Incorporating Fluorescent Nanomaterials in Organically Modified Sol-Gel Materials – Creating Single Composite Optical pH Sensors

Optical sensors hold the promise of providing the coupling between the tangible and the digital world that we are currently experiencing with physical sensors. The core of optical sensor development...

In situ Interlamellar Production of Amide Based Functional Copolymer/Clay Nanocomposites

Functional amide based copolymer/clay nanocomposites were synthesized by in situ radical-initiated interlamellar copolymerization from acrylamide and citraconic anhydride monomers in the presence of organically modified montmorillonite (O-MMT) clay. To investigate...

Improving Fracture Toughness of Tetrafunctional Epoxy with Functionalized 2D Molybdenum Disulfide Nanosheets

In this work, improved fracture toughness of tetra-functional epoxy polymer was obtained using two-dimensional (2H polytype) molybdenum disulfide (MoS2) nano-platelets as a filler. Simultaneous in-situ exfoliation and functionalization of MoS2 were achieved in the presence of cetyltrimethylammonium bromide (CTAB) via sonication. The aim was to improve the dispersion of MoS2 nanoplatelets in epoxy and enhance the interfacial interaction between nanoplatelets and epoxy matrix. Epoxy nanocomposites with CTAB functionalized MoS2 (f-MoS2) nanoplatelets, ranging in content from 0.1 wt% up to 1 wt%, were fabricated. Modified MoS2 improved the fracture properties (81%) of tetrafunctional epoxy nanocomposites. The flexural strength and compressive strength improved by 64% and 47%, respectively, with 0.25 wt% loading of f-MoS2 nanoplatelets compared to neat epoxy. The addition of f-MoS2 nanoplatelets enhanced the thermomechanical properties of epoxy. This work demonstrated the potential of organically modified MoS2 nanoplatelets for improving the fracture and thermal behavior of tetrafunctional epoxy nanocomposites.

Preparation and characteristics of sepiolite-waterborne polyurethane composites

A kind of organic/inorganic composite material composed of waterborne polyurethane and sepiolite was prepared in this work. Sepiolite was organically modified by three kinds of silane coupling agents, and then compounded with waterborne polyurethane through layer-by-layer method in order to prepare composite materials. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) show the crystal and chemistry structure of sepiolite samples, and confirmed the preparation of organic sepiolite. Scanning electron microscope (SEM) and energy dispersive X-ray spectroscopy (EDS) showed the surface microstructure and elemental content of sepiolite and organic sepiolite, and was consistent with the XRD results. Transmission electron microscope (TEM) examination of waterborne polyurethane composites surfaces showed that sepiolite particles were regularly dispersed in the waterborne polyurethane matrix. Thermal resistance of waterborne polyurethane composites was determined by thermogravimetry analyzer (TG) and derivative thermogravimetry analyzer (DTG), differential scanning calorimetry (DSC), gas chromatography (GC), and mass chromatography (MS). Mechanical behavior was examined by tensile strength tester, showed higher break strength than that of the control waterborne polyurethane. Therefore, organically modified sepiolite was considered to be a kind of wonderful inorganic material that could be used to improve the thermal stability and mechanical property of polymer.

Maghnite: an innovative inorganic reinforcement utilized in the synthesis of polyamide 12 nanocomposites with optimized thermal and mechanical properties

This study will contribute to the identification and understanding of the reinforcement mechanisms of thermoplastic matrices by nanofillers. This aspect is addressed through the investigation of the thermal and mechanical properties of nanocomposites consisting of a polyamide 12 (PA12) matrix crammed with organically modified clay nanoparticles. An efficient approach to the synthesis of polyamide 12 (PA12) nanocomposites was investigated; Maghnite may be a processed Algerian mineral clay which will act both as a catalyst and as an inorganic reinforcement. Two sorts of organic substances were used, labeled CTA-Mag (1CEC) and CTA-Mag (2CEC), modified by cetyltrimethylammonium (CTA) ions. However, PA12/CTA-Mag nanocomposites are characterized by various physico-chemical techniques, XRD, FTIR, TGA, scanning and transmission electron microscopy (SEM and TEM). Measurements of tensile modulus, yield strength, lastingness, elongation at break and toughness were done to assess the behavior of the mechanical properties. Furthermore, we have analyzed the consequences of the mass fraction of the fillers on the structural, thermal and mechanical properties of those nanocomposites. Specific attention has been paid to the study of relationships between the macroscopic properties and therefore the structure of nanocomposites. Thermomechanical tests showed a big improvement within the properties of the nanocomposites compared to neat PA12.

“Doing More with Less”: Ni(II)@ORMOSIL, a Novel Sol-Gel Pre-Catalyst for the Reduction of Nitrobenzene

Reduction of nitrobenzene with NaBH4 using zero-valent iron nanoparticles (ZVI-NPs) and NiCl2∙6H2O incorporated in organically modified hybrid silica matrices as ZVI@ORMOSIL and Ni(II)@ORMOSIL catalysts is proposed as a remediation strategy. Ni(II)@ORMOSIL is prepared by ion-exchanging H+ of the ORMOSIL matrix with NiII. Ni(II)@ORMOSIL is a pre-catalyst that undergoes reduction by NaBH4 by an in-situ reaction and promotes nitrobenzene reduction by the unconsumed NaBH4, leading to sparing use of the catalyst. Ni(II)@ORMOSIL undergoes color change from green to black in this process, returning to a green hue after washing and drying. Nitrobenzene reductions were examined in aqueous acetonitrile solvent mixtures, and the reduction cascade produced the reaction end-products with catalytic implications. Plausible mechanisms of ZVI@ORMOSIL and Ni(II)@ORMOSIL catalyzed reductions of nitrobenzene are discussed. This work is the first to report M(II)@ORMOSIL pre-catalysts for in-situ reduction of nitrobenzene, and expands the scope of the ORMOSIL series of catalysts for the reduction of polluting compounds. This approach enables the development of catalysts that use very low concentrations of transition metal cations.

A CRYSTAL CHEMISTRY OF HYDROXYAPATITE : A REVIEW

In chemistry of inorganic crystals, the octacalcium phosphate (OCP) is an apatite based crystals and having a hydrated layers which used in producing of needle or plate-shaped hydroxyapatite (HAP) nanocrystals. Although, the crystals is prepared by a dissolution precipitation reaction. These reaction led to a hexagonal HAP nanocrystals formation under hydrothermal condition from OCP at 180 for 3 hours with pH of solution adjusted to 5.5 and incorporating dicarboxylate e.g. succinate (OOC.(CH2)2.COO)2- ions having Ca/P molar ratio is expected to be 1.56±0.02, where the morphology of OCP are retained. During incorporating of succinate ions in OCP crystals, the hydrogen phosphate (HPO42-) ions in the hydrated layers of OCP are being substituted by succinate ions. Since the crystal system of HAP is hexagonal and its crystalline size in the longitudinal direction of various (a,b,c) axes depending on the thickness of the laminated plate-shaped HAP crystals. Here, their size as perpendicular to the (100) plane which is calculated by introducing of Scherrers equation, D100 = Kλ/(β cos ). The organically modified OCP which generated to HAP have unique nanostructure with micrometer thickness are characterized by using of SEM, FTIR and X-ray diffraction analysis.