Effect of plasma treatment on the surface properties of polydimethylsiloxane

In this work, the analysis of the plasma modification of polydimethylsiloxane (PDMS) substrates was conducted. The influence of the modification onto the changes occurred within the geometrical structure and chemical composition of the surface was analyzed. Due to the study of the atomic force microscopy, it was possible to determine the relationships between the surface development and applied process parameters, defining the conditions facilitating to obtain isotropic or anisotropic orientations of wrinkles. A precise analysis of the chemical composition of the surface, executed before and after the modification processes, enabled to define the changes in their elementary composition. Moreover, the modification influence onto the changes of the contact angle and the surface free energy were also analyzed. So, based on the research it was stated that the increase of value of the surface free energy is proportional to the sp³ phase contents in the DLC coatings. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41635.     

Mechanisms of non-toxic anticorrosive pigments in organic waterborne coatings

Investigations have been carried out concerning the mechanism of the behaviour of non-toxic anticorrosive pigments belonging to the group of phosphates, ferrites and ion exchange pigments in waterborne systems. The mechanism controlling the protective effectiveness of organic coatings is complex and results from simultaneous activity of various agents, from among which the kind of the corrosion inhibitor and the structure of the coating are of fundamental importance. The effect of pigments on the protective properties of coatings was tested by means of electrochemical impedance spectroscopy (EIS), scanning vibrating electrode technique (SVET) as well as the salt spray and Prohesion tests. For the investigation of the structure of coatings the porosymetric method and modulated-force thermomechanical analysis (mf TMA) were applied. The results of these investigations have shown that calcium zinc phosphate and zinc ferrite are the most effective. These pigments take part in the passivation of steel, which has been proved by the results of electrochemical investigations and by the presence of the passive layers as has been found out by X-ray diffraction (XRD), energy dispersive X-ray analysis (EDXA) and scanning electron microscopy (SEM). Calcium zinc phosphate and zinc ferrite affect the structure of the coatings, increasing the glass transition temperature (Tg) of the coatings. Zinc phosphate and calcium-exchanged silica do not act in compliance with electrochemical mechanism neither do they improve the barrier properties of the binder.     

Shewanella sp. O23S as a Driving Agent of a System Utilizing Dissimilatory Arsenate-Reducing Bacteria Responsible for Self-Cleaning of Water Contaminated with Arsenic

The purpose of this study was a detailed characterization of Shewanella sp. O23S, a strain involved in arsenic transformation in ancient gold mine waters contaminated with arsenic and other heavy metals. Physiological analysis of Shewanella sp. O23S showed that it is a facultative anaerobe, capable of growth using arsenate, thiosulfate, nitrate, iron or manganite as a terminal electron acceptor, and lactate or citrate as an electron donor. The strain can grow under anaerobic conditions and utilize arsenate in the respiratory process in a broad range of temperatures (10–37 °C), pH (4–8), salinity (0%–2%), and the presence of heavy metals (Cd, Co, Cr, Cu, Mn, Mo, Se, V and Zn). Under reductive conditions this strain can simultaneously use arsenate and thiosulfate as electron acceptors and produce yellow arsenic (III) sulfide (As₂S₃) precipitate. Simulation of As-removal from water containing arsenate (2.5 mM) and thiosulfate (5 mM) showed 82.5% efficiency after 21 days of incubation at room temperature. Based on the obtained results, we have proposed a model of a microbially mediated system for self-cleaning of mine waters contaminated with arsenic, in which Shewanella sp. O23S is the main driving agent.     

Thermal,hydrolytic, anticorrosive,and tribological properties of alkyd‐silicone hyperbranched resins with high solid content

Novel alkyd hyperbranched resins (AHBRs) modified with a Z‐6018 silicone (a polysiloxane intermediate) and with high solid content were synthesized by etherification reaction using an acid catalyst. Different molar ratios of AHBR to silicone were used. Structural, thermal, hydrolytic, anticorrosive, and tribological properties were studied using infrared (IR) analysis, nuclear magnetic resonance (NMR), vapor pressure osmometry (VPO), thermogravimetric analysis (TGA), acid value, electrochemical impedance spectroscopy (EIS), and pin‐on‐disk friction. IR and NMR provide evidence of grafting of the silicone on AHBR; the efficiency of grafting was quantified by TGA. Thermal stability was studied also by acid value analysis. Grafting increases the number average molecular mass, enhances thermal stability, and improves significantly hydrolytic stability. Corrosion resistance on steel is improved by two orders of magnitude, hence our modified materials can be used as highly effective anticorrosion coatings. Grafting lowers dynamic friction dramatically, more so at higher concentrations of silicone. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Tribological properties of ethylene–propylene–diene rubber + polypropylene + thermal‐shock‐resistant ceramic composites

This work is part of a program on composites used in thermoelectric devices. Tribological properties of dynamic vulcanizate blends of polypropylene and ethylene‐propylene‐diene rubber filled with 5 wt% of microscale powder have been studied. The microscale thermal‐shock‐resistant ceramic filler contains α‐Al₂O₃, mullite (3Al₂O₃ · 2SiO₂ or 2Al₂O₃SiO₂), β‐spodumene glass‐ceramic and aluminium titanate. We found that our ceramic particles are abrasive; they cause strong abrasion of softer steel ball surfaces during dry sliding friction. To overcome the difficulty of particle dispersion and adhesion, the filler was modified through grafting using three types of organic molecules. Dry sliding friction was measured using four types of counter‐surfaces: tungsten carbide, Si₃N₂, 302 steel and 440 steel. Thermoplastic vulcanizate filled with neat ceramic powder shows the lowest friction compared to composites containing the same but surface‐treated powder. We introduce a ‘bump’ model to explain the tribological responses of our composites. ‘Naked’ or untreated ceramic particles protrude from the polymer surface and cause a decrease of the contact area compared to neat polymer. The ball partner surface has only a small contact area with the bumps. As contact surface area decreases, so does friction and the amount of heat generated during sliding friction testing. Chemical coupling of the ceramic to the matrix smoothens the bumps and increases the contact surface, giving a parallel increase in friction. Copyright © 2012 Society of Chemical Industry     

Hydrostatic pressure influence on electric relaxation response of bismuth manganite ceramics

Electrical impedance of bismuth manganite ceramics was studied under ambient and high hydrostatic pressure. Local disorder of crystal lattice was confirmed using XRD and DSC. Two relaxation processes were discerned. One was attributed to small polarons, which showed a changeover from variable range hopping features related to Fermi glass and structural disorder to the nearest neighbor hopping behavior in higher temperature range related to uniform distribution of energy levels. Hydrostatic pressure shortened relaxation times that would be interesting for applications. The second process, which was assigned to the nearest neighbor hopping of polarons, also exhibited a changeover to glassy features in a high-temperature range.     

Organic sulphur in the hard coal of the stratigraphic layers of the Upper Silesian coal basin

The paper presents the results of investigation of organic sulphur occurrence in the coal of Upper Silesian coal basin. Six hundred coal samples from 52 mines were tested. It has been found that the content of organic sulphur in the coal depends on the stratigraphic layer, coalification grade and geographic location in the Upper Silesia region. The highest mean content of organic sulphur has been found in the most recent (ca. 0.85%) and in the oldest (ca. 0.5%) strata. The lowest mean contents of organic sulphur have been found in the intermediate strata. In the case of the most recent coals, the content of organic sulphur decreases with increasing of coalification grade. When the carbon content (C^daf) exceeds 82%, the increase of coalification grade causes no further decrease of the mean content of organic sulphur. The share of organic sulphur in the total sulphur is lower in the case of more recent (<50%) and higher in the case of older coals (>50%).     

Single amino acid substitutions can further increase the stability of a thermophilic L-lactate dehydrogenase

Lactate dehydrogenases are of considerable interest as stereospecificcatalysts in the chemical preparation of enantiomerically pure-hydroxyacid synthons. For such applications in synthetic organicchemistry it would be desirable to have enzymes which tolerateelevated temperatures for prolonged reaction times, to increaseproductivity and to extend then applicability to poor substrates.Here, two examples are reported of significant thermostabilizations,induced by sitedirected mutagenesis, of an already thermostableprotein, the L-lactate dehydrogenase (EC 1.1.1.27 [EC] , 35 kDa permonomer subunit) from Bacillus stearothermophilus. Thermal inactivationof this enzyme is accompanied by irreversible unfolding of thenative protein structure. The replacement of Argl71 by Tyr stabilizesthe enzyme against thermal inactivation and unfolding. Thisstabilizing effect appears to be based on improved interactionsbetween the subunits in the core of the active dimeric or tetramericforms of the enzyme. The thermal stability of L-lactate dehydrogenasevariants with an active site Arg residue, either in the 171(wild-type) or in the 102 position, is further increased bysulfate ions. The two stabilizing effects are additive, as foundfor the Argl71Tyr/ Gln1O2Arg double mutant, for which the stabilityof the protein in 100 mM sulfate solution reaches that of L-lactatedehydrogenases from extreme thermophiles. All mutant proteinsretain significant catalytic activity, both in the presenceand absence of stnhilfoing salts, and are viable catalysts inpreparative scale reactions.