煅烧对粉煤灰合成4A沸石的作用

研究了煅烧对粉煤灰合成4A沸石除炭(有机物)增白和活化的两个作用,试验确定了粉煤灰最佳的锻烧条件:温度为850℃,时间为2h。在此条件下煅烧,通过XRD、SEM分折和白度测定,结果显示:破坏了粉煤灰中的晶相结构和溶解了玻璃体,白度达到了63。     

生物炭基非金属过硫酸盐活化剂的开发与应用

生物炭驱动的过硫酸盐高级氧化技术近几年来受到了环境科学界的广泛关注.本文对当前生物炭基非金属过硫酸盐活化剂开发过程中采取的调控措施与改性手段进行了总结,汇总了生物炭基过硫酸盐高级氧化技术在难降解有机污染物削减方面的应用,同时阐述了生物炭活化过硫酸盐的机理,展望了生物炭基过硫酸盐活化剂未来的发展方向与挑战.     

景区典型树种的热解特性及动力学研究

为了研究山林或景区中不同植物的热稳定性,选取了景区种植数量较多的6种典型树种:女贞、枇杷、竹子、松树、柏树和法桐的枝干和叶作为样品。借助同步热分析仪,在温升速率20℃/min的条件下,对未经干燥处理的样品进行热解特性及热解反应动力学研究。通过TG、DTG以及DSC曲线分析各样品的热解过程,并采用分阶段一级反应动力学模型Coats-Redfern法求得相应参数。研究结果表明:所取样品的热解过程都出现4个明显的热解阶段,即脱水阶段、综纤维素热解阶段、木质素热分解阶段、炭化阶段。根据6个树种的主要热解阶段和动力学分析,6种树种的热稳定性从低到高顺序依次为竹子、女贞、枇杷、法桐、柏树、松树。     

Electrochemical decolorization of dye wastewater by surface-activated boron-doped nanocrystalline diamond electrode

Complex organics contained in dye wastewater are difficult to degrade and often require electrochemical advanced oxidation processes (EAOPs) to treat it. Surface activation of the electrode used in such treatment is an important factor determining the success of the process. The performance of boron-doped nanocrystalline diamond (BD-NCD) film electrode for decolorization of Acid Yellow (AY-36) azo dye with respect to the surface activation by electrochemical polarization was studied. Anodic polarization found to be more suitable as electrode pretreatment compared to cathodic one. After anodic polarization, the originally H-terminated surface of BD-NCD was changed into O-terminated, making it more hydrophilic. Due to the oxidation of surface functional groups and some portion of sp² carbon in the BD-NCD film during anodic polarization, the electrode was successfully being activated showing lower background current, wider potential window and considerably less surface activity compared to the non-polarized one. Consequently, electrooxidation (EO) capability of the anodically-polarized BD-NCD to degrade AY-36 dye was significantly enhanced, capable of nearly total decolorization and chemical oxygen demand (COD) removal even after several times of re-using. The BD-NCD film electrode favored acidic condition for the dye degradation; and the presence of chloride ion in the solution was found to be more advantageous than sulfate active species.     

Utilization of Arachis hypogaea hull,an agricultural waste for the production of activated carbons to remove phenol from aqueous solutions

Arachis hypogaea hulls, an agricultural waste, were used to prepare activated carbon by chemical activation with zinc chloride under four different activation atmospheres. The most important parameter in chemical activation was found to be the chemical ratio (activating agent/precursor). Carbonization temperature and time are the other two important variables, which had significant effect on the pore structure of carbon. The maximum Brunquer-Emmett-Teller (BET) surface area and micropore volume of the activated carbon was found to be 418 m²/g and 0.28 cm³/g, respectively. The activated carbon developed shows substantial capability to adsorb phenol from aqueous solutions. The kinetic data were fitted to the models of intraparticle diffusion, pseudo-second-order, and Lagergren, and followed more closely the pseudo-second-order chemisorption model. The isotherm equilibrium data were well fitted by the Langmuir and Freundlich models. Solution pH has significant effect on adsorption and the maximum uptake of phenol was reported at pH 3.5.     

Distribution of toxic and essential elements in various chicken organs

An instrumental neutron activation technique was applied to determine toxic, essential and other elements in various chicken organs namely; liver, heart, gizzard, breast and leg. The range, arithmetic mean, geometric mean and median were computed which indicate normal distribution pattern for Hg, Se, Cl, Fe, Zn, Mn, Na, K and Cs in the five chicken organs. The concentration of Hg, Se, As, Fe, Zn and Mn in local chicken liver were also compared with the literature values. Dietary intake value for toxic and essential elements were also computed and compared with the recommended values.     

模拟酸雨及其活化Al~（3＋）构成的复合污染对中小型土壤动物的毒杀效果

酸雨可引起土壤中铝离子的活化而造成铝毒问题,因此酸雨及其活化的金属铝离子势必造成对土壤中小型动物的复合污染与影响。为此,通过室内模拟试验,研究3种优势土壤动物直接暴露在4种不同酸度的模拟酸雨和4种不同铝离子浓度梯度组合而构成的复合污染处理条件下的死亡率,以探明酸雨通过降低土壤酸度同时活化Al3＋对土壤动物的叠加影响效应。研究结果表明：弹尾目、线虫、蜱螨目等土壤动物直接暴露在酸水和铝离子的复合溶液中,其死亡率总体上均会随着酸水pH值的降低和Al3＋离子浓度的升高而增加。通过单因素和双因素方差分析还发现,不同类群的土壤动物对模拟酸雨pH和溶液中Al3＋含量的敏感性各不相同,其中酸水和铝离子复合胁迫对线虫和蜱螨目动物死亡率的影响并没有表现出明显的交互作用,但对弹尾目土壤动物死亡率存在显著的交互作用影响。     

机械力化学活化HPW-TiO_2/膨润土光催化降解甲基橙

采用溶胶-凝胶法制备了磷钨酸(HPW)改性TiO_2,并固载于膨润土上,再经机械力化学活化,得到机械力化学活化HPW-TiO_2/膨润土(MCA-HPW-TiO_2/膨润土)复合光催化剂。采用XRD,SEM,EDS技术对复合光催化剂进行了表征,并将其用于甲基橙的紫外光催化降解。表征结果显示:活性组分TiO_2和HPW成功固载于膨润土上;在机械力化学活化作用下,膨润土层间结构遭到破坏,TiO_2的XRD特征峰形呈弥散状态。实验结果表明:机械力化学活化作用对HPW-TiO_2/膨润土的光催化性能提升效果显著;在酸性及近中性条件下MCA-HPWTiO_2/膨润土均具有较高的催化活性;在溶液p H 6.2、初始甲基橙质量浓度10 mg/L、反应时间180 min、MCAHPW-TiO_2/膨润土投加量1 g/L的条件下,甲基橙去除率达88.27%;该光催化降解过程符合一级动力学模型。     

神经毒剂沙林的破坏机理研究

采用VAMP和密度泛函程序DMol3计算了沙林的生成热,并用VAMP-PM3/UHF半经验方法对沙林裂解的过渡态进行了优化计算,共发现9种过渡态,据此判断化学键断裂的难易顺序为P=O＞P-F＞P-O＞C-O＞P-C＞C-C＞C-H; C-H键断裂的活化能最小,可能与氢原子迁移到氧原子上有关.活化能小于相应的键解离能,计算结果能解释沙林的质谱数据.计算结果对使用低当量小型核武器破坏沙林等生化武器(核除剂)的可行性提供了能量上的参考,即试图通过计算得出有效的原位破坏沙林等生化战剂所需的最低能量,进而研究使用低当量小型核武器破坏沙林等生化武器的可行性.     

Activation of sulfite by metal-organic framework-derived cobalt nanoparticles for organic pollutants removal

Sulfite (SO₃²⁻) activation is one of the most potential sulfate-radical-based advanced oxidation processes, and the catalysts with high efficiency and low-cost are greatly desired. In this study, the cobalt nanoparticles embedded in nitrogen-doped graphite layers (Co@NC), were used to activate SO₃²⁻ for removal of Methyl Orange in aqueous solution. The Co@NC catalysts were synthesized via pyrolysis of Co²⁺-based metal-organic framework (Co-MOF), where CoO was firstly formed at 400℃ and then partially reduced to Co nanoparticles embedded in carbon layers at 800℃. The Co@NC catalysts were more active than other cobalt-based catalysts such as Co²⁺, Co₃O₄ and CoFe₂O₄, due to the synergistic effect of metallic Co and Co_xO_y. A series of chain reaction between Co species and dissolved oxygen was established, with the production and transformation of SO₃^•−, SO₅²⁻, and subsequent active radicals SO₄^•− and HO•. In addition, HCO₃⁻ was found to play a key role in the reaction by complexing with Co species on the surface of the catalysts. The results provide a new promising strategy by using the Co@NC catalyst for SO₃²⁻ oxidation to promote organic pollutants degradation.