Process optimization for the production of biodiesel from Azolla Microphylla oil and its fuel characterization

The most competent and operative use of renewable feedstock is super critical for the production of biodiesel which has increased attention worldwide pertaining to aquatic fern Azolla. Maximizing the biodiesel yield by optimizing the process parameters of the low-frequency ultrasonic energy-assisted transesterification process of Azolla oil is the need of the hour for minimizing the production cost of biodiesel. Response Surface Methodology (RSM) was applied using central composite rotatable design (CCRD) to find the best optimum reaction parameters for this transesterification process. The optimized reaction parameters arrived from the design of experiments were as following: methanol/Azolla oils molar ratio (A) = 6.49 mole/mole, KOH catalyst concentration (B) = 1.69 (weight% of oil), reactiion time (C) = 34.74 min and reaction temperature (D) = 38.87°C. The best higher theoretical predicted Azolla Fatty Acid Methyl Ester (FAME) yield was Y = 99.76% which is in well coincidence with the actual yield. The extracted Azolla biodiesel was tested for various fuel properties with standard test procedures and found to be in agreement with various Biodiesel standards and the results are promising in terms of utilizing Azolla oil as an inexhaustible and potentially economical source of biodiesel.

3 Methods and Materials Applied in Electrosynthesis

This chapter is intended as a tutorial for the organic chemist and to serve as an introductory guide to the technical and methodological aspects of electrosynthesis. The most important reaction parameters, methods, and materials are covered both from a practical point of view and in their physicochemical context.

Wavelength Dependence of the Transformation Mechanism of Sulfonamides Using Different LED Light Sources and TiO2 and ZnO Photocatalysts

The comparison of the efficiency of the commercially available photocatalysts, TiO2 and ZnO, irradiated with 365 nm and 398 nm light, is presented for the removal of two antibiotics, sulfamethazine (SMT) and sulfamethoxypyridazine (SMP). The •OH formation rate was compared using coumarin, and higher efficiency was proved for TiO2 than ZnO, while for 1,4-benzoquinone in O2-free suspensions, the higher contribution of the photogenerated electrons to the conversion was observed for ZnO than TiO2, especially at 398 nm irradiation. An extremely fast transformation and high quantum yield of SMP in the TiO2/LED398nm process were observed. The transformation was fast in both O2 containing and O2-free suspensions and takes place via desulfonation, while in other cases, mainly hydroxylated products form. The effect of reaction parameters (methanol, dissolved O2 content, HCO3− and Cl−) confirmed that a quite rarely observed energy transfer between the excited state P25 and SMP might be responsible for this unique behavior. In our opinion, these results highlight that “non-conventional” mechanisms could occur even in the case of the well-known TiO2 photocatalyst, and the effect of wavelength is also worth investigating.

Preparation of Hierarchical Structure Au/ZnO Composite for Enhanced Photocatalytic Performance: Characterization, Effects of Reaction Parameters, and Oxidizing Agent Investigations

Zinc oxide (ZnO) has been shown as a potential photocatalyst under ultraviolet (UV) light but its catalytic activity has a limitation under visible (Vis) light due to the wide bandgap energy and the rapid recombination of electrons and holes. Thus, hierarchical structure Au/ZnO composites were fabricated by the hydrothermal method and chemical reduction method for enhanced photocatalytic performance under visible light. As-prepared composites were characterized by UV-vis diffuse reflectance spectra (DR/UV-Vis), field emission scanning electron microscope (FESEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and electron paramagnetic resonance (EPR). The Au/ZnO-5 composite showed the highest adsorption among as-prepared samples in the range of 250-550 nm, having bandgap energy of 0.13 eV. Au nanoparticles of about 3-5 nm were well dispersed on hierarchical flower ZnO with approximately 10-15 μm. The EPR signal at g = 1.965 on both ZnO and Au/ZnO samples was attributed to oxygen vacancy Vo•, but the presence of Au led to a decrease in signal strength of Au/ZnO composite, showing the degradation efficiency (DE) and reaction rate of 99.2% and 0.109 min-1, respectively; these were larger than those of other samples. The effects of reaction parameters and oxidizing agents on photocatalytic performance were investigated and showed that the presence of H2O2 and O2 could improve the reaction of composite. In addition, the kinetic and photocatalytic mechanism of tartrazine (TA) on catalysts were studied by the first-order kinetic model and characterized analyses.

Towards understanding kraft lignin depolymerisation under hydrothermal conditions

Kraft lignin depolymerisation using hydrothermal liquefaction suffers from the formation of char, resulting in a decreased product yield as well as causing operational problems. While this may be mitigated by the addition of capping agents such as phenol and isopropanol, other reaction parameters, for example reaction time and temperature, are also important for the product yields. In this work, the effect of short reaction times on the hydrothermal liquefaction of kraft lignin in an alkaline water and isopropanol mixture was investigated at 1–12 min and 290 °C. The results show that there were swift initial reactions: the major ether bonds in the lignin were broken within the first minute of reaction, and the molecular weight of all product fractions was halved at the very least. Longer reaction times, however, do not cause as pronounced structural changes as the initial reaction, indicating that a recalcitrant carbon-carbon skeleton remained in the products. Nevertheless, the yields of both char and monomers increased slowly with increasing reaction time. The swift initial depolymerising reactions were therefore followed by slower repolymerisation as well as a slow formation of monomers and dimers, which calls for careful tuning of the reaction time.

Amine-based synthesis of Fe3C nanomaterials: mechanism and impact of synthetic conditions

Iron-based catalysts are a preferred variant of metal catalysts due to the high abundance of iron on earth. Iron carbide has been investigated in recent times as an electrochemical catalyst due to its potential as a great ORR catalyst. Using a unique amine-metal complex anion composite (AMAC) method, iron carbide/nitride nanoparticles (Fe3C and Fe3−x N) were synthesized through varying several reaction parameters. While the synthesis is generally quite robust and can easily afford phase pure Fe3C, it now has been shown that the particle size, morphology, excess carbon, and amount of nitrogen in the resulting nanomaterials can readily be tuned. In addition, it was discovered that Fe2N can be synthesized as an intermediate by stopping the reaction at a lower heating temperature. These nanomaterials were tested for their electrochemical activity in oxygen evolution reactions (OER).