Parameters Influencing the Pyrotechnic Reaction

Phenomena (reaction effects) such as varied light emissions, sound, varied burning rates, varied heats of reaction and reaction products occur during the reaction of inorganic redox systems used for pyrotechnics. The peculiarity of these redox reactions is, that they take place as solid‐solid, solid‐liquid or solid‐gaseous state reactions. In opposite the theoretical redox reaction normally postulated in inorganic chemistry takes place in a solvent. By variation of different parameters as for example the reducing agent, the oxidizer, the oxygen balance and the particle size, it is possible to create the above‐mentioned effects in a wide range.     

我国成功研制机载大气污染探测系统

正中国科学院合肥物质科学研究院安徽光学精密机械研究所成功研制出1种用于机载、可快速获取区域环境大气污染成分的环境大气成分探测系统,并通过了安徽省科技成果转化服务中心组织的科技成果鉴定。该机载环境大气成分探测系统由大气环境激光雷达、差分吸收光谱仪和多角度偏振辐射计及主控管理器等4个子系统组成。研究人员研制出了国内首台探测气溶胶和云的双波长偏振航空遥感激光雷达。     

Enzymatic esterification of glycerol I. Lipase-catalyzed synthesis of regioisomerically pure 1,3-sn-diacylglycerols

Regioisomerically pure 1,3-sn-diacylglycerols are conveniently prepared in high yields (>80%) and in large quantities by enzymatic esterification of glycerol in the presence of various 1,3-selective lipases(Chromobacterium viscosum, Rhizopus delemar, Rhizomucor miehei) and a variety of different acyl donors like free fatty acids, fatty acid alkyl esters and vinyl esters. All reactions are carried out in aprotic organic solvents of low water content, namelyn-hexane, diethyl ether or tBuOMe. The creation of an artificial interphase between the solvent-immiscible hydrophilic glycerol and the hydrophobic reaction media by the adsorption of glycerol onto a solid support prior to use was essential for the success of these transformations. The effects of reaction conditions and the regioselectivities of the lipases on the product yields are described in detail.     

TEM of Dislocations in AIN

Sintered AIN specimens were deformed by Vickers hardness (HV) indentations. Compared with Al₂O₃ the HV hardness values indicate a much higher plasticity of AIN at room temperature, but above 600°C a higher ductility for Al₂O₃. Deformed AIN specimens were examined by transmission electron microscopy. Basal and prismatic glide with the slip systems (0001) 〈1120〉 and {1 1 00}〈11 2 0〉 were frequently observed. This results in four linearly independent slip systems. The critical resolved shear stress for single prismatic slip seems to be even smaller than for basal slip. However, thermally activated dislocation reactions are frozen up to at least 1000°C. Thus, prismatic slip is suppressed as soon as more than one slip direction is activated.     

Mechanical properties of anatase and semi-metallic TiO2 nanotubes

We report for the first time on mechanical properties of anodically formed, self-organized TiO₂ nanotube layers on titanium. We compare their behavior in their virgin state and after conversion to their semi-metallic form by an acetylene treatment. We show that the acetylene treatment leads to significant enhanced hardness, tensile strength and friction behavior.     

Separation of Extracellular Esterases from Pellet Cultures of the Basidiomycete Pleurotus sapidus by Foam Fractionation

Two extracellular esterases were produced in submerged cultures of the basidiomycete Pleurotus sapidus. A foam fractionation device was designed and employed for the isolation of the esterolytic enzymes. The recovery of enzyme activity in the liquefied foam strongly depended on the superficial gas velocity. High purification and enrichment factors (E _a = 62.0, P = 15.5) were achieved using nitrogen at 1.87 cm min⁻¹ within 100 min. Increasing the superficial gas velocity to 2.49 cm min⁻¹ improved the recovery of total esterase activity in the foam to >95% at the expense of reduced enrichment and purification factors. Differences in their physicochemical characteristics resulted in differing foaming properties of the two esterases secreted by P. sapidus. By variation of the pH value of the culture medium and addition of Triton X-100, both esterases were successively and quantitatively transferred into the foam in a two-step fractionation process.     

A flexible method for the conjugation of aminooxy ligands to preformed complexes of nucleic acids and lipids

Attachment of targeted ligands to nonviral DNA or RNA delivery systems is a promising strategy that seeks to overcome the poor target selectivity generally observed in systemic delivery applications. Several methods have been developed for the conjugation of ligands to lipids or polymers, however, direct conjugation of ligands onto lipid- or polymer-nucleic acid complexes is not as straightforward. Here, we examine an oximation approach to directly label a lipoplex formulation. Specifically, we report the synthesis of a cationic diketo lipid DMDK, and its use as a convenient ligation tool for attachment of aminooxy-functionalized reagents after its complexation with DNA. We demonstrate the feasibility of direct lipoplex labeling by attaching an aminooxy-functionalized fluorescent probe onto pre-formed plasmid DNA-DMDK lipoplexes (luciferase, GFP). The results reveal that DMDK protects DNA from degradation on exposure to either DNase or human cerebral spinal fluid, and that simple mixing of DMDK lipoplexes with the aminooxy probe labels the complexes without sacrificing transfection efficiency. The biocompatibility and selectivity of this method, as well as the ease of bioconjugation, make this labeling approach ideal for biological applications.     

Microstructure of mayenite 12CaO·7Al2O3 and electron emission characteristics

Electron emission characteristic, electrical conductivity of polycrystalline mayenite (12CaO·7Al₂O₃) electride, formation of [Ca₂₄Al₂₈O₆₄]⁴⁺(e⁻)₄ framework as a function of phase content, and microstructure have been investigated. The mayenite microstructure was investigated using high-resolution transmission microscopy which revealed the type cage structure of 12CaO·7Al₂O₃ partially filled by extra-framework oxygen ions. Incorporation of electrons by means of carbon ion template 12CaO·7Al₂O₃ produces complex structure, and an incomplete ion template 12CaO·7Al₂O₃ structure consisting of mixture of a [Ca₂₄Al₂₈O₆₄]⁴⁺(e⁻)₄ and [Ca₂₄Al₂₈O₆₄]⁴⁺(O²⁻)₂ framework had a direct effect on the electron emission. Surface chemistry and stability of the 12CaO·7Al₂O₃ electride have been studied using x-ray photoelectron spectroscopy. The work function of phase pure 12CaO·7Al₂O₃ electride was determined from direct thermionic emission data and compared to the measurement from ultraviolet photoelectron spectroscopy (UPS). Depending on the extent of ion template of 12CaO·7Al₂O₃ structure, a work function of 0.9–1.2 eV and 2.1–2.4 eV has been measured and thermionic emission initiating at 600°C.