Changes In Surface Chemical Properties Research Articles

Changes in the Properties of Precipitated Silica Depending on the Modification Process of Silica Hydrogel Originated from Rice Husk

In this study, the changes in the properties of the prepared precipitated silica were evaluated depending on the conditions of the modification process of the silica hydrogel originated from rice husks. Rice husk silica hydrogel was prepared through a sol-gelation process after alkali soaking extraction of rice husk. The silica hydrogel was modified by adjusting the solution concentration and temperature conditions in acidic and alkali solutions. As a result, the changes in surface chemical properties and the improvement of quality characteristics such as whiteness and impurity removal were confirmed through the modification process. The modification treatment in an acidic atmosphere minimized the decrease in production yield and showed great effects on the whiteness and the removal of impurities such as alkali metals. In a alkaline condition, the improvement in the whiteness was clearly shown, but the reduction in yield increased. It was shown that the effects of the residual alkali metals and the organic substances on the properties of the precipitated silica could be controlled by the control of the modification process conditions.

Ultrasensitive quantum dot fluorescence quenching assay for selective detection of mercury ions in drinking water.

Mercury is one of the most acutely toxic substances at trace level to human health and living thing. Developing a rapid, cheap and water soluble metal sensor for detecting mercury ions at ppb level remains a challenge. Herein, a metal sensor consisting of MPA coated Mn doped ZnSe/ZnS colloidal nanoparticles was utilized to ultrasensitively and selectively detect Hg2+ ions with a low detection limit (0.1 nM) over a dynamic range from 0 to 20 nM. According to strong interaction between thiol(s) and mercury ions, mercaptopropionic acid (MPA) was used as a highly unique acceptor for mercury ions in the as-obtained ultrasensitive sensor. In the presence of mercury ions, colloidal nanoparticles rapidly agglomerated due to changes of surface chemical properties, which results in severe quenching of fluorescent intensity. Meanwhile, we find that the original ligands are separated from the surface of colloidal nanoparticles involving strongly chelation between mercury ion and thiol(s) proved by controlled IR analysis. The result shows that the QD-based metal ions sensor possesses satisfactory precision, high sensitivity and selectivity, and could be applied for the quantification analysis of real samples.

Surface chemical properties and pedogenesis of tropical soils derived from basalts with different ages in Hainan, China

Abstract Limited information is available on the changes of surface chemical properties of tropical soils with time during the pedogenesis. Soil samples of three profiles derived from basalts of 10, 1330 and 2290 kilo annum (ka) in age were collected from adjacent locations in a tropical region of Hainan Province, China. The changes in soil surface chemical properties and the mineralogy of the soil clay fraction with time were investigated using ion adsorption, micro-electrophoresis, and X-ray diffraction analysis. The content of 2:1-type clay minerals decreased, while those of kaolinite and gibbsite increased with increasing basalt age and degree of soil development. The content of pedogenic free iron (Fe) oxides and the ratio of free Fe oxides/total Fe oxides increased with soil development stage, while soil poorly crystalline Fe and aluminum (Al) oxides had an opposite trend. The positive surface charge of the soils increased with increasing basalt age and degree of soil development; this was consistent with the change in their contents of free Fe/Al oxides. However, the value of negative surface charge had an opposite behavior. The soil derived from 10-ka-basalt had much more negative charge than soils derived from 1330- and 2290-ka-basalt. Soil net surface charge and zeta potential of the soil clay-fraction decreased with the increase in basalt age. Both net charge–pH curves and zeta potential–pH curves shifted to positive values with increased basalt age and degree of soil development. Increasing age also elevated the point of zero net charge of the soil and the isoelectric point of soil colloids.

Surface Characterization of Acidithiobacillus ferrooxidans Adapted to High Copper and Zinc Ions Concentration

Changes in surface chemical properties of Acidithiobacillus ferrooxidans after adaptation to high copper and zinc ion concentration were studied by surface sensitive techniques such as zeta-potential, XPS and FT-IR measurements. The adapted bacteria were also characterized by their surface energies and adhesion capacities on different sulphide minerals. Their surface negative charge was decreased due to changes in the structure of bacterial surface layers. The metal ions adapted cells secreted more extracellular polymeric substances with a modified composition compared to unadapted ferrous ions grown cells. Bacterial cells hydrophilic property increased after adaptation and altered their adhesion behavior to sulphide mineral.

Crystal Structures of Flax Rust Avirulence Proteins AvrL567-A and -D Reveal Details of the Structural Basis for Flax Disease Resistance Specificity

The gene-for-gene mechanism of plant disease resistance involves direct or indirect recognition of pathogen avirulence (Avr) proteins by plant resistance (R) proteins. Flax rust (Melampsora lini) AvrL567 avirulence proteins and the corresponding flax (Linum usitatissimum) L5, L6, and L7 resistance proteins interact directly. We determined the three-dimensional structures of two members of the AvrL567 family, AvrL567-A and AvrL567-D, at 1.4- and 2.3-A resolution, respectively. The structures of both proteins are very similar and reveal a beta-sandwich fold with no close known structural homologs. The polymorphic residues in the AvrL567 family map to the surface of the protein, and polymorphisms in residues associated with recognition differences for the R proteins lead to significant changes in surface chemical properties. Analysis of single amino acid substitutions in AvrL567 proteins confirm the role of individual residues in conferring differences in recognition and suggest that the specificity results from the cumulative effects of multiple amino acid contacts. The structures also provide insights into possible pathogen-associated functions of AvrL567 proteins, with nucleic acid binding activity demonstrated in vitro. Our studies provide some of the first structural information on avirulence proteins that bind directly to the corresponding resistance proteins, allowing an examination of the molecular basis of the interaction with the resistance proteins as a step toward designing new resistance specificities.

Comprehensive study of polymer fiber surface modifications Part 1: high‐fluence UV‐excimer‐laser‐induced structures

AbstractRecently, there has been great interest in physico‐chemical surface treatments for modifying polymer surfaces. Ultraviolet (UV)‐excimer‐laser irradiation of polymers is of particular interest. In this study, polyamide was irradiated by a 193 nm excimer laser with a fluence above its ablation threshold (high‐fluence). Morphological changes of the resulting samples were characterized by scanning electron microscopy (SEM) and tapping mode atomic force microscopy (TM‐AFM). Chemical modifications by laser treatment were studied by X‐ray photoelectron spectroscopy (XPS), time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS) and chemical force microscopy (CFM). Topographical results indicated that ‘ripple‐like’ structures of micrometer size were formed after laser irradiation. XPS and Tof‐SIMS results showed that bond scission occurred on the polymer surface under the action of high‐fluence. Changes in surface chemical properties of the laser‐irradiated polyamide were supported by CFM experiments. Copyright © 2004 Society of Chemical Industry

Comprehensive study of pulsed UV-laser modified polyamide fibers

Polyamide fibers (nylon 6) are modified by UV-radiation using a pulsed excimer laser with different treatment parameters. The treated samples are characterized by using a scanning electron microscopy (SEM), tapping mode atomic force microscopy (TM-AFM), x-ray photoelectron spectroscopy (XPS), and chemical force microscopy (CFM). Depending on the conditions during the irradiation, different surface modifications are obtained which can generally be distinguished as high-fluence (above the ablation threshold) and low-fluence (below the ablation threshold). Topographical results indicate that ripple-like structures of micrometer size are developed under high-fluence laser irradiation. On the contrary, smaller sub-micron structures are formed by low-fluence treatment. XPS results show that bond scission occurs on the polymer surface under the action of high-fluence while low-fluence modifies the sample by an oxidative process. Changes in surface chemical properties of the laser-irradiated polyamide are supported by chemical force microscopy experiments with gold-coated AFM tips modified with -COOH terminated self-assembled alkanethiol monolayers (SAMs).

Surface chemical characterisation of Paenibacillus polymyxa before and after adaptation to sulfide minerals

A heterotroph Paenibacillus polymyxa bacteria is adapted to pyrite, chalcopyrite, galena and sphalerite minerals by repeated subculturing the bacteria in the presence of the mineral until their growth characteristics became similar to the growth in the absence of mineral. The unadapted and adapted bacterial surface have been chemically characterised by zeta-potential, contact angle, adherence to hydrocarbons and FT-IR spectroscopic studies. The surface free energies of bacteria have been calculated by following the equation of state and surface tension component approaches. The aim of the present paper is to understand the changes in surface chemical properties of bacteria during adaptation to sulfide minerals and the projected consequences in bioflotation and bioflocculation processes. The mineral-adapted cells became more hydrophilic as compared to unadapted cells. There are no significant changes in the surface charge of bacteria before and after adaptation, and all the bacteria exhibit an iso-electric point below pH 2.5. The contact angles are observed to be more reliable for hydrophobicity assessment than the adherence to hydrocarbons. The Lifschitz–van der Waals/acid–base approach to calculate surface free energy is found to be relevant for mineral–bacteria interactions. The diffuse reflectance FT-IR absorbance bands for all the bacteria are the same illustrating similar surface chemical composition. However, the intensity of the bands for unadapted and adapted cells is significantly varied and this is due to different amounts of bacterial secretions underlying different growth conditions.

Changes in physico‐chemical properties during decomposition of nonionic surfactant solutions

AbstractThe decomposition and accompanying changes in surface chemical properties of nonionic surfactants were investigated. The decomposition of nonionic surfactants occurs in the polyoxyethylene and ester chains. Ester chains were susceptible to decomposition with an increase in the polyoxyethylene chain length, but polyoxyethylene chains were not. Surface chemical properties such as solubilizing power, surface tension, effective specific volume, and intrinsic viscosity also deteriorated during decomposition of the surfactants.

Surface analysis using complementary electronic and chemical measurements

Surface electronic properties using scanning low energy electron probe (SLEEP) techniques have been studied in conjunction with surface chemical properties using Auger electron spectroscopy (AES). Some examples of SLEEP measurements such as scanning TV surface work function and secondary emission displays, work function and surface field distributions using sampling techniques, and determination of thin film dielectric constant and resistivity will be described. Observed correlation between the variation of work function from SLEEP and changes in surface chemical properties using AES will be shown for some electronic applications. The use of SLEEP as a means for determining surface changes caused by other techniques such as AES will also be discussed.