壳聚糖-TiO_2吸附剂对银的吸附及纳米银的生成

将生物选择性吸附和光催化技术耦合合成一种新型的多功能壳聚糖-二氧化钛吸附剂(CTA),这种新型的多功能壳聚糖-二氧化钛吸附剂能够同时吸附重金属和降解有机污染物。实验发现,CTA对银离子有较好的吸附容量,在初始浓度为1 000 mg/L时吸附容量为100.3 mg/g,且吸附了银离子的吸附剂对甲基橙有更好的降解效果。扫描电镜表明,CTA紫外条件下吸附银以后表面会有纳米银的生成,能谱显示纳米银颗粒在一定条件下可以由CTA表面自行脱落。     

载银TiO2催化剂的制备与性能研究

本文是采用负载金属银对TiO2改性后得到了载银TiO2,利用不同反应时间的胭脂红降解率反映光催化氧化反应的速率,结果表明,载银TiO2比TiO2的催化反应速率提高了3倍.通过实验确定最佳含银量和催化剂最佳投加量,并讨论了载银TiO2的催化机理,提出了制取载银TiO2催化剂的方法.     

Ag~+-TiO_2/AC复合材料的可见光吸附-光催化协同作用

采用水热法制备活性炭负载银掺杂纳米Ti O2复合材料(Ag+-Ti O2/AC),对样品进行了TEM、XRD、FT-IR和UV-Vis表征,分析了Ag+-Ti O2/AC的微结构、吸收谱特性和掺杂银离子后的半导体带隙变化,并研究了其在可见光下对甲基橙溶液(MO)的降解性能。结果表明,水热法不需要高温处理即可得到高活性的锐钛矿相纳米Ti O2,Ag+掺杂和AC负载均明显提高Ti O2光催化剂的光催化活性,在可见光下光照180 min,0.2 g/L的Ag+-Ti O2/AC对10 mg/L的甲基橙溶液的降解率为73.7%,主要由于存在持续的活性炭局域强吸附-Ti O2光催化降解协同作用,明显提高了甲基橙的降解效率。     

Ag/TiO2-SiO2的制备及其光催化降解有机污染物的研究

结合溶胶凝胶法和光还原法制备了Ag/TiO2-SiO2光催化材料,采用X射线衍射(XRD)、扫描电子显微镜(SEM)、N2吸附-脱附曲线、紫外—可见漫反射等测试技术对材料形貌、结构等进行了表征,并测试了其对2×10-5 mol/L亚甲基蓝(MB)溶液及实际废水的光催化降解性能。结果表明,适量的Ag负载可有效提高材料的光催化活性。以Ag负载量为5%(质量分数)的Ag/TiO2-SiO2(记为TS-A5)为例,TS-A5与商用光催化剂P25相比具有更优越的可见光催化活性;在500 W氙灯做为光源条件下,5次重复使用后TS-A5对MB仍能保持较高的光催化活性,应用于实际废水中可使其COD明显下降,表明该材料具有较好的实际应用潜力。     

还原剂对Ag/Al2O3催化剂上NO还原的影响

在富氧条件下,研究了CH4、C3H8、C 3H6、C8H18、CH 3OH、C2H5OH,以及C3H6与CH3OH、C3H6与C2H5OH组合作还原剂时,在Ag/Al2O3催化剂上NO的还原活性.结果表明,不同碳氢化合物还原NO的活性温度存在较大的差异.SO2的存在会导致CH3OH还原NO的活性提高,而其他碳氢化合物还原NO的活性降低.随着还原剂浓度提高,NOx转化率增大,不过,过高的还原剂浓度对NO还原不利.组合使用CH3OH与C3H6或C2H5OH与C3H6作为还原剂,能显著拓宽活性温度范围.     

Enhanced photocatalytic removal of amoxicillin with Ag/TiO2/mesoporous g-C3N4 under visible light: property and mechanistic studies

In present study, an efficient ternary Ag/TiO₂/mesoporous g-C₃N₄ (M-g-C₃N₄) photocatalyst was successfully synthesized through depositing Ag nanoparticles (NPs) on the surface of TiO₂/M-g-C₃N₄ heterojunction. Ag/TiO₂/M-g-C₃N₄ nanocomposite displayed the highest degradation efficiency for amoxicillin (AMX) compared to TiO₂/M-g-C₃N₄ heterojunction, M-g-C₃N₄, and bulk-g-C₃N₄ (B-g-C₃N₄). The removal efficiency of AMX in real situation, surface water (SW), hospital wastewater (HW), and waste water treatment plant (WWTP) also were studied to illustrate the effectiveness of Ag/TiO₂/M-g-C₃N₄ photocatalysts. The vulnerable atoms in AMX structure were revealed through DFT calculation. Additionally, the dominating active groups produced in time of the photocatalytic procedure were determined on account of free radical trapping experiments and ESR spectra. The mechanism of photocatalytic degradation was proposed and verified. The transfer of the electrons and the inhibition of the recombination of photogenerated electron-holes were enhanced effectively under the synergistic effect of the Ag NPs and TiO₂. As a consequence, the catalytic activity of the composite was improved under visible light.

     

模拟阳光下Ag／I-TiO2光催化预处理山核桃加工废水

研究了在模拟太阳光下,采用银修饰的碘掺杂二氧化钛光催化剂（Ag／I—TiO2）对某食品厂山核桃加工废水进行光催化预处理的效果。结合x射线衍射（XRD）、比表面积分析（BET）、紫外-可见漫反射光谱（uV—Vis）的表征结果,来分析催化剂结构对于废水处理效果的影响。探讨了Ag含量、废水初始pH（pHi）和光照时间等因素对化学需氧量（COD）去除及水质可生化性（B／C）提高的影响。并得出适宜的反应参数为：3％Ag含量;pHi为6;光照时间为240min。在最佳条件下,COD去除率45％,废水B／C比由0．17上升到0．31。光催化氧化法能够有效降低山核桃加工废水的COD含量,并达到显著提高废水可生化性的目的。     

Synthesis of heterojunction photocatalysts composed of Ag 2 S quantum dots combined with Bi 4 Ti 3 O 12 nanosheets for the degradation of dyes

Environmental Science and Pollution Research - Facilitating the separation of photogenerated electron/hole pairs and widening the light-responsive region are crucial to enhance the overall...     

Catalytic performance of Ag/Al2O3-C2H5OH-Cu/Al2O3 system for the removal of NOx from diesel engine exhaust

The selective catalytic reduction (SCR) of NOx by C(2)H(5)OH was studied in excess oxygen over Ag/Al(2)O(3) catalysts with different Ag loadings at lab conditions. The 4% Ag/Al(2)O(3) has the highest activity for the C(2)H(5)OH-SCR of NOx with a drawback of simultaneously producing CO and unburned THC in effluent gases. An oxidation catalyst 10% Cu/Al(2)O(3) was directly placed after the Ag/Al(2)O(3) to remove CO and unburned THC. Washcoated honeycomb catalysts were prepared based on the 4% Ag/Al(2)O(3) and 10% Cu/Al(2)O(3) powders and tested for the C(2)H(5)OH-SCR of NOx on a diesel engine at the practical operating conditions. Compared with the Ag/Al(2)O(3) powder, the Ag/Al(2)O(3) washcoated honeycomb catalyst (SCR catalyst) has a similar activity for NOx reduction by C(2)H(5)OH and the drawback of increasing the CO and unburned THC emissions. Using the SCR+Oxi composite catalyst with the optimization of C(2)H(5)OH addition, the diesel engine completely meets EURO III emission standards.     

模拟阳光下Ag/I-TiO_2光催化预处理山核桃加工废水

研究了在模拟太阳光下,采用银修饰的碘掺杂二氧化钛光催化剂(Ag/I-TiO2)对某食品厂山核桃加工废水进行光催化预处理的效果。结合X射线衍射(XRD)、比表面积分析(BET)、紫外-可见漫反射光谱(UV-Vis)的表征结果,来分析催化剂结构对于废水处理效果的影响。探讨了Ag含量、废水初始pH(pHi)和光照时间等因素对化学需氧量(COD)去除及水质可生化性(B/C)提高的影响。并得出适宜的反应参数为:3%Ag含量;pHi为6;光照时间为240 min。在最佳条件下,COD去除率45%,废水B/C比由0.17上升到0.31。光催化氧化法能够有效降低山核桃加工废水的COD含量,并达到显著提高废水可生化性的目的。     

Facile fabrication of highly catalytic-active Ag2CO3/AgBr/graphene oxide ternary composites towards the photocatalytic wastewater treatment

Environmental Science and Pollution Research - Ag2CO3/AgBr/graphene oxide (Ag2CO3/AgBr/GO) ternary composites with different percentages of GO were fabricated by a facile co-precipitation strategy....     

Novel visible-light-driven SrCoO3/Ag3PO4 heterojunction with enhanced photocatalytic performance for tetracycline degradation

Environmental Science and Pollution Research - The semiconductor photocatalytic technology has been considerably studied due to its excellent catalytic performance in water pollution control....     

Studies on electrochemical recovery of silver from simulated waste water from Ag(II)/Ag(I) based mediated electrochemical oxidation process

In the Ag(II)/Ag(I) based mediated electrochemical oxidation (MEO) process, the spent waste from the electrochemical cell, which is integrated with the scrubber columns, contains high concentrations of precious silver as dissolved ions in both the anolyte and the catholyte. This work presents an electrochemical developmental study for the recovery of silver from simulated waste water from Ag(II)/Ag(I) based MEO process. Galvanostatic method of silver deposition on Ti cathode in an undivided cell was used, and the silver recovery rate kinetics of silver deposition was followed. Various experimental parameters, which have a direct bearing on the metal recovery efficiency, were optimized. These included studies with the nitric acid concentration (0.75-6M), the solution stirring rate (0-1400 rpm), the inter-electrode distance between the anode and the cathode (2-8 cm), the applied current density (29.4-88.2 mA cm(-2)), and the initial Ag(I) ion concentration (0.01-0.2M). The silver recovered by the present electrodeposition method was re-dissolved in 6M nitric acid and subjected to electrooxidation of Ag(I) to Ag(II) to ascertain its activity towards Ag(II) electrogeneration from Ag(I), which is a key factor for the efficient working of MEO process. Our studies showed that the silver metal recovered by the present electrochemical deposition method could be reused repeatedly for MEO process with no loss in its electrochemical activity. Some work on silver deposition from sulfuric acid solution of different concentrations was also done because of its promising features as the catholyte in the Ag(II) generating electrochemical cell used in MEO process, which include: (i) complete elimination of poisonous NO(x) gas liberation in the cathode compartment, (ii) reduced Ag(+) ion migration across Nafion membrane from anolyte to catholyte thereby diminished catholyte contamination, and (iii) lower cell voltage and hence lesser power consumption.     

Adsorption and desorption of 2,4,6-trichlorophenol onto and from ash as affected by Ag+, Zn2+, and Al3+

Metal cations and organic pollutants mostly co-exist in the natural environment. However, their interactions in adsorption processes have yet to be adequately addressed. In the current study, the effect of inorganic cations with different charges (Ag⁺, Zn²⁺, and Al³⁺) on the adsorption and desorption of 2,4,6-trichlorophenol (TCP) onto and from processed ash derived from wheat (Triticum aestivum L.) straw was investigated. The adsorption and desorption of TCP were both nonlinear; the isotherm and kinetics curves fitted well using the Freundlich equation and a pseudo-second-order model, respectively. The presence of Ag⁺ promoted TCP adsorption, while Zn²⁺ and Al³⁺ reduced TCP adsorption onto ash. The desorption of TCP from ash showed obvious hysteresis, and the presence of Ag⁺, Zn²⁺, and Al³⁺ caused the desorption to be less hysteretic. The suppression of TCP adsorption by Zn²⁺ and Al³⁺ was ascribed to the partial overlapping of adsorption groups between TCP and metal ions. Al³⁺ had a stronger inhibition effect than that of Zn²⁺ due to its higher binding capacity and larger hydrated ionic radius than those of Zn²⁺. Enhanced adsorption of TCP onto ash by Ag⁺ was ascribed to its ability to reduce the competitive adsorption of water molecules on ash surface by replacing the original ions, such as Na⁺ and Ca²⁺, and compressing the hydrated ionic radius of these metal ions. In addition, Ag⁺ was able to bind with the aromatic organic compounds containing π-electrons, which resulted in a further increase of TCP adsorption by ash.     

Ag／ZnO光催化降解甲基对硫磷研究

描述了掺杂体系Ａｇ／ＺｎＯ用于甲基对硫磷水溶液光催化降解,有氧存在下,经ＵＶ照射对甲基对硫磷光降解是有效的,并讨论了影响光降解中甲基硫磷诸因素,初步探讨了光降解机理和动力学,起始降解物为Ｃ２Ｈ６Ｐ＾＋Ｓ和Ｏ２ＮＨ４Ｏ,且是一级反应,半衰期为１．８２ｍｉｎ。     

Photocatalytic degradation of phenol using Ag core-TiO<Subscript>2</Subscript> shell (Ag@TiO<Subscript>2</Subscript>) nanoparticles under UV light irradiation

Ag@TiO₂ nanoparticles were synthesized by one pot synthesis method with postcalcination. These nanoparticles were tested for their photocatalytic efficacies in degradation of phenol both in free and immobilized forms under UV light irradiation through batch experiments. Ag@TiO₂ nanoparticles were found to be the effective photocatalysts for degradation of phenol. The effects of factors such as pH, initial phenol concentration, and catalyst loading on phenol degradation were evaluated, and these factors were found to influence the process efficiency. The optimum values of these factors were determined to maximize the phenol degradation. The efficacy of the nanoparticles immobilized on cellulose acetate film was inferior to that of free nanoparticles in UV photocatalysis due to light penetration problem and diffusional limitations. The performance of fluidized bed photocatalytic reactor operated under batch with recycle mode was evaluated for UV photocatalysis with immobilized Ag@TiO₂ nanoparticles. In the fluidized bed reactor, the percentage degradation of phenol was found to increase with the increase in catalyst loading.     

A rapid green synthesis of Ag/AgCl-NC photocatalyst for environmental applications

Environmental Science and Pollution Research - The present study focuses on extract-mediated Ag nanoparticles (NPs), AgCl-NPs, and Ag/AgCl nanocomposites (NCs) as photocatalysts along with its...     

Ag-DDC光度法测砷影响因素的研究

Ag-DDC光度法测定水体中的砷具有较高的准确度和精密度，是环境监测中常用的方法。根据该法的反应机理和多年的实践，对Ag-DDC光度法测砷过程中各种影响因素进行了研究探讨，并提出了行之有效的控制方法。     

Ag/Cu合金触点废料回收铜粉的工艺研究

Ag/Cu合金触点废料含Ag量在30%(质量分数)以上,含Cu量在60%(质量分数)以上、含Sn量在2%(质量分数)以上.先将Ag/Cu合金触点废料中的Cu分离,然后采用葡萄糖预还原、水合肼再还原制得了粒径在0.3～O.6 pm的类球形超细铜粉(纯度≥99.9%).研究表明,适量聚乙烯吡咯烷酮(PVP)的加入有助于超细铜粉粒径均匀且形貌趋于一致;量佳反应温度为70℃;抗氧化剂苯并三氮唑可以有效防止超细铜粉的表面氧化.