(2E)-N-Methyl-2-[(2E)-3-phenyl-prop-2-en-1-yl-idene]hydrazinecarbothio-amide.

The title compound, C(11)H(13)N(3)S, is close to being planar, with a dihedral angle of 9.64 (3)° between the benzene ring and the thio-semicarbazone mean plane, maintained by the presence of π-conjugation in the chain linking the the two systems. In the crystal, N-H⋯S hydrogen bonds form centrosymmetric dimers through a cyclic association [graph-set R(2) (2)(8)].

Sodium alginate/magnetic hydrogel microspheres from sugarcane bagasse for removal of sulfamethoxazole from sewage water: Batch and column modeling.

Magnetic carbon were synthesized from sugarcane bagasse using hydrothermal carbonization followed by thermal activation was converted to solid state as beads (hydrogels SACFe) using sodium alginate and applied as adsorbent in removal sulfamethoxazole in batch and column mode. From adsorption parameter analysis it was confirmed that 0.6 g L-1 SACFe was effective in removing 50 mg L-1 of SMX at pH 6.2. Sorption of SMX on SACFe beads followed Elovich kinetics and Freundlich isotherm. It was further confirmed that sorption occurred on heterogeneous surface of SACFe beads with chemisorption as rate limiting step. Maximum adsorption capacity was obtained as 58.439 mg g-1 pH studies revealed that charged assisted hydrogen bonding, EDA interactions are some of the mechanism that favoured removal of SMX. From column studies it was found that bead height of 2 cm and flow rate of 1.5 mL min-1 found to be best in removing pollutant. Thomas model fitted better the experimental data stating that improved interaction between adsorbent and adsorbate act as major driving force tool in obtaining maximum sorption capacity. Breakthrough curve was completely affected by varied flow rate and bed height. Column adsorption was effective in reducing COD and BOD levels of sewage which are affected by toxic pollutants and miscellaneous compounds. Feasibility analysis showed that SACFe beads could be employed for real-time applications as it is cost, energy effective and easy recovery.

6-Methyl-N-(4-methoxy-phen-yl)-2-[(E)-(4-methyl-phen-yl)methyl-eneamino]-4,5,6,7-tetra-hydro-thieno[2,3-c]pyridine-3-carboxamide.

The molecular structure of the title compound, C(24)H(25)N(3)O(2)S, is stabilized by intra-molecular N-H⋯N, C-H⋯O and C-H⋯S hydrogen bonds. There are no significant inter-molecular inter-actions.

2-Amino-N-(2-methoxy-phen-yl)-4,5-dimethyl-thio-phene-3-carboxamide.

In the title compound, C(14)H(16)N(2)O(2)S, the two aromatic rings make a dihedral angle of 13.9 (1)°. The crystal structure is stabilized by both inter- and intra-molecular N-H⋯O, C-H⋯O and C-H⋯N hydrogen bonds.

Synthesis, luminescence properties and EPR investigation of hydrothermally derived uniform ZnO hexagonal rods.

One-dimensional (1D) zinc oxide (ZnO) hexagonal rods have been successfully synthesized by surfactant free hydrothermal process at different temperatures. It can be found that the reaction temperature play a crucial role in the formation of ZnO uniform hexagonal rods. The possible formation processes of 1-D ZnO hexagonal rods were investigated. The zinc hydroxide acts as the morphology-formative intermediate for the formation of ZnO nanorods. Upon excitation at 325 nm, the sample prepared at 180°C show several emission bands at 400 nm (∼3.10 eV), 420 nm (∼2.95 eV), 482 nm (∼2.57 eV) and 524 nm (∼2.36 eV) corresponding to different kind of defects. TL studies were carried out by pre-irradiating samples with γ-rays ranging from 1 to 7 kGy at room temperature. A well resolved glow peak at ∼354°C was recorded which can be ascribed to deep traps. Furthermore, the defects associated with surface states in ZnO nano-structures are characterized by electron paramagnetic resonance.

Luminescence studies and EPR investigation of solution combustion derived Eu doped ZnO.

ZnO:Eu (0.1 mol%) nanopowders have been synthesized by auto ignition based low temperature solution combustion method. Powder X-ray diffraction (PXRD) patterns confirm the nanosized particles which exhibit hexagonal wurtzite structure. The crystallite size estimated from Scherrer's formula was found to be in the range 35-39 nm. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies reveal particles are agglomerated with quasi-hexagonal morphology. A blue shift of absorption edge with increase in band gap is observed for Eu doped ZnO samples. Upon 254 nm excitation, ZnO:Eu nanopowders show peaks in regions blue (420-484 nm), green (528 nm) and red (600 nm) which corresponds to both Eu2+ and Eu3+ ions. The electron paramagnetic resonance (EPR) spectrum exhibits a broad resonance signal at g=4.195 which is attributed to Eu2+ ions. Further, EPR and thermoluminescence (TL) studies reveal presence of native defects in this phosphor. Using TL glow peaks the trap parameters have been evaluated and discussed.

EPR and photoluminescence studies of ZnO:Mn nanophosphors prepared by solution combustion route.

Nanocrystalline ZnO:Mn (0.1 mol%) phosphors have been successfully prepared by self propagating, gas producing solution combustion method. The powder X-ray diffraction of as-formed ZnO:Mn sample shows, hexagonal wurtzite phase with particle size of ∼40 nm. For Mn doped ZnO, the lattice parameters and volume of unit cell (a=3.23065 Å, c=5.27563 Å and V=47.684 (Å)(3)) are found to be greater than that of undoped ZnO (a=3.19993 Å, c=5.22546 Å and V=46.336 (Å)(3)). The SEM micrographs reveal that besides the spherical crystals, the powders also contained several voids and pores. The TEM photograph also shows the particles are approximately spherical in nature. The FTIR spectrum shows two peaks at ∼3428 and 1598 cm(-1) which are attributed to O-H stretching and H-O-H bending vibration. The PL spectra of ZnO:Mn indicate a strong green emission peak at 526 nm and a weak red emission at 636 nm corresponding to (4)T(1)→(6)A(1) transition of Mn(2+) ions. The EPR spectrum exhibits fine structure transition which will be split into six hyperfine components due to (55)Mn hyperfine coupling giving rise to all 30 allowed transitions. From EPR spectra the spin-Hamiltonian parameters have been evaluated and discussed. The magnitude of the hyperfine splitting (A) constant indicates that there exists a moderately covalent bonding between the Mn(2+) ions and the surrounding ligands. The number of spins participating in resonance (N), its paramagnetic susceptibility (χ) have been evaluated.

Combustion synthesis, characterization and Raman studies of ZnO nanopowders.

Spherical shaped ZnO nanopowders (14-50 nm) were synthesized by a low temperature solution combustion method in a short time <5 min. Rietveld analysis show that ZnO has hexagonal wurtzite structure with lattice constants a=3.2511(1) Å, c=5.2076(2) Å, unit cell volume (V)=47.66(5) (Å)(3) and belongs to space group P63mc. SEM micrographs reveal that the particles are spherical in shape and the powders contained several voids and pores. TEM results also confirm spherical shape, with average particle size of 14-50 nm. The values are consistent with the grain sizes measured from Scherrer's method and Williamson-Hall (W-H) plots. A broad UV-vis absorption spectrum was observed at ∼375 nm which is a characteristic band for the wurtzite hexagonal pure ZnO. The optical energy band gap of 3.24 eV was observed for nanopowder which is slightly lower than that of the bulk ZnO (3.37 eV). The observed Raman peaks at 438 and 588 cm(-1) were attributed to the E(2) (high) and E(1) (LO) modes respectively. The broad band at 564 cm(-1) is due to disorder-activated Raman scattering for the A(1) mode. These bands are associated with the first-order Raman active modes of the ZnO phase. The weak bands observed in the range 750-1000 cm(-1) are due to small defects.

EPR, thermo and photoluminescence properties of ZnO nanopowders.

Nanocrystalline ZnO powders have been synthesized by a low temperature solution combustion method. The photoluminescence (PL) spectrum of as-formed and heat treated ZnO shows strong violet (402, 421, 437, 485 nm) and weak green (520 nm) emission peaks respectively. The PL intensities of defect related emission bands decrease with calcinations temperature indicating the decrease of Zn(i) and V(o)(+) caused by the chemisorptions of oxygen. The results are correlated with the electron paramagnetic resonance (EPR) studies. Thermoluminescence (TL) glow curves of gamma irradiated ZnO nanoparticles exhibit a single broad glow peak at ∼343°C. This can be attributed to the recombination of charge carriers released from the surface states associated with oxygen defects, mainly interstitial oxygen ion centers. The trapping parameters of ZnO irradiated with various γ-doses are calculated using peak shape method. It is observed that the glow peak intensity increases with increase of gamma dose without changing glow curve shape. These two characteristic properties such as TL intensity increases with gamma dose and simple glow curve structure is an indication that the synthesized ZnO nanoparticles might be used as good TL dosimeter for high temperature application.