UASB反应器处理染料及印染废水的研究进展

综述了国内外UASB反应器处理染料及印染废水的研究概况.分析了UASB反应器处理废水存在的问题,并给出了相应的建议.展望了UASB反应器处理染料及印染废水的发展趋势,指出厌氧UASB-好氧法组合工艺是目前处理染料及印染废水的一种经济而有效的方法.     

催化湿式氧化处理造纸废水的研究

以过渡金属氧化物CuO为活性组分,采用催化湿式氧化法处理造纸废水,考察Cu负载量、催化剂用量、反应温度对废水COD去除率的影响。结果表明:固定氧气分压在2.5MPa和反应时间3h,催化剂用量为3g,Cu负载量为4%,反应温度为220℃,500mL浓度为3250mg/L造纸废水的COD去除率为90%,色度去除率为89%,pH值由9.6变为7.8。另外,对催化剂进行再生处理和稳定性测试。结果表明:450℃下活化3h,在上述相同反应条件下,对原废水的COD去除率降低为88%,重复使用9次后对废水的COD去除率仍能保持在85%左右。     

2005年中国燃煤大气砷排放清单

燃煤排放的砷是引起大气环境污染和经济损失的重要痕量元素之一.对燃煤大气砷排放进行估算可以为砷排放法规政策的制定和选择适宜的燃煤砷污染控制技术提供依据.采用基于燃料消耗的排放因子法,按照经济部门、燃烧方式和除尘设施将燃煤排放源进行分类,根据各省区不同排放类型的煤炭消耗量和燃煤平均砷含量,建立了2005年中国燃煤大气砷排放清单. 2005年中国燃煤生产和消耗量分别为2 119.8和2 099.8 Mt.燃煤导致的大气砷排放总量估算约为1 564.4 t,其中排放量最大的省区是山东（144.4 t）,其次是湖南（141.1 t）、河北（108.5 t）、河南（77.7 t）、江苏（77.0 t）等,燃煤大气砷排放主要集中在中东部省区;绝大部分燃煤大气砷排放来自工业（818.8 t）和电力部门（303.4 t）,分别占燃煤大气砷排放总量的52.3%和19.4%;2005年中国燃煤排放的砷大约有375.5 t是以气态形式排放到大气中,占排放总量的24%.总体上,在全国范围内燃煤大气砷污染排放控制的重点是电力和工业部门;而对于新疆、甘肃、青海、贵州等地区,还应关注生活消费燃煤引起的砷中毒事件.     

Ru/AC催化臭氧氧化难生物降解有机物

研究了臭氧单独氧化和Ru/AC催化臭氧氧化DMP、酚类物质和消毒副产物前体物.结果表明,Ru/AC能显著提高臭氧氧化中有机物的矿化效果.在DMP降解中,反应100 min后TOC的去除率由单独臭氧氧化的28.84%提高到66.13%.在23种酚类物质降解中,反应60min后TOC的去除率由单独臭氧的9.57%~56.08%提高到41.81%~82.32%.相对于单独臭氧,Ru/AC催化臭氧氧化更能有效地降低水源水中消毒副产物的生成势,以卤乙酸生成势的降低最为明显,100 min后卤乙酸生成势由144.02μg/L降到58.50μg/L,低于美国环保局规定的限制浓度60μg/L.而使用单独臭氧处理并不能使卤乙酸生成势降到符合美国EPA的规定.比较了BAC、O3+BAC、O3/AC+BAC以及Ru/AC+O3+BAC工艺处理水源水的效果,TOC平均去除率分别为3.80%、20.14%、27.45%和48.30%;COD平均去除率分别为4.37%、27.22%、39.91%和50.00%;UV254去除率分别为8.16%、62.24%、67.03%和84.95%.Ru/AC+O3+BAC工艺相比其他工艺,更能有效地...     

新型真空膜渗透结晶工艺初探

真空膜渗透结晶工艺(vacuum membrane percrystallization, VMPC)是一种新型膜结晶工艺,可同步实现溶质的结晶及其与溶剂的分离回收。以NaCl溶液为目标物系,对VMPC过程的原理进行了分析,初步考察了进料液温度、浓度和操作压力对该工艺产能的影响。结果表明：VMPC过程是膜渗透和真空压差闪蒸结晶的协同作用的过程,随进料液温度的升高,结晶盐通量和水通量均增大;随进料液浓度的升高,结晶盐通量增大,水通量降低;而操作压力对工艺产能影响较小,但对生成晶体的形貌影响显著;当进料液温度为34 ℃,进料质量分数为25%,操作压力为0.5 kPa时,可获得高达8.04 kg·(m²·h)⁻¹的盐通量和30 L·(m²·h)⁻¹的水通量,远高于现有太阳能驱动膜结晶技术的产能。针对现有膜滤浓缩液类高浓盐水结晶工艺流程复杂、能耗高、效率和产能低的问题,VMPC工艺为新型高效处置技术的开发及应用提供了可行的解决方案。     

恐惧诉求对职业驾驶员安全驾驶态度和行为意向的影响

研究以EPPM模型作为理论框架,探讨恐惧诉求对危险驾驶行为(超速和不系安全带)态度和行为意向的作用。54名职业驾驶员在观看交通安全恐惧诉求录像后,完成安全驾驶行为问卷。回归分析表明恐惧诉求的交通事故录像能够改变驾驶员对超速及不系安全带驾驶的态度和行为意向,但作用不完全一致。恐惧情绪唤起通过恐惧情感所引发的威胁评估过程中介对不超速行为意向的影响。最后,对研究的局限和未来的研究进行讨论。     

电化学还原-氧化工艺降解4-氯酚的毒性研究

采用紫外光还原法制备了Pd-Fe/石墨烯催化阴极,并以Ti/IrO_2/RuO_2为阳极,构成三电极体系(双阴极)和两电极体系(单阴极)的电化学还原-氧化降解工艺,分别对4-氯酚进行降解.采用离子色谱、高效液相色谱、TOC仪对4-氯酚降解过程中中间产物及其浓度进行测定.根据公式计算降解过程中理论计算毒性值,应用发光细菌法测定降解过程中的实际毒性值,对理论计算毒性值与实际毒性值进行比较,分析不同体系下降解过程中毒性的变化规律.结果表明,两种工艺体系在最佳降解条件下,阴极室毒性均呈下降的趋势,由于降解过程中在阳极室生成高毒性的苯醌,阳极室毒性均先升高后降低.通过相关性分析得到,两种体系理论计算毒性与实际毒性在P=0.01水平下,相关性系数均为1,显著相关,表明降解过程中实际毒性的测定结果真实可靠.降解至120 min时,三电极体系毒性小于两电极体系,表明三电极体系优于两电极体系.据此提出实际毒性测定方法在电化学还原-氧化工艺降解氯酚类有机废水毒性测试的工业应用中有着广泛的前景.     

Dynamic risk assessment for underground gas storage facilities based on Bayesian network

Loss of the underground gas storage process can have significant effects, and risk analysis is critical for maintaining the integrity of the underground gas storage process and reducing potential accidents. This paper focuses on the dynamic risk assessment method for the underground gas storage process. First, the underground gas storage process data is combined to create a database, and the fault tree of the underground gas storage facility is built by identifying the risk factors of the underground gas storage facility and mapping them into a Bayesian network. To eliminate the subjectivity in the process of determining the failure probability level of basic events, fuzzy numbers are introduced to determine the prior probability of the Bayesian network. Then, causal and diagnostic reasoning is performed on the Bayesian network to determine the failure level of the underground gas storage facilities. Based on the rate of change of prior and posterior probabilities, sensitivity and impact analysis are combined to determine the significant risk factors and possible failure paths. In addition, the time factor is introduced to build a dynamic Bayesian network to perform dynamic assessment and analysis of underground gas storage facilities. Finally, the dynamic risk assessment method is applied to underground gas storage facilities in depleted oil and gas reservoirs. A dynamic risk evaluation model for underground gas storage facilities is built to simulate and validate the dynamic risk evaluation method based on the Bayesian network. The results show that the proposed method has practical value for improving underground gas storage process safety.     

Effects of typical additives on the thermal stability of ammonium peroxydisulfate

Ammonium peroxydisulfate (APS), one of the most widely used inorganic peroxides in the process industries, is a thermally unstable peroxide and potent oxidizer due to the presence of peroxy bond in the molecule and is incompatible with most substances. To investigate the effect of typical additives on the thermal decomposition of APS, in this paper, diamine phosphate (DAP), monoamine phosphate (MAP), and aluminum hydroxide (AH) were selected as additives; pure APS and samples with 10 wt% and 20 wt% of additives were first tested by differential scanning calorimetry (DSC). The experiments and analysis showed that the samples with 10 wt% of additive had better thermal stability than those with 20 wt% of additive. After screening, the three groups of 10 wt% AH, 10 wt% MAP, and 20 wt% MAP additive conditions could be considered to have a better thermal stability effect on the thermal decomposition of APS. Four groups of samples were, in turn, tested by Phi-Tec II. The adiabatic results showed two discontinuous exothermic processes; 10 wt% AH promoted the weak exothermic effect in the first stage. In contrast, the three groups of additives in the main exothermic stage showed different degrees of inhibition, and the inhibiting effect was ranked as 10 wt% AH, 10 wt% MAP, and 20 wt% MAP in order. Finally, the self-accelerated decomposition temperature (SADT) was calculated under the 25 kg standard package. The adiabatic results, including SADT, were combined to render feasible recommendations for the use of additives, which provides references for the packaging and transportation of additives and their applications.     

A thermal hazard risk evaluation of emulsion polymerisation and vinyl acetate monomers in the latex manufacturing process

Latex is extensively used in industrial products. However, completing some processes at scale leads to unacceptable levels of risk that need to be quantified and mitigated. Systemic risks must be eliminated wherever possible, and safety takes priority over efficiency and quality. To assess the process risks accurately, four raw materials were examined in this study: polyvinyl acetate (PVA), latex process-initiator-ammonium persulfate (APS) and hydrogen peroxide (H₂O₂), and vinyl acetate monomer (VAM). The physicochemical composition of the PVA latex process was determined via calorimeters, including differential scanning calorimetry (DSC) and vent sizing package 2 (VSP2). The calorimetry results showed that the protective colloid was a critical component in the polymerisation reaction. In addition, when adding initiators to the system, it is vital to observe the normal ratio of materials and keep the stirring system operating. The scenario system also simulated the effects of shutting down various inhibitory programs, including the build-up of free radicals that could result in a runaway reaction when the initiator was added in excess. On the other hand, the result of the risk matrix displayed as a medium level, indicating that although the probability of an accident is low, the resulting severity is at disaster level. As a result, this study provides process safety engineers with a reliable frame of reference for assessing the potential dangers in the PVA latex manufacturing process.