3 research outputs found
Production of Liquid Hydrocarbon Fuel from Catalytic Cracking of Rubber Seed Oil Using New Mesoporous Molecular Sieves
New mesoporous molecular sieves MMS-11,
MMP-12, MNS-16, MNP-10,
and MNC-13 were synthesized successfully using zeolite β as
a silica–alumina source and different ionic liquids as templates.
The structure and catalytic activity of the mesoporous molecular sieves
as heterogeneous catalysts for the cracking of rubber seed oil (RSO)
were studied in detail. MNC-13 exhibited excellent catalytic performance
for the cracking of RSO, and the cracked oil had a chemical composition
and properties similar to those of diesel-based fuels. Furthermore,
the catalyst MNC-13 is of such outstanding stability that it retains
high activity even after being used five times. Therefore, this research
provides a new type of catalytic result for the same type of high-temperature
cracking reaction
Comparative Study of the Structure of Hydroproducts Derived from Loblolly Pine and Straw Grass
The
structural characteristics of products derived from the hydrothermal
carbonization (HTC) of loblolly pine (LP) and straw grass (SG) were
investigated via solid-state cross-polarization/magic angle spinning
nuclear magnetic resonance (CP/MAS <sup>13</sup>C NMR), heteronuclear
single-quantum correlation nuclear magnetic resonance (HSQC-NMR),
and solution <sup>13</sup>C NMR and <sup>31</sup>P NMR techniques.
Results revealed that after HTC, hydrochars from both LP and SG mainly
consisted of a combination of lignin, furfural, and condensed polyaromatic
structures with a high level of fixed carbon content and higher heating
value (HHV). Hydrochar from LP exhibited a higher aryl to furan ratio,
and those from SG contained more aliphatic functional groups. Solution <sup>13</sup>C NMR and HSQC revealed that both liquid chemicals were condensed
polyphenolic structures with aliphatic groups that exist mainly in
the form of side chains. Although the LP products exhibited a higher
proportion of aromatic structures, the types of polyphenol and aliphatic
C–H were more diverse in the SG products. Results also indicated
that reactions such as chain scission and condensation occurred during
hydrothermal carbonization processes. Overall, HTC was found to be
an effective refinery treatment for converting different waste biomass
into valuable energy materials and chemicals
Liquid Hydrocarbon Fuels from Catalytic Cracking of Waste Cooking Oils Using Basic Mesoporous Molecular Sieves K<sub>2</sub>O/Ba-MCM-41 as Catalysts
Mesoporous molecular sieves K<sub>2</sub>O/Ba-MCM-41, which feature
base sites, were prepared under hydrothermal conditions. The structure,
base properties, and catalytic activity of the mesoporous molecular
sieves as heterogeneous catalysts for the cracking of waste cooking
oil (WCO) were then studied in detail. K<sub>2</sub>O/Ba-MCM-41 exhibited
higher catalytic performance for the cracking of WCO than traditional
base catalysts such as Na<sub>2</sub>CO<sub>3</sub> and K<sub>2</sub>CO<sub>3</sub>. Moreover, the cracking of WCO generates fuels (main
composition is C<sub>12</sub>∼C<sub>17</sub> alkane or olefin)
that have similar chemical compositions to diesel-based fuels, and
K<sub>2</sub>O/Ba-MCM-41 is of excellent stability. The catalyst could
be recycled and reused with negligible loss in activity for four cycles.
K<sub>2</sub>O/Ba-MCM-41 is an environmentally benign heterogeneous
basic catalyst for the production of liquid hydrocarbon fuels from
low quality feed stocks