Visual search performance among persons with schizophrenia as a function of target eccentricity.

The current study investigated one possible mechanism of impaired visual attention among patients with schizophrenia: a reduced visual span. Visual span is the region of the visual field from which one can extract information during a single eye fixation. This study hypothesized that schizophrenia-related visual search impairment is mediated, in part, by a smaller visual span. To test this hypothesis, 23 patients with schizophrenia and 22 healthy controls completed a visual search task where the target was pseudorandomly presented at different distances from the center of the display. Response times were analyzed as a function of search condition (feature vs. conjunctive), display size, and target eccentricity. Consistent with previous reports, patient search times were more adversely affected as the number of search items increased in the conjunctive search condition. It was important however, that patients’ conjunctive search times were also impacted to a greater degree by target eccentricity. Moreover, a significant impairment in patients’ visual search performance was only evident when targets were more eccentric and their performance was more similar to healthy controls when the target was located closer to the center of the search display. These results support the hypothesis that a narrower visual span may underlie impaired visual search performance among patients with schizophrenia. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The time course of word frequency and case alternation effects on fixation times in reading: Evidence for lexical control of eye movements.

Participants' eye movements were monitored while they read sentences in which high-frequency and low-frequency target words were presented either in normal font (e.g., account) or case alternated (e.g., aCcOuNt). The influence of the word frequency and case alternation manipulations on fixation times was examined. Although both manipulations had comparable effects on standard first-pass fixation measures, word frequency, but not case alternation was found to influence the duration of the first fixation in trials with multiple first-pass fixations. Assuming that lexical processing is more often incomplete at the termination of the first in multiple first-pass fixations than at the end of single first-pass fixations, the present findings provide strong evidence for an influence of word frequency on early lexical processing. Importantly, such a demonstration of a fast acting influence of a lexical variable on fixation times satisfies a critical prerequisite for establishing lexical control of eye movements in reading. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Complexation with starch for encapsulation and controlled release of menthone and menthol

A platform of starch complexes for the oral release of aroma substances by salivary fluids was studied. Menthone, menthol and limonene were used as model flavor compounds for complexation with starches with different amylose content. Complexes were characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC), dynamic light scattering (DLS), and atomic force microscopy (AFM). Aroma retention was tested under pH, temperature and storage challenges. Furthermore, the kinetic of aroma release in simulated saliva fluids (SSF) was also tested. Both menthone and menthol form V-amylose complexes in a ’food grade’ process while limonene does not form such complexes efficiently. Complexation yield was higher, with more included aroma and less free core content, as the amylose content increased. The complexes had melting temperature of over 90 °C. Digestion results suggest that the complexes can release the aroma in the oral cavity.     

Irradiation‐induced grafting of poly(vinylidene fluoride)‐graft‐poly(styrene sulfonic acid) for the preparation of planar and tube‐shaped air‐drying membranes

A novel air‐drying membrane was developed and investigated as an alternative for planar and tube‐shaped drying membranes composed of Nafion^®. The new membrane is based on poly(vinylidene fluoride) (PVDF) polymer types grafted with polystyrene sulfonic acid. Modification of the PVDF membrane by chemical grafting was initiated via γ‐irradiation of pre‐made film and tube‐shaped samples. The grafting was conducted while the pre‐irradiated PVDF samples were immersed in styrene monomer solution. Three unique characterization methods were introduced to evaluate the ion exchange and barrier functions of the membrane. This investigation focuses on optimizing the degree of grafting yield, and subsequently the control of the membrane's overall functional performances, through (1) monitoring the PVDF's degree of crystallinity and (2) monitoring the styrene monomer solution temperature, respectively. Different levels of crystallinity were achieved by melt blending the PVDF‐copolymer with PVDF‐homopolymer, in various mixing ratios. Another variable examined in this investigation was the introduction of an ionic complex on the sulfonic acid end groups, and its effect on the membrane functional performance was studied. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

The role of interfacial viscoelasticity in the stabilization of an electrospun jet

Stabilization of the jet is necessary for the successful fabrication of continuous fibers from solutions via electrospinning. Although intensively studied over the past decade, the mechanisms underlying jet stabilization are still not precisely understood. The traditional explanation for jet stabilization emphasizes the role of the elastic response of the polymer coil in creating a sufficiently high extensional viscosity, which prevents the breakup of the filament under extension. However, comprehensive rheological studies of bovine serum albumin (BSA) solutions that can be electrospun into continuous fibers show an absence of any significant bulk elasticity in shear and extension that would account for the stabilization of the jet. In order to explain this discrepancy, it is proposed that a complex jet structure, composed of a liquid core surrounded by a viscoelastic interface, is formed during the spinning process, where the surface viscoelasticity is responsible for the jet stabilization. These rheological properties of the surface are experimentally verified using novel interfacial rheometry. It is also shown that the surface viscoelasticity is further enhanced by varying the protein conformation (unfolding), as well as its concentration in solution.     

Bacterial community composition and structure of biofilms developing on nanofiltration membranes applied to wastewater treatment

The structure and microbial communities of biofilms developing on cross-flow nanofiltration (NF) membranes at different temperatures (20, 25 or 34 degrees C) and operation lengths (8h-24days) were studied. Feedwater comprised tertiary quality wastewater effluent or synthetic media mimicking effluents of intermediate quality. After each run, the membranes were autopsied for bacterial enumeration, bacterial community composition and microscopy visualization (SEM, CLSM and AFM/NSOM). Community composition was analyzed by polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) coupled with sequence analysis of 16S rRNA gene fragments from dominant bands. Deposition of polysaccharides and initial bacterial colonization were observed within 8h, whereas developed biofilms markedly affecting membrane permeability were evident from days 2-3 onwards. Regardless of applied conditions, the heterotrophic plate counts in the biofilm were 3-4x10(6)CFU/cm(2) and the thickness of the biofouling layer was 20-30microm. From a total of 22 sequences obtained from 14 independent experiments, most species identified were Gram negative (19 of 22 sequences). Proteobacteria were found to be a prevalent group in all cases (16 of 22 sequences) and among it, the beta-subclass was the most predominant (8 sequences), followed by the gamma-subclass (5 sequences). Pseudomonas/Burkholderia, Ralstonia, Bacteroidetes and Sphingomonas were the dominant groups found in most cases. Even though the microbial population might be important with respect to biofouling patterns, membrane permeability decline seems to be more substantially influenced by the formation and accumulation of exopolymeric substances (EPS).     

Very high thermopower of Bi nanowires with embedded quantum point contacts

Quantum confinement effects in bismuth (Bi) nanowires (NWs) are predicted to impart them with high thermopower values and hence make them efficient thermoelectric materials. Yet, boundary scattering of charge carriers in these NWs operating in the diffusion transport regime mask any quantum effects and impede their use for nanoscale thermoelectric applications. Here we demonstrate quantum confinement effects in Bi NWs by forming in their structure ballistic quantum point contacts (QPCs) leading to exceptionally high thermopower values (S > 2 mV/K). The power factor, S(2)G, of the QPCs is maximized at G ~ 0.25G(0) (where G(0) is the quantum of conductance) within agreement with a one-band model with step edge characteristics.     

Influence of partial charge on the material removal rate during chemical polishing

A partial charge-based chemical polishing model has been developed, which can serve as metric for describing the relative polishing material removal rate for different combinations of slurries and workpieces. A series of controlled polishing experiments utilizing a variety of colloidal polishing slurries (SiO₂, CeO₂, ZrO_2, MgO, Sb₂O₅) and optical materials [single crystals of Al₂O₃ (sapphire), SiC, Y₃Al₅O₁₂ (YAG), CaF₂, and LiB₃O₅ (LBO); a SiO₂-Al₂O₃-P₂O₅-Li₂O glass ceramic (Zerodur); and glasses of SiO₂:TiO₂ (ULE), SiO₂ (fused silica), and P₂O₅-Al₂O₃-K₂O-BaO (Phosphate)] was performed and its material removal rate was measured. As previously proposed by Cook (J Non-Cryst Solids. 1990;120:152), for many polishing systems, the removal rate is governed by a series of chemical reactions which include the formation of a surface hydroxide, followed by condensation of that hydroxyl moiety with the polishing particle, and a subsequent hydrolysis reaction. The rate of condensation can often be the rate limiting step, thus it can determine the polishing material removal rate. By largely keeping the numerous other factors that influence material removal rate fixed (such as due to particle size distributions, interface interactions, pad topography, kinematics, and applied pressure), the material removal rate is shown to scale exponentially with the partial charge difference (δ_wp-s) between the workpiece and polishing slurry particle for many of the slurry-workpiece combinations indicating that condensation rate is the rate limiting step. The partial charge (δ) describes the equilibrium distribution of electron density between chemically bonded atoms and is related to the electronegativity of the atoms chemically bonded to one another. This partial charge model also explains the age-old experimental finding of why cerium oxide is the most effective polishing slurry for chemical removal of many workpieces. Some of the slurry-workpiece combinations that did not follow the partial charge dependence offer insight to other removal mechanisms or rate limiting reaction pathways.     

EXTRACTION OF TITANIUM(IV) BY MIXTURES OF MONO- AND DH(2-ETHYLHEXYL) PHOSPHORIC ACID ESTERS

ABSTRACT

Solvent extraction of titanium(IV) from hydrochloric acid solutions by mixtures of mono- and di-2-ethylhexyl phosphoric acid esters (MEHPA and DEHPA) has been investigated as a function of HC1 concentration in the aqueous phase and extractants concentration in the organic phase

It was found that MEHPA extracts Ti, 3 orders of magnitude more efficiently than DEHPA. Efficiency of extraction by MEHPA does not depend on acid concentration in the aqueous phase in the range of 0·1 – 8·8 mole/Kg. As a rule Ti/MEHPA ratio in the complex is 1/2. At low aqueous phase acidities (0·1–1·0 mole/Kg HCl) formation of six- (or eight-) coordinate bidentate hydrated Ti(IV)-2MEHPA complexes is suggested. At acidities above 7·0 mole/Kg HC1 titanium forms tridentate six- (or eight-) coordinate complexes. At medium acidities (2·0–6·0 mole/Kg HCl) mixtures of these complexes are formed. Prolonged mixing of the phases or aging of the organic phase leads to dehydration and to transformation of bidentate to tridentate Ti-2MEHPA complexes. Ti-2MEHPA complexes are colorless

At ratios Ti/MEHPA<0·5 formation of Ti-MEHPA hydrated or solvated complex ions is suggested which form emulsion in the aqueous phase. These species slowly react with DEHPA and formation of Ti:MEHPA:DEHPA=1:1:2 complex is realized. This complex is yellow.