02226nas a2200217   4500008004100000022001400041245014600055210006900201260006800270300001400338490000800352520138100360653002601741653001901767653001501786653001401801653002301815100002501838700002301863856012201886       2007                        eng d  a0021-899500aInfluence of organic modification on mechanical properties of melt processed intercalated poly(methyl methacrylate)-organoclay nanocomposites0 aInfluence of organic modification on mechanical properties of me  a111 RIVER ST, HOBOKEN, NJ 07030 USAbJOHN WILEY & SONS INCcSEP  a2433-24430 v1053 a<p>The influence of organic modifiers on intercalation extent, structure, thermal and mechanical properties of poly(methyl methacrylate) (PMMA)-clay nanocomposites were studied. Two different organic modifiers with varying hydrophobicity (single tallow versus ditallow) were investigated. The nanocomposites were prepared from melt processing method and characterized using wide angle X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, differential scanning calorimetry (DSC), and tensile tests. Mechanical properties such as tensile modulus (E), break stress (sigma(brk)), and 0% break strain (epsilon(brk)) were determined for nanocomposites at various clay loadings. Extent of PMMA intercalation is sufficient and in the range 9-15 angstrom depending on organoclay and filler loading. Overall thermal stability of nanocomposites increases by 16-30 degrees C. The enhancement in T-g of nanocomposite is merely by 2-4 degrees C. With increase in clay loading, tensile modulus increases linearly while % break strain decreases. Break stress is found to increase till 4 wt % and further decreases at higher clay loadings. The overall improvement in thermal and mechanical properties was higher for the organoclay containing organic modifier with lower hydrophobicity and single tallow amine chemical structure. (c) 2007 Wiley Periodicals, Inc.</p>10amechanical properties10aNanocomposites10aorganoclay10astructure10aThermal properties1 aTiwari, Rajkiran, R.1 aNatarajan, Upendra  uhttps://library.ncl.res.in/content/influence-organic-modification-mechanical-properties-melt-processed-intercalated-002294nas a2200241   4500008004100000022001400041245012300055210006900178260006800247300001400315490000800329520139100337653002601728653001901754653001501773653002601788653001601814653002301830100002501853700002301878700002301901856012801924       2008                        eng d  a0021-899500aNew poly(phenylene oxide)/polystyrene blend nanocomposites with clay: intercalation, thermal and mechanical properties0 aNew polyphenylene oxidepolystyrene blend nanocomposites with cla  a111 RIVER ST, HOBOKEN, NJ 07030 USAbJOHN WILEY & SONS INCcMAY  a1818-18280 v1083 a<p>We present the first study and results on the preparation and characterization of montmorillonite clay filter based polymer blend nanocomposites of the miscible poly(phenylene oxide)/polystyrene blend. Intercalated nanocomposites, prepared by a melt-processing method with 2-6 wt % commercially available organically modified sodium montmorillonite, have been characterized with wide-angle X-ray diffraction, transmission electron microscopy analysis, thermal analysis (thermogravimetric analysis and differential scanning calorimetry), and mechanical tensile tests. We show that nanocomposites can be successfully prepared in a batch mixer at temperatures much below the conditions conventionally used for this blend without organic degradation. Thermal stability is enhanced by nanoscale hybrid formation. The level of intercalation (change in the d-spacing) does not change with the clay loading. Better dispersion of clay in the blend matrix has been observed at a low level of clay content. The nanocomposites show improved tensile modulus (by 31%) in comparison to the blend, whereas the tensile strength (stress at break) and elongation decrease in the presence of the filler with an increase in the clay loading. The Halpin-Tsai model is able to predict the modulus of the nanocomposites in very good agreement with the experimental data. (c) 2008 Wiley Periodicals, Inc.</p>10amechanical properties10aNanocomposites10aorganoclay10apoly(phenylene oxide)10aPolystyrene10aThermal properties1 aTiwari, Rajkiran, R.1 aKhilar, Kartic, C.1 aNatarajan, Upendra  uhttps://library.ncl.res.in/content/new-polyphenylene-oxidepolystyrene-blend-nanocomposites-clay-intercalation-thermal-and-001998nas a2200229   4500008004100000022001400041245007300055210006900128260005700197300001200254490000700266520118700273653002201460653001501482653003301497653003101530653003701561100002001598700001901618700002101637856011001658       2009                        eng d  a0170-083900aPolypropylene-organoclay nanocomposites containing nucleating agents0 aPolypropyleneorganoclay nanocomposites containing nucleating age  a233 SPRING ST, NEW YORK, NY 10013 USAbSPRINGERcDEC  a897-9090 v633 a<p>Polypropylene/organoclay nanocomposites containing nucleating agents, viz., aluminum hydroxybis[2,2-methylenebis(4,6-di-tert-butylphenyl) phosphate (NA21) and 1,3:2,4-bis(3,4-dimethylbenzylidene)sorbitol (Millad 3988), were prepared by direct melt intercalation in a twin-screw extruder. Nucleating agents were added to polypropylene during compounding and their effect on the properties of the nanocomposites was studied. X-ray diffraction (XRD) and transmission electron microscopy (TEM) exhibited clay layers to be intercalated and partially exfoliated. The expansion of inter-gallery distance of the clay layers was governed by the interaction between polypropylene, compatibilizer, and different nucleating agents. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) indicated higher thermal stability and crystallization temperature for nanocomposites compared to virgin polymer. Even a small addition of the nanoscale filler with 0.2% nucleating agents was found to promote concurrently several PP material properties, including improved tensile characteristics, higher Young's modulus, increased thermal stability and rate of crystallization.</p>10aNucleating agents10aorganoclay10aPolypropylene nanocomposites10aThermogravimetric analysis10atransmission electron microscopy1 aGhugare, S., V.1 aGovindaiah, P.1 aAvadhani, C., V.  uhttps://library.ncl.res.in/content/polypropylene-organoclay-nanocomposites-containing-nucleating-agents-002307nas a2200205   4500008004100000022001400041245013300055210006900188260006800257300001400325490000800339520148100347653003401828653001901862653001501881653001701896100003101913700002501944856013201969       2010                        eng d  a0021-899500aInfluence of structure of organic modifiers and polyurethane on the clay dispersion in nanocomposites via in situ polymerization0 aInfluence of structure of organic modifiers and polyurethane on   a111 RIVER ST, HOBOKEN, NJ 07030 USAbJOHN WILEY & SONS INCcNOV  a1774-17860 v1183 a<p>Influence of polyurethane (PU) structure on the nature of PU/clay nanocomposite was studied using varying amounts of trimethylol propane (TMP) as branching agent. The effect of hydroxyl groups in the modifier of organoclays on the structure of PU/clay nanocomposites was studied. Nanocomposites were characterized using wide-angle X-ray diffraction measurements (WAXD) and transmission electron microscopy (TEM). The results show that formation of completely exfoliated and well dispersed polyurethane/clay nanocomposites via in situ polymerization, is facilitated by the presence of tethering groups on the clay surface and an ability to form branched and crosslinked structures. Incorporation of long alkyl chains in addition to tethering hydroxyl groups in the modifier structure of the clay did not significantly improve the compatibility of linear PU with the clay. Intercalated thermoplastic polyurethane/clay nanocomposites, prepared using poly(caprolactone diol) as soft segment and isophorone diisocyanate and 1,4-butanediol as hard segments show increase in storage tensile moduli at temperatures before glass transition temperature when functional groups capable of chemically reacting with the growing polymer chains are present in the clay modifier. This is indicative of improved interaction of the polymer with the clay surface when the modifier has larger number of hydroxyl groups. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 118: 1774-1786, 2010</p>10aintercalation and exfoliation10aNanocomposites10aorganoclay10apolyurethane1 aRama, Mallikarjuna, Shroff1 aSwaminathan, Sivaram  uhttps://library.ncl.res.in/content/influence-structure-organic-modifiers-and-polyurethane-clay-dispersion-nanocomposites-situ-002147nas a2200229   4500008004100000022001400041245013000055210006900185260000800254300001400262490000700276520134400283653001101627653002601638653002001664653001901684653001501703653003001718100002501748700002301773856012101796       2020                        eng d  a0032-388800aCritical organic modifier aliphatic tail length for the formation of poly(methyl methacrylate)-montmorillonite nanocomposites0 aCritical organic modifier aliphatic tail length for the formatio  cJUL  a1604-16170 v603 a<p>In this article, we report the influence of organic modifier structure (alkyl chain length C8-C20, single vs ditallow) and thereby, the effect of hydrophobicity on the structure, thermal and mechanical properties of poly(methyl methacrylate) (PMMA)-clay hybrids. Melt processed PMMA-clay hybrids were characterized using wide-angle X-ray diffraction, transmission electron microscopy, and differential scanning calorimetry. The organoclays having an alkyl chain length of more than 12 CH2 groups resulted in the formation of nanocomposites. The glass transition temperature (T-g) of PMMA increased in the presence of clay. The mean-field lattice model was used to predict the free energy for nanocomposite formation, which showed a reasonable match with the experimental results and provided a general guideline for the proper selection of polymer and organoclay (ie, organic modifier) to obtain nanocomposite. Tensile modulus showed maximum improvement of 58% for the nanocomposites compared to 9% improvement for the composites. Tensile modulus increased with increases in the alkyl chain length of the organic modifier and clay loading. The level of improvement for the tensile properties of nanocomposites prepared from primary and secondary ammonium-modified clay is the same as that obtained with the commercial organoclays.</p>
10ahybrid10amechanical properties10aMontmorillonite10aNanocomposites10aorganoclay10apoly(methyl methacrylate)1 aTiwari, Rajkiran, R.1 aNatarajan, Upendra  uhttps://library.ncl.res.in/content/critical-organic-modifier-aliphatic-tail-length-formation-polymethyl-methacrylate01872nas a2200253   4500008004100000022001400041245010100055210006900156260000900225300001000234490000800244520103000252653002601282653001401308653001801322653002401340653001101364653001501375100002301390700001801413700002501431700003201456856013001488       2023                        eng d  a0920-586100aHydrogenation of levulinic acid to gamma-valerolactone over nickel supported organoclay catalyst0 aHydrogenation of levulinic acid to gammavalerolactone over nicke  cJAN   a36-490 v4083 a<p>
	In this work, a series of Ni/Organoclay catalysts with different Nickel loadings were prepared by the wetimpregnation method for the catalytic hydrogenation of levulinic acid (LA) to gamma-valerolactone (GVL). Reaction parameters such as reaction temperature, pressure, solvent effect, and wt% of catalyst were optimized to get excellent conversion of levulinic acid selectively to gamma-valerolactone. Ni/Organoclay with 30% Nickel loading exhibited 100% conversion of LA with 100% selectivity towards GVL at 140 degrees C and 3.0 MPa H2 pressure using 1,4-dioxane as a solvent in 5 h. Different bulk and surface characterization techniques such as XRD, BET, FE-SEM, HR-TEM, XPS, XRF, NH3-TPD, and H2-Chemisorption were used to characterize the Ni/Organoclay catalyst. BET and NH3-TPD analysis showed that the pre-treatment of bentonite with surfactant (CTAB) improved the pore volume, surface area, and acidity of Organoclay which assisted in improving the conversion and selectivity of LA and GVL respectively.</p>
10a?-Valerolactone (GVL)10aBentonite10aHydrogenation10aLevulinic acid (LA)10aNickel10aorganoclay1 aKamble, Paresh, A.1 aVinod, C., P.1 aRathod, Virendra, K.1 aKantam, Mannepalli, Lakshmi  uhttps://library.ncl.res.in/content/hydrogenation-levulinic-acid-gamma-valerolactone-over-nickel-supported-organoclay-catalyst01791nas a2200241   4500008004100000022001400041245010500055210006900160260000900229300001100238490000800249520097500257653001301232653001801245653001101263653001501274653003101289100002301320700001801343700002501361700003201386856013101418       2024                        eng d  a0926-860X00aHydrogenation of furfural to tetrahydrofurfuryl alcohol over nickel-supported on organoclay catalyst0 aHydrogenation of furfural to tetrahydrofurfuryl alcohol over nic  cMAR   a1196210 v6743 a<p>
	Nickel supported on organoclay prepared by the impregnation method provides excellent catalytic activity for the hydrogenation of furfural to tetrahydrofurfuryl alcohol. The relative amount of metal and acidic sites influences the hydrogenation reaction. Additionally, by varying the temperature and the H-2 pressure, we can regulate the interaction of furfural with the active sites. And this may decide the fate of the reaction whether it will undergo a two-step hydrogenation to form tetrahydrofurfuryl alcohol or a rearrangement reaction to form cyclopentanone/cyclopentanol. Water was found to be the best solvent for the selective formation of tetrahydrofurfuryl alcohol. Even though alcohols inhibited rearrangement reaction, the hydrogenation of furfural was more selective towards furfuryl alcohol. Ni/O-clay30A under the optimum conditions of 120 degrees C, 4.0 MPa, and in 1 h offered complete conversion of furfural to tetrahydrofurfuryl alcohol.</p>
10afurfural10aHydrogenation10aNickel10aorganoclay10aTetrahydrofurfuryl alcohol1 aKamble, Paresh, A.1 aVinod, C., P.1 aRathod, Virendra, K.1 aKantam, Mannepalli, Lakshmi  uhttps://library.ncl.res.in/content/hydrogenation-furfural-tetrahydrofurfuryl-alcohol-over-nickel-supported-organoclay-catalyst