臭氧氧化—湿式钙法吸收工艺对烟气的同时脱硫脱硝

采用臭氧氧化—湿式钙法吸收工艺对模拟烟气进行同时脱硫脱硝处理。O₃于150 ℃下具有较高的热稳定性,可将NO氧化为高价态氮氧化物,且NO氧化率随n（O₃）∶n（NO）的增大而逐渐提高。烟气中SO₂和H₂O的存在对NO氧化率的影响不大。O₃对SO₂的氧化率较低,约为5%。3%（w）石灰石浆液对SO₂的吸收率接近100%,NO_x吸收率随n（O₃）∶n（NO）的增大而逐渐提高,当n（O₃）∶n（NO）为1.6时NO_x吸收率可达约65%。SO₂能促进吸收液对NO_x的脱除。石灰石浆液中加入0.2%（w）的（NH₄）₂SO₃或Na₂SO₃后NO_x吸收率可达约85%或82%,且吸收率随添加剂加入量的增加而提高,添加（NH₄）₂SO₃的NO_x吸收率略高于添加Na₂SO₃。     

煤与瓦斯共采在错层位巷道布置中的机理研究及应用构想

为了完善现有煤与瓦斯共采技术，创新煤与瓦斯共采方法，对错层位巷道布置下的煤与瓦斯共采系统展开研究，利用相似模拟试验，分析错层位巷道布置覆岩运动情况，预测其开采围岩裂隙发育和瓦斯运移形式，提出了创新煤与瓦斯共采技术构想。研究结果表明:采空区覆岩三带高度随接续工作面的增加而增大，相邻采空区垮落矸石压实区呈现“O-L-O”形变化，多个相邻采空区覆岩出现大“O”形圈裂隙带；相邻采空区内瓦斯可实现相互运移，大“O”形圈裂隙带内赋存大量瓦斯气体；研究提出了地面钻井抽采瓦斯、走向高位瓦斯抽采巷和外错尾巷穿层钻孔3种煤与瓦斯共采技术，比传统巷道布置情况下的煤与瓦斯共采技术在安全、经济等方面更具优势。     

Estimate on spillover effect of environmental pollution between peripheral areas

ABSTRACT

Interaction of environmental pollution between peripheral areas has become a central topic in the field of resources and environment but little is known about the actual impact on peripheral areas in the current literature. This paper sets out a simultaneous equation model to investigate the spillover effect of environmental pollution between China’s peripheral areas utilizing the panel data of 218 cities in China. Making use of indicators for measuring the impact on environmental pollution, it identifies that environmental pollution between cities of China has a significant two-way spillover effect. After standardization of variables, it is found that the spillover effect of peripheral areas on urban environmental pollution cannot be neglected. Nearly, a third of the environmental pollution level in a city is induced by the environmental pollution in peripheral areas. If the indicator of environmental pollution in peripheral areas is missing, wrong conclusions will be drawn. Therefore, government should shift the emphasis of environmental regulation from local to global, and improve the overall environmental quality through coordinated management of regional environment.     

气相色谱法测定水中的三氯乙醛

建立了一种用气相色谱法测定水体中三氯乙醛的方法。水样先以石油醚萃取,除去高沸点化合物,加入氯化钠破乳,然后再用石油醚—乙醚混合溶剂(V/V=2:1)萃取3次,萃取液经色谱柱分离,用电子捕获检测器检测。最低检出浓度可达0.008 mg/L,线性关系良好(相关系数γ=0.992~0.998),一般共存物质不干扰测定。     

K_2Cr_2O_7法和紫外分光光度法测定污水COD的对比研究

分别利用重铬酸钾法、重铬酸钾紫外分光光度法和紫外分光光度法测定污水的COD极差分别为2.43mg/L、1.19 mg/L和4.72 mg/L,RE%分别为0.84%、0.53%和1.36%,重铬酸钾紫外分光光度法和紫外分光光度法的线性范围分别在0~280 mg/L和0~400 mg/L.结果表明:重铬酸钾紫外分光光度法测定的准确度和精密度最高,简化了用标准溶液进行标定的步骤,缩短了实验时间;紫外分光光度法测定的结果准确度和精密度相对差一些,但是快速、操作简单、节省试剂,为广大环境工作者提供借鉴参考的实例。     

亚甲基蓝分光光度法测定废水硫化物的不确定度评定研究

分析了应用亚甲基蓝分光光度(GB/T16489-1996)测定废水硫化物测试过程中不确定度影响因素,主要来源为硫化物标准溶液、标准曲线拟合、随机效应、分光光度计和取样体积这五部分。本测量合成相对标准不确定度0.025 9;其中由测定样品质量引入的不确定度为0.024 7;由样品体积引入的不确定度为0.007 7。本次废水中硫化物测量结果为:0.110±0.006 mg/L,k=2(包含概率约为95%)。     

静置/好氧/缺氧序批式反应器（SBR）脱氮除磷效果研究

以静置段代替传统厌氧段,采用后置缺氧方式,考察了静置/好氧/缺氧序批式反应器(SBR)(R1)的生物脱氮除磷(BNR)性能,并与传统厌氧/好氧/缺氧序批式反应器(SBR)(R2)进行对比.两反应器进水乙酸钠、氨氮(NH+4-N)及磷酸盐(PO3-4-P)浓度均分别为350 mg·L-1(以COD计)、40 mg·L-1及12 mg·L-1,水力停留时间(HRT)为12 h.研究结果表明,R1长期运行中磷的去除率与R2相当,分别为92.4%和92.1%,而总氮(TN)去除率则较R2高,分别为83.5%和77.0%.R1静置段省去搅拌但仍能起到厌氧段的作用,为好氧快速摄磷奠定了基础,同时R1缺氧段发生反硝化摄磷,使出水磷降至0.91 mg·L-1.好氧段内R1发生了同步硝化-反硝化(SND),贡献了18.0%的TN去除量,R2也存在SND,但脱氮贡献率较少,仅为9.8%.R1和R2后置缺氧反硝化均以糖原驱动,反硝化速率分别为0.98、0.84 mg·g-1·h-1(以每g VSS产生的N(mg)计),出水TN分别为6.62、9.21 mg·L-1.研究表明,静置段代替传统厌氧段后,可获得更好的脱氮效果,且工艺更为简化.     

高效液相色谱-电感耦合等离子体质谱联用测定生物样品中的有机汞

建立了酸提取-高效液相色谱-电感耦合等离子体质谱联用技术(HPLC-ICP-MS)测定生物样品中甲基汞、乙基汞、苯基汞等3种有机汞的分析方法。鱼肉和贝类样品经盐酸消解,苯萃取,硫代硫酸钠溶液反萃取后,采用醋酸铵/L-半胱氨酸缓冲盐及甲醇体系组成的流动相按一定比例进行梯度洗脱,经前处理的生物样品在液相色谱中经C18柱分离后,进入电感耦合等离子体质谱检测其甲基汞、乙基汞和苯基汞的浓度。3种有机汞化合物均在0.50~50.0μg/L范围内呈现良好的线性关系,线性相关系数(r)均大于0.9998。方法检出限为0.010~0.038mg/kg;3种有机汞样品加标的RSD均小于12.2%;两个水平的加标回收率在50.8~129%。     

Rapid and simple spectrophotometric determination of persulfate in water by microwave assisted decolorization of Methylene Blue

A rapid and simple method for determination of persulfate in aqueous solution was developed. The method is based on the rapid reaction of persulfate with Methylene Blue(MB) via domestic microwave activation, which can promote the activation of persulfate and decolorize MB quickly. The depletion of MB at 644 nm(the maximum absorption wavelength of MB) is in proportion to the increasing concentration of persulfate in aqueous solution. Linear calibration curve was obtained in the range 0–1.5 mmol/L, with a limit of detection of 0.0028 mmol/L. The reaction time is rapid(within 60 sec), which is much shorter than that used for conventional methods. Compared with existing analytical methods, it need not any additives, especially colorful Fe2+, and need not any pretreatment for samples, such as p H adjustment.     

MFC强化同步短程硝化反硝化工艺的启动

微生物燃料电池(MFC)可在阴极实现反硝化、短程反硝化和同步硝化反硝化并产生电能,但在MFC阴极实现同步短程硝化反硝化的研究尚未见到报道。为了探讨MFC阴极同步短程硝化反硝化工艺的性能,将双室曝气阴极MFC与A/O脱氮工艺结合处理人工模拟低碳氮比废水。通过静置运行15 d使得MFC阴极室亚硝态氮得以积累,氨氧化菌得以富集。随即改为连续运行后第21天成功启动同步短程硝化反硝化MFC;阴极出水氨氮浓度为0.3 mg/L,亚硝态氮浓度为15.9 mg/L,硝态氮浓度为0.6 mg/L,亚硝化率达到95%以上,阴极电极自养反硝化去除率达到50%以上,COD去除率达到85%以上。结果表明,将MFC与同步短程硝化反硝化工艺结合,通过阴极室中氧气得电子获得高p H,可以强化同步短程硝化反硝化工艺,完成生物脱氮的同时回收电能,并具有减少外加碱度的优势。