大化肥煤代油CO耐硫变换工艺流程的设计

分析石脑油制氨装置改扩建为水煤浆制氨装置ＣＯ耐硫变换工艺的特点，具体阐述其工艺流程优化设计中需考虑的主要技术问题。     

炭粒床高效工业除尘装置的设计与开发

The new dust removal technical route using the carbon-granular bed filter,packed of carbon particles with appropriate grade derive from an online-process vibration sieve,to replace the traditional baggy filter had been developed successfully for capturing the micro-carbon dusts produced from pulverization of petroleum coke,and the green close loop of carbon materials is thus completed in the combined pulverizing and classifying system and pulverized carbon dust removal process.The high dust removal efficiency greater than 99%,low outlet dust concentration less than 100 mg.m-3,low pressure drop through dust filtration chamber less than 980 Pa,simple and easy design,and flexible and stable operation were achieved also with the carbon-granular bed filter in both bench and industrial scale operations.     

利用ADCP回波强度估算河流悬移质含沙量的应用研究

通过简要介绍利用声学多普勒水流剖面仪(ADCP)回波强度估算悬移质含沙量的基本原理,结合梧州水文站的应用实例,利用ADCP的回波强度数据和现场采集的水样含沙量建立相关关系,根据相关关系由回波强度反演估算的水体悬移质含沙量验证了利用ADCP的回波强度估算悬移质含沙量的可行性。应用于梧州水文站的实践表明,左河道推算的系统误差为-0.1%,右河道推算的系统误差为1.5%。这种方法具有不扰动流场、测量剖面同步性较好、数据空间分辨率较高的优点,与传统的取样过滤称量法相比,计算效率显著提高。     

大面积水域浓度场测试方法及系统研究

针对大面积水域浓度场难以实现实时测量、测量精度不高等问题,采用了一种多通道荧光测试系统和方法。首先,基于单色光诱导荧光检测浓度(LIF)原理,使用探头获取离散点的浓度参数。然后,经总线或通信网络技术,将数百个测点连接起来。最后,通过数据总线或网络将采集的数据输送到中央测控计算机中,处理离散的数据后形成完整的浓度场。在恒定流浓度场中的试验结果表明,污染物测量相对误差均值不超过5%,单次测量相对误差最高值为8.33%,传感器线性度不超过5%,可检测的荧光素钠溶液浓度分辨率为0.001 ppm,系统测量稳定、精度较高。相较于其他浓度测量方法,该系统具有测量面积大、实时测量的优势,可为水污染防治等领域提供可靠的技术支撑。     

PARTICLE FLOW PATTERNS IN THE RISER AND DOWNER OF CIRCULATING FLUIDIZED BED

This paper presents an experimental study on the flow patterns of FCC particles in a 140 mm ID Circulating Fluidized Bed with concurrent upflow and downflow gas-solid suspension. Based on the distribution of local particle velocity and particle concentration measured by a Fiber-Optical Probe Laser Doppler Velocimeter and a Fiber Optical Probe System respectively, the different flow patterns of local particls concentration, local particle velocity, local particle fluctuating velocity and sectionally average particle velocity in concurrent upflow and downflow gas-solid system have been investigated. It is found that the particle flow in the concurrent downflow is much more uniform radially than that in the concurrent upflow riser. The investigation of flow patterns in different flow systems is of significance to the development of a new gas-solid reactor.     

臭氧氧化处理法对聚丙烯表面涂装性的改良 Ⅱ.臭氧浓度及臭氧发生气组成对聚丙烯表面氧化过程的影响

讨论了用臭氧氧化法对聚丙烯表面进行涂装性改良时,臭氧浓度和臭氧发生气组成对聚丙烯表面氧化过程的影响。我们发现,随臭氧浓度的增加,各种聚丙烯表面上COOH基的生成速率变大,而OH基的生成速率变小,且表面上COOH基和OH基的生成比变大。在相同的臭氧浓度下,COOH基的生成速率和聚丙烯种类无关,各种聚丙烯表面上COOH的生成速率大体相等。而OH基的生成速率及COOH基、OH基生成比和聚丙烯的种类有关,就COOH基和OH基生成比而言,其大小顺序为均聚物>嵌段共聚物>无规共聚物。臭氧发生气组成对聚丙烯表面氧化过程有很大的影响。和臭氧发生气为空气时的情况相比,当臭氧发生气为氧气时,即使其体系中臭氧浓度的变化很小,也会引起较大的表面氧吸收量或表面氧化分解量的变化。     

Characterization and Catalytic Properties of Combustion Synthesized Au/CeO2 Catalyst

Ceria-supported Au catalyst has been synthesized by the solution combustion method for the first time and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Au is dispersed as Au⁰ as well as Au³⁺ states on CeO₂ surface of 20-30 nm crystallites. On heating the as-prepared 1% Au/CeO₂ in air, the concentration of Au³⁺ ions on CeO₂ increases at the expense of Au⁰. Catalytic activities for CO and hydrocarbon oxidation and NO reduction over the as-prepared and the heat-treated 1% Au/CeO₂ have been carried out using a temperature-programmed reaction technique in a packed bed tubular reactor. The results are compared with nano-sized Au metal particles dispersed on -Al₂O₂ substrate prepared by the same method. All the reactions over heat-treated Au/CeO₂ occur at lower temperature in comparison with the as-prepared Au/CeO₂ and Au/Al₂O₂. The rate of NO + CO reaction over as-prepared and heat-treated 1% Au/CeO₂ are 28.3 and 54.0 mol g^-1 s^-1 at 250 and 300 °C respectively. Activation energy (E _a) values are 106 and 90 kJ mol^-1 for CO + O₂ reaction respectively over as-prepared and heat-treated 1% Au/CeO₂ respectively.     

Surface activity of quaternary ammonium salts derived from jojoba oil

A number ofcis andtrans quatenary ammonium salts were synthesized from jojoba oil. All derivatives were found to be surface active agents, i.e., they reduced the surface tension to 35 dynes/cm⁻¹, at very low concentrations. The relationship between the surface activity and the molecular structure is discussed.     

Kinetics of the methanation of carbon dioxide over a supported Ni-La2O3 catalyst

The kinetics of the methanation of carbon dioxide was investigated using an alumina supported Ni-La₂O₂ catalyst in a differential and integral reactor. In the differential reactor the molar ratio of H₂ to CO₂ was varied from 0.6 to 30. In the integral reactor the rates were measured with up to 90% conversion. Both reactor tests were carried out at temperatures between 513 and 593 K. The experimental results were described by a Langmuir-Hinshelwood type equation. The kinetics can be explained by assuming equilibrium of dissociative carbon dioxide and hydrogen adsorption, and assuming hydrogenation of surface carbon as the rate determining step.     

IR study of the interaction of hydroxyl groups of silica gel with Cr species of Phillips' type catalysts

Spectroscopic evidence for the interaction of hydroxyl groups and chromium ions was obtained using a catalyst prepared from chromyl chloride. A new OH peak, observed at 3705 cm^–1 after pumping away CO gas, is attributed to the direct interaction of OH with the low-valent chromium. This peak shifts to 3590 cm^–1 on contact with O₂ at room temperature and it is assigned to a hydroxyl interacting with the oxidized chromium. New assignments are also proposed for IR bands of CO presorbed on the catalyst. The peak due to CO at 2188 cm^–1 decreases as the OH intensity at 3705 cm^–1 increases, suggesting that the former peak arises from adsorption on Cr(II) species to which two oxygen atoms are attached.