scholarly journals Dynamical Effects and Product Distributions in Simulated CN + Methane Reactions

2016 ◽  
Vol 120 (27) ◽  
pp. 4672-4682 ◽  
Author(s):  
Thomas J. Preston ◽  
Balázs Hornung ◽  
Shubhrangshu Pandit ◽  
Jeremy N. Harvey ◽  
Andrew J. Orr-Ewing
2018 ◽  
Vol 5 (3) ◽  
Author(s):  
Mohamad Yusman

Water at the supercritical state is a new process for the chemical recycling. At this thermodynamic state i.e. Pc = 218 atmospheres and Tc = 374oC , water behaves very differently from its everyday temperament and it is a very good solvent for organic components. Experimental studies show that supercritical water can decompose hydrocarbons/polymers and produce useful products like 2-Azacyclotridecanone /lactam-1 from Nylon-12 (batch process). The decomposition process itself was carried out in batch reaction system in order to get more information about product distributions, time dependence, and scale-up possibilities.Keywords: supercritical water, decomposition, batch, polymer, hydrocarbon


2018 ◽  
Vol 3 (44) ◽  
pp. 12415-12423 ◽  
Author(s):  
Zhipeng Tian ◽  
Chenguang Wang ◽  
Zhan Si ◽  
Yachen Wang ◽  
Lungang Chen ◽  
...  

Fuel ◽  
1994 ◽  
Vol 73 (6) ◽  
pp. 789-794 ◽  
Author(s):  
Dominique Brodzki ◽  
Gérald Djéga-Mariadassou ◽  
Chun-Zhu Li ◽  
Rafael Kandiyoti

2019 ◽  
Author(s):  
Wendell Dilling

<p>Photocycloaddition of fullerene-C<sub>60 </sub>to the isomeric 2,4-hexadienesreported by Orfanopoulos and co-workers gave a series of 2 + 2 cycloadducts in which bond rotation had occurred in some products. Relative rates of bond rotation and ring closure in the biradical intermediates were calculated from the product distributions using equations developed by Bartlett and co-workers. These data are reinterpreted to show that the ratio of the rate of bond rotation in the intermediate to the rate of ring closure to the cyclobutane product is ~70 for the <i>trans</i>-1-propenyl intermediate formed in the initial cis conformation. Data are inconsistent for the analogous <i>cis</i>-1-propenyl intermediate. The relative rate for the <i>trans</i>-1-propenyl intermediate formed in the initial trans conformation is ~9. Accurate relative rate determinations are highly dependent on very accurate product distribution determinations.</p>


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