Trimetallic NiFeCr-LDH/MoS2composites as novel electrocatalyst for OER

The development of efficient and stable oxygen evolution reaction (OER) catalysts is an ongoing challenge. In order to solve the problem of low oxygen evolution efficiency of the current OER catalysts, a novel material was synthesized by the incorporation of NiFeCr-LDH and MoS₂, and its structural and electrochemical properties were also investigated. The introduction of MoS₂ improves the electrochemical performance of NiFeCr-LDH. The polarization curve shows that the potential of composite material is only 1.50 V at a current density of 10 mA cm^?2, which is far superior to commercial precious metal catalysts. In addition, the stability experiment shows that the composite material has excellent stability, and the current density has little change after 500 cycles. Furthermore, we found that some metal ions, such as Ni, Cr and Mo, exist in the form of high valence on the surface of NiFeCr-LDH@MoS₂, which is also conducive to the occurrence of oxygen evolution reaction.     

Mn-containing catalytic materials for the total combustion of toluene: The role of Mn localisation in the structure of LDH precursor

Mg/Mn/Al mixed oxide systems of similar atomic ratios close to 2/0.5/1 were obtained by calcination of Mg,Al layered double hydroxide (LDH) type precursors containing Mn either in the cationic form within the brucite layer or as permanganate anions in the interlayer. The materials were characterised with PXRD, thermal analysis, XPS, ESR, TPR and BET. In mixed oxides derived from interlayer-doped precursor PXRD identified MgO–MnO solid solution and poorly crystalline Al-rich spinel phase, while those obtained from layer-doped LDH contained a better crystalline Mn-rich spinel. Surface of both materials was covered with poorly crystalline and/or amorphous Mn⁴⁺-containing phases. Higher reducibility of this surface coat in calcined layer-doped catalyst, as compared to interlayer-doped one, was attributed to the differences in the nature of underlying crystalline phases, and was considered the chief reason for the higher catalytic activity of this catalyst in the total oxidation of toluene.     

水滑石材料处理工业废水的研究进展

工业废水主要由工业生产过程中产生的污水和废液组成,具有成分复杂、种类繁多、差异性大、难以处理等特点。主要综述了水滑石常用的制备方法,利用壳聚糖法、等离子体法、农业废弃物法进行改性制备复合材料。水滑石材料在吸附过程中多呈粉末状,难以回收,且工业化应用较少。针对以上问题,可采用引入Fe离子产生磁性,利于回收;通过开发更低廉的合成材料、简单快捷的制备方法、稳定的理化性质使水滑石材料得以工业化应用。水滑石复合材料在层板中引入磁性物质有助于回收,随着水滑石技术的深入研究和新工艺的发展,处理有毒污染物的前景必定会更广阔。     

Selective oxidation of ammonia to nitrogen on transition metal containing mixed metal oxides

The selective catalytic oxidation of ammonia to nitrogen (NH₃-SCO) has been studied over hydrotalcite derived mixed metal oxides containing Cu, Co, Fe or Ni. XRD, BET, NH₃-TPD and TPR techniques were used for catalysts characterization. Results of NH₃-SCO were compared with those of selective catalytic reduction of NO with NH₃ (NO-SCR). Reaction mechanism was studied by temperature-programmed surface reaction (TPSR) and activity tests with a various contact time. Catalytic performance of the studied samples depends on both kind and loading of transition metals in the mixed metal oxide system. The Cu-containing samples have been found to be the most active catalysts of the NH₃-SCO process. Transition metal loading strongly influences distribution of ammonia oxidation products. The highest selectivity to N₂ was measured for the catalysts with the lowest transition metal content.     

Aldol condensation of campholenic aldehyde and MEK over activated hydrotalcites

In this paper, activated Mg-Al hydrotalcites were used as catalysts in the aldol condensation of campholenic aldehyde and methyl ethyl ketone (MEK). These materials represent an attractive alternative to less environmentally friendly liquid bases in a number of base-catalyzed reactions involved in the pharmaceutical and fragrance industries. The presence of basic hydroxyl groups in the interlayer space leads to very active materials. However, the relation between the activity of reconstructed hydrotalcites and the rehydration procedure is still not well understood. Different rehydration protocols in combination with extensive characterization studies were performed, including XRD, SEM, IR spectroscopy and TPD of CH₃CN and CH₃NO₂. The materials were tested as catalysts in the aldol condensation of campholenic aldehyde and MEK, and relationships between the catalytic performance of the activated hydrotalcites and the rehydration procedure were derived. Several factors may influence the activity and selectivity of this reaction, such as the reaction temperature, the molar ratio of the reactants and the degree of rehydration of the hydrotalcite-like catalysts. The selectivity towards the formation of the desired branched isomer increases when performing the reaction at low temperatures.     

NOx storage-reduction catalysts based on hydrotalcite: Effect of Cu in promoting resistance to deactivation

Novel NO_x storage-reduction (NO_xSR) catalysts prepared by Pt and/or Cu impregnation of Mg–Al (60:40) hydrotalcite (HT)-type compounds show better performances in NO_x storage than Pt–Ba/Al₂O₃ Toyota-type NO_xSR catalysts at reaction temperatures lower than 250 °C. The presence of Pt or Cu considerably enhances the activity, with the former more active. The nature of the HT source, however, also influences performance. The co-presence of Pt and Cu slightly worsens the low temperature activity, but considerably promotes the resistance to deactivation after severe hydrothermal treatment and in the presence of SO₂. This effect is attributed to both the possibility of formation of a Pt–Cu alloy after reduction, and the modification of the HT induced during the deposition of Cu. The overall Pt–Cu/HT performances are thus superior to those of the Pt–Ba/Al₂O₃ Toyota-type NO_xSR catalysts.     

Improving the yield of Jatropha curcas's FAME through sol–gel derived meso-porous hydrotalcites

The conversion of fatty acid methyl ester (FAME) from triglycerides using heterogeneous catalysis has gained increasing interest due to the prospect of increased yield at reduced operating costs and reaction conditions. In this paper, meso-porous hydrotalcite was used to catalyze jatropha oil into FAME with relatively higher yield at atmospheric pressure and relatively low reaction temperature. The molar ratio of methanol to oil required was relatively low and the conversion was completed within few hours of reaction time. The reaction was promoted when moderate calcination temperature was applied, the disordered structure of the catalyst was maintained, counterbalance anions was removed, and phase transitions within the oxide lattice was induced. Despite the observed deactivation during successive reaction cycles due to adsorption of residual triglycerides, the catalyst performance was restored effectively by air-re-calcination.     

Reconstruction and hydration of hydrotalcite response to thermal activation temperature: Enhancement of properties for magnesia castables

Optimization binding system for refractory castables is significant to enhance the service performance. Hydrotalcite has been considered a promoter for high-temperature performance of basic castables, however, its binding property remains to be improved before practical application. In this work, the thermal activated Mg–Al hydrotalcites were incorporated in magnesia castables, and the mutual influence of pre-calcination temperature on the hydration, microstructure, and strength of castables was investigated. The obtained results indicated that the reconstruction of calcined hydrotalcite took place in the hydration process and effectively motivated the hydrolysis. Hydrate was thus promoted and a relatively dense microstructure of magnesia castables was confirmed by X-ray computed tomography analysis. Hydrotalcite pre-calcinated at 300 °C contributed to the highest early strength for castable, and the high-temperature properties also performed better than that of other pre-calcinated hydrotalcite-adding. The enhancement mechanisms of calcined hydrotalcite were attributed to the two following reasons: (ⅰ) the modified microstructure of magnesia castables from the early stage by hydration process, (ⅱ) the further enhanced sinterability inspired by the appropriate thermal activation effect.     

Surfactant-assisted synthesis and catalytic activity for SOx abatement of high-surface-area CuMgAlCe mixed oxides

CuMgAlCe mixed oxides were prepared by a modified coprecipitation–calcination method using CTAB as surfactant template. All the precursors showed hydrotalcite-like layered structure and mixed oxides with mainly periclase phase were obtained after calcination. Catalytic activity for SO₂ removal of mixed oxides was examined through adsorption–reduction cycles under the conditions similar to those of FCC units. The results showed that incorporation of both Ce and Cu could improve SO_x oxidative chemisorption. CTAB/metal molar ratio during synthesis had a significant influence on the structural properties of mixed oxides. Sample CuMgAlCe-0.1 prepared by CTAB/metal molar ratio of 0.1 had the highest specific area 142.2 m²/g and also presented the best SO₂ adsorption rate and capacity. This behavior is mainly due to its exposed more adsorption sites provided by high specific surface area, facilitating SO₂ diffusion and contact with active components. It still possessed excellent cyclic stability that is beneficial for industrial application.     

焙烧还原条件下硬脂酸钠改性水滑石的制备及应用

以镁铝碳酸根型水滑石MgAl-CO₃-LDHs(LDHs)为前驱体,硬脂酸钠(NaSt)为改性剂,通过焙烧还原法在硬脂酸钠的溶液中制备硬脂酸钠改性水滑石LDHs-NaSt,采用X射线衍射仪(XRD)、傅里叶转变红外光谱仪(FTIR)和扫描电镜(SEM)对结构进行表征,并研究不同改性剂加入量条件下得到的改性水滑石对聚氯乙烯(PVC)热稳定性能的影响。结果表明,在氮气保护下,焙烧后的水滑石可以成功复原,硬脂酸钠对LDHs的改性为表面改性,但影响复原水滑石的结晶度。改性水滑石可以改善PVC的初期着色性和长期热稳定性,随着改性剂浓度的增大,当NaSt与LDHs质量比为1∶4时,静态热老化时间可以达到370 min,比未改性水滑石热稳定性能提升了61%。