阻断漏风供氧的脱氧剂在密闭中的应用研究

工作面回采过程中产生的超前支撑压力,会对上区段回采过程中在联络巷构筑的密闭造成破坏,使之产生裂隙出现漏风,向采空区供氧。为解决目前密闭出现裂隙后只能采取措施减少漏风而不能将漏风中氧气消耗、除去的弊端,利用具有耗氧功能的脱氧剂,设计了主动脱氧型密闭,并通过数值模拟将普通密闭与该密闭漏风时氧浓度分布进行对比。研究表明:相同漏风情况下,普通密闭中添加脱氧剂成为主动脱氧型密闭后,使漏出密闭风流的氧浓度大幅降低,有效减少了进入采空区的氧气量;另外,经过脱氧的密闭漏风,剩余高浓度的N2,对采空区起到了惰化效果,降低了采空区附近的氧浓度。     

基于FLACS的CH4/CO2/air混合气爆炸参数分析

利用FLACS软件分析初始压力、初始温度对CH4/CO2/air混合气的爆炸温度、最大爆炸压力的影响;并与计算值对比。结果表明:①初始压力对爆炸温度、爆炸前后压力比影响可以忽略。常温变压条件下二氧化碳浓度增加,爆炸温度与爆炸前后压力比基本呈线性降低。常压变温条件较复杂,二氧化碳浓度升高爆炸温度降低;初始温度对低浓度（<15%）二氧化碳混合气爆炸温度几乎没有影响,而高浓度（>15%）二氧化碳混合气爆炸温度随初始温度增加而升高;最大爆炸压力随二氧化碳浓度以及温度升高而降低。②在设定条件下,低浓度（5%~10%）二氧化碳混合气爆炸温度计算值与模拟值相对误差小于5.5%,吻合较好;最大爆炸压力计算值与模拟值相对误差在6.5%～10.5%之间。     

烟气注入采空区封存的可行性与安全性分析

采用自制的煤大样量吸附实验装置测定了常温常压条件下煤对每种烟道气体成分 的饱和吸附量,并根据电厂烟气流量与工作面配风量的计算对井下注入烟气的安全性进 行了分析。实验数据结果显示,煤是一种多孔性物质,将电厂烟气注入井下采空区,每 吨煤可封存烟气中CO2约1.2 m3, N2约0.26 m3,其中烟气中SO2和NO2可全部被煤样封 存,揭示了利用烟气替代传统N2及CO2预防煤炭自燃的可行性;根据对电厂烟气流量及 回采工作面配风量的计算发现,在假定注入采空区的烟气与煤、岩没有任何吸附的情况 下,按照规定流量注入烟气未造成工作面回风巷中CO2、SO2气体浓度超标,NO2则超出 规定允许最高浓度,因此应对注入井下的烟气进行进一步脱硝处理。     

The determination of partition coefficients of organic compounds in technical products and waste waters for the estimation of their bioaccumulation potential using reversed phase thin layer chromatography

Reversed phase thin layer chromatography (RPTLC) has been investigated for the estimation of octanol/water partition coefficients (P), an important parameter for the prediction of the environmental behaviour of organic chemicals. A strong correlation between P derived from the traditional octanol/water system and RPTLC has been established over five orders of magnitude. RPTLC data are likewise correlated to results obtained by high performance chromatography (HPLC). Due to the low costs, simplicity and separation power RPTLC is especially suited for the investigation and screening of mixtures of compounds before more complicated tests are involved.

Results from a round robin test on the determination of partition coefficients by HPLC, RPTLC and the batch method indicate the simplicity and accuracy of the RPTLC technique. Applications of the RPTLC‐technique on technical products and industrial waste waters are described.     

进水氨氮浓度对静置/好氧/缺氧SBR脱氮除磷性能的影响

在4个序批式反应器(SBR)R1、R2、R3和R4中,以静置段代替传统厌氧段,采用后置缺氧,考察进水氨氮浓度分别为20,30,40,50mg/L对静置/好氧/缺氧SBR脱氮除磷性能的影响.结果表明,R1、R2、R3和R4长期运行中磷去除率分别为82.3%、92.8%、92.6%和89.1%,总氮(TN)去除率分别为97.2%、88.6%、84.5%和72.6%.静置段省却搅拌,但仍起厌氧段作用,仍可实现生物强化除磷.4个反应器好氧段均发生同步硝化-反硝化(SND),分别贡献14.7%、16.6%、17.8%和14.8%的进水后TN量,且后置缺氧段利用糖原驱动反硝化,脱氮效果较好,出水TN分别为0.57,4.43,6.61,13.70mg/L.研究表明,进水氨氮浓度可影响静置释磷、好氧摄磷、反硝化除磷.静置段代替厌氧段的后置缺氧工艺可取得较好脱氮除磷效果,且节约成本,简化工艺.     

障碍物对气体爆炸压力场影响数值模拟

气体爆炸是工业生产和生活领域中爆炸灾害的主要形式之一,研究障碍物对管道内可燃气体爆炸的影响规律具有十分重要的现实意义。运用计算流体动力学软件AutoReaGas,定量地研究了障碍物阻塞率、个数等因素对管道中预混乙炔/空气混和物爆炸压力场的影响规律。计算结果表明,障碍物的个数和阻塞比对管道内乙炔气体爆炸峰值超压均有显著影响。本文的研究结果对于预防和控制气体爆炸灾害有一定的借鉴作用。     

城市供水管网健康监测与诊断:IV.监测点压力在线预测

供水管网运行状态的准确把握,对供水管网的健康监测与诊断至关重要,而监测点压力是管网运行状态最重要的标志之一。提出用于供水管网监测点压力在线预测的EMD(经验模态分解)与自回归模型相结合的方法,并对EMD组合模态所蕴含的物理意义进行了阐述。通过一实际供水管网中某监测点压力的在线预测与实际监测值的比较,验证了方法的有效性,此方法可提高城市供水管网健康的在线监测与诊断的效率。     

Social vulnerability and pneumonic plague: revisiting the 1994 outbreak in Surat,India

The 1994 outbreak of pneumonic plague in Surat, India is revisited and analyzed using the pressure and release (PAR) model. Overviews of the outbreak, of India's experience with plague, and of the disease are provided and the PAR model is used to trace the production of vulnerability via root causes, dynamic pressures, and unsafe conditions and to explain the why, when, and where of the epidemic. The emergence of plague in Surat was an unfortunate amalgam of prior hazard events and of factors generating vulnerability. Root causes include the country's colonial legacy and a complex and pervasive social hierarchy promoting caste and class interests over the common good. Dynamic pressures include: a curative-focused healthcare system; a weak civil society; misplaced spending priorities; and public and private corruption that deprived public health programs of needed funds and which compelled workers to live and labor in unhealthy environments. Unhealthy public, residential and workplace environments; fragile economic conditions; and a lack of surveillance and preparation are immediately linked to the outbreak and to the transmission of pneumonic plague.     

Ligand-less in situ surfactant-based solid phase extraction for preconcentration of silver from natural water samples prior to its determination by atomic absorption spectroscopy

A simple and rapid ligand-less in situ surfactant-based solid phase extraction method for preconcentration of silver from water samples is developed. In this method, a cationic surfactant containing a proper alkyl group (n-dodecyltrimethylammonium bromide) is dissolved in the aqueous sample and then a proper ion-pairing agent (ClO₄^?) is added. Due to the interaction between surfactant and ion-pairing agent, solid particles are formed and used for adsorption of silver carbonate. After centrifugation, the sediment is dissolved in 2.0 mL 1 M HNO₃ in ethanol and then aspirated directly into the flame atomic absorption spectrometer. Variables affecting the extraction efficiencies such as pH, concentrations of surfactant and CO₃^2?, ion pair concentration, and extraction time, are optimized. Under such conditions, the calibration curve is linear from 3 to 700 μg L^?1. Detection limit is 1.1 μg L^?1 with an enrichment factor of 37. The relative standard deviation for eight replicate measurements of 100 μg L^?1 is 2.1%. The method has been applied for the determination of silver in water samples.     

Preconcentration of samarium with modified yeast cells for its determination by atomic emission spectroscopy

A chelating-modified biosorbent is produced by coupling of a dye, procion red, to yeast cells. The resulting modified cells have been characterized by Fourier transform infrared, elemental analysis and thermogravimetric analysis and studied for preconcentration and determination of trace Sm(III). The optimum pH value for sorption of the samarium ions is 6.2. The sorption capacity of functionalized modified yeast cells is 7.2 mg g^?1. Recovery was 99% when Sm(III) was eluted with an aqueous solution of 0.1 mol L^?1 ethylenediaminetetraacetic acid. Scatchard analysis suggested that binding sites were homogeneous. The equilibrium data were analyzed using Langmuir, Freundlich, Temkin, and Redlich–Peterson isotherm models, and the respective constants were determined as 1.0 (L mg^?1), 2.9 [(mg g^?1) (L mg^?1)^1/n], 2.4 × 10⁸ (L g^?1), and 30 (dm³ g^?1) at 20 °C. The method was applied for an Sm(III)-containing sample of ceramic industry effluent.