NIR spectroscopic study of the complexation of neptunium(V) with humic acids: influence of phenolic OH groups on the complex formation

2005 ◽  
Vol 93 (3) ◽  
Author(s):  
S. Sachs ◽  
G. Bernhard

SummaryThe influence of phenolic OH groups on the Np(V) complexation by humic acids was studied at pH 7 and pH 8 under nitrogen atmosphere applying chemically modified humic acids with blocked phenolic OH groups in comparison to their corresponding unmodified humic acids. The studies were performed by near-infrared (NIR) absorption spectroscopy using the metal ion charge neutralization model for evaluation of the experimental data. For all humic acids under investigation comparable complexation constants were determined. However, the studied modified humic acids Aldrich and M42 show significantly lower loading capacities for NpO

2016 ◽  
Vol 13 (3) ◽  
pp. 507 ◽  
Author(s):  
Rachel D. Deese ◽  
Madeline R. LeBlanc ◽  
Robert L. Cook

Environmental context Surfactants, a pollutant class routinely introduced into aquatic environments, can be toxic to a variety of species. It is thus important to understand how surfactants’ toxicity is influenced by their interactions with other environmental constituents, including natural organic matter. We report the changes in toxicity of three surfactants to brine shrimp in the presence of unmodified and chemically modified humic acids. Abstract Surfactants can be extremely toxic to aquatic species and are introduced to the environment in a variety of ways. It is thus important to understand how other environmental constituents, in this case humic acids (HAs), may alter the toxicity of anthropogenic surfactants. Hatching and mortality assays of Artemia Franciscana were performed for three different toxic surfactants: Triton X-100 (Tx-100, non-ionic), cetylpyridinium chloride (CPC, cationic) and sodium dodecyl sulfate (SDS, anionic). HAs of varying composition and concentrations were added to the assays to determine the toxicity mitigating ability of the HAs. Tx-100 had a significant toxic effect on Artemia mortality rates and HAs from terrestrial sources were able to mitigate the toxicity, but an aquatic HA did not. CPC and SDS limited hatching success of the Artemia and, as HAs were added, the hatching percentages increased for all HA sources, indicating toxicity mitigation. In order to determine which functional groups within HAs were responsible for the interaction with the surfactants, the HAs were chemically modified by: (i) bleaching to reduce aromatics, (ii) Soxhlet extraction to reduce lipids and (iii) acid hydrolysis to reduce O- and N-alkyl groups. Although most of the modified HAs had some toxicity mitigating ability for each of the surfactants, there were two notable differences: (1) the lipid-extracted HA did not reduce the toxicity of Tx-100 and (2) the bleached HA had a lower toxicity mitigating ability for CPC than the other modified HAs.


2005 ◽  
Vol 93 (1) ◽  
Author(s):  
S. Sachs ◽  
K. Schmeide ◽  
T. Reich ◽  
V. Brendler ◽  
K. H. Heise ◽  
...  

AbstractThe structure of Np(V) humic acid (HA) complexes at pH 7 was studied by extended X-ray absorption fine structure analysis (EXAFS). For the first time, the influence of phenolic OH groups on the complexation of HA and Np(V) in the neutral pH range was investigated using modified HAs with blocked phenolic OH groups and Bio-Rex70, a cation exchange resin having only carboxyl groups as proton exchanging sites.The formation of Np(V) humate complexes was verified by near-infrared (NIR) spectroscopy. Axial Np-O bond distances of 1.84–1.85 Å were determined for the studied Np(V) humate complexes and the Np(V)-Bio-Rex70 sorbate. In the equatorial plane Np(V) is surrounded by about 3 oxygen atoms with bond lengths of 2.48–2.49 Å. The comparison of the structural parameters of the Np(V) humates with those of Np(V)-Bio-Rex70 points to the fact that the interaction between HA and Np(V) in the neutral pH range is dominated by carboxylate groups. However, up to now a contribution of phenolic OH groups to the interaction process cannot be excluded completely. The comparison of the obtained structural data for the Np(V) humates to those of Np(V) carboxylates and Np(V) aquo ions reported in the literature indicates that humic acid carboxylate groups predominantly act as monodentate ligands. A differentiation between equatorial coordinated carboxylate groups and water molecules using EXAFS spectroscopy is impossible.


Author(s):  
Leonid Perelomov ◽  
Binoy Sarkar ◽  
David Pinsky ◽  
Yury Atroshchenko ◽  
Irina Perelomova ◽  
...  

2000 ◽  
Vol 88 (9-11) ◽  
Author(s):  
S. Pompe ◽  
K. Schmeide ◽  
M. Bubner ◽  
Gerhard Geipel ◽  
K. H. Heise ◽  
...  

We investigated the influence of phenolic OH groups on the complexation behavior of humic acid (HA) with UO


1997 ◽  
Vol 506 ◽  
Author(s):  
Jiang Wei

ABSTRACTBatch sorption experiments were carried out to investigate the adsorption of humic acids (HA) and Eu-humate colloids onto repository components: Boom clay, bentonite and Fe2O3 as a function of pH. The concentration of humic acids is 150 mg/l and the bulk concentration of Eu is 10−6 M. Radioactive 152Eu was used as a tracer. The adsorption of humic acids onto bentonite and Fe2O3 decreased with increasing pH. Humic acids were probably complexed to Al/Fe sites on the adsorbents through COOH and phenolic OH groups. It is difficult to interpret the adsorption of humic acids onto Boom clay because Boom clay itself contains high content of organic matters. The adsorption of Eu-humate colloids onto repository components were performed near neutral pH conditions. Eu was strongly adsorbed by three adsorbents, and pH had little effect on the adsorption in the neutral pH range. The strong complexation of Eu with humic acids did not prevent Eu from being adsorbed. Eu is likely bound to solid surfaces via humic acids. The adsorption of Eu-humate colloids onto mixed adsorbents (Boom clay + bentonite, Boom clay + Fe2O3, bentonite + Fe2O3, and Boom clay + bentonite + Fe2O3) was investigated. Most of Eu-humate colloids was adsorbed by the mixed adsorbents. The desorption of humic acids and Eu from repository components was also examined.


2012 ◽  
Vol 50 (12) ◽  
pp. 1032-1037
Author(s):  
D. A. Malikov ◽  
T. A. Goryacheva ◽  
A. P. Novikov ◽  
V. V. Platonov ◽  
R. Z. Treityak

2019 ◽  
Vol 70 (9) ◽  
pp. 3103-3107 ◽  
Author(s):  
Ioana Glevitzky ◽  
Gabriela Alina Dumitrel ◽  
Mirel Glevitzky ◽  
Bianca Pasca ◽  
Pavel Otrisal ◽  
...  

Using different methods of statistics, this paper aims to highlight the potential link between the antioxidant activity of flavonoids and the corresponding molecular descriptors. By calculating the descriptors (van der Waals surface (A), molar volume (V), partition coefficient (LogP), refractivity (R), polarizability (a), forming heat (Hformation), hydration energy (Ehidr), the dipole moment (mt)), together with antioxidant activities (RSA) calculated or taken from the literature, number of phenolic -OH groups and the presence (2) or absence (1) of C2=C3 double bond) for 29 flavonoid compounds and by intercorrelation between the studied parameters, the link between the number of phenolic groups grafted to the basic structure of flavonoids and their antioxidant activity was confirmed. Simultaneously, by using the chi-squared test and the intercorrelations matrix, a satisfactorily correlation coefficient (r2=0.5678; r=0.7536) between the structure of the flavonoids and their activity was obtained, fact that confirms the correlation of the antioxidant activity with the number of -OH phenolic groups.


2021 ◽  
Author(s):  
Abhineet Verma ◽  
Sk Saddam Hossain ◽  
Sailaja S Sunkari ◽  
Joseph Reibenspies ◽  
Satyen Saha

Lanthanides (LnIII) are well known for their characteristic emission in the Near-Infrared Region (NIR). However, direct excitation of lanthanides is not feasible as described by Laporte’s parity selection rule. Here,...


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