Is isobutane a greenhouse gas?
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| Papers (8) | Insight |
|---|---|
25 Citations | The results indicated that the greenhouse gas emission, especially for the CO 2 and CH 4 , showed a distinctly spatial variation. |
29 Citations | While this is a significant component, the CH4 associated with imported embodied energy should also be included in national greenhouse gas (GHG) inventories. |
| The experimental results indicated that isobutane was formed by a propane intermediate and isobutyraldehyde was formed by a propionaldehyde intermediate in the reaction. | |
39 Citations | The greenhouse with CO2 supplied from bottles turns out to be superior to tthe greenhouse with CO2 supplied by burning gas. |
155 Citations | Furthermore, in a range of temperatures and pressures, the affinity of Cu-BTC for isobutane was observed to be intermediate to that of propane and propylene which suggest that isobutane is a promising desorbent in SMB processes for propane/propylene separations. |
94 Citations | Evidently hydrogen transfer is more important in the conversion of isobutane than of neopentane. |
22 Citations | Isobutane presents a smaller sensitivity to residence time than other investigated hydrocarbon systems. |
22 Citations | Dehydrogenation of saturated isobutane provides an alternative process to produce isobutene from nonpetroleum resources. |
Related Questions
What are the biomedical applications of isobutyric acid?5 answersIsobutyric acid has several biomedical applications. It can be used as a raw material for perfumes and other fragrance products. Additionally, it can be collected from a culture material by cultivating a fungus belonging to the genus Candida. Isobutyric acid is also produced through the oxidation of isobutyl aldehyde, and it can be used as a food additive or as a starting material for methacrylic acid. Furthermore, isobutyric acid can be obtained through the liquid phase air oxidation of isobutylaldehyde in the presence of a basic compound, making the purification process easier. Finally, isobutyric acid can be prepared through the Koch synthesis method, which involves reacting propylene, carbon monoxide, and water or a lower alcohol in the presence of hydrogen fluoride.
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