CN106832671A - The resin expanded transfer door and its preparation technology of a kind of use calcium zinc stabilizer - Google Patents
The resin expanded transfer door and its preparation technology of a kind of use calcium zinc stabilizer Download PDFInfo
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- CN106832671A CN106832671A CN201710080259.5A CN201710080259A CN106832671A CN 106832671 A CN106832671 A CN 106832671A CN 201710080259 A CN201710080259 A CN 201710080259A CN 106832671 A CN106832671 A CN 106832671A
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- 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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B7/00—Mixing; Kneading
- B29B7/002—Methods
- B29B7/005—Methods for mixing in batches
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0012—Combinations of extrusion moulding with other shaping operations combined with shaping by internal pressure generated in the material, e.g. foaming
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0022—Combinations of extrusion moulding with other shaping operations combined with cutting
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0023—Combinations of extrusion moulding with other shaping operations combined with printing or marking
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/022—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
- C08J9/08—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing carbon dioxide
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
- C08J9/10—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
- C08J9/102—Azo-compounds
- C08J9/103—Azodicarbonamide
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- E—FIXED CONSTRUCTIONS
- E06—DOORS, WINDOWS, SHUTTERS, OR ROLLER BLINDS IN GENERAL; LADDERS
- E06B—FIXED OR MOVABLE CLOSURES FOR OPENINGS IN BUILDINGS, VEHICLES, FENCES OR LIKE ENCLOSURES IN GENERAL, e.g. DOORS, WINDOWS, BLINDS, GATES
- E06B1/00—Border constructions of openings in walls, floors, or ceilings; Frames to be rigidly mounted in such openings
- E06B1/04—Frames for doors, windows, or the like to be fixed in openings
- E06B1/34—Coverings, e.g. protecting against weather, for decorative purposes
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- E—FIXED CONSTRUCTIONS
- E06—DOORS, WINDOWS, SHUTTERS, OR ROLLER BLINDS IN GENERAL; LADDERS
- E06B—FIXED OR MOVABLE CLOSURES FOR OPENINGS IN BUILDINGS, VEHICLES, FENCES OR LIKE ENCLOSURES IN GENERAL, e.g. DOORS, WINDOWS, BLINDS, GATES
- E06B1/00—Border constructions of openings in walls, floors, or ceilings; Frames to be rigidly mounted in such openings
- E06B1/04—Frames for doors, windows, or the like to be fixed in openings
- E06B1/52—Frames specially adapted for doors
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- E—FIXED CONSTRUCTIONS
- E06—DOORS, WINDOWS, SHUTTERS, OR ROLLER BLINDS IN GENERAL; LADDERS
- E06B—FIXED OR MOVABLE CLOSURES FOR OPENINGS IN BUILDINGS, VEHICLES, FENCES OR LIKE ENCLOSURES IN GENERAL, e.g. DOORS, WINDOWS, BLINDS, GATES
- E06B3/00—Window sashes, door leaves, or like elements for closing wall or like openings; Layout of fixed or moving closures, e.g. windows in wall or like openings; Features of rigidly-mounted outer frames relating to the mounting of wing frames
- E06B3/70—Door leaves
- E06B3/7001—Coverings therefor; Door leaves imitating traditional raised panel doors, e.g. engraved or embossed surfaces, with trim strips applied to the surfaces
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92009—Measured parameter
- B29C2948/92209—Temperature
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92323—Location or phase of measurement
- B29C2948/92361—Extrusion unit
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92857—Extrusion unit
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/724—Doors
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/02—CO2-releasing, e.g. NaHCO3 and citric acid
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/04—N2 releasing, ex azodicarbonamide or nitroso compound
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/18—Binary blends of expanding agents
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised 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
- C08J2327/02—Characterised 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
- C08J2327/04—Characterised 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
- C08J2327/06—Homopolymers or copolymers of vinyl chloride
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2423/02—Characterised 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
- C08J2423/04—Homopolymers or copolymers of ethene
- C08J2423/06—Polyethene
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- 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
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/14—Applications used for foams
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- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
Abstract
The invention provides the resin expanded transfer door and its preparation technology of a kind of use calcium zinc stabilizer, compared with prior art, the application uses calcium zinc stabilizer, re-establishes formula system framework;According to formula adjustment mixing time control, preplasticizing effect is improved;By reducing first three area's temperature in terms of expressing technique, discharging speed is controlled, find out the modes such as rational production capacity interval;Transfer temperature is especially paid close attention in terms of transfer printing process, in the case of the change in size that fully research second time of foaming causes, rational transfer temperature control interval is set, to transfer speed, platen pressure, the link such as preheating temperature is strictly controlled.The transfer door of preparation is formaldehydeless, without toxic chemical substance, environmental protection, solve the precipitation that easily occurs in calcium zinc stabilizer production, zinc burn, transfer when second time of foaming the problems such as, while expansion ratio and properties of product aspect are satisfied by coherent detection requirement.
Description
Technical field
The invention belongs to building materials field, and in particular to a kind of resin expanded transfer door of use calcium zinc stabilizer and its preparation
Technique.
Background technology
As market user's demand is continually changing, finishing material day of the people to the harmful substance such as environmental protection, formaldehydeless
Plus favor, in this wheel ornament materials revolution, resin expanded Men Yiqi environmental protection, reusable edible, transfer film paste formaldehydeless etc.
Advantage, and its its excellent sound insulation, heat-insulated, moistureproof, processability and decorative effect lead the interior door trend of a new generation.It is excellent
The hollow skinning PVC foam door-plate and its transfer printing wood grain technique of matter assign resin expanded door environmental protection ecosystem characterization, and with excellent
Good physical property and diversified product design, are adapted to all kinds of architectural styles, are increasingly received by the market, and disappear as vast
The first-selection of the asepsis environment-protecting interior door of the person of expense.
PVC foam door-plate has excellent processing characteristics, can be bored, be sawed, being followed closely, being dug, being glued etc. processing, be applicable to heat into
Type, heating bending and folding are processed, can welded according to general Plastic Welding program, also can be Nian Jie with other PVC materials, with wood
, compared to there is stronger superiority, product service life reaches more than 50 years for plate, glued board.
At this stage in the production of conventional resins foamed products, lead salt formula system is used mostly, and in lead salt formula system
Containing heavy metals such as a certain amount of lead, for a long time using being possible to separate out, the most stabilizer of the state such as America and Europe is produced at this stage
Product, for a long time due to intellectual property and production-supply-marketing, it is first lead system to form European main flow formula in polyvinyl chloride resin industry
It is afterwards calcium zinc system, North America main flow formula is formulated for organotin system.
Organotin system is formulated plasticizing capacity, product surface gloss, physical and mechanical properties, stability, weatherability and is superior to lead
It is formula system product, but tin still belongs to heavy metal, and the feature of environmental protection is queried, and process taste is big, and formulation cost is high;Lead system matches somebody with somebody
Side contains toxic heavy metal, and easy sulfide staining, environmental-protecting performance is poor, and mechanical property discreteness is big.Calcium zinc system formula is near European countries
Over year and future development main flow formula, with the continuous progress of technology, tended to ripe, and as environmental protection stabilizer
Standard.
But when the precipitation, zinc burning, the transfer that at present, easily occur in calcium zinc stabilizer production the problems such as second time of foaming, together
When expansion ratio and properties of product aspect be satisfied by that coherent detection requirement can not be met.
The content of the invention
It is formaldehydeless, do not contain it is an object of the invention to provide a kind of resin expanded transfer door of use calcium zinc stabilizer
Malicious chemical substance, environmental protection, second time of foaming when solving the precipitation, zinc burning, the transfer that easily occur in calcium zinc stabilizer production
The problems such as, while expansion ratio and properties of product aspect are satisfied by coherent detection requirement.
Present invention also offers a kind of preparation technology of the resin expanded transfer door of use calcium zinc stabilizer, coordinate in being formulated
Property of raw material, develop manufacturing process and design optimization technological parameter, simple to operate, stability and high efficiency.
A kind of resin expanded transfer door of use calcium zinc stabilizer that the present invention is provided, contains following raw material:
The PVC trades mark are SG-7;
A kind of preparation technology of the resin expanded transfer door of use calcium zinc stabilizer that the present invention is provided, including following step
Suddenly:
1), batch mixing heat is mixed:Each component is weighed by formula, according to PVC-- precipitated calcium carbonates under 300rpm rotating speeds -- it is compound
Bag -- K718--AC foaming agents -- NaHCO3Order under enter the mixed pot of heat after, then rotating speed control high-speed stirring under 680-720rpm
Mix, make material temperature that more than 110 DEG C were promoted within 200 seconds, realize the preplasticizing of dry blend;
It is described it is compound bag by formula ratio PE waxes, pentaerythritol fatty acid ester ST220/ or F210, phosphite ester, acetylacetone,2,4-pentanedione
Zinc, hydrotalcite, zeolite, K123, K385, interior lubrication prescription G60, ZnO, calcium stearate, zinc stearate, beta-diketon zinc and AC316A groups
Into;
2) batch mixing is cold mixed:After through the mixed preplasticizing of heat, by cold mixed 50rpm stirring at low speed, material temperature was dropped at 350-400 seconds
To less than 50 DEG C, prevent material accumulated heat from degrading, while eliminating the electrostatic that high-speed stirred is produced;
3) extrude:Extrusion forming after material plasticizing, then cooling and shaping;
4) blanking, end of door plate is cut according to customer demand size;
5) transfer:By temperature control heating transfer apparatus, transfer film is covered on resin expanded door base material;
Door-plate transfer printing process state modulator:1 temperature (plate is taken turns in 0.2 ± 0.05N of winder tension force, hauling speed 3-5m/min, face
The big face thermoprint wheel of material) 185 ± 5 DEG C, 185 ± 5 DEG C of 2 temperature of face wheel, side scald 170 ± 5 DEG C of 1 temperature, side scald 170 ± 5 DEG C of 2 temperature and
Scald 130 ± 5 DEG C of 3 temperature in side.
Further, step 1) in it is preferred, material temperature is promoted to 115-118 DEG C;Dry blend is pre- solidifying at a temperature of this
Gel degree highest;
Further, step 1) in material incorporation time 300-420 seconds in the mixed machine of heat, obtain uniform quality, mainstream property
Good dry blend;
Step 1) in it is preferred, batch mixing amount accounts for the 65%-68% of the mixed pot pot volume of 800L heat, the pregelatinized of compound
Preferably, sheet material production is stable for effect.
Step 1) in it is preferred, the mixed flow deflector side of heat should be wide apart from pot wall 3-5cm, and now material seethes effect in pot
Most preferably.
Step 2) in it is preferred, cold doing time should be at 330-420 seconds, while blanking temperature should be arranged on 45 DEG C;
Further, because of foaming agent containing sodium acid carbonate in calcium zinc ecological door formula, easily water suction is decomposed, therefore calcium zinc is ecological
Door formula storage time is shut down and in advance should be finished remaining dry blend for a long time no more than 72 hours, such as, hair otherwise easily occurs
Bubble multiplying power it is impacted, extrusion load fluctuation it is big the problems such as.
Step 3) include:First stage:Plasticizing, the effect for passing through barrel zone temperature and screw rod, material are changed by graininess
It is the process of the uniformly continuous melt with certain fluidity;Second stage:Shaping, the improving uniformity of melt with mobility, utilize
The rotary squeezing of screw rod enters head by porous plate, and is the effigurate parison of tool by mouth mold and mandrel molding;3rd
Stage:Cooling and shaping:That is parison under extrusion pressure and draw, by after vacuum cooled stock mould, formed have it is certain
The product of intensity, rigidity and dimensional accuracy.
Step 3) in specific process parameter be:16 ± 2rpm of screw speed, 50 ± 5rpm of charging rate, hauling speed 0.6
± 0.2m/min, extrusion load 40~70%, the temperature 150 of 145 ± 10 DEG C, tin area of extruder temperature, 1 temperature, 150 ± 10 DEG C, tin area 2
The temperature 170 of 3 temperature, 150 ± 10 DEG C, tin area of ± 10 DEG C, tin area, 4 temperature, 150 ± 10 DEG C, tin area, 5 temperature, 170 ± 10 DEG C, tin area 6
± 10 DEG C, 170 ± 10 DEG C of 1 temperature of connector, 170 ± 10 DEG C of 2 temperature of connector, mold temperature (1-11):190 ± 10 DEG C, mould
Tool temperature (12-13):170 ± 10 DEG C, 180 ± 10 DEG C of melt temperature, 180 ± 10 DEG C of core oil temperature, mouth mold oil temperature 180 ± 10
DEG C, 60~80 DEG C of core water temperature, 30~50 DEG C of mouth mold water temperature, 14~18 DEG C of coolant water temperature, vacuum hydrofuge negative pressure -0.03~-
0.07Mpa and dry 0~-0.06Mpa of negative-pressure shaping.
Step 4) blanking:Because foaming doors blank size precise requirements are high, using relatively accurate cross-cut saw according to visitor
Family requires to carry out cutting small powder;
Step 5) in also include doorframe material transferring technique, design parameter control:0.2 ± 0.05N of winder tension force, traction speed
Degree 3-7m/min, 140 ± 5 DEG C of 1 temperature of perming, 170 ± 5 DEG C of 2 temperature of perming and 160 ± 5 DEG C of 3 temperature of perming.
Also include step 6) packaging shipping, according to《Ecological door Package Management specifies》Entered by the way of pearl cotton+carton
Row packaging, blend compounds band is tightened, and order shipment is carried out according to entrucking specification.
Calcium zinc stabilizer formula system is applied in resin expanded product in the present invention, uses hollow low foaming knot
Skin production technology, it is high to stabilizer heat stabilizing system, lubricating system requirement, fully studied to all calcium zinc raw material mechanisms of action
On the basis of grasp, formula system framework is redesigned.In heat stabilizing system design, using beta-diketon zinc and ST-220/
Used as core stable agent, be aided with phosphite ester and zinc acetylacetonate carries out stable regulation to F210, uses calcium stearate and stearic acid
Zinc improves formula plasticizing capacity, and Related product is formulated consumption and calculates by accurate Theory and practical proof, after emphasis solves transfer
Second time of foaming, mould zinc burn problem and meet the satisfaction requirement of product associated materials performance.In lubricating system design, using G60 Inner
, used as core lubricant, being aided with OPE carries out inside and outside sliding collaboration, and the system must agree with for lubrication prescription and the outer lubrication prescription of PE waxes
Resin expanded door long-term production stability, in the case where release property is ensured, reduces and separates out, and improves product stability and production week
Phase.Calcium stearate and zinc stearate adjust plasticizing effect in passing through formula in foaming process, make do not influenceing the feelings of gas release
Improve melt strength under condition, it is to avoid occur foaming doors surface crater, by adjust AC foam dosage and sodium bicarbonate content, regulation produce
Product rice proportion and expansion ratio, it is ensured that product meets use requirement.
It is whole due to the difference of calcium zinc formula system and traditional lead salt system in terms of technology controlling and process in preparation technology
Change production technology has specific technique matched from batch mixing-extrusion-later stage transfer film transfer, by technical research team
Grope tackling key problem, analyzed in the main points of processes control such as each operation operation mechanism and temperature by formula each component, formulated a set of
It is adapted to the technology controlling and process route of the product.According to the proterties of different material, physical characteristic, preformed in formula in terms of mixing procedure
Change the key parameters such as requirement etc., the mixed mixing time of adjustment heat, improve preplasticizing effect.The morphogenetic change of material during heat is mixed
Change:(1) apparent density for being compacted usual polyvinyl chloride resin is only 0.45~0.55g/ml.Due to phase mutual friction in high-speed mixer
The frictional heat of generation, makes temperature of charge constantly rise, and PVC granule and other components are constantly interpenetrated, and PVC particle surfaces are gradually
The various auxiliary agents such as Vapor recovery unit agent and molten lubricant etc., making the apparent density of compound can increase to 0.58~0.65g/
ml.(2) in high-speed mixer, each component can not only reach good mechanical mixture to homogenizing, also can obtain good between each component
Stable dispersion.As temperature is constantly raised, PVC particles can constantly Vapor recovery unit agent, lubricant etc., gradually wrapped by each component
Cover, when temperature rises to 110~118 DEG C, the dry mixed powder of uniform stabilization can be formed.(3) hydrofuge:When temperature of charge rises to 100 DEG C
During left and right, the moisture that is included in resin and adjuvant component and other volatile substances are easy to remove, it is to avoid in extrusion type
Bubble and defect are produced during material.(4) pregelatinized:The gelation of PVC refers to that resin progressively melts modeling in process
Change, then recrystallization forms the process of network morphology structure, during high speed hot mixing, it is seen that the existing particle of polyvinyl chloride resin
Refinement, the metamorphosis of uniform particle sizes, show again density increase, partial gelation the characteristics of.Therefore PVC material high-speed heat is mixed
Conjunction process, is also the process of polyvinyl chloride resin homogenization, densification and partial gelation, though material gelation is not the main mesh of batch mixing
, but in mixed process, there is gelation in existing part PVC particles.There are the small particles of large surface area, be vulnerable to larger
Friction, reaches gelation state, shows similar transparence, and little particle is gradually melted at relatively high temperatures, is flocked together,
Become larger particle, the PVC of surface gelling can be very good to absorb various auxiliary agents, finally give our common homogeneity
With the preferable dry blend of mainstream property.(5) influence of the mixing temperature to mixture performance:The mixing temperature of material is influence dry blend
One of most important factor of performance, mixture temperature be less than 80 DEG C when, material it is closely knit closely knit mainly by mechanical force, make each group subpackage
It is trapped among PVC particle peripheries.When temperature is to higher than polyvinyl chloride resin glass transition temperature Tg (about 80 DEG C), PVC granule starts to soften, and inhales
Other components are received, it is gradually closely knit, when temperature rises to 110~120 DEG C, less particle gradually gel in PVC particles, we pass through
Feedstock property design studies, at 115-118 DEG C, the ecological transfer door formula compounding effect of calcium zinc is optimal, dry blend for temperature
Pregelatinized degree highest.(6) incorporation time influence:Compacting, homogenizing, partial gelation mistake that material experiences in mixed process
Journey, is required to certain hour completion.The extension of mixing time contributes to stabilizer and other additives to be more uniformly diffused into
In resin, further to improve material stability and uniformity coefficient.Rule of thumb, incorporation time is extremely in high-speed mixer for material
Less between 300~420 seconds, uniform quality, the dry blend of dry good fluidity can be just obtained.(7) feeding quantity in high-speed mixer
Influence:The feeding quantity selected in high-speed mixer, should be able to be conducive to production efficiency on the premise of mixed material quality is ensured
Improve.Too small per batch materials inventory, such as volume of material is only less than the 50% of high-speed mixer, and material seethes poor, generation
Frictional heat it is low, temperature rise is slow, and time-consuming, reaches default mixing temperature and about want more than 15min, while also the mixing of influence material is
It is even.Conversely, inventory is excessive, motor load is too high, and the speed of mainshaft declines, and equally influence material seethes situation and batch mixing matter
Amount, programming rate is also no longer significantly improved.Usual feeding quantity is in mixer volume 60%~80%, and mixed effect is preferable.This
Batch mixing amount accounts for the 65%-68% of pot volume in application, and preferably, sheet material production is steady for the pregelatinized effect of calcium zinc formula compound
It is fixed.(8) the mixed flow deflector of heat will directly affect material and be seethed in pot in semiellipse cambered surface, therefore flow deflector angle in batch mixing pot
Effect, so as to influence matter homogenizing and pregelatinized effect, by design studies, excessively middle flow deflector side of device itself should be apart from pot
Wall 1-23-5cm is a width of preferably, and now material seethes best results in pot.
By reducing first three area's temperature (temperature control is at 150 ± 10 DEG C) in terms of expressing technique, discharging speed is controlled
(0.6 ± 0.2m/min) finds out the modes such as rational production capacity interval, the problems such as preventing zinc and burn, and reduces to a certain extent
The generation of precipitate, improves production stability.Extrude control technology in the present invention to be mainly reflected in temperature control, on the one hand
To suppress foaming too early in early stage, while cylinder area temperature will match with calcium zinc formula feature, while by investigation and comparison, calcium zinc
Using the positive setting of temperature, than using, temperature parabola is set ecological door extrusion foaming technique and reverse setting of temperature discharges uniformly
Degree, surface skining effect is even more ideal.
Transfer temperature is especially paid close attention in terms of transfer printing process, in the situation of the fully change in size that research second time of foaming causes
Under, rational transfer temperature control interval is set, to transfer speed (sheet material is controlled in 3-5m/min), (control of platen pressure scale
System is in 39.2mm), the link such as preheating temperature (185 ± 5 DEG C) is strictly controlled.
Compared with prior art, the present invention provide use calcium zinc stabilizer resin expanded transfer door, calcium zinc-base material with
Transfer printing process all meets environment-friendly materials requirement, and base material is free of heavy metal, and transfer materials are free of formaldehyde;Anti-corrosion, protection against the tide, Anti-moth-eating,
It is indeformable, due to main material polyvinyl chloride self performance used, influenceed smaller by soda acid;Water absorption rate is only 0.5%;It is effectively anti-
Only damage by worms.It is highly suitable for the environment of southern humidity.Processing install convenient, sheet material inside use hollow structure and core layer foaming skill
Art, makes the density of foamed products close to timber.The xyloid processing request of class, the installation than wooden door is more quick, is not required to nail
Nail, smear putty, brush paint etc. traditional work mode, factory normalization production, Digit Control Machine Tool milling hinge, lockhole, decorated dormer
Hole, dimensional standard is accurate, it is ensured that overall tight during in-site installation.Using bulk-breaking modular construction, it is readily transported, in-site installation side
Just, it is to avoid numerous and diverse at the scene manual processing and making process, the road of batch production pipelining is walked, improves the making of door
Installation effectiveness.Manufacturing process variation, without professional, machining tool highly versatile used.
Brief description of the drawings
Fig. 1 is the preparation technology schematic flow sheet of resin expanded transfer door;
Fig. 2 is the preparation technology schematic diagram of batch mixing.
Specific embodiment
Primary product board is as follows in the present invention:
PVC(SG-7):Qilu Petrochemical SG-7;Fine particle calcium carbonate:Jiangxi Daewoo;Calcium stearate and zinc stearate:Nanjing Nanjing;
ST220:Aginomoto;;Phosphite ester:Wuxi Ju Wang;Hydrotalcite and zeolite:Aluminium in Shandong;AC316A:Honeywell;AC foams
Agent:Upper sea light is abundant;K385、K718:The inscription of Weihai hundred million reaches;PE waxes:Nation Buddhist nun BN208.
Embodiment 1
A kind of resin expanded transfer door of use calcium zinc stabilizer, contains following raw material:
The PVC trades mark are SG-7.
A kind of preparation technology of the resin expanded transfer door of use calcium zinc stabilizer, comprises the following steps:
1) feed proportioning
Accurate weighing is carried out to each component raw material using Automatic weighing equipment, weighing precision is 0.01KG, and weighing is finished
Enter the mixed pot of heat in units of part by programme-control afterwards.
2) batch mixing heat is mixed
Batch mixing heat is mixed:Each component is weighed by formula, according to PVC-- precipitated calcium carbonates under 300rpm rotating speeds -- compound bag --
K718--AC foaming agents -- NaHCO3Order under enter the mixed pot of heat after, then rotating speed control high-speed stirred under 680-720rpm,
Make material temperature that more than 110 DEG C were promoted within 200 seconds, realize the preplasticizing of dry blend;
It is described it is compound bag by formula ratio PE waxes, pentaerythritol fatty acid ester ST220/ or F210, phosphite ester, acetylacetone,2,4-pentanedione
Zinc, hydrotalcite, zeolite, K123, K385, interior lubrication prescription G60, ZnO, calcium stearate, zinc stearate, beta-diketon zinc and AC316A groups
Into;Batch mixing amount accounts for the 65%-68% of pot volume, and the mixed flow deflector side of heat should be wide apart from pot wall 3-5cm, by bed plate, middle knife,
The synergy of angle knife high-speed stirred is raised, material temperature is stepped up to 115-118 DEG C, dry blend pregelatinized at a temperature of this
Degree highest, incorporation time 300-420 seconds in high-speed mixer;Realize the preplasticizing of dry blend.
3) batch mixing is cold mixed
After through the mixed preplasticizing of heat, by cold mixed stirring at low speed, cold doing time should be between 330-420 seconds, with present
Material temperature degree should be arranged on 45 DEG C, and material now decomposes the stage more optimal than reaching relative equilibrium containing static content and foaming agent, prevents
Only material accumulated heat degraded, foaming agent foam is decomposed, while eliminating the electrostatic that high-speed stirred is produced.
4) deposit
Because of foaming agent containing sodium acid carbonate in calcium zinc ecological door formula, easily water suction is decomposed, therefore calcium zinc ecological door formula is stored up
The time is deposited no more than 72 hours, such as shutting down for a long time in advance should be finished remaining dry blend, expansion ratio otherwise easily occur and receive
Influence, extrusion load fluctuation it is big the problems such as.
5) extrude
First stage:Plasticizing.I.e. by the effect of barrel zone temperature and screw rod, material is changed into a constant current by graininess
The process of the uniformly continuous melt of dynamic property.Second stage:Shaping.Improving uniformity of melt with mobility, is squeezed using the rotation of screw rod
Pressure enters head by porous plate, and is the effigurate parison of tool by mouth mold and mandrel molding.Phase III:Cooling is fixed
Type.That is parison under extrusion pressure and draw, by after vacuum cooled stock mould, formed have some strength, rigidity and
The product of dimensional accuracy.
Extrusion control technology is mainly reflected in temperature control, on the one hand to suppress foaming too early in early stage, while cylinder area
Temperature will match with calcium zinc formula feature, while by investigation and comparison, calcium zinc ecological door extrusion foaming technique is using temperature just
To setting than setting the setting discharging uniformity reverse with temperature using temperature parabola, surface skining effect is even more ideal.This Shen
Please technological control temperature such as table 1 below:
The procession parameters of table 1 are controlled
5) blanking:Because foaming doors blank size precise requirements are high, will according to client using relatively accurate cross-cut saw
Asking carries out cutting stock
6) transfer:By temperature control heating transfer apparatus, transfer film is covered on resin expanded door base material, this operation is complete
By thermal transfer, formaldehyde materials are contained without the use of glue etc..
Transfer printing process is especially it is noted that temperature control, it is to avoid the second time of foaming phenomenon that calcium zinc formula easily occurs.
Controlled for door-plate transfer printing process as follows:
Winder tension force | (0.2±0.05)N |
Hauling speed: | (3-5)m/min |
Take turns 1 temperature in face: | (185±5)℃ |
Take turns 2 temperature in face: | (185±5)℃ |
Scald 1 temperature in side: | (170±5)℃ |
Scald 2 temperature in side: | (170±5)℃ |
Scald 3 temperature in side: | (130±5)℃ |
Controlled for auxiliary material transfer printing process as follows:
Product performance index
1) produced in strict accordance with inner quality standard, properties meet user's use requirement.
2) calcium zinc-base material and transfer printing process all meet environment-friendly materials requirement, and base material is free of heavy metal, and transfer materials are free of first
Aldehyde.
3) anti-corrosion, protection against the tide, Anti-moth-eating, indeformable, due to main material polyvinyl chloride self performance used, is influenceed by soda acid
It is smaller;Water absorption rate is only 0.5%;Effectively prevent from damaging by worms.It is highly suitable for the environment of southern humidity.
4) processing install convenient, sheet material inside use hollow structure and core layer foaming technology, connect the density of foamed products
Nearly timber.The xyloid processing request of class, the installation than wooden door is more quick, is not required to nail, smears the biographies such as putty, brush paint
System operating type, factory normalization production, Digit Control Machine Tool milling hinge, lockhole, decoration fenestra, dimensional standard is accurate, it is ensured that existing
It is overall tight when field is installed.Using bulk-breaking modular construction, it is readily transported, in-site installation is convenient, it is to avoid numerous and diverse at the scene
Manual processing and making process, walks the road of batch production pipelining, improves the fabrication and installation efficiency of door.Manufacturing process is various
Change, without professional, machining tool highly versatile used.
Claims (9)
1. a kind of resin expanded transfer of use calcium zinc stabilizer, it is characterised in that the resin of the use calcium zinc stabilizer
Foaming transfer door contains following raw material:
2. the use calcium zinc stabilizer described in a kind of claim 1 resin expanded transfer door preparation technology, it is characterised in that
The preparation technology is comprised the following steps:
1), batch mixing heat is mixed:Each component is weighed by formula, according to PVC-- precipitated calcium carbonates under 300rpm rotating speeds -- compound bag --
K718--AC foaming agents -- NaHCO3Order under enter the mixed pot of heat after, then rotating speed control high-speed stirred under 680-720rpm,
Make material temperature that more than 110 DEG C were promoted within 200 seconds, realize the preplasticizing of dry blend;
It is described it is compound bag by formula ratio PE waxes, pentaerythritol fatty acid ester ST220/ or F210, phosphite ester, zinc acetylacetonate, water
Talcum, zeolite, K123, K385, interior lubrication prescription G60, ZnO, calcium stearate, zinc stearate, beta-diketon zinc and AC316A composition;
2) batch mixing is cold mixed:After through the mixed preplasticizing of heat, by cold mixed 50rpm stirring at low speed, material temperature was down to 50 at 350-400 seconds
Below DEG C, prevent material accumulated heat from degrading, while eliminating the electrostatic that high-speed stirred is produced;
3) extrude:Extrusion forming after material plasticizing, then cooling and shaping;
4) blanking, end of door plate is cut according to customer demand size;
5) transfer:By temperature control heating transfer apparatus, transfer film is covered on resin expanded door base material;
Door-plate transfer printing process state modulator:1 temperature 185 ± 5 is taken turns in 0.2 ± 0.05N of winder tension force, hauling speed 3-5m/min, face
DEG C, 185 ± 5 DEG C of 2 temperature of face wheel, side scald that 170 ± 5 DEG C of 1 temperature, side scald 170 ± 5 DEG C of 2 temperature and 130 ± 5 DEG C of 3 temperature is scalded in side.
3. preparation technology according to claim 2, it is characterised in that step 1) in material temperature is promoted to 115-118
℃。
4. the preparation technology according to Claims 2 or 3, it is characterised in that step 1) in material when mixing in the mixed machine of heat
Between 300-420 seconds.
5. the preparation technology according to claim any one of 2-4, it is characterised in that step 1) in batch mixing amount to account for 800L heat mixed
The 65%-68% of pot volume.
6. the preparation technology according to claim any one of 2-5, it is characterised in that step 1) in the mixed flow deflector side of heat should
It is wide apart from pot wall 3-5cm.
7. the preparation technology according to claim any one of 2-6, it is characterised in that step 2) in cold doing time should be
330-420 seconds, while blanking temperature should be arranged on 45 DEG C.
8. the preparation technology according to claim any one of 2-7, it is characterised in that step 3) in specific process parameter be:
16 ± 2rpm of screw speed, 50 ± 5rpm of charging rate, 0.6 ± 0.2m/min of hauling speed, extrusion load 40~70%, screw rod
DEG C, tin area 4 of 145 ± 10 DEG C, tin area of temperature, 1 temperature, 150 ± 10 DEG C, tin area, 2 temperature, 150 ± 10 DEG C, tin area, 3 temperature 150 ± 10
170 ± 10 DEG C of 150 ± 10 DEG C, tin area of temperature, 5 temperature, 170 ± 10 DEG C, tin area, 6 temperature, 170 ± 10 DEG C of 1 temperature of connector, connection
170 ± 10 DEG C of 2 temperature of body, mold temperature (1-11):190 ± 10 DEG C, mold temperature (12-13):170 ± 10 DEG C, melt temperature
180 ± 10 DEG C, 180 ± 10 DEG C of core oil temperature, 180 ± 10 DEG C of mouth mold oil temperature, 60~80 DEG C of core water temperature, mouth mold water temperature 30~50
DEG C, 14~18 DEG C of coolant water temperature, vacuum -0.03~-0.07Mpa of hydrofuge negative pressure and dry 0~-0.06Mpa of negative-pressure shaping.
9. the preparation technology according to claim any one of 2-8, it is characterised in that step 5) in also turn including doorframe material
Print technique, design parameter control:0.2 ± 0.05N of winder tension force, hauling speed 3-7m/min, 140 ± 5 DEG C of 1 temperature of perming, scald
170 ± 5 DEG C of first 2 temperature and 160 ± 5 DEG C of 3 temperature of perming.
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CN113088014A (en) * | 2021-03-25 | 2021-07-09 | 台州联成新材料有限公司 | Ultraviolet-resistant PVC (polyvinyl chloride) sunlight material and preparation method thereof |
CN113583300A (en) * | 2021-09-03 | 2021-11-02 | 江西宝泰聚科技协同创新有限公司 | Moistureproof calcium-zinc stabilizer and preparation method thereof |
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CN108586975A (en) * | 2018-03-30 | 2018-09-28 | 芜湖海螺新材料有限公司 | A kind of PVC furniture-plates and preparation method thereof |
CN110845811A (en) * | 2019-12-03 | 2020-02-28 | 芜湖海螺新材料有限公司 | Formaldehyde-free odorless PVC (polyvinyl chloride) foamed sheet and processing method thereof |
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CN113583300A (en) * | 2021-09-03 | 2021-11-02 | 江西宝泰聚科技协同创新有限公司 | Moistureproof calcium-zinc stabilizer and preparation method thereof |
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