scholarly journals Cracking of the paraffins on catalysts from natural zeolite of Kazakhstan Shankanay field

2021 ◽  
pp. 20-27
Author(s):  
Lazat Krebayeva ◽  
Zhannur Algabas ◽  
Akerkem Еssenbayeva ◽  
Alexandr Brodskyi ◽  
Sapargali Konuspayev
Keyword(s):  
Atmospheric Pressure ◽  
Natural Zeolite ◽  
Reaction Products ◽  
Gaseous Reaction ◽  
X Ray ◽  
Gaseous Products ◽  
Iron Form ◽  
Group Compositions ◽  
Zeolite Modification ◽  
Partial Destruction

Cracking of paraffins was held to obtain long chain α-olefins using the catalysts from natural zeolite of Shankanay field modified with 1N HCl at the temperature range of 500-570°С and atmospheric pressure on a fixed layer. Liquid and gaseous reaction products were analyzed by gas chromatography; regeneration of the catalyst was carried out with a steam-air mixture until total absence of CO2 in the contact gases. To evaluate the structure and texture of the obtained catalysts, the methods of Mössbauer spectroscopy, X-Ray diffractometry analysis, and elemental analysis using scanning electron microscopy were used. As results, zeolite modification allowed doubling the activity of the catalysts and increasing the selectivity by 23.8-44.8%. The group compositions of olefins, alkanes and gaseous products were detected. Iron form under α-Fe2O3, ε-FeOOH and γ-FeOOH was present. The modified and blank form of catalysts under 1N hydrochloric acid solution washing phase content was detected; partial destruction of the crystalline carcass of clinoptilolite was observed.

MODEL AND METHOD OF CONTROLLED PYROLYSIS OF ORGANIC SUBSTANCES OF VARIABLE COMPOSITION

2021 ◽  
Vol 1 ◽  
pp. 134
Author(s):  
Konstantin V. Beglov ◽  
◽  
Alexander I. Brunetkin ◽  
Maxim M. Maximov ◽  
Elena O. Ulitskaya ◽  
...  
Keyword(s):  
Water Vapor ◽  
Calorific Value ◽  
Variable Composition ◽  
Simultaneous Increase ◽  
Organic Substances ◽  
Reaction Products ◽  
Gaseous Reaction ◽  
Energy Value ◽  
Gaseous Products ◽  
Gasification Process

The issues of organization of the process of slow pyrolysis of organic substances, in the general case of unknown and variable composition, are considered. The relevance of the work is determined by considering the possibility of using various organic waste (domestic, agricultural, industrial) without their preliminary sorting and drying to obtain secondary energy resources of a known (controlled) composition. The novelty of the work is due to the development of a model for the method of controlled pyrolysis or gasification of organic substances with a minimum amount of solid residues at a maximum calorific value of the resulting mixture of combustible gases. A process based on filtration combustion in superadiabatic mode is considered. In existing devices, when this mode is implemented, a counter flow of the feedstock and reaction products is organized. As a result, a part of the water vapor generated at the drying stage is part of the mixture of reaction products and, accordingly, reduce their energy value. The scheme of the process proposed for consideration is based on the organization of the associated flow of feedstock and reaction products. As a result, the resulting carbon dioxide and water vapor are used as additional oxidizing agents. As a result, the carbonaceous residue decreases with a simultaneous increase in the composition of the mixture of gaseous products of carbon monoxide and hydrogen. A scheme for real-time monitoring of the composition of the feedstock during pyrolysis (gasification) is proposed. Knowledge of the composition makes it possible to control the process of its processing in order to: a) organize the optimal gasification process in terms of maximizing the amount and energy value of the mixture of gaseous reaction products; b) control the consumption of the processed feedstock in order to produce the required amount of product gas at any given time.

Kinetics of the catalytic hydrodesulphurization reaction system; hydrogenolysis of thiophene

1980 ◽  
Vol 45 (10) ◽  
pp. 2728-2741 ◽  
Author(s):  
Pavel Fott ◽  
Petr Schneider
Keyword(s):  
Atmospheric Pressure ◽  
Active Sites ◽  
Flow Reactor ◽  
Kinetic Equations ◽  
Reaction System ◽  
Reaction Products ◽  
Molybdenum Catalyst ◽  
Cobalt Molybdenum Catalyst ◽  
Kinetics Of ◽  
Reaction Schemes

Kinetics have been studied of the reaction system taking place during the reaction of thiophene on the cobalt-molybdenum catalyst in a gradientless circulation flow reactor at 360 °C and atmospheric pressure. Butane has been found present in a small amount in the reaction products even at very low conversion. In view of this, consecutive and parallel-consecutive (triangular) reaction schemes have been proposed. In the former scheme the appearance of butane is accounted for by rate of desorption of butene being comparable with the rate of its hydrogenation. According to the latter scheme part of the butane originates from thiophene via a different route than through hydrogenation of butene. Analysis of the kinetic data has revealed that the reaction of thiophene should be considered to take place on other active sites than that of butene. Kinetic equations derived on this assumption for the consecutive and the triangular reaction schemes correlate experimental data with acceptable accuracy.

scholarly journals First Report on the Geologic Occurrence of Natural Na–A Zeolite and Associated Minerals in Cretaceous Mudstones of the Paja Formation of Vélez (Santander), Colombia

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 218
Author(s):  
Carlos Alberto Ríos-Reyes ◽  
German Alfonso Reyes-Mendoza ◽  
José Antonio Henao-Martínez ◽  
Craig Williams ◽  
Alan Dyer
Keyword(s):  
Natural Zeolite ◽  
Scanning Electron Micrographs ◽  
Total Sulfur ◽  
Zeolite A ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mineral Phases ◽  
The World ◽  
Porosity And Permeability ◽  
First Time

This study reports for the first time the geologic occurrence of natural zeolite A and associated minerals in mudstones from the Cretaceous Paja Formation in the urban area of the municipality of Vélez (Santander), Colombia. These rocks are mainly composed of quartz, muscovite, pyrophyllite, kaolinite and chlorite group minerals, framboidal and cubic pyrite, as well as marcasite, with minor feldspar, sulphates, and phosphates. Total organic carbon (TOC), total sulfur (TS), and millimeter fragments of algae are high, whereas few centimeters and not biodiverse small ammonite fossils, and other allochemical components are subordinated. Na–A zeolite and associated mineral phases as sodalite occur just beside the interparticle micropores (honeycomb from framboidal, cube molds, and amorphous cavities). It is facilitated by petrophysical properties alterations, due to processes of high diagenesis, temperatures up to 80–100 °C, with weathering contributions, which increase the porosity and permeability, as well as the transmissivity (fluid flow), allowing the geochemistry remobilization and/or recrystallization of pre-existing silica, muscovite, kaolinite minerals group, salts, carbonates, oxides and peroxides. X-ray diffraction analyses reveal the mineral composition of the mudstones and scanning electron micrographs show the typical cubic morphology of Na–A zeolite of approximately 0.45 mμ in particle size. Our data show that the sequence of the transformation of phases is: Poorly crystalline aluminosilicate → sodalite → Na–A zeolite. A literature review shows that this is an unusual example of the occurrence of natural zeolites in sedimentary marine rocks recognized around the world.

scholarly journals Combined Influence of Low-Grade Metakaolins and Natural Zeolite on Compressive Strength and Heavy Metal Adsorption of Geopolymers

Minerals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 486
Author(s):  
Alcina Johnson Sudagar ◽  
Slávka Andrejkovičová ◽  
Fernando Rocha ◽  
Carla Patinha ◽  
Maria R. Soares ◽  
...  
Keyword(s):  
Heavy Metals ◽  
Heavy Metal ◽  
Compressive Strength ◽  
Natural Zeolite ◽  
Metal Adsorption ◽  
Low Grade ◽  
Heavy Metal Adsorption ◽  
Adsorption Model ◽  
X Ray ◽  
Adsorption Capacities

Metakaolins (MKs) prepared from low-grade kaolins located in the Alvarães (A) and Barqueiros (B) regions of Portugal were used as the aluminosilicate source to compare their effect on the compressive strength and heavy metal adsorption of geopolymers. Natural zeolite, an inexpensive, efficient adsorbent, was used as an additive in formulations to enhance geopolymers’ adsorption capacities and reduce MK utilization’s environmental footprint. Geopolymers were synthesized with the replacement of MK by zeolite up to 75 wt.% (A25, B25—25% MK 75% zeolite; A50, B50—50% MK 50% zeolite; A75, B75—75% MK 25% zeolite; A100, B100—100% MK). The molar ratios of SiO2/Al2O3 and Na2O/Al2O3 were kept at 1 to reduce the sodium silicate and sodium hydroxide environmental impact. Geopolymers’ crystallography was identified using X-ray diffraction analysis. The surface morphology was observed by scanning electron microscopy to understand the effect of zeolite incorporation. Chemical analysis using X-ray fluorescence spectroscopy and energy dispersive X-ray spectroscopy yielded information about the geopolymers’ Si/Al ratio. Compressive strength values of geopolymers obtained after 1, 14, and 28 days of curing indicate high strengths of geopolymers with 100% MK (A100—15.4 MPa; B100—32.46 MPa). Therefore, zeolite did not aid in the improvement of the compressive strength of both MK-based geopolymers. The heavy metal (Cd2+, Cr3+, Cu2+, Pb2+, and Zn2+) adsorption tests exhibit relatively higher adsorption capacities of Barqueiros MK-based geopolymers for all the heavy metals except Cd2+. Moreover, zeolite positively influenced divalent cations’ adsorption on the geopolymers produced from Barqueiros MK as B75 exhibits the highest adsorption capacities, but such an influence is not observed for Alvarães MK-based geopolymers. The general trend of adsorption of the heavy metals of both MK-based geopolymers is Pb2+ > Cd2+ > Cu2+ > Zn2+ > Cr3+ when fitted by the Langmuir isotherm adsorption model. The MK and zeolite characteristics influence geopolymers’ structure, strength, and adsorption capacities.

scholarly journals Preparation and Characterization of the Sulfur-Impregnated Natural Zeolite Clinoptilolite for Hg(II) Removal from Aqueous Solutions

Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 217
Author(s):  
Marin Ugrina ◽  
Martin Gaberšek ◽  
Aleksandra Daković ◽  
Ivona Nuić
Keyword(s):  
Chemical Modification ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Natural Zeolite ◽  
Contact Time ◽  
Liquid Ratio ◽  
X Ray ◽  
Solid Liquid

Sulfur-impregnated zeolite has been obtained from the natural zeolite clinoptilolite by chemical modification with Na2S at 150 °C. The purpose of zeolite impregnation was to enhance the sorption of Hg(II) from aqueous solutions. Chemical analysis, acid and basic properties determined by Bohem’s method, chemical behavior at different pHo values, zeta potential, cation-exchange capacity (CEC), specific surface area, X-ray powder diffraction (XRPD), scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetry with derivative thermogravimetry (TG-DTG) were used for detailed comparative mineralogical and physico-chemical characterization of natural and sulfur-impregnated zeolites. Results revealed that the surface of the natural zeolite was successfully impregnated with sulfur species in the form of FeS and CaS. Chemical modification caused an increase in basicity and the net negative surface charge due to an increase in oxygen-containing functional groups as well as a decrease in specific surface area and crystallinity due to the formation of sulfur-containing clusters at the zeolite surface. The sorption of Hg(II) species onto the sulfur-impregnated zeolite was affected by the pH, solid/liquid ratio, initial Hg(II) concentration, and contact time. The optimal sorption conditions were determined as pH 2, a solid/liquid ratio of 10 g/L, and a contact time of 800 min. The maximum obtained sorption capacity of the sulfur-impregnated zeolite toward Hg(II) was 1.02 mmol/g. The sorption mechanism of Hg(II) onto the sulfur-impregnated zeolite involves electrostatic attraction, ion exchange, and surface complexation, accompanied by co-precipitation of Hg(II) in the form of HgS. It was found that sulfur-impregnation enhanced the sorption of Hg(II) by 3.6 times compared to the natural zeolite. The leaching test indicated the retention of Hg(II) in the zeolite structure over a wide pH range, making this sulfur-impregnated sorbent a promising material for the remediation of a mercury-polluted environment.

scholarly journals Biodiesel Production on Monometallic Pt, Pd, Ru, and Ag Catalysts Supported on Natural Zeolite

Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 48
Author(s):  
Pawel Mierczynski ◽  
Magdalena Mosińska ◽  
Lukasz Szkudlarek ◽  
Karolina Chalupka ◽  
Misa Tatsuzawa ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Natural Zeolite ◽  
Noble Metals ◽  
Methyl Esters ◽  
Physicochemical Characteristics ◽  
Biodiesel Production ◽  
X Ray Diffraction ◽  
X Ray ◽  
Yield Values ◽  
Temperature Programmed

Biodiesel production from rapeseed oil and methanol via transesterification reaction facilitated by various monometallic catalyst supported on natural zeolite (NZ) was investigated. The physicochemical characteristics of the synthesized catalysts were studied by X-ray diffraction (XRD), Brunauer–Emmett–Teller method (BET), temperature-programmed-reduction in hydrogen (H2-TPR), temperature-programmed-desorption of ammonia (NH3-TPD), Scanning Electron Microscope equipped with EDX detector (SEM-EDS), and X-ray photoelectron spectroscopy (XPS) methods. The highest activity and methyl ester yields were obtained for the Pt/NZ catalyst. This catalyst showed the highest triglycerides conversion of 98.9% and fatty acids methyl esters yields of 94.6%. The activity results also confirmed the high activity of the carrier material (NZ) itself in the investigated reaction. Support material exhibited 90.5% of TG conversion and the Fatty Acid Methyl Esters yield (FAME) of 67.2%. Introduction of noble metals improves the TG conversion and FAME yield values. Increasing of the metal loading from 0.5 to 2 wt.% improves the reactivity properties of the investigated catalysts.

scholarly journals Observations of X-rays from Laboratory Sparks in Air at Atmospheric Pressure under Negative Switching Impulse Voltages

Atmosphere ◽  
2019 ◽  
Vol 10 (4) ◽  
pp. 169 ◽  
Author(s):  
Mahbubur Rahman ◽  
Pasan Hettiarachchi ◽  
Vernon Cooray ◽  
Joseph Dwyer ◽  
Vladimir Rakov ◽  
...  
Keyword(s):  
Rise Time ◽  
Atmospheric Pressure ◽  
Opposite Polarity ◽  
X Rays ◽  
X Ray ◽  
Impulse Voltage ◽  
First Time ◽  
Switching Impulses ◽  
Low Rate

We present observations of X-rays from laboratory sparks created in the air at atmospheric pressure by applying an impulse voltage with long (250 µs) rise-time. X-ray production in 35 and 46 cm gaps for three different electrode configurations was studied. The results demonstrate, for the first time, the production of X-rays in gaps subjected to switching impulses. The low rate of rise of the voltage in switching impulses does not significantly reduce the production of X-rays. Additionally, the timing of the X-ray occurrence suggests the possibility that the mechanism of X-ray production by sparks is related to the collision of streamers of opposite polarity.

scholarly journals Joining of SiO2 glass and 316L stainless steel using Bi–Ag-based active solders

2020 ◽  
Vol 56 (4) ◽  
pp. 3444-3454
Author(s):  
Felix Weber ◽  
Markus Rettenmayr
Keyword(s):  
Stainless Steel ◽  
Cross Sections ◽  
316L Stainless Steel ◽  
Dissimilar Materials ◽  
Intermetallic Phases ◽  
Reaction Products ◽  
Cast State ◽  
Metallic Component ◽  
X Ray ◽  
Solder Interface

Abstract Active brazing is a commonly used method for joining dissimilar materials with at least one non-metallic component. In the present study, joining of SiO2 glass to 316L stainless steel was performed utilizing Bi–Ag-based solders. Ti up to a concentration of 4 and Mg up to 1 wt.% were added as active elements. Microstructures of the solder alloys in the as-cast state and of cross sections of the joined compounds were analysed using scanning electron microscopy and energy-dispersive X-ray spectroscopy. In the as-cast state of the solder, Ti is found in Bi–Ti intermetallic phases; Mg is partially dissolved in the fcc-(Ag) phase and additionally contained in a ternary Ag-Bi-Mg phase. After soldering, a tight joint was generated using several alloy compositions. Ti leads to the formation of reaction products at the steel/solder and glass/solder interfaces, and Mg is exclusively accumulated at the glass/solder interface.

Microtexture of shock reaction products of niobium and silica mixtures

1999 ◽  
Vol 14 (7) ◽  
pp. 3169-3174 ◽  
Author(s):  
Reiko Murao ◽  
Masae Kikuchi ◽  
Kiyoto Fukuoka ◽  
Eiji Aoyagi ◽  
Toshiyuki Atou ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Electron Microscope ◽  
Shock Compression ◽  
Pressure Range ◽  
Reaction Products ◽  
Small Particles ◽  
Powder Mixtures ◽  
X Ray ◽  
Transmission Electron

Shock compression experiments on powder mixtures of niobium metal and quartz were conducted for the pressure range of 30–40 GPa by a 25-mm single-stage propellant gun. Chemical reaction occurred above 35 GPa, and products were found to be mainly so-called “Cu3Au-type” Nb3Si, which contained a small amount of oxygen. Microtextures of the specimen were examined by scanning and transmission electron microscopy. A field-emission transmission electron microscope was used for energy-dispersive x-ray analysis of microtextures in small particles found in the SiO2 matrix, and various species with different Nb/Si ratio and oxygen content were shown to be produced through the nonequilibrium process of shock compression.

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