Differences in prevalence of tobacco use among Indian urban youth: the role of socioeconomic status

This study examined whether the distribution of tobacco use and related psychosocial risk factors among youth in urban India vary by socioeconomic status (SES). Data were derived from a cross-sectional survey of students enrolled in the 6th and 8th grades in 32 schools in Delhi and Chennai (N = 11,642). The survey was conducted in 2004, before the implementation of a program designed to prevent and reduce tobacco use (MYTRI). Mixed-effect regression models were used (a) to determine the prevalence of tobacco use among private (higher SES) and government (lower SES) school students, (b) to investigate whether certain psychosocial factors were associated with increased tobacco use, and (c) to determine how these factors varied by school type. Ever-use of multiple forms of tobacco (e.g., gutkha, bidis, and cigarettes) was more prevalent among government school students than private school students. After adjusting for city, gender, grade, and age, we found the prevalence rate for ever-use of any tobacco product to be 18.9% for government school students, compared with 12.2% for private school students (p<.01). Students in government schools scored lower than private school students on most psychosocial risk factors for tobacco use studied here, indicating higher risk. Government school students scored the lowest for refusal skills, self-efficacy, and reasons not to use tobacco. Social susceptibility to chewing tobacco and social susceptibility to smoking were strong correlates of current tobacco use among government school students. Exposure to tobacco advertising was also a strong correlate of current tobacco use for government school students but not private school students. In two large cities of India, students attending government schools are using many forms of tobacco at higher rates than private school students. The psychosocial risk profile of government school students suggests they are more vulnerable to initiation and use and to outside influences that encourage use.     

Characterization of Thermal-Sprayed HAP and HAP/TiO<Subscript>2</Subscript> Coatings for Biomedical Applications

In the present study, hydroxyapatite (HAP) coating along with HAP/TiO₂ coating has been deposited by high-velocity flame spray (HVFS) technique onto 316LSS. Titania was used as a bond coat and HAP as top coat in HAP/TiO₂ coating. The main aim of the study is to investigate the corrosion behavior of thermal spray coating of HAP and HAP/TiO₂ on steel. Electrochemical corrosion testing was carried out using potentiodynamic polarization test. The corrosion behavior of bare and as-sprayed specimens was analyzed in simulated body fluid known as Hank’s solution. As-sprayed specimens along with corroded specimens were further characterized by XRD, SEM/EDS, and x-ray mapping analysis. It was observed that the HAP/TiO₂ coating possessed higher microhardness (280 Hv) as compared to HAP coating (254 Hv). Surface roughness also got enhanced in case of HAP/TiO₂ coating (9.35 μm) as compared to pure HAP coating (7.37 μm). The porosity of the HAP coating was found to be higher than the bond coating. It was observed that the Ca/P ratio almost resembled that of the natural bone composition. The corrosion resistance of steel increased after the deposition of HAP and HAP/TiO₂ coatings. The maximum corrosion resistance was exhibited by HAP/TiO₂ coating.     

Interaction of lanthanide and actinide with BaHfO3 perovskite: A case study with cerium and uranium

Speciation of actinide (An) and lanthanide (Ln) in technologically important ceramics is very important from both fundamental as well as technological aspects. The intrinsic structural flexibility of perovskite containing AO₆ and BO₁₂ polyhedra makes them suitable and rich hosts for An and Ln. In this work, emphasis was given to deciphering information such as oxidation state, local dopant site, charge compensating defects, excited state kinetics, and so forth in BaHfO₃ (BHO) related to dopant uranium (BHO-U) and cerium (BHO-Ce). Several spectroscopic techniques namely, time-resolved photoluminescence (TRPL), positron annihilation lifetime spectra (PALS), and thermoluminescence (TL) spectroscopy coupled with density functional theory (DFT) were employed to probe the same. Ce and U though are distributed at both Ba and Hf sites, Ce prefers the former, while U prefers the latter site. Uranium on the other hand stabilizes as U⁶⁺ in the form of octahedral uranate ion giving green emission. PALS suggested the formation of defects in BHO-Ce and BHO-U with oxygen vacancies predominating in the former whereas BHO-U perovskites are loaded with cation vacancies and vacancy clusters. These cation vacancies are responsible for lower TL output in BHO-U. TL measurements also suggested cerium doping leads to a higher density of deeper traps in BHO-Ce compared to uranium doping in BHO-U which is in concurrence with DFT results and may have implications in designing afterglow phosphors based on perovskite. We believe this work would have a long-term impact on exploring the potential of perovskite for nuclear waste host and afterglow phosphors applications.     

Estimation of vapour pressure and partial pressure of subliming compounds by low-pressure thermogravimetry

A method for the estimation of vapour pressure and partial pressure of subliming compounds under reduced pressure, using rising temperature thermogravimetry, is described in this paper. The method is based on our recently developed procedure to estimate the vapour pressure from ambient pressure thermogravimetric data using Langmuir equation. Using benzoic acid as the calibration standard, vapour pressure-temperature curves are calculated at 80, 160 and 1000 mbar for salicylic acid and vanadyl bis-2,4-pentanedionate, a precursor used for chemical vapour deposition of vanadium oxides. Using a modification of the Langmuir equation, the partial pressure of these materials at different total pressures is also determined as a function of temperature. Such data can be useful for the deposition of multi-metal oxide thin films or doped thin films by chemical vapour deposition (CVD).     

Hybrid polymer networks of unsaturated polyester–urethane as composite matrices for jute reinforcement

Reactions of unsaturated polyester resin and 4,4′ diphenyl methane diisocyanate were carried out at different NCO/OH ratios in presence of catalysts to form the hybrid polymer networks. Chain extender (1,4 butanediol) added in the hybrid network (NCO/OH ratio: 0.76) was optimized at a level of ～ 3 wt % only of the polyester resin. The curing of these networks was studied by a rigid body pendulum type (RPT) method in terms of reduced damping ratio and increased frequency. Lack of multiple glass transition temperatures, sharp Tan delta peak, and particulate composite type morphology clearly demonstrated the formation of phase mixed domains in the hybrid networks. The storage modulus and loss modulus master curves obtained by dynamic mechanical analysis indicate that hybrid polymer networks retained higher modulus at lower and intermediate frequencies over the polyester resin showing their superior time‐dependent response. Efficacy of these hybrid network resins was examined as matrices in the jute composites and compared with those of polyester resin and unsaturated polyester–polyurethane interpenetrating network matrices. It is found that the hybrid polymer network matrix composites exhibited superior physicomechanical properties under both dry and boiling water age test. Fractographic evidences such as fiber–matrix adhesion, hackle markings, and fiber breakage also supported their superior behavior over other composite matrices. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

SPECTROSCOPIC CHARACTERIZATION OF SOLVENT SOLUBLE FRACTIONS OF PETROLEUM VACUUM RESIDUES

ABSTRACT

NMR and FTIR spectroscopic techniques were used to investigate the effect of different solvent extraction schemes on the composition and chemical nature of species of vacuum residues of two Indian crude oils (namely Jodhpur and Heera) extractable into polar (ethyl acetate) and non-polar (n-pentane and n-heptane) solvents. The obtained soluble fractions were found to consist of mainly simple aliphatic and naphthenic ring structures, while insoluble fractions consisted primarily aromatic compounds. The results were used to draw inferences on the relative utility of different extraction schemes to upgrade vacuum residues as feedstocks for secondary conversion processes in petroleum industry.     

Pressure dependent phase transitions in (Pb,Ca)TiO3: Determination of structure using high pressure synchrotron X-ray and Raman studies

Pressure dependent studies on technologically important ferroelectric material Pb_0.70Ca_0.30TiO₃ show the occurrence of a new hitherto unreported pressure dependent phase transition around 4 GPa. In the pressure range 4–14 GPa, the parent tetragonal (P4mm) phase of Pb_0.70Ca_0.30TiO₃ transforms in to a monoclinic (Cm) phase before attaining its paraelectric cubic (Pm3m) phase around 15 GPa. High pressure Raman studies reveal the presence of a critical pressure above which the ferroelectric phase starts to reappear in the paraelectric phase. This critical pressure is found to be much lower than the critical pressure observed in pure PbTiO₃. Possible reasons for this lowering of the critical pressure are presented.