Alumina-supported CuCl2, the basic catalyst for ethylene oxychlorination, has been investigated 1 hour after preparation by UV-vis spectroscopy, a solubility test, EPR, EXAFS, and XRD in a wide range (0.25-9.0 wt%) of Cu concentration. We have evidenced that, at low Cu content, the formation of a surface aluminate species takes place, where isolated Cu(II) ions occupy octahedral vacancies of the alumina surface, having (within experimental errors) five oxygen ligands at 1.92 +/- 0.02 A. The chlorine released by copper chloride during its interaction with alumina gives >Al-Cl species. The formation of this surface copper aluminate stops at 0.95 wt% Cu/100 m(2); at higher Cu concentrations excess copper chloride precipitates directly from solution during the drying step, forming an amorphous CuCl2. 2H(2)O phase, overlapping progressively the surface aluminate. A slow hydrolysis, giving traces of paratacamite, an insoluble Cu hydroxochloride, also occurs. A room temperature dehydration process up to 10(-3) Torr implies the evolution of CuCl2. 2H(2)O into anhydrous CuCl2 as a consequence of the loss of the crystallization water.

ALUMINA SUPPORTED COPPER CHLORIDE PART 1: CHARACTERIZATION OF FRESHLY PREPARED CATALYST

ZECCHINA, Adriano;SPOTO, Giuseppe;BORDIGA, Silvia;LAMBERTI, Carlo
2000-01-01

Abstract

Alumina-supported CuCl2, the basic catalyst for ethylene oxychlorination, has been investigated 1 hour after preparation by UV-vis spectroscopy, a solubility test, EPR, EXAFS, and XRD in a wide range (0.25-9.0 wt%) of Cu concentration. We have evidenced that, at low Cu content, the formation of a surface aluminate species takes place, where isolated Cu(II) ions occupy octahedral vacancies of the alumina surface, having (within experimental errors) five oxygen ligands at 1.92 +/- 0.02 A. The chlorine released by copper chloride during its interaction with alumina gives >Al-Cl species. The formation of this surface copper aluminate stops at 0.95 wt% Cu/100 m(2); at higher Cu concentrations excess copper chloride precipitates directly from solution during the drying step, forming an amorphous CuCl2. 2H(2)O phase, overlapping progressively the surface aluminate. A slow hydrolysis, giving traces of paratacamite, an insoluble Cu hydroxochloride, also occurs. A room temperature dehydration process up to 10(-3) Torr implies the evolution of CuCl2. 2H(2)O into anhydrous CuCl2 as a consequence of the loss of the crystallization water.
2000
189
91
104
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WHJ-45FC5R2-7R&_user=525216&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000026382&_version=1&_urlVersion=0&_userid=525216&md5=8ee1ea22fa8c12dfe94e916a9bbe90b5
OXYCHLORINATION CATALYSTS; HYDROGEN CHLORIDE; UV-Vis SPECTROSCOPY; EPR SPECTROSCOPY; CuCl2; EXAFS
G. LEOFANTI; M. PADOVAN; M. GARILLI; D. CARMELLO; A. ZECCHINA; G. SPOTO; S. BORDIGA; G. TURNES PALOMINO; C. LAMBERTI
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/6886
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