✦ LIBER ✦

Flash pyrolysis of coal sub-structures. A mechanistic and kinetic evaluation

✍ Scribed by Jesper V. Christiansen; Anders Feldthus; Helge Egsgaard; Peter Bo; Lars Carlsen

Book ID: 107905784
Publisher: Elsevier Science
Year: 1993
Tongue: English
Weight: 799 KB
Volume: 25
Category: Article
ISSN: 0165-2370
DOI: 10.1016/0165-2370(93)80042-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Flash pyrolysis of coal sub-structures a

Flash pyrolysis of coal sub-structures adsorbed on a carbosieve

✍ Jesper V. Christiansen; Anders Feldthus; Helge Egsgaard; Lars Carlsen 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 692 KB

Time-resolved pyrolysis mass spectrometr

Time-resolved pyrolysis mass spectrometry of coal: a new tool for mechanistic and kinetic studies

✍ Chakravarty, Tanmoy; Windig, Willem; Hill, George R.; Meuzelaar, Henk L. C.; Kha 📂 Article 📅 1988 🏛 American Chemical Society 🌐 English ⚖ 756 KB

Kinetics of tetrabromobisphenol A pyroly

Kinetics of tetrabromobisphenol A pyrolysis. Comparison between correlation and mechanistic models

✍ Rafael Font; Julia Moltó; Nuria Ortuño 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 844 KB

Kinetics of coal and catalytic coal pyro

Kinetics of coal and catalytic coal pyrolysis reactions in a fixed bed reactor

✍ P.K. Dey 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 174 KB

Flash pyrolysis of coal, coal maceral, a

Flash pyrolysis of coal, coal maceral, and coal-derived pyrite with on-line characterization of volatile sulfur compounds

✍ Mei-in M. Chou; Michael A. Lake; Robert A. Griffin 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 562 KB

Comparative studies on the pyrolysis of

Comparative studies on the pyrolysis of N-arylideneaminoamides: Kinetic and mechanistic studies

✍ Nouria A. Al-Awadi; Yehia A. Ibrahim; Mehul Patel; Bobby J. George; Alya M. Al-E 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 207 KB

## Abstract Rates of thermal decomposition of title compounds have been measured using a static reaction system. They undergo a unimolecular first‐order elimination to give arylnitrile and the corresponding substituted amides. The decomposition parallels that of __N__‐arylidenamino cyclic amide. Th