Characterisation of Organic Matter and Carbon Cycling in Rehabilitated Lignite-rich Mine Soils

Open-cast lignite mining in the Lusatian mining district resulted in rehabilitated mine soils containing up to four organic matter types: (1) recent plant litter, (2) lignite deposited by mining activity, (3) carbonaceous ash particles deposited during amelioration of the lignite-containing parent substrate and (4) airborne carbonaceous particles deposited during contamination. The influence of lignite-derived carbon types on the organic matter development and their role in the soil carbon cycle was unknown. This paper presents the findings obtained during a six year project concerning the impact of lignite on soil organic matter composition and the biogeochemical functioning of the ecosystem. The organic matter development after rehabilitation was followed in a chronosequence of rehabilitated mine soils afforested in 1966, 1981 and 1987. A differentiation of the organic matter types and an evaluation of their role within the ecosystem was achieved by the use of ¹⁴C activity measurements, ¹³C CPMAS NMR spectroscopy and wet chemical analysis of plant litter compounds. The results showed that the amount and degree of decomposition of the recent organic matter derived from plant material of the 30 year old mine soil was similar to natural uncontaminated forest soil which suggests complete rehabilitation of the ecosystem. The decomposition and humification processes were not influenced by the presence of lignite. On the other hand it was shown that lignite, which was thought to be recalcitrant because of its chemical structure, was part of the carbon cycle in these soils. This demonstrates the need to elucidate further the stabilisation mechanisms of organic matter in soils.     

Effect of Cross-Linking Waste Protein with Dialdehydes on Its Biodegradation Under Anaerobic Conditions

Most native polymers used in processing and application technologies are admittedly disposable from the environment in a biologic manner, but products possess low mechanical strength. One of the paths to increasing this attribute (if feasible) is their cross-linking, which may, however, affect their readiness to biodegradation. In the presented work this condition was observed on the example of waste protein (Hykol B) cross-linking by means of glutardialdehyde and glyoxal. Degree and course of cross-linking were determined through impedance spectroscopy. The objective of this work also was to obtain data for constructing a sensor capable of following the cross-linking course in real time, for potential industrial application of Hykol in continuous production. Impedance spectroscopy proved to be applicable even to this kind of material marked by considerable water content and exhibiting relatively high electric conductivity; so far it had been used only for materials of low conductivity. An aqueous environment inoculated with digested anaerobic sludge from a municipal wastewater treatment plant was selected for modeling anaerobic conditions. The relation was studied between cross-linking degree given by content of cross-linking agent (determined by impedance spectroscopy) and biodegradation degree under anaerobic conditions. It was confirmed that network density as given by quantity of added agent not only reduced breakdown degree but also slowed the course of the process. This fact is particularly obvious with cross-linking by means of glyoxal; network density is thus dependent on type of employed substance, which affect type and structure of created network. That not merely forms an obstacle during polymer swelling and dissolution but also prevents access of bacteria to source of metabolized organic carbon.     

红外光度法测定石油类和动植物油常见问题探讨

根据石油类在波数为2930cm-1、2960 cm-1、3030 cm-1全部或部分谱带处有物征吸收的原理,采用红外光度测油仪和水样絮凝富集技术测定石油类、动植物油。     

红外和热分析联用在化工产品研究中的应用

运用实例论述了红外光谱分析与热分析联用在化工产品的产品开发和检测方面的应用。     

ACCURACY OF LAKE AND STREAM TEMPERATURES ESTIMATED FROM THERMAL INFRARED IMAGES1

Emitted thermal infrared radiation (TIR, λ= 8 to 14 μm) can be used to measure surface water temperatures (top approximately 100 μm). This study evaluates the accuracy of stream (50 to 500 m wide) and lake (300 to 5,000 m wide) radiant temperatures (15 to 22°C) derived from airborne (MASTER, 5 to 15 m) and satellite (ASTER 90 m, Landsat ETM+ 60 m) TIR images. Applied atmospheric compensations changed water temperatures by ?0.2 to +2.0°C. Atmospheric compensation depended primarily on atmospheric water vapor and temperature, sensor viewing geometry, and water temperature. Agreement between multiple TIR bands (MASTER ‐ 10 bands, ASTER ‐ 5 bands) provided an independent check on recovered temperatures. Compensations improved agreement between image and in situ surface temperatures (from 2.0 to 1.1°C average deviation); however, compensations did not improve agreement between river image temperatures and loggers installed at the stream bed (from 0.6 to 1.6°C average deviation). Analysis of field temperatures suggests that vertical thermal stratification may have caused a systematic difference between instream gage temperatures and corrected image temperatures. As a result, agreement between image temperatures and instream temperatures did not imply that accurate TIR temperatures were recovered. Based on these analyses, practical accuracies for corrected TIR lake and stream surface temperatures are around 1°C.     

具有变频器的矿井低压漏电保护研究

为了解决移动变电站低压侧为变频器供电时漏电保护装置误动的问题，提出了基于傅式算法的附加直流原理漏电保护新方法。通过理论分析和MATLAB/Simulink仿真，研究了具有变频器的矿井低压供电系统附加直流原理漏电保护，提出由傅式算法分解出采样电压直流分量以反映电缆绝缘水平的保护方法；同时分析了其他因素对直流分量的影响。研究结果表明:变频器对传统附加直流保护整定值有较大影响，易造成漏电保护装置误动且无法实现电缆的在线绝缘监测；所提出的直流分量法能准确测量电缆对地绝缘电阻，且可消除电缆分布电容、变频器载波频率、变频器输出频率等其他因素的干扰；采用该漏电保护方法，可承受变频器投入时对采样电压造成的较大冲击，不必在启动期间解除漏电保护装置，能够消除在此期间存在的人身触电安全隐患。     

长期施肥下浙江稻田不同颗粒组分有机碳的稳定特征

依托浙江水网地区稻田长期定位施肥试验(1996~2013年),利用固态13C核磁共振波谱技术,研究长期不同施肥措施下土壤各颗粒组分有机碳含量及其化学结构特征.结果表明,与不施肥对照(CK)相比,秸秆与化肥配施(NPKRS)、栏肥与化肥配施(NPKOM)、单施化肥(NPK)和单施栏肥(OM)处理均显著(P0.05)增加了砂粒(2~0.02 mm)、粉粒(0.02~0.002mm)和黏粒(0.002 mm)组分中有机碳含量;而单施秸秆(RS)处理仅显著增加砂粒组分有机碳含量.此外,与单施化肥处理相比,有机肥和化肥配施促进了新增有机碳在粉粒和黏粒组分的分配,更有利于新增有机碳的稳定.应用13C-NMR波谱技术进行结构表征,结果表明粉粒和黏粒组分有机碳的化学结构存在明显差异,粉粒组分烷氧碳、芳香碳的相对含量高于黏粒,而烷基碳、羰基碳的相对含量低于黏粒.长期有机肥与化肥配施下粉粒和黏粒烷基碳相对含量较单施有机肥处理分别降低9.1%~11.9%和13.7%~19.9%,烷氧碳的相对含量则分别增加2.9%~6.3%和13.4%~22.1%,表明有机肥与化肥配施处理降低了粉粒和黏粒组分有机碳的分解程度.长期单施化肥处理下粉粒和黏粒组分有机质的芳化度和疏水性低于单施有机肥处理和不施肥处理,有机质的矿化稳定性较低.长期有机肥与化肥配施,尤其是NPKOM处理,通过增加化学抗性化合物和碳水化合物的积累,并且减缓活性组分的分解提高粉粒和黏粒组分有机碳含量,是促进稻田土壤有机碳可持续积累的有效措施.     

Effect of oxide nanoparticles on the morphology and fluidity of phospholipid membranes and the role of hydrogen bonds

Engineered oxide nanoparticles (NPs) are widely applied in insulators, catalyzers, paints, cosmetic products, textiles and semiconductors. Their attachment on cell membrane may lead to cytotoxicity. The effects of Al₂O₃, Fe₂O₃, SiO₂, TiO₂ and ZnO NPs on membrane integrity and fluidity were studied using giant or small unilamellar vesicles in this study. Al₂O₃ and SiO₂ NPs disrupted the oppositely charged membrane, indicating the important role of electrostatic attraction. However, Fe₂O₃, TiO₂ and ZnO NPs did not cause serious membrane disruption as Al₂O₃ and SiO₂ NPs. Membrane fluidity was evaluated by the generalized polarity (GP) values of Laurdan fluorescent emission. SiO₂ NPs induce the membrane gelation of both positively and negatively charged membrane. Al₂O₃ and ZnO NPs induced the gelation of the oppositely charged membrane, but did not cause obvious membrane gelation to the like charged membrane. The phospholipid molecular structural changes after NP exposure were analyzed by Fourier transform infrared (FT-IR) spectroscopy. FT-IR spectra revealed the hydrogen bond formation between NPs and the carbonyl/phosphate groups of phospholipids. Al₂O₃ and SiO₂ NPs showed strongest evidence of hydrogen bonding on their FT-IR spectra. It was consistent with the microscopic observation and fluorescent data that Al₂O₃ and SiO₂ NPs caused more serious membrane disruption and gelation. This study on membrane damage provides further knowledge on the cytotoxicity of nanomaterials and the safety of NP application.     

覆盖金属氧化物对湖泊沉积物溶解性有机质特征的影响

为揭示不同金属氧化物对湖泊沉积物DOM（溶解性有机质）影响机制,通过室内模拟试验,在沉积物表层分别覆盖Fe、Al、Mn氧化物及湖沙后培养1 a,并利用三维荧光和紫外光谱方法进行表征.结果表明:① 覆盖Al、Fe、Mn氧化物和湖沙主要降低了0~3 cm沉积物的w（DOC）,降幅分别为8.61%、6.27%、22.38%和0.44%. ② 沉积物中DOM的类络氨酸峰（peak B₁）和类色氨酸峰（peak T₂）均产生较大变化.其中三种氧化物均显著降低了上层沉积物中DOM的peak T₂,使底层DOM的peakT₂显著增加. Mn氧化物使DOM的peak B₁降低,Fe和Al氧化物使DOM的peak B₁增加,湖沙则使两类峰均降低. ③ 覆盖金属氧化物改变了沉积物DOM结构特征,其中覆盖Fe氧化物增强了其芳香性,而覆盖Mn氧化物和Al氧化却降低其芳香性,但三者均使DOM腐质化程度及官能团数量增加,并使FI（Fluorescence Index,荧光指数）增大,表明DOM向生物源转化.研究显示,沉积物表层覆盖金属氧化物影响了沉积物中DOM迁移和转化,并促进了其降解,导致其分子量和腐殖化程度增加.      

基于各向异性粒子介电常数张量重构的散射特性研究

目的简化各向异性介质中的光电传播、目标散射识别等问题。方法基于电场强度矢量和电位移矢量的关系,提出将各向异性介质的介电常数张量重构为对角张量通用方法。结果给出了对角张量元素的表达式和对应单位特征矢量,并作了详细的数值计算。得到了单位特征矢量坐标系中电磁场与原坐标系中电磁场的变换关系以及磁导率张量的变换关系;所用方法具有通用性,所得结果具有实用性。结论在各向异性介质研究领域,可实现特征坐标系中的电磁场及介质参数与主坐标系的电磁场与介质参数的相互定量转换。