4.7 Article

Stability of ZSM-11 and BETA zeolites during the catalytic cracking of low-density polyethylene

Journal

JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS
Volume 92, Issue 2, Pages 450-455

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jaap.2011.08.008

Keywords

H-ZSM-11; H-BETA; LDPE; Deactivation; Coke

Funding

  1. Foncyt [PICT 2007-00303]
  2. Ministerio de Ciencia y Tecnologia de la Provincia de Cordoba [PID 000121]
  3. CONICET
  4. [UTN-PID 25E129]

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The stability of H-ZSM-11 (H-Z) and H-BETA (H-B) zeolites during the catalytic degradation of low-density polyethylene (LDPE) was studied using the same sample of catalyst in eleven consecutive cycles. The gaseous hydrocarbons, liquid hydrocarbons and waxes generated in each cycle were analyzed as well as the used catalyst. The zeolites were characterized by XRD. FTIR of adsorbed pyridine and N(2) adsorption, while the physical mixtures of LDPE/zeolites were subjected to TG-DTG analysis. The H-Z zeolite exhibited an important stability during the successive cycles of LDPE conversion. On the contrary, the behavior H-B zeolite was completely different: from the sixth cycle the yields of products changed progressively, approaching to that obtained in a purely thermal process. The yields of accumulated coke increased steadily throughout the cycles up to maximum values in the eleventh cycle of similar to 6 and similar to 15 wt% for H-Z and H-B, respectively. These results were confirmed by TG under air flow. (C) 2011 Elsevier B.V. All rights reserved.

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