scholarly journals Isolation of Soil Bacteria Adapted To Degrade Humic Acid-Sorbed Phenanthrene

2005 ◽  
Vol 71 (7) ◽  
pp. 3797-3805 ◽  
Author(s):  
D. J. Vacca ◽  
W. F. Bleam ◽  
W. J. Hickey
Keyword(s):  
Humic Acid ◽  
Humic Acids ◽  
Contaminated Soils ◽  
Soil Bacteria ◽  
Polynuclear Aromatic Hydrocarbons ◽  
Aerobic Bacteria ◽  
Substrate Uptake ◽  
Bacterial Phylotypes ◽  
Selective Interaction ◽  
Different Levels

ABSTRACT The goal of these studies was to determine how sorption by humic acids affected the bioavailability of polynuclear aromatic hydrocarbons (PAHs) to PAH-degrading microbes. Micellar solutions of humic acid were used as sorbents, and phenanthrene was used as a model PAH. Enrichments from PAH-contaminated soils established with nonsorbed phenanthrene yielded a total of 25 different isolates representing a diversity of bacterial phylotypes. In contrast, only three strains of Burkholderia spp. and one strain each of Delftia sp. and Sphingomonas sp. were isolated from enrichments with humic acid-sorbed phenanthrene (HASP). Using [14C]phenanthrene as a radiotracer, we verified that only HASP isolates were capable of mineralizing HASP, a phenotype hence termed “competence.” Competence was an all-or-nothing phenotype: noncompetent strains showed no detectable phenanthrene mineralization in HASP cultures, but levels of phenanthrene mineralization effected by competent strains in HASP and NSP cultures were not significantly different. Levels and rates of phenanthrene mineralization exceeded those predicted to be supported solely by the metabolism of phenanthrene in the aqueous phase of HASP cultures. Thus, competent strains were able to directly access phenanthrene sorbed by the humic acids and did not rely on desorption for substrate uptake. To the best of our knowledge, this is the first report of (i) a selective interaction between aerobic bacteria and humic acid molecules and (ii) differential bioavailability to bacteria of PAHs sorbed to a natural biogeopolymer.

Changes in the Humic Acid–Metal Complexation Characteristics Depending on Humification Degree / Humīnskābju – Metālu Kompleksveidošanās Rakstura Izmaiņas Atkarībā No Humifikācijas Pakāpes

2012 ◽  
Vol 51 (3) ◽  
pp. 228-237
Author(s):  
D. Dudare ◽  
M. Klavins
Keyword(s):  
Humic Acid ◽  
Stability Constants ◽  
Humic Acids ◽  
Complex Stability ◽  
Peat Layer ◽  
Raised Bog ◽  
Complexing Capacity ◽  
Humification Degree ◽  
Complexation Process ◽  
Complex Stability Constants

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.

EFFECT OF IRRIGATION AND GRASSING TO CHANGE SOME OF THE BIOLOGICAL PROPERTIES OF THE MINING OF BROWN CALCAREOUS SOILS

2019 ◽  
Vol 1 (1) ◽  
pp. 29-32
Author(s):  
Ruzimurod B. Boimurodov ◽  
Zebinisso Q. Bobokhonova
Keyword(s):  
Folic Acid ◽  
Humic Acid ◽  
Humic Acids ◽  
Rapid Growth ◽  
Growth And Development ◽  
Sharp Increase ◽  
Humus Content ◽  
Calcareous Soils ◽  
Biological Properties ◽  
Humus Accumulation

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.

Kinetic Adsorption of Humic Acids Mixture Obtained from Microalgae on Exfoliated Graphite Nanoplatelets

2018 ◽  
Vol 69 (1) ◽  
pp. 191-195
Author(s):  
Elena Radu ◽  
Elena Emilia Oprescu ◽  
Cristina Emanuela Enascuta ◽  
Catalina Calin ◽  
Rusandica Stoica ◽  
...  
Keyword(s):  
Humic Acid ◽  
Humic Acids ◽  
Alkali Treatment ◽  
Exfoliated Graphite ◽  
Acid Mixture ◽  
Acidic Ph ◽  
Graphite Nanoplatelets ◽  
Mixture Concentration ◽  
Ft Ir ◽  
Exfoliated Graphite Nanoplatelets

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.

Effective Treatment of Humic Acid Foulants in SAGD Produced Water

2021 ◽  
Author(s):  
Chunli Li ◽  
Zhiwei David Yue ◽  
Xiaohong Tian ◽  
John Hazlewood
Keyword(s):  
Humic Acid ◽  
Humic Acids ◽  
Produced Water ◽  
Chelating Agent ◽  
Cost Effective ◽  
Efficiency Factor ◽  
Alcohol Ethoxylate ◽  
Major Type ◽  
Chemical Solution ◽  
Well Injectivity

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.

scholarly journals Genome reduction in an abundant and ubiquitous soil bacterial lineage

2016 ◽  
Author(s):  
Tess E Brewer ◽  
Kim M Handley ◽  
Paul Carini ◽  
Jack A Gibert ◽  
Noah Fierer
Keyword(s):  
Soil Bacteria ◽  
Large Population ◽  
Metabolic Reconstruction ◽  
Soil Environment ◽  
Genomic Databases ◽  
Bacterial Phylotypes ◽  
Bacterial Lineage ◽  
Metabolic Versatility ◽  
Soil Metagenome ◽  
Soil Bacterial

AbstractAlthough bacteria within theVerrucomicrobiaphylum are pervasive in soils around the world, they are underrepresented in both isolate collections and genomic databases. Here we describe a single verrucomicrobial phylotype within the classSpartobacteriathat is not closely related to any previously described taxa. We examined >1000 soils and found this spartobacterial phylotype to be ubiquitous and consistently one of the most abundant soil bacterial phylotypes, particularly in grasslands, where it was typically the most abundant phylotype. We reconstructed a nearly complete genome of this phylotype from a soil metagenome for which we propose the provisional name ‘CandidatusUdaeobacter copiosus’. TheCa. U. copiosus genome is unusually small for soil bacteria, estimated to be only 2.81 Mbp compared to the predicted effective mean genome size of 4.74 Mbp for soil bacteria. Metabolic reconstruction suggests thatCa. U. copiosus is an aerobic chemoorganoheterotroph with numerous amino acid and vitamin auxotrophies. The large population size, relatively small genome and multiple putative auxotrophies characteristic ofCa. U. copiosus suggests that it may be undergoing streamlining selection to minimize cellular architecture, a phenomenon previously thought to be restricted to aquatic bacteria. Although many soil bacteria need relatively large, complex genomes to be successful in soil,Ca. U. copiosus appears to have identified an alternate strategy, sacrificing metabolic versatility for efficiency to become dominant in the soil environment.

scholarly journals Isolation of humic acid from oxidized lignite and complexation with metal cations

2017 ◽  
Vol 71 (4) ◽  
pp. 319-327
Author(s):  
Benjamin Catovic ◽  
Minela Sisic ◽  
Majda Srabovic ◽  
Melita Huremovic
Keyword(s):  
Humic Acid ◽  
Metal Ions ◽  
Humic Acids ◽  
Metal Binding ◽  
Base Material ◽  
Metal Cations ◽  
Biological Properties ◽  
Metal Nitrate ◽  
Chemical Difference ◽  
The Difference

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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