CN1478818A - Synthesis method of PBO/carbon nanometer pipe composite material - Google Patents
Synthesis method of PBO/carbon nanometer pipe composite material Download PDFInfo
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- CN1478818A CN1478818A CNA031325122A CN03132512A CN1478818A CN 1478818 A CN1478818 A CN 1478818A CN A031325122 A CNA031325122 A CN A031325122A CN 03132512 A CN03132512 A CN 03132512A CN 1478818 A CN1478818 A CN 1478818A
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Abstract
A process for synthesizing PBO/carbon nanotube composition includes such steps as proportional adding 4,6-diamino resorcinol hydrochloride and terephthalic acid derivative to polyphosphoric acid while stirring in inertial gas, removing hydrogen chloride, adding P2O5 several times, and raising temp under 210 deg.C while adding dispersed carbon nanotubes. Its advantage is high tension strength and tension modulus.
Description
Technical field: the synthesis technique that the present invention relates to polymer-based carbon/inorganic nano composite material.
Background technology: PBO (to the penylene benzo-dioxazole) base polymer is tool advantage aspect fibrous physical property and raw materials cost, it is with extremely excellent mechanical property, thermal characteristics, flame retardant resistance, solvent resistance, is applied in aerospace matrix material and civilian some performance application fields; Carbon nanotube has high length-to-diameter ratio and superpower mechanical property, for machinery, electricity, the thermal characteristics that makes full use of the carbon nanotube excellence, strengthen or improve polymkeric substance or other base matter performance with carbon nanotube, synthesizing into polymer-based carbon/carbon nano tube compound material is the problem that a lot of people are studying.Polymer-based carbon/carbon nanotube (CNTs) matrix material synthetic has two kinds of methods usually: a kind of is in-situ polymerization in the presence of CNTs, this method is to utilize the functional group on CNTs surface to participate in polymerization, or utilize initiator to open the π key of CNTs, make it participate in polymerization and reach excellent compatibility with organic phase; Another kind is a physical blending, is divided into solution blending and melt blended again, and it is to utilize the avidity of functional group on the CNTs and organic phase or space steric effect to reach excellent compatibility with organic phase.For PBO, PBO is not molten, melt blended far from.PBO can only be dissolved in strong protonic acid solvent such as methylsulfonic acid (MSA), chlorsulfonic acid (ClA), polyphosphoric acid (PPA), trifluoroacetic acid, 100% sulfuric acid, adopt the synthetic PBO/ carbon nano tube compound material of method of solution blending, the PBO polymkeric substance must be dissolved in again in the above-mentioned strong protonic acid solvent, with the carbon nanotube blend.One side PBO dissolution process again can cause molecular weight to reduce, and time-consuming, loaded down with trivial details; On the other hand, if material has the liquid crystal property that excellent performance must be utilized PBO, high-molecular weight PBO liquid crystal solution viscosity is very high, and carbon nanotube and its blend must efficiently be stirred, even also be difficult to the carbon nanotube good distribution under the efficient stirring state.
Summary of the invention: the synthetic method that the purpose of this invention is to provide a kind of PBO/ carbon nano tube compound material, it is simple and convenient that it has method, carbon nanotube is scattered, the molecular weight height, specific tensile strength and tensile modulus all have the characteristics that significantly improve mutually with synthetic PBO material under this method synthetic PBO/ carbon nano tube compound material and the equal conditions.The present invention calculates required 4 by 6～20% polymer concentrations under protection of inert gas, normal pressure agitation condition; 6-diamino resorcin hydrochlorate monomer and etc. mole proportioning or join in the polyphosphoric acid by the excessive terephthalic acid derivatives monomer of mole proportioning; controlled temperature removes hydrogenchloride between 60～120 ℃, remove hydrogenchloride fully after gradation add P
2O
5, with P
2O
5Concentration is controlled between 82.5～83.5%, control is lower than 210 ℃ of temperature programmings, the carbon nanotube through dispersion treatment that accounts for polymer quality 1～20% added or be lower than in 180 ℃ of temperature programming processes when the PBO polymeric solution is deviate from hydrogenchloride fully be added in the PBO polymeric solution, form liquid crystal in 6～36 hours behind the adding carbon nanotube, after precipitating, washing, drying, obtain matrix material of the present invention then.Described rare gas element is a nitrogen; Described by the excessive terephthalic acid derivatives monomer of mole proportioning excessive＜5%; The derivative of described terephthalic acid is terephthalic acid, p-phthaloyl chloride and poly-(terephthalic anhydride); The temperature rise rate of described temperature programming is 5～10 ℃/2～4h; Described carbon nanotube through dispersion treatment accounts for 1～10% of polymer quality; Described carbon nanotube through dispersion treatment accounts for 3% of polymer quality.The present invention adopts the method for original position polymerizable mesogenic to synthesize the PBO/ carbon nano tube compound material, and the carbon nanotube of refinement dispersion treatment added at PBO polymerization initial stage or mid-term, and carbon nanotube adds the back and generated liquid crystal in 6～36 hours.Be scattered at carbon nanotube that the PBO molecular weight slowly increases in the process of polymeric solution system, carbon nanotube can further be activated in strong protonic acid solution in addition, produce functional group and participate in certain polymerization, factors all make carbon nanotube can effectively reach the purpose that is dispersed in the PBO polymkeric substance, this method is simple, convenient, carbon nanotube is scattered, the molecular weight height, under this method synthetic PBO/ carbon nano tube compound material and the equal conditions synthetic PBO material mutually specific tensile strength improve 10～70%, tensile modulus improves 10～30%.
Embodiment one: present embodiment is adding 9.149g85% phosphoric acid and 5.848gP in the 250ml four-hole bottle under nitrogen protection, the agitation condition
2O
5Be made into concentration and be 77% poly phosphoric acid solution, add 4.261g (0.020mol) 4 when being cooled to 90 ℃, the 6-diamino resorcin hydrochlorate, 3.323g (0.020mol) terephthalic acid, deviate from hydrogenchloride till the liquid level calmness in vacuum under this temperature, add the carbon nanotube of 0.468g afterwards, be warming up to 100 ℃ and kept 6 hours through dispersion treatment, be cooled to room temperature afterwards, add P
2O
56.329g 80 ℃ kept 2 hours, were cooled to room temperature and added P
2O
56.00g, being lower than 210 ℃ of temperature programmings, opalescence appears in the temperature-rise period stirring, to 200 ℃ of maintenances 4 hours, stop heating, be cooled to 100 ℃, press mold solidifies in distilled water, and massive laundering is until neutrality.With the methylsulfonic acid is that solvent is made into 0.05g/dL solution, utilizes one-point method to measure intrinsic viscosity in 30 ℃ and is 12dL/g.
Embodiment two: present embodiment is adding 39.40g85% phosphoric acid and 50.63g P in the 250ml four-hole bottle under nitrogen protection, the agitation condition
2O
5Be made into concentration and be 83% poly phosphoric acid solution, add 8.521g (0.040mol) 4,6-diamino resorcin hydrochlorate when being cooled to 90 ℃, 6.896g (0.042mol) terephthalic acid kept this temperature 4 hours, was warming up to 120 ℃ and kept 24 hours, be cooled to 90 ℃ afterwards, add P
2O
514.55g, kept 2 hours, temperature programming to 160 ℃ adds the carbon nanotube of 0.187g through dispersion treatment, kept this temperature 6 hours, be lower than 210 ℃ of temperature programmings afterwards, be warming up to 180 ℃ and opalescence occurs stirring, to 200 ℃ of maintenances 4 hours, stop heating, be cooled to 100 ℃, press mold solidifies in distilled water, and massive laundering is until neutrality.With the methylsulfonic acid is that solvent is made into 0.05g/dL solution, utilizes one-point method to measure intrinsic viscosity in 30 ℃ and is 14dL/g.
Claims (7)
1, a kind of synthetic method of PBO/ carbon nano tube compound material; it is characterized in that under protection of inert gas, normal pressure agitation condition calculating required 4 by 6～20% polymer concentrations; 6-diamino resorcin hydrochlorate monomer and etc. mole proportioning or join in the polyphosphoric acid by the excessive terephthalic acid derivatives monomer of mole proportioning; controlled temperature removes hydrogenchloride between 60～120 ℃, remove hydrogenchloride fully after gradation add P
2O
5, with P
2O
5Concentration is controlled between 82.5～83.5%, control is lower than 210 ℃ of temperature programmings, the carbon nanotube through dispersion treatment that accounts for polymer quality 1～20% added or be lower than in 180 ℃ of temperature programming processes when the PBO polymeric solution is deviate from hydrogenchloride fully be added in the PBO polymeric solution, form liquid crystal in 6～36 hours behind the adding carbon nanotube, make matrix material of the present invention through precipitating, washing, drying then.
2, the synthetic method of a kind of PBO/ carbon nano tube compound material according to claim 1 is characterized in that described rare gas element is a nitrogen.
3, the synthetic method of a kind of PBO/ carbon nano tube compound material according to claim 1, it is characterized in that described by the excessive terephthalic acid derivatives monomer of mole proportioning excessive＜5%.
4, the synthetic method of a kind of PBO/ carbon nano tube compound material according to claim 1, the derivative that it is characterized in that described terephthalic acid are terephthalic acid, p-phthaloyl chloride and poly-(terephthalic anhydride).
5, the synthetic method of a kind of PBO/ carbon nano tube compound material according to claim 1, the temperature rise rate that it is characterized in that described temperature programming are 5～10 ℃/2～4h.
6, the synthetic method of a kind of PBO/ carbon nano tube compound material according to claim 1 is characterized in that described carbon nanotube through dispersion treatment accounts for 1～10% of polymer quality.
7, the synthetic method of a kind of PBO/ carbon nano tube compound material according to claim 1 is characterized in that described carbon nanotube through dispersion treatment accounts for 3% of polymer quality.
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| Application Number | Priority Date | Filing Date | Title |
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| CN 03132512 CN1226326C (en) | 2003-07-18 | 2003-07-18 | Synthesis method of PBO/carbon nanometer pipe composite material |
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| CN 03132512 CN1226326C (en) | 2003-07-18 | 2003-07-18 | Synthesis method of PBO/carbon nanometer pipe composite material |
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| CN1478818A true CN1478818A (en) | 2004-03-03 |
| CN1226326C CN1226326C (en) | 2005-11-09 |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100430443C (en) * | 2006-08-02 | 2008-11-05 | 哈尔滨工业大学 | Preparation method for composite material of silicon resin and quartz fibrous coating with polybenzdioxazole |
| CN101338463B (en) * | 2008-08-08 | 2010-06-02 | 哈尔滨工业大学 | Method for preparing PBO/single-wall carbon nanotube composite fiber |
| CN101274983B (en) * | 2008-05-21 | 2010-06-02 | 哈尔滨工业大学 | Preparation for single wall carbon nano-tube monomer-containing compound for PBO polymerization |
| CN101338073B (en) * | 2008-08-08 | 2011-06-22 | 哈尔滨工业大学 | Process for preparing PBO/single-wall carbon nanotube polymer |
| CN102296376A (en) * | 2011-07-05 | 2011-12-28 | 深圳市中晟创新科技股份有限公司 | Production method of poly-p-phenylene benzodioxazole fibers |
| CN103014901A (en) * | 2012-12-12 | 2013-04-03 | 哈尔滨工业大学 | Preparation method of graphene/PBO (Poly-P-Phenylene Benzobisoxazazole) composite fiber |
| CN103923316A (en) * | 2014-04-28 | 2014-07-16 | 哈尔滨工业大学 | Carbon nano ring-grafted modified plumbous oxide (PBO) polymer and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101358385B (en) * | 2008-04-09 | 2011-02-23 | 北京服装学院 | Modified polybenzoxazole fiber and preparation method thereof |
-
2003
- 2003-07-18 CN CN 03132512 patent/CN1226326C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100430443C (en) * | 2006-08-02 | 2008-11-05 | 哈尔滨工业大学 | Preparation method for composite material of silicon resin and quartz fibrous coating with polybenzdioxazole |
| CN101274983B (en) * | 2008-05-21 | 2010-06-02 | 哈尔滨工业大学 | Preparation for single wall carbon nano-tube monomer-containing compound for PBO polymerization |
| CN101338463B (en) * | 2008-08-08 | 2010-06-02 | 哈尔滨工业大学 | Method for preparing PBO/single-wall carbon nanotube composite fiber |
| CN101338073B (en) * | 2008-08-08 | 2011-06-22 | 哈尔滨工业大学 | Process for preparing PBO/single-wall carbon nanotube polymer |
| CN102296376A (en) * | 2011-07-05 | 2011-12-28 | 深圳市中晟创新科技股份有限公司 | Production method of poly-p-phenylene benzodioxazole fibers |
| CN103014901A (en) * | 2012-12-12 | 2013-04-03 | 哈尔滨工业大学 | Preparation method of graphene/PBO (Poly-P-Phenylene Benzobisoxazazole) composite fiber |
| CN103014901B (en) * | 2012-12-12 | 2014-12-24 | 哈尔滨工业大学 | Preparation method of graphene/PBO (Poly-P-Phenylene Benzobisoxazazole) composite fiber |
| CN103923316A (en) * | 2014-04-28 | 2014-07-16 | 哈尔滨工业大学 | Carbon nano ring-grafted modified plumbous oxide (PBO) polymer and preparation method thereof |
| CN103923316B (en) * | 2014-04-28 | 2016-03-09 | 哈尔滨工业大学 | A kind of carbon nano ring graft modification PBO polymkeric substance and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN1226326C (en) | 2005-11-09 |
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