CN103834166A - Mineral reinforced high-performance PPA (Polyphthal Amide) material and preparation method thereof - Google Patents
Mineral reinforced high-performance PPA (Polyphthal Amide) material and preparation method thereof Download PDFInfo
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- CN103834166A CN103834166A CN201410113405.6A CN201410113405A CN103834166A CN 103834166 A CN103834166 A CN 103834166A CN 201410113405 A CN201410113405 A CN 201410113405A CN 103834166 A CN103834166 A CN 103834166A
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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- B29B9/00—Making granules
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- B29B9/14—Making granules characterised by structure or composition fibre-reinforced
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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
- B29B7/30—Mixing; Kneading continuous, with mechanical mixing or kneading devices
- B29B7/58—Component parts, details or accessories; Auxiliary operations
- B29B7/72—Measuring, controlling or regulating
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B29B7/00—Mixing; Kneading
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- B29B7/7461—Combinations of dissimilar mixers
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- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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- B29B7/00—Mixing; Kneading
- B29B7/80—Component parts, details or accessories; Auxiliary operations
- B29B7/88—Adding charges, i.e. additives
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- B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
- B29C48/395—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
- B29C48/40—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
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- C08J3/00—Processes of treating or compounding macromolecular substances
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- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
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- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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Abstract
The invention relates to the technical field of the high polymer materials, and in particular relates to a mineral reinforced high-performance PPA (Polyphthal Amide) material and a preparation method thereof. The mineral reinforced high-performance PPA material comprises the following raw materials in parts by weight: 35-60 parts of polyphthalamide, 10-20 parts of polyhexamethylene terephthalamide, 10-15 parts of a filling and strengthening agent, 5-8 parts of a main flame retardant, 1-5 parts of an auxiliary flame retardant, 0.3-0.5 part of an antioxidant, 0.4-0.7 part of a lubricant, 0.5-0.8 part of a nucleating agent and 0.6-0.9 part of a shrink resisting agent. The mineral reinforced high-performance PPA material has excellent mechanical strength; the tensile strength and the bending strength of the mineral reinforced high-performance PPA material are improved; the PPA modified material further has high impact resistance and processability; the product is stable in quality, and is particularly applicable to LED (Light Emitting Diode) support manufacture. The preparation method of the mineral reinforced high-performance PPA material is simple, easy to implement, low in production cost and beneficial to popularization and application.
Description
Technical field
The present invention relates to technical field of polymer materials, relate in particular to a kind of mineral and strengthen high-performance PPA material and preparation method thereof.
Background technology
Polyphtalamide (Polyphthalamide, PPA) is the semiaromatic polyamide composition taking terephthalic acid or phthalic acid as raw material.PPA is a kind of hemicrystalline thermoplasticity aromatic polyamide, is commonly called as aromatic series high-temperature nylon, and it is a kind of resistant to elevated temperatures material, and fusing point is between 310~325 DEG C.PPA has following fundamental characteristics: 1, as more solid in PA66 hard than fats polymeric amide; 2, lower to the susceptibility of moisture, thermal characteristics is better; 3, resistance to creep, fatigue and chemical resistance are outstanding; 4, the PPA resin of glass strengthening has very high heat-drawn wire (Heat Deflection Temperature, HDT) value, can tolerate the very shortterm effect of high-temperature; 5,, under home condition, PPA resin shows outstanding non-fusibility to aliphatic hydrocarbon, aromatic hydrocarbon, hydrochloric ether, ester, ketone, alcohol and most of aqueous solution conventionally.
Under humid tropical condition, the tensile strength of PPA is higher by 20% than nylon 6, higher than nylon 66; The modulus in flexure of PPA material is higher by 20% than nylon, and hardness is larger, can resist long tensile creep; And the ability of resistance to gasoline, grease resistance and the refrigerant of PPA is also strong than PA; PPA has superior environmental-protecting performance, can reach U.S. FDA level.The water-intake rate of PPA is more much lower than general enhancing PA6 or PA66, even soak in cold water several years, its tensile strength also can keep more than 80%.
Polymeric amide all absorbs certain moisture, causes that plastification and size change.For example PA66, it when relative humidity is 100%, can absorb 8~9% moisture at-5 DEG C, and this makes its second-order transition temperature (Tg) drop to-20 DEG C by 6.5 DEG C, and size increases by 2~3%.Poor because of its dimensional stability, processing is difficulty comparatively, has limited its use range.And higher, the ageing-resistant weak effect of the price of existing MODIFIED PP A material.
summary of the invention
The object of the invention is to for the deficiencies in the prior art, and provide a kind of and reduce production costs, strengthen the mineral of mechanical property to strengthen high-performance PPA material.
Another object of the present invention is to provide a kind of mineral to strengthen the preparation method of high-performance PPA material.
The present invention is achieved through the following technical solutions.
A kind of mineral strengthen high-performance PPA material, and it comprises the raw material of following weight part:
Polyphtalamide 35-60 part
Poly-hexamethylene terephthalamide 10-20 part
Fill toughener 10-15 part
Main flame retardant 5-8 part
Auxiliary fire retardant 1-5 part
Antioxidant 0.3-0.5 part
Lubricant 0.4-0.7 part
Nucleator 0.5-0.8 part
Shrinkproof aqua 0.6-0.9 part.
Preferably, it comprises the raw material of following weight part:
Polyphtalamide 35-40 part
Poly-hexamethylene terephthalamide 10-15 part
Fill toughener 10-15 part
Main flame retardant 5-8 part
Auxiliary fire retardant 3-5 part
Antioxidant 0.3-0.5 part
Lubricant 0.4-0.7 part
Nucleator 0.5-0.8 part
Shrinkproof aqua 0.6-0.9 part.
More preferably, it comprises the raw material of following weight part:
Polyphtalamide 55-60 part
Poly-hexamethylene terephthalamide 15-20 part
Fill toughener 10-15 part
Main flame retardant 5-8 part
Auxiliary fire retardant 1-3 part
Antioxidant 0.3-0.5 part
Lubricant 0.4-0.7 part
Nucleator 0.5-0.8 part
Shrinkproof aqua 0.6-0.9 part.
Wherein, described filling toughener is long glass fiber; Described main flame retardant is antimonous oxide; Described auxiliary fire retardant is inorganic combustion inhibitor aluminium hydroxide or magnesium hydroxide; Described antioxidant is antioxidant 1098; Described lubricant oxidation polyethylene wax; Described nucleator is the special nucleator P22 of nylon; Described shrinkproof aqua is the shrinkproof aqua of polymeric amide.Inorganic combustion inhibitor aluminium hydroxide or magnesium hydroxide its there is weighting agent, fire retardant, the inhibitor triple functions of being fuming.
The shrinkproof aqua of polymeric amide is made by nano-scale fiber, effectively improve the crystallization of polymeric amide, promote the mechanical property of material, thermal characteristics and processing characteristics, it has following characteristics: 1, high-crystallinity makes the mechanical property of material, thermal characteristics is increased dramatically, 2, significantly promote the resist displacement ability of stablizing, the anti-warpage performance of dimensional stabilizing is outstanding, improve product size stability, 3, the crystallization rate being exceedingly fast, product approval stability is improved, shorten shaping cycle, enhance productivity, demolding performace excellence (formed product time shorten 30%-50%), 4, reduce goods post shrinkage, prevent goods stress cracking, promote and improve product surface glossiness, 5, pass through food, pharmaceutical grade certification, meet compared with high-environmental requirement, 6, excellent surface treatment, surface can efficiently, impel nano material to be dispersed in material, do not reunite, overcoming material easily reunites, disperse an inhomogeneous difficult problem, discharge nano effect completely.The shrinkproof aqua of polymeric amide of the optional model GSC-3239 with Dongguan City GaoSun Chemical Co., Ltd. of the shrinkproof aqua of polymeric amide.
Further, it also comprises the UV light absorber UV-234 of 0.1-0.3 weight part.UV light absorber UV-234 is a kind of efficient protective agent, can absorb UV-light, has that look shallow is, nontoxic, consistency is good, transport property is little, be easy to the features such as processing.It has maximum provide protection to polymkeric substance, and contributes to reduce look change, delays and the blocker rationality loss of energy simultaneously.Act synergistically with oxidation inhibitor 1098, can significantly promote ageing-resistant performance of the present invention, extend product work-ing life.
Further, it also comprises the nano hydrotalcite of 1-5 weight part.Described nano hydrotalcite is interlayer anion, is specially the hydrotalcite of one of borate ion, phosphate anion and 3-hydroxy phenyl phosphoroso-propionate ion; The particle diameter of described nano hydrotalcite is 200-500nm, and nano hydrotalcite can improve the flame retardant properties of PPA material.
Mineral strengthen a preparation method for high-performance PPA material, and it comprises following preparation process:
A, take raw material by weight, and described raw material is carried out respectively to drying treatment; 120 DEG C-140 DEG C of polyphtalamide drying treatment temperature, drying treatment time 2.5-3.5h, 100 DEG C-110 DEG C of poly-hexamethylene terephthalamide drying treatment temperature, drying treatment time 3.5-4.5h;
B, dried polyphtalamide and poly-hexamethylene terephthalamide are added in high-speed mixer, and add except main flame retardant and auxiliary fire retardant, fill the surplus stock of toughener, carry out high-speed mixing 6-10min;
C, main flame retardant and auxiliary fire retardant are put into and in high-speed mixer, mixed 5-12min and obtain mixing fire retardant, mixing fire retardant is joined in the material mixing in B step and fully mixes 10-15min, the material mixing is put into 100-110 DEG C of dry 2-3h in loft drier;
D, will fully mix and dry raw material is put in twin screw extruder, add and fill toughener and strengthens and fill extruding pelletization, make mineral enhancing high-performance PPA material.
Wherein, in described step D, each section of Temperature Setting of twin screw extruder is: 270~290 DEG C of district's temperature, two 280~295 DEG C of district's temperature, three 280~295 DEG C of district's temperature, four 280~295 DEG C of district's temperature, five 280~295 DEG C of district's temperature, six 280~295 DEG C of district's temperature, seven 280~295 DEG C of district's temperature, eight 280~295 DEG C of district's temperature, head temperature is 295~300 DEG C.
Wherein, in described step D, well-mixed raw material residence time in described twin screw extruder is 1~2 minute, and the internal pressure of twin screw extruder is 12~18MPa.
Beneficial effect of the present invention: the present invention introduces poly-hexamethylene terephthalamide, poly-hexamethylene terephthalamide can merge with polyphtalamide material well, thereby increases its mobility, and the course of processing is simplified; Add auxiliary agent by choose reasonable, obtain the PPA material of excellent combination property, not only intensity is high for it, heat-resisting good, difficult combustion, there is preferably physical strength, tensile strength, flexural strength are improved, and also have stronger shock resistance and processing characteristics, constant product quality, the price of PPA material prepared by the present invention is 20,000 yuan/ton of left and right, reduce more than 67% than ten thousand yuan/ton of the 6-8 of existing PPA material, greatly reduce production costs, cost performance is high, be convenient to promote and recycle, be particularly useful for the application in LED support is manufactured.
A kind of mineral of the present invention strengthen the preparation method of high-performance PPA material, and preparation method is simple, are easy to processing, and production cost is low, is conducive to generally apply.
Embodiment
Below in conjunction with embodiment, the present invention is further illustrated.
embodiment 1.
A kind of mineral strengthen high-performance PPA material, and it comprises the raw material of following weight part: 35 parts of polyphtalamides, 20 parts of poly-hexamethylene terephthalamides, fill 0.6 part of 10 parts of toughener long glass fiber, 8 parts of main flame retardant antimonous oxides, 1 part, auxiliary fire retardant aluminium hydroxide, 10980.5 parts of antioxidants, 0.4 part of lubricant oxidation polyethylene wax, nucleator P220.8 part, the shrinkproof aqua of polymeric amide.Mineral strengthen a preparation method for high-performance PPA material, and it comprises following preparation process:
A, take raw material by weight, and described raw material is carried out respectively to drying treatment; 120 DEG C of polyphtalamide drying treatment temperature, drying treatment time 3.5h, 100 DEG C of poly-hexamethylene terephthalamide drying treatment temperature, drying treatment time 4.5h;
B, dried polyphtalamide and poly-hexamethylene terephthalamide are added in high-speed mixer, and add except main flame retardant and auxiliary fire retardant, fill the surplus stock of toughener, carry out high-speed mixing 6min;
C, main flame retardant and auxiliary fire retardant are put into and in high-speed mixer, mixed 12min and obtain mixing fire retardant, mixing fire retardant is joined in the material mixing in B step and fully mixes 10min, the material mixing is put into 100 DEG C of dry 3h in loft drier;
D, will fully mix and dry raw material is put in twin screw extruder, add and fill toughener and strengthens and fill extruding pelletization, make mineral enhancing high-performance PPA material.
Wherein, in described step D, each section of Temperature Setting of twin screw extruder is: 270 DEG C of district's temperature, two 280 DEG C of district's temperature, three 280 DEG C of district's temperature, four 280 DEG C of district's temperature, five 280 DEG C of district's temperature, six 280 DEG C of district's temperature, seven 280 DEG C of district's temperature, eight 280 DEG C of district's temperature, head temperature is 297 DEG C.
Wherein, in described step D, well-mixed raw material residence time in described twin screw extruder is 1 minute, and the internal pressure of twin screw extruder is 12MPa.
embodiment 2.
A kind of mineral strengthen high-performance PPA material, and it comprises the raw material of following weight part: 40 parts of polyphtalamides, 10 parts of poly-hexamethylene terephthalamides, fill 15 parts of toughener long glass fibers, 5 parts of main flame retardant antimonous oxides, 5 parts of auxiliary fire retardant magnesium hydroxides, 0.3 part of antioxidant, 0.7 part of lubricant oxidation polyethylene wax, 0.5 part of the special nucleator P22 of nylon, 0.9 part, the shrinkproof aqua of polymeric amide.
Mineral strengthen a preparation method for high-performance PPA material, and it comprises following preparation process:
A, take raw material by weight, and described raw material is carried out respectively to drying treatment; 125 DEG C of polyphtalamide drying treatment temperature, drying treatment time 3h, 10 DEG C of poly-hexamethylene terephthalamide drying treatment temperature, drying treatment time 4h;
B, dried polyphtalamide and poly-hexamethylene terephthalamide are added in high-speed mixer, and add except main flame retardant and auxiliary fire retardant, fill the surplus stock of toughener, carry out high-speed mixing 7min;
C, main flame retardant and auxiliary fire retardant are put into and in high-speed mixer, mixed 12min and obtain mixing fire retardant, mixing fire retardant is joined in the material mixing in B step and fully mixes 10min, the material mixing is put into 105 DEG C of dry 2.5h in loft drier;
D, will fully mix and dry raw material is put in twin screw extruder, add and fill toughener and strengthens and fill extruding pelletization, make mineral enhancing high-performance PPA material.
Wherein, in described step D, each section of Temperature Setting of twin screw extruder is: 275 DEG C of district's temperature, two 285 DEG C of district's temperature, three 285 DEG C of district's temperature, four 285 DEG C of district's temperature, five 285 DEG C of district's temperature, six 285 DEG C of district's temperature, seven 285 DEG C of district's temperature, eight 285 DEG C of district's temperature, head temperature is 298 DEG C.
Wherein, in described step D, well-mixed raw material residence time in described twin screw extruder is 1.5 minutes, and the internal pressure of twin screw extruder is 14MPa.
embodiment 3.
A kind of mineral strengthen high-performance PPA material, and it comprises the raw material of following weight part: 50 parts of polyphtalamides, 12 parts of poly-hexamethylene terephthalamides, fill 13 parts of toughener long glass fibers, 6 parts of main flame retardant antimonous oxides, 3 parts of auxiliary fire retardant magnesium hydroxides, 1,098 0.4 parts of antioxidants, 0.5 part of lubricant oxidation polyethylene wax, 0.7 part of nucleator, 0.7 part, the shrinkproof aqua of polymeric amide, UV light absorber UV-2340.2 part.Mineral strengthen a preparation method for high-performance PPA material, and it comprises following preparation process:
A, take raw material by weight, and described raw material is carried out respectively to drying treatment; 130 DEG C of polyphtalamide drying treatment temperature, drying treatment time 2.5h, 110 DEG C of poly-hexamethylene terephthalamide drying treatment temperature, drying treatment time 4h;
B, dried polyphtalamide and poly-hexamethylene terephthalamide are added in high-speed mixer, and add except main flame retardant and auxiliary fire retardant, fill the surplus stock of toughener, carry out high-speed mixing 8min;
C, main flame retardant and auxiliary fire retardant are put into and in high-speed mixer, mixed 9min and obtain mixing fire retardant, mixing fire retardant is joined in the material mixing in B step and fully mixes 12min, the material mixing is put into 110 DEG C of dry 2h in loft drier;
D, will fully mix and dry raw material is put in twin screw extruder, add and fill toughener and strengthens and fill extruding pelletization, make mineral enhancing high-performance PPA material.
Wherein, in described step D, each section of Temperature Setting of twin screw extruder is: 280 DEG C of district's temperature, two 290 DEG C of district's temperature, three 290 DEG C of district's temperature, four 290 DEG C of district's temperature, five 290 DEG C of district's temperature, six 290 DEG C of district's temperature, seven 290 DEG C of district's temperature, eight 290 DEG C of district's temperature, head temperature is 295 DEG C.
Wherein, in described step D, well-mixed raw material residence time in described twin screw extruder is 2 minutes, and the internal pressure of twin screw extruder is 15MPa.
embodiment 4.
A kind of mineral strengthen high-performance PPA material, and it comprises the raw material of following weight part: 55 parts of polyphtalamides, 18 parts of poly-hexamethylene terephthalamides, fill 12 parts of toughener long glass fibers, 7 parts of main flame retardant antimonous oxides, 2 parts, auxiliary fire retardant aluminium hydroxide, 1,098 0.3 parts of antioxidants, 0.6 part of lubricant oxidation polyethylene wax, the special nucleator P220.6 of nylon part, 0.8 part, the shrinkproof aqua of polymeric amide, 3 parts of nano hydrotalcites; Described nanomete talc powder particle diameter is 300nm.Mineral strengthen a preparation method for high-performance PPA material, and it comprises following preparation process:
A, take raw material by weight, and described raw material is carried out respectively to drying treatment; 135 DEG C of polyphtalamide drying treatment temperature, drying treatment time 3h, 105 DEG C of poly-hexamethylene terephthalamide drying treatment temperature, drying treatment time 4h;
B, dried polyphtalamide and poly-hexamethylene terephthalamide are added in high-speed mixer, and add except main flame retardant and auxiliary fire retardant, fill the surplus stock of toughener, carry out high-speed mixing 7min;
C, main flame retardant and auxiliary fire retardant are put into and in high-speed mixer, mixed 8min and obtain mixing fire retardant, mixing fire retardant is joined in the material mixing in B step and fully mixes 13min, the material mixing is put into 105 DEG C of dry 2.5h in loft drier;
D, will fully mix and dry raw material is put in twin screw extruder, add and fill toughener and strengthens and fill extruding pelletization, make mineral enhancing high-performance PPA material.
Wherein, in described step D, each section of Temperature Setting of twin screw extruder is: 285 DEG C of district's temperature, two 290 DEG C of district's temperature, three 290 DEG C of district's temperature, four 290 DEG C of district's temperature, five 290 DEG C of district's temperature, six 290 DEG C of district's temperature, seven 290 DEG C of district's temperature, eight 290 DEG C of district's temperature, head temperature is 295 DEG C.
Wherein, in described step D, well-mixed raw material residence time in described twin screw extruder is 2 minutes, and the internal pressure of twin screw extruder is 12MPa.
embodiment 5.
A kind of mineral strengthen high-performance PPA material, and it comprises the raw material of following weight part: 60 parts of polyphtalamides, 17 parts of poly-hexamethylene terephthalamides, fill 14 parts of toughener long glass fibers, 8 parts of main flame retardant antimonous oxides, 1 part, auxiliary fire retardant aluminium hydroxide, 1,098 0.5 parts of antioxidants, 0.5 part of lubricant oxidation polyethylene wax, the special nucleator P220.8 of nylon part, 0.9 part, the shrinkproof aqua of polymeric amide, 5 parts of nano hydrotalcites; Described nanomete talc powder particle diameter is 500nm.Mineral strengthen a preparation method for high-performance PPA material, and it comprises following preparation process:
A, take raw material by weight, and described raw material is carried out respectively to drying treatment; 140 DEG C of polyphtalamide drying treatment temperature, drying treatment time 2.5h, 110 DEG C of poly-hexamethylene terephthalamide drying treatment temperature, drying treatment time 3.5h;
B, dried polyphtalamide and poly-hexamethylene terephthalamide are added in high-speed mixer, and add except main flame retardant and auxiliary fire retardant, fill the surplus stock of toughener, carry out high-speed mixing 7min;
C, main flame retardant and auxiliary fire retardant are put into and in high-speed mixer, mixed 8min and obtain mixing fire retardant, mixing fire retardant is joined in the material mixing in B step and fully mixes 15min, the material mixing is put into 100 DEG C of dry 2.5h in loft drier;
D, will fully mix and dry raw material is put in twin screw extruder, add and fill toughener and strengthens and fill extruding pelletization, make mineral enhancing high-performance PPA material.
Wherein, in described step D, each section of Temperature Setting of twin screw extruder is: 290 DEG C of district's temperature, two 295 DEG C of district's temperature, three 295 DEG C of district's temperature, four 295 DEG C of district's temperature, five 295 DEG C of district's temperature, six 295 DEG C of district's temperature, seven 295 DEG C of district's temperature, eight 295 DEG C of district's temperature, head temperature is 300 DEG C.
Wherein, in described step D, well-mixed raw material residence time in described twin screw extruder is 1.5 minutes, and the internal pressure of twin screw extruder is 18MPa.
Mineral prepared by embodiment 1 ~ embodiment 5 strengthen high-performance PPA material to be tested, in table 1.
Table 1.
。
By table 1, can find out excellent combination property of the present invention, not only intensity is high for it, heat-resisting good, has preferably physical strength, and tensile strength, flexural strength are improved, and also have stronger shock resistance and processing characteristics, constant product quality.
Finally should be noted that; above embodiment is only in order to illustrate technical scheme of the present invention; but not limiting the scope of the invention; although the present invention has been done to explain with reference to preferred embodiment; those of ordinary skill in the art is to be understood that; can modify or be equal to replacement technical scheme of the present invention, and not depart from essence and the scope of technical solution of the present invention.
Claims (9)
1. mineral strengthen a high-performance PPA material, it is characterized in that: it comprises the raw material of following weight part:
Polyphtalamide 35-60 part
Poly-hexamethylene terephthalamide 10-20 part
Fill toughener 10-15 part
Main flame retardant 5-8 part
Auxiliary fire retardant 1-5 part
Antioxidant 0.3-0.5 part
Lubricant 0.4-0.7 part
Nucleator 0.5-0.8 part
Shrinkproof aqua 0.6-0.9 part.
2. a kind of mineral according to claim 1 strengthen high-performance PPA material, it is characterized in that: it comprises the raw material of following weight part:
Polyphtalamide 35-40 part
Poly-hexamethylene terephthalamide 10-15 part
Fill toughener 10-15 part
Main flame retardant 5-8 part
Auxiliary fire retardant 3-5 part
Antioxidant 0.3-0.5 part
Lubricant 0.4-0.7 part
Nucleator 0.5-0.8 part
Shrinkproof aqua 0.6-0.9 part.
3. a kind of mineral according to claim 1 strengthen high-performance PPA material, it is characterized in that: it comprises the raw material of following weight part:
Polyphtalamide 55-60 part
Poly-hexamethylene terephthalamide 15-20 part
Fill toughener 10-15 part
Main flame retardant 5-8 part
Auxiliary fire retardant 1-3 part
Antioxidant 0.3-0.5 part
Lubricant 0.4-0.7 part
Nucleator 0.5-0.8 part
Shrinkproof aqua 0.6-0.9 part.
4. strengthen high-performance PPA material according to a kind of mineral described in claim 1 ~ 3 any one, it is characterized in that: described filling toughener is long glass fiber; Described main flame retardant is antimonous oxide; Described auxiliary fire retardant is inorganic combustion inhibitor aluminium hydroxide or magnesium hydroxide; Described antioxidant is antioxidant 1098; Described lubricant is oxidized polyethlene wax; Described nucleator is the special nucleator P22 of nylon; Described shrinkproof aqua is the shrinkproof aqua of polymeric amide.
5. a kind of mineral according to claim 1 strengthen high-performance PPA material, it is characterized in that: it also comprises the UV light absorber UV-234 of 0.1-0.3 weight part.
6. a kind of mineral according to claim 1 strengthen high-performance PPA material, it is characterized in that: it also comprises the nano hydrotalcite of 1-5 weight part.
7. a kind of mineral described in claim 1-6 any one strengthen the preparation method of high-performance PPA material, it is characterized in that: it comprises following preparation process:
A, take raw material by weight, and described raw material is carried out respectively to drying treatment; 120 DEG C-140 DEG C of polyphtalamide drying treatment temperature, drying treatment time 2.5-3.5h, 100 DEG C-110 DEG C of poly-hexamethylene terephthalamide drying treatment temperature, drying treatment time 3.5-4.5h;
B, dried polyphtalamide and poly-hexamethylene terephthalamide are added in high-speed mixer, and add except main flame retardant and auxiliary fire retardant, fill the raw material toughener, carry out high-speed mixing 6-10min;
C, main flame retardant and auxiliary fire retardant are put into and in high-speed mixer, mixed 5-12min and obtain mixing fire retardant, mixing fire retardant is joined in the material mixing in B step and fully mixes 10-15min, the material mixing is put into 100-110 DEG C of dry 2-3h in loft drier;
D, will fully mix and dry raw material is put in twin screw extruder, add and fill toughener and strengthens and fill extruding pelletization, make mineral enhancing high-performance PPA material.
8. a kind of mineral according to claim 7 strengthen the preparation method of high-performance PPA material, it is characterized in that: in described step D, each section of Temperature Setting of twin screw extruder is: 270~290 DEG C of district's temperature, two 280~295 DEG C of district's temperature, three 280~295 DEG C of district's temperature, four 280~295 DEG C of district's temperature, five 280~295 DEG C of district's temperature, six 280~295 DEG C of district's temperature, seven 280~295 DEG C of district's temperature, eight 280~295 DEG C of district's temperature, head temperature is 295~300 DEG C.
9. a kind of mineral according to claim 7 strengthen the preparation method of high-performance PPA material, it is characterized in that: in described step D, fully mixing dry raw material residence time in described twin screw extruder are 1~2 minute, and twin screw extruder internal pressure is 12~18MPa.
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020006998A1 (en) * | 2000-06-12 | 2002-01-17 | Haruhiko Furukawa | Thermoplastic elastomer composition, method of preparation, and molded products thereof |
CN101817978A (en) * | 2010-04-21 | 2010-09-01 | 深圳市科聚新材料有限公司 | High temperature nylon PPA reinforcing material and preparation method thereof |
CN101885914A (en) * | 2010-07-13 | 2010-11-17 | 东莞市意普万工程塑料有限公司 | Composite material special for automobile engine oil pan and preparation method thereof |
CN102634189A (en) * | 2011-02-15 | 2012-08-15 | 汉达精密电子(昆山)有限公司 | PPA (polyphthalamide) reinforced material and preparation method thereof |
WO2013091737A1 (en) * | 2011-12-23 | 2013-06-27 | Ems-Patent Ag | Polyamide moulding compound, use thereof and moulded parts produced therefrom |
-
2014
- 2014-03-25 CN CN201410113405.6A patent/CN103834166B/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020006998A1 (en) * | 2000-06-12 | 2002-01-17 | Haruhiko Furukawa | Thermoplastic elastomer composition, method of preparation, and molded products thereof |
CN101817978A (en) * | 2010-04-21 | 2010-09-01 | 深圳市科聚新材料有限公司 | High temperature nylon PPA reinforcing material and preparation method thereof |
CN101885914A (en) * | 2010-07-13 | 2010-11-17 | 东莞市意普万工程塑料有限公司 | Composite material special for automobile engine oil pan and preparation method thereof |
CN102634189A (en) * | 2011-02-15 | 2012-08-15 | 汉达精密电子(昆山)有限公司 | PPA (polyphthalamide) reinforced material and preparation method thereof |
WO2013091737A1 (en) * | 2011-12-23 | 2013-06-27 | Ems-Patent Ag | Polyamide moulding compound, use thereof and moulded parts produced therefrom |
Non-Patent Citations (1)
Title |
---|
沈开猷: "《不饱和聚酯树脂及其应用》", 28 February 2002, 化学工业出版社 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113652084A (en) * | 2021-08-16 | 2021-11-16 | 创合新材料科技江苏有限公司 | Corrosion-resistant plastic PA and preparation method thereof |
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