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海域水质模型长周期数值模拟中,模型参数全时段统一赋值的方法忽略了参数随时间动态变化的物理特性,降低了模型的可靠性,增加了海域水质模型验证工作的难度.本文建立了将数据驱动模型和水质模型有机结合的参数动态反演的新方法:以水质模型多参数设计工况的数值模拟,构建海域内部观测点污染物浓度响应解集,并将解集划分为若干时段;应用基于人工神经网络的数据驱动模型归纳建立观测点每一时段内污染物浓度同多个模型参数之间的非线性关系;将实测资料带入关系中,进行模型参数随时间变化的动态反演.以渤海海域水质模型为例,采用“孪生”实验验证参数动态反演新方法的可行性,结果表明该方法是有效的,能够保证模拟周期内较高的数值精度,提高了模型的准确性. 相似文献
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地下水多组分反应运移模型是刻画解释微生物降解地下水有机污染物的水文地质、生物地球化学耦合过程并对各组分分布特征进行预测的重要工具.反应运移模型往往包含多个参数,并含有多种不同生物化学组分的观测数据,高维参数和观测数据类型的多样性给模型参数的反演带来了极大的困难.因此,本文以反应运移软件PHT3D模拟某污染场地地下水中有机污染物生物降解的理想正问题为例,对比讨论了不同观测数据权重对反应运移模型参数估计的影响.结果表明:未考虑观测数据权重时参数估计结果与真实值相差较大,而采用反映观测误差的权重时参数估计值与真实值更接近.敏感性分析表明,参数对于不同观测组数据的敏感度有明显差异.对于本例,生物降解模型中的降解反应参数最敏感,其次是溶解速率迁移常数,多相溶解度摩尔分数敏感度较小. 相似文献
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腐植质与有机污染物作用研究进展 总被引:6,自引:0,他引:6
综述了腐殖质的结构特性、与有机污染物的结合性质以及腐殖质对有机污染物毒性和生物可利用率的影响。已有的研究表明:腐殖质与有机污染物的结合能力受到下列因素的影响———腐殖质的结构、腐殖质的分子量和浓度、有机物的结构、水环境条件以及光化学降解作用等;腐殖质的存在通常降低了有机污染物的毒性,但在少数情况下例外,其推测性的机理还有待于实验进一步验证;有机污染物的生物可利用率不仅与腐殖质的浓度和组成有关,还受水体PH值的影响。本文同时对腐殖质的结构和多样性的研究、腐殖质对极性有机污染物的迁移、毒性和生物可利用率的研究、腐殖质增强某些有机物毒性的机理的研究进行了展望。 相似文献
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室外空气污染对室内空气质量的影响研究 总被引:1,自引:0,他引:1
利用数值模拟方法,研究了单个建筑物外存在点污染源时室外空气污染对室内空气质量的影响.首先利用点污染源时单个建筑物周围污染物扩散的风洞实验验证了计算模型和方法的正确性,再利用自然通风的风洞实验,计算了不同污染源位置和建筑物进风口时的室内外速度场和污染物浓度场.结果表明:速度场的计算结果与风洞实验结果基本吻合,无量纲通风量的计算值略小于实验值;建筑物迎风面回流区上方的气流进入室内;当点污染源位于建筑物前的距离和建筑物高度之比约等于1时,污染源在地面处的室内污染物浓度要小于源在建筑物高度一半处的;建筑物进风口的挡风板对室内污染物浓度的影响不大;根据壁面上污染物浓度的分布来改变进风口位置,是减少室内空气受室外污染影响的有效方法. 相似文献
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数值风洞与物理风洞对烟塔合一排烟的比较研究 总被引:1,自引:0,他引:1
热电厂"烟塔合一"排烟技术因其初期投资和运行维护费用少,排烟效果好、SO2落地浓度低等优势,特别是在机场附近的净空限高和对景观环境有特殊要求的地区具有广阔的发展空间。目前国内外广泛使用的大气污染物预测模型——德国模式在烟塔合一排烟方式的预测上尚存在许多问题,如大风下洗条件下,冷却塔附近空腔区的大小和范围、空腔区污染物最大地面浓度等难以给出准确的预测结果。为准确预测烟塔合一排烟方式的大气污染物扩散情况,一种新的大气污染物扩散预测模式——数值风洞模型以及物理风洞实验被用于模拟烟塔合一的环境影响,分析数值风洞模式和物理风洞实验在大气环境预测领域应用的适用性和优缺点。2个预测方法的结果表明:在烟塔合一排烟方式下,大气污染物最大落地浓度随风速增加而增加同时在冷却塔下风向存在负压区,污染物在该区域高浓度聚集。对2种方法进行比较,物理风洞实验由于受到物质和气象等条件的限制,无法得到精确的预测结果以及无法直观地描述空腔区的产生和变化规律。而数值风洞模拟具有更大的自由度和灵活性,预测出在夏季6 m/s风速下,冷却塔下风向最大落地浓度出现峰值,属于最不利的气象条件。同时该方法可利用图形化手段实现对空腔区产生、变化、破碎至再生成的全过程描述,从而建立了一种大气污染预测的重要手段。 相似文献
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以某含1,2-二氯乙烷等10种有机物污染土壤回填项目为例,介绍了2种方法(三相平衡耦合地下水稀释模型和Sesoil耦合地下水稀释模型)在评估土壤污染对地下水影响中的具体应用并进行了比较. 结果表明,采用US EPA(美国国家环境保护局)推荐的三相平衡耦合地下水稀释模型预测的地下水中目标污染物浓度高于新泽西州推荐的Sesoil耦合地下水稀释模型的3~10倍,污染物亨利常数及碳水分配系数越高,二者的差异越明显,达到1个数量级. 对于多环芳烃类的强疏水性有机污染物,2种方法的评估结论无本质差异. 出于保守性及调查成本的考虑,在制订国家或区域范围基于保护地下水的土壤通用筛选值时,建议采用所需参数相对较少的三相平衡耦合地下水稀释模型的方法,以节约调查成本. 对于具体评估项目,当污染物浓度超过通用筛选值时,建议进一步对场地水文地质条件进行调查,采用Sesoil耦合地下水稀释模型重新评估并计算该特定场地的筛选值,以节约修复成本. 相似文献
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使用多介质模型建模方法,构建了针对疏水性液体物质的顶空被动加标系统的动力学模型,以浮萍生长抑制试验系统和鱼类胚胎毒性试验系统为例,得出了3种不同性质的疏水性液体物质正壬烷、十甲基环五硅氧烷(D5)和邻苯二甲酸(2-乙基己基)酯(DEHP)在顶空被动加标系统中的浓度变化,并使用实测浓度对模型进行验证.结果表明,正壬烷和D5在两类系统中平衡24h后,水中浓度便已达到完全平衡时浓度的80%以上,而DEHP的平衡时间很长,不适合使用顶空被动加标系统开展试验,原因是DEHP的挥发性极低.实测浓度和模型预测结果偏差较小.敏感性分析表明,试验系统参数中容器直径对待测物质在水中浓度影响较大,因此可通过调整容器直径来缩短平衡时间,或提高平衡后化学物质在水中的浓度.使用所构建的模型可确定试验系统平衡时间、水中待测物质浓度和待测物质添加体积是否满足试验需求,并可通过敏感性分析来优化试验系统参数,提升试验效率和质量.以上结果完善了顶空被动加标系统应用的理论基础. 相似文献
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Ion adsorption components in liquid/solid systems 总被引:6,自引:2,他引:4
Experiments on Zn^2+ and Cd^2+ adsorptions on vermiculite in aqueous solutions were conducted to investigate the widely observed adsorbent concentration effect on the traditionally defined adsorption isotherm in the adsorbate range 25--500 mg/L and adsorbent range 10--150 g/L. The results showed that the equilibrium ion adsorption density did not correspond to a unique equilibrium ion concentration in liquid phase. Three adsorbate/adsorbent ratios, the equilibrium adsorption density, the ratio of equilibrium adsorbate concentration in liquid phase to adsorbent concentration, and the ratio of initial adsorbate concentration to adsorbent concentration, were found to be related with unique values in the tested range. Based on the assumption that the equilibrium state of a liquid/solid adsorption system is determined by four mutually related components: adsorbate in liquid phase, adsorbate in solid phase, uncovered adsorption site and covered adsorption site, and that the equilibrium chemical potentials of these components should be equalized, a new model was presented for describing ion adsorption isotherm in liquid/solid systems. The proposed model fit well the experimental data obtained from the examined samples. 相似文献
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水溶液中磷的吸附与预测模型 总被引:2,自引:2,他引:0
用红壤和水滑石作为吸附剂,进行了水溶液中磷的等温吸附试验,目的是研究吸附剂(W)0效应和起始吸附质浓度(C)0效应对经典方程参数变异的影响,分析经典Langmuir和Freundlich方程在液/固离子吸附体系中的适用性和验证新吸附模型的预测精确度。试验结果显示,红壤和水滑石在吸附磷的过程中存在明显的吸附剂和吸附质浓度效应,单一的经典方程仅适用于给定吸附剂或吸附质浓度的体系,因此,用其参数来表征不同吸附剂的吸附能力或描述不同吸附剂或吸附质浓度水平上的吸附规律具有一定的局限性。数据分析表明,单位吸附剂的平衡吸附量qe不唯一由初始浓度C0或液相平衡浓度Ce所决定,而是C0/W0或Ce/W0的函数,新吸附预测模型能较好的反映红壤和水滑石磷吸附的总体趋势。新的预测模型用来描述红壤和水滑石的磷吸附曲线时具有较高的精确度。在实践中,新模型可用来预测给定条件下磷的吸附量和所需吸附剂的用量。 相似文献
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为了定量生态相关物种基因组中低丰度的5-甲基-2-脱氧胞苷(5-mdC),建立了一种采用高效液相色谱串联质谱(HPLC-MS/MS)的无标记方法.全基因组DNA甲基化计算公式5-mdC (mole)/(5-mdC (mole)+dC (mole)可以转化为1/(1+dC (mole)/5-mdC (mole)),然后通过HPLC-MS/MS得到DNA样品中5-mdC和dC的物质的量比(dC (mole)/5-mdC (mole))即可得到基因组DNA甲基化值.此外,还对HPLC条件进行了优化使正常核苷和修饰核苷基线分离,消除分析物的交叉干扰.本方法避免了使用昂贵的稳定同位素标记内标,在等度高效液相色谱条件下实现了正常和修饰核苷基线分离,5-mdC和dC的保留时间分别为5.50和3.06min.5-mdC和dC的定量限分别为14.2和19.1pg/mL.日内和日间偏差和准确性(相对误差)都≤ 10%.该方法测定的小牛胸腺DNA和大型蚤及秀丽线虫的全基因组DNA甲基化值分别为(6.44 ±0.25)%,(0.097 ±0.010)%和(0.025 ±0.002)%.采用HPLC-MS/MS技术建立并验证了一种快速、高精密度和灵敏度的DNA样品全基因组DNA甲基化测定方法,适用于评估环境污染物对生态学相关物种的潜在表观遗传风险. 相似文献
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Solubility data of recalcitrant contaminants in cosolvents is essential to determine their potential applications in enhanced soil remediation. The solubilities of phenanthrene, anthracene, fluoranthene and benzo[a]pyrene in ethyl lactate/water and ethanol/water mixtures were measured using equilibrium techniques. The cosolvency powers derived from solubility data were then applied to the model developed from the solvophobic approach to predict the capability of ethyl lactate and ethanol in enhancing the desorption of contaminants from soils. Both ethyl lactate and ethanol cosolvents were shown to be able to enhance the solubilisation of the tested four polycyclic aromatic hydrocarbons by > 4 orders of magnitude above the levels obtained with water alone. However, ethyl lactate demonstrated a greater capacity to enhance PAH solubility than ethanol. The cosolvency powers of ethyl lactate/water system obtained from the end-to-end slope (σ) and the end-to-half slope (σ0.5) of the solubilisation curve were 1.0--1.5 and 2.0--2.9 higher than ethanol/water system respectively. In line with this, ethyl lactate/water was demonstrated to enhance the desorption of contaminants from soil by 20%--37% and 18%--61% higher compared to ethanol/water system in low organic content and high organic content soils respectively, with a 2:1 (V/W) ratio of solution:soil and with cosolvent fraction as low as 0.4. With the exception of benzo[a]pyrene, the experimental desorption results agreed fairly with the predicted values, under an applied solution:soil ratio that was enough to hold the capacity of released contaminants. 相似文献
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Electrokinetic movement of multiple chlorobenzenes in contaminated soils
in the presence of β-cyclodextrin 总被引:1,自引:0,他引:1
This study investigated the electrokinetic(EK)behavior of multiple chlorobenzenes,including 1,2,3,4-tetrachlorobenzene(TeCB), 1,2,4,5-tetrachlorobenzene(i-TeCB),and 1,2,3-trichlorobenzene(TCB)in contaminated clayed soils.The effect ofβ-cyclodextrin(β- CD)on the EK removal of the chlorobenzenes was studied.The largest removal was obtained when Na_2CO_3/NaHCO_3 buffer was used as anodic purging solution withoutβ-CD.The removal efficiencies were related to the aqueous solubilities of chlorobenzenes. With the same cumulative electroosmotic flow,greater solubility led to higher removal efficiency.The addition ofβ-CD inhibited the EK removal efficiency of all chlorobenzenes.The inhibition increased with the increase ofβ-CD concentration.With the sameβ-CD concentration,the inhibition increased with the rise of electric potential.It was found that the inclusion compounds betweenβ-CD and chlorobenzenzes were less soluble than chlorobenzenes.The formation of the less soluble inclusion compounds reduced the aqueous solubility of chlorobenzenes and led to the partial immobilization of the chlorobenzenes that desorbed from soil.It was feasible to use the EK technology to remove ehlorobenzenes in contaminated soils using water as the anodic flushing solution.The addition ofβ-CD was not recommended for the EK removal of chlorobenzenes. 相似文献
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采用批量平衡法,比较研究了苹果角质结合蜡质、分离蜡质和重建蜡质对极性有机污染物甲萘酚的吸附作用,并探讨了不同负载量的重建蜡质的吸附性能,以期为准确预测有机污染物在不同状态蜡质组分上的吸附行为提供依据.结果表明,甲萘酚在苹果角质层、脱蜡角质层、分离蜡质(IW)、重建蜡质(BW)上的等温吸附线呈非线性,符合Freundlich方程.植物蜡质对甲萘酚的吸附作用与蜡质所处状态密切相关,吸附能力(Koc)大小顺序为:重建蜡质(321.2) > 分离蜡质(190.4) > 角质结合蜡质(128.4),表明植物角质层进入土壤后发生演化过程中,其中不易降解的蜡质的吸附能力逐渐增大.重建蜡质(BW)的吸附系数(Kd)与甲萘酚的浓度呈负相关,与蜡质的负载量呈正有关.在低浓度时,甲萘酚的有机碳标化吸附系数Koc值随有机碳含量(foc)增大先增大后减小,存在一些强的特殊作用;而高浓度时, Koc-基本为一常数,不随蜡质负载量而变化,主要吸附机理为分配作用.角质结合蜡质(CW)对角质层的总吸附作用的贡献较小,但随甲萘酚平衡浓度的增大而逐渐增大,并于高浓度时, CW的吸附能力与IW相当. 相似文献
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This study investigated the electrokinetic (EK) behavior of multiple chlorobenzenes, including 1,2,3,4-tetrachlorobenzene (TeCB), 1,2,4,5-tetrachlorobenzene (i-TeCB), and 1,2,3-trichlorobenzene (TCB) in contaminated clayed soils. The effect of β-cyclodextrin (β-CD) on the EK removal of the chlorobenzenes was studied. The largest removal was obtained when Na2CO3/NaHCO3 buffer was used as anodic purging solution without β-CD. The removal efficiencies were related to the aqueous solubilities of chlorobenzenes. With the same cumulative electroosmotic flow, greater solubility led to higher removal efficiency. The addition of β-CD inhibited the EK removal efficiency of all chlorobenzenes. The inhibition increased with the increase of β-CD concentration. With the same β-CD concentration, the inhibition increased with the rise of electric potential. It was found that the inclusion compounds between β-CD and chlorobenzenzes were less soluble than chlorobenzenes. The formation of the less soluble inclusion compounds reduced the aqueous solubility of chlorobenzenes and led to the partial immobilization of the chlorobenzenes that desorbed from soil. It was feasible to use the EK technology to remove chlorobenzenes in contaminated soils using water as the anodic flushing solution. The addition of β-CD was not recommended for the EK removal of chlorobenzenes. 相似文献