Enalapril-induced renal artery thrombosis in unilateral renal artery stenosis

Intravascular adhesion of leucocytes plays a role in the pathogenesis of acute and chronic vascular disease. Regular aerobic exercise seems to protect against vascular disease. Since leucocyte adhesion is mediated by integrins, we tested the hypothesis that surface expression of the integrin adhesive receptors LFA-1 (cd11a/cd18), MAC-1 (cd11b/cd18), gp 150/95 (cd11c/cd18), and VLA-4 (cd29/cd49) is decreased by moderate endurance exercise. Surface expression of integrins was measured by FACS analysis in 19 healthy subjects (16 males, 3 females, 36.6 +/- 8.7 years, 177.1 +/- 7.5 cm, 70.3 +/- 8.1 kg) before and after submaximal exercise (3 h run) using monoclonal antibodies against cd11a, cd11b, cd11c, cd18, cd29 and cd49. In addition, we compared resting integrin expression in this group with a group of sedentary subjects (19 males, 6 females, 29.3 +/- 5.3 years). White blood cell count increased from 5300 ml(-1) to 9740 ml(-1) during exercise (P < 0.001). Nevertheless, the expression (indicated by the mean log fluorescence) of cd11a (94 +/- 24 vs. 78 +/- 14) and cd18 (128 +/- 31 vs. 102 +/- 21) on lymphocytes and of cd11a (104 +/- 25 vs. 85 +/- 16), cd11c (497 +/- 171 vs. 408 +/- 126) cd29 (109 +/- 16 vs. 89 +/- 16), cd49 (69 +/- 8 vs. 54 +/- 11) on monocytes was decreased after exercise (all P < 0.05). In contrast, integrin expression on granulocytes was not altered by exercise. Comparison of exercising and sedentary subjects showed a significantly decreased expression of integrins in exercising subjects. Our results demonstrate that moderate exercise leads to decreased expression of integrin receptors on leucocytes. This decreased expression of adhesion molecules may result in decreased adhesion and infiltration of leucocytes into the vessel wall. This phenomenon may play a role in the beneficial effect of moderate exercise in prevention of acute and chronic vascular disease.     

Synthesis and compressive behavior of Cr2GeC up to 48 GPa

M_n+1AX_n compounds have gathered huge momentum because of its exciting properties. In this paper we report the synthesis of ternary layered ceramic Cr₂GeC, a 211 M_n+1AX_n compound by hot-pressing. Scanning electron microscopy and X-ray diffraction have been employed to characterize the new synthesized phase. High-pressure compressibility of Cr₂GeC were measured using diamond anvil cell and synchrotron radiation at room temperature up to 48 GPa. No phase transformation was observed in the experimental pressure range. The bulk modulus of Cr₂GeC calculated using the Birch–Murnaghan equation of state is 169 ± 3 GPa, with K′ = 3.05 ± 0.15.     

Oligoaniline intermediates in the aniline-peroxydisulfate system

Chemical oxidative polymerization of aniline using peroxydisulfate oxidant in aqueous pH 2.5–10.0 buffers yields electrically insulating brown powders that are believed to be mixtures of Michael-type adducts of benzoquinone monoimine and aniline at various stages of hydrolysis. A spectroscopically similar product is formed when solid 1,4-benzoquinone is added to an aqueous solution of aniline at room temperature in the absence of peroxydisulfate. This suggests that the peroxydisulfate oxidant in the aniline/S₂O₈^2? system provides a pathway for the formation of benzoquinone monoimine as an intermediate. Benzoquinone monoimine intermediate could be formed as a result of a Boyland–Sims rearrangement of aniline proceeding via the intermediacy of p-aminophenyl sulfate. Benzoquinone monoimine undergoes a series of conjugate 1,4-Michael-type addition/reoxidation/coupling steps with aniline or p-aminophenyl sulfate yielding the oligoaniline product. The precipitate that is isolated is also in the midst of two simultaneous pH dependent hydrolysis reactions: (i) hydrolysis of the imine groups to quinone, and (ii) hydrolysis of arylsulfates to phenols. The ratio of hydrolysis in each case was determined by the C/N ratio and sulfur elemental analysis values yielding analytical data that is consistent with experimentally determined values and also with our proposed reaction scheme. These findings offer a rationale for the high C/N ratios (>6.0) frequently observed in these systems while tracing the genesis of the residual sulfur in the product to unhydrolyzed arylsulfate. The oligoaniline product has previously been reported to have a novel poly-aza structure consisting of continuously linked –N–N–N– bonds, and alternately also reported to consist of phenazine-type linkages. This study is consistent with the latter and describes a pathway to phenazine coupling through a second and third stage hydrolysis of the arylsulfate and reoxidation with peroxydisulfate. There is no pathway for the formation of linear –N–N–N– linkages in the aniline/benzoquinone adduct and the striking similarity between its spectroscopic properties and the aniline/S₂O₈^2? adduct suggests that it is not a preferred pathway under these experimental conditions.     

Effects of various hydrocarbons on micellar growth

The effect of aliphatic and aromatic hydrocarbons on surfactant micellar growth has been investigated by viscosity measurements at 40°C. Aqueous and aqueous KBr (0.1 M) solutions of 0.1 M cetylpyridinium bromide (CPB) showed that the viscosity behavior changed substantially in the presence of KBr. This is attributed to favorable conditions produced by KBr that assist micellar growth by addition of hydrocarbons. Reasons for the effectiveness of the solubilized hydrocarbons are suggested and supported by theoretical arguments. The causes of viscosity decrease at higher aromatic hydrocarbon concentrations are also explained. Micellar growth with soluble aromatic/aliphatic hydrocarbons could also be initiated if a moderate salt concentration is present in CPB micellar solutions. The chainlength, solubilization site, and molar volume of the soluble hydrocarbons all affect the bulk viscosity of the solution. Such surfactant and hydrocarbon combinations may find use in micellar-enhanced ultrafiltration of benzene and its derivatives, but it should be kept in mind that micellar shape may change and be more curved at higher benzene derivative concentrations.     

Hydrogen peroxide sensing properties of PVA/TiO2/I2 nanocomposite‐based free standing membranes

The nanocomposite of titanium‐di‐oxide (TiO₂)/iodine (I₂) in polyvinyl alcohol (PVA) matrix has been explored to be used in hydrogen peroxide (H₂O₂) sensing applications for the first time. The proposed nanocomposite can be easily casted in the form of thin film on glass substrates as well as free standing membranes. These nanocomposite films and membranes exhibit reduced resistance values and easily observable colour changes in the presence of H₂O₂. The films also exhibit significant quenching in photoluminescence emission properties upon H₂O₂ exposure. These sensor responses have been attributed to redox reactions at nanocomposite films and H₂O₂ interface. This study indicates an easy to fabricate, flexible and environmental friendly sensing platform for H₂O₂. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42257.     

Studies on corrosion control of naphtha fractions in overhead condensing system using laboratory distillation device

Corrosion in the overhead condensing system of atmospheric distillation units is a common occurrence in petroleum refineries worldwide. These corrosion problems are influenced by the presence of three phases: vapours, liquid hydrocarbons and aqueous phase containing hydrochloric acid formed during distillation by decomposition of chloride salts of calcium and magnesium.Present studies highlight the corrosion control of naphtha fractions of Bombay High and Dubai crude oils in laboratory distillation device by chemical treatment using various corrosion inhibitors having different functional groups. These studies were carried out using two phase systems (aqueous-hydrocarbon) in the distillation device having facilities for monitoring the corrosion and temperatures in vapour condensing region and liquid condensate. Corrosion monitoring was carried out by potentiodynamic polarization technique and dissolved iron analysis using inductively coupled plasma atomic emission spectroscopy (ICPAES). Experimental findings indicate that Dubai naphtha fraction is more corrosive in nature when compared to Bombay High naphtha. This observation can also be explained on the basis of characterization of both crude oils and their naphtha fractions. At normally recommended dosage level as in refinery overhead systems, water soluble corrosion inhibitors are more effective than hydrocarbon soluble ones in the vapour condensing region as well as in the liquid condensate of both naphtha fractions.     

On the solution and applicability of bivariate population balance equations for mixing in particle phase

New benchmarks are used to test two classes of discretization methods available in the literature to solve bivariate population balance equations (2-d PBEs), and the applicability of these mean-field equations to finite size systems. The new benchmarks, different from the extensions of their 1-d counterparts, relate to prediction of kinetics of mixing in particle phase under: (i) pure aggregation of particles, called aggregative mixing, and (ii) simultaneous breakup and coalescence of drops. The discretization methods for 2-d PBEs, derived from the widely used 1-d solution methods, are first classified into two classes. We choose one representative method from each class. The results show that the extensions based on minimum consistency of discretization perform quite well with respect to both the new and the old benchmarks, in comparison with the geometrical extensions of 1-d methods. We next revisit aggregative mixing using Monte-Carlo simulations. The simulations show that (i) the time variation of the extent of mixing in finite size systems has power law scaling with the system size, and (ii) the mean-field PBEs fail to capture the evolution of mixing for reduced population of particles at long times. The sum kernel limits the applicability of PBEs to substantially larger particle populations than that seen for the constant kernel. Interestingly, these populations are orders of magnitude larger than those at which the PBEs fail to capture the evolution of total particle population correctly.     

A near infrared optical reflector using one-dimensional photonic crystal structure containing chalcogenide glasses

The reflectivity of one-dimensional chalcogenide photonic crystal (CGPC) structure with the first order reflection band in near infrared (NIR) region is theoretically studied. Sb-Se and Ge-S chalcogenide glasses are used as high and low refractive index layers respectively, because these materials have zero absorption in NIR region. The transfer matrix method (TMM) is employed to calculate the reflective spectra of the proposed structure. The theoretical results of reflective spectra of bulk chalcogenide materials with the composition of Sb₄₀Se₆₀ and Ge₃₀S₇₀ for 4, 8, 12 and 15 layers and thicknesses of 117 nm and 183 nm respectively, at normal incidence, are close agreement with the experimental results. Furthermore, by increasing the number of layers of Sb₄₀Se₆₀ and Ge₃₀S₇₀, the reflection bands can be enhanced in the wider range of the NIR region for the polarization at different angles and thus the broadband omnidirectional reflector can be designed.