固相萃取富集高压液相色谱分析饮用水中的苯并(a)

本文以高压液相色谱仪作为样品分析手段,对Ｃ１８键合相吸附剂富集饮用水中苯并（ａ）芘回收效率的影响因素逐一进行系统研究。实验结果显示,在优化的样品富集和样品分析条件下,该方法具有快速、安全、高效和低耗等优点,在绝对进样量００２５～０３ｍｇ之间,线性良好,方法最低检出限为０５ｎｇ／Ｌ,同时准确度和精密度也得到很好地控制。另外,该方法在自来水及其源水的样品分析中获得了良好的结果。     

非等间隔GM（1，1）模型在液相色谱保留值研究中的应用

本文运用灰色系统理论思想,建立非等间隔ＧＭ（１,１）模型,对色谱中的流动相组成及容量因子的关系进行预测研究,所建立模型能实现对各实验点值进行模拟和合理地预测。     

水样中痕量有机物分析的前处理方法

对几种常用或新近发展起来的水中有机物分析的前处理方法作了简要论述 ,着重讨论了它们的应用特点、优缺点以及发展前景     

Effect of aging level on viscoelastic properties of asphalt binder containing waste polyethylene

Due to inherent advantages, waste polyethylene (generated from domestic sources) has been used as asphalt modifier. This article discusses viscoelastic properties of the polyethylene modified asphalt binder. Several asphalt concrete mixtures were designed by varying polyethylene and asphalt content. Shredded polyethylene incorporated into asphalt concrete by dry mixing process. Using optimised asphalt content (at several polyethylene percentages), mixtures were prepared and compacted. These compacted specimens were aged for different duration in convection oven. Asphalt binder (from aged specimens) was extracted and tested for its viscoelastic properties using dynamic shear rheometer. Comparison of mastercurves indicated increase in complex modulus and decrease in phase angle values with addition of polyethylene at all reduced frequencies. However, the extent of change was highly dependent on frequency, aging duration and polyethylene content. This indicates that the addition of polyethylene provides more resilience to asphalt binder especially with less aging time. Storage modulus mastercurves (at lower frequencies) and relaxation modulus values (at longer time) indicate polyethylene provides additional stiffening to binder. Further, changes in viscous modulus with addition of polyethylene were marginal. Overall results indicate that waste polyethylene improves the properties of asphalt binder over extended loading period when heated for less time during mixing.     

Sample Preparation Followed by High Performance Liquid Chromatographic (HPLC) Analysis for Monitoring Muconic Acid as a Biomarker of Occupational Exposure to Benzene

Factors affecting solid phase extraction (SPE) of trans,trans-muconic acid (ttMA), as a benzene biomarker, including sample pH, sample concentration, sample volume, sample flow rate, washing solvent, elution solvent, and type of sorbent were evaluated. Extracted samples were determined by HPLC-UV(highperformance liquid chromatography-ultraviolet). The analytical column was C18, UV wave length was 259 nm, and the mobile phase was H2O/methanol/acetic acid run at flow rate of 1 ml/min. A strong anion exchange silica cartridge was found successful in simplifying SPE. There was a significant difference between recoveries of ttMA when different factors were used (p < .001). An optimum recovery was obtained when sample pH was adjusted at 7. There was no significant difference when different sample concentrations were used (p > .05). The optimized method was then validated with 3 different pools of samples showing good reproducibility over 6 consecutive days and 6 within-day experiments.     

时效对高导耐热铝合金导线第二相析出及其性能的影响

目的 开展时效过程中61.5%IACS高导耐热铝合金导线析出第二相特性及其电导率与拉伸力学性能变化规律的研究,评价其热稳定性。方法 经过150~230 ℃长达630 h时效,揭示第二相的组成、形态与分布及其对时效态铝合金导线电导率与拉伸力学性能的影响规律。结果 时效态铝合金导线中,颗粒状及针状A13Zr(Y, Er)、A13(Zr(Y)xErl?x)第二相在Al晶内、晶界析出,A13Fe相颗粒弥散分布于Al晶界。伴随着时效过程,铝合金导线的抗拉强度与伸长率先上升、再逐渐下降;同时,铝合金导线的电导率先增大、后逐渐趋于稳定。该趋势随时效温度的升高而越加明显。结论 第二相的析出、长大是影响时效态铝合金导线力学性能及电导率的主要原因。经230 ℃、1 h时效,铝合金导线的强度保持率高达94%,满足GB/T 30551—2014的要求。所有时效态铝合金导线的电导率均高于其初始值,该高导耐热铝合金导线的热稳定性良好。     

Coliquefaction of coal and polystyrene in supercritical water

The coliquefaction of coal and polystyrene (PS) in supercritical water (SCW) was carried out in a 50-mL batch stainless steel autoclave reactor, and the effects of the polymer ratio by weight (10–40%), reaction temperature (633.5–703.5 K), and reaction time (30–120 min) were investigated. The main products were analyzed qualitatively by Fourier transform infrared spectroscopy and high-performance liquid chromatography. The results show that polystyrene stimulates coal liquefaction as a hydrogen donor, and the synergistic effects during coliquefaction in SCW were confirmed. The conversion reached a maximum of 62.26% after 60 min at 673.5 K. The phase behavior during coliquefaction was observed in a fused silica capillary reactor using a combined microscope and video recorder system.     

Testing for thresholds of ecosystem collapse in seagrass meadows

Although the public desire for healthy environments is clear‐cut, the science and management of ecosystem health has not been as simple. Ecological systems can be dynamic and can shift abruptly from one ecosystem state to another. Such unpredictable shifts result when ecological thresholds are crossed; that is, small cumulative increases in an environmental stressor drive a much greater change than could be predicted from linear effects, suggesting an unforeseen tipping point is crossed. In coastal waters, broad‐scale seagrass loss often occurs as a sudden event associated with human‐driven nutrient enrichment (eutrophication). We tested whether the response of seagrass ecosystems to coastal nutrient enrichment is subject to a threshold effect. We exposed seagrass plots to different levels of nutrient enrichment (dissolved inorganic nitrogen) for 10 months and measured net production. Seagrass response exhibited a threshold pattern when nutrient enrichment exceeded moderate levels: there was an abrupt and large shift from positive to negative net leaf production (from approximately 0.04 leaf production to 0.02 leaf loss per day). Epiphyte load also increased as nutrient enrichment increased, which may have driven the shift in leaf production. Inadvertently crossing such thresholds, as can occur through ineffective management of land‐derived inputs such as wastewater and stormwater runoff along urbanized coasts, may account for the widely observed sudden loss of seagrass meadows. Identification of tipping points may improve not only adaptive‐management monitoring that seeks to avoid threshold effects, but also restoration approaches in systems that have crossed them.     

Single-solute and bi-solute sorption of phenanthrene and pyrene onto pine needle cuticular fractions

To better understand interaction mechanisms of pine needles with persistent organic pollutants, single-solute and bi-solute sorption of phenanthrene and pyrene onto isolated cuticular fractions of pine needle were investigated. The structures of cuticular fractions were characterized by elemental analysis, Fourier transform infrared spectroscopy and solid-state ¹³C NMR. Polymeric lipids (cutin and cutan) exhibited notably higher sorption capabilities than the soluble lipids (waxes), while cellulose showed little affinity with sorbates. With the coexistence of the amorphous cellulose, the sorption of cutan (aromatic core) was completely inhibited, so the cutin components (nonpolar aliphatic moieties) dominated the sorption of bulk needle cuticle. By the consumption of the amorphous cellulose under acid hydrolysis, sorption capacities of the de-sugared fractions were dramatically enhanced, which controlled by the exposed aromatic cores and the aliphatic moieties. Furthermore, the de-sugared fractions demonstrated nonlinear and competitive sorption due to the specific interaction between aromatic cores and polycyclic aromatic hydrocarbon.