高安全AZH——20型化学氧自救器的研究

介绍了高安全ＡＺＨ——２０ 型化学氧自救器科研成果。重点阐述了该自救器的结构设计、选材、氧烛起动装置和提高ＫＯ２ 片状生氧剂性能等方面的技术创新和改进,对应用高新技术提高自救器的防护性能和安全可靠性作了有益的探索     

微孔扩散管曝气试验

本文综术字在污水处理站使用离心鼓风机穿孔管大气泡浅 支暴气所引起的溶解氧不足。     

分光光度法测定COD_(Cr)的试验条件选择

用分光光度法测定水中化学需氧量ＣＯＤＣｒ,通过正交试验选择氧化的最佳选择。试验结果表明对ＣＯＤＣｒ值为５０～１０００ｍｇ／Ｌ的水样：氧化剂Ｋ２Ｃｒ２Ｏ７用量为０．２０～０．４０ｍｏｌ／Ｌ,催化剂Ａｇ２ＳＯ４用量为１０ｇ／ＬＨ２ＳＯ４,消解时间１０ｍｉｎ,加热温度１８０℃。用ＣＯＤＣｒ为１３８ｍｇ／Ｌ的质控标样进行验证试验,其绝对误差为０．５～３．０ｍｇ／Ｌ。与标准方法相比用分光光度法测定ＣＯＤＣｒ具有分析误差小,省时、省力,节约药剂的特点。     

COD_(Cr)测定中排除氯离子干扰的进一步探讨

废水中化学需氧量的测定采用重铬酸钾法［１］,大多数情况下都存在Ｃｌ－干扰,其排除方法用ＨｇＳＯ４掩蔽,通过实验探讨不用剧毒药品ＨｇＳＯ４掩蔽Ｃｌ－的干扰,而用ＣＯＤＣｒ总量减去Ｃｌ－的量。实验结果表明：当测定化学需氧量较低而Ｃｌ－含量高的水样时,即使采用掩蔽Ｃｌ－也会产生较大的误差,而用测定值减去０．２２６［Ｃｌ－］之值更接近真值。     

汽车尾气催化转化器模型研究进展

本文主要介绍汽车尾气催化转化器模型的研究进展 ,包括反应器内气体流动特性、单通道反应器内的传递现象和反应动力学、通道间的热传递和反应行为的模拟 ;并指出认识反应器内的各种特性和规律对设计汽车尾气催化转化器的必要性和意义     

Modelling the environmental degradation of water contaminants. Kinetics and mechanism of the riboflavin-sensitised-photooxidation of phenolic compounds

The aerobic visible-light-photosensitised irradiation of methanolic solutions of either of the phenolic-type contaminants model compounds (ArOH) p-phenylphenol (PP), p-nitrophenol (NP) and phenol (Ph), and for two additional phenolic derivatives, namely p-chlorophenol (ClP) and p-methoxyphenol (MeOP), used in some experiments, was carried out. Employing the natural pigment riboflavin (Rf) as a sensitiser, the degradation of both the ArOH and the very sensitiser was observed. A complex mechanism, common for all the ArOH studied, operates. It involves superoxide radical anion (O₂^√−) and singlet molecular oxygen (O₂(¹Δ_g)) reactions. Maintaining Rf in sensitising concentrations levels (≈0.02 mM), the mechanism is highly dependent on the concentration of the ArOH. Kinetic experiments of oxygen and substrate consumption, static fluorescence, laser flash photolysis and time-resolved phosophorescence detection of O₂(¹Δ_g) demonstrate that at ArOH concentrations in the order of 10 mM, no chemical transformation occurs due to the complete quenching of Rf singlet excited state. When ArOH is present in concentrations in the order of mM or lower, O₂^√− is generated from the corresponding Rf radical anion, which is produced by electron transfer reaction from the ArOH to triplet excited Rf. The determined reaction rate constants for this step show a fairly good correlation with the electron-donor capabilities for Ph, PP, NP, ClP and MeOP. In this context, the main oxidative species is O₂^√−, since O₂(¹Δ_g) is quenched in an exclusive physical fashion by the ArOH. The production of O₂^√− regenerates Rf impeding the total degradation of the sensitiser. This kinetic scheme could partially model the fate of ArOH in aquatic media containing natural photosensitisers, under environmental conditions.     

Atmospheric lead deposition to Okefenokee Swamp, Georgia, USA

Contamination of the environment from atmospheric deposition during the twentieth century is pervasive even in areas ostensibly considered pristine or remote from point sources. In this study, Pb concentrations in a 210Pb-dated peat core collected from the Okefenokee Swamp, GA were used to assess historical contaminant input via atmospheric deposition. Lead isotope ratios were determined by dynamic reaction cell ICP-MS (DRC-ICP-MS). Increases in Pb concentration occurred in the late nineteenth century and a marked rise in Pb concentrations pre-dated the widespread use of leaded gasoline within the US. The 206Pb/207Pb ratios of 1.19 during this period were consistent with coal combustion emissions. A later increase in Pb concentration, concurrent with a trend toward more radiogenic 206Pb/207Pb ratios in gasoline is consistent with an increased input of Pb from leaded gasoline emissions. However, it appears that coal combustion emissions remain a major source of Pb to the Okefenokee.     

有机负荷和溶解氧的变化对SBR污泥膨胀的影响及控制方法

本文研究SBR工艺处理汽车电泳废水在不同有机负荷、溶解氧条件下污泥膨胀的现象 ,分析膨胀发生机理 ,分别提出控制方法。实验结果表明 ,在低、中、高负荷时 ,只要溶解氧发生变化 ,均有可能发生膨胀。低负荷、正常溶解氧时发生的膨胀可以通过前联好氧生物选择器加以控制 ;中负荷、低溶解氧及高负荷、低溶解氧活性污泥发生膨胀时可以通过强化曝气得到控制     

污水厂Carrousel氧化沟溶解氧和速度分布的研究

对长沙某污水处理厂的Carrousel氧化沟进行现场测试，获得不同截面的溶解氧和速度的数据，探讨了表曝机台数、沟深、沟的长宽比、进出水位置对溶解氧和速度的影响。初步掌握了该Carrousel氧化沟内溶解氧和速度的变化规律，认为通过调节倒伞形表面曝气机，可以在沟内不同区段创造好氧与缺氧的环境，为最终实现同步硝化反硝化的高效运行做准备。     

PM2.5 chemical source profiles for vehicle exhaust, vegetative burning, geological material, and coal burning in Northwestern Colorado during 1995

PM_2.5 (particles with aerodynamic diameters less than 2.5 μm) chemical source profiles applicable to speciated emissions inventories and receptor model source apportionment are reported for geological material, motor vehicle exhaust, residential coal (RCC) and wood combustion (RWC), forest fires, geothermal hot springs; and coal-fired power generation units from northwestern Colorado during 1995. Fuels and combustion conditions are similar to those of other communities of the inland western US. Coal-fired power station profiles differed substantially between different units using similar coals, with the major difference being lack of selenium in emissions from the only unit that was equipped with a dry limestone sulfur dioxide (SO₂) scrubber. SO₂ abundances relative to fine particle mass emissions in power plant emissions were seven to nine times higher than hydrogen sulfide (H₂S) abundances from geothermal springs, and one to two orders of magnitude higher than SO₂ abundances in RCC emissions, implying that the SO₂ abundance is an important marker for primary particle contributions of non-aged coal-fired power station contributions. The sum of organic and elemental carbon ranged from 1% to 10% of fine particle mass in coal-fired power plant emissions, from 5% to 10% in geological material, >50% in forest fire emissions, >60% in RWC emissions, and >95% in RCC and vehicle exhaust emissions. Water-soluble potassium (K⁺) was most abundant in vegetative burning profiles. K⁺/K ratios ranged from 0.1 in geological material profiles to 0.9 in vegetative burning emissions, confirming previous observations that soluble potassium is a good marker for vegetative burning.