A review on selected heterogeneous photocatalysts for hydrogen production

In this study, visible light‐driven heterogeneous photocatalysts for hydrogen production are comparatively assessed based on technical, environmental, and cost criteria. The photocatalysis systems are compared with respect to their (i) rate of hydrogen generation per gram; (ii) rate of hydrogen generation per m² of the specific surface area; and (iii) the band gap energy. The photocatalysis systems are also compared and discussed in terms of flammability, reactivity, and their impact on living systems' health. Furthermore, the costs of the required components of the photocatalysis systems are ranked. In addition to individual photocatalyst comparison, seven photocatalyst groups are ranked and compared. The results show that TiO₂‐C‐362 and Ag_0.03Mn_0.40Cd_0.60S show the highest in terms of µmol/h‐g_cat and µmol/h‐m²_cat, respectively, and TiO₂‐C‐362 has the highest overall rankings. The Zn/In/S‐based photocatalyst groups show the highest hydrogen production rate in terms of µmol/h‐gcat and µmol/h‐m²_cat. Overall, Cd/S/Zn has the highest rankings when cost and health and environmental impact criteria are taken into account. Copyright © 2014 John Wiley & Sons, Ltd.     

MHD flow in a rectangular duct with a perturbed boundary

The unsteady magnetohydrodynamic (MHD) flow of a viscous, incompressible and electrically conducting fluid in a rectangular duct with a perturbed boundary, is investigated. A small boundary perturbation $\epsilon$ is applied on the upper wall of the duct which is encountered in the visualization of the blood flow in constricted arteries. The MHD equations which are coupled in the velocity and the induced magnetic field are solved with no-slip velocity conditions and by taking the side walls as insulated and the Hartmann walls as perfectly conducting. Both the domain boundary element method (DBEM) and the dual reciprocity boundary element method (DRBEM) are used in spatial discretization with a backward finite difference scheme for the time integration. These MHD equations are decoupled first into two transient convection–diffusion equations, and then into two modified Helmholtz equations by using suitable transformations. Then, the DBEM or DRBEM is used to transform these equations into equivalent integral equations by employing the fundamental solution of either steady-state convection–diffusion or modified Helmholtz equations. The DBEM and DRBEM results are presented and compared by equi-velocity and current lines at steady-state for several values of Hartmann number and the boundary perturbation parameter.     

Road to Metastasis: The TWEAK Pathway as a Discriminant between Metastasizing and Non-Metastasizing Thick Melanomas

Cutaneous melanoma (CM) is the most aggressive form of skin cancer, and its worldwide incidence is rapidly increasing. Early stages can be successfully treated by surgery, but once metastasis has occurred, the prognosis is poor. However, some 5–10% of thick (≥2 mm) melanomas do not follow this scenario and run an unpredictable course. Little is known about the factors that contribute to metastasis in some patient with thick melanomas and the lack thereof in thick melanoma patients who never develop metastatic disease. We were therefore interested to study differential gene expression and pathway analysis and compare non-metastatic and metastatic thick melanomas. We found that the TNF-like weak inducer of apoptosis (TWEAK) pathway was upregulated in thick non-metastasizing melanomas. MAP3K14 (NIK1), BIRC2 (cIAP1), RIPK1, CASP7, CASP8, and TNF play an important role in inhibiting proliferation and invasion of tumor cells via the activation of the non-canonical NF-κB signaling pathway. In particular, this pathway sensitizes melanoma cells to TNF-alpha and activates the apoptosis module of the TWEAK pathway in thick non-metastasizing melanomas. Hence, our study suggests a potential role of the TWEAK pathway in inhibiting thick melanoma from metastasis. Exploitation of these genes and the pathway they control may open future therapeutic avenues.     

Obtaining Butter Oil Triacylglycerols Free from β-Carotene and α-Tocopherol via Activated Carbon Adsorption and Alumina-Column Chromatography Treatments

It is difficult to remove β-carotene from oils with alumina-column chromatography, because β-carotene is even less-polar than triacylglycerols (TAGs) are. The objective of this study was to obtain butter oil TAGs free from β-carotene and antioxidants via sequential treatments with activated carbon (AC) adsorption and alumina column chromatography. The AC used was prepared from waste apricots. The effects of AC dosages, temperatures and time courses on β-carotene adsorption were studied. The Langmuir and Freundlich isotherms were used to describe the adsorption of β-carotene onto AC, and it was found to be more consistent with the Freundlich isotherm with a higher R ² value (0.9784). Adsorption kinetics of β-carotene was analyzed by pseudo-first order and pseudo-second order models. The pseudo-second order model was found to explain the kinetics of β-carotene adsorption more effectively (R ² = 0.9882). The highest β-carotene reduction was achieved (from 31.9 to 1.84 mg/kg) at an AC dosage of 10 wt%, temperature of 50 °C, and adsorption time of 240 min. A considerable amount of α-tocopherol was also adsorbed during the AC treatment. Remaining portions of α-tocopherol were completely removed with alumina adsorption chromatography. The method described may be used for purification of vegetable oil TAGs, which will be used as model compounds in model oxidation studies.     

Preparation and characterization of ciprofloxacin‐loaded alginate/chitosan sponge as a wound dressing material

The aim of this study is preparation and characterization of alginate/chitosan sponges including a model antibiotic (i.e., ciprofloxacin) to use in wound and/or burn treatment. Sponges were prepared firstly by the gelation of sodium alginate followed by lyophilization, crosslinking with calcium chloride, and finally coating with chitosan. Sponges were characterized with respect to morphology, water uptake, in vitro drug release behavior, and antimicrobial activity. Investigated and evaluated parameters in all of these studies were selected as the concentration of calcium chloride, alginate viscosity, drug content, and molecular weight of chitosan. Drug release and water uptake were found to be greatly influenced by these parameters. Water uptake and drug release rate were decreased by increasing the crosslinking density, chitosan molecular weight, and alginate viscosity. In the antimicrobial tests, it was obtained that the antimicrobial activity is directly proportional with the release rates and water uptake. Morphological studies showed a highly porous structure with interconnected pores. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1602–1609, 2006     

Sorption and Preconcentration of Vanadium,Chromium, Manganese,and Lead on Silica Gel Modified with (3‐Mercaptopropyl) Trimethoxysilane

Abstract

3‐mercaptopropyltrimethoxysilane, (CH₃O)₃SiCH₂CH₂CH₂SH, loaded on silica gel was used as a preconcentration sorbent for V, Cr, Mn and Pb prior to their determination by graphite furnace atomic absorption spetrometry (GFAAS). Surface characteristics and surface area of the silica gel before and after chemical modification were determined by elemental analysis. The retention and recovery of the analyte elements were studied by applying batch and column techniques. The experimental parameters, such as the effect of pH of the sample, shaking time in batch technique, flow rate of the eluent, the concentration of acid solution in the column section, and the amount of silica on retention and elution have been investigated. All elements were quantitatively (≥90%) recovered in the batch technique with R.S.D. values of 3.0 for vanadium, 1.8 for chromium, 1.7 for manganese, and 0.4 for lead. The same recoveries were obtained in the column techniques for all elements, while manganese in sea water could not be succesfully recovered. Detection limits of the method for vanadium, chromium, manganese, and lead are 1.1, 1.4, 1.3, and 0.8 ng, respectively.     

Lot-splitting approach of a hybrid manufacturing system under CONWIP production control: a mathematical model

This paper discusses the advantages of lot splitting in hybrid manufacturing environments where cellular and functional layouts are combined under Constant Work in Process (CONWIP) production control. The proposed model fills a research gap in the related literature by applying lot splitting and pull production simultaneously. A linear CONWIP control mathematical model that minimises the average flow time is developed in case of lot splitting. The developed model has sequence-dependent set-up times. The demand level, coefficient of variation (CV) impact and set-up time reduction effect on CONWIP production control are also investigated. The model is solved using GAMS21.6 optimisation software; the optimal backlog list, the number and size of sublots are reported. The proposed model is compared with lot production under push control in different settings as well as with two different heuristics from the literature. Experimental results indicate that in all settings, the lot splitting is more advantageous than lot production in terms of average flow time. CV has a greater effect than set-up time reduction on average flow time.     

Concomitant Crystallization of Copper(II) Sachharinato Complexes with 2-methylpyrazine as a Monomer and an One-dimensional Polymer: Syntheses,Crystal Structures,Spectroscopic and Thermal Properties

The reaction of [Cu(sac)₂(H₂O)₄] · 2H₂O with 2-methylpyrazine (mpyz) leads two complexes, concomitant crystallization of a mononuclear complex [Cu(sac)₂(mpyz)(H₂O)₂] (1) and a polymeric complex [Cu(sac)₂(μ-mpyz)]_n (2). Both complexes have been characterized by elemental analyses, magnetic measurements, FT-IR and ESR, TG-DTA and single-crystal X-ray diffraction analyses. Single-crystal X-ray analyses show that complex 1 consists of discrete molecules in which the copper(II) ions exhibits a square-pyramidal coordination geometry. The individual molecules of 1 are connected into a hydrogen-bonded chain structure, which is further assembled to form a three-dimensional network by π–π stacking interactions. Complex 2 is an 1D coordination polymer in which copper(II) centers are bridged by the mpyz ligand. The chains are further assembled to form two-dimensional frameworks by π–π and C–H···π stacking interactions.