SIMOP: Efficient reactive distillation optimization using stochastic optimizers

A methodology to improve the efficiency of stochastic methods applied to the optimization of chemical processes with a large number of equality constraints is presented. The methodology is based on two steps: (a) the optimization of the simulation step, which involves the optimum choice of design variables and subsystems to be simultaneously solved; (b) the optimization of the nonlinear programming (NLP) problem using stochastic methods. For the first step a flexible tool (SIMOP) is used, whereby different numerical procedures can be easily obtained, taking into account the problem formulation and specific characteristics, the need for specific initialization schemes and the efficient solution of systems of nonlinear equations. This methodology was applied to the optimization of a reactive distillation process for the production of ethylene glycol. Due to the complexity of the mathematical model, several different numerical procedures were generated, and their influence on the computational burden and on the reliability and accuracy of the optimization to reach the global optimum were studied. The results obtained suggest that in addition to the choice of design variables, the structure of subsystems associated to numerical procedures has a considerable impact on the performance of the optimizers.     

球磨时间对钛酸钡介电性能的影响

通过改变混料的秩序以及采用沉降、水煮损耗、温度特性、电导率和化学分析等测试手段，研究了制备钛酸钡的球磨工艺中球磨时间对钛酸钡粉体均匀性及钛酸钡介电性能的影响。研究结果表明：采用不同的球磨时间制得的钛酸钡性能差别较大，球磨时间达12小时时，能减少球磨引起的团聚，极大地改善了固相合成BaTiO3粉体均匀性，并最终提高了钛酸钡的介电性能。     

浅析加快300 MW机组启动速度的方法及措施

随着电网的装机容量日益增大,机组的启动次数也在逐日增多。从保证机组安全经济运行的角度出发,结合笔者直接或间接参与制定的技术措施,简要分析了影响机组启动速度的因素和改善措施,以期为其他发电厂在机组启动方面提供一些参考和建议。     

Reactively compatibilised polyamide6/ethylene-co-vinyl acetate blends: mechanical properties and morphology

Mechanical properties and morphological studies of compatibilised blends of PA6/EVA-g-MA and PA6/EVA/EVA-g-MA were studied as functions of maleic anhydride content (MA) and dispersed phase (EVA-g-MA) concentrations, respectively at blending composition of 20 wt% dispersed phase (EVA-g-MA or combination of EVA and EVA-g-MA). The maleic anhydride (MA) was varied from 1 to 6 wt% in the PA6/EVA-g-MA blend, whereas MA concentration was fixed at 2 wt% in the ternary compositions with varying level of EVA-g-MA. ATR-IR spectroscopy revealed the formation of in situ copolymer during reactive compatibilisation of PA6 and EVA-g-MA. It was found that notched Izod impact strength of PA6/EVA-g-MA blends increased significantly with MA content in EVA-g-MA. The brittle to tough transition temperature of reactively compatibilised blends was found to be at 23 °C. The impact fractured surface topology reveals extensive deformation in presence of EVA-g-MA whereas; uncompatibilised PA6/EVA blend shows dislodging of EVA domains from the matrix. Tensile strength of the PA6/EVA-g-MA blends increased significantly as compared to PA6/EVA blends. Analysis of the tensile data using predictive theories showed an enhanced interaction of the dispersed phase and the matrix. It is observed from the phase morphological analysis that the average domain size of the PA6/EVA-g-MA blends is found to decrease gradually with increase in MA content of EVA-g-MA. A similar decrease is also found to observe in PA6/EVA/EVA-g-MA blends with increase in EVA-g-MA content, which suggest the coalescence process is slower in presence of EVA-g-MA. An attempt has been made to correlate between impact strength and morphological parameters with regard to the compatibilised system over the uncompatibilised system.     

Fatty acid esterification by reactive distillation: Part 2—kinetics-based design for sulphated zirconia catalysts

In a previous study on the basis of reaction equilibrium, it was demonstrated that the synthesis of fatty acids esters of heavy alcohols by catalytic reactive distillation (RD) is basically feasible. Presently, the analysis is expanded to the kinetics-based design applied to the synthesis of 2-ethylhexyl dodecanoate. Experimental data for a super-acidic sulphated zirconia catalyst are employed. It is shown that this catalyst is highly selective even for the high alcohol/acid ratios as prevail in a RD column. To avoid catalyst deactivation, liquid-liquid segregation into an organic and an aqueous phase must be prevented, and operating temperatures beyond must be chosen. A kinetic model based on liquid activities is proposed, with parameters determined from both kinetic and equilibrium measurements. A typical column design has 13 reactive stages with a catalyst loading of , temperature profile of 400-, and a space velocity of for 99.9% purity product ester. A modified Damköhler number is proposed.     

Reactive compatibilization of PE/PS blends. Effect of copolymer chain length on interfacial adhesion and mechanical behavior

This paper deals with in situ compatibilization of PE/PS blends via Friedel-Crafts reaction, performed at the interphase. Two polyethylenes having different molecular weights, and the same PS, were used along a wide range of catalyst concentration. The influence of the graft copolymer architecture and content on the efficiency of blend compatibilization was studied. The emulsifying effect, morphological aspects and mechanical behavior were also assessed for these blends. The amount of copolymer formed increases with catalyst concentration and the short chain length fraction of the homopolymers. The high molecular weight (MW) copolymers behaved as better compatibilizers as they showed, at the cmc, greater graft copolymer concentration than the low MW ones. A substantial increase in interfacial adhesion and particle size reduction was observed, even at catalyst concentrations as low as 0.3 wt%. In correspondence, mechanical properties, like ductility and yield strength, were enhanced by the effect of this Friedel-Crafts reaction's compatibilization.     

Magnetoelectric coupling in multiferroic BiFeO3 by co-doping with strontium and nickel

We report the effects of the Sr²⁺ and Ni²⁺ co-doping of BiFeO₃ on the crystal structure and multiferroic properties of Bi_1?xSr_xFe_1-yNi_yO₃ (x?=?0.05, 0.0?≤?y?≤?0.10, and Δy?=?0.05) that is synthesized using assisted high-energy ball milling. The mixtures of Bi₂O₃, Fe₂O₃, SrO and NiO were milled for 5?h, pressed at 900?MPa, and sintered at 800?°C in order to obtain cylindrical test pieces. X-ray diffraction and Rietveld refinement elucidated the effects of Sr²⁺ and Ni²⁺ on the crystal structure. Co-doping with SrNi in suitable proportions stabilizes rhombohedral BiFeO₃. High contents of Ni²⁺ promote the precipitation of secondary phases in the forms of NiFe₂O₄ and Bi₂₅FeO₄₀. The magnetic behavior was examined by means of vibrating sample magnetometry. The results showed a change in the magnetic order from antiferromagnetic for the undoped sample to the ferromagnetic order for the co-doped samples. This change is attributed to the modulations in the magnetic moment due to crystal structure distortions. All samples show high relative permittivity values, which were enhanced by doping with Sr²⁺. Ni²⁺ cations increase the dielectric dissipation factor; this enhancement is related to their interactions with cations of a different oxidation state, such as Fe³⁺, Fe²⁺, Ni²⁺, Bi³⁺ and Sr²⁺ in the crystal structure of BiFeO₃. The magnetoelectric coupling that was evaluated using magnetodielectric measurements was above 4% at 1?kHz for the higher applied magnetic field of 18?kOe.     

A reactive extension of the OpenMusic visual programming language

Objectives: OpenMusic (OM) is a domain-specific visual programming language designed for computer-aided music composition. This language based on Common Lisp allows composers to develop functional processes generating or transforming musical data, and to execute them locally by demand-driven evaluations. As most historical computer-aided composition environments, OM relies on a transformational declarative paradigm, which is hard to conciliate with reactive data-flow (an evaluation scheme more adequate to the development of interactive systems). We propose to link these two evaluation paradigms in the same and consistent visual programming framework.Methods: We establish a denotational semantics of the visual language, which gives account for its demand-driven evaluation mechanism and the incremental construction of programs. We then extend this semantics to enable reactive computations in the functional graphs.Results: The resulting language merges data-driven executions with the existing demand-driven mechanism. A conservative implementation is proposed.Conclusions: We show that the incremental construction of programs and their data-driven and demand-driven evaluations can be smoothly integrated in the visual programming workflow. This integration allows for the propagation of changes in the programs, and the evaluation of graphically designed functional expressions as a response to external events, a first step in bridging the gap between computer-assisted composition environments and real-time musical systems.