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Increasing the efficiency of transfer processes when using inhomogeneous fluidization 使用非均匀流化时,提高传递过程的效率
Yaroslav M. Kornienko, S. Haidai, Oleksandr Sameliuk
The processes of dehydration and granulation are associated with the heat transfer to the solid particles from the gas coolant, which acts as a fluidizing agent and causes the stochastic movement of the granular material in the apparatus. To implement the layered structure mechanism of granulation of organic-mineral fertilizers it is necessary to ensure intensive circulation of granular material with intensive gradual passage through the appropriate technological zones of the apparatus. The main problem is the low efficiency of interphase exchange in the gas-liquid-solid system and the formation of agglomerates during granulation with the injection of a liquid heterogeneous solution into the bed of solid granular material. In this work the conditions for increasing the efficiency of the transfer processes when using an inhomogeneous jet-pulsating mode of fluidization were determined. Analysis of the intensity of renewal of the contact surface of the phases when using inhomogeneous jet-pulsating fluidization in the self-oscillating mode was carried out. It was established that the use of this mode of fluidization allows getting a significant intensification of heat and mass transfer processes due to the activation of diffusion-controlled processes and an increase in the dynamics of interphase contact exchange by 1.9÷2.9 m2/s, which is 27÷41% of the total surface of the material in device.
脱水和造粒过程与气体冷却剂向固体颗粒的传热有关,气体冷却剂作为流化剂并引起颗粒材料在装置中的随机运动。为了实现有机无机肥料造粒的分层结构机制,必须保证颗粒物料的密集循环,密集地逐步通过设备的适当工艺区域。主要问题是气-液-固系统的界面交换效率低,以及在造粒过程中向固体颗粒物料床中注入液体非均质溶液会形成团块。在这项工作中,确定了使用非均匀射流脉动流化模式时提高传递过程效率的条件。分析了非均匀射流脉动流化在自振荡模式下的接触面更新强度。已经确定,由于扩散控制过程的激活,使用这种流化模式可以显著增强传热和传质过程,并使界面接触交换的动力学增加1.9÷2.9 m2/s,这是装置中材料总表面的27÷41%。
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引用次数: 0
Disposal of short-lived low- and intermediate-level waste: analysis of foreign experience 短寿命低、中水平废物的处置:国外经验分析
B. Shabalin, O. Lavrynenko, N. Mitsiuk
The article summarizes and analyzes the main approaches and practical experience of foreign countries regarding the disposal of short-lived low- and medium-level waste. Their place in the category of low-level waste according to the recommended classification of the IAEA, for which disposal in near-surface storage facilities is provided, is shown. Currently, in countries that operate nuclear facilities and develop nuclear technologies, there is no one approach to the disposal of such waste. The type of repository and its structural and technological solutions are determined by the specifics of the waste itself, the nature of the site, the state strategy in the nuclear industry, as well as social and economic factors. To date, several types of storage facilities have been developed for the disposal of short-lived low- and medium-level waste: relatively simple trench-type near-surface storage facilities; modular-type near-surface storage facilities with a complicated system of engineering barriers and criteria for selecting containing rocks (natural barriers) compared to the trench type; geological storages, which are mainly built in mining operations with a complex system of tunnels and barrier protection. Bentonite clays are widely used as components of engineering barriers. In the simplest case of near-surface repositories, the bentonite layer serves as the base material of the repositories and helps to reduce filtration and increase the sorption of radionuclides and other components. In the organization of geological repositories, the bentonite layer contributes to the reduction of water filtration into the repositories, increases the sorption of radionuclides, prevents the destruction of concrete structures during a shift by containing rocks, and, in the event of the destruction of cement-concrete structures of engineering barriers, leads to a decrease in the removal of radionuclides from the repositories into the environment. The work gives examples of different types of storage facilities in countries around the world.
本文总结和分析了国外处理短寿命中、低放废物的主要方法和实践经验。根据原子能机构建议的分类,它们属于低水平废物类别,在近地面储存设施中进行处置。目前,在运行核设施和发展核技术的国家,没有一种处理这类废物的办法。储存库的类型及其结构和技术解决办法取决于废物本身的特点、场址的性质、核工业的国家战略以及社会和经济因素。迄今为止,已为处置短期低、中水平废物开发了几种类型的储存设施:相对简单的沟渠式近地表储存设施;与沟式相比,模块化近地表储存设施具有复杂的工程屏障系统和选择含岩(天然屏障)的标准;地质储库,主要是在采矿作业中建造的,具有复杂的隧道和屏障保护系统。膨润土粘土被广泛用作工程屏障的组成部分。在最简单的近地表储存库的情况下,膨润土层作为储存库的基础材料,有助于减少过滤,增加放射性核素和其他成分的吸收。在地质储存库的组织中,膨润土层有助于减少进入储存库的水过滤,增加放射性核素的吸收,防止在转移期间因含有岩石而破坏混凝土结构,并且在工程屏障的水泥-混凝土结构遭到破坏的情况下,导致放射性核素从储存库转移到环境中的减少。这项工作给出了世界各国不同类型的储存设施的例子。
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引用次数: 0
Numerical analysis of the thermal-elastic-plastic state of electrical contact gasket made from dispersion-reinforced composite materials using the fusioned deposition modeling method 采用熔融沉积建模方法对分散增强复合材料电接触垫片的热弹塑性状态进行了数值分析
V. Soloveǐ
The article presents the results of a theoretical study on determining the suitability of using electrical contact gaskets (ECG) in industrial conditions (Castner direct graphitization furnaces), made of coke-pitch composite using additive technologies based on the Fused Deposition Modeling (FDM) method. Numerical analysis of the physical state of ECG under the conditions of industrial application was performed on the basis of the mathematical statement of the thermo-elastic-plasticity problem and the algorithm of implicit inverse mapping of its solution based on the finite element method in the Mathcad programming environment. To construct the geometry and tetraid mesh of the ECG model, a freely open program code was used - the Gmsh CAD system for grid generation, and for the visualization of the results of physical field calculations, the free open program code ParaView was used. The study of the thermo-elastic-plastic state of ECG under the conditions of the graphitization process in Castner furnaces was carried out in the temperature range up to 900 °С, at which the thermoplastic properties of the material are manifested. At the same time, such physical fields of ECG were analyzed as temperature distribution, resulting displacements, equivalent elastic stresses according to Mises, equivalent total, elastic and plastic deformations according to Mises, and the volume fraction of ECG material in a plastic state, depending on the temperature level and radial gradient temperatures (radial temperature difference) of electrical contact gaskets. Numerical simulation of the thermo-elastic-plastic state of the ECG was carried out under the conditions of force loading by external pressure on the lateral surface of the gasket of 2.5 MPa and different values ​​of the radial temperature difference in the range of 15–90 °C in the temperature range up to 900 °C. It was established that: at the stages of formation of semi-coke and coke in the material of the coke-pitch composite ECG under the thermomechanical conditions of operation of the Kastner furnace, a margin of strength of not less than unity was obtained; with the subsequent increase in the temperature level in the Castner furnace to 3000 °C and above, the raw material of ECG, as a result of thermal destruction, has already turned into coke and, therefore, its mechanical properties have become close to the mechanical properties of electrode blanks in columns that are subjected to graphitization. This gives reason to assert that the ECGs will not be mechanically destroyed during the entire graphitization campaign of the Castner furnace. On the basis of the analysis of the results of numerical simulation, the possibility of using ECGs made from dispersion-reinforced composite materials (coke-pitch mixtures) by the FDM method in the technology of graphitizing electrode products according to the Сastner method is substantiated.
本文介绍了基于熔融沉积建模(FDM)方法的添加剂技术在工业条件下(Castner直接石墨化炉)确定使用电接触垫片(ECG)的适用性的理论研究结果。在Mathcad编程环境中,基于热弹塑性问题的数学表述和基于有限元法的隐式逆映射求解算法,对工业应用条件下心电的物理状态进行了数值分析。为了构建心电模型的几何网格和四分体网格,使用了自由开放的程序代码- Gmsh CAD系统进行网格生成,并使用了自由开放的程序代码ParaView对物理场计算结果进行可视化。在高达900°С的温度范围内,对Castner炉石墨化工艺条件下ECG的热弹塑性状态进行了研究,在此温度范围内,材料的热塑性性能得到了体现。同时,根据电接触垫的温度水平和径向梯度温度(径向温差),分析了ECG的温度分布、产生位移、等效弹性应力(Mises)、等效总变形、弹性变形和塑性变形(Mises)以及ECG材料处于塑性状态的体积分数等物理场。在高达900℃的温度范围内,在衬垫侧面施加2.5 MPa的外力载荷和15 ~ 90℃不同的径向温差值的条件下,对ECG的热弹塑性状态进行了数值模拟。结果表明:在Kastner炉热工条件下,焦沥青复合ECG材料在半焦和焦炭形成阶段,得到的强度余量不小于1;随着Castner炉内温度水平进一步提高到3000℃及以上,ECG原料由于热破坏已经变成焦炭,因此其力学性能已经接近于石墨化的柱内电极坯的力学性能。这就有理由断言,在卡斯特纳炉的整个石墨化过程中,ecg不会被机械破坏。在对数值模拟结果进行分析的基础上,论证了用FDM方法将分散增强复合材料(焦炭-沥青混合料)制成的电芯应用于Сastner方法石墨化电极产品工艺的可能性。
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引用次数: 0
Method for PID-tuning via feedback control system pole placement 通过反馈控制系统极点配置的pid整定方法
A. Zhuchenko, Redrikh Putiatin
Pole placement is the only PID-tuning technic that allows one to obtain a control system with desired, and, moreover, highly predictable performance and control quality. Number of controller tuning parameters is equal to number of poles closed-loop poles it can precicely place, so that PID-controller can place exactly three poles, and PI- can place only two. For this reason PI-controller is best used with first-order processes (second-order closed loop system), and PID-controller with second-orded ones (third-order closed loop system). However, many processes have higher order than two, and still are controlled with PID-controllers. To tune it using pole placement techniques, it is necessary to consider only dominant poles, which affect performance of the system to the greatest extent. First, it is necessary to study a PI-controller with a second-order process, which is the most basic case. Tuning is performed using global optimization methods to fit dominant poles of a tuned system to dominant poles of a reference system.
极点放置是唯一的pid调谐技术,它允许人们获得具有期望的控制系统,而且,高度可预测的性能和控制质量。控制器整定参数的个数等于闭环极点精确放置的极点数,使得pid控制器可以精确放置三个极点,而PI-只能放置两个极点。因此,pi控制器最适合用于一阶过程(二阶闭环系统),而pid控制器适合用于二阶过程(三阶闭环系统)。然而,许多过程的阶数高于2,并且仍然由pid控制器控制。要使用极点放置技术对其进行调谐,必须只考虑对系统性能影响最大的主导极点。首先,有必要研究具有二阶过程的pi控制器,这是最基本的情况。采用全局优化方法进行调谐,使调谐系统的主导极点拟合到参考系统的主导极点。
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引用次数: 0
The dependence of the efficiency of the ion exchange of manganese ions from water on the type and form of the ionite and its hardness 水中锰离子交换效率与离子石类型、形态及其硬度的关系
M. Gomelya, I. Trus, M. Tverdokhlib, Viktor Kamaiev
Drinking water must comply physical, chemical, bacteriological and radiochemical guidelines therefore its quality should be continuously monitored before being introduced into the distribution system. Water used for human consumption may come from various sources: groundwater, spring water; water from rivers, streams, lakes, among other. A large part of the population of Ukraine uses drinking water that does not meet hygienic requirements according to various indicators. Manganese compounds are quite often present in natural waters. Their quantitative content can vary in a wide range, depending on the region, it can be 0,5-10 mg/dm3. It is worth noting that with a high content of manganese compounds in water, their removal is a rather difficult task. Removal of manganese compounds from water can be implemented using the ion exchange method, which consists of filtering water through loading in salt or acidic form. At the same time, softening and desalination of water can occur simultaneously. Therefore, the ion exchange method should be used for comprehensive water purification, softening, and removal of manganese compounds. The article presents the results of obtained during the extraction of manganese ions from distilled and tap water using the strongly acidic cationite KU-2-8 and the weakly acidic cationite Dowex MAC-3. Cationites were used in Na+ and Ca2+ form. The concentration of manganese ions (Mn2+) was varied from 5 to 500 mg/dm3. It was shown that the sorption capacity of the cationite KU-2-8 depended on the concentration of manganese ions, the form of the ionite, the presence of hardness ions in water and was little dependent on the pH of the medium. The sorption capacity of the weakly acidic cationite increased with the increase in the concentration of manganese ions and with the increase in the pH of the medium, which changed with the change in the concentration of magnesium sulfate in distilled water. Sorption of manganese ions from tap water decreases for strongly acidic and weakly acidic cations, compared to solutions in distilled water, which is associated with competitive sorption of hardness ions. This is especially noticeable when using ionites in Ca2+ form in solutions in tap water. The use of ionites in Ca2+ form reduces their sorption capacity for Mn2+ and in distilled water to a certain extent. But this effect is smaller compared to tap water. The Thomas model was used in the work to estimate the full exchange capacity of weakly acidic cationite at low concentrations of MnSO4 solution in distilled water.
饮用水必须符合物理、化学、细菌学和放射化学准则,因此在进入分配系统之前应不断监测其质量。用于人类消费的水可能来自各种来源:地下水、泉水;来自河流、小溪、湖泊等的水。根据各种指标,乌克兰人口的很大一部分使用的饮用水不符合卫生要求。天然水体中经常存在锰化合物。它们的定量含量变化范围很广,根据地区不同,可为0、5-10 mg/dm3。值得注意的是,由于水中锰化合物含量高,去除它们是一项相当困难的任务。可以使用离子交换法从水中去除锰化合物,该方法包括通过盐或酸性形式的负载过滤水。同时,水的软化和淡化可以同时发生。因此,应采用离子交换法进行水的综合净化、软化和锰化合物的去除。本文介绍了用强酸性阳离子矿KU-2-8和弱酸性阳离子矿Dowex MAC-3从蒸馏水和自来水中提取锰离子的结果。阳离子以Na+和Ca2+形式使用。锰离子(Mn2+)浓度在5 ~ 500 mg/dm3之间变化。结果表明:cu -2-8的吸附能力与锰离子的浓度、离子的形态、水中硬度离子的存在有关,而与介质pH的关系不大。弱酸性阳离子矿的吸附量随锰离子浓度的增加和介质pH的增加而增加,随蒸馏水中硫酸镁浓度的变化而变化。与蒸馏水溶液相比,强酸性和弱酸性阳离子对自来水中锰离子的吸附减少,这与硬度离子的竞争性吸附有关。当在自来水溶液中使用Ca2+形式的离子离子时,这一点尤其明显。Ca2+形式离子离子的使用在一定程度上降低了它们对Mn2+和蒸馏水的吸附能力。但与自来水相比,这种影响较小。本文采用Thomas模型估算了弱酸性阳离子矿在低浓度MnSO4溶液中蒸馏水的全交换容量。
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引用次数: 0
Characteristics of nano-sized composites based on rare earth orthoferrites and hematite 稀土正铁氧体与赤铁矿纳米复合材料的特性
O. Lavrynenko, O. Pavlenko, O. Olifan
Photocatalysts based on orthoferrites of rare earth elements are used to neutralize a number of harmful substances and organic dyes under the influence of visible light, which makes them to promise the introduction of resource-saving water purification technologies. The thermal-gravimetric analysis, X-ray phase analysis, scanning electron microscopy, and energy-dispersive spectroscopy was used to study nanoscale samples of orthoferrites of rare earth elements and hematite obtained by the chemical precipitation of aqueous solutions of inorganic salts of ferrum with lanthanides (La, Er, Sm, Dy, Nd, Yb ) and Y in a weakly alkaline environment and subsequent heat treatment of sediments at 800 and 1100 °C. It was found that during the simultaneous precipitation of hydroxide phases of ferrum and REE, their transformation under the influence of temperature is spatially separated due to the differences in the temperatures of phase transformations and the hydrogen index of the precipitation of precursor phases. It is shown that, depending on the chemical composition of the initial solutions, goethite is formed in the temperature range of 190-250 °C, and the formation of hematite takes place at 425-450 °C. Dehydroxylation of lanthanum hydroxide is observed at 300-330 °С, and the formation of lanthanum oxides continues in the range from 390 to 900 °С. The perovskite phase crystallizes at 960 °C. Using the X-ray phase analysis method, it was established that hematite and a mixture of REE oxygen phases are present in the sediments heat-treated at 800 °C. At 1100 °C, the structure of perovskite and hematite with particle sizes from 25 to 40 nm was identified in the composition of the powders. It was determined that the removal of auxiliary substances takes place at temperatures of 650-770 °C and no impurities of K, Na, S, Cl, or C in the powders fired at 1100 °C. Hematite and perovskite particles are well crystallized and form fragile aggregates, the specific surface area of the samples is several m2/h.
基于稀土元素的正铁氧体光催化剂在可见光的作用下可以中和多种有害物质和有机染料,这使得它们有望引入资源节约型水净化技术。采用热重分析、x射线物相分析、扫描电镜、能谱分析等方法,对铁的无机盐与镧系元素(La、Er、Sm、Dy、Nd、Yb)和Y的水溶液在弱碱性环境下化学沉淀,并在800℃和1100℃下对沉积物进行热处理,得到稀土元素和赤铁矿的纳米级正铁氧体样品进行了研究。研究发现,在铁和稀土的氢氧化物相同时析出过程中,由于相变温度和前驱相析出氢指数的差异,它们在温度影响下的转变在空间上是分离的。结果表明,根据初始溶液的化学组成,针铁矿在190 ~ 250℃的温度范围内形成,赤铁矿在425 ~ 450℃形成。在300-330°С观察到氢氧化镧的脱羟基作用,在390 - 900°С范围内继续形成氧化镧。钙钛矿相在960℃时结晶。通过x射线物相分析,确定了800℃热处理后的沉积物中存在赤铁矿和稀土氧混合物相。在1100℃时,粉末的组成中有25 ~ 40 nm的钙钛矿和赤铁矿结构。测定了在650 ~ 770℃的温度下辅助物质的去除,1100℃烧制的粉末中没有K、Na、S、Cl、C等杂质。赤铁矿和钙钛矿颗粒结晶良好,形成脆弱的团聚体,样品的比表面积为几m2/h。
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引用次数: 0
Efficiency of magnesium ions removal from water in processes of its mitigation 缓释过程中水中镁离子的去除效率
Yaroslav Radovenchyk, Kateryna Hordiienko, T. Krysenko, V. Radovenchyk
Significant concentrations of calcium and magnesium ions in natural waters force the majority of domestic drinking and energy waters to undergo preliminary softening. Therefore, mitigation technologies are becoming particularly acute today, and research in this field is increasing every year. Since water hardness is determined by the total content of calcium and magnesium ions, these elements are the focus of such research. Traditionally, it is believed that calcium ions are the first to be removed, and magnesium ions are less likely to form a solid phase. However, the effectiveness of softening technology depends equally on both cations. Therefore, sufficient attention should also be paid to magnesium ions. Sodium phosphate is considered a promising reagent in this direction. Its use in the processes of removing calcium ions allows to ensure the residual hardness of water at the level of 0.1 - 0.2 mg-eq/dm3 in a wide range of temperatures and hydrogen index. Detailed studies of the use of sodium phosphate in the processes of removing magnesium ions showed its insufficient efficiency. The effectiveness of soda-sodium softening allows to ensure at pH 11.0 - 11.5 the residual hardness of water at the level of 0.4 - 0.6 mg-eq/dm3. But the need to adjust the hydrogen index and the high consumption of reagents make this technology unsuitable for widespread use. The determining factor in water softening processes using phosphate ions is the ratio between the concentrations of phosphate ions and magnesium ions K = [PO43-, mg-eq] / [Mg2+, mg-eq]. Taking into account the strict requirements of current regulatory documents for the content of phosphates in treated waters, it is desirable to carry out the treatment with stoichiometric ratios of reagents for a more complete reaction between the components. The advantage of sodium phosphate as a reagent for removing magnesium ions can be considered the fact that in the pH range of 3.16 - 10.07 at K = 1, the residual hardness ranges from 1.8 to 3.4 mg-eq/dm3. At the same time, the minimum value of the residual stiffness was recorded at the level of 0.75 mg-eq/dm3 at pH 10.07 and K = 2. As the pH decreases, a stable decrease in efficiency is observed, although it is not very significant. Thus, during the transition from an alkaline to an acidic medium, the residual concentration of magnesium ions increases by a factor of 2, regardless of the value of the coefficient K. Similar trends persist in the case of a change in the initial hardness of water. The biggest difference is observed at values ​​of K ≤ 1, which is explained by the deficiency of phosphate anions and the impossibility of forming a solid phase of stoichiometric composition. However, even with a stoichiometric ratio of reactants (K = 1), the residual hardness of treated water is quite significant and ranges from 2.5 to 3 mg-eq/dm3. A further increase in the dose of sodium phosphate allows to slightly reduce the residual hardness of the treated wate
天然水中钙和镁离子的显著浓度迫使大多数家庭饮用水和能源水经过初步软化。因此,缓解技术在今天变得特别紧迫,这一领域的研究每年都在增加。由于水的硬度是由钙和镁离子的总含量决定的,所以这些元素是这类研究的重点。传统上,人们认为钙离子首先被去除,而镁离子不太可能形成固相。然而,软化技术的有效性同样取决于这两种阳离子。因此,对镁离子也应给予足够的重视。磷酸钠被认为是一种很有前途的试剂。它用于去除钙离子的过程中,可以确保在广泛的温度和氢指数范围内,水的剩余硬度在0.1 - 0.2 mg-eq/dm3的水平。对磷酸钠在脱除镁离子过程中的应用进行了详细的研究,表明其效率不足。钠-钠软化的有效性可以确保在pH 11.0 - 11.5时,水的剩余硬度在0.4 - 0.6 mg-eq/dm3的水平。但由于需要调整氢指数和试剂的高消耗,使得该技术不适合广泛应用。磷酸盐离子软化水过程的决定因素是磷酸盐离子与镁离子浓度之比K = [PO43-, mg-eq] / [Mg2+, mg-eq]。考虑到当前法规文件对处理水中磷酸盐含量的严格要求,为了使各组分之间的反应更完全,需要使用试剂的化学计量比进行处理。磷酸钠作为脱除镁离子试剂的优势在于,在pH为3.16 ~ 10.07,K = 1时,残余硬度为1.8 ~ 3.4 mg-eq/dm3。同时,在pH 10.07、K = 2条件下,在0.75 mg-eq/dm3水平下,记录了残余刚度的最小值。随着pH值的降低,可以观察到效率的稳定下降,尽管不是很显著。因此,在从碱性介质到酸性介质的转变过程中,镁离子的残留浓度增加了2倍,而与系数k的值无关。在水的初始硬度发生变化的情况下,也存在类似的趋势。K≤1时差异最大,这是由于磷酸盐阴离子缺乏,不可能形成化学计量组成的固相。然而,即使在反应物的化学计量比(K = 1)下,处理后的水的剩余硬度也相当显著,范围在2.5至3 mg-eq/dm3之间。进一步增加磷酸钠的剂量可以稍微降低处理过的水的残余硬度。因此,当K = 2.0时,处理水的最小剩余硬度固定在0.7 mg-eq/dm3,初始硬度为22.9 mg-eq/dm3。还注意到处理过的水的残余硬度增加而其初始硬度降低。在我们看来,这种情况是由于固相质量的显著增加和pH值随着磷酸钠剂量的增加而增加造成的。磷酸钠作为钙离子沉淀剂的一个显著优点是,在很宽的温度范围内,水的温度实际上不影响工艺的效率。这种趋势也是镁离子的特征。在5 ~ 70℃的温度范围内,软化效率保持稳定。此外,固相在排干溶液后立即形成。如果我们考虑到磷酸盐去除钙离子的高效率,那么一般来说,只要形成的固相与水完全分离,就可以允许使用磷酸盐软化水。通过沉淀或过滤分离磷酸镁颗粒的效率的详细研究与固相形成过程同样重要。
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引用次数: 0
Algorithm of coordinated control of an open-type headbox 开式头箱协调控制算法
A. Zhuchenko, Mykola Pirhach, Y. Zhurakovskyi, Roman Sadovnychyi
The control system of an open-type headbox has a high complexity, which is associated with the need not only to stabilize the parameters of the object, but also to carry out coordinated control of it in the case of automatic transfer of a paper machine from one type of product to another for a minimum time. A mathematical model of an open-type headbox as an object of mass level control has been developed. In the model, the output variable of the control object is the level of mass in the injection chamber, and the control action is the mass flow rate supplied to the injection chamber. The model takes into account the disturbing action - the area of the discharge slot. On the basis of the developed model, two options for constructing an algorithm for controlling the pressure box during its transfer from one mode to another are considered. The structure of the algorithm for coordinated control of the pressure box is developed. An illustrative example of application of the developed algorithm is given. The calculations of the optimal transient process in the object confirm the effectiveness of the developed control algorithm. The algorithm of coordinated control is applied to the standard pressure box YANO-180. The development of the algorithm for transferring the pressure box from the working (0.485 m) to the maximum (0.575 m) height of the mass level in the pressure box for 180 seconds is demonstrated. The calculation results show that the coordinated control algorithm provides the transfer of the mass level to the maximum height for a given time. The algorithm developed on the basis of the obtained mathematical model allows to control the level of mass in such a complex object as an open-type headbox when transferring a paper machine from one mode of operation to another for the time specified by the coordinated control system.
开式封头箱的控制系统具有较高的复杂性,不仅需要稳定对象的参数,而且需要在最短时间内实现纸机从一种产品自动转移到另一种产品的情况下对其进行协调控制。建立了作为质量水平控制对象的开式顶箱的数学模型。在模型中,控制对象的输出变量为注射腔内的质量水平,控制作用为注射腔内供给的质量流量。该模型考虑了扰动作用-放电槽面积。在此基础上,考虑了压力箱从一种模式转换到另一种模式的控制算法的两种构建方案。给出了压力箱协调控制算法的结构。最后给出了该算法的应用实例。通过对目标中最优暂态过程的计算,验证了所提控制算法的有效性。将协调控制算法应用于标准压力箱YANO-180。演示了将压力箱从工作高度(0.485 m)转移到压力箱中质量水平的最大高度(0.575 m) 180秒的算法的发展。计算结果表明,该协调控制算法能在给定时间内将质量水平传递到最大高度。在得到的数学模型的基础上开发的算法允许在协调控制系统规定的时间内控制纸机从一种操作模式转换到另一种操作模式时,诸如开式头箱这样的复杂物体的质量水平。
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引用次数: 0
Parameters of crack resistance of nanoreinforced polymeric engineering products 纳米增强聚合物工程产品的抗裂性能参数
Oleksandr Gondlyakh, Oleksandr Mamchur
Currently, structural elements made of polymer and rubber materials are widely used in various branches of mechanical engineering. One of the leading directions for improving the properties of such elements is the procedure of strengthening them by nanomodification with carbon nanotubes. The analysis of literary sources allows us to state that the process of nanomodification is a reliable tool for increasing the parameters of strength and crack resistance of polymer products. The purpose of this work is to build and numerically implement a model for physical prediction of the properties of nanomodified materials in order to determine the strength parameters of nanomodified objects. To analyze the mechanisms of formation and propagation of defects at the nano-, micro- and macro-levels, the method of discrete-virtual crack propagation was used, which allows for effective investigation of the strength of spatial systems of polymer nanocomposites. As a result of the conducted numerical experiments, it was established that the process of pulling out a carbon nanotube, which is under the action of an asymmetric load, is accompanied by a complex process of accumulation of defects, which depends on the change in conditions load and significantly affects the evolutionary scheme of the destruction of the nanocomposite. The developed methods make it possible to reliably assess the strength of nanomodified polymer materials and can be used in the development and implementation of information support systems for their life cycle elements of machine-building equipment.
目前,高分子材料和橡胶材料制成的结构元件广泛应用于机械工程的各个分支。提高这类元素性能的主要方向之一是用碳纳米管对其进行纳米改性。对文献资料的分析使我们能够指出,纳米改性过程是提高聚合物产品强度和抗裂性参数的可靠工具。本工作的目的是建立并数值实现纳米改性材料性能的物理预测模型,以确定纳米改性物体的强度参数。为了从纳米、微观和宏观三个层面分析缺陷的形成和扩展机制,采用离散虚拟裂纹扩展方法对聚合物纳米复合材料空间体系的强度进行了有效的研究。数值实验结果表明,在非对称载荷作用下,碳纳米管的拔出过程伴随着一个复杂的缺陷积累过程,该过程取决于条件载荷的变化,对纳米复合材料破坏的演化方案有重要影响。所开发的方法可以可靠地评估纳米改性聚合物材料的强度,并可用于机械制造设备中其生命周期元件的信息支持系统的开发和实施。
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引用次数: 0
Potential impact of dispersion products of magnetite quartzites on the environment 磁铁矿石英岩分散产物对环境的潜在影响
O. Lavrynenko, V. Yatsenko, B. Shabalin, I. Yatsenko
Using XRF, TG-DTA, chemical and sedimentation analysis of the products of processing of magnetite quartzites from the N Ore Processing Plant of Krivorozhye, changes in the phase and chemical composition of samples of four stages of magnetic separation and tailings were traced compared to a sample of the raw ore, and the potential impact of the dispersion process on the environment was revealed. Thermogravimetric studies indicate phase transformations of magnetite to maghemite (250-340 ° C), polymorphic transformations of iron oxides and destruction of rock-forming minerals (430-480 ° C), conversion of alpha quartz to beta-form (564-568 ° C), dehydroxylation of iron and magnesium oxyhydroxides (385 ° C), conversion of beta-quartz to beta-cristobalite (970 ° C). In the process of enrichment, there is an increase in the loss of mass of the samples, which is %: 0.06 (I); 1.46 (II); 1.9 (III), and 2.6 (IV). According to X-ray diffraction, the main ore mineral is magnetite, the rock-forming mineral is quartz. Among the secondary minerals are sulfides, cummingtonite, actinolite, and others. It is shown that at the first stage of enrichment all primary and secondary minerals are present in the samples, at the 2nd stage sulfides disappear from the sample, at the 3rd stage secondary minerals disappear, and at the 4th stage quartz remains in the sample and it forms aggregates with magnetite. The parameter of the crystal lattice of magnetite varies between 8.397-8.403 nm, its coherent scattering region (CSR) is 31.4-35.6 nm. It is found that in the course of ore grinding the destruction of secondary minerals takes place with the removal of destruction products, as evidenced by the occurrence of disperse quartz in the tailings. According to sedimentation analysis data, in the first 20 seconds, more than half of the particles with a size of 24-28 μm were deposited from the pulp, after 3 minutes, particles with a size of 8-9 μm settled, after 6 minutes - particles with a size of 6-7 μm. Within 30 minutes, almost complete precipitation of particles with sizes of 4.5-2.7 μm was observed. Hydraulic classification of the tailings showed the deposition of mainly quartz particles in the first and second chambers of the separator, actinolite and muscovite particles were separated in the third chamber, and cummingtonite, biotite and chlorite in the fourth chamber. Analysis of the chemical composition of the dispersion products indicates that Si, Ca, and Na accumulate in the tailings, whereas Ti is removed, and could potentially enter the environment. It is shown that the tailings and separation products increase the content of Zn, and the tailings accumulate environmentally hazardous As, and Nb. At the same time, the concentrations of other elements remain stable at all stages of processing.
利用XRF、TG-DTA、化学和沉积分析等方法,对克罗热热N矿选矿厂磁铁矿石英岩的选矿产物进行了对比分析,对比原矿样品,追踪了磁选4个阶段的样品和尾矿的物相和化学组成的变化,揭示了分散过程对环境的潜在影响。热重研究显示阶段转换的磁铁矿磁赤铁矿(250 - 340°C),多态转换的铁氧化物和破坏矿物(430 - 480°C),α-石英转换成测试阶段(564 - 568°C),脱羟基铁和镁氢氧化物(385°C),转换的石英beta-cristobalite(970°C)。在浓缩过程中,有一个损失的增加样品的质量,这是%:0.06(我);1.46 (2);1.9 (III)和2.6 (IV).根据x射线衍射,矿石矿物主要为磁铁矿,造岩矿物为石英。次生矿物有硫化物、明矾、放光石等。结果表明:在第1阶段,原生矿物和次生矿物全部存在于样品中;在第2阶段,硫化物从样品中消失;在第3阶段,次生矿物消失;在第4阶段,石英保留在样品中,并与磁铁矿形成团聚体。磁铁矿的晶格参数在8.397 ~ 8.403 nm之间变化,其相干散射区域(CSR)为31.4 ~ 35.6 nm。研究发现,在磨矿过程中,二次矿物的破坏是伴随着破坏产物的去除而发生的,尾矿中出现了分散的石英。根据沉降分析数据,在前20秒内,24-28 μm的颗粒有一半以上从矿浆中沉降,3分钟后,8-9 μm的颗粒沉降,6分钟后- 6-7 μm的颗粒沉降。在30分钟内,4.5 ~ 2.7 μm的颗粒几乎完全析出。尾矿水力分级结果表明,分选机第一室和第二室主要沉积石英颗粒,第三室分离放线石和白云母颗粒,第四室分离明辉石、黑云母和绿泥石颗粒。分散产物的化学成分分析表明,Si、Ca和Na在尾矿中积累,而Ti被去除,可能进入环境。结果表明,尾矿和分离产物使锌含量增加,尾矿中富集了对环境有害的砷和铌。同时,其它元素的浓度在加工的各个阶段都保持稳定。
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引用次数: 0
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Proceedings of the NTUU “Igor Sikorsky KPI”. Series: Chemical engineering, ecology and resource saving
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