Comparative evaluation of sorption kinetics and isotherms of pyrene onto microplastics

Chemosphere ◽  
2018 ◽  
Vol 193 ◽  
pp. 567-573 ◽  
Author(s):  
Wenfeng Wang ◽  
Jun Wang
2018 ◽  
Vol 131 ◽  
pp. 191-196 ◽  
Author(s):  
Baile Xu ◽  
Fei Liu ◽  
Philip C. Brookes ◽  
Jianming Xu

2016 ◽  
Vol 73 (8) ◽  
pp. 2007-2016 ◽  
Author(s):  
N. Contreras Olivares ◽  
M. C. Díaz-Nava ◽  
M. Solache-Ríos

The sorption processes of red 5 (R5) and yellow 5 (Y5) dyes by iron modified and sodium bentonite in aqueous solutions was evaluated. The modified clay was prepared, conditioned and characterized. The sodium clay did not remove any of either dye. The sorption kinetics and isotherms of R5 and Y5 dyes by iron modified clay were determined. The maximum removal percentages achieved were 97% and 98% for R5 and Y5, respectively, and a contact time of 72 h; the experimental data were best adjusted to Ho model. The isotherms of both dyes were best adjusted to the Langmuir model and the maximum adsorption capacities of the modified clay were 11.26 mg/g and 5.28 mg/g for R5 and Y5, respectively. These results indicate that adsorption processes have a high probability to be described as chemisorption on a homogeneous material. Temperature range between 283 and 213 K does not affect the adsorption of Y5 by the iron modified clay, but the adsorption process of R5 was affected, and the thermodynamic parameters could be calculated, which indicate a chemisorption mechanism.


2020 ◽  
Vol 20 (10) ◽  
pp. 3644-3655 ◽  
Author(s):  
Tatjana Schneckenburger ◽  
Sören Thiele-Bruhn

Abstract Purpose Sorption of organic compounds to soil largely determines their mobility and bioavailability in ecosystems. It is well known that molecular properties of the organic sorbates affect the sorbed amounts and sorption kinetics. But also changes in the hydration status of soils alter the physicochemical and sorptive properties of soil organic matter (SOM), which is the main sorbent for organic compounds in soils. This study elucidates the effects of varying SOM prehydration status on sorption of PAHs and PAH derivatives in peat soil. Materials and methods For sorption experiments, topsoil samples of a peat soil with 51% SOM were adjusted to water contents of 15, 30, and 50% (w/w based on dry soil mass) and conditioned for different water contact times of up to 2 years at one constant water content. Sorption kinetics and isotherms of naphthalene, three naphthalene derivatives, phenanthrene, and pyrene to these samples were investigated in batch experiments. Effects of the sorbates’ properties and SOM hydration on sorption were analyzed. Results and discussion Sorption to the peat soil was nonlinear and varied among sorbates and differently prehydrated soil samples. Sorbate polarizability, molecular volume, and weight increased the sorbed amount. Sorption kinetics were two-phased with a fast and a slow sorbing fraction. Hydroxyl groups in sorbates acting as H-donor or acceptor led to an increase of the slow sorbing fraction. Increasing total water contents, amounts of non-freezable water in SOM, increasing pore sizes, and decreasing hydrophobicity of SOM decreased the total sorbed amount and the fast sorbing fraction while increasing the slow sorbing fraction. The latter effects increased with increasing polarity and dipole moment of the sorbate. The SOM matrix rigidity varied with prehydration status; higher SOM matrix rigidity led to non-ideal sorption processes, namely, higher sorption nonlinearity and slower sorption. Conclusions The study revealed the effects and interplay of SOM prehydration status and molecular properties of the sorbates on sorption of PAHs and PAH derivatives. As sorbed amounts may decrease and become non-ideal upon aging at the presence of water, estimations of the mobility of organic compounds in the environment need to consider SOM prehydration status in high organic soils.


2019 ◽  
Vol 254 ◽  
pp. 112927 ◽  
Author(s):  
Wenwen Gong ◽  
Mengyun Jiang ◽  
Ping Han ◽  
Gang Liang ◽  
Tingting Zhang ◽  
...  

2014 ◽  
Vol 69 (11) ◽  
pp. 2265-2271 ◽  
Author(s):  
A. H. M. G. Hyder ◽  
Shamim A. Begum ◽  
Nosa O. Egiebor

The characteristics of sorption of hexavalent chromium (Cr(VI)) onto bio-char derived from wood chips (spruce, pine, and fir) were evaluated as a function of pH, initial Cr(VI) concentration and bio-char dosage using synthetic wastewater in batch tests. The initial Cr(VI) concentrations were varied between 10 and 500 mg/L to investigate equilibrium, kinetics, and isotherms of the sorption process. About 100% of Cr(VI) was removed at pH 2 with initial Cr(VI) concentration of 10 mg/L using 4 g of bio-char after 5 hours of sorption reaction. The maximum sorption capacity of the bio-char was 1.717 mg/g for an initial Cr(VI) concentration of 500 mg/L after 5 hours. The sorption kinetics of total Cr onto bio-char followed the second-order kinetic model. The Langmuir isotherm model provided the best fit for total Cr sorption onto bio-char. The bio-char used is a co-product of a down draft gasifier that uses the derived syngas to produce electricity. Bio-char as a low cost adsorbent demonstrated promising results for removal of Cr(VI) from aqueous solution. The findings of this study would be useful in designing a filtration unit with bio-char in a full-scale water and wastewater treatment plant for the Cr(VI) removal from contaminated waters.


2008 ◽  
Vol 2008 ◽  
pp. 1-7 ◽  
Author(s):  
Peter J. Holliman ◽  
Beatriz Vaca Velasco ◽  
Ian Butler ◽  
Maarten Wijdekop ◽  
David A. Worsley

Sorption kinetics and isotherms have been measured for a commercial dye (Direct Red 23) on different samples of powdered Titania, and the data were analysed to better understand the dye sensitization process for dye sensitised solar cells (DSSCs). For the sorption kinetics, the data show rapid initial sorption (<1 hour) followed by slower rate of increasing uptake between 1 and 24 hours. While higher initial concentrations of dye correspond to higher sorption overall, less dye is absorbed from higher initial dye concentrations when considered as percentage uptake. The correlation between the sorption data and model isotherms has been considered with time. The Langmuir model shows better correlations compared to the Freundlich isotherm. The dye uptake data has also been correlated with Titania characterization data (X-ray diffraction, scanning electron microscopy, BET and zero point charge analysis). Kinetic data show significantly better fits to second-order models compared to first order. This suggests that chemisorption is taking place and that the interaction between the dye sorbate and the Titania sorbent involves electron sharing to form an ester bond.


RSC Advances ◽  
2016 ◽  
Vol 6 (74) ◽  
pp. 69947-69955 ◽  
Author(s):  
Lilan Hao ◽  
Hualin Wang ◽  
Ruizhi Cai ◽  
Junfeng Cheng ◽  
Min Sun ◽  
...  

We fabricated mesoporous hydroxylapatite/activated carbon bead-on-string nanofibers from electrospun nanofibers by a hydrothermal method and evaluated their sorption towards Co(ii) via sorption kinetics and isotherms.


2012 ◽  
Vol 30 (No. 5) ◽  
pp. 446-455 ◽  
Author(s):  
S. Galus ◽  
A. Turska ◽  
A. Lenart

The water vapour sorption kinetics and isotherms of pectin films prepared by the casting method were determined. The measurement of water vapour sorption kinetics was conducted using a saturated sodium chloride solution to obtain constant relative humidity of the environment (75.3%). The measurement was carried out at the temperature of 25&deg;C over a 24 h period. The water vapour adsorption rate was the highest in the first hours of the process. The exponential equation fitted well the experimental data of water vapour adsorption with time. Glycerol concentration in the analysed films affected the increasing water vapour adsorption. The water vapour sorption isotherms were analysed using the saturated salt solutions with water activity from 0.113 to 0.901 for 3 months at 25&deg;C. The sorption isotherms curves had a sigmoidal shape for all films. Glycerol content affected water vapour adsorption during 3 months. Peleg&rsquo;s equation was appropriate for the mathematical description of the sorption isotherms. The microstructure of pectin films showed different internal arrangement as a function of the film composition. &nbsp;


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