02393nas a2200253   4500008004100000022001400041245010600055210006900161260007300230300001200303490000700315520145300322653003101775653002801806653002201834653002201856653002001878100002901898700001801927700001401945700002801959700002601987856012602013       2007                        eng d  a1387-181100aSynthesis and characterization of mesoporous carbon through inexpensive mesoporous silica as template0 aSynthesis and characterization of mesoporous carbon through inex  aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcJAN  a189-1990 v983 a<p>Mesoporous silica materials have been synthesized through sol-gel reaction using inexpensive sodium silicate as source of silica and low cost hydroxy carboxylic acid compounds as templates/pore forming agents. The material measured surface area of 1014 m(2)/g, pore diameter of 65 angstrom and pore volume of 1.4 cc/g when parameters like time and temperature of synthesis along with mole ratio of TA/SiO(2) were optimized. Here TA stands for tartaric acid. Carbonization of sucrose inside the pores of above silica material at 900 degrees C followed by removal of silica framework using aqueous ethanoic solution of NaOH gave rise to mesoporous carbon material. The resulting materials were characterized by N(2)-sorption, FTIR spectroscopy, X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, thermal analysis and cyclic voltammetry. Three dimensional interconnecting wormhole channel arrangement of mesoporous silica template leads to mesoporous carbon replica with surface area of 1200 m(2)/g. X-ray photoelectron spectroscopic study (XPS) of the mesoporous carbon material shows the concentration of carbon atom in the range of 97-98% with 1-2% oxygen and negligible amount of silica. The electrochemical double layer capacitance behavior of carbon material with the specific capacitance value of 88.0 F/g at the scan rate of 1 mV/s appears to be promising. (C) 2006 Elsevier Inc. All rights reserved.</p>10aElectrochemical properties10ahydroxy carboxylic acid10amesoporous carbon10aMesoporous silica10asodium silicate1 aKarandikar, Prashant, R.1 aPatil, K., R.1 aMitra, A.1 aKakade, Bhalchandra, A.1 aChandwadkar, Asha, J.  uhttps://library.ncl.res.in/content/synthesis-and-characterization-mesoporous-carbon-through-inexpensive-mesoporous-silica02260nas a2200229   4500008004100000022001400041245015300055210006900208260000800277520139800285653001801683653002101701653001901722653002301741653002201764653002201786100002101808700002901829700002601858700002301884856012301907       2020                        eng d  a1380-222400aSynthesis, characterization and catalytic study of mesoporous carbon materials prepared via mesoporous silica using non-surfactant templating agents0 aSynthesis characterization and catalytic study of mesoporous car  cNOV3 a<p>Mesostructured silica materials with surface area in the range of similar to 700-900 m(2)/g have been prepared using hydroxy-carboxylic acid compounds such as tartaric acid, malic acid and citric acid (low cost non-surfactant template/pore forming agents) and tetraethylorthosilicate (TEOS) as silica source by sol-gel reaction. The templates were removed by either soxhlet extraction or calcination method. Mesoporous carbon molecular sieves were then prepared by carbonizing sucrose inside the pores of the above prepared mesoporous silica using sulfuric acid as a catalyst. The materials were characterized by FTIR spectroscopy, powder X-ray diffraction (XRD), N-2-sorption studies, microanalysis, thermal analysis and transmission electron microscopy (TEM). The resulting carbon material shows relatively higher surface area (similar to 1100 m(2)/g), narrow pore size distribution and pore diameter of 4-5 nm. The mesoporosity of carbon material arises from interconnecting channels arrangements of mesoporous silica template. The mesoporous carbon material was used as a support for the immobilization of rhodium complex [HRhCO(TPPTS)(3)] by ossification method. The prepared catalyst has been tested for the hydroformylation of higher olefins. The activity of the catalyst was improved by 20-30% as compared to the catalyst prepared from a conventional activated carbon support.</p>
10aCarbonization10aHydroformylation10aImmobilization10aLow cost templates10amesoporous carbon10aMesoporous silica1 aPagar, Nitin, S.1 aKarandikar, Prashant, R.1 aChandwadkar, Asha, J.1 aDeshpande, Raj, M.  uhttps://library.ncl.res.in/content/synthesis-characterization-and-catalytic-study-mesoporous-carbon-materials-prepared