海藻酸钙固定化零价铁抗团聚及堵塞的作用机制

以海藻酸钠（SA）、氯化钙、微米零价铁（MZVI）为原料，制备了海藻酸钙（CA）固定化MZVI填料（CAZ），通过静态烧杯实验和动态PRB模型实验，探讨了CA运用对Cr(Ⅵ)的去除性能的影响，并通过电镜扫描分析了CA避免团聚、堵塞机制。实验结果表明，CA凝胶颗粒的运用能显著提升MZVI的除Cr(Ⅵ)性能，CAZ相比MZVI对Cr(Ⅵ)的去除率和反应速率分别提升7.1倍、23.0倍；MZVI利用率的提高是CAZ反应器处理Cr(Ⅵ)水量显著大于MZVI反应器的主要原因，MZVI反应速率的提高是CAZ反应器出水Cr(Ⅵ)浓度显著低于MZVI反应器的主要原因。电镜扫描结果表明，SA与氯化钙交联形成的CA具有丰富的骨架孔道结构，具有骨架支撑作用，能有效克服MZVI颗粒因重力作用导致团聚、降低比表面积的缺陷。CA表层固定的MZVI颗粒与Cr(Ⅵ)反应生成的(Fe_xCr_1-x)(OH)₃ 络合沉淀会冲破CA表层外壳，释放到零价铁-渗透反应墙（Fe⁰-PRB）系统中，导致PRB反应初期出现堵塞现象；大部分MZVI颗粒被固定在CA内部，CA内部有较多孔隙结构，这些孔隙结构会控制(Fe_xCr_1-x)(OH)₃ 络合沉淀释放，从而缓解了Fe⁰-PRB后期长期运行持续堵塞的问题。     

LTE系统DVRB和DPRB映射的研究与实现

通过对分布式虚拟资源块(Distributed Virtual Resource Block,DVRB)与物理资源块(Distributed Physical Resource Block,PRB)的研究,结合LTE系统特性,提出了一种适用于LTE系统的分布式虚拟资源块映射到物理资源块的DSP实现方案。该算法可直接计算出已排好序的物理资源块索引,最后将多个虚拟资源块映射模块的结果进行级联得到所需的物理资源块的索引,算法简单,计算量小,且便于在TMS320C64x DSP中实现。将该方案应用于TD-LTE射频一致性测试系统的开发中,实际运行验证了该方案的可行性、高效性。     

基于生物阴极MFC的PRB中试系统处理AMD研究

为研究基于SRB生物阴极微生物电池(MFC)的固定化硫酸盐还原菌可渗透反应墙(PRB)对提高PRB处理酸性矿井废水(AMD)效果的影响,构建了中试系统,考察了进水不同p H值、重金属离子浓度及不同HRT对系统处理AMD效果的影响。结果表明:(1)MFC区有很好的调节p H功能,进水p H=3,仍能调节PRB生化反应区进水及系统出水稳定在6.5左右。(2)重金属离子的去除以MFC区为主,系统最终出水重金属离子去除率在95%左右;调节HRT=4~2 d,Fe~(2+),Cu~(2+),Zn~(2+),Ni~(2+)去除速率750~1 500 mg/(m~3·h),而Mn~(2+)去除速率略低为600~1 000 mg/(m~3·h)。(3)硫酸根的去除速率随碳源减少呈下降趋势;MFC外电压随碳源以及菌量的变化而显著变化。     

高氟地下水PRB修复介质的选择

高氟地下水在我国分布广泛,直接作饮用水对当地居民健康产生很大危害.为了开发出经济高效的PRB介质,研究了沸石、骨炭、黏土矿物(海泡石、蒙脱石、高岭土、硅藻土等)、活性氧化铝、石灰石、分子筛、PAM、树脂等介质材料的特点,分析了PRB用于高氟地下水修复的技术关键-PRB介质选择.结果表明:活性氧化铝结构及出水氟含量稳定、...     

Evaluation of polyaromatic hydrocarbon removal from aqueous solutions using activated carbon and hyper‐crosslinked polymer (Macronet MN200)

BACKGROUND: Sorption of polycyclic aromatic hydrocarbons (PAHs) on activated carbon and the Macronet polymeric sorbent MN200 was investigated to determine the effectiveness of each sorbent for removal of pollutants from aqueous solution and their possible use as sorbent materials for groundwater. Experiments were carried out to determine the loading capacities of a family of PAHs (acenaphthene, anthracene, fluoranthene, fluorene, naphthalene and pyrene). RESULTS: Activated carbon was the more effective sorbent, with maximum loadings of PAHs between 90 and 230 g kg^?1, while MN200 resin showed values of 25–160 g kg^?1. Loading isotherms based on the Langmuir, Freundlich and Redlich–Peterson models were determined. The hydrophobic character of the pollutants appeared as an important parameter related to the sorption process. Equilibrium and kinetic parameters were used to determine the retardation factors for each PAH. CONCLUSION: The calculated values for the simulation of barrier thickness using both sorbents, taking into account EU requirements for PAHs in groundwater effluent, were perfectly reasonable as a first estimate. The better kinetic properties of MN200 are evident in lower hydraulic residence times and consequently in a lower barrier thickness. Copyright © 2008 Society of Chemical Industry     

SCR deactivation in a full-scale cofired utility boiler

The Energy and Environmental Research Center installed a portable slipstream selective catalytic reduction (SCR) reactor in the convective pass of a utility boiler cofiring wood waste and Powder River Basin (PRB) coal. Catalyst sections were removed after 43, 128, and 171 days of operation. SCR catalytic activity was determined for each section, and a sample of one section was examined under a scanning electron microscope to look for signs of catalyst blinding and/or poisoning. The catalyst deactivated at an apparently inverse rate with an initial deactivation rate of 18% every 1000 h. The major mode of deactivation appeared to be pore blocking by combined alkali and calcium sulfate deposition and growth.     

地下水污染修复的活性渗滤墙技术

活性渗滤墙是一种现场修复受污染地下水的新型技术，具有原理简单，施工方便，运行费用低廉等特点，活性渗滤墙垂直于地下水流动方向设置，当地下水流通过活性渗滤墙时，污染物与墙体材料发生化学反应，从而达到环境修复的目的。文中综述了活性渗滤墙技术的修复机理和实际应用，大量研究表明，应用金属铁作为活性渗滤墙材料，可以去除地下水中的重金属以及有机污染物，目前活性渗滤墙已经在世界各地应用，是一种非常有发展前景的环境污染修复技术。     

Evaluation of matrices for the sorption and biodegradation of phenanthrene

Permeable reactive barriers (PRBs), a new cost effective technology for the remediation of contaminated groundwater, have rarely been considered for PAH contamination. We evaluated three candidate matrices (activated carbon (AC), pouzzolana coated (PzF) or not (Pz) with heavy fuel oil) for phenanthrene (PHE) sorption capacity and the biodegradation of adsorbed PHE. Adsorption-desorption batch experiments showed higher sorption capacity of AC than PzF (60 fold) and Pz (1,500 fold). Sorption isotherms were not linear for all matrices as described by a Freundlich model. Phenanthrene desorption from AC and PzF within 48 h was limited (1-3%). Mineralization of (14)C-PHE by a PAH-degrading bacterial strain increased in the presence of AC and Pz (+16 and +12%). Among the three matrices, AC may be a good candidate for PRBs due to high adsorption, low desorption and increased PHE degradation.     

羟基磷灰石复合材料对地下水中铀吸附去除研究进展

铀矿山尾矿库周边地下水在铀矿的风化、淋滤、渗漏等作用下,给地下水和人类带来长期的健康隐患。可渗透反应墙(PRB)作为一种原位修复技术,具有无动力运行、环境影响小和成本低等优点,已经在地下水污染修复中得到了应用。羟基磷灰石(HAP)因具有成本低、原料广泛、生物相容性等优点,成为去除地下水中铀废水的最具潜力介质材料。综述了羟基磷灰石在处理含铀废水中的影响因素,主要包括羟基磷灰石制备方法、改性方法,对含铀废水去除影响研究。并对羟基磷灰石除铀进行机理分析,包括羟基磷灰石形貌、铀溶液pH、共存阴离子等对铀的去除影响。羟基磷灰石(HAP)因具有成本低、原料广泛、生物相容性等优点,成为去除地下水铀的最具潜力介质材料。     

沸石负载纳米氧化铁处理氮磷污水研究

采用共沉淀法制备了沸石负载纳米氧化铁复合材料(沸石@Fe_3O_4),并采用静态吸附试验探究了pH、吸附动力学、等温吸附模型及热力学等对沸石@Fe_3O_4吸附模拟氨氮废水溶液的影响。试验表明,当溶液pH为6时,沸石@Fe_3O_4对水中氨氮的吸附能力达到最高值,随溶液中pH的升高,沸石@Fe_3O_4对水中磷的吸附能力逐渐降低。可采用准二级动力学模型描述沸石@Fe_3O_4对水中氨氮和磷的吸附动力学过程。Langmuir吸附等温线模型的线性拟合结果表明,氨氮和磷最大理论单位吸附量分别为7.92和9.09mg/g。