n-Butane Isomerization Over SO4 =/NiO/Al2O3/ZrO2 Catalysts. Effect of the Reaction Pressure and Metal Loading

The effect of alumina and nickel in sulfated ZrO₂ as a catalyst for n-butane isomerization was investigated. Samples were synthesized by supporting nickel sulfated zirconia on boehmite and then calcining the material. The crystalline structure of ZrO₂ was studied by X-ray powder diffraction and refined by the Rietveld method. Surface areas were determined by N₂ adsorption and BET analysis, while the acid properties were studied by NH₃ adsorption. The chemical reaction was carried out in a fixed-bed microreactor at 338 K under atmospheric (78 kPa) or 245 kPa total pressure. Results showed that either nickel or alumina improved the catalytic activity, but a synergic effect was observed when both components assisted. The catalytic activity was related to the relative content of tetragonal zirconia and acid site density. Alumina stabilized tetragonal zirconia increased the acid site density and presumably led to a better dispersion of nickel oxide. The catalytic activity could be related to both oxidation and acid sites produced by nickel. A bimolecular reaction mechanism helps explain the observed trends. The increase in the reaction rate would be explained by the increase in the rate of the initial step of dehydrogenation either caused by a better dispersion of nickel or higher operating pressure.     

The SMSI between supported platinum and CeO2–ZrO2–La2O3 mixed oxides in oxidative atmosphere

CeO₂–ZrO₂–La₂O₃ (CZL) mixed oxides were prepared by citric acid sol–gel method. The as-received gel was calcined at 500, 700, 900 and 1050 °C to obtain the so-called C5, C7, C9 and CK, respectively. The C5, C7 and C9 powders were impregnated with H₂PtCl₆ and then calcined at 500 °C to prepare P5C5, P5C7 and P5C9, respectively. The impregnated CK powders were calcined at 500, 700 and 900 °C to prepare P5CK, P7CK and P9CK, respectively. The XRD and XPS analyses show that the surface distribution of Pt is evidently influenced by the structural and textural properties of the support. The CO adsorption followed by FTIR reveals that the dispersion and the chemisorption sites of Pt are reduced as the calcination temperature of CZL support increases. The chemisorption ability of the CK samples is even completely deactivated. The encapsulation mechanism, which has been applied to explain the so-called strong metal–support interaction (SMSI) after reductive treatment, is introduced here to demonstrate the abnormal observations though the samples were prepared in oxidative atmosphere. The HRTEM results also confirm this explanation. The effects of oxygen vacancies, the chemisorption sites on the Pt surface and Pt/Ce interfacial sites on the three-way catalytic activities are discussed.     

醇酮装置废酸水中副产物的回收利用探讨

分析了醇田装置副产物的生成过程和借鉴国外辞酮装置废酸水和皂化废碱液的回收利用技术，提出了合并浓缩、脱过氧化氢生产混合二元酸及硝酸后氧化、结晶、真空间歇精馏相结合分高己二酸、戊二酸、丁二酸的两种回收利用的工艺方法，并提出了两个工业化装置的设想，对治理废酸水提出了建设性意见。     

基于循环检测的气动退化图像混合域去噪算法

气动退化图像中存在先验信息未知以及噪声成分复杂不易进行滤波处理的问题,为此,提出一种气动退化图像混合域去噪算法。设计针对高斯噪声、泊松噪声、固定值脉冲噪声和随机值脉冲噪声的混合检测方法,使用改进的滤波方法在空域去除固定值脉冲噪声和随机值脉冲噪声,进行非下采样轮廓波变换多层分解,在变换域使用阈值方法去除高斯噪声和泊松噪声。进行噪声循环检测,设定迭代停止条件控制算法循环从而实现算法自适应。仿真实验结果表明,该算法的噪声检测性能和滤波性能较好,图像细节信息得到正确恢复。同时,算法复杂度较低,实时性较好,可满足气动退化图像去噪处理的需要。     

混炼硅橡胶的配合技术(四)

介绍了几种胶辊用混炼硅橡胶的配制,包括低硬度胶辊用混炼硅橡胶、低环硅氧烷含量的胶辊用混炼硅橡胶、送纸胶辊用混炼硅橡胶及工业胶辊用混炼硅橡胶的配制。     

Coordination between strategic forest management and tactical logistic and production planning in the forestry supply chain

In this paper, we study the coordination mechanism in the forestry supply chain between strategic forest management and tactical production planning. We first formulate an integrated model to establish a theoretical benchmark for performance of the entire supply chain. It is a mixed integer programming model that involves harvesting, bucking, transportation, production, and sales decisions for both tactical and strategic planning levels. We then present two sequential approaches S‐A and S‐B where the coordination is done through internal pricing. S‐A is the approach currently used in practice where harvesting in the forest is the main driver of the supply chain activities and internal pricing is introduced to control bucking decision in a separate stage. In contrast, S‐B takes downstream demand information into consideration and internal pricing directly influences harvesting decision in the first stage. In order to find the appropriate setting of internal pricing that leads to the system optimum, we suggest two heuristics H‐I and H‐II. The internal pricing in H‐I is based on dual values and in H‐II, it is derived from a Lagrangian decomposition. A real‐life case study in the Chilean forestry industry is used to compare the results of different approaches. It is shown that the new sequential approach S‐B generates as good feasible solution as that obtained from the integrated approach but in much less time. Both heuristics H‐I and H‐II bring about near‐optimal feasible solutions. H‐II also provides optimistic bound of the optimal objective function value, which can be used as a measure of the solution quality.     

高气速选择性分离氨碳混和气模拟实验

采用二级串联鼓泡吸收器对NH3／CO2摩尔比为2：1的混和气体进行高气速选择性吸收，获得氨的总吸收率为96．7％，二氧化碳的总吸收率为33．1％，二级吸收器出口气相CO2摩尔含量达90．9％，液相氨碳摩尔比为5．85。将此吸收液在加压下精馏分离氨，基本可以把吸收液中游离氨回收。分离游离氨后的溶液在常压下进行解吸，蒸馏塔出口液体含NH3和CO2量仅为0．014％和0．006％，解吸气回串联吸收器进行循环吸收分离。对预计工业分离过程进行物料和能量衡算，分离1kg液氨需1MPa的蒸汽约3.2kg。     

一类混合延迟混沌神经网络的同步

时滞混沌神经网络系统是解空间为无穷维系统,可生成多个正向Lyapunov指数,产生具有高度随机性和不可预测性的混沌甚至超混沌序列,这种特性使得时滞混沌神经网络系统特别适用于保密通信中,混沌同步是保密通信中的关键技术。基于Lyapunov稳定性理论和线性矩阵不等式(LMI)方法,研究了一类具有时变延迟和分布式延迟的混沌神经网络系统的同步问题,考虑系统的内部参数不确定性和外部干扰及混合时滞等因素,将系统时滞项加入所设计的控制器中,给出了保证误差系统的全局均方渐近稳定的充分条件和控制律,实现驱动系统和响应系统的同步。与其它方法相比,所设计的含有时滞项的控制器提高了系统误差精度及反应速率。最后,通过仿真实例,验证了所提方法的有效性。     

Ethanol combustion over strontium- and cerium-doped LaCoO3 catalysts

Ce- or Sr-doped LaCoO₃ bulk perovskites were prepared by citric acid method as well as 10 wt.% of LaCoO₃ was deposited on alumina carrier stabilized with lanthanum. Properties of prepared materials were characterized by determination of surface area, acid-basic properties and XRD, XPS, TPDO₂, H₂-TPR measurements as well as catalytic activity and selectivity for ethanol combustion was tested. It was found that substitution of La in LaCoO₃ with either Sr or Ce has only small effect on its activity in ethanol combustion. Strontium inserted into LaCoO₃ structure increases basic character of the perovskite surface as well as selectivity to acetaldehyde (ACA). Substitution of La with cerium has no effect on the concentration of basic sites and does not affect the selectivity to ACA. Activity of LaCoO₃-based catalysts in ethanol combustion and their selectivity to ACA formation can be explained on the basis of the presence of both -oxygen species and sites with basic character on the material surface.

Acid-basic properties of supported LaCoO₃ are dominated by acidic character of the carrier. Results of XPS and H₂-TPR measurements of LaCoO₃ supported on La–Al₂O₃ suggest that perovskite remains in strong interaction with carrier and probably is partially decomposed. Deposition of perovskite on stabilized carrier significantly increases the rate of ethanol combustion.     

同时发生初次和二次成核且为聚结控制的沉淀过程多定态及稳定性分析

The possibility of multiplicity in an isothermal continuous mixed suspension-mixed product removal crystallizer is explored using the bifurcation theory.A process involving agglomeration controlled precipitation is considered in which secondary nucleation occurs simultaneously with primary nucleation.The determinant equations for the existence of multiple steady states are developed and the multiplicity boundaries dependent on the physical and kinetic properties and operational parameters of the process are obtained by resolving these determinant equations.The number of steady states in the precipitator for various multiplicity regions is determined and the linear stability of these steady states is analyzed by using the Routh criterion.