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1.
文章以河北沧县高氟水灌溉区土壤氟的积累与分布特征、氟等温吸附试验、吸附动力学试验、土柱模拟试验以及农作物含氟量为依据，对高氟水灌溉区水－土壤－植物系统氟迁移转化环境效应进行讨论分析，并提出了防止氟环境恶化的对策。 相似文献
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文章以河北沧县高氟水灌溉区土壤氟的积累与分布特征、氟等温吸附试验、吸附动力学试验、土柱模拟试验以及农作物含氟量为依据，对高氟水灌溉区水－土壤－植物系统氟迁移转化环境效应进行讨论分析，并提出了防止氟环境恶化的对策。 相似文献
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氟铝交互作用对茶园土壤氟吸附动力学特征的影响 总被引：1，自引：0，他引：1
在氟的不同初始浓度及不同水土比情况下,茶园土壤对氟的吸附平衡时间均在25min左右,但对动力学方程拟合效果有一定差异,除了初始浓度为4.0mg/L(水土比10∶1)、20.0mg/L(水土比40∶1)、100.0mg/L(水土比40∶1和20∶1)处理氟的吸附动力学不能用一级动力学方程或二级动力学方程描述外,其余处理均可以用双常数方程、Elovich方程、一级动力学方程、二级动力学方程和抛物线方程这5个动力学方程描述。在铝存在下,不同氟铝比对氟的吸附动力学过程有明显影响,表现为吸附速率下降,吸附平衡时间延长,50min左右达吸附平衡。动力学方程拟合效果虽然有一定差异,但均可以用这5个动力学方程描述。在有无铝存在下,茶园土壤氟的吸附动力学特征用双常数方程和Elovich方程描述的效果更好。 相似文献
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通过该区太古界一新生界氟的地层地球化学剖面及岩浆岩和土壤中氟的丰度的研究,论证了该区为一高氟的地球化学区。根据重矿物对比研究和地貌分析,阐明了泰沂隆起区太古界和元古界的高氟古老岩系为该区土壤沉积物源,黄河多次泛滥堆积（粘土矿物对氟的吸附）对土壤氟起了叠加富集的作用。研究揭示该区土壤水溶氟较高,经降水淋滤和浸取作用氟转入地下水,并在凹陷区或河间洼地中聚集,水体停泄、蒸发浓缩形成高氟地下水区。 相似文献
6.
氟与聚合羟基铝-蒙脱石复合体相互作用机理及土壤环境意义 总被引：5，自引：1，他引：4
在一定条件下利用钠基蒙脱石 (Na- Mt)合成了 OH/Al比为 1.6的聚合羟基铝-蒙脱石 (HyAl- Mt)复合体,并研究了弱酸性和强酸化条件下 HyAl- Mt与氟之间的相互作用及土壤环境意义.结果表明, pH在 5.0～ 9.0之间时, HyAl- Mt对氟的吸附受 pH影响小;当 pH < 4.5时,吸附能力随 pH减小迅速增大. pH 6.62时, HyAl- Mt对氟的吸附主要是络合交换机制,而 pH 3.02及高氟浓度条件下是表面吸附、矿物溶解及共沉淀-卷扫等协同作用机制,并使 HyAl- Mt具有异常高的氟去除能力.与蒙脱石粘土相比, HyAl- Mt的氟吸附能力明显提高,土壤中的 HyAl- Mt组分可有效地降低氟污染土壤中氟的迁移性并减少其生物有效性.在酸性氟污染的土壤中,氟与 HyAl- Mt相互作用还可一定程度抑制土壤的酸化.土壤酸度越大,这种抑制作用越明显.施用合成的 HyAl- Mt 可作为酸性氟污染土壤修复并控制土壤酸化的有效途经之一. 相似文献
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贵州省西部广泛分布上二叠统煤系地层,燃煤型氟中毒严重影响当地居民的身体健康。引起氟中毒的氟是多来源的,影响氟中毒的因素是多方面的。高氟含量的岩石粘土岩、煤、页岩等是氟的初始来源体;高氟含量土壤是氟第二个层次的来源;高氟含量土壤中种植的农作物是第三个层次的来源;燃煤烟尘直接排放室内空气中和用燃煤烘烤食物等,使空气、食物和水中氟含量增高,是一重要的人为氟来源。人通过呼吸高氟含量的空气和食(饮)用高氟含量的食物(水)将氟沉淀在体内,造成氟中毒。 相似文献
9.
土壤对氟离子吸附与解吸的动态土柱法研究 总被引：6，自引：0，他引：6
用饱水动态土柱法对氟离子的吸附与解吸特征及其反应动力学特征进行了初步探讨。结果表明，氟离子的吸附与解吸特征可分别用Ｌａｎｇｍｉｕｒ模型和Ｆｒｅｎｄｌｉｃｈ模型来表征，而氟的吸附与解吸反应动力学均可用Ｅｌｏｖｉｃｈ方程来述。吸附与解吸过程是一个由反应速率控制的不可逆过程。 相似文献
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不同茶园茶叶氟含量及土壤氟的形态分布 总被引：7，自引：0，他引：7
通过对我国中西南产茶区12个茶园土壤样品和茶叶样品的采集,探讨了不同茶园茶叶氟含量和茶园土壤氟的形态分布规律。老叶和嫩叶氟含量分别为221～1 504 mg/kg和49.0～602 mg/kg,老叶氟含量是嫩叶的2.5～8.1倍。各形态氟含量随土壤层次加深没有统一变化规律,但各层土壤不同形态氟含量均为残渣态铁锰氧化物态＞有机结合态＞水溶态＞交换态。土壤pH值、有机质含量和阳离子交换量对茶园土壤氟的形态分布有不同程度的影响。老叶和嫩叶氟含量随水溶态氟含量的增加均呈显著增加趋势,但与其他形态氟含量没有显著的相关关系。 相似文献
12.
为揭示冲积与湖积成因土壤镉的吸附特征,以安徽省当涂县冲积成因的江心洲和冲积、湖积成因的大陇乡根际土壤为研究对象,开展土壤镉的等温吸附实验和吸附动力学实验.等温吸附实验结果表明,冲积土壤镉的吸附量（S）、等温吸附常数（K）和固液分配系数（Kd）均较湖积土壤明显偏大,显示冲积土壤对镉的吸附能力较湖积土壤强;吸附动力学实验表明,冲积土壤的最大吸附量、平衡吸附量均较湖积土壤大,吸附速率也明显偏大,尤其在吸附实验早期更为显著;等温吸附常数K和平衡吸附速率Vb与土壤理化性质的分析表明,土壤pH是造成研究区土壤镉吸附能力差异的主要原因,其次为物理性粘粒含量;土壤pH是影响研究区冲积土壤镉吸附能力的主要因素;湖积土壤镉的吸附能力受土壤pH、有机质含量、Cd含量、物理性粘粒含量等因素的综合影响.研究对于揭示Cd在水土系统的迁移转化规律以及土壤Cd的污染防治具有重要的指导意义. 相似文献
13.
Reza Dehbandi Farid Moore Behnam Keshavarzi Ahmad Abbasnejad 《Environmental Earth Sciences》2017,76(4):177
Presence of fluoride in groundwater is a public health problem in the so-called endemic fluorosis belt of the central Iran, where the groundwater is the major source of drinking water in most urban and rural areas. Therefore, an attempt has been made to determine the hydrogeochemical factors controlling fluoride enrichment in the groundwater resources at this belt. Fluoride concentrations ranged from 0.20 to 1.99 mg/L (1.02 ± 0.47) in groundwater samples. The presence of different F-bearing minerals and also clay minerals in the soils and aquifer materials was confirmed using XRD analysis. To identify probable sources of dissolved F? and investigate groundwater quality, multivariate statistical analyses were carried out. Geochemical modeling indicated that all samples were undersaturated with respect to fluorite, halite, gypsum and anhydrite and mostly oversaturated with respect to calcite and dolomite. Contrary to most high-fluoride regions in the World, the high F? content was dominated by Na–Cl- and Ca–SO4-type groundwater in the study area. Besides, fluoride showed negative relationship with pH and HCO3 ? in groundwater. In order to assess the bioavailability of fluoride in soils, a two-step chemical fractionation method was applied. The results showed that fluoride in soils mostly accompanied with the residual and water-soluble fractions and was poorly associated with soil’s bonding sites. Calculated aqueous migration coefficient demonstrated that fluoride in the studied soils was mobile to easily leachable to the groundwater. Finally, the results demonstrated that combination of water–rock interaction and influence of clay minerals is geochemical mechanism responsible for controlling fluoride enrichment in groundwater. 相似文献
14.
用饱水动态土柱法对氟离子的吸附与解吸特征及其反应动力学特征进行了初步探讨。结果表明，氟离子的吸附与解吸特征可分别用Ｌａｎｇｍｉｕｒ模型和Ｆｒｅｎｄｌｉｃｈ模型来表征。而氟的吸附与解吸反应动力学均可用Ｅｌｏｖｉｃｈ方程来描述。吸附与解吸过程是一个由反应速率控制的不可逆过程。 相似文献
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岩溶区典型土壤对Cd2+的吸附特性 总被引：2，自引：2，他引：0
文章采用有序批试验,就岩溶区两种典型石灰土（棕色、黑色石灰土）对Cd2+的吸附行为进行研究。试验结果表明:石灰土对重金属Cd2+具有较强的吸附能力（平均吸附率范围89.84~98.84）,黑色石灰土的吸附能力高于棕色石灰土,吸附量随平衡浓度的增加而增大;Langmuir和Freundlich方程均能很好地描述两种石灰土对Cd2+的等温吸附过程,Freundlich方程拟合最优;两种石灰土吸附镉的动力学特征相似,吸附过程可分为快速反应、慢速反应和吸附平衡3个阶段,棕色石灰土对Cd2+吸附动力学的最优模型为Elovich方程和双常数方程（R>0.9）,黑色石灰土仅在Cd2+初始浓度为100 mg/L条件下,Elovich方程、双常数方程和W-M方程的模拟达到较显著水平（R>0.8）;有机质、碳酸钙含量及CEC值是影响石灰土对Cd2+吸附能力的主控因素,铁、铝、硅氧化物含量对Cd2+吸附影响不大;综合热力学、动力学及影响因素分析认为石灰土对Cd2+吸附机理包括土壤颗粒表面官能团的专性吸附及不均匀粒内扩散、静电作用等非专性吸附过程。 相似文献
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中国和世界上许多国家（地区） 都面临着饮用水氟含量超标的问题,因此研究氟的环境地球化学行为以及探索除氟
技术和原理至关重要。本实验采用廉价的非金属矿物羟基磷灰石作为吸附材料,研究羟基磷灰石吸附溶解态F-的地球化学
行为和机制,考察反应时间、pH、初始F-浓度等环境参数对吸附反应的影响。实验结果发现羟基磷灰石对F-的吸附反应需
进行到48 h以上时才接近反应平衡。在实验条件下（pH≥4）,F-的吸附量随pH升高而降低,羟基磷灰石对F-的吸附受pH
调控。同时还发现羟基磷灰石在pH=6条件下对F-的吸附等温线既满足Langmuir等温模式（R2=0.89） 同时也满足Freundlich
等温模式（R2=0.99）,并推导出该条件的理论最大吸附量为21.6×10-3。本研究还进一步采用了先进的XRD、SEM、
HR-TEM、19F NMR手段,系统地表征了反应前后吸附产物的形态和成分变化,发现在高F-浓度条件下,F-在羟基磷灰石表
面的吸附机制不再是单层的表面配位。核磁共振的结果表明F-可部分取代羟基磷灰石结构中的隧道羟基而形成含氟羟基磷
灰石。研究结果表明羟基磷灰石是一种相当具有潜力的除氟材料,值得进一步开发。 相似文献
17.
Fluorine adsorption by volcanic soils at Mt. Etna,Italy 总被引：1，自引：0，他引：1
Fluorine adsorption experiments were performed on 28 samples of the first 5 cm of topsoil collected on the flanks of Mt. Etna. The soil samples were equilibrated with F-rich rainwater (3.25 mg/L) at a soil/water weight ratio of 1/25. Aliquots of the supernatant were collected after 1, 7, 72, 720 and 5640 h and analysed for F content. The soil samples could be subdivided into three groups based on their F-adsorption behaviours after 1 h and at the end of the experiment: (1) negative adsorption (F released from the soil to the solution) after 1 h and negative or moderately positive adsorption at the end, (2) from negative after 1 h to strongly positive adsorption at the end, and (3) always strong positive adsorption. The adsorption capacity of the soils was positively correlated with the soil pH, the contents of finer granulometric fractions (clay and silt) and the weathering stage (as quantified by the chemical alteration index). The most F adsorbing soils are found at the periphery of the volcano where aquifers are more vulnerable to contamination due to the shallower depth of the water table. This study further evidences the importance of the Etnean soils in protecting groundwater from an excessive magmatic F input. 相似文献
18.
Dental fluorosis occurs because of fluoride over-absorption during tooth calcification and maturation. We studied fluoride concentration in water and soil samples of the Koohbanan region in Kerman province of southeastern Iran and the effects of calcium chloride and gypsum treatments in decreasing the amount of fluoride in water samples of this region. The results indicate that the high amount of fluoride in the water samples of Koohbanan region is not in agreement with the recommended amount of fluoride concentration for drinking water by World Health Organization (that is 1–1/5 mg/l). Applying calcium chloride and gypsum treatments decreased the amount of fluoride in the water samples showing that utilizing calcium chloride (6 mg/l) or gypsum (12 mg/l) can lower the fluoride concentration in the water samples of Koohbanan, and thus solve the observed dental fluorosis problem. 相似文献
19.
Bamidele I. Olu-Owolabi Paul N. Diagboya Chukwunonso P. Okoli Kayode O. Adebowale 《Environmental Earth Sciences》2016,75(24):1494
In order to predict exposure risks as well as appropriate remediation strategies for pesticides in soils, knowledge of pesticides sorption processes onto various representative soils is vital. Hence, laboratory batch experiments were carried out to study sorption of a pesticide, pentachlorophenol (PCP), on five soils obtained from different sub-Saharan agro-ecological zones (AEZs) in order to understand sorption equilibrium, kinetics, and thermodynamics. Experimental data showed that sorption equilibrium was attained within 24 h. The fitting of kinetic results and equilibrium data to different models suggested partly surface adsorption and partly partitioning of PCP within voids of the various soil components. Sorption was mainly attributed to sharing or exchange of valence electrons between negatively charged PCP molecules and positively charged soil sorption sites. The sorption process was spontaneous and accompanied by decreased entropy, but was pH and temperature dependent, reducing with increase in pH and temperature. The various soils’ PCP sorption capacities were directly proportional to their cation exchange capacities. The low PCP sorption observed in these soils suggested high risk of PCP being present in soil water solution, especially at higher temperatures, which can lead to contamination of the aquifer. This risk may be higher for soils obtained from AEZs with warmer natural temperatures. 相似文献
20.
Phosphorus transport in shallow groundwater in peri-urban Kampala, Uganda: results from field and laboratory measurements 总被引：1，自引：0，他引：1
To understand Phosphorus (P) sources and transport processes in the subsurface in Bwaise III Parish, Kampala, P attenuation
and adsorption capacities of soils were studied in situ and from laboratory measurements. Relationships between sorption parameters
and soil matrix properties, rates and mechanism of the adsorption process and soil P fractions were also investigated. P was
generally higher in the wet than the dry season, but for both seasons, the maximum was 5 mgP/l. P transport mechanisms appeared
to be a combination of adsorption, precipitation, leaching from the soil media and by colloids with the latter two playing
an important role in the wet season. The sorption process comprised two phases with the first stage rate constants being about
fourfold those of the second stage. The Langmuir isotherm described the sorption data well (R
2 ≥ 0.95) with the second soil layer exhibiting the highest sorption maximum (C
max) (average value 0.6 ± 0.17 mgP/gDW). The best prediction of C
max had organic carbon, Ca, available P and soil pH. Residual P consisting mostly of organics was the main fraction in all the
layers followed by inorganic HCl-P and NaOH-P in the top and middle layers, respectively. Loosely bound P (NH4Cl-P) was the least fraction (<0.4% of total P) in all layers indicating the high binding capacity of P by the soils. The
study results suggest that P dynamics is related to Ca, Fe and organic carbon content of the soils. 相似文献