scholarly journals SYNTHESIS OF ZEOLITE-ACTIVATED CARBON COMPOSITE FOR REMOVAL OF AMMONIUM FROM AQUEOUS SOLUTION

2020 ◽  
Vol 58 (5A) ◽  
pp. 75
Author(s):  
Pham Thi Yen ◽  
Nguyen Thanh Dong ◽  
Pham Tuan Linh ◽  
Nguyen Viet Hoang ◽  
Nguyen Tien Vinh ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Hydrothermal Reaction ◽  
Carbon Composite ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
Equilibrium And Kinetics ◽  
Adsorption Equilibrium And Kinetics ◽  
Area X ◽  
Synthesized Materials

In this study, zeolite-activated carbon composite (Z/AC) was synthesized by hydrothermal reaction using kaolin as a source of silica and alumina. The synthesized materials were characterized by Brunner-Emmet-Teller (BET) surface area to calculate surface area, X-ray diffraction (XRD) to study the crystal structure of materials, Infrared spectroscopy (IR) to indicate the presence of functional groups on the surface and scanning electron microscopy (SEM) to determine the morphology of the composites. In this paper, adsorption equilibrium and kinetics for the removal of ammonium by prepared Z/AC materials were evaluated.

scholarly journals Antibacterial properties of AgNO3-activated carbon composite on Escherichia coli: inhibition action

2018 ◽  
Vol 6 (1) ◽  
pp. 46
Author(s):  
Nkwaju Yanou Rachel ◽  
Baçaoui Abdelaziz ◽  
Ndi Julius Nsami ◽  
Kouotou Daouda ◽  
Yaacoubi Abdelrani ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Total Pore Volume ◽  
Carbon Composite ◽  
Micropore Volume ◽  
Bet Surface Area ◽  
Activation Temperature ◽  
X Ray ◽  
Impregnation Time ◽  
Methylene Blue Number

AgNO3- activated carbon composite based palm kernel shell was prepared by hydrothermal carbonization. The concentration of AgNO3, activation temperature and impregnation time were investigated on five responses (iodine number, methylene blue number, BET surface area, micropore volume and total pore volume). The most influential parameters of the preparation process were optimized using the Doehlert optimal design. From the ANOVA, the following optimal conditions of preparation were retained: 0.068 mol/L, 210°C and 3.7 h for AgNO3 concentration, activation temperature and impregnation time respectively. The activated carbon (AC) and the composite (AC-AgNO3) were characterized using Fourier Transform infrared spectroscopy, X-Ray diffraction, Scanning Electron Microscopy coupled to Energy Dispersive X-ray spectroscopy and measurements of the surface area. The XRD pattern and SEM-EDX clearly confirmed the presence of silver in the composite. The experimental parameters of AC- AgNO3 composite were as followed: 708.44 mg/g; 293.09 mg/g; 713.0 m2/g; 0.49 cm3/g and 0.76 cm3/g, for iodine number, methylene blue number, BET surface area, micropore volume and total pore volume of AC- AgNO3 respectively. The antibacterial test carried on Escherichia Coli showed that AC-AgNO3 composite has a high-improved antibacterial property of 99.99% fixation with a dosage of 1500 ppm for 5 hours of contact time.

scholarly journals Adsorptive Removal of Methylene Blue and Crystal Violet onto Micro-Mesoporous Zr3O/Activated Carbon Composite: A Joint Experimental and Statistical Modeling Considerations

2018 ◽  
Vol 2018 ◽  
pp. 1-14 ◽  
Author(s):  
H. Ait Ahsaine ◽  
Z. Anfar ◽  
M. Zbair ◽  
M. Ezahri ◽  
N. El Alem
Keyword(s):  
Methylene Blue ◽  
Activated Carbon ◽  
Surface Area ◽  
Crystal Violet ◽  
Zirconium Oxide ◽  
Carbon Composite ◽  
Bet Surface Area ◽  
Sem Images ◽  
X Ray ◽  
Pseudo Second Order

Zirconium oxide/activated carbon (Zr3O/AC) composite was synthesized to remove methylene blue (MB) and crystal violet (CV) from the aqueous medium. The Zr3O/AC sample was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analyses (EDS), Raman spectroscopy (RS), BET surface area, and Fourier transform infrared spectroscopy (FTIR). XRD profiles confirmed the successful synthesis of the zirconium oxide/activated carbon composite. SEM images showed multideveloped walls with irregular particle size with channel arrays. The nitrogen physisorption combines I and IV types with a calculated BET surface area of 1095 m2/g. Raman spectrum illustrated a disorder of both crystalline structure and the graphitic structure. The adsorption was better fitted to the pseudo-second-order (PSO) kinetic model. Langmuir model fitted better the experimental results of MB adsorption, whereas the CV was better consistent with the Freundlich model. The obtained results suggested that the MB and CV adsorption might be influenced by the mass transfer that involves multiple diffusion steps. The maximum adsorption capacities are 208.33 and 204.12 mg/g for MB and CV, respectively. The MB and CV removal mechanisms were proposed, and statistical optimization was performed using central composite design combined with the response surface methodology.

scholarly journals Removal of Congo Red Dye using Synthesised Copper(II) Activated Carbon from Date Seeds

2021 ◽  
Vol 14 ◽  
pp. 1-9
Author(s):  
Nur rahimah Said ◽  
Hazirah Syahirah Zakria ◽  
Siti Nor Atika Baharin ◽  
Nurul' Ain Jamion
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Congo Red ◽  
Bet Surface Area ◽  
Activation Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Effective Removal ◽  
Vis Spectroscopy ◽  
Red Dye

Azo dyes are recognised as contaminants from the textile and printing industries that lead to human toxicity. Copper(II) activated carbon (CuAC) is an effective removal agent of dyes in these industries. The purpose of this study is to synthesise and characterise CuAC from date seeds. In addition, the efficiency of CuAC as a removal of Congo red (CR) in aqueous solution is also studied. Activated carbon (AC) was prepared from date seeds using phosphoric acid as activating agent, followed by activation process in a furnace at 500 ℃ for 2 hours. Copper(II) nitrate was used in the impregnation of AC to produce CuAC. The AC and CuAC were characterised using Attenuated Total Reflectance Fourier-Transform Infrared Spectroscopy (ATR-FTIR), BET surface area (SBET), Scanning Electron Microscope-Energy Dispersive X-Ray Spectroscopy (SEM-EDX), Atomic Absorption Spectroscopy (AAS) and X-Ray Diffraction (XRD). UV-VIS Spectroscopy was used to determine dye concentrations after treatment with removal agent of CuAC. The characterisation data proved that the CuAC has been successfully synthesised with 0.33% Cu(II) loaded onto AC and its surface area increased from 8.37 m2/g to 384.82 m2/g. The dye removal study was conducted at 10 ppm concentration of dye. Result revealed that 0.2 g of CuAC at pH 2 in 90 min removed 100% of CR dye.

scholarly journals Preparation of Terminalia catappa Shell Based Activated Carbon by Microwave Assisted Chemical Activation

2019 ◽  
Vol 1 (1) ◽  
pp. 54-60
Author(s):  
Awitdrus Awitdrus
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Chemical Activation ◽  
Bet Surface Area ◽  
Koh Activation ◽  
X Ray Diffraction ◽  
Scanning Microscope ◽  
Terminalia Catappa ◽  
Electron Scanning Microscope ◽  
Adsorption Desorption

Activated carbon was prepared from Terminalia catappa shells using microwave asissted KOH activation. The ratio of mass percentages of Terminalia catappa and KOH were 4:1, 4:2, and 4:3. Terminalia catappa based activated carbon was prepared by KOH activation at the room temperature for 24 hours and followed by microwave irradiation at the out put power of 630 Watt for 20 minutes. The physical properties of activated carbon i.e. surface morphology, micro structure, and BET surface area were characterized by electron scanning microscope, X-ray diffraction and N2 adsorption-desorption isotherm at 77K, respectively. The highest BET surface area was 312 m2/g with adsorption of activated carbon towards methylene blue by 84.4 mg/g. The BET surface area was directly correlated with the stack height (Lc) of the activated carbon.

Adsorption Equilibrium and Kinetics of CO2 and H2O on Activated Carbon

2012 ◽  
Vol 27 (2) ◽  
pp. 139-145 ◽  
Author(s):  
Dong XU ◽  
Jun ZHANG ◽  
Gang LI ◽  
Penny XIAO ◽  
Paul WEBLEY ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Adsorption Equilibrium ◽  
Equilibrium And Kinetics ◽  
Adsorption Equilibrium And Kinetics ◽  
Kinetics Of

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.

Carbon Dioxide Sequestration Using Activated Carbon From Agro Waste-Waste Bamboo

2021 ◽  
Author(s):  
Emmanuel Ayodele ◽  
Victoria Ezeagwula ◽  
Precious Igbokwubiri
Keyword(s):  
Activated Carbon ◽  
Fly Ash ◽  
Greenhouse Gases ◽  
Surface Area ◽  
Carbon Capture ◽  
Agricultural Waste ◽  
High Surface ◽  
Research Work ◽  
High Surface Area ◽  
Bet Surface Area

Abstract Bamboo trees are one of the fastest growing trees in tropical rainforests around the world, they have various uses ranging from construction to fly ash generation used in oil and gas cementing, to development of activated carbon which is one of the latest uses of bamboo trees. This paper focuses on development of activated carbon from bamboo trees for carbon capture and sequestration. The need for improved air quality becomes imperative as the SDG Goal 12 and SDG Goal13 implies. One of the major greenhouse gases is CO2 which accounts for over 80% of greenhouse gases in the environment. Eliminating the greenhouse gases without adding another pollutant to the environment is highly sought after in the 21st century. Bamboo trees are mostly seen as agricultural waste with the advent of scaffolding and other support systems being in the construction industry. Instead of burning bamboo trees or using them for cooking in the local communities which in turn generates CO2 and fly ash, an alternative was considered in this research work, which is the usage of bamboo trees to generate activated, moderately porous and high surface area carbon for extracting CO2 from various CO2 discharge sources atmosphere and for water purification. This paper focuses on the quality testing of activated carbon that can effectively absorb CO2. The porosity, pore volume, bulk volume, and BET surface area were measured. The porosity of the activated carbon is 27%, BET surface area as 1260m²/g. Fixed carbon was 11.7%, Volatility 73%, ash content 1.7%.

scholarly journals Synthesis and Characterization of Co-Mo/γ-Alumina Catalyst from local Kaolin clay for Hydrodesulfurization of Iraqi Naphtha

2021 ◽  
Vol 11 (1) ◽  
pp. 84-106
Author(s):  
Nada Sadoon Ahmed zeki ◽  
Sattar Jalil Hussein ◽  
Khalifa K. Aoyed ◽  
Saad Kareem Ibrahim ◽  
Ibtissam K. Mehawee
Keyword(s):  
Surface Area ◽  
Sulfur Removal ◽  
Sulfuric Acid Concentration ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mo Catalyst ◽  
Pressure Time ◽  
Al2o3 Catalyst

This work deals with the hydrodesulfurization of three types of naphtha feedstocks; mixednaphtha (WN), heavy naphtha (HN) & light naphtha (LN) with a sulfur content of 1642.1,1334.9 & 709 ppm respectively, obtained from Missan refinery using prepared Co-Mo/γ-Al2O3catalyst. The Iraqi white kaolin was used as a starting material for the preparation of γ-Al2O3support, transferring kaolin to meta-kaolin was studied through calcination at differenttemperatures and durations, kaolin structure was investigated using X-Ray diffractiontechniques.High purity 94.83%. Crystalline γ-Al2O3 with a surface area of 129.91 m2/gm, pore volume0.9002 cm3/g was synthesized by extraction of Iraqi kaolin with H2SO4 at different acid to clayweight ratios, acid concentrations & leaching time. Ethanol was used as precipitating agent; theresultant gel was dried and calcined at 70OC, 10 hrs & 900 OC, 2 hrs respectively.The effects of different parameters on the average crystallinity and extraction % ofsynthesized γ-Al2O3 were studied like; acid: clay ratio, sulfuric acid concentration, leachingtime, leaching temperature & kaolin conversion to metakaolin. Characterization of prepared γ-Al2O3 & Co-Mo catalyst were achieved by X-ray diffraction, FTIR-spectra, texture properties& BET surface area, BJH N2 adsorption porosity, AFM, SEM, crush strength & XRF tests. Co-Mo/ γ-Al2O3 catalyst with final loading 5.702 wt% and 21.45 wt% of Co and Mo oxidesrespectively was prepared by impregnation methods.The activity of prepared Co-Mo/γ-Al2O3 catalyst after moulding to be tested forhydrodesulfurization (HDS) of naphtha feedstock W.N, H.N & L.N was performed using apilot hydrotreating unit at petroleum research & development centre, at different operatingconditions. Effects of temperature, LHSV, pressure, time & pore size distribution were studied,the best percentage of sulfur removal is increased with decreasing LHSV to 2 hr-1 as a generaltrend to be 89.71, 99.72, 99.20 % at 310oC for the whole naphtha, heavy naphtha and lightnaphtha feedstocks respectively, at 34 bar pressure and 200/200 cm3/cm3 H2/HC ratio.

scholarly journals The Elusive Nitro-Functionalised Member of the IRMOF-9 Family

2019 ◽  
Vol 72 (10) ◽  
pp. 811 ◽  
Author(s):  
Luke Conte ◽  
Tian-You Zhou ◽  
Omid T. Qazvini ◽  
Lujia Liu ◽  
David R. Turner ◽  
...  
Keyword(s):  
Dicarboxylic Acid ◽  
Surface Area ◽  
Metal Organic Framework ◽  
Bet Surface Area ◽  
Solvothermal Reaction ◽  
X Ray Diffraction ◽  
Secondary Building Unit ◽  
Initial Product ◽  
Building Unit ◽  
Metal Organic

The solvothermal reaction of 2-nitro-[1,1′‐biphenyl]‐4,4′‐dicarboxylic acid (H2bpdcNO2) with Zn(NO3)2·6H2O in DMF solvent does not give a functionalised variant of IRMOF-9. Single-crystal X-ray diffraction analysis shows the major initial product of this reaction, WUF-21 (WUF=Wollongong University Framework), is a porous interpenetrated diamondoid metal–organic framework (MOF) with a secondary building unit that ‘doubly straps’ eight bridging bpdcNO2 ligands in a distorted tetrahedral shape around an unusual pentazinc core. A second porous MOF phase (WUF-23) containing a large and novel dodecazinc secondary building unit forms in the same reaction and eventually predominates in solutions containing formate anion, which arises from the hydrolysis of DMF. Doping the starting ligand with [1,1′‐biphenyl]‐4,4′‐dicarboxylic acid (H2bpdc) provides a facile way to grow nitro-functionalised IRMOF-9, hereafter denoted as WUF-22, where the dopant is carried through into the product. Activated WUF-22 is a microporous solid with an apparent Brunauer–Emmett–Teller (BET) surface area of 2497m2g−1, which matches well with geometric surface area calculations. The CO2 adsorption properties of WUF-22 are reported.

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