CN112409728A - High-strength polyvinyl chloride film and preparation method thereof - Google Patents

High-strength polyvinyl chloride film and preparation method thereof Download PDF

Info

Publication number
CN112409728A
CN112409728A CN202011352759.8A CN202011352759A CN112409728A CN 112409728 A CN112409728 A CN 112409728A CN 202011352759 A CN202011352759 A CN 202011352759A CN 112409728 A CN112409728 A CN 112409728A
Authority
CN
China
Prior art keywords
polyvinyl chloride
parts
chloride film
mixture
ethylene
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.)
Pending
Application number
CN202011352759.8A
Other languages
Chinese (zh)
Inventor
黄舒文
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.)
Nantong Gibson Technology Co ltd
Original Assignee
Nantong Gibson Technology 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 Nantong Gibson Technology Co ltd filed Critical Nantong Gibson Technology Co ltd
Priority to CN202011352759.8A priority Critical patent/CN112409728A/en
Publication of CN112409728A publication Critical patent/CN112409728A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • C08J2327/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
    • C08J2327/02Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2327/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08J2327/06Homopolymers or copolymers of vinyl chloride
    • 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
    • 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
    • C08J2423/08Copolymers of ethene
    • 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
    • C08J2467/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2467/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • 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
    • C08J2471/00Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
    • C08J2471/02Polyalkylene oxides
    • 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
    • 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
    • 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
    • C08K2201/00Specific properties of additives
    • C08K2201/017Additives being an antistatic agent
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/346Clay
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • 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
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • 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
    • C08K5/17Amines; Quaternary ammonium compounds
    • C08K5/19Quaternary ammonium compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention discloses a high-strength polyvinyl chloride film and a preparation method thereof, wherein the polyvinyl chloride film comprises, by weight, 70-100 parts of polyvinyl chloride resin, 4-10 parts of a plasticizer, 5-12 parts of an ethylene-propylene copolymer, 1-3 parts of an antistatic agent, 4-10 parts of kaolin and 5-15 parts of silicon micropowder.

Description

High-strength polyvinyl chloride film and preparation method thereof
Technical Field
The invention relates to the technical field of polyvinyl chloride film preservation, in particular to a high-strength polyvinyl chloride film and a preparation method thereof.
Background
The polyvinyl chloride film comprises polyvinyl chloride resin, a plasticizer, a stabilizer, a filler and a pigment, can be prepared by processing technologies such as high-temperature calendering or high-temperature tape casting, can be used as a base material for preparing polyvinyl chloride adhesive tapes, labels and the like due to the characteristics of good insulation and flame retardant properties, higher tensile strength, excellent extensibility and the like, can be widely used for packaging and industrial insulation protection, and is particularly suitable for manufacturing electric adhesive tapes for covering and bundling cable bundles.
The existing polyvinyl chloride film preparation process is complex, and the final finished product has poor overall mechanical properties and short service life, so that improvement is necessary.
Disclosure of Invention
The invention aims to provide a high-strength polyvinyl chloride film and a preparation method thereof, so as to solve the problems in the background technology.
In order to achieve the purpose, the invention provides the following technical scheme: the high-strength polyvinyl chloride film comprises, by weight, 70-100 parts of polyvinyl chloride resin, 4-10 parts of a plasticizer, 5-12 parts of an ethylene-propylene copolymer, 1-3 parts of an antistatic agent, 4-10 parts of kaolin and 5-15 parts of silica micropowder.
Preferably, the polyvinyl chloride film comprises 85 parts of polyvinyl chloride resin, 7 parts of plasticizer, 9 parts of ethylene-propylene copolymer, 2 parts of antistatic agent, 7 parts of kaolin and 10 parts of silicon powder.
Preferably, the plasticizer is one or a mixture of more of ethylene-vinyl acetate copolymer, ethylene-methyl acrylate copolymer and ethylene-ethyl acrylate copolymer.
Preferably, the antistatic agent consists of 30% of allyl trimethyl ammonium bromide, 20% of polyethylene glycol acrylate, 10% of polyethylene glycol, 20% of linolenic acid and 20% of polyethylene terephthalate.
Preferably, the preparation method comprises the following steps:
A. mixing polyvinyl chloride resin, plasticizer and ethylene-propylene copolymer, adding the mixture into a stirring kettle, heating and stirring to obtain a mixture A;
B. adding an antistatic agent, kaolin and silica micropowder into the mixture A, and fully mixing to obtain a mixture B;
C. adding the mixture B into a double-screw extruder for extrusion to obtain polyvinyl chloride film material particles;
D. adding the granules of the polyvinyl chloride film material into a calender to prepare the polyvinyl chloride film.
Preferably, the stirring temperature of the stirring kettle in the step A is 55-70 ℃, the time is 20min-30min, and the stirring speed is 1200-2000 rpm.
Preferably, the extrusion temperature in the step C is 190-210 ℃.
Compared with the prior art, the invention has the beneficial effects that: the preparation method is simple, and the prepared polyvinyl chloride film has high strength, good tensile property, low cost and good environmental protection property, is not easy to damage, is easy to degrade and has good industrialization prospect; the added antistatic agent has excellent antistatic performance, long-acting antistatic performance and better transparency, and can improve the hydrophilicity of the polyester film and further improve the performance of the polyvinyl chloride film.
Detailed Description
The technical solutions in the embodiments of the present invention are clearly and completely described below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
The invention provides the following technical scheme: the high-strength polyvinyl chloride film comprises, by weight, 70-100 parts of polyvinyl chloride resin, 4-10 parts of a plasticizer, 5-12 parts of an ethylene-propylene copolymer, 1-3 parts of an antistatic agent, 4-10 parts of kaolin and 5-15 parts of silica micropowder.
The first embodiment is as follows:
the polyvinyl chloride film comprises, by weight, 70 parts of polyvinyl chloride resin, 4 parts of plasticizer, 5 parts of ethylene-propylene copolymer, 1 part of antistatic agent, 4 parts of kaolin and 5 parts of silicon micropowder.
In this example, an ethylene-vinyl acetate copolymer was used as the plasticizer.
In this example, the antistatic agent was composed of 30% allyl trimethyl ammonium bromide, 20% polyethylene glycol acrylate, 10% polyethylene glycol, 20% linolenic acid, and 20% polyethylene terephthalate.
The preparation method of this example includes the following steps:
A. mixing polyvinyl chloride resin, plasticizer and ethylene-propylene copolymer, adding the mixture into a stirring kettle, heating and stirring to obtain a mixture A;
B. adding an antistatic agent, kaolin and silica micropowder into the mixture A, and fully mixing to obtain a mixture B;
C. adding the mixture B into a double-screw extruder for extrusion to obtain polyvinyl chloride film material particles;
D. adding the granules of the polyvinyl chloride film material into a calender to prepare the polyvinyl chloride film.
In this example, the stirring temperature of the stirring kettle in step A was 55 ℃, the stirring time was 20min, and the stirring rate was 1200 rpm.
In this example, the extrusion temperature in step C was 190 ℃.
Example two:
the polyvinyl chloride film comprises 100 parts of polyvinyl chloride resin, 10 parts of plasticizer, 12 parts of ethylene-propylene copolymer, 3 parts of antistatic agent, 10 parts of kaolin and 15 parts of silicon micropowder according to parts by weight.
In this example, a mixture of an ethylene-methyl acrylate copolymer and an ethylene-ethyl acrylate copolymer was used as the plasticizer.
In this example, the antistatic agent was composed of 30% allyl trimethyl ammonium bromide, 20% polyethylene glycol acrylate, 10% polyethylene glycol, 20% linolenic acid, and 20% polyethylene terephthalate.
The preparation method of this example includes the following steps:
A. mixing polyvinyl chloride resin, plasticizer and ethylene-propylene copolymer, adding the mixture into a stirring kettle, heating and stirring to obtain a mixture A;
B. adding an antistatic agent, kaolin and silica micropowder into the mixture A, and fully mixing to obtain a mixture B;
C. adding the mixture B into a double-screw extruder for extrusion to obtain polyvinyl chloride film material particles;
D. adding the granules of the polyvinyl chloride film material into a calender to prepare the polyvinyl chloride film.
In this example, the stirring temperature of the stirring kettle in the step A is 70 ℃, the stirring time is 30min, and the stirring speed is 2000 rpm.
In this example, the extrusion temperature in step C was 210 ℃.
Example three:
the polyvinyl chloride film comprises 76 parts of polyvinyl chloride resin, 6 parts of plasticizer, 8 parts of ethylene-propylene copolymer, 2 parts of antistatic agent, 5 parts of kaolin and 7 parts of silicon micropowder according to parts by weight.
In this example, the plasticizer was a mixture of ethylene-vinyl acetate copolymer and ethylene-ethyl acrylate copolymer.
In this example, the antistatic agent was composed of 30% allyl trimethyl ammonium bromide, 20% polyethylene glycol acrylate, 10% polyethylene glycol, 20% linolenic acid, and 20% polyethylene terephthalate.
The preparation method of this example includes the following steps:
A. mixing polyvinyl chloride resin, plasticizer and ethylene-propylene copolymer, adding the mixture into a stirring kettle, heating and stirring to obtain a mixture A;
B. adding an antistatic agent, kaolin and silica micropowder into the mixture A, and fully mixing to obtain a mixture B;
C. adding the mixture B into a double-screw extruder for extrusion to obtain polyvinyl chloride film material particles;
D. adding the granules of the polyvinyl chloride film material into a calender to prepare the polyvinyl chloride film.
In this example, the stirring temperature of the stirring kettle in the step A is 58 ℃, the stirring time is 23min, and the stirring speed is 1400 rpm.
In this example, the extrusion temperature in step C was 195 ℃.
Example four:
the polyvinyl chloride film comprises 96 parts by weight of polyvinyl chloride resin, 9 parts by weight of plasticizer, 10 parts by weight of ethylene-propylene copolymer, 2 parts by weight of antistatic agent, 8 parts by weight of kaolin and 12 parts by weight of silicon micropowder.
In this example, the plasticizer is a mixture of ethylene-vinyl acetate copolymer, ethylene-methyl acrylate copolymer, and ethylene-ethyl acrylate copolymer.
In this example, the antistatic agent was composed of 30% allyl trimethyl ammonium bromide, 20% polyethylene glycol acrylate, 10% polyethylene glycol, 20% linolenic acid, and 20% polyethylene terephthalate.
The preparation method of this example includes the following steps:
A. mixing polyvinyl chloride resin, plasticizer and ethylene-propylene copolymer, adding the mixture into a stirring kettle, heating and stirring to obtain a mixture A;
B. adding an antistatic agent, kaolin and silica micropowder into the mixture A, and fully mixing to obtain a mixture B;
C. adding the mixture B into a double-screw extruder for extrusion to obtain polyvinyl chloride film material particles;
D. adding the granules of the polyvinyl chloride film material into a calender to prepare the polyvinyl chloride film.
In this example, the stirring temperature of the stirring kettle in the step A was 68 ℃, the stirring time was 28min, and the stirring rate was 1800 rpm.
In this example, the extrusion temperature in step C was 205 ℃.
Example five:
the polyvinyl chloride film comprises 85 parts of polyvinyl chloride resin, 7 parts of plasticizer, 9 parts of ethylene-propylene copolymer, 2 parts of antistatic agent, 7 parts of kaolin and 10 parts of silicon micropowder according to parts by weight.
In this example, the plasticizer is a mixture of ethylene-vinyl acetate copolymer, ethylene-methyl acrylate copolymer, and ethylene-ethyl acrylate copolymer.
In this example, the antistatic agent was composed of 30% allyl trimethyl ammonium bromide, 20% polyethylene glycol acrylate, 10% polyethylene glycol, 20% linolenic acid, and 20% polyethylene terephthalate.
The preparation method of this example includes the following steps:
A. mixing polyvinyl chloride resin, plasticizer and ethylene-propylene copolymer, adding the mixture into a stirring kettle, heating and stirring to obtain a mixture A;
B. adding an antistatic agent, kaolin and silica micropowder into the mixture A, and fully mixing to obtain a mixture B;
C. adding the mixture B into a double-screw extruder for extrusion to obtain polyvinyl chloride film material particles;
D. adding the granules of the polyvinyl chloride film material into a calender to prepare the polyvinyl chloride film.
In this example, the stirring temperature of the stirring kettle in the step A is 62 ℃, the stirring time is 25min, and the stirring speed is 1800 rpm.
In this example, the extrusion temperature in step C was 200 ℃.
Experimental example:
the films prepared by the embodiments of the invention are used for performance test, and the obtained data are as follows:
Figure DEST_PATH_IMAGE002
in conclusion, the preparation method is simple, and the prepared polyvinyl chloride film has high strength, good tensile property, difficult damage, good environmental protection property, easy degradation and low cost, and has good industrialization prospect; the added antistatic agent has excellent antistatic performance, long-acting antistatic performance and better transparency, and can improve the hydrophilicity of the polyester film and further improve the performance of the polyvinyl chloride film.
Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.

Claims (7)

1. A high strength polyvinyl chloride film characterized by: the polyvinyl chloride film comprises, by weight, 70-100 parts of polyvinyl chloride resin, 4-10 parts of a plasticizer, 5-12 parts of an ethylene-propylene copolymer, 1-3 parts of an antistatic agent, 4-10 parts of kaolin and 5-15 parts of silica powder.
2. A high strength polyvinyl chloride film according to claim 1, wherein: the preferable component proportion of the polyvinyl chloride film component comprises 85 parts of polyvinyl chloride resin, 7 parts of plasticizer, 9 parts of ethylene-propylene copolymer, 2 parts of antistatic agent, 7 parts of kaolin and 10 parts of silicon micropowder.
3. A high strength polyvinyl chloride film according to claim 1, wherein: the plasticizer is one or a mixture of ethylene-vinyl acetate copolymer, ethylene-methyl acrylate copolymer and ethylene-ethyl acrylate copolymer.
4. A high strength polyvinyl chloride film according to claim 1, wherein: the antistatic agent consists of 30% of allyl trimethyl ammonium bromide, 20% of polyethylene glycol acrylate, 10% of polyethylene glycol, 20% of linolenic acid and 20% of polyethylene glycol terephthalate.
5. The preparation method for realizing the high-strength polyvinyl chloride film of claim 1 is characterized by comprising the following steps of: the preparation method comprises the following steps:
A. mixing polyvinyl chloride resin, plasticizer and ethylene-propylene copolymer, adding the mixture into a stirring kettle, heating and stirring to obtain a mixture A;
B. adding an antistatic agent, kaolin and silica micropowder into the mixture A, and fully mixing to obtain a mixture B;
C. adding the mixture B into a double-screw extruder for extrusion to obtain polyvinyl chloride film material particles;
D. adding the granules of the polyvinyl chloride film material into a calender to prepare the polyvinyl chloride film.
6. The method for preparing a high-strength polyvinyl chloride film according to claim 5, wherein: in the step A, the stirring temperature of the stirring kettle is 55-70 ℃, the time is 20-30 min, and the stirring speed is 1200-2000 rpm.
7. The method for preparing a high-strength polyvinyl chloride film according to claim 5, wherein: the extrusion temperature in the step C is 190-210 ℃.
CN202011352759.8A 2020-11-26 2020-11-26 High-strength polyvinyl chloride film and preparation method thereof Pending CN112409728A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202011352759.8A CN112409728A (en) 2020-11-26 2020-11-26 High-strength polyvinyl chloride film and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202011352759.8A CN112409728A (en) 2020-11-26 2020-11-26 High-strength polyvinyl chloride film and preparation method thereof

Publications (1)

Publication Number Publication Date
CN112409728A true CN112409728A (en) 2021-02-26

Family

ID=74842583

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202011352759.8A Pending CN112409728A (en) 2020-11-26 2020-11-26 High-strength polyvinyl chloride film and preparation method thereof

Country Status (1)

Country Link
CN (1) CN112409728A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110158325A (en) * 2019-05-20 2019-08-23 宁波全泰环保科技有限公司 A kind of the lamination equipment and its production technology of versatility production PVC adhesive plaster

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102827435A (en) * 2012-09-04 2012-12-19 天津盛天利材料科技有限公司 Polrvinyl chloride preservative film and preparation method thereof
CN104312034A (en) * 2014-09-19 2015-01-28 金发科技股份有限公司 Polyvinyl chloride anti-counterfeiting film and preparation method thereof
CN106188930A (en) * 2016-06-24 2016-12-07 河北华夏实业有限公司 A kind of polyvinyl chloride film being applicable to hot-fusible pressure-sensitive adhesive coating and preparation method thereof
CN111548544A (en) * 2020-03-20 2020-08-18 深圳市华中通用技术有限公司 High-temperature-resistant stable protective film material and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102827435A (en) * 2012-09-04 2012-12-19 天津盛天利材料科技有限公司 Polrvinyl chloride preservative film and preparation method thereof
CN104312034A (en) * 2014-09-19 2015-01-28 金发科技股份有限公司 Polyvinyl chloride anti-counterfeiting film and preparation method thereof
CN106188930A (en) * 2016-06-24 2016-12-07 河北华夏实业有限公司 A kind of polyvinyl chloride film being applicable to hot-fusible pressure-sensitive adhesive coating and preparation method thereof
CN111548544A (en) * 2020-03-20 2020-08-18 深圳市华中通用技术有限公司 High-temperature-resistant stable protective film material and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110158325A (en) * 2019-05-20 2019-08-23 宁波全泰环保科技有限公司 A kind of the lamination equipment and its production technology of versatility production PVC adhesive plaster

Similar Documents

Publication Publication Date Title
CN109251399B (en) Soft low-smoke halogen-free high-flame-retardant oil-resistant cable material for high-voltage line in vehicle and preparation method thereof
CN110862598B (en) 90-DEG C low-shrinkage ultraviolet-proof medium-density polyethylene sheath material and preparation method thereof
WO2024002274A1 (en) Packaging adhesive film for photovoltaic module, packaging adhesive film preparation method, and photovoltaic module
WO2021114753A1 (en) Silane cross-linked polyethylene insulation material having high carbon black content and good tracking resistance, and preparation method therefor
CN112409728A (en) High-strength polyvinyl chloride film and preparation method thereof
CN113637258A (en) Silane crosslinked polyethylene insulating material with 70-year service life and preparation method thereof
CN107418041A (en) A kind of socket ultra-toughness flame-proof polyethylene and preparation method
CN115107341B (en) High-transmittance low-fog optical base film and preparation method thereof
CN105778206B (en) A kind of softness PE cable protective cover material and preparation method thereof
CN111331985A (en) Polyolefin heat shrinkable sleeve film and preparation method and application thereof
CN105778326B (en) A kind of communication cable environment-friendly high fire-retardant PVC sheath material and its preparation method and application
CN105907031A (en) Environment-friendly power cable insulating material
CN113480820B (en) PVA high-barrier composite material and preparation method thereof
CN108285586A (en) A kind of weather proof cable protective cover material and preparation method thereof
CN110483915B (en) 105 ℃ semiconductive PVC material for automobile coaxial cable and preparation method thereof
CN112851862A (en) Environment-friendly flame-retardant plastic and preparation method thereof
CN111253694A (en) PVC (polyvinyl chloride) cable material for 5G photoelectric hybrid cable
CN111394006A (en) Preparation method of infrared-blocking EVA (ethylene-vinyl acetate copolymer) film
CN109627666A (en) A kind of oil resistant EVA CABLE MATERIALS and its preparation process
CN115785558B (en) PP/PBS biodegradable antistatic plastic and preparation method thereof
CN113105722B (en) Improved TPEE wire and cable sheath material and sheath thereof
CN115181370B (en) Flame-retardant and aging-resistant cable material and preparation process thereof
CN108410183A (en) A kind of conductive plastic material and preparation method thereof
CN116082762B (en) Flame-retardant polyvinyl chloride material for battery connecting wire and preparation method thereof
CN116554404A (en) Ageing-resistant high-temperature-resistant cold-resistant polyvinyl chloride cable material and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20210226