<?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%">Dandekar, M. S.</style></author><author><style face="normal" font="default" size="100%">Arabale, G.</style></author><author><style face="normal" font="default" size="100%">Vijayamohanan, K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation and characterization of composite electrodes of coconut-shell-based activated carbon and hydrous ruthenium oxide for supercapacitors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Power Sources</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">activated carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">Composite</style></keyword><keyword><style  face="normal" font="default" size="100%">Electrochemical characterization</style></keyword><keyword><style  face="normal" font="default" size="100%">pseudocapacitance</style></keyword><keyword><style  face="normal" font="default" size="100%">specific capacitance</style></keyword><keyword><style  face="normal" font="default" size="100%">supercapacitor</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style  face="normal" font="default" size="100%">FEB</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">1</style></number><publisher><style face="normal" font="default" size="100%">ELSEVIER SCIENCE BV</style></publisher><pub-location><style face="normal" font="default" size="100%">PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS</style></pub-location><volume><style face="normal" font="default" size="100%">141</style></volume><pages><style face="normal" font="default" size="100%">198-203</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The relationship between the structure-specific capacitance (F g(-1)) of a composite electrode consisting of activated coconut-shell carbon and hydrous ruthenium oxide (RuOx(OH)(y)) has been evaluated by impregnating various amounts of RuOx(OH)(y) into activated carbon that is specially prepared with optimum pore-size distribution. The composite electrode shows an enhanced specific capacitance of 250 F g(-1) in 1 M H2SO4 with 9 wt.% ruthenium incorporated. Chemical and structural characterization of the composites reveals a homogeneous distribution of amorphous RuOx(OH)(y) throughout the porous network of the activated carbon. Electrochemical characterization indicates an almost linear dependence of capacitance on the amount of ruthenium owing to its pseudocapacitive nature. (C) 2004 Elsevier B.V. All rights reserved.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</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;</style></custom3><custom4><style face="normal" font="default" size="100%">6.333</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%">Mane, Rasika B.</style></author><author><style face="normal" font="default" size="100%">Patil, S.</style></author><author><style face="normal" font="default" size="100%">Shirai, Masayuki</style></author><author><style face="normal" font="default" size="100%">Rayalu, Sadhana S.</style></author><author><style face="normal" font="default" size="100%">Rode, Chandrashekhar V.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of carbon based supports on selectivity behavior of diols and propanol in Ru catalyzed glycerol hydrogenolysis</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Catalysis B: Environmental</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">activated carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">Amorphous carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">catalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Glycerol</style></keyword><keyword><style  face="normal" font="default" size="100%">Glycerol conversions</style></keyword><keyword><style  face="normal" font="default" size="100%">Glycerol hydrogenolysis</style></keyword><keyword><style  face="normal" font="default" size="100%">graphite composites</style></keyword><keyword><style  face="normal" font="default" size="100%">Graphite supports</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogenolysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrolysis</style></keyword><keyword><style  face="normal" font="default" size="100%">layered structures</style></keyword><keyword><style  face="normal" font="default" size="100%">Particle size</style></keyword><keyword><style  face="normal" font="default" size="100%">Product distributions</style></keyword><keyword><style  face="normal" font="default" size="100%">Propanediols</style></keyword><keyword><style  face="normal" font="default" size="100%">Propanol</style></keyword><keyword><style  face="normal" font="default" size="100%">Selectivity behavior</style></keyword><keyword><style  face="normal" font="default" size="100%">Structural characteristics</style></keyword><keyword><style  face="normal" font="default" size="100%">Structural effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Structural effects</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAY</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">204</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Activated carbon (AC) and three graphite materials were studied as supports for Ru catalyzed glycerol hydrogenolysis to propanediols and 1-propanol. Structural characteristics of AC and graphite materials were found to greatly affect the reducibility and particle size of supported Ru and hence, the activity and product distribution in glycerol hydrogenolysis. XRD of graphite materials showed distinctly (002) plane having highly organized layered structure and the peak intensity decreased in the order of Ru/KS150 &amp;gt; Ru/HSAG100 &amp;gt; Ru/KS6 due to decrease in the graphite sheet thickness. In Raman, the intense D band in HSAG100 compared to that in KS6 and KS150 samples indicated its highly amorphous nature or mixed carbon hybridization. Glycerol conversion for Ru on AC was higher than that on graphite and among different graphites, it showed a descending activity order of Ru/KS6 &amp;gt; Ru/HSAG100 &amp;gt; Ru/KS150. The product distribution for AC and HSAG100 supported Ru was similar, giving 1-propanol (45%) alongwith 1,2-propanediol (1,2-PDO) (37%) and 1,3-propanediol (1,3-PDO) (9–11%). For graphite supports, availability of Ru although bigger in size (4–5 nm), would be higher on the surface than in case of AC which formed deep hydrogenolysis products like 1-, 2- propanol, ethanol etc.&lt;/p&gt;</style></abstract><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">11.698</style></custom4><section><style face="normal" font="default" size="100%">134-146</style></section></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%">Jadhav, A.</style></author><author><style face="normal" font="default" size="100%">Mohanraj, G.T.</style></author><author><style face="normal" font="default" size="100%">Gokarn, A.</style></author><author><style face="normal" font="default" size="100%">Mayadevi, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis of biomass waste derived activated carbon-NBR composites for automobile application</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry and Chemical Technology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">activated carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">composites</style></keyword><keyword><style  face="normal" font="default" size="100%">hardness</style></keyword><keyword><style  face="normal" font="default" size="100%">NBR</style></keyword><keyword><style  face="normal" font="default" size="100%">Phosphoric acid</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">236-243</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;This paper reports on usability of activated carbon obtained from areca nut shell, coconut shell, and coconut leaves as a filler to prepare NBR based composite for automobile based application. The carbon was activated by phosphoric acid (H3PO4) as dehydrating agent. The stoichiometric ratio of biomass and phosphoric acid was found to be 3:1 for the batch size of 300 g. As compared to commercially available carbon filler, the activated carbon derived from biomass waste responded better to the petrol swelling test. Among three biomass waste sources, namely, areca nut shell, coconut shell, and coconut leaves, activated carbon derived from coconut shell was appeared to be the best for percent swelling and percent deviation in hardness. The results obtained are confirmed by proximate analysis.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Journal Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;3.135&lt;/p&gt;</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%">Jadhav, Abhijit</style></author><author><style face="normal" font="default" size="100%">Mohanraj, Govindraj</style></author><author><style face="normal" font="default" size="100%">Gokarn, Ashok</style></author><author><style face="normal" font="default" size="100%">Mayadevi, Susheeladevi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ferets diameter estimation of activated carbon for effluent treatment application</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Indian Chemical Society</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">activated carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">Arecanut shell</style></keyword><keyword><style  face="normal" font="default" size="100%">Phosphoric acid</style></keyword><keyword><style  face="normal" font="default" size="100%">teret diameter</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">96</style></volume><pages><style face="normal" font="default" size="100%">1067-1074</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In this paper, activated carbon was produced of by chemical activation with phosphoric acid of agricultural wastes such as Arecanut shell of 25 micronmeter at 400 degrees C by slow pyrolysis. The BET surface area and iodine number surface area is calculated and compared. The FTIR spectra show the presence of activated carbon. The TGA revealed, activated carbon is thermally stable at 480 degrees C. The SEM shows the incorporation of activated carbon particles leads to the systematic change in morphology of activated carbon. Surface area plot shows the details of morphological change caused by iodine number surface area. Ferets diameter is estimated to know circularity of the particle. Methylene blue number, acid adsorption value is calculated to know adsorption capacity of the carbon. Thus results proves selection of ferets diameter, activation temperature, and impregnation ratio is important in determining the quality of activated carbon obtained and its use in industrial waste water treatment.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">8</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;Indian&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;0.158&lt;/p&gt;
</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%">Sharma, Preeti</style></author><author><style face="normal" font="default" size="100%">Sharma, Geeta</style></author><author><style face="normal" font="default" size="100%">Punia, Rajesh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis of graphene from activated carbon at liquid nitrogen temperature and its detailed structural analysis</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Physics A-Materials Science &amp; Processing</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">activated carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">Amorphous carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">graphene</style></keyword><keyword><style  face="normal" font="default" size="100%">H-2 storage applications</style></keyword><keyword><style  face="normal" font="default" size="100%">Raman spectroscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Supercapacitors</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAY</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">127</style></volume><pages><style face="normal" font="default" size="100%">319</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The present study deals with the synthesis of graphene using thermal quenching of pre-heated activated carbon (a-C) (1370 K for 3 h) at liquid nitrogen temperature and its detailed structural analysis using XRD, TEM, FTIR and Raman spectroscopy. The analysis of lattice parameters (L-a, L-c,L- and d) of constituent nanographitic domains using XRD shows restoration of graphene-like structure in the resultant product (a-CL). TEM image reveals porosity and partially crystallinity (from SAED) in a-C. While thin layers of graphene are observed in the TEM images of a-CL Deconvoluted Raman spectra have been used to investigate the evolution of crystalline behaviour of a-C with temperature in view of Ferrari and Robertson's three-stage model. The evolution of G peak and increase in I-D/I-G reveals restoration of crystallinity in a-CL. The development of the D peak indicates disordering of graphite but ordering of amorphous carbon. The reported method is technologically beneficial for graphene synthesis for large number of applications such as supercapacitors, H-2 storage, gas separation and purification.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</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;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;1.810&lt;/p&gt;</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%">Patil, Suryakant A.</style></author><author><style face="normal" font="default" size="100%">Suryawanshi, Umesh P.</style></author><author><style face="normal" font="default" size="100%">Harale, Namdev S.</style></author><author><style face="normal" font="default" size="100%">Patil, Sandip K.</style></author><author><style face="normal" font="default" size="100%">Vadiyar, Madgonda M.</style></author><author><style face="normal" font="default" size="100%">Luwang, Meitram N.</style></author><author><style face="normal" font="default" size="100%">Anuse, Mansing A.</style></author><author><style face="normal" font="default" size="100%">Kim, Jin H.</style></author><author><style face="normal" font="default" size="100%">Kolekar, Sanjay S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Adsorption of toxic Pb(II) on activated carbon derived from agriculture waste (Mahogany fruit shell): isotherm, kinetic and thermodynamic study</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Environmental Analytical Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">activated carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">Adsorption</style></keyword><keyword><style  face="normal" font="default" size="100%">mahogany fruit shell</style></keyword><keyword><style  face="normal" font="default" size="100%">Pb(II)</style></keyword><keyword><style  face="normal" font="default" size="100%">sulphuric acid</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</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%">102</style></volume><pages><style face="normal" font="default" size="100%">8270-8286</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;An adsorbent, mahogany fruit shell activated carbon(MFSAC), was derived from environmental friendly raw material, i.e. agriculture waste and explored for bench scale adsorption of toxic Pb(II). A facile MFSAC material was synthesised using a chemical activation method using concentrated sulphuric acid as an impregnating (activating) reagent. So derived adsorbent material was characterised by FTIR, XRD, BET, SEM, EDAX, TGA and XPS techniques to know the properties and plausible adsorption mechanism. Bench scale adsorption of toxic Pb(II) and maximum adsorption capacity of MFSAC were exhibited through batch adsorption experiments. The effect of physico-chemical parameters such as pH (1-7), MFSAC amount (0.5-5.0 g L-1), Pb(II) concentration (200-1000 mgL(-1)), contact period (60-600 min) and orbital shaking speed (60-200 rpm) was studied for maximum removal of Pb(II) upto 99.70 +/- 0.17%. The experimental data follow the Langmuir adsorption isotherm with a maximum monolayer adsorption capacity 322.28 mg g(-1)and pseudo-second-order kinetic uptake rate. The thermodynamic and temperature study revealed that the adsorption process was spontaneous and endothermic in nature (Delta H-o = 43.37 kJ mole(-1), Delta S-o = 158.02 J mol(-1)K(-1)). Most importantly, the MFSAC adsorbent was successfully regenerated and reused with conspicuous performance up to five consecutive cycles. The bench-scale adsorption with simple synthesis route, good stability and remarkable regeneration capability makes the MFSAC as an encouraging adsorbent for wastewater treatment.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">19</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;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;2.731&lt;/p&gt;
</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%">Bobade, Rushikesh G.</style></author><author><style face="normal" font="default" size="100%">Dabke, Niteen B.</style></author><author><style face="normal" font="default" size="100%">Shaikh, Shoyebmohamad F.</style></author><author><style face="normal" font="default" size="100%">Lokhande, Balkrushna J.</style></author><author><style face="normal" font="default" size="100%">Mane, Rajaram S.</style></author><author><style face="normal" font="default" size="100%">Ambare, Revanappa C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Facile chemical synthesis of BaO:MgO nanorods for designing distinctive solid-state asymmetric supercapacitor device with activated carbon</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Energy Storage</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">activated carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">ASSD device</style></keyword><keyword><style  face="normal" font="default" size="100%">BaO:MgO</style></keyword><keyword><style  face="normal" font="default" size="100%">SILAR</style></keyword><keyword><style  face="normal" font="default" size="100%">supercapacitor</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">APR</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">84</style></volume><pages><style face="normal" font="default" size="100%">110776</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	The successive ionic layer adsorption and reaction (SILAR) technique was adapted to produce the interconnected complex network of BaO:MgO nanorods on a flexible stainless-steel (SS) substrate surface. The phase and surface morphology of the BaO:MgO electrode were examined from the X-ray diffraction and scanning electron microscopy measurements, respectively, which endowed electrochemical specific capacitance (SC) of 528.77 F/g at a 2 mV/s scan rate with great rate capability and cycling performance of 94.33 % over 5000 cyclic voltammetry cycles. Fabricated BaO:MgO//AC asymmetric solid-state supercapacitor device, using polyvinyl alcohol and potassium hydroxide gel as an electrolyte, demonstrated distinctive energy storage performance, i.e., a specific capacitance (SC) of 259.07 F/g with an energy density of 57.27 Wh/kg and a power density of 2.34 kW/kg at a current density of 4 mA/cm(2). The results demonstrated the facile method for synthesizing a spherical nanorod network of BaO:MgO and made them promising electrode materials for energy storage applications. The use of a solid-state supercapacitor device to illuminate an LED demonstrated the commercial feasibility of both the materials utilized and the design type.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">Part A</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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	9.4&lt;/p&gt;
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