基于Landsat-8数据和劈窗算法的地表温度反演及城市热岛效应研究

陆地表面温度(Land Surface Temperature,LST)是地表能量平衡组分中的一个重要参数。随着卫星遥感技术的快速发展,遥感反演成为获取区域LST的一个重要手段。目前已有学者提出多种基于遥感数据反演LST的算法,其中劈窗算法被证明是一种精度较高的算法。基于Landsat-8卫星30 m空间分辨率的陆地成像仪(OLI)数据和100 m分辨率的热红外传感器(TIRS)数据,采用劈窗算法计算了无锡地区的LST,并采用地面实测水温数据和同步的MODIS温度产品对Landsat-8的计算结果进行了验证和对比分析。结果表明:基于Landsat-8数据和劈窗算法获取的LST精度较高,误差1K。在计算的LST结果基础上,进一步提取了热场变异指数来分析城市热岛空间分布特征,给出了城市热岛效应的定量化描述,并就不同地表覆盖类型对热岛效应的影响进行了分析。     

热脱附-GC/MS法测定垃圾填埋场周围空气中氯代烃

采用热脱附-冷阱捕集-GC/MS法测定垃圾填埋场周围空气中24种氯代烃,通过试验优化并确定热脱附质谱的最佳处理条件。方法在5.00 mg/L～100 mg/L范围内线性良好,24种氯代烃的方法检出限为0.060μg/m~3～0.200μg/m~3,测定下限为0.240μg/m~3～0.800μg/m~3。空白加标回收率为91.8%～110%,6次测定结果的RSD均5%。实际样品测定结果为0.112 mg/m~3～0.412 mg/m~3,表明离垃圾填埋场最近的居民区环境中氯代烃为未检出或痕量分布,对生命体危害极低。     

原油在土壤中的吸附和解吸研究

用振荡平衡法研究了原油在土壤中的吸附和解吸行为，测得了吸附常数，给出了吸附等温线。结果表明，Linear吸附关系可较好地描述原油在土壤中的吸附状况；土壤有机质含量影响原油的吸附量；其解吸行为则明显受到溶液pH的影响，表面活性剂的加入有助于原油解吸。     

Role of NO and SO2 in mercury oxidation over a La2O3/Fe2O3 catalyst with high thermal stability

In this study, the thermal stability of a ferric oxide catalyst for mercury oxidation was found to be considerably promoted by doping with La₂O₃. The catalysts doped with La₂O₃ maintained a higher surface area when subjected to high-temperature calcination, with lower average pore size and a narrower pore size distribution. X-ray diffraction (XRD) results revealed that La₂O₃ doping hinders the growth of catalyst particles and crystallization of the material at high temperatures. Both NO and SO₂ inhibited Hg⁰ oxidation over the La₂O₃/Fe₂O₃ catalyst. Fourier transform infrared (FTIR) spectra revealed that SO₂ reacts with O₂ over the catalysts to form several species that are inert for mercury oxidation, such as SO₄^2?, HSO₄^?, or other related species; these inert species cover the catalyst surface and consequently decrease Hg⁰ oxidation capacity. In addition, NO or SO₂ competed with Hg⁰ for active sites on the La₂O₃/Fe₂O₃ catalyst and hindered the adsorption of mercury, thereby inhibiting subsequent Hg⁰ oxidation. Hg⁰ oxidation on the La₂O₃/Fe₂O₃ catalyst mainly followed the Eley–Rideal mechanism. Moreover, the inhibition effects of NO and SO₂ were at least partially reversible, and the catalytic activity was temporarily restored after eliminating NO or SO₂.     

空调器印剧电路板(PCB)无铅焊点寿命评估研究

由于无铅焊料的应用,无铅焊点的可靠性问题得到了关注.本文针对无铅焊点的空调器印刷电路板(PCB),结合实际使用条件,采用加速寿命的方式,测试了焊点的寿命.并针对温度循环条件下的焊点,使用有限元模拟技术计算测定了其寿命,并与实验的结果进行了比较,取得了较吻合的结果.     

二硫化铁(FeS2)纳米颗粒对聚苯乙烯(PS)热稳定性和燃烧性能的影响

采用熔融共混法制备聚苯乙烯(PS)/二硫化铁(FeS2)纳米复合材料研究FeS2对PS热稳定性和燃烧性能的影响。扫描电镜(SEM)结果表明FeS2能够很好地分散在PS基体中。热重分析(TGA)的数据显示,FeS2可以显著地提高残余炭量。锥形量热仪(CONE)结果表明,FeS2可以改变PS的分解,从而在复合材料的表面上形成炭层,导致燃烧和烟气方面的参数有效降低,如热释放速率(HRR)、总热释放(THR)、烟释放率(SPR)、烟释放总量(TSR)、平均质量损失速率(AMLR)和平均烟消光面积(ASEA)等。此外,极限氧指数也得到了提高。拉曼(LRS)的结果证实了残余炭中有石墨碳的存在,热降解过程中石墨碳的形成有利于对热扩散的抑制,从而改善了PS的热稳定和燃烧性能。     

Effects of thermal radiation heat transfer on flame acceleration and transition to detonation in particle-cloud hydrogen flames

The current work examines regimes of the hydrogen–oxygen flame propagation and ignition of mixtures heated by radiation emitted from the flame. The gaseous phase is assumed to be transparent for the radiation, while the suspended particles of the dust cloud ahead of the flame absorb and reemit the radiation. The radiant heat absorbed by the particles is then lost by conduction to the surrounding unreacted gaseous phase so that the gas phase temperature lags that of the particles. The direct numerical simulations solve the full system of two phase gas dynamic time-dependent equations with a detailed chemical kinetics for a plane flames propagating through a dust cloud. It is shown that depending on the spatial distribution of the dispersed particles and on the value of radiation absorption length the consequence of the radiative preheating of the mixture ahead of the flame can be either the increase of the flame velocity for uniformly dispersed particles or ignition either new deflagration or detonation ahead of the original flame via the Zel'dovich gradient mechanism in the case of a layered particle-gas cloud deposits. In the latter case the ignited combustion regime depends on the radiation absorption length and correspondingly on the steepness of the formed temperature gradient in the preignition zone that can be treated independently of the primary flame. The impact of radiation heat transfer in a particle-laden flame is of paramount importance for better risk assessment and represents a route for understanding of dust explosion origin.     

Applications of thermal hazard analyses on process safety assessments

In 2011, a large petrochemical complex in Taiwan incurred several fire and explosion accidents, which had considerable negative impact for the industry on both environmental and safety issues. Reactive substances are widely used in many chemical industrial fields as an initiator, hardeners, or cross-linking agents of radical polymerization process with unsaturated monomer. However, the unpredictable factors during the process having risk to runaway reaction, thermal explosion, fire, and exposure to harmful toxic chemicals release due to the huge heat and gas products by thermal decomposition could not be removed from the process. This study used differential technology of thermal analysis to characterize the inherent hazard behaviors of azo compounds and organic peroxides in the process, to seek the elimination of the source of the harmful effects and achieve the best process safety practices with zero disaster and sound business continuity plan.     

On equilibration of pore water in column leaching tests

Column leaching tests are closer to natural conditions than batch shaking tests and in the last years have become more popular for assessing the release potential of pollutants from a variety of solids such as contaminated soils, waste, recycling and construction materials. Uncertainties still exist regarding equilibration of the percolating water with the solids, that might potentially lead to underestimation of contaminant concentrations in the effluent. The intention of this paper is to show that equilibration of pore water in a finite bath is fundamentally different from release of a certain fraction of the pollutant from a sample and that equilibrium is reached much faster at low liquid-to-solid ratios typical for column experiments (<0.25) than in batch tests with much higher liquid-to-solid ratios (e.g. 2–10). Two mass transfer mechanisms are elucidated: First-order type release (film diffusion) and intraparticle diffusion. For the latter, mass transfer slows down with time and sooner or later non-equilibrium conditions are observed at the column outlet after percolation has been started. Time scales of equilibrium leaching can be estimated based on a comparison of column length with the length of the mass transfer zone, which is equivalent to a Damköhler number approach. Mass transfer and diffusion coefficients used in this study apply to mass transfer mechanisms limited by diffusion in water, which is typical for release of organic compounds but also for dissolution of soluble minerals such as calcite, gypsum or similar. As a conclusion based on these theoretical considerations column tests (a) equilibrate much faster than batch leaching tests and (b) the equilibrium concentrations are maintained in the column effluent even for slow intraparticle diffusion limited desorption for extended periods of time (>days). Since for equilibration the specific surface area is crucial, the harmonic mean of the grain size is relevant (small grain sizes result in high concentrations even after short pre-equilibration of a column). The absolute time scales calculated with linear sorption and aqueous diffusion aim at organic compounds and are not valid for sparingly soluble mineral phases (e.g. metal oxides and silicates). However, the general findings on how different liquid-to-solid ratios and specific surface area influence equilibration time scales also apply to other mass transfer mechanisms.     

Thermal behaviors, combustion mechanisms, evolved gasses, and ash analysis of spent potlining for a hazardous waste management

An unavoidable but reusable waste so as to enhance a more circular waste utilization has been spent potlining (SPL) generated by the aluminum industry. The combustion mechanisms, evolved gasses, and ash properties of SPL were characterized dynamically in response to the elevated temperature and heating rates. Differential scanning calorimetric (DSC) results indicated an exothermic reaction behavior probably able to meet the energy needs of various industrial applications. The reaction mechanisms for the SPL combustion were best described using the 1.5-, 3- and 2.5-order reaction models. Fluoride volatilization rate of the flue gas was estimated at 2.24%. The SPL combustion emitted CO₂, HNCO, NO, and NO₂ but SO_x. The joint optimization of remaining mass, derivative thermogravimetry, and derivative DSC was achieved with the optimal temperature and heating rate combination of 783.5°C, and 5 °C/min, respectively. Interaction between temperature and heating rate exerted the strongest and weakest impact on DSC and remaining mass, respectively. The fluorine mainly as the formation of substantial NaF and CaF₂ in the residual ash. Besides, the composition and effect of environment of residual solid were evaluated. The ash slagging tendency and its mineral deposition mechanisms were elucidated in terms of turning SPL waste into a benign input to a circular waste utilization.