炼厂外排污水回用于循环冷却水腐蚀影响因素初探

从单因素、多因素和复杂水系考察了炼厂外排污水回用于循环冷却水腐蚀的影响因素，结果表明，碳钢腐蚀的主要影响因素取决于离子特性、氧化膜的形成和溶解氧的扩散等综合协同作用，其中以离子特性的,影响为最大（如：Cl^-、Ca^2 、CO3^2-的腐蚀性较强）。碳钢腐蚀反应又可由以上三种主要影响因素分为三个反应控制区，而当电导率在0．1－2．0mS/cm范围时，其水质属于腐蚀危险高发区。从而也进一步说明水质的低电导率处理，其防腐效果并不理想，相反在高电导率情况下却表现出相对较好的低腐蚀性能。     

FOF-18结构与性能的量子化学研究

用B3LYP法,在6-31G基组水平上优化了FOF-18的几何构型,得其稳定的几何构型;在振动分析的基础上求得体系的振动频率、IR谱;采用Monte-Carlo方法预估了密度;设计等键等电子反应计算了生成焓;运用Kamlet公式预测爆速、爆压和爆热;将计算性能与CL-20的性能作比较。结果表明,FOF-18整个分子呈N字形,且存在7个强吸收峰,密度2.06g/cm3、生成焓501.03kJ/mol、爆速9411.82m/s、爆压42440.76MPa、爆热6637.46kJ/kg,该化合物的性能与CL-20接近。     

Simulation of swirling combustion and NO formation using a USM turbulence-chemistry model

A unified second-order moment (USM) turbulence-chemistry model is used to simulate methane-air swirling combustion and NO formation for different swirl numbers. The simulation results are compared with those using the EBU-Arrhenius (E-A) combustion model, the simplified PDF model of NO formation in turbulent flows and the corresponding experimental results. The comparison indicates that the USM model is obviously better than the E-A model and the simplified PDF model. The E-A model cannot reasonably simulate the finite-rate kinetics, while the simplified PDF model, using a product of two single-variable PDF's instead of a joint PDF, remarkably under-predicts the NO reaction rate. The USM model gives the best agreement with the experimental results. Predictions show that as the swirl number increases the total NO formation at first decreases and then increases, which is in agreement with the experimental results.     

Glass Formation and Properties in the System Calcia-Gallia-Silica

The glass-formation region of the calcia-gallia-silica system was determined. The glasses within this region were measured to have a density of 3 to 4 g/cm³, a refractive index of 1.6 to 1.73, an Abbe number between 35 and 58, a thermal expansion coefficient of 6.5 × 10⁻⁷/°C to 11.5 × 10⁻⁷/°C, softening temperatures between 730° and 790°C, and a Vickers microhardness of 5.2 to 7.3 GPa. Crystalline phases were identified along the glass-formation boundary. Infrared transmission spectra were used to explain glass structures and their effect on glass properties. The results suggest that the role of calcia in the glass structure is similar to that for calcia in calcium aluminosilicate glasses.     

湿塑性水泥土增强研究

从水泥在水泥-水-粘土系统中水化的特点出发，阐述了湿塑性水泥土的强度形成过程，主要是依赖于水泥石的强度骨架与粘土之间的结构连接。通过实验，研究了几种外加剂对湿塑性水泥土的增强作用及其增强机理，结果表明，外加剂能改善水泥土的水化介质环境和结构粘接，可改善水泥土的稠度和强度。     

PET高速纺丝方法及超高速纺丝纤维成形机理

综述了 PET高速纺丝热辊法生产工艺 (MG)、冷辊拉伸蒸汽定型法生产工艺 (H 4S)、热管法生产工艺 (TCS)、热管拉伸法生产工艺 (HCS)以及超高速纺丝工艺 (SHSS) ;阐明了超高速纺在纺程上结构的发展与成形机理 ,以及超高速纺纺程上的细颈现象 ,超高速纺的成形机理与高速纺是不同的 ,明显区别在于细颈点的出现     

肥皂霜的成分分析及成因研讨

采用红外光谱、气相色谱 ,X-射线能谱、原子吸收光谱、紫外分光光度法及化学法分析了肥皂霜中脂肪酸盐、硅、磷、碳酸盐等成分。其结果如下 :RCOONa:94.82 %;Si O2 :2 .43%;PO3-4:0 .40 %;Na2 CO3:1 .0 8%、水份及挥发物余量。依据测试结果 ,对肥皂冒霜的原因进行了探讨     

Mixed monolayer and mixed micelle formation in binary mixture of surfactants—Systems for trioxyethylenated dodecyl sulfonate and some polyoxyethylenated fatty alcohol ether nonionic surfactants

The interaction and synergism of some polyoxyethylenated fatty alcohol ether (POE) nonionic surfactants (C₁₂E₂, C₁₂E₃, C₁₀E₅, C₁₀E₇, where C_x indicates number of carbon atoms in the chain and E_y indicates number of oxyethylene glycol ethers) with trioxyethylenated dodecyl sulfonate (C₁₂E₃S) in mixed monolayer formation at the surface and in mixed micelle formation in aqueous solutions were studied at 25 and 40°C by calculating interaction parameters (β_α, β_M) from surface tension-concentration data by use of Rosen's equations based on the nonideal solution theory. All the systems investigated adapt reasonably well to the nonideal model, with negative values of β_σ and β_M (where M means micelle and σ refers to the air-liquid interface) indicating a favorable interaction between the mixed surfactants. Either at a monolayer or in a mixed micelle, the attractive interaction becomes stronger when the alkyl chain in the POE surfactant is longer, i.e., when the POE becomes more hydrophobic. The interaction increases in the order C₁₀E₇<C₁₀E₅<C₁₂E₃, C₁₂E₂. For the two C₁₀E _n (n= 5,7)/C₁₂E₃S systems, as temperature increases from 25 to 40°C, the interaction increases in a mixed micelle, but it decreases in a mixed monolayer. Synergism in mixed micelle formation exists for C₁₂E₃S/C₁₀E _n mixtures when X₁ ^M , the mole fraction of POE in a mixed micelle, is ≈0.4–0.8, whereas synergism does not occur in the systems of C₁₂E₃S/C₁₂E _m due to the large difference between CMC₁ and CMC₂, i.e., large |In(C ₁ ^M /C ₂ ^M )| value (where CMC=critical micelle concentration). The degree of synergism in mixed micelle formation is temperature independent and is 0.23, 0.18, and close to zero for C₁₀E₅/C₁₂E₃S, C₁₀E₇/C₁₂E₃S, and C₁₂E _m (m=2,3)/C₁₂E₃S systems, respectively. Synergism in surface tension reduction effectiveness occurs in C₁₂E₃S/C₁₂E₂ and C₁₂E₃S/C₁₂E₃ systems. The mole fractions of POE in the solution phase are 0.302 and 0.333 for the two mixtures at the point of maximum synergism.     

Combustion and structure formation in the Ti-Ta-C-Ca<Subscript>3</Subscript>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript> system

Biocompatible composites (Ti, Ta)C _x + Ca₃(PO₄)₂ for deposition of nanofilms onto load-bearing implants by ion-plasma sputtering were prepared from Ti + Ta + C + Ca₃(PO₄)₂ mixtures by forced SHS compaction. The effect of Ta + C addition to green mixtures (characterized by parameter z) on the structure/phase formation in combustion products was explored. The addition of tantalum and carbon was found to have little or no influence on the burning velocity U and combustion temperature T _c. Two thermal spikes exhibited by thermograms were associated with the occurrence of two consecutive reactions leading to formation of titanium and tantalum carbides. With increasing z, the grain size of (Ti, Ta)C was found to diminish, its relative density to decrease, while the hardness to markedly grow.      

Effect of natural antioxidants in virgin olive oil on oxidative stability of refined,bleached, and deodorized olive oil

The factors influencing the oxidative stability of different commercial olive oils were evaluated. Comparisons were made of (i) the oxidative stability of commercial olive oils with that of a refined, bleached, and deodorized (RBD) olive oil, and (ii) the antioxidant activity of a mixture of phenolic compounds extracted from virgin olive oil with that of pure compounds andα-tocopherol added to RBD olive oil. The progress of oxidation at 60°C was followed by measuring both the formation (peroxide value, PV) and the decomposition (hexanal and volatiles) of hydroperoxides. The trends in antioxidant activity were different according to whether PV or hexanal were measured. Although the virgin olive oils contained higher levels of phenolic compounds than did the refined and RBD oils, their oxidative stability was significantly decreased by their high initial PV. Phenolic compounds extracted from virgin olive oils increased the oxidative stability of RBD olive oil. On the basis of PV, the phenol extract had the best antioxidant activity at 50 ppm, as gallic acid equivalents, but on the basis of hexanal formation, better antioxidant activity was observed at 100 and 200 ppm.α-Tocopherol behaved as a prooxidant at high concentrations (>250 ppm) on the basis of PV, but was more effective than the other antioxidants in inhibiting hexanal formation in RBD olive oil.o-Diphenols (caffeic acid) and, to a lesser extent, substitutedo-diphenols (ferulic and vanillic acids), showed better antioxidant activity than monophenols (p- ando-coumaric), based on both PV and hexanal formation. This study emphasizes the need to measure at least two oxidation parameters to better evaluate antioxidants and the oxidative stability of olive oils. The antioxidant effectiveness of phenolic compounds in virgin olive oils can be significantly diminished in oils if their initial PV are too high.