Treatment of 2,4-Dichlorophenol by Solar Photocatalysis: Comparison of Coupled Photocatalytic-Active Carbon vs. Active Carbon

2000 ◽  
Vol 123 (2) ◽  
pp. 138-142 ◽  
Author(s):  
Sixto Malato ◽  
Julia´n Blanco ◽  
Pilar Ferna´ndez-Iba´n˜ez ◽  
Julia Ca´ceres

The photocatalytic oxidation of 2,4-Dichlorophenol (DCP), using TiO2 suspensions under solar radiation, has been studied at pilot-plant scale at the Plataforma Solar de Almerı´a (PSA). This compound is used as a model to demonstrate the practical application of the treatment. Total Organic Carbon (TOC) analysis is applied to confirm the total mineralization of the contaminants. The pilot plant has a volume of 247 L and consists of 9 m2 of CPC modules (with transparent tubes) connected to a recirculation tank. DCP at 20, 50 and 200 mg/L is completely photodegraded in the presence of 200 mg/L of TiO2, but mineralization is slow when organics concentration is small. The results obtained from these experiments have been used to decide the dimensions of a solar photocatalytic plant for treating wastewater contaminated with different concentration of DCP. Due to the slow kinetic obtained in the photodegradation last steps, a combination with GAC treatment is proposed. Besides, this article attempts to compare the advantages, disadvantages and costs of photocatalytic treatment, versus other more conventional technologies such as active carbon adsorption.

2019 ◽  
Vol 166 ◽  
pp. 115037 ◽  
Author(s):  
Alejandro Cabrera-Reina ◽  
Ana B. Martínez-Piernas ◽  
Yannis Bertakis ◽  
Nikolaos P. Xekoukoulotakis ◽  
Ana Agüera ◽  
...  

2018 ◽  
Vol 25 (35) ◽  
pp. 34995-35007 ◽  
Author(s):  
Nuria Vela ◽  
May Calín ◽  
María J. Yáñez-Gascón ◽  
Isabel Garrido ◽  
Gabriel Pérez-Lucas ◽  
...  

2005 ◽  
Vol 128 (3) ◽  
pp. 331-337 ◽  
Author(s):  
Mahmut Kus ◽  
Wolfgang Gernjak ◽  
Pilar Fernández Ibáñez ◽  
Sixto Malato Rodríguez ◽  
Julián Blanco Gálvez ◽  
...  

The degradation of gallic acid and imidacloprid with supported Millennium PC500 and Degussa P25 TiO2 is reported. TiO2 particles were immobilized using a titanium sol-solution and direct deposition on glass supports. The film characterization was done by x-ray diffraction, scanning electron microscopy, and atomic force microscopy, and degradation of organic compounds was monitored by high-performance liquid chromatography, total organic carbon analyzer, and ion chromatography. The experiments were performed under sunlight in compound parabolic collector plants with flat supports inside the glass tubes. Photocatalytic activity of the films was compared and identified. Although sol-gel coatings had better mechanical properties, mineralization was observed to be approximately five times slower than paste-deposited films. Photoactivity of the films decreased with silver deposition due to the nature of the organic compounds. The rate constants were calculated to be between 2×10−1 and 6×10−2mgm2∕kJ for organic compounds, and 6×10−2 and 6×10−3 for total organic carbon.


1997 ◽  
Vol 35 (4) ◽  
pp. 157-164 ◽  
Author(s):  
S. Malato ◽  
J. Blanco ◽  
C. Richter ◽  
D. Curcó ◽  
J. Giménez

The photocatalytic oxidation of 2,4-Dichlorophenol (DCP), using TiO2 suspensions under solar radiation, has been studied at pilot-plant scale at the Plataforma Solar de Almería (PSA). Two different reactor designs were tested: a medium concentrating radiation system called a Parabolic-Trough-Collector Reactor, PTCR, equipped with two motors (azimuth and elevation) to adjust the position of the module perpendicular to the sun, and a low-concentrating radiation system, the Compound-Parabolic-Concentrator Reactor, CPCR, facing south and inclined 37 degrees. Substrates were dissolved in water to required mg L−1 levels in a reservoir tank. In both cases, 0.2 g L−1 of the suspended TiO2 catalyst was used in a 250 L solution of the contaminant, which was recirculated through the photoreactors using a centrifugal pump and an intermediate reservoir tank. The advantages and disadvantages of the two types of photoreactors in DCP oxidation are compared and discussed. The strong potential of photocatalytic peroxydisulphate-assisted degradation in high DCP concentrations was demonstrated in both systems, and chemical actinometry (the decomposition reaction of oxalic acid by radiated uranyl salts) in the CPC reactor is compared with the results obtained in the PTC.


2008 ◽  
Vol 6 (1) ◽  
Author(s):  
Markus Heryanto Langsa

<p>Penelitian ini bertujuan untuk menentukan senyawa organik khususnya organic karbon terlarut (DOC) dari dua spesies daun tumbuhan (<em>wandoo eucalyptus </em>and <em>pinus radiate, conifer</em>) yang larut dalam air selama periode 5 bulan leaching eksperimen. Kecepatan melarutnya senyawa organic ditentukan secara kuantitatif dan kualitatif menggunakan kombinasi dari beberapa teknik diantaranya Total Organic Carbon (TOC) analyser, Ultraviolet-Visible (UV-VIS) spektrokopi dan pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS).</p><p>Hasil analisis DOC dan UV menunjukkan peningkatan yang tajam dari kelarutan senyawa organic di awal periode pengamatan yang selanjutnya berkurang seiring dengan waktu secara eksponensial. Jumlah relatif senyawa organic yang terlarut tergantung pada luas permukaan, aktifitas mikrobiologi dan jenis sampel tumbuhan (segar atau kering) yang digunakan. Fluktuasi profil DOC dan UV<sub>254</sub> disebabkan oleh aktifitas mikrobiologi. Diperoleh bahwa daun kering lebih mudah terdegradasi menghasilkan senyawa organic dalam air dibandingkan dengan daun segar. Hasil pyrolysis secara umum menunjukkan bahwa senyawa hidrokarbon aromatic dan fenol (dan turunannya) lebih banyak ditemukan pada residue sampel setelah proses leaching kemungkinan karena adanya senyawa lignin atau aktifitas humifikasi mikrobiologi membuktikan bahwa senyawa-senyawa tersebut merupakan komponen penting dalam proses karakterisasi DOC.</p>


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