Laser pulse optimization for practical laser drilling

Laser drilling is a common commercially developed technique for material processing. From the application viewpoint, it is the end product for a laser system, for instance a drilled hole, that matters. Laser pulse profile is the most important parameter controlling the laser hole drilling process. An efficient and practical method is therefore needed to develop a relationship between the pulse parameters and the depth of hole produced in a known material. In the present study, dimensionless groups are developed to optimize laser pulse parameters to give information on workpiece materials. Consequently, an optimal laser pulse for drilling an aluminum workpiece is predicted.     

Radioactivity levels in some wild edible mushroom species in Turkey

Eleven different wild-growing edible mushroom species collected from various regions of Turkey were analysed for their content of 137Cs, 40K, 226Ra and 232Th using a high-resolution gamma-ray spectrometry. Specific activities of 226Ra and 232Th were generally below detection limits. The specific activities of 137Cs and 40K ranged from 2.4+/-0.3 to 109.0+/-7.3 Bq kg-1 with a mean of 28.4+/-27.2 Bq kg-1 (dry matter) and 715.5+/-50.1 to 1779.0+/-163.7 Bq kg-1 with a mean of 1150.8+/-315.2 Bq kg-1 (dry matter), respectively. The mean annual effective dose of 137Cs and 40K through mushrooms were estimated to be (7.0+/-6.0)x10(-3) microSv and 0.13+/-0.03 microSv, respectively. The overall intake of 137Cs is quite low and no significant contamination was found in collected mushroom species. The highest contents of 137Cs and 40K among the analysed mushrooms were in Morchella esculenta and Stropharia coronilla, respectively.     

Experimental and theoretical FT‐IR and FT‐Raman spectroscopic analysis of N1‐methyl‐2‐chloroaniline

In this work, the experimental and theoretical vibrational spectra of N1‐methyl‐2‐chloroaniline (C₇H₈NCl) were studied. FT‐IR and FT‐Raman spectra of the title molecule in the liquid phase were recorded in the region 4000–400 cm^?1 and 3500–50 cm^?1, respectively. The structural and spectroscopic data of the molecule in the ground state were calculated by using density functional method (B3LYP) with the 6‐311++G(d,p) basis set. The vibrational frequencies were calculated and scaled values were compared with experimental FT‐IR and FT‐Raman spectra. The observed and calculated frequencies are found to be in good agreement. The complete assignments were performed on the basis of the total energy distribution (TED) of the vibrational modes, calculated with scaled quantum mechanics (SQM) method. ¹³C and ¹H NMR chemical shifts results were compared with the experimental values. The optimized geometric parameters (bond lengths and bond angles) were given and are in agreement with the corresponding experimental values of aniline and p‐methyl aniline. Copyright © 2008 John Wiley & Sons, Ltd.     

Investigation of soliton solutions with different wave structures to the(2+1)-dimensional Heisenberg ferromagnetic spin chain equation

The principal objective of this article is to construct new and further exact soliton solutions of the(2+1)-dimensional Heisenberg ferromagnetic spin chain equation which investigates the nonlinear dynamics of magnets and explains their ordering in ferromagnetic materials.These solutions are exerted via the new extended FAN sub-equation method.We successfully obtain dark,bright,combined bright-dark,combined dark-singular,periodic,periodic singular,and elliptic wave solutions to this equation which are interesting classes of nonlinear excitation presenting spin dynamics in classical and semi-classical continuum Heisenberg systems.3D figures are illustrated under an appropriate selection of parameters.The applied technique is suitable to be used in gaining the exact solutions of most nonlinear partial/fractional differential equations which appear in complex phenomena.     

Cyclobutane-substituted diacetamido sulfides and 2,5-diacylthiophenes

A general and convenient route for the synthesis of 2,5-di[1-methyl-1-arylcyclobutane-3-yl]- thiophenes 4a–c and bis[1-methyl-1-arylcyclobutane-3-yl]-2-(2-oxyethtylamido)thiazole sulfides 7a–c is reported. The characterization of these compounds was obtained by elemental analyses, IR, ¹³C, and ¹H NMR techniques. © 2003 Wiley Periodicals, Inc. 15:26–31, 2004; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/.hc10207     

Combining Step-Growth and Chain-Growth Polymerizations in One Pot: Light-Induced Fabrication of Conductive Nanoporous PEDOT-PCL Scaffold

A novel method based on light-induced fabrication of a poly (3,4-ethylenedioxythiophene)-polycaprolactone (PEDOT-PCL) scaffold using phenacyl bromide (PAB) as a single-component photoinitiator is presented. HBr released from the step-growth polymerization of EDOT is utilized as an in situ catalyst for the chain-growth polymerization of ε-caprolactone. Detailed investigations disclose the formation of a self-assembled nanoporous electroconductive scaffold (1.2 mS cm⁻¹). Fluorescence emission spectra of the fabricated scaffold exhibit a mixed solvatochromic behavior, indicating specific interactions between the self-assembled scaffold and solvents with varying polarities, as evidenced by transmission electron microscopy (TEM). Moreover, the same light-induced technique can also be applied for bulk photopolymerization showcasing the versatility and wide-ranging scope of the originated method. In brief, this study introduces a novel approach for light-induced polymerization reactions that is merging step-growth and chain-growth mechanisms. This innovative approach is promising to facilitate in situ polymerization of monomers possessing diverse functionalities.