尾气余热制氢柴油机的燃烧特性分析

设计了一种利用发动机尾气余热制取氢气的装置,该装置可以利用发动机余热,将乙醇水溶液催化反应为富含氢气的重整气。该重整气通入发动机供其燃烧使用,可以有效的提高发动机的燃烧效率。主要考虑该重整气对柴油燃烧的影响,依据美国加州劳伦斯利弗莫尔国家实验室反应机理,通过Chemkin软件计算该装置生成的重整气加入发动机以后对发动机燃烧特性的影响,分析了不同重整气掺混比例下的火焰传播速度,研究了柴油燃烧和柴油混合重整气燃烧的区别,总结了重整气在改善发动机燃烧方面所发挥的作用。     

爆炸法回收废旧轮胎实验研究

利用爆破法处理废旧轮胎,通过观察测量废旧轮胎爆破后的橡胶碎片量,考察了不同炸药对轮胎回收效果的影响。通过测量加入不同比例消焰剂的TNT爆破回收量,确定了最佳配比范围。研究表明,在TNT中加入消焰剂可有效提高轮胎爆破回收效果,消焰剂加入量10%~15%时效果最佳。     

Experimental and LES investigation of premixed methane/air flame propagating in a chamber for three obstacle BR configurations

The paper aims at revealing the effect of blockage ratio (BR) on the flame acceleration process and the flame-vortex mechanism in an obstructed chamber based essentially on the experimental and numerical methods. In the experiments, high-speed video photography and pressure transducer are used to study the flame shape changes and pressure dynamics. In the numerical simulations, large eddy simulation (LES) with the flame surface density (FSD) model is applied to investigate the interaction between the moving flame and vortices induced by obstacle. The results demonstrate that the flame propagation process can be divided into four stages, namely spherical flame, finger-shaped flame, jet flame and volute flame for three obstacle BR configurations, and a small recirculation zone is observed above the obstacle only for BR = 0.5. The peak of flame tip speed and pressure growth rate increases with the blockage ratio. The generation and evolution of the vortex behind the obstacle can be attributed to the initial flame acceleration, while the subsequent flame deceleration is due to the flame-vortex interaction. In addition, the transition from a “thin reaction zones” to a “broken reaction zones” is also observed in the simulation.     

管道压力对天然气射流火热辐射灾害的影响

天然气管道时常受到破坏,并诱发巨大的射流火焰,可能引燃周围建构物体。系统地分析了管道压力对天然气射流火热辐射灾害的影响,以建立天然气射流火热辐射灾害的系统定量分析方法。基于压力管道小孔泄漏模型和权重-多点源热辐射计算模型,建立了目标物体最大入射热辐射通量、管道压力和目标物与泄漏小孔水平距离的定量关系式。进而选定10 k W/m~2和31.5 k W/m~2作为城镇建筑物遭受引燃和机械破坏的热辐射通量阈值,得到了不同管道压力下天然气射流火热辐射灾害范围。计算结果表明,GB 50028—2006《城镇燃气设计规范》依据管道压力所规定的燃气管道与建筑物的安全间距不能完全满足天然气管道破坏时射流火焰的安全要求,与某武汉天然气管道射流火事故后果一致。     

氢氧化镁/红磷对硅橡胶/黏土纳米复合物阻燃性能的研究

选用甲基乙烯基硅橡胶(MVMQ)和十六烷基三甲基溴化铵(C16BrN)改性的蒙脱土(OMMT)纳米复合材料为原料,以氢氧化镁/微胶囊化红磷(MH/MRP)为阻燃剂,以气相法白炭黑为补强剂,用熔融共混法制备了无卤阻燃MVMQ纳米复合材料。笔者采用XRD表征制备的MVMQ/OMMT纳米复合物的结构,用机械性能测试研究气相法白炭黑和OMMT对MVMQ的协效补强作用,通过极限氧指数、UL94 V垂直燃烧法、环境扫描电镜(ESEM)和热重分析(TG)等分析测试手段研究其燃烧性能和热性能,结合材料宏观燃烧性能的改变,推断OMMT和MH/MRP对MVMQ的阻燃作用机理。     

立体结构障碍物对甲烷预混火焰传播影响的研究

使用自行设计的火焰加速试验系统,研究了3种立体结构障碍物对管道内预混火焰传播速度和超压的影响。选用长方体、正四棱柱和圆柱,其阻塞比均为40%。结果表明,管道内障碍物对火焰传播的初始阶段起阻碍作用,当火焰越过障碍物后,障碍物加速火焰传播过程。有障碍物时管道内最大火焰传播速度和峰值超压比无障碍物时要大。随着点火距离的增大,管道中最大火焰传播速度和超压先变大后减小。当障碍物位于约6倍管径处时,对管道中火焰传播速度和超压影响最大。点火距离的改变对火焰传播速度的影响大于对管道内超压的影响。     

本质阻燃PA纤维及纤维（织物）阻燃技术最近进展

本文首先概论了纤维（织物）阻燃技术，其次重点讨论了两种含磷本质阻燃PA纤维，一种是由含磷羟基羧酸或含磷二元羧酸与己二胺及己二酸共缩聚而后纺丝制得．另一种是用螺环磷酰氯与PA66及PA6纤维反应制得，后者具膨胀性。最后是综述了纤维（织物）阻燃技术的最新进展，包括新型表面改性技术及纳米技术等。     

管道内瓦斯爆炸传播的试验研究

运用大型试验管道对瓦斯爆炸传播规律进行试验研究,并对瓦斯爆炸压力峰值、火焰速度和呈现时间进行分析,得出:在不出现爆轰的前提下,爆源点附近的压力峰值是全管道的最大值;爆炸压力峰值在沿管道的传播过程中从爆源点附近是先增大后减小,然后再逐渐增大且压力峰值最早呈现在出口附近;火焰传播速度随着传播距离的增大而逐渐增大且在爆炸初期增大速率更快;瓦斯浓度对爆炸压力峰值、火焰传播速度和呈现时间等都有重要影响。     

半密闭空间油气爆炸初期火焰特性研究

为了研究半密闭空间内部油气着火爆炸初期火焰特性，进行了不同油气体积分数下的油气着火爆炸实验，通过高速摄影等技术手段对爆炸过程中火焰形态进行了捕捉，分析了不同油气体积分数下爆炸初期火焰着火模式、火焰形态、传播过程和火焰浮力稳定性的变化规律。结果表明:油气体积分数为决定容器内部着火模式的关键因素，随着油气体积分数的逐渐增大，着火模式呈现出燃烧-爆炸-爆燃后持续燃烧的转变；爆炸下的火焰具有明显的分区现象，而其他的着火模式则没有；随着油气体积分数的增加，越靠近化学当量比，纵向和横向火焰阵面速度越大；油气体积分数小于等于1.1%或大于等于2.6%时，火焰稳定性受浮力影响显著。     

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.