When simulated environments make the difference: the effectiveness of different types of training of car service procedures

An empirical analysis was performed to compare the effectiveness of different approaches to training a set of procedural skills to a sample of novice trainees. Sixty-five participants were randomly assigned to one of the following three training groups: (1) learning-by-doing in a 3D desktop virtual environment, (2) learning-by-observing a video (show-and-tell) explanation of the procedures, and (3) trial-and-error. In each group, participants were trained on two car service procedures. Participants were recalled to perform a procedure either 2 or 4 weeks after the training. The results showed that: (1) participants trained through the virtual approach of learning-by-doing performed both procedures significantly better (i.e. p < .05 in terms of errors and time) than people of non-virtual groups, (2) the virtual training group, after a period of non-use, were more effective than non-virtual training (i.e. p < .05) in their ability to recover their skills, (3) after a (simulated) long period from the training—i.e. up to 12 weeks—people who experienced 3D environments consistently performed better than people who received other kinds of training. The results also suggested that independently from the training group, trainees’ visuospatial abilities were a predictor of performance, at least for the complex service procedure, adj R ² = .460, and that post-training performances of people trained through virtual learning-by-doing are not affected by learning styles. Finally, a strong relationship (p < .001, R ² = .441) was identified between usability and trust in the use of the virtual training tool—i.e. the more the system was perceived as usable, the more it was perceived as trustable to acquire the competences.     

The fine structure of bicomponent polyester fibers

The application of alkaline hydrolysis to study the change in the fine structure of bicomponent polyester fibers as their surface is removed progressively was explored. The samples were prepared with a poly(butylene terephthalate) (PBT) sheath and a poly(ethylene terephthalate) (PET) core. The reagent used to hydrolyze the PBT was 1M NaOH in 75/25 methanol to water since it appeared to react topochemically with the fiber. The solution reacted more rapidly with PET than with PBT. Thus, when necessary to retard the weight loss of the bicomponent fibers, after a 2‐h hydrolysis with this reagent to remove PBT, it was replaced with aqueous 1M NaOH solution containing 0.1% cetrimmonium bromide. Unlike homofil PET or PBT fibers, where alkaline attack appeared to be confined to the surface and left the residue relatively smooth, the bicomponent fiber was attacked unevenly, and penetration to the PET core occurred before all the PBT at the surface was removed. Nevertheless, most of the reaction was confined initially to the PBT sheath. The tenacity and extension at break of the PBT–PET fiber passed through a maximum as hydrolysis progressed. The fall in tenacity at high weight losses is ascribed to increasing surface defects in the fiber surface. After removal of the PBT by the hydrolysis, the birefringence of the residue became progressively higher. The synergistic effect of the PBT sheath on the properties of the PET core and the possible causes of the nonuniform hydrolysis at the PBT surface are discussed. An equation is proposed that includes an interaction parameter, which can be utilized to determine which property is affected most by the hydrolysis of a bicomponent fiber. In this instance, it appears from the parameters that the order is strength > extension at break ≈ birefringence. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1163–1173, 1999     

Environment-friendly and cost-effective solution for flexible packaging printing process by advancement in engraving process

Clean Technologies and Environmental Policy - Organic solvents have been commonly used in the printing process for a long time in gravure printing applications. Using organic solvents in...     

Propagation modes and regimes of intense laser beam in magnetized plasma

This paper presents an analytical and numerical investigation of a circularly polarized beam propagating along the static magnetic field parallel to oscillating magnetic field in plasma at relativistic intensities. In the high intensity regime, such a magnetic field is created by the pulse itself. The authors have identified three regimes of propagation taking into account the relativistic mass correction. Based on WKB and paraxial ray theory, an appropriate expression for a dielectric tensor has been evaluated in the presence of an externally applied magnetic field. The natural electromagnetic modes are circularly polarized. Consequently, extraordinary and ordinary modes propagate, which are significantly affected due to the relativistic mechanism. The regimes are characterized by dimensionless power and beamwidth, characterizing the nature of propagation as steady divergence, oscillatory divergence and self-focusing. Numerical computations are presented and discussed for typical parameters of laser plasma interaction; defined through critical parameters, namely cyclotron-to-beam frequency (Ω _c ), plasma-to-beam frequency (Ω _p ) and beam power for arbitrary large intensities.     

Techniques to develop and characterize nanosized formulation for salbutamol sulfate

The present study relates to enhancing the dosing efficiency of pharmaceutical dry powder formulations administered by pulmonary inhalation. In particular, the study relates to the provision of dry powder inhalers (DPI) by forming nanosized particles of salbutamol sulfate (SBM) in order to augment the drug penetrability and deposition in the lungs. SBM, an antiasthmatic was selected to be developed into a nanosized formulation by different techniques like solvation, high-pressure homogenization, and spray drying, which were then compared on the basis of particle shape, particle size, and particle size distribution. In case of solvation method the nanosuspension was prepared by dispersing SBM into a nonsolvent and adding Tween-80 as a surfactant to prevent the agglomeration, the particles obtained therein were in the range of 2-10 mu. The second attempt was made by passing the suspension of SBM through high-pressure homogenizer at 10,000-15,000 psi. A treatment of six cycles of homogenization in presence of a Tween-80 as surfactant was found to give a nanosuspension within a size range 50-100 nm. The only drawback seemed with this technique was the low-product yield and high-processing time (3-4 h). In order to overcome this drawback spray-drying technique was further explored; the solution of SBM containing Tween-80 was stirred on magnetic stirrer at 1,200 rpm and finally dried by using spray dryer at an inlet and outlet temperature of 75 degrees C and 56 degrees C, respectively. The feed rate for spray dryer was kept to be 91 ml/h. The sample was collected and analyzed for particle size distribution which was found to be in the range of 50-100 nm. Keeping in view the positive outcomes in terms of higher yield and lower processing time, the spray-drying technique was taken to give the optimized formulation. Nanosized particles, thus obtained were evaluated for particle size, surface topology and particles size distribution, by Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), and Quasi-elastic light scattering (QELS) technique, respectively. The nanosized particles were subjected to investigate changes on the physical stability of the powder, for this different analytical method was used as: Fourier transform infrared spectroscopy (FT-IR), Differential Scanning Calorimetry (DSC) and X-ray diffraction (XRD) analysis and thus the result indicates that there was no physical disparity when compared with the commercial SBM sample.     

Preparation,characterization, in vivo biodistribution and pharmacokinetic studies of donepezil-loaded PLGA nanoparticles for brain targeting

Objective: Alzheimer’s disease (AD) is a progressive neurodegenerative disorder manifested by cognitive, memory deterioration and variety of neuropsychiatric symptoms. Donepezil is a reversible cholinesterase inhibitor used for the treatment of AD. The purpose of this work is to prepare a nanoparticulate drug delivery system of donepezil using poly(lactic-co-glycolic acid) (PLGA) for sustained release and efficient brain targeting.

Materials and methods: PLGA nanoparticles (NPs) were prepared by the solvent emulsification diffusion–evaporation technique and characterized for particle size, particle-size distribution, zeta potential, entrapment efficiency, drug loading and interaction studies and in vivo studies using gamma scintigraphy techniques.

Results and discussion: The size of drug-loaded NPs (drug polymer ratio 1:1) was found to be 89.67?±?6.43?nm. The TEM and SEM images of the formulation suggested that particle size was within 20–100?nm and spherical in shape, smooth morphology and coating of Tween-80 on the NPs was clearly observed. The release behavior of donepezil exhibited a biphasic pattern characterized by an initial burst release followed by a slower and continuous sustained release. The biodistribution studies of donepezil-loaded PLGA NPs and drug solution via intravenous route revealed higher percentage of radioactivity per gram in the brain for the nanoparticulate formulation as compared with the drug solution (p?Conclusion: The high concentrations of donepezil uptake in brain due to coated NPs may help in a significant improvement for treating AD. But further, more extensive clinical studies are needed to check and confirm the efficacy of the prepared drug delivery system.     

Correlation between structural,ferroelectric, piezoelectric and dielectric properties of Ba0.7Ca0.3TiO3-xBaTi0.8Zr0.2O3 (x = 0.45, 0.55) ceramics

We report on the correlation between structural, ferroelectric, piezoelectric and dielectric properties of the (1-x)Ba_0.7Ca_0.3TiO₃-xBaTi_0.8Zr_0.2O₃ (x?=?0.45, 0.55; abbreviated as 55BCT30 and 45BCT30) ceramics close to morphotropic phase boundary (MPB) region. The 55BCT30 and 45BCT30 ceramics were synthesized by the standard, high-temperature solid state ceramic method. X-ray diffraction (XRD) along with Rietveld refinement indicate that the 55BCT30 ceramics exhibit rhombohedral (R, space group R3m), orthorhombic (O, space group Amm2) and tetragonal (T, space group P4mm) phases while 45BCT30 ceramics exhibit only T and O phases. The temperature dependent Raman spectroscopy measurements confirm the structure and phase transformations observed from XRD. All the ceramics are chemically homogeneous and exhibit a dense microstructure with a grain size of 5–7?µm. The presence of polarization-electric field and strain-electric field hysteresis loops confirm the ferroelectric and piezoelectric nature of the ceramics. The polarization current density-electric field curves show the presence of two sharp peaks in opposite directions indicating the presence of two stable states with opposite polarity. Higher values of direct piezoelectric coefficient (d₃₃ ~?360 pC/N) were observed due to the existence of low energy barrier near MPB region and polymorphism. The 55BCT30 ceramics exhibit a higher value of electrostrictive coefficient (Q₃₃ ~?0.1339?m⁴/C²) compared to the well-known lead-based materials. The temperature dependent dielectric measurements indicate the O to T phase transition for 55BCT30 and 45BCT30. These ceramics exhibit a Curie temperature (T_c) of 380?K with a dielectric maximum of ~ 4500.     

Sorptive sequestration of 2‐chlorophenol by zeolitic materials derived from bagasse fly ash

BACKGROUND: Water pollution by toxic organic compounds is of great concern and increasingly there are demands for effective sorbents to remove them. Bagasse fly ash, a sugar industry solid waste with disposal problems, was utilized as a source for the synthesis of zeolitic material. The efficiency of virgin and synthesized material was examined for the sorption of 2‐chlorophenol. RESULTS: Zeolitic materials have been synthesized by alkaline hydrothermal and fusion methods. Zeolite P and Analcime were the major components of the zeolitic material. These materials were characterized by XRF, PXRD, FTIR and SEM and were found to have improved morphology with new crystalline phases. Batch sorption experiments for the removal of 2‐chlorophenol by virgin and zeolitic materials were carried out to evaluate isotherm capacities and kinetics of sorption processes. The Langmuir isotherm better fits the equilibrium data which concur with physical sorption. Kinetic studies showed better correlation coefficients for pseudo‐second‐order and intraparticle diffusion model, confirming that the sorption rate was controlled by film diffusion followed by pore diffusion. Desorption studies were performed to regenerate the activity of the spent sorbents. The practical utility of sorbents was tested by column study. CONCLUSION: Bagasse fly ash, readily available at very low cost was successfully converted into zeolitic material. The synthesized zeolitic material showed enhanced capacities for the sorption of 2‐chlorophenol and can be utilized as a low cost sorbent for treatment of phenolic waste‐water. Copyright © 2011 Society of Chemical Industry     

Synthesis of waterborne acrylic copolymer resin as a binding agent for the development of water-based inks in the printing application

In this study, a new waterborne acrylic copolymer resin (acrylic-co-resin) was synthesized to develop water-based printing inks on polyester (PET) film. The synthesized acrylic resin showed good water solubility, high acid value (120 mg KOH/g), about 57% solid content. The developed water-based inks (cyan, magenta, and yellow) exhibited small particle size (<1 μm) and optimum surface energy within required values (31.5, 32, and 30 mN/m) for good adhesion of ink upon PET films. The developed inks also showed good storage stability for 30 days. Further, to evaluate the application performance, the inks were printed on corona-treated PET films at room temperature, and the ink drying time was measured. Further, the inks were printed on the corona-treated PET film to evaluate the application performance. The developed inks showed a short drying time (7–9 s), which indicates their fast drying nature. Moreover, the developed inks showed good printability, color strength, high adhesion, and excellent rub-resistant properties. Thus, the overall results demonstrated the potential of water-based inks in printing applications.