CN106280425A - A kind of high glaze nylon reinforcements and preparation method thereof - Google Patents
A kind of high glaze nylon reinforcements and preparation method thereof Download PDFInfo
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- CN106280425A CN106280425A CN201610798130.3A CN201610798130A CN106280425A CN 106280425 A CN106280425 A CN 106280425A CN 201610798130 A CN201610798130 A CN 201610798130A CN 106280425 A CN106280425 A CN 106280425A
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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
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
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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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- 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
- B29C2948/9258—Velocity
- B29C2948/9259—Angular velocity
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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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- 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
- C08K2201/002—Physical properties
- C08K2201/003—Additives being defined by their diameter
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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
- C08K2201/011—Nanostructured additives
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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
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Abstract
The invention discloses a kind of high glaze nylon reinforcements and preparation method thereof.This high glaze nylon reinforcements is by the PA6 of 60 70% by weight percentage, glass microballoon 10 15%, coupling agent 0.2 1%, composite nucleating agent 0.5 1%, antioxidant 0.2 0.8%, flow ability modifying agent 0.5 1.5%, glass fibre 15 25% is prepared from.High glaze nylon reinforcements of the present invention has that surface gloss is good, coloring is good, all can keep the advantages such as higher dimensional stability at different conditions；Can use steadily in the long term under high/low temperature, and have stable mechanical property and chemical resistance.
Description
Technical field
The invention belongs to macromolecular material and processing technique field thereof, be specifically related to a kind of high glaze nylon reinforcements and
Its preparation method.
Background technology
Nylon 6 (PA6) is the linear polymer of caprolactam, the hydrogen that in a strand, amide group is connected with nitrogen-atoms
The oxygen atom of the amide group on atomic energy and another strand associates and forms hydrogen bond, the formation of hydrogen bond increase strand it
Between active force, beneficially macromole aligning to a certain extent.So PA intermolecular force is relatively strong, strand has
Having compliance, easily crystallize, have higher degree of crystallinity and high-melting-point, the methylene embedded between amide group is nonpolar hydrophobic
Group, it is provided that molecular flexibility, gives material excellent toughness.
In recent years, dynamo-electric and the plasthetics shell of automobile industry, such as electronic apparatus component enclosure, automotive rim cover,
Motor cases etc., more and more different field product needed high gloss could meet the demand of product, is also easy to meet and sprays paint
With the late stage process demand such as dyeing, the most also will more excellent mechanical property and life-time service stability, and these products pair
The most increasing in demand and the dependence of nylon material.
The nylon material used in the market is mainly the modified and mineral-filled modified material of PA6 or PA66 glass fibre filling
Material.PA6 due to the difference of glass fibre filling content, its material flowability can also have the biggest difference, although glass fibre filling material
Shrinkage factor is relatively low, but the technology controlling and process of forming temperature and processing is relatively difficult, and goods are difficult to saturated, and product appearance is coarse
Rough, easy floating fibre and lines.Elapsed time passage and long-time use, product in appearance it may happen that turn yellow existing
As, mineral-filled it is easily controlled processing and forming although single, preferably improves mobility and the surface superiority of material, but
Mechanical property includes that the toughness of material and intensity hardness aspect are the most poor, and shrinkage factor is the biggest, it is impossible to meet high finish surface product
Machinery and physical property requirements.
Summary of the invention
In order to overcome the deficiencies in the prior art, it is an object of the invention to provide a kind of high glaze nylon reinforcements, tool
Have that surface gloss is good, coloring is good, all can keep the advantages such as higher dimensional stability at different conditions；Can be in high/low temperature
Lower use steady in a long-term, and have stable mechanical property and chemical resistance.
Further object is that the preparation method that a kind of high glaze nylon reinforcements is provided, pass through the method
Obtain a kind of high glaze nylon reinforcements.
For solving the problems referred to above, the technical solution adopted in the present invention is as follows:
A kind of high glaze nylon reinforcements, it is to be prepared from by following raw material by weight percentage:
PA6 60-70%,
Glass microballoon 10-15%,
Coupling agent 0.2-1%,
Composite nucleating agent 0.5-1%,
Antioxidant 0.2-0.8%,
Flow ability modifying agent 0.5-1.5%,
Glass fibre 15-25%；
Wherein, the percetage by weight summation of above-mentioned raw materials is 100%.
In high glaze nylon reinforcements of the present invention, as further scheme, the viscosity of described PA6 is 2.3-
2.52dl/g。
In high glaze nylon reinforcements of the present invention, as further scheme, described flow ability modifying agent is silicon
In ketone powder, dendritic, PE wax, TAF powder, one or more are with any ratio mixing.
In high glaze nylon reinforcements of the present invention, as further scheme, described composite nucleating agent is selected from
In nano silicon, 30000 mesh superfine talcum powders, sodium benzoate, long-chain linear saturated carboxylic acid sodium salt two or three with
On with any than mixing.
In high glaze nylon reinforcements of the present invention, as further scheme, described glass fibre is alkali-free
Roving glass fiber, a diameter of 5-14 μm of alkali-free roving glass fiber.
In high glaze nylon reinforcements of the present invention, as further scheme, described coupling agent is that silane is even
Join agent, mix with any ratio for one or more in amino silicane coupling agent, epoxy silane coupling.
In high glaze nylon reinforcements of the present invention, as further scheme, described antioxidant is hindered phenol
Kind antioxidant and phosphoric acid ester antioxidant are that 1:1 is compounding according to weight ratio to be formed.
In high glaze nylon reinforcements of the present invention, as further scheme, described glass microballoon granularity is
10-250 micron, wall thickness 1-2 micron.
A kind of preparation method of high glaze nylon reinforcements, this preparation method comprises the following steps:
1) raw material disposal and mixing: dried by PA6 according to composition of raw materials amount, controls moisture below 0.04%；Then
Add with coupling agent in high speed mixer to stir and mix, obtain mixture；
2) in said mixture, it is sequentially added into glass microballoon, antioxidant, composite nucleating agent, flow ability modifying agent, continues to stir
Mix and make each component fully dispersed uniformly, obtain premix material；
3) melt extrude: above-mentioned premix material is added in double screw extruder and melt extrudes；
4) pelletize and post processing: obtain finished product after the material after extrusion is sequentially passed through cooling, air-dried, pelletizing, packaging.
The preparation method of high glaze nylon reinforcements of the present invention, as further scheme, step 3) in, molten
Melting extrusion temperature and be 250-280 DEG C, screw speed is 200-900r/min.
Compared to existing technology, the beneficial effects of the present invention is:
High glaze nylon reinforcements the most of the present invention has that surface gloss is good, coloring is good, in different condition
Lower all can keep the advantages such as higher dimensional stability；Can use steadily in the long term under high/low temperature, and have stable mechanical property
Energy and chemical resistance；
High glaze nylon reinforcements the most of the present invention with the addition of glass microballoon mineral material fill, make material stream
Dynamic property is more preferable, thus so that surface gloss is more preferable during injecting products product, goes floating fine effect obvious, makes surface smooth,
Effectively reduce cost simultaneously；
High glaze nylon reinforcements the most of the present invention, by adding composite nucleating agent, makes material internal crystal grain uniform
Distribution, crystallizes more perfect, better crystallinity degree, obtains more excellent mechanical property and dimensional stability during injecting products product；
High glaze nylon reinforcements the most of the present invention, by adding flow ability modifying agent, makes the interior lubricant effect of material
Significantly, obtain more preferable product surface effect, and during injecting products product, have more extensive and stable process adjustments scope；
High glaze nylon reinforcements the most of the present invention can be widely applied to make the horse used under various environment
Reach shell, automotive rim cover, electronic apparatus component enclosure etc..
Below in conjunction with detailed description of the invention, the present invention is described in further detail.
Detailed description of the invention
High glaze nylon reinforcements of the present invention, it is by following raw material preparation by weight percentage
Become:
PA6 60-70%,
Glass microballoon 10-15%,
Coupling agent 0.2-1%,
Composite nucleating agent 0.5-1%,
Antioxidant 0.2-0.8%,
Flow ability modifying agent 0.5-1.5%,
Glass fibre 15-25%；
Wherein, the percetage by weight summation of above-mentioned raw materials is 100%.
" PA6 " mentioned in the present invention refers to polyamide 6.Owing to the viscosity of PA6 is very sensitive for variations in temperature,
And the shrinkage factor of PA6 is had a certain impact by viscosity.Therefore, the nylon material moderate in order to obtain shrinkage factor, institute of the present invention
In the high glaze nylon reinforcements stated, as further scheme, the viscosity of described PA6 is 2.3-2.52dl/g.
In high glaze nylon reinforcements of the present invention, as further scheme, described flow ability modifying agent is silicon
In ketone powder, dendritic, PE wax, TAF powder, one or more are with any ratio mixing.Preferably, flow ability modifying agent is
Above two is with compounding.
High glaze nylon reinforcements of the present invention uses composite nucleating agent, PA material internal crystal grain can be made equal
Even distribution, crystallizes more perfect, better crystallinity degree, obtains more excellent mechanical property and dimensionally stable during injecting products product
Property.In high glaze nylon reinforcements of the present invention, it is preferred that described composite nucleating agent selected from nano silicon,
(product type that Clariant Corporation produces is for 30000 mesh superfine talcum powders, sodium benzoate, long-chain linear saturated carboxylic acid sodium salt
NAV101) more than two or three in is with any ratio mixing.Wherein, optimal, use at least one inorganic nucleator with extremely
Few a kind of organic nucleating agent is combined, such as, can be the composite nucleating agent or 30000 of nano silicon and sodium benzoate
Mesh superfine talcum powder and the composite nucleating agent of sodium benzoate.Should be the composite nucleating agent of inorganic nucleator and organic nucleating agent, two
Collaborative effect is had between person.Such as, in the composite nucleating agent of nano silicon and sodium benzoate, due to nanometer titanium dioxide
Silicon exist, sodium benzoate in PA6 matrix will not undue concentration, agglomeration reduce, make nucleation excessively to concentrate, be conducive to
Improve the mechanical property of PA6；And the existence of sodium benzoate, make again nano silicon rise while potentiation, PA6 can be
Faster crystallize in the presence of nucleator, it is thus achieved that ratio is individually added into the mechanical property that nano silicon is more excellent.
Owing to due to PA6 water absorption relatively greatly, dimensional stability is poor, and intensity is not as good as metallic aluminium, limits it at some
Application in structural material；The mechanical property of PA 6 depends primarily on chemical bond and the intermolecular force of its molecular backbone；Add
After adding certain filler, the water absorption rate of PA6 declines, and dimensional stability improves, and intensity is affected by filling intensity and affine degree and
Corresponding rising.Roving glass fiber is to be interleaved with each other lack of alignment together in the composite, and multiple unlike short glass fiber
Streamwise arrangement in condensation material；Compared with short glass fiber composite, the most this lack of alignment state and Length of Glass Fiber
Increase, make roving glass fiber composite material exhibits go out higher mechanical property, excellent thermostability, fatigue durability and wearability, and
Preferably fillibility, low warpage properties and isotropism etc.；Owing to long stapled fibrous termination is less, compare short glass fiber composite
Contributed in performance excellent.Therefore, in high glaze nylon reinforcements of the present invention, described glass fibre is
Alkali-free roving glass fiber, a diameter of 5-14 μm of alkali-free roving glass fiber.Along with the raising of glass fiber content, on the arbitrary cross section of PA composite
Glass increased number, when by impulsive force, the stress of material internal is disperseed, and the mean stress that every glass is subject to subtracts
Few, so more energy can be absorbed during fracture of composite materials so that impact strength becomes big.Meanwhile, along with glass fiber content
Increasing, the matrix between glass and glass is thinning, is more beneficial for the stress transmission at material internal, and meanwhile, the stress of glass is more
Add all so that the impact property of composite is improved.Can also learn that the bending property of PA6 resin is for glass simultaneously
Addition very sensitive.With pure PA6 resin-phase ratio, glass fibre reinforced composite material under external force, the arbitrary cross section of composite
On have substantial amounts of glass bear external force, and to make extraction or the fracture of these glasses, need to apply bigger load and go to overcome glass
Motive power between fibre and matrix material.Therefore, the addition of glass improves the hot strength of composite and bends strong
Degree.
In high glaze nylon reinforcements of the present invention, as further scheme, described coupling agent is that silane is even
Join agent, mix with any ratio for one or more in amino silicane coupling agent, epoxy silane coupling.
In high glaze nylon reinforcements of the present invention, as further scheme, described antioxidant is hindered phenol
Kind antioxidant and phosphoric acid ester antioxidant are that 1:1 is compounding according to weight ratio to be formed.
Glass microballoon (GB), as a kind of novel silicate material, is shaped as the spherical of rule, and draw ratio is fixed, simultaneously
Have light weight, low heat conduction, nontoxic, do not fire, chemical stability is good, high dispersive, sound insulation, high-low temperature resistant, electrical insulating property and thermally-stabilised
Property the advantage high glaze of the present invention nylon reinforcements such as good in.The research of the present invention finds: glass microballoon conduct
A kind of silicate fillers, surface, with the polar group such as hydroxyl etc. of certain content, has preferably with the PA6 matrix with polarity
Interface interaction, PA6 can be served enhancing simultaneously and increase firm effect；Therefore, add glass microballoon and can make material flowability
More preferably, thus so that surface gloss is more preferable during injecting products product, go floating fine effect obvious, make surface smooth.Preferably
, the glass microballoon granularity used in the present invention is 10-250 micron, wall thickness 1-2 micron.
A kind of preparation method of high glaze nylon reinforcements, this preparation method comprises the following steps:
1) raw material disposal and mixing: dried by PA6 according to composition of raw materials amount, controls moisture below 0.04%；Then
Add with coupling agent in high speed mixer to stir and mix, obtain mixture；
2) in said mixture, it is sequentially added into glass microballoon, antioxidant, composite nucleating agent, flow ability modifying agent, continues to stir
Mix and make each component fully dispersed uniformly, obtain premix material；
3) melt extrude: above-mentioned premix material is added in double screw extruder and melt extrudes；
4) pelletize and post processing: obtain finished product after the material after extrusion is sequentially passed through cooling, air-dried, pelletizing, packaging.
The research of the present invention finds, improves screw speed and increase the active force between glass and resin, it is easier to
Causing the fracture of glass, Length of Glass Fiber reduces accordingly, and mechanical property can decline accordingly.Therefore, in order to ensure the mechanics of PA material
Performance；In the preparation method of high glaze nylon reinforcements of the present invention, it is preferred that step 3) in, melt extrude temperature
For 250-280 DEG C, screw speed is 200-900r/min.
The following is some embodiments of the present invention, in the following embodiments, at raw material, reagent and the equipment used
Outside particular determination, all can be obtained by commercial channel.
Embodiment 1-embodiment 3
High glaze nylon reinforcements described in embodiment 1-embodiment 3, is prepared by the following method and forms:
1) raw material disposal and mixing: dried by PA6 according to composition of raw materials amount, controls moisture below 0.04%；Then
Add with coupling agent and high speed mixer stirs 1min, obtain mixture；
2) in said mixture, it is sequentially added into glass microballoon, antioxidant, composite nucleating agent, flow ability modifying agent, continues to stir
Mixing 2min makes each component fully dispersed uniformly, obtains premix material；
3) melt extrude: above-mentioned premix material is added in double screw extruder and melt extrudes；Wherein, extruder melt extrudes
In the range of temperature is set in 250-280 DEG C, vacuum is 0.08Pa, and main-machine screw rotating speed is 500r/min；
4) pelletize and post processing: obtain finished product after the material after extrusion is sequentially passed through cooling, air-dried, pelletizing, packaging.
In embodiment 1-embodiment 3, proportioning raw materials sees table 1.
Table 1: proportioning raw materials in embodiment 1-embodiment 3
Performance detects
High glaze nylon reinforcements obtained by embodiment 1-3 is carried out performance test event, the mark of test institute foundation
Accurate and test result sees table 2.
Table 2: the test result of embodiment 1-3
It can be seen that the high glaze nylon reinforcements not only surface gloss prepared of the present invention is good in the result of table 2, and
And cost performance is high, properties is excellent.Hot strength is high, bending modulus is maximum up to 5674MPa, bending strength most preferably up to
237MPa, Izod notched impact strength is good up to 14KJ/M2, mobile performance (melt index)) may be up to 36g/10min.
Above-mentioned embodiment is only the preferred embodiment of the present invention, it is impossible to limit the scope of protection of the invention with this,
The change of any unsubstantiality that those skilled in the art is done on the basis of the present invention and replacement belong to institute of the present invention
Claimed scope.
Claims (10)
1. a high glaze nylon reinforcements, it is characterised in that it is by following raw material preparation by weight percentage
Become:
PA6 60-70%,
Glass microballoon 10-15%,
Coupling agent 0.2-1%,
Composite nucleating agent 0.5-1%,
Antioxidant 0.2-0.8%,
Flow ability modifying agent 0.5-1.5%,
Glass fibre 15-25%；
Wherein, the percetage by weight summation of above-mentioned raw materials is 100%.
High glaze nylon reinforcements the most according to claim 1, it is characterised in that the viscosity of described PA6 is 2.3-
2.52dl/g。
High glaze nylon reinforcements the most according to claim 1, it is characterised in that described flow ability modifying agent is silicone
In powder, dendritic, PE wax, TAF powder, one or more are with any ratio mixing.
High glaze nylon reinforcements the most according to claim 1, it is characterised in that described composite nucleating agent is nanometer two
In silicon oxide, 30000 mesh superfine talcum powders, sodium benzoate, long-chain linear saturated carboxylic acid sodium salt more than two or three is to appoint
Meaning is than mixing.
High glaze nylon reinforcements the most according to claim 1, it is characterised in that described glass fibre is the long glass of alkali-free
Fibre, a diameter of 5-14 μm of alkali-free roving glass fiber.
High glaze nylon reinforcements the most according to claim 1, it is characterised in that described coupling agent is silane coupled
Agent, in amino silicane coupling agent, epoxy silane coupling one or more with any than mixing.
High glaze nylon reinforcements the most according to claim 1, it is characterised in that described antioxidant is that Hinered phenols resists
Oxygen agent and phosphoric acid ester antioxidant are that 1:1 is compounding according to weight ratio to be formed.
High glaze nylon reinforcements the most according to claim 1, it is characterised in that described glass microballoon granularity is 10-
250 microns, wall thickness 1-2 micron.
9. the preparation method of the high glaze nylon reinforcements as described in any one of claim 1-8, it is characterised in that should
Preparation method comprises the following steps:
1) raw material disposal and mixing: dried by PA6 according to composition of raw materials amount, controls moisture below 0.04%；Then with idol
Connection agent adds stirring mixing in high speed mixer, obtains mixture；
2) in said mixture, it is sequentially added into glass microballoon, antioxidant, composite nucleating agent, flow ability modifying agent, continues stirring and make
Each component is fully dispersed uniformly, obtains premix material；
3) melt extrude: above-mentioned premix material is added in double screw extruder and melt extrudes；
4) pelletize and post processing: obtain finished product after the material after extrusion is sequentially passed through cooling, air-dried, pelletizing, packaging.
Preparation method the most according to claim 9, it is characterised in that step 3) in, melt extruding temperature is 250-280
DEG C, screw speed is 200-900r/min.
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106810849A (en) * | 2017-02-20 | 2017-06-09 | 四川久远科技股份有限公司 | A kind of superelevation light nylon composite materials for motor intake manifold and preparation method thereof |
| CN106916445A (en) * | 2017-04-21 | 2017-07-04 | 金旸（厦门）新材料科技有限公司 | One kind exempts from spraying transparent glass fiber reinforced nylon resin material and preparation method thereof |
| CN109401287A (en) * | 2018-10-22 | 2019-03-01 | 滁州吉胜新材料科技有限公司 | A kind of smooth nylon of lightweight and preparation method thereof |
| CN109825077A (en) * | 2019-03-14 | 2019-05-31 | 金旸（厦门）新材料科技有限公司 | One kind is heat-resisting to be exempted to spray bloom nylon material and preparation method thereof |
| CN110305469A (en) * | 2019-05-27 | 2019-10-08 | 中广核俊尔(浙江)新材料有限公司 | A kind of polyamide compoiste material and its preparation method and application for gas assisted molding |
| WO2021058769A1 (en) * | 2019-09-27 | 2021-04-01 | Solvay Specialty Polymers Usa, Llc | Thermoplastic polymer composition |
| CN115926444A (en) * | 2022-11-26 | 2023-04-07 | 郑州倍耐防护材料有限公司 | Hollow glass microsphere continuous long fiber blending modified nylon-based composite material, and preparation method and application thereof |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106810849A (en) * | 2017-02-20 | 2017-06-09 | 四川久远科技股份有限公司 | A kind of superelevation light nylon composite materials for motor intake manifold and preparation method thereof |
| CN106916445A (en) * | 2017-04-21 | 2017-07-04 | 金旸（厦门）新材料科技有限公司 | One kind exempts from spraying transparent glass fiber reinforced nylon resin material and preparation method thereof |
| CN106916445B (en) * | 2017-04-21 | 2019-06-18 | 金旸（厦门）新材料科技有限公司 | One kind is exempted to spray transparent glass fiber reinforced nylon resin material and preparation method thereof |
| CN109401287A (en) * | 2018-10-22 | 2019-03-01 | 滁州吉胜新材料科技有限公司 | A kind of smooth nylon of lightweight and preparation method thereof |
| CN109825077A (en) * | 2019-03-14 | 2019-05-31 | 金旸（厦门）新材料科技有限公司 | One kind is heat-resisting to be exempted to spray bloom nylon material and preparation method thereof |
| CN110305469A (en) * | 2019-05-27 | 2019-10-08 | 中广核俊尔(浙江)新材料有限公司 | A kind of polyamide compoiste material and its preparation method and application for gas assisted molding |
| CN110305469B (en) * | 2019-05-27 | 2021-04-09 | 中广核俊尔(浙江)新材料有限公司 | Polyamide composite material for gas-assisted molding and preparation method and application thereof |
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| CN114430764A (en) * | 2019-09-27 | 2022-05-03 | 索尔维特殊聚合物美国有限责任公司 | Thermoplastic polymer composition |
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Application publication date: 20170104 |