氯化钾结晶器搅拌选型探研

反浮选冷结晶氯化钾生产的关键在于DTB结晶器中的控速分解和控速结晶,而控速的关键在于搅拌器的调速,因此本文通过对搅拌工作原理、类型及机理的粗浅分析,在保证不影响分解和结晶速率的情况下选用合适的搅拌型式,生产实践证明:推进式轴流型搅拌较之折叶式径漉型搅拌在提高氯化钾产品的粒度方面有极大的优越性.     

Thin-film reactions during diffusion soldering of Cu/Ti/Si and Au/Cu/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> with Sn interlayers

The multilayer thin-film systems of Cu/Ti/Si and Au/Cu/Al₂O₃ were diffusion-soldered at temperatures between 250°C and 400°C by inserting a Sn thin-film interlayer. Experimental results showed that a double layer of intermetallic compounds (IMCs) η-(Cu_0.99Au_0.01)₆Sn₅/δ-(Au_0.87Cu_0.13)Sn was formed at the interface. Kinetics analyses revealed that the growth of intermetallics was diffusion-controlled. The activation energies as calculated from Arrhenius plots of the growth rate constants for (Cu_0.99Au_0.01)₆Sn₅ and (Au_0.87Cu_0.13)Sn are 16.9 kJ/mol and 53.7 kJ/mol, respectively. Finally, a satisfactory tensile strength of 132 kg/cm² could be attained under the bonding condition of 300°C for 20 min.     

水泥水化动力学模型

水泥的水化是一个复杂的变化过程,很难建立起一套直接用于描述水泥水化完整过程的动力学模型.依据水泥水化过程特点及化学反应动力学原理,明确了成核与产物生长、界面化学反应及扩散控制反应三种基本动力学方式对水泥水化的控制作用过程及转换条件,建立了水泥水化动力学模型.该模型能够直接依据水泥水化程度随时间的变化曲线确定水泥颗粒的水化速度,或在已知有关颗粒水化速度的基础上测算水泥在不同时间的水化程度.与其它模型相比,所建模型更加直观和准确.应用结果表明,提出的理论及方法具有良好的适用性和准确性.     

The combustion characteristics of high-heating-rate chars from untreated and torrefied biomass fuels

Torrefaction of biomass is of great interest at the present time, because of its potential to upgrade biomass into a fuel with improved properties. This study considers the fundamentals of combustion of two biomass woods: short rotation willow coppice and eucalyptus and their torrefied counterparts. Chars were prepared from the untreated and torrefied woods in a drop tube furnace at 1100 °C. Fuels and chars were characterised for proximate, ultimate and surface areas. Thermogravimetric analysis was used to derive pyrolysis and char combustion kinetics for the untreated and treated fuels and their chars. It was found that the untreated fuels devolatilise faster than their torrefied counterparts. Similarly, the chars from the untreated biomass were also found to be more reactive than chars from torrefied fuels, when comparing reaction rates. However, the activation energy value (Ea) for combustion of the untreated eucalyptus char was higher than that for the torrefied eucalyptus chars. Moreover, the eucalyptus chars were more reactive than the willow char analogues, although they had seen a lower extent of burn off, which is also a parameter indicative of reactivity. Similar trends in were also observed from their intrinsic reactivities; i.e. chars from the untreated fuel were more reactive than chars from the torrefied fuel and eucalyptus chars were more reactive than willow chars. Chars were also studied using scanning electron microscopy with energy-dispersive X-ray analysis. This latter method enabled a semi-quantitative analysis of char potassium contents, which led to an estimation of potassium partitioning during char formation and burnout. Results show a good correlation between potassium release and percent burnout. With respect to the effect of torrefaction on fuel-N, findings suggest that torrefaction would be beneficial for pf combustion in terms of nitrogen emissions, as it resulted in lower fuel-N contents and ∼72–92% of the fuel-nitrogen was released with the volatile fraction upon devolatilisation at 1100 °C.     

The oxidation of benzene under conditions encountered in waste incinerators

The oxidation of benzene was studied as a function of residence time (τ_res=0–2.5 s), temperature (850–960 K), and oxygen concentration (O₂=0.2–2.3%) in a heated laminar flow reactor at atmospheric pressure. Nitrogen, doped with 350 ppm benzene, was injected downstream of the burned gas from a near stoichiometric flame of methane + air. Gas samples were taken at different heights up the reactor and analyzed using GC-FID/TCD and HPLC techniques. Phenol and partially oxidized hydrocarbons such as acetaldehyde, formaldehyde, and acrolein were found with concentrations up to 50 ppm. At relatively low temperatures, the conversion of benzene was observed to proceed considerably more slowly at higher oxygen concentrations. Measured concentration profiles were modeled using detailed reaction schemes. A modified mechanism for the oxidation of benzene called BenWas was constructed from the mechanism of Zhang and McKinnon (Combust. Sci. Technol. 107 (1995) 261) by incorporating a submechanism for benzoquinone (OC₆H₄O) and by updating and enlarging the reaction scheme of cyclopentadiene (C₅H₆). The agreement between observed and predicted concentration profiles, e.g., of phenol (C₆H₅OH), acetylene (C₂H₂), and carbon monoxide (CO), was considerably improved by the use of the BenWas mechanism for rich and lean conditions, mainly due to the introduction of an additional pathway for phenyl oxidation (C₆H₅ + O₂ = OC₆H₄O + H) and due to the changed kinetics of the oxidation of cyclopentadienyl (C₅H₅) in C₅H₅ + O₂ = C₅H₄O + OH. The measured retardation of benzene oxidation with higher amounts of oxygen can be explained by the formation and reactions of peroxy radicals.     

基于仿真设计的坦克炮发射动力学研究

本文首先分析了坦克炮发射全过程动力学仿真技术,并通过运用计算机仿真技术,构建了坦克炮发生全过程的各种模型,以此为坦克炮设计人员运用计算机对坦克炮的核心心梗进行分析,就设计方案予以修改与确定,以及我国后续装甲装备的评估、论证与研制,提供了全面、科学且多元的技术途径与科学方法。     

A study of the kinetics of nucleation in a palm oil melt

Nucleation from a supercooled melt of palm oil was studied by optical microscopy and differential scanning calorimetry (DSC). Despite being a multicomponent system, palm oil exhibits a rather simple cooling thermogram with its high- and low-T exotherms exclusively related to the “hard” and “soft” components of the oil. As the “hard” components are being removed, the position of the high-T peak shifts down toward the low-T peak with diminishing peak intensity, while the position of the latter remains virtually unchanged. At 288°K, nucleation in a palm oil melt is instantaneous. Its induction time-temperature curve shows an abrupt discontinuity at 297°K, which demarcates the occurrence of one polymorph from another. Nucleation data fit very well into the Fisher-Turnbull equation. Its larger activation free energy of nucleation is accompanied by lowering of the melting point and an increase in the crystal/melt interfacial free energy as compared to palm stearin. The slow rate of nucleation in palm oil is attributed to intermolecular interaction between its “hard” and “soft” components. Partly presented at the 1989 PORIM International Palm Oil Development Conference, September 5–9, Kuala Lumpur, Malaysia.     

Nonequiiibrium Surface Segregation in Aluminum-Doped TiO2 under an Oxidizing Potential: Effects on Redox Color-Boundary Migration

During the oxidation of redued single crystals of Al-doped rutile, unusual anisotropies in color-boundary migration have been observed that are opposite to those predicted from published diffusion data. Analysis of the redox kinetics and of surface segregation (using ESCA and AES) shows that rapid transport of minority Al interstitials in the c -axis direction occurs under an oxidation potential, resulting in a surface segregation layer inhibiting further reoxidation. This surface segregation is nonequilibrium in nature, is driven by oxidation, and bears similarities to the phenomena of kinetic demixing in ionic systems. The results show that minority defects can play critical roles in demixing at the local scale; in their absence this system would not be expected to demix. This thus appears to be an additional mechanism for nonequilibrium interfacial segregation in ionic systems.     

Silica to Silicon: Key Carbothermic Reactions and Kinetics

The primary carbothermic reactions for the reduction of silica to produce silicon were defined and the reaction kinetics were determined. Most possible reactions between silicon oxide and carbon or carbon compounds were studied by a series of thermogravimetric analyses at temperatures up to 2000°C. Four key sequential reactions occur with SiC and SiO as intermediate reactants; two reactions involve SiO₂ and two involve SiO. Reaction rate versus temperature, activation energy, and preexponential factors were determined for each of six reactions involving SiO₂ or SiO. These kinetic studies show that SiO, when combined with either carbon or Sic, reacts in the gaseous state, and the sublimation of SiO is not the rate-limiting reaction for forming silicon.