SYNTHESIS AND EVALUATION OF ETHYL (4-(N-(THIAZOL-2-YL) SULFAMOYL) PHENYL)CARBAMATE (TSPC) AS A CORROSION INHIBITOR FOR MILD STEEL IN 0.1M HCL

Laboratory synthesized ethyl (4-(N-(thiazol-2-yl)sulfamoyl)phenyl)carbamate (TSPC), characterized by 1H NMR spectroscopy, was evaluated as corrosion inhibitor of mild steel in 0.1M HCl using electrochemical techniques. Open circuit potential, potentiodynamic polarization and impedance spectroscopy were used to evaluate the inhibition efficiency of (TSPC) at various concentrations. The obtained electrochemical data indicated that (TSPC) acts as moderate corrosion inhibitor for mild steel in acidic media. It is found that the inhibition efficiency increases with the concentration of the inhibitor till 400ppm. The adsorption isotherm involving physisorption of (TSPC) at room temperature and the experimental data complied to the Langmuir adsorption isotherms and the negative values of the Gibb’s free energy of adsorption obtained suggested that inhibitor molecules have been spontaneously adsorbed onto the mild steel surface

New Longitudinal Waves in Electron-Positron-Ion Quantum Plasmas

A general quantum dispersion equation for electron-positron(hole)-ion quantum plasmas is derived and studied for some interesting cases. In an electron-positron degenerate Fermi gas, with or without the Madelung term, a new type of zero sound waves are found. Whereas in an electron-hole plasmas a new longitudinal quantum waves are revealed, which have no analogies in quantum electron-ion plasmas. The excitation of these quantum waves by a low-density monoenergetic straight electron beam is examined. Furthermore, the KdV equation for novel quantum waves is derived and the contribution of the Madelung term in the formation of the KdV solitons is discussed

Comparative Hepatotoxicity of Aflatoxin B1 among Workers Exposed to Different Organic Dust with Emphasis on Polymorphism Role of Glutathione S-Transferase Gene

AIM: The study aimed to investigate effects of organic dust exposure from different sources on aflatoxin B1-albumin adducts (AFB1/Alb), and role of glutathione S-transferase (GST) gene polymorphism in hepatotoxicity of (AFB1) among exposed workers. MATERIAL AND METHODS: Liver enzymes, AFB1/Alb, and GST polymorphism were estimated in 132 wheat flour dust and 87 woods sawmill workers, and 156 controls.RESULTS: Results revealed that AFB1/Alb and liver enzymes were significantly elevated in exposed workers compared to controls, and were significantly higher in sawmill workers compared to flour workers. AFB1/Alb in flour and sawmill workers with GSTT1 and GSTM1&GSTT1 null genotypes were significantly higher than controls, and in sawmill workers with GSTM1&GSTT1 null than flour workers. Liver enzymes (ALT and AST) in sawmill workers were significantly higher than flour workers and controls in all GST polymorphism; except in GSTT1 polymorphism, where these enzymes were significantly higher in the two exposed groups than controls.CONCLUSIONS: In conclusion, organic dust exposure may cause elevation in AFB1/Alb and liver enzymes of exposed workers, and GST gene polymorphism plays an important role in susceptibility to hepatic parenchymal cell injury; except in workers with GSTT1&GSTM1 null genotype, gene susceptibility seemed to have little role and the main role was for environmental exposures

The Correlation Between Hepatitis B Virus Precore/Core Mutations and the Progression of Severe Liver Disease

Viral mutations acquired during the course of chronic hepatitis B virus (HBV) infection are known to be associated with the progression and severity of HBV-related liver disease. This study of HBV-infected Saudi Arabian patients aimed to identify amino acid substitutions within the precore/core (preC/C) region of HBV, and investigate their impact on disease progression toward hepatocellular carcinoma (HCC). Patients were categorized according to the severity of their disease, and were divided into the following groups: inactive HBV carriers, active HBV carriers, liver cirrhosis patients, and HCC patients. Two precore mutations, W28* and G29D, and six core mutations, F24Y, E64D, E77Q, A80I/T/V, L116I, and E180A were significantly associated with the development of cirrhosis and HCC. Six of the seven significant core mutations that were identified in this study were located within immuno-active epitopes; E77Q, A80I/T/V, and L116I were located within B-cell epitopes, and F24Y, E64D, and V91S/T were located within T-cell epitopes. Multivariate risk analysis confirmed that the core mutations A80V and L116I were both independent predictors of HBV-associated liver disease progression. In conclusion, our data show that mutations within the preC/C region, particularly within the immuno-active epitopes, may contribute to the severity of liver disease in patients with chronic hepatitis. Furthermore, we have identified several distinct preC/C mutations within the study population that affect the clinical manifestation and progression of HBV-related disease. The specific identity of HBV mutations that are associated with severe disease varies between different ethnic populations, and so the specific preC/C mutations identified here will be useful for predicting clinical outcomes and identifying the HBV-infected patients within the Saudi population that are at high risk of developing HCC