油箱明火烤燃下燃爆危险性分析与安全对策

为预防交通事故中油箱燃爆危险的发生,利用摄像机、高速照相机和红外热成像仪观测油箱在烤燃过程中的燃爆特性,得到爆炸火球参数和油箱内部温度变化,并针对油箱烤燃的危险性,利用爆炸火球辐射总能量和热剂量来评判热效应严重程度。结果表明:明火烤燃状态17min左右,油箱发生爆炸;爆炸火球的体积、表面最高温度和辐射总能量分别为150.46m~3、1 490.4℃和2.10×10~4kJ,距爆炸火球中心1m、5m和10m处的热剂量分别为1 978.8kJ/m~2、99.4kJ/m~2和25.1kJ/m~2。最后,从油箱本质安全设计和点火源控制方面提出了相应的安全对策与措施。     

南昌市固定燃烧点源大气污染物排放清单及特征

大气污染物排放清单是了解区域污染物排放特征、准确模拟空气质量的重要资料,而工业点源是大气污染的重点排放源.通过收集相关活动水平信息和合理的排放因子,采用"自下而上"的方法建立了南昌市2014年点源大气污染物排放清单.结果表明,SO_2、NO_x、CO、PM_(10)、PM_(2.5)和VOC排放总量分别为29576.2、17115.1、25946.6、4689.4、922.9和1190.4 t,其中,金属炼制行业对SO_2、CO和VOC的贡献最高,分别占37.75%、30.59%和38.45%;火电行业是NO_x的主要来源,其贡献率为47%;水泥等建材制造行业对PM_(10)和PM_(2.5)排放贡献最高,分别为26%和25%.根据排放源污染物排放量及地理坐标信息,建立了0.4 km×0.4 km的污染物排放量空间分布特征图,结果表明,南昌市大气污染物排放较为集中,青山湖区北部和新建区北部是SO_2、NO_x、CO和VOC的主要排放区,而PM_(10)和PM_(2.5)的排放量相对分散,并在安义县出现排放高值区.通过将计算结果与统计数据结果进行对比,了解所估算清单的准确程度.对SO_2和NO_x的计算值和统计值进行统计分析,结果显示,NMB(标准化平均偏差)和NME(标准化平均误差)值均小于50%,清单计算精度较高.同时,为了解清单数据质量,对清单的不确定性进行定量分析,结果显示,SO_2和VOC不确定性较低而PM_(10)和PM_(2.5)的不确定性相对较高,清单整体不确定性与其他研究结果相差不大.建议后期研究可以从提升基础数据质量和建立具有区域代表性的排放因子数据库着手,从而减小排放量的不确定性,获得精准可靠的大气污染物清单并应用于空气质量模型预报等更深入的研究.     

企业低碳制造战略分类研究:以水泥企业为例

随着气候变化加剧,低碳发展已成为政府和学者关注的重要议题。降低工业碳排放成为实现我国经济可持续发展的当务之急。低碳制造战略是工业企业实现战略转型、应对碳排放约束和提升市场竞争力的可行策略之一,但企业低碳制造战略的研究正处于起步阶段,还缺乏低碳制造战略类型的认识。为此,本文在拓展企业制造战略竞争优先权结构要素的基础上,增加能源利用率和单位产品二氧化碳排放量为竞争优先权结构要素,构建低碳制造战略竞争优先权分类指标,由此探索企业低碳制造战略类型。本文以国内22个省(自治区、直辖市)所辖的137家水泥企业为研究对象,运用聚类分析方法,识别企业低碳制造战略的类型,结果表明:企业低碳制造战略可划分为三种类型,分别是设计者、看守者和低碳践行者。研究结果不仅有助于深入了解水泥企业低碳制造战略特点,为我国水泥企业低碳制造战略制定和实施提供决策依据,而且其理论成果也可推广至其他高耗能产业,创新引导企业有效实施基于产品全生命周期的企业低碳制造战略。     

从6-APA和7-ADCA生产废液中回收苯乙酸

采用溶剂萃取、水法提取等方法从6-氨基青霉烷酸和7-氨基-3-去乙酰氧基头孢烷酸生产废液（简称废液）中回收苯乙酸（PAA）,考察了各种因素对回收效果的影响。实验结果表明：以甲苯为萃取剂,在萃取温度30℃、萃取时间15m in、500mL废液中萃取剂加入量130mL的最佳条件下,萃取率为96.5%;在提取温度为65℃左右、结晶温度低于10℃的条件下,PAA收率大于89%,纯度大于99%;所得PAA产品质量好,可用于青霉素G等医药产品的生产。     

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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Degradation of rizazole in water–sediment systems

This study investigated the degradation of rizazole in water-sediment systems (West Lake system, WL; Beijing–Hangzhou Grand Canal system, BG) with two different types of sediments under aerobic and anaerobic conditions. The half-lives of rizazole in the WL water phase (14.59–15.13 d) were similar to those in the BG water phase (15.90–16.46 d). Within 3–7 d, the rizazole concentration in the sediments reached the maximum values, i.e., equilibrium. Rizazole dissipation was faster in the WL sediment phase with higher organic matter content (T_1/2 = 18.99–19.09 d) compared with the BG sediment phase (T_1/2 = 31.08–33.32 d). Rizazole degradation was slightly faster in the West Lake water-sediment system (WL system) (T_1/2 = 17.11–18.05 d) than in the Beijing–Hangzhou Grand Canal water—sediment system (BG system) (T_1/2 = 20.51–25.02 d). The aerobic degradation of rizazole was similar to its anaerobic degradation in the water-sediment system. The findings are useful to understand the behavior of pesticide in environment.     

黑藻对铅离子的生物吸附

研究了黑藻对Pb^2＋的生物吸附作用,考察了溶液pH、Pb^2＋初始质量浓度、黑藻加入量和吸附时间对吸附效果的影响。实验结果表明,溶液pH在2．5～5．0时吸附效果最好,吸附20min基本达到平衡。在溶液pH为4．0、黑藻加入量为2g／L、吸附时间为60min、Pb^2＋初始质量浓度为100mg／L的条件下,黑藻对Pb^2＋的吸附量为47．5mg／g。通过元素分析和等温吸附模型对黑藻吸附Pb^2＋的机理进行了研究,发现黑藻吸附Pb“是阳离子交换过程,吸附符合Langmuir、Freundlich和D—R等温吸附模型。考察了Cd^2＋、Cu^2＋和Ni^2＋对黑藻吸附Pb^2＋的影响,结果表明,Cd^2＋、Cu^2＋和Ni^2＋的存在不干扰黑藻对Pb^2＋的吸附。     

Effect of heavy metals (Cu, Pb, and As) on the ultrastructure of Sargassum pallidum in Daya Bay, China

Concentrations of Cu, Pb, and As were determined in seawater, surface sediment, Sargassum pallidum collected from the Daya Bay, China. The influence of metal contamination on the marine alga was investigated at chemical and ultrastructural level. Mean concentrations of Cu (19.44 mg kg^?1) and Pb (33.99 mg kg^?1) were found to be high in sediment, whereas concentration of As (122.29 mg kg^?1) in S. pallidum was higher than that in water and sediment. The ultrastructure of S. pallidum cells was anomalous and aberrant. Energy-dispersive x-ray spectroscopic analysis revealed that the nanometal particles in the form of comparatively high-electron density substance diffused in the cell structures constituted by Cu, Pb, As, etc. There is a remarkable similarity or correspondence in the anomalous elements between the geochemistry and the botanic cell, and the heavy metals have potential hazardous effect on the ocean ecology system in Daya Bay.     

Low-reactive circulating fluidized bed combustion (CFBC) fly ashes as source material for geopolymer synthesis

In this contribution, low-reactive circulating fluidized bed combustion (CFBC) fly ashes (CFAs) have firstly been utilized as a source material for geopolymer synthesis. An alkali fusion process was employed to promote the dissolution of Si and Al species from the CFAs, and thus to enhance the reactivity of the ashes. A high-reactive metakaolin (MK) was also used to consume the excess alkali needed for the fusion. Reactivities of the CFAs and MK were examined by a series of dissolution tests in sodium hydroxide solutions. Geopolymer samples were prepared by alkali activation of the source materials using a sodium silicate solution as the activator. The synthesized products were characterized by mechanical testing, scanning electron microscopy (SEM), X-ray diffractography (XRD), as well as Fourier transform infrared spectroscopy (FTIR). The results of this study indicate that, via enhancing the reactivity by alkali fusion and balancing the Na/Al ratio by additional aluminosilicate source, low-reactive CFAs could also be recycled as an alternative source material for geopolymer production.