In situ electron-induced reduction of NOx via CNTs activated by DBD at low temperature

• An in situ electron-induced deNO_x process with CNT activated by DBD was achieved. • Carbon atoms on CNT surface were verified to be excited by plasma in DBD-CNT system. • Reactions between NO_x and excited C result in synergistic effect of DBD-CNT system. In this study, a new in situ electron-induced process is presented with carbon nanotubes (CNTs) as a reduction agent activated by dielectric barrier discharge (DBD) for nitrogen oxide (NO_x) abatement at low temperature (<407 K). Compared with a single DBD system and a DBD system with activated carbon (DBD-AC), a DBD system with carbon nanotubes (DBD-CNT) showed a significant promotion of NO_x removal efficiency and N₂ selectivity. Although the O₂ content was 10%, the NO_x conversion and N₂ selectivity in the DBD-CNT system still reached 64.9% and 81.9% at a specific input energy (SIE) of 1424 J/L, and these values decreased to 16.8%, 31.9% and 43.2%, 62.3% in the single DBD system and the DBD-AC system, respectively. X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) were utilized to investigate surface changes in the CNTs after activation by DBD to explore the NO_x reduction abatement mechanism of this new process. Furthermore, the outlet gas components were also observed via Fourier transform infrared spectroscopy (FTIR) to help reveal the NO_x reduction mechanism. Experimental results verified that carbon atoms excited by DBD and the structure of CNTs contributed to the synergistic activity of the DBD-CNT system. The new deNO_x process was accomplished through in situ heterogenetic reduction reactions between the NO_x and carbon atoms activated by the plasma on the CNTs. In addition, further results indicated that the new deNO_x process exhibited acceptable SO₂ tolerance and water resistance.     

Investigation on the interaction between triclosan and bovine serum albumin by spectroscopic methods

Abstract

Multi-spectroscopic and molecular docking methods were used to study the interaction between triclosan (TCS) and bovine serum albumin (BSA). The results indicated that the fluorescence quenching of BSA by TCS was due to the formation of TCS–BSA complex through static quenching. This result was also demonstrated by time-resolved fluorescence experiment. The binding constants and number of binding sites between TCS and BSA were 1.30?×?10⁵ M^?1 and 1.17 at 298?K, respectively. The thermodynamic parameters were studied in detail which suggested that hydrophobic forces and hydrogen bond played major roles in the TCS–BSA interaction. Moreover, the site marker competitive experiments and docking studies revealed that TCS could bind BSA into site I in subdomain IIA. All the results of UV–vis spectrophotometry, circular dichroism spectroscopy and synchronous fluorescence spectroscopy showed that interaction between TCS and BSA induced conformation changes of BSA.     

好氧触媒在造纸法再造烟叶污水处理中的应用分析

本文围绕好氧触媒在造纸法再造烟叶污水处理中的应用展开分析。如对好氧触媒在再造烟叶污水处理中的应用必要性及好氧触媒作用原理予以介绍,并对好氧触媒在造纸法再造烟叶污水处理中应用展开试验。     

空区处理与残矿回采对围岩及地表影响的数值模拟分析

为了提高矿山企业开采的生产效益及确保施工中设备人员的生命财产安全,采用现场声波测试试验与室内物理力学试验得出的力学参数,应用FLAC3D数值模拟软件,在空区顶板-矿柱体系简化为弹性矩形薄板-H-K体流变力学模型的基础上,分析空区处理与残矿回采对围岩及地表的影响规律。结果表明:矿区三中段充填回采过程中压应力最大值出现在Ⅲ-10开采之后,右帮壁形成了9. 8 MPa的压应力集中区;拉应力区域主要存在于充填体内,且大部分拉应力超过了充填体抗拉强度幅值0. 12 MPa;地表移动带范围内垂直方向位移保持在0～1 mm。实际施工中应采取加强充填体强度达0. 27 MPa以上或保留部分矿体支撑顶板等措施确保回采安全。     

空区隐患爆破治理方案及延期时间的数值模拟分析

为了防止矿山空区引起地表塌陷造成建构（筑）物的破坏以及降低矿柱塌落振动对井下开采的威胁,采用现场试验与数值模拟相结合的方法,优选爆破治理方案和延期时间。根据炮孔布置和爆破参数,建立实际比例数值模型;在岩石物理力学指标测试的基础上,确定模型材料参数;采用LS-DYNA数值模拟软件,对比分析方案优劣以及确定爆破延期时间。研究结果表明:在满足空区隐患爆破治理效果的前提下,同一节点处A方案质点振速峰值为0.923 9 m/s小于B方案质点振速峰值1.225 3 m/s;而且当延期时间为100 ms时,通过模型垂直方向的位移云图可知岩石的破坏范围最大,塌落区域更加分散。现场应用结果显示空区隐患治理工程爆破效果良好,形成了隔离缓冲层,可以保证露天和井下的安全。