嗜酸氧化亚铁硫杆菌对煤炭脱硫影响的研究

嗜酸氧化亚铁硫杆菌(Acidithiobacillus ferrooxidans)广泛应用于湿法冶金和煤炭脱硫。不同的实验条件对煤炭脱硫效率的影响很大。以QXS菌株为实验对象,分别考查了处理时间、初始pH、煤样粒度、煤浆质量分数等因素对煤炭脱硫效率的影响,结果表明:处理时间达到10d后,全硫脱除率达到65%且不再继续增加;初始pH的影响符合钟罩形曲线,最佳pH条件为2.0左右;伴随煤样粒度和煤浆质量分数的增加,脱硫的效果均呈现减弱趋势。此外,对具有不同Fe2+氧化能力的菌株的脱硫能力进行了对比分析,结果表明它们的脱硫效率与Fe2+氧化能力呈正相关。采用QXS菌株,煤浆质量分数为20%,煤样粒度为200目(<0.074mm),初始pH为2.0,温度30℃,摇床转速为175r/min,接种量为1010～1011·g-1时,10d后煤炭的全硫脱除效率可达65.1%。

影响浸铀细菌活性的因素初探

微生物浸铀技术可以大幅度提高难浸铀矿石的浸出率 ,其关键技术是培养高活性的菌种。为了培养能适应多种恶劣条件的高活性菌种 ,必须对影响浸铀微生物活性的各种因素进行研究。通过实验室对浸铀细菌硫杆菌属中的氧化亚铁硫杆菌的活性因素的研究 ,并结合实际对从江西山南矿区的野外矿样中分离筛选出的菌株的活性的影响因素作了初步探讨 ,认为pH值为 1 8、温度为 30℃、接种量为 2 0 %及 90r/min的充气条件是该硫杆菌最佳的培养条件。通过对磷、铀两种元素在不同浓度下对细菌活性影响的试验 ,得出高浓度的磷、铀对细菌有明显的抑制作用 ,但通过驯化可以降低及弱化这种抑制作用。

A.f菌生物转盘反应器的工艺特性研究

采用嗜酸氧化亚铁硫杆菌(A.f菌)生物转盘反应器处理矿山酸性废水,研究了反应器转盘表面上固定化细菌的特性,同时还考察了HRT、进水的Fe2+浓度及转盘转速对Fe2+氧化率的影响。结果表明,以5%(体积分数)的接种量接种,进行接续性循环培养,随着培养次数的增加,Fe2+的氧化周期不断缩短(由最初的100h降至70h),反应器的氧化性能逐渐增强,连续6次循环培养后可完成反应器的启动;反应器运行稳定后,其对Fe2+的氧化速率最高可达2.32g/(L.h);Fe2+的氧化率随进水Fe2+浓度的增加而降低,在实际工程中,当进水的Fe2+浓度较高时,宜采用多级处理方式;该试验条件下,反应器的最佳HRT为4h、最佳转盘转速为7r/min。

氨基酸营养对At.f菌生长迟缓期的影响

[目的]研究氨基酸营养对At.f菌生长迟缓期的影响。[方法]将At.f在分别加入20种氨基酸的培养基中培养,利用重铬酸钾滴定法测定各时段Fe2+利用情况,并检测添加氨基酸后培养基pH的变化。[结果]非极性氨基酸对缩短At.f菌的迟缓期的效果较明显;苯丙氨酸、酪氨酸、脯氨酸、色氨酸四种成环氨基酸有较好的效果;丝氨酸、谷氨酰胺、组氨酸有明显的抑制作用。[结论]非极性氨基酸能有效缩短At.f菌生长迟缓期,部分极性氨基酸则起到相反效果。

微生物法脱除煤炭中黄铁矿硫

用微生物法脱除四川松藻煤矿煤样中黄铁矿硫的初步试验已经完成。氧化亚铁硫杆菌(Thiobacillus ferrooxidans)在煤炭脱硫过程中起着重要作用。根据 pH 值、接种量、煤浆浓度、摇床转速、营养成分以及培养时间对微生物煤炭脱硫的影响,确定了微生物煤炭脱硫的最佳条件。氧化亚铁硫杆菌在8天时间内,可脱除70%左右的黄铁矿硫,使煤的总含硫量从2.45%降到1,12%,低于国家规定标准(燃煤含硫量1.50%以下)。另外,还对提高微生物煤炭脱硫的一些措施及脱硫的机理进行了研究,发现在黄铁矿上适应后的菌体比非适应菌体的脱硫能力强;吸附在黄铁矿上的菌体比游离菌体的活性高;微生物直接氧化机理在脱硫过程中起着主要作用;同时还探讨了细菌处理后的煤样中还残留一部分不能被进一步作用的黄铁矿的原因。

Electrochemical oxidation behavior of pyrite bioleaching by Acidthiobacillus ferrooxidans

The electrochemical oxidation behavior of pyrite in bioleaching system of Acidthiobacillusferrooxidans was investigated by cyclic voltammetry （CV）, polarization curve and electrochemical impedance spectroscopy （EIS）. The results show that in the presence or absence of A. ferrooxidans, the oxidation reaction of pyrite is divided into two steps： the first reaction step involves the oxidation of pyrite to S, and the second reaction step is the oxidation of S to SO4^2-. The oxidation mechanism of pyrite is not changed in the presence of A. ferrooxidans, but the oxidation rate of pyrite is accelerated. With the extension of reaction time of A. ferrooxidan with pyrite, the polarization current density of pyrite increases and the breakdown potential at which the passive film dissolves decreases. The impedance in the presence ofA. ferrooxidans is obviously lower than that in the absence of A. ferrooxidans, further indicating that microorganism accelerates the corrosion process of pyrite.

Enhancement of bio-oxidation of refractory arsenopyritic gold ore by adding pyrolusite in bioleaching system

Pyrolusite was added in the bioleaching process to enhance the bio-oxidation process. Bioleaching tests at different dosages of pyrolusite ore, pH and inoculation amounts of Acidithiobacillus ferrooxidans were studied. The results showed that the time of the bio-oxidation process was decreased obviously and the arsenic leaching rate reached 94.4% after the bioleaching. The bio-oxidation of arsenopyrite and the effective extraction of manganese from pyrolusite were achieved by the bioleaching process. After bioleaching, the leaching rate of gold from the reaction residues reached 95.8% by cyanide leaching. In the bio-oxidation process, pyrolusite increased the redox potential of the solution to accelerate the bioleaching rate. The experiment showed that there were two reaction modes in the bioleaching process.

Decomposition mechanism of pentlandite during electrochemical bio-oxidation process

Electrochemical measurements were carried out to elucidate decomposition mechanism of pentlandite using modified powder microelectrode with Acidithiobacillus ferrooxidans attached or without on the mineral powder surface.Cyclic voltammetry（CV） results show that at a low potential of about-0.2 V（vs SCE）,the pentlandite was transformed to an intermediated phase like Fe4.5-yNi4.5-xS8-z when Fe and Ni ions were evacuated from mineral lattice;when the potential was changed from-0.2 V to 0.2 V,the unstable violarite（Fe3Ni3S4） and FeNi2S4 were formed which was accompanied by element sulfur formed on the mineral surface;when the potential increased over 0.2 V,the unstable intermediated phase decomposed entirely;at a higher potential of 0.7 V,the evacuated ferrous ion was oxidized to ferric ion.The presence of Acidithiobacillus ferrooxidans made the oxidation peak current increase with initial peak potential negatively moving,and the bacteria also contributed to the sulfur removing from mineral surface,which was demonstrated by the reduction characteristic at potential ranging from-0.75 to-0.5 V.Leaching experiments and electrochemical results show that the solution acidity increasing when pH2 may impede the oxidation process slightly.

Acidthiobacillus ferrooxidans中磁小体的提取(英文)

At.f和趋磁细菌在生理特性和生长环境有一定的相似性,而且镜检发现At.f具有趋磁性,所以本文采用了趋磁细菌中磁小体的提取方法尝试提取At.f中的磁小体,用超声波破碎At.f后,以磁铁吸取其体内的磁性颗粒,经过检测,发现其体内确实存在含铁元素的磁性颗粒。提取粗样品经过电镜分析,证实其体内存在着少量由脂质包裹的磁小体。磁小体悬浮液经过蔗糖密度梯度离心纯化后,对其作透射电镜,可以清晰的看到磁小体。实验结果表明,At.f体内存在少量的磁小体,正是由于磁小体的存在,才使得At.f在外加磁场作用下发生磁生物效应。这是首次发现从酸性矿坑水分离的At.f具有趋磁性,并从中提取到了磁小体,可以利用At.f的趋磁性将其按照不同磁性进行分离,从而获得活性高的、对不同磁性矿物有特异性的高效浸矿菌种。

Preservation efficiency of new cryoprotectant used for Acidithiobacillus ferrooxidans in liquid nitrogen

The efficiency of a new cryoprotectant,GP,for the preservation of Acidithiobacillus ferrooxidans（A.ferrooxidans） strain DC in liquid nitrogen was investigated.The optimal concentration of this new cryoprotectant for the maximal viable cell recovery and the highest ferrous ion oxidation activity was determined.The results show that 30%（volume fraction） GP is optimal for the cryopreservation with 84.4% of cells surviving,completely oxidizing ferrous ions within 120 h,and growing to a final density of 5.8×107 cell/mL after 6 d in the culture.Furthermore,the optimal residual GP concentration for viable cell recovery after culture of thawed cells in 9K medium for 6 d is 0.6%（volume fraction）.At this concentration,strain DC completely oxidizes ferrous ions within 108 h and grows to a final cell density of 6.8×107 mL-1.Thus,GP is a simple,effective cryoprotectant for the preservation of A.ferrooxidans strain DC in liquid nitrogen.

Effect of pH values on extracellular protein and polysaccharide secretions of Acidithiobacillus ferrooxidans during chalcopyrite bioleaching

The effect of pH values on the extracellular protein and polysaccharide secretions of Acidithiobacillus ferrooxidans was comparatively investigated in different phases of bacterial growth during chalcopyrite bioleaching. The results indicate that the extracellular protein is always more than the extracellular polysaccharide secreted by attached cells on the chalcopyrite, on the contrary, and is always less than the extracellular polysaccharide secreted by free cells in the solution at bacterial adaptive phase, logarithmic phase and stationary phase whenever pH value is at 1.0, 1.5, 2.0 or 2.5; free cells are mainly through the secretion of extracellular polysaccharide rather than the extracellular protein to fight against disadvantageous solution environment, such as high concentration of metal ions and unsuitable pH solution; both amounts of polysaccharide and protein secreted by attached cells are mainly positively related to the solution acidity rather than the total concentration of soluble metal ions. The experimental results imply that bacteria are mainly through secreting more extracellular polysaccharide to fight against disadvantageous environment and the extracellular protein perhaps plays an important role in oxidation？reduction reactions in the bioleaching system.

Comparison of Fe^(2+) oxidation by Acidithiobacillus ferrooxidans in rotating-drum and stirred-tank reactors

Fe2＋ oxidation by Acidithiobacillus ferrooxidans（At.ferrooxidans） under different solid contents by adding inert Al2O3 powder was examined in rotating-drum and stirred-tank reactors.The results show that the bioactivity of At.ferrooxidans in the stirred-tank is higher than that in the rotating-drum in the absence of Al2O3 powder,but the biooxidation rate of Fe2＋ decreases markedly from 0.23 g/（L·h） to 0.025 g/（L·h） with increasing the content of Al2O3 powder from 0 to 50%（mass fraction） in the stirred-tank probably due to the deactivation of At.ferrooxidans resulting from the collision and friction of solid particles.The increase in Al2O3 content has a little adverse effect on the bioactivity of At.ferrooxidans in the rotating-drum due to different mixing mechanisms of the two reactors.The biooxidation rate of Fe2＋ in the rotating-drum is higher than that in the stirred-tank at the same content of Al2O3 powder,especially at high solid content.The higher bioactivity of At.ferrooxidans can be maintained for allowing high solid content in the rotating-drum reactor,but its application potential still needs to be verified further by the sulfide bioleaching for the property differences of Al2O3 powder and sulfide minerals.

Really active form of fluorine toxicity affecting Acidithiobacillus ferrooxidans activity in bioleaching uranium

In order to determine the mechanism of bacterial tolerance to fluorine,Acidithiobacillus ferrooxidans ATCC 23270 was domesticated and studied under the conditions of different fluorine concentrations and pH values with or without treatment by Proteinase K.The bacterial activities were observed through measuring the changes of solution potentials by platinum electrode with Ag/AgCl reference electrode and the intracellular fluorine was determined by-uorine ion-selective electrode.The results indicated that the tolerance of Acidithiobacillus ferrooxidans ATCC 23270 to fluorine could be obviously improved by domestication,HF was the effective form of fluorine to affect the bacterial activity,and pH increase or concentration change of ions of strong complex ability with fluorine ions in solution could result in false appearance of high fluorine-resistant strain.Some proteins located in cell wall or cell membrane were intimately relative with the bacterial fluorine tolerance.

Catalytic effect of visible light and Cd^2+on chalcopyrite bioleaching

The effects of visible light and Cd^2+ion on chalcopyrite bioleaching in the presence of Acidithiobacillus ferrooxidans(A.ferrooxidans)were studied by scanning electron microscopy(SEM),synchrotron radiation X-ray diffraction(SR-XRD),and X-ray photoelectron spectroscopy(XPS).The results of bioleaching after 28 days showed that the copper dissolution increased by 4.96%with only visible light,the presence of Cd2+alone exerted slight inhibition effect on chalcopyrite dissolution and the concentration of dissolved copper increased by 14.70%with visible light and 50 mg/L Cd^2+.The results of chemical leaching showed that visible light can promote the circulation of iron.SEM results showed that Cd^2+promoted the attachment of A.ferrooxidans on chalcopyrite surface under visible light.SR-XRD and XPS results indicated that visible light and Cd^2+promoted chalcopyrite dissolution,but did not inhibit the formation of passivation.Finally,a model of synergistic catalysis mechanism of visible light and Cd2+on chalcopyrite bioleaching was proposed.

Bioleaching of low-grade copper sulfide ores by Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans

The grown conditions of Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans were investigated,and then experiments were conducted to research the bioleaching behaviors of crude ore of copper sulfide and hand-picked concentrates of chalcopyrite by Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans.The experimental results show that the bacteria grow best when the temperature is(30±1) °C and the pH value is 2.0.The bacteria concentration is 2.24×107 mL-1 in this condition.It is found that the copper extraction yield is affected by the inoculum size and the pulp density and the extraction yield increases as the inoculum size grows.The bioleaching rates reach their highest point in sulfide copper and chalcopyrite with a pulp density of 5% and 10%,respectively.Column flotation experiments of low-grade copper sulfide ores show that the bioleaching recovery reaches nearly 45% after 75 days.

Photogenerated-hole scavenger for enhancing photocatalytic chalcopyrite bioleaching

The effects of photogenerated-hole scavengers(ascorbic acid,oxalic acid,humic acid and citric acid)on chalcopyrite bioleaching in the presence of visible light were studied using Acidithiobacillus ferrooxidans(A.ferrooxidans).Four sets of bioleaching experiments were performed:(1)visible light+0 g/L scavenger,(2)visible light+0.1 g/L of different scavenger(ascorbic acid,oxalic acid,humic acid and citric acid),(3)dark+0.1 g/L of different scavenger(ascorbic acid,oxalic acid,humic acid and citric acid),and(4)dark+0 g/L scavenger(control group).The results showed that ascorbic acid and oxalic acid could act as photogenerated-hole scavengers and significantly enhance chalcopyrite bioleaching under visible light.The dissolved copper in the light group without scavenger was only 18.7%higher than that of the control group.The copper extraction rates of the light groups with oxalic acid and ascorbic acid were respectively 30.1%and 32.5%higher than those of the control group.Scanning electron microscopy(SEM),X-ray diffraction(XRD)and Fourier transform infrared spectroscopy(FT-IR)analyses indicated that ascorbic acid and oxalic acid as photogenerated-hole scavenger could capture photo-generated holes and inhibit jarosite formation on the chalcopyrite surface,thereby enhancing bioleaching of chalcopyrite under visible light.

Bioleaching of chalcopyrite by UV-induced mutagenized Acidiphilium cryptum and Acidithiobacillus ferrooxidans

The original strains Acidithiobacillusferrooxidans GF and Acidiphilium cryptum DXI-1 were isolated from the drainage of some caves riched in chalcopyrite in Dexing Mine in Jiangxi Province of China. The optimum temperature and pH for growth were 30 ℃ and 3.5 for Ac. cryptum DXI-1, and 30 ℃ and 2.0 for At. ferrooxidans GF, respectively. For Ac. cryptum DXI-1, the optimum UV radiating time was 60 s and the positive mutation rate was 22.5%. The growth curves show that Ac. cryptum after mutagenesis reached stationary phase within 60 h, which was 20 h earlier than the original strain. For At. ferrooxidans GF, the optimum mutation time was 60 s and the positive mutation rate was 35%. The most active UV-mutated strain At. ferrooxidans GF oxidized all the ferrous after 48 h. The bioleaching experiments showed that bioleaching with the mixture of UV-mutated strains of At. ferrooxidans GF and A c. cryptum DX1-1 （1：1） could extract 3.01 g/L of copper after 30 d, while the extracted copper was 2.63 g/L with the mixture of the original strains before UV-mutation. At the end of the bioleaching experiments, the proportion of the cell density in the cultures ofAc. cryptum DXI-1 andAt.ferrooxidans GF was approximately 1：5.

Enhancing recovery of uranium column bioleaching by process optimization and kinetic modeling

This research aimed to enhance the column bioleaching recovery of uranium ore by Acidithiobacillus ferrooxidans.Seven factors were examined for their significance on bioleaching using a Plackett-Burman factorial design.Four significant variables([Fe2+]initial,pH,aeration rate and inoculation percent)were selected for the optimization studies.The effect of these variables on uranium bioleaching was studied using a central composite design(CCD).The optimal values of the variables for the maximum uranium bioleaching recovery(90.27±0.98)%were as follows:[Fe2+]initial=2.89g/L,aeration rate420mL/min,pH1.45and inoculation6%(v/v).[Fe2+]initial was found to be the most effective parameter.The maximum uranium recovery from the predicted models was92.01%.This value was in agreement with the actual experimental value.The analysis of bioleaching residue of uranium ore under optimum conditions confirmed the formation of K-jarosite on the surface of minerals.By using optimal conditions,uranium bioleaching recovery is increased at column and jarosite precipitation is minimized.The kinetic model showed that uranium recovery has a direct relation with ferric ion concentration.

Mechanism of bioleaching chalcopyrite by Acidithiobacillus ferrooxidans in agar-simulated extracellular polymeric substances media

The mechanism of leaching chalcopyrite by Acidithiobacillus ferrooxidans （,4. ferrooxidans） in agar-simulated extracellular polymeric substances （EPS） media was investigated. The results indicate that bacterial EPS can release H＋ and concentrate Fe3＋; Fe2＋ is movable between agar-simulated EPS phase and bulk solution phase, but it is difficult for Fe3＋ to move due to its hydroxylation and EPS complex action; A. ferrooxidans first prefer Fe2＋ as energy to metabolize compared with chalcopyrite, and a suitable simulated EPS environment for bacterial living is at about pH 1.8; the iron precipitates and jarosites formed by a lot of biologically oxidized Fe3 cover the simulated EPS easily and form an impermeable deposit acting as a limited barrier of ion transport that attenuates the aggressiveness of the bioleaching attack. The EPS layer blocked by iron precipitates or jarosites is responsible for the chalcopyrite passivation.

Formation of jarosite and its effect on important ions for Acidithiobacillus ferrooxidans bacteria

The precipitation of jarosite adversely affects the bio-leaching of copper sulfides in the Sarcheshmeh heap bio-leaching process. The variables of the initial concentration of ferrous iron in the growth medium, pH, and temperature were examined in the laboratory to determine how they affect the precipitation of jarosite in the presence of Acidithiobacillus ferrooxidans bacteria. It was found that the maximum ferric precipitate occurred at a ferrous sulfate concentration of 50 g/L, a temperature of 32 ℃, and an initial pH value of 2.2. The effects of the precipitation of ferric iron on the quantities of ions that are important for A. ferrooxidans bacteria in aqueous phase, i.e., ferric, sulfate, potassium, phosphate, and magnesium ions, also were assessed. The results showed relatively similar patterns for the ferric and potassium ions, and then reason might have been the co-precipitation of these ions as constituent elements of jarosite mineral. At pH values greater than 1.6, the solubility of phosphate ions decreased dramatically due to the co-precipitation of phosphate ions with the jarosite precipitate and due to the significant growth rate of A. ferrooxidans bacteria in this pH range. Due to the dissolution of a gangue constituent in the ore, the magnesium levels increased in the first few days of the bio-leaching process;thereafter, it decreased slightly.