Polymer matrix composite material with high PTC strength and stability and preparation method thereof
A technology of composite materials and polymers, which is applied in the field of PTC composite materials and its preparation, can solve the problems that it is difficult to realize the control of material structure and evolution of materials, the electrothermal performance of polymer PTC products is not stable enough, and the function of electronic devices is difficult to realize. Good repetitive stability, significant PTC performance, and NTC effect reduction effect
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example 1
[0027] (1) Dissolve 0.06g of titanate coupling agent in 50ml of ethanol, and stir it with magnetic force to fully dilute it evenly. Put 6g of CB into titanate coupling agent solution, modify it with 1% coupling agent by mass fraction, ball mill for 2h, and then put it in an oven at 120°C to evaporate the solvent. The dried CB was placed in a vacuum oven, evacuated at 120°C for 1 hour, and allowed to fully react and dry to obtain the desired surface-functionalized CB;
[0028] (2) Weigh 34.37g of PVDF, 17.95g of UHMWPE, and 2.98g of CB (f CB =4%) and 0.52 g of antioxidant 1010. In the Hakke Torque Rheometer, first, the molten PVDF was heated for 2 minutes; then UHMWPE and Antioxidant 1010 were added. Mix the mixture of the two bases for 10 minutes; then add CB in batches, and knead for 15 minutes at 250°C; after the melt blending is completed, discharge;
[0029] (3) The composite material obtained in step (2) was kept at 250°C and 18MPa for 10 minutes at constant temperatur...
example 2
[0039] (1) The surface treatment process of the CB particles is the same as in Example 1.
[0040] (2) Dissolve 0.06g of titanate coupling agent in 50ml of ethanol, and stir it with magnetic force to fully dilute it evenly. Put 6g of CB into the titanate coupling agent solution, ultrasonically disperse it for 2h, and then put it in an oven at 120°C to evaporate the solvent. The dried MWNTs were placed in a vacuum oven, evacuated and kept at 120°C for 1 hour to allow them to fully react and dry to obtain the desired surface-functionalized MWNTs;
[0041] (2) Weigh 34g of PVDF, 17.77g of UHMWPE, 0.52g of antioxidant 1010, and 2.98g of CB (f CB =4%), and the MWNT (f MWNT= 1%). In the Hakke torque rheometer, first, heat and melt PVDF for 2 minutes; then add UHMWPE and antioxidant 1010, and mix the mixture of the two matrices for 10 minutes; then add CB and MWNT in batches, and mix for 15 minutes at 250°C Minutes; after the melt blending is completed, discharge;
[0042] (3) P...
example 3
[0046] (1) The surface treatment process of CB particles is the same as Example 1, and the surface treatment process of MWNT is the same as Example 2.
[0047] (2) Weigh 33.65g PVDF, 17.58g UHMWPE, 0.51g antioxidant 1010 and 2.98g CB (f CB =4%), and the MWNT (f MWNT = 2%). In the Hakke torque rheometer, first, heat and melt PVDF for 2 minutes; then add UHMWPE and antioxidant 1010, and mix the mixture of the two matrices for 10 minutes; then add CB and MWNT in batches, and mix for 15 minutes at 250°C Minutes; after the melt blending is completed, discharge;
[0048] (3) Put the composite material obtained in step (2) on a hot press at 250°C and 18MPa under constant temperature and pressure for 10 minutes, cool naturally, and press it into (MWNT / CB) co-filled (PVDF / CB) with a thickness of 1mm and a diameter of 12mm. UHMWPE)((MWNT / CB)-co-filled-(PVDF / UHMWPE))(f CB = 4%, f MWNT =2%) of the disc sample;
[0049] (4) Coat the two ends of the sample obtained in step (3) with co...
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