高效液相色谱串联大气压化学电离源质谱(HPLC-APCI-MS)法测定水中三氯生

建立了高效液相色谱串联大气压化学电离源质谱(HPLC-APCI-MS)测定水中三氯生的方法,预处理采用正己烷液液萃取法萃取三氯生,回收率达99.6%;优化的色谱质谱联机分析条件为:检测波长230 nm,流动相乙腈/水(75∶25),离子源APCI源,负离子模式;该分析方法能在5 min内实现对水中三氯生的定性与定量分析.质量保证(Quality Assurance,QA)与质量控制(Quality Control,QC)研究得出,仪器检测限为0.18μg·L-1,相对标准偏差(relative standard deviations,RSD)为0.59%;空白加标实验回收率为103%,RSD为1.2%;以城市生活污水、河水和自来水为加标基质实验回收率为96.6%—108%,方法检测限为0.26—0.61μg·L-1,RSD为0.28%—0.81%.该方法操作简便,分析方法准确性、精密性与可靠性均较高.     

Modeling quenching distance and flame propagation speed through an iron dust cloud with spatially random distribution of particles

In this research combustion of iron dust particles in a medium with spatially discrete sources distributed in a random way has been studied using a numerical approach. A new thermal model is generated to estimate flame propagation speed and quenching distance in a quiescent reaction medium. The flame propagation speed is studied as a function of iron dust concentration and particle diameter. The predicted propagation speeds as a function of these parameters are shown to agree well with experimental measurements. In addition, the minimum ignition energy has also been investigated as a function of equivalence ratio and particle diameter. The quenching distance has been studied as a function of particle diameter and validated by the experiment. Considering random distribution of particles, the obtained results provide more realistic and reasonable predictions of the combustion physics compared to the results of the uniform distribution of particles.     

双火源条件下的XPS火蔓延速率研究

为研究挤塑聚苯乙烯泡沫板(XPS)双火源火焰迁移规律,在不同间距(0.5cm~8cm)的情况下,进行了竖直和水平方向的系列实验。研究发现:火蔓延速率和质量损失速率均随间距先上升后缓慢下降;在竖直方向实验中,火蔓延速率极值点右偏移于质量损失极值点。基于双火源条件下所得到的热解区传热系数,计算出火蔓延速率,进而分析火蔓延速率计算式中对流项和辐射项,得出火蔓延速率随间距的变化主要受控于传热系数。依据此结论解释了火蔓延速率和质量损失趋势相似但两者极值点偏移不同的原因。     

试样放置角度与外加辐射强度对可碳化固体表面火蔓延的影响

选取了尺寸为400mm×90mm×3mm质地较为均匀的白木作为研究对象,对不同试样放置角度和不同外加辐射强度作用下的火焰高度、火蔓延速率和失重速率等火蔓延参数进行了测量,以研究试样放置角度和辐射强度对可炭化固体表面火蔓延的作用规律。研究发现,试样表面的火蔓延速率随辐射强度的增加而增加。当角度在负角度范围内时,角度的变化对火蔓延速率的影响不大,当角度在正角度范围内时,火蔓延速率随着角度的增加而迅速上升。试样失重速率随着辐射强度以及试样放置角度的增加而增加。火焰高度会随着外加辐射强度的增加而增加,并与试样失重速率的0.4次方呈正比关系。     

羟基锡酸锌阻燃聚氯乙烯电缆材料及其潜在火灾危险性评价

采用氧指数、成炭率、烟密度、垂直燃烧(UL 94)、热重分析、环境扫描电镜和锥形量热的方法测试了羟基锡酸锌(ZHS)对PVC的阻燃抑烟作用。ZHS用量为15%时即可以满足对PVC电缆材料燃烧烟密度的要求,燃烧等级可以达到UL94 V0级。PVC/ZHS电缆材料的热稳定性能、成炭性能和燃烧性能表明,ZHS在PVC电缆材料燃烧时,可以促进PVC交联成炭,生成的炭具有较好的隔氧、隔热及抑制可燃性气体逸出的作用,提高了PVC电缆材料的热稳定性能,有效降低了PVC电缆材料的潜在火灾危险性。     

火焰原子吸收光谱法测定水中银

采用硝酸消解样品,氘灯背景校正技术消除非特征吸收和光散射影响,火焰原子吸收光谱法测定水中银,方法简便可靠,检出限为0.010 mg/L,RSD为0.9%～6.6%,加标回收率为93.0%～101%.     

火焰原子吸收法测定饮用水中银的改进

对火焰原子吸收分光光度法测定饮用水中银的方法作了改进。试验发现在酸性条件下,不利于银的测定,改加氨水氰化钾溶液则取得满意的结果,提高了测定灵敏度。银的特征质量浓度为0 016mg·L-1/1%吸收,检测限为0 001mg/L,相对标准差<2.5%,加标回收率在98%～103%之间。     

等离子体发射光谱法等三种方法测定马铃薯中镉

采用IRISER/SDuoICP测定马铃薯中的镉元素含量,并与火焰原子吸收法和石墨炉原子吸收法的测定作一比较,3种方法的检测限分别为0 001mg/L、0 004mg/L和0 25ng/L,加标回收率均在95%～102%范围内,相对标准差<10%。     

垂直壁面火蔓延速率的实验测量

垂直壁面火蔓延过程受材料本身的热物理性质以及外加辐射等复杂因素条件的影响很大,论文研究建立了可测量不同材料存在外加辐射条件下的垂直方向火蔓延实验台,来研究典型可燃物的垂直方向火蔓延特性,观察不同材料之间火蔓延行为的不同,同时测定可燃物的火焰到达高度随时间的变化情况,得到相应的火焰蔓延速率。同时考虑外辐射情况下对不同材料垂直方向火蔓延过程的影响,实验数据可为进一步的模拟研究工作提供很好的参考。     

Behavior of bromine on the thermal decomposition of paper-based phenolic laminate wastes

We investigated the thermal properties and behavior of bromine on the thermal decomposition of paper-based phenolic laminate wastes containing polybrominated flame retardants. The thermal properties of the phenolic laminate wastes were measured with a thermogravimeter and a conduction-type scanning calorimeter (TG-CSC). The weight loss of the wastes on thermal decomposition was mainly in three phases between 40°C and 600°C. The enthalpy (ΔH) of the thermal decomposition was 104 cal/g. The material balance of the decomposition components was measured with batch-type thermal decomposition equipment. The ratios of carbon residue, liquid, and gas on decomposition at 800°C in a vacuum were 37 wt. %, 48 wt. %, and 15 wt. %, respectively. The bromine contents in the carbon residue and liquid were less than 0.02 wt. % and 10 wt. %, respectively. These results are useful both in the carbonization process of these wastes and in the application of carbon residue as carbon materials. Received: August 11, 2000 / Accepted: March 7, 2001