Studies on Hot Corrosion of the Microstructurally Different Regions of 2.25Cr-1Mo (T22) Boiler Tube Steel Weldment

This study examines the effect of microstructurally different regions on the hot corrosion of tungsten inert gas weldment in 2.25Cr-1Mo (T22) boiler tube steel. Various regions of weldment were oxidized in molten salt Na₂SO₄-60% V₂O₅ environment at 900 °C. The base metal was found to oxidize at much higher rates than the weld metal and the heat-affected zone. Oxide scales formed in the three regions were compared by scanning electron microscopy with energy dispersive of X-ray analysis, X-ray diffraction pattern, and electron probe microanalysis. The research investigates the formation of inner scales with free Cr over the HAZ.     

Performance of carbon dioxide vent for direct methanol fuel cells

Direct methanol fuel cells have potentially high energy density if the balance of plant and fuel losses can be kept to a minimum. CO₂ accumulation in the fuel tank can lower the efficiency and performance of closed-tank methanol fuel cells. This report discusses the implementation of a passive CO₂ vent fabricated with poly(1-trimethyl silyl propyne) and 1,6-divinylperfluorohexane. The performance of the membrane as a selective vent for carbon dioxide in the presence of methanol has been studied at various operating conditions. First, the selectivity of the vent membrane improved with temperature. Second, the activation energy for permeation through the polymer membrane corresponded to diffusion controlled transport of CO₂ and sorption controlled transport for methanol vapor. The activation energy for CO₂ transport through the poly(1-trimethyl silyl propyne) and 1,6-divinylperfluorohexane membrane was less than that for a pure poly(1-trimethyl silyl propyne) membrane. Finally, the polymer had a high selectivity for carbon dioxide compared to both liquid and vapor phase methanol.     

Amplitude comparator based algorithm for directional comparisonprotection of transmission lines

A high-speed directional comparison relay based on an evaluation of the locally measured deviations of the voltage and the phase-shifted current from their prefault values is described. The operation of the relay depends on the power frequency components of the voltage and phase-shifted current deviation signals. The direction to a fault is determined by an amplitude comparator technique which compares a discriminant value with a positive or negative threshold. Simulation studies on a three-phase power system model show that the direction to a fault is determined within the first few milliseconds following the inception of a fault. Studies over a wide range of faults and source impedance angles show that the proposed amplitude comparator technique performs better than an analogous phase comparator technique     

Laboratory investigation of an amplitude comparator baseddirectional comparison digital protection scheme

A directional comparison digital protection scheme has been implemented with a 16-b single-board computer at each end of a physical model of a transmission line, with communication between the two ends. The protection algorithm makes use of the fundamental frequency components of the deviation signals of the voltage and phase-shifted current. Software routines have been developed for fault monitoring, directional determination, and the trip/block decision. Graphics features incorporated in the software are explained. Tests for various faults conducted on the physical model of a double-circuit transmission line show that the direction to a fault is determined in 3 to 7 ms. The blocking features of the relay are demonstrated     

Peat swamps at Giral lignite field of Barmer basin,Rajasthan, Western India: understanding the evolution through petrological modelling

International Journal of Coal Science & Technology - The lignite samples collected from Giral lignite field of Barmer basin have been subjected to petrological investigation. The data generated...     

Easy Access to 1‐Amino and 1‐Carbon Substituted Isoquinolines via Cobalt‐Catalyzed C?H/N?O Bond Activation

A green atom‐economical method for the synthesis of highly functionalized 1‐amino and 1‐carbon substituted isoquinolines from the reaction of N′‐hydroxybenzimidamides and aryl ketoximes, respectively, with alkynes via pentamethylcyclopentadienylcobalt(III)‐catalyzed C H/N O bond activation is described. The external oxidant‐free annulation reaction uses the =NOH moiety in N′‐hydroxybenzimidamides or N‐aromatic ketone oximes as the directing group and internal oxidant. This first row transition metal‐catalyzed annulation serves as an efficient alternative for the synthesis of isoquinolines, as water is the only by‐product and expensive noble metals such as rhodium(III), iridium(III), palladium(II), and ruthenium(II) are not required. The reaction proceeds via C H activation, alkyne insertion, reductive elimination, and N O activation.

     

Copper‐Catalyzed C–N,C–O Coupling Reaction of Arylglyoxylic Acids with Isatins

The copper(II)‐catalyzed decarboxylative coupling reactions of arylglyoxylic acids with isatins afford 4H‐benzo[d][1,3]oxazin‐4‐ones via decarbonylation and concurrent C–N, C–O bond formation.

     

Through‐the‐glass spectroscopic ellipsometry for analysis of CdTe thin‐film solar cells in the superstrate configuration

Polycrystalline CdS/CdTe thin‐film solar cells in the superstrate configuration have been studied by spectroscopic ellipsometry (SE) using glass side illumination. In this measurement method, the first reflection from the ambient/glass interface is rejected, whereas the second reflection from the glass/film‐stack interface is collected; higher order reflections are also rejected. The SE analysis incorporates parameterized dielectric functions ε for solar cell component materials obtained by in situ and variable‐angle SE. In the SE analysis of the complete cells, a step‐wise procedure ranks the fitting parameters, including thicknesses and those defining the spectra in ε, according to their ability to reduce the root‐mean‐square deviation between the simulated and measured SE spectra. The best fit thicknesses from this analysis are found to be consistent with electron microscopy. Based on the SE results, the solar cell quantum efficiency (QE) can be simulated without any free parameters, and comparisons with measured QE enable optical model refinements as well as identification of optical and electronic losses. These capabilities have wide applications in photovoltaic module mapping and in‐line monitoring. Copyright © 2016 John Wiley & Sons, Ltd.     

Synthesis and characterization of new aromatic polyesters containing pendent naphthyl units

Two bisphenols, viz., 4,4′‐[1‐(2‐naphthalenyl)ethylidene]bisphenol and 4,4′‐[1‐(2‐naphthalenyl) ethylidene]bis‐3‐methylphenol were prepared by condensation of commercially available 2‐acetonaphthanone with phenol and o‐cresol, respectively. A series of new aromatic polyesters containing pendent naphthyl units was synthesized by phase‐transfer‐catalyzed interfacial polycondensation of these bisphenols with isophthaloyl chloride, terephthaloyl chloride, and a mixture of isophthaloyl chloride/terephthaloyl chloride (50 : 50 mol %). Inherent viscosities of polyesters were in the range 0.83–1.76 dL g⁻¹, while number average molecular weights (M_n) were in the range 61,000–235,000 g mol⁻¹. Polyesters were readily soluble in organic solvents such as dichloromethane, chloroform, tetrahydrofuran, m‐cresol, pyridine, N,N‐dimethylformamide, N,N‐dimethylacetamide, and 1‐methyl‐2‐pyrrolidinone at room temperature. Tough, transparent, and flexible films were cast from a solution of polyesters in chloroform. X‐Ray diffraction measurements displayed a broad halo at 2θ ≅ 19° indicating the amorphous nature of polyesters. Glass transition temperatures of polyesters were in the range 209–259°C. The temperature at 10% weight loss (T₁₀), determined by TGA in nitrogen atmosphere, of polyesters was in the range 435–500°C indicating their good thermal stability. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010