CN104312094B - Composite material for preparing connecting pieces - Google Patents

Composite material for preparing connecting pieces Download PDF

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CN104312094B
CN104312094B CN201410432585.4A CN201410432585A CN104312094B CN 104312094 B CN104312094 B CN 104312094B CN 201410432585 A CN201410432585 A CN 201410432585A CN 104312094 B CN104312094 B CN 104312094B
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epoxy resin
connector
polyamide
glass fibre
composite
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CN104312094A (en
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温雨
彭磊
杨硕
张蒙蒙
陈博宇
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QINGDAO HILYWILL ADVANCED MATERIALS TECHNOLOGY Co Ltd
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QINGDAO HILYWILL ADVANCED MATERIALS TECHNOLOGY Co Ltd
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Abstract

A novel composite material for preparing connecting pieces comprises, in percent by mass, 4-8% of aluminium particle, 6-12% of carbon nanoparticle, 24-35% of low-viscosity polyamide, 13-25% of glass fiber, and 33-52% of epoxy resin. A connecting piece prepared by employing the above composite material has mechanical strength, hardness and other performances similar to those of cast iron, the mass is reduced by 40%-50%, and the connecting piece is excellent in mechanical performances, and is simple in manufacturing and installation. The production cost is reduced and the composite material is suitable for wide popularization.

Description

A kind of connector making composite
Technical field
The present invention relates to Material Field, especially, relate to a kind of novel connector making composite.
Background technology
Mechanical field it is frequently necessary to connector, in connecting at pipeline, it will usually use the connector of plugging-in type attachment structure one class.In prior art, the connector of above-mentioned plugging-in type attachment structure one class generally uses ironcasting or rustless steel to manufacture, but its weight is big, inconvenience is all there is in manufacture, installation, although existing connector also has some to use aluminium alloy to manufacture, but its typically cost is higher, and its mechanical strength there is also certain gap compared with the connector that ironcasting or rustless steel make, it is impossible to realizes large-scale application.Therefore, it is badly in need of the connector of the new material making of a kind of light weight, intensity height, low cost, to meet the needs being easily installed and reducing entreprise cost.
Summary of the invention
It is an object of the invention to provide a kind of novel connector making composite, its light weight, the connector quality made than conventional ironcasting or rustless steel alleviates 40%-50%, and intensity is high, and manufacture method is simple, reduces production cost.
Present invention employs techniques below scheme:
A kind of novel connector making composite, including aluminum particulate, carbon nano-particles, low-viscosity polyamides, glass fibre and epoxy resin, by weight percentage, the mass content of above-mentioned each material is aluminum particulate 4-8%, carbon nano-particles 6-12%, low-viscosity polyamides 24-35%, glass fibre 13-25%, epoxy resin 33-52%.
Further, the group of described polyamide choosing freely following polyamide composition: polyamide 6, polyamide 46, polyamide 66, polyamide 11, polyamide 12, polyamide 1212, polyamide 1010, polyamide 1012, polyamide 1112, polyamide 610, polyamide 612, polyamide 69, polyamide 810 or its mixture.
Further, described glass fibre is flat glass fibers, and it is selected from E glass fibre, A glass fibre, C glass fibre, D glass fibre, M glass fibre, S glass fibre, R glass fibre or its mixture.
Further, described flat glass fibers preferably has amino and is coated or epoxy silane is coated.
Further, described epoxy resin is bifunctional epoxy resin, the epoxy resin of trifunctional or the epoxy resin of four senses.
Further, bifunctional epoxy resin includes bifunctional epoxy resin based on following material: the diglycidyl ether of Bisphenol F, the diglycidyl ether of (optional bromination) bisphenol-A, the glycidyl ether of phenol-aldehyde adducts, the glycidyl ether of aliphatic diol, diglycidyl ether, diethylene glycol diglycidyl ether, Epikote, Epon, aromatic epoxy resin, epoxidised alkene, brominated resins, aromatic glycidyl amine, the glycidyl acid imide (glycidyl imidine) of heterocycle and amide, glycidyl ether, fluorinated epoxy resin, or their combination in any;
Further, this bifunctional epoxy resin is preferably selected from the diglycidyl ether of Bisphenol F, the diglycidyl ether of bisphenol-A, diglycidyl dihydroxy naphthlene, or their any combination, the most preferably diglycidyl ether of Bisphenol F.
Further, also include the thermoplastic component dissolving in epoxy resin, being calculated in mass percent, described thermoplastic component accounts for the content 3-6% of composite, and described thermoplasticity includes arbitrary following thermoplastic that must be soluble in epoxy component: polyether sulfone, Polyetherimide and polysulfones.
Further, also include at least one firming agent, be calculated in mass percent, described firming agent accounts for the 2-3% of composite, and described firming agent is multi-carboxy anhydride, aromatic amine or polyhydric alcohol, and at least one accelerator, it accounts for 2-4% in the composite, and suitable accelerator is urea ketone compounds.
The invention still further relates to the manufacture method of a kind of preceding claim composite, it is characterised in that comprise the steps:
(1). manufacture high-quality carbon nano-particles, and by carbon nano-particles functionalization;
(2). in liquid aluminium spray atomization to inert atmosphere, and by aluminum metal powder high energy milling, pass through mechanical alloying subsequently by carbon nano-particles mechanical dispersion in step 1 in aluminum, the nano microcrystalline of formation aluminum particulate-carbon nano-particles;
(3). glass fibre processing is made it have the staple glass precursor form of a length of 2~5mm;
(4). by low-viscosity polyamides and epoxy resin room temperature mix homogeneously;
(5). nano microcrystalline in step 2 is uniformly mixed to step 4 in the mixture of low-viscosity polyamides and epoxy resin with chopped glass strand in step 3, i.e. forms the connector making composite of the present invention.
The invention still further relates to the purposes of above-mentioned composite, by described composite, utilize injection mo(u)lding, extrusion, pultrusion, blowing or other plastic technology, make connector, connector uses plugging-in type connected mode.
The method have the advantages that the connector that the composite of the present invention is made has the performances such as the mechanical strength similar to ironcasting and hardness, and quality alleviates 40%-50%, good mechanical performance, making, simple installation, reduce production cost, be suitable to large-scale popularization.
Detailed description of the invention:
A kind of novel connector making composite of the present invention, including aluminum particulate, carbon nano-particles, low-viscosity polyamides, glass fibre, epoxy resin, by weight percentage, the mass content of the most each material is aluminum particulate 4-8%, carbon nano-particles 6-12%, low-viscosity polyamides 24-35%, glass fibre 13-25%, epoxy resin 33-52%.
In the composite of the present invention, it is calculated in mass percent, aluminum particulate 4-8%, carbon nano-particles 6-12%, preferably, wherein aluminum particulate 5-6%, carbon nano-particles 8-10%, having the micro structure comprising the microcrystalline at least partly separated by carbon nano-particles, the size of microcrystalline is that 10 nanometers are to 100 nanometers.Owing to making nano microcrystalline nanometer stabilisation by carbon nano-particles, can be in the temperature holding position dislocation density of the fusing point of some phases close to this aluminum particulate and the hardness of relative raising.This means can keep the certain mechanical strength of this connector and hardness by manufacturing this connector in the hot-working of the temperature of the fusing point of some phases close to this carbon nano-particles or extrusion molding simultaneously.Due to above-mentioned nanometer stabilisation, under hot-working, even also keep Young's modulus and the hardness improved, simultaneously because carbon nano-particles is along little, the preferably crystal boundary location of nano level metal crystallite, dislocation motion can be suppressed and the dislocation in carbon nano-particles stable metal can be passed through, due to the very high surface/volume ratio of nano-sized crystal, this stabilisation is highly effective.If additionally, use the alloy that strengthened by solution hardening as metal ingredient, can by with the engaging or interlock and stablize the phase of mixed crystal or solid solution of carbon nano-particles.In the microcrystalline used by this connector, nanoparticle not only part is spaced from each other by carbon nano-particles, and some carbon nano-particles also comprise or are embedded in crystallite.This can be considered as carbon nano-particles prominent from crystallite as " hair ".These carbon nano-particles embedded play a significant role in terms of preventing dislocation density reduction.Use existing Mechanic Alloying Technology, the crystallite less than 100 nanometers of the size containing the carbon nano-particles embedded can be manufactured.In some cases, according to the diameter of carbon nano-particles, embedding carbon nano-particles in the crystallite of size 100 nanometer to 200 nanometers may be easier to.Especially, by the additional stabilization effect of the carbon nano-particles embedded, it has been found that nanometer stabilisation is the most highly effective to the crystallite of 200 nanometers to size 100 nanometer.
Using low-viscosity polyamides and glass fibre as amplified medium in the present invention, the combination of glass fibre and above-mentioned crystallite can further enhance hardness and the intensity of the connector that composite is made simultaneously.Simultaneously, find through test, flat glass fibers (the ratio > 2 of transverse axis) demonstrates significant advantage compared to the glass fibre of circular cross section in mechanical performance, processing and surface quality, and this is the most true for the high content of glass fiber of > 50%.Therefore, in the novel connector making composite of the present invention, find, compared to the glass fibre with circular configuration, to use the high notch impact strength that flat glass fibers has 2 times.
The toughness value lower than higher molecular weight polyamide is found in low molecular polyamides.But, at high fill level, owing to the viscosity of more high-molecular polyamide is higher, so molding history is complicated.It is poor that this is embodied in formation filling difficulty, shrink mark and surface quality.Simultaneously, it is further discovered that the flat glass fibers particularly with high percentage composition, when the moulding material using the present invention, preferably there is low viscosity, aliphatic partially crystallizable polyamide, compared to the material containing circular cross section glass fibre, made connector has good processability, low warpage, great surface quality and the product of the most more high tenacity.Compared with the glass fibre with circular cross section, cross section main shaft and secondary axes have the glass fibre (flat glass fibers) of different numerical value and have considerably higher packed density when high level strengthens, this causes higher modulus and intensity, especially transverse fibers direction.
The low-viscosity polyamides that the novel connector making composite of the present invention is used includes at least one aliphatic partially crystallizable polyamide, as fatty polyamide, it is possible to use the group of polyamide choosing freely following polyamide composition: polyamide 6, polyamide 46, polyamide 66, polyamide 11, polyamide 12, polyamide 1212, polyamide 1010, polyamide 1012, polyamide 1112, polyamide 610, polyamide 612, polyamide 69, polyamide 810 or its mixture.
Described flat glass fibers has the staple glass precursor form of a length of 2~5mm, flat glass fibers is added as staple glass precursor, main transverse cutting shaft a diameter of 6~40 μm of described flat glass fibers and secondary transverse cutting shaft a diameter of 3~20 μm, the ratio of the most orthogonal transverse cutting shaft is between 2 and 5, preferably, the ratio of the most orthogonal transverse cutting shaft is between 3 and 4.Preferably, described flat glass fibers preferably has amino selected from E glass fibre, A glass fibre, C glass fibre, D glass fibre, M glass fibre, S glass fibre, R glass fibre or its mixture, and wherein said flat glass fibers and is coated or epoxy silane is coated.
Containing epoxy resin 33-52% in the composite of the present invention, epoxy resin is for improving toughness and the injection performance of composite, and epoxy resin ingredient can include bifunctional epoxy resin, can use any suitable bifunctional epoxy resin.It is understood that this any suitable epoxy resin including there are two epoxy-functionals.This bifunctional epoxy resin can be saturated, undersaturated, (cylcoaliphatic) of cyclic aliphatic, alicyclic or heterocyclic.Exemplary bifunctional epoxy resin include based on following material those: the diglycidyl ether of Bisphenol F, the diglycidyl ether of (optional bromination) bisphenol-A, the glycidyl ether of phenol-aldehyde adducts, the glycidyl ether of aliphatic diol, diglycidyl ether, diethylene glycol diglycidyl ether, Epikote, Epon, aromatic epoxy resin, epoxidised alkene, brominated resins, aromatic glycidyl amine, the glycidyl acid imide (glycidyl imidine) of heterocycle and amide, glycidyl ether, fluorinated epoxy resin, or their combination in any.This bifunctional epoxy resin is preferably selected from the diglycidyl ether of Bisphenol F, the diglycidyl ether of bisphenol-A, diglycidyl dihydroxy naphthlene, or their any combination.The most preferably diglycidyl ether of Bisphenol F.The diglycidyl ether of Bisphenol F can be purchased from Huntsman Advanced Materials (Brewster, NY) with trade name AralditeGY281 and GY285.Bifunctional epoxy resin can be by individually or to use in the way of any proper combination of other bifunctional epoxy resin.Although bifunctional epoxy resin can be used, it is preferred that epoxy resin ingredient includes the combination of the combination of polyfunctional epoxy resin, specifically trifunctional epoxy resin and tetrafunctional epoxy resin.This polyfunctional epoxy resin can be saturated, undersaturated, cyclic aliphatic, alicyclic or heterocyclic.As an example, be suitable for polyfunctional epoxy resin include based on following material those: phenol-epoxy novolac and cresol-epoxy novolac, the glycidyl ether of phenol-aldehyde adducts, the glycidyl ether of two aliphatic diols (dialiphatic diol), diglycidyl ether, diethylene glycol diglycidyl ether, aromatic epoxy resin, two aliphatic series triglycidyl group ether (dialiphatic triglycidyl ether), the many glycidyl ethers of aliphatic series, epoxidised alkene, brominated resins, aromatic glycidyl amine, the glycidyl acid imide of heterocycle and amide, glycidyl ether, fluorinated epoxy resin, or their combination in any.Epoxy resin ingredient should account for 40wt%~65wt% of substrate.Three epoxy radicals in para-position that the epoxy resin of trifunctional can be understood as having the benzyl ring of the main chain being either directly or indirectly substituted in compound or meta (meta orientation).Meta orientation is preferred.The epoxy resin of four senses can be understood as four epoxy radicals having in the meta or para position of the benzyl ring of the main chain being either directly or indirectly substituted in compound.
Described benzyl ring can additionally replace other suitable non-ethoxyl substitution.As an example, suitable substituent group includes hydrogen, hydroxyl, alkyl, thiazolinyl, alkynyl, alkoxyl, aryl, aryloxy group, aralkoxy, aralkyl, halogen, nitro or cyano group.Suitable non-ethoxyl substitution can be attached on benzyl ring in para-position or ortho position, or in not meta combination for epoxy radicals occupied by.The epoxy resin of four suitable senses includes N, N, N ', N '-four glycidyl group-m-xylene diamine (can be with trade name Tetrad-X purchased from Mitsubishi Gas Chemical Company (Chiyoda-Ku, Tokyo,) and ErisysGA-240 (deriving from CVC Chemicals, Moorestown, New Jersey) Japan).As an example, the epoxy resin of suitable trifunctional include based on following material those: phenol-epoxy novolac and cresol-epoxy novolac, the glycidyl ether of phenol-aldehyde adducts, aromatic epoxy resin, two aliphatic series triglycidyl group ethers, aliphatic many glycidyl ethers, epoxidised alkene, brominated resins, aromatic glycidyl amine and glycidyl ether, the glycidyl acid imide of heterocycle and amide, glycidyl ether, fluorinated epoxy resin, or their combination in any.Preferably trifunctional epoxy resin is triglycidyl meta-aminophenol.
The novel connector making composite of the present invention also includes the thermoplastic component dissolving in epoxy resin, it is calculated in mass percent, described thermoplastic component accounts for the content 3-6% of composite, can use any suitable soluble thermoplastic polymer already functioning as toughener.The exemplary thermoplastic that can be used as soluble thermoplastic component includes arbitrary following thermoplastic that must be soluble in epoxy component: polyether sulfone, Polyetherimide and polysulfones.
Polyether sulfone (PES) is preferably used as soluble thermoplastic component.PES is sold by trade name Sumikaexcel5003P, and it is purchased from Sumitomo Chemicals.The alternative of 5003P is Solvay polyether sulfone 105RP, or the grade such as Solvay1054P of non-hydroxyl end-blocking.
The novel connector making composite of the present invention can also include that at least one firming agent, described firming agent are calculated in mass percent, account for the 2-3% of composite.In particularly preferred embodiments, this firming agent is included in the ring-opening polymerisation of epoxy functional compounds those compounds being polymerized with this epoxy functional compounds.Two or more these firming agent can use in combination.
nullSuitable firming agent includes acid anhydride,Particularly multi-carboxy anhydride,Such as nadic anhydride (NA)、Methyl norbornene dioic anhydride (MNA-derives from Aldrich)、Phthalic anhydride、Tetrabydrophthalic anhydride、(HHPA-derives from Anhydrides and ChemicalsInc. to hexahydrophthalic anhydride,Newark,NJ.)、Methyl tetrahydrophthalic anhydride (MTHPA-derives from Anhydrides andChemicals Inc.)、Methylhexahydrophthalic anhydride (MHHPA-derives from Anhydrides andChemicals Inc.)、Nadic anhydride、Chlordene Nadic anhydride (chlorendic anhydride (Chlorentic Anhydride)-derive from Velsicol Chemical Corporation,Rosemont,Ill.)、Trimellitic anhydride、Pyromellitic acid dianhydride、Maleic anhydride (MA-derives from Aldrich)、Succinic anhydrides (SA)、Nonenyl succinic acid acid anhydride、Dodecenylsuccinic anhydride (DDSA-derives from Anhydridesand Chemicals Inc.)、The many acid anhydrides of poly-decanedioic acid (polysebacic polyanhydride) and the many acid anhydrides of poly-Azelaic Acid.
Other suitable firming agent is amine, including aromatic amine, such as 1,3-diaminobenzene, Isosorbide-5-Nitrae-diaminobenzene, 4,4'-diaminodiphenyl-methane and polyamino sulfone, such as 4,4'-diamino diphenyl sulfone (4,4'-DDS-derive from Huntsman), 4-aminophenyl sulfone and 3,3'-diamino diphenyl sulfone (3,3'-DDS).
Suitable firming agent can also include polyhydric alcohol, such as ethylene glycol (EG-derives from Aldrich), polypropylene glycol and polyvinyl alcohol;Phenol-formaldehyde resin, such as mean molecule quantity is about the phenolic resin of 550-650, mean molecule quantity is about the p-tert-butylphenol-formaldehyde resin of 600-700, mean molecule quantity is about the p-n-octyl resinox of 1200-1400, these resins can derive from Schenectady Chemicals with HRJ2210, HRJ-2255 and SP-1068 respectively, Inc., Schenectady, N.Y..Combination (deriving from Ajinomoto USA Inc. (Teaneck, NJ.) with CG-125) additionally for the phenolic resin that phenolic resin, CTU guanamines and molecular weight are 398 is also suitable.
The firming agent being additionally suitable for includes imidazoles (1,3-diaza-2,4-cyclopentadiene), derives from SigmaAldrich (St.Louis, Missouri);2-ethyl-4-methylimidazole, derives from Sigma Aldrich;And boron trifluoride amine complex, such as Anchor1170, derive from AirProducts&Chemicals, Inc.Firming agent is selected to make them provide the solidification of this resin Composition when with resin Composition combination in composite in applicable temperature.The amount providing the firming agent required by abundant solidification of resin Composition can become, including the resinous type being cured, desired solidification temperature and hardening time with many factors.Firming agent generally includes cyanoguanidines, aromatics and aliphatic amine, anhydride, lewis acid, substituted urea, imidazoles and hydrazine.Needed for every kind of concrete situation, the specified quantitative of firming agent can be determined by ripe normal experiment.
The preferred consolidation agent of example includes 4,4'-diamino diphenyl sulfone (4,4'-DDS) and 3, and 3'-diamino diphenyl sulfone (3,3'-DDS) all derives from Huntsman.The amount of firming agent should be 10wt%~30wt% of uncured resinous substrates.Preferably, the amount of firming agent is 15wt%~25wt% of uncured resinous substrates.3,3'-DDS is preferred firming agent.It is preferably used as unique firming agent, in an amount of from 16wt%~25wt%.The 4,4'-DDS using substantial amounts of reactivity relatively low is not preferred as firming agent.Using reactive higher by 3,3'-DDS solidifies the resinous substrates formulation of the present invention provides the intensity of raising in solidification composite, but does not reduces damage toleration and interlayer toughness.Additionally, the external life-span of the character of prepreg such as viscosity and prepreg is affected the most inadequately.Uncured matrix resin can also include other composition, such as performance enhancement or modifying agent and other thermoplastic polymer, as long as they the most deleteriously affect the viscosity of prepreg and external life-span, or the intensity of the composite component of solidification and damage toleration.This performance enhancement or modifying agents are as being selected from softening agent (flexibilizer), toughener/toughness reinforcing particle, accelerator, core shell rubber, fire retardant, wetting agent, pigment/dye, UV absorbent, antifungal compound, filler, conducting particles and viscosity modifier.
Can also include at least one accelerator in the novel connector making composite of the present invention, by mass percentage, it accounts for 2-4% in the composite, and suitable accelerator is the most normally used any urea ketone (urone) compound.The instantiation of the accelerator that can use individually or in combination includes N, N-dimethyl, N'-3,4-Dichlorobenzene base urea (Diuron), N'-3-chlorphenyl urea (Monuron) and preferably N, N-(4-methyl-metaphenylene two [N', N'-dimethyl urea] (such as, deriving from the DyhardUR500 of Degussa).
The manufacture method of a kind of novel connector making composite of the present invention comprises the steps:
1. manufacture high-quality carbon nano-particles, and by carbon nano-particles functionalization;
2. liquid aluminium spray atomization is in inert atmosphere, and by the high energy milling of aluminum metal powder, subsequently by mechanical alloying by carbon nano-particles mechanical dispersion in step 1 in aluminum, form the nano microcrystalline of aluminum particulate-carbon nano-particles;
3. glass fibre processing is made it have the staple glass precursor form of a length of 2~5mm;
4. by low-viscosity polyamides and epoxy resin room temperature mix homogeneously;
5. nano microcrystalline in step 2 is uniformly mixed to step 4 in the mixture of low-viscosity polyamides and epoxy resin with chopped glass strand in step 3, i.e. form the connector making composite of the present invention;
6. utilizing injection mo(u)lding, extrusion, pultrusion, blowing or other plastic technology, make connector, connector uses plugging-in type connected mode.
Embodiment:
Embodiment 1:
Aluminum particulate 4%, carbon nano-particles 6%, polyamide 66 26%, cylindrical cross-section glass fibre 13%, the diglycidyl ether 51% of Bisphenol F is used in the composite of this embodiment.Using after the mixing of above-mentioned each material and utilize injection mo(u)lding, extrusion, pultrusion, blowing or other plastic technology, make connector, connector uses plugging-in type connected mode.
Embodiment 2:
Aluminum particulate 6%, carbon nano-particles 8%, polyamide 1010 26%, A glass fibre 20%, aromatic glycidyl amine 37%, Polyetherimide 3%.Use after the mixing of above-mentioned each material and utilize injection mo(u)lding, extrusion, pultrusion, blowing or other plastic technology, make connector.
Embodiment 3:
Aluminum particulate 8%, carbon nano-particles 12%, polyamide 1010 24%, S glass fibre 15%, the glycidyl ether 36% of aliphatic diol, polyether sulfone 5%.Use after the mixing of above-mentioned each material and utilize injection mo(u)lding, extrusion, pultrusion, blowing or other plastic technology, make connector.
Embodiment 4:
Aluminum particulate 4%, carbon nano-particles 6%, polyamide 81024%, M glass fibre 15%, glycidyl ether 43%, polyether sulfone 5%, trimellitic anhydride 3%.Use after the mixing of above-mentioned each material and utilize injection mo(u)lding, extrusion, pultrusion, blowing or other plastic technology, make connector.
Embodiment 5:
Aluminum particulate 4%, carbon nano-particles 10%, polyamide 81025%, C glass fibre 15%, fluorinated epoxy resin 37%, polysulfones 5%, tetrabydrophthalic anhydride 4%.Use after the mixing of above-mentioned each material and utilize injection mo(u)lding, extrusion, pultrusion, blowing or other plastic technology, make connector.
The connector making the various embodiments described above carries out measuring mechanical property, its mechanical properties data such as following table:
Embodiment 1 2 3 4 5
Longitudinal stretching fracture strength Mpa 201 189 197 188 204
Cross directional stretch fracture strength Mpa 135 152 125 142 138
Impact flexibility kJ/m2 75 65 77 68 69
Hardness/HB 135 143 144 138 139
From table it can be seen that, the connector that the composite of the present invention is made has the performances such as the mechanical strength similar to ironcasting and hardness, and quality alleviates 40%-50%, good mechanical performance, making, simple installation, assessing through expert, unanimously think the connector of the making such as its alternative cast iron commonly used in the prior art, it is sturdy and durable, and it is corrosion-resistant, easily processing and fabricating, reduces production cost, is suitable to large-scale popularization.
Finally it should be noted that, above example is only in order to describe technical scheme rather than to limit the technical program, the present invention can extend to other amendment in application, change, applies and embodiment, and it is taken as that all such amendments, change, apply, embodiment is all in the range of the spirit or teaching of the present invention.

Claims (2)

1. the connector that a composite is fabricated to, it is characterised in that described composite is made up of the component of following weight ratio: aluminum particulate 4%, Carbon nano-particles 6%, polyamide 81024%, M glass fibre 15%, glycidyl ether 43%, polyether sulfone 5%, trimellitic anhydride 3%; Described glass fibre has amino and is coated or epoxy silane is coated;By described composite, utilize injection mo(u)lding, extrusion, pultrusion, blowing Or other plastic technology, make connector, connector uses plugging-in type connected mode.
2. the connector that a composite is fabricated to, it is characterised in that described composite is made up of the component of following weight ratio: aluminum particulate 4%, Carbon nano-particles 10%, polyamide 81025%, C glass fibre 15%, fluorinated epoxy resin 37%, polysulfones 5%, tetrahydrophthalic acid Acid anhydride 4%;Wherein, described glass fibre has amino and is coated or epoxy silane is coated;By described composite, utilize injection mo(u)lding, extrusion, Pultrusion, blowing or other plastic technology, make connector, and connector uses plugging-in type connected mode.
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