<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Solanki, Bhanupratap Singh</style></author><author><style face="normal" font="default" size="100%">Rode, V. Chandrashekhar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Selective hydrogenation of 5-HMF to 2,5-DMF over a magnetically recoverable non-noble metal catalyst</style></title><secondary-title><style face="normal" font="default" size="100%">Green Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">DEC</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">6390-6406</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A non-noble bimetallic catalyst Cu-Fe (1 : 2) was magnetically recoverable, highly selective and efficient for 5-(hydroxymethyl) furfural (5-HMF) hydrogenation to 2,5-dimethyl furan (DMF). The structure-activity correlation was established by characterising the prepared catalyst by XRD, XPS, TEM, ESEM, BET surface area, N-2-adsorption, NH3-TPD, pyridine-IR and H-2-TPR measurements. The high catalytic efficiency was attributed to the oxophilic nature and Lewis acidity of Fe, whereas the selectivity towards DMF was attributed to the Bronsted acidity of CuO and its affinity towards the C-O bond which was further confirmed by NH3-TPD and Py-IR analyses. XPS and XRD revealed the presence of Cu/CuFe2O4 species which catalyzed the hydrogenolysis pathway. TEM and SEM images evidenced the presence of a Cu-Fe nanomorph in which Cu/CuFe2O4 was present. The size of the Cu-Fe nanomorph was found to be between 15.4-17.6 nm. Under the optimised reaction conditions, the highest conversion of 97% and selectivity of 93% were achieved.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">23</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;
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</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Solanki, Bhanupratap Singh</style></author><author><style face="normal" font="default" size="100%">Roh, Hyun-Seog</style></author><author><style face="normal" font="default" size="100%">V. Rode, Chandrashekhar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Selective oxidation of 5-HMF to DFF over alkali promoted Mn nanocomposite</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Catalysis A-General</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">5-HMF</style></keyword><keyword><style  face="normal" font="default" size="100%">Biomass</style></keyword><keyword><style  face="normal" font="default" size="100%">heterogeneous catalyst</style></keyword><keyword><style  face="normal" font="default" size="100%">polyurethane</style></keyword><keyword><style  face="normal" font="default" size="100%">Selective oxidation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JUN</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">659</style></volume><pages><style face="normal" font="default" size="100%">119180</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Various compositions of Cs promoted Mn catalysts were synthesized and investigated for selective oxidation of 5HMF to DFF, among which Mn-Cs(80:20) was found to be most efficient giving 91 % conversion of 5-HMF and 99 % selectivity to DFF. Detail characterization like N2-sorption, BET surface area, TG-DTA, XRD, XPS, FE-SEM-EDX, TEM, HR-TEM, CO2-TPD, H2-TPR, O2-TPO, FTIR, Raman spectra and CH3OH-IR were done to establish structureactivity correlation. Enhanced surface area, porosity, thermal stability, dual morphologies were observed due to inclusion of Cs in Mn lattice domain which further enhanced the crystallinity, and oxygen diffusion on the surface. Mixed morphologies comprising nanoparticles (4-5 nm) and nanocubes (50-60 nm) were observed with enhanced redox potential and reduced work function due to weakening of Mn-O bonds. Significant increase in the basicity of catalyst, interfacial redox properties and lattice oxygen led to highly efficient oxidation of 5-HMF to DFF via Mars-van Krevelen mechanism at relatively milder conditions i.e. T = 90 degrees C and PO2= 200 psig. The catalyst was easily recyclable up to 7 times with minor loss in activity which was regenerated heat treatment protocol.&lt;/p&gt;
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	Foreign&lt;/p&gt;
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	5.5&lt;/p&gt;
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