Recalcitrance as a catalyst for new developments

2001 ◽  
Vol 44 (8) ◽  
pp. 33-40 ◽  
Author(s):  
J.A. Field

Humic substances are very recalcitrant in anaerobic environments as substrates, mostly due to their non-hydrolyzable high molecular weight structure, which is incompatible for cell uptake. The recalcitrant nature can be applied towards immobilizing pollutants into non-toxic humic substances. Certain anaerobic bioconversions such as demethylation of lignin and reduction of nitro- or azo groups can activate pollutants for humification processes upon subsequent exposure to air. Although humic substances provide no carbon or energy for microorganisms, the evidence presented here indicates that they are very active as terminal electron acceptors and redox mediators promoting the anaerobic degradation and biotransformation of priority pollutants.

2000 ◽  
Vol 42 (5-6) ◽  
pp. 215-222 ◽  
Author(s):  
J.A. Field ◽  
F.J. Cervantes ◽  
F.P. van der Zee ◽  
G. Lettinga

Evidence is accumulating that inert humic substances can play important roles in the anaerobic degradation of priority pollutants by shuttling electrons. This paper reviews the roles of humus and quinone analogues as electron acceptors, redox mediators and electron donors for microbial and abiotic degradation processes. An eventual technology based on pumping quinones as terminal electron acceptors into aquifers and sediments to stimulate xenobiotic degradation offers promising potential. Also quinone redox mediators can be considered to accelerate reductive transformations (e.g. dechlorination, azo cleavage) of priority pollutants.


2002 ◽  
Vol 54 (11) ◽  
pp. 1471-1479 ◽  
Author(s):  
J. Rau ◽  
B. Maris ◽  
R. Kinget ◽  
C. Samyn ◽  
G. van den Mooter ◽  
...  

2020 ◽  
Author(s):  
Colin R. Bridges ◽  
Andryj M. Borys ◽  
Vanessa Béland ◽  
Joshua R. Gaffen ◽  
Thomas Baumgartner

Low molecular weight organic molecules that can accept multiple electrons at high<br>reduction potentials are sought after as electrode materials for high-energy sustainable batteries. To date their synthesis has been difficult, and organic scaffolds for electron donors significantly outnumber electron acceptors. Herein, we report two highly electron deficient phosphaviologen derivatives from a phosphorus-bridged 4,4-bipyridine and characterize their electrochemical properties. Phosphaviologen sulfide (PVS) and P-methyl phosphaviologen (PVM) accept two and three electrons at high reduction potentials, respectively. PVM can reversibly accept 3 electrons between 3-3.6 V vs. Li/Li+ with an equivalent molecular weight of 102 g/(mol e-) (262 mAh/g), making it a promising scaffold for sustainable organic electrode materials having high specific energy densities.


Agronomy ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1067
Author(s):  
Aleksandra Ukalska-Jaruga ◽  
Romualda Bejger ◽  
Guillaume Debaene ◽  
Bożena Smreczak

The objective of this paper was to investigate the molecular characterization of soil organic matter fractions (humic substances (HS): fulvic acids-FAs, humic acids-HAs, and humins-HNs), which are the most reactive soil components. A wide spectrum of spectroscopic (UV–VIS and VIS–nearIR), as well as electrochemical (zeta potential, particle size diameter, and polydispersity index), methods were applied to find the relevant differences in the behavior, formation, composition, and sorption properties of HS fractions derived from various soils. Soil material (n = 30) used for the study were sampled from the surface layer (0–30 cm) of agricultural soils. FAs and HAs were isolated by sequential extraction in alkaline and acidic solutions, according to the International Humic Substances Society method, while HNs was determined in the soil residue (after FAs and HAs extraction) by mineral fraction digestion using a 0.1M HCL/0.3M HF mixture and DMSO. Our study showed that significant differences in the molecular structures of FAs, Has, and HNs occurred. Optical analysis confirmed the lower molecular weight of FAs with high amount of lignin-like compounds and the higher weighted aliphatic–aromatic structure of HAs. The HNs were characterized by a very pronounced and strong condensed structure associated with the highest molecular weight. HAs and HNs molecules exhibited an abundance of acidic, phenolic, and amine functional groups at the aromatic ring and aliphatic chains, while FAs mainly showed the presence of methyl, methylene, ethenyl, and carboxyl reactive groups. HS was characterized by high polydispersity related with their structure. FAs were characterized by ellipsoidal shape as being associated to the long aliphatic chains, while HAs and HNs revealed a smaller particle diameter and a more spherical shape caused by the higher intermolecular forcing between the particles. The observed trends directly indicate that individual HS fractions differ in behavior, formation, composition, and sorption properties, which reflects their binding potential to other molecules depending on soil properties resulting from their type. The determined properties of individual HS fractions are presented as averaged characteristics over the examined soils with different physico-chemical properties.


2004 ◽  
Vol 52 (1) ◽  
pp. 29-32 ◽  
Author(s):  
Toshiyuki SHINOZUKA ◽  
Mitsuhiro SHIBATA ◽  
Tatsuaki YAMAGUCHI

Author(s):  
Francesca Della Sala ◽  
Teresa Silvestri ◽  
Assunta Borzacchiello ◽  
Laura Mayol ◽  
Luigi Ambrosio ◽  
...  

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