CN104987708A - Fiber-reinforced nylon composite material and preparation method therefor - Google Patents

Fiber-reinforced nylon composite material and preparation method therefor Download PDF

Info

Publication number
CN104987708A
CN104987708A CN201510479584.XA CN201510479584A CN104987708A CN 104987708 A CN104987708 A CN 104987708A CN 201510479584 A CN201510479584 A CN 201510479584A CN 104987708 A CN104987708 A CN 104987708A
Authority
CN
China
Prior art keywords
composite material
weight part
reinforced nylon
nylon composite
fiber reinforced
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201510479584.XA
Other languages
Chinese (zh)
Inventor
李明华
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jin Baoli Technology (suzhou) Co Ltd
Original Assignee
Jin Baoli Technology (suzhou) Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jin Baoli Technology (suzhou) Co Ltd filed Critical Jin Baoli Technology (suzhou) Co Ltd
Priority to CN201510479584.XA priority Critical patent/CN104987708A/en
Publication of CN104987708A publication Critical patent/CN104987708A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

Abstract

The present invention discloses a fiber-reinforced nylon composite material and a preparation method therefor. The fiber-reinforced nylon composite material is prepared by using the following components in parts by weight: 80-90 parts of nylon, 25-30 parts of glass fibers, 18-20 parts of polyvinyl butyral, 8-12 parts of polyethylene glycol, 8-11 parts of calcium chloride, 8 11 parts of diglycidyl ether, 6-8 parts of maleic anhydride grafted polypropylene, 5-9 parts of zinc stearate, 3-7 parts of trimethylol propane triacrylate and 1-2 parts of mirabilite. The present invention also provides a preparation method for the fiber-reinforced nylon composite material.

Description

A kind of fiber reinforced nylon composite material and preparation method thereof
Technical field
The invention belongs to field of compound material, particularly a kind of fiber reinforced nylon composite material and preparation method thereof.
Background technology
Tynex is commonly called as nylon, and be called for short PA, a class is the PA 66 obtained by diamines and diacid polycondensation, is another kind ofly obtained by hexanolactam polycondensation or ring-opening polymerization.The rigidity of nylon is higher, and thermotolerance is better, and frictional coefficient is low, good springiness, and resistance to fatigue is good, and wear resistance is good, good corrosion resistance, but water absorbability is large, and dimensional stability is inadequate.
Booster stage nylon is mainly used in the fields such as automobile, mechanical industry, electronic apparatus, precision instrument, is generally used for manufacturing nut, bolt, screw, nozzle, production chain, travelling belt, flabellum, gear, impeller and scaffolding and fixes climbers etc.
Summary of the invention
For above-mentioned demand, invention especially provides a kind of fiber reinforced nylon composite material and preparation method thereof.
Object of the present invention can be achieved through the following technical solutions:
A kind of fiber reinforced nylon composite material, be made up of the component comprising following weight part:
Nylon 8 0-90 part,
Glass fibre 25-30 part,
Polyvinyl butyral acetal 18-20 part,
Polyoxyethylene glycol 8-12 part,
Calcium chloride 8-11 part,
Diglycidylether 8-11 part,
Maleic anhydride inoculated polypropylene 6-8 part,
Zinic stearas 5-9 part,
Viscoat 295 3-7 part,
Saltcake 1-2 part.
Described glass fibre is alkali free glass fibre.
The diameter of described alkali free glass fibre is 12-18 micron.
Described component also comprises urea 0-2 weight part.
A preparation method for fiber reinforced nylon composite material, the method comprises the following steps:
(1) take nylon 8 0-90 weight part, glass fibre 25-30 weight part, polyvinyl butyral acetal 18-20 weight part, polyoxyethylene glycol 8-12 weight part, diglycidylether 8-11 weight part, maleic anhydride inoculated polypropylene 6-8 weight part, Zinic stearas 5-9 weight part, Viscoat 295 3-7 weight part and saltcake 1-2 weight part, mix;
(2) said components is added in high pressure homogenizer mix, regulate pH to 7.8-8.6, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 8-11 weight part and urea 0-2 weight part is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The mixing temperature of described high pressure homogenizer is 65-75 DEG C, and pressure is 20-23Mpa.
The each zone temperatures of described twin screw extruder is: a district temperature 180-200 DEG C, two district temperature 210-220 DEG C, three district temperature 220-230 DEG C, four district temperature 230-240 DEG C.
compared with prior art, its beneficial effect is in the present invention:
(1) fiber reinforced nylon composite material that the present invention obtains take nylon as main raw material.By adding glass fibre, polyvinyl butyral acetal, polyoxyethylene glycol, calcium chloride, diglycidylether, maleic anhydride inoculated polypropylene, Zinic stearas, Viscoat 295 and saltcake, the fiber reinforced nylon composite material obtained is made to have good mechanical strength, and there is good weather resistance and break resistance, there will not be metachromatism.
(2) fiber reinforced nylon composite material that obtains of the present invention, has good mechanical property.
(3) fiber reinforced nylon composite material of the present invention, its preparation method is simple, is easy to suitability for industrialized production.
Embodiment
Below in conjunction with embodiment, the present invention is further illustrated.
Embodiment 1
(1) take nylon 8 0kg, diameter be 12 microns alkali free glass fibre 25kg, polyvinyl butyral acetal 18kg, polyoxyethylene glycol 8kg, diglycidylether 8kg, maleic anhydride inoculated polypropylene 6kg, Zinic stearas 5kg, Viscoat 295 3kg and saltcake 1kg, mix;
(2) said components to be added in high pressure homogenizer 65 DEG C, 20Mpa mixes under regulating, regulate pH to 7.8, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 8kg and urea 2kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 180 DEG C, two district's temperature 210 DEG C, three district's temperature 220 DEG C, four district's temperature 230 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
Embodiment 2
(1) take nylon 8 0kg, diameter be 12 microns alkali free glass fibre 25kg, polyvinyl butyral acetal 18kg, polyoxyethylene glycol 8kg, diglycidylether 8kg, maleic anhydride inoculated polypropylene 6kg, Zinic stearas 5kg, Viscoat 295 3kg and saltcake 1kg, mix;
(2) said components to be added in high pressure homogenizer 65 DEG C, 20Mpa mixes under regulating, regulate pH to 7.8, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 8kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 180 DEG C, two district's temperature 210 DEG C, three district's temperature 220 DEG C, four district's temperature 230 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
Embodiment 3
(1) take nylon 9 0kg, diameter be 18 microns alkali free glass fibre 30kg, polyvinyl butyral acetal 20kg, polyoxyethylene glycol 12kg, diglycidylether 11kg, maleic anhydride inoculated polypropylene 8kg, Zinic stearas 9kg, Viscoat 295 7kg and saltcake 1kg, mix;
(2) said components to be added in high pressure homogenizer 75 DEG C, 23Mpa mixes under regulating, regulate pH to 8.6, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 11kg and urea 2kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 200 DEG C, two district's temperature 220 DEG C, three district's temperature 230 DEG C, four district's temperature 240 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
Embodiment 4
(1) take nylon 9 0kg, diameter be 18 microns alkali free glass fibre 30kg, polyvinyl butyral acetal 20kg, polyoxyethylene glycol 12kg, diglycidylether 11kg, maleic anhydride inoculated polypropylene 8kg, Zinic stearas 9kg, Viscoat 295 7kg and saltcake 2kg, mix;
(2) said components to be added in high pressure homogenizer 75 DEG C, 23Mpa mixes under regulating, regulate pH to 8.6, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 11kg and urea 2kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 200 DEG C, two district's temperature 220 DEG C, three district's temperature 230 DEG C, four district's temperature 240 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
Embodiment 5
(1) take nylon 8 5kg, diameter be 14 microns alkali free glass fibre 28kg, polyvinyl butyral acetal 19kg, polyoxyethylene glycol 10kg, diglycidylether 9kg, maleic anhydride inoculated polypropylene 7kg, Zinic stearas 6kg, Viscoat 295 5kg and saltcake 1.5kg, mix;
(2) said components to be added in high pressure homogenizer 70 DEG C, 22Mpa mixes under regulating, regulate pH to 8, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 9kg and urea 1kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 190 DEG C, two district's temperature 215 DEG C, three district's temperature 225 DEG C, four district's temperature 235 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
Comparative example 1
(2) take nylon 9 0kg, diameter be 30 microns alkali free glass fibre 30kg, polyvinyl butyral acetal 20kg, polyoxyethylene glycol 12kg, diglycidylether 11kg, maleic anhydride inoculated polypropylene 8kg, Zinic stearas 9kg, Viscoat 295 7kg and saltcake 1kg, mix;
(2) said components to be added in high pressure homogenizer 75 DEG C, 23Mpa mixes under regulating, regulate pH to 8.6, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 11kg and urea 2kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 200 DEG C, two district's temperature 220 DEG C, three district's temperature 230 DEG C, four district's temperature 240 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
Comparative example 2
(3) take nylon 9 0kg, diameter be 18 microns alkali free glass fibre 30kg, polyoxyethylene glycol 12kg, diglycidylether 11kg, maleic anhydride inoculated polypropylene 8kg, Zinic stearas 9kg, Viscoat 295 7kg and saltcake 1kg, mix;
(2) said components to be added in high pressure homogenizer 75 DEG C, 23Mpa mixes under regulating, regulate pH to 8.6, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 11kg and urea 2kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 200 DEG C, two district's temperature 220 DEG C, three district's temperature 230 DEG C, four district's temperature 240 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
Comparative example 3
(4) take nylon 9 0kg, diameter is alkali free glass fibre 30kg, polyvinyl butyral acetal 20kg, polyoxyethylene glycol 12kg, diglycidylether 11kg, maleic anhydride inoculated polypropylene 8kg, Zinic stearas 9kg, the Viscoat 295 7kg of 18 microns, mix;
(2) said components to be added in high pressure homogenizer 75 DEG C, 23Mpa mixes under regulating, regulate pH to 8.6, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 11kg and urea 2kg is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
The each zone temperatures of described twin screw extruder is: district's temperature 200 DEG C, two district's temperature 220 DEG C, three district's temperature 230 DEG C, four district's temperature 240 DEG C.
The performance test results of obtained fiber reinforced nylon composite material is as shown in table 1.
The fiber reinforced nylon composite material of embodiment 1-5 and comparative example 1-3 is tested.
Table 1
Test event Flexural strength (MPa) Pencil hardness (level) Tensile strength (MPa)
Embodiment 1 87 2H 179
Embodiment 2 89 2H 175
Embodiment 3 91 2H 188
Embodiment 4 88 2H 182
Embodiment 5 83 2H 185
Comparative example 1 38 H 111
Comparative example 2 43 H 124
Comparative example 3 37 H 120
The invention is not restricted to embodiment here, those skilled in the art, according to announcement of the present invention, do not depart from improvement that scope makes and amendment all should within protection scope of the present invention.

Claims (7)

1. a fiber reinforced nylon composite material, is characterized in that, is made up of the component comprising following weight part:
Nylon 8 0-90 part,
Glass fibre 25-30 part,
Polyvinyl butyral acetal 18-20 part,
Polyoxyethylene glycol 8-12 part,
Calcium chloride 8-11 part,
Diglycidylether 8-11 part,
Maleic anhydride inoculated polypropylene 6-8 part,
Zinic stearas 5-9 part,
Viscoat 295 3-7 part,
Saltcake 1-2 part.
2. fiber reinforced nylon composite material according to claim 1, is characterized in that, described glass fibre is alkali free glass fibre.
3. fiber reinforced nylon composite material according to claim 2, is characterized in that, the diameter of described alkali free glass fibre is 12-18 micron.
4. fiber reinforced nylon composite material according to claim 1, is characterized in that, described component also comprises urea 0-2 weight part.
5. a preparation method for fiber reinforced nylon composite material, is characterized in that, the method comprises the following steps:
(1) take nylon 8 0-90 weight part, glass fibre 25-30 weight part, polyvinyl butyral acetal 18-20 weight part, polyoxyethylene glycol 8-12 weight part, diglycidylether 8-11 weight part, maleic anhydride inoculated polypropylene 6-8 weight part, Zinic stearas 5-9 weight part, Viscoat 295 3-7 weight part and saltcake 1-2 weight part, mix;
(2) said components is added in high pressure homogenizer mix, regulate pH to 7.8-8.6, ultrasonic removing bubble, add in twin screw extruder, calcium chloride 8-11 weight part and urea 0-2 weight part is added at the side loading mouth of twin screw extruder, melting, extrude, dry, pelletizing, obtain fiber reinforced nylon composite material.
6. the preparation method of fiber reinforced nylon composite material according to claim 5, it is characterized in that, the mixing temperature of described high pressure homogenizer is 65-75 DEG C, and pressure is 20-23Mpa.
7. the preparation method of fiber reinforced nylon composite material according to claim 5, it is characterized in that, each zone temperatures of described twin screw extruder is: a district temperature 180-200 DEG C, two district temperature 210-220 DEG C, three district temperature 220-230 DEG C, four district temperature 230-240 DEG C.
CN201510479584.XA 2015-08-03 2015-08-03 Fiber-reinforced nylon composite material and preparation method therefor Pending CN104987708A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510479584.XA CN104987708A (en) 2015-08-03 2015-08-03 Fiber-reinforced nylon composite material and preparation method therefor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510479584.XA CN104987708A (en) 2015-08-03 2015-08-03 Fiber-reinforced nylon composite material and preparation method therefor

Publications (1)

Publication Number Publication Date
CN104987708A true CN104987708A (en) 2015-10-21

Family

ID=54299613

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510479584.XA Pending CN104987708A (en) 2015-08-03 2015-08-03 Fiber-reinforced nylon composite material and preparation method therefor

Country Status (1)

Country Link
CN (1) CN104987708A (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1249704A (en) * 1997-03-07 2000-04-05 美国3M公司 Abrasive article for providing clear surface finish on glass
CN1761719A (en) * 2003-03-14 2006-04-19 纳幕尔杜邦公司 Comprise the composition of polymeric amide, polyvinyl butyral acetal and mineral filler and from the goods of its manufacturing
CN102660090A (en) * 2012-05-17 2012-09-12 贵州省复合改性聚合物材料工程技术研究中心 Heat-resistant polyvinyl chloride blend and preparation method thereof
CN103849141A (en) * 2012-12-06 2014-06-11 上海杰事杰新材料(集团)股份有限公司 Long glassfiber reinforced nylon composite material and preparation method thereof
CN104610717A (en) * 2015-02-10 2015-05-13 海安县中山合成纤维有限公司 Glass fiber reinforced nylon 66 composite
CN104710778A (en) * 2015-02-11 2015-06-17 铜陵向尚电气有限公司 Electric coupler made of material less prone to deformation

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1249704A (en) * 1997-03-07 2000-04-05 美国3M公司 Abrasive article for providing clear surface finish on glass
CN1761719A (en) * 2003-03-14 2006-04-19 纳幕尔杜邦公司 Comprise the composition of polymeric amide, polyvinyl butyral acetal and mineral filler and from the goods of its manufacturing
CN102660090A (en) * 2012-05-17 2012-09-12 贵州省复合改性聚合物材料工程技术研究中心 Heat-resistant polyvinyl chloride blend and preparation method thereof
CN103849141A (en) * 2012-12-06 2014-06-11 上海杰事杰新材料(集团)股份有限公司 Long glassfiber reinforced nylon composite material and preparation method thereof
CN104610717A (en) * 2015-02-10 2015-05-13 海安县中山合成纤维有限公司 Glass fiber reinforced nylon 66 composite
CN104710778A (en) * 2015-02-11 2015-06-17 铜陵向尚电气有限公司 Electric coupler made of material less prone to deformation

Similar Documents

Publication Publication Date Title
CN104725780B (en) Hybrid basalt fiber and glass fiber reinforced resin
CN103834161A (en) High-temperature resistant semi aromatic nylon composite material and preparation method thereof
CN103013045B (en) Novel preparation method of epoxy tooling board
CN106397932A (en) Composite for fiber-reinforced plastic inspection chamber and preparation method thereof
CN107337808A (en) A kind of carbon fiber strengthens emulsion-type sizing agent and preparation method thereof with interface
CN105315474A (en) Preparation method of enhancing PEEK by treating carbon fibers with special coupling agent
CN104726048A (en) Compound toughening bisphenol-A epoxy resin inserted-bar glue high in adhesive capability in high-temperature environment and preparation method of bispheonl-A epoxy resin inserted-bar glue
CN105175991A (en) Preparation method of high strength polyether ether ketone composite material
JP6658986B1 (en) Epoxy resin composition, molding material for fiber reinforced composite material, and fiber reinforced composite material
CN110894356A (en) High-strength modified nylon material for automobile
CN106566042A (en) Corrosion-resistant carbon fiber resin-based composite material used for pump
CN103030934B (en) Novel epoxy wood substitute
CN104987708A (en) Fiber-reinforced nylon composite material and preparation method therefor
EP2905302A1 (en) Fiber reinforced thermoset composites and methods of making
CN111171516A (en) Preparation method of antibacterial toughened plant functional glass fiber reinforced plastic
CN103772839B (en) A kind of polystyrene composite plastic and preparation method thereof
CN104292828A (en) Reinforced nylon 66 composite material and preparation method thereof
CN110066508A (en) Vehicle outer door knob fiberglass reinforced modification of nylon
CN105420845A (en) Modified polyoxymethylene fiber for concrete and preparation method thereof
CN105733180A (en) Preparation method of special coupling agent-treated SiO2-enhanced PEEK
CN107604469A (en) A kind of nano combined foaming rope and preparation method
CN105647182B (en) A kind of heat-barrier material used for textiles and preparation method thereof
CN102850784A (en) Nylon 6 modified material and preparation method thereof
CN113999484A (en) Light-weight high-strength high-impact-resistance high-modulus nano modified epoxy resin composition for wind power blade main beam and preparation method thereof
CN104962072A (en) Flame-retardant PPO/PA (poly-p-phenylene oxide /poly-A) alloy

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20151021

RJ01 Rejection of invention patent application after publication