Catalytic performance and industrial test of HY zeolite for alkylation of naphthalene and α-tetradecene

As a synthetic lubricant with excellent properties, alkyl naphthalene is widely used in petrochemical and manufacturing industries. Alkyl naphthalene is formed by naphthalene and α-tetradecene under the action of alkylation...

n-Heptane isomerization activities of Pt catalyst supported on micro/mesoporous composites

Pt loaded on a series of MCM-48 silica and composites with HZSM-5 zeolite, HY zeolite, or TiO2 has been prepared and studied for n-heptane isomerization reaction at 200–350 °C. The structural characterization, acid distribution, and morphology of these catalysts were characterized by X-ray diffraction, Fourier transform infrared, UV–Vis diffuse reflectance, scanning electron microscope, temperature-programmed desorption of NH3, and nitrogen adsorption–desorption methods. The results show that these catalysts have a good selectivity to multi branched isomers, while producing low aromatic compounds. Also, these new composite catalysts prove the catalytic stability during the time of reaction. The most desirable results, and significantly higher n-heptane conversion and isomerization selectivity were achieved with Pt/MCM48-HZSM5 catalyst.

Py-GC-MS Study on Catalytic Pyrolysis of Biocrude Obtained via HTL of Fruit Pomace

Herein, we proposed new two-stage processing of blackcurrant pomace toward a value-added, hydrocarbon-rich biocrude fraction. The approach consisted of thermochemical liquefaction of a wet-type organic matter into liquid biocrude followed by its upgrade by thermal and catalytic pyrolysis. Particularly, we put effort into investigating the effect of selected catalysts (ZSM-5 and HY zeolite) on the composition of the volatiles released during the pyrolysis of the biocrude. The latter was obtained through liquefaction of the raw material in the binary solvent system of water and isopropanol. The biocrude yield accounted for ca. 45 wt.% of the initial dry biomass. It was a complex mixture of various component groups with an abundant share of oxygenates, especially carboxylic acids and esters. Thereafter, the biocrude was subjected to a pyrolysis study performed by means of the microscale coupled pyrolysis-gas chromatography-mass spectrometry technique (Py-GC-MS). The dominant components identified in the catalytic pyrolytic volatiles were unsaturated hydrocarbons (both cyclic and aliphatic ones) and, to a lesser extent, oxygen and nitrogen compounds. The addition of the ZSM-5 and HY zeolite allowed us to attain the relative total share of hydrocarbons in the volatile fraction equal to 66% and 73%, respectively (in relation to identified compounds). Thus, catalytic pyrolysis over zeolites seems to be particularly prospective due to the promotion of the deoxygenation reactions, which manifested in the noticeable decrease in the share of oxygen compounds in the evolved volatiles. The developed innovative two-stage processing of blackcurrant pomaces allows for obtaining value-added products that could serve as chemicals, biocomponents, and self-contained biofuels as well as bioplastic precursors. The presented contribution brings some new insights into the field of valorization of residuals generated by the food industry sector.

Biodiesel Production using Synthesized HY Zeolite Catalyst

Biodiesel was produced using oleic acid esterification and transesterification of the sunflower oil methods. Many different factors affecting production procedures were studied such as reaction temperature, the molar ratio of ethanol to oil, reaction time and concentration of HY catalyst. Different techniques such as TGA, FTIR and Mass spectroscopy were used to syntheses biodiesel. Results showed that 78% of oleic acid maximum conversion was obtained at a temperature of 70oC with molar ratio 12:1 ethanol: oil with 5 wt.% catalysts at 90 min reaction time, while for sunflower oil conversion of 98% at 200oC with 5 weight ratio of ethanol: oil at a time of 3 h was successfully obtained.

Stabilitas Zeolit HY Hidrofobik terhadap Uji Hot Liquid Water (HLW)

Initially, zeolite catalysts cannot be used for reactions involving hot liquid water, so it is necessary to modify the zeolite to be stable under these conditions. The synthesis of HY and hydrophobic zeolites aimed to determine the stability of zeolite in hot liquid water (HLW). The stability of zeolite in HLW is related to zeolite hydrophobicity. In this study, the main raw materials for the synthesis of HY zeolite were sodium aluminate (NaAlO2) and Ludox HS-40 by calcining the product at 350 oC for 1 hour. Furthermore, increasing the hydrophobicity of HY zeolite was carried out by modifying the external zeolite surface using organosilanes (aminopropyltriethoxysilane). The stability of two zeolites in HLW was set at 200 oC. Zeolite analysis used physical test and Fourier Transform-Infra Red (FTIR) Spectrometer. The results of the zeolite distribution in two phases confirmed that HY zeolite was completely dispersed in the water phase, while the zeolite one was dispersed in the organic phase. Moreover, the IR spectra of HY zeolite showed that the wide peak detection at wave number 720 cm-1 for beginning to disappear. This means that the HLW condition could be damaged to the d6r unit. Another result was shown by hydrophobic zeolite spectra with a stable peak for 72 hours. This indicates that the hydrophobic zeolite has thermal stability in HLW so that it can be used in chemical reaction catalytic applications that use on phase.

Ceric Ammonium Nitrate supported on Hy-Zeolite Catalyzed Oxidative Condensation Reaction and its Docking Studies

The chemistry of chalcone has been recognized as a significant field of study. Chalcone serve as to prepare starting materials for the synthesis of various heterocyclic compounds. From the backbone of reported literature, we have developed an alternative heterogeneous and simple catalytic system for the synthesis of chalcones via the oxidative condensation of benzyl alcohol with substituted acetophenone using metal nitrate supported HY-Zeolite as a catalyst. 30 mol% CAN supported HY-zeolite has been efficiently used as a catalyst for the oxidative condensation reaction of benzyl alcohol with substituted acetophenones in the presence of hydrogen peroxide as an oxidant in toluene to afford the corresponding chalcones in good to moderate yields. Docking studies were carried out for the synthesized compounds towards the protein Lysine aminotransferase using the software.

Sustainable production of benzene from lignin

Benzene is a widely used commodity chemical, which is currently produced from fossil resources. Lignin, a waste from lignocellulosic biomass industry, is the most abundant renewable source of benzene ring in nature. Efficient production of benzene from lignin, which requires total transformation of Csp2-Csp3/Csp2-O into C-H bonds without side hydrogenation, is of great importance, but has not been realized. Here, we report that high-silica HY zeolite supported RuW alloy catalyst enables in situ refining of lignin, exclusively to benzene via coupling Bronsted acid catalyzed transformation of the Csp2-Csp3 bonds on the local structure of lignin molecule and RuW catalyzed hydrogenolysis of the Csp2-O bonds using the locally abstracted hydrogen from lignin molecule, affording a benzene yield of 18.8% on lignin weight basis in water system. The reaction mechanism is elucidated in detail by combination of control experiments and density functional theory calculations. The high-performance protocol can be readily scaled up to produce 8.5 g of benzene product from 50.0 g lignin without any saturation byproducts. This work opens the way to produce benzene using lignin as the feedstock efficiently.