Molecular hydrogen occurs in two isomeric forms, one with its two proton nuclear spins aligned parallel (orthohydrogen), the other with its two proton spins aligned antiparallel (parahydrogen).[1] These two forms are often referred to as spin isomers[2] or as nuclear spin isomers.[3]
Parahydrogen is in a lower energy state than is orthohydrogen. At room temperature and thermal equilibrium, thermal excitation causes hydrogen to consist of approximately 75% orthohydrogen and 25% parahydrogen. When hydrogen is liquified at low temperature, there is a slow spontaneous transition to a predominantly para ratio, with the released energy having implications for storage. Essentially pure parahydrogen form can be obtained at very low temperatures, but it is not possible to obtain a sample containing more than 75% orthohydrogen by heating.
A mixture or 50:50 mixture of ortho- and parahydrogen can be made in the laboratory by passing it over an iron(III) oxide catalyst at liquid nitrogen temperature (77 K)[4] or by storing hydrogen at 77 K for 2–3 hours in the presence of activated charcoal.[5] In the absence of a catalyst, gas phase parahydrogen takes days to relax to normal hydrogen at room temperature while it takes hours to do so in organic solvents.[5]
^P. Atkins and J. de Paula, Atkins' Physical Chemistry, 8th edition (W.H.Freeman 2006), p. 451–2 ISBN0-7167-8759-8
^Matthews, M.J.; Petitpas, G.; Aceves, S.M. (2011). "A study of spin isomer conversion kinetics in supercritical fluid hydrogen for cryogenic fuel storage technologies". Appl. Phys. Lett. 99 (8): 081906. Bibcode:2011ApPhL..99h1906M. doi:10.1063/1.3628453.
^Matsumoto, Mitsuru; Espenson, James H. (2005). "Kinetics of the Interconversion of Parahydrogen and Orthohydrogen Catalyzed by Paramagnetic Complex Ions". Journal of the American Chemical Society. 127 (32): 11447–11453. doi:10.1021/ja0524292. ISSN0002-7863. PMID16089474.
^ abAroulanda, Christie; Starovoytova, Larisa; Canet, Daniel (2007). "Longitudinal Nuclear Spin Relaxation ofOrtho- andPara-Hydrogen Dissolved in Organic Solvents". The Journal of Physical Chemistry A. 111 (42): 10615–10624. Bibcode:2007JPCA..11110615A. doi:10.1021/jp073162r. ISSN1089-5639. PMID17914761.