Investigating the properties and performance of 3A molecular sieves as an adsorbent to prevent coke formation in olefin dehydration process

Author(s):  
Zoya Moslempour ◽  
Sepehr Sadighi ◽  
Ali Dashti ◽  
Ali Ahmadpour

Abstract To study the affinity of 3A aluminosilicate adsorbents to prevent oligomerization of olefin molecules and forming green oil, physical and chemical properties of 3A molecular sieves are measured by using characterization techniques such as temperature-programmed desorption (TPD), nitrogen (N2) and water adsorptions, X-ray diffraction (XRD), X-ray fluorescence (XRF), crushing strength, and carbon dioxide (CO2) adsorption. Moreover, coke formation affinities of the understudy adsorbents are evaluated in a bench-scale system using 1-butene and 1,3-butadiene at temperatures of 220 and 260 °C, and outcomes are validated against the actual data gathered from an industrial scale olefin dehydration plant. Results confirm that the type of binder and the amount of ion exchange affect the performance of a 3A molecular sieve nominated for dehydrating olefinic streams. The binder with the least amount of acidity is preferred, and at least 35% of Na ions of the 4A zeolite should be exchanged with K ions to make it applicable for synthesizing an appropriate 3A molecular sieve. Furthermore, to control the oligomerization and inhibit green oil formation, the CO2 adsorption and acidity of Trisiv shape molecular sieves with the sizes of 1/4 inch should be less than 0.5 wt % and 1.7 mmol NH3/g, respectively. For extrudate shape with the sizes of 1/16 inch CO2 adsorption and acidity should be less than 0.2 wt % and 2.2 mmol NH3/g, respectively.

Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 580
Author(s):  
Kai Zhang ◽  
Yuze Bai ◽  
Zhijun Gong ◽  
Zengwu Zhao ◽  
Baowei Li ◽  
...  

Acid leaching and alkali roasting were used to remove impurities such as Ca and Si in Baiyun Obo rare earth concentrate. The effects of acid–base treatment on the physical and chemical properties of the samples were analyzed by scanning electron microscopy, X-ray diffraction, Brunauer–Emmett–Teller characterization, X-ray photoelectron spectroscopy, H2-temperature-programmed reduction, NH3-temperature-programmed desorption (TPD), and NO-TPD. Results showed that the content of Ce7O12 in the rare earth concentrates increased and the dispersion was uniform. The grains became smaller, the specific surface area of rare earth concentrates increased, and the active sites were more exposed. Ce coexisted in the form of Ce3+ and Ce4+, whereas Fe coexisted in the form of Fe3+ and Fe2+. The content of Fe3+ was increased. The acid–base-treated rare earth concentrates had a denitration efficiency of 87.4% at a reaction temperature of 400 °C.


2010 ◽  
Vol 64 (1) ◽  
Author(s):  
Yunfei Bi ◽  
Shuangqin Zeng ◽  
Dadong Li ◽  
Hong Nie

AbstractAmmonium dioxothiotungstate was synthesized using different tungsten sources and characterized in detail by powder X-ray diffraction, energy dispersive X-ray spectrometry, transmission electron microscopy, nitrogen adsorption, and temperature-programmed sulfidation. It was found that tungsten oxide nanobelts are superior to ammonium metatungstate as tungsten source for the synthesis of ammonium dioxothiotungstate due to a time-consuming aging step being excluded from the synthesis route. Moreover, detailed characteristic data reveal that, when tungsten oxide nanobelts are used, the physical and chemical properties of the resulting ammonium dioxothiotungstate including particles size, specific surface area, and sulfidation pattern were improved. Also, the hydrodesulfurization measurements showed higher catalytic activity and balanced selectivity of the resulting ammonium dioxothiotungstate.


2019 ◽  
Vol 17 (1) ◽  
pp. 1459-1465
Author(s):  
Xuedong Feng ◽  
Jing Yi ◽  
Peng Luo

AbstractWith the purpose of studying the influence of NO/O2 on the NOx storage activity, a Pt-Ba-Ce/γ-Al2O3 catalyst was synthesized by an acid-aided sol-gel method. The physical and chemical properties of the catalyst were characterized by X-ray diffraction (XRD) and Transmission Electron Microscope (TEM) methods. The results showed that the composition of the catalyst was well-crystallized and the crystalline size of CeO2 (111) was about 5.7 nm. The mechanism of NO and NO2 storage and NOx temperature programmed desorption (NO-TPD) experiments were investigated to evaluate the NOx storage capacity of the catalyst. Pt-Ba-Ce/γ-Al2O3 catalyst presented the supreme NOx storage performance at 350℃, and the maximum value reached to 668.8 μmol / gcat. Compared with O2-free condition, NO oxidation to NO2 by O2 had a beneficial effect on the storage performance of NOx. NO-TPD test results showed that the NOx species stored on the catalyst surface still kept relatively stable even below 350℃.


1987 ◽  
Vol 113 ◽  
Author(s):  
Scott Schlorholtz ◽  
Ken Bergeson ◽  
Turgut Demirel

ABSTRACTThe physical and chemical properties of fly ash produced at Ottumwa Generating Station have been monitored since April, 1985. The fly ash is produced from burning a low sulfur, sub-bituminous coal obtained from the Powder River Basin near Gillette, Wyoming. One-hundred and sixty samples of fly ash were obtained during the two year period. All of the samples were subjected to physical testing as specified by ASTM C 311. About one-hundred of the samples were also subjected to a series of tests designed to monitor the self-cementing properties of the fly ash. Many of the fly ash samples were subjected to x-ray diffraction and fluorescence analysis to define the mineralogical and chemical composition of the bulk fly ash as a function of sampling date. Hydration products in selected hardened fly ash pastes, were studied by x-ray diffraction and scanning electron microscopy. The studies indicated that power plant operating conditions influenced the compressive strength of the fly ash paste specimens. Mineralogical and morphological studies of the fly ash pastes indicated that stratlingite formation occurred in the highstrength specimens, while ettringite was the major hydration product evident in the low-strength specimens.


Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 436
Author(s):  
Denis Leybo ◽  
Dmitry Arkhipov ◽  
Konstantin Firestein ◽  
Denis Kuznetsov

Chemical and morphological transformations during Ni2Mo3N synthesis were studied in this work. Nitride samples were synthesized from oxide precursors in H2/N2 flow and were analyzed by thermogravimetry, X-ray diffraction analysis, scanning electron microscopy, and energy dispersive X-ray spectroscopy methods. In addition, physical and chemical adsorption properties were studied using low-temperature N2 physisorption and NH3 temperature-programmed desorption. It was shown that nitride formation proceeds through a sequence of phase transformations: NiMoO4 + MoO3 → Ni + NiMo + MoO2 → Ni + NiMo + Mo2N → Ni2Mo3N. The weight changes that were calculated from the proposed reactions were in agreement with the experimental data from thermogravimetry. The morphology of the powder changed from platelets and spheres for the oxide sample, to aggregates of needle-like particles for the intermediate product, to porous particles with an extended surface area for the nitride final product. The obtained results should prove useful for subsequent Ni2Mo3N based catalysts production process optimization.


2019 ◽  
Vol 942 ◽  
pp. 40-49
Author(s):  
Yulia Murashkina ◽  
Olga B. Nazarenko

Natural zeolite of Shivirtui deposit (Russia) was modified with nanofibers of aluminum oxyhydroxide AlOOH. Aluminum oxyhydroxide nanofibers were produced at the heating and oxidation of aluminum powder with water. The properties of modified zeolite were investigated by means of X-ray diffraction, transmission electronic microscopy, scanning electronic microscopy, low-temperature nitrogen adsorption, thermal analysis, and Fourier transform infrared spectroscopy. It was found that water content in the modified sample of zeolite was about 15 %. Based on the study of the physical and chemical properties, shivirtui zeolite modified with nanofibers of aluminum oxyhydroxide can be proposed for use as a flame-retardant additive to polymers.


2007 ◽  
Vol 361-363 ◽  
pp. 463-466
Author(s):  
T. Lin ◽  
S.M. Zhang ◽  
J. Li ◽  
L. Zhang ◽  
Y.H. Liu ◽  
...  

The composite scaffolds with nine different ratios of nano-HA and ß-TCP content were fabricated by using lyophilization method. Their microscopy, physical and chemical properties were investigated by using scanning electron microscopy (SEM), X-ray diffraction (XRD), and fourier transformed infrared (FTIR) spectroscopy. MTT test was applied to quantitatively assess the number of viable cells attached and grown on the scaffolds. And the result showed that the amount of cells on the scaffold containing 30% by mass of nano-HA was significantly higher than the other samples.


2014 ◽  
Vol 979 ◽  
pp. 440-443
Author(s):  
W. Siriprom ◽  
K. Teanchai ◽  
S. Kongsriprapan ◽  
J. Kaewkhao ◽  
N. Sangwaranatee

The chemical and physical properties of topsoil and subsoil which collected from the cassava cropping area in Chonburi Province have been investigated. The characterization of both soil sample were used X-Ray Diffraction (XRD), Energy Dispersive X-Ray Fluorescence (EDXRF) while FTIR used to confirmed the formation of intermolecular bonding and Thermo-Gravimetric Analysis (TGA) used for investigated the crystalline. It was found that, the XRD pattern indicated quartz phase. The chemical composition by XRF reported that the soils samples consist of Si, Al, Ca, Fe, K, Mn, Ti, Cr, Zn, Ag and Cu. and TGA results, noticed that the removal of moisture and organics material.


2016 ◽  
Vol 14 (5) ◽  
pp. 945-954 ◽  
Author(s):  
Anamol Tripathi ◽  
Kajornsak Faungnawakij ◽  
Apirat Laobuthee ◽  
Suttichai Assabumrungrat ◽  
Navadol Laosiripojna

Abstract In the present work, the catalytic conversion of ethanol to 1,3-butadiene (1,3-BD) was studied over monometallic of Cu and Ag, and bimetallic Cu-Ag supported on MgO-SiO2 (with MgO/SiO2 ratio of 2.0) under the temperature range from 250 to 325 °C. All catalysts were prepared by 4 different techniques including (i) conventional impregnation, (ii) microwave-assisted method, (iii) polyvinyl alcohol/sodium borohydride (PVA/NaBH4) assisted method, and (iv) benzoxaxine-assisted method to elucidate the effect of catalyst preparation method on their catalytic performance. All fresh and spent catalysts were also characterized by X-ray diffraction (XRD), N2 adsorption and Temperature-programmed reduction (TPR) techniques to understand the relation between their physical/chemical properties and catalytic performance. From the reaction test, it was found that 5 %Ag/MgO-SiO2 showed greater activity towards 1,3-BD production than 5 %Cu/MgO-SiO2; nevertheless, higher deactivation after 6 h of operation was observed from 5 %Ag/MgO-SiO2. Importantly, this study revealed that bimetallic 2.5 %Cu-2.5 %Ag/MgO-SiO2 enhanced significantly higher activity and stability towards the reaction than monometallic catalysts. In addition, 2.5 %Cu-2.5 %Ag/MgO-SiO2 prepared by benzoxaxine-assisted method enhanced significantly higher reaction activity and stability than other preparation techniques, from which 1,3-BD yield of 46.40 % after 6 h of operation can be achieved. From the characterization, the good activity of this catalyst is mainly due to the dispersion improvement of metal over MgO-SiO2 support.


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