scholarly journals Preparasi katalis nafta hidritreating dengan fasa aktif Ni-Mo pada penyangga lempung berpilar

2018 ◽  
Vol 7 (2) ◽  
pp. 761
Author(s):  
Nino Rinaldi ◽  
S Subagjo ◽  
IGBN Makertihartha ◽  
Hery Haerudin

Research on a subject of the preparation of Ni-Mo catalyst on pillared clay support by wetness impregnation method will be investigated in laboratory. The metal concentration of Mo, which will be treated, is roughly 20 %wt and of Ni is 3 %wt. Due to using MoO3 as the metal active catalyst; therefore the support has to contain a specific surface area more than 210 m2/gr in order to achieve the high dispersion of active metal on the support. Also, the effect of the pH of the Mo impregnation solution to the metal active dispersion and activity for Coker naphtha hydrodesulfurization (HDS) will be studied. Characterization of the catalyst will be conducted by using X-ray Diffraction, FT-Infrared, X-ray fluorescence and nitrogen sorption measurement. It is found that the surface area of the support is generated almost 280 m2/gr by pillarization with the oxide composition of the catalyst was 12%-wt of MoO3 and 1.4%-wt of NiO. NiMo-PILC pH-10 catalyst had higher dispersion of active metal on the support than NiMo-PILC pH-1 catalyst. On NiMo-PILC pH-10 catalyst, there was a substantial part of Mo species in the interlayer space of the Al-pillared lay, probably in interaction with the alumina pillar.  Although, it has to be more detail investigated. From the result of the activity test for Coker naphtha HDS showed that NiMo­ PILC pH-10 catalyst had slightly higher activity than NiMo-PILC pH-1 catalyst. However, the both of catalyst still had not good enough activity if compare with the commercial catalyst.Keywords: Montmorillonite-Pillared Clay, Ni-Mo catalyst, Preparation Abstrak Suatu penelitian mengenai preparasi katalis Ni-Mo pada penyangga lempung berpilar dengan metoda impregnasi basah dirancang dan dilakukan dalam skala laboratorium. Konsentrasi logam Mo yang digunakan sebesar 13%-b MoO3 dan logam Ni 4%-b NiO. Karena fasa aktif katalis yang digunakan adalah MoO3 maka luas permukaan penyangga yang dibutuhkan adalah lebih besar dari 210 m2/gr guna mendapatkan dispersi yang tinggi. Selain itu, dipelajari juga efek pH larutan impregnasi Mo terhadap dispersi fasa aktif dan aktivitas katalis pada reaksi hidrodesulfurisasi coker nafta. Karakterisasi katalis berpenyangga dilakukan dengan menggunakan alat difraksi sinar-x, FT-IR, XRF serta dilakukan pengukuran luas permukaan spesifiknya. Dari penelitian ini, didapatkan luas permukaan penyangga lempung berpilar sebesar 277 m2/gr dengan komposisi okasida katalis NiMo yang dihasilkan adalah 12%-b MoO3 dan 1.4%-b NiO. Katalis NiMo-PILC pH-1O memiliki dispersi logam aktif yang lebih tinggi pada penyangga jika dibandingkan dengan katalis NiMo-PILC pH-1. Selain itu, pada katalis NiMo-PILC pH-10 ditemukan adanya sebagian logam Mo yang masuk kedalam ruang interlayer dari lempung, yang diduga menjadi pilar. Namun hal ini harus diteliti lebih detail. Hasil uji aktivitas katalis pada reaksi HDS coker nafta menunjukan bahwa katalis NiMo-PILC pH-10 memiliki aktivitas yang lebih tinggi jika dibandingkan dengan katalis NiMo-PILC pH-1. Namun aktivitas dari kedua katalis tersebut masih di bawah dari katalis hidrotreating komersial. Kata kunci: Coker Nafta, Katalis Ni-Mo, Lempung Berpilar, Preparasi

2021 ◽  
Vol 11 (1) ◽  
pp. 84-106
Author(s):  
Nada Sadoon Ahmed zeki ◽  
Sattar Jalil Hussein ◽  
Khalifa K. Aoyed ◽  
Saad Kareem Ibrahim ◽  
Ibtissam K. Mehawee

This work deals with the hydrodesulfurization of three types of naphtha feedstocks; mixednaphtha (WN), heavy naphtha (HN) & light naphtha (LN) with a sulfur content of 1642.1,1334.9 & 709 ppm respectively, obtained from Missan refinery using prepared Co-Mo/γ-Al2O3catalyst. The Iraqi white kaolin was used as a starting material for the preparation of γ-Al2O3support, transferring kaolin to meta-kaolin was studied through calcination at differenttemperatures and durations, kaolin structure was investigated using X-Ray diffractiontechniques.High purity 94.83%. Crystalline γ-Al2O3 with a surface area of 129.91 m2/gm, pore volume0.9002 cm3/g was synthesized by extraction of Iraqi kaolin with H2SO4 at different acid to clayweight ratios, acid concentrations & leaching time. Ethanol was used as precipitating agent; theresultant gel was dried and calcined at 70OC, 10 hrs & 900 OC, 2 hrs respectively.The effects of different parameters on the average crystallinity and extraction % ofsynthesized γ-Al2O3 were studied like; acid: clay ratio, sulfuric acid concentration, leachingtime, leaching temperature & kaolin conversion to metakaolin. Characterization of prepared γ-Al2O3 & Co-Mo catalyst were achieved by X-ray diffraction, FTIR-spectra, texture properties& BET surface area, BJH N2 adsorption porosity, AFM, SEM, crush strength & XRF tests. Co-Mo/ γ-Al2O3 catalyst with final loading 5.702 wt% and 21.45 wt% of Co and Mo oxidesrespectively was prepared by impregnation methods.The activity of prepared Co-Mo/γ-Al2O3 catalyst after moulding to be tested forhydrodesulfurization (HDS) of naphtha feedstock W.N, H.N & L.N was performed using apilot hydrotreating unit at petroleum research & development centre, at different operatingconditions. Effects of temperature, LHSV, pressure, time & pore size distribution were studied,the best percentage of sulfur removal is increased with decreasing LHSV to 2 hr-1 as a generaltrend to be 89.71, 99.72, 99.20 % at 310oC for the whole naphtha, heavy naphtha and lightnaphtha feedstocks respectively, at 34 bar pressure and 200/200 cm3/cm3 H2/HC ratio.


2016 ◽  
Vol 1141 ◽  
pp. 190-195
Author(s):  
Hitesh Saravaia ◽  
Hariom Gupta ◽  
Vaibhav Kulshreshtha

Barium Titanate (BaTiO3) nanostructures are synthesized by the molten salt-hydroxide reaction. The crystalline phase and chemical structure of the synthesized material are analyzed using powder x-ray diffraction (XRD) and FT-IR techniques, revealing the tetragonal BaTiO3 crystalline structure. Morphology and thermal stability of the material are characterized using TEM and TG-DTG analysis. BET surface area analysis shows significant active surface available for adsorption and its surface area value is found to be 14.8427 m2 g-1. The maximum adsorption of strontium metal is found to be 56.3 for the 1.2 g L-1 BaTiO3 adsorbent dose which reveals a remarkable separation property of the BaTiO3.


2021 ◽  
Author(s):  
Zohreh Razmara

Abstract A 2D heterometallic copper(II)–sodium(I) complex based on pyridine 2,6-dicarboxylato (dipic2-) formulated as [Cu(μ-dipic)2{Na2(µ-H2O)4}]n. 2nH2O (1) has been synthesized. Thermal stability of complex 1 was studied by thermo gravimetric analysis (TGA) and differential thermal analysis (DTA). Single-crystal X-ray diffraction (SC-XRD) analysis showed that the parallelepiped colorless crystal of complex 1 crystallizes in a monoclinic system with the space group P2/c . A highly dispersed truncated octahedral catalyst formulated as Cu-Na/Al2O3 (CNM) was prepared by thermal decomposition of complex 1. Besides, the reference catalyst of Cu-Na/Al2O3 (CNR) was prepared by impregnation conventional method. The catalysts were examined by FT-IR, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) surface area, and subjected to water-gas shift (WGS) reaction in the temperature range of 150-400 °C. The catalysts showed strong surface structure-activity dependence in WGS reaction. Improved catalytic performance during the water-gas shift reaction was observed for CNM compared to CNR due to its high dispersion, smaller particle size, and higher BET specific surface area.


2010 ◽  
Vol 4 (2) ◽  
pp. 69-73 ◽  
Author(s):  
Marija Milanovic ◽  
Ivan Stijepovic ◽  
Ljubica Nikolic

Titanate structures were synthesized in highly alkaline solution using hydrothermal procedure. As-prepared powders were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). A specific surface area of the powders was measured by BET method. Results confirmed formation of layered trititanates, already after one hour of hydrothermal synthesis. To examine the photocatalytic activity of the as-prepared layered titanates, methylene blue (MB) was employed as a target compound in response to visible light at ambient temperature. It was observed that the specific surface area, size distribution and crystallinity are important factors to get high photocatalytic activity for the decomposition of MB. .


2012 ◽  
Vol 455-456 ◽  
pp. 1053-1059
Author(s):  
Xue Hai Fan ◽  
Guo Min Xiao

Multi-walled carbon nanotubes (MWCNTs), potassium dichromate (K2Cr2O7) and sulphuric acid were used for the preparation of Cr/MWCNT composite by impregnation method. The composites were comprehensively characterized by transmission electron microscopy (TEM),energy dispersive X-ray analysis (EDX), infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and thermal gravity analysis (TGA). Due to its unique electrical and structural properties, this composite was applied to the synthesis of biodiesel (FAME) as a catalyst, showing effectively catalytic performance.


Author(s):  
Eko Supriadi ◽  
Danawati Hadi Prajitno ◽  
Mahfud Mahfud ◽  
Ngatijo Ngatijo ◽  
Rahmat Basuki

Metal doping plays important role in increasing catalytic activity of catalyst materials. In this work, Ca and K were doped to the γ-Al2O3 by dry impregnation method to study the crystallinity, surface area, activation energy, and yield in the coconut oil transesterification reaction. The success of doping was shown in the characterization of Ca/γ-Al2O3 and K/γ-Al2O­3 using X-Ray Diffraction (XRD) which increasing in crystallinity from 62.2% (γ-Al2O3) to 69.3 (K/γ-Al2O3) and 76.0 (Ca/γ-Al2O3). The emerging peak of 2θ characteristics of K (29.70° and 32.65°) and Ca (25.35°, 26.77°, and 27.17°) on the γ-Al2O3 (37.66°, 45.82° and 67.22 °) was also observed. Characterization by the Surface Area Analyzer (SAA) shows that the K/γ-Al2O3 catalyst has a smaller surface area (34.03 m2/g) than Ca/γ-Al2O3 (83.77 m2/g), but a higher pore diameter (66.12 Å) than Ca/γ-Al2O3 (35.22 Å). The K/γ-Al2O­3 catalyst produced greater FAME yield (93.19%) than Ca/γ-Al2O3 (29.76%) at a catalyst concentration of 2.5%, reaction time 150 s, and ultrasonic frequency of 40 kHz. The quality of the FAME catalyzed by K/γ-Al2O­3 fulfills four test parameters: density, kinematic viscosity, flash point, and pour point according to SNI 04-7182-2006 standards.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Hua Chen ◽  
Jianhua Wang ◽  
Huajun Wang ◽  
Fei Yang ◽  
Jia-nan Zhou ◽  
...  

TiO2/stellerite composite photocatalysts were prepared by dispersing TiO2 onto the surface of HCl, NaOH, or NaCl treated stellerite using a sol-gel method. The materials were characterized by scanning electron microscopy (SEM), energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FT-IR), BET surface area analysis, and X-ray diffraction (XRD). HCl and NaCl modification result in the promotion of the pore formation at the stellerite surfaces and induced the microscopic changes, while the surface morphology and structure of the stellerite were almost ruined by NaOH modification. Supported TiO2 calcinated at 200°C presented anatase structure. The photocatalytic degradation activities of TiO2 loaded HCl and NaCl modified stellerite were better than that of natural stellerite, accompanied with increasing specific surface area. On the contrary, NaOH modification induced the loss of photocatalytic ability of composite due to the generation of silicates.


2020 ◽  
Vol 843 ◽  
pp. 116-121
Author(s):  
Tanushree Choudhury

Titania pillared clay membranes exhibit unique charge characteristics which are dependent on the solution pH. Doping of such membranes with precious metal like Pt induces a positive charge on the surface of the membranes, thus increasing its resistance against fouling. X-ray Diffraction (XRD) and Fourier Transform Infra-Red Spectroscopy (FT-IR) confirm the complete intercalation of anatase titania in the interlayer spaces of Montmorillonite in the present work. These membranes efficiently removed 83% of the dye from the real textile effluent in a one filtration cycle.


2020 ◽  
Vol 841 ◽  
pp. 312-316
Author(s):  
Ratu Ulfiati ◽  
Donanta Dhaneswara ◽  
Jaka Fajar Fatriansyah ◽  
Sri Harjanto

The effect of Metakaolinization on the thermal and physicochemical properties of Badau Belitung kaolin is presented. Calcination of Badau Belitung kaolin indicated that kaolin was transformed to metakaolin at temperature above 500°C. The metakaolin was characterized using X-ray Diffraction (XRD), Fourier Transform Infrared (FT-IR) and Brunauer-Emmett-Teller (BET). The XRD diffraction pattern of the metakaolin was highly amorphous as a result of calcination effect on the raw kaolin. The FTIR spectra of the metakaolin produced showed that the material was thermally stable at temperature range of 500–700°C, whereas the specific surface area values of the raw kaolin and the metakaolin formed were increased with increasing calcination temperature from 500°C to 700°C.


Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1027
Author(s):  
Dandan Yang ◽  
Haiyan Wang ◽  
Wenhua Wang ◽  
Sihua Peng ◽  
Xiuzhen Yang ◽  
...  

In this paper, five kinds of transition metal-modified titanium silicalite-1 (M-TS-1) were prepared by an ultrasonic impregnation method. We studied their catalytic performances in the ammoximation of methyl ethyl ketone (MEK). The various M-TS-1 catalysts revealed distinct differences in their MEK ammoximation activity. The nickel-modified TS-1 (Ni-TS-1), especially 3 wt % Ni-TS-1, exhibited a satisfactory conversion of MEK (99%) associated with a high selectivity of methyl ethyl ketoxime (MEKO) (99.3%), which was 6% higher than that of TS-1 under the same conditions. Moreover, the catalyst showed excellent recyclability and the reactivity could be completely recovered after regeneration. The catalysts were characterized by Powder X-ray Diffraction (XRD), Fourier Transformed Infrared Spectra (FT-IR), X-ray photoelectron spectroscopy (XPS), and so on. It was demonstrated that the skeleton structure of TS-1 was basically maintained and the electron environment of the Ti active site was changed after the nickel modification, which can optimize the adsorption capacity and the activation for H2O2. Meanwhile, the surface nickel species reduced the surface acidity of the catalyst, which provided an appropriate pH and inhibited the deep oxidation of oxime.


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