Brominated flame retardants and heavy metals in automobile shredder residue (ASR) and their behavior in the melting process

The End-of-life Vehicles Recycling Act went into effect on January 1, 2005, in Japan and requires the proper treatment of airbags, chlorofluorocarbons (CFCs), and automobile shredder residue (ASR). The need for optimal treatment and recycling of ASR, in particular, has been increasing year after year because ASR is regarded as being difficult to treat. Dioxin-related compounds, brominated flame retardants (BFRs), heavy metals, chlorine and organotin compounds are all present in high concentrations in ASR. The authors conducted ASR melting treatment tests using a 10-tons/day-scale direct melting system (DMS), which employs shaft-type gasification and melting technology. The results obtained showed that dioxin-related compounds and BFRs were decomposed by this melting treatment. The high-temperature reducing atmosphere in the melting furnace moved volatile heavy metals such as lead and zinc into the fly ash where they were distributed at a rate of more than 90% of the input amount. This treatment was also found to be effective in the decomposition of organotin, with a rate of decomposition higher than 99.996% of the input amount. Via the recovery of heavy metals concentrated in the fly ash, all the products discharged from this treatment system were utilized effectively for the complete realization of an ASR recycling system that requires no final disposal sites.     

火焰原子吸收分光光度法测定废水中总铬

研究环境样品中总铬用火焰原子吸收分光光度法测定。选择不同实验条件 ,确定了最佳的分析条件 ,并通过标准样品和实验样品的分析 ,验证了方法的准确度和精密度。实验证明 ,此方法快速方便、准确度高、精密度好。     

阻燃剂废水的处理及回收利用

采用电化学氧化、电气浮与Fenton强氧化性协同作用的电解Fenton法预处理难降解阻燃剂废水(CODCr=17108mg/L),CODCr去除率达98.34%,色度去除率达74.19%。其适宜操作条件是:pH=2.0～2.6;电流密度10.8～14.3A/dm2;H2O2起始摩尔浓度27～42mmol/L;FeSO4起始质量浓度660～990mg/L;电解5h。处理后取废水50mL,HCl(1∶1)67mL,NaAlO230g,FeCl3·6H2O4g,加热回流反应2h制成聚合氯化铝铁无机高分子絮凝剂(Al2O39.93%、Fe2O30.75%、盐基度68.0%左右)。该絮凝剂在pH=7～9时有良好的絮凝效果。     

Effects of a carbon monoxide-dominant gas mixture on the explosion and flame propagation behaviors of methane in air

This work aimed to experimentally evaluate the effects of a carbon monoxide-dominant gas mixture on the explosion characteristics of methane in air and report the results of an experimental study on explosion pressure measurement in closed vessel deflagration for a carbon monoxide-dominant gas mixture over its entire flammable range. Experiments were performed in a 20-L spherical explosion tank with a quartz glass window 110 mm in diameter using an electric spark (1 J) as the ignition source. All experiments were conducted at room temperature and at ambient pressure, with a relative humidity ranging from 52 to 73%. The peak explosion pressure (P_max), maximum pressure rise rate ((dp/dt)_max), and gas deflagration index (K_G) were observed and analyzed. The flame propagation behavior in the initial stage was recorded using a high-speed camera. The spherical outward flame front was determined on the basis of a canny method, from which the maximum flame propagation speed (S_n) was calculated. The results indicated that the existence of the mixture had a significant effect on the flame propagation of CH₄-air and increased its explosion risk. As the volume fraction of the mixed gas increases, the P_max, (dp/dt)_max, K_G and S_n of the fuel-lean CH₄-air mixture (7% CH₄-air mixture) increase nonlinearly. In contrast, addition of the mixed gas negatively affected the fuel-rich mixture (11% CH₄-air mixture), exhibiting a decreasing trend. Under stoichiometric conditions (9.5% CH₄-air mixture), the mixed gas slightly lowered P_max, (dp/dt)_max, K_G, and S_n. The P_max of CH₄-air mixtures at volume fractions of 7%, 9.5%, and 11% were 5.4, 6.9, and 6.8 bar, respectively. The S_n of CH₄-air mixtures at volume fractions of 7%, 9.5%, and 11% were 1.2 m/s, 2.0 m/s, and 1.8 m/s, respectively. The outcome of the study is comprehensive data that quantify the dependency of explosion severity parameters on the gas concentration. In the storage and transportation of flammable gases, the information is required to quantify the potential severity of an explosion, design vessels able to withstand an explosion and design explosion safety measures for installations handling this gas.     

基于1 m3泄爆装置的墨粉爆炸泄压机制研究*

为了研究墨粉在爆炸泄压过程中燃烧与流动的变化机制,通过改变泄爆片尺寸、墨粉浓度以及泄爆片的惯性力等参数对爆炸泄放过程中反应釜中压力以及外场火焰形态变化进行试验研究,同时与完全封闭空间内不同墨粉浓度的压力曲线对比。研究结果表明:相同泄爆开口尺寸下,粉尘浓度与受控爆炸压力（采用爆炸泄压保护措施后工业腔体内产生的压力）负相关;开口尺寸增加可以提升泄压效率;结合外场火焰形态的变化情况揭示声动火焰不稳定性对反应釜中压力发展的影响;通过无惯性泄爆试验的对比证明泄爆片惯性对受控爆炸压力的影响不可忽视。     

MPP协同MF@ADP阻燃低密度聚乙烯性能研究*

为提高低密度聚乙烯（LDPE）阻燃性能和阻燃LDPE复合材料的力学性能与抑烟性能,采用原位聚合法制备三聚氰胺-甲醛（MF）树脂包覆二乙基次磷酸铝（ADP）的MF@ADP微胶囊,再引入三聚氰胺聚磷酸（MPP）与MF@ADP进行协效复配,熔融共混制备阻燃LDPE复合材料。通过氧指数、热重分析、力学测试和烟密度测试等研究复合材料的阻燃、力学和抑烟性能。研究结果表明:MF@ADP微胶囊能改善阻燃剂与复合材料之间的相容性,与MPP复配构成的磷-氮膨胀阻燃体系能有效提高LDPE的抑烟性能;当MF@ADP∶MPP的质量比为2∶1时,材料的LOI达到了30.6%,垂直燃烧测试达到UL-94 V0级,拉伸强度为11.8 MPa,且形成的P/N/O高聚物炭层稳定性更高,可减少LDPE燃烧释放的烟雾量。     

超细CaCO3惰化剂对铝合金抛光伴生粉尘爆炸的防控效果*

为探究超细粉体惰化剂对铝合金抛光伴生粉尘爆炸特性的影响规律,利用标准化实验装置及自行搭建的实验平台,在对爆炸基本参数进行测试的基础上,分别研究超细CaCO3粉体对抛光废弃物粉尘点燃敏感度的钝化作用以及对爆炸火焰传播进程的惰化效果,并在相同条件下与同等粒径高纯度铝粉的实验效果进行比对。研究结果表明:铝合金抛光废弃物粉尘最小点火能量为280 mJ,而同等粒径高纯度铝粉最小点火能量为35 mJ;在铝合金抛光废弃物粉尘质量浓度为300 g/m3条件下,发生爆炸的火焰传播速度峰值为7.4 m/s,约为高纯度铝粉的57%,铝合金抛光废弃物粉尘的爆炸敏感度及猛烈度均低于高纯度铝粉;当超细CaCO3粉体的惰化比为30%时,可将铝合金抛光废弃物粉尘的最小点火能量钝化至约1 J,爆炸火焰失去持续传播能力,惰化作用效果充分显现。     

横向风作用下喷口间距对射流扩散火焰特征的影响研究*

为研究横向风作用下喷口间距对射流扩散火焰特征的影响,以双喷口火焰为研究对象,利用CCD摄像机拍摄火焰几何形态,研究横向风条件下喷口间距对火焰形态演化、火焰长度和火焰吹熄极限的影响。研究结果表明:喷口间距较小时,2束火焰因空气夹带竞争和压差作用,彼此相互倾斜融合,火焰融合概率随喷口间距增加而逐渐降低,火焰临界融合间距随横向风的增加先增大后减小;由于火焰的空气夹带和热反馈处于较高水平,2束火焰被少量拉伸,火焰长度先增加后减小;喷口间距较小时,火焰吹熄极限显著增加。     

便携式气相色谱-氢火焰离子化检测器法测定低浓度总烃的氧气干扰特征研究

研究了采用便携式气相色谱-氢火焰离子化检测器法测定气体中的总烃浓度时,氧气浓度对测定结果的影响,并采用多元线性回归模型对总烃的测定结果进行了校准。当总烃的实际浓度不低于9 mg/m³时,氧气的干扰较小(相对标准偏差≤2%)。在试验的所有总烃实际浓度下(1~200 mg/m³),当氧气浓度为1%~7%时,也无需考虑氧气干扰的影响(相对标准偏差≤2%)。当总烃的实际浓度低于9 mg/m³且氧气浓度为9%~21%时,需依据多元线性回归分析原理并采用模型对测得的总烃浓度进行校准。线性回归方程分析结果显示,模型拟合情况良好(R²=0.999),可以用来修正测试结果,从而得到更加准确的总烃实际浓度。     

胃肠模拟体外法的生理参数对室内灰尘中邻苯二甲酸酯与磷系阻燃剂的生物有效性的影响

室内灰尘吞食暴露是邻苯二甲酸酯与磷系阻燃剂的主要暴露途径,测定室内灰尘中该类有机污染物的生物有效性对其暴露风险评价至关重要.本研究选择胃肠模拟体外方法-生理原理提取法(PBET)法测定室内灰尘中邻苯二甲酸二正丁酯(Dibutyl phthalate,DBP)、邻苯二甲酸丁基苄基酯(Butyl benzyl phthalate,BBP)、邻苯二甲酸二(2-乙基己基)酯(Di(2-ethylhexyl)phthalate,DEHP)和三(2-氯乙基)磷酸酯(Tris(2-chloroethyl)phosphate,TCEP)的生物有效性.研究了PBET法中胆盐含量、模拟肠液p H值、液固比及同时摄入奶粉等生理参数对生物有效性的影响.结果表明,4种有机污染物的生物有效性从1.5%(DEHP)到52%(TCEP),随污染物辛醇水分配系数的增加而降低.随着模拟液胆盐含量增加,DBP、BBP与DEHP的生物有效性逐渐增加,并在10 g·L~(-1)附近达到最大值后趋于平稳.TCEP由于其较好的水溶性,生物有效性并未随着胆盐含量的增加而明显变化.奶粉含量的增加则显著增加了DBP、BBP、DEHP和TCEP的生物有效性,在10 g·L~(-1)附近达到最大值后普遍呈现下降趋势.随着液固比的增加,DBP和DEHP的生物有效性显著提升,然而BBP与TCEP的生物有效性却未发生明显改变.在p H 6~8范围内,均未对4种有机物的生物有效性产生显著影响.