浏阳河长沙段CODMn、NH3-N和TP综合降解系数研究

采用现场水团追踪法,研究了浏阳河长沙段COD_Mn、NH₃-N和TP的综合降解系数与河段水流流速之间的相关关系,并通过河段历史水文和水质监测数据对所建立的相关方程进行了验证.结果表明,浏阳河长沙段COD_Mn、NH₃-N和TP的综合降解系数与流速之间呈明显的线性相关关系,相关方程形式分别为K（COD_Mn）=0.037+0.635v、K（NH₃-N）=0.059+0.315v和K（TP）=0.004+0.140v.所建立的线性相关方程对研究河段COD_Mn、NH₃-N和TP浓度预测结果的决定系数均大于0.90、相对均方根误差均小于0.10.受风浪作用、紊动水流和弯道环流的影响,当流速小于0.35m/s时,顺直河段的污染物综合降解系数均大于弯曲河段的污染物综合降解系数;当流速大于0.46m/s时,弯曲河段污染物综合降解系数均大于顺直河段的污染物综合降解系数.研究成果对浏阳河长沙段水质管理与水环境保护具有重要的参考价值.     

木耳菌糠生物炭对阳离子染料的吸附性能研究

为了有效处理印染废水,以废弃木耳菌糠（AG）为原料,采用限氧热解法在350、550、750℃的温度下制备木耳菌糠生物炭（AGBC）,处理含有孔雀石绿（MG）、番红花红T （ST）的有色废水.考察了不同初始pH值、吸附时间、初始浓度对AGBC吸附MG、ST的影响,讨论了吸附动力学及等温吸附特性.并利用傅里叶变换红外光谱（FTIR）、X射线衍射仪（XRD）、扫描电子显微镜（SEM）等技术对吸附前后的菌糠生物炭进行表征,探究吸附机理.结果表明：随着热解温度的升高,吸附剂表面的含氧官能团数量逐渐减少,而比表面积和芳香化程度逐渐增加.MG的平衡吸附量随溶液pH值的升高而增大,而ST的平衡吸附量呈现相反趋势.AGBC对MG、ST的吸附分别在8h和4h基本达到平衡.AGBC对MG的吸附过程符合准一级动力学模型与Freundlich模型,说明吸附过程以物理吸附为主;对ST的吸附过程符合准二级动力学模型与Freundlich模型,说明吸附过程以化学吸附为主.与AG350和AG550相比,AG750对MG和ST的吸附量更高,经Langmuir模型拟合,其对MG和ST的最大吸附量分别为10249.79mg/g、3353.49mg/g.吸附机理表明,AGBC对MG的吸附主要为静电引力和π-π共轭作用,对ST的吸附主要为氢键作用、π-π共轭作用以及静电引力.说明AGBC对阳离子染料具有一定的吸附潜力,是一种经济高效的吸附材料.     

氯和紫外消毒过程中胞外抗性基因的产生特征

考察了城市污水氯和紫外消毒过程中不同物理形态的胞外抗性基因的产生行为与及微生物群落的关联特征.结果表明,氯消毒尽管使胞内抗性基因丰度下降,但使结合型胞外抗性基因丰度明显上升（0.7±0.1）log,而游离型胞外抗性基因丰度下降（0.2±0.1）log.紫外消毒也使胞内抗性基因下降,但使游离型胞外抗性基因显著上升（0.4±0.2）log,而结合型胞外抗性基因丰度下降（0.3±0.1）log.氯消毒后,结合型胞外DNA（a-eDNA）中变形菌门丰度下降而其他菌门的丰度上升,细菌多样性指数由4.2上升到4.7;而游离型胞外DNA（f-eDNA）中变形菌门上升了6.6%,多样性指数则从3.5降低到2.8.紫外消毒后,a-eDNA中变形菌门丰度下降了36.6%,多样性则上升到4.8,而f-eDNA中细菌丰度变化较小.分子生态网络分析揭示了抗性基因与细菌间广泛的寄存关系,tetA、tetX、sulI和sulII分别与17、15、15和5种菌属间存在共现性,表明抗性基因潜在宿主的变化是导致消毒后胞外抗性基因产生的关键原因.本研究表明氯和紫外消毒不能消除抗性基因风险,反而通过导致不同胞外抗性基因的大量产生,使风险的形式发生变化.     

螺形龟甲轮虫形态结构对环境变化的响应

以螺形龟甲轮虫为研究对象,于2015年7月至2018年12月,选取广东南澳岛及湖南常德中营养至中度富营养水体共14个样点进行采样,对螺形龟甲轮虫进行了形态特征测量分析.结果表明,水温是螺形龟甲轮虫形态变化最主要影响因子,且与背甲长、背甲宽、棘刺长度均呈显著负相关（P<0.01）.不同纬度条件下螺形龟甲轮虫形态参数差异显著,常德地区螺形龟甲轮虫个体显著大于南澳地区（P<0.05）.螺形龟甲轮虫形态存在显著季节性变化,各形态参数随季节波动呈现夏秋、冬春分化模式.螺形龟甲轮虫后棘刺长随水体营养程度增加而减小（F=159.4,P<0.01）,富营养条件下后棘刺长度占全长的比例减小（F=167.5,P<0.01）.研究结果表明,螺形龟甲轮虫棘刺长度可作为水质生物监测指标,并为研究全球气候变暖提供重要参考.     

Distribution and chemical speciation of arsenic in different sized atmospheric particulate matters

The distribution and chemical speciation of arsenic (As) in different sized atmospheric particulate matters (PMs), including total suspended particles (TSP), PM₁₀, and PM_2.5, collected from Baoding, China were analyzed. The average total mass concentrations of As in TSP, PM₁₀, and PM_2.5 were 31.5, 35.3, and 54.1 µg/g, respectively, with an order of PM_2.5 >PM ₁₀ > TSP, revealing that As is prone to accumulate on fine particles. Due to the divergent toxicities of different As species, speciation analysis of As in PMs is further conducted. Most of previous studies mainly focused on inorganic arsenite (iAs^III), inorganic arsenate (iAs^V), monomethylarsonate (MMA), and dimethylarsinate (DMA) in PMs, while the identification and sensitive quantification of trimethylarsine oxide (TMAO) were rarely reported. In this study, a high-performance liquid chromatography coupled to inductively coupled plasma mass spectrometry system was optimized for As speciation including TMAO in PMs. An anion exchange column was used to separate MMA, DMA and iAs^V, while a cation exchange column to separate TMAO and iAs^III. Results showed that iAs^V was the dominate component in all the samples, corresponding to a portion of 79.2% ± 9.3% of the total extractable species, while iAs^III, TMAO and DMA made up the remaining 21%. Our study demonstrated that iAs^III accounted for about 14.4% ± 11.4% of the total extracted species, with an average concentration of 1.7 ± 1.6 ng/m³. It is worth noting that TMAO was widely present in the samples (84 out of 97 samples), which supported the assumption that TMAO was ubiquitous in atmospheric particles.     

Impact of meteorological condition changes on air quality and particulate chemical composition during the COVID-19 lockdown

Stringent quarantine measures during the Coronavirus Disease 2019 (COVID-19) lockdown period (January 23, 2020 to March 15, 2020) have resulted in a distinct decrease in anthropogenic source emissions in North China Plain compared to the paralleled period of 2019. Particularly, 22.7% decrease in NO₂ and 3.0% increase of O₃ was observed in Tianjin, nonlinear relationship between O₃ generation and NO₂ implied that synergetic control of NO_x and VOCs is needed. Deteriorating meteorological condition during the COVID-19 lockdown obscured the actual PM_2.5 reduction. Fireworks transport in 2020 Spring Festival (SF) triggered regional haze pollution. PM_2.5 during the COVID-19 lockdown only reduced by 5.6% in Tianjin. Here we used the dispersion coefficient to normalize the measured PM_2.5 (DN-PM_2.5), aiming to eliminate the adverse meteorological impact and roughly estimate the actual PM_2.5 reduction, which reduced by 17.7% during the COVID-19 lockdown. In terms of PM_2.5 chemical composition, significant NO₃^? increase was observed during the COVID-19 lockdown. However, as a tracer of atmospheric oxidation capacity, odd oxygen (O_x = NO₂ + O₃) was observed to reduce during the COVID-19 lockdown, whereas relative humidity (RH), specific humidity and aerosol liquid water content (ALWC) were observed with noticeable enhancement. Nitrogen oxidation rate (NOR) was observed to increase at higher specific humidity and ALWC, especially in the haze episode occurred during 2020SF, high air humidity and obvious nitrate generation was observed. Anomalously enhanced air humidity may response for the nitrate increase during the COVID-19 lockdown period.     

Identification of close relationship between atmospheric oxidation and ozone formation regimes in a photochemically active region

Understanding ozone (O₃) formation regime is a prerequisite in formulating an effective O₃ pollution control strategy. Photochemical indicator is a simple and direct method in identifying O₃ formation regimes. Most used indicators are derived from observations, whereas the role of atmospheric oxidation is not in consideration, which is the core driver of O₃ formation. Thus, it may impact accuracy in signaling O₃ formation regimes. In this study, an advanced three-dimensional numerical modeling system was used to investigate the relationship between atmospheric oxidation and O₃ formation regimes during a long-lasting O₃ exceedance event in September 2017 over the Pearl River Delta (PRD) of China. We discovered a clear relationship between atmospheric oxidative capacity and O₃ formation regime. Over eastern PRD, O₃ formation was mainly in a NO_x-limited regime when HO₂/OH ratio was higher than 11, while in a VOC-limited regime when the ratio was lower than 9.5. Over central and western PRD, an HO₂/OH ratio higher than 5 and lower than 2 was indicative of NO_x-limited and VOC-limited regime, respectively. Physical contribution, including horizontal transport and vertical transport, may pose uncertainties on the indication of O₃ formation regime by HO₂/OH ratio. In comparison with other commonly used photochemical indicators, HO₂/OH ratio had the best performance in differentiating O₃ formation regimes. This study highlighted the necessities in using an atmospheric oxidative capacity-based indicator to infer O₃ formation regime, and underscored the importance of characterizing behaviors of radicals to gain insight in atmospheric processes leading to O₃ pollution over a photochemically active region.     

控制回路的多维度性能评估方法研究

为评价炼化装置中各控制回路的性能,基于控制回路关键品质指标要求,采用控制回路的设定值、输出值、测量值、控制模式等过程参数设计了准确性指标、稳定性指标及快速性指标等性能评估指标。辅助技术人员在线进行控制回路性能评估,识别性能较差的控制回路,诊断异常原因并进行优化,提高装置的自动化水平。     

油田井口加热炉烟尘排放超标原因分析及治理方法

针对井口加热炉燃用套管气出现的烟尘排放超标问题,从燃烧方式及燃料组成方面分析发现,加热炉所采用的扩散式燃烧,火焰面燃料侧缺少氧气,燃料产生热分解生成炭黑颗粒;另外,套管气含有大量的重碳烷烃,其稳定性差、分解温度低,加剧了热分解反应。因此,控制套管气质量和改变燃烧方式是治理烟尘排放超标的基本途径。但是井口加装轻烃回收装置,分离出套管气中的重碳烷烃,成本高不可行。最终,基于预混燃烧理论,设计了双调风预混燃烧装置,现场实施结果表明,不仅烟尘排放降低了87.8%,而且NOx排放降低了58.6%、热效率提升了8.2%。实践证明,预混燃烧是治理井口加热炉烟尘排放超标的有效方法。