Neutral aqueous system liquid flow battery system
A technology of flow battery and flow battery stack, which is applied to fuel cells, regenerative fuel cells, circuits, etc., can solve the problems of prone to water electrolysis side reactions, limited solubility of active materials, and easy cross-contamination of electrolytes, and achieves cost-effectiveness. Low, high solubility, high safety performance
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Embodiment 1
[0078] Synthesis of 1,1'-bis(3-(trimethylamino)propyl)-[4,4'-bipyridyl]tetrabromosalt
[0079] 0.47g (3.0mmol) of 4,4'-bipyridine and 1.27g (7.0mmol) of (3-bromopropyl)trimethylammonium bromide were mixed and dissolved in 30mL of acetonitrile. The temperature was raised slowly to reflux, and a light yellow solid was produced after 24 hours of reflux. Then the reaction solution was left standing overnight in the refrigerator. The precipitated product was filtered, washed and dried with ethanol, and recrystallized with methanol / ethanol (1:1, v / v) to obtain a solid. The product was characterized by NMR, and 1.43 g of the product was obtained with a yield of 92%.
[0080] Pale yellow solid, 1 HNMR (400MHz,D 2 O), δ9.25(d, J=7.0Hz, 4H), 8.67(d, J=6.9Hz, 4H), 5.04–4.85(m, 4H), 3.77–3.54(m, 4H), 3.24(s ,18H),2.87–2.60(m,4H); 13 C NMR (101MHz, D 2 O) δ 150.58, 145.73, 127.59, 62.43, 58.29, 53.30, 24.67.
Embodiment 2
[0082] Synthesis of (3-(trimethylamino)propyl)-[4,4'-bipyridyl]tribromide
[0083] 0.47g (3.0mmol) of 4,4'-bipyridine and 0.54g (3.0mmol) of (3-bromopropyl)trimethylammonium bromide were mixed and dissolved in 30mL of acetonitrile. The temperature was raised slowly to reflux, and a white solid was produced after reflux for 24 hours. Then the reaction solution was left standing overnight in the refrigerator. The precipitated product was filtered, washed and dried with ethanol, and recrystallized with methanol / ethanol (1:1, v / v) to obtain a solid. The product was characterized by NMR, and 0.91 g of the product was obtained with a yield of 90%.
[0084] white solid, 1 H NMR (400MHz,D 2 O)δ9.10(d, J=6.9Hz, 2H), 8.90–8.63(m, 2H), 8.48(d, J=6.9Hz, 2H), 8.04–7.80(m, 2H), 4.86(t, J=7.7Hz, 2H), 3.78–3.49(m, 2H), 3.25(s, 9H), 2.89–2.46(m, 2H); 13 C NMR (101MHz, D 2 O) δ154.32, 150.02, 144.99, 142.27, 126.45, 122.55, 62.50, 57.73, 53.35, 24.66.
Embodiment 3
[0086] Synthesis of 1,1'-bis(4-bromobutyl)-[4,4'-bipyridyl]dibromide
[0087] 0.47g (3.0mmol) of 4,4'-bipyridine and 1.51g (7.0mmol) of 1,4-dibromobutane were mixed and dissolved in 30mL of acetonitrile. The temperature was raised slowly to reflux, and a light yellow solid was produced after 24 hours of reflux. Then the reaction solution was left standing overnight in the refrigerator. The precipitated product was filtered, washed and dried with ethanol, and recrystallized with methanol / ethanol (1:1, v / v) to obtain a solid. The product was characterized by NMR, and 1.66 g of the product was obtained with a yield of 94.1%.
[0088] Pale yellow solid, 1 HNMR (400MHz,D 2 O), δ9.21(t, J=6.2Hz, 4H), 8.63(d, J=5.5Hz, 4H), 5.06–4.70(m, 7H), 3.60(t, J=6.4Hz, 2H), 2.52–2.20(m,4H),2.19–1.91(m,2H); 13 C NMR (101MHz,D 2 O) δ145.59, 127.38, 127.19, 61.33, 33.27, 29.41, 28.53.
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