Isomerization of α-Pinene over Alumina-Pillared Montmorillonite

2013 ◽  
Vol 746 ◽  
pp. 49-52 ◽  
Author(s):  
Peng Quan Yao ◽  
Lin Hua Zhu ◽  
Jin Yang ◽  
Tian Si

In this work, the liquid phase catalytic isomerization of α-pinene over alumina-pillared montmorillonitewas investigated, and the influence of reaction temperature, reaction time and amount of the catalyston the conversion of α-pinenewere discussed systematically, and the optimum reaction conditions forisomerization of α-pineneover alumina-pillared montmorillonitewere obtained. The basal spacing of thealumina-pillared montmorillonite was characterized by X-ray diffraction, and the liquid reactant was separated and identified by gas chromatography. The result showed that alumina-pillared montmorillonite with 1.83nm of basal spacing exhibited a high catalytic activity for the isomerization of α-pinene, and 97.4% conversion of α-pinene was achievedat 373K for 3hwhen the mass ratio of catalyst to α-pinene was 1/10.

2011 ◽  
Vol 189-193 ◽  
pp. 1275-1279
Author(s):  
Ying Wang ◽  
Gao Yang Zhao ◽  
Li Yuan

The crystalline phase and morphology of the products formed during the synthesis of yttrium oxide via the hydrothermal treatment yttrium nitrate were characterized by X-ray diffraction, transmission electron microscopy and scanning electron microscopy. Products with high OH/NO3ratios are formed with the increasing of hydrothermal treatment. The crystalline phases are evolved from Y2(OH)5.14(NO3)0.86•H2O toY4O(OH)9(NO3) and finally Y(OH)3. The hydrothermal reaction conditions play an important role in the synthesis of the microstructures. Results show the particle size and final morphology of samples could be controlled by reaction temperature, reaction time, and OH-concentration. Sheets, hexagonal and needle-like Y2O3powders are obtained with the hydrothermal treatment of yittrium nitrate at 180 oC to 200oC for 2-8 hours at pH 9-13.


2015 ◽  
Vol 50 (1) ◽  
pp. 1-6 ◽  
Author(s):  
ASM A Islam ◽  
T Ferdous ◽  
AK Das ◽  
MM Karim ◽  
SM Masum

The ZnO nanoparticle was prepared by using Zn(NO3)2.6H2O and NaOH under optimum reaction conditions and the prepared nanoparticle was characterized by UV-visible spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), energy dispersion X-ray spectroscopy (EDX) and scanning electron microscopy (SEM). The sunlight irradiated photocatalytic degradation of Direct Brown RN dye was studied using ZnO nanoparticle. The results of this investigation revealed that in the presence of sunlight, catalyst load of 0.5 g?L-1 and time of contact of 40 min, ZnO nanoparticle showed substantial capability of destroying Direct Brown RN dye from solution. An actual leather effluent containing Brown RN as a major constituent along with other dyes and dyeing auxiliaries was treated using ZnO and the reduction in the chemical oxygen demand (COD) of the treated effluent revealed almost complete destruction of the organic molecules along with color removal.Bangladesh J. Sci. Ind. Res. 50(1), 1-6, 2015


2012 ◽  
Vol 557-559 ◽  
pp. 1629-1632
Author(s):  
Xing Shun Cong ◽  
Min Li

A set of pillared montmorillonite (PILM) catalysts were prepared by exchanging Na+ with iron pillars, chromium pillars, complexes pillars of iron and chromium with different proportion, as well as complexes pillar of silica sol and iron and chromium, respectively. X-ray diffraction (XRD), X-ray fluorescence (XRF), thermogravimetry (TG) and differential thermal analysis (DTA) were used to characterize the catalysts. The XRD results reveal that Fe-Cr complexes pillared montmorillonites (Fe/Cr-PILM) have the basal spacing of about 2.04 nm after calcination at 300 °C for 2 h, while sole metal PILM have that of about 1.0 nm; in particular, the basal spacing of silica sol complexes pillared montmorillonite (Fe-Cr-Si-PILM) are expanded up to 4.33 nm. The TG-DTA results show that both Fe-Cr-PILM and Fe-Cr-Si-PILM have high thermal stability up to 640 °C. Catalytic activity of Fe/Cr-Si-PILM in Longkou lignite (LL) and ShengLi coal residue (SCR) liquefaction was studied, which showed that PILM had a good catalytic performance in coal conversion field.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Is Fatimah ◽  
Dwiarso Rubiyanto ◽  
Thorikul Huda

Preparation of sulfated zirconia-pillared montmorillonite was carried out in two steps; zirconia pillarization and sulfation to zirconia-pillared montmorillonite. The prepared materials were characterized by using X-ray diffraction (XRD), measurement of the specific surface area, total pore volume and pore size distribution by the N2adsorption method, scanning electron microscopy-energy dispersive X-ray (SEM-EDX), and surface acidity determination by using pyridine adsorption-FTIR analysis. The activity of the materials as catalysts was evaluated for a microwave-assisted conversion of citronellal. The results showed that the prepared materials had a physicochemical character that promoted high catalytic activity to convert citronellal. From varied Zr content and study of the effect of sulfation on the activity, it was found that Zr content and sulfation increase the surface acidity of the material as shown by the higher total conversion and tendency to produce menthol as a product of the tandem cyclization-hydrogenation mechanism.


2011 ◽  
Vol 71-78 ◽  
pp. 1118-1122
Author(s):  
Hong Shao ◽  
Ning Cao ◽  
Hong Kang Xiao

A novel adsorption material was synthesized and characterized by the methods of X-ray diffraction and scanning electron microscopy. The optimum reaction conditions of the 8-hydroxyquinoline modified bentonites were studied. And the modified bentonite was applied into the treatment of dyeing wastewater. The decoloration rate was invested as index. The effects of pH, adsorbent dosage, stirring speed, sedimentation time on adsorption have also been studied. The result showed that the decoloration rate of direct light turquoise blue dye on modified bentonites reached 94.12%, and the decoloration rate of acid orange dyeing wastewater reached 74.46%. So this type of modified bentonite was suitable for the treatment of dyeing wastewater.


2008 ◽  
Vol 5 (1) ◽  
pp. 163-168 ◽  
Author(s):  
Susheel Kalia ◽  
B. S. Kaith

Graft copolymerization of methyl methacrylate (MMA) onto flax fiber under the influence of microwave radiations (MWR) was carried out. 24.64% grafting was found at 210W microwave power under optimum reaction conditions. The graft copolymers were characterized with FTIR spectroscopy, scanning electron microscopy (SEM) and X-ray diffraction (XRD) techniques. Graft copolymers thus prepared were used in the preparation of phenol-formaldehyde (PF) composites. Modulus of rupture (MOR), modulus of elasticity (MOE) and stress at the limit of proportionality (SP) of composites were measured and it has been found that composites reinforced with Flax-g-poly(MMA) showed better mechanical properties in comparison to composites reinforced with raw flax.


2008 ◽  
Vol 15 (03) ◽  
pp. 329-336 ◽  
Author(s):  
YIMIN ZHANG ◽  
SHAOXIAN SONG ◽  
MIN ZHANG ◽  
BIYANG TUO

In this work, a Ti -pillared montmorillonite with high thermal stability has been prepared by using a Na -montmorillonite as the host clay and polyhydroxy-titania ions as the pillaring precursor. The formation of Ti -pillared montmorillonite has been confirmed from the characterizations through X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric–differential scanning calorimeter, and specific surface area analyses. In the preparation of Ti -pillared montmorillonite several parameters, such as the type of solvent in which the synthesis is realized, the ratio of polyhydroxy-titania ions and montmorillonite, the intercalation time, the calcining temperature, and calcining time, were tested to understand their effects on the basal spacing. It was shown that this method could produce a Ti -pillared montmorillonite with the basal spacing of 3.74 nm, specific surface area of 409 m2/g, and mean pore size of 2.94 nm, as well as a high thermal stability up to 900°C.


2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Claudia Maria Simonescu ◽  
Valentin Serban Teodorescu ◽  
Camelia Capatina

This paper presents the obtaining of copper sulfide CuS (covelite) from Cu(CH3COO)2.H2O and thioacetamide (TAA) system. The reaction was conducted in presence or absence of sodium-bis(2-ethylhexyl) sulfosuccinate (Na-AOT). The effects of various reaction parameters on the size and on the shape of nanoparticles have been examined. CuS obtained was characterized by X ray diffraction, IR spectroscopy, TEM � transmission electron microscopy and SAED selected area electron diffraction. The influence of surfactant to the shape and size of CuS (covellite) nanocrystals was established. The size of the nanocrystals varied from 10-60 nm depending on the reaction conditions such as quantity of surfactant.


2013 ◽  
Vol 634-638 ◽  
pp. 1968-1976 ◽  
Author(s):  
Shi Han Shen ◽  
Yu Yu Zhang ◽  
Tian Bin Li ◽  
Qing Le Zeng

In this paper, a novel superabsorbent composite material based on acrylic acid (AA), acrylic amide (AM) and inorganic kaolin was synthesized via solution polymerization in aqueous medium with N,N’-methylene bisacrylamide (MBA) as crosslinker and potassium persulfate (KPS) as initiator. The effects of water absorbency of the composite variables, such as neutralization, kaolin concentration and MBA concentration, on the water absorbency were systematically optimized. Evidence of compositing was obtained by a comparison of the Fourier transform infrared spectra of the initial reactants with that of the superabsorbent composites, and its complex structure was confirmed with scanning electron microscope. The water absorbing mechanism was also discussed. The results indicated that the superabsorbent composite material was successfully synthesized and the optimum reaction conditions were as follows: the neutralization degree was 80%, the dosage of kaolin, crosslinker and initiator were 4%, 0.11%, and 0.9% respectively and the mass ratio of AA and AM was 3∶2. The optimum absorbency of the superabsorbent composite material in distilled water could reach 815.6g/g.


Plants ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 6
Author(s):  
Asma Tabasum ◽  
Mousa Alghuthaymi ◽  
Umair Yaqub Qazi ◽  
Imran Shahid ◽  
Qamar Abbas ◽  
...  

Pesticides are one of the main organic pollutants as they are highly toxic and extensively used worldwide. The reclamation of wastewater containing pesticides is of utmost importance. For this purpose, GO-doped metal ferrites (GO-Fe3O4 and GO-CoFe2O4) were prepared and characterized using scanning electron microscopy, X-ray diffraction and Fourier transform infrared spectroscopic techniques. Photocatalytic potentials of catalysts were investigated against acetamiprid’s degradation. A detailed review of the parametric study revealed that efficiency of overall Fenton’s process relies on the combined effects of contributing factors, i.e., pH, initial oxidant concentration, catalyst dose, contact time, and acetamiprid load. ~97 and ~90% degradation of the acetamiprid was achieved by GO-CoFe2O4 and GO-Fe3O4, respectively during the first hour under UV radiations at optimized reaction conditions. At optimized conditions (i.e., pH:3, [H2O2]: 14.5 mM (for Fe3O4, GO-Fe3O4, and GO-CoFe2O4) and 21.75 mM (for CoFe2O4), catalysts: 100 mgL−1, time: 60min) the catalysts exhibited excellent performance, with high degradation rate, magnetic power, easy recovery at the end, and efficient reusability (up to 5 cycles without any considerable loss in catalytic activity). A high magnetic character offers its easy separation from aqueous systems using an external magnet. Moreover, the combined effects of experimental variables were assessed simultaneously and justified using response surface methodology (RSM).


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