稀溶液中硝基烷烃的介电弛豫

B. Singh, J.K. Vij
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引用次数: 4

摘要

测量了(a)硝基乙烷、(b) 1-硝基丙烷、(c) 2-硝基丙烷和(d) 1-硝基丁烷在环己烷中的稀溶液在10°、20°、30°和40°c下在10kHz和10GHz频率下的相对介电常数和折射率。材料(b)和(c)以及(e)2-硝基- 1-丙醇和(f) 2-硝基- 1-丁醇也在不同的非极性溶剂中进行了研究。计算了电偶极矩、介电弛豫时间和摩尔活化能参数。结果表明,在硝基醇的羟基和硝基的氧原子之间存在内部氢键。对于溶剂正庚烷、环己烷和十氢化萘,材料(b)和(c)的log τ与log η曲线呈线性关系。讨论了这些材料与对二甲苯、四氯化碳和对二恶烷相互作用的可能性。观察到这些材料的活化焓(ΔHε)在稀溶液中比在纯液体中高,并且硝化丁烷的活化焓(ΔHε)也明显低于其他材料。
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Dielectric relaxation of nitroalkanes in dilute solutions

The relative permittivity at frequencies of 10kHz and 10GHz and the refractive indices have been measured for dilute solutions of (a) nitroethane, (b) 1-nitropropane, (c) 2-nitropropane, and (d) 1-nitrobutane in cyclohexane at 10°, 20°, 30° and 40°C. Materials (b) and (c) together with (e)2-nitro 1-propanol and (f) 2-nitro-l-butanol, have also been studied in different nonpolar solvents. The electric dipole moments, the dielectric relaxation times, and the molar activation energy parameters have been calculated. The results for nitroalcohols show the existence of internal hydrogen bonding between the hydroxyl group and an oxygen atom of the nitro group. The plots of log τ versus log η for materials (b) and (c) are linear for the solvents n-heptane, cyclohexane and decalin. The possibility of interaction of these materials with p-xylene, carbon tetrachloride and p-dioxane are discussed. Activation enthalpy (ΔHε) of these materials is observed to be higher in dilute solutions than in pure liquids, and also ΔHε for nitrobutane is significantly lower than for the other materials.

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