CN1858116A - Glass microfiber and super micro nano particle reinforced tenacity increased nylon composite material and its preparing method - Google Patents
Glass microfiber and super micro nano particle reinforced tenacity increased nylon composite material and its preparing method Download PDFInfo
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Abstract
The present invention relates to glass microfiber and nanometer particle reinforced and toughened nylon composite material and its preparation process, and belongs to the field of nylon material modifying technology. The glass microfiber and nanometer particle reinforced and toughened nylon composite material is prepared with nylon 400-600 weight portions, glass microfiber 100-300 weight portions, nanometer particle 40-160 weight portions, toughening agent 5-25 weight portions and assistant 0.1-10 weight portions. The preparation process includes mixing the materials except glass microfiber, melting and extruding in a double screw extruder at temperature 210-285 deg.c while adding glass microfiber, cooling in water, pelletizing, and stoving. The modified nylon material has 3-12 raised strength and may be used in making water meter casing, water pipeline fitting, etc.
Description
Technical field
The invention belongs to the modification technology field of nylon composite materials, more particularly relate to a kind of glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material, and relate to the preparation method of above-mentioned materials.
Background technology
Because nylon has that wear resistance is good, tensile strength is high, anti-combustion, excellent comprehensive performance that electrical insulation properties is good, heat-resisting and mostly nontoxic, therefore purposes is comparatively extensive, but, when the amide monomer in the resin is too high, then should not contact with skin and food for a long time, and because of the strong occasion in special light requirement (heat) stability, dimensional stability and resistance to impact shock of water absorbability, pure nylon does not just satisfy requirement.Present terms of settlement is to make its modification by add an amount of additive in the nylon polymerization process or the course of processing, method or other similar approach modification by copolymerization are also arranged, use the oxidation-resistance, dimensional stability, minimizing molding shrinkage, the increase hardness that improve nylon products.External the appearance substitutes other engineering materials with the nylon material of modification, and constantly extends to new Application Areas.
Chinese patent literature for example Granted publication CN1175038C discloses that primitive fiber/ultramicro powder/polypropylene composite material, publication number CN1511872A disclose a kind of nylon particle toughened polypropylene composite and preparation method, Granted publication CN1068022C discloses a kind of high-toughness polypropylene composite material and preparation method thereof.But the enlightenment of the technology of above-mentioned all patent documentations can't be referred from glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon and obtain high strength, high tenacity, anti-oxidant, low temperature resistant, nylon composite materials that dimensional stability is good; Although Chinese patent literature for example the patent No. 02138152.6 disclose positive from the polymerization nylon nano composite material technical scheme and application number 03106526.0 discloses nylon 66/ Nanometer Composite Material Of Montmorillonite And Its Preparation Method and periodical has been reported " nylon 6/ nano-TiO of being write by people such as Li Ying, Yu Jian as " polymeric amide communication " 2005 the 5th phases the 21st volume
2And the technology of the modification of nylon 6/ nanometer Al2O3 in-situ composite enlightenment, yet the technology contents that above-mentioned document is instructed is and adopts a specific class (single) substance modification nylon, improve to obtain nylon characteristic in one aspect. therefore, do not see so far and adopt the above material of a class (a kind of) for example to adopt glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon to obtain to integrate the relevant report of the nylon composite materials of high strength, high-tenacity, anti-oxidant, low temperature resistant, chemical physics performance such as dimensional stability is good simultaneously.In addition, the applicant also entrusts State Intellectual Property Office patent information center to retrieve, and has not detected the similar techniques enlightenment equally.Yet make various components of machine, bearing, tubing, wrapping material or the like for adopting nylon, necessarily require nylon to possess chemistry, the physicals of above-mentioned excellence, especially for pipe element for example water meter case, water distributing pipe (industrial, civilian), if use nylon, so, tensile yield strength, flexural strength, shrinkage coefficient, these mechanical and physical performances of notched Izod impact strength to nylon all are very harsh.Therefore, in recent years, for the enhancing of nylon, the toughness reinforcing problem that has just become that industry is paid close attention to and expected to solve.
Summary of the invention
Task of the present invention be to provide a kind of have excellent tensile yield strength, flexural strength, notched Izod impact strength, little, the antioxidant property ideal glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material of shrinkage coefficient.
Task of the present invention also is to provide the preparation method of above-mentioned materials, and method technology is simple, can ensure the modification to nylon.
Task of the present invention is finished like this, a kind of glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material, it includes the raw material of following (in weight ratio): nylon 400-600 part, glass microfiber 100-300 part, super micro nano particle 40-160 part, toughner 5-25 part, auxiliary agent 0.1-10 part.
Nylon of the present invention is any one in nylon 6, nylon 66, the nylon 1010.
Glass microfiber of the present invention is an alkali free glass fibre.
The metric system number of alkali free glass fibre of the present invention is the 1000-2500 tex, and diameter is 10-16 μ m.
Super micro nano particle of the present invention is the mixture of any one or two kinds in the wollastonite, mica powder, talcum powder of mean particle size 0.5-10 μ m.
Super micro nano particle of the present invention is the mixture of any one or two kinds in the lime carbonate, wollastonite, silicon-dioxide, kaolin of mean particle size 50-400 μ m.
Toughner of the present invention is any one or two kinds in ethyl phthalate(DEP), dioctyl phthalate (DOP), dibutyl phthalate, diethyl phthalate, the Methyl Benzene-o-dicarboxylate.
Auxiliary agent of the present invention is a silane coupling agent, interfacial compatibilizer, oxidation inhibitor, the mixture of one or more in the lubricant, wherein silane coupling agent comprises Γ-aminopropyltriethoxywerene werene, Γ-propyl methacrylate base Trimethoxy silane, Γ-Racemic glycidol oxygen propyl trimethoxy silicane, the sulfonyl azide Trimethoxy silane, interfacial compatibilizer comprises MALEIC ANHYDRIDE, vinylformic acid, methacrylic acid and methylene-succinic acid, oxidation inhibitor comprises antioxidant 1010, oxidation inhibitor 168, antioxidant CA, carbon black, lubricant comprises polyethylene wax, paraffin, naphthenic oil, oleic acid and ester thereof, stearic acid and ester thereof.
The preparation method of glass primitive fiber provided by the invention and super micro nano particle reinforced tenacity increased nylon composite material, at first, raw material nylon 400-600 part, super micro nano particle 40-160 part, toughner 5-25 part, auxiliary agent 0.1-10 part of following weight part ratio are carried out pre-mixing, obtain Preblend; Then Preblend is delivered to twin screw extruder fusion coextrusion, 210-285 ℃ of screw rod melt temperature, screw speed 25-50 rev/min, and add glass microfiber 100-300 part in extrusion obtain the melt extrusion thing and enter in the water and cool off; After pelletizing, oven dry obtain finished product.
Screw rod melt temperature of the present invention is a district 210-230 ℃, two district 225-240 ℃, three district 240-250 ℃, four district 250-260 ℃, five district 260-275 ℃, six district 270-285 ℃, the particle diameter of described pelletizing is 3-5mm, and the oven temperature of described oven dry is that 105-115 ℃, drying time are 100-140 minute.
The tensile yield strength of nylon composite materials disclosed in this invention, flexural strength, notched Izod impact strength, shrinkage coefficient are respectively 73.6-170.7 (MPa), 65-216 (MPa), 160-584 (J/m), 0.3-1.2 (* 10
-4/ ℃), having improved 3-12 doubly than the modification index of pure nylon, can be suitable for fully making such as water meter case, water distribution tubing etc.; Step of preparation process is few, and it is effective to strengthen toughening modifying.
Embodiment
Embodiment 1:
At first, with the raw material nylon 6 of following weight part meter is that 600 parts, mean particle size are that 0.8 part of input homogenizer of 1.5 parts of 2 parts of 0.8 part of 12 parts of 8 parts of 45 parts of wollastonites, ethyl phthalate(DEP)s, phthalic ester dioctyl esters, Γ-aminopropyltriethoxywerene werene, antioxidant 1010s, methacrylic acids, whiteruss of 0.5-10 μ m carries out pre-temperature fully and closes, and obtains Preblend; Then Preblend is delivered in the barrel of twin screw extruder, by twin screw extruder fusion coextrusion, each section temperature to the head discharge port is controlled to be a district 210-230 ℃, two district 225-240 ℃, three district 240-250 ℃, four district 250-260 ℃, five district 250-275 ℃, six district 270-285 ℃ respectively from charging opening to twin screw extruder, screw speed is 30 rev/mins, in extrusion, add the metric system number and be 1000-2500 tex, diameter and be 110 parts of the non-alkali glass primitive fibers of 10-16 μ m, obtain the melt extrusion thing and enter in the water and cool off; Last dicing machine is cut into the granule of 3-5mm, through baking oven 105-115 ℃ of baking 120 minutes, obtains by the nylon composite materials with ideal physical and mechanical property shown in the table 1.
To be processed into water meter case by the resulting nylon composite materials of the foregoing description through the applicant, and send Changshu City, Jiangsu Province product quality supervision and testing institute to detect physical and mechanical property water meter case with the excellence shown in the table 2.In addition, the applicant also will be sent country to specify to detect unit Henan Province Zhengzhou City's quality technical supervision verification test center in December, 2005 and carry out the water test (test number is S0512201001) by the water meter case that nylon composite materials was processed into that the foregoing description obtained, and test-results is: bear 1.6 times of water meter nominal pressures and continue the 1.5min ne-leakage, bear 2.0 times of water meter nominal pressure time length 1min and do not have damage.
Embodiment 2:
Only raw material and corresponding weight part are changed into: nylon 6 is 420 parts, 105 parts of alkali free glass fibres, 63 parts of talcum powder, 6 parts of diethyl phthalates, Γ-0.5 part of propyl methacrylate base Trimethoxy silane, 0.5 part of antioxidant 1010,1 part in vinylformic acid, 0.5 part in paraffin, all the other are with embodiment 1, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 3:
Only raw material and corresponding weight part are changed into: nylon 6 is 480 parts, 200 parts of alkali free glass fibres, 82 parts of talcum powder, 10 parts of ethyl phthalate(DEP)s, Γ-1 part of propyl methacrylate base Trimethoxy silane, 168 0.5 parts in oxidation inhibitor, 0.5 part of antioxidant CA, 0.8 part of whiteruss, all the other are with embodiment 1, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 4:
Only raw material and corresponding weight part are changed into: nylon 66 is 550 parts, 160 parts of alkali free glass fibres, 135 parts of kaolin, 15 parts of dibutyl phthalates, Γ-2 parts of Racemic glycidol oxygen propyl trimethoxy silicanes, 168 1.05 parts in oxidation inhibitor, 3 parts of MALEIC ANHYDRIDE, 1.2 parts of oleic acid, all the other are with embodiment 1, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 5:
Only raw material and corresponding weight part are changed into: nylon 66 is 500 parts, 240 parts of alkali free glass fibres, 45 parts of the mica powders of median size 0.5-10 μ m, 50 parts of the silicon-dioxide of median size 50-400 μ m, 12 parts of Methyl Benzene-o-dicarboxylates, 12 parts of dioctyl phthalate (DOP)s, 2.5 parts of Γ-Racemic glycidol oxygen propyl trimethoxy silicane, 1 part of antioxidant 1010,0.8 part of carbon black, 4.8 parts of MALEIC ANHYDRIDE, 1 part of whiteruss, screw speed changes 40 rev/mins into, drying time changes 100 minutes into, all the other are with embodiment 1, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 6:
Only raw material and corresponding weight part are changed into: nylon 1010 is 530 parts, 270 parts of alkali free glass fibres, 100 parts of the wollastonites of median size 0.5-10 μ m, 55 parts of mica powders, 18 parts of dioctyl phthalate (DOP)s, 1.4 parts of Γ-aminopropyltriethoxywerene werene, 4 parts of MALEIC ANHYDRIDE, 1.3 parts of stearic acid, all the other are with embodiment 5, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 7:
Only raw material and corresponding weight part are changed into: nylon 66 is 550 parts, 180 parts of alkali free glass fibres, 70 parts of the silicon-dioxide of median size 50-400 μ m, 8 parts of diethyl phthalates, 0.2 part of Γ-aminopropyltriethoxywerene werene, 168 0.5 parts in oxidation inhibitor, 4 parts of methacrylic acids, 1.8 parts of oleic acid, all the other are with embodiment 5, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 8:
Only raw material and corresponding weight part are changed into: nylon 1010 is 550 parts, 120 parts of alkali free glass fibres, 120 parts of the wollastonites of median size 0.5-10 μ m, 10 parts of dimethyl phthalates, 12 parts of ethyl phthalate(DEP)s, 1.5 parts of Γ-Racemic glycidol oxygen propyl trimethoxy silicane, 3 parts of antioxidant 1010s, 1 part of whiteruss, screw speed changes 50 rev/mins into, drying time changes 135 minutes into, all the other are with embodiment 1, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 9:
Only raw material and corresponding weight part are changed into: nylon 6 is 600 parts, 294 parts of alkali free glass fibres, 57 parts of mica powders, 14 parts of dibutyl phthalates, Γ-1.5 parts of Racemic glycidol oxygen propyl trimethoxy silicanes, 2 parts of MALEIC ANHYDRIDE, 1.5 parts of whiterusss, all the other are with embodiment 8, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Embodiment 10:
Only raw material and corresponding weight part are changed into: nylon 66 is 600 parts, 224 parts of alkali free glass fibres, 70 parts of the mica powders of median size 0.5-10 μ m, 70 parts of the kaolin of median size 50-400 μ m, 24 parts of dioctyl phthalate (DOP)s, 2 parts of Γ-aminopropyltriethoxywerene werene, 1681 parts in oxidation inhibitor, 4 parts in vinylformic acid, 1 part of whiteruss, 0.6 part of oleic acid, all the other are with embodiment 8, obtain that this materials processing becomes the physical and mechanical property of the excellence of product institute tool with the usefulness shown in the table 2 by the nylon composite materials with ideal physicals shown in the table 1.
Table 1
Project | Tensile yield strength (MPa) | Flexural strength (MPa) | Notched Izod impact strength (J/M) | Shrinkage coefficient (* 10 -4℃) |
Embodiment 1 | 126.8 | 189.6 | 468.3 | 0.51 |
Embodiment 2 | 73.6 | 65.3 | 183.6 | 1.13 |
Embodiment 3 | 84.8 | 88.1 | 399.1 | 0.76 |
Embodiment 4 | 140.3 | 129.4 | 451.5 | 0.64 |
Embodiment 5 | 137.1 | 171.9 | 428.7 | 0.47 |
Embodiment 6 | 170.7 | 197.3 | 583.4 | 0.32 |
Embodiment 7 | 92.3 | 108.6 | 283.1 | 0.83 |
Embodiment 8 | 118.5 | 154.5 | 322.8 | 0.95 |
Embodiment 9 | 106.4 | 136.8 | 376.3 | 0.61 |
Embodiment 10 | 158.6 | 215.7 | 401.9 | 0.55 |
Table 2
Sequence number | Test item | Technical requirements | Detected result | The individual event evaluation | |
1 | Carrying capacity requires test | Cover and watchcase | Should bear 2MPa and continue the water pressure test of 1min, and do not reveal, seepage or damage. | No leakage, seepage and damage | Qualified |
Tube stub | Should bear 1.6MPa and continue the water pressure test of 1min, and do not reveal, seepage or damage. | No leakage, seepage and damage | Qualified | ||
2 | Heat aging property | Cover and watchcase | Through behind 80 ℃, the heat ageing test of 168h, should meet the requirement of carrying capacity requirement test. | No leakage, seepage and damage | Qualified |
Tube stub | The same | No leakage, seepage and damage | Qualified | ||
3 | Anti-anti-freezing property | Cover and watchcase | Behind the freezing test of-20 ℃ of processes, 24h, should meet the requirement of carrying capacity requirement test | No leakage, seepage and damage | Qualified |
Tube stub | The same | No leakage, seepage and damage | Qualified |
Claims (10)
1, a kind of glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material is characterized in that it includes the raw material of following (in weight ratio): nylon 400-600 part, glass microfiber 100-300 part, super micro nano particle 40-160 part, toughner 5-25 part, auxiliary agent 0.1-10 part.
2, glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 1 is characterized in that described nylon is any one in nylon 6, nylon 66, the nylon 1010.
3, glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 1 is characterized in that described glass microfiber is an alkali free glass fibre.
4, glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 2, the metric system number that it is characterized in that described alkali free glass fibre is the 1000-2500 tex, diameter is 10-16 μ m.
5, glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 1 is characterized in that described super micro nano particle is the mixture of any one or two kinds in the wollastonite, mica powder, talcum powder of mean particle size 0.5-10 μ m.
6, glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 1 is characterized in that described super micro nano particle is the mixture of any one or two kinds in the lime carbonate, wollastonite, silicon-dioxide, kaolin of mean particle size 50-400 μ m.
7, glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 1 is characterized in that described toughner is any one or two kinds in ethyl phthalate(DEP), dioctyl phthalate (DOP), dibutyl phthalate, diethyl phthalate, the Methyl Benzene-o-dicarboxylate.
8, glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 1, it is characterized in that described auxiliary agent is a silane coupling agent, interfacial compatibilizer, oxidation inhibitor, the mixture of one or more in the lubricant, wherein silane coupling agent comprises г-aminopropyltriethoxywerene werene, г-propyl methacrylate base Trimethoxy silane, г-Racemic glycidol oxygen propyl trimethoxy silicane, the sulfonyl azide Trimethoxy silane, interfacial compatibilizer comprises MALEIC ANHYDRIDE, vinylformic acid, methacrylic acid and methylene-succinic acid, oxidation inhibitor comprises antioxidant 1010, oxidation inhibitor 168, antioxidant CA, carbon black, lubricant comprises polyethylene wax, paraffin, naphthenic oil, oleic acid and ester thereof, stearic acid and ester thereof.
9, a kind of method for preparing glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material as claimed in claim 1, it is characterized in that: at first, raw material nylon 400-600 part, super micro nano particle 40-160 part, toughner 5-25 part, auxiliary agent 0.1-10 part of following weight part ratio are carried out pre-mixing, obtain Preblend; Then Preblend is delivered to twin screw extruder fusion coextrusion, 210-285 ℃ of screw rod melt temperature, screw speed 25-50 rev/min, and add glass microfiber 100-300 part in extrusion obtain the melt extrusion thing and enter in the water and cool off; After pelletizing, oven dry obtain finished product.
10, the preparation method of glass micro-fibers peacekeeping super micro nano particle reinforced tenacity increased nylon composite material according to claim 9, it is characterized in that described screw rod melt temperature is a district 210-230 ℃, two district 225-240 ℃, three district 240-250 ℃, four district 250-260 ℃, five district 260-275 ℃, six district 270-285 ℃, the particle diameter of described pelletizing is 3-5mm, and the oven temperature of described oven dry is that 105-115 ℃, drying time are 100-140 minute.
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