Concentrations Of Heavy Metal Ions Research Articles

Electrochemical sensing platform for detection of heavy metal ions without electrochemical signal.

Heavy metal pollution has attracted global attention because of its high toxicity, non-biodegradability, and carcinogenicity. Electrochemical sensors are extensively employed for the detection of low concentrations of heavy metal ions (HMIs). However, their applicability is often limited to the detection of ions that exhibit electrochemical signals exclusively in aqueous solutions. In this study, we proposed a multi-responsive detection platform based on the modification of horseradish peroxidase@zeolitic imidazolate frameworks-8/thionine/gold/ionic liquid-reduced graphene oxide (HRP@ZIF-8/THI/Au/IL-rGO). This platform demonstrated its capability to detect various metal ions, including those without conventional electrochemical signals. The Au/IL-rGO composite structure enhanced the specific surface area available for the reaction. Furthermore, the in situ growth of HRP@ZIF-8 not only shielded the THI signal prior to detection but also protected the electrode material. It was important to note that the introduced edetate disodium dihydrate (EDTA) had the ability to complex with various HMIs. When excess EDTA was present, it could cleave ZIF-8 and release HRP. In the presence of hydrogen peroxide (H2O2), HRP promoted the oxidation of THI previously reduced by the electrode and thus showed excellent sensitivity for HMIs detection. The proposed method overcame the limitation of traditional electrochemical sensors, which solely relied on electrochemical signals for detecting metal ions. This offers a novel approach to enhance electrochemical ion sensing detection.

The effect of acid mine drainage on the properties of an all-solid waste paste backfill body based on oil shale residue

The complex environment of mine water is closely linked to the effect of the backfill body. The goal of this study was to establish a method with which to reduce carbon emissions from cementitious materials while addressing the large amount of unutilized solid waste, such as oil shale residue, which lies on the surface of the planet, and pollutes the environment. Oil shale residue, fly ash, slag and coal gangue were used to produce an oil shale residue-based all-solid waste paste backfill (OSGPB) to study the changes in strength and environmental impact with corrosion time under acid mine drainage conditions. The development of cracks was monitored using digital image correlation (DIC) technology. The corrosion mechanism of OSGPB was analysed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). This study revealed that in an acid mine drainage environment, the unconfined compressive strength (UCS) decreased by 38.58% and 15.66% after 24 d of wetdry cycling and complete immersion corrosion, respectively. A significant quantity of corrosive gypsum was produced in the OSGPB, which expanded the internal micropores and gradually formed cracks. This led to more severe internal structural damage during wetdry cycles. Changes in the UCS of the OSGPB over 60 d were predicted using established grey models. The leached concentrations of heavy metal ions met the groundwater quality standard (class III) after the OSGPB was completely immersed in acid mine drainage and subjected to wetdry corrosion cycles. OSGPB showed great potential as a green backfilling material for mines.

The migration process and temperature effect of aqueous solutions contaminated by heavy metal ions in unsaturated silty soils

Adsorption-desorption experiments of three heavy metal ions (i.e., lead, copper, cadmium) in silty soil were carried out at different temperatures, and the microscopic characteristics of silty soil loaded with the three heavy metal ions were analyzed. A one-dimensional soil column was used to discuss the influences of heavy metal ion types and concentrations on the soil moisture distribution and the migration level of different heavy metal ions, especially during the dynamic change process from an unsaturated state to a saturated state. Studies show that the adsorption of heavy metal ions onto silty soil is closely related to the mineral composition and functional groups in silty soil. In addition to physical adsorption, the adsorption of heavy metal ions is closely related to the hydrolysis reaction of mineral components such as kaolinite, calcite, dolomite, plagioclase and quartz. Under constant temperature, the types and concentrations of heavy metal ions play an important role in the moisture migration of unsaturated soil. In the presence of heavy metal ions, the penetration of lead ions is the greatest, followed by copper ions and then cadmium ions. The greater the ion concentration is, the stronger the penetration of heavy metal ions in silty soils.

Efficient separation of Cd2+ and Pb2+ by Tetradesmus obliquus: Insights from cultivation conditions with competitive adsorption modeling

Microalgae serve as efficient biosorbents for the removal of heavy metals. This study investigates the adsorption and desorption behavior of Tetradesmus obliquus FACHB-14 (T. obliquus) under various culture conditions. Glucose cultivation enhances adsorption, with Pb2+ exhibiting higher capacity than Cd2+, reaching a maximum of 80.24 mg/g at an initial heavy metal ion concentration of 64 mg/L. Kinetic modeling favors the pseudo-second-order kinetics. The Langmuir model is more suitable for describing the adsorption process of Cd2+ in BG11 and Pb2+ in glucose, with maximum adsorption capacities of 6.48 mg/g and 86.29 mg/g, respectively. The Temkin model is more suitable for describing the adsorption process of Pb2+ in BG11 and Cd2+ in glucose. Competitive adsorption reduces the maximum capacity by 42.60 % for Cd2+ and 55.61 % for Pb2+. The Extended Freundlich model fits competitive behavior. Analysis reveals increased extracellular polymer secretion under glucose conditions, which aids adsorption. Na2EDTA achieves up to 97.37 % recovery of heavy metal ions. Overall, T. obliquus cultured with glucose shows promise for heavy metal removal, especially in mixed systems.

Magnesium source with function of slowly releasing Mg and pH control for impurity-resistance synthesis ultra-large struvite from wastewater

Struvite (MgNH4PO4·6H2O, Magnesium ammonium phosphate, MAP), recovered from wastewater, has potential application as a slow-release fertilizer. However, crystal size distribution (CSD) of recovered MAP typically lied in the range of 50–300 μm, due to fast nucleation rate and notably narrow metastable zone width (MSZW) of MAP, with purity levels 40–90 %. In order to control the rate of nucleation, a novel magnesium source with the form of MgHPO4·3H2O wrapped with Mg(OH)2 was prepared, referred to as P-3. This compound gradually released Mg2+ and PO43−, regulating solution concentration kept in MSZW to promote crystal growth. The inherent Mg(OH)2 within P-3 also acted as a pH regulator in wastewater, eliminating the necessity for additional acid or alkali adjustments during crystallization process. The MAP precipitated by P-3 exhibited an impressive CSD of 5000–7000 μm, with a maximum size reaching 10,000 μm. This represented the largest CSD reported in literature for recovered MAP from wastewater. The significance of the ultra-large MAP precipitated by P-3 lied in its enhanced resistance to impurity adsorption, resulting in MAP with a remarkable purity 97 %, under conditions of low heavy metal ion concentration approximately 5 mg/L. Furthermore, the removal efficiency of ammonia nitrogen (NH4+) can reach 92 %. In comparison, two other magnesium sources, soluble salts (MgCl2 and Na2HPO4, P-1) and a combination of insoluble salts (Mg(OH)2 and MgHPO4, P-2) were evaluated alongside P-3. The CSD of MAP precipitated from P-1, P-2 was both <100 μm, with purity levels of 90 and 92 % and NH4+ removal efficiency of 92 and 90 %, respectively. Importantly, the strategy of obtaining ultra-large size MAP from wastewater in this study provided novel insights into the crystallization of other insoluble salts with large sizes.

Effects of Polyether Amine Canopy Structure on Heavy Metal Ions Adsorption of Magnetic Solvent-Free Nanofluids.

Three Fe3O4 magnetic solvent-free nanofluids with different amine-based coronal layer structures are synthesized and characterized by using magnetic Fe3O4 as the core, silane coupling agent as the corona, and polyether amines with different graft densities and chain lengths as the canopy. The concentration of heavy metal ions after adsorption is measured by atomic absorption spectrometry (AAS) to study the effect of Fe3O4 magnetic solvent-free nanofluids on the adsorption performance of the heavy metal ions lead (Pb(II)) and copper (Cu(II)) in water. The adsorption of Fe3O4 magnetic solvent-free nanofluid was explored by changing external condition factors such as adsorption contact time and pH. Additionally, the adsorption model is established. The magnetic solvent-free nanofluid is separated from water by applying an external magnetic field to the system, and desorption and cyclic adsorption tests are carried out. Based on the adsorption mechanism, the structure design of Fe3O4 magnetic solvent-free nanofluid was optimized to achieve optimal adsorption performance.

Development of MXene for removal of lead (Pb+) ions from wastewater

Abstract A new family of 2D materials with enhanced properties than graphene plays a crucial role in environmental remediation and sustainability. The concentration of heavy metal ions in wastewater is an emerging issue in the global scenario. Heavy metals such as lead, chromium, cadmium, etc. are natural carcinogens and adversely affect environmental species, which tend to have potential activities on the surface of the new families. Lead poisoning is a very raising issue in some parts of India and is a major effluent disposed of to the waterbodies from various industrial streams. The removal of the lead components is studied in this research using adsorption experimentation using MXene as the surface-active adsorbent. The possible mechanism for lead removal from wastewater is also discussed, as well as the effective regeneration and reusability of the adsorbent over long adsorption cycles. MXenes were applied after the confirmation using X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy and zeta-potential. The induced coupled plasma–optical emission spectroscopy confirms the lead remediation by over 96% in the first adsorption cycle, which was then reduced to over 92% in the second adsorption cycle. The lead contamination was under the permissible limits as per the water standards.

Heavy metal decontamination by ion exchange polymers for water purification: counterintuitive cation removal by an anion exchange polymer

Ion exchange polymers were used for mercury and lead ions removal in water. The heavy metal ion concentration was analyzed by two independent methods: inductively coupled plasma–optical emission spectroscopy (ICP-OES) and gravimetry. The studied cation exchange polymer (CEP) was sulfonated poly(ether ether ketone) (SPEEK), and the anion exchange polymer (AEP) was poly(sulfone trimethylammonium) chloride (PSU-TMA). The removal capacity was connected with the ion exchange capacity (IEC) equal to 1.6 meq/g for both polymers. The concentration ranges were 0.15–0.006 mM for Hg2+ and 10.8–1.0 mM for Pb2+. SPEEK achieved 100% removal efficiency for mercury and lead if the concentration was below the maximum sorption capacity (Qmax), which was about 210 mg/g for Pb2+ with SPEEK. For PSU-TMA, the surprising removal efficiency of 100% for Hg2+, which seemed incompatible with ion exchange, was related to the formation of very stable complex anions that can be sorbed by an AEP. Langmuir adsorption theory was applied for the thermodynamic description of lead removal by SPEEK. A second-order law was effective to describe the kinetics of the process.

Experimental study on environmental chemical effect and purification treatment of waste slurry in horizontal directional drilling

The waste slurry generated during Horizontal Directional Drilling (HDD) has detrimental effects on water sources, soil, and organisms. Existing studies lack quantitative analysis and assessment of the environmental hazards of waste slurry. The treatment of waste slurry is usually done by physical curing or chemical curing agents. The treatment effect of these treatments is unsatisfactory or not environmentally friendly enough. Research on the application of Microbially Induced Calcite Precipitation (MICP) in waste slurry purification can help provide innovative solutions. This study began by acquiring the basic properties, mineral composition, and particle size distribution of the waste slurry through experiments. The effects of different concentrations of waste slurry on soil chemical properties were compared, including the measurement of total dissolved solids (TDS), turbidity, and heavy metal ion concentrations of waste slurry supernatant. Additionally, the environmental impact of the waste slurry was assessed from an electrochemical, turbidity, and ionic composition perspectively. A combination formulation containing 2.8 wt% urease, 5 wt% urea, and 3.5 wt% calcium chloride was used to purify the waste slurry. The supernatant of the MICP treated waste slurry undergoes electrochemical testing to evaluate the effectiveness of MICP technology for slurry treatment. The findings indicate that both chemical additives and stratum contaminants significantly contribute to slurry pollution. When the waste slurry constitutes more than 40 wt% of the soil mass fraction, the electrical conductivity (EC) of the soil surpasses the threshold of 1000 μs/cm, and the pH level rises to approximately 9.5, rendering it unsuitable for plant growth. Moreover, the TDS, turbidity, and heavy metal ion concentrations in the waste slurry supernatant exceed the permissible environmental discharge limits. Notably, the concentration of arsenic (As) exceeds the national standard by 18 times, cadmium (Cd) by 20 times, and selenium (Se) by 208 times, posing a high risk of environmental pollution. However, the comparison of ion concentrations in the supernatant before and after MICP treatment reveals that MICP demonstrates effective cementation and co-precipitation of heavy metal ions. MICP purified 66.6 % of arsenic (As), all cadmium (Cd), 75 % of phosphorus (P), and 76 % of selenium (Se) from the waste slurry supernatant. The results of this research contribute to the quantitative evaluation of the environmental hazards of waste slurry. It also helps to promote the application of MICP in waste slurry purification.

Characterization, Efffects and Chemical Treatment of Heavy Metals in Produced Water from Injection Wells using Hydroxide Precipitation

Produced water obtained from five (5) water injection Wells in the Niger Delta area Nigeria were analysed for heavy metal ion concentrations using Themo Elemental Flame Atomic Absorption Spectrophotometer (AAS). Results obtained show that concentrations of lead (Pb2+), cadmium (Cd2+), chromium (Cr2+), nickel (Ni2+), cobalt (Co2+), vanadium (V2+), zinc (ZN2+), mercury (Hg+), silver (Ag+) and copper (Cu2) were above acceptable limits as specified by Environmental Guidelines and Standard for Petroleum Industries in Nigeria (EGASPIN). The concentrations of As2+, Fe2+, K+ and Mn2+ were within specification. Commingled produced water from the five water injection Wells were subjected to hydroxide precipitation using Ca(OH)2 at concentrations of 10, 20, 30, 40 and 50 ppm respectively. Results obtained show that all the heavy metal ions reduced within acceptable limit at 30 ppm chemical concentration. Heavy metal ions reduced with increase in chemical concentration with a corresponding increase in the pH of the solution which was however still within specification. The hydroxide converts the metal ions dissolved in solution into solid particles for easy sedimentation. Ca(OH)2 precipitates metal ions by changing the pH and electro-oxidizing potential of the solution. Properly treated produced water can be reinjected into the reservoir to enhance oil recovery, used in agriculture for irrigation purposes, discharged into the sea and other water bodies during offshore operations or even used in drilling services. Produced water discharged into the soil are non-biodegradable so must be adequately treated before discharge. Plants pick up heavy metals through their roots by the release of a variety of root exudates which changes the rhizosphere pH of the metal ion in solution thereby making them bioavailable for plant uptake by osmosis. Heavy metals in plants can exert a variety of toxic actions by damaging plant chloroplast thereby disturbing photosynthesis. Humans take in heavy metals into their system by consuming contaminated plants, water as well as inhaling contaminated air. Consumption, ingestion and inhalation of heavy metals by humans can cause a wide range of ailments such as cardiovascular diseases, kidney related problems, neurocognitive diseases, renal damage, heart disease, coronary artery disease, lung fibrosis, nasal cancer.

High-sensitivity detection of low-concentration heavy metal ions in solution by multiple reflection enhanced absorption (MREA) spectroscopy.

Heavy metal ions (Cr6+, Co2+, Ni2+, and Cu2+) in the electroplating and electrolysis industries are significantly related to process parameters and product quality, even at lower concentrations. Absorption spectroscopy is widely used for substance qualitative and quantitative analysis, which is an analytical method with the potential for real-time monitoring of heavy metal ions concentration in industrial processes. In this paper, a low-concentration heavy metal ion analysis method based on multiple reflection enhanced absorption (MREA) is proposed. Compared with traditional absorption, MREA has the advantages of low concentration detection limit and high-sensitivity. First, a reflective film (Al-SiO2) was prepared and a multiple reflection optical structure was designed to realize multiple parallel reflections of light in the solution medium. Then absorption spectra of low-concentration Cr6+, Co2+, Ni2+ and Cu2+ solutions were measured by MREA and traditional absorption methods. Finally, spectral bandwidth and incident light spots were optimized to obtain a superior absorption enhancement effect. The results showed that MREA could effectively increase the substance absorbance compared with traditional absorption. At the same time, with the optimal spectral bandwidth (0.4 nm) and incident light spot (1 mm), the detection limit of Cr6+, Co2+, Ni2+ and Cu2+ was reduced by 81.48%, 82.52%, 80.92% and 82.93%, respectively. The sensitivity was improved by 5-6 times, which was more obvious for low-concentration detection. In addition, the MREA method can achieve ion concentration analysis when Cr6+, Co2+, Ni2+, and Cu2+ coexist, and the linear correlative coefficients of the C-A curves were all greater than 0.999. Moreover, by adjusting reflectivity of the reflective film and the number of reflections in the optical structure, the results of the MREA method can be further optimized for the low-concentration heavy metal ion analysis. The MREA method has the advantages of simplicity, rapidity and versatility, which can provide the technical foundation for real-time monitoring method development of low-concentration heavy metal ions in industrial processes.

Curcumin-based ratiometric electrochemical sensing interface for the detection of Cd2+ and Pb2+ in grain products

The conventional electrochemical detection in food samples often suffers from low stability and poor reproducibility. The construction of ratiometric sensor is regarded as an effective means to overcome the issues. Herein, poly-curcumin (p-CCM)-Multi walled carbon nanotubes (MWCNTs)-layered double hydroxides (LDHs) was constructed as a novel rationmetric sensing material for detection of Cd2+ and Pb2+ in grain samples. Under the synergistic effect of MWCNTs and the adsorption capacity of LDHs, the p-CCM/MWCNTs/LDHs can significantly enhance the electrochemical responses of heavy metals. In the differential pulse voltammetry test, the ratio of oxidation peak currents between heavy metal ions and curcumin was directly proportional to the concentration of heavy metal ions. This has formed the basis of a new ratiometric electrochemical sensor for the detection of the levels of Cd2+ and Pb2+ in grain products. Under optimal conditions, the limits of detection for Cd2+ and Pb2+ were found to be 0.61 μg mL−1 and 0.74 μg mL−1, respectively. It is worth mentioning that the method was additionally utilized to detect Cd2+ and Pb2+ in rice and flour samples. The satisfactory recovery outcomes in both samples demonstrated minimal interference of the food matrix with the obtained ratiometric sensor. In this work, a CCM-based ratiometric electrochemical sensor was presented, which could potentially replace the widely used ferrocene-based ratiometric electrochemical sensor, thereby enhancing the exploration of electrode materials for ratiometric electrochemical sensors.

The apple Ca2+/H+ exchanger MdCAX2L-2 functions positively in modulation of Ba2+ tolerance

Calcium is an essential element for plant growth and development, and it plays an important role in the responses of plants to abiotic stress. High concentrations of heavy metal ions in soil significantly affect the yield and quality of crops and pose human health threats when these ions accumulate in edible organs. The Ca2+/H+ exchanger (CAX) family is a class of transporters that mediate the transmembrane transport of both Ca2+ and metal ions, and they are widely involved in regulating plant growth and development and stress responses. Here, we cloned an AtCAX2 ortholog, MdCAX2L-2, from apple. It is constitutively expressed in various apple tissues and significantly induced by Ca2+ and Ba2+ treatments. The MdCAX2L-2 protein is located in the vacuolar membrane in both plant and yeast cells. Overexpression of MdCAX2L-2 enhanced the tolerance of the yeast mutant K667 to high concentrations of Ca2+ and Ba2+. In addition, the role of MdCAX2L-2 in modulating Ba2+ tolerance was identified using MdCAX2L-2-overexpressing transgenic Arabidopsis plants and apple calli. Comparison of growth phenotypes and stress-related physiological indexes under BaCl2 treatment indicated that MdCAX2L-2 could enhance the Ba2+ tolerance of plants by promoting Ba2+ compartmentalization into the vacuoles and eliminating excess ROS. Our results provide insights that will aid future studies examining the function of CAX proteins in regulating stress tolerance in fruit crops, as well as their underlying mechanisms.

Effects of biochar-derived dissolved organic matter on the gut microbiomes and metabolomics in earthworm Eisenia fetida

The ecological risks of biochar-derived dissolved organic matter (DOM) to soil invertebrates at different organismal levels remains limited. This study comprehensively explored the ecological risks of biochar-derived DOM on earthworm gut through assessments of enzyme activity response, histopathology, gut microbiomes, and metabolomics. Results demonstrated that DOM disturbed the digestive enzymes in earthworm, especially for 10% DOM300 groups. The integrated biomarker response v2 (IBRv2) indicated that the perturbation of earthworm digestive enzymes induced by DOM was both time-dependent and dose-dependent. Pathological observations revealed that 10% DOM300 damaged intestinal epithelium and digestive lumen of earthworms. The significant damage and injury to earthworms caused by DOM300 due to its higher concentrations of heavy metal ions and organic substrates (e.g., toluene, hexane, butanamide, and hexanamide) compared to DOM500 and DOM700. Analysis of 16S rRNA from the gut microbiota showed a significant decrease in genera (Verminephrobacter, Bacillus, and Microbacteriaceae) associated with inflammation, disease, and detoxification processes. Furthermore, 10% DOM300 caused the abnormality of metabolites, such as glutamate, fumaric acid, pyruvate, and citric acid, which were involved in energy metabolism, These findings contributed to improve our understanding of the toxic mechanism of biochar DOM from multiple perspectives.

The content of heavy metal ions in ash from waste incinerated in domestic furnaces

The content of heavy metal ions in ash from waste incinerated in domestic furnaces

Investigation on the effect of Cu2+, Mn2+ and Fe3+ on biotreatment of Cr(VI) by Shewanella oneidensis and Bacillus subtilis in bimetallic system

Coexistence of chromium and iron, manganese and copper in industries is common, which may affect the microbial treating efficiency and toxicity to microorganisms, thus restricting the application of microbial treatment technology. In this research, Cu2+ promoted the reduction of Cr(VI) and the fixation of total chromium in bimetallic systems for both Shewanella oneidensis MR-1 and Bacillus subtilis, while Mn2+ and Fe3+ exhibited inhibition effects. Generally, groups with coexisting heavy metal of 0.1 mM were most affected, no matter promotive or inhibitive. Toxicity analysis revealed that high concentration of heavy metal ions led to damage to the cell membranes and reduction of their survival rate. To clarify the optimal condition for microbial treatment, response surface methodology was used to investigate the influencing factors of Cr(VI) reduction by S. oneidensis. The total chromium concentration in the supernatant was correlated with three factors, and the significant order of influence was: culture time > culture temperature > pH.

Synthesis and application of EDTA grafed metal-organic frameworks (MOFs) and graphene composite for the electrochemical detection of lead(II)

ABSTRACTThe rapid and sensitive detection of heavy metal ion concentrations in water holds significant importance for water resource quality control and protection. In this study, we developed a novel electrochemical sensor utilising a composite material consisting of ethylene diamine tetraacetic acid (EDTA) grafted metal-organic frameworks (MOFs NH2-UiO-66) and graphene to detect Pb2+ in water. The NH2-UiO-66 material exhibited a large specific surface area and porous structure, which was advantageous for the pre-enrichment of the heavy meatal ions. EDTA contained abundant – COOH groups, enabling it to chelate metal ions and increase the reaction sites of redox reactions. The introduction of graphene improved the conductivity of the composite, facilitating electron transfer and enhancing the sensitivity of the electrochemical sensor. Under optimal conditions, the linear range for Pb2+ detection was 0.1 μM–50 μM, and the limit of detection was achieved at 0.052 μM. Furthermore, simultaneous detection of Pb2+ and Cd2+ was successfully accomplished. The fabricated sensor also exhibited excellent selectivity, reproducibility and stability.

Biomass derived green carbon dots for sensing applications of effective detection of metallic contaminants in the environment

The rapid consumption of metals and unorganized disposal have led to unprecedented increases in heavy metal ion concentrations in the ecosystem, which disrupts environmental homeostasis and results in agricultural biodiversity loss. Mitigation and remediation plans for heavy metal pollution are largely dependent on the discovery of cost-effective, biocompatible, specific, and robust detectors because conventional methods involve sophisticated electronics and sample preparation procedures. Carbon dots (CDs) have gained significant importance in sensing applications related to environmental sustainability. Fluorescence sensor applications have been enhanced by their distinctive spectral properties and the potential for developing efficient photonic devices. With the recent development of biomass-functionalized carbon dots, a wide spectrum of multivalent and bivalent transition metal ions responsible for water quality degradation can be detected with high efficiency and minimal toxicity. This review explores the various methods of manufacturing carbon dots and the biochemical mechanisms involved in metal detection using green carbon dots for sensing applications involving Cu (II), Fe (III), Hg (II), and Cr (VI) ions in aqueous systems. A detailed discussion of practical challenges and future recommendations is presented to identify feasible design routes.

Recycling of the waste battery: Effect of waste battery on property of asphalt and environmental impact evaluation

A waste battery is a kind of hazardous solid waste, and traditional recycling methods can cause serious environmental pollution. In this paper, a pilot study was conducted to reduce the leaching of heavy metals in waste battery power (WBP) by using the wrapping effect of asphalt and explored the feasibility of adding waste battery as a modifier to asphalt. The main components of WBP are determined through microscopic experiments, and its compatibility with asphalt and microscopic mechanism are analyzed; The influence of WBP on asphalt properties are analyzed through routine tests and mixture tests; The leaching test of toxicity is used to analyze the impact of WBP and WBP modified asphalt on the environment. The experimental results indicate that WBP is mainly composed of MnO2, C, and ZnO; There are many wrinkles and grooves on the surface of WBP, which can effectively adsorb asphalt during the modification process, produce anchoring effect, and have good compatibility with asphalt; The components of waste battery adsorb the aging light components in asphalt through their folds and swelling, so that the proportion of heavy components is relatively increased, improving the property indicators of asphalt; From the perspective of engineering property, WBP modified asphalt mixture has strong resistance to deformation and water damage. The leaching concentration of heavy metal ions from bare WBP in soil seriously exceeded the standard. In contrast, when WBP was added to asphalt, the cumulative leaching concentration of heavy metal ions was significantly reduced due to the wrapping effect of asphalt, and the WBP leaching toxicity was greatly suppressed; The method of recycling waste battery and adding it to asphalt as a modifier can prevent the release of heavy metal ions from waste battery into the environment and reduce the risk of the total environmental harm to soil, groundwater and human health.

FACTORS ON THE BIOSYNTHESIS OF AMYLOLITIC ENZYMES OF STREPTOMYCETE ORIGIN

Modern enzyme biotechnology is a promising and rapidly developing field that requires the latest research on the conditions of enzyme biosynthesis. Optimizing the composition of the nutrient medium depending on the needs of microorganisms and physicochemical factors directly affect the increase in the efficiency of the biosynthesis of amylolytic enzymes, namely the biosynthetic capacity of the strain Streptomyces recifensis var. lyticus 2P-15. Modulation of the biosynthetic activity of strains producing amylolytic enzymes will allow to significantly increase their economic yield. Aim. The purpose of this work is to optimize the biosynthetic capacity of the strain Streptomyces recifensis var. lyticus 2P-15 in terms of the synthesis of amylolytic enzymes and the study of the dynamics of the influence of physical and chemical factors on optimization. Methods. The object of the study is the strain Streptomyces recifensis var. lyticus 2P-15, obtained by three-stage selection of the producer. The simplex method of selecting the composition of the environment was used for the research. The ratio of amylolytic activity to the level of biomass accumulation was taken as the biosynthetic capacity of the strain. A photocolometric method was used to determine amylolytic activity. The level of biomass accumulation was determined by the weight method. Results. It was established that as a result of optimizing the composition of the simplex nutrient medium by the method of mathematical modeling, the biosynthetic capacity increased by 3.63 compared to the control variant. It was also investigated that the optimal concentration of such a component of the nutrient medium as monosodium glutamate С5Н8NO4Na・H2O is 1.5%, which increases the amylolytic activity by 2.63 and increases the accumulation of biomass. Separately, it should be noted the obtained results of the study of the optimal concentrations of heavy metal ions added to the optimized version of the nutrient medium, which allow further research in this aspect to be continued and the use of Co, Mo, Cd ions in the composition of the nutrient medium. With the obtained results, there is an increase in amylolytic activity in the best response by 3.54. The obtained results have theoretical and practical significance for further research in the biotechnology of enzymes. Conclusions. The prospect of further research into the optimization of the biosynthesis of actinomycetes by the simplex method of other aspects of its regulation will be to increase the biosynthetic capacity of the studied strain, which will have a positive effect on the economic output of the production of amylolytic enzyme preparations by obtaining microbial synthesis.