scholarly journals Treatment of Mining and Thermoelectric Waste Through the Geopolymerization Process

2021 ◽  
Vol 100 ◽  
pp. 05003
Author(s):  
Morales-Aranibar Carlos ◽  
Linares Nataniel ◽  
Soto Tolomeo ◽  
Morales-Aranibar Luis
Keyword(s):  
Fly Ash ◽  
Mine Tailings ◽  
Room Temperature ◽  
Hydroelectric Plant ◽  
Chemical Characterization ◽  
Second Stage ◽  
Pyrite Content ◽  
Two Stages ◽  
Sem Morphology

Currently, energy and extraction activities generate large amounts of highly polluting waste, so there is a need for sustainable and environmentally friendly technologies. The aim of the study is to treat mining tailings and fly ash through the process of geopolymerization. The samples studied were obtained from the Toquepala mine, Tacna and from the ENGIE-Moquegua hydroelectric plant (Peru). The methodology was based on two stages, the first characterization of Fly Ash (FA) and mine tailings (MT) by EDX chemical characterization, SEM morphology, the second was prepared mixtures of MT and FA in 10 M alkaline solution, cured in 35 days at room temperature and the characterization of the geopolymer by organoleptic analysis, SEM and TCLP. The first stage shows high aluminosilicate content 20.44% Al2O3 and 53.39 % SiO2 for (MT); 22.11% Al2O3 and 51.76% SiO2 for (FA), presents metal and pyrite content. In the second stage, the samples show health and environmental harmlessness, with the formation of tetragonal structures typical of the geopolymer, the samples show a significant reduction of Sr, Ca, Fe, Pb, Ba, Be, and Cu, demonstrating the effectiveness of treatment by means of geopolymerization opening a new field for the environmental passive treatment.

Processing by Pulsed Laser Deposition and Structural, Morphological and Chemical Characterization of Bi-Pb-Sr-Ca-Cu-O and Bi-Pb-Sb-Sr-Ca-Cu-O Thin Films

2010 ◽  
Vol 75 ◽  
pp. 202-207
Author(s):  
Victor Ríos ◽  
Elvia Díaz-Valdés ◽  
Jorge Ricardo Aguilar ◽  
T.G. Kryshtab ◽  
Ciro Falcony
Keyword(s):  
Thin Films ◽  
Pulsed Laser Deposition ◽  
Room Temperature ◽  
Pulsed Laser ◽  
Chemical Characterization ◽  
Laser Deposition ◽  
Nominal Composition ◽  
Deposition Parameters ◽  
The Relationship

Bi-Pb-Sr-Ca-Cu-O (BPSCCO) and Bi-Pb-Sb-Sr-Ca-Cu-O (BPSSCCO) thin films were grown on MgO single crystal substrates by pulsed laser deposition. The deposition was carried out at room temperature during 90 minutes. A Nd:YAG excimer laser ( = 355 nm) with a 2 J/pulse energy density operated at 30 Hz was used. The distance between the target and substrate was kept constant at 4,5 cm. Nominal composition of the targets was Bi1,6Pb0,4Sr2Ca2Cu3O and Bi1,6Pb0,4Sb0,1Sr2Ca2Cu3OSuperconducting targets were prepared following a state solid reaction. As-grown films were annealed at different conditions. As-grown and annealed films were characterized by XRD, FTIR, and SEM. The films were prepared applying an experimental design. The relationship among deposition parameters and their effect on the formation of superconducting Bi-system crystalline phases was studied.

Growth mechanism and characterization of ZnO nano-tubes synthesized using the hydrothermal-etching method

2009 ◽  
Vol 63 (6) ◽  
Author(s):  
Yan Li ◽  
Chuan-Sheng Liu ◽  
Yun-Ling Zou
Keyword(s):  
Room Temperature ◽  
Morphological Analysis ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Etching Method ◽  
Nano Rods ◽  
Two Stages

AbstractZnO nano-tubes (ZNTs) have been successfully synthesized via a simple hydrothermal-etching method, and characterized by X-ray diffraction, field emission scanning electron microscopy and room temperature photoluminescence measurement. The as-synthesized ZNTs have a diameter of 500 nm, wall thickness of 20–30 nm, and length of 5 µm. Intensity of the plane (0002) diffraction peak, compared with that of plane (10$$ \bar 1 $$0) of ZNTs, is obviously lower than that of ZnO nano-rods. This phenomenon can be caused by the smaller cross section of plane (0002) of the nano-tubes compared with that of other morphologies. On basis of the morphological analysis, the formation process of nano-tubes can be proposed in two stages: hydrothermal growth and reaction etching process.

Physico-Chemical Characterization of Alumina Sols Prepared From Aluminum Alcoxides

1986 ◽  
Vol 73 ◽  
Author(s):  
William L. Olson
Keyword(s):  
Room Temperature ◽  
Gel Filtration ◽  
Chemical Characterization ◽  
Process Conditions ◽  
Chemical Processing ◽  
Rotary Evaporation ◽  
Physico Chemical ◽  
Elution Curves ◽  
Alumina Sol

ABSTRACTAlumina sols derived from aluminum sec-butoxide (Yoldas) were characterized. The distribution of the polymer sizes within the sol, determined by gel filtration chromatography (GFC), was found to be dramatically affected by small changes in the chemical processing or preparative procedure. Aging the sol at room temperature for two weeks produced no significant change in the GFC elution curves of the alumina sol. Sols with a “milky” appearance were found to exhibit a wider distribution of polymers by GFC than transparent sols. Rotary evaporation of the sol followed by redissolution of the residue was found to change the polymer size distribution described by the gel filtration elution curves. These observations coupled with 27Al NMR spectroscopy and viscometry measurements were used to elucidate the effects of process conditions and aging on the molecular structure of the sol.

The Influence of Heat and Two Stages Precipitation in the Process of Natural Polymer Purification from the Byproduct of Bioethanol Process Base on Empty Palm Fruit Bunch

2015 ◽  
Vol 1123 ◽  
pp. 177-181
Author(s):  
Achmad Hanafi ◽  
Harry Budiman ◽  
Fauzan Aulia
Keyword(s):  
Sulfuric Acid ◽  
Sodium Hydroxide ◽  
Room Temperature ◽  
Black Liquor ◽  
Ash Content ◽  
Natural Polymer ◽  
Palm Fruit ◽  
Second Stage ◽  
Direct Precipitation ◽  
Two Stages

The biopolymer material, lignin, was recovered from the black liquor by acidification of the black liquor using sulfuric acid. Several purification techniques were carried out to produce the high purity of lignin such as gradual precipitation of lignin from black liquor (first stage: precipitation at pH 7, second stage: precipitation at pH 2) and the diluting of crude lignin by sodium hydroxide then followed by re-precipitation at different temperature. Subsequently, the impurities of lignin product resulted from each purification techniques was determined as ash content that analyzed using temperature program furnace; and the content of lignin was investigated using spectrophotometer UV-Vis. The result showed that the content of lignin of material produced from gradual precipitation was approximately 77.6%. It was higher than the content of lignin about 3.4% of material produced from direct precipitation to pH 2. In addition, the elevating of temperature from 40 to 60°C was no considerably affect to the content of lignin in precipitate produced from re-precipitation of crude lignin solution in sodium hydroxide. Nonetheless, the content of lignin of precipitate improved 15% when the temperature of re-precipitation of crude lignin solution in sodium hydroxide was raised from room temperature to 40-60°C.

Chemical Characterization of Fly Ash Aqueous Systems

1980 ◽  
Vol 9 (3) ◽  
pp. 424-428 ◽  
Author(s):  
Ahmed A. Elseewi ◽  
A. L. Page ◽  
Sabine R. Grimm
Keyword(s):  
Fly Ash ◽  
Chemical Characterization ◽  
Aqueous Systems

3D Chemical Characterization of Micron-Sized Coal Fly Ash Particles

1985 ◽  
Vol 65 ◽  
Author(s):  
Richard W. Linton ◽  
Scott R. Bryan ◽  
X. B. Cox ◽  
Dieter P. Griffis
Keyword(s):  
Trace Elements ◽  
Fly Ash ◽  
Secondary Ion Mass Spectrometry ◽  
Coal Fly Ash ◽  
Three Dimensional ◽  
Depth Profiling ◽  
Chemical Characterization ◽  
Detection Sensitivity ◽  
3D Analysis

The surface layers on coal fly ash particles are of special environmental interest in that concentration enrichments of trace elements may occur [1], thereby enhancing the potential bioavailability of toxic species. Little research, however, has been devoted to the analytical characterization of intraparticle and interparticle distributions of trace elements. The high detection sensitivity, spatial resolution, and depth profiling capabilities of secondary ion mass spectrometry (SIMS), coupled to digital image acquisition and processing [2], permit three-dimensional (3D) compositional maps for collections of individual micron-sized particles. The 3D analysis of trace element distributions in coal fly ash particles is the subject of this SIMS investigation

scholarly journals Characterization and compressive strength of fly ash based-geopolymer paste

2018 ◽  
Vol 195 ◽  
pp. 01023 ◽  
Author(s):  
Ari Widayanti ◽  
Ria Asih Aryani Soemitro ◽  
Hitapriya Suprayitno ◽  
Januarti Jaya Ekaputri
Keyword(s):  
Compressive Strength ◽  
Fly Ash ◽  
Room Temperature ◽  
Chemical Resistance ◽  
Combustion Process ◽  
Mass Ratio ◽  
Alkali Activator ◽  
Compressive Strength Test ◽  
Geopolymer Paste

Fly ash is a by-product obtained from coal combustion process. Some of the utilization of fly ash is to produce geopolymer products which have high compressive strength, fire, chemical resistance. This paper proposes fly ash from unit 1-7 Suralaya Power Plant Indonesia. The aims of this study are to obtain characterization of fly ash and mechanical properties of geopolymer paste based on variations of the alkali activator ratio. The method was based on previous research and laboratory investigation. XRF and compressive strength were analysed in this study. Alkali activator was obtained from NaOH and Na2SiO3 mixture. The ratio of Na2SiO3 to NaOH was in the range of 0.5-2.5. Geopolymer paste was casted in acrylic cylinders with a diameter of 2 cm and a height of 4 cm. The curing was conducted at room temperature until the day for the compressive strength test at 28 days. The result showed that the fly ash is classified as F class. Increasing the alkali activator ratio influenced the strength. The best composition of geopolymer paste is made with NaOH 8M, and the mass ratio of Na2SiO3 to NaOH is 2.5. This composition produced compressive strength of 98.6 MPa.

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