01672nas a2200229   4500008004100000022001400041245011000055210006900165260009900234300001200333490000800345520083000353653002301183653001401206653000801220653001501228653001801243653000801261100002501269700002301294856012501317       2014                        eng d  a0144-861700aFunctionalized celluloses and their nanoparticles: morphology, thermal properties, and solubility studies0 aFunctionalized celluloses and their nanoparticles morphology the  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLANDbELSEVIER SCI LTDcAPR  a135-1420 v1043 a<p>Agricultural residues derived cellulose was used to synthesize a new series of carboxy functionalized cellulosic nanoparticles (quasi-spherical shaped, 13.2-21.5% carboxyl content) and macro-sized 6-carboxycelluloses (long-fibril shaped, 1.7-22% carboxyl content). The DP (50-70) and yield (upto 46%) of nanoparticles were manipulated by controlling the reaction temperature and time. TGA/DTG thermographs of the carboxycelluloses gave thermostability data and co-related well with the residual crystalline, amorphous, and anhydroglucuronic acid content. The particle shape and size had no effect on the thermal stability. Some derivatives were fully or partially soluble in aqueous alkali and non-aqueous solvents, which can lead to increased versatility of these polymers. (C) 2014 Elsevier Ltd. All rights reserved.</p>10a6-Carboxycellulose10acellulose10aDTG10aMorphology10aNanoparticles10aTGA1 aSharma, Priyanka, R.1 aVarma, Anjanikumar  uhttps://library.ncl.res.in/content/functionalized-celluloses-and-their-nanoparticles-morphology-thermal-properties-and-002266nas a2200229   4500008004100000022001400041245015400055210006900209260009900278300001200377490000800389520136000397653002101757653001401778653001801792653000801810653001001818100002501828700003501853700002301888856012501911       2014                        eng d  a0144-861700aSupramolecular transitions in native cellulose-I during progressive oxidation reaction leading to quasi-spherical nanoparticles of 6-carboxycellulose0 aSupramolecular transitions in native celluloseI during progressi  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLANDbELSEVIER SCI LTDcNOV  a615-6230 v1133 a<p>Cellulose-I swells considerably in phosphoric acid, and converts to amorphous cellulose via a cellulose-II transition state. Controlled oxidation of cellulose-I to 6-carboxycellulose (6CC) using HNO3-H3PO4-NaNO2 oxidation system led to the selective production of 6CC's of varying carboxyl contents (1.7-22%) as well as various shapes and sizes (macro-sized fibrils of several micron length and/or spherical nanoparticles of 25-35 nm), depending on the reaction conditions. 6CC's having less than 14% carboxyl content were largely in cellulose-II form (WAXRD values in-between cellulose I and cellulose II), whereas at 14-22% the 6CC's were largely amorphous; only trace crystallinity was observed at 19% and 22% carboxyl 6CC. Spherical nanoparticles retained a high degree of crystallinity having cellulose-I structure, whereas the macro-sized fibrils were largely converted to cellulose-II structure. Analysis by WAXRD as well as by CP-MAS C-13 NMR studies gave similar conclusions. Reduced molecular weight with progressive oxidation, including presence of oligomers, was also evident from an increase in the reducing-end carbon peak at similar to 92 ppm. For high oxidation levels (&gt;14%) the NMR 92-96 ppm peaks disappeared on extracting with dilute alkali, due to soluble oligomers being removed. (C) 2014 Elsevier Ltd. All rights reserved.</p>10aCarboxycellulose10acellulose10aNanoparticles10aNMR10aWAXRD1 aSharma, Priyanka, R.1 aRajamohanan, Pattuparambil, R.1 aVarma, Anjanikumar  uhttps://library.ncl.res.in/content/supramolecular-transitions-native-cellulose-i-during-progressive-oxidation-reaction-002292nas a2200241   4500008004100000022001400041245012400055210006900179260009900248300001200347490000800359520139000367653000601757653000601763653002701769653002301796653002601819653001401845653001201859100002501871700002301896856013101919       2014                        eng d  a0144-861700aThermal stability of cellulose and their nanoparticles: Effect of incremental increases in carboxyl and aldehyde groups0 aThermal stability of cellulose and their nanoparticles Effect of  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLANDbELSEVIER SCI LTDcDEC  a339-3430 v1143 a<p>Oxidized cellulose containing carboxyl and aldehyde functional groups represent an important class of cellulose derivatives. In this study effect of incrementally increasing COOH and CHO groups at C2, C3, and C6 positions of cellulose and nanocellulose has been investigated, with a view to understanding their effect on thermal treatment of cellulose. The results show that 2,3-dialdehyde cellulose (DAC) is the most thermally stable oxidized product of cellulose while the most unstable derivatives contain carboxyl group at the C6 position (6CC). Carboxymethylcellulose (CMC), with carboxymethyl group on C6 position, is more stable than 6CC. Multi-functionalized celluloses 2,3,6-tricarboxycellulose and 6-carboxy-2,3-dialdehyde, have the same level of thermal stability as 6CC, showing that the presence of carboxyl at the C6 is a key destabilizing factor in the thermal stability of oxidized cellulose products. More the number of reducing end groups on the polymer chain, lower the thermal stability of the cellulose, as proved by comparing the TGA/DTG of monomeric analogs dextrose, cellobiose and glucuronic acid with the oxidized celluloses. The thermal stability trend observed for oxidized celluloses was DAC &gt; DCC &gt; nanoparticles &gt; dextrose &gt;glucuronic acid, caused by extent of reducing ends and COOH groups. (C) 2014 Elsevier Ltd. All rights reserved.</p>10a210a310a3-Dialdehyde cellulose10a6-Carboxycellulose10a6-Tricarboxycellulose10acellulose10aTGA/DTG1 aSharma, Priyanka, R.1 aVarma, Anjanikumar  uhttps://library.ncl.res.in/content/thermal-stability-cellulose-and-their-nanoparticles-effect-incremental-increases-carboxyl-002057nas a2200241   4500008004100000022001400041245009800055210006900153260007300222300001200295490000700307520118200314653001901496653001401515653002801529653002401557100002501581700001801606700001901624700001901643700002301662856013001685       2016                        eng d  a0141-813000aShape and size engineered cellulosic nanomaterials as broad spectrum anti-microbial compounds0 aShape and size engineered cellulosic nanomaterials as broad spec  aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcJUN  a460-4650 v873 a<p>Oxidized celluloses have been used for decades as antimicrobial wound gauzes and surgical cotton. We now report the successful synthesis of a next generation narrow size range (25-35 nm) spherical shaped nanoparticles of 2,3,6-tricarboxycellulose based on cellulose I structural features, for applications as new antimicrobial materials. This study adds to our previous study of 6-carboxycellulose. A wide range of bacteria such as Escherichia coli, Staphloccocus aureus, Bacillus subtilis and Mycobacterium tuberculosis (non-pathogenic as well as pathogenic strains) were affected by these polymers in in vitro studies. Activity against Mycobacteria were noted at high concentrations (MIC99 values 250-1000 mu g/ml, as compared to anti-TB drug Isoniazid 0.3 mu g/ml). However, the broad spectrum activity of oxidized celluloses and their nanoparticles against a wide range of bacteria, including Mycobacteria, show that these materials are promising new biocompatible and biodegradable drug delivery vehicles wherein they can play the dual role of being a drug encapsulant as well as a broad spectrum anti-microbial and anti-TB drug. (C) 2016 Published by Elsevier B.V.</p>10aAnti-microbial10acellulose10aSpherical nanoparticles10aTricarboxycellulose1 aSharma, Priyanka, R.1 aKamble, Sunil1 aSarkar, Dhiman1 aAnand, Amitesh1 aVarma, Anjanikumar  uhttps://library.ncl.res.in/content/shape-and-size-engineered-cellulosic-nanomaterials-broad-spectrum-anti-microbial-compounds