scholarly journals A Comprehensive Study of Coke Deposits on a Pt-Sn/SBA-16 Catalyst during the Dehydrogenation of Propane

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 128
Author(s):  
Jose P. Ruelas-Leyva ◽  
Luis F. Maldonado-Garcia ◽  
Alfonso Talavera-Lopez ◽  
Iván A. Santos-López ◽  
Lorenzo A. Picos-Corrales ◽  
...  

Catalytic propane dehydrogenation is an attractive method to produce propylene while avoiding the issues of its traditional synthesis via naphtha steam cracking of naphtha. In this contribution, a series of Pt-Sn/SBA-16 catalysts were synthesized and evaluated for this purpose. Bimetallic Pt-Sn catalysts were more active than catalysts containing only Pt. The catalyst with the best performance was assessed at different reaction times of 0, 60, 180, and 300 min. The evolution of coke deposits was also studied. Thermogravimetric analysis demonstrated the presence of two types of coke on the catalyst surface at low and high temperature, respectively. Raman results showed an increased coke’s crystal size from 60 to 180 min on stream, and from 180 to 300 min under reaction, Raman suggested a reduction in the crystal size of coke. Also transmission electron microscopy confirmed a more evident agglomeration of metallic particles with reaction times higher than 180 min. These results are consistent with the phenomena called “coke migration” and the cause is often explained by coke movement near the particle to the support; it can also be explained due to sintering of the metallic particle, which we propose as a more suitable explanation.

1993 ◽  
Vol 311 ◽  
Author(s):  
Chih M. Yang ◽  
Harry A. Atwater

ABSTRACTIn this paper we discuss the size-dependent shrinkage rate of nanometer-size Si crystals in amorphous Si thin films during ion irradiation. We obtain shrinkage rate of nanometersize crystals at low temperature under ion irradiation by studying the evolution of the crystal size distribution using transmission electron microscopy. Our results indicate that crystals less than 10 nm in diameter decrease in size faster than larger crystals under ion irradiation. In addition, we fit our data to a capillary model for growth of Si crystals in amorphous Si under ion irradiation.


Polymers ◽  
2018 ◽  
Vol 10 (8) ◽  
pp. 865 ◽  
Author(s):  
Ewa Serwicka ◽  
Małgorzata Zimowska ◽  
Dorota Duraczyńska ◽  
Bogna Napruszewska ◽  
Małgorzata Nattich-Rak ◽  
...  

The effect of synthesis parameters on the physicochemical properties of clay/ polydiallyldimethylammonium (PDDA)/Ru composites and their applicability in hydrogenation of 2-butanone under very mild conditions (room temperature, atmospheric pressure, and aqueous solution) was studied. Three synthetic procedures were employed, differing in the order of addition of components and the stage at which metallic Ru species were generated. The materials were characterized with XRD (X-ray diffraction), XRF (X-ray fluorescence), EDS (energy-dispersive spectroscopy), AFM (atomic force microscopy), TEM/HRTEM (transmission electron microscopy/high resolution transmission electron microscopy), and TG/DSC (thermal gravimetry/differential scanning microscopy techniques. The study revealed that the method of composite preparation affects its structural and thermal properties, and controls the distribution and size of Ru particles. All catalysts are active in hydrogenation of 2-butanone. For best catalytic performance (100% conversion within 30 min) both the size of Ru particles and the load of polymer had to be optimized. Superior catalytic properties were obtained over the composite with intermediate crystal size and intermediate PDDA load, prepared by generation of metallic Ru species in the polymer solution prior to intercalation. This method offers an easy way of controlling the crystal size by modification of Ru/PDDA ratio.


1986 ◽  
Vol 74 ◽  
Author(s):  
Y. Goto ◽  
K. Utsumi ◽  
A. Ushioda ◽  
I. Tsugawa ◽  
N. Koshino

AbstractWritten and erased bits of the In-Sb phase change type optical disk medium were studied using transmission electron microscopy (TEN) and electron probe microanalysis (EPMA). Both the bits were separated into inner and outer areas and were composed of only rhombohedral Sb crystals and zinc blende In50Sb50 crystals. The difference between the two bits were in crystal size and atomic distribution of the inner area. Models of the writing and erasing processes were derived from these observations and the In-Sb phase diagram. With these models, the thicknesses, grain sizes and optical contrasts of the both bits were consistently explained.


2006 ◽  
Vol 21 (4) ◽  
pp. 807-810 ◽  
Author(s):  
C. Angeles-Chavez ◽  
M.A. Cortes-Jácome ◽  
E. Torres-Garcia ◽  
J.A. Toledo-Antonio

Direct evidence of the transformation of WOx species in WO3 nanoclusters on WOx–ZrO2 system was achieved by high-resolution transmission electron microscopy (HRTEM) and Raman spectroscopy on samples obtained by a conventional precipitation method and annealed from 560 to 800 °C. WO3 Nanoclusters with 2-nm crystal size orthorhombic structure were identified on the ZrO2 surface after annealing at 800 °C.


Author(s):  
G. G. Shaw

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.


Author(s):  
R. W. Anderson ◽  
D. L. Senecal

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.


Author(s):  
S. Fujishiro

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.


Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).


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