𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Pyrolysis of acetylene-vinylacetylene mixtures between 400 and 500°C

✍ Scribed by Chellappah Chanmugathas; Julian Heicklen


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
559 KB
Volume
18
Category
Article
ISSN
0538-8066

No coin nor oath required. For personal study only.

✦ Synopsis


Acetylene and vinylacetylene mixtures were pyrolyzed at 400-500°C in the absence and presence of O2 or NO. The major product of the interaction between CzH2 and C4H4 is polymer, but benzene is also produced. Both the C2H2 removal and CsHs formation rates are first-order in C2Hz and C4H4. The rate coefficients are log(k{CzHZ}, M-' s -~) = 6.26 2 0.20 -(70.6 2 3.6)/2.3RT log(k{C,jH,j}, M-' s-') = 8.65 * 0.39 -(125.9 2 5.4)/2.3RT where R is the ideal gas constant in kJ/mol-K. Benzene formation occurs by two processes: a concerted molecular mechanism (=60%) and a singlet diradical mechanism (=40%).


📜 SIMILAR VOLUMES


Pyrolysis of 2-butyne/vinylacetylene mix
✍ Charles Harper; Julian Heicklen 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 523 KB

Vinylacetylene and 2-butyne mixtures were pyrolyzed a t 350-450°C in the absence and presence of 0, and NO. The major product of the reaction is a polymer, but o-xylene is also produced and was studied as the species of interest. The C,H,,i formation rate is first-order in C,H, and C,H,. The rate co

Pyrolysis of vinylacetylene between 300
✍ Richard Lundgard; Julian Heicklen 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 1014 KB

Vinylacetylene was pyrolyzed at 300-450°C in a packed and an unpacked static reactor with a pinhole bleed to a quadrupole mass spectrometer. The reactant and C,H, products were monitored continuously during a reaction by mass spectrometry. In some runs, the products were also analyzed by gas chromat

The pyrolysis of acetylene-styrene mixtu
✍ C. Chanmugathas; Julian Heicklen 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 630 KB

The pyrolysis of acetylene-etyrene mixtures has been studied from 450-550°C in a quartz reaction vessel in the absence and presence of 0, or NO. The rates of disappearance of reactants and formation of adducts are first-order in each reactant. The major product is polymer, with the adducts accountin

Pyrolysis of Propyne/2-Methylbut-1-ene-3
✍ Charles Harper; Julian Heicklen 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 626 KB

2-Methylbut-1-ene-3-yne and Propyne mixtures were pyrolyzed at 350-450°C in the absence and presence of O2 and NO. The major product of the reaction is a polymer, but rn-xylene andp-xylene are also produced and were studied as the species of interest. The CsHIo formation rate is first-order in C3H4