Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, COA of Formula: C9H12O2702-23-8, Name is 2-(4-Methoxyphenyl)ethanol, SMILES is COC1=CC=C(CCO)C=C1, belongs to alcohols-buliding-blocks compound. In a article, author is Cai, Dongren, introduce new discover of the category.
Design and synthesis of novel amphipathic ionic liquids for biodiesel production from soapberry oil
Biodiesel produced from non-edible oils has received intensive attention in recent years. Herein, a series of novel amphipathic ionic liquids (ILs) based on the 4-dimethylaminopyridine (DMAP) were prepared for the transesterification of soapberry oil and methanol. The structures of the prepared ILs were systematically characterized by both Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (NMR, H-1 NMR and C-13 NMR). In addition, the effects of side-chain length of cation and the number of active site (H+) of ILs on the biodiesel yield were investigated, and the results suggested that 1-dodecyl-(4-dimethylammonium)-pyridinium bisulfate ([C12-DMAPH][HSO4](2)) exhibited the highest catalytic efficiency. Meanwhile, [C12-DMAPH][HSO4](2) was proven to be amphipathic, and the corresponding catalytic mechanism was proposed. Under the catalysis of [C12-DMAPH][HSO4](2), the optimum operating conditions of transesterification of soapberry oil and methanol were explored via the combination of single factor experiment and response surface methodology, obtaining the high biodiesel yield of (98.02 +/- 0.36)% under the optimum operating conditions. Importantly, [C12-DMAPH][HSO4](2) exhibited high stability in the transesterification of soapberry oil and methanol in five consecutive runs. Furthermore, the catalytic activities of [C12-DMAPH][HSO4](2) towards other transesterification of non edible oils and lower alcohols were also investigated, which indicated a general applicability of the prepared IL. (c) 2020 Elsevier Ltd. All rights reserved.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 702-23-8. COA of Formula: C9H12O2.
Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts