二维层状纳米片材料制备及在电解水中应用的研究进展

高效、清洁的氢能被认为是化石能源最有潜力的替代能源之一。制氢方法中电解水制氢是非常简便、且易于规模化的一种方法,但是电解水过程中存在制氢能耗增加、成本升高等问题,因此制备能耗低、具有稳定催化效率的催化剂成为能源领域的研究热点。层状双金属氢氧化物（LDHs）由于具有独特的二维层状结构,使其组成易于调节、结构易于调控,因此具有高效的电催化活性。但是,LDHs存在尺寸大、厚度高的问题,导致电催化剂的活性位点的数目受限、本征活性低和电导率低,最终会影响LDHs的电催化性能。主要论述了LDHs的结构和电解机理以及作为电解水催化剂的研究现状,对目前存在的问题以及解决方法进行了归纳,并对未来的研究方向进行了展望。     

影响LDHs改性LDPE膜性能的因素

通过对薄膜力学和光学性能的测试,研究不同载体、不同分散剂、不同粉体及不同粉体含量对薄膜性能的影响,再结合其对纳米粉体在聚合物中分散效果的影响,寻找合适的配方与工艺条件,研制出性能优越的薄膜.     

焙烧温度对CuMgAl催化剂催化糠醇加氢制戊二醇的影响

采用共沉淀法制得物质的量比为n(Cu²⁺)∶n(Mg²⁺)∶n(Al³⁺)=10∶65∶25的CuMgAl类水滑石前体（CMA-HT），经过不同温度焙烧制得CuMgAl水滑石催化剂。通过傅里叶变换红外光谱（FTIR）、热重分析（TG）、X射线粉末衍射（XRD）、扫描电子显微镜（SEM）、透射电子显微镜（TEM）、N₂-物理吸附、程序升温还原（H₂-TPR）、H₂-程序升温脱附（H₂-TPD）、CO₂-程序升温脱附（CO₂-TPD）和NH₃-程序升温脱附（NH₃-TPD）等对催化剂的结构进行表征，在高压反应釜中考察了CuMgAl水滑石催化剂催化糠醇（FFA）加氢制1,2-戊二醇（1,2-PeD）和1,5-戊二醇（1,5-PeD）的催化性能。研究结果表明，焙烧温度对催化剂的结构及其催化性能具有显著的影响，金属活性中心和碱性位随焙烧温度的升高先增加后减少。经600℃焙烧的CMA催化剂表面存在适宜的金属中心和碱性位，在金属位和碱性中心的协同催化下，表现出了优异的催化性能。在140℃，H₂压力为4 MPa的条件下，反应8 h，糠醇的转化率和戊二醇的收率分别达74.13%和58.36%。     

Hierarchically structured Mg–Al mixed metal oxides templated from pine sawdust: fabrication,Congo red adsorption and antibacterial properties

ABSTRACT

Biomorphic Mg–Al layered double hydroxides (LDHs) templated from pine sawdust as precursors, hierarchically structured Mg–Al mixed metal oxides (MMOs) with well-developed porosity were prepared through biological template method and hydrothermal process. As-synthesized composites were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction and nitrogen adsorption measurements. Adsorption conditions including different Congo red concentration, contact time, pH and temperature were investigated. Antibacterial ability and mechanism against Escherichia coli and Staphylococcus aureus were analyzed. MMOs exhibited higher adsorption and stronger antibacterial ability as compared with biomorphic LDHs. The concept provides new insight into design and preparation efficient adsorption and antibacterial materials.     

Theoretical Evaluation of the Microporosity of Pillared Layered Double Hydroxides

Over the last ten years, the concept of pillaring has frequently been applied on layered double hydroxides (LDHs). Due to the variety of possible anionic pillaring species and the adjustable layer charge density, LDHs offer good perspectives with regard to the creation of porous adsorbents and catalysts. But despite these possibilities, their porosity properties can still not compete with those of industrially applicable materials like zeolites. In this study, theoretical calculations based on geometrical models and performed on both Fe(CN)₆-MgAl-LDHs (A) and [PV₂W¹⁰ O⁴⁰]-ZnAl-LDHs (B) were reported. Properties such as the micropore volume and the interpillar distance were calculated, and compared to experimental data. For a M(II)/M(III) ratio in the layers of 3, the theoretical maximum micropore volumes were 0.3843 cm³/g (A) and 0.1497 cm³/g (B), respectively. By implementing parameters like the stack size, pillars on the outside of the stacks and the possibility of collapse, the model was adjusted in order to create a realistic picture of the microstructure of pillared LDHs. This led to a better understanding of the limiting factors, and gave an explanation for the relatively low micropore volumes of pillared LDHs. For the Fe(CN)₆-MgAl-LDHs, small interpillar distances were responsible for the partial inaccessibility of the interlayer regions by N₂. This effect was the most pronounced for high charge density LDHs. The situation for the [PV₂W¹⁰O⁴⁰]-ZnAl-LDHs is more complex. Probably due to an incomplete pillaring process, the theoretical maximum values are not reached.     

纳米金催化剂Au/ZnAl-LDHs的制备及在CO常温氧化反应中的活性及稳定性

以人工合成的双羟基金属氢氧化物ZnAl-LDHs为载体,将预先制备的金溶胶通过静电吸附的方式负载到载体上,获得了纳米金催化剂Au/ZnAl-LDHs,用X射线粉末衍射(XRD)表征了催化剂的物相,用透射电镜(TEM)观察了纳米金颗粒的粒径分布,以CO的常温催化氧化为模型反应,分别考察了金溶胶制备过程中金前体HAuCl4·6H2O的浓度和还原剂THPC的用量、负载过程的pH值以及金的负载量等因素对金催化剂的活性和稳定性的影响。结果表明:在制备金溶胶的过程中,降低HAuCl4·6H2O的浓度并提高还原剂THPC的用量,可以制备出粒径分布处于1~7nm之间、平均粒径仅3.87nm的负载型纳米金颗粒,其对CO的常温转化率为100%,且其催化活性的稳定性明显提高;而在金溶胶的吸附负载过程中,使体系的pH值处于6~7的范围,有利于金溶胶在ZnAl-LDHs载体上的吸附负载,从而得到实际负载量更接近理论负载量的金催化剂样品,当金的实际负载量接近1%(质量分数)时,能够确保对CO的常温氧化转化率达到100%。     

水滑石类光催化剂在污水处理中的应用

双金属复合氢氧化物（LDHs,又叫水滑石）因具有层状结构、稳定的物化性质和电子特性等优点,可以大范围地应用在污水处理中。目前,水滑石作为光催化剂及其复合材料在污水处理上的应用受到越来越多的关注。综述了水滑石光催化剂的制备及其改性,着重介绍了不同类型水滑石对水中不同污染物的去除效果,并简要阐述了水滑石光催化剂的作用机理和研究现状。最后,展望了水滑石光催化剂的发展趋势,以期为后续水滑石在污水处理上的应用提供借鉴。     

氧化石墨烯/类水滑石基复合催化剂的可控制备及其催化性能

针对纳米催化剂在有机染料氧化降解反应中存在的问题,开发高效纳米Fe基催化剂成为当前研究的重点。基于"创新纳米结构调变催化功能"的新策略,利用类水滑石层板金属离子和层间阴离子与氧化石墨烯(GO)表面官能团之间的静电作用,采用水热法制备氧化石墨烯复合类水滑石Fe-LDH@GO纳米催化剂。利用XRD、N_2吸附-脱附和TEM对催化剂的形貌、尺寸、孔道及FeO_x粒子尺寸等物化性质进行表征,发现氧化石墨烯的引入不改变水滑石纳米片结构和形貌,但能够增加催化剂的比表面积,有效锚定FeO_x纳米粒子,使其粒径减小并均匀分散在载体表面,提供更多的有效活性位点。XPS结果表明,催化剂表面存在的Fe^(2+)是芬顿反应的活性中心,氧化石墨烯的引入提高含氧官能团数量,使其在RhB降解反应中表现出优异的催化活性,反应14 min时,RhB转化率100%。     

水滑石/废橡胶粉复合改性沥青的制备及其性能研究

以克拉玛依90号沥青作为基质沥青、废橡胶粉和水滑石（LDHs）作为改性剂,制备了LDHs/废橡胶粉复合改性沥青,在废橡胶粉加入量不变的条件下,考察LDHs加入量对复合改性沥青的物理性能、抗紫外老化性能和流变性能的影响。结果表明：当废橡胶粉加入量（w）为15%时,随着LDHs的加入,复合改性沥青的软化点升高,针入度和延度有所下降,两种改性剂相互结合,使复合改性沥青的物理性能得到改善,并且满足国家聚合物改性沥青标准的要求,考虑到改性剂成本,选取LDHs加入量（w）为3%～4%;LDHs的加入使复合改性沥青的软化点增量减小,残留针入度比和延度保留率上升,表明LDHs可明显提高复合改性沥青的抗紫外老化性能;LDHs的加入可使复合改性沥青复数模量和车辙因子增加,相位角下降,说明LDHs可提高复合改性沥青的抗车辙性能。     

Preparation,structure-property relationships of zinc oxide pillared organic layered double hydroxides and its effect on the performance of poly (lactic acid)

Zinc oxide pillared organic layered double hydroxides (ZnO-LDHs-S) were synthesized with sodium dodecyl sulfate (SDS) via a intercalation method. Meanwhile, the properties of ultraviolet (UV) absorbance and antibacterial of ZnO-LDHs-S were investigated. To improve the performances of poly (lactic acid) (PLA), PLA/ZnO-LDHs-S nanocomposites were prepared by melt blending using ZnO-LDHs-S as nucleating agent. Structure and properties of PLA/ZnO-LDHs-S nanocomposites were investigated by Fourier transform infrared spectra, transmission electron microscopy, mechanical properties testing, differential scanning calorimetry, polarized optical microscopy and rheological analysis. It was shown that the introduction of ZnO-LDHs-S improved the comprehensive performance of PLA.