Thermophysical property prediction of supercritical multiple mixtures fluid by molecular dynamics simulation

IF 5.3 2区 化学 Q2 CHEMISTRY, PHYSICAL
Tete Gui, Jiasunle Li, Zhiwei Ge, Liejin Guo
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Abstract

Supercritical multiple mixtures (H2O/CO2) fluids are produced in the poly-generation system based on supercritical water gasification (SCWG). Understanding the thermophysical property of supercritical multiple mixtures fluid is rather essential to design and industrialize the poly-generation system. At present, the selection of force field models for H2O/CO2 mixtures are rather complicated, chaotic and inconsistent, the calculation of each parameter necessitates the use of one force field model. There is no universal force field model to calculate and conduct thermophysical property of H2O/CO2 at one time in a wide range of temperature within SCW. In this paper, heat capacity, viscosity and thermal conductivity of multiple mixtures in supercritical and near-critical water (575 K–1075 k) are first investigated via a novel common force field model with molecular dynamics (MD) simulations. The effects of different factors including the pressure, temperature and CO2 mass fraction on thermophysical properties of H2O/CO2 at a wide range of temperature were first analyzed and conducted in detail. The calculated results indicate that the phenomenon “critical point drift” for viscosity and thermal conductivity of H2O/CO2 mixtures migrating toward the low temperature region occurs. The drift values of viscosity and thermal conductivity are about 10 K and 28 K. The variation of heat capacity and viscosity of H2O/CO2 mixtures increases with increasing pressures only in low temperatures region (700 K-–800 K), while the thermal conductivity always increases with increasing pressures. When the mass fractions of CO2 increases from 20 % to 40 % and 60 %, the drift values for thermal conductivity and viscosity of H2O/CO2 mixtures decreases from 628 K to 624 K and 620 K, and from 627 K to 618 K and 610 K, respectively, and the peak heat capacity decreases from 64.9 J/mol·K to 52.4 J/mol·K and 45.1 J/mol·K. The fitting polynomial to determine conductivity, viscosity and heat capacity H2O/CO2 mixtures as a functional relationship with temperature were first obtained. The research data of this paper could facilitate the industrialized application of the poly-generation system.
分子动力学模拟超临界多元混合流体热物性预测
超临界多元混合物(H2O/CO2)流体是在基于超临界水气化(SCWG)的多联产系统中产生的。了解超临界多组分混合流体的热物理性质对多组分联产系统的设计和工业化至关重要。目前,H2O/CO2混合物力场模型的选择比较复杂、混沌和不一致,每个参数的计算都需要使用一个力场模型。目前还没有一个通用的力场模型来计算和计算超临界水内大温度范围内H2O/CO2的一次热物理性质。本文首先利用分子动力学(MD)模拟的新通用力场模型研究了超临界和近临界水(575 k - 1075 k)中多种混合物的热容、粘度和导热系数。首先详细分析了压力、温度、CO2质量分数等不同因素对大范围温度下H2O/CO2热物性的影响。计算结果表明,H2O/CO2混合物的黏度和导热系数存在向低温区迁移的“临界点漂移”现象。粘度和导热系数漂移值分别为10 K和28 K左右。仅在低温区(700 ~ 800 K), H2O/CO2混合物的热容量和粘度随压力的增加而增加,而导热系数则随压力的增加而增加。当CO2质量分数从20%增加到40%和60%时,H2O/CO2混合物的导热系数和粘度漂移值分别从628 K减小到624 K和620 K,从627 K减小到618 K和610 K,峰值热容从64.9 J/mol·K减小到52.4 J/mol·K和45.1 J/mol·K。首先得到了确定H2O/CO2混合物的电导率、粘度和热容量随温度的函数关系的拟合多项式。本文的研究数据可为多联产系统的工业化应用提供参考。
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来源期刊
Journal of Molecular Liquids
Journal of Molecular Liquids 化学-物理:原子、分子和化学物理
CiteScore
10.30
自引率
16.70%
发文量
2597
审稿时长
78 days
期刊介绍: The journal includes papers in the following areas: – Simple organic liquids and mixtures – Ionic liquids – Surfactant solutions (including micelles and vesicles) and liquid interfaces – Colloidal solutions and nanoparticles – Thermotropic and lyotropic liquid crystals – Ferrofluids – Water, aqueous solutions and other hydrogen-bonded liquids – Lubricants, polymer solutions and melts – Molten metals and salts – Phase transitions and critical phenomena in liquids and confined fluids – Self assembly in complex liquids.– Biomolecules in solution The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include: – Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.) – Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.) – Light scattering (Rayleigh, Brillouin, PCS, etc.) – Dielectric relaxation – X-ray and neutron scattering and diffraction. Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.
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