scholarly journals A Bio-Based Alginate Aerogel as an Ionic Liquid Support for the Efficient Synthesis of Cyclic Carbonates from CO2 and Epoxides

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 872
Author(s):  
Ana B. Paninho ◽  
Ana N. Mustapa ◽  
Kamran T. Mahmudov ◽  
Armando J. L. Pombeiro ◽  
M. Fátima C. Guedes da Silva ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Cycloaddition Reaction ◽  
X Ray Diffraction ◽  
Wet Impregnation ◽  
X Ray ◽  
Support Materials ◽  
Ionic Liquid Support ◽  
Limonene Oxide ◽  
Adsorption Desorption ◽  
High Pressure Apparatus

In this work, the ionic liquid [Aliquat][Cl] was supported into alginate and silica aerogel matrices and applied as a catalyst in the cycloaddition reaction between CO2 and a bio-based epoxide (limonene oxide). The efficiency of the alginate aerogel system is much higher than that of the silica one. The method of wet impregnation was used for the impregnation of the aerogel with [Aliquat][Cl] and a zinc complex. The procedure originated a well-defined thin solvent film on the surface of support materials. Final materials were characterised by Fourier Transform Infrared Spectroscopy, N2 Adsorption–Desorption Analysis, X-ray diffraction, atomic absorption and Field Emission Scanning Microscopy. Several catalytic tests were performed in a high-pressure apparatus at 353.2 K and 4 MPa of CO2.

scholarly journals SYNTHESIS, CHARACTERIZATION, AND APPLICATION OF ZnO/ZSM-5 AS CATALYST IN THE CRACKING PROCESS OF PALM METHYL ESTERS

2021 ◽  
pp. 1-8
Author(s):  
Nina Haryani ◽  
Taslim Taslim ◽  
Irvan ◽  
Renita Manurung ◽  
Rondang Tambun
Keyword(s):  
Alternative Fuels ◽  
Methyl Esters ◽  
Environmentally Friendly ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Wet Impregnation ◽  
X Ray ◽  
Temperature Programmed ◽  
Cracking Process ◽  
Adsorption Desorption

Biofuels as environmentally friendly alternative fuels such as biogasoline, biokerosene and others are generally obtained through a cracking process and take place more effectively to attend a catalyst. In this study, the synthesis of ZnO/ZSM-5 aims to obtain a catalyst that can be used in the cracking process of Palm Methyl Esters (PME) into hydrocarbon fuels especially biogasoline. This catalyst is environmentally friendly, easy to separate, has good selectivity, and can increase the conversion of cracking products. The wet impregnation method followed by drying and calcination is the method used to synthesize the catalyst. Furthermore, several analyzes were carried out to determine the characteristics of the catalyst. The analysis is the Scanning Electron Microscopy-Energy Dispersive X-Ray (SEM-EDX), X-Ray Diffraction (XRD), N2 adsorption-desorption with BET-BJH, Temperature Programmed Desorption-NH3 (TPD-NH3) and the Temperature Programmed Reduction (TPR). Based on synthesis results obtained ZnO/ZSM-5 catalyst with ZnO content of 11.77 wt%, 13.61 wt% and 18.22 wt%. The use of this catalyst in the cracking process can result in the conversion of liquid fuel by 88.57%, heavy hydrocarbon (8.57%) and gas product (2.86%).

scholarly journals Influence of the Presence of Different Alkali Cations and the Amount of Fe(CN)6 Vacancies on CO2 Adsorption on Copper Hexacyanoferrates

Materials ◽  
2019 ◽  
Vol 12 (20) ◽  
pp. 3371 ◽  
Author(s):  
Svensson ◽  
Grins ◽  
Eklöf ◽  
Eriksson ◽  
Wardecki ◽  
...  
Keyword(s):  
Thermogravimetric Analysis ◽  
Prussian Blue ◽  
Co2 Adsorption ◽  
X Ray Diffraction ◽  
Alkali Cations ◽  
Prussian Blue Analogue ◽  
X Ray ◽  
Infra Red ◽  
Adsorption Desorption ◽  
Adsorption Capability

The CO2 adsorption on various Prussian blue analogue hexacyanoferrates was evaluated by thermogravimetric analysis. Compositions of prepared phases were verified by energy-dispersive X-ray spectroscopy, infra-red spectroscopy and powder X-ray diffraction. The influence of different alkali cations in the cubic Fm3m structures was investigated for nominal compositions A2/3Cu[Fe(CN)6]2/3 with A = vacant, Li, Na, K, Rb, Cs. The Rb and Cs compounds show the highest CO2 adsorption per unit cell, 3.3 molecules of CO2 at 20 C and 1 bar, while in terms of mmol/g the Na compound exhibits the highest adsorption capability, 3.8 mmol/g at 20 C and 1 bar. The fastest adsorption/desorption is exhibited by the A-cation free compound and the Li compound. The influence of the amount of Fe(CN)6 vacancies were assessed by determining the CO2 adsorption capabilities of Cu[Fe(CN)6]1/2 (Fm3m symmetry, nominally 50% vacancies), KCu[Fe(CN)6]3/4 (Fm3m symmetry, nominally 25% vacancies), and CsCu[Fe(CN)6] (I-4m2 symmetry, nominally 0% vacancies). Higher adsorption was, as expected, shown on compounds with higher vacancy concentrations.

scholarly journals Adsorption of malic acid at the hydroxyapatite/aqueous NaCl solution interface

2021 ◽  
Author(s):  
Władysław Janusz ◽  
Ewa Skwarek
Keyword(s):  
Zeta Potential ◽  
Malic Acid ◽  
Particle Sizes ◽  
Nacl Solution ◽  
X Ray Diffraction ◽  
Radioisotope Method ◽  
X Ray ◽  
Solution Interface ◽  
Adsorption Desorption ◽  
Kinetics Of

AbstractThe aim of the study was the basic incidence on the phenomenon of adsorption that occurs at the hydroxyapatite/malic acid interface, leading to a change in the surface properties of hydroxyapatite, Analytical methods used in the research: X-ray diffraction (XRD) as well as by the, adsorption–desorption of nitrogen (ASAP), potentiometric titration. The specific adsorption of malic acid ions at the hydroxyapatite interface was investigated by means of the radioisotope method. The zeta potential of hydroxyapatite dispersions was determined by electrophoresis with Zetasizer Nano ZS90 by Malvern. The particle sizes of hydroxyapatite samples were analyzed using Masteriszer 2000 Malvern. Studies on the kinetics of malic acid on hydroxyapatite from a solution with an initial concentration of 1 mmol/dm3 have shown that the adsorption process is initially fast, followed by a slow adsorption step. An increase in the pH of the solution causes a decrease in the malic acid adsorption as a result of competition with hydroxyl ions. The presence of adsorbed malic acid was confirmed by the FTIR measurements. The effect of malic acid adsorption on the zeta potential and particle size distribution of hydroxyapatite in the NaCl solution was investigated.

Behaviours of direct yellow 12 adsorption on mesoporous carbons with different pore geometries

2018 ◽  
Vol 2017 (1) ◽  
pp. 219-228
Author(s):  
Fengling Liu ◽  
Ziyan Guo ◽  
Hui Qiu ◽  
Xia Lu ◽  
Hua Fang ◽  
...  
Keyword(s):  
Mesoporous Carbons ◽  
X Ray Diffraction ◽  
Pore Characteristics ◽  
X Ray ◽  
Transmission Electron ◽  
Cylindrical Pores ◽  
Pseudo Second Order ◽  
Hexagonally Ordered ◽  
Adsorption Desorption ◽  
Interconnected Pore

Abstract Four kinds of mesoporous carbons, C1-h-w, C2-h-h, C3-s-w, and C4-s-h, with different pore geometries were prepared and characterised, and their adsorption behaviours with aqueous direct yellow 12 (DY-12) were investigated. The results of X-ray diffraction and transmission electron microscopy show that C1-h-w and C3-s-w have wormlike pore characteristics, whereas C2-h-h and C4-s-h have 2-D hexagonally arranged pores. According to the N2 adsorption/desorption results, the specific surface area of C1-h-w (1,378 m2/g) is the largest among the four carbons. The adsorption isotherms could be effectively fitted using the Langmuir model. The maximum adsorption amounts of C1-h-w, C2-h-h, C3-s-w and C4-s-h are 0.968 mmol/g, 0.726 mmol/g, 0.161 mmol/g and 0.156 mmol/g, respectively. The pseudo-second-order rate constants of C1-h-w (39.8 g/(mmol·min)) and C2-h-h (7.28 g/(mmol·min)) are substantially larger than those of C3-s-w (0.0046 g/(mmol·min)) and C4-s-h (0.014 g/(mmol·min)), indicating that an open and interconnected pore geometry is favourable for DY-12 adsorption. Furthermore, DY-12 diffusion in 2-D hexagonally ordered cylindrical pores is superior to that in wormlike pores due to the smoothness of the channels in the former. External mass transfer and intraparticle diffusion both play roles in the adsorption process.

FeYO3@rGO nanocomposites: Synthesis, characterization and application in photooxidative degradation of atrazine under visible light

2021 ◽  
Vol 11 (5) ◽  
pp. 706-716
Author(s):  
Nada D. Al-Khthami ◽  
Tariq Altalhi ◽  
Mohammed Alsawat ◽  
Mohamed S. Amin ◽  
Yousef G. Alghamdi ◽  
...  
Keyword(s):  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Bandgap Energy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Structural Surface ◽  
Adsorption Desorption

Different organic pollutants have been remediated photo catalytically by applying perovskite photocatalysts. Atrazine (ATR) is a pesticide commonly detected as a pollutant in drinking, surface and ground water. Herein, FeYO3@rGO heterojunction was synthesized and applied for photooxidation decomposition of ATR. First, FeYO 3nanoparticles (NPs) were prepared via routine sol-gel. After that, FeYO3 NPs were successfully incorporated with different percentages (5, 10, 15 and 20 wt.%) of reduced graphene oxide (rGO) in the synthesis of novel FeYO3@rGO photocatalyst. Morphological, structural, surface, optoelectrical and optical characteristics of constructed materials were identified via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), adsorption/desorption isotherms, diffusive reflectance (DR) spectra, and photoluminescence response (PL). Furthermore, photocatalytic achievement of the constructed materials was evaluated via photooxidative degradation of ATR. Various investigations affirmed the usefulness of rGO incorporation on the advancement of formed photocatalysts. Actually, novel nanocomposite containing rGO (15 wt.%) possessed diminished bandgap energy, as well as magnified visible light absorption. Furthermore, such nanocomposite presented exceptional photocatalytic achievement when exposed to visible light as ATR was perfectly photooxidized over finite amount (1.6 g · L-1) from the optimized photocatalyst when illuminated for 30 min. The advanced photocatalytic performance of constructed heterojunctions could be accredited mainly to depressed recombination amid induced charges. The constructed FeYO3@rGO nanocomposite is labelled as efficient photocatalyst for remediation of herbicides from aquatic environments.

STRUCTURAL AND ELECTROCHEMICAL PROPERTIES OF THIN LAYERS OF BINARY Ni–Fe ALLOYS ELECTRODEPOSITED BY TWO DIFFERENT BATHS: ACID AND IONIC LIQUID

2018 ◽  
Vol 25 (08) ◽  
pp. 1950025
Author(s):  
RAFIK MAIZI ◽  
ATHMANE MEDDOUR ◽  
CÉLINE ROUSSE
Keyword(s):  
Ionic Liquid ◽  
Nickel Content ◽  
Deposition Potential ◽  
Thin Layers ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Different Shapes ◽  
Fe Alloys ◽  
Irregular Behavior

The deposition of Ni–Fe thin layers in boric acid and ionic liquid ([BuMePyr][Tf2N]) baths were successfully prepared. The obtained materials have been characterized by X-ray diffraction (XRD), Energy Dispersive X-ray spectroscopy (EDX) and SEM. Meanwhile, these materials were carried out by chronoamperometry or chronopotentiometry by varying the intensity of the current and the deposition potential. The results indicate that the coatings of Ni–Fe alloys were successfully obtained by electroplating on the copper substrates, and the alloys composition shows irregular behavior with polarization. The nickel content in the samples is in the range of 55–90%, but the iron content ranges from 10–30%, when potential deposits were varied from [Formula: see text]2[Formula: see text]V to [Formula: see text]4[Formula: see text]V vs Ni electrode. The results also showed that the thin layers are monophased; they contain the Ni3Fe phase. Further, SEM images of Ni–Fe alloys show the different shapes of particles.

Improved Enzymatic Depolymerization of Chitosan by Ionic Liquid Pretreatment and the Effect of Oligo-Chitosan on Intestinal Flora In Vitro

2011 ◽  
Vol 391-392 ◽  
pp. 1319-1323
Author(s):  
Cui Zheng ◽  
Lin Li ◽  
Hao Pang ◽  
Zhao Mei Wang ◽  
Na Li
Keyword(s):  
Ionic Liquid ◽  
Hydrogen Bonds ◽  
Molecular Hydrogen ◽  
Intestinal Flora ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrolysis Of ◽  
Positive Effect ◽  
Enzymatic Depolymerization

It still remains challenging for effective hydrolysis of chitosan into chitosan oligomers. In this work, a pretreatment was conducted on chitosan by an ionic liquid 1-butyl-3-methylimidazolium chloride ([C4mim]Cl), aiming at improving enzymatic depolymerization of chitosan. X-ray diffraction analysis indicated that the inter- and intra-molecular hydrogen bonds within chitosan molecules were broken by [C4mim]Cl and the crystalline was destroyed. The oligo-chitosan hydrolyzed from IL-pretreated chitosan, coded as COS-IL, showed a DP of 3~5, in contrast to DP 5~8 with oligo-chitosan obtained from untreated chitosan(coded as COS-UN). COS-IL was more effective than COS-UN in inhibiting intestinal spoilage bacterials growth and it has positive effect on the growth of intestinal probiotic bacterials.

Removeal of Arsenic(III) from Water by Using a New Class of Zero-Valent Iron Modified Mesoporous Silica Molecular Sieves SBA-15

2011 ◽  
Vol 356-360 ◽  
pp. 423-429
Author(s):  
Meng Ye ◽  
Jin Huang ◽  
Rui Chen ◽  
Qi Zhuang He
Keyword(s):  
Molecular Sieves ◽  
Cost Effective ◽  
Zero Valent Iron ◽  
Preparation Process ◽  
X Ray Diffraction ◽  
Wet Impregnation ◽  
X Ray ◽  
New Class ◽  
Transmission Electron ◽  
Removal Of Arsenic

An elevated arsenic (As) content in groundwater imposes a great threat to people worldwide. Thus, developing new and cost-effective methods to remove As from groundwater and drinking water becomes a priority. Using Zero-Valent iron (ZVI) to remove As from water is a proven technology. In this study, ZVI modified SBA-15 mesoporous silicamolecular sieves (ZVI-SBA-15), was prepared, characterized, and used for removing arsenic from water. Wet impregnation, drying, and calcination steps led to iron inclusion within the mesopores. Iron oxide was reduced to ZVI by NaBH4, and the ZVI modified SBA-15 was obtained. Fourier-transform infrared spectroscopy confirmed the preparation process of the nitrate to oxide forms. The structure of the materials was confirmed by Powder X-ray diffraction. Its data indicated that the structure of ZVI-SBA-15 retained the host SBA-15 structure. Brunauer-Emmett-Teller analysis revealed a decrease in surface area and pore size, indicating ZVI-SBA-15 coating on the inner surfaces. Transmission electron micrographs also confirmed that modified SBA-15 retained the structure of the parent SBA-15 silica.It has a high uptake capability(more than 90 pecent) make it potentially attractive absorbent for the removal of arsenic from water.

Facile hydrothermal synthesis of Fe3O4 nanoparticle and effect of crystallinity on performances for supercapacitor

2019 ◽  
Vol 12 (02) ◽  
pp. 1950019 ◽  
Author(s):  
Yue Xu ◽  
Ying Zhang ◽  
Xiaolan Song ◽  
Hanjun Liu
Keyword(s):  
Hydrothermal Method ◽  
Reaction Times ◽  
Amorphous Structure ◽  
Electrochemical Performances ◽  
X Ray Diffraction ◽  
Oxide Electrode ◽  
Facile Hydrothermal Method ◽  
X Ray ◽  
Pseudocapacitive Behavior ◽  
Adsorption Desorption

Fe3O4 nanoparticles were synthesized by a facile hydrothermal method using triethanolamine. Effects of reaction times (2–8[Formula: see text]h) on crystallinity and electrochemical performances of Fe3O4 were investigated. Samples were analyzed by X-ray diffraction, infrared spectroscopy, N2 adsorption–desorption, scanning electron microscope, galvanostatic charge/discharge, and cyclic voltammetry. Results showed that the crystallinity of Fe3O4 was increased with hydrothermal time, and the sample prepared at 2[Formula: see text]h displayed amorphous structure with small grain size and large surface area of 165.0[Formula: see text]m2[Formula: see text]g[Formula: see text]. The sample exhibited typical pseudocapacitive behavior with capacitance of 383.2[Formula: see text]F[Formula: see text]g[Formula: see text] at 0.5 Ag[Formula: see text] in Na2SO3 electrolyte. After 2000 cycles, the capacitance retention of Fe3O4 at 2[Formula: see text]h was recorded as 83.6%, much higher than 26.3% for sample at 8[Formula: see text]h. It indicated that hydrothermal method was an effective approach to obtain amorphous Fe3O4, implying the potential application for preparing metal oxide electrode for supercapacitors.

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