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Nitrogen-enriched carbon nanofibers containing Cu-loaded porous carbon beads for the abatement of NO emissions Bhaskar Bhaduri1 and Nishith Verma1,2 1 Department of Chemical Engineering, Indian Institute of Technology Kanpur, Kanpur (India) 2 Center for Environmental Science and Engineering, Indian Institute of Technology Kanpur, Kanpur (India) Experimental Set-up SEM and EDX Introduction Various stationary and mobile sources such as thermal power plants, nitric acid plants, and automobiles emit significant amounts of nitric oxide (NO), responsible for several environmental hazards such as acid rain, photochemical smog, and the depletion of ozone layer. Among several methods used for the abatement of NO emissions, selective catalytic reduction (SCR) has been extensively studied using ammonia, urea, and hydrocarbon gases as the reducing agents. A wide variety of catalysts containing noble metals, transition metal oxides, and zeolites modified with metals have been used for the SCR of NO. Schematic illustration of the experimental set-up used for catalyst activity test SEM images of (a) CBs, (b) Cu-CBs and (c) Cu-CNFs/CBs, (d) EDX spectra of Fig. c SEM images of (a-a/) N-Cu-CNFs/CBs, (b-b/) NO exposed N-Cu-CNFs/CBs. Fig. c shows the EDX spectra of NO exposed N-Cu-CNFs/CBs. Characterization Techniques XPS and Raman analysis The prepared materials were characterized using several analytical and spectroscopic techniques such as atomic absorption spectroscopy (AAS), scanning electron microscopy (SEM), temperature programmed reduction (TPR) and so on. Objective Results and Discussion Catalytic activity studies Synthesis of N-enriched Cu nanoparticles grown carbon nanofibers (CNFs) containing porous carbon beads (CBs) for the removal of NO emissions by reduction. Reaction Conditions: TPR analysis (W = 0.5 g, CNO = 400 ppm, reaction time = 5 h) Optimum reduction temperature for the reduction of CuxOy -CBs is 270 oC Schematic for Material Preparation Interaction of NO molecules with the catalyst Cu NPs CBs CNF N+ e- +2 NO + Heat - Hyponitrite species N2 XRD Pattern Scherrer Equation: r (nm) = Kλ/βCosθ Avg. Cu crystallite size rages from 19- 37 nm Conclusions Cu NPs-doped porous activated carbon beads (~0.8 mm) decorated with CNFs were synthesized. The Cu NPs in situ incorporated into the PVA polymeric matrix during the synthesis step acted as the CVD catalyst for growing the CNFs. The high catalytic activity of the material was attributed to the combined roles of the catalytic Cu NPs, reactive CNFs, large N-contents of the material, and the porous activated carbon bead. AAS measurements to evaluate Cu loadings of the prepared materials Materials loadings (mg/g) PhB - Cu_PhB 3.4 CuxOy-CB 20.0 Cu-CNF/CB 14.0 Textural properties of the prepared materials Sample SBET (m2/g) VT (cm3/g) PSD (%) Micro Meso Macro PhB Cu-PhB 1.97 0.50 0.001 CB (without pre- oxidation) 998 0.531 88.17 5.24 6.59 CB (with pre-oxidation) 1748 0.918 78.48 8.26 13.26 CuxOy-CB Cu-CB 1056 1172 0.568 0.615 75.82 72.40 9.28 12.19 14.90 15.41 Cu-CNF/CB 733 0.462 70.12 15.88 14.00 N-Cu-CNF/CB 648 0.411 69.51 12.23 18.26 References B. Bhaduri, N. Verma. Preparation of asymmetrically distributed bimetal CeO2 and Cu NPs in nitrogen-doped ACF/CNF for the removal of NO by reduction. Journal of Colloid and Interface Science 436 (2014)
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