CN106188936A - A kind of high-barrier PVC pharmaceutical pack film and production technology thereof - Google Patents

A kind of high-barrier PVC pharmaceutical pack film and production technology thereof Download PDF

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Publication number
CN106188936A
CN106188936A CN201610540146.4A CN201610540146A CN106188936A CN 106188936 A CN106188936 A CN 106188936A CN 201610540146 A CN201610540146 A CN 201610540146A CN 106188936 A CN106188936 A CN 106188936A
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CN
China
Prior art keywords
pharmaceutical pack
stabilizer
pvc
pack film
barrier
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
CN201610540146.4A
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Chinese (zh)
Inventor
谢四海
王玮
吴康胜
蔡静
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JIANGSU GOLDEN MATERIAL TECHNOLOGY Co Ltd
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JIANGSU GOLDEN MATERIAL TECHNOLOGY Co Ltd
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Priority to CN201610540146.4A priority Critical patent/CN106188936A/en
Publication of CN106188936A publication Critical patent/CN106188936A/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions 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; Compositions of derivatives of such polymers
    • C08L27/02Compositions 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; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions 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; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/14Gas barrier composition
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/02Applications for biomedical use
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/16Applications used for films
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

A kind of high-barrier PVC pharmaceutical pack film and production technology thereof, relate to acceptable packaging material field.According to mass fraction ratio, it is made up of following raw material: PVC resin powder: 100 parts, stabilizer: 1.0 2.5, interior lubrication prescription: 0.5 1.5 parts, outer lubrication prescription: 0.2 1.0 parts, processing aid: 1.0 4.0 parts, MBS resin: 3.0 9.0 parts, Graphene: 0.1 3.0 parts.The PVC pharmaceutical pack film of the present invention has relative to prior art that thickness is uniform, surface gloss is high and has the advantage of high barrier;Steam penetrating capacity is from 1 2g/m2* about 24h is reduced to 0.5 1g/m2*24h;Oxygen transit dose is from 14 18g/m2* 24h*0.1mpa is reduced to 3g/m2* within 24h*0.1mpa.

Description

A kind of high-barrier PVC pharmaceutical pack film and production technology thereof
Technical field
The present invention relates to acceptable packaging material field, be specially a kind of high-barrier PVC pharmaceutical pack film and production technology thereof.
Background technology
The most the most frequently used PTP pharmaceutical pack film packaging is all the base material made of PVC, and PVC low cost, combination property is excellent Different.
But in the middle of actually used, Some Drugs is very sensitive to humidity, oxygen, and the barrier property of existing PVC can not be expired Foot needs.
Summary of the invention
It is an object of the invention to provide a kind of high-barrier PVC pharmaceutical pack film and production technology thereof, there is technique simple, resistance to Corrode the advantages such as strong, lighter in weight and high obstructing performance.
The technical scheme realizing above-mentioned purpose is: a kind of high-barrier PVC pharmaceutical pack film, it is characterised in that: according to quality Portion rate, is made up of following raw material: PVC resin powder: 100 parts, stabilizer: 1.0-2.5, interior lubrication prescription: 0.5-1.5 part, outer lubrication prescription: 0.2-1.0 part, processing aid: 1.0-4.0 part, MBS resin: 3.0-9.0 part, Graphene: 0.1-3.0 part.
Further, described stabilizer be Methyltin stabiliser, octyl tin stabilizer, rare-earth stabilizer, calcium zinc stabilizer, One or more in barium zinc stabilizer.
Further, processing aid is methyl methacrylate-acrylate copolymer.
Further, the degree of polymerization of PVC resin powder is 700 or 800.
Further, the model of described interior lubrication prescription is G16.
The production technology of above-mentioned high-barrier PVC pharmaceutical pack film, it is characterised in that comprise the following steps:
A, material put in high-speed mixer by dosage and mix, make temperature of charge by the physical friction between raw material Rising to 100-120 DEG C, the rotating speed of high-speed mixer is: 2000-3000 rev/min;
B, the material after mixed at high speed is sent in low speed mixer remix, make temperature of charge be down to 40-60 DEG C, low The rotating speed of speed mixer is 50-500 rev/min;
Extruder extrusion plasticizing sent into by c, material after mixed on low speed, and extruder temperature is 140-200 DEG C;
Material after d, plasticizing is delivered to calender, is processed into thin film, calendering workshop section temperature by the calendering workshop section of calender Degree 150-220, then it is cooled to 30-60 DEG C by the chill roll group of calender.
Further, the outer wall of the hybrid chamber of described low speed mixer is provided with water-cooling jacket.
Preferably, above-mentioned steps a is initially charged PVC resin powder, treats that the temperature of high-speed mixer hybrid chamber rises to 45-50 DEG C Time, add stabilizer and interior lubrication prescription, rise to add outer lubrication prescription, processing aid, MBS resin and Graphene when 75-80 DEG C.
Stabilizer is mainly used in maintaining the stability of product, and outer lubrication prescription, processing aid, MBS resin and Graphene are such as Fruit and stabilizer are simultaneously introduced meeting Vapor recovery unit agent, cause the effectiveness of stabilizer normally not play, affect product quality.
Beneficial effects of the present invention:
1, the PVC pharmaceutical pack film of the present invention has relative to prior art that thickness is uniform, surface gloss is high and has The advantage having high barrier;Steam penetrating capacity is from 1-2g/m2* about 24h is reduced to 0.5-1g/m2*24h;Oxygen transit dose from 14-18g/m2* 24h*0.1mpa is reduced to 3g/m2* within 24h*0.1mpa.
2, the preparation technology of the present invention is simple, low cost.
3, the PVC pharmaceutical pack film of the present invention is widely used, and can apply to the various occasion high to barrier requirement.
Detailed description of the invention
In order to make the purpose of the present invention, technical scheme clearer, below in conjunction with specific embodiment, the present invention is entered Row further describes.
Below one high-barrier PVC pharmaceutical pack film of the present invention and production technology thereof are described in detail below.
Embodiment 1
A kind of high-barrier PVC pharmaceutical pack film, according to mass fraction ratio, is made up of following raw material: PVC resin powder: 100 Part, stabilizer: 1.0, interior lubrication prescription: 1.0 parts, outer lubrication prescription: 1.0 parts, processing aid: 1.0 parts, MBS resin: 6.0 parts, Graphene: 3.0 part.
Wherein, processing aid is methyl methacrylate-acrylate copolymer;The degree of polymerization of PVC resin powder is 700; The model of interior lubrication prescription is G16.
The production technology of above-mentioned high-barrier PVC pharmaceutical pack film, it is characterised in that comprise the following steps:
A, first PVC resin powder is put into by dosage high-speed mixer stirring, treat the temperature of high-speed mixer hybrid chamber When rising to 45 DEG C, add stabilizer and interior lubrication prescription, rise to add outer lubrication prescription, processing aid, MBS resin and graphite when 75 DEG C Alkene, makes temperature of charge rise to 100 DEG C by the physical friction between raw material, and the rotating speed of high-speed mixer is: 2000 revs/min;
B, material after mixed at high speed is sent in low speed mixer and remixed, the outer wall of the hybrid chamber of low speed mixer Being provided with water-cooling jacket, make temperature of charge be down to 40 DEG C, the rotating speed of low speed mixer is 50 revs/min;
Extruder extrusion plasticizing sent into by c, material after mixed on low speed, and extruder temperature is 140 DEG C;
Material after d, plasticizing is delivered to calender, is processed into thin film, calendering workshop section temperature by the calendering workshop section of calender Degree 150, then it is cooled to 30 DEG C by the chill roll group of calender.
Embodiment 2
A kind of high-barrier PVC pharmaceutical pack film, according to mass fraction ratio, is made up of following raw material: PVC resin powder: 100 Part, stabilizer: 2.5, interior lubrication prescription: 0.5 part, outer lubrication prescription: 0.6 part, processing aid: 4.0 parts, MBS resin: 3.0 parts, Graphene: 1.5 part.
Wherein, processing aid is methyl methacrylate-acrylate copolymer;The degree of polymerization of PVC resin powder is 800; The model of interior lubrication prescription is G16.
The production technology of above-mentioned high-barrier PVC pharmaceutical pack film, it is characterised in that comprise the following steps:
A, first PVC resin powder is put into by dosage high-speed mixer stirring, treat the temperature of high-speed mixer hybrid chamber When rising to 50 DEG C, add stabilizer and interior lubrication prescription, rise to add outer lubrication prescription, processing aid, MBS resin and graphite when 80 DEG C Alkene, makes temperature of charge rise to 120 DEG C by the physical friction between raw material, and the rotating speed of high-speed mixer is: 3000 revs/min;
B, material after mixed at high speed is sent in low speed mixer and remixed, the outer wall of the hybrid chamber of low speed mixer Being provided with water-cooling jacket, make temperature of charge be down to 60 DEG C, the rotating speed of low speed mixer is 500 revs/min;
Extruder extrusion plasticizing sent into by c, material after mixed on low speed, and extruder temperature is 200 DEG C;
Material after d, plasticizing is delivered to calender, is processed into thin film, calendering workshop section temperature by the calendering workshop section of calender Degree 185, then it is cooled to 60 DEG C by the chill roll group of calender.
Embodiment 3
A kind of high-barrier PVC pharmaceutical pack film, according to mass fraction ratio, is made up of following raw material: PVC resin powder: 100 Part, stabilizer: 1.8, interior lubrication prescription: 1.5 parts, outer lubrication prescription: 0.2 part, processing aid: 2.5 parts, MBS resin: 9.0 parts, Graphene: 0.1 part.
Wherein, processing aid is methyl methacrylate-acrylate copolymer;The degree of polymerization of PVC resin powder is 700; The model of interior lubrication prescription is G16.
The production technology of above-mentioned high-barrier PVC pharmaceutical pack film, it is characterised in that comprise the following steps:
A, first PVC resin powder is put into by dosage high-speed mixer stirring, treat the temperature of high-speed mixer hybrid chamber When rising to 47 DEG C, add stabilizer and interior lubrication prescription, rise to add outer lubrication prescription, processing aid, MBS resin and graphite when 78 DEG C Alkene, makes temperature of charge rise to 110 DEG C by the physical friction between raw material, and the rotating speed of high-speed mixer is: 2500 revs/min;
B, material after mixed at high speed is sent in low speed mixer and remixed, the outer wall of the hybrid chamber of low speed mixer Being provided with water-cooling jacket, make temperature of charge be down to 50 DEG C, the rotating speed of low speed mixer is 270 revs/min;
Extruder extrusion plasticizing sent into by c, material after mixed on low speed, and extruder temperature is 170 DEG C;
Material after d, plasticizing is delivered to calender, is processed into thin film, calendering workshop section temperature by the calendering workshop section of calender Degree 220, then it is cooled to 45 DEG C by the chill roll group of calender.
Stabilizer in above-mentioned 3 embodiments can be Methyltin stabiliser, octyl tin stabilizer, rare-earth stabilizer, calcium One or more in zinc stabilizer, barium zinc stabilizer.
The foregoing is only embodiments of the invention, not thereby limit the scope of the claims of the present invention, every utilize this The equivalent transformation that bright description is made, or directly or indirectly it is used in other relevant technical fields, the most in like manner it is included in this In bright scope of patent protection.

Claims (8)

1. a high-barrier PVC pharmaceutical pack film, it is characterised in that: according to mass fraction ratio, it is made up of following raw material: PVC tree Cosmetics: 100 parts, stabilizer: 1.0-2.5, interior lubrication prescription: 0.5-1.5 part, outer lubrication prescription: 0.2-1.0 part, processing aid: 1.0-4.0 Part, MBS resin: 3.0-9.0 part, Graphene: 0.1-3.0 part.
A kind of high-barrier PVC pharmaceutical pack film the most according to claim 1, it is characterised in that: described stabilizer is methyl One or more in stannum stabilizer, octyl tin stabilizer, rare-earth stabilizer, calcium zinc stabilizer, barium zinc stabilizer.
A kind of high-barrier PVC pharmaceutical pack film the most according to claim 1, it is characterised in that: processing aid is methyl-prop E pioic acid methyl ester-acrylate copolymer.
A kind of high-barrier PVC pharmaceutical pack film the most according to claim 1, it is characterised in that: the degree of polymerization of PVC resin powder It is 700 or 800.
A kind of high-barrier PVC pharmaceutical pack film the most according to claim 1, it is characterised in that: the model of described interior lubrication prescription For G16.
6., according to the production technology of the high-barrier PVC pharmaceutical pack film described in claim any one of claim 1-5, it is special Levy and be, comprise the following steps:
A, material put in high-speed mixer by dosage and mix, make temperature of charge rise to by the physical friction between raw material 100-120 DEG C, the rotating speed of high-speed mixer is: 2000-3000 rev/min;
B, being sent in low speed mixer by the material after mixed at high speed and remix, make temperature of charge be down to 40-60 DEG C, low speed mixes The rotating speed of conjunction machine is 50-500 rev/min;
Extruder extrusion plasticizing sent into by c, material after mixed on low speed, and extruder temperature is 140-200 DEG C;
Material after d, plasticizing is delivered to calender, is processed into thin film, calendering workshop section temperature by the calendering workshop section of calender 150-220, then it is cooled to 30-60 DEG C by the chill roll group of calender.
The production technology of high-barrier PVC pharmaceutical pack film the most according to claim 6, it is characterised in that described low speed mixes The outer wall of the hybrid chamber of conjunction machine is provided with water-cooling jacket.
The production technology of high-barrier PVC pharmaceutical pack film the most according to claim 6, it is characterised in that first add in step a Enter PVC resin powder, when the temperature of high-speed mixer hybrid chamber rises to 45-50 DEG C, add stabilizer and interior lubrication prescription, rise to 75- Outer lubrication prescription, processing aid, MBS resin and Graphene is added when 80 DEG C.
CN201610540146.4A 2016-07-08 2016-07-08 A kind of high-barrier PVC pharmaceutical pack film and production technology thereof Pending CN106188936A (en)

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Application Number Priority Date Filing Date Title
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107226973A (en) * 2017-06-20 2017-10-03 苏州奥宇包装科技有限公司 A kind of preparation method of woodwork packaging film
CN107226978A (en) * 2017-06-20 2017-10-03 苏州奥宇包装科技有限公司 A kind of preparation method of woodwork packaging material
CN107353561A (en) * 2017-06-20 2017-11-17 苏州奥宇包装科技有限公司 A kind of preparation method of packaging film
CN110819028A (en) * 2018-08-10 2020-02-21 江苏永润包装材料有限公司 Cold stamping forming composite film for medicine packaging and preparation process thereof
CN111675868A (en) * 2020-06-03 2020-09-18 无锡宏义高分子材料科技有限公司 High-glossiness low-transmittance PVC (polyvinyl chloride) base material and preparation method thereof
CN114644771A (en) * 2022-04-15 2022-06-21 山东金阳光医药包装有限公司 Polyvinyl chloride medicine package sheet with anti-fouling and antibacterial functions and preparation method thereof

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CN104231468A (en) * 2014-01-03 2014-12-24 江苏金材科技有限公司 Anti-radiation medicinal polyvinyl chloride (PVC) hard sheet and preparation method thereof
CN105295254A (en) * 2015-11-23 2016-02-03 青岛友诚高新技术有限公司 Medical film material and preparation method thereof

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CN104231468A (en) * 2014-01-03 2014-12-24 江苏金材科技有限公司 Anti-radiation medicinal polyvinyl chloride (PVC) hard sheet and preparation method thereof
CN104059312A (en) * 2014-05-21 2014-09-24 河北凯鹏包装材料有限公司 PVC (Polyvinyl Chloride) hard sheet for packaging solid medicine bubble cap
CN105295254A (en) * 2015-11-23 2016-02-03 青岛友诚高新技术有限公司 Medical film material and preparation method thereof

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107226973A (en) * 2017-06-20 2017-10-03 苏州奥宇包装科技有限公司 A kind of preparation method of woodwork packaging film
CN107226978A (en) * 2017-06-20 2017-10-03 苏州奥宇包装科技有限公司 A kind of preparation method of woodwork packaging material
CN107353561A (en) * 2017-06-20 2017-11-17 苏州奥宇包装科技有限公司 A kind of preparation method of packaging film
CN110819028A (en) * 2018-08-10 2020-02-21 江苏永润包装材料有限公司 Cold stamping forming composite film for medicine packaging and preparation process thereof
CN111675868A (en) * 2020-06-03 2020-09-18 无锡宏义高分子材料科技有限公司 High-glossiness low-transmittance PVC (polyvinyl chloride) base material and preparation method thereof
CN114644771A (en) * 2022-04-15 2022-06-21 山东金阳光医药包装有限公司 Polyvinyl chloride medicine package sheet with anti-fouling and antibacterial functions and preparation method thereof

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Application publication date: 20161207