Machinability of Elongated Coarse Grain Fe-Based Superalloys

□ In conventional metal cutting process, materials are assumed to be homogeneous and isotropic structure. However, some materials with a single crystal or coarse elongated polycrystalline demonstrate strong anisotropic behavior in physical and mechanical properties in machining of some superalloy materials. The anisotropic structure always leads to variation at machinability properties of the material. In this study, machinability properties of ferritic superalloy PM2000, which had elongated a few coarse grains, were investigated. These properties were determined by investigation of chip formation, cutting forces and surface roughness. Machinability was assessed by single-point turning on a CNC lathe and turning forces were measured by using a Kistler Lathe Dynamometer. The chip formation mechanisms in machining of PM2000 at various cutting speeds were determined by using a quick-stop device (QSD). Chip roots and machined surfaces were analyzed by means of scanning electron microscopy (SEM). The results indicated that the machinability properties of the PM2000 were changed by orientated coarse grain structure. Three types chip formation mechanism were determined at the same cutting conditions. Also, surface roughness on the machined each grain changed with changing the grain to be cut. Surface roughness and force fluctuations decreased with increasing the cutting speed; however, tool wearing increased.     

Activities of MFI-Supported Rhenium Catalysts for the Aromatization of Methane: Effect of Cationic Form of the Inorganic Carrier

MFI type inorganic carrier was used in two different cationic forms, hydrogen and calcium respectively. MFI-supported molybdenum and rhenium catalysts were prepared. The activities of the catalysts were compared for the aromatization reaction of methane. Higher activity values were attained with the catalysts supported on HZSM-5. Aromatics were also observed with the catalysts supported on CaZSM-5, despite their deficiency in acid sites. Highly dispersed rhenium is expected to be formed with the use of the inorganic carrier in calcium form. On the other hand, lower reaction rates were observed with rhenium supported on CaZSM-5, in spite of the improved dispersion of the active rhenium species on this catalyst. This was interpreted in terms of the critical role of the acid sites in the conversion of methane to aromatics, compared to the improved dispersion of the active metal.     

Effects of some additives on the corrosion behaviour and preferred orientations of zinc obtained by continuous current deposition

The effect of thiourea, urea and guanidin on zinc deposits obtained from chloride baths under continuous current conditions are described and discussed. The corrosion behaviour of the deposits was investigated in an aerated 3.5% NaCl solution; anodic polarization curves, polarization resistance (R _p) measurements and weight-loss studies were performed. The corrosion resistance of zinc deposits improved in the presence of urea. The deposit morphology was analyzed using Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD) was used to determine the preferred crystallographic orientations of the deposits. The preferred crystallographic orientations of zinc deposits (112) do not change in the presence of urea and guanidin except for an increase in the peak intensity of the (112) plane. In the presence of thiourea, zinc deposits crystallise in two textures; (100) and (110). The influence of each additive and the difference between additives on the zinc deposits are also discussed.     

Predicting and tuning physicochemical properties in lead optimization: amine basicities

This review describes simple and useful concepts for predicting and tuning the pK(a) values of basic amine centers, a crucial step in the optimization of physical and ADME properties of many lead structures in drug-discovery research. The article starts with a case study of tricyclic thrombin inhibitors featuring a tertiary amine center with pK(a) values that can be tuned over a wide range, from the usual value of around 10 to below 2 by (remote) neighboring functionalities commonly encountered in medicinal chemistry. Next, the changes in pK(a) of acyclic and cyclic amines upon substitution by fluorine, oxygen, nitrogen, and sulfur functionalities, as well as carbonyl and carboxyl derivatives are systematically analyzed, leading to the derivation of simple rules for pK(a) prediction. Electronic and stereoelectronic effects in cyclic amines are discussed, and the emerging computational methods for pK(a) predictions are briefly surveyed. The rules for tuning amine basicities should not only be of interest in drug-discovery research, but also to the development of new crop-protection agents, new amine ligands for organometallic complexes, and in particular, to the growing field of amine-based organocatalysis.     

Experimental Tests and Modelling of an Electrodeionization Cell for the Treatment of Dilute Copper Solutions

The paper presents the results of experimental and theoretical investigations of an electrodeionization process for the removal of metal cations from dilute solutions. The ability of this technique to treat 100 ppm copper solutions using cationic membranes and ion‐exchange resins between the membranes was studied. Fair abatement yields were obtained in the 100 mm high resin bed in long‐term runs, and solutions of an appreciable copper ion concentration could be produced in the cathode chamber. The process capacity was limited by significant deposition of copper at the cathode, non‐even distribution of current density, and side‐diffusion to the anode chamber. Additional tests were then carried out using a 15 mm resin bed. The more even current distributions allowed the effect of the resin stiffness and the current density on the removal yield to be thoroughly observed. Steady‐state operation of the resin bed was modelled using generalized expressions of the various transport rates. Results of the model clearly showed the significance of solid‐liquid interactions on the transport processes.     

A novel method for color determination of edible oils in L*a*b* format

A simple method that uses visible spectrophotometer data and an artificial neural network (ANN) was developed to determine edible oil color based on the L*a*b* format. The 100 oil samples consisted of nine pure oils, a sesame oil blend and three heated oils. Binary, ternary and quaternary mixtures of these 13 oils in different ratios were prepared, and absorbance values of the samples were measured in the visible region (380–700 nm). The absorbance values at wavelengths of 416, 456, 483, 537, 611 and 672 nm were used to train, validate and test the network. Strong correlations between the instrumental L*a*b*ΔE and the estimated L*a*b*ΔE were found for the test samples, with correlation coefficients (R²) of 0.989, 0.984, 0.996 and 0.992 for L*, a*, b*, and ΔE, respectively. The effects of number and combination of the wavelengths used for training of the ANN on the estimation capability of the network for the test samples were also investigated. Although a good agreement, average R² of 0.991– 0 993 for L*a*b*, was obtained for combinations composed of three to six wavelengths with 483 and 537 nm in common, the best R² value was obtained when all six wavelengths were used to train the ANN. The developed method is objective, cost effective and simple, and allows the color measurement with a basic visible spectrophotometer and disposable cuvettes.     

Determination of tocopherols and phytosterols in sunflower seeds by NIR spectrometry

The objective of this work was to develop a near‐infrared reflectance spectrometry (NIRS) calibration estimating the tocopherol and phytosterol contents in sunflower seeds. Approximately 1000 samples of grinded sunflower kernels were scanned by NIRS at 2‐nm intervals from 400 to 2500 nm. For each sample, standard measurements of tocopherol and phytosterol contents were performed. The total tocopherol content was obtained by high‐performance liquid chromatography coupled with a fluorescence detector, while the total phytosterol content was assessed by gas chromatography. For tocopherol, the calibration data set ranged from 175 to 1005 mg/kg oil (mean value around 510 ± 140 mg/kg oil), whereas for the phytosterol content, the calibration data set ranged from 180 to 470 mg/100 g oil (mean value of 320 ± 50 mg/100 g oil). The NIRS calibration showed a relatively good correlation (R² = 0.64) between predicted by NIRS and real values for the total tocopherol content but a poor correlation for the total phytosterol content (R² = 0.27). These results indicate that NIRS could be useful to classify samples with high and low tocopherol content. In contrast, the estimation of phytosterol contents by NIRS needs further investigation. Moreover, in this study, calibration was obtained by a modified partial least‐squares method; the use of other mathematical treatments can be suitable, particularly for total phytosterol content estimation.     

Bioactive Sheath/Core nanofibers containing olive leaf extract

This study aimed at producing silk fibroin (SF)/hyaluronic acid (HA) and olive leaf extract (OLE) nanofibers with sheath/core morphology by coaxial electrospinning method, determining their antimicrobial properties, and examining release profiles of OLE from these coaxial nanofibers. Optimum electrospinning process and solution parameters were determined to obtain uniform and bead‐free coaxial nanofibers. Scanning electron microscopy and transmission electron microscopy (TEM) were used to characterize the morphology of the nanofibers. The antimicrobial activities of nanofibers were tested according to AATCC test method 100. Total phenolic content and total antioxidant activity were tested using in vitro batch release system. The quality and quantity of released components of OLE were determined by high‐performance liquid chromatography. The changes in nanofibers were examined by Fourier‐transform infrared spectroscopy. Uniform and bead‐free nanofibers were produced successfully. TEM images confirmed the coaxial structure. OLE‐loaded nanofibers demonstrated almost perfect antibacterial activities against both of gram‐negative and gram‐positive bacteria. Antifungal activity against C. albicans was rather poor. After a release period of 1 month, it was observed that ～70–95% of the OLE was released from nanofibers and it was still bioactive. Overall results indicate that the resultant shell/core nanofibers have a great potential to be used as biomaterials. Microsc. Res. Tech. 79:38–49, 2016. © 2015 Wiley Periodicals, Inc.