Kholin Kirill V, Sabirova Aigul F, Kadirov Danis M, Khamatgalimov Ayrat R, Khrizanforov Mikhail N, Nizameev Irek R, Morozov Mikhail V, Gainullin Radis R, Sultanov Timur P, Minzanova Salima T, Nefed'ev Eugene S, Kadirov Marsil K
Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Kazan 420088, Russia.
Department of Physics, Kazan National Research Technological University, Kazan 420015, Russia.
Membranes (Basel). 2023 Jun 30;13(7):635. doi: 10.3390/membranes13070635.
Sodium pectate derivatives with 25% replacement of sodium ions with nickel ions were obtained by carbonization to temperatures of 280, 550, and 800 °C, under special protocols in an inert atmosphere by carbonization to temperatures of 280, 550, and 800 °C. The 25% substitution is the upper limit of substitution of sodium for nickel ions, above which the complexes are no longer soluble in water. It was established that the sample carburized to 550 °C is the most effective active element in the hydrogen-oxidation reaction, while the sample carbonized up to 800 °C was the most effective in the oxygen-reduction reaction. The poor performance of the catalytic system involving the pectin coordination biopolymer carbonized up to 280 °C was due to loss of proton conductivity caused by water removal and mainly by two-electron transfer in one catalytic cycle of the oxygen-reduction reaction. The improved performance of the system with coordination biopolymer carbonized up to 550 °C was due to the better access of gases to the catalytic sites and four-electron transfer in one catalytic cycle. The (Ni-NaPG) sample contains metallic nickel nanoparticles and loose carbon, which enhances the electrical conductivity and gas capacity of the catalytic system. In addition, almost four-electron transfer is observed in one catalytic cycle of the oxygen-reduction reaction.
通过在惰性气氛中按照特殊规程将温度分别碳化至280、550和800℃,获得了钠离子被镍离子25%取代的果胶酸钠衍生物。25%的取代率是钠被镍离子取代的上限,超过此上限,配合物不再溶于水。已确定碳化至550℃的样品在氢氧化反应中是最有效的活性元素,而碳化至800℃的样品在氧还原反应中最有效。碳化至280℃的果胶配位生物聚合物催化体系性能不佳,这是由于脱水导致质子传导性丧失,主要是由于氧还原反应的一个催化循环中的双电子转移。碳化至550℃的配位生物聚合物体系性能的改善归因于气体更易到达催化位点以及一个催化循环中的四电子转移。(Ni-NaPG)样品包含金属镍纳米颗粒和疏松碳,这提高了催化体系的电导率和气体容量。此外,在氧还原反应的一个催化循环中观察到几乎四电子转移。