Effects of street tree configuration and placement on roadside thermal environment within a tropical urban canyon.

The Urban Heat Island (UHI) effect increases surface and air temperatures, affecting urban health and well-being. A well-known UHI mitigation measure is the increased roadside tree vegetation facilitating evapotranspiration and shade. In its implementation, the identification of thermally optimal street tree configurations and a quantitative assessment of how various street tree configurations impact the roadside thermal environment were deemed essential and were chosen as the main aims of the study. Twelve tropical urban canyons were categorized into three clusters representative of different street tree placement and configuration scenarios. A control cluster devoid of any roadside trees was also selected. The CFD-based 3-D microclimate model 'ENVI-met' was used to identify suitable roadside urban tree planting scenarios for better microclimate regulation. From a tree planting scenario analysis done as part of the study, the greening scenario of using a 'Continuous tree row (Densely foliated - high Leaf Area Density - LAD)' tree configuration was recognized with the highest ambient temperature reduction of 1.41 °C. The study outcomes reveal that tree configuration of high LAD street trees placed in closer spacing contributes towards the better cooling effect of roadside environments and thus improves thermal comfort for warmer tropical climates of higher humidity levels. The study's findings offer valuable insights for urban planning professionals and policymakers involved in designing future cities and urban developments. They emphasize the importance of strategic tree-planting designs and configurations to enhance thermal comfort and livability in urban areas. This highlights the need to avoid ad-hoc procedures and instead prioritize well-planned roadside tree configurations within urban canyons.

Enhanced Photo-Catalytic and Antibacterial Properties of Ni-Doped Cd0.9Zn0.1S Nanostructures.

The present work describe the synthesis of Cd0.9Zn0.1S and Cd0.87Zn0.1Ni0.03S nanostructures by chemical co-precipitation method. The XRD profile proved the cubic crystal structure of the samples without any impurity related phases. The reduced size from 63 to 51 Å and the dissimilarities in lattice parameters and micro-strain has been discussed by Ni addition in Cd0.87Zn0.1Ni0.03S structure. The noticed anomalous optical studies and the elevated transmittance at Ni doped sample suggested them for the fabrication of efficient opto-electronic devices. The energy gap reduction during the substitution of Ni = 3% is explained by the generation of extra energy levels associated with defects within the two bands. The release of additional charge carriers, improved optical property, reduced particle size and more defect generation are responsible for the enhanced photo-catalytic performance of Ni doped Cd0.9Zn0.1S. The enhanced anti-bacterial capacity in Cd0.87Zn0.1Ni0.03S is described by the collective response of reduced particle size and higher reactive oxygen species (ROS) like O2 ⋅- , H2O2 and OH ⋅ generating capacity.

Influence of Ni2+ ions on the structural, morphological, photoluminescence, photo-catalytic and anti-bacterial studies of Cd0.9Zn0.1S nanostructures.

The present investigation reported the controlled synthesis of Cd0.9Zn0.1S and Cd0.89Zn0.1Ni0.01S nanostructures by simple chemical co-precipitation route. The XRD analysis confirmed the cubic structure of CdS on Zn doped CdS and Zn, Ni dual doped CdS without any secondary/impurity phases and no alteration in CdS cubic phase was noticed by Zn/Ni addition. The shrinkage of crystallite size from 69 to 43 Å and the variation in lattice constants and micro-strain were described by the addition of Ni and the defects associated with Ni2+ ions. Microstructural and optical studies of the prepared films were carried out using scanning electron microscope (SEM), UV-visible spectrometer and photoluminescence (PL) spectra. The enhanced optical absorbance in the visible wavelength and the reduced energy gap by Ni substitution showed that Cd0.89Zn0.1Ni0.01S nanostructures are useful to improve the efficiency of opto-electronic devices. The functional groups of Cd-S/Zn-Cd-S/Zn/Ni-Cd-S and their chemical bonding were verified by Fourier transform infrared (FTIR) studies. The elevated visible PL emissions such as blue and green emissions by Ni addition was explained by decreasing of crystallite size and generation of more defects. Zn, Ni dual doped CdS nanostructures are identified as the probable an efficient photo-catalyst for the degradation of methylene blue dye. The liberation of more charge carriers, better visible absorbance, improved surface to volume ratio and the creation of more defects are accountable for the current photo-catalytic activity in Zn/Ni doped CdS which exhibited better photo-catalytic stability after sex cycling process. The better bacterial killing ability is noticed in Ni doped Cd0.9Zn0.1S nanostructure which is due to the collective effect of lower particle/grain size and also higher ROS producing capacity.

Metal concentration and its ecological risk assessment in the beach sediments of Coromandel Coast, Southern India.

The present study investigates the concentration of acid leachable trace metals (ALTMs) and their ecological risk in the beach sediments of Coromandel Coast, Southern India. In total, thirty-six beach sediments (eighteen samples from low tide and eighteen samples from high tide) were collected from the study area. The results of the study of the ALTMs suggest that the sediments are enriched by natural processes with significant anthropogenic influences. The distribution of ALTMs in beach sediments is in the following descending order: Fe > Cr > Mn > Pb > Ni > Cu > Co > Zn. The statistical results indicate that the metal concentrations were chiefly originated from natural processes such as leaching, weathering, and fluvial action. In addition, the textural characteristics, organic matter, and calcium carbonate percentage play an important role in the distribution of metals in the beach sediments.

Structural, optical and antibacterial investigation of La, Cu dual doped ZnO nanoparticles prepared by co-precipitation method.

La, Cu dual doped ZnO with Cu = 0%-4% were prepared by co-precipitation route. The XRD pattern optimized the Cu content as 2% which restrict the secondary phase formation. The new phase at 38.7° corresponding to CuO (111) and the another phase at 42.3° related to Zn (101) came from un-reacted Zn2+ ions appeared in Cu = 4% doped sample. Zeta potential measurements confirms the stability of the particles. The blue shift of absorption edge and the energy gap from 3.66 eV to 3.99 eV by Cu doping was discussed by the shape of the particles, the distortion of the host lattice and generation of defect concentrations. The characteristic IR peaks around 470-489 cm-1 was related to the octahedral sites of Zn-O for Cu = 0 and 2% which is shifted to 616 cm-1 corresponding to the tetrahedral site at Cu = 4%. The shift in frequency was originated from the dissimilarity in the volume and bond lengths by the substitution of La and Cu in Zn-O. Based on the antibacterial report, it can be concluded that the Cu-doped Zn-La-O solid solution compose an effectual antimicrobial agent against pathogenic microorganisms. Cu = 4% doped sample possessed highest bacterial killing capacity because of the enhanced crystallite size and high density of oxygen vacancies which led the higher ROS values. Tuning of crystallite size and energy gap and the enhanced bactericial killing capacity by Cu addition is useful for opto-electronic device and medical applications.

Computing the effective diffusion coefficient of solutes in a multi-salts solutions during forward osmosis (FO) membrane filtration: Experiments and mathematical modelling.

Diffusion coefficient of solutes through a porous membrane media is different from diffusion coefficient through a free homogenous media. Porosity, tortuosity and the thickness of the membrane significantly affect the diffusion through a specific thickness of a membrane and therefore it is termed as effective diffusion coefficient (Deff) which is lower than the actual diffusion coefficient, D. The Deff of single or dual solutes through a porous membrane layer are well documented but not for multiple salts. Therefore, in this study, single, dual and multiple salt mixtures were passed through a flat sheet cellulose triacetate Forward Osmosis (FO) membrane to obtain a semi-empirical relationship with the Deff and its water flux. This will allow computing the structural coefficient of FO membranes. Research community have spent tremendous efforts in membrane modification to reduce the structural coefficient to improve FO process efficiency. Our finding suggests that optimising the draw solution chemistry can achieve this goal.

Structural, optical, dielectric and antibacterial studies of Mn doped Zn0.96Cu0.04O nanoparticles.

Zn(0.96-x)Cu0.04Mn(x)O (0⩽x⩽0.04) nanoparticles were synthesized by sol-gel method. The X-ray diffraction pattern indicated that doping of Mn and Cu did not change the ZnO hexagonal wurtzite structure. The Mn doped nanoparticles had smaller average crystallite size than un-doped Zn0.96Cu0.04O nanoparticles due to the distortion in the host ZnO lattice. This distortion prevented the subsequent growth and hence the size reduced by Mn doping. The changes in lattice parameters, average crystallite size, peak position and peak intensity confirmed the Mn substitution in Zn-Cu-O lattice. The Mn and Cu co-doping increased the charge carrier density in ZnO nanoparticles which led to increase the dielectric constant. The dielectric constant also varied by depend the size of the nanoparticles. The change in morphology by Mn-doping was studied by transmission electron microscope. The optical absorption and band gap were changed with respect to both compositional and size effects. The band gap was initially increased from 3.65 to 3.73 eV at 1% of Mn doping, while decreasing trend in band gap was noticed for further increase of Mn. The band gap was decreased from 3.73 to 3.48 eV when Mn concentration was increased from 2% to 4%. Presence of chemical bonding and purity of the nanoparticles were confirmed by FTIR spectra. The antibacterial study revealed that that the antibacterial activity of Zn0.96Cu0.04O is enhanced by Mn doping.

Structural studies on AIPL1 and its functional interactions with NUB1 to identify key interacting residues in LCA4.

Leber congenital amaurosis (LCA) is an autosomal recessive disorder that causes visual impairment in children due to fifteen different gene mutations. Of these, mutations in Aryl-Hydrocarbon Receptor Interacting Protein-like 1 (AIPL1) cause the most severe form of LCA (LCA4) leading to the degeneration of photoreceptor cells. NEDD8 Ultimate Buster 1 (NUB1), a protein that regulates cell cycle progression, interacts with AIPL1 to prevent the over expression of NUB1. In the case of over expression, cell cycle progression is disrupted and may lead to LCA. The studies on interactions between these two proteins will aid in identifying potential modulators for this condition. Since no three-dimensional structure is currently available for these two proteins, in this study we predicted the structures of these two proteins by molecular modelling methods. Moreover, we also modelled the three proven significant mutant forms of AIPL1 spanning the tetratricopeptide domain. Finally, both the modelled wild and mutant structures of AIPL1 (A197P, C239R and G262S) were computationally docked to NUB1, so as to map the potential molecular interactions. This is the first study on modelling the structure-function relationship of AIPL1-NUB1 interactions which shall aid in discovery of novel therapeutic agents.

Chemical inhibition of fatty acid synthase: molecular docking analysis and biochemical validation in ocular cancer cells.

Fatty acid biosynthesis is an attractive target for anti-cancer therapeutics. The ocular cancer, retinoblastoma cells were treated with fatty acid synthase (FASN) enzyme inhibitors: cerulenin, triclosan and orlistat. The IC(50) and dose-dependent sensitivity of cancer cells to FASN inhibitors decrease in biologic enzyme activity, and cell morphology alterations were analysed. Molecular interactions of enzyme-inhibitor complexes were studied by molecular modelling and docking simulations. The crystal structures of ketoacyl synthase (PDB ID:3HHD) (cerulenin) and thioesterase (PDB ID:2PX6) (orlistat) domains of human FASN were utilized for docking, while for the non-crystallised human FASN enoyl reductase domain (triclosan), homology model was built and used for docking. All three inhibitors showed significant binding energy indicating stable complex formation with their respective FASN subunits. The predicted Ki value of the FASN inhibitors corroborated well with their corresponding anti-cancer effects.