Application of GaN-based ultraviolet-C light emitting diodes--UV LEDs--for water disinfection

GaN-based ultraviolet-C (UV-C) light emitting diodes (LEDs) are of great interest for water disinfection. They offer significant advantages compared to conventional mercury lamps due to their compact form factor, low power requirements, high efficiency, non-toxicity, and overall robustness. However, despite the significant progress in the performance of semiconductor based UV LEDs that has been achieved in recent years, these devices still suffer from low emission power and relatively short lifetimes. Even the best UV LEDs exhibit external quantum efficiencies of only 1-2%.The objective of this study was to investigate the suitability of GaN-based UV LEDs for water disinfection. The investigation included the evaluation of the performance characteristics of UV LEDs at different operating conditions as well as the design of a UV LED module in view of the requirements for water treatment applications. Bioanalytical testing was conducted using Bacillus subtilis spores as test organism and UV LED modules with emission wavelengths of 269 nm and 282 nm.The results demonstrate the functionality of the developed UV LED disinfection modules. GaN-based UV LEDs effectively inactivated B. subtilis spores during static and flow-through tests applying varying water qualities. The 269 nm LEDs reached a higher level of inactivation than the 282 nm LEDs for the same applied fluence. The lower inactivation achieved by the 282 nm LEDs was compensated by their higher photon flux. First flow-through tests indicate a linear correlation between inactivation and fluence, demonstrating a well designed flow-through reactor. With improved light output and reduced costs, GaN-based UV LEDs can provide a promising alternative for decentralised and mobile water disinfection systems.     

Laboruntersuchungen zur Freisetzung von Unat aus einem Gestein unter oxischen naturnahen Bedingungen

Kurzfassung Im Labor wurden verschiedene Größen (pH-Wert, HCO ₃ —Gehalt, Präsenz von Fe(OH) ₃ ) untersucht, von denen angenommen werden konnte, dass sie die umweltrelevante Freisetzung von Uran aus Gesteinen (z. B. Haufwerken, Halden, Tailings) im neutralen und schwach basischen pH-Bereich (6 bis 9) beeinflussen. Hierzu wurde der Austrag von U _nat aus einem schwach vererzten Urangestein (2,31 %) in Batchversuchen untersucht. Diese Versuche wurden mit 8, 10 oder 40 g/l Gestein und Leitungs- bzw. Mineralwasser durchgeführt. Zum Vergleich wurden parallele Standversuche in deionisiertem Wasser, 0,1 M Na ₂ CO ₃ und 0,1 M H ₂ SO ₄ durchgeführt. Die Ergebnisse zeigen eine Begünstigung der Uranfreisetzung in Anwesenheit von Carbonat (gelöst oder in situ durch Dolomitauflösung entstanden), während die Rolle des Pyrits auf die Freisetzung deutlich komplexer ist. Das Erreichen eines Gleichgewichtszustands kann unter Umständen durch sorptive Einflüsse verzögert werden.

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Investigations for the release of U_nat from ore bearing rock under natural near oxic conditions

Abstract The effects of carbonate concentration and the presence of iron hydroxide phases on uranium release into the environment were investigated under oxic conditions and in the pH range from 6 to 9. For this purpose not-shaken batch experiments were conducted with a constant amount (8, 10 or 40 g/l) of a uranium bearing rock and different types of water (deionised, tap and mineral water). For comparison parallel experiments were conducted with 0.1 M Na ₂ CO ₃ and 0.1 M H ₂ SO ₄ . The use of dolomite confirmed the favourable role of carbonate bearing minerals for U transport while the presence of pyrite on Uranium mobilisation was shown to be considerably more complex. This study shows that the approach of equilibrium conditions can be strongly delayed by sorption processes.

     

Resources and reserves of European gravel deposits

Contrary to public opinion, gravel and sand are mineral raw materials that are not available in unlimited quantities, and, at any place. In quantity and economic value they belong to the top-ranking resources on a world scale. Supplies are not unlimited: lifetime is very short in some regions. Being very vulnerable to changes in transport costs and sensitive with respect to conflicts between environmental protection and mining, sand and gravel require scientific effort in order that new deposits be found and the lifetime of reserves increased.     

城市发展战略规划研究中的空间拓展方向分析方法

通过对沈阳市铁西新区发展战略规划的实践,提出一种从外部环境拉动、内部需求推动、自身现有基础三个视角,分别考察产业发展、空间结构、城市形象、行政效率等相关要素,来确定城市空间拓展方向的系统分析方法.     

砖混结构构造柱及圈梁的设置与功能分析

介绍了构造柱、圈梁的主要功能,从多层砖房中构造柱和圈梁的设置、构造措施,分析了设计中应注意的有关问题,以提高多层砖房的有效抗震能力,引起设计人员的重视.     

玻璃结构体系应用与抗震性能分析

结合国内外新型玻璃建筑结构的典型工程实例 ,介绍了玻璃结构体系的应用现状与发展趋势 ,分析了玻璃结构体系抗震方案的选择与应用 ,为玻璃建筑结构的设计提供了参考     

利用混凝土施工标准离差评价施工管理水平

通过对公路工程施工中混凝土施工质量的标准离差分析，来评价施工企业的施工管理水平，评价阶段的施工质量，并进行数据分析，查找不足和整个系统中的每个环节可能出现的问题，从而能够及时改进管理措施，使得工程质量管理水平持续提高，更大程度地提高工程质量。     

某教学楼墙体裂缝原因分析及加固处理

通过对某教学楼墙体裂缝的鉴定分析,提出了造成墙体裂缝的地质原因和外在原因,并给出了基于沉降控制的防沉锚杆基础托换加固方案,经观测,该方案是合理可行的。     

Phenols in anaerobic digestion processes and inhibition of ammonia oxidising bacteria (AOB) in soil

This study focuses on the presence of phenols in digestate from seven Swedish large-scale anaerobic digestion processes and their impact on the activity of ammonia oxidising bacteria (AOB) in soil. In addition, the importance of feedstock composition and phenol degradation capacity for the occurrence of phenols in the digestate was investigated in the same processes. The results revealed that the content of phenols in the digestate was related to the inhibition of the activity of AOB in soil (EC(50)=26 microg phenols g(-1) d.w. soil). In addition, five pure phenols (phenol, o-, p-, m-cresol and 4-ethylphenol) inhibited the AOB to a similar extent (EC(50)=43-110 microg g(-1) d.w. soil). The phenol content in the digestate was mainly dependent on the composition of the feedstock, but also to some extent by the degradation capacity in the anaerobic digestion process. Swine manure in the feedstock resulted in digestate containing higher amounts of phenols than digestate from reactors with less or no swine manure in the feedstock. The degradation capacity of phenol and p-cresol was studied in diluted small-scale batch cultures and revealed that anaerobic digestion at mesophilic temperatures generally exhibited a higher degradation capacity compared to digestion at thermophilic temperature. Although phenol, p-cresol and 4-ethylphenol were quickly degraded in soil, the phenols added with the digestate constitute an environmental risk according to the guideline values for contaminated soils set by the Swedish Environmental Protection Agency. In conclusion, the management of anaerobic digestion processes is of decisive importance for the production of digestate with low amounts of phenols, and thereby little risks for negative effects of the phenols on the soil ecosystem.     

Formation of alkylated aromatic acids in groundwater by anaerobic degradation of alkylbenzenes

Evidence for the presence of previously unreported alkylated aromatic acids in anaerobic groundwater samples from a jet fuel-contaminated site is presented. The redox conditions are dominated by sulfate reduction. A gas chromatography/mass spectrometry screening showed a composition of aromatic hydrocarbons ranging from BTEX (C(0)-C(2)-substituted benzenes) up to C(7)-benzenes. Known metabolites like methylbenzoates (C(1)-BA), C(2)-BA, C(3)-BA as well as methylbenzylsuccinates (C(1)-BSA) were detected. Additionally, previously unreported metabolites of higher alkylated benzenes have been identified in the extracts: those are C(2)-BSA to C(5)-BSA as well as C(4)-BA to C(6)-BA, which were detected in the microg/l-concentration range. The formation of C(1)- and C(2)-BSA as well as the C(1)- and C(2)-BA can be linked to structurally corresponding parent contaminants like the xylene isomers and the trimethylbenzene isomers. The C(3)-BSA and C(3)-BA represent metabolites of C(4)-benzenes. The occurrence of C(4)-C(5)-BSA and C(4)-C(6)-BA is attributed to C(5)-C(7)-benzenes acting as parent compounds. The concentration of total aromatic contaminants decreased along the plume centre line. In contrast, benzoates and benzylsuccinates (BA and BSA) showed constant concentrations over a distance of 84 m. BA concentrations were up to 162 times higher compared to BSA, as indicated by the ratio f(BA/BSA). A pronounced transient behaviour of BSA or an overall persistent behaviour of BA can explain this. Hence, along the plume centre line, f(BA/BSA) was constant over a distance of 128 m. The degradation products detected in a monitoring well are not necessarily tied to contaminants detected in that well. Therefore, the metabolite plume is partly located in front of the contaminant plume, but does not significantly migrate downstream the plume toe.