Probing CO on a rutile TiO2(110)surface using atomic force microscopy and Kelvin probe force microscopy

Probing CO at a specific site on a metal oxide surface is essential for characterizing various applications such as CO oxidation,hydrogenation,and water-gas shi...     

Protein Modification with Ribose Generates Nδ-(5-hydro-5-methyl-4-imidazolone-2-yl)-ornithine

Advanced glycation end products (AGEs) are associated with diabetes and its complications. AGEs are formed by the non-enzymatic reactions of proteins and reducing sugars, such as glucose and ribose. Ribose is widely used in glycation research as it generates AGEs more rapidly than glucose. This study analyzed the AGE structures generated from ribose-modified protein by liquid chromatography–quadrupole time-of-flight mass spectrometry. Among these AGEs, N^δ-(5-hydro-5-methyl-4-imidazolone-2-yl)-ornithine (MG-H1) was the most abundant in ribose-glycated bovine serum albumin (ribated-BSA) among others, such as N^ε-(carboxymethyl) lysine, N^ε-(carboxyethyl) lysine, and N^ω-(carboxymethyl) arginine. Surprisingly, MG-H1 was produced by ribated-BSA in a time-dependent manner, whereas methylglyoxal levels (MG) were under the detectable level. In addition, Trapa bispinosa Roxb. hot water extract (TBE) possesses several anti-oxidative compounds, such as ellagic acid, and has been reported to inhibit the formation of MG-H1 in vivo. Thus, we evaluated the inhibitory effects of TBE on MG-H1 formation using ribose- or MG-modified proteins. TBE inhibited MG-H1 formation in gelatin incubated with ribose and ribated-BSA, but not in MG-modified gelatin. Furthermore, MG-H1 formation was inhibited by diethylenetriaminepentaacetic acid. These results demonstrated that ribose reacts with proteins to generate Amadori compounds and form MG-H1 via oxidation.     

Cytocompatible and multifunctional polymeric nanoparticles for transportation of bioactive molecules into and within cells

Multifunctional polymeric nanoparticles are materials with great potential for a wide range of biomedical applications. For progression in this area of research, unfavorable interactions of these nanoparticles with proteins and cells must be avoided in biological environments, for example, through treatment of the nanoparticle surfaces. Construction of an artificial cell membrane structure based on polymers bearing the zwitterionic phosphorylcholine group can prevent biological reactions at the surface effectively. In addition, certain bioactive molecules can be immobilized on the surface of the polymer to generate enough affinity to capture target biomolecules. Furthermore, entrapment of inorganic nanoparticles inside polymeric matrices enhances the nanoparticle functionality significantly. This review summarizes the preparation and characterization of cytocompatible and multifunctional polymeric nanoparticles; it analyzes the efficiency of their fluorescence function, the nature of the artificial cell membrane structure, and their performance as in-cell devices; and finally, it evaluates both their chemical reactivity and effects in cells.     

Decomposition of a cyanine dye in binary nanosheet colloids of photocatalytically active niobate and inert clay

Binary colloids of inorganic nanosheets prepared by exfoliation of two different layered crystals form phase-separated structures with demixing of the two nanosheets. The phase-separated colloids of photocatalytic niobate and photochemically inert clay nanosheets exhibit unusual photochemical reactions based on the phase-separated structure. The present paper reports photocatalytic decomposition of a cyanine dye in this binary colloid, where the dye is selectively adsorbed on the clay nanosheets to be spatially separated from the photocatalytic nanosheets. Upon UV irradiation, the dye is photocatalytically decomposed in the colloids containing the niobate nanosheets, but self-photolysis of the dye is observed in the colloid lacking the photocatalytic nanosheets. Faster decomposition in nitrogen than in air suggests contribution of the conduction-band electrons generated in the niobate nanosheets to the photocatalytic reaction. In the binary colloid, the degradation is retarded compared with the single-component niobate colloid. Larger clay content more stabilized the dye against the decomposition. In contrast, irradiation of the colloids with visible light causes self-photolysis of the dye even in the presence of the niobate nanosheets, indicating the absence of electron transfer from the photoexcited dye to the photocatalytic nanosheets.     

FATIGUE MICROCRACKS IN A LOW CARBON STEEL

Abstract— The behaviour of a low carbon steel has been studied, in particular the initiation, growth and coalescence of fatigue microcracks on the surfaces of smooth specimens via surface replicas and photomicrographs. From the study, quantitative information on the initiation period, growth and coalescence of cracks, statistical distributions of crack length and crack depth, density of cracks, distribution pattern and characteristics of the major crack, were obtained. Knowledge of these parameters is critical for non-destructive inspection during service life and the application of fracture mechanics to life assessment.     

Corrosion products of tin in humid air containing sulfur dioxide and nitrogen dioxide at room temperature

To obtain a fundamental understanding of the corrosion behavior of tin in corrosive gas environments, in situ infrared reflection absorption spectroscopy measurements were carried out on tin in humid air containing SO₂ and NO₂ at room temperature. A series of time-resolved in situ IR spectra in air of 90% relative humidity (RH) containing 10-22 ppm SO₂ suggested that the oxide films on tin specimens had a protective effect and that no significant corrosion occurred. The corrosion products in air of 80-90% RH containing 10-22 ppm NO₂ were SnO₂, SnO, nitrate and hyponitrite. The synergistic effect of SO₂ and NO₂ on corrosion of tin was not observed in humid air (RH of 90%) containing 0.84 ppm SO₂ and 1.8 ppm NO₂.     

Automatic FeO activity determinator for slag control

An automatic facility for rapid determination of the activities of FeO in metallurgical slags has been developed, by employing an electrochemical technique incorporating stabilized zirconia as solid electrolyte, a mixture of Mo + MoO₂ as reference electrode and an Mo rod as an electrical contact. With this equipment, one datum is obtainable within 5 minutes. In the present article, discussions were held on potential applications of this system to steelmaking process control. A particular emphasis is given to the control of FeO levels in slags used for secondary steelmaking and chromium levels in stainless steelmaking slags.     

Efficient error estimation and adaptive meshing method for boundary element analysis

This paper describes a new and efficient error estimator by using the Direct Regular Method and h or h-r adaptive meshing for BEM analysis. This posteriori error estimator correctly indicates the discretization errors on each element. Based on the error distribution, and the adaptive meshing is generated automatically. The accuracy and convergence of this method are demonstrated by the numerical results on the stress concentration problem and the crack problem.     

Performance of thermal energy storage unit using CaCl2-NH3 system mixed with Ti

In order to develop an energy storage system using the reaction of solid CaCl₂ with ammonia gas, various properties such as volume expansion of CaCl₂ with ammoniation, activity of the chemical reaction for repeated cycles and influence of a metal additive on the heat transfer rate of the ammoniated salt were studied experimentally. The maximum volume after the reaction was 14–16 times of the ideal volume of CaCl₂. No deactivation was observed on repeated cycles. The heat transfer rate of ammoniated salts (CaCl₂ · nNH₃) was improved by adding the metal, titanium. The time required for ammoniation of CaCl₂ mixed with Ti was 10–30% shorter than for CaCl₂ alone. Similar results were obtained by repeating the cycles of ammoniation and deammoniation.     

Occurrence and production of chloramines in the chlorination of creatinine in aqueous solution

Occurrence and production of stable chloramines in the chlorination of creatinine, a constituent of perspiration and urine, in aqueous media were studied. Creatinine (5 x 10(-5)M) was treated with free chlorine in aqueous solutions at molar ratios of 0.5-8 (chlorine/creatinine) at pH 7.0 at room temperature for several days. At lower ratios of chlorine, two stable N-chlorocreatinine derivatives, which were determined as dichloramine fractions by the DPD method, were isolated by HPLC and identified by EI-MS and (1)H-NMR. One was 2-chloroamino-1-methylimidazolin-4-one (creatinine chloramine) and the other was 2-chloroamino-5-hydroxy-1-methylimidazolin-4-one (hydroxycreatinine chloramine). In addition, the formation of methylamine was identified by GC-MS analyses of its imine derivative formed with pentafluorobenzaldehyde. Methylamine forms stable chloramines, which might be determined as mono- and/or di-chloramine fractions together with free chlorine by the DPD method in the reaction mixtures at higher molar ratios of chlorine. In practice, small amounts of methylamine (ca. 19 microg/L) were detected in water samples collected from several swimming pools. Hence, methylamine may be an origin of elusive organic chloramine formed in the chlorination of swimming pools. A probable mechanism of the occurrence and processing of chlorination products of creatinine is suggested.