Evaluating Sediment Phosphorus Exchange in Rural Ontario Headwaters by Paired Sequential Extraction and Sorption Isotherms

2021 ◽  
Vol 232 (10) ◽  
Author(s):  
Nicholas Falk ◽  
Matthew Day ◽  
Christopher G. Weisener
2018 ◽  
Vol 10 (7) ◽  
pp. 2491 ◽  
Author(s):  
Jianxin Fan ◽  
Guoliang Zhao

Sorption properties play a key role in the mobility of selenium (Se) and fraction distribution changes, leading to the bioavailability of Se in the soil environment. Thus, the effect of soil physicochemical properties on the sorption of exogenous selenite was investigated to predict the rate and capacity of sorption. Correlation analysis and multiple linear regression were used to observe the relationship between sorption characteristics and soil properties. Sequential extraction was used to observe the fractions of Se at different ages in soil. Results indicated that sorption isotherms followed the Langmuir equation, and the sorption capacity ranged from 50.7 to 567 mg·kg−1 with pseudo-second-order sorption kinetics. The correlation and multiple linear regression analyses showed that sorption parameters were significantly positively correlated with dithionite–citrate–bicarbonate-extracted Fe (FeDCB), dithionite–citrate–bicarbonate-extracted Al (AlDCB), amorphous Fe (FeOX), and soil organic matter (SOM), whereas pH was negatively correlated. Sequential extraction analyses revealed that the fraction distribution of Se in soil varied with the age, and the content of elemental Se increased with prolonged aging. FeDCB, AlDCB, FeOX, pH, and SOM play important roles in selenite sorption onto soils. Selenite sorption onto soil can be reduced to a lower-state Se, such as elemental Se and selenides, during the aging process. This information on the environmental behavior of Se is used to develop agronomic strategies for increasing Se levels in food crops and improving human health.


2013 ◽  
Vol 58 (2) ◽  
pp. 449-463 ◽  
Author(s):  
Mieczysław Żyła ◽  
Agnieszka Dudzińska ◽  
Janusz Cygankiewicz

Ethane constitutes an explosive gas. It most often accompanies methane realizing during exploitation and mining works. In this paper the results of ethane sorption have been discussed on three grain classes of six selected hard coal samples collected from active Polish coalmines. On the basis of obtained results, it has been stated that the tested hard coals prove differentiated sorption power with reference to ethane. Te extreme amount of ethane is sorbed by low carbonized hard coal from “Jaworzno” coalmine. This sort of coal shows great porosity, and great content of oxygen and moisture. The least amount of ethane is sorbed by hard coal from “Sośnica” coalmine. This sort of coal possesses relatively a great deal of ash contents. Together with the process of coal disintegration, the amount of sorbed ethane increases for all tested coal samples. Between tested coals there are three medium carbonized samples collected from “Pniówek”, “Chwałowice” “Zofiówka” coalmines which are characterized by small surface values counted according to model BET from nitrogen sorption isotherms determined at the temperature of 77.5 K. The samples of these three coals prove the highest, from between tested coals, increase of ethane sorption occurring together with their disintegration. These samples disintegrated to 0,063-0,075 mm grain class sorb ethane in the amount corresponding with the sorption quantity of low carbonized coal from “Jaworzno” coalmine in 0.5-0.7 mm grain class. It should be marked that the low carbonized samples collected from “Jaworzno” and Wesoła” coalmines possess large specific surface and great porosity and belong to coal group of “loose” spatial structure. Regarding profusion of sorbed ethane on disintegrated medium carbonized samples from “Pniówek”, “Zofiówka”, “Chwałowice” coalmines it can be supposed that in the process of coal disintegration, breaking their “compact’ structure occurs. Loosened structure of medium carbonized coals results in increasing accessibility of ethane particles to sorption centres both electron donors and electron acceptors which are present on hard coal surface. The surface sorption centre increase may result in formation a compact layer of ethane particles on coal surface. In the formed layer, not only the strengths of vertical binding of ethane particles with the coal surface appear but also the impact of horizontal strengths appears which forms a compact layer of sorbed ethane particles. The surface layer of ethane particles may lead to explosion.


2014 ◽  
Vol 59 (2) ◽  
pp. 509-516
Author(s):  
Andrzej Olajossy

Abstract Methane sorption capacity is of significance in the issues of coalbed methane (CBM) and depends on various parameters, including mainly, on rank of coal and the maceral content in coals. However, in some of the World coals basins the influences of those parameters on methane sorption capacity is various and sometimes complicated. Usually the rank of coal is expressed by its vitrinite reflectance Ro. Moreover, in coals for which there is a high correlation between vitrinite reflectance and volatile matter Vdaf the rank of coal may also be represented by Vdaf. The influence of the rank of coal on methane sorption capacity for Polish coals is not well understood, hence the examination in the presented paper was undertaken. For the purpose of analysis there were chosen fourteen samples of hard coal originating from the Upper Silesian Basin and Lower Silesian Basin. The scope of the sorption capacity is: 15-42 cm3/g and the scope of vitrinite reflectance: 0,6-2,2%. Majority of those coals were of low rank, high volatile matter (HV), some were of middle rank, middle volatile matter (MV) and among them there was a small number of high rank, low volatile matter (LV) coals. The analysis was conducted on the basis of available from the literature results of research of petrographic composition and methane sorption isotherms. Some of those samples were in the form (shape) of grains and others - as cut out plates of coal. The high pressure isotherms previously obtained in the cited studies were analyzed here for the purpose of establishing their sorption capacity on the basis of Langmuire equation. As a result of this paper, it turned out that for low rank, HV coals the Langmuire volume VL slightly decreases with the increase of rank, reaching its minimum for the middle rank (MV) coal and then increases with the rise of the rank (LV). From the graphic illustrations presented with respect to this relation follows the similarity to the Indian coals and partially to the Australian coals.


MethodsX ◽  
2020 ◽  
Vol 7 ◽  
pp. 100888
Author(s):  
Margit H. Simon ◽  
Daniel P. Babin ◽  
Steven L. Goldstein ◽  
Merry Yue Cai ◽  
Tanzhuo Liu ◽  
...  

2020 ◽  
Vol 65 (6) ◽  
pp. 1921-1934 ◽  
Author(s):  
Samara Alves Testoni ◽  
Vander Freitas Melo ◽  
Lorna Anne Dawson ◽  
Joice Malakoski ◽  
Edimar Cunico ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1157
Author(s):  
Daniele Tammaro ◽  
Lorenzo Lombardi ◽  
Giuseppe Scherillo ◽  
Ernesto Di Maio ◽  
Navanshu Ahuja ◽  
...  

Optimization of post polymerization processes of polyolefin elastomers (POE) involving solvents is of considerable industrial interest. To this aim, experimental determination and theoretical interpretation of the thermodynamics and mass transport properties of POE-solvent mixtures is relevant. Sorption behavior of n-hexane vapor in a commercial propylene-ethylene elastomer (V8880 VistamaxxTM from ExxonMobil, Machelen, Belgium) is addressed here, determining experimentally the sorption isotherms at temperatures ranging from 115 to 140 °C and pressure values of n-hexane vapor up to 1 atm. Sorption isotherms have been interpreted using a Non Random Lattice Fluid (NRLF) Equation of State model retrieving, from data fitting, the value of the binary interaction parameter for the n-hexane/V8880 system. Both the cases of temperature-independent and of temperature-dependent binary interaction parameter have been considered. Sorption kinetics was also investigated at different pressures and has been interpreted using a Fick’s model determining values of the mutual diffusivity as a function of temperature and of n-hexane/V8880 mixture composition. From these values, n-hexane intra-diffusion coefficient has been calculated interpreting its dependence on mixture concentration and temperature by a semi-empiric model based on free volume arguments.


Author(s):  
Sara Sandström ◽  
Martyn N. Futter ◽  
David W. O'Connell ◽  
Emma E. Lannergård ◽  
Jelena Rakovic ◽  
...  

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