道路用聚氨酯改性沥青的制备工艺探讨

结合不同改性剂掺量单因素试验,确定了采用88mm叶轮、115mm容器、圆盘锯齿式搅拌器(转速1400r/min)、175℃共混温度、改性剂掺量4.27%、单次搅拌300g的制备工艺参数。在此条件下制备的聚氨酯改性沥青具有优异的水稳定性、储存稳定性且耐老化、耐高温,拥有比普通聚合物改性沥青更高的车辙因子G*/sinδ和15℃动态模量,基本满足高模量沥青要求。     

Effect of preparation method on physicochemical properties and catalytic performances of LaCoO_3 perovskite for CO oxidation

Perovskite oxides LaCoO_3 prepared by templating, co-precipitation and sol-gel method with different complexants were systematically characterized and its catalytic performances for CO oxidation were investigated. The samples were characterized by X-ray diffraction, thermogravimetry analysis and differential scanning calorimetry, N_2 physisorption, transmission electron microscopy, temperature program reduction of hydrogen, temperature program desorption of oxygen and X-ray photoelectron spectroscopy measurement, results of which show that the properties of LaCoO_3, such as surface morphology, surface area, surface compositions, redox capability, oxygen vacancy, as well as the calcination temperature and formation mechanism, depend intimately on the preparation method. Catalytic tests indicate that the sample prepared by carbon templating method shows the best activity for CO oxidation, with full CO conversion obtained at 135 ℃. In particular, the catalyst can be activated and significant increase of activity can be obtained with the increase of reaction time. The cyclic and longterm stability of catalysts were discussed and compared.     

海洋非成岩天然气水合物原位快速制备实验及评价

我国的海洋天然气水合物（以下简称水合物）资源主要分布在沿海大陆架水深介于300～3 000 m的深水区，具有弱胶结、非成岩的特征，为了测试和研究该类型水合物必须原位、大量、快速制备样品，而目前常用的搅拌法、喷淋法、鼓泡法等制备技术却存在着生成速度慢、储气密度低等问题。为此，自主设计、研制了1 062 L非成岩水合物快速制备釜，针对我国南海非成岩水合物的物性特征，开展了搅拌法、鼓泡法、喷淋法单一制备方法及“三合一”法（上述3种方法相结合）水合物制备实验，测试了实验过程中温度、压力、电阻率及反应时间等数据，分析比较了几种不同制备方法的水合物生成情况与制备效率。实验结果表明：①搅拌法、鼓泡法、喷淋法制备水合物过程中，生成的水合物均缓慢增加并逐渐铺满整个液面；②搅拌法制备过程中可以观测到明显的诱导期，而喷淋法、鼓泡法及“三合一”法却无明显的诱导期；③单一制备方法及“三合一”法制备水合物过程中，电阻率均随反应时间的增加而增加，其变化趋势亦与水合物制备速率基本一致；④“三合一”法的制备周期明显短于单一制备方法（搅拌法、喷淋法、鼓泡法单一方法的制备时间分别约为“三合一”法的5.14倍、3.59倍、3.16倍）。结论认为，所研制的1 062 L水合物快速制备釜能够实现海洋非成岩水合物样品的原位、快速制备；较之于单一制备方法，“三合一”法大大提高了水合物的制备效率。     

Preparation and properties of Eu and Dy co-doped strontium aluminate long afterglow nanomaterials

The long afterglow nanomaterials of strontium aluminate co-doped by Eu and Dy have been synthesized by co-precipitation combined hydrothermal method. The effects of hydrothermal time, calcination time, pH value, the amount of aluminum nitrate, activator, co-activator and flux H₃BO₃ on the fluorescence properties of the product were investigated by means of single factor optimization experiment. Then the orthogonal experiment was employed to obtain the optimal synthesis conditions that are as follows: n_Dy/n_Eu = 2.5, t_c = 2.5?h, n_Eu/n_Sr = 0.02, t_h = 8?h. Subsequently, the optimal synthesis conditions were verified by three repeated experiments, and the obtained products were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX) and fluorescence spectrometer. The results showed that the synthesized target products all were the mixed crystal phase of SrAl₂O₄ and Sr₄Al_l4O₂₅. The particles presented regular spherical-like with size ~ 100?nm. The dopants Eu and Dy were confirmed existed in the SrAl₂O₄ powders. The fluorescence and afterglow data of the target products were better than that in the orthogonal experiment scheme. The primary emission spectra band was in the range of 400–600?nm with characteristic peak located at ~ 460?nm corresponding to the transitions of Eu²⁺ ions from 4f⁶5d→4f⁷, and the blue light can be observed by naked eyes. The similar fast-decaying and slow-decaying processes were displayed in all the afterglow curves, and the initial afterglow brightness of the target product is apparently higher than that of products synthesized by the orthogonal experiment. The synthesized target products, which show excellent long afterglow performance, present a great application prospects in the aspects of ceramics, plastics, arts and crafts, ink and coating.     

An excellent universal catalyst support-mesoporous silica: Preparation,modification and applications in energy-related reactions

As a kind of versatile, excellent catalyst carriers, mesoporous silicas (mSiO₂) have been widely applied for preparing various supported catalysts with ideal catalytic properties due to their uniform and regular channels, adjustable medium pore size, big surface area, controllable wall composition, high hydrothermal stability, easy functional modification and good accessibility of larger reactant molecules. mSiO₂ not only enhances the dispersity of the active phase and generates more active sites for superior catalytic activity but also improves resulted selectivity and cyclic lifespan for enhanced interaction. And high adsorption capacity of mSiO₂ also increases the reactant molecule enrichment. In addition, mesoporous feature of the mSiO₂ pore wall can ensure diffusion of the substrate molecules and prevent leaching of active components. Thus, related investigation and application have been rapidly growing in the past decades. In this review, the development of mesoporous silica based catalysts on preparation, modification, pore size tune and energy-related applications, especially in hydrogenation reaction, esterification reaction, hydrogen production by alkane dry reforming and alcohol steam reforming and photocatalytic water splitting, is introduced in detail and the design ideas, preparation strategies and corresponding mechanism of different composite catalysts are discussed.     

Preparation and Application of Perovskite Catalysts for Diesel Soot Emissions Control: An Overview

The diesel engines are energy efficient (1), but their particulate matter (soot) emissions are still a matter of concern even though major advances in their control are being made. For soot abatement, catalytic diesel particulate filter (DPF) technique is widely employed to trap and burn the soot. Many types of catalysts have been investigated for the soot combustion i.e. platinum group metal (PGM) based, perovskite-type oxides, spinel-type oxides, rare earth metal oxides, and mixed transient metal oxides etc. The cost of PGM catalysts is high and their availability is questionable. Further they are susceptible to poisoning and have low thermal stability. On the other hand perovskite catalysts show potential as effective soot oxidation catalyst for the DPF because of their low cost, high thermal stability and tailoring flexibility. Many papers related to soot oxidation over perovskite catalysts have been published but no review paper appears in the literature that is dedicated to soot oxidation. Thus, this article provides a summary of published information regarding pure and substituted perovskite catalyst, preparation methods, properties, and their application for diesel soot emission control.     

Preparation and characterization of NaBiO3 nanopowders by different methods for photocatalytic reduction of CO2

In this work we prepared NaBiO₃ nanopowders via three synthesis methods (sol-precipitation, dehydration and hydrothermal methods). To evaluate and compare the physical properties of the prepared materials X-ray diffraction analysis, BET measurements, UV–vis spectroscopy and TEM were applied. The results showed changes to the NaBiO₃ crystallinity, the specific surface area and the particle shape and size, depending on the method of synthesis. To determine the photocatalytic efficiency of the prepared materials, we evaluated the photocatalytic reduction of CO₂.     

超高分缔合聚合物驱注聚站的监测

针对高温高盐油藏,胜利油田开展了超高分缔合聚合物驱先导试验。试验研究发现,超高分缔合聚合物需要在高温下溶解,注聚站必需密切监测污水温度,保证矿场的配制温度。注聚站的沿程剪切及污水水质严重影响聚合物的黏度,矿场需要进行母液沿程损失及配制水水质的监测。同时,注聚站进行聚合物浓度及注入液的黏度监测,以保证矿场实施效果。     

Preparation and Characterization of C10–C14 Alkyl Cellulose Ester Sulfate Surfactant

The aim of this work is to synthesize surfactants based on cellulose with different molecular weights. Raw cotton cellulose was tailored into cellulose segments with different molecular weights by a hydrothermal process, then the average degree of polymerization (DP) was determined by viscosimetry and the molecular weight distribution was estimated by gel permeation chromatography. The C₁₀–C₁₄ alkyl cellulose ester sulfate surfactants were prepared by hydrophilic sulfonation and hydrophobic esterification. The surface tension of the surfactants solution was obtained by the Wilhelmy plate method. Results showed that the cellulose segments presented a broader distribution compared with the raw material. The critical micelle concentration (CMC) value decreased from 1.08 to 0.86 wt% as the hydrophobic chain length was increased from 10 to 14. The CMC values of cellulose surfactants with C₁₄-acyl chloride hydrophobization decreased from 1.32 to 0.86 wt% as the DP was decreased from 2,700 to 296.     

Preparation of a Novel Class of Cationic Gemini Imidazolium Surfactants Containing Amide Groups as the Spacer: Their Surface Properties and Antimicrobial Activity

A class of novel cationic Gemini imidazolium surfactants containing amide groups as the spacer were synthesized from ethylenediamine and 1-bromoalkane(C₈, C₁₀, C₁₂, C₁₄, C₁₆) by N-alkylation to get N,N′-dialkyl ethylenediamine (1a–e), 1a–e was further reacted with chloroacetyl chloride by N-acylation to get N,N′-(ethane-1,2-diyl)bis(2-chloro-N-alkylacetamide) (2a–e), which was further reacted respectively with 1-methyl imidazole by quaternized to form the surfactant molecule, N,N′-((ethane-1,2-diyl)bis(alkyl-azanediyl)bis(2-oxoethane-2,1-diyl)) bis(1-methyl-1H-imidazol-3-ium) dichloride. The structures of intermediates (1a–e) and (2a–e) were characterized by IR and ¹H NMR. The structures of the surfactants (3a–e) were characterized by IR, ¹H-NMR and ¹³C-NMR and element analysis. The critical micelle concentrations (CMC) of 3a–e were determined by the conductivity method at 25 °C. The CMC values decreased with increasing the length of the hydrophobic chain. The surfactants (3a–e) showed good foaming stability, emulsion ability and wetting ability. The surfactants (3a–e) also have good antimicrobial activity against Staphylococcus aureus, Escherichia coli and Bacillus subtilis.