Synthesis and Evaluation of Levulinic Ester as Biodiesel Additives

2020 ◽  
Vol 71 (8) ◽  
pp. 21-26
Author(s):  
Elena-Emilia Oprescu ◽  
Cristina-Emanuela Enascuta ◽  
Elena Radu ◽  
Vasile Lavric

In this study, the SO42-/TiO2-La2O3-Fe2O3 catalyst was prepared and tested in the conversion of fructose to ethyl levulinate . The catalyst was characterized from the point of view of the textural analysis, FT-IR analysis, acid strength distribution, X-ray powder diffraction and pyridine adsorption IR spectra. The influence of the reaction parameters on the ethyl levulinate yield was study. The maximum yield of 37.95% in levulinate esters was obtained at 180 �C, 2 g catalyst and 4 h reaction time. The effect of ethyl levulinate addition to diesel-biodiesel blend in different rates, i.e, 0.5, 1, 2.5, 5 (w.t %) on density, kinematic viscosity and flash point was evaluated and compared with the European specification.

2007 ◽  
Vol 21 (30) ◽  
pp. 2089-2094
Author(s):  
N. A. PAREY ◽  
M. A. SHAH

The effect of L-methionine doping on the optical properties of potassium acid phthalate have been studied. Bulk single crystals of L-methionine-doped potassium acid phthalate (LMDKAP) were grown by a slow cooling method using a constant temperature bath. X-ray powder diffraction study has revealed the significant variation in the cell parameter values and the shift in peak positions, which confirms the presence of dopant in the sample. The UV-VIS cut off wavelength of LMDKAP was found to be 300 nm and it is slightly less than KAP. The presence of functional groups present in LMDKAP were confirmed through FT-IR analysis.


Minerals ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. 341 ◽  
Author(s):  
Yu Zheng ◽  
Yating Cui ◽  
Weiqing Wang

The activation mechanism of lead ions (Pb2+) in perovskite flotation with an octyl hydroxamic acid collector was systematically investigated using microflotation experiments, zeta-potential measurements, adsorption tests, Fourier transform infrared (FT-IR) analysis, and X-ray photoelectron spectroscopy (XPS) analysis. The results of microflotation experiments and adsorption tests indicate that the presence of Pb2+ can promote the adsorption of octyl hydroxamic acid (OHA) on the perovskite surface and enhance the flotability of perovskite under weakly acidic conditions. The maximum recovery of 79.62% was obtained at pH 6.5 in the presence of Pb2+, and the maximum recovery of 57.93% was obtained at pH 5.7 without Pb2+. At pHs below 7, lead species are mainly present as Pb2+ and PbOH+ in the solution; besides this, the relative content of titanium increases on the perovskite surface. The adsorption of Pb2+ and PbOH+ on the perovskite surface makes the zeta-potential of perovskite shift positively, and increases the number of activated sites on the perovskite surface. FT-IR and XPS analyses confirm that OHA chemisorbs on the surface of Pb2+-activated perovskite and forms hydrophobic Pb-OHA complexes, which improve the flotability of perovskite.


Polymers ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 4187
Author(s):  
Huifang Xie ◽  
Xin Ma ◽  
Wenbin Lin ◽  
Shiting Dong ◽  
Qiang Liu ◽  
...  

In the current study, linear dextrin (LD) was prepared using waxy potato starch debranched with pullulanase, which has attracted immense interest in the food, pharmaceutical, and cosmetic industries as a versatile ingredient. Various LDs were separated on the basis of their differential solubility in aqueous/ethanol solutions of different volumetric ratios. Three LD products—LD Fabrications with 40% ethanol (F-40); LD Fabrications with 50% ethanol (F-50); and LD Fabrications with 60%, 70%, and 80% ethanol (F-M)—were obtained with an average degree of polymerization (DP) values of 31.44, 21.84, and 16.10, respectively. The results of Fourier transform infrared spectroscopy (FT-IR) analysis revealed that the reaction mainly involved hydrogen bonding and a hydrophobic interaction between LD and insulin in the process of inclusion complex formation. X-ray diffraction (XRD) results indicated that insulin was encapsulated in LD. The results of circular dichroism (CD) showed that the changes in the secondary structure of insulin were negligible during the release from the inclusion complexes. The order of encapsulation capacity is as follows: the complex composed of F-M and insulin (F-M-INS) > the complex composed of LD and insulin (LD-INS) > the complex composed of F-50 and insulin (F-50-INS) > and the complex composed of F-40 and insulin (F-40-INS). F-M-INS inclusion complexes showed a better effect on reducing the release of insulin in gastric juice and promoting the release of insulin in intestinal juice and blood plasma than LD-INS.


2012 ◽  
Vol 68 (5) ◽  
pp. 467-479 ◽  
Author(s):  
Esther García-Tuñón ◽  
Bruno Dacuña ◽  
Guillermo Zaragoza ◽  
Jaime Franco ◽  
Francisco Guitián

We have synthesized large chlorapatite [ClAp, Ca5(PO4)3Cl x (OH)1 − x , where x = 1] single crystals using the molten salt method. We have corroborated that the hexagonal symmetry P63/m describes the crystal structure best, even though the crystals are synthetic and stoichiometric. Moreover, we have performed several thermal treatments on these ClAp crystals, generating new single crystals in the apatite system [Ca5(PO4)3Cl x (OH)1 − x , where x ≤ 1], where the chloride anions (Cl−) were systematically substituted by hydroxyl anions (OH−). These new single crystals were methodically characterized by powder and single-crystal X-ray diffraction (SXRD), scanning electron microscopy (SEM), Fourier transform–IR spectroscopy (FT–IR), and energy-dispersive X-ray spectroscopy (EDS). We have discovered a previously unreported OH− inclusion site substituting the Cl− anion during the ion-exchanging process. Finally, we evaluated the atomic rearrangements of the other species involved in the structure. These movements are associated with ionic exchange, which can be justified from an energetic point of view. We also found a novel phase transformation at high temperature. When the crystals are heated over 1753 K the apatite system evolves to a less ordered monoclinic structure, in which the complete loss of the species in the anionic channel (Cl−, OH−) has been confirmed.


2014 ◽  
Vol 14 ◽  
pp. 12-19
Author(s):  
B Purevsuren ◽  
S Jargalmaa ◽  
B Bat-Ulzil ◽  
B Avid ◽  
T Gerelmaa

On the basis of proximate, ultimate, petrographic and IR analysis results have been confirmed that the Tavan tolgoi coal is a high-rank G mark stone coal. The results of X-ray fluorescence analysis of coal ash show that the Tavan tolgoi coal is a subbituminous coal. The ash of Tavan tolgoi coal has an acidic character. The results of pyrolysis of Tavan tolgoi coal at different heating temperatures show that a maximum yield - 5.0% of liquid product can be obtained at 700°C. The results of thermal dissolution of Tavan tolgoi coal in tetralin with constant mass ratio between coal and tetralin (1:1.8) at 450°C show that 50.0% of liquid product can be obtained after thermal decomposition of the COM (coal organic matter). DOI: http://dx.doi.org/10.5564/mjc.v14i0.191 Mongolian Journal of Chemistry 14 (40), 2013, p12-19


Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1772 ◽  
Author(s):  
Georgeta Voicu ◽  
Andreea C. Didilescu ◽  
Andrei B. Stoian ◽  
Cristina Dumitriu ◽  
Maria Greabu ◽  
...  

This paper aims to investigate the composition, surface, and microstructural characteristics, and bioactivity of two commercially available pulp capping materials known as TheraCal LC and BIO MTA+. The materials were prepared as cylindrical samples and assessed by X-ray diffraction (XRD) and complex thermal analysis for mineralogical characterization, and by scanning electron microscopy (SEM) coupled with energy dispersive of X-ray (EDX), Fourier-Transformed Infrared Spectroscopy (FT-IR), and atomic force microscopy (AFM) for microstructural and surface characteristics. The in vitro bioactivity was highlighted by surface mineralization throughout SEM coupled with EDX and FT-IR analysis. XRD analysis performed on both materials showed calcium silicate phases and different radiopacifying compounds. AFM measurements indicated a smoother and more homogenous surface with a lower average roughness for TheraCal LC due to the resin matrix from its composition. FT-IR analysis displayed bands for several compounds in both materials. Both materials exhibited bioactive properties showing surface mineralization after being immersed in solution similar to the human physiological environment. However, the MTA cement showed a better mineralization due to the anhydrous and hydrated phases.


Author(s):  
Katlakanti Mohan Reddy ◽  
Kajal Goswami

AbstractNanocomposites plays a very significant role in the catalysis and photocatalysis. Our aim is to synthesize multiphase nanocomposite material with advanced catalytic properties that are useful in the energy and environmental applications. Nano silver (Ag0) decorated Zinc-Cobalt/Titania composite (Ag decorated Zn-Co/TiO2, AZCT) with nonporous in nature as well as single grain size of 10–15 nm with beautiful morphological in nature. The material has multiphase crystalline in nature predicted from the powdered X-ray diffraction studies (PXRD) and FT-IR analysis, which illustrate the multiphase crystalline powder with high surface area of nanoporous in nature. The synthesized nanocomposite material is labelled as AZCT.


2016 ◽  
Vol 16 (4) ◽  
pp. 3969-3972 ◽  
Author(s):  
Yongde Meng ◽  
Yanjie Sun

In the present study, biosynthesis of silver nanoparticles was carried out using Rosa chinensis flower extract as reducing agent. The characterization of silver nanoparticles was done by UV-VIS spectrum. The morphology and size of silver nanoparticles were determined by transmission electron microscope (TEM) image. The crystallization of silver nanoparticles was confirmed by X-ray diffraction (XRD) measurements. The Fourier transform infrared (FT-IR) analysis was used to confirm the possible involvement in the formation and stabilization of synthesized silver nanoparticles by the extract of Rosa chinensis flower. Antibacterial activity of silver nanoparticles was studied against Gram positive Staphycoccus aureus and Gram negative Escherichia coli.


2021 ◽  
Vol 21 (4) ◽  
pp. 2212-2220
Author(s):  
T. S. Gokul Raja ◽  
S. Balamurugan ◽  
A. Reshma

In this work, several attempts were made to prepare nanoceramic zirconate (Nd2Zr2O7) powder for pigment applications. The single pyrochlore phase, Nd2Zr2O7 was successfully synthesized with the aid of flux at relatively low temperature (1000 °C) upon milling the reaction mixture made from Nd2O3 and ZrO2 in a tungsten carbide vial. Several characterizations were done on the thermal analysis (TG/DTA), X-ray diffraction (XRD), High-resolution scanning electron microscope (HRSEM), energy dispersive X-ray (EDX) analysis, Fourier-transform infrared (FT-IR) analysis, and near-infrared (NIR spectroscopy). A single-phase nanocrystalline (˜28 nm) pyrochlore structure (Fd3m) was confirmed through XRD analysis. A highly uniform particle in the size of ˜110 nm was observed for the Nd2Zr2O7 phase in the microimages. The vibrational (FT-IR) peaks at 423 cm-1 and 510 cm-1 in FTIR spectroscopic study confirmed the formation of pyrochlore structure. Higher NIR reflectivity recorded for this material in the 750–2500 nm region shows its novel application in color cool pigments for energy-saving paints reminiscent of Bi2−xYxCe2O7, Bi2Ce2−xTbxO7, and Gd2Ti2O7.


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