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Detail of "13772-29-7"

  • CAS Number:
  • 13772-29-7
  • Name:
  • Phosphoric acid,zirconium(4+) salt (2:1)

  • Molecular Structure:
  • Formula:
  • H3O4 P . 1/2 Zr
  • Molecular Weight:
  • 283.18
  • Synonyms:
  • Zirconiumphosphate (6CI,7CI); Phosphoric acid zirconium salt (2:1); Zirconiumbis(monohydrogen orthophosphate); Zirconium bis(monohydrogen phosphate);Zirconium hydrogen orthophosphate; Zirconium hydrogen phosphate (Zr(HPO4)2);Zirconium monohydrogen phosphate (Zr(HPO4)2); Zirconium phosphate (Zr(HPO4)2); a-Zirconium phosphate; g-Zirconium phosphate
  • Density:
  • g/cm3
  • Boiling Point:
  • 158°Cat760mmHg
  • Flash Point:
  • °C

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CAS No.13772-29-7 Phosphoric acid,zirconium(4+) salt (2:1)

Gladys Structure and surface chemistry of crystalline zirconium phosphate catalysts Structure and surface chemistry of crystalline zirconium phosphate catalysts. Segawa, K.Several substances are used for example 13772-29-7 and 54914-24-8 which are their

Supplier:Aoruide International Chemicals Co.,Ltd [ China (Mainland)]

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CAS No.13772-29-7 ZIRCONIUM(IV) HYDROGENPHOSPHATE

Molecular Formula: H2O8P2Zr Molecular Weight: 283.18

Supplier:Shanghai Phosland Chemie Co.,Ltd [ China (Mainland)]

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Reference

Structure and surface chemistry of crystalline zirconium phosphate catalysts
Structure and surface chemistry of crystalline zirconium phosphate catalysts. Segawa, K.Several substances are used for example 13772-29-7 and 54914-24-8 which are their cas registry numbers.; Nakata, S.; Asaoka, S. (Fac. Sci. Technol., Sophia Univ., Tokyo 102, Japan). Mater. Chem. Phys., 17(1-2), 181-200 (English) 1987. CODEN: MCHPDR. DOCUMENT TYPE: Journal CA Section: 67 (Catalysis, Reaction Kinetics, and Inorganic Reaction Mechanisms) Section cross-reference(s): 22 The catalytic activities of isomerization of butenes and cyclopropane on cryst. Zr phosphates (ZrP) were examd. The ZrP catalyst calcined at ~800 K exhibited high catalytic activities. The coisomerization of d0- and d8-1-butene suggests that isomerization would proceed on protonic acid sites even after heat treatment at 1100 K. After evacuation of ~800K, most of the phosphate groups were removed, with consequent loss of H2O due to the condensation of phosphate groups between each Zr atom layer. However, a trace amt. of residual phosphate groups still remained on the surface. 31P magic-angle spinning NMR was employed to study the P micro-environments. The catalysts which showed higher activities showed higher 31P chem. shifts, suggesting that the phosphate groups remaining after evacuation at ~800 K may enhance the protonic acidity. .
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