Villora-Picó Juan-José, Sepúlveda-Escribano Antonio, Pastor-Blas María-Mercedes
Laboratory of Advanced Materials, Department of Inorganic Chemistry-University Institute of Materials of Alicante, University of Alicante, P.O. Box 99, E-03080 Alicante, Spain.
Int J Mol Sci. 2024 Feb 21;25(5):2515. doi: 10.3390/ijms25052515.
Metal-free catalysts based on nitrogen-doped porous carbons were designed and synthesized from mixtures of melamine as nitrogen and carbon sources and calcium citrate as carbon source and porogen system. Considering the physicochemical and textural properties of the prepared carbons, a melamine/citrate ratio of 2:1 was selected to study the effect of the pyrolysis temperature. It was observed that a minimum pyrolysis temperature of 750 °C is required to obtain a carbonaceous structure. However, although there is a decrease in the nitrogen amount at higher pyrolysis temperatures, a gradual development of the porosity is produced from 750 °C to 850 °C. Above that temperature, a deterioration of the carbon porous structure is produced. All the prepared carbon materials, with no need for a further activation treatment, were active in the hydrogenation reaction of 1-chloro-4-nitrobenzene. A full degree of conversion was reached with the most active catalysts obtained from 2:1 melamine/citrate mixtures pyrolyzed at 850 °C and 900 °C, which exhibited a suitable compromise between the N-doping level and developed mesoporosity that facilitates the access of the reactants to the catalytic sites. What is more, all the materials showed 100% selectivity for the hydrogenation of the nitro group to form the corresponding chloro-aniline.
基于氮掺杂多孔碳的无金属催化剂是由三聚氰胺作为氮源和碳源以及柠檬酸钙作为碳源和致孔剂体系的混合物设计合成的。考虑到所制备碳材料的物理化学和结构性质,选择三聚氰胺/柠檬酸盐比例为2:1来研究热解温度的影响。观察到需要至少750℃的热解温度才能获得含碳结构。然而,尽管在较高热解温度下氮含量会降低,但从750℃到850℃会逐渐产生孔隙率的发展。高于该温度,会产生碳多孔结构的劣化。所有制备的碳材料无需进一步活化处理,在1-氯-4-硝基苯的氢化反应中都具有活性。由在850℃和900℃热解的2:1三聚氰胺/柠檬酸盐混合物获得的最活性催化剂实现了完全转化,这些催化剂在氮掺杂水平和发达的介孔率之间表现出合适的平衡,有利于反应物进入催化位点。此外,所有材料对硝基氢化形成相应的氯苯胺均表现出100%的选择性。