Hamad Hesham, Bailón-García Esther, Morales-Torres Sergio, Carrasco-Marín Francisco, Pérez-Cadenas Agustín F, Maldonado-Hódar Francisco J
Carbon Materials Research Group, Department of Inorganic Chemistry, Faculty of Sciences, University of Granada, Avda, Fuente Nueva, s/n. ES18071 Granada, Spain.
Fabrication Technology Department, Advanced Technology and New Materials Research Institute (ATNMRI), City of Scientific Research and Technology Applications (SRTA-City), New Borg El-Arab City 21934, Egypt.
Nanomaterials (Basel). 2020 Apr 11;10(4):729. doi: 10.3390/nano10040729.
Carbon-Ti nanocomposites were prepared by a controlled two-step method using microcrystalline cellulose as a raw material. The synthesis procedure involves the solubilization of cellulose by an acid treatment (HPO or HNO) and the impregnation with the Ti precursor followed of a carbonization step at 500 or 800 °C. The type of acid treatment leads to a different functionalization of cellulose with phosphorus- or oxygen-containing surface groups, which are able to control the load, dispersion and crystalline phase of Ti during the composite preparation. Thus, phosphorus functionalities lead to amorphous carbon-Ti composites at 500 °C, while TiPO crystals are formed when prepared at 800 °C. On the contrary, oxygenated groups induce the formation of TiO rutile at an unusually low temperature (500 °C), while an increase of carbonization temperature promotes a progressive crystal growth. The removal of Orange G (OG) azo dye in aqueous solution, as target pollutant, was used to determine the adsorptive and photocatalytic efficiencies, with all composites being more active than the benchmark TiO material (Degussa P25). Carbon-Ti nanocomposites with a developed micro-mesoporosity, reduced band gap and TiO rutile phase were the most active in the photodegradation of OG under ultraviolet irradiation.
以微晶纤维素为原料,采用可控两步法制备了碳钛纳米复合材料。合成过程包括通过酸处理(HPO或HNO)使纤维素溶解,并用钛前驱体浸渍,随后在500或800℃下进行碳化步骤。酸处理的类型导致纤维素与含磷或含氧表面基团发生不同的官能化,这些表面基团能够在复合材料制备过程中控制钛的负载量、分散性和晶相。因此,磷官能团在500℃时导致形成无定形碳钛复合材料,而在800℃制备时形成TiPO晶体。相反,含氧基团在异常低的温度(500℃)下诱导形成TiO金红石,而碳化温度的升高促进晶体的逐步生长。以水溶液中的橙色G(OG)偶氮染料作为目标污染物的去除来测定吸附和光催化效率,所有复合材料都比基准TiO材料(德固赛P25)更具活性。具有发达微介孔结构、减小的带隙和TiO金红石相的碳钛纳米复合材料在紫外光照射下对OG的光降解最具活性。