一种适用于深水压试验的传压隔热装置设计

目的真实高效地进行深水压环境的温度模拟。方法提出一种深水压试验压力加载过程中的恒温实现方法,通过开展基于皮囊的结构设计、密封性设计、导热性研究等工作,设计一种适用于深水压试验的传压隔热装置,对其进行理论分析和仿真计算。结果该装置可以实现液体温度在较长时间内基本恒定,具有良好的传压隔热性能。结论在建立的实验系统上进行了试验研究,实现了深水压环境模拟试验中压力载荷同步条件下液体温度小范围恒定功能,该技术为深水压环境试验的相关技术研究提供了技术储备。     

油田用钨合金镀层腐蚀性能评价研究

目的评价钨合金镀层油管的腐蚀性能。方法利用高压釜模拟高压气井和高含硫气井的腐蚀环境,进行高压高温腐蚀试验,以及标准的氢致开裂(HIC)和硫化氢应力腐蚀试验。采用电子扫描显微镜(SEM)及其能谱仪(EDS)和X射线衍射分析仪(XRD),分析或检测钨合金镀层和基管的腐蚀形貌、腐蚀产物的组成。结果油管表面的钨合金镀层平整而致密,其主要组成元素为W和Ni。高温高压腐蚀试验后,镀层仍然致密平整,腐蚀程度轻微。在60、90、120、140℃试验7天时,镀层和基材的H_2S/CO_2腐蚀速率分别为0.0179、0.0093、0.0102、0.0369 mm/a和1.030、1.272、1.183、0.991 mm/a。试验30天,在120℃时,其H_2S/CO_2腐蚀速率分别为-0.0085、0.1789 mm/a;在160℃时,其CO_2腐蚀速率分别为0.0091、0.8976 mm/a。该钨合金镀层均通过了标准的氢致开裂和硫化氢应力腐蚀试验。结论该钨合金镀层具有很好的耐腐蚀性能。     

天津市郊夏季VOCs化学特征及其时间精细化的来源解析

夏季为环境空气中臭氧污染事件的频发时期,针对挥发性有机化合物(VOCs)及其臭氧生成潜势(OFP)的时间精细化的来源解析研究,对有效地进行臭氧污染防控具有非常重要的作用.利用2019年夏季(6～8月)天津市郊区点位监测的小时分辨率VOCs在线数据,分析臭氧污染事件和非臭氧污染时期环境受体中VOCs及其OFP的变化特征,并利用正定矩阵因子分解(PMF)模型进行精细化的来源解析研究.结果表明,夏季环境受体中VOCs平均体积分数为24.42×10-9,臭氧污染事件中的VOCs平均体积分数为27.72×10-9,较非臭氧污染时期增加15.69％.夏季总VOCs(TVOCs)的OFP为87.92×10-9,其中烯烃的OFP最高,对TVOCs的OFP的贡献达58.28％.臭氧污染事件中TVOCs的OFP为102.68×10-9,较非臭氧污染时期增加19.59％.臭氧污染事件中VOCs的来源分别为石化工业及汽油挥发(29.44％)、柴油车尾气(23.52％)、液化石油气及汽油车尾气(22.00％)、天然气及燃烧(13.41％)、溶剂使用(6.14％)和植物排放(5.49％).相比于非臭氧污染时期,液化石油气及汽油车尾气和柴油车尾气分别增长4.84％和5.29％.石化工业及汽油挥发和植物排放的贡献均表现为08:00开始上升,11:00达到最高,这与太阳辐射增强和温度不断上升密切相关.液化石油气及汽油车尾气和柴油车尾气均具有明显的早晚高峰特征,并在夜间(00:00～06:00)保持较高贡献水平.根据PMF结果并结合OFP的计算方法,解析了不同源类对臭氧生成潜势的 贡献.石化工业及汽油挥发(31.01％)和柴油车尾气(36.64％)是较高贡献源类,相比非臭氧污染时期分别增加了 1.74％和8.27％;并且石化工业及汽油挥发贡献率在臭氧污染事件发生过程的上升阶段显著增加,而在下降阶段明显下降.     

基于PMF-PCA/APCS与PERI的菏泽油用牡丹种植区表层土壤重金属潜在来源识别及生态风险评估

研究特色农产品产区土壤重金属来源及其潜在风险,对科学管理、安全利用土壤和作物资源具有重要意义.以菏泽油用牡丹种植区为研究对象,采集并测定了254件表层土壤样品As、Cd、Cr、Cu、Hg、Ni、Pb和Zn等8种重金属的含量.采用多元统计法分析了重金属的含量特征及相关性,利用地累积指数（I_geo）、正定矩阵因子分解法（PMF）和主成分分析/绝对主成分分数法（PCA/APCS）相结合的手段解析了表层土壤中重金属的来源,借助潜在生态风险指数（PERI）对该8种重金属的生态风险进行了评估.结果表明,土壤中除Cd元素的平均值高于菏泽市背景值1.44倍之外,其余7种重金属的平均含量均与菏泽市土壤元素背景值基本一致;经相关分析和聚类分析,土壤中Pb、Hg和Cd元素受后期人为活动的干扰影响较大;研究区8种重金属的来源为自然源、农业化肥源、工业燃煤源和生活交通源,贡献率分别为81.31%、15.45%、2.74%和0.50%;研究区84.25%的点位处于轻微生态风险,而中度风险和强风险点位占比分别为14.96%和0.79%,其中Cd和Hg是研究区生态风险主导元素.     

动态膜压法测定江、污混合水体中有机物含量的探讨

用双驱动动态膜压仪测定江、污混合水中有机物含量。通过测定白龙港污水和长江水混合后的膜压和滞回环面积，用它们与相应的经典法CODCr作图，获得了滞回环面积和CODCr之间良好地线性关系，表明用动态膜压法可快速测定混合水中的有机物含量，不须加任何试剂，不会产生二次污染。同时，对实验结果进行了初步的机理探讨。     

Optimization of the high-pressure, near-critical liquid-based microsortation of recyclable post-consumer plastics

High-pressure, near-critical liquids were used as float-sink separation media for the microsortation of polyolefin mixtures and PET/PVC mixtures. Near-critical carbon dioxide was used for the refinement of the polyolefins, and sulfur hexafluoride was used to separate post-consumer PVC from PET. Preliminary experiments indicated that there was no overlap in the density ranges of post-consumer HDPE, LDPE and PP containers. There was no overlap in the PET and PVC densities, with the exception of a single PVC packaging material with a density in the PET range. These initial results indicated that a float-sink separation was a viable means of microsortation. Separations of 91% LDPE (1/8′ beads)/9% PP (1/8′ chopped strands) resin mixtures and mixed post-consumer polyolefin flakes were then conducted in a laboratory-scale, 1-I batch apparatus. This apparatus not only permitted the observation of the separation, but also enabled the separated fractions to be removed from the high-pressure environment. The results indicated that LDPE purity of greater than 98.9% was obtained in 3 min or less if (a) the fluid density was 0.018 g/cm³ greater than the PP density and only 0.002 g/cm³ less than the LDPE density, thereby providing the greatest buoyancy force for the removal of the PP, (b) the fluid was recirculated upward through the bed of mixed plastics, facilitating the upward movement of the PP, and (c) the loading was kept at levels below 40% by volume. HDPE purity of 99% was also attained with clean, dry, post-consumer mixed plastic flakes. The loadings for these separations were very low, however, due to the difficulty in agitating the mixed bed of plastics using fluid recirculation. An economic analysis of these microsortation processes indicated that the value of the sorted plastics relative to the mixed feed must increase by approx. $0.08/lb for the CO₂-based separation and approx. $0.27/lb for the SF₆-based separation to justify the implementation of these high-pressure processes.     

江淮流域大洪水的因子分析及成因链初步构造

结合 1998年长江流域的特大洪水 ,提出了洪水成因链的概念 ,分析了各个物理因子对江淮洪水的影响。指出影响江淮洪水的物理因子都是层层相接、环环相扣的 ,它们组成了一个互相联系、互为因果的洪水成因链。成因链上物理因子之间的正反馈作用和消长作用 ,导致成因链上各个因子的致洪理论都不能完全地自圆其说 ,因而也无法完全确定地用于洪水预测。只有深入探讨洪水成因链上物理因子之间的正反馈作用和消长作用 ,对它们进行全面综合的诊断分析 ,才能提高江淮洪水预测的准确率。     

Study of metabolites from the degradation of polycyclic aromatic hydrocarbons (PAHs) by bacterial consortium enriched from mangrove sediments

The PAH metabolites produced during degradation of fluorene, phenanthrene and pyrene by a bacterial consortium enriched from mangrove sediments were analyzed using the on-fiber silylation solid-phase microextraction (SPME) combining with gas chromatography–mass spectrometry (GC–MS) method. Seventeen metabolites at trace levels were identified in different PAH degradation cultures based on the full scan mass spectra. In fluorene degradation cultures, 1-, 2-, 3- and 9-hydroxyfluorene, fluorenone, and phthalic acid were detected. In phenanthrene and pyrene degradation cultures, various common metabolites such as phenanthrene and pyrene dihydrodiols, mono-hydroxy phenanthrene, dihydroxy pyrene, lactone and 4-hydroxyphenanthrene, methyl ester, and phthalic acid were found. The detection of various common and novel metabolites demonstrates that SPME combining with GC–MS is a quick and convenient method for identification as well as monitoring the real time changes of metabolite concentrations throughout the degradation processes. The knowledge of PAH metabolic pathways and kinetics within indigenous bacterial consortium enriched from mangrove sediments contributes to enhance the bioremediation efficiency of PAH in real environment.     

Vapour pressures, aqueous solubility, Henry's law constants and air/water partition coefficients of 1,8-dichlorooctane and 1,8-dibromooctane

New data on the vapour pressures and aqueous solubility of 1,8-dichlorooctane and 1,8-dibromooctane are reported as a function of temperature between 20 °C and 80 °C and 1 °C and 40 °C, respectively. For the vapour pressures, a static method was used during the measurements which have an estimated uncertainty between 3% and 5%. The aqueous solubilities were determined using a dynamic saturation column method and the values are accurate to within ±10%. 1,8-Dichlorooctane is more volatile than 1,8-dibromooctane in the temperature range covered (p_sat varies from 3 to 250 Pa and from 0.53 to 62 Pa, respectively) and is also approximately three times more soluble in water (mole fraction solubilities at 25 °C of 5.95 × 10⁻⁷ and 1.92 × 10⁻⁷, respectively). A combination of the two sets of data allowed the calculation of the Henry’s law constants and the air water partition coefficients. A simple group contribution concept was used to rationalize the data obtained.     

Phytoremediation of Cadmium-Contaminated Soils by Rorippa globosa Using Two-Phase Planting (5 pp)

Background Phytoextraction of contaminated soils by heavy metals can provide a great promise of commercial development. Although there are more than 400 species of hyperaccumulators found in the world, phytoremediation technology is rarely applied in field practice for remedying contaminated soils, partially due to low biomass and long growth duration for most of discovered hyperaccumulating plants. In order to enhance the metal-removing efficiency in a year, the two-phase planting countermeasure of phytoextraction by harvesting anthesis biomass was investigated on the basis of the newly found Cd-hyperaccumulator Rorippa globosa (Turcz.) Thell. with 107.0 and 150.1 mg/kg of the Cd accumulation in stems and leaves, respectively, when soil Cd added was concentrated to 25.0 mg/kg. Methods The field pot-culture experiment was used to observe the distribution property of R. globosa aboveground biomass and to examine characteristics of accumulating Cd by the plant at different growth stages. The concentration of Cd in plants and soils was determined using atomic absorption spectrophotometry (AAS). Results and Discussion The results indicated that the total dry stem and leaf biomass of R. globosa harvested at the flowering phase was up to 92.3% of that at its full maturity and the concentration of Cd in stems and leaves harvested at the flowering phase was up to 73.8% and 87.7% of that at the mature phase, respectively. The Cd-removing ratio by shoots of R. globosa harvested at the flowering phase was up to 71.4% of that at the mature phase. It was also found, by observing the growth duration of R. globosa, that the frostless period at the experiment site was twice as long as the growth time from the seedling-transplanted phase to the flowering phase of the hyperaccumulator. Conclusion R. globosa could be transplanted into contaminated soils twice in one year by harvesting the hyperaccumulator at its flowering phase based on climatic conditions of the site and traits of the plant growth. In this sense, the extraction efficiency of Cd in shoots of R. globosa increased 42.8% compared to that of at its single maturity when the plant was transplanted into contaminated soils after it had been harvested at its flowering phase and the plant accumulated Cd from soil at the same extraction ratio at its second flowering phase. Thus, the method of anthesis biomass regulation by the two-phase planting is very significant to increase the Cd-removing efficiency by phytoremediation used in practice over the course of a year. Recommendation and Outlook As for some hyperaccumulators that the growth duration from the seedling-transplanted phase to the flowering phase are short and the concentrations of heavy metals accumulated in their shoots at the flowering phase are high, the efficiency of phytoremediation can greatly be improved using the method of the two-phase planting.