Preparation and Catalytic Performance of Ti(SO4)2/γ-Al2O3 Catalysts for Oligomerization of 1-Butene

2013 ◽  
Vol 634-638 ◽  
pp. 696-700
Author(s):  
Lin Jiu Xiao ◽  
Peng Li ◽  
Yong Gang Sheng

A series of Ti(SO4)2/γ-Al2O3 catalysts were prepared by impregnation method and the catalytic performance of these catalysts in 1-butene oligomerization was investigated. The heat treatment temperature played great influences on the catalytic performance of these catalysts in the oligomerization. 90.1 wt.% conversion of 1-butene and 92.2 wt.% selectivity of dimers were obtained on Ti(SO4)2/γ-Al2O3(450) catalyst at 80 °C, 1.0 Mpa and LHSV=0.6 h−1. The heat treatment temperature determined the crystallinity of TiOSO4 and specific surface area of these catalysts, which affected the catalytic performance of these catalysts in 1-butene oligomerization. In addition, the physicochemical properties of these catalysts were comparatively characterized by powder X-ray diffraction (XRD), N2 isothermal adsorption-desorption techniques.

Coatings ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 858
Author(s):  
Shenglin Liu ◽  
Yongsheng Zhu ◽  
Xinyue Lai ◽  
Xueping Zheng ◽  
Runnan Jia ◽  
...  

Fe-based amorphous/nanocrystalline coatings with smooth, compact interior structure and low porosity were fabricated via supersonic plasma spraying (SPS). The coatings showed outstanding corrosion resistance in a 3.5% NaCl solution at room temperature. In order to analyze the effect of annealing treatment on the microstructure, corrosion resistance and microhardness, the as-sprayed coating was annealed for 1 h under different temperatures such as 350, 450, 550 and 650 °C, respectively. The results showed that the number of oxides and cracks in the coatings presented an obvious increase with increasing annealing temperature, and the corrosion resistance of the coatings showed an obvious reduction. However, the microhardness of coatings showed an important increase. The microhardness of the coating could reach 1018 HV when the heat treatment temperature reached 650 °C. The X-ray diffraction (XRD) results showed that there appeared a number of crystalline phases in the coating when the heat treatment temperature was at 650 °C. The crystalline phases led to the increase of the microhardness.


2012 ◽  
Vol 624 ◽  
pp. 134-137 ◽  
Author(s):  
Ping Zhai ◽  
Xiao Feng Duan ◽  
Da Qian Chen ◽  
Chong Hai Wang

In this paper, β-eucryptite glass ceramics were synthesized by using solid reaction method. Phase constitution, structure and properties of the material were studied by X-ray diffraction (XRD) and differential thermal analysis (DTA). Furthermore, the effects of heat treatment temperature and preservation time on the thermal expansion coefficient were also analyzed. The results showed that the crystallization temperature of β-eucryptite glass ceramics was in the range of 810-860 °C and the content was more than 90%. With the increase of heat treatment temperature, the material expansion coefficient decreased.


1994 ◽  
Vol 346 ◽  
Author(s):  
A.W. Reid ◽  
B. Rand ◽  
R.J.P. Emsley

ABSTRACTIt is shown that ceramics derived from polycarbosilane polymers may develop an open nanoporous network after heat treatment to a temperatures between 1300 and 1550°C in argon. The resulting SiC-based ceramics were characterised by N2 gas adsorption analysis and X-ray diffraction. The apparent surface area, and pore volume increase with increasing heat treatment temperature, reaching values of 170 m2g-1 and 0.12 cm3-1 respectively. The pore network develops as the SiC crystals grow and as carbon is ejected from the structure. It is thought that the porosity may reside within the carbon phase, but this remains to be confirmed.


1991 ◽  
Vol 246 ◽  
Author(s):  
Ming-Yuan Kao ◽  
Sepehr Fariabi ◽  
Paul E. Thoma ◽  
Husnu Ozkan ◽  
Louis Cartz

AbstractThe reversible transformations between the Austenite (A) and Martensite (M) phases of NITI shape memory wires having a 78°C austenlte finish temperature (950°C annealed) were studied In the cold work and heat treatment ranges between 14 to 62% and 400 to 525°C respectively. The ranges of peak Transformation Temperatures (TI), determined by Differential Scanning Calorimetry (DSC) at a 10°C/min rate, were found to be 56 to 75°C, -28 to 33°C, and 38 to 52°C for the respective high temperature A, low temperature M, and the Intermediate Rhombohedral (R) phases. The degree of cold work and heat treatment had significant effects on the TT of NITI wires. The peak TT of A and M decreases with Increasing cold work. Except for the 14% cold worked wires, the peak TT Increases with Increasing heat treatment temperature for M, and Increases with Increasing heat treatment temperature for A for temperatures higher than 450°C. The peak IT of R Increases with Increasing cold work and decreasing heat treat temperature.Using MoKα radiation, transmission x-ray diffraction analysis was utilized to determine the phases at room temperature on wires thinned down to 0.05 to 0.01 mm in diameter. The diffraction patterns of body-centered cubic austenite (132) and monodlinic martenslte (B19) for NITi were both Identified. In addition, extra diffraction lines observed for various samples were tentatively assigned to M and the Intermediate R-phase. Depending on the thermal history and the processing conditions, the NITI wires consist of either a pure M, a mixture of A and R, or a mixture of A, R, and M at room temperature.


Author(s):  
Parisa Sadeghpour ◽  
Mohammad Haghighi ◽  
Mehrdad Esmaeili

Aim and Objective: Effect of two different modification methods for introducing Ni into ZSM-5 framework was investigated under high temperature synthesis conditions. The nickel successfully introduced into the MFI structures at different crystallization conditions to enhance the physicochemical properties and catalytic performance. Materials and Methods: A series of impregnated Ni/ZSM-5 and isomorphous substituted NiZSM-5 nanostructure catalysts were prepared hydrothermally at different high temperatures and within short times. X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), Energy dispersive X-ray (EDX), Brunner, Emmett and Teller-Barrett, Joyner and Halenda (BET-BJH), Fourier transform infrared (FTIR) and Temperature-programmed desorption of ammonia (TPDNH3) were applied to investigate the physicochemical properties. Results: Although all the catalysts showed pure silica MFI–type nanosheets and coffin-like morphology, using the isomorphous substitution for Ni incorporation into the ZSM-5 framework led to the formation of materials with lower crystallinity, higher pore volume and stronger acidity compared to using impregnation method. Moreover, it was found that raising the hydrothermal temperature increased the crystallinity and enhanced more uniform incorporation of Ni atoms in the crystalline structure of catalysts. TPD-NH3 analysis demonstrated that high crystallization temperature and short crystallization time of NiZSM-5(350-0.5) resulted in fewer weak acid sites and medium acid strength. The MTO catalytic performance was tested in a fixed bed reactor at 460ºC and GHSV=10500 cm3 /gcat.h. A slightly different reaction pathway was proposed for the production of light olefins over impregnated Ni/ZSM-5 catalysts based on the role of NiO species. The enhanced methanol conversion for isomorphous substituted NiZSM-5 catalysts could be related to the most accessible active sites located inside the pores. Conclusion: The impregnated Ni/ZSM-5 catalyst prepared at low hydrothermal temperature showed the best catalytic performance, while the isomorphous substituted NiZSM-5 prepared at high temperature was found to be the active molecular sieve regarding the stability performance.


MRS Advances ◽  
2018 ◽  
Vol 3 (11) ◽  
pp. 563-567 ◽  
Author(s):  
Quentin Altemose ◽  
Katrina Raichle ◽  
Brittani Schnable ◽  
Casey Schwarz ◽  
Myungkoo Kang ◽  
...  

ABSTRACTTransparent optical ZnO–Bi2O3–B2O3 (ZBB) glass-ceramics were created by the melt quenching technique. In this work, a melt of the glass containing stoichiometric ratios of Zn/Bi/B and As was studied. Differential scanning calorimeter (DSC) measurements was used to measure the thermal behavior. VIS/NIR transmission measurements were used to determine the transmission window. X-ray diffraction (XRD) was used to determine crystal phase. In this study, we explore new techniques and report a detailed study of in-situ XRD of the ZBB composition in order to correlate nucleation temperature, heat treatment temperature, and heat treatment duration with induced crystal phase.


2012 ◽  
Vol 184-185 ◽  
pp. 1175-1180
Author(s):  
Guo Liang Li ◽  
Xiao Hua Jie ◽  
Bi Xue Yang

Amorphous Cr–C alloy coating was prepared by electrodepositing. The microhardness of the coating was tested after annealing from 100°C to 800°C and the crystallization evolution was studied by the analysis of X-ray diffraction (XRD) and differential scanning caborimetry (DSC). The results showed that the crystallization evolution of the coating began at 300°C and finished around 450°C, and intermetallic compound Cr7C3and Cr23C6appeared when heat treatment temperature reached around 600°C. The microhardness, corrosion resistance as well as the adhesion of the coating all increased first with the temperature and then dropped until it attained the proper values. The microhardness reached the maximum of 1610HV0.025at 600°C. While the corrosion resistance and the adhesion force attained the peak value at about 400°C.


2000 ◽  
Vol 663 ◽  
Author(s):  
P. Loiseau ◽  
D. Caurant ◽  
N. Baffier ◽  
C. Fillet

ABSTRACTThe investigations on enhanced reprocessing of nuclear spent fuel, and notably on separating the long-lived minor actinides, such as Am and Cm, from the other fission products have led to the development of highly durable specific matrices such as glass-ceramics for their immobilization. This study deals with the characterization of zirconolite (CaZrTi2O7) based glass-ceramics synthesized by devitrification of an aluminosilicate parent glass. Trivalent actinide ions were simulated by neodymium, which is a paramagnetic local probe. Glass-ceramics with Nd2O3 contents ranging from 0 to 10 weight % were prepared by heat treatment of a parent glass at two different growth temperatures: 1050° and 1200°C. X-ray diffraction (XRD), energy dispersive X-ray analysis (EDX) and electron spin resonance (ESR) measurements clearly indicate that Nd3+ ions are partly incorporated in zirconolite crystals formed in the bulk of the glass-ceramic samples. The amount of neodymium in the crystalline phase was estimated using ESR results and was found to decrease with increasing either heat treatment temperature or total Nd2O3 content.


2010 ◽  
Vol 93-94 ◽  
pp. 22-26 ◽  
Author(s):  
Surachai Artkla ◽  
Won Yong Choi ◽  
Jatuporn Wittayakun

This work compared properties and catalytic performance of two hybrid photocatalysts, TiO2/RH-MCM-41 and TiO2/TEOS-MCM-41 prepared by loading nanoparticles of TiO2 (10 wt.%) on MCM-41 synthesized with rice husk silica and tetraethyl orthosilicate respectively. The supports and catalysts were characterized by X-ray diffraction, N2 adsorption-desorption, transmission electron microscopy and zeta potential. The photocatalytic activities of the TiO2/RH-MCM-41 and TiO2/TEOS-MCM-41 for the degradation of tetramethylammonium (TMA) in aqueous slurry were similar with a complete conversion after irradiation time of 90 min at pH 7.


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