CN107163441A - A kind of preparation method of PVC packaging materials - Google Patents
A kind of preparation method of PVC packaging materials Download PDFInfo
- Publication number
- CN107163441A CN107163441A CN201710471224.4A CN201710471224A CN107163441A CN 107163441 A CN107163441 A CN 107163441A CN 201710471224 A CN201710471224 A CN 201710471224A CN 107163441 A CN107163441 A CN 107163441A
- Authority
- CN
- China
- Prior art keywords
- parts
- pvc
- packaging materials
- preparation
- pvc packaging
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions 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
- C08L27/02—Compositions 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
- C08L27/04—Compositions 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
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2237—Oxides; Hydroxides of metals of titanium
- C08K2003/2241—Titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3045—Sulfates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a kind of preparation method of PVC packaging materials, raw material is:PVC, vinyl chloride, POM, titanium dioxide, tribasic lead sulfate, dibasic lead phosphite, lubricating oil, zinc oxide, sorbierite monopalmitate, PDOP, POP, dibutyl tin mercaptides, phosphenylic acid dioctyl ester, silver system antibacterial matrices and pigment;The 11MPa of longitudinal tensile strength 9, the 10MPa of transverse tensile strength 8, longitudinal tensile strain rate 88 92%, cross direction elongation 75 85%;The 125s of melting time 105, the 13.8kV/mm of breakdown voltage 11.4, the 112MPa of tearing strength 108, the 6.7kJ/m of notch impact strength 5.32;The 35MPa of bending strength 30, Brinell hardness 22 24, after the gamma-ray irradiation that 40kGy is measured, gel fraction 75 85%.
Description
Technical field
The present invention relates to packing material technical field, more particularly to a kind of preparation method of PVC packaging materials.
Background technology
Polyvinyl chloride, English abbreviation PVC is in initiators such as peroxide, azo-compounds;Or pressed certainly under light, heat effect
The polymer being polymerized by base polymerization reaction mechanism.Ryuron and vinyl chloride copolymer system are referred to as vinyl chloride tree
Fat;PVC is the white powder of impalpable structure, and the degree of branching is smaller, relative density 1.4 or so, 77 ~ 90 DEG C of glass transition temperature, 170
DEG C or so start to decompose, the stability to light and heat is poor, more than 100 DEG C or through long-time exposure in sunshine, will decompose and produce
Raw hydrogen chloride, and further autocatalysis is decomposed, and causes discoloration, physical and mechanical properties also declines rapidly, in actual applications must
Stabilizer must be added to improve the stability to light and heat.
Packaging film is main to be formed by the polyvinyl resin mixing extrusion of several different trades mark, and with puncture resistant, super-strength is high
Performance, packaging is wound to the goods being deposited on supporting plate, packing material is more consolidated clean and tidy, more superpower waterproof action, quilt
Widely use, in foreign export, papermaking, hardware, plastics chemical industry, building materials, food pharmaceuticals industry.
Polyvinyl chloride can be substituted reaction by ethene, chlorine and catalyst and be made.Due to the effect of its fireproofing and heat resistant, polyvinyl chloride
It is widely used in all trades and professions product of all kinds:Wire outer skin, optical cable coating, footwear, handbag, bag, jewelry, signboard and advertisement
Board, building decoration articles for use, furniture, ornament, roller, trunnion, toy, door curtain, rolling door, medical assistance articles for use, gloves, some foods
Tin foil.
Industrial PVC molecular weight is general in the range of 50,000~110,000, with larger polydispersity, molecular weight with
The reduction of polymerization temperature and increase;Without definite melting point, 80~85 DEG C start softening, and 130 DEG C are changed into viscoelastic state, and 160~180 DEG C are opened
Beginning is changed into viscous state;There are preferable mechanical performance, tensile strength 60MPa or so, there are excellent dielectric properties.
PVC was once the general-purpose plastics of yield maximum in the world, using widely.In construction material, industrial product, daily
In terms of product, flooring laminate, floor tile, artificial leather, tubing, electric wire, packaging film, bottle, expanded material, encapsulant, fiber
It is widely used.
PVC typically will first be modified granulation, be prepared into Screw Extrusion unit after particle, and plasticizing is more abundant, and processing is also more held
Easily, especially technique is the product of injection.Screw extruder is one of topmost equipment of plastics processing, and it passes through outside
Power transmits the Solid Conveying and Melting with the heat transfer progress plastics of external heat element, compacting, melting, shearing mixing extrusion shaping.Spiral shell
Strictly speaking bar extruder all occupies critical role as plasticizing granulation machinery or processing and forming machinery, there is special want
The PVC product asked, PVC modified formulas, makes to measure according to customer requirement.Also it is exactly the copolymerization in PVC production processes
Derivative, the kind of such modification has vinyl chloride copolymer, polyvinyl chloride blend and chliorinated polyvinyl chloride etc..
PVC is prepared with radical addition polymerization method, and polymerization is broadly divided into suspension polymerization, emulsion polymerization and sheet
Body polymerization, based on suspension polymerization, accounts for 80% or so of PVC total outputs.By pure water, liquefied VCM monomers, dispersant
It is added in reactor, then adds initiator and other auxiliary agents, is warming up to VCM monomers after certain temperature and occurs radical polymerization
Reaction generation PVC granule.Lasting stirring causes the epigranular of particle, and the particle of generation is suspended in water.In addition,
Also useful microsuspending method production PVC paste resin, properties of product and good into paste property.
Thermal stability of polyvinyl chloride and light resistance are poor.Start to decomposite hydrogen chloride at 150 DEG C, with plasticizer loading
How much generation adverse reactions.In addition, influence of the pigment to PVC, be embodied in pigment whether with PVC and composition PVC product its
Its component reacts and pigment resistance to migration itself, heat resistance.Some of colouring agent composition may promote resin
Degraded.If iron ion and zinc ion are the catalyst of polyvinyl chloride resin degradation reaction.Therefore, using iron oxide(It is red, yellow, brown and black)
Pigment or zinc oxide, zinc sulphide and lithopone off-white color pigment can reduce the heat endurance of polyvinyl chloride resin.Some colouring agents may
Had an effect with the catabolite of polyvinyl chloride resin.As ultramarine class pigment acid resistance it is poor, therefore PVC coloring process in, understand with
PVC, which decomposes the hydrogen chloride produced, to be occurred interaction and loses due color.Therefore for PVC colorings, it is contemplated that used
The feature of resin and related auxiliaries, with reference to the characteristics of pigment.
PVC material is a kind of amorphism material.PVC material is frequently added stabilizer in actual use, lubricant, auxiliary
Helps processing agent, colorant, impact modifier and other additives.PVC material have low flammability, high intensity, resistance to climate variability with
And excellent geometrical stability.PVC has very strong resistance to oxidant, reducing agent and strong acid.But it can be by dense oxygen
Change the acid such as concentrated sulfuric acid, concentrated nitric acid and corrode and also do not apply to the occasion contacted with aromatic hydrocarbon, chlorinated hydrocabon.PVC is molten in processing
It is a very important technological parameter to change temperature, if this parameter is improper will to cause the problem of material is decomposed.PVC flowing is special
Property is mutually on duty, and its processing range is very narrow.The PVC material of particularly macromolecule is more difficult to processing, therefore usually used is all
The PVC material of small-molecular-weight.PVC shrinkage factor is at a fairly low, and generally 0.2 ~ 0.6%.
The content of the invention
The present invention provides the system of high a kind of heat-proof aging, tensile strength, impact strength height and the high PVC packaging materials of hardness
Preparation Method, solve existing waterproofing packing material preparation method hardness is low and the low technical problem of tensile strength.
The present invention uses following technical scheme:A kind of preparation method of PVC packaging materials, comprises the following steps:
The first step:PVC100 parts, 0.1-0.3 parts of vinyl chloride, POM10-50 parts, titanium dioxide 2- are weighed according to mass fraction proportioning
6 parts, 1-3 parts of tribasic lead sulfate, dibasic lead phosphite is 2-4 parts, 4-8 parts of lubricating oil, 1-5 parts of zinc oxide, sorbierite list
2-6 parts of palmitate, PDOP1-5 parts, POP2-8 parts, dibutyl tin mercaptides are 10-30 parts, phosphenylic acid dioctyl ester 0.5-2.5
Part, antibacterial matrices 0.3-0.5 parts of silver system, 0.002-0.006 parts of pigment;
Second step:PVC is put into high-speed kneading machine, 95-105 DEG C is warming up to, surplus stock is added, is warming up to 110-120 DEG C,
Speed 800-1000r/min is mediated, 15-25min is mediated;
3rd step:The roller of material two after kneading is plasticated, and preceding roll temperature is 170-190 DEG C, rotating speed 16-20 r/min, back roller 160-
170 DEG C, rotating speed 26-28 r/min knead 15-25min, vulcanizing press tabletting, and temperature is 180-220 DEG C, pressure 25-
35MPa, time 10-30min, cooling crimps to obtain PVC packaging materials after press polish, and thickness is 0.5-2.5mm.
It is used as a preferred technical solution of the present invention:The raw material of the preparation method of the PVC packaging materials presses mass parts
Number proportioning is as follows:PVC100 parts, 0.1 part of vinyl chloride, POM10 parts, 2 parts of titanium dioxide, 1 part of tribasic lead sulfate, two alkali formulas are sub-
Lead phosphate is 2 parts, 4 parts of lubricating oil, 1 part of zinc oxide, 2 parts of sorbierite monopalmitate, PDOP1 parts, POP2 parts, dibutyl mercaptan
Tin is 10 parts, 0.5 part of phosphenylic acid dioctyl ester, 0.3 part of silver system antibacterial matrices, 0.002 part of pigment.
It is used as a preferred technical solution of the present invention:The raw material of the preparation method of the PVC packaging materials presses mass parts
Number proportioning is as follows:PVC100 parts, 0.3 part of vinyl chloride, POM50 parts, 6 parts of titanium dioxide, 3 parts of tribasic lead sulfate, two alkali formulas are sub-
Lead phosphate is 4 parts, 8 parts of lubricating oil, 5 parts of zinc oxide, 6 parts of sorbierite monopalmitate, PDOP5 parts, POP8 parts, dibutyl mercaptan
Tin is 30 parts, 2.5 parts of phosphenylic acid dioctyl ester, 0.5 part of silver system antibacterial matrices, 0.006 part of pigment.
It is used as a preferred technical solution of the present invention:The raw material of the preparation method of the PVC packaging materials presses mass parts
Number proportioning is as follows:PVC100 parts, 0.2 part of vinyl chloride, POM30 parts, 4 parts of titanium dioxide, 2 parts of tribasic lead sulfate, two alkali formulas are sub-
Lead phosphate is 3 parts, 6 parts of lubricating oil, 3 parts of zinc oxide, 4 parts of sorbierite monopalmitate, PDOP3 parts, POP5 parts, dibutyl mercaptan
Tin is 20 parts, 1.5 parts of phosphenylic acid dioctyl ester, 0.4 part of silver system antibacterial matrices, 0.004 part of pigment.
It is used as a preferred technical solution of the present invention:The pigment uses phthalocyanine blue.
Beneficial effect
A kind of preparation method of PVC packaging materials of the present invention using above technical scheme compared with prior art, with
Lower technique effect:1st, preparation method is simple, uses manpower and material resources sparingly, longitudinal tensile strength 9-11MPa, transverse tensile strength 8-
10MPa, longitudinal tensile strain rate 88-92%, cross direction elongation 75-85%;2nd, burn from fiery self-extinguishment, melting time 105-125s, puncture
Voltage 11.4-13.8kV/mm, tearing strength 108-112MPa, notch impact strength 5.3-6.7kJ/m2;3rd, bending strength 30-
35MPa, Brinell hardness 22-24, raw material sources are extensive, with low cost, natural light aging after-drawing loss of strength in 12 months
0.015-0.035%;4th, it can be widely used in various extreme environments, 100 DEG C of heat ageings loss of tensile strength after two months
0.08-0.12%, after the gamma-ray irradiation that 40kGy is measured, gel fraction 75-85% can extensively be produced and constantly be replaced existing
There is packaging material.
Embodiment
Below in conjunction with example, the invention will be further described, and embodiment is only used for that the present invention will be described, not
Constitute limitation to right, it may occur to persons skilled in the art that other alternative means, in right of the present invention
In claimed range.
Embodiment 1:
The first step:PVC100 parts, 0.1 part of vinyl chloride, POM10 parts, 2 parts of titanium dioxide, three alkali are weighed according to mass fraction proportioning
1 part of formula lead sulfate, dibasic lead phosphite is 2 parts, 4 parts of lubricating oil, 1 part of zinc oxide, 2 parts of sorbierite monopalmitate, PDOP1
Part, POP2 parts, dibutyl tin mercaptides are 10 parts, 0.5 part of phosphenylic acid dioctyl ester, 0.3 part of silver system antibacterial matrices, phthalocyanine blue
0.002 part.
Second step:PVC is put into high-speed kneading machine, 95 DEG C are warming up to, surplus stock is added, 110 DEG C, kneading are warming up to
Speed 800r/min, mediates 15min.
3rd step:The roller of material two after kneading is plasticated, and preceding roll temperature is 170 DEG C, rotating speed 16r/min, and 160 DEG C of back roller turns
Fast 26r/min, kneads 15min, vulcanizing press tabletting, and temperature is 180 DEG C, and pressure 25MPa, time 10min are cooled down after press polish
PVC packaging materials are crimped to obtain, thickness is 0.5mm.
Preparation method is simple, uses manpower and material resources sparingly, longitudinal tensile strength 9MPa, transverse tensile strength 8MPa, longitudinal direction elongation
Rate 88%, cross direction elongation 75%;Burn from fiery self-extinguishment, melting time 105s, breakdown voltage 11.4kV/mm, tearing strength
108MPa, notch impact strength 5.3kJ/m2;Bending strength 30MPa, Brinell hardness 22, raw material sources are extensively, with low cost, from
Right light aging after-drawing loss of strength 0.015% in 12 months;It can be widely used in various extreme environments, 100 DEG C of heat ageings two
After-drawing loss of strength 0.12% in individual month, after the gamma-ray irradiation that 40kGy is measured, gel fraction 75% can be produced simultaneously extensively
Constantly instead of existing packaging material.
Embodiment 2:
The first step:PVC100 parts, 0.3 part of vinyl chloride, POM50 parts, 6 parts of titanium dioxide, three alkali are weighed according to mass fraction proportioning
3 parts of formula lead sulfate, dibasic lead phosphite is 4 parts, 8 parts of lubricating oil, 5 parts of zinc oxide, 6 parts of sorbierite monopalmitate, PDOP5
Part, POP8 parts, dibutyl tin mercaptides are 30 parts, 2.5 parts of phosphenylic acid dioctyl ester, 0.5 part of silver system antibacterial matrices, phthalocyanine blue
0.006 part.
Second step:PVC is put into high-speed kneading machine, 105 DEG C are warming up to, surplus stock is added, is warming up to 120 DEG C, pinches
Sum velocity 1000r/min, mediates 25min.
3rd step:The roller of material two after kneading is plasticated, and preceding roll temperature is 190 DEG C, the r/min of rotating speed 20, and 170 DEG C of back roller turns
28 r/min of speed, knead 25min, vulcanizing press tabletting, temperature is 220 DEG C, and pressure 35MPa is time 30min, cold after press polish
But PVC packaging materials are crimped to obtain, thickness is 2.5mm.
Preparation method is simple, uses manpower and material resources sparingly, longitudinal tensile strength 11MPa, transverse tensile strength 10MPa longitudinally stretch
Long rate 92%, cross direction elongation 85%;Burn from fiery self-extinguishment, melting time 125s, breakdown voltage 13.8kV/mm, tearing strength
112MPa, notch impact strength 6.7kJ/m2;Bending strength 35MPa, Brinell hardness 24, raw material sources are extensively, with low cost, from
Right light aging after-drawing loss of strength 0.035% in 12 months;It can be widely used in various extreme environments, 100 DEG C of heat ageings two
After-drawing loss of strength 0.1% in individual month, after the gamma-ray irradiation that 40kGy is measured, gel fraction 80% can be produced not extensively
Existing packaging material is replaced in the division of history into periods.
Embodiment 3:
The first step:PVC100 parts, 0.2 part of vinyl chloride, POM30 parts, 4 parts of titanium dioxide, three alkali are weighed according to mass fraction proportioning
2 parts of formula lead sulfate, dibasic lead phosphite is 3 parts, 6 parts of lubricating oil, 3 parts of zinc oxide, 4 parts of sorbierite monopalmitate, PDOP3
Part, POP5 parts, dibutyl tin mercaptides are 20 parts, 1.5 parts of phosphenylic acid dioctyl ester, 0.4 part of silver system antibacterial matrices, phthalocyanine blue
0.004 part.
Second step:PVC is put into high-speed kneading machine, 100 DEG C are warming up to, surplus stock is added, is warming up to 115 DEG C, pinches
Sum velocity 900r/min, mediates 20min.
3rd step:The roller of material two after kneading is plasticated, and preceding roll temperature is 180 DEG C, rotating speed 18r/min, and 165 DEG C of back roller turns
Fast 27r/min, kneads 20min, vulcanizing press tabletting, and temperature is 200 DEG C, and pressure 30MPa, time 20min are cooled down after press polish
PVC packaging materials are crimped to obtain, thickness is 1.5mm.
Preparation method is simple, uses manpower and material resources sparingly, longitudinal tensile strength 11MPa, transverse tensile strength 10MPa longitudinally stretch
Long rate 92%, cross direction elongation 85%;Burn from fiery self-extinguishment, melting time 125s, breakdown voltage 13.8kV/mm, tearing strength
112MPa, notch impact strength 6.7kJ/m2;Bending strength 35MPa, Brinell hardness 24, raw material sources are extensively, with low cost, from
Right light aging after-drawing loss of strength 0.015% in 12 months;It can be widely used in various extreme environments, 100 DEG C of heat ageings two
After-drawing loss of strength 0.08% in individual month, after the gamma-ray irradiation that 40kGy is measured, gel fraction 85% can be produced simultaneously extensively
Constantly instead of existing packaging material.
Claims (5)
1. a kind of preparation method of PVC packaging materials, it is characterised in that comprise the following steps:
The first step:PVC100 parts, 0.1-0.3 parts of vinyl chloride, POM10-50 parts, titanium dioxide 2- are weighed according to mass fraction proportioning
6 parts, 1-3 parts of tribasic lead sulfate, dibasic lead phosphite is 2-4 parts, 4-8 parts of lubricating oil, 1-5 parts of zinc oxide, sorbierite list
2-6 parts of palmitate, PDOP1-5 parts, POP2-8 parts, dibutyl tin mercaptides are 10-30 parts, phosphenylic acid dioctyl ester 0.5-2.5
Part, antibacterial matrices 0.3-0.5 parts of silver system, 0.002-0.006 parts of pigment;
Second step:PVC is put into high-speed kneading machine, 95-105 DEG C is warming up to, surplus stock is added, is warming up to 110-120 DEG C,
Speed 800-1000r/min is mediated, 15-25min is mediated;
3rd step:The roller of material two after kneading is plasticated, and preceding roll temperature is 170-190 DEG C, rotating speed 16-20 r/min, back roller 160-
170 DEG C, rotating speed 26-28 r/min knead 15-25min, vulcanizing press tabletting, and temperature is 180-220 DEG C, pressure 25-
35MPa, time 10-30min, cooling crimps to obtain PVC packaging materials after press polish, and thickness is 0.5-2.5mm.
2. a kind of preparation method of PVC packaging materials according to claim 1, it is characterised in that the PVC packaging materials
Preparation method raw material by mass fraction match it is as follows:PVC100 parts, 0.1 part of vinyl chloride, POM10 parts, 2 parts of titanium dioxide,
1 part of tribasic lead sulfate, dibasic lead phosphite is 2 parts, 4 parts of lubricating oil, 1 part of zinc oxide, 2 parts of sorbierite monopalmitate,
PDOP1 parts, POP2 parts, dibutyl tin mercaptides are 10 parts, 0.5 part of phosphenylic acid dioctyl ester, 0.3 part of silver system antibacterial matrices, pigment
0.002 part.
3. a kind of preparation method of PVC packaging materials according to claim 1, it is characterised in that the PVC packaging materials
Preparation method raw material by mass fraction match it is as follows:PVC100 parts, 0.3 part of vinyl chloride, POM50 parts, 6 parts of titanium dioxide,
3 parts of tribasic lead sulfate, dibasic lead phosphite is 4 parts, 8 parts of lubricating oil, 5 parts of zinc oxide, 6 parts of sorbierite monopalmitate,
PDOP5 parts, POP8 parts, dibutyl tin mercaptides are 30 parts, 2.5 parts of phosphenylic acid dioctyl ester, 0.5 part of silver system antibacterial matrices, pigment
0.006 part.
4. a kind of preparation method of PVC packaging materials according to claim 1, it is characterised in that the PVC packaging materials
Preparation method raw material by mass fraction match it is as follows:PVC100 parts, 0.2 part of vinyl chloride, POM30 parts, 4 parts of titanium dioxide,
2 parts of tribasic lead sulfate, dibasic lead phosphite is 3 parts, 6 parts of lubricating oil, 3 parts of zinc oxide, 4 parts of sorbierite monopalmitate,
PDOP3 parts, POP5 parts, dibutyl tin mercaptides are 20 parts, 1.5 parts of phosphenylic acid dioctyl ester, 0.4 part of silver system antibacterial matrices, pigment
0.004 part.
5. the preparation method of a kind of PVC packaging materials according to claim 1, it is characterised in that the pigment uses phthalein
Cyanines are blue.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710471224.4A CN107163441A (en) | 2017-06-20 | 2017-06-20 | A kind of preparation method of PVC packaging materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710471224.4A CN107163441A (en) | 2017-06-20 | 2017-06-20 | A kind of preparation method of PVC packaging materials |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107163441A true CN107163441A (en) | 2017-09-15 |
Family
ID=59818835
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710471224.4A Pending CN107163441A (en) | 2017-06-20 | 2017-06-20 | A kind of preparation method of PVC packaging materials |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107163441A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109435267A (en) * | 2018-10-29 | 2019-03-08 | 枣庄金茂塑业科技有限公司 | A kind of firecrackers film self-control technique and preparation method thereof |
CN113897002A (en) * | 2021-10-29 | 2022-01-07 | 四川天邑康和通信股份有限公司 | Environment-friendly polyvinyl chloride optical cable sheathing compound and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102199329A (en) * | 2010-03-25 | 2011-09-28 | 中国石油化工股份有限公司 | Polyvinyl-chloride-containing material for waterproof coiled felt |
CN104194211A (en) * | 2014-08-06 | 2014-12-10 | 郭良来 | PVC wrapping film |
CN105968635A (en) * | 2016-05-31 | 2016-09-28 | 苏州市鼎立包装有限公司 | Waterproof packaging material and preparing method thereof |
-
2017
- 2017-06-20 CN CN201710471224.4A patent/CN107163441A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102199329A (en) * | 2010-03-25 | 2011-09-28 | 中国石油化工股份有限公司 | Polyvinyl-chloride-containing material for waterproof coiled felt |
CN104194211A (en) * | 2014-08-06 | 2014-12-10 | 郭良来 | PVC wrapping film |
CN105968635A (en) * | 2016-05-31 | 2016-09-28 | 苏州市鼎立包装有限公司 | Waterproof packaging material and preparing method thereof |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109435267A (en) * | 2018-10-29 | 2019-03-08 | 枣庄金茂塑业科技有限公司 | A kind of firecrackers film self-control technique and preparation method thereof |
CN113897002A (en) * | 2021-10-29 | 2022-01-07 | 四川天邑康和通信股份有限公司 | Environment-friendly polyvinyl chloride optical cable sheathing compound and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104194211A (en) | PVC wrapping film | |
EP0138121B1 (en) | Moulding composition based on vinyl chloride polymers and process for preparing films from these moulding compositions for the preparation of securities protected against falsification | |
CN107163441A (en) | A kind of preparation method of PVC packaging materials | |
CN105623153A (en) | Nano-silicon dioxide toughened PVC (polyvinyl chloride) corrugated pipe and preparation method therefor | |
DE2055751C3 (en) | Process for the production of chlorinated ethylene polymers and their use | |
CN105602159A (en) | PVC master batch and preparation method thereof | |
CN104371219B (en) | A kind of medical heat-resisting ageing-resisting composite plastic and preparation method thereof | |
EP3105267B1 (en) | Use of methyl methacrylate vinylaromate copolymers | |
CN104893183A (en) | Hard antibacterial pharmaceutical PVC (polyvinyl chloride) sheet and production method thereof | |
CN104744849B (en) | A kind of Environmental-friendantistatic antistatic high-flame-retardantPVC PVC sheath material and preparation method thereof | |
CN107459735B (en) | Environment-protective polychloroethylene material composition and its preparation method and application | |
DE1067595B (en) | Process for the production of vulcanizable elastomers by chlorosulfonation of polyolefins | |
CN105331002B (en) | A kind of PVC polymer membranes | |
CN105778337A (en) | PVC (polyvinyl chloride) elastomer and method for preparing same | |
CN107353531A (en) | A kind of preparation method of PVC packaging films | |
CN107325431A (en) | A kind of fire-retardant long glass fiber reinforced polyvinyl chloride(PVC)Composite and preparation method thereof | |
CN108503975A (en) | PVC composite materials and its preparation process for luggage | |
CN107177134A (en) | A kind of preparation method of PVC waterproof packaging films | |
CN103724876B (en) | polyvinyl chloride/chlorinated polyethylene blend and processing method thereof | |
DE1745411A1 (en) | Process for the production of a rubbery crosslinked polyethylene copolymer | |
CN106751205A (en) | A kind of medicinal stiff sheet formulas of PVC | |
CN105602161A (en) | PVC (polyvinyl chloride) alloy | |
DE1494917A1 (en) | Compounds hardenable to elastomers | |
CN102504467B (en) | Reactive extrusion production double-component graft modified polyvinyl chloride plastic and preparation method thereof | |
CN107189264A (en) | A kind of preparation method of packaging material |
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 |
Application publication date: 20170915 |
|
RJ01 | Rejection of invention patent application after publication |