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Functionalized Nanomaterials for Catalytic Application


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Sono assisted | Chemical precipitation UV pH (10.5) | 90 min VBR (> 95%) | 6 Langmuir-Hinshelwood | pseudo-1st-order [209] ZnS: Fe QDs (Capping agent: 2-ME) Chemical precipitation UV pH (8.0) | 90 min MG (98%) | 6 Langmuir-Hinshelwood | pseudo-1st-order [210]

      1.5.1 Carbon-Based FNMs as Photocatalysts

       1.5.1.1 CNT-Based FNMs

      In a similar manner, ZnO/NiO coated MWCNTs photocatalytically degraded (azo dye) MO efficiently, where a comparative study was done by the authors at different combinations of the trio component, at pH 7, for 6 h, using UV (280 nm) and visible radiation (480 nm) [131]. Exposure of hydrothermally formed TiO2-NRs/CNTs/braced with FeCo-Al2O3 catalytic agent was a potent remover of MB (97.5%), when the medium was photocatalytically degraded by natural sunlight, was later proved for its sustainability up to six trials with lesser doses in kinetic runs [132]. In a different situation, functionalized MWCNTs/TiO2 got by sol-gel method as per the reporters of El-Sayed, B.A. et al. had a versatile photocatalytic decomposition under variable conditions of sunlight, UV, and Xenon light-irradiation. Later, these were proven for their activity over the textile dye effluents Vat Green dyes and Dianix Blue dye in different trial runs [133].

       1.5.1.2 Fullerene-Based FNMs

       1.5.1.3 Graphene (G)/Graphene Oxide (GO)–Based FNMs

      The supply of graphene/graphene oxide–based functionalization resolves the constraints delivered by metal oxide PCs. Of late, attentions are focused on FNMs of graphene/graphene oxide–based semi-conductor materials as functionalized PC due to their smaller size with larger specific surface area supported by high electron (e) conductivity and high adsorption capacity [141]. Advanced research work has been augmented on MO-G/GO FMNs photocatalytic systems [142] for oxidativereduction of pollutants (BG) [143] and (MB) [144]. The unstable and aggregation tendency of the NMs are retarded by the advantages raised due to FNMs.

      In one of their studies, researchers Rao, G. et al. synthesized TiO2-NW/Fe2O3-NP/GO FNM sheets by colloid-blending scheme, where the material was found to have 93% efficacy in getting rid of humic acid from water photocatalytically at a pH 6. TiO2 furnished h+ required for ·OH and GO the e needed for ·O2− needed for the activity [145]. GO/MCU-C3N4/PVDF materials synthesized by vacuumized self-assembly and cross-linking process had exceptional self-cleaning property, which was proven fit for separating oil-in-water colloidal emulsions. Photocatalytic degrading capabilities were attributed to the e transferences from CB (1.61 eV) to VB (1.18 eV), with π-π* transition giving h+ in VB. h+, ·O2−, and ·OH were controllers in the reaction for eradicating oil-foulants as observed by the researchers Shi, Y. et al. [146].

      Scientific workers Gnanamoorthy, G. et al. synthesized AF-Bi2Sn2O7/rGO (AF-amine functionalized) FNMs for photocatalytic degradation of organic dye MB in the visible region was 75% (20 min). Bandgap between pure (2.6 eV) and FNMs (1.6 eV) decreased. VB with h+ and CB with e that favored the reaction were supported by the formation of radicals ·O2− and ·OH. Stability and reusability of FNMs were persistent up to four cycles [147]. In one of their methods, the authors Liu, H. et al. used FNMs of Bi2Sn2O7/RGO to reduce and degrade Rh B and phenol photocatalytically in the bright visible region (420 nm) and noticed that the degrading efficiencies were 95.8% (125 min) and 81.1% (200 min) for Rh B and phenol, respectively. On embedding RGO on Bi2Sn2O7 (pure), they observed that there was a decrease in the bandgap from 2.48 eV (pure) to 1.85 eV FNM which served well for degrading the contaminant, where the active radicals involved for the reaction was h+ and ·OH [148].

       1.5.1.4 Graphene-Carbon Nitride/Metal or Metalloid Oxide–Based FNMs

      Recently, conjugation of C and N in a metal-free graphitic polymer is a hotspot that captivates the research workers to utilize the visible energy for the receptive photocatalytic zone in redemption of water pollutants [149]. Normally, hetero-junctions of g-C3N4–based PC are obtained by fusing g-C3N4 (semiconductor) PC and a co-catalyst (semiconductor). Significantly, type II hetero-junction and Z-scheme PC are predominantly employed by many co-workers for removing OPs. Z-scheme have been extensively utilized in BiOI/Pt/g-C3N4 [150], MoO3/g-C3N4 [151], g-C3N4/FeWO4 [152], g-C3N4/Ag/MoS2 [153], TiO2/g-C3N4