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降膜蒸发用齿形螺纹调节液体分布器 总被引:1,自引:0,他引:1
几年来生产实践证明了,用于二甲基硅油生产时重要设备脱低分子降膜蒸发器的设计是合理的。它与国内外已知的同类蒸发器最不同之处是,所设计的液体分布器为齿形螺纹调节式的,见图1。用此种液体分布器的降膜蒸发器生产的二甲基硅油产品不仅超过了国家标准,而且不低于同类的日本产品。该液体分布器的特点:成膜完整均匀,产量高,稳定可靠,结构简单,安装方便,不易堵塞,造价低廉等。 相似文献
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本文对顺酐生产中升膜蒸发器结垢的原因进行了分析,指出顺丁烯二酸溶液长时间在130℃的温度下生成反丁烯二酸,反丁烯二酸稍溶于水,而以针状结晶物析出,从而在升膜蒸发器换热管内形成结垢。解决办法是降低蒸汽温度,改进升膜蒸发器结构,提高换热管束内流体分布均匀程度,缩短溶液在升膜蒸发器内的停留时间。 相似文献
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落条式脱挥发物设备液体分布装置的研究 总被引:1,自引:0,他引:1
以糖浆为实验介质,采用接液法和电导探针法,研究了落条式脱挥发物设备中的列管式蒸发器用液体分布装置。该装置由一倒置的圆锥形分布器和一成膜器组成。前者用以实施管间的流体流量分布,后者用以实施管内流体的液膜分布。成膜器的最佳环隙宽为1.9~2.5mm,相应的底圆直径约为46mm。分布的结构参数与进料流量、流体物性之间的关联式为H=0.039QηL/ρb^3(b+d1)-0.118。该液体分布装置具有结构 相似文献
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1 问题的提出 我公司的焦油蒸馏采用切取三混馏分的一塔式工艺。在二段蒸发器底部采出沥青,侧线切取二蒽油,一蒽油则在馏分塔底采出。二段蒸发器由5层弓型隔板的蒸发段和6层圆形泡 相似文献
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The removal of a volatile organic compound (VOC) from high viscous liquid was carried out in a rotating packed bed (RPB) in this study. The mixed liquid of syrup and acetone was used as simulated high viscous polymer solution with acetone as the volatile compound. The influence of the rotating speed of RPB, liquid viscosity, liquid flow rate, vacuum degree, and initial acetone content in the liquid on acetone removal efficiency was investigated. The experimental results indicated that the removal efficiency increased with increasing rotating speed and initial acetone content in the viscous liquid and decreased with increasing liquid viscosity and flow rate. It was also observed that acetone removal efficiency increased with an increasing vacuum degree and reached 58% at a vacuum degree of 0.1 MPa. By the comparison with a flash tank devolatilizer, it was found that acetone removal ef-ficiency in RPB increased by about 67%. 相似文献
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论述了聚酯,聚酰胺缩聚反应装置及高粘流体脱挥设备。在简述其选型原理及设备结构的基础上,介绍和推荐了一些新型缩聚反应器和脱挥装置。 相似文献
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轴流式强制内循环表面更新设备在有机硅生产中的应用 总被引:2,自引:1,他引:2
介绍了新型脱低设备-轴流式强制内循环表面更新设备的结构、工作原理、生产工艺,试验表明,该设备可用于生产超低挥发分的高粘度硅油的硅橡胶。 相似文献
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Michael J. Misovich Eric A. Grulke Robert F. Blanks 《Polymer Engineering and Science》1987,27(4):303-312
Polymer devolatilizers are in widespread use in the polymer industry for removing solvents and monomers from polymer melts prior to product fabrication. Design equations for describing the solvent flux usually include both the diffusion coefficient of the solvent in the polymer melt and the equilibrium concentration of the solvent at the polymer-vapor interface. Several models make the as sumption that the solvent diffusivity is constant over the ranges of solvent concentrations and temperatures in the devolatilizer. This is a critical assumption that may be difficult to check without obtaining diffusivity data at the operating temperatures and concentrations of the process equipment. There are three models that can be used for diffusion coefficients in devolatilizer design: the free volume model developed by Duda, Vrentas, and coworkers; a new linear model proposed in this study; and a constant diffusivity model, The linear model is obtained by combining a new correlation for solvent activity coefficients in molten polymers with free volume theory and linearizing the resulting equation. The error between using the complete free volume theory and using the linear model, or alternatively, using a constant diffusion coefficient, is calculated for several solvent-polymer systems. The linear model is convenient to use for determining the effects of the solvent activity coefficient on the diffusion coefficient. A method is presented for determining whether the complete model, the linear model, or the constant diffusivity model is appropriate for a given devolatilizer design. 相似文献
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An experimental investigation was conducted into elucidating the mechanism of foam devolatilization. For the investigation, we have constructed two separate apparatuses of Plexiglas—one simulating the partially filled flow channel in a single-screw devolatilizer, and the other simulating the partially filled, closed-chamber (often referred to as the “C-chamber),” in a twin-screw devolatilizer. The test fluids employed were aqueous solutions of polyacrylamide having various concentrations. During the preparation of the test fluids, we controlled the amount of air entrapped in the liquid phase by varying the level of vacuum applied. The entrapped air stayed as fine gas bubbles dispersed in the polymer solution, and mixtures of the polymer solution and air bubbles were subjected to devolatilization experiments. In the use of a single-screw devolatilizer, we have observed that: 1. The streamlines show circulatory flow patterns forming a singular point at a position slightly below the free surface, where small gas bubbles are trapped initially and become stationary, and 2. The small gas bubbles trapped at the stationary position coalesce later to form large gas bubbles, which then move slowly toward the free surface and are removed under vacuum from the system. In the use of twin-screw devolatilizers, we have found that the degree of fill, the rotational direction of the screws, and the degree of intermeshing, (i. e., partially or fully intermeshing) greatly influence the amount of free surface available for the removal of volatiles, as well as the flow patterns in the liquid pool, and thus the devolatilization efficiency. 相似文献
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