金属氧化物对Ca(OH)_2脱硫影响的研究

1前言鉴于钙基吸收剂干法烟气脱硫技术在脱硫产物处理等方面的优势，本文开展了Ca（O）。中低温干燥状态下的反应特性、活化能及其影响因素的试验研究，以求进一步增强对其反应特性的了解并弄清金属氧化物的作用。2装置及样品试验装置如图1示，采用硫化床形式以强化吸收剂与气相反应物之间传质。床层温度由理入反应器内的热电偶测出并由温控仅控制。SOZ气体经稀释气体稀释并混合、预热后流入反应管进行反应，反应后气体由尾部的SOZ吸收水箱吸收后排入大气。冷却室可防止水蒸气进入气体分析仪。通过记录SOZ浓度随时间的变化规律即可得到…     

地脉动作用下主机装置靶室结构稳定性分析与评估

在大型固体激光器结构稳定性设计中,数值模拟结果是结构稳定性设计的主要依据,故数值模拟的可信度至关重要。为了评估装置稳定性计算结果的可信度,基于现代模型验证与确认技术中关于不确定性源的量化及传播分析方法、模型形式误差与预测推断的叠加方法研究,对靶球结构的最大位移响应进行了预测推断。稳定性分析中为了快速进行不确定性参数的传播和灵敏度分析,使用二次响应面模型作为代理模型,灵敏度分析结果表明模态阻尼比对靶球结构的稳定性影响更大。对关心量的稳定性预测结果表明,靶球结构最大位移响应的上界与稳定性设计指标相比,安全裕度仍大于7,说明主机装置的稳定性设计具有足够的可信度。     

Rotation speed measurement of moving particles in a CFB riser

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循环流化床热电气三联产装置研究

循环流化床热电气三联产装置研究岑可法，方梦祥，骆仲泱，李绚天，陈飞，王勤辉，陈冠益，倪明江（浙江大学热能工程研究所杭州３１００２７）关键词循环流化床，气化，煤气蒸汽联产１前言在近几年来，我国能源仍主要以煤炭为主，而目前煤炭的绝大部分作为燃料直接燃用，...     

The maximum principles for partially observed risk-sensitive optimal controls of Markov regime-switching jump-diffusion system

ABSTRACT

This paper studies partially observed risk-sensitive optimal control problems with correlated noises between the system and the observation. It is assumed that the state process is governed by a continuous-time Markov regime-switching jump-diffusion process and the cost functional is of an exponential-of-integral type. By virtue of a classical spike variational approach, we obtain two general maximum principles for the aforementioned problems. Moreover, under certain convexity assumptions on both the control domain and the Hamiltonian, we give a sufficient condition for the optimality. For illustration, a linear-quadratic risk-sensitive control problem is proposed and solved using the main results. As a natural deduction, a fully observed risk-sensitive maximum principle is also obtained and applied to study a risk-sensitive portfolio optimization problem. Closed-form expressions for both the optimal portfolio and the corresponding optimal cost functional are obtained.     

Relationship between surface microstructure and properties of supported catalyst Rh/Ys

The inner structure of Rh/Ys,a novel high efficiency supported catalyst,and the spreading of Rh on the Ys surface were analyzed through electron transmission microscopy and scanning tunnel microscopy.The relationship between the distribution of Rh over the support and the preparation temperature of th catalyst was determined.The formation of Rh-C bond was confirmed by XPS and far-IR spectra.The loss of Rh from the surface of the support and the catalytic activity under different preparation conditions have been compared.The internal factors for the high activity and high stability of the novel Rh/Ys catalyst have been discussed.     

Kinetic studies on vapor phase carbonylation of methanol to acetic acid over Rh/Ys catalyst

A novel catalyst Rh/Ys for the carbonylation of methanol to acetic acid with CH3I as the promoter shows excellent activity and selectivity.The reaction is kinetically controlled.The reaction rate is in proportion to the concentration of Rh and CH3I but has nothing to do with those of CH3OHH and CO.The surface active energy is Ea ~51.02 kJ/mol.A mechanism is also proposed.     

复合掺杂氧化物La0.5Sr0.5CoO2.91的性能和稳定性

采用固相反应法和柠檬酸-硝酸盐溶胶-凝胶低温自蔓延燃烧法（简称柠檬酸法）合成了La0.5Sr0.5CoO2．91（LSC）复合氧化物。借助XRD和SEM对不同制备方法合成粉体的晶体结构和晶粒形貌进行了研究。结果表明：固相反应法可制得均一钙钛矿结构的LSC氧化物，柠檬酸法除制得LSC氧化物外，还有LaSrCoO4相的生成。柠檬酸-硝酸盐溶胶-凝胶低温自蔓延燃烧法合成粉体的粒度相对较小。为研究以Ce0．9Gd0.1O1．95（GDC）为电解质的固体氧化物燃料电池阴极材料的性能，将LSC粉体与GDC粉体按6：4（质量比）制备了固体氧化物燃料电池（SOFC）的阴极片。在空气气氛下使用直流四探针法研究了烧结样品300～800℃的电导率，发现由柠檬酸法得到粉体制备的阴极片的电导率值较高。将制备的样品置于马弗炉中800℃条件下烧结800h，比较失效前后电导率的变化情况，并借助XRD，SEM等测试手段分析样品电导率变化的原因。分析发现，失效后两种样品的电导率值都有所降低，且样品中都有新相生成，晶体形貌有较大的变化。     

Mechanism of Formation and Consequent Evolution of Active Cellulose during Cellulose Pyrolysis

An intermediate product that was yellow, soluble, and solid was obtained in a high-radiation flash pyrolysis reactor. Under two different radiant heat fluxes, the yields tended to both increase initially until achieving a steady state, and then increase again with the progress of reaction. The compositional analysis of the yellow product was performed on high performance liquid chromatography (HPLC). It was indicated that the product mainly consisted of oligosaccharides, glucose, levoglucosan, methylglyoxal and so on. The compounds including oligosaccharides such as cellobiose and cellotriose, and monosaccharides such as glucose were regarded as active cellulose. Under the higher heat flux, the relative yield of the active cellulose increased initially, followed by a decreasing trend, and achieved a maximum mass fraction of 68% (w) in the soluble yellow product. The oligosaccharides with higher degree of polymerization (DP) were the primary components. Under the lower heat flux the yield of active cellulose was relatively lower, achieving a maximum of about 57% (w), and more saccharides with lower DP were contained. It was suggested that active cellulose was quite unstable at high temperature, and easily decomposed into saccharides with lower DP, even char, volatiles, and gaseous products. Finally an improved mechanism was proposed to describe the reaction route of formation and consequent evolution of active cellulose during cellulose pyrolysis.