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TESTING RESULTS
TABLE 1
PROCESSING OF N-DECANE
_____________________________________
NO NAME
INITIAL TREATMENT
MIX,
MIX,
% by
mass % by mass
______________________________________
1. 1.2-Dimethylhexane
----- 1.43482
2. N - Octane
0.04844 0.28183
3. N - Nonane
0.04610 0.24178
4. 2 - Methylnonane
0.05085 0.26179
5. 3 - Methylnonane
0.13862 0.55417
6. 4 - Methylnonane
0.21275 0.66980
7. N - Decane 99.50323
96.55574
______________________________________
CONCLUSION:
We observed isomerization of the hydrocarbon
output with formation
of volatile 2-, 3-, 4- methylene-nonane,
n-nonane.
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TABLE 2
PROCESSING OF N-OCTANE
______________________________________
NO NAME
INITIAL TREATMENT
MIX,
MIX,
% by
mass % by mass
______________________________________
1. N - Heptanes
0.11504 0.14879
2. 1.2 - Dimethylhexane ----
0.68847
3. 2 - Methylnonane
0.61088 0.51834
4. 4 - Methylnonane
0.25901 0.22089
5. 3 - Methylnonane 0.88853
0.83008
6. N - Octane
97.25901 93.28211
7. Don't…
-
0.03763
8. 2.4 - Methyloctane 0.13545
0.29003
9. 3 - Methyloctane
0.05794 0.08449
10. N - Nonane
0.54939
0.86537
11. 2 - Methylnonane 0.06818
0.07128
12. N - Decane
0.05657
0.63418
______________________________________
CONCLUSION:
The mechanism of reaction differs from
classic hydrocarbon creaking separation of CH3 groups from molecular
saturated hydrocarbons with carbon atom
Number greater that 7, and not
breaking molecules in the middle part.
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