Cupric ion binding by coal humic acids at pH's 1–3

1977 ◽  
Vol 55 (18) ◽  
pp. 3248-3254 ◽  
Author(s):  
John B. Green ◽  
Stanley E. Manahan

The extent and mechanism of cupric ion binding by humic acid (HA) at low pH's where the material was insoluble in aqueous media was investigated. It was shown that significant amounts of Cu(II) were bound by HA even at pH's as low as 1.35. Two major types of HA—Cu2+ binding were observed. Binding which was accompanied by exchange of H+ was more prevalent at high pH's and [Cu2+]. Nonexchange bonding occurred at all pH's, but assumed greater importance at low pH's. Since the pattern of Cu(II) uptake could not be interpreted in terms of basic ion exchange or surface adsorption theory, a new model was proposed which qualitatively explained the dependence of Cu(II) on pH and [Cu2+]. The model assumed that the intermolecular bonding in flocculated HA was determined by the relative amounts of H+ and Cu2+ available for forming bridging bonds between the HA molecules. The model suggested that at high concentrations of Cu(II) and/or high pH's, the floc structure was such that the formation of copper bridge bonds was maximized.

2012 ◽  
Vol 51 (3) ◽  
pp. 228-237
Author(s):  
D. Dudare ◽  
M. Klavins

The aim of this study is to determine the Cu(II) complexing capacity and stability constants of Cu(II) complexes of humic acids isolated from two well-characterized raised bog peat profiles in respect to the basic properties and humification characteristics of the studied peats and their humic acids. The complex stability constants significantly change within the studied bog profiles and are well correlated with the age and decomposition degree of the peat layer from which the humic acids have been isolated. Among factors that influence this complexation process, molecular mass and ability to form micellar structures (supramolecules) of humic substances are of key importance.


2019 ◽  
Vol 1 (1) ◽  
pp. 29-32
Author(s):  
Ruzimurod B. Boimurodov ◽  
Zebinisso Q. Bobokhonova

In this article is showing, that the irrigation mountain brown carbonate soils prone methods of irrigation and grassing comes the rapid growth and development of natural vegetation, which leads to intensive humus accumulation. Humus content in the upper layer is increased by 0.98% and a significantly smaller severely eroded. Increasing the amount of humus promotes accumulation mainly humic acids, that conducts to expansion of relations the content of humic acid: The content of folic acid. When grassing of soil traced sharp increase in the number associated with the related and R2 O3 humic acid.


2018 ◽  
Vol 69 (1) ◽  
pp. 191-195
Author(s):  
Elena Radu ◽  
Elena Emilia Oprescu ◽  
Cristina Emanuela Enascuta ◽  
Catalina Calin ◽  
Rusandica Stoica ◽  
...  

The dehydration of polysaccharides fraction in the presence of acid catalysts, is a chemical process in which results as secondary product humic matter. In our work, the humic acid mixture was for the first time based on our knowledge extracted from defatted microalgae biomass rich in polysaccharides by standard alkali treatment, followed by precipitation at acidic pH. The dried humic acid mixture has been characterized using infrared spectroscopic measurements (FT-IR). Exfoliated graphite nanoplatelets (xGnP) were used as new adsorbents for this type of humic acids mixture, their adsorption being investigated. The effect of several parameters such as: contact time, concentration of humic acid mixture, concentration of xGnP, temperature and pH of the solutions were studied. The process of adsorption took place with good results, in the following conditions: at a concentration of humic acid mixture of 18.6 mg L-1, an xGnP amount of 0.01 mg in 25 mL of solution, at a temperature of 25 �� and at acidic pH values, in aqueous solution.


Chemosphere ◽  
2021 ◽  
Vol 273 ◽  
pp. 129678
Author(s):  
Yingjie He ◽  
Lei Huang ◽  
Baocheng Song ◽  
Bichao Wu ◽  
Lvji Yan ◽  
...  

2001 ◽  
Vol 35 (12) ◽  
pp. 2512-2517 ◽  
Author(s):  
Iso Christl ◽  
Chris J. Milne ◽  
David G. Kinniburgh ◽  
Ruben Kretzschmar

2012 ◽  
Vol 442 ◽  
pp. 54-57
Author(s):  
Heng Li

The ion-exchanger Li0.6Zn1.2PO4of spinel type was prepared by a solid state reaction crystallization method. The extraction/insertion reaction with this material was investigated by X-ray, saturation capacity of exchange, and Kd measurement. The experimental results have proved that the acid-treated sample has a capacity of exchange 2.4mmol•g-1for Li+in the solution, The chemical analysis showed that the Li+extraction/insertion progressed mainly by ion-exchange mechanism and surface adsorption.


2021 ◽  
Author(s):  
Chunli Li ◽  
Zhiwei David Yue ◽  
Xiaohong Tian ◽  
John Hazlewood

Abstract Humic acids, one major type of organic foulants in steam assisted gravity drainage (SAGD) produced water, can precipitate on surface and downhole equipment in SAGD facilities, resulting in high cleaning costs, potential equipment damage and decrease of injectivity of disposal wells. In this paper, a cost-effective chemical solution is presented where an alcohol ethoxylate surfactant/chelating agent package can efficiently disperse the organic fouling molecules in SAGD produced water; therefore, the approach is expected to significantly mitigate the humic acid related fouling issues in the SAGD system. In this study, a variety of commercially available surfactant products were evaluated for their aids in well injectivity on humic acid molecules in the freshly obtained SAGD produced water. The lab testing filtration apparatus was specially designed to simulate the sandstone formation geology of SAGD disposal wells. An "efficiency factor" was defined to grade the dispersing performance of the surfactant and/or surfactant/chelating agent package in the lab filtration tests. The efficiency factor provides a reasonable estimation regarding how well the chemical can reduce the plugging risk in a disposal well as compared to the untreated produced water. Among all the surfactant products tested, an alcohol ethoxylate surfactant with the appropriate molecular structure shows distinguished dispersing performance on humic acids in SAGD produced water. However, the surfactant alone was found inconsistent in the dispersing performance when different batches of the produced water were involved. Inclusion of the specific metal chelating agents to the above surfactant formulation improved the dispersing performance consistency. The chelator molecules presumably help destroy the intermolecular bridges among humic acid molecules in the SAGD produced water; thereby, increasing the dispersing effectiveness of the alcohol ethyoxylate surfactants. Tests show that the efficiency factor of the surfactant/chelating agent package is higher than 8, which implies that the formulation could lead to eight times extension of the interval between workovers on SAGD disposal wells, a significant reduction for the operational downtime and costs. This study presented a cost-effective chemical solution to help disperse the humic acid molecules in SAGD produced water, which can help significantly reduce the fouling risk caused by organic foulants, improve injectivity and extend the intervals between workovers of SAGD disposal wells.


2017 ◽  
Vol 71 (4) ◽  
pp. 319-327
Author(s):  
Benjamin Catovic ◽  
Minela Sisic ◽  
Majda Srabovic ◽  
Melita Huremovic

Lignite is brown coal, which in its composition contains humic acids. Humic acids are produced by coal combustion, which leads to the enrichment of coal humic acids. Lignite, from the opet pit mine Sikulje, lignite ore ?Kreka?, Bosnia and Herzegovina, was fragmented and sieved to the appropriate size and used as a base material. The isolation of humic acid was carried out from pre-oxidized and dried lignite after which it was refined. Identification thus obtained humic acids was carried out by FTIR spectroscopy and its characterization of UV analysis which is determined by optical density of isolated humic acid and its complexation with metal cations. Data obtained by FTIR spectroscopic analysis of isolated humic acids show no significant structural and chemical difference in relation to the spectrum obtained for standard humic acids (Sigma Aldrich). UV analysis showed that isolated and standard humic acid have E4/E6 ratio in an appropriate range of 3?5, which indicates the presence of a large number of aliphatic structure. Based on the degree of humification was found that the isolated humic acids belong to the type B standard while humic acids belong to type A. The most important property of the humic substances is the ability to interact with the metal ions forming soluble or insoluble complexes which possess different chemical and biological properties and stability. The nature of the complex between humic acid and metal cation derived from the heterogeneous, polyelectric and polydispersive character humic acids that occurs due to the presence of a large number of functional groups. Complexation of humic acid is carried out with different concentrations of metal nitrate solutions and at different pH values. Different amounts of humic acids were used for the complexation. The amount of the free metal ions was measured with the ICP-OES methode. The data were also statistically analyzed with ANOVA. The results showed that increasing the pH reduces the concentration of metal ions adsorbed on humic acid and by increasing the concentrations and amounts of metal humic acid that power increases. On the basis of the difference in absorbance between metals and humic acids can be said that there is an interaction between the metal and the ligand and is based on absorbance values obtained can be determine the next set of metal binding to humic acids Pb>Zn>Ni>Cu.


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