污泥与煤混烧动力学及常规污染物排放分析

采用热重分析法研究了不同污泥掺烧比例及不同加热速率时污泥与煤的热失重特性.探讨了掺烧污泥对煤燃烧特性的影响,分析了掺入污泥对煤的燃烧变化规律,并进行了动力学分析.结果表明,加热速率增加时,样品的失重速率增大,开始失重温度及最终燃尽温度升高.掺烧时的TG曲线在400~600℃时有一个明显的失重阶段.失重速率峰值随着掺烧比的提高而升高,对应的温度降低.掺烧污泥后的混合样品的燃烧温度范围比单一燃煤时少20~100℃.非等温动力学模型分析可得,少量的污泥与煤掺烧时所需的活化能与煤较接近,对煤的正常燃烧影响不大.不同比例掺烧时产生的烟气中NOx、SO2、CO2生成量及减排规律因N、S、C含量不同而各有差异.热重分析及模型分析法可以为不同理化特性的煤与污泥掺烧提供初始理论依据.     

空气整段间隔流动注射-催化动力学光度法测定天然水中痕量钒

应用空气整段间隔流动注射法与改进的钒-溴酸钾-没食子酸催化动力学反应体系相结合,建立了测定天然水体中痕量钒的催化动力学光度FIA法。通过使用一个自制的进样阀,使样品带在反应管道中的留存时间得到延长,加热允许温度得到提高。在温度80℃,反应留存时间4.75min条件下,可测定0—10ppb的钒,检出限达0.1ppb。测定2ppb钒样品时,RSD为2.7％(n=10),测定频率达90次/h,方法的平均回收率在80—109％之间。     

Stable chlorine intramolecular kinetic isotope effects from the abiotic dehydrochlorination of DDT

INTENTION, GOAL, SCOPE, BACKGROUND: Identifying different sources and following reaction pathways of chlorinated organic contaminants in the environment can be challenging, especially when only their concentrations are available. Compound-specific stable chlorine measurements of some contaminants have recently been shown to provide additional information and an increased understanding of their biogeochemistry. These studies, however, have been generally limited to volatile molecules. OBJECTIVE: Here, the stable chlorine isotope ratios of the semi-volatile pesticide, 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane (DDT) were investigated. Specifically, the intramolecular stable chlorine isotopic compositions of DDT and the kinetic isotope effect (KIE) for the abiotic dehydrochlorination of DDT to 2,2-bis(p-chlorophenyl)-1,1-dichloroethene (DDE) were determined. METHODS: Selective chemical oxidation of DDT to dichlorobenzophenone (DCBP) and analysis of each compound was used to calculate the stable chlorine isotope ratios of the alkyl and aromatic chlorines in DDT. To determine the KIE for dehydrochlorination, DDT was reacted in a basic solution to yield DDE at 52 degrees C, 60 degrees C, and 72 degrees C for 3, 5, and 5 days, respectively. RESULTS AND DISCUSSION: Significant intramolecular stable chlorine isotopic differences were observed in one sample of DDT where the alkyl and aromatic delta 37Cl values were -5.76 +/- 0.45 and -2.21 +/- 0.24%@1000, respectively. Dehydrochlorination of DDT to DDE in basic solutions at 52, 60, and 70 degrees C resulted in a substantial intramolecular KIE where the alkyl chlorines of DDE shifted by approximately 3%@1000 relative to the alkyl chlorines in DDT. However, no temperature dependence was observed. The KIE, calculated by an iterative program, was 1.009. CONCLUSIONS: Intramolecular differences in the stable chlorine isotope ratios were observed in DDT and this is the first such finding. Dehydrochlorination of DDT yields a measurable and distinct intramolecular stable chlorine KIE. RECOMMENDATION AND OUTLOOK: The results of this study demonstrate the existence of significant intramolecular differences in chlorinated organic compounds. Many other chlorinated semi-volatile and volatile organic contaminants are synthesized from multiple sources of chlorine, and we recommend that similar studies be performed on many such molecules in order to attain a clear understanding of their intramolecular chlorine isotopic differences. The existence of a measurable KIE for the dehydrochlorination of DDT to DDE shows the potential strength of using isotopic measurements to investigate the biogeochemistry of these important compounds. For example, the isotopically depleted aqueous chloride produced by dehydrochlorination of DDT to DDE may be a useful tracer of these reactions in freshwater environments.     

柠檬酸固态发酵过程的研究

本文研究了以甘薯为原料，以黑曲霉为菌种，固态发酵制柠檬酸的最佳发酵条件和发酵动力学。探讨了接种方式、灭菌与否以及温度、含水量、ｐＨ值、颗粒度、通气速率等因素对柠檬酸固态发酵过程的影响，提出了适宜的发酵参数。在此基础上，进一步研究甘薯固态发酵制取柠檬酸的动力学模型，确定了模型参数与操作条件的关系。该模型反映了基质消耗、产物生成、菌体生长及ＣＯ２释放速率的变化过程和温度、颗粒度的影响。模型的模拟结果与     

Mg/Fe水滑石吸附水中磷的动力学及热力学研究

以MgCl2和FeCl3为原料通过共沉淀法制备了Mg/Fe水滑石,并对其进行焙烧得到了焙烧态Mg/Fe水滑石。采用X射线衍射(XRD)和傅里叶红外光谱(FTIR)对所得产物进行了结构表征。利用焙烧前后的水滑石作吸附剂吸附处理含磷废水,比较了两者对磷的吸附能力,并在不同温度和pH条件下进行了吸附动力学实验。结果表明,焙烧前后的水滑石对磷都具有很好的吸附能力,但300℃焙烧后水滑石的吸附能力提高了约5%。动力学实验表明,水滑石对磷的吸附可很好地用准二级动力学方程进行描述,其线性相关系数达0.999以上。在15~35℃下进行了等温吸附实验,结果发现水滑石对磷的吸附更符合Langmuir方程。经热力学研究发现,标准吸附焓变(ΔH0)0J/mol、标准吸附自由能(ΔG0)0J/mol和标准吸附熵变(ΔS0)0J/(mol·K),说明水滑石对磷的吸附反应是自发的吸热反应,且是一个熵增加的过程。     

Energy-efficient removal of carbamazepine in solution by electrocoagulation-electrofenton using a novel P-rGO cathode

In this study,carbamazepine(CBZ) decay in solution has been studied by coupling electrocoagulation with electro-Fenton(EC-EF) with a novel P-rGO/carbon felt(CF) cathode,aiming to accelerate the in-situ generation of ·OH,instead of adding Fe²⁺ and H₂ O₂.Firstly,the fabricated P-rGO and its derived cathode were characterized by XRD,SEM,AFM,XPS and electrochemical test(EIS,CV and LSV).Secondly,it was confirmed that the performance in removal efficiency and electric ...     

热水解-厌氧消化工艺中污泥的触变性分析

采用触变动力学系数作为评价指标,通过流变试验研究了热水解-厌氧消化联合工艺中污泥标准化黏度和触变性的变化规律,并探讨了屈服应力和触变性二者间的联系,从触变性角度为热水解-厌氧消化污泥的处理处置提供参考依据。结果表明:与滞后环相比,用触变动力学系数K更适合表征污泥的触变性;调配污泥、热水解污泥和厌氧消化污泥的标准化黏度均随时间增大逐渐减小;3种污泥的触变性随TSS质量分数增大而减小,经热水解-厌氧消化后污泥的触变性增大,流动性增强;污泥屈服应力越大,触变性越小,稳定性越强。     

基于动力学与混合核函数LS-SVM的厌氧发酵产气量预测模型研究

利用农业生产中产生的牲畜粪便牛粪和秸秆进行厌氧发酵试验,以产气量为参考指标,研究牛粪和秸秆厌氧发酵的产气量预测模型。试验过程中测量发酵物的氧化还原电位(ORP)、p H值、挥发性脂肪酸(VFA)、氨氮含量、化学需氧量(COD)、电导率及产气量,并用灰色关联分析法筛选出与产气量关联较强的参数,将筛选出的参数作为多项式核函数和高斯径向基核函数构建的混合核函数LS-SVM模型的输入量,训练出预测能力较强的混合核函数LS-SVM模型,然后在混合核函数LS-SVM模型中融入微生物动力学构建产气量预测模型,并用验证集验证模型性能。仿真结果表明,筛选得到关联较强的参数为ORP、p H值、VFA、氨氮含量;融入动力学的混合核函数LS-SVM模型与混合核函数LS-SVM模型相比,产气量的预测更准确,误差更小,最小误差减少了近一个数量级,试验证明该模型有效。     

Gas-phase thermal explosions in catalytic direct oxidation of alkenes

The metal-based catalytic oxidation of alkenes to the corresponding epoxides is playing a significant role in the modern chemical industry. Nevertheless, these key processes are still lacking proper understanding with respect to the gas-phase runaway behaviour (thermal explosion) and to the hot spot formation on the catalytic surface, under the typical process conditions.This work aims to enlighten these aspects by considering either the catalytic or the gas-phase chemistry for the development of reactor operative diagrams, in order to define the best-operating conditions with respect to the selectivity, the productivity, and the process safety aspects.The proposed methodology has been applied to the oxidation of ethylene and propylene for the direct oxidation process by pure oxygen, considering a detailed kinetic model accounting for the homogeneous reactions, coupled with the heterogeneous catalytic mechanisms.Sensitivity and reaction path analyses were performed to individuate the ruling species and reactions determining the transition to runaway conditions.     

超临界流体萃取固体物料动力学模型的研究进展(英文)

文章总结与讨论了超临界流体萃取固体物料的动力学模型。这些动力学模型包括经验模型,基于热传递类推的模型以及基于微分质量平衡的模型。所有这些都有助于实现过程的数学模拟放大,有助于投资前的经济预算,有效减小投资风险,也可作为超临界流体萃取过程的研究手段,减少实验探索的工作量。