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Crystal Structure and Chemical Stabilization of the Triple Salt (KHSO5)2⋅KHSO4⋅K2SO4

✍ Scribed by Otto Ermer; Christof Röbke


Publisher
John Wiley and Sons
Year
2003
Tongue
German
Weight
131 KB
Volume
86
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The title compound, a versatile and chemically stabilized oxidant, which is used technologically on a large scale, builds up an intercalation‐type of crystal structure with alternating sheets of sulfate and peroxomonosulfate anions, interspersed by the potassium cations. The sulfate ions are joined by a very short but nonetheless probably asymmetric hydrogen bond. At room temperature, the HSO$\rm{_{5}^{-}}$ ions show dynamic orientational/conformational disorder in the area of the hydrogenperoxo group, which disappears at 100 K. The chemical stabilization of the triple salt is ascribed to shielding of the HSO$\rm{_{5}^{-}}$ ions effected by the intercalation between the sulfate sheets and, furthermore, by the large and abundant K^+^ ions of this potassium‐rich compound.


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High-Temperature Structural Phase Transi
✍ T.M. Chen; R.H. Chen 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 476 KB

High-temperature structural phase transitions in \(\mathrm{K}_{2} \mathrm{SO}_{4}\) and \(\mathrm{K}_{2} \mathrm{SeO}_{4}\) crystals have been studied by \(\mathrm{X}\)-ray diffraction. Laue and precession photographs were taken with Mo radiation at several high temperatures. Results indicate that t