Using Titania Photocatalysts to Degrade Toluene in a Combined Adsorption and Photocatalysis Process

2007 ◽  
Vol 10 (1) ◽  
Author(s):  
Linda Y. Zou ◽  
Yonggang Luo ◽  
Eric J. Hu

AbstractThree types of titania supported materials including titanium dioxide and silicon dioxide composite, titania-coated activated carbon and titania-coated glass beads were prepared and used as photocatalysts to remove toluene from an air stream. Their surface areas were analysed. TEM image reveals titania-silica composites were nanostructured aggregates. XRD was used to determine their crystalline phase which was 100% anatase for the titania component. A fixed bed reactor was designed and built in the laboratory, the toluene with initial concentration of 300 ppm (1149 mg/m

2013 ◽  
Vol 11 (1) ◽  
pp. 569-576 ◽  
Author(s):  
Djamila Djedouani ◽  
Malika Chabani ◽  
Abdeltif Amrane ◽  
Aicha Bensmaili

Abstract Batch experiments were carried out for the adsorption of oxytetracycline (OTC) onto powdered activated carbon (PAC). The operating variables examined were the initial concentration (20–150 mg L−1) and the adsorbent concentration (0.75–1.75 g L−1). As observed increasing the initial concentration, while decreasing the adsorbent dosage, had a positive impact on the amount of OTC uptake (mg g−1). The kinetics was examined in a closed-loop fixed bed adsorber to propose an adsorption mechanism, to understand the dynamic interactions of OTC with ECA08 activated carbon and to predict its fate with time. The sorption results were analyzed using chemical and physical kinetics models. For concentrations lower than 70 mg L−1, the sorption process was found to be controlled by both surface reactions and mass transfer. The average external mass transfer coefficient and intraparticle diffusion coefficient were found to be 0.0051 min−1 and 1.97 mg g−1 min−0.5, respectively. For concentrations higher than 70 mg L−1, mass transfer became rapid and the chemical reaction at the surface of the solid phase was the rate-limiting step. The results showed that the adsorption reaction was accurately described by the pseudo-second-order model.


Fuel ◽  
1996 ◽  
Vol 75 (2) ◽  
pp. 227-237 ◽  
Author(s):  
Ajay K. Dalai ◽  
Jasimuz Zaman ◽  
E.Stanley Hall ◽  
Eric L. Tollefson

2012 ◽  
Vol 1 (3) ◽  
pp. 81 ◽  
Author(s):  
A Buasri ◽  
B Ksapabutr ◽  
M Panapoy ◽  
N Chaiyut

: The continuous production of ethyl ester was studied by using a steady-state fixed bed reactor (FBR). Transesterification of palm stearin (PS) and waste cooking palm oil (WCPO) with ethanol in the presence of calcium oxide impregnated palm shell activated carbon (CaO/PSAC) solid catalyst was investigated. This work was determined the optimum conditions for the production of ethyl ester from PS and WCPO in order to obtain fatty acid ethyl ester (FAEE) with the highest yield. The effects of reaction variables such as residence time, ethanol/oil molar ratio, reaction temperature, catalyst bed height and reusability of catalyst in a reactor system on the yield of biodiesel were considered. The optimum conditions were the residence time 2-3 h, ethanol/oil molar ratio 16-20, reaction temperature at 800C, and catalyst bed height 300 mm which yielded 89.46% and 83.32% of the PS and WCPO conversion, respectively. CaO/PSAC could be used repeatedly for 4 times without any activation treatment and no obvious activity loss was observed. It has potential for industrial application in the transesterification of triglyceride (TG). The fuel properties of biodiesel were determined. Keywords: biodiesel, calcium oxide, ethyl ester, fixed bed reactor, palm shell activated carbon


2019 ◽  
Vol 9 (7) ◽  
pp. 1371 ◽  
Author(s):  
Stefano Cimino ◽  
Jessica Apuzzo ◽  
Luciana Lisi

MgO supported on activated carbon (AC) with a load ranging from 10% to 30% has been investigated as catalyst for the conversion of ethanol into butanol at 400 °C in a fixed bed reactor at different GHSV. Catalysts have been characterized by XRD, SEM/EDX, and N2 physisorption at 77 K. The high dispersion of MgO into the pores of the support provides strongly enhanced performance with respect to bulk MgO. MgO/AC catalysts have been also tested under wet feed conditions showing high water tolerance and significantly larger butanol yield with respect to an alumina supported Ru/MgO catalyst. After wet operation, the increased surface area of the catalyst leads to better performance once dry feed conditions are restored.


Author(s):  
Yanbing Li ◽  
Rui Xiao ◽  
Baosheng Jin ◽  
Huiyan Zhang

As one of the fundamental issues of the new poly-generation system on the basis of gasification gas and coke oven gas, carbon dioxide reforming of methane experiments have been performed over coal chars derived from different parent coals in a lab-scale fixed-bed reactor (internal diameter 12 mm, length 700 mm). The char derived from TongChuan coal exhibited higher activity than other samples employed under the same conditions. After the reforming reaction, the char samples were covered with different amounts of carbon deposition which resulted in the surface areas decrease. As the flow rate of feed gas increased from 200 ml/min to 600 ml/min over the Xuzhou char sample at 1050 degrees Celsius, the conversion of methane decreased from 52.7% to 17.5% and the H2 /CO dropped from 0.75 to 0.55. While maintaining the flow rate of CO2 at 20ml/min at 1050 degrees Celsius, the mole ratio of reactants CH4/CO2 was varied from 1 to 1.75 which led to the H2/CO ratio increase from 0.75 to 1.2.


2014 ◽  
Vol 955-959 ◽  
pp. 2169-2172 ◽  
Author(s):  
Bing Li ◽  
Jian Ming Xue ◽  
Yue Yang Xu ◽  
Hong Liang Wang ◽  
Chun Yuan Ma ◽  
...  

Five kinds of powder activatedcarbons were studied to investigate the removal of SO2 from flue gasin a fixed bed reactor. The fractal dimension of activated carbon was determined by N2 adsorption isothermat 77Kand SO2 adsorptioncapacity was correlated with thefractal dimension. The results show thatthe activated carbons prepared from different precursors by differentactivation methods have different fractal dimension. Big differences in SO2 adsorption capacity are found between fivekinds of activated carbons. SO2 adsorption capacity increases with the fractaldimension increasing. The results indicate that the fractal dimension could be used as a indicator of SO2removal capacity on powder activated carbon.


Materials ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2047 ◽  
Author(s):  
Katarzyna Januszewicz ◽  
Paweł Kazimierski ◽  
Maciej Klein ◽  
Dariusz Kardaś ◽  
Justyna Łuczak

Pyrolysis of straw pellets and wood strips was performed in a fixed bed reactor. The chars, solid products of thermal degradation, were used as potential materials for activated carbon production. Chemical and physical activation processes were used to compare properties of the products. The chemical activation agent KOH was chosen and the physical activation was conducted with steam and carbon dioxide as oxidising gases. The effect of the activation process on the surface area, pore volume, structure and composition of the biochar was examined. The samples with the highest surface area (1349.6 and 1194.4 m2/g for straw and wood activated carbons, respectively) were obtained when the chemical activation with KOH solution was applied. The sample with the highest surface area was used as an adsorbent for model wastewater contamination removal.


Catalysts ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 752 ◽  
Author(s):  
Yingquan Wu ◽  
Li Tan ◽  
Tao Zhang ◽  
Hongjuan Xie ◽  
Guohui Yang ◽  
...  

Two types of amorphous ZrO2 (am-ZrO2) catalysts were prepared by different co-precipitation/reflux digestion methods (with ethylenediamine and ammonia as the precipitant respectively). Then, copper and potassium were introduced for modifying ZrO2 via an impregnation method to enhance the catalytic performance. The obtained catalysts were further characterized by means of Brunauer-Emmett-Teller surface areas (BET), X-ray diffraction (XRD), H2-temperature-programmed reduction (H2-TPR), and In situ diffuse reflectance infrared spectroscopy (in situ DRIFTS). CO hydrogenation experiments were performed in a fixed-bed reactor for isobutanol synthesis. Great differences were observed on the distribution of alcohols over the two types of ZrO2 catalysts, which were promoted with the same content of Cu and K. The selectivity of isobutanol on K-CuZrO2 (ammonia as precipitant, A-KCZ) was three times higher than that on K-CuZrO2 (ethylenediamine as precipitant, E-KCZ). The characterization results indicated that the A-KCZ catalyst supplied more active hydroxyls (isolated hydroxyls) for anchoring and dispersing Cu. More importantly, it was found that bicarbonate species were formed, which were ascribed as important C1 species for isobutanol formation on the A-KCZ catalyst surface. These C1 intermediates had relatively stronger adsorption strength than those adsorbed on the E-KCZ catalyst, indicating that the bicarbonate species on the A-KCZ catalyst had a longer residence time for further carbon chain growth. Therefore, the selectivity of isobutanol was greatly enhanced. These findings would extend the horizontal of direct alcohols synthesis from syngas.


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