01904nas a2200241   4500008004100000022001400041245008400055210006900139260007300208300000900281490000700290520107400297653002301371653001601394653001501410653002601425653001301451100002301464700001701487700002201504700001901526856011701545       2006                        eng d  a1387-181100aClaisen rearrangement of allyl phenyl ether over zeolites beta, mordenite and Y0 aClaisen rearrangement of allyl phenyl ether over zeolites beta m  aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcOCT  a8-160 v953 a<p>The Claisen rearrangement of allyl phenyl ether (APE) to o-allylphenol was investigated over zeolites beta (BEA), mordenite (MOR) and Y (FAU) with different Si/Al ratios. Over the zeolite catalysts, the allylphenol cyclized to produce 2,3-dihydro-2-methyl benzofuran. Larger catalyst loading, higher reaction temperatures and longer run duration favored the formation of the ring compound. Conversion was small over MOR and FAU although they possessed higher acidity (as measured by the temperature programmed desorption of ammonia) compared to BEA. Studies using BEA revealed that the nature of the solvent influenced the reaction rate. The order of reactivity in the solvents was, benzene &gt; EDC (1,2-dichloroethane) &gt; toluene &gt; TCE (1, 1,2,2-tetrachloroethane) &gt;&gt; ACN (acetonitrile). The intermediate allylphenol reacted with the aromatic solvents to produce byproducts when benzene and toluene were used as solvents. A kinetic analysis assuming first order series and parallel reactions is presented. (c) 2006 Elsevier Inc. All rights reserved.</p>10aallyl phenyl ether10aallylphenol10aBenzofuran10aClaisen rearrangement10azeolites1 aWagholikar, S., G.1 aMayadevi, S.1 aJacob, Nalini, E.1 aSivasanker, S.  uhttps://library.ncl.res.in/content/claisen-rearrangement-allyl-phenyl-ether-over-zeolites-beta-mordenite-and-y-001754nas a2200205   4500008004100000022001400041245010300055210006900158260010600227300001200333490000700345520096500352653001501317653001401332653001301346653002901359100001901388700001701407856012401424       2008                        eng d  a0045-653500aCellulose supported layered double hydroxides for the adsorption of fluoride from aqueous solution0 aCellulose supported layered double hydroxides for the adsorption  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcJUN  a995-9980 v723 a<p>Cellulose supported layered double hydroxides (CSLDHs) were synthesized and tested for adsorption of fluoride in aqueous medium. Three samples of cellulose supported LDHs were synthesized by varying the LDH loading on cellulose. The raw cellulose, unsupported LDH and cellulose supported LDHs were characterized by XRD, SEM and BET surface area. Batch adsorption as well as fixed-bed column experiments were performed for determining the fluoride adsorption characteristics of CSLDHs. The fluoride adsorption properties of CSLDHs were found to be superior to that of reported adsorbents, including activated alumina and carbon nanotubes. Defluoridation capacity of the CSLDHs was 2-4 times higher than that of unsupported LDH. The cellulose supported LDH, CSLDH-50, having an LDH loading of 27% showed maximum fluoride uptake capacity (5.29 mg g(-1) of CSLDH, 25.18 mg g(-1) of LDH) in fixed-bed column study. (C) 2008 Elsevier Ltd. All rights reserved.</p>10aAdsorption10acellulose10aFluoride10aLayered double hydroxide1 aMandal, Sujata1 aMayadevi, S.  uhttps://library.ncl.res.in/content/cellulose-supported-layered-double-hydroxides-adsorption-fluoride-aqueous-solution-0