板栗壳对重金属Cr（Ⅵ）吸附性能的研究

从废弃的植物材料中筛选出一种Cr(Ⅵ)高效吸附剂——板栗壳。研究了pH、接触时间、板栗壳用量、温度和Cr (Ⅵ)初始浓度对Cr(Ⅵ)吸附活性的影响。结果表明, 板栗壳的最佳pH为2～3。在pH 2时,Cr(Ⅵ)的去除率达99.7%。在15～35℃的温度范围内,板栗壳对Cr(Ⅵ)的去除率随温度的升高而增加。30℃时,Cr(Ⅵ)的去除率可达99%。板栗壳用量对Cr(Ⅵ)的去除有明显影响。由0.2 g增加到0.4 g时, Cr(Ⅵ)的去除率从90.6%提高到99%。在较宽的铬初始浓度范围内,板栗壳对Cr (Ⅵ)有明显的去除作用。     

Improved performance of a biomaterial-based cation exchanger for the adsorption of uranium(VI) from water and nuclear industry wastewater

The amine-modified polyhydroxyethylmethacrylate (poly(HEMA))-grafted biomaterial (tamarind fruit shell, TFS) carrying carboxyl functional groups at the chain end (PGTFS-COOH) was prepared and used as an adsorbent for the removal of uranium(VI) from water and nuclear industry wastewater. FTIR spectral analysis revealed that U(VI) ions and PGTFS-COOH formed a chelate complex. The adsorption process was relatively fast, requiring only 120 min to attain equilibrium. The adsorption kinetic data were best described by the pseudo-second-order equation. The equilibrium adsorption data were correlated with the Sips isotherm model. The maximum U(VI) ions uptake with PGTFS-COOH was estimated to be 100.79 mg/g. The complete removal of 10 mg/L U(VI) from simulated nuclear industry wastewater was achieved by 3.5 g/L PGTFS-COOH. The reusability of the adsorbent was demonstrated over 4 cycles using NaCl (1.0 M) + HCl (0.5 M) solution mixture to de-extract the U(VI). The results show that the PGTFS-COOH tested is very promising for the recovery of U(VI) from water and wastewater.     

低压稳流过滤器的研制及在油田污水处理中的应用

为了解决大庆油田现有核桃壳、石英砂过滤器反冲洗憋压、跑料和滤料再生困难等问题，在对原有过滤装置分析的基础上，根据反冲洗特性，对过滤器进行了改造，开发出低压稳流核桃壳过滤器和低压稳流石英砂过滤器。经现场测试，核桃壳过滤器反冲洗压力由原来的0.15～0.5 MPa降低到0.03～0.08 MPa，石英砂过滤器反冲洗压力由原来的0.27～0.46 MPa降低到0.17～0.20 MPa，且均能实现罐群水反冲洗。改造后核桃壳过滤器出水油平均含量13.4 mg/L，平均去除率为78.1%；出水悬浮物平均含量20.5 mg/L，平均去除率为55%。改造后石英砂过滤器出水油平均含量5 mg/L以下，平均去除率达到75%以上；出水悬浮物平均含量为9.8 mg/L，去除率达到80%以上。为了进一步提高过滤效果，在二级滤前投加絮凝剂形成微絮凝过滤工艺，出水悬浮物可达到3 mg/L，通过两级过滤达到特低渗透地层回注水标准。     

椰壳活性炭吸附消除VOCs

对一种椰壳活性炭对甲基丙烯酸甲酯的吸附消除行为进行了研究,重点考察了甲基丙烯酸甲酯的浓度、流速和吸附温度等条件以及水汽存在时对活性炭吸附行为的影响。结果表明,该颗粒活性炭对甲基丙烯酸甲酯有良好的吸附效果,甲基丙烯酸甲酯进口浓度和进气量的改变均会影响吸附饱和时间,导致其增加或减少。通过变温吸附实验确定降低环境温度对其吸附有促进作用。湿度为50%时吸附量相对干气饱和吸附量影响较小,说明该活性炭抗水汽能力较好。经多次重复再生实验,其饱和吸附量未见明显下降。     

Recovery of gold by chicken egg shell membrane-conjugated chitosan beads

We have successfully prepared a bead-type adsorbent from two materials with different adsorption characteristics. Heavy metals were removed by greatly swollen egg shell membrane-conjugated chitosan beads. The egg shell membrane accumulated and removed precious metal ions from a dilute aqueous solution with a high affinity in a short contact time. Experiments suggested that chitosan beads could take up gold ions with great capacity and selectivity by conjugation with egg shell membrane. Under certain conditions, the selective removal of gold and copper in a mixture of gold and copper ions by egg shell membrane-conjugated chitosan beads was 100% and 2%, respectively. Egg shell membrane-conjugated chitosan beads can be seen as a promising material to recover gold in wastewater from various industries, such as electroplating.     

核桃壳粉对水溶液中Pb2＋的吸附

实验通过间歇吸附方式研究了核桃壳粉对水溶液中Pb^2＋的吸附特性，探讨了核桃壳粉粒径及用量、溶液pH、Pb^2＋初始浓度等参数对吸附的影响，并讨论了吸附过程的热力学和动力学特征。结果表明，核桃壳粉对Pb^2＋吸附的最佳pH为5．0，去除率随吸附剂粒径的减小、用量的增加、Pb^2＋初始浓度的减小而增加。优化实验条件下，0～0．3mm15g／L的吸附剂在298K时，对pH=5的50mL50mg／LPb^2＋溶液的去除率达96．98％。核桃壳粉对Pb^2＋的吸附等温线符合Sips模型，在283、293和303K的最大吸附量分别为18．25、18．27和20．94mg／g。吸附过程是放热的、混乱度减小的自发过程，且符合准二级动力学模型。吸附速率常数随温度升高而减小，在293和303K时分别在90和120min基本达到平衡。结合FTIR和SEM手段发现核桃壳对Pb^2＋的吸附以物理吸附为主，同时包括离子交换、螯合等化学吸附以及颗粒内扩散步骤，是一个复杂的过程。     

基于几何参数的优化对双层柱面网壳结构动力性能的影响

以双层柱面网壳为研究对象,采用参数化设计语言APDL对AN SY S进行二次开发,实现了任意跨度双层柱面网壳的自动建模、加载、施加约束及求解。借此平台对柱面网壳结构进行模态和地震反应分析。首先,分析了结构自振特性随几何参数变化的特点,研究了结构的基频随矢跨比和网壳厚度的变化规律,结果表明,当矢跨比在1/3.6~1/5该范围内,结构的整体刚度较大;网壳厚度在1.8~2.1 m时,网壳整体刚度较大;对于矢跨比一定的网壳,随着厚度的增加,杆件的动内力大多增加,横向弦杆的二维与单维动内力比值有所增加,而纵向弦杆的二维与单维动内力则变化不大。然后,对网壳进行不同几何参数下的地震反应分析,给出了最大节点位移和最大杆件轴应力随几何参数变化的时程响应曲线,揭示了这类网壳的地震反应特点。     

Removal of Se(IV) from aqueous solution using sulphuric acid-treated peanut shell

A carbonaceous sorbent was prepared from peanut shell via sulphuric acid treatment. Se(IV) removal from aqueous solution on the sorbent was studied varying time, pH, Se(IV) concentration, temperature and sorbent status (wet and dry). Se(IV) removal was faster using the wet sorbent than the dry sorbent following a pseudo-first-order model. Se(IV) removal increases at low pH values, and decreases as pH increases until pH 7. Sorption was found to fit the Langmuir equation and sorption capacity for the wet sorbent was higher than that for the dry one. Both sorbents showed an increased selenium sorption by rising the temperature. Redox processes between Se(IV) and the carbon sorbent are involved. Analysis by scanning electron microscope and X-ray powder diffraction for the sorbent after the reaction with acidified Se(IV) confirmed the availability of elemental selenium as particles on the sorbent surface as a result of Se(IV) reduction. Physicochemical tests showed an increase in sorbent acidity, cation exchange capacity (CEC) and surface functionality after the reaction with acidified Se(IV), indicating the oxidation processes occurring on the sorbent surface. Due to its reduction properties, the sorbent seems efficient for Se(IV) removal from aqueous solution.     

牡蛎壳粉和石灰改良酸性水稻土对磷有效性、形态和酶活性的影响

我国南方粮食主产区土壤酸化治理是提升耕地地力促进粮食增产的重要内容,目的是探究酸化土壤改良剂牡蛎壳粉和石灰对水稻土酸度、磷有效性和形态以及酶活性和相关功能基因的影响.盆栽试验设计2种改良剂的3个施用量（0.05%、0.10%和0.15%）,以水稻为试验作物.结果表明：①牡蛎壳粉和石灰均显著提高土壤pH,降低土壤交换性酸,且改良效果随着改良剂用量增加而提高,相同用量下石灰对土壤酸性的改良效果高于牡蛎壳粉;② 4种有效磷提取剂提取的土壤有效磷测定结果表明,牡蛎壳粉和石灰显著提高H₂SO₄-P、Bray-1 P和Olsen-P含量,其中Olsen-P含量随改良剂用量的增加而提高.③土壤中不同形态无机磷含量表现为：Fe-P>Al-P>Ca-P,石灰和牡蛎壳粉显著提高Al-P和Fe-P含量,分别提高26.3%~37.4%和7.9%~23.7%;0.15%改良剂显著增加Ca-P含量;④石灰和牡蛎壳粉对土壤DHA、ALP、IPP活性和phoD基因拷贝数具有提高作用,而对土壤ACP活性、phoC和pqqC拷贝数表现为降低;⑤改良剂（0.10%和0.15%）显著提高水稻产量,0.15%用量的石灰和牡蛎壳粉分别提高水稻产量34.2%和46.8%,但对秸秆生物量无显著影响.相关分析表明,土壤无机磷和有效磷含量与pH和ALP活性呈显著正相关,改良剂通过消除土壤酸化和提高土壤磷酸酶活性来改善土壤磷营养状况,这对促进作物产量具有积极作用.     

Zero-valent iron nanoparticles in treatment of acid mine water from in situ uranium leaching

Acid mine water from in situ chemical leaching of uranium (Straz pod Ralskem, Czech Republic) was treated in laboratory scale experiments by zero-valent iron nanoparticles (nZVI). For the first time, nZVI were applied for the treatment of the real acid water system containing the miscellaneous mixture of pollutants, where the various removal mechanisms occur simultaneously. Toxicity of the treated saline acid water is caused by major contaminants represented by aluminum and sulphates in a high concentration, as well as by microcontaminants like As, Be, Cd, Cr, Cu, Ni, U, V, and Zn. Laboratory batch experiments proved a significant decrease in concentrations of all the monitored pollutants due to an increase in pH and a decrease in oxidation-reduction potential related to an application of nZVI. The assumed mechanisms of contaminants removal include precipitation of cations in a lower oxidation state, precipitation caused by a simple pH increase and co-precipitation with the formed iron oxyhydroxides. The possibility to control the reaction kinetics through the nature of the surface stabilizing shell (polymer vs. FeO nanolayer) is discussed as an important practical aspect.