特种服装特殊性的研究

本文通过对特种服装的广泛调查,总结、归纳出它们与一般服装的不同之处,也即它们的特殊性.本文对这些特殊性进行了详细地分析研究,并深入地研究出这些特殊性之间的内部联系,对特种服装的生产、管理、开发乃至应用有指导性的作用.     

单兵装备系统人机工效仿真评价技术初步研究

本文结合士兵系统的发展概况,阐述了单兵装备人机工程仿真评价技术研究的重要性,并总结了目前的研究进展情况,进而重点介绍单兵装备人机工效仿真评价系统的最新研究成果,首次在三维仿真环境和基础数据库的支持下对单兵装备系统的可视性、可达性、舒适性等指标进行综合研究和评价。     

环境温度对喷头响应时间特性影响的研究

洒水喷头的热响应特性直接影响整个自动喷水灭火系统的效率,而喷头的响应时间不仅与喷头安装高度、响应时间指数、喷头距火源径向距离等参数有关,还受环境温度的影响.本文以环境温度对普通高度建筑中喷头响应时间的影响为研究对象,使用软件DETACT 12计算得到不同场景下喷头的启动时间,并使用统计分析软件SPSS 13.0进行分析,得出环境温度与喷头启动时间之间的关系式,并研究了综合考虑喷头响应时间指数、安装高度和环境温度影响的情况下,喷头启动时间的变化规律,研究结果表明,喷头启动时间随环境温度的升高而减小,环境温度越低,喷头的启动时间越长.在其他条件相同的情况下,喷头响应时间指数越大、安装高度越高,其启动时间受环境的影响越明显.     

火电汽轮机组热电解耦技术研究

针对供热机组受传统“以热定电”运行模式限制,单机调峰能力低(最大仅有50%),无法满足深度调峰的问题,以国电集团西北地区所辖火电供热机组的实际运行情况为出发点,结合汽轮机组节能诊断及机组改造经验,提出了高、低压旁路联合供热,低压缸切缸运行两种热电解耦技术方案,通过比选得出两种技术方案的优缺点及适用范围。     

Competition for electrons between reductive dechlorination and denitrification

It is common that 2,4,6-trichlorophenol (TCP) coexists with nitrate or nitrite in industrial wastewaters. In this work, simultaneous reductive dechlorination of TCP and denitrification of nitrate or nitrite competed for electron donor, which led to their mutual inhibition. All inhibitions could be relieved to a certain degree by augmenting an organic electron donor, but the impact of the added electron donor was strongest for TCP. For simultaneous reduction of TCP together with nitrate, TCP’s removal rate value increased 75% and 150%, respectively, when added glucose was increased from 0.4 mmol?L^–1 to 0.5 mmol?L^–1 and to 0.76 mmol?L^–1. For comparison, the removal rate for nitrate increased by only 25% and 114% for the same added glucose. The relationship between their initial biodegradation rates versus their initial concentrations could be represented well with the Monod model, which quantified their half-maximum-rate concentration (K _S value), and K _S values for TCP, nitrate, and nitrite were larger with simultaneous reduction than independent reduction. The increases in K _S are further evidence that competition for the electron donor led to mutual inhibition. For bioremediation of wastewater containing TCP and oxidized nitrogen, both reduction reactions should proceed more rapidly if the oxidized nitrogen is nitrite instead of nitrate and if readily biodegradable electron acceptor is augmented.

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Urinary metabolomic profiling in rats exposed to dietary di(2-ethylhexyl) phthalate (DEHP) using ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS)

Di(2-ethylhexyl) phthalate (DEHP) is an omnipresent environmental chemical with widespread nonoccupational human exposure through multiple ways. Although considerable efforts have been invested to investigate mechanisms of DEHP toxicity, the key metabolic biomarkers of DEHP toxicity remain to be identified. The aim of this study was to assess the urinary metabonomics of dietary DEHP in rats using the technique of ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS). Fourteen female Wistar rats were divided into two groups and given increasing dietary doses of DEHP for 30 consecutive days. The urinary metabolite profile was studied using ultra-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry. Principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) enabled clusters to be clearly separated. Eleven principal urinary metabolites were identified as contributing to the clusters. The clusters in the positive electrospray ionization (ESI) mode were xanthurenic acid, kynurenic acid, nonate, N6-methyladenosine, and L-isoleucyl-L-proline. The clusters in the negative ESI mode were hippuric acid, tetrahydrocortisol, citric acid, phenylpropionylglycine, cPA(18:2(9Z, 12Z)/0:0), and LysoPC(14:1(9Z)). The urinary metabonomic changes indicated that exposure to dietary DEHP can affect energy-related metabolism, liver and renal function, fatty acid metabolism, and cause DNA damage in rats. The findings of this study on the urinary metabolites and metabolic pathways of DEHP may form the basis for future studies on the mechanisms of toxicity of this commonly found environmental chemical.     

太阳翼驱动机构的扰振力矩测试与分析

为了研究太阳翼驱动机构(solar array drive assembly,SADA)驱动太阳翼运行期间所产生的扰振力矩特性,设计了一套地面测试系统,包括应变式微振动测试平台、柔性负载以及模拟SADA在轨无重力工作环境的重力卸载装置。阐述了所设计测试系统的工作原理,并利用该测试系统进行了试验测试。测试结果表明:SADA驱动柔性负载运行期间所产生扰振力矩的扰振频率成分主要包含两部分,即:1)SADA驱动柔性负载耦合系统的低阶扭转固有频率;2)SADA电脉冲信号的输入频率及其高阶谐波。     

Fate of caffeine in mesocosms wetland planted with Scirpus validus

Uptake, accumulation and translocation of caffeine by Scirpus validus grown in hydroponic condition were investigated. The plants were cultivated in Hoagland’s nutrient solution spiked with caffeine at concentrations of 0.5–2.0 mg L^?1. The effect of photodegradation on caffeine elimination was determined in dark controls and proved to be negligible. Removal of caffeine in mesocosms without plants showed however that biodegradation could account for about 15–19% of the caffeine lost from solutions after 3 and 7 d. Plant uptake played a significant role in caffeine elimination. Caffeine was detected in both roots and shoots of S. validus. Root concentrations of caffeine were 0.1–6.1 μg g^?1, while the concentrations for shoots were 6.4–13.7 μg g^?1. A significant (p < 0.05) positive correlation between the concentration in the root and the initial concentrations in the nutrient solution was observed. The bioaccumulation factors (BAFs) of caffeine for roots ranged from 0.2 to 3.1, while BAFs for shoots ranged from 3.2 to 16.9. Translocation from roots to shoots was the major pathway of shoot accumulation. The fraction of caffeine in the roots as a percentage of the total caffeine mass in solution was limited to 0.2–4.4% throughout the whole experiment, while shoot uptake percentage ranged from 12% to 25% for caffeine at the initial concentration of 2.0 mg L^?1 to 50–62% for caffeine at the initial concentration of 0.5 mg L^?1. However, a marked decrease in the concentration of caffeine in the shoots between d-14 and d-21 suggests that caffeine may have been catabolized in the plant tissues subsequent to plant uptake and translocation.     

Modeling cold soak evaporative vapor emissions from gasoline-powered automobiles using a newly developed method

ABSTRACT

Volatile organic compounds (VOCs) evaporate and vent from a vehicle’s fuel tank to its evaporative control system when the vehicle is both driven and parked. VOCs making it past the control system are emissions. Driving and parking activity, fuel volatility, and temperature strongly affect vapor generation and the effectiveness of control technologies, and the wide variability in these factors and the sensitivity of emissions to these factors make it difficult to estimate evaporative emissions at the macro level. Established modeling methods, such as COPERT and MOVES, estimate evaporative emissions by assuming a constant in-use canister condition and consequently contain critical uncertainty when real conditions deviate from that standard condition. In this study, we have developed a new method to model canister capacity as a representative variable, and estimated emissions for all parking events based on semi-empirical functions derived from real-world activity data and laboratory measurements. As compared to chamber measurements collected during this study, the bias of the MOVES diurnal tank venting simulation ranges from ?100% to 129%, while the bias for our method’s simulation is 1.4% to 8.5%. Our modeling method is compared to the COPERT and MOVES models by estimating evaporative emissions from a Euro-3/4/5 and a Tier 2 vehicle in conditions representative for Chicago, IL, and Guangzhou, China. Estimates using the COPERT and MOVES methods differ from our method by ?56% to 120% and ?100% to 25%, respectively. The study highlights the importance for continued modeling improvement of the anthropogenic evaporative emission inventory and for tightened regulatory standards.

Implications: The COPERT and MOVES methodologies contain large uncertainties for estimating evaporative emissions, while our modeling method is developed based on chamber measurements to estimate evaporative emissions and can properly address those uncertainties. Modeling results suggested an urgent need to complete evaporative emissions inventories and also indicated that tightening evaporative emission standards is urgently needed, especially for warm areas.     

常温低基质厌氧氨氧化反应器启动及其稳定性

以上向流生物滤池为反应器,以实验室内氧化沟回流污泥为接种污泥,采用先培育好氧生物膜,后转为厌氧环境培育厌氧氨氧化生物膜的方式,成功实现了常温低基质浓度下厌氧氨氧化反应器的启动。控制反应器进水pH为7.50～7.80,NH4+-N为30～40 mg/L,NO2--N为35～50 mg/L,温度为20～25℃。224 d以后,反应器启动成功。在稳定运行阶段,出水亚硝氮和氨氮的平均浓度分别为1.4 mg/L和4.6 mg/L,平均去除率分别为95.3%和90.1%,去除比例为1～1.8∶1,主要集中在1.4～1.5∶1,亚硝氮和氨氮去除的容积负荷分别为104.2 mg/(L.d)和146.0 mg/(L.d)。