 parts of toluene di-isocyanate(TDI), 0.2 part of polybutadiene, metallocene 5 Part is 3 in mass ratio by melamine, ammonium polyphosphate, pentaerythrite and organo montmorillonite:1:1:The halogen-free flame retardants of 2 compositions 1.2 parts, 0.3 part of dioctyl phthalate, modified 0.6 part of polyisobutene, the wherein melting means of low density polyethylene (LDPE) is 3.5g/ 10min, density 0.926g/cm3, very low density polyethylene melting means be 2g/10min, density 0.891g/cm3, high density The melting means of polyethylene is 6.3g/10min, density 0.953g/cm3;Modified polyisobutene is prepared by following methods:It weighs Mass ratio is 3:1:1:2:1 isobutene, bis- (2- chloro isopropyls) benzene of Isosorbide-5-Nitrae-, vanadium tetrachloride, 2- picolines and triphenyl alkene Bis- (2- chloro isopropyls) benzene of isobutene, Isosorbide-5-Nitrae-, vanadium tetrachloride and 2- picolines are placed in blender and are stirred by propyl silane Polymerisation is brought it about, modified polyisobutene is made triphenyl allyl silicane is added into blender;The stretched film Preparation method includes the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replacement mesh number is 100 purpose, two layers of strainer, will Reaction temperature is set in 80 DEG C, and 5 parts of polypropylene, 4 parts of very low density polyethylene and high density polyethylene (HDPE) 2 are weighed according to weight ratio Part, it stirs and keeps the temperature 20 minutes at 80 DEG C;
(2) it feeds:Reaction temperature is risen to 95 DEG C, 15 parts of low density polyethylene (LDPE), first are sequentially added into the raw material stirred evenly 1.1 parts of phenylene diisocyanate, 0.2 part of polybutadiene, 5 parts of metallocene, by melamine, ammonium polyphosphate, pentaerythrite and organic Montmorillonite is 3 in mass ratio:1:1:1.2 parts of halogen-free flame retardants, 0.3 part of dioctyl phthalate, the modified poly- isobutyl of 2 compositions 0.6 part of alkene, is sufficiently stirred, and stir speed (S.S.) is 900 revs/min, and mixing time is 50min, and keeps the temperature 2 at 95 DEG C Hour;
(3) it squeezes out:By the raw material in step (2) a diameter of 50mm, draw ratio 15:1 twin-screw carries out high temperature extrusion, high Warm Extrusion is divided into 4 stages, and first stage temperature range is 154 DEG C, and second stage temperature range is 174 DEG C, phase III temperature It is 186 DEG C to spend section, and fourth stage temperature range is 200 DEG C;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
Embodiment 2:A kind of stretched film, by the material composition of following parts by weight:20 parts of low density polyethylene (LDPE), polypropylene 6.5 Part, 6.5 parts of very low density polyethylene, 3.5 parts of high density polyethylene (HDPE), 1.3 parts of toluene di-isocyanate(TDI), 0.35 part of polybutadiene, 6 parts of metallocene is 3 in mass ratio by melamine, ammonium polyphosphate, pentaerythrite and organo montmorillonite:1:1:The Halogen of 2 compositions 1.55 parts of fire retardant, 0.55 part of repefral, modified 0.85 part of polyisobutene, the wherein melting means of low density polyethylene (LDPE) For 3.5g/10min, density 0.926g/cm3, very low density polyethylene melting means be 2g/10min, density 0.891g/cm3、 The melting means of high density polyethylene (HDPE) is 6.3g/10min, density 0.953g/cm3;Modified polyisobutene prepared by following methods and At:It is 3 to weigh mass ratio:1:1:2:1 isobutene, bis- (2- chloro isopropyls) benzene of Isosorbide-5-Nitrae-, vanadium tetrachloride, 2- picolines and three Bis- (2- chloro isopropyls) benzene of isobutene, Isosorbide-5-Nitrae-, vanadium tetrachloride and 2- picolines are placed on blender by allyl base silane Middle stirring brings it about polymerisation, and modified polyisobutene is made triphenyl allyl silicane is added into blender;The drawing The preparation method for stretching film includes the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replacement mesh number is 100 purpose, two layers of strainer, will Reaction temperature is set in 80 DEG C, and 6.5 parts of polypropylene, 6.5 parts of very low density polyethylene and high-density polyethylene are weighed according to weight ratio 3.5 parts of alkene, stirs, and stir speed (S.S.) is 1050 revs/min, and mixing time is 40min, and is kept the temperature at 80 DEG C 20 minutes;
(2) it feeds:Reaction temperature is risen to 95 DEG C, 20 parts of low density polyethylene (LDPE), first are sequentially added into the raw material stirred evenly 1.3 parts of phenylene diisocyanate, 0.35 part of polybutadiene, 6 parts of metallocene, by melamine, ammonium polyphosphate, pentaerythrite and organic Montmorillonite is 3 in mass ratio:1:1:1.55 parts of the halogen-free flame retardants of 2 compositions, 0.55 part of repefral, modification are poly- different 0.85 part of butylene, is sufficiently stirred, and stir speed (S.S.) is 1050 revs/min, and mixing time is 40min, and at 95 DEG C Heat preservation 2 hours;
(3) it squeezes out:By the raw material in step (2) a diameter of 50mm, draw ratio 15:1 twin-screw carries out high temperature extrusion, high Warm Extrusion is divided into 4 stages, and first stage temperature range is 154-166 DEG C, and second stage temperature range is 174-181 DEG C, the Three phase temperature sections are 186-198 DEG C, and fourth stage temperature range is 200-210 DEG C;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
Embodiment 3:A kind of stretched film, by the material composition of following parts by weight:25 parts of low density polyethylene (LDPE), 8 parts of polypropylene, 9 parts of very low density polyethylene, 5 parts of high density polyethylene (HDPE), 1.5 parts of toluene di-isocyanate(TDI), 0.5 part of polybutadiene, metallocene 7.5 Part is 3 in mass ratio by melamine, ammonium polyphosphate, pentaerythrite and organo montmorillonite:1:1:The halogen-free flame retardants of 2 compositions 1.7 parts, 0.8 part of dicyclohexyl phthalate, modified 1.1 parts of polyisobutene, the wherein melting means of low density polyethylene (LDPE) is 3.5g/ 10min, density 0.926g/cm3, very low density polyethylene melting means be 2g/10min, density 0.891g/cm3, high density The melting means of polyethylene is 6.3g/10min, density 0.953g/cm3;Modified polyisobutene is prepared by following methods:It weighs Mass ratio is 3:1:1:2:1 isobutene, bis- (2- chloro isopropyls) benzene of Isosorbide-5-Nitrae-, vanadium tetrachloride, 2- picolines and triphenyl alkene Bis- (2- chloro isopropyls) benzene of isobutene, Isosorbide-5-Nitrae-, vanadium tetrachloride and 2- picolines are placed in blender and are stirred by propyl silane Polymerisation is brought it about, modified polyisobutene is made triphenyl allyl silicane is added into blender;The stretched film Preparation method includes the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replacement mesh number is 100 purpose, two layers of strainer, will Reaction temperature is set in 80 DEG C, and 8 parts of polypropylene, 9 parts of very low density polyethylene and high density polyethylene (HDPE) 5 are weighed according to weight ratio Part, it stirs, stir speed (S.S.) is 1200 revs/min, and mixing time is 30min, and 20 points are kept the temperature at 80 DEG C Clock;
(2) it feeds:Reaction temperature is risen to 95 DEG C, 25 parts of low density polyethylene (LDPE), first are sequentially added into the raw material stirred evenly 1.5 parts of phenylene diisocyanate, 7.5 parts of metallocene, by melamine, ammonium polyphosphate, pentaerythrite and has 0.5 part of polybutadiene Machine montmorillonite is 3 in mass ratio:1:1:1.7 parts of the halogen-free flame retardants of 2 compositions, is modified and gathers 0.8 part of dicyclohexyl phthalate 1.1 parts of isobutene, is sufficiently stirred, and stir speed (S.S.) is 1200 revs/min, and mixing time is 30min, and at 95 DEG C Heat preservation 2 hours;
(3) it squeezes out:By the raw material in step (2) a diameter of 50mm, draw ratio 15:1 twin-screw carries out high temperature extrusion, high Warm Extrusion is divided into 4 stages, and first stage temperature range is 154-166 DEG C, and second stage temperature range is 174-181 DEG C, the Three phase temperature sections are 186-198 DEG C, and fourth stage temperature range is 200-210 DEG C;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
Comparative example:A kind of stretched film, by the material composition of following parts by weight:20 parts of low density polyethylene (LDPE), toluene diisocyanate 1.3 parts of acid esters, 6 parts of metallocene, is pressed by melamine, ammonium polyphosphate, pentaerythrite and organo montmorillonite 0.35 part of polybutadiene Mass ratio is 3:1:1:1.55 parts of halogen-free flame retardants, 0.55 part of repefral, the modified polyisobutene 0.85 of 2 compositions Part, wherein the melting means of low density polyethylene (LDPE) is 3.5g/10min, density 0.926g/cm3, very low density polyethylene melting means be 2g/10min, density 0.891g/cm3, high density polyethylene (HDPE) melting means be 6.3g/10min, density 0.953g/cm3;It is modified Polyisobutene is prepared by following methods:It is 3 to weigh mass ratio:1:1:2:1 isobutene, Isosorbide-5-Nitrae-are bis- (2- chloro isopropyls) Benzene, vanadium tetrachloride, 2- picolines and triphenyl allyl silicane, by bis- (2- chloro isopropyls) benzene of isobutene, Isosorbide-5-Nitrae-, four chlorinations Vanadium and 2- picolines are placed on stirring in blender and bring it about polymerisation, and triphenyl allyl is being added into blender Modified polyisobutene is made in silane;The preparation method of the stretched film includes the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replacement mesh number is 100 purpose, two layers of strainer;
(2) it feeds:Reaction temperature is risen to 95 DEG C, 20 parts of low density polyethylene (LDPE), first are sequentially added into the raw material stirred evenly 1.3 parts of phenylene diisocyanate, 0.35 part of polybutadiene, 6 parts of metallocene, by melamine, ammonium polyphosphate, pentaerythrite and organic Montmorillonite is 3 in mass ratio:1:1:1.55 parts of the halogen-free flame retardants of 2 compositions, 0.55 part of repefral, modification are poly- different 0.85 part of butylene, is sufficiently stirred, and stir speed (S.S.) is 1050 revs/min, and mixing time is 40min, and at 95 DEG C Heat preservation 2 hours;
(3) it squeezes out:By the raw material in step (2) a diameter of 50mm, draw ratio 15:1 twin-screw carries out high temperature extrusion, high Warm Extrusion is divided into 4 stages, and first stage temperature range is 154-166 DEG C, and second stage temperature range is 174-181 DEG C, the Three phase temperature sections are 186-198 DEG C, and fourth stage temperature range is 200-210 DEG C;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
Comparative example 2:A kind of stretched film, by the material composition of following parts by weight:20 parts of low density polyethylene (LDPE), polypropylene 6.5 Part, 6.5 parts of very low density polyethylene, 3.5 parts of high density polyethylene (HDPE), 1.3 parts of toluene di-isocyanate(TDI), 0.35 part of polybutadiene, 6 parts of metallocene is 3 in mass ratio by melamine, ammonium polyphosphate, pentaerythrite and organo montmorillonite:1:1:The Halogen of 2 compositions 1.55 parts of fire retardant, 0.55 part of repefral, the wherein melting means of low density polyethylene (LDPE) are 3.5g/10min, and density is 0.926g/cm3, very low density polyethylene melting means be 2g/10min, density 0.891g/cm3, high density polyethylene (HDPE) melting means For 6.3g/10min, density 0.953g/cm3;The preparation method of the stretched film includes the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replacement mesh number is 100 purpose, two layers of strainer, will Reaction temperature is set in 80 DEG C, and 6.5 parts of polypropylene, 6.5 parts of very low density polyethylene and high-density polyethylene are weighed according to weight ratio 3.5 parts of alkene, stirs, and stir speed (S.S.) is 1050 revs/min, and mixing time is 40min, and is kept the temperature at 80 DEG C 20 minutes;
(2) it feeds:Reaction temperature is risen to 95 DEG C, 20 parts of low density polyethylene (LDPE), first are sequentially added into the raw material stirred evenly 1.3 parts of phenylene diisocyanate, 0.35 part of polybutadiene, 6 parts of metallocene, by melamine, ammonium polyphosphate, pentaerythrite and organic Montmorillonite is 3 in mass ratio:1:1:1.55 parts of halogen-free flame retardants, 0.55 part of repefral, the polyisobutene of 2 compositions It 0.85 part, is sufficiently stirred, stir speed (S.S.) is 1050 revs/min, and mixing time is 40min, and keeps the temperature 2 at 95 DEG C Hour;
(3) it squeezes out:By the raw material in step (2) a diameter of 50mm, draw ratio 15:1 twin-screw carries out high temperature extrusion, high Warm Extrusion is divided into 4 stages, and first stage temperature range is 154-166 DEG C, and second stage temperature range is 174-181 DEG C, the Three phase temperature sections are 186-198 DEG C, and fourth stage temperature range is 200-210 DEG C;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
Comparative example 3:Embodiment 2:A kind of stretched film, by the material composition of following parts by weight:20 parts of low density polyethylene (LDPE), first 1.3 parts of phenylene diisocyanate, 0.35 part of polybutadiene, 6 parts of metallocene, by melamine, ammonium polyphosphate, pentaerythrite and organic Montmorillonite is 3 in mass ratio:1:1:1.55 parts of halogen-free flame retardants, 0.55 part of the repefral of 2 compositions, wherein low close The melting means for spending polyethylene is 3.5g/10min, density 0.926g/cm3, very low density polyethylene melting means be 2g/10min, it is close Degree is 0.891g/cm3, high density polyethylene (HDPE) melting means be 6.3g/10min, density 0.953g/cm3;The preparation of the stretched film Method includes the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replacement mesh number is 100 purpose, two layers of strainer;
(2) it feeds:Reaction temperature is risen to 95 DEG C, 20 parts of low density polyethylene (LDPE), first are sequentially added into the raw material stirred evenly 1.3 parts of phenylene diisocyanate, 0.35 part of polybutadiene, 6 parts of metallocene, by melamine, ammonium polyphosphate, pentaerythrite and organic Montmorillonite is 3 in mass ratio:1:1:1.55 parts of halogen-free flame retardants, 0.55 part of the repefral of 2 compositions carry out abundant Stirring, stir speed (S.S.) is 1050 revs/min, and mixing time is 40min, and keeps the temperature 2 hours at 95 DEG C;
(3) it squeezes out:By the raw material in step (2) a diameter of 50mm, draw ratio 15:1 twin-screw carries out high temperature extrusion, high Warm Extrusion is divided into 4 stages, and first stage temperature range is 154-166 DEG C, and second stage temperature range is 174-181 DEG C, the Three phase temperature sections are 186-198 DEG C, and fourth stage temperature range is 200-210 DEG C;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
The tensile strength of stretched film and tearing toughness made from embodiment 1-3 and comparative example 1-3 are detected, detected The results are shown in Table 1:
The testing result of stretched film made from table 1 embodiment 1-3 and comparative example 1-3
As shown in Table 1, various embodiments of the present invention are by being added polypropylene part, very low density polyethylene part and high density polyethylene (HDPE) The tensile strength of stretched film and tearing toughness made from blend and the modified polyisobutene of addition are above in comparative example 1 and make With the tensile strength and tearing toughness of the stretched film that conventional low density polyethylene (LDPE) is fabricated to, and modified poly- isobutyl is only added The comparative example 1 of alkene and be only added polypropylene part, very low density polyethylene, high density polyethylene (HDPE) the comparative example 2 of blend be made Stretched film, although tensile strength and tearing toughness all increase, that polypropylene is not added simultaneously in each embodiment The effect that stretched film is made in part, the blend of very low density polyethylene part and high density polyethylene (HDPE) and modified polyisobutene is good.
The above is only a preferred embodiment of the present invention, protection scope of the present invention is not limited merely to above-mentioned implementation Example, all technical solutions belonged under thinking of the present invention all belong to the scope of protection of the present invention.It should be pointed out that for the art Those of ordinary skill for, several improvements and modifications without departing from the principles of the present invention, these improvements and modifications It should be regarded as protection scope of the present invention.

Claims (10)

1. a kind of stretched film, it is characterised in that:By the material composition of following parts by weight:15-25 parts of low density polyethylene (LDPE), polypropylene 5-8 parts, 4-9 parts of very low density polyethylene, 2-5 parts of high density polyethylene (HDPE), 1.1-1.5 parts of toluene di-isocyanate(TDI), polybutadiene 0.2-0.5 parts, 5-7.5 parts of metallocene, 1.2-1.7 parts of halogen-free flame retardants, 0.3-0.8 parts of plasticizer, modified polyisobutene 0.6- 1.1 parts, the melting means of the low density polyethylene (LDPE) is 3.5g/10min, density 0.926g/cm3, the very low density polyethylene Melting means be 2g/10min, density 0.891g/cm3, the melting means of high density polyethylene (HDPE) is 6.3g/10min, and density is 0.953g/cm3
2. the stretched film according to claim 1, it is characterised in that:The modified polyisobutene is prepared by following methods It forms:It is 3 to weigh mass ratio:1:1:2:1 isobutene, bis- (2- chloro isopropyls) benzene of Isosorbide-5-Nitrae-, vanadium tetrachloride, 2- picolines and Bis- (2- chloro isopropyls) benzene of isobutene, Isosorbide-5-Nitrae-, vanadium tetrachloride and 2- picolines are placed on stirring by triphenyl allyl silicane Stirring brings it about polymerisation in device, and modified polyisobutene is made triphenyl allyl silicane is added into blender.
3. stretched film according to claim 1, it is characterised in that:By the material composition of following parts by weight:Low density polyethylene 20 parts of alkene, 6.5 parts of polypropylene, 6.5 parts of very low density polyethylene, 3.5 parts of high density polyethylene (HDPE), 1.3 parts of toluene di-isocyanate(TDI), 0.35 part of polybutadiene, 6 parts of metallocene, 1.55 parts of halogen-free flame retardants, 0.55 part of plasticizer, modified 0.85 part of polyisobutene, institute The melting means for stating low density polyethylene (LDPE) is 3.5g/10min, density 0.926g/cm3, the melting means of the very low density polyethylene is 2g/10min, density 0.891g/cm3, the melting means of high density polyethylene (HDPE) is 6.3g/10min, density 0.953g/cm3
4. stretched film according to claim 1, it is characterised in that:Plasticizer refers to dioctyl phthalate, adjacent benzene two One or more of formic acid dimethyl ester, dicyclohexyl phthalate.
5. stretched film according to claim 1, it is characterised in that:The halogen-free flame retardants is by melamine, polyphosphoric acid Ammonium, pentaerythrite and organo montmorillonite are 3 in mass ratio:1:1:2 compositions.
6. the method for preparing the stretched film as described in claim 1-5 any one, it is characterised in that:Include the following steps:
(1) mold is cleared up:Go deep into die orifice 2-3cm with soft cutter and remove material residue 3 times, replaces strainer, reaction temperature is set in 80 DEG C, 2-5 parts of 5-8 parts of polypropylene, 4-9 parts of very low density polyethylene and high density polyethylene (HDPE) are weighed according to weight ratio, is sufficiently stirred Uniformly and keep the temperature 20 minutes at 80 DEG C;
(2) it feeds:Reaction temperature is risen to 95 DEG C, sequentially added into the raw material stirred evenly 15-25 parts of low density polyethylene (LDPE), 1.1-1.5 parts of toluene di-isocyanate(TDI), 0.2-0.5 parts of polybutadiene, 5-7.5 parts of metallocene, 1.2-1.7 parts of halogen-free flame retardants, 0.3-0.8 parts of plasticizer, modified 0.6-1.1 parts of polyisobutene, are sufficiently stirred, and keep the temperature 2 hours at 95 DEG C;
(3) it squeezes out:Raw material in step (2) is subjected to Couble screw rod high-temp extruding;
(4) it is cast:Casting temperature by raw material after extrusion casting machine casting film-forming, the firstth area to the 9th area is 220 DEG C, stream It delays to obtain stretched film;
(5) it winds:Stretched film is subjected to volume packet with winder, is stretched film finished product after volume packet.
7. the preparation method of stretched film according to claim 6, it is characterised in that:The mesh number of strainer in the step (1) For 100 mesh, and it is arranged two layers.
8. the preparation method of stretched film according to claim 6, it is characterised in that:Twin-screw extrusion in the step (3) The screw diameter of machine is 55mm, draw ratio 15:1.
9. the preparation method of stretched film according to claim 6, it is characterised in that:Step (3) high temperature, which squeezes, divides For 4 stages, first stage temperature range is 154-166 DEG C, and second stage temperature range is 174-181 DEG C, phase III temperature It is 186-198 DEG C to spend section, and fourth stage temperature range is 200-210 DEG C.
10. the preparation method of stretched film according to claim 6, it is characterised in that:In the step (1) and step (2) Stir speed (S.S.) is 900-1200 revs/min, and mixing time is 30-50min.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108976772A (en) * 2018-07-25 2018-12-11 苏州清之绿新材料有限公司 A kind of wear-resisting antistatic composite sheet and preparation method thereof
CN110685032A (en) * 2019-08-19 2020-01-14 浙江海洋大学 Preparation method of polyethylene mesh wire monofilament with marine fouling prevention characteristic
CN111573000A (en) * 2020-05-29 2020-08-25 佛山市驰力科技有限公司 Wrapping film applied to PE mattress and preparation method
CN111592708A (en) * 2020-06-16 2020-08-28 潍坊众合安美包装科技有限公司 Metal nano stretching and winding film and preparation method thereof
CN112406238A (en) * 2020-12-01 2021-02-26 昆山金盟塑料薄膜有限公司 Green environment-friendly cold-stretched film and preparation method thereof
CN114085449A (en) * 2021-11-11 2022-02-25 宁波市鄞州冰雨塑料制品有限公司 High-tensile winding film and processing technology
CN114316424A (en) * 2021-11-22 2022-04-12 金发科技股份有限公司 Transparent weather-resistant PP/PS composite material and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998003586A1 (en) * 1996-07-22 1998-01-29 Crc For Polymers Pty. Ltd. Polymer blend
CN101503537A (en) * 2008-12-31 2009-08-12 孙国锦 Easy-to-uncover heat sealable films special for sanitary bag
CN103724791A (en) * 2014-01-02 2014-04-16 苏州艾兴无纺布制品有限公司 Ultrahigh-performance plastic film as well as preparation method and composite material thereof
CN106065116A (en) * 2016-06-01 2016-11-02 石狮市炎英塑胶制品有限公司 A kind of cold-resistant, shock resistance casting films and preparation method thereof and production line
CN107418033A (en) * 2017-06-19 2017-12-01 苏州锐耐洁电子科技新材料有限公司 A kind of waterproof and dampproof type packaging material

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998003586A1 (en) * 1996-07-22 1998-01-29 Crc For Polymers Pty. Ltd. Polymer blend
CN101503537A (en) * 2008-12-31 2009-08-12 孙国锦 Easy-to-uncover heat sealable films special for sanitary bag
CN103724791A (en) * 2014-01-02 2014-04-16 苏州艾兴无纺布制品有限公司 Ultrahigh-performance plastic film as well as preparation method and composite material thereof
CN106065116A (en) * 2016-06-01 2016-11-02 石狮市炎英塑胶制品有限公司 A kind of cold-resistant, shock resistance casting films and preparation method thereof and production line
CN107418033A (en) * 2017-06-19 2017-12-01 苏州锐耐洁电子科技新材料有限公司 A kind of waterproof and dampproof type packaging material

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108976772A (en) * 2018-07-25 2018-12-11 苏州清之绿新材料有限公司 A kind of wear-resisting antistatic composite sheet and preparation method thereof
CN110685032A (en) * 2019-08-19 2020-01-14 浙江海洋大学 Preparation method of polyethylene mesh wire monofilament with marine fouling prevention characteristic
CN111573000A (en) * 2020-05-29 2020-08-25 佛山市驰力科技有限公司 Wrapping film applied to PE mattress and preparation method
CN111592708A (en) * 2020-06-16 2020-08-28 潍坊众合安美包装科技有限公司 Metal nano stretching and winding film and preparation method thereof
CN112406238A (en) * 2020-12-01 2021-02-26 昆山金盟塑料薄膜有限公司 Green environment-friendly cold-stretched film and preparation method thereof
CN114085449A (en) * 2021-11-11 2022-02-25 宁波市鄞州冰雨塑料制品有限公司 High-tensile winding film and processing technology
CN114316424A (en) * 2021-11-22 2022-04-12 金发科技股份有限公司 Transparent weather-resistant PP/PS composite material and preparation method thereof
CN114316424B (en) * 2021-11-22 2023-08-25 金发科技股份有限公司 Transparent weather-proof PP/PS composite material and preparation method thereof

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