Polyarylene sulfide resin composition
A technology of polyarylene sulfide and resin composition, which is applied in the field of polyarylene sulfide resin composition, can solve the problems of reduced mechanical properties, lack of sufficient functional groups, low adhesion of filling materials, etc., and achieve high melting point, The effect of dramatic improvement in chemical resistance
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[0171] Hereinafter, the method of the present invention will be described more concretely by way of examples and comparative examples, but the present invention is not limited only to these examples. In addition, the measuring method of a physical property is as follows.
[0172] [Carboxyl content]
[0173] The carboxyl group content of the PAS resin was calculated using a Fourier transform infrared spectrometer (hereinafter abbreviated as FT-IR).
[0174] First, measure benzoic acid as a standard substance by FT-IR, and read 3066 cm as the absorption of the C-H bond of the benzene ring -1 The absorption intensity of the peak (b1) and 1704cm as the absorption of the carboxyl group -1 From the absorption intensity (c1) of the peak of , the amount of carboxyl group (U1) relative to one unit of the benzene ring was obtained, (U1)=(c1) / [(b1) / 5]. Next, the PAS resin was melt-pressed at 320° C. for 1 minute, then quenched, and FT-IR measurement of the resulting amorphous film was...
Synthetic example 1
[0200] [Synthesis Example 1 (Synthesis of PPS-1)]
[0201] In a 70-liter autoclave with a stirrer and a bottom plug valve, add 47.5% sodium hydrosulfide 8.26kg (70.00 moles), 96% sodium hydroxide 3.03kg (72.69 moles), N-methyl-2-pyrrolidone (NMP ) 11.45 kg (115.50 moles) and 5.50 kg of ion-exchanged water, while passing nitrogen gas under normal pressure, the reaction vessel was slowly heated to 225° C. for about 3 hours to perform the dehydration process. Heating was terminated when 9.82 kg of water and 0.28 kg of NMP distilled out, and cooling was started. The amount of water remaining in the system per 1 mol of the alkali metal hydrosulfide added at this time was 1.01 mol including the water consumed by the hydrolysis of NMP. In addition, since the amount of hydrogen sulfide scattered was 1.4 mol, the amount of the sulfidizing agent in the system after this dehydration step was 68.6 mol. In addition, 1.4 moles of sodium hydroxide were regenerated in the system with the sc...
Synthetic example 2
[0208] [Synthesis Example 2 (Synthesis of PPS-2)]
[0209] The same operation as in Synthesis Example 1 was performed except that Step 1 and Step 2 were performed under the following reaction conditions.
[0210] The temperature was raised from 230°C to 238°C over 13 minutes at 0.6°C / min. The reaction was performed at a constant temperature of 238°C for 128 minutes, and then the temperature was raised from 238°C to 245°C over 9 minutes at 0.8°C / min. T1 is 188 minutes and T1a is 150 minutes. The conversion of p-DCB was 94.5%.
[0211] Following Step 1, the temperature was raised from 245°C to 255°C over 12 minutes at 0.8°C / min. The polymerization time (T2) of the process 2 was 12 minutes.
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