CN100487053C - Composite material of fibrous nanometer clay and high viscosity polyamide - Google Patents
Composite material of fibrous nanometer clay and high viscosity polyamide Download PDFInfo
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- CN100487053C CN100487053C CNB2003101090914A CN200310109091A CN100487053C CN 100487053 C CN100487053 C CN 100487053C CN B2003101090914 A CNB2003101090914 A CN B2003101090914A CN 200310109091 A CN200310109091 A CN 200310109091A CN 100487053 C CN100487053 C CN 100487053C
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- clay
- matrix material
- polyamide
- viscosity polyamide
- fibrous nano
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Abstract
The invention relates to a composite material of fibrous nanometer clay and high viscosity polyamide whose raw material includes, (a) a monomer oligomer for preparing polyamides, (b) clay mainly in the shape of fibrous rod or corresponding at least one compound capable of dispersing homogeneously into component (a), (c) dispersing agent (c) participating in dispersion and catalyst, catalyst promoter D,E etc. capable of participating in synthesizing. The preparing process is characterized in configuring the raw material and auxiliary agent, mainly utilizing monomer hydrolytic open loop polycondensation to prepare the high viscosity nano composite polyamide resin.
Description
Technical field
The present invention relates to the matrix material that a kind of inorganic nano material compound macromolecular polymer forms, specially refer to the matrix material of fibrous nano clay and high-viscosity polyamide.
Background technology
Polymeric amide (nylon PA) be in the engineering plastics exploitation early, one of bigger, the most widely used kind of output, have intensity height, good toughness, excellent electrical properties, wear-resisting, damping sound-absorbing, oil resistant and weak acid alkali, be easy to advantages such as forming process, high comprehensive performance.But defectives such as shock strength was low when nylon existed dry state and low temperature, water-intake rate is big, thereby influence its product size stability and electrical property.As engineering plastics, nylon is applied in aspects such as trolley part, mechanical component, decoration bar section in large quantities.In order fully to satisfy the needs in the practical application, improve the over-all properties of nylon, using inorganic materials (as glass, lime carbonate, talcum powder etc.) that nylon is carried out modification has become the nylon trend of application.But because problems such as associativity that exists between inorganic materials and the organic polymer and consistency and appearance effect, machine-shapings, inorganic materials usually makes the user attend to one thing and lose sight of another to the modification of nylon.In recent years, along with developing rapidly of whole world industry, especially more and more higher to the requirement of synthetic material to material.In addition, increase sharply as the demand of structured material, engineering materials, functional materials, blow, squeeze, draw engineering materials more and more obvious as structural articles, seeking increasing substantially of polymeric amide (nylon PA) performance becomes instant thing.
In recent years, the material supply section scholar invests the compound of nano material and high molecular polymer with the common eye, and particularly nano material and polymeric amide (nylon PA) is compound.During this time, many relevant theory, patent even products have also appearred both at home and abroad.
Abroad, Toyota Motor company has at first announced PA/ layered silicate (inorganic clay) matrix material achievement in 1991, developed the PA nano composite material cooperatively with company of space portion emerging product (UBE) afterwards, is nanoclay mishmash (NCH
S), and be applied to timer cover and engine decorative shell.Japan You Niqika company also releases PA/ layered silicate (inorganic clay) matrix material that the trade mark is M1030D; Clear and electrician releases PA6/ synthetic mica nano composite material SystemerFE2010z.
U.S. Solutia Corp has applied for " polyamide nano material compositions " (international application: PCT/US98/02768; China's application number: 98813964.2), wherein with layered silicate material with contain ammonia from salt handle.Germany BASF AG has applied for " thermoplastic nanocomposites " (international application: PCT/EP00/01088; China's application number: 00806107.6), electronegative layered silicate is embedded in the compound of positively charged ion formation.
At home, the chemistry QiZongNeng researcher of institute of the Chinese Academy of Sciences waits and has also applied for " a kind of polyamide/nano clay composite material and preparation method thereof " (application number: 96105362.3), the stratiform polynite is prepared into the polyamide nano material composite with in-situ inserted polymeric principle, but does not have product at present; Ba Ling petrochemical industry general petrochemical works has applied for " a kind of nm-class composite polyamide/silicate material and manufacture method thereof " (application number: 97108360.6), prepare nano composite material by ion-exchange and two processes of polymerization, but do not have product to appear on the market; The Wang Xiuying of Shiyan east wind etc. has applied for " a kind of method for preparing nano-class polyamide/laminated silicate composition ", obtains matrix material with melt intercalated method, does not have product equally.
In sum, the compounding technology of present nano material and polymeric amide (nylon PA), no matter be abroad or domestic, all be confined to this field of intercalation polymeric, promptly based on two-dimensional nano material (as layered silicate, sheet mica etc.), the interlayer that inserts inorganic materials by the polymer organic molecular chain forms matrix material.And the matrix material that forms of this technology does not show outstanding advantage yet on performance at present, so the popularization of product and the situation that appears on the market can not form.
To the high molecular enhanced mechanism of random orientation, reinforced effects depends on rigidity, length-to-diameter ratio and strongthener and the high molecular cohesiveness of matrix of strongthener according to the staple fibre strongthener.Conventional this type of material of using comprises glass fibre after the organic process, carbon fiber etc., the yardstick that their common problems that exists are reinforcing fibers is at micron order, there is unsurmountable obstacle in processing to polymer fiber and film etc., and the ratio of matrix material is great, and processing characteristics is bad, products appearance is poor, the polymer performance descends to some extent.The fiber nano material has the rigidity of staple fibre strongthener concurrently, and length-to-diameter ratio and also improve a lot with the high molecular consistency of matrix, and inorganic fibre is in the nanoscale scope simultaneously, and what do not influence matrix material makes fiber and processing film.This is the characteristics of this patent resin just.
Summary of the invention
The matrix material that the purpose of this invention is to provide a kind of fibrous nano clay and polymeric amide (nylon PA).
The matrix material of a kind of fibrous nano clay and high-viscosity polyamide, the feed composition of described matrix material and content (content is in weight part) are as follows:
Monomer of polyamide 100
Clay 1-30
Dispersion agent 0.01-50
Catalyzer 0.01-20
Additive 0.01-5
Described clay is sepiolite, sloping aluminium stone or attapulgite clay, preferred attapulgite clay.
Described monomer of polyamide is ε-Ji Neixianan, laurolactam, hexanediamine or hexanodioic acid, preferred ε-Ji Neixianan or laurolactam.
Described dispersion agent is phosphoric acid salt or polyacrylate.
Described catalyzer is a deionized water, hydrochloric acid, phosphoric acid and hexanodioic acid.
Described additive is oxidation inhibitor and stabilizer molecule, is mainly 1010,1098.
Carry out following steps according to above-mentioned raw material and content and prepare this matrix material:
A) clay is pulverized, in 90-900 ℃ of air and rare gas element, calcined 0.5-10.0 hours;
B) add dispersion agent, and add catalyzer and oxidation inhibitor, mix the high-speed stirring decentralized system down at 90-150 ℃ and get nanoparticle active agent;
C) monomer of polyamide is put into reactor, add nanoparticle active agent and stablizer, heat, distillation is anhydrated, and the off-response still is heated and entered hydrolytic polymerization then, and in this process, the processing parameter of hydrolytic polymerization: still is pressed 0.6-1.2MPa; 250-290 ℃ of hydrolysis temperature of charge; Vacuum hydro-extraction is pressed and is-0.4-0.9MPa, and keeping polymerization time under the vacuum is 30-180 minutes, promptly makes described matrix material.
The present invention compared with prior art, this material has excellent mechanical property, thermotolerance, processing characteristics and exterior surface features and high cost performance.
Embodiment
Below in conjunction with embodiment the present invention is further described.The cited case does not limit protection domain of the present invention.
Embodiment 1
Present embodiment is preparation attapulgite and hexanolactam compound polyamide resin.
The raw material composition and the content of 1 preparation fibrous nano clay composite polyamide resin are as follows: (weight part)
A) ε-Ji Neixianan: 100g
B) fibrous nano clay material (attapulgite) is respectively: 3g,
C) 0.1% phosphoric acid salt dispersion treating agent: 50g
D) phosphoric acid: 0.1g
E) antioxidant 1010: 0.2g
F) stablizer 1098:0.2g
2 preparation process:
Getting attapulgite 3g respectively pulverizes, calcining was incorporated in the 0.1%50g phosphoric acid salt dispersion treatment liquid after 6.0 hours in 400 ℃ of rare gas elementes, and add phosphoric acid 0.1g, oxidation inhibitor 0.2g, disperse and reacted 40 minutes 95 ℃ of 6000 rev/mins of high-speed stirring, under 90 ℃, stablize later on to make in 100 minutes and make nanoparticle active agent.
Hexanolactam is put in the reactor, and slowly adds nanoparticle active agent and stablizer is just heated later on, distillation is anhydrated, and when aquifer yield reached 45g, the off-response still was heated and entered hydrolytic polymerization.Processing parameter is in the process: still is pressed 0.9Mpa; 270 ℃ of hydrolysis temperature of charge; Vacuum hydro-extraction is pressed and is-0.5Mpa, and keeping polymerization time under the vacuum is 120 minutes.Last discharging, moulding extraction and oven dry become fibrous nano clay composite polyamide resin.Get performance after tested and see Table 1 (embodiment 1).
Embodiment 2-5
With embodiment 1, wherein nanoclay material (attapulgite) is respectively: 5g, 10g, 20g, 30g, different clay contents see Table 1 (embodiment 2--5) to the influence of material relative viscosity and mechanical property after its Combined Processing, can see that clay content is to changes of properties.
Embodiment 6
Present embodiment is preparation attapulgite and laurolactam compound polyamide resin.
With embodiment 1, wherein monomer of polyamide is that laurolactam nanoclay material (attapulgite) is: 3g, different monomers sees Table 1 (embodiment 6) to the influence of material relative viscosity and mechanical property after its Combined Processing, can see that monomer changes Effect on Performance.
Table 1
| Embodiment | Fibrous native content (g) | Relative viscosity | Tensile strength MPa | Flexural strength MPa | Modulus in flexure MPa | Heat-drawn wire ℃ (1.8Mpa) | Notch shock KJ/m 2 |
| 1 | 3 | 3.2 | 79 | 130 | 2305 | 115 | 11.0 |
| 2 | 5 | 3.5 | 85 | 140 | 2710 | 132 | 9.5 |
| 3 | 10 | 3.2 | 92 | 145 | 3525 | 155 | 8.5 |
| 4 | 20 | 3.1 | 115 | 155 | 3950 | 182 | 7.0 |
| 5 | 30 | 3.0 | 125 | 165 | 4865 | 196 | 6.5 |
| 6 | 3 | 3.2 | 75 | 125 | 2200 | 105 | 15.0 |
Embodiment 7,8
With embodiment 1, wherein dispersion agent is respectively phosphoric acid salt and polypropylene hydrochlorate, and different dispersion agents see Table 2 (embodiment 7,8) to the influence of material relative viscosity and mechanical property during its Combined Processing, can see that phosphoric acid salt is best as dispersant effect.
Table 2
| Embodiment | Clay content (g) | The component agent | Tensile strength MPa | Flexural strength MPa | Modulus in flexure MPa | Notch shock KJ/m 2 |
| 7 | 3 | Phosphoric acid salt | 80 | 130 | 2300 | 11.0 |
| 8 | 3 | The polypropylene hydrochlorate | 75 | 120 | 2100 | 10.0 |
Claims (9)
1, the matrix material of a kind of fibrous nano clay and high-viscosity polyamide is characterized in that the feed composition of described matrix material and content are as follows:
Monomer of polyamide 100
Clay 1～30
Dispersion agent 0.01～50
Catalyzer 0.01～20
Additive 0.01～5
Wherein: described clay is sepiolite, sloping aluminium stone or attapulgite clay, and content is in weight part.
2. the matrix material of a kind of fibrous nano clay as claimed in claim 1 and high-viscosity polyamide is characterized in that described clay is an attapulgite clay.
3. the matrix material of a kind of fibrous nano clay as claimed in claim 1 and high-viscosity polyamide is characterized in that described monomer of polyamide is ε-Ji Neixianan, laurolactam, hexanediamine or hexanodioic acid.
4. the matrix material of a kind of fibrous nano clay as claimed in claim 1 and high-viscosity polyamide is characterized in that described dispersion agent is phosphoric acid salt or polyacrylate.
5. the matrix material of a kind of fibrous nano clay as claimed in claim 1 and high-viscosity polyamide is characterized in that described catalyzer is a deionized water, hydrochloric acid, phosphoric acid and hexanodioic acid.
6. the matrix material of a kind of fibrous nano clay as claimed in claim 1 and high-viscosity polyamide is characterized in that described additive is oxidation inhibitor and stabilizer molecule.
7, the matrix material of a kind of fibrous nano clay as claimed in claim 1 and high-viscosity polyamide is characterized in that described additive is antioxidant 1010 and stabilizer molecule 1098.
8. the matrix material of a kind of fibrous nano clay as claimed in claim 3 and high-viscosity polyamide is characterized in that described monomer of polyamide is ε-Ji Neixianan or laurolactam.
9. method for preparing the matrix material of a kind of fibrous nano clay as claimed in claim 1 and high-viscosity polyamide is characterized in that raw material according to claim 1 and content carry out following steps:
A) clay is pulverized, in 90～900 ℃ of air and rare gas element, calcined 0.5～10.0 hour;
B) add dispersion agent, and add catalyzer and oxidation inhibitor, mix the high-speed stirring decentralized system down at 90～150 ℃ and get nanoparticle active agent;
C) monomer of polyamide is put into reactor, add nanoparticle active agent and stablizer, heat, distillation is anhydrated, and the off-response still is heated and entered hydrolytic polymerization then, and in this process, the processing parameter of hydrolytic polymerization: still is pressed 0.6～1.2Mpa; 250～290 ℃ of hydrolysis temperature of charge; Vacuum hydro-extraction presses to-0.4～-0.9Mpa, keeping polymerization time under the vacuum is 30～180 minutes, promptly makes described matrix material.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2003101090914A CN100487053C (en) | 2003-12-04 | 2003-12-04 | Composite material of fibrous nanometer clay and high viscosity polyamide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2003101090914A CN100487053C (en) | 2003-12-04 | 2003-12-04 | Composite material of fibrous nanometer clay and high viscosity polyamide |
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| Publication Number | Publication Date |
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| CN1546570A CN1546570A (en) | 2004-11-17 |
| CN100487053C true CN100487053C (en) | 2009-05-13 |
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Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1329337C (en) * | 2005-02-28 | 2007-08-01 | 江苏南大紫金科技集团有限公司 | Preparation method of one-dimensional nano silicate clay |
| CN100412108C (en) * | 2005-07-27 | 2008-08-20 | 上海杰事杰新材料股份有限公司 | Material for making toothbrush bristle and its preparation method |
| CN100430442C (en) * | 2005-11-17 | 2008-11-05 | 复旦大学 | Reinforced toughened antiwear composite polyimide material |
| JP5832296B2 (en) * | 2009-12-09 | 2015-12-16 | ユニチカ株式会社 | Polyamide resin composition and method for producing polyamide resin composition |
| JP5911426B2 (en) * | 2010-09-30 | 2016-04-27 | ユニチカ株式会社 | Polyamide resin composition and molded product obtained therefrom |
| CN102618030B (en) * | 2012-03-20 | 2014-09-10 | 杭州鑫福纺织有限公司 | Fragrant chinlon masterbatch, fragrant chinlon fiber and preparation methods thereof |
| US10053611B2 (en) * | 2016-03-22 | 2018-08-21 | Saudi Arabian Oil Company | In situ generation of nano-clay drilling fluid |
| CN110144040A (en) * | 2019-05-14 | 2019-08-20 | 东华大学 | A kind of drop sticks additive agent modified nylon 66 composite material and its preparation and application |
| CN113527670B (en) * | 2021-08-06 | 2023-10-13 | 东莞市凯泰汽车零部件有限公司 | 1200H xenon lamp aging resistant urea pipe and preparation method thereof |
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