四钛酸钾晶须处理含铀废水实验研究

实验研究新型无机离子交换剂——四钛酸钾晶须(K2Ti4O9)处理含铀废水。通过静态交换实验优化影响铀去除率的因子,并测定四钛酸钾晶须对铀的饱和交换容量;利用制备的四钛酸钾-PVC膜进行动态交换实验;初步实验研究了四钛酸钾在不同温度和配方下的烧结固化。结果表明,在酸性条件下,四钛酸钾对铀的去除率>95%,最佳pH为3～4,对铀的静态饱和交换容量约为894μg/g;制备的四钛酸钾-PVC膜对铀的动态交换容量约为185μg/g;80%K2Ti4O9+20%高岭土在1200℃下烧结效果良好。     

基于水体交换模拟的白洋淀围堤围埝拆除方案比选

白洋淀是华北平原最大的浅水湖泊,因水产养殖等社会经济活动需要,淀内高密度建设围堤围埝,不利于水体交换,影响了水体环境和生态功能.基于MIKE 21软件,构建了白洋淀二维水动力模拟模型,选取水力滞留时间、滞水区面积比、流线分布均匀度等指标,提出了水体交换能力综合改善率计算方法,模拟了基准与低、中、高3种围堤围埝拆除强度情景的水体交换能力变化,进行了方案比选.结果表明,与基准情景相比,3种拆除强度情景下,流线分布均匀度均有增加,滞水区面积比分别减少6.17%、9.04%、9.24%,水力滞留时间分别缩短约1、2、3 d,水体交换能力综合改善率分别为34.37%、42.84%、47.25%,3种拆除情景对水体交换能力提升均有明显效果.本研究可为湖泊阻水构筑物拆除方案比选提供技术方法,为湖泊水体交换能力提升、水生态修复提供技术依据.     

基于IRGA通量箱法的草坪夏季晴天CO_2净交换量日动态

利用红外气体箱式法(Infrared Gas Analyze,IRGA),于2008年8月晴天对福州市马尼拉草坪(Zoysia matrel-la)的生态系统CO2净交换(NEE)和环境因子进行观测,阐明NEE及其组分的昼夜动态变化特征和影响因子。马尼拉草坪NEE的昼夜变化呈现为单峰型曲线,昼间其变化规律较强,夜间呈波动状态。NEE(取绝对值)最大值出现在10:00,最小值出现在16:00左右。太阳辐射、腔室内空气相对湿度和气温与NEE的相关性均为极显著(p<0.01),太阳辐射、腔室内空气相对湿度和5cm土壤温度共同解释NEE速率昼夜变异的89.30%。太阳辐射和腔室内空气相对湿度是影响草坪生态系统CO2净交换量日动态的主导环境因子;其中,太阳辐射可以单独解释NEE速率昼夜变化的79.70%,腔室内空气相对湿度可以单独解释NEE速率昼夜变化的50.40%;夏季晴天草坪生态系统在日尺度上表现为净吸收,平均CO2净交换速率为-4.11μmol/(m2.s)(负值表示吸收),平均日总通量为-0.18 mol/(m2.d)。     

黄河水中悬浮粒子对镉离子的交换吸附等温线

研究了黄河水中悬浮粒子对 Cd²⁺ 的交换吸附等温线以及赖氨酸和门冬氨酸对吸附作用的影响．研究结果得到一类具有一个“拐点”、两个“平台”的新型河流等温线,用分级离子交换等温式求出平衡常数 K₁ 和 K₂ ．当低浓度的氨基酸存在时,对镉与悬浮粒子的交换吸附起促进作用．促进作用的程度与氨基酸的等电点有关,赖氨酸的促进作用较门冬氨酸大．     

水中微量甲基膦酸类化合物的树脂富集与GC／MS分析

本文使用三种阴离子交换树脂（即大孔弱碱型Ｄ－３０１－Ｒ,强碱型Ｄ－２９６,２０１Ｘ７）柱对水中微量甲基膦酸类化合物的富集方法进行了研究。含磷毒剂降解产物的水样用气相色谱／质谱法进行定性定量分析。结果表明,Ｄ－３０１－Ｒ阴离子交换树脂柱对甲基膦酸的富集回收率高于６０％。     

镁盐改性活性炭对普拉红B的吸附性能研究

运用化学沉淀-原位复合法制得氢氧化镁/活性炭复合材料(Mg(OH)2/AC),对其比表面积和XRD谱进行了表征,考察了该复合材料对普拉红B的脱色性能.结果表明,在293～313 K下,Langmuir模型和Freundlich模型都能很好地描述Mg(OH)2/AC对普拉红B的等温吸附过程,而Langmuir模型更为合适...     

Capturing the lost phosphorus

Minable phosphorus (P) reserves are being depleted and will need to be replaced by recovering P that currently is lost from the agricultural system, causing water-quality problems. The largest two flows of lost P are in agricultural runoff and erosion (∼46% of mined P globally) and animal wastes (∼40%). These flows are quite distinct. Runoff has a very high volumetric flow rate, but a low P concentration; animal wastes have low flow rates, but a high P concentration together with a high concentration of organic material. Recovering the lost P in animal wastes is technically and economically more tractable, and it is the focus for this review of promising P-capture technologies. P capture requires that organic P be transformed into inorganic P (phosphate). For high-strength animal wastes, P release can be accomplished in tandem with anaerobic treatment that converts the energy value in the organic matter to CH₄, H₂, or electricity. Once present as phosphate, the P can be captured in a reusable form by four approaches. Most well developed is precipitation as magnesium or calcium solids. Less developed, but promising are adsorption to iron-based adsorbents, ion exchange to phosphate-selective solids, and uptake by photosynthetic microorganisms or P-selective proteins.     

Sorption of dissolved lead from shooting range soils using hydroxyapatite amendments synthesized from industrial byproducts as affected by varying pH conditions

For immobilization technologies to be successful, the use of readily available and cost advantageous amendment is important when the remediation targets vast amounts of contaminated soils. The objectives of this study were to investigate whether the byproduct-synthesized hydroxyapatite can be used as an immobilizing amendment for dissolved Pb from a shooting range soil, and to model the kinetic data collected from dissolution experiments. A soil–solution kinetic experiment was conducted under fixed pH conditions as a function of time. A Pb-contaminated soil was reacted with various hydroxyapatite amendments to determine the dissolution rate and mineral products of soil Pb. Three types of amendments used were pure hydroxyapatite (HA), and poorly crystalline hydroxyapatites synthesized from gypsum waste (CHA), and synthesized from incinerated poultry litter (PHA). The dissolved Pb concentration decreased with the addition of amendments at pH 3–7. Both CHA and PHA were more effective than HA for attenuating Pb dissolution at pH 6 and above. According to the thermodynamic calculation at pH 6, the dissolved Pb concentration for CHA and PHA treatments was predicted to be 66% and 50% lower than that of HA treatment, respectively. A better Pb immobilization effect demonstrated by CHA and PHA resulted in their greater solubility at higher pH, which may promote the formation of chloropyromorphite precipitates. Dissolution kinetics of soil Pb was adequately explained by pseudo-first order and pseudo-second order equations in acid pH ranges. According to the ion exchange model, an adequate agreement between the experimental data and regression curves was shown in the initial 40 min of the reaction process, but the accuracy of model predictability decreased thereafter. According to kinetic models and dissolution phenomena, CHA and PHA amendments had better Pb sorption capacity with rapid kinetics than pure hydroxyapatite at weak acid to neutral pH.     

碱激发胶凝材料及其固化Pb2+的试验研究

对碱激胶凝材料（碱-偏高岭土、碱-矿渣和碱-粉煤灰）与水-水泥体系固化Pb²⁺进行了试验研究,其中水-水泥体系为对比样。结果表明：对于相同稠度的碱激发胶凝材料,即使Pb²⁺含量达到2.4%,除了碱-粉煤灰的抗压强度略低外,其他都达到30 MPa以上,满足填埋或做建筑基材的使用要求;与水泥相比,碱激发胶凝材料能显著降低重金属离子（Pb²⁺）浸出浓度,其规律性与其NH⁺₄交换容量大小的规律性一致,与其固化体的抗压强度的大小没有相关性。