化工行业危险废物调查方法的建立与应用研究

在化工行业危险废物调查实践基础上,建立了适用于化工行业危险废物调查的快速浏览法.该法通过对化工企业工业流程的每一工序的物料投入与产出分析,得到产品整个生产工艺的物料平衡图,据此可分析物料转化率、危险废物产生环节、产生量、产废系数等.介绍了该方法的建立过程、主要调查步骤及其在化学农药厂的实际应用案例.     

石灰石湿法烟气脱硫添加剂的实验研究

利用双搅拌釜，作石灰石浆液脱硫的实验，测定添加剂强化前后石灰石浆液脱硫过程中气液两相传质系数的变化，对比气液两相传质系数的大小。并结合国内外脱硫技术现状，提出了以石灰石作为脱硫剂，以硫酸镁、硫酸钠、腐残酸钠为添加剂，应用双搅拌釜为主设备的湿法脱硫方法，对添加剂的脱硫机理进行了基础性研究。     

湿法烟气脱硫法鼓泡反应器的气液传质建模

利用双膜理论对湿法烟气脱硫法鼓泡反应器气液传质建立数学模型。通过鼓泡反应的钠碱脱硫实验来验证模型，得到的模型计算结果和实验相吻合。利用模型，通过改变的初始参数来研究对传质的影响。结果表明，提高气流速度、进气浓度、吸收液柱高度和吸收液浓度，有利于传质吸收，提高鼓泡反应器的传质系数和脱硫效率。     

摩擦对板料极限拉深系数的影响

通过对板料拉深法兰变形区和直壁传力区的应力分析 ,应用功平衡法 ,推导了极限拉深系数与摩擦系数之间的关系式 ,并讨论了摩擦对拉深性能的影响。     

室温平衡顶空气相色谱法测定水中挥发性卤代烃影响因素的研究

对室温下用顶空气相色谱法测定水听军发性卤代烃的影响因素进行了研究，结果表明，随着样品浓度的增高，平衡时间缩短；气液平衡瓶体积增大，平衡时间加长；同一瓶样品重复进样次数不得多于2次；适宜的气液体积比为1：2。室温平衡顶空气相色谱法简单易行。     

石油化工废水中有机组分剖析

采用二氯甲烷液—液萃取预处理水样，气相色谱—质谱联用技术分析了炼油厂生化曝气池进、出水，腈纶厂干法纺丝废水及其经ＳＢＲ小试处理的出水中二氯甲烷可萃取的有机组分，并半定量地评估了生化处理对这些有机组分的去除效果。结果表明，炼油厂生化曝气池对酚类及芳烃类化合物的去除效果较好，而长链脂肪烃的去除率相对较低；腈纶干法纺丝工艺废水中可萃取的有机组分主要为Ｎ，Ｎ二甲基甲酰胺，其相对含量大于９５％（ｍ／ｍ），该废水经ＳＢＲ小试处理后，原水中各种可萃取的有机化合物均得到分解，结构发生了变化，但不能全部彻底地转化为ＣＯ２和水。     

自然资源资产负债表编制中生态损益核算

生态损益核算是自然资源资产负债表的重要部分,是对自然资源分类核算的扩展和补充。本文梳理生态损益核算的总体思路,系统总结生态损益核算技术,以围场县为例进行实证,遵循先实物后价值的核算原则,选择森林、草地、湿地生态系统,按不同的生态服务指标进行实物量和价值量的核算,并在已有的核算基础上计算各类型生态系统的实物量参数和价值量参数,以便根据面积统计数据进行快速简洁的核算比较。研究发现：围场县2015年生态系统服务功能价值量总值为338.99亿,与2013年相比增加了0.04%。生态系统服务功能价值量从大到小依次为草地、森林、湿地,核算期间森林和草地生态系统价值量分别下降0.06%和0.22%,湿地生态系统价值量增加4.47%。研究成果有助于全面理解和量化自然资源数量变化和质量变化带来的生态效应,并为自然资源资产负债表中的负债核算提供数据基础。     

Hydroclimatology of the Mississippi River Basin

Model estimated monthly water balance (WB) components (i.e., potential evapotranspiration, actual evapotranspiration, and runoff [R]) for 848 United States (U.S.) Geological Survey 8‐digit hydrologic units located in the Mississippi River Basin (MRB) are used to examine the temporal and spatial variability of the MRB WB for water years 1901 through 2014. Results indicate the MRB can be divided into nine subregions with similar temporal variability in R. The WB analyses indicated ~79% of total water‐year MRB runoff is generated by four of the nine subregions and most of the R in the basin is derived from surplus (S) water during the months of December through May. Furthermore, the analyses showed temporal variability in S is largely controlled by the occurrence of negative atmospheric pressure anomalies over the western U.S. and positive atmospheric pressure anomalies over the eastern U.S. coast. This combination of atmospheric pressure anomalies results in an anomalous flow of moist air from the Gulf of Mexico into the MRB. In the context of paleo‐climate reconstructions of the Palmer Drought Severity Index, since about 1900 the MRB has experienced wetter conditions than were experienced during the previous 500 years.     

Distinct potential aerosol masses under different scenarios of transport at a suburban site of Beijing

In order to evaluate the secondary aerosol formation potential at a suburban site of Beijing,in situ perturbation experiments in a potential aerosol mass(PAM) reactor were carried out in the winter of 2014.The variations of secondary aerosol formation as a function of time,OH exposure,and the concentrations of gas phase pollutants and particles were reported in this study.Two periods with distinct secondary aerosol formation potentials,marked as Period Ⅰ and Period Ⅱ,were identified during the observation.In Period Ⅰ,the secondary aerosol formation potential was high,and correlated well to the air pollutants,i.e.,SO_2,NO_2,and CO.The maximal secondary aerosol formation was observed with an aging time equivalent to about 3 days of atmospheric oxidation.In period Ⅱ,the secondary aerosol formation potential was low,with no obvious correlation with the air pollutants.Meanwhile,the aerosol mass decreased,instead of showing a peak,with increasing aging time.Backward trajectory analysis during the two periods confirmed that the air mass in Period Ⅰwas mainly from local sources,while it was attributed mostly to long distance transport in Period Ⅱ.The air lost its reactivity during the long transport and the particles became highly aged,resulting in a low secondary aerosol formation potential.Our experimental results indicated that the in situ measurement of the secondary aerosol formation potential could provide important information for evaluating the contributions of local emission and long distance transport to the aerosol pollution.     

丁苯橡胶生产废水的生物降解特性

为研究丁苯橡胶生产废水的好氧生物降解特性,对某石化企业丁苯橡胶生产装置的生产废水进行好氧处理,并采用液液萃取-气相色谱/质谱、三维荧光光谱、紫外吸收光谱等手段对水质指标进行表征. 结果表明:经好氧生物降解后,丁苯橡胶废水中ρ(COD_Cr)和ρ(DOC)分别降至155和76 mg/L,COD_Cr和DOC去除率分别为76.07%和70.08%;废水中二苄胺、苯乙烯和十二烷基二甲基叔胺等9种主要特征有机物19 d内可被完全降解. 丁苯橡胶生产废水在λ_Ex/λ_Em(激发波长/发射波长)为225 nm/340 nm、215 nm/290 nm,275 nm/340 nm处有3个荧光峰,分别由二苄胺、十二烷基二甲基叔胺、苯乙烯、甲苯和苯甲醛等胺类、苯乙烯和芳香族化合物等有机物产生,好氧生物降解能去除废水中的绝大部分荧光物质,荧光峰强度的总去除率达到93.87%;废水中二苄胺、十二烷基二甲基叔胺、4-甲基环己酮、苯甲醛,苯乙烯、甲苯等有机物使丁苯橡胶生产废水分别在波长190~230、230~250、250~400 nm处有紫外吸收,好氧生物降解对UV₂₅₄的去除率达到52%. 研究显示,丁苯橡胶废水经单独好氧生物处理不能达到GB 31572—2015《合成树脂工业污染物排放标准》的要求,需结合其他方式进行联合处理.