First Evidence of Active Sulphate Reduction in a Lignite Mine Dump Site at Low pH Values – the Plessa Site

2007 ◽  
Vol 20-21 ◽  
pp. 201-204 ◽  
Author(s):  
Annett Storch ◽  
Katja Tröger ◽  
Nils Hoth ◽  
Kay Knöller

It has been postulated that bacterial sulphate reduction is related to pH-values above 5.5 (e.g. [1]). First investigations for the 80-year old dump Plessa in the Lower Lusatian mining district (East Germany) show evidence for active sulphate reduction. Mining dump waters from the Plessa site have pH values of 2.4 to 4.9 and pe values between 2 and 6. Measured sulphide concentrations range from 50 to 1200 -g/L. The influence of bacterial sulphate reduction on the development of sulphate concentrations in the dump waters is supported by increasing δ34S and δ18O values with decreasing sulphate concentrations. These findings document that sulphate reduction under natural conditions is not exclusively related to neutral pH values and strongly reducing conditions. Furthermore the tertiary organic matter contained in the dump sediments is the main carbon source for sulphate reducing bacteria.

2019 ◽  
Vol 98 ◽  
pp. 01015
Author(s):  
Feng’e Zhang ◽  
Sheng Zhang ◽  
Miying Yin ◽  
Ze He ◽  
Xinxin Geng

The present work is designed to simulate the dissolution of sulphate rock under various conditions of different bacterial cell numbers, temperatures and reaction times both in water-rock system and water-rock-bacteria systems by laboratory experiment. The rate of sulphate reduction were estimated using the experimental data. The results suggested that the sulphate-reducing bacteria promote the sulphate rock dissolution and increase the amount of dissolved sulphate. The dissolution of sulphate rock driven by bacterial sulphate reduction results in the formation of sulphate rock karst. The research is an insight into biokarst, which provides a new perspective for the field of petroleum geology.


1985 ◽  
Vol 22 (12) ◽  
pp. 1910-1918 ◽  
Author(s):  
P. A. Trudinger ◽  
L. A. Chambers ◽  
J. W. Smith

Sulphate is considered to have been a major source of sulphide in strata-bound and stratiform base-metal sulphide deposits. Many of these deposits, however, appear to have been formed at moderate temperatures (<200 °C), which poses the question, By what mechanism(s) was sulphate reduced to sulphide? Two modes of reduction have been established experimentally: (1) catalysis by sulphate-reducing bacteria, which at present is only known to occur below ca. 100 °C; and (2) abiological reduction by ferrous iron or organic matter, which has only been clearly shown above ca. 250 °C.Several attempts have been made to demonstrate abiological reduction below 200 °C, and some new data are presented here. Although the results do not exclude the possibility that such a reaction may be geochemically significant, there has been no unequivocal demonstration of nett sulphide formation from sulphate at these temperatures.Recent studies of the microbiology of hydrothermal regions have opened up the prospect of bacterial sulphate reduction at much higher temperatures than had earlier been thought possible.


2021 ◽  
Vol 9 (2) ◽  
pp. 147-154
Author(s):  
Alena Luptakova ◽  
Eva Macingova ◽  
Vlasta Harbulakova

The submitted work is oriented on the study of two aspects of the sulphate-reducing bacteria metabolism: the metals bioprecipitation and the concrete biodeterioration. The bioprecipitation of metals with the bacterially produced hydrogen sulphide by sulphate-reducing bacteria (SRB) represents the positive effect of the SRB existence in the environment. It allows the industrial exploitation in the area of the removal metals from industrial wastewaters. Referred method involves principal stages such as: hydrogen sulphide bacterial production, metals precipitation by biologically produced hydrogen sulphide, metal sulphides separation, setting pH of the filtrate from previous steps by 1M NaOH and metal hydroxides separation. The basis of the first stage i.e. the hydrogen sulphide bacterial production is the cultivation of SRB. In the laboratory conditions the sodium lactate is the energetic substrate for the growth of bacteria. Its price is not economic for the application in the practice and is needed investigate the alternative substitutes. Therefore was studied the cultivation of sulphate-reducing bacteria to using the selected energetic substrates such as: calcium lactate, glycerol and whey. Experimental studies confirm that all chosen substrates are suitable alternative substrates of sodium lactate for the bacterial sulphate-reduction. In the regard to the efficiency of bacterial sulphate reduction the calcium lactate is the best. The biodeterioration of the concrete presents the negative effect of the SRB existence in the environment. The research was oriented on the simulation of the biodeterioration of concrete samples under the simultaneous influence of the sulphur-oxidising bacteria genera Acidithiobacillus thiooxidans and sulphatereducing bacteria genera Desulfovibrio in the environs of the waste water, the acid mine drainage, the nutrient medium and the distilled water. The observation of the surface structure changes of concrete samples confirms the highest biodeterioration influences in the case of the acid mine drainage application.


1991 ◽  
Vol 31 (3) ◽  
pp. 415 ◽  
Author(s):  
FC Miller ◽  
BJ Macauley ◽  
ER Harper

Investigations of hydrogen sulfide and ammonia concentrations, pH and redox potential were carried out within Phase I mushroom composting stacks in conjunction with measurements of temperature and oxygen concentrations. Gypsum-derived sulfate supported significant microbial activity by sulfate-reducing bacteria in anaerobic core areas. Ammonia concentrations up to 800 ppm were strongly associated with pH values up to 8.8 in aerobic stack areas. Anaerobic areas had pH values of 5-7, with little or no ammonia. Redox potential generally agreed with oxygenation history, with stacks exhibiting reducing conditions overall and with potential rising with compost maturity. Anomalously negative redox potentials in aerobic, outer stack areas were associated with actinomycete colonisation. Physical factors such as temperature, oxygen availability and water potential, which determine microbial and chemical activity in stacks, are distributed very unevenly, both spatially and temporally.


2021 ◽  
Vol 62 (08) ◽  
pp. 887-903
Author(s):  
D.A. Novikov ◽  
A.V. Chernykh ◽  
L.N. Konstantinova ◽  
F.F. Dultsev ◽  
I.I. Yurchik

Abstract —The Vendian deposits of the Siberian Platform are represented by four regional horizons (from bottom to top): Nepa, Vilyuchan, Tira, and Danilovka. The TDS of brines in the Nepa and Vilyuchan horizons varies from 170.3 to 470.1 g/L, and the TDS in the overlying Tira and Danilovka horizons, from 84.6 to 583.1 g/L. Brines of Cl Na, Cl Na–Ca, Cl Ca–Na, Cl Ca, and Cl Ca–Mg types have been identified. The pH values of the brines vary from 3.0 to 7.0; acidic and weakly acidic brines (pH = 3.0–5.5) prevail. The redox potential Eh varies from –440 mV (highly reducing conditions) to +130 mV (oxidizing conditions), averaging –176 mV. Areal regional hydrogeochemical zoning is controlled by the outer (on the periphery of the Siberian Platform, where infiltration of meteoric waters took place) and inner feeding areas. The outer feeding areas bear infiltrogenic brines of different ages (group I), mostly of Cl Na composition. They are characterized by TDS ≤ 280 g/L, rNa/rCl ≤ 1.55, Cl/Br ≤ 2512, and average Ca/Cl = 0.3. The average values of the integrated brine metamorphization index S (according to S.L. Shvartsev) range from 50 to 200. In the intraplatform feeding areas, there are several phases of brines that underwent gravitational sinking into the Vendian horizons in the periods when Cambrian salt-bearing basins existed on the platform. These brines were metamorphosed during filtration along the fracture and fault zones. The intrusion of traps in the late Permian–early Triassic was accompanied by hydrothermal activity. The waters of the enclosing Cambrian dolomite horizons were heated to 800–1000 °C; their subsequent interaction with carbonate rocks and evaporites (in particular, chlorides) resulted in extrastrong saturated brines. These brines were also subjected to gravitational sinking into the Vendian reservoirs, which was the main cause of the inverse vertical hydrogeochemical zoning in the hydrogeologic subsalt formation. The brine metamorphism processes and temperature changes in the rock horizons during the intrusion of traps and their subsequent cooling led to a significant alteration of the enclosing rocks under interaction with brines and to salinization of the reservoirs, an increase in the total salinity of the brines, and catagenetic changes in their composition. The brines closest to the maximum saturation with halite were found in reservoir zones with the highest salinization and near faults and boundaries of intrusive bodies. During the pre-Vilyuchan, pre-Nepa, pre-Tira, and pre-Danilovka sedimentation breaks, infiltrogenic waters penetrated into the Vendian sediments. Geochemically, the sedimentogenic, infiltrogenic, and metamorphic strong brines (group II) have a predominantly Cl Ca or Cl Ca–Mg composition with TDS &gt; 350 g/L. They are characterized by low rNa/rCl ratios (on average, 0.3), Cl/Br ≤ 100, high Ca/Cl values (on average, 0.4), and S &gt; 250.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Sarah B. Duckworth ◽  
Xavier Gaona ◽  
Alexander Baumann ◽  
Kathy Dardenne ◽  
Jörg Rothe ◽  
...  

Abstract The solubility of 99Tc(IV) was investigated from undersaturation conditions in NaCl–Na2SO4 (0.3 M ≤ I ≤ 5.0 M), MgCl2–MgSO4 (I = 13.5 M) and CaCl2–CaSO4 (I = 13.5 M) systems with 0.001 M ≤ [SO4 2−]tot ≤ 1.0 M and 1 ≤ pH m  ≤ 12 (with pH m  = −log[H+], in molal units). Reducing conditions were set by either Sn(II) or Fe(0). Special efforts were dedicated to accurately characterize the correction factors A m required for the determination of pH m from the experimentally measured pH values in the mixed salt systems investigated, with pH m  = pHexp + A m . The combination of (pe + pH m ) measurements with Pourbaix diagrams of Tc suggests that technetium is present in its +IV redox state. This hypothesis is confirmed by XANES, which unambiguously shows the predominance of Tc(IV) both in the aqueous and solid phases of selected solubility samples. XRD and SEM–EDS support the amorphous character of the solid phase controlling the solubility of Tc(IV). EXAFS data confirm the predominance of TcO2(am, hyd) at pH m  > 1.5, whereas the formation of a Tc(IV)–O–Cl solid phase is hinted at lower pHm values in concentrated NaCl–Na2SO4 systems with ≈5 M NaCl. Solubility data collected in sulfate-containing systems are generally in good agreement with previous solubility studies conducted in sulfate-free NaCl, MgCl2 and CaCl2 solutions of analogous ionic strength. Although the complexation of Tc(IV) with sulfate cannot be completely ruled out, these results strongly support that, if occurring, complexation must be weak and has no significant impact on the solubility of Tc(IV) in dilute up to highly saline media. Solubility upper-limits determined in this work can be used for source term estimations including the effect of sulfate in a variety of geochemical conditions relevant in the context of nuclear waste disposal.


2017 ◽  
Vol 17 (2) ◽  
pp. 203 ◽  
Author(s):  
Endah Retnaningrum ◽  
Wahyu Wilopo

The present research was conducted to investigate sulphate and manganese removal from synthetic wastewater. The continuous laboratory scale of down-flow fluidized-bed reactor (DFBR) using sulphate reducing bacteria (SRB) consortium and Indonesian natural zeolite as a bacterial support material was designed. At 9 days operation, maximum sulphate and manganese removal was observed to be 23% and 15.4%, respectively. The pH values were also changed to neutral. The population of SRB increased which effect on the raising of their activity for removing sulphate and manganese. Using the scanning electronic microscopy (SEM), it was observed that natural zeolite possesses excellent physical characteristics as a bacterial support material in DFBR. The imaging SEM result of SRB consortium on zeolite surface clearly showed the developed SRB biofilm on that particle. Analysis result of EDX confirmed that manganese was precipitated as manganese–sulfides.


Microbiology ◽  
1989 ◽  
Vol 135 (1) ◽  
pp. 175-187 ◽  
Author(s):  
R. J. PARKES ◽  
G. R. GIBSON ◽  
I. MUELLER-HARVEY ◽  
W. J. BUCKINGHAM ◽  
R. A. HERBERT

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