scholarly journals Synthesis of Ce-Mesoporous Silica Catalyst and Its Lifetime Determination for the Hydrocracking of Waste Lubricant

2018 ◽  
Vol 18 (3) ◽  
pp. 441
Author(s):  
Wega Trisunaryanti ◽  
Triyono Triyono ◽  
Iip Izul Falah ◽  
Andreas David Siagian ◽  
Muhammad Fajar Marsuki
Keyword(s):  
Electron Microscope ◽  
Mesoporous Silica ◽  
Surface Area ◽  
Liquid Product ◽  
Total Pore Volume ◽  
Bet Surface Area ◽  
Bovine Bone ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Transmission Electron

The synthesis of Ce/mesoporous silica (Ce/MS) and its lifetime determination for the hydrocracking of waste lubricant has been carried out. The MS was synthesized using tetraethyl orthosilicate (TEOS) and gelatin extracted from bovine bone as a template. Cerium was impregnated onto the MS by wet impregnation method using Ce(NO3)3.6H2O. The MS and Ce/MS were then characterized by means of acidity using ammonia base vapor adsorption, Fourier Transform Spectrophotometer (FTIR), Transmission Electron Microscope (TEM), Scanning Electron Microscope-Energy Dispersive X-ray Spectrometer (SEM-EDX), and surface area analyzer (SAA) based on the BET and BJH equation. The Ce/MS catalyst was tested in hydrocracking of waste lubricant in three runs. Lifetime of Ce/MS catalyst was determined using a linear regression of the liquid product yields vs hydrocracking time. The Ce/MS catalyst showed an acidity of 2.79 mmol/g, BJH desorption pore diameter of 3.84 nm, BET surface area of 246.55 m2/g, and total pore volume of 0.44 cm3/g. The yield of liquid product obtained from hydrocracking of waste lubricant using the Ce/MS catalyst for the first, second, and third runs was 21.42, 17.23 and 10.54 wt.%, respectively for 2.5 h per each run. Lifetime of Ce/MS catalyst in hydrocracking of waste lubricant was 12.54 h.

scholarly journals Mesoporous silica from Parangtritis beach sand templated by CTAB as a support of Mo Metal as a catalyst for hydrocracking of waste palm cooking oil into biofuel

2021 ◽  
Author(s):  
Gesha Desy Alisha ◽  
Wega Trisunaryanti ◽  
Akhmad Syoufian
Keyword(s):  
Mesoporous Silica ◽  
Surface Area ◽  
Weight Ratio ◽  
Beach Sand ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Cooking Oil ◽  
Liquid Products ◽  
Hydrocarbon Compound ◽  
Wet Impregnation Method

Abstract In this study, natural source Parangtritis beach sand was extracted into mesoporous silica (MS). Synthesis of mesoporous silica (MS) was carried out at sodium silicate: CTAB ratio of 1:0.5 (w/w). Monometallic catalyst was used to improve the performance of the catalyst. The monometallic used was Mo metal, which was synthesized using the wet impregnation method. Catalysts were characterized using FTIR, XRD, Surface Area Analyzer (SAA), SEM-EDX, and TEM. MS has pore diameters and surface area of 2.62 nm and 897.3 m2/g. Mo/MS has pore diameters, surface area, and Mo metal concentration of 2.46 nm, 593 m2/g, and 4.75 %. Catalytic activity and selectivity were evaluated in hydrocracking of waste palm cooking oil at 500, 550, and 600 oC, and catalyst: waste palm cooking oil ratio of 1:100, 1:200, and 1:300. The best catalyst will be tested for reusability 3 times through the hydrocracking process. Mo/MS produces better liquid products and hydrocarbon compounds than MS. The results of the conversion of liquid products analyzed using GCMS. The yield of liquid products obtained in the hydrocracking of waste palm cooking oil using Mo/MS with the optimum temperature and the weight ratio of catalyst: feed at 550oC and 1: 300 was 66.99 wt.% with consists of hydrocarbon compound as 62.79 wt.%. The yield of liquid products obtained in the hydrocracking waste palm cooking oil using the used Mo/MS catalyst in the last run was 80.26 wt.% with consist of hydrocarbon compound as 74.13 wt.%.

scholarly journals Hydrotreatment of Cellulose-Derived Bio-Oil Using Copper and/or Zinc Catalysts Supported on Mesoporous Silica-Alumina Synthesized from Lapindo Mud and Catfish Bone

2020 ◽  
Author(s):  
Fahri Swasdika ◽  
Wega Trisunaryanti ◽  
Iip Izul Falah
Keyword(s):  
Mesoporous Silica ◽  
Liquid Product ◽  
Impregnation Method ◽  
Total Acidity ◽  
Wet Impregnation ◽  
Catalytic Application ◽  
Bio Oil ◽  
Silica Alumina ◽  
Metal Addition ◽  
Wet Impregnation Method

Catalysts comprising copper and/or zinc supported on mesoporous silica-alumina (MSA) with a high Si/Al ratio were prepared by wet impregnation method. This study investigated the preparation, characterization, and catalytic application of the prepared catalysts for hydrotreatment cellulose-derived bio-oil. The wet impregnation was performed by directly dispersing Cu(NO3)2·3H2O and/or Zn(NO3)2·4H2O aqueous solution into MSA, followed by calcination and reduction under H2 gas stream. The acidity test revealed that metal addition on MSA support increases the acidity of catalysts. During hydrotreatment of cellulose-derived bio-oil CuZn/MSA with total acidity, copper loading, zinc loading, and specific surface area of 24.86 mmol g–1, 5.23 wt.%, 3.15 wt.%, and 170.77 m2 g–1, respectively, exhibited the best performance compared to other prepared catalysts with 90.49 wt.% conversion of liquid product.

Nickel-Hydroxyapatite as Biomaterial Catalysts for Hydrogen Production via Glycerol Steam Reforming

2010 ◽  
Vol 447-448 ◽  
pp. 770-774 ◽  
Author(s):  
Hakim Lukman ◽  
Zahira Yaakob ◽  
Ismail Manal ◽  
Wan Ramli Wan Daud
Keyword(s):  
Hydrogen Production ◽  
Surface Area ◽  
Steam Reforming ◽  
Bet Surface Area ◽  
Feed Ratio ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Production Of Hydrogen ◽  
Catalytic Steam Reforming ◽  
Wet Impregnation Method

Nickel-hydroxyapatite as biomaterial catalysts exhibited high activity and selectivity in glycerol steam reforming. The catalytic steam reforming of glycerol (C3H8O3) for the production of hydrogen is carried out over nickel supported on hydroxyapatite [Ca5(PO4)3(OH)] catalyst at 600 oC with atmospheric pressure and 120 minute time reaction. The catalysts were prepared by mean of wet impregnation method and varied nickel loadings (3, 6, 12 %) on hydroxyapatite. It is found that the 3% wt% Ni/HAP show higher hydrogen production rate over the other nickel loadings on hydroxyapatite, which is correlated with Ni/HAP catalyst surface area measured by BET adsorbtion and morphology of catalysts. Glycerol steam reforming with water-to-glycerol feed ratio 8/1 much more hydrogen production (77-82%) compared feed ratio 4/1. The catalysts were characterised by BET surface area and SEM-EDX techniques.

Synthesis and Characterization of Florfenicol-silver Nanocomposite and its Antibacterial Activity against some Gram Positive and Gram-negative Bacteria

2020 ◽  
Keyword(s):  
Silver Nanoparticles ◽  
Electron Microscope ◽  
Zeta Potential ◽  
Surface Area ◽  
Spherical Shape ◽  
Bet Surface Area ◽  
Sonochemical Method ◽  
Raman Spectrometry ◽  
Silver Nanocomposite ◽  
Morphology Characterization

In this paper, easy, rapid and cheap synthetic method was described for florfenicol-silver nanocomposite by sonochemical method. Florfenicol-silver nanocomposite was characterized based on three classes namely index, identification and morphology class. Index characterization was carried out by zeta sizing, BET surface area and zeta potential. Identification characterization was performed using X-ray diffraction (XRD) and Raman spectrometry. Morphology characterization was done utilizing transmission electron microscope (TEM), scanning electron microscope (SEM) and atomic force microscope (AFM). Characterization results showed zeta sizing of florfenicol was 30.44nm, while florfenicol-silver nanocomposite was 33.5 nm with zeta potential -14.1 and -18, respectively. BET surface area was found to be 13.3, 73.2 and 103.69 m2/g for florfenicol, silver nanoparticles and florfenicol-silver nanocomposite respectively. XRD and Raman charts confirmed the formation of florfenicol-silver nanocomposite without any contamination. TEM, SEM and AFM spectral data illustrated spherical to sub spherical shape of silver nanoparticles on cubic to sheet shape of florfenicol with size less than 50 nm. Antimicrobial activity was screened where the average zone of inhibitions caused by the prepared nanocomposite were 28.3 mm, 24 mm, 27.3 mm and 24 mm compared to 17.7 mm, 16 mm, 18.7 mm and 13.3 mm of the native drug and 13 mm, 10 mm, 14.3 mm and 15 mm of the used positive reference standards against E. coli, Salmonella typhymurium, Staphylococcus aureus and Staph.aureus MRSA respectively.

scholarly journals An Eco-Friendly Process for Removal of Lead from Aqueous Solution

2017 ◽  
Vol 11 (5) ◽  
pp. 47 ◽  
Author(s):  
Heman A. Smail ◽  
Kafia M. Shareef ◽  
Zainab H. Ramli
Keyword(s):  
Heavy Metal ◽  
Oxalic Acid ◽  
Surface Area ◽  
Pore Volume ◽  
Metal Ion ◽  
Adsorption Equilibrium ◽  
Total Pore Volume ◽  
Heavy Metal Ion ◽  
Bet Surface Area ◽  
Barley Husk

The adsorption of lead (Pb II) ion on different types of synthesized zeolite was investigated. The BET surface area, total pore volume & average pore size distribution of these synthesized zeolites were determined by adsorption isotherms for N2, the surface area & total pore volume of their sources were found by adsorption isothermN2.The adsorption equilibrium was measured after 24h at room temperature (RT) & concentration 10mg.L-1 of Pb (II) was used. The adsorption of heavy metal Pb (II) on four different prepared zeolites (LTA from Montmorillonite clay, FAU(Y)-B.H (G2) from Barley husk, Mordenite (G1) from Chert rock, FAU(X)-S.C (G3) from shale clay & modified Shale clay by oxalic acid (N1) & sodium hydroxide (N2)), were compared with the adsorption of their sources by using static batch experimental method. The major factors affecting the heavy metal ion sorption on different synthesized zeolites & their sources were investigated. The adsorption equilibrium capacity (Qm) of Pb (II) ion for different synthesized zeolites ordered from (N1>N2>LTA>G3>G2>G1&for their sources ordered Shale clay >Montmorilonite> Barley husk>Chert rock. The atomic absorption spectrometry was used for analysis of lead heavy metal ion, the obtained results in this study showed that the different synthesized zeolites were efficient ion exchanges for removing heavy metal, in particular, the modified zeolite from shale clay by oxalic acid.

scholarly journals Synthesis of Mesoporous Carbon from Merbau Wood (Intsia spp.) by Microwave Method as Ni Catalyst Support for α-Cellulose Hydrocracking

2019 ◽  
Author(s):  
Andaru Dena Prasiwi ◽  
Wega Trisunaryanti ◽  
Triyono Triyono ◽  
Iip Izul Falah ◽  
Darma Santi ◽  
...  
Keyword(s):  
Microwave Irradiation ◽  
Surface Area ◽  
Mesoporous Carbon ◽  
Catalyst Support ◽  
Liquid Product ◽  
Total Pore Volume ◽  
Ni Catalyst ◽  
Microwave Method ◽  
Average Pore ◽  
Impregnation Technique

Synthesis of mesoporous carbon from Merbau wood (Intsia spp.) waste by microwave method as nickel catalyst support for α-cellulose hydrocracking had been carried out. The Merbau wood sawdust was carbonized at 800 °C to produce C800 and the C800 was treated by microwave irradiation (399 W) for 5 min to produce C800MW. The Merbau wood flakes, which were only treated by microwave irradiation (399 Watts) for 30 min produced CMW. Wet impregnation technique was carried out to disperse the Ni metal (1.0, 1.5, and 2.0 wt.%) onto the best mesoporous carbon. The mesoporous carbons were analyzed by Fourier Transform Infra-Red Spectroscopy (FTIR), Surface Area Analyzer (SAA) and Scanning Electron Microscopy (SEM). The hydrocracking of pyrolyzed α-cellulose was carried out at 400 °C. The liquid product was analyzed by Gas Chromatograph-Mass Spectrometer (GC-MS). The results showed that the C800MW was the best performance carbon and it had a specific surface area, total pore volume, average pore diameter and acidity of 364.12 m2/g, 0.28 cm3/g, 3.03 nm, and 2.18 mmol/g, respectively. The Ni1.5/C800MW catalyst produced the highest conversion of liquid product (58.76 wt.%) than the Ni1/C800MW (57.51 wt.%) and Ni2/C800MW (34.18 wt.%).

scholarly journals Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV-Irradiation

2018 ◽  
Author(s):  
Irwing M. Ramírez-Sánchez ◽  
Erick R. Bandala
Keyword(s):  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Bet Surface Area ◽  
Doped Tio2 ◽  
X Ray ◽  
Transmission Electron ◽  
Iron Doped

Iron Doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV-radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-Ray Photoelectron Spectroscopy (XPS) technique. The XPS evidenced that ferric ion (Fe3+) was in the lattice of TiO2 and co-dopants no intentionally added were also present due to the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radical (•OH) and estriol (E3) degradation. Fe-TiO2 materials accomplished E3 degradation, and it was found that the catalyst with 0.3 at. % content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV-irradiation compared with no intentionally Fe-added TiO2 (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV-irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.

scholarly journals Activated Carbons from Thermoplastic Precursors and Their Energy Storage Applications

Nanomaterials ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 896 ◽  
Author(s):  
Hye-Min Lee ◽  
Kwan-Woo Kim ◽  
Young-Kwon Park ◽  
Kay-Hyeok An ◽  
Soo-Jin Park ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Field Emission ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Activated Carbons ◽  
Total Pore Volume ◽  
Cross Linking ◽  
Mesopore Volume

In this study, low-density polyethylene (LDPE)-derived activated carbons (PE-AC) were prepared as electrode materials for an electric double-layer capacitor (EDLC) by techniques of cross-linking, carbonization, and subsequent activation under various conditions. The surface morphologies and structural characteristics of the PE-AC were observed by field-emission scanning electron microscope, Cs-corrected field-emission transmission electron microscope, and X-ray diffraction analysis, respectively. The nitrogen adsorption isotherm-desorption characteristics were confirmed by Brunauer–Emmett–Teller, nonlocal density functional theory, and Barrett–Joyner–Halenda equations at 77 K. The results showed that the specific surface area and total pore volume of the activated samples increased with increasing the activation time. The specific surface area, the total pore volume, and mesopore volume of the PE-AC were found to be increased finally to 1600 m2/g, 0.86 cm3/g, and 0.3 cm3/g, respectively. The PE-AC also exhibited a high mesopore volume ratio of 35%. This mesopore-rich characteristic of the activated carbon from the LDPE is considered to be originated from the cross-linking density and crystallinity of precursor polymer. The high specific surface area and mesopore volume of the PE-AC led to their excellent performance as EDLC electrodes, including a specific capacitance of 112 F/g.

scholarly journals Surface and Catalytic Properties of γ-Irradiated Cr2O3/Al2O3 Solids

1997 ◽  
Vol 15 (6) ◽  
pp. 465-476 ◽  
Author(s):  
G.A. El-Shobaky ◽  
A.M. Ghozza ◽  
G.M. Mohamed
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Surface Area ◽  
Pore Volume ◽  
Active Sites ◽  
Catalytic Properties ◽  
Total Pore Volume ◽  
Bet Surface Area ◽  
Two Samples ◽  
Γ Rays

Two samples of Cr2O3/Al2O3 were prepared by mixing a known mass of finely powdered Al(OH)3 with a calculated amount of CrO3 solid followed by drying at 120°C and calcination at 400°C. The amounts of chromium oxide employed were 5.66 and 20 mol% Cr2O3, respectively. The calcined solid specimens were then treated with different doses of γ-rays (20–160 Mrad). The surface and catalytic properties of the different irradiated solids were investigated using nitrogen adsorption at −196°C and the catalysis of CO oxidation by O2 at 300–400°C. The results revealed that γ-rays brought about a slight decrease in the BET surface area, SBET (15%), and in the total pore volume, Vp (20%), of the adsorbent containing 5.66 mol% Cr2O3. The same treatment increased the total pore volume, Vp (36%), and the mean pore radius, r̄ (43%), of the other adsorbent sample without changing its BET surface area. The catalytic activities of both catalyst samples were found to increase as a function of dose, reaching a maximum value at 80–160 Mrad and 40 Mrad for the solids containing 5.66 and 20 mol% Cr2O3, respectively. The maximum increase in the catalytic activity measured at 300°C was 59% and 100% for the first and second catalyst samples, respectively. The induced effect of γ-irradiation on the catalytic activity was an increase in the concentration of catalytically active sites taking part in chemisorption and in the catalysis of CO oxidation by O2 without changing their energetic nature. This was achieved by a progressive removal of surface hydroxy groups during the irradiation process.

scholarly journals Elemental Composition of Biochar Obtained from Agricultural Waste for Soil Amendment and Carbon Sequestration

2019 ◽  
Vol 9 (19) ◽  
pp. 3980 ◽  
Author(s):  
Saowanee Wijitkosum ◽  
Preamsuda Jiwnok
Keyword(s):  
Surface Area ◽  
Soil Amendment ◽  
Agricultural Sector ◽  
Crop Residues ◽  
Low Cost ◽  
Agricultural Waste ◽  
Total Pore Volume ◽  
Appropriate Technology ◽  
Bet Surface Area ◽  
Agricultural Crop

For an agricultural country such as Thailand, converting agricultural waste into biochar offers a potential solution to manage massive quantities of crop residues following harvest. This research studied the structure and chemical composition of biochar obtained from cassava rhizomes, cassava stems and corncobs, produced using a patented locally-manufactured biochar kiln using low-cost appropriate technology designed to be fabricated locally by farmers. The research found that cassava stems yielded the highest number of Brunauer-Emmett-Teller (BET) surface area in the biochar product, while chemical analysis indicated that corncobs yielded the highest amount of C (81.35%). The amount of H in the corncob biochar was also the highest (2.42%). The study also showed biochar produced by slow pyrolysis was of a high quality, with stable C and low H/C ratio. Biochar’s high BET surface area and total pore volume makes it suitable for soil amendment, contributing to reduced soil density, higher soil moisture and aeration and reduced leaching of plant nutrients from the rhizosphere. Biochar also provides a conducive habitat for beneficial soil microorganisms. The findings indicate that soil incorporation of biochar produced from agricultural crop residues can enhance food security and mitigate the contribution of the agricultural sector to climate change impacts.

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