景观水体表观污染成因分析

景观水体的表观污染已经成为一个普遍面临的水环境污染问题,探寻其产生的原因具有非常重要的意义。文章在前人研究成果的基础上,从化学、物理、生态等方面对表观污染成因进行分析。目的是为了更好地维持景观水体生态平衡,控制水体污染,预防水体表观污染的发生提供参考。     

Heterogeneously doped polyethylene glycol as nano-composite soft matter electrolyte

We have applied the concept of heterogeneous doping [1] to prepare and examine composite electrolytes, consisting of silica particles, low molecular weight polyethylene glycol solvents and lithium perchlorate salt. These “soggy sand” electrolytes combine high ionic conductivities (on the order of mS cm⁻¹) and high Li transference numbers (typically 60–80%) with improved mechanical properties. They were characterized using differential scanning calorimetry, dc-polarization and ac-impedance spectroscopy, zeta potential measurements and viscosimetry. Oxide, size and concentration as well as solvent molecular weight were varied to better understand the influence of ceramic oxide fillers on the ion conduction in these systems. As regarding the filler content, we observe that both conductivity and transference number of Li⁺ start increasing already at low volume fractions of oxide particles, reach a maximum and subsequently decrease to low values. The percolating network is – after initial partial coarsening – found to be stable within the time periods of the measurements.     

Yield behavior of gelled waxy oil in water-in-oil emulsion at temperatures below ice formation

Paraffinic waxes precipitate from bulk oil when oil temperatures are lower than the oil wax appearance temperature. The oil can form a gel if the temperature goes below the pour point, especially under quiescent conditions. The strength of the gelled waxy oil increases as temperature decreases further. Application of a mechanical shear deforms and fractures the gel. It is shown that this strength reduction in the gel is irreversible under isothermal conditions. In subsequent cooling, the prior fractured gel even showed much less yield stress than the gel from the shear-free condition at measured temperature. This study explored the gel strength behavior in water-in-oil (w/o) emulsion state. Three different model oils, water-free oil, 10 wt.% w/o and 30 wt.% w/o, were used to determine the yield stress using vane method. Both emulsified oils showed less yield stress values at temperatures between the pour points and ice temperature. Compared to water-free oil at temperatures below ice formation, the higher yield stresses were observed in 10 wt.% w/o oil; however, the lower yield stresses in 30 wt.% w/o oil. Subsequent cooling option after prior gel breakage was also examined.     

Aging and Thermal Stability of the Mixed Product of the Ether‐Soluble Fraction of Bio‐Oil and Bio‐Diesel

The storage and thermal stability of blends of the ether‐soluble fraction of bio‐oil (ES) and bio‐diesel are reported. Fuel properties such as viscosity, water content, acid number and average molecular weight of the ES/bio‐diesel blends were measured before and after aging. Compared to the aging properties of bio‐oil alone, very small changes in water content and viscosity were shown for the blends aged at 80 °C for 180 h. Chemical changes were characterized using gel permeation chromatography, showing a slight increase in the molecular weight over time. Further confirmation of the changes was provided through Fourier transform infrared spectrometry, thermal decomposition analysis using a thermogravimetric analyzer, proton assignment using proton nuclear magnetic resonance, and carbon assignment using carbon nuclear magnetic resonance. Overall, the study indicates that ES/bio‐diesel blends are stable as fuel under the conditions tested in this paper.     

Modeling of the bulk free radical polymerization up to high conversion—three stage polymerization model. II. Number-average molecular weight and apparent initiator efficiency

The equations for predicting the number-average molecular weight are derived on the basis of the three stage polymerization model (TSPM) in this paper. By applying the equations, a plotting approach is proposed to determine the apparent initiator efficiency defined as f[(α_td+1)/2] and the constant of chain transfer to monomer, where f is the initiator efficiency and α_td denotes the fraction of the termination rate constants by disproportionation. Using the approach to plot the experimental data in the literature, it is found that the chain transfer to monomer can be neglected for both methylmethacrylate (MMA) and styrene (St) polymerizations, but it can exert a significant effect on ethylmethacrylate (EMA) polymerization. In addition, the apparent initiator efficiency is found to be independent of reaction temperature and initiator concentration at each stage. The values of f[(α_td+1)/2] at gel effect stage are slightly reduced as compared with that at low conversion stage for MMA and EMA polymerizations. However, it decreases significantly at gel effect stage for St polymerization. Using the equations derived and the apparent initiator efficiencies obtained from TSPM plots, the number-average molecular weights at different conversions can be predicted. Comparisons show that the agreement between predictions and experimental data is satisfactory.     

Influence of selective filling on rheological properties and phase inversion of two-phase polymer blends

We investigate the phase inversion of selectively filled polystyrene (PS)/poly(methyl methacrylate) (PMMA) blends prepared by melt mixing. As we have shown by transmission electron microscopy analysis and by the calculation of different selectivity criteria, the filler used (glass spheres of submicron dimensions) resides exclusively in the PMMA-phase and modifies its rheological properties correspondingly.Four blend series made of PS and PMMA with different filler content are analyzed for the location of phase inversion concentration, φ_PI, and the width of the cocontinuity interval, CCI, in the concentration range where cocontinuity is predominant. Upon addition of filler a shift of φ_PI to higher concentrations of the filled PMMA-phase has been observed. This shift is in agreement with the predictions of a recently proposed equation defining the phase inversion concentration as that concentration where the maximum of the blends' extra elasticity occurs. The qualitative morphological analysis of these blends confirms this result.Moreover, it was found that the cocontinuity interval is widened significantly at increased filler content. We explain the appearance of a wider CCI for filled blends on the basis of a slowdown of processes leading to morphology destruction. Corresponding Tomotika experiments (stability of fibrils) substantiate these findings.     

搪瓷烧成温度计算方法的探讨

搪瓷釉的烧成过程是一种“液相烧结”过程,其传质有赖于熔体的粘性流动。根据玻璃态物质化学组成—结构—粘度—温度的一般关系,推导出计算瓷釉烧成温度(T_烧)的经验公式。     

纳米聚甲基丙烯酸十八酯降粘剂的合成及其降粘性能

通过微乳液聚合方法合成了纳米聚甲基丙烯酸十八酯降粘剂,并且通过傅立叶变换红外光谱仪和透射电子显微镜（TEM）进行表征。将纳米聚甲基丙烯酸十八酯（NPOMA）降粘剂分别应用于胜利19号井稠油和大庆丹东站稠油进行降粘性能研究,结果表明,在40℃时,叫（降粘剂）-500×10^-6时胜利稠油的表观粘度下降70．88mm^2／s,表观降粘率为70．53％,净降粘率为23．04％;w（降粘剂）=300×10^-5时大庆稠油的表观粘度下降26．44mm2／s,表观降粘率为66．26％,净降粘率为37．59％。因此该种降粘剂更适用于大庆稠油。     

浸渍沥青性能的影响因素研究

优质的浸渍沥青要求低QI（喹啉不溶物）、高残碳和低黏度。研究了低QI浸渍沥青的β组分（甲苯不溶喹啉可溶物）以及添加剂对其残碳和黏度的影响。实验表明,β组分含量对浸渍沥青性能的影响比添加剂更大。     

油品二元掺混黏度预测模型评价研究

为较好的控制和预测石油化工过程中油品掺混后的黏度,获得对于不同工艺情形的精度较高的掺混黏度预测模型,以黏度比为工况划分标准,相对误差的绝对值及工程允许误差为评价准则,评价了8种二元油品掺混黏度的预测模型。得到了各个模型在全黏度比1～106内的黏度预测特性。计算分析了各个模型的预测精度。按黏度比,对掺混黏度预测做了模型的优选。结果表明,Arrhenius、Bingham、Kendall等基本模型的预测结果波动及误差较大,不推荐使用,黏度比在1～103时优选Chevron模型,黏度比在104～105时优选Cragoe模型,而黏度比在105～106时各模型都超出允许范围,且波动及偏差较大,预测效果不好,亟待开发出一种适用模型。