变坡度条件下正丁醇定常流淌火非稳态燃烧行为研究*

为探究流淌火在变坡度地面的蔓延特性,丰富火灾研究理论,推进流淌火预防和风险评估的发展,采用1套自制矩形小尺度油槽系统,研究正丁醇变坡度、变泄漏速率情况下溢油定常流淌火的蔓延特性。结果表明:当泄漏速率相同时,坡度越大,正丁醇的加速过程越明显,当坡度从1°上升到4°,正丁醇扩散速率增大了40.8%;不同坡度下,正丁醇的平均火焰高度随泄漏速率的变化均呈现“上升-下降-稳定”趋势;流淌火蔓延过程中脉动方式分为2种:“跳跃-爬行”和“跳跃-爬行-回缩”;当泄漏速率较小时,流淌火蔓延过程中的脉动频率随油槽坡度的增大而增大,当泄漏速率较大时,脉动频率不再随油槽坡度的改变而发生明显趋势变化。     

多元可燃性气体爆炸压力与中间产物发射光谱特性的耦合研究

工业生产中爆炸事故往往是由多元可燃气体与空气混合后遇到明火而引起的,为研究乙烷（C₂H₆）、乙烯（C₂H₄）、一氧化碳（CO）、氢气（H₂）对甲烷爆炸特性的影响,选取多组分可燃气体甲烷爆炸压力特性和自由基发射光谱的影响进行研究,利用陕西省工业过程安全与应急救援工程技术研究中心重点实验室搭建的多功能球形气体/粉尘爆炸实验装置和单色仪进行爆炸实验测试,同步采集时间—压力曲线、中间产物（OH,CH₂O）的发射光谱信号,考察多组分可燃气体浓度对甲烷爆炸压力特性和中间产物的影响。结果表明:在富氧状态下,多组分可燃气体加剧了甲烷—空气混合体系的爆炸剧烈程度,随着体系中氧气含量的减少、由富氧状态变为贫氧状态、促进作用逐渐减弱转变为阻尼作用,爆炸压力特性与中间产物发射光谱参数的影响规律基本保持一致,均呈高度正相关;多元混合体系爆炸剧烈程度越大,自由基发射光谱达到峰值的速度越快,自由基更早、更快的积累是加剧爆炸程度的原因之一。     

Organochlorines, brominated flame retardants and mercury levels in six seabird species from the Gulf of St. Lawrence (Canada): Relationships with feeding ecology, migration and molt

Concentrations of organochlorines (OCs), brominated flame retardants (BFRs) and mercury (Hg) were measured in eggs of six seabird species breeding in the Gulf of St. Lawrence, Canada. Stable nitrogen (δ¹⁵N) and carbon (δ¹³C) isotopes were used as ecological tracers to measure trophic level and connectivity with benthos, respectively. Concentrations, patterns as well as ecological tracers varied significantly between species. The sum of polychlorinated biphenyls (ΣPCBs) was the most important group measured in all seabird species based on concentration followed generally by the sum of chlorinated pesticides (ΣCPs), the sum of brominated flame retardants (ΣBFRs) and finally total Hg (THg). ΣPCBs, ΣCPs and ΣBFRs increased with trophic level, whereas THg did not. Only ΣBFRs increased with a higher connectivity with the benthos. Seabird species resident to the Great Lakes-St. Lawrence ecosystem showed higher Hg and BFR levels than migratory species. Molt patterns were used to explain variations of contaminant levels.     

侧开缝对竖通道内旋转热流场影响的实验研究

为了掌握竖通道两侧开缝对于通道内热流场的影响,在一32cm(长)×32cm(宽)×200cm(高)的竖通道内进行了旋转热流场实验研究,对比了在不同热源条件下,竖通道侧开缝宽度为3.0cm和3.5cm时,侧开缝底部5cm高区域被遮挡前后通道内热流场的变化。实验结果表明,与遮挡前相比,遮挡通道侧开缝底部对火焰燃烧和热流场的运动状态都会产生影响。遮挡通道侧开缝底部区域,会在一定程度上限制外界冷空气进入通道内,从而减弱通道内的火焰旋转程度,致使燃料燃尽的耗时更长,平均火焰高度降低,其影响程度随着燃料池增大而减弱;遮挡侧开缝底部区域后,造成通道内下部区域中心轴线处的温度降低,最大影响区域在50cm高度附近,而在150cm高度以上基本没有影响;平均火焰高度与燃料池直径之比的无量纲量H/Φ与Peclet数之间的比例系数近似为1.732,并且是否遮挡侧开缝底部区域对于两者之间比例关系的影响不大。     

2,5,6,9,10-Pentabromocyclododecanols (PBCDOHs): a new class of HBCD transformation products

Pentabromocyclododecanols (PBCDOHs) are potential environmental transformation products of hexabromocyclododecanes (HBCDs). They are also potential stage one metabolites of biological HBCD transformations. Herein, we present analytical evidence that PBCDOHs are also constituents of technical HBCDs and flame-proofed polystyrenes (FP-PSs). PBCDOHs are possibly formed during the synthesis of technical HBCD, presumably during the bromination of cyclododecatrienes in aqueous isobutanol together with isobutoxypentabromocyclododecanes (iBPBCDs), which have been identified in these materials recently. Of the 64 stereoisomers possible, eight pairs of enantiomers, named α-, β-, γ-, δ-, ε-, ζ-, η-, and θ-PBCDOHs were separated with a combination of normal-, reversed- and chiral-phase LC. Crystal structure analysis revealed the stereochemistry of the α-PBCDOH pair of enantiomers, which was assigned to (1S,2S,5R,6S,9S,10R)-2,5,6,9,10-pentabromocyclododecanol and its enantiomer. Mass spectrometric data are in accordance with the expected isotope patterns. On a C₁₈-RP-column, the polar PBCDOHs eluted before the HBCD and iBPBCD classes of compounds. PBCDOHs were also found in FP-PS materials. The stereoisomer patterns varied considerably in these materials like those of HBCDs and iBPBCDs. Expanded polystyrenes were rich in late-eluting stereoisomers, similar to technical HBCD mixtures. Extruded polystyrenes contained more of the polar, faster-eluting isomers. The presented chromatographic and analytical methods allow a stereoisomer-specific search for PBCDOHs in biota samples, which might have experienced metabolic HBCD transformation reactions. Besides this potential source, it has to be recognized that PBCDOHs are by-products in technical HBCDs and in flame-proofed polystyrenes. Therefore, it is likely that PBCDOHs and iBPBCDs are released to the environment together with HBCD-containing plastic materials.     

Contamination and potential sources of polybrominated diphenyl ethers (PBDEs) in water and sediment from the artificial Lake Shihwa, Korea

Concentrations of polybrominated diphenyl ethers (PBDEs) were determined in water and sediment collected from the artificial Lake Shihwa and surrounding creeks. Total concentrations of 23 PBDE congeners in water and sediment ranged from 0.16 to 11.0 ng L⁻¹ and from 1.3 to 18 700 ng g⁻¹ dry weight, respectively. The concentrations of BDE 209 in water and sediment were 1-2 orders of magnitude higher than the total concentrations of other PBDE congeners. The concentrations of total PBDEs and BDE 209 in sediments were the highest compared to previously reported worldwide levels. The highest concentrations of PBDEs in water and sediments were found in creeks near industrial complexes. The PBDE concentrations gradually decreased with increasing distance from the creeks to the inshore and then offshore regions of the lake. BDE 209 was a major congener, accounting for 80% of the total PBDEs in water and sediment, consistent with a high consumption of deca-BDE for the brominated flame retardant market in Korea. Non-parametric multidimensional scaling ordination showed that surrounding creeks are major pathways of PBDE contamination associated with deca-BDE technical mixtures used in industrial complexes around Lake Shihwa. A significant correlation between total organic carbon and total PBDE concentration was found in sediments, and the correlation coefficients for individual PBDE congeners relatively increased from lower to higher brominated congeners.     

W火焰炉低氮燃烧改造可行性研究

对黔北电厂1～4号W火焰锅炉实际运行状态进行分析,得出NO。排放浓度偏高的主要原因,并提出1—4号机组W火焰炉低氮改造的方案,即在拱下燃烧室内组织大回流长火焰燃烧方式,并通过SOFA风形成炉内深度空气分级低氮燃烧。同时针对1、2号炉和3、4号炉各自特性提出具体的改造方案,保证在锅炉效率不降低的条件下,1～4号W火焰锅炉的NOx排放浓度不高于850mg／m3,从而为W火焰锅炉低氮燃烧改造提供可行性方案,保证W火焰锅炉下一步烟气脱硝的顺利进行。     

超临界丙酮降解废弃线路板中的溴化环氧树脂简

探讨废弃线路板中溴化环氧树脂在超临界丙酮中的脱溴降解特性,重点考察了温度、反应时间和有机溶剂添加量对溴化环氧树脂降解特性的影响,确立的最佳实验条件为：温度260℃、保温时间1~2 h、丙酮添加量20~40 mL,系统压强3~6 MPa,此时溴化环氧树脂能够快速降解,脱溴率达到97.94%,降解产物主要为苯酚和异丙基苯酚,含量分别为60.99%和3.12%,降解产物中溴主要以HBr的形式存在于油相中,可以用碱液从油相中萃取脱除。线路板经超临界丙酮处理后,铜箔与玻璃纤维自动分层解离便于后续破碎回收,为废弃线路板的无害化处理和资源回收利用提供了一条新途径。     

火焰原子吸收分光光度法测定饮用水中铁和锰的不确定度评定

分析了测试过程中不确定度影响因素,其主要来源为标准溶液、标准曲线拟合、样品重复测定、分光光度计4部分。本次测量结果为:铁(0.232±0.012)mg/L;锰(0.092±0.004)mg/L,k=2(约95%置信水平)。     

环境中“新型”持久性有机污染物的质谱分析

“新型”持久性有机污染物逐渐受到环境科研工作者的重视,这类物质包括溴代阻燃剂、全氟化合物、多氯萘、多氯代正构烷烃和药物以及个人护理用品等,综述了目前对这类环境污染物的检测分析技术。