煤化工用水及废水处理分析

概述了煤化工高能耗、高污染、高耗水的产业特点,从工艺、意识、来源分析了造成产业特点的原因。为了减少煤化工废水中有毒害物质的含量,介绍了常用的废水处理方法,展望了煤化工用水及废水处理发展趋势。     

微波条件下氯化锌对乙醇抽提神府煤的影响

微波条件下,研究了在乙醇抽提神府煤中加入氯化锌对其结果的影响。采用气相色谱/质谱联用的方法分析了乙醇和乙醇-氯化锌抽提物的组成;利用傅里叶红外光谱技术分析了神府脱矿物质煤、乙醇抽余煤和乙醇-氯化锌抽余煤的结构。分析结果显示:在乙醇溶剂中添加少量的氯化锌,其抽提物的组成发生了改变;乙醇-氯化锌抽余煤与原脱矿物质煤和乙醇抽余煤相比,芳环吸收强度降低,表明在抽提过程中可能伴随着烷基化反应的发生。     

三相气升式环流反应器内上升区相含率轴向分布与循环液速的研究

常温常压下,在三相气升式内环流反应器中,将硅铝球、石英砂和瓷球分别与空气、水组成三相物系,考察了细颗粒与大颗粒物系中上升区相含率轴向分布规律、固体装载率和颗粒粒径对该规律的影响,以及各物系中上升区循环液速随表观气速的变化规律。结果表明:随轴向高度的增加,瓷球物系中上升区固含率εsr先增大后减小;硅铝球物系中εsr减小;石英砂物系中εsr均匀分布。随轴向高度的增加,瓷球物系中上升区气含率εgr增大;硅铝球物系中εgr减小;石英砂物系中εgr先增大后减小。固定表观气速,各轴向位置处的上升区气含率随固体装载率、颗粒粒径的增大而增大。当固体装载率相同时,各物系中上升区循环液速随表观气速的增大而增大。     

Influence of ash agglomerating fluidized bed reactor scale‐up on coal gasification characteristics

To study the influence of fluidized‐bed reactor scale‐up on coal gasification characteristics, a model of the ash agglomerating fluidized‐bed reactor has been developed using an equivalent reactor network method. With the reactor network model, the scale‐up effects of a gasifier were studied in terms of the characteristics of the chemical reactions in the jet zone, the annulus dense‐phase zone and the freeboard zone. Results showed that the changes occurred in the inequality proportion of the volume of the jet zone during the reactor scale‐up. Taking into consideration the utilization of a portion of the backflow gas, the expansion of the jet zone volume and the coal particle residence time, the temperature of the jet zone was increased from 1592 to 1662 K. Also, both the annulus dense‐phase zone temperature and the freeboard zone temperature decreased, causing subsequent decrease in the carbon conversion efficiency. © 2014 American Institute of Chemical Engineers AIChE J, 60: 1821–1829, 2014     

Regime transition in viscous and pseudo viscous systems: A comparative study

A comprehensive quantitative study on the effect of liquid viscosity (1 ≤ µ_L ≤ 1149 mPa‐s) on the local flow phenomena of the gas phase in a small diameter bubble column is performed using ultrafast electron beam X‐ray tomography. The internal dynamic flow structure and the bubble size distribution shows a dual role of the liquid viscosity on the hydrodynamics. Further, the effect of solid concentration (C_s = 0.05, 0.20) on the local flow behavior of the gas phase is studied for the pseudo slurry viscosities similar to the liquid viscosities of the gas–liquid systems. The effects of liquid and pseudo slurry viscosities on flow structure, bubble size distribution, and gas phase distribution are compared. The bubble coalescence is significantly enhanced with the addition of particles as compared to the system without particles for apparently same viscosity. The superficial gas velocity at which transition from homogeneous bubbly to slug flow regime occurs is initiated by the addition of particles as compared to the particle free system for apparently same viscosity. © 2014 American Institute of Chemical Engineers AIChE J, 60: 3079–3090, 2014     

Rapid and large‐scale separation of magnetic nanoparticles by low‐field permanent magnet with gas assistance

Bubbles can be used to greatly improve the speed of magnetic separation (MS) and overcome the limitation of magnetic force on the capture distance, making low‐field MS highly efficient and easily scalable. This novel method leads to the development of a medium‐free continuous gas‐assisted magnetic separator on small pilot scale using low‐field permanent magnet. This separator is demonstrated highly efficient for recovery of proteins‐loaded magnetic nanoparticles from large volume biosuspension. © 2014 American Institute of Chemical Engineers AIChE J, 60: 3101–3106, 2014     

Insight into the intraparticle diffusion of residue oil components in catalysts during hydrodesulfurization reaction

Well‐defined and uniform pore structure catalysts were used to study the intraparticle diffusion of fractionated Saudi vacuum residue under hydrodesulfurization (HDS) reaction conditions. HDS rates of residue oil cuts with different molecular weights are determined as functions of pore size, temperature, and pressure in a trickle‐bed reactor. Credible intrinsic and bulk diffusivities of organosulfur compounds in residue oil were obtained for the first time, from the apparent and intrinsic reaction kinetic constants. Intrinsic diffusivities ranged from 2 × 10^?7 to 8 × 10^?7 cm²/s for the residual oil molecules; diffusivity decreases with increasing molecular weight of the residual oil. The intrinsic diffusivity for molecular weights ～1000 Daltons increases with pore size for pores <70 nm, but is nearly independent of pore size for pores >70 nm. The diffusivity dependences on pore size and molecular weight suggest that the onset of restricted diffusion occurs for ratios of molecular diameter to pore diameter of ～0.04. © 2014 American Institute of Chemical Engineers AIChE J, 60: 3267–3275, 2014