Real time correlation filter for optical particle counter

Particle signals are detected by two parallel measuring chains which consist of a detector and analog to digital converter. We have used OPT101 as photodiode and ADS7870 for A/D converter and the output signal from two parallel measuring chains is processed by on line correlation filter. This filter works as real time systems. A correlation algorithm has been applied for this work. The signal to noise ratio has been increased by applying correlation filter. The gain of the filter has been improved by introducing digital signal processing.     

Colorizing mechanism of brass surface by femtosecond laser induced microstructures

In this paper, we exhibit the colorizing of brass surfaces by forming femtosecond laser induced microstructures on the sample surfaces. A variety of single colors such as brown, yellow, green, and black are introduced on brass surfaces by engineering periodic microgratings, microholes, and ring-shaped micro-patterns using Single Beam Direct Laser Writing (SBDLW) technique. The color of the micro-structured brass surfaces is certainly dependent on the width, depth, and period of the microstructures. Finally, we explain, in brief, the colorizing mechanism of metals by femtosecond laser induced microstructures.     

Influence of Macro-pores on DNAPL Migration in Double-Porosity Soil Using Light Transmission Visualization Method

Double porosity is a substantial microstructure characteristic in a wide range of geomaterials. It is a natural phenomenon that can be found in many types of soil, and it can result from biological, chemical or mechanical damage. In this paper, the influence of macro-pores on dense non-aqueous phase liquid (DNAPL) migration in double-porosity medium was investigated using light transmission visualization technique. Three experiments were carried out in two-dimensional flow chambers filled with a double-porosity medium composed of a mixture of local sand and sintered kaolin clay spheres arranged in a periodic manner. In each experiment, a different volumetric fraction of macro-pores and micropores was used. Tetrachloroethylene (PCE) was used to simulate DNAPL, and it was dyed using Oil-Red-O for better visualization. A predetermined amount of PCE was injected into the flow chambers and this amount was re-calculated using image analysis. A very strong correlation was found between the PCE amount injected and the amount calculated from image analysis in each experiment. The experiment was repeated by filling the flow chamber with silica sand to represent single-porosity medium. The results show that the macro-pores have a considerable effect on the PCE migration in double-porosity soil as the PCE movement was the fastest in the third experiment which contained the largest macro-pores volume. The accuracy of the method was validated using statistical analysis. The results show a slight difference between the means of the three experiments, indicating that the method is viable for monitoring NAPL migration in double-porosity medium under different volumetric fractions of macro-pores and micropores.     

Validated HPLC method for simultaneous quantification of mutant IDH1/2 inhibitors (enasidenib,ivosidenib and vorasidenib) in mouse plasma: Application to a pharmacokinetic study

Isocitrate dehydrogenase (IDH) inhibitors comprise a novel class of anticancer drugs, which are approved to treat acute myeloid leukemia patients having mutations on IDH1/2. We report the development and validation of a high‐performance liquid chromatography (HPLC) method for the simultaneous quantitation of IDH inhibitors, namely enasidenib (EDB), ivosidenib (IDB) and vorasidenib (VDB), in mouse plasma as per the US Food and Drug Administration regulatory guidelines. The method involves extraction of EDB, IDB and VDB along with internal standard (IS; phenacetin) from mouse plasma (100 μl) using a simple protein precipitation process. The chromatographic analysis was performed on an HPLC system using a gradient mobile phase (comprising 10 mm ammonium acetate and acetonitrile in a flow‐gradient) and an X‐Terra Phenyl column. The UV detection wave length was set at λ_max 265 nm. EDB, IDB, VDB and the IS eluted at 7.36, 8.60, 9.50 and 5.12 min, respectively, with a total run time of 10 min. The calibration curve was linear over a concentration range of 0.20–12.5 μg/ml for EDB and 0.50–12.5 μg/ml for IDB and VDB (r² = ≥0.998 for all of the analytes). Validation results met the acceptance criteria. The validated HPLC method was successfully applied to a pharmacokinetic study in mice.     

Regression and ANN models for estimating minimum value of machining performance

Surface roughness is one of the most common performance measurements in machining process and an effective parameter in representing the quality of machined surface. The minimization of the machining performance measurement such as surface roughness (R_a) must be formulated in the standard mathematical model. To predict the minimum R_a value, the process of modeling is taken in this study. The developed model deals with real experimental data of the R_a in the end milling machining process. Two modeling approaches, regression and Artificial Neural Network (ANN), are applied to predict the minimum R_a value. The results show that regression and ANN models have reduced the minimum R_a value of real experimental data by about 1.57% and 1.05%, respectively.     

QbD approached comparison of reaction mechanism in microwave synthesized gold nanoparticles and their superior catalytic role against hazardous nirto‐dye

Microwave irradiation (MI) process characteristically enables extremely rapid “in‐core” heating of dipoles and ions, in comparison to conventional thermal (conductance) process of heat transfer. During the process of nanoparticles synthesis, MI both modulates functionality behaviors as well as dynamic of reaction in favorable direction. So, MI providing a facile, favorable and alternative approach during nanoparticles synthesis nanoparticles with enhanced catalytic performances. Although, conventionally used reducing and capping reagents of synthetic origin, are usually environmentally hazardous and toxic for living organism. But, in absence of suitable capping agent; stability, shelf life and catalytic activity of metallic nanoparticles adversely affected. However, polymeric templates which emerged as suitable choice of agent for both reducing and capping purposes; bearing additional advantages in terms of catalyst free one step green synthesis process with high degree of biosafety and efficiency. Another aspect of current works was to understand role of process variables in growth mechanism and catalytic performances of microwave processed metallic nanoparticles, as well as comparison of these parameters with conventional heating method. However, due to poor prediction ability with previously published architect OFAT (One factor at a time) design with these nanoparticles as well as random selection of process variables with their different levels, such comparison couldn't be possible. Hence, using gum Ghatti (Anogeissus latifolia) as a model bio‐template and under simulated reaction conditions; architect of QbD design systems were integrated in microwave processed nanoparticles to establish mechanistic role these variables. Furthermore, in comparison to conventional heating; we reported well validated mathematical modeling of process variables on characteristic of nanoparticles as well as synthesized gold nanoparticles of desired and identical dimensions, in both thermal and microwave‐based processes. Interestingly, despite of identical dimension, MI processed gold nanoparticles bearing higher efficiency (kinetic rate) against remediation of hazardous nitro dye (4‐nitrophenol), into safer amino (4‐aminophenol) analogues.     

Electrophilicity Scale of Activated Amides: 17O NMR and 15N NMR Chemical Shifts of Acyclic Twisted Amides in N−C(O) Cross-Coupling

The structure and properties of amides are of tremendous interest in organic synthesis and biochemistry. Traditional amides are planar and the carbonyl group non-electrophilic due to n_N→π*_C=O conjugation. In this study, we report electrophilicity scale by exploiting ¹⁷O NMR and ¹⁵N NMR chemical shifts of acyclic twisted and destabilized acyclic amides that have recently received major attention as precursors in N-C(O) cross-coupling by selective oxidative addition as well as precursors in electrophilic activation of N-C(O) bonds. Most crucially, we demonstrate that acyclic twisted amides feature electrophilicity of the carbonyl group that ranges between that of acid anhydrides and acid chlorides. Furthermore, a wide range of electrophilic amides is possible with gradually varying carbonyl electrophilicity by steric and electronic tuning of amide bond properties. Overall, the study quantifies for the first time that steric and electronic destabilization of the amide bond in common acyclic amides renders the amide bond as electrophilic as acid anhydrides and chlorides. These findings should have major implications on the fundamental properties of amide bonds.