Carbon material precursor and method for producing carbon material using the same
a carbon material and precursor technology, applied in the direction of carbon preparation/purification, etc., can solve the problem of low carbonization yield of carbon material precursor prepared using polyacrylamide, and achieve high carbonization yield, high carbonization yield, and enhanced carbonization yield of carbon material precursor
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synthetic example 1
[0032]Dissolved into 190 ml of water was 8.52 g (120 mmol) of acrylamide (manufactured by Wako Pure Chemical Industries, Ltd. and for electrophoresis). After that, 366 mg (1.20 mmol) of 4,4′-azobis(4-cyanovaleric acid) was added as a polymerization initiator, followed by radical polymerization for 3 hours at 70° C. The obtained aqueous solution was introduced into methanol, followed by precipitation of polyacrylamide. Polyacrylamide was collected and subjected to vacuum drying.
example 1
[0033]Polyacrylamide obtained in Synthetic Example 1 was dissolved into water so as to be a concentration of 10% by mass. Phosphoric acid was added to the obtained polyacrylamide aqueous solution so that the content of phosphoric acid was 2% by mass relative to 100% by mass of carbon material precursor. Freeze drying was performed using the obtained phosphoric acid-containing polyacrylamide aqueous solution. As a result, a carbon material precursor containing polyacrylamide and phosphoric acid was obtained.
example 2
[0034]A carbon material precursor was obtained in the same manner as that in Example 1 except that diammonium hydrogen phosphate was used instead of the phosphoric acid. Note that the content of diammonium hydrogen phosphate was 2% by mass relative to 100% by mass of carbon material precursor.
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