2014
DOI: 10.1016/j.cej.2013.10.064
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Prediction of the removal efficiency of pharmaceuticals by a rapid spectrophotometric method using Rhodamine B in the UV/H2O2 process

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Cited by 20 publications
(21 citation statements)
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“…The photodegradation experiments were carried out using a bench-scale quasi-collimated beam apparatus [15] equipped with two 11-W low-pressure lamps (Philips, Amsterdam, The Netherland), which primarily emit light at 253.7 nm. A 50 mL geosmin and 2-MIB aliquot was placed in a Petri dish at a depth of about 0.786 cm [15][16][17]. The solution was stirred using a cross-shaped stirring bar with a diameter of 1 cm to ensure that it was homogenously exposed to UV light, and the solution is well mixed in the system.…”
Section: Lab-scale Experimentsmentioning
confidence: 99%
See 1 more Smart Citation
“…The photodegradation experiments were carried out using a bench-scale quasi-collimated beam apparatus [15] equipped with two 11-W low-pressure lamps (Philips, Amsterdam, The Netherland), which primarily emit light at 253.7 nm. A 50 mL geosmin and 2-MIB aliquot was placed in a Petri dish at a depth of about 0.786 cm [15][16][17]. The solution was stirred using a cross-shaped stirring bar with a diameter of 1 cm to ensure that it was homogenously exposed to UV light, and the solution is well mixed in the system.…”
Section: Lab-scale Experimentsmentioning
confidence: 99%
“…The UV transmittance was increased (85 → 4%). This could be explained by the decreased DOC and UV 254 after the PMC process because DOMs are the main water constituents considered in the estimation of •OH scavenging rates in natural waters [16]. Moreover, removal of turbidity could increase the performance of UV based AOPs because turbidity causing particles can act as a 'screen' that reduces the amount of light reaching H 2 O 2 or Cl 2 ; therefore, those oxidants do not receive sufficient UV photons for •OH production [12].…”
Section: Uv/h 2 O 2 and Uv/cl 2 Process In Pilot Scalementioning
confidence: 99%
“…In another set of experiments, 0.2 mg·L −1 MC-LR was also spiked. The ensemble was incubated under 2.3 W·m −2 at 25 • C, and the residual OH radicals' concentrations were estimated against a calibration curve plotted in Figure S4 of the Supplementary Information for 8100 s. Equation (2), as presented by Kwon et al (2014) [49], was used for the calculation of residual [·OH]. …”
Section: Quantification Of Residual Hydroxyl Radicalsmentioning
confidence: 99%
“…Measurement of residual OH radicals was performed using a spectrophotometric method with Rhodamine B (RhB, Sigma-Aldrich Chemie GmbH, Riedstr, Germany) as the probe chemical, according to the protocol described by Kwon et al (2014) [49]. Different concentrations of RhB (10 −3 , 0.5 10 −3 , 10 −4 , 0.5 10 −4 , 10 −5 , 10 −6 M) were read for their absorbance at 554 nm (Hach DR-3900, Loveland, CO, USA).…”
Section: Quantification Of Residual Hydroxyl Radicalsmentioning
confidence: 99%
“…Pharmaceutical treatment technologies including ozonation, photo‐catalytic degradation and other advanced oxidation processes (AOPs) have been investigated by many researchers . Recently ferrate (VI) has been studied comprehensively, as it could be an alternative to the other AOPs for the removal of pharmaceutical residuals .…”
Section: Introductionmentioning
confidence: 99%