Humic acid

腐殖酸
  • 文章类型: Journal Article
    如何解决多孔材料吸附污染物的效率与吸附速率之间的矛盾一直是人们关注的焦点问题之一。在这项研究中,利用腐殖酸(HA)设计并合成了小型景观柏树仿生结构的分层和双重形态三维多孔HA气凝胶,以果胶(PE)和壳聚糖(CTS)为原料,它是由3D空间中由纤维网络组成的薄片的无序重叠形成的。由于其特殊的微观结构,它可以像分离膜一样使用,这允许在水流快速通过时快速吸附水中的污染物。总的来说,本工作为具有快速吸附速率和高效吸附多孔材料的制备方法采用绿色方法提供了新的思路。
    How to solve the contradiction between the efficiency and adsorption rate of porous materials in adsorbing pollutants has always been one of the focus issues. In this study, the small landscape cypress trees structure like biomimetic of a hierarchical and dual morphology 3D porous HA-based aerogel was designed and synthesized to use humic acid (HA), pectin (PE) and chitosan (CTS) as raw materials, which it was formed by the disorderly overlapping of lamella composed of fiber networks in 3D space. Due to its special microstructure, it can be used like separation membrane, which allowing for rapid adsorption of pollutants in the water while the water flow passes through quick. In general, this work provides a new concept for owning fast adsorption rate and efficient adsorption of porous materials of preparation to use green method.
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  • 文章类型: Journal Article
    一致认为,高铝含量的一致存在,对其生长和人类健康构成了越来越大的威胁。本研究重点探讨了影响因素,影响,以及使用腐殖酸从肠苔中去除铝的过程。结果表明,在腐殖酸浓度为0.0330g·L-1的实验条件下,pH3.80,34°C,持续时间为40分钟,去除率可达80.18%。主要风味成分的含量,蛋白质,并且经过治疗后,Enteromorpha中的氨基酸显着增加,而多糖和微量元素如钙和镁显著下降。红外光谱研究表明,腐殖酸吸附过程中与Al3+结合的主要官能团为羟基,羧基,苯酚,和其他含氧基团。腐殖酸对Al3+的吸附过程是一个自发现象,分为三个关键阶段:快速吸附,缓慢吸附,和吸附平衡,这是由物理和化学吸附效应引起的。本研究为藻类金属去除提供了一种安全高效的方法。
    High level of aluminum content in Enteromorpha prolifera posed a growing threat to both its growth and human health. This study focused on exploring the factors, impacts, and process of removing aluminum from Enteromorpha prolifera using humic acid. The results showed that under experimental conditions of 0.0330 g·L-1 humic acid concentration, pH 3.80, 34 °C, and a duration of 40 min, the removal rate was up to 80.18%. The levels of major flavor components, proteins, and amino acids in Enteromorpha prolifera increased significantly after treatment, while polysaccharides and trace elements like calcium and magnesium decreased significantly. Infrared spectroscopy demonstrated that the main functional groups involved in binding with Al3+ during humic acid adsorption were hydroxyl, carboxyl, phenol, and other oxygen-containing groups. The adsorption process of Al3+ by humic acid was a spontaneous phenomenon divided into three key stages: fast adsorption, slow adsorption, and adsorption equilibrium, which resulted from both physical and chemical adsorption effects. This study provided a safe and efficient method in algae metal removal.
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  • 文章类型: Journal Article
    酒石酸泰乐菌素,大环内酯类抗生素,是一类在自然水体中检测到的新兴污染物之一,因为它们不容易通过常规处理工艺去除。在这项研究中,分析了泰乐菌素酒石酸盐的直接和间接光降解,以了解可能存在于地表水中的活性氧和有机物的作用。而直接光解引起的降解可以忽略不计(k=(9.4±1.8)×10-5s-1),添加0.4M过氧化氢(k=(2.18±0.01)×10-4s-1)或使用光芬顿工艺(k=(2.96±0.02)×10-4s-1)导致更大的降解。通过将酒石酸泰乐菌素与实验确定的最佳腐殖酸浓度(15mg/L)相结合,使降解最大化。通过间接光解容易产生单线态氧,并增加了总体降解(k=1.31±0.05)×10-3s-1)。用单线态氧[(4.7936±0.0001)×105M-1s-1]和羟基自由基[(5.2693±0.0002)×109M-1s-1]测量了酒石酸泰乐菌素的绝对伪一级双分子反应速率常数。使用竞争动力学,当结合活性氧的浓度数据时,表明羟基自由基对降解的贡献比单线态氧大大约11个数量级。
    Tylosin tartrate, a macrolide antibiotic, is one of a class of emerging contaminants that have been detected in natural bodies of water since they are not easily removed by conventional treatment processes. In this study, the direct and indirect photodegradation of tylosin tartrate was analyzed to understand the role of reactive oxygen species and organic matter that may be present in surface waters. While direct photolysis caused negligible degradation (k = (9.4 ± 1.8) × 10-5 s-1), the addition of 0.4 M hydrogen peroxide (k = (2.18 ± 0.01) × 10-4 s-1) or usage of the photo-Fenton process (k = (2.96 ± 0.02) × 10-4 s-1) resulted in greater degradation. The degradation was maximized by combining tylosin tartrate with an experimentally determined optimal concentration of humic acid (15 mg/L), which readily produced singlet oxygen and increased the overall degradation (k = 1.31 ± 0.05) × 10-3 s-1) by means of indirect photolysis. Absolute pseudo-first-order bimolecular reaction rate constants for tylosin tartrate were measured with singlet oxygen [(4.7936 ± 0.0001) × 105 M-1 s-1] and hydroxyl radical [(5.2693 ± 0.0002) × 109 M-1 s-1] using competition kinetics, and when combined with data on concentration of the reactive oxygen species, showed that the hydroxyl radical makes a contribution to the degradation that is approximately eleven orders of magnitude greater than singlet oxygen.
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  • 文章类型: Journal Article
    废水中新兴污染物和溶解有机物的共存使氯化处理过程中消毒副产物(DBPs)的转化和生成变得复杂,这对于有效的水质评价和氯化优化至关重要。本研究以氟西汀(FLX)和腐殖酸(HA)为代表物质,分析其在不同氯化条件下的化学特性变化和斑马鱼胚胎发育毒性。荧光特性和傅里叶变换离子回旋共振质谱分析表明,氯化处理增加了HA溶液中芳香族化合物的含量。加入FLX进一步增加了芳香环结构和氧化分子的存在,导致形成许多具有高度不饱和和酚类结构的Cl-DBPs。此外,用FLX发现斑马鱼胚胎发育和行为的不同反应,HA,和FLX+HA曝光。心脏毒性与cTn-I蛋白浓度和各种基因表达的变化有关。长时间的氯化条件显示出更高的毒性。相关分析发现化学指标与毒性数据之间的关系较弱,这表明在分析氯化的影响时需要考虑这两种分析方法。Further,化学分析和毒性试验相结合表明,在本实验中,氯化条件为3mg/L的FLXHA溶液30分钟具有较低的化学和毒性作用。这项研究为含FLX和溶解有机物的氯化水的安全排放提供了宝贵的科学见解,以及优化废水处理中氯化参数的指导。
    The coexistence of emerging pollutants and dissolved organic matter in wastewater complicates the transformation and generation of disinfection byproducts (DBPs) during chlorination treatment, which is essential for effective water quality evaluation and chlorination optimization. This study used fluoxetine (FLX) and humic acid (HA) as representative substances to analyze changes in their chemical characteristics and zebrafish embryonic developmental toxicity under different chlorination conditions. The analysis of the fluorescence characteristics and Fourier transform ion cyclotron resonance mass spectrometry indicated that chlorination treatment increased the aromatic compound content of the HA solution. FLX addition further increased the presence of aromatic ring structures and oxidized molecules, resulting in the formation of numerous Cl-DBPs with highly unsaturated and phenolic structures. Moreover, different responses in zebrafish embryo development and behavior were found with FLX, HA, and FLX + HA exposures. Cardiotoxicity was linked to changes in the concentration of cTn-I protein and expression of various genes. Prolonged chlorination conditions showed higher toxicities. Correlation analysis found a weak relation between chemical indicators and toxicity data, indicating that both analysis methods need to be considered when analyzing the impact of the chlorination. Further, a combination of chemical analyses and toxicity tests revealed that the FLX + HA solution with chlorination conditions of 3 mg/L for 30 min had lower chemical and toxic effects in this experiment. This study provides valuable scientific insights for the safe discharge of chlorinated water containing FLX and dissolved organic matter, as well as guidance for optimizing chlorination parameters in wastewater treatment.
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  • 文章类型: Journal Article
    氧化锌纳米颗粒(ZnO-NP)在许多消费产品中的日益增加的利用是值得关注的,因为它们最终释放到自然环境中并诱导潜在的不利影响。ZnO-NP的行为和环境影响可以通过它们与环境共存物质的相互作用来改变。这项研究调查了在共存有机污染物(例如全氟辛酸[PFOA])存在下ZnO-NP行为的变化,天然有机物质(即,腐殖酸[HA]),和电解质(即,NaCl和CaCl2)在模拟水中。大小,形状,纯度,结晶度和不同相互作用间隔后模拟水中ZnO-NPs的表面电荷(如1天,1周,2周,和3周)在控制的pH值为7时使用各种表征技术进行检查。结果表明尺寸发生了变化(如162.4nm,1天相互作用至>10µm,3周相互作用)和ζ电位(例如-47.2mV,1天相互作用至-0.2mV,3周相互作用)单独的ZnO-NP和当PFOA,电解质,和HA存在于悬浮液中。对于固定浓度(5mM)的不同电解质,观察到对纳米颗粒尺寸和表面电荷的不同影响。HA分散的ZnO-NP的存在影响ζ电位。在PFOA和盐的存在下,由于它们的大的脂肪族碳含量和复杂的结构,也观察到这种分散效应。阳离子桥接效应,疏水相互作用,氢键,静电相互作用,范德华力可能是导致PFOA吸附的潜在相互作用力。有机污染物(PFOA)和天然有机物质(HA)的存在可以改变天然和海水中ZnO-NP的表面特征和命运。
    The increasing utilization of zinc oxide nanoparticles (ZnO-NPs) in many consumer products is of concern due to their eventual release into the natural environment and induction of potentially adverse impacts. The behaviour and environmental impacts of ZnO-NPs could be altered through their interactions with environmentally coexisting substances. This study investigated the changes in the behaviour of ZnO-NPs in the presence of coexisting organic pollutants (such as perfluorooctanoic acid [PFOA]), natural organic substances (i.e., humic acid [HA]), and electrolytes (i.e., NaCl and CaCl2) in simulated waters. The size, shape, purity, crystallinity, and surface charge of the ZnO-NPs in simulated water after different interaction intervals (such as 1 day, 1 week, 2 weeks, and 3 weeks) at a controlled pH of 7 were examined using various characterization techniques. The results indicated alterations in the size (such as 162.4 nm, 1 day interaction to >10 µm, 3 weeks interaction) and zeta potential (such as -47.2 mV, 1 day interaction to -0.2 mV, 3 weeks interaction) of the ZnO-NPs alone and when PFOA, electrolytes, and HA were present in the suspension. Different influences on the size and surface charge of the nanoparticles were observed for fixed concentrations (5 mM) of the different electrolytes. The presence of HA-dispersed ZnO-NPs affected the zeta potential. Such dispersal effects were also observed in the presence of both PFOA and salts due to their large aliphatic carbon content and complex structure. Cation bridging effects, hydrophobic interactions, hydrogen bonding, electrostatic interactions, and van der Waals forces could be potential interaction forces responsible for the adsorption of PFOA. The presence of organic pollutants (PFOA) and natural organic substances (HA) can transform the surface characteristics and fate of ZnO-NPs in natural and sea waters.
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  • 文章类型: Journal Article
    2H相二硫化钼(2H-MoS2)被认为是化学稳定的二维(2D)纳米材料。尽管如此,2H-MoS2在环境氧化还原活性基质存在下的持久性,例如天然存在的氧化剂(例如,二氧化锰(MnO2)和天然有机物(NOM),仍然很大程度上未知。在这里,我们研究了2H-MoS2、MnO2(一种常见的天然氧化剂)之间的相互作用,和NOM物种(即,奥尔德里奇腐殖酸(ALHA)和苏万尼河天然有机物(SRNOM))。结果表明,无论是否存在溶解氧,MnO2都会加速2H-MoS2的氧化溶解。发现NOM对MnO2诱导的2H-MoS2命运的影响取决于其对2H-MoS2的亲和力和NOM的功能。由于还原性多环芳烃和多酚成分的富集,ALHA优先吸附在疏水性2H-MoS2纳米片上。优先的ALHA吸附抵消了MnO2触发的2H-MoS2的氧化转化,如2H-MoS2的阴极响应所示(即,添加ALHA后,开路电位降低了0.0338V),并在228.8和231.9eV处出现了还原性Mo-C键。这项工作评估了2H-MoS2的持久性,说明了其对天然氧化剂分解的敏感性以及NOM对其的影响。这些发现对于揭示MoS2在水生环境中的命运和运输至关重要,并为MoS2和潜在的其他2D材料在天然或工程系统中的相关应用提供了指南。
    2H-phase molybdenum disulfide (2H-MoS2) has been considered to be a chemically stable two-dimensional (2D) nanomaterial. Nonetheless, the persistence of 2H-MoS2 in the presence of environmental redox-active matrices, such as naturally occurring oxidants (e.g., manganese dioxide (MnO2)) and natural organic matter (NOM), remains largely unknown. Herein, we examined the interplay between 2H-MoS2, MnO2 (a common natural oxidant), and NOM species (i.e., Aldrich humic acid (ALHA) and Suwannee River natural organic matter (SRNOM)). The results show that MnO2 accelerates the oxidative dissolution of 2H-MoS2, regardless of the presence of dissolved oxygen. The effect of NOM on the MnO2-induced fate of 2H-MoS2 was found to depend on its affinity for 2H-MoS2 and the functionality of NOM. ALHA preferentially adsorbed on hydrophobic 2H-MoS2 nanosheets due to the enrichment of reductive polycyclic aromatics and polyphenolic constituents. The preferential ALHA adsorption counteracted the MnO2-triggered oxidative transformation of 2H-MoS2, as revealed by the cathodic response of 2H-MoS2 (i.e., decreased the open circuit potential by 0.0338 V) and the emergence of reductive Mo‒C bonds at 228.8 and 231.9 eV upon the addition of ALHA. This work evaluated the persistence of 2H-MoS2, illustrating its susceptibility to decomposition by naturally occurring oxidants and the influence of NOM on it. These findings are crucial for revealing the fate and transport of MoS2 in aquatic environments and provide guidelines for related applications in natural or engineered systems for MoS2 and potentially other 2D materials.
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  • 文章类型: Journal Article
    土壤有机碳(SOC)在不同的生态系统和土壤景观之间存在差异。然而变化的程度仍然不确定。将森林等未受干扰的生态系统中的SOC水平与逐渐改变的生态系统中的SOC水平进行比较,可以为土地利用对碳动态的影响提供有价值的见解。本研究旨在评估喀拉拉邦热带地区不同土地利用方式对土壤肥力参数的影响,专注于森林以及种植的农业景观,如椰子,胡椒,木薯,相思种植园,和混合家庭花园种植系统。在土壤肥力方面,在不同作物和土地利用系统之间观察到显着差异。森林的SOC含量最高,为3.78gkg-1,而金合欢人工林的SOC含量最低,为0.76gkg-1。此外,各种土壤特性,如不同的碳分数(例如,腐殖酸,富里酸),总氮,碳,可用的营养素,物理性质,骨料尺寸分数,微生物生物质碳,和光谱特征在不同的土地利用中存在显着差异。这些发现表明,与邻近的森林土壤相比,改变的生态系统中的土壤肥力有所下降,强调森林在保护自然资源和保持土壤健康方面的重要作用。此外,在研究的不同景观中,家庭花园的混作系统比单作系统更好地维持土壤肥力。观察到的不同土地利用类型之间土壤理化性质的变化表明对可持续作物生产的威胁。在这些改变的生态系统中,旨在提高土壤肥力和维持作物产量的有效管理做法至关重要。这项研究强调了在喀拉拉邦等热带景观中采取适当的管理策略以保护土壤健康并确保可持续作物生产的重要性。本研究采用的整体方法,涵盖各种土地用途的土壤肥力参数,以及它对可持续土地管理的影响,为喀拉拉邦等热带地区的土壤动力学现有文献增加了新颖性和相关性。
    Soil organic carbon (SOC) is known to vary among different ecosystems and soilscapes, yet the degree of variation remains uncertain. Comparing SOC levels in undisturbed ecosystems like forests with those in gradually altered ecosystems can provide valuable insights into the impact of land use on carbon dynamics. This study aimed to evaluate the effects of different land uses on soil fertility parameters in the tropical region of Kerala, focusing on forests as well as cultivated agricultural landscape such as coconut, pepper, tapioca, acacia plantations, and mixed home garden cropping systems. Significant variations were observed among different crops and land use systems in terms of soil fertility. Forests exhibited the highest SOC content at 3.78 g kg-1, while acacia plantations showed the lowest at 0.76 g kg-1. Additionally, various soil properties such as different carbon fractions (e.g., humic acid, fulvic acid), total nitrogen, carbon, available nutrients, physical properties, aggregate size fractions, microbial biomass carbon, and spectral signatures differed significantly across the different land uses. These findings suggest a decline in soil fertility in altered ecosystems compared to adjacent forest soils, highlighting the vital role of forests in conserving natural resources and maintaining soil health. In addition, among the different landscapes studied, mixed cropping systems of home gardens sustained soil fertility better than monocropping systems. The observed variations in soil physicochemical properties among different land use types indicate a threat to sustainable crop production. Effective management practices aimed at improving soil fertility and sustaining crop production in these altered ecosystems are essential. This study highlights the importance of adopting appropriate management strategies to conserve soil health and ensure sustainable crop production in tropical landscapes like Kerala. The holistic approach adopted in this study, encompassing a wide range of soil fertility parameters across various land uses, along with its implications for sustainable land management, adds significant novelty and relevance to the existing literature on soil dynamics in tropical regions like Kerala.
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  • 文章类型: Journal Article
    背景:随着工业化和城市化的进展,农田镉(Cd)污染日益严重,极大地影响人类健康。向日葵对Cd胁迫具有很高的抗性,在Cd污染土壤的植物修复中具有巨大的潜力。先前的研究表明,腐殖酸(HA)有效地减轻了Cd对植物的伤害;然而,其对Cd胁迫下向日葵植物的缓解作用尚不清楚。
    结果:我们通过叶面施用使用了四种不同浓度的HA(50、100、200和300mgL-1),以检查它们减轻Cd胁迫对向日葵植物生长的能力,叶绿素合成,和生化防御系统。结果表明,Cd胁迫不仅降低了株高,阀杆直径,新鲜和干重,和向日葵植物中的叶绿素含量,但与对照组相比,它们的叶绿素荧光特性也发生了变化。Cd胁迫后,光合结构被破坏,每单位PSII反应中心的数量发生变化。施用200mgL-1HA促进向日葵生长并增加叶绿素含量。HA显著增强抗氧化酶活性(SOD,POD,CAT,和APX)并降低ROS含量(O2-,H2O2和-OH)。完全正确,施用200mgL-1HA对缓解向日葵植物Cd诱导的胁迫效果最好。
    结论:叶面施用一定浓度的HA对向日葵植物表现出最有效的缓解Cd诱导的胁迫。它可以增强光能利用率和抗氧化酶活性,同时降低向日葵植物中的ROS含量。这些发现为利用HA缓解向日葵Cd胁迫提供了理论依据。
    BACKGROUND: With the progress of industrialization and urbanization, cadmium (Cd) pollution in farmland is increasingly severe, greatly affecting human health. Sunflowers possess high resistance to Cd stress and great potential for phytoremediation of Cd-contaminated soil. Previous studies have shown that humic acid (HA) effectively mitigates plant damage induced by Cd; however, its alleviating effects on sunflower plants under Cd stress remain largely unknown.
    RESULTS: We employed four different concentrations of HA (50, 100, 200, and 300 mg L-1) via foliar application to examine their ability to alleviate Cd stress on sunflower plants\' growth, chlorophyll synthesis, and biochemical defense system. The results revealed that Cd stress not only reduced plant height, stem diameter, fresh and dry weight, and chlorophyll content in sunflower plants but also altered their chlorophyll fluorescence characteristics compared to the control group. After Cd stress, the photosynthetic structure was damaged and the number of PSII reactive centers per unit changed. Application of 200 mg L-1 HA promotes sunflower growth and increases chlorophyll content. HA significantly enhances antioxidant enzyme activities (SOD, POD, CAT, and APX) and reduces ROS content (O2 -, H2O2 and -OH). Totally, Application of 200 mg L-1 HA had the best effect than other concentrations to alleviate the Cd-induced stress in sunflower plants.
    CONCLUSIONS: The foliar application of certain HA concentration exhibited the most effective alleviation of Cd-induced stress on sunflower plants. It can enhance the light energy utilization and antioxidant enzyme activities, while reduce ROS contents in sunflower plants. These findings provide a theoretical basis for using HA to mitigate Cd stress in sunflowers.
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  • 文章类型: Journal Article
    重金属在天然土壤系统中的迁移可能受到这些系统的性质和组成的影响:有机物的含量和质量以及无机成分的特征。在这项工作中,铜(II)离子在掺入钙(II)的腐殖质水凝胶中的扩散,镁(II),和铁(III)离子进行了研究。使用了瞬时平面源和恒定源的方法。实验数据得出了水凝胶中浓度的时间发展和有效扩散系数的值。系数包括水凝胶结构的影响和扩散颗粒与水凝胶的相互作用。我们的结果表明,天然金属离子如钙的存在,镁,或铁可以强烈影响铜在腐殖质系统中的扩散率。它们表明铜离子的迁移率取决于它们的浓度。系统中较高的铜含量可以支持迁移率。虽然Ca和Mg的掺入导致铜离子扩散系数的降低,与纯腐殖质水凝胶相比,Fe(III)掺入腐殖质水凝胶导致Cu(II)在水凝胶中的扩散系数增加。
    The mobility of heavy metals in natural soil systems can be affected by the properties and compositions of those systems: the content and quality of organic matter as well as the character of inorganic constituents. In this work, the diffusion of copper(II) ions in humic hydrogels with incorporated calcium(II), magnesium(II), and iron(III) ions was investigated. The methods of instantaneous planar source and of constant source were used. Experimental data yielded the time development of the concentration in hydrogels and the values of effective diffusion coefficients. The coefficients include both the influence of the hydrogel structure and the interaction of diffusing particles with the hydrogel. Our results showed that the presence of natural metal ions such as calcium, magnesium, or iron can strongly affect the diffusivity of copper in humic systems. They indicate that the mobility of copper ions depends on their concentration. The mobility can be supported by higher contents of copper in the system. While the incorporation of Ca and Mg resulted in the decrease in the diffusivity of copper ions, the incorporation of Fe(III) into humic hydrogel resulted in an increase in the diffusivity of Cu(II) in the hydrogel in comparison with pure humic hydrogel.
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  • 文章类型: Journal Article
    废旧锂电池有价金属的资源化回收是可持续发展的必然趋势。在这项研究中,通过外部调节来增强废旧锂电池浸出中菌株的耐受性和稳定性,以从根本上提高生物浸出效率。Li的浸出,Ni,Co和Mn增加到100%,85.06%,与未驯化菌株相比,用HA靶向培养后分别为74.25%和69.44%。在废旧锂电池的微生物浸出过程中,Ⅰ中的代谢物,Ⅳ,未驯化细菌菌落的代谢和Ⅴ区与废旧锂电池的溶解呈正相关。Ⅰ的代谢物,Ⅱ,HA驯化菌群对废锂电池的溶解有直接影响。蛋白质物质的过量代谢可以显著促进Ni的减少,Co,锰浸出,同时在体系中大量的腐殖质络合了有毒金属离子,以确保细菌菌落的活性。可以看出,该细菌是由腐殖酸驯化的,促进细菌自身的新陈代谢,超代谢EPS促进废旧锂电池的溶解。
    Resource recovery of valuable metals from spent lithium batteries is an inevitable trend for sustainable development. In this study, external regulation was used to enhance the tolerance and stability of strains in the leaching of spent lithium batteries to radically improve the bioleaching efficiency. The leaching of Li, Ni, Co and Mn increased to 100 %, 85.06 %, 74.25 % and 69.44 % respectively after targeted cultivation with HA as compared to the undomesticated strain. In the process of microbial leaching of spent lithium batteries, the metabolites in the Ⅰ, Ⅳ, and Ⅴ regions of the metabolism of the undomesticated bacterial colony had a positive correlation to the dissolution of spent lithium batteries. The metabolites of Ⅰ, Ⅱ, and Ⅴ regions were directly affected by the HA domesticated flora on the dissolution of spent lithium batteries. The excess metabolism of protein substances can significantly promote the reduction of Ni, Co, Mn leaching, and at the same time in the role of a large number of humic substances complexed the toxic metal ions in the system, to ensure the activity of the bacterial colony. It can be seen that the bacteria were domesticated by humic acid, which promoted the bacteria\'s own metabolism, and the super-metabolised EPS promoted the solubilisation of spent lithium batteries.
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