Pesticides Removal Using Conventional and Low‐Cost Adsorbents: A Review     

Javad Zolgharnein  Ali Shahmoradi  Jahanbakhsh Ghasemi 《洁净——土壤、空气、水》2011,39(12):1105-1119

Worldwide pesticide usage has increased dramatically during the last three decades, coinciding with changing practices and increasing by intensive agriculture. This widespread use of pesticides for agricultural and non‐agricultural purposes has resulted in the presence of their residues in various environmental matrices. The occurrence of pesticides and their metabolite transported in rivers, channels, lakes, sea, air, soils, groundwater, and even drinking water, proves the high risk of these chemicals to human health and the environment. Therefore, pesticide removal is of an increasing concern. In this study, a review of the published literature dealing with pesticides removal process is presented. Firstly, pesticide removal by conventional means is briefly considered. Secondly, the use of the low‐cost sorbent through biosorption process is discussed comprehensively. The effect of factors such as pH, contact time, sorbent dosage, initial pesticide concentration, and optimization of biosorption conditions is also discussed. Kinetic, thermodynamic, and mechanism studies are also given. This study shows that both microorganisms and other materials with biological origin like agricultural by‐products may be used to this end. There is a significant potential for pesticide uptake by the use of various pristine and especially modified biosorbents. In the case of living organisms used as removal agents, degradation may also play a role in the total removal observed.  相似文献   

Performance of Carbon Xerogels in the Production of Environmentally Friendly Urea Formaldehyde‐Bagasse Composites     

《洁净——土壤、空气、水》2017,45(6)

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On the relevance of iron adsorption to container materials in small-volume experiments on iron marine chemistry: Fe-aided assessment of capacity, affinity and kinetics     

A.C. Fischer  J.J. Kroon  T.G. Verburg  T. Teunissen  H.Th. Wolterbeek 《Marine Chemistry》2007,107(4):533-546

Iron chemistry in seawater has been extensively studied in the laboratory, mostly in small-volume sample bottles. However, little has been reported about iron wall sorption in these bottles. In this paper, radio-iron ⁵⁵Fe was used to assess iron wall adsorption, both in terms of capacity, affinity and kinetics. Various bottle materials were tested. Iron sorption increased from polyethylene/polycarbonate to polymethylmetacrylate (PMMA)/high-density polyethylene/polytetrafluoroethylene to glass/quartz, reaching equilibrium in a 25–70 h period. PMMA was studied in more detail: ferric iron (Fe(III)) adsorbed on the walls of the bottles, whereas ferrous iron (Fe(II)) did not. Considering that in seawater the inorganic iron pool mostly consists of ferric iron, the wall will be a factor that needs to be considered in bottle experiments.The present data indicate that for PMMA with specific surface (S)-to-volume (V) ratio S/V, both iron capacity (42 ± 16 × 10^− 9 mol/m² or 1.7 × 10^− 9 mol/L recalculated for the S/V-specific PMMA bottles used) and affinity (log K_Fe'W = 11.0 ± 0.3 m²/mol or 12.4 ± 0.3 L/mol, recalculated for the S/V-specific PMMA bottles used) are of similar magnitude as the iron capacity and -affinity of the natural ligands in the presently used seawater and thus cannot be ignored.Calculation of rate constants for association and dissociation of both Fe'L (iron bound to natural occurring organic ligands) and Fe'W (iron adsorbed on the wall of vessels) suggests that the two iron complexes are also of rather similar kinetics, with rate constants for dissociation in the order of 10 ⁻⁴–10^− 5 L/s and rate constants for association in the order of 10⁸ L/(mol s). This makes that iron wall sorption should be seriously considered in small-volume experiments, both in assessments of shorter-term dynamics and in end-point observations in equilibrium conditions. Therefore, the present data strongly advocate making use of iron mass balances throughout in experiments in smaller volume set-ups on marine iron (bio) chemistry.  相似文献   

污水-海水混合过程中磷转移的动力学   总被引：5，自引：0，他引：5       下载免费PDF全文

陈松  林汝健  廖文卓 《海洋与湖沼》1993,24(1):59-64

模拟研究厦门市污水排海时污水-海水混合过程中磷含量和形态的变化,及其在海水-颗粒物界面交换的动力学过程;提供转移模式,确定转移速率,进行磷的容量校正,为厦门西海域环境容量估算和水质控制提供定量参数和理论依据。  相似文献   

天然水体中酚的降解动力学     

吴欣然  夏福兴  吴玲  陈邦林 《海洋科学》1992,16(1):33-37

本文报道了天然水体中低浓度酚的降解动力学;计算了它的降解速率常数、降解活化能等。降解半表期是t_(1/2)=1.5d~(-1)(10℃),t_(1/2)=O.74d~(-1)(30℃)。低浓度酚的降解动力学跟天然水体中酚的降解情况比较接近。本文的结果对环境评价、蓄水库工程设计等很有参考价值。  相似文献   

Practical kinetic modeling of petroleum generation and expulsion     

John G. Stainforth 《Marine and Petroleum Geology》2009

Models for petroleum generation used by the industry are often limited by (a) sub-optimal laboratory pyrolysis methods for studying hydrocarbon generation, (b) over-simple models of petroleum generation, (c) inappropriate mathematical methods to derive kinetic parameters by fitting laboratory data, (d) primitive models of primary migration/expulsion and its coupling with petroleum generation, and (e) insufficient use of subsurface data to constrain the models. Problems (a), (b) and (c) lead to forced compensation effects between the activation energies and frequency factors of reaction kinetics that are wholly artificial, and which yield poor extrapolations to geological conditions. Simple switch or adsorption models of expulsion are insufficient to describe the residence time of species in source rocks. Yet, the residence time controls the thermal stresses to which the species are subjected for cracking to lighter species.  相似文献   

Kinetic and equilibrium studies of copper-dissolved organic matter complexation in water column of the stratified Krka River estuary (Croatia)     

Yoann Louis  Cdric Garnier  Vronique Lenoble  Stphane Mounier  Neven Cukrov  Dario Omanovi&#x;  Ivanka Pieta 《Marine Chemistry》2009,114(3-4):110-119

An interaction of dissolved natural organic matter (DNOM) with copper ions in the water column of the stratified Krka River estuary (Croatia) was studied. The experimental methodology was based on the differential pulse anodic stripping voltammetric (DPASV) determination of labile copper species by titrating the sample using increments of copper additions uniformly distributed on the logarithmic scale. A classical at-equilibrium approach (determination of copper complexing capacity, CuCC) and a kinetic approach (tracing of equilibrium reconstitution) of copper complexation were considered and compared. A model of discrete distribution of organic ligands forming inert copper complexes was applied. For both approaches, a home-written fitting program was used for the determination of apparent stability constants (K_i^equ), total ligands concentration (L_iT) and association/dissociation rate constants (k_i¹,k_i^- 1).A non-conservative behaviour of dissolved organic matter (DOC) and total copper concentration in a water column was registered. An enhanced biological activity at the freshwater–seawater interface (FSI) triggered an increase of total copper concentration and total ligand concentration in this water layer. The copper complexation in fresh water of Krka River was characterised by one type of binding ligands, while in most of the estuarine and marine samples two classes of ligands were identified. The distribution of apparent stability constants (log K₁^equ: 11.2–13.0, log K₂^equ:8.8–10.0) showed increasing trend towards higher salinities, indicating stronger copper complexation by autochthonous seawater organic matter.Copper complexation parameters (ligand concentrations and apparent stability constants) obtained by at-equilibrium model are in very good accordance with those of kinetic model. Calculated association rate constants (k₁¹:6.1–20 × 10³ (M s)^− 1, k₂¹: 1.3–6.3 × 10³ (M s)^− 1) indicate that copper complexation by DNOM takes place relatively slowly. The time needed to achieve a new pseudo-equilibrium induced by an increase of copper concentration (which is common for Krka River estuary during summer period due to the nautical traffic), is estimated to be from 2 to 4 h.It is found that in such oligotrophic environment (dissolved organic carbon content under 83 µM_C, i.e. 1 mg_CL^− 1) an increase of the total copper concentration above 12 nM could enhance a free copper concentration exceeding the level considered as potentially toxic for microorganisms (10 pM).  相似文献   

南海北部神狐区域 SH2 站位甲烷水合物成藏动力学模拟研究     

关进安  梁德青  万丽华  谷任国 《工程地质学报》2014,22(5):997-1002

南海北部神狐区域海底的高丰度水合物储层与生物成因为主的甲烷气源表明该区域很可能是一种特殊的复合型海洋水合物系统,其成藏动力学机制有待进一步的研究和澄清。建立了一个耦合沉积层地质属性-流体流动过程-水合物反应动力学的传输-反应模型,区别了两种不同类型的水合物形成(分解)动力学过程:(1)在通常情况下溶解甲烷和游离气共同形成水合物,(2)特殊情况下游离气直接生成水合物,结果表明在神狐海域热力学环境下游离气形成水合物速度比溶解甲烷快约4倍,气体含量和动力学常数比值越大生成水合物越快,而对比水合物分布的模拟结果与实测数据表明该区域水合物储层聚集和产状很可能受到了其他地质活动的影响。  相似文献   

t-BAMBP/磺化煤油萃取体系从盐湖卤水中萃取铷的动力学研究          下载免费PDF全文

黄东方  郑红  宝阿敏  刘泽宇  段东平  王舒娅  李波  王斌  杨晋生  范承亮 《盐湖研究》2017,25(1):49-56

采用上升单液滴法,进行盐湖卤水中萃取铷的动力学研究,主要考察了比界面积、水相铷浓度和油相(t-BAMBP/磺化煤油)浓度对萃取速率的影响。通过比界面积的研究发现,t-BAMBP萃取铷的过程由界面化学反应和相内化学反应共同控制;通过对实验数据的非线性拟合,得到了萃取体系的动力学方程,R=9.936×10-7[Rb+]1.134[t-BAMBP]2.190,萃取速率对铷的反应级数为a=1.134,对t-BAMBP反应级数b=2.190,实验值和计算值的均方根误差为1.735%。  相似文献   

封闭体系有机质与有机碳氢氮恢复动力学研究   总被引：3，自引：0，他引：3  

彭平安  秦艳  张辉  刘大永  张善文  隋风贵  李钜源  李政 《海相油气地质》2008,13(2):27-36

在封闭体系的条件下,对典型的Ⅰ、Ⅱ、Ⅲ型干酪根在热演化过程中的损失进行生烃动力学研究,获得了Ⅰ、Ⅱ、Ⅲ型干酪根的总量、有机碳、氢以及氮质量损失动力学参数。用Kinetics软件计算了封闭体系干酪根有机碳丰度、氢碳原子比和氮碳原子比的恢复系数。认为在对高成熟—过成熟干酪根进行生烃评价时,Ⅰ、Ⅲ型干酪根残余有机碳丰度需要进行恢复,而Ⅱ型干酪根残余有机碳丰度不需要恢复。三种类型干酪根的氢碳原子比均需要进行恢复。  相似文献