首页> 外文期刊>Fluid Phase Equilibria >Solid–liquid equilibrium and hydrogen solubility of trans-decahydronaphthalene + naphthalene and cis-decahydronaphthalene + naphthalene for a new hydrogen storage medium in fuel cell system
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Solid–liquid equilibrium and hydrogen solubility of trans-decahydronaphthalene + naphthalene and cis-decahydronaphthalene + naphthalene for a new hydrogen storage medium in fuel cell system

机译:反式十氢萘+萘和顺式十氢萘+萘的固液平衡和氢溶解度,用于燃料电池系统中的新型储氢介质

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Solid–liquid equilibrium was measured for benzene + cyclohexane, trans-decahydronaphthalene + naphthalene and cis-decahydronaphthalene + naphthalene under the atmospheric pressure in the temperature range from 226.69 to 353.14 K. The apparatus was specially designed in this study, and it was based on a cooling method. The phase diagram with the complete immiscible solids was observed for the three systems, and the eutectic point was found at x2 = 0.2709 and Teu = 232.11 K for benzene + cyclohexane, x2 = 0.9816 and Teu = 241.98 K for trans-decahydronaphthalene + naphthalene, and x3 = 0.9822 and Teu = 225.74 K for cis-decahydronaphthalene + naphthalene, respectively. Hydrogen solubility was also measured for the two pure substances, trans-decahydronaphthalene and cis-decahydronaphthalene, and the three mixtures, trans-decahydronaphthalene + cis-decahydronaphthalene, trans-decahydronaphthalene + naphthalene, and cis-decahydronaphthalene + naphthalene, in the pressure range from 1.702 to 4.473 MPa at 303.15 K. Considering the solid–liquid equilibrium data, mole ratio of trans-decahydronaphthalene:cis-decahydronaphthalene was set to 50:50, and those of trans-decahydronaphthalene + naphthalene, and cis-decahydronaphthalene + naphthalene to 85:15. The hydrogen solubility increased linearly with the pressure following the Henry's law for all systems. The experimental solubility data were correlated or predicted with the Peng–Robinson equation of state [D.Y. Peng, D.B. Robinson, Ind. Eng. Chem. Fundam. 15 (1976) 59–64; R. Stryjek, J.H. Vera, Can. J. Chem. Eng. 64 (1986) 323–333].
机译:在226.69至353.14 K的大气压下,对苯+环己烷,反式十氢萘+萘和顺式十氢萘+萘的固液平衡进行了测量。冷却方法。观察到三个系统具有完全不混溶的固体的相图,对于苯+环己烷,共晶点位于x2 = 0.2709和Teu = 232.11 K,对于反式十氢萘+萘,x2 = 0.9816和Teu = 241.98 K,对于顺式十氢萘+萘,x3 = 0.9822,Teu = 225.74K。在压力范围为在303.15 K时1.702到4.473 MPa。考虑到固液平衡数据,反式十氢萘:顺式十氢萘的摩尔比设置为50:50,反式十氢萘+萘和顺式十氢萘+萘的摩尔比设置为85 :15。对于所有系统,氢溶解度均随遵循亨利定律的压力而线性增加。实验溶解度数据与Peng-Robinson状态方程相关联或预测。彭德宝罗宾逊,工业工程。化学丰达15(1976)59-64;斯特里耶克(R. Stryjek)维拉,可以。 J.化学。 64(1986)323–333]。

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