Review: recent advances in biogas purifying technologies

Biomethane production through biogas upgrading is a promising renewable energy for some industries which could be part of the equilibrium needed with fossil fuels consumption to achieve a sustainable society. This paper presents a comprehensive list of biogas upgrading technologies focused on carbon dioxide removal as well as recent advances reported by researcher with wide expertise in this topic. Additionally, an extensive costs–performance comparison among the technologies studied is discussed. Among the different alternatives, chemical scrubbing stood out to achieve high biomethane purities while cryogenic technologies proved to be effective against methane losses. Regarding the different costs, water scrubbing and membrane separation seem to be the most affordable techniques.     

重金属离子对肺表面活性物质单层膜的影响

为了探究重金属对肺表面活性物质（PS）膜的影响,利用Langmuir–Wilhelmy膜天平,研究了不同种类和浓度的重金属离子与PS单层膜的相互作用.发现Cr³⁺、Cu²⁺、Hg²⁺、Pb²⁺、Cd²⁺、Ni²⁺6种重金属离子均使PS单层的π-A等温线G-LE相变阶段外扩,而Fe³⁺可诱导单层缩合.随后,选取Cd²⁺,Cu²⁺,Hg²⁺,Fe³⁺4种离子进一步探究了重金属浓度对PS单层膜表面活性的影响规律,进行了可压缩模量分析,并结合红外光谱（FTIR）和原子力显微镜（AFM）探究其作用机理,发现Cu²⁺,Fe³⁺和Hg²⁺均会以浓度依赖的方式与PS单层的极性头部发生络合作用,形成复合物,改变膜的稳定性;而Cd²⁺的影响明显弱于其他3种金属离子,但也能使得PS单层有序性增强.     

螯合树脂在线富集——火焰原子吸收光度法测定水中微量Cu,Pb,Zn,Cd

对螯合树脂在线富集，火焰原子吸收光度法进行了条件试验。试验证实方法对Ｃｕ、Ｐｂ、Ｚｎ、Ｃｄ４个元素检出浓度可达μｇ／Ｌ级，校准曲线性、样品重现性及准确度可满足测定要求。     

火焰原子吸收分光光度法测定鱼内脏及河流底泥中的铜

采用火焰原子吸收分光光度法测定鱼内脏及河流底泥中的铜。鱼内脏经组织捣碎机捣成匀浆后，加硝酸消解；底泥则经氢氟酸和高氯酸消化。该方法具有灵敏度高，精密度和回收率较好等特点。     

Comparison of Two Manual Methods of Nitrogen Dioxide Determination in Ambient Air

Sodium arsenite (modified Jacobs and Hochheiser method; hereafter referred as SA), the most widely used manual monitoring method for determination of nitrogen dioxide (NO₂) in ambient air, particularly in developing countries has been evaluated and compared with US EPA recommended equivalent method of TGS-ANSA (hereafter referred as ANSA). NO₂ concentrations generated from laboratory test atmosphere were analyzed by these two methods and were compared statistically. Laboratory evaluations showed that SA method has high sensitivity to different sampling conditions, which normally vary during actual field monitoring. Hence, correction factors for absorption efficiency were estimated for SA and ANSA methods. Absorption efficiency of NO₂ in SA method was found to be much lower (64%) as against the reported value of 82% at the method recommended sampling conditions, whereas for ANSA method, it was found 1.0 as against the reported value of 0.93. After applying derived correction factors, both the methods produced almost similar concentration values of NO₂.     

离子交换树脂光度法测定微量铁的研究

研究了以阳离子交换树脂为显色载体，利用直接吸附在树脂上有色络合物－Fe(II)邻二氮菲的吸光度，借以检测水和火腿肠中铁的新方法，本法具有比原子吸收法更高的灵敏度，稳定性和选择性，并对成络及树脂吸附条件作了较详细研究。     

表面活性剂存在下铁-邻菲罗啉-曙红分光光度法的研究

研究了表面活性剂(乳化剂OP)存在下,铁、邻菲罗啉、曙红的显色反应.该离子缔合物的最大吸收波长为545 nm,摩尔吸光系数为9.4×104 L·mol-1·cm-1,铁含量在0-0.4 mg/L内符合比耳定律.以自来水为基体进行铁的回收实验,回收率在99%以上.     

Simultaneous determination of parathion and p-nitrophenol in vegetable tissues by derivative spectrophotometry

A first derivative spectrophotometric method has been developedfor the determination of parathion and p-nitrophenol in vegetabletissues. Ethanol was used as solvent for extracting the compoundsfrom the tissues and subsequently the samples were evaluated against a vegetable tissue blank, directly by derivative spectrophotometry. The simultaneous determination of these compounds can be carried out using the zero-crossing approach for parathion at 253.0 nm and for p-nitrophenol at 273.1 nm. In the samples each analyte was determined in the presence of one another in the ranges between 4.9 to 3883.5 g g^-1 forparathion and 4.9 to 3285.3 g g^-1 for p-nitrophenol.The detection limits (3) were found to be 1.5 and 1.4 g g^-1 for parathion and p-nitrophenol, respectively. The relative standard deviations were in all instances less than1.8%. The proposed method was applied to the determination ofthe analytes in spiked leafs of corn. The results show a goodrecovery and they are in agreement with those obtained bypolarography.     

氢化物发生原子荧光法测定饮用水中的微量硒

氢化物发生原子荧光法测定饮用水中的微量硒时。仪器条件和试剂的浓度选择很重要。本文对条件的最佳化进行了实验。并对方法的精密度、准确度和检出限进行了讨论。     

过硫酸钾氧化-紫外光度法测定总氮方法的改进

过硫酸钾氧化紫外光度法测定总氮的空白吸光度高的主要原因是：K2S2O3是220nm波长上有特征吸收，适当降低K2S2O3、NaOH的用量，延长消解时间，使用二次蒸馏水，用低浓度亚砷酸钠溶液，还原消解后剩余的极少量的K2S2O3，可以降低空白吸光度。K2S2O3-NaOH碱溶液不稳定，使用期短，三天后氧化能力迅速降低，原因是：K2S2O3溶液中，加入NaOH，加速了K2S2O3的分解。K2S2O3和NaOH分别配制，并在K2S2O3溶液中，加入少量HCl，抑制其水解。两种溶液可使用半年以上时间。