scholarly journals Synthesis of Zeolite-A and Zeolite-Y Using Silica Gel Waste as Silica Source and Modifying with Fe

2018 ◽  
Vol 7 (4.38) ◽  
pp. 1376
Author(s):  
Pornnipa Khaosomboon ◽  
Kulyakorn Khuanmar ◽  
Panomchai Weerayutsil
Keyword(s):  
Surface Area ◽  
Silica Gel ◽  
Zeolite Y ◽  
Physical Adsorption ◽  
Lower Surface ◽  
Zeolite A ◽  
Silica Source ◽  
Bet Specific Surface Area ◽  
Silica Gel Waste ◽  
Modified Zeolites

The purpose of this research was to synthesize zeolite-A (Ze-A) and zeolite-Y (Ze-Y) using silica sources from silica gel waste, and also improving adsorption capacity with Fe which was trapped in the synthesized zeolites:  Ze-Fe-A and Ze-Fe-Y. All synthesized zeolites were tested with lead solution of 40 mg/L at pH 5. For BET specific surface area, the parent Ze-A and Ze-Y presented surface area of 27.02 and 211.42 m2/g, respectively, whereas Ze-Fe-A and Ze-Fe-Y presented a lower surface area of 10.90 and 28.22 m2/g, respectively. SEM and TEM image demonstrated the cubic and polygon shapes for Ze-A and Ze-Y, respectively, while their modification with Fe presented more round shape. Additionally, both modified zeolites with Fe presented higher adsorption efficiency than their parents. Although the modified zeolites gave lower surface area, the efficiency removal of lead showed higher capacity than zeolite without Fe. It could be concluded that the adsorption mechanism of modified zeolites did not only rely on physical adsorption, but also on chemical adsorption.      

scholarly journals Hydrochloric Acid Modification and Lead Removal Studies on Naturally Occurring Zeolites from Nevada, New Mexico, and Arizona

Processes ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 1238
Author(s):  
Garven M. Huntley ◽  
Rudy L. Luck ◽  
Michael E. Mullins ◽  
Nick K. Newberry
Keyword(s):  
New Mexico ◽  
Surface Area ◽  
Bet Surface Area ◽  
Lead Removal ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Naturally Occurring ◽  
27Al Mas Nmr ◽  
Modified Zeolites

Four naturally occurring zeolites were examined to verify their assignments as chabazites AZLB-Ca and AZLB-Na (Bowie, Arizona) and clinoptilolites NM-Ca (Winston, New Mexico) and NV-Na (Ash Meadows, Nevada). Based on powder X-ray diffraction, NM-Ca was discovered to be mostly quartz with some clinoptilolite residues. Treatment with concentrated HCl (12.1 M) acid resulted in AZLB-Ca and AZLB-Na, the chabazite-like species, becoming amorphous, as confirmed by powder X-ray diffraction. In contrast, NM-Ca and NV-Na, which are clinoptilolite-like species, withstood boiling in concentrated HCl acid. This treatment removes calcium, magnesium, sodium, potassium, aluminum, and iron atoms or ions from the framework while leaving the silicon framework intact as confirmed via X-ray fluorescence and diffraction. SEM images on calcined and HCl treated NV-Na were obtained. BET surface area analysis confirmed an increase in surface area for the two zeolites after treatment, NM-Ca 20.0(1) to 111(4) m2/g and NV-Na 19.0(4) to 158(7) m2/g. 29Si and 27Al MAS NMR were performed on the natural and treated NV-Na zeolite, and the data for the natural NV-Na zeolite suggested a Si:Al ratio of 4.33 similar to that determined by X-Ray fluorescence of 4.55. Removal of lead ions from solution decreased from the native NM-Ca, 0.27(14), NV-Na, 1.50(17) meq/g compared to the modified zeolites, 30 min HCl treated NM-Ca 0.06(9) and NV-Na, 0.41(23) meq/g, and also decreased upon K+ ion pretreatment in the HCl modified zeolites.

scholarly journals Band Engineering and Morphology Control of Oxygen-Incorporated Graphitic Carbon Nitride Porous Nanosheets for Highly Efficient Photocatalytic Hydrogen Evolution

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Yunyan Wu ◽  
Pan Xiong ◽  
Jianchun Wu ◽  
Zengliang Huang ◽  
Jingwen Sun ◽  
...  
Keyword(s):  
Surface Area ◽  
Hydrogen Evolution ◽  
Carbon Nitride ◽  
Separation Efficiency ◽  
Physical Adsorption ◽  
Graphitic Carbon ◽  
Graphitic Carbon Nitride ◽  
Photocatalytic Hydrogen Evolution ◽  
Band Engineering ◽  
Highly Efficient

AbstractGraphitic carbon nitride (g-C3N4)-based photocatalysts have shown great potential in the splitting of water. However, the intrinsic drawbacks of g-C3N4, such as low surface area, poor diffusion, and charge separation efficiency, remain as the bottleneck to achieve highly efficient hydrogen evolution. Here, a hollow oxygen-incorporated g-C3N4 nanosheet (OCN) with an improved surface area of 148.5 m2 g−1 is fabricated by the multiple thermal treatments under the N2/O2 atmosphere, wherein the C–O bonds are formed through two ways of physical adsorption and doping. The physical characterization and theoretical calculation indicate that the O-adsorption can promote the generation of defects, leading to the formation of hollow morphology, while the O-doping results in reduced band gap of g-C3N4. The optimized OCN shows an excellent photocatalytic hydrogen evolution activity of 3519.6 μmol g−1 h−1 for ~ 20 h, which is over four times higher than that of g-C3N4 (850.1 μmol g−1 h−1) and outperforms most of the reported g-C3N4 catalysts.

Synthesis and Characterization of Hematite Nanoparticles as Active Photocatalyst for Water Splitting Application

2013 ◽  
Vol 594-595 ◽  
pp. 73-77 ◽  
Author(s):  
Sze Mei Chin ◽  
Suriati Sufian ◽  
Jeefferie Abd Razak
Keyword(s):  
Surface Area ◽  
Water Splitting ◽  
Combustion Method ◽  
Hydrogen Gas ◽  
Bet Surface Area ◽  
Synthesis And Characterization ◽  
Hematite Nanoparticles ◽  
X Ray ◽  
Bet Specific Surface Area

This paper highlights on the hydrogen production through photocatalytic activity by using hematite nanoparticles synthesized from self-combustion method based on different stirring period. The morphologies and microstructures of the nanostructures were determined using Field-Emission Scanning Electron Microscope (FESEM), X-Ray Diffractometer (XRD) and Particle Size Analyser (PSA). Besides that, surface area analyser was used to determine the BET surface area of the hematite samples. The hematite nanocatalyst as-synthesized are proven to be rhombohedral crystalline hematite (α-Fe2O3) with particle diameters ranging from 60-140 nm. The BET specific surface area of hematite samples increased from 5.437 to 7.6425 m2/g with increasing stirring period from 1 to 4 weeks. This caused the amount of hydrogen gas produced from photocatalytic water splitting to increase as well.

Preparing of Silica Aerogel and Adsorption Performance on Nitrobenzene

2012 ◽  
Vol 512-515 ◽  
pp. 1980-1985
Author(s):  
Ya Jun Luo ◽  
Xue Li ◽  
Xiao Li Hu ◽  
Deng Liang He ◽  
Peng Lin
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Ph Value ◽  
Adsorption Property ◽  
Infrared Absorption Spectrum ◽  
Nitrobenzene Solution ◽  
Silica Source ◽  
Electron Microscopes ◽  
Scanning Electron Microscopes

SiO2aerogel is prepared under normal conditions by taking tetraethyl orthosilicate (TEOS) as the silica source, N-hexane as the displacer, trimethylchlorosilane hexane as the modifier and hydrolysis environment provided by hydrochloric acid and ammonia water. The effect of pH value, time, temperature, initial concentration on the adsorption of nitrobenzene by aerogel has been studied. The results show that the best range of the pH value for adsorption is 10.72. When adsorption time is 100 min, adsorption equilibrium can be reached. The best temperature for adsorption is 40 °C. The adsorption capacity becomes larger with the concentration increasing of the nitrobenzene solution. When the concentration reaches 500 mg/L, the adsorption reaches 32.402 mg/g. The adsorption equation matches Langmuir model. Scanning Electron Microscopes (SEM), infrared absorption spectrum and specific surface area measurements have shown that the adsorption property of SiO2aerogel for the nitrobenzene is related to cellular structure of the aerogel and large specific surface area.

Decomposition of Dioxins in Gas and Water Using Photocatalytic Silica-Gel

2005 ◽  
Vol 486-487 ◽  
pp. 41-44 ◽  
Author(s):  
Hiroshi Taoda
Keyword(s):  
Surface Area ◽  
Silica Gel ◽  
Catalyst Layer ◽  
Dip Coating ◽  
Organic Substances ◽  
Titanium Tetraisopropoxide ◽  
Oxidative Potential ◽  
Uv Lamp ◽  
Waste Incinerators ◽  
Almost All

Dioxins are extremely toxic, and it is difficult to treat them with the conventional method. When irradiated by light, photocatalysts generate strong oxidative potential and decomposes almost all organic substances containing dioxins to water, carbon dioxide and others. Silica-gel has high adsorptive activity as well as large surface area, and it is transparent to ultraviolet light. Photocatalytic silica-gel was prepared by a dip coating method using TiO2 sol obtained by hydrolyzing titanium tetraisopropoxide on silica-gel bead (about 3mm in diameter) and heat-treated at 550°C. Since the surface area of the photocatalytic silica-gel is 300m2/g, the reaction area is large and allows the highly efficient decomposition of harmful organic substances, unpleasant odors and colored matters contained in waste water. The photocatalytic apparatus for decomposition of dioxins in emission gas from waste incinerators is composed of the catalyst layer consisting of 95dm3 photocatalytic silica-gel and 16 units of UV lamp. The photocatalytic apparatus was connected to the bypass line led from the outlet duct of cyclone, and the concentration of dioxins in the exhaust gas was measured. Decomposition test of dioxins in scrubber water was also performed using a photocatalytic apparatus with 150g photocatalytic silica-gel and 8 units of UV lamp. After 0.5dm3 of scrubber water containing dioxins was circulated in the photocatalytic apparatus for 1, 2 and 24 hour, each concentration of dioxins in the water was measured. As a result, the removal efficiency over 99% of dioxins in emission gas and scrubber water from waste incinerators has been obtained.

scholarly journals The Effect of Various Hydroxide and Salt Additives on the Reduction of Fluoride Ion Mobility in Industrial Waste

2021 ◽  
Vol 13 (3) ◽  
pp. 1554
Author(s):  
Tadas Dambrauskas ◽  
Kestutis Baltakys ◽  
Agne Grineviciene ◽  
Valdas Rudelis
Keyword(s):  
Liquid Medium ◽  
Silica Gel ◽  
Ion Mobility ◽  
Fluoride Removal ◽  
Dynamic Conditions ◽  
Treatment Conditions ◽  
Medium Flow ◽  
Silica Gel Waste ◽  
Fluorine Ions ◽  
Static Conditions

In this work, the influence of various hydroxide and salt additives on the removal of F− ions from silica gel waste, which is obtained during the production of AlF3, was examined. The leaching of the mentioned ions from silica gel waste to the liquid medium was achieved by the application of different techniques: (1) leaching under static conditions; (2) leaching under dynamic conditions by the use of continuous liquid medium flow; and (3) leaching in cycles under dynamic conditions. It was determined that the efficiency of the fluoride removal from this waste depends on the w/s ratio, the leaching conditions, and the additives used. It was proven that it is possible to reduce the concentration of fluorine ions from 10% to <5% by changing the treatment conditions and by adding alkaline compounds. The silica gel obtained after the leaching is a promising silicon dioxide source.

scholarly journals PENGARUH KONSENTRASI NaOH DAN WAKTU PENAHANAN TERHADAP KARAKTERISTIK ZEOLIT YANG DISINTESIS DARI LIMBAH GEOTHERMAL

REAKTOR ◽  
2017 ◽  
Vol 17 (1) ◽  
pp. 17
Author(s):  
Sulardjaka Sulardjaka ◽  
Deni Fajar Fitriana
Keyword(s):  
Crystal Size ◽  
Holding Time ◽  
Zeolite A ◽  
Zeolite Structure ◽  
Silica Source ◽  
Zeolite P

Abstract THE EFFECT OF CONCENTRATION OF NaOH AND HOLDING TIME ON CHARACTERISTIC OF ZEOLIT SINTHESIZED FROM GEOTHERMAL WASTE. Objective of this research is to investigate the effect of concentration of NaOH and holding time on the characteristic of synthesized zeolite from geothermal waste. Geothermal waste was used as silica source and hydrothermally processed for zeolite synthesized. Variation concentration of NaOH was 1.67, 3, and 5 M and variation of holding time are 1, 3, and 5 hours. Synthesized products were characterized by XRD, FTIR and SEM photomicrograph. It can be concluded that the rise of concentration of NaOH reduce the cristalization time and crystal size. Increasing of concentration of NaOH and holding time produce divers zeolite structure. At holding time 5 h and NaOH 1.67 M produces zeolite A. At holding time 5 h and NaOH concentration 3 M produce zeolite P. Sodalite is produced at concentration NaOH 5 M with holding time 5 h. Keywords: hydrothermal; geothermal waste; zeolite   Abstrak Penelitian ini bertujuan untuk meneliti pengaruh konsntrasi NaOH dan waktu penahanan terhadap karakteristik zeolit yang disintesis dari limbah geothermal. Limbah geothermal dipilih sebagai bahan silika pada sintesis zeolit dengan metode hidrothermal. Penelitian dilakukan dengan variasi konsentrasi NaOH: 1,67, 3, dan 5 M, dan variasi waktu penahanan 1, 3 dan 5 jam. Produk hasil sintesis dikarakterisasi dengan XRD, FTIR dan foto SEM. Hasil dari penelitian ini menunjukkan bahwa  tinggi konsentrasi NaOH kristalisasi zeolit A semakin cepat, sehingga ukuran kristal semakin kecil. Konsentrasi NaOH yang semakin tinggi dan waktu penahanan yang semakin lama, menghasilkan  jenis struktur zeolit yang lebih beragam. Pada waktu penahanan 5 jam, variasi konsentrasi NaOH 1,67 M menghasilkan zeolit A, variasi konsentrasi NaOH 3M menghasilkan zeolit P (NaP1) dan pada variasi konsentrasi NaOH 5M menghasilkan sodalit. Kata kunci: hydrothermal; limbah geothermal; zeolit

Studies on the surface area of zeolites, as determined by physical adsorption and X-ray crystallography

1968 ◽  
Vol 46 (10) ◽  
pp. 1695-1701 ◽  
Author(s):  
D. J. C. Yates
Keyword(s):  
Surface Area ◽  
Physical Adsorption ◽  
Independent Method ◽  
Linear Portion ◽  
Adsorbed Molecules ◽  
X Ray ◽  
X Ray Crystallography ◽  
Surface Areas

The determination of the surface areas of zeolites is discussed. It is shown that it is incorrect to use the multilayer isotherm method of Brunauer, Emmett, and Teller for solids where only little more than one monolayer can be adsorbed, in cavities little larger than the adsorbed molecules. The areas of such materials can, however, be determined from the beginning of the linear portion of their isotherms (point B). In addition, X-ray spectra can provide an independent method of measuring changes in the surface areas of zeolites.

scholarly journals Catalytic Cracking of n-Hexadecane Using Carbon Nanostructures/Nano-Zeolite-Y Composite Catalyst

Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1385
Author(s):  
Botagoz Zhuman ◽  
Shaheen Fatima Anis ◽  
Saepurahman ◽  
Gnanapragasam Singravel ◽  
Raed Hashaikeh
Keyword(s):  
Surface Area ◽  
Catalytic Cracking ◽  
Carbon Nanostructures ◽  
Active Sites ◽  
Zeolite Y ◽  
High Surface ◽  
High Surface Area ◽  
Composite Catalyst ◽  
Homogeneous Distribution ◽  
Binding Material

Zeolite-based catalysts are usually utilized in the form of a composite with binders, such as alumina, silica, clay, and others. However, these binders are usually known to block the accessibility of the active sites in zeolites, leading to a decreased effective surface area and agglomeration of zeolite particles. The aim of this work is to utilize carbon nanostructures (CNS) as a binding material for nano-zeolite-Y particles. The unique properties of CNS, such as its high surface area, thermal stability, and flexibility of its fibrous structure, makes it a promising material to hold and bind the nano-zeolite particles, yet with a contemporaneous accessibility of the reactants to the porous zeolite structure. In the current study, a nano-zeolite-Y/CNS composite catalyst was fabricated through a ball milling approach. The catalyst possesses a high surface area of 834 m2/g, which is significantly higher than the conventional commercial cracking catalysts. Using CNS as a binding material provided homogeneous distribution of the zeolite nanoparticles with high accessibility to the active sites and good mechanical stability. In addition, CNS was found to be an effective binding material for nano-zeolite particles, solving their major drawback of agglomeration. The nano-zeolite-Y/CNS composite showed 80% conversion for hexadecane catalytic cracking into valuable olefins and hydrogen gas, which was 14% higher compared to that of pure nano-zeolite-Y particles.

scholarly journals The Prospective Approach for the Reduction of Fluoride Ions Mobility in Industrial Waste by Creating Products of Commercial Value

2019 ◽  
Vol 11 (3) ◽  
pp. 634 ◽  
Author(s):  
Valdas Rudelis ◽  
Tadas Dambrauskas ◽  
Agne Grineviciene ◽  
Kestutis Baltakys
Keyword(s):  
Liquid Medium ◽  
Silica Gel ◽  
Reaction Temperature ◽  
Industrial Waste ◽  
Adsorption Properties ◽  
Raw Material ◽  
Fluoride Ions ◽  
Dynamic Conditions ◽  
Stable Compound ◽  
Silica Gel Waste

In this work, we present the possibility to reduce the amount of fluoride ions in silica gelwaste by using different techniques or to immobilize these ions by creating products ofcommercial value. The leaching of fluoride ions from silica gel waste to the liquid medium wasdone under static and dynamic conditions. It was determined that the removal of fluoride ionsfrom this compound depends on various factors, such as dissociation, solubility, the w/s ratio,reaction temperature, leaching conditions, the adsorption properties of silica gel waste, and others.The obtained results showed that, by applying different techniques, the quantity of fluoride ionscan be reduced by 60%, while obtained water was neutralized by calcium hydroxide.Additionally, it was determined that silica gel waste is a promising raw material for thehydrothermal synthesis of a stable compound containing fluoride ions – cuspidine.

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