scholarly journals Comparison of CaO-NPs and Chicken Eggshell-Derived CaO in the Production of Biodiesel from Schinziophyton rautanenii (Mongongo) Nut Oil

2021 ◽  
Vol 2021 ◽  
pp. 1-15
Author(s):  
Keene Carlvin Mmusi ◽  
Sebusi Odisitse ◽  
Florence Nareetsile

The ever-increasing population growth and economic developments have heightened demand for energy. This has resulted in depletion and ever-rising prices of petroleum diesel, thus increasing environmental degradation. These complications have motivated this study for the search of an alternative eco-friendly and renewable source of energy such as biodiesel. Biodiesel has been found to be a potential alternative fuel for diesel. Biodiesel was produced by transesterification reaction of Schinziophyton rautanenii (mongongo) nut oil in the presence of a base heterogeneous catalyst: CaO derived from eggshell ash and synthesised CaO-nanoparticles (CaO-NPs). The catalysts were calcined at a temperature of 800°C for 3 h and characterized by scanning electron microscope-energy dispersive X-ray (SEM-EDX) where both catalysts showed agglomerated particles and high elemental composition of Ca and O. Powder X-ray diffraction (XRD) showed that CaO was present in both catalysts, and the average crystalline size obtained was 42 and 50 nm for CaO-NPs and eggshell ash, respectively. Fourier transmission infrared (FTIR) spectrometer showed absorption bands of CaO in both catalysts which were at 875 and 713.46 cm−1 for CaO-NPs and eggshell ash, respectively. The analysis of mongongo nut oil (MNO) and mongongo methyl esters (MMEs) was done according to the European biodiesel specification (EN 1421) and American Society for Testing and Materials (ASTM D675). Statistically, there was no significant difference between CaO-NPs and eggshell in terms of optimum yield ( P > 0.05 ) using a sample t-test. However, in terms of catalyst loading, the eggshell was a better catalyst as it required a low catalyst load to obtain an optimum yield of 83% at 6 wt.% compared to CaO-NPs with an optimum yield of 85% at 12 wt.%. The reactions were all performed at constant reaction conditions of 9 : 1 methanol to oil ratio, 3 h reaction time, and 65°C reaction temperature.

2021 ◽  
Vol 75 (5) ◽  
pp. 257-276
Author(s):  
Ana Velickovic ◽  
Jelena Avramovic ◽  
Milan Kostic ◽  
Jugoslav Krstic ◽  
Olivera Stamenkovic ◽  
...  

Wheat straw ash (WSA) was investigated as a new catalyst in biodiesel production from sunflower oil. The catalyst was characterized by temperature-programmed decomposition, X- ray powder diffraction, Hg porosimetry, N2 physisorption, and scanning electron microscopy - energy dispersive X-ray spectroscopy methods. The methanolysis reaction was tested in the temperature range of 55?65?C, the catalyst loading range 10?20 % of the oil weight, and the methanol-to-oil molar ratio range 18 : 1?24 : 1. The reaction conditions of the sunflower oil methanolysis over WSA were optimized by using the response surface methodology in combination with the historical experimental design. The optimum process conditions ensuring the highest fatty acid methyl esters (FAME) content of 98.6 % were the reaction temperature of 60.3?C, the catalyst loading of 11.6 % (based on the oil weight), the methanol-to-oil molar ratio of 18.3 :1, and the reaction time of 124 min. The values of the statistical criteria, such as coefficients of determination (R2 = 0.811, R2 = 0.789, R2 = 0.761) and the mean relative percent deviation (MRPD) value of 10.6 % (66 data) implied the acceptability and precision of the developed model. The FAME content after 4 h of reaction under the optimal conditions decreased to 37, 12, and 3 %, after the first, second, and third reuse, respectively.


2022 ◽  
Author(s):  
M Sukumar ◽  
M. Mathankumar ◽  
Chandra Sekhar Dash ◽  
M. Sundararajan ◽  
Mohd Ubaidullah ◽  
...  

Abstract We report the synthesis of multiferroic BiFeO3 perovskite nanoparticles using the microwave combustion technique. Phase evolution is investigated by X-ray diffraction (XRD), which confirms that the formation of a secondary α-Bi2O3 phase with a monoclinic structure along with the existing rhombohedral (BiFeO3) structure. The average crystalline size has been found at 50 nm. The optical band gap was calculated from the Tauc’s plot it has been found 2.18 eV, as measured by diffuse reflectance spectroscopy (DRS). The appearances of Fourier transform infrared spectroscopy (FT-IR) absorption bands at 550 and 444 cm-1 were correlated to the rhombohedral stretching modes of bismuth ferrite nanostructure. The morphology observations using scanning electron microscopy (SEM) showed the formation of nanosized grains with pores. Energy-dispersive X-ray analysis (EDX) was done to confirm the extent of Bi3+, Fe3+, and O2- in the samples. The magnetization-Field (M-H) hysteresis curves recorded from the vibrating sample magnetometer (VSM) revealed the appearance of ferrimagnetic behavior at room temperature. The specific surface area characterized by N2 adsorption-desorption isotherm is found 44.86 m2 g-1 using Brunauer-Emmett-Teller (BET) technique. The as-fabricated BiFeO3 perovskite nanoparticles were investigated for their superior catalytic activity in two applications, which include (i) the conversion of glycerol to formic acid in a selective liquid phase batch reactor at atmospheric pressure. This bismuth-based nanoparticles exhibit as an efficient multifunctional catalyst with high conversion and selectivity efficiency around 99.2% and 98.5%, respectively, (ii) the photocatalytic degradation of rhodamine B under visible light irradiation is found maximum efficiency (99.9%), when a small amount of H2O2 was added during photocatalysis, indicating the samples possessed photo-Fenton like catalytic activity. Finally, we concluded that the BiFeO3 perovskite nanoparticles' high performance in future multifunctional devices is demonstrated by the simultaneous enhancement of catalytic and photocatalytic activities.


Molecules ◽  
2021 ◽  
Vol 26 (19) ◽  
pp. 5772
Author(s):  
Ala’a H. Al-Muhtaseb

Waste eggshells were considered for synthesising a precursor (CaO) for a heterogeneous catalyst, further impregnated by alkali caesium oxide (Cs2O). The following techniques were used to characterise the synthesised catalysts: X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS) and Temperature Programmed Desorption (CO2-TPD). The synthesised catalyst revealed its suitability for transesterification to produce biodiesel. The biodiesel production process was optimised, and it showed that the optimal biodiesel yield is 93.59%. The optimal set of process parameters is process temperature 80 °C, process time 90 min, methanol-to-oil molar ratio 8 and catalyst loading 3 wt.%. It has been found that the high basicity of the catalyst tends to give a high biodiesel yield at low methanol-to-oil ratio 8 when the reaction time is also less (90 min). The fuel properties of biodiesel also satisfied the standard limits defined by ASTM and the EN standards. Thus, the synthesised catalyst from waste eggshells is highly active, improved the biodiesel production conditions and PPSS oil is a potential nonedible source.


MRS Advances ◽  
2020 ◽  
Vol 5 (62) ◽  
pp. 3273-3282
Author(s):  
I. Cosme-Torres ◽  
M.G. Macedo-Miranda ◽  
S.M. Martinez-Gallegos ◽  
J.C. González-Juárez ◽  
G. Roa-Morales ◽  
...  

AbstractThe heterogeneous catalyst HTCMgFe was used in the degradation of the IC, through the heterogeneous photo-fenton treatment, this material in combination with H2O2 and UV light degraded the dye in 30 min at pH 3. As the amount of HTCMgFe increases the degradation it was accelerated because there are more active catalytic sites of Fe2+ on the surface of the material, which generates a greater amount of •OH radicals. The HTCMgFe was characterized by infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and X-ray energy dispersive elemental analysis (EDS). The UV-vis spectrum shows that the absorption bands belonging to the chromophore group of the IC disappear as the treatment time passes, indicating the degradation of the dye.


2020 ◽  
Vol 3 (2) ◽  
Author(s):  
Kavipriya K C ◽  
Sudha A P ◽  
Sujatha K ◽  
Sowmya Lakshmi K

The interest in miniaturization of particles revealed the hidden applications of metal oxides. The potential applications of the particles may vary when the size of the particle is reduced. One of the alternative routes to the conventional approach is the use of plant extract for the synthesis of metal oxides NPs. In the framework of this study, the ecofriendly MgO nanoparticles were synthesized using Acalypha Indica leaf extract,functioning as reducing and capping agent by co-precipitation method. The predecessor taken here was Magnesium Nitrate. The biologically synthesized MgO NPs were characterized by various techniques like X ray diffraction(XRD), Fourier Transform infrared spectroscopy(FTIR), Scanning electron microscope (SEM) with Energy Dispersive X-ray spectroscopy(EDX) profile and its antibacterial activity is evaluated against causative organisms. XRD studies confirmed the face centered cubic crystalline structure of MgO NPs and the average crystalline size of MgO NPs calculated using Scherer’s formula was found to be 13 nm. FTIR spectrum shows a significant Mg-O vibrational band. Purity, surface morphology and chemical composition of elements were confirmed by SEM with EDX. The SEM result shows the fine spherical morphology with the grain size range between 43nm to 62nm. Antimicrobial assay of MgO NPs was examined against gram positive and negative bacteria. Appreciated activity was observed on the Staphylococcus aureus bacterial species. In general, the renewed attempt of this facile approach gave the optimum results of multifunctional MgO NPs.


2020 ◽  
Vol 3 (2) ◽  
Author(s):  
Aarth R ◽  
Sudha A P ◽  
Sujatha B ◽  
Sowmya Lakshmi K

The phytosynthesis of n-type Cadmium Oxide Nanoparticles reduces the toxicity of the substance and makes it Eco-friendly. This Eco-friendly biosynthesis of CdO NPs was synthesized for the first time from the Queen of herbs, Ocimum Sanctum (holy basil).The biosynthesized Cadmium oxide was prepared using Ocimum leaf extract as a reductant and Cadmium Chloride and hydroxide as cadmium and oxide source materials by Co- Precipitation method. Thus obtained Cadmium Oxide Nanoparticles were characterized by different techniques such as X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR), Scanning electron microscope (SEM),Energy dispersive X-ray spectroscopy(EDS) to study the structural and morphological properties. XRD pattern exhibited the formation of face centered cubic structure of CdO NPs with an average crystalline size of 11.5nm .The chemical bond formation of CdO NPs were confirmed by FTIR spectrum in the range of (400-4000cm-1). The SEM micrographs revealed the predominant formation of Cauliflower shape with a particle size in the range of 61-142nm. The high purity of the biosynthesized nanoparticles were confirmed by EDS analysis. Further it was tested against gram positive and gram negative bacterial strains and showed significant antibacterial activity. This biosynthetic research study opens an innovative window to progress our understanding of how CdO NPs shows resistance to different bacterial strains.


2020 ◽  
Vol 3 (3) ◽  
Author(s):  
Jothi M ◽  
Sowmiya K

Nickel Oxide (NiO) is an important transition metal oxide with cubic lattice structure. NiO is thermally stable that is suitable for tremendous applications in the field of optic, ceramic,glass, electro-chromic coatings, plastics, textiles, nanowires, nanofibers, electronics,energy technology, bio-medicine, magnetism and so on. In this present study, NiO nanoparticles were successfully synthesized by sol-gel technique. Nano-sols were prepared by dissolving Nickel-Chloride [NiCl2.6H2O] in NaOH solvent and were converted into nano structured gel on precipitation. A systematic change in preparation parameters like calcination temperature, time, pH value has been noticed in order to predict the influence on crystallite size. Then the prepared samples were characterized by the X-ray Diffraction Spectroscopic (XRD), UV-VIS Spectroscopy, Fourier Transform Infra-Red Spectroscopy (FTIR), Energy Dispersive X-ray Spectroscopy (EDX), Scanning Electron Microscopy (SEM) and Particle Size Analyzer (PSA). From XRD, the average crystalline-size has been calculated by Debye-Scherrer Equation and it was found to be 12.17 nm and the band gap energy of Nickel oxide (NiO) from UV studies reveals around 3.85 eV. Further, EDX and FTIR studies, confirm the presences of NiO nanoparticles. The SEM study exhibits the spherical like morphology of Nickel oxide (NiO). Further from PSA, the mean value of NiO nanoparticles has been determined.


2021 ◽  
Vol 22 (13) ◽  
pp. 6787
Author(s):  
Constantin I. Tănase ◽  
Constantin Drăghici ◽  
Miron Teodor Căproiu ◽  
Anamaria Hanganu ◽  
Gheorghe Borodi ◽  
...  

β-Ketophosphonates with pentalenofurane fragments linked to the keto group were synthesized. The bulky pentalenofurane skeleton is expected to introduce more hindrance in the prostaglandin analogues of type III, greater than that obtained with the bicyclo[3.3.0]oct(a)ene fragments of prostaglandin analogues I and II, to slow down (retard) the inactivation of the prostaglandin analogues by oxidation of 15α-OH to the 15-keto group via the 15-PGDH pathway. Their synthesis was performed by a sequence of three high yield reactions, starting from the pentalenofurane alcohols 2, oxidation of alcohols to acids 3, esterification of acids 3 to methyl esters 4 and reaction of the esters 4 with lithium salt of dimethyl methanephosphonate at low temperature. The secondary compounds 6b and 6c were formed in small amounts in the oxidation reactions of 2b and 2c, and the NMR spectroscopy showed that their structure is that of an ester of the acid with the starting alcohol. Their molecular structures were confirmed by single crystal X-ray determination method for 6c and XRPD powder method for 6b.


2020 ◽  
pp. 000313482097338
Author(s):  
Elizabeth McCarthy ◽  
Benjamin L. Gough ◽  
Michael S. Johns ◽  
Alexandra Hanlon ◽  
Sachin Vaid ◽  
...  

Introduction Robotic colectomy could reduce morbidity and postoperative recovery over laparoscopic and open procedures. This comparative review evaluates colectomy outcomes based on surgical approach at a single community institution. Methods A retrospective review of all patients who underwent colectomy by a fellowship-trained colon and rectal surgeon at a single institution from 2015 through 2019 was performed, and a cohort developed for each approach (open, laparoscopic, and robotic). 30-day outcomes were evaluated. For dichotomous outcomes, univariate logistic regression models were used to quantify the individual effect of each predictor of interest on the odds of each outcome. Continuous outcomes received a similar approach; however, linear and Poisson regression modeling were used, as appropriate. Results 115 patients were evaluated: 14% (n = 16) open, 44% (n = 51) laparoscopic, and 42% (n = 48) robotic. Among the cohorts, there was no statistically significant difference in operative time, rate of reoperation, readmission, or major complications. Robotic colectomies resulted in the shortest length of stay (LOS) (Kruskal-Wallis P < .0001) and decreased estimated blood loss (EBL) (Kruskal-Wallis P = .0012). Median age was 63 years (interquartile range [IQR] 53-72). 54% (n = 62) were female. Median American Society of Anesthesiologists physical status classification was 3 (IQR 2-3). Median body mass index was 28.67 (IQR 25.03-33.47). A malignant diagnosis was noted on final pathology in 44% (n = 51). Conclusion Among the 3 approaches, there was no statistically significant difference in 30-day morbidity or mortality. There was a statistically significant decreased LOS and EBL for robotic colectomies.


Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 48
Author(s):  
Pawel Mierczynski ◽  
Magdalena Mosińska ◽  
Lukasz Szkudlarek ◽  
Karolina Chalupka ◽  
Misa Tatsuzawa ◽  
...  

Biodiesel production from rapeseed oil and methanol via transesterification reaction facilitated by various monometallic catalyst supported on natural zeolite (NZ) was investigated. The physicochemical characteristics of the synthesized catalysts were studied by X-ray diffraction (XRD), Brunauer–Emmett–Teller method (BET), temperature-programmed-reduction in hydrogen (H2-TPR), temperature-programmed-desorption of ammonia (NH3-TPD), Scanning Electron Microscope equipped with EDX detector (SEM-EDS), and X-ray photoelectron spectroscopy (XPS) methods. The highest activity and methyl ester yields were obtained for the Pt/NZ catalyst. This catalyst showed the highest triglycerides conversion of 98.9% and fatty acids methyl esters yields of 94.6%. The activity results also confirmed the high activity of the carrier material (NZ) itself in the investigated reaction. Support material exhibited 90.5% of TG conversion and the Fatty Acid Methyl Esters yield (FAME) of 67.2%. Introduction of noble metals improves the TG conversion and FAME yield values. Increasing of the metal loading from 0.5 to 2 wt.% improves the reactivity properties of the investigated catalysts.


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