Formation of organo-mineral complexes as affected by particle size, pH, and dry - wet cycles

Soil Research ◽  
2010 ◽  
Vol 48 (8) ◽  
pp. 713 ◽  
Author(s):  
B. Pan ◽  
S. Tao ◽  
R. W. Dawson ◽  
B. S. Xing

The formation of organo-mineral complexes is an important process controlling carbon cycling and the properties of soil particles. However, differences between the complexes formed in aqueous systems and those found in terrestrial systems have not been clearly recognised. This study simulated the formation of organo-mineral complexes between dissolved humic acid (DHA) and mineral particles using a solid/aqueous adsorption experiment (aqueous system) and a wet–dry cycling methodology (terrestrial system). The clay fraction of mineral particles contributed greatly (>90%) to overall DHA adsorption on soil particles in adsorption experiments where DHA fractionation was clearly observed. Aromatic content was found to be less favourable for adsorption under all conditions. For particles of different sizes, the significance of fractionation increased with adsorption. High adsorption was observed under acid conditions, although there was less fractionation as a result of the acid-facilitated ligand exchange process. When using a wet–dry cycling methodology, a much higher fOC was observed for the complexes than when using the adsorption experiment, and DHA fractionation was not significant. Further, the distinctly decreased E465/E665 ratio suggests that the DHA washed off from acid complexes was different from the original DHA and most likely the result of DHA precipitation during wet–dry cycles under acid conditions.

2020 ◽  
Vol 10 (3) ◽  
pp. 975 ◽  
Author(s):  
Hyung Ryul You ◽  
Jin Young Park ◽  
Duck Hoon Lee ◽  
Younghoon Kim ◽  
Jongmin Choi

Colloidal quantum dots (CQDs) are considered as next-generation semiconductors owing to their tunable optical and electrical properties depending on their particle size and shape. The characteristics of CQDs are mainly governed by their surface chemistry, and the ligand exchange process plays a crucial role in determining their surface states. Worldwide studies toward the realization of high-quality quantum dots have led to advances in ligand exchange methods, and these procedures are usually carried out in either solid-state or solution-phase. In this article, we review recent advances in solid-state and solution-phase ligand exchange processes that enhance the performance and stability of lead sulfide (PbS) CQD solar cells, including infrared (IR) CQD photovoltaics.


2013 ◽  
Vol 1547 ◽  
pp. 161-166 ◽  
Author(s):  
Ying Li ◽  
Peng Tao ◽  
Richard W. Siegel ◽  
Linda S. Schadler

ABSTRACTThe addition of high refractive index (RI) inorganic nanoparticles (NPs) to LED encapsulation materials can lead to higher light extraction efficiency. In addition, the NPs can be carriers for additional functionality such as color conversion. Using a simple “grafting-to” approach, bimodal polydimethylsiloxane (PDMS) brushes were grafted onto high-RI ZrO2 NPs. Subsequently, an organic phosphor, 6-[fluorescein-5(6)-carboxamido]hexanoic acid (FCHA), was attached onto the PDMS-grafted ZrO2 NPs via a facile ligand exchange process. The bimodal polymer brush design enables homogenous dispersion of the surface functionalized NPs within the silicone matrix. The functionalized NPs with ∼53 wt% ZrO2 core have a ∼0.08 higher RI than neat silicone, and the NP-filled silicone nanocomposites exhibit a transparency of ∼ 90% in the 550-800 nm wavelength range. In addition, the nanocomposites could be excited at a wavelength around 455 nm by a blue LED and undergo secondary yellow emission at around 571 nm. It is expected that the prepared nanocomposites can be used as high-efficiency, non-scattering, color-tuned materials for advanced LED encapsulation.


2019 ◽  
Vol 80 (7) ◽  
pp. 1357-1366
Author(s):  
Jianming Liu ◽  
Runying Bai ◽  
Junfeng Hao ◽  
Bowen Song ◽  
Yu Zhang ◽  
...  

Abstract This study investigated a magnetically recycled modified polishing powder (CMIO@PP) as an adsorbent of phosphate; the CMIO@PP was synthesized by combining the modified La/Ce-containing waste polishing powder with CaO2-modified Fe3O4 (CMIO). Results indicate that the CMIO@PP nanocomposite presents a crystal structure comprising La (OH)3, Ce (OH)3, and Fe3O4, and that CMIO is uniformly dispersed in the modified polishing powder. The CMIO@PP (1:3) is a suitable choice considering its magnetism and adsorption capacity. The magnetic adsorbent exhibits a high adsorption capacity of 53.72 mg/g, a short equilibrium time of 60 min, and superior selectivity for phosphate. Moreover, the adsorbent strongly depends on the pH during the adsorption process and maintains a large adsorption capacity when the pH level is between 2 and 6. The adsorption of phosphate by the CMIO@PP (1:3) accords with the Langmuir isotherm model, and the adsorption process follows the pseudo-second order model. Meanwhile, adsorption–desorption experiments show that the adsorbent could be recycled a few times and that a high removal efficiency of phosphate from civil wastewater was achieved. Finally, mechanisms show that the adsorption of phosphate by the CMIO@PP (1:3) is mainly caused by electrostatic attraction and ligand exchange.


2015 ◽  
Vol 17 (11) ◽  
pp. 7214-7223 ◽  
Author(s):  
Yin Tian ◽  
Jia Fu ◽  
Yi Zhang ◽  
Kecheng Cao ◽  
Chiyao Bai ◽  
...  

The extraction mechanism is an exchange process between the ligands on Urea-GO and the coordinated water molecules of uranyl.


2017 ◽  
Vol 53 (4) ◽  
pp. 728-731 ◽  
Author(s):  
S. J. Oh ◽  
D. B. Straus ◽  
T. Zhao ◽  
J.-H. Choi ◽  
S.-W. Lee ◽  
...  

We develop a hybrid ligand exchange process to enhance both mobility and lifetime of carriers in nanocrystal thin films.


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