Low Concentrations Of Heavy Metals Research Articles

Enhanced removal of lead ions from wastewaters by electrochemical adsorption using nitrogen-doped Ti3C2Tx MXene

As a two-dimensional material containing transition metal carbides and nitrides, MXene is often used in capacitive deionization for its excellent hydrophilic and pseudocapacitive properties. Nitrogen doping is widely used to improve the adsorption properties of certain materials. However, the effect of nitrogen doping on the electrochemical adsorption properties of MXene remains unclear. In this work, nitrogen-doped Ti3C2Tx MXene was synthesized using a simple hydrothermal method to achieve highly selective and efficient removal of Pb(II) at a constant cell voltage. The concentration of Pb(II) decreased from 4.95 to 0.02 mg L−1 in a 100 mg L−1 NaCl supporting electrolyte after electrosorption. The removal efficiency of Pb(II) reached 99.5 %, whereas it was only 15.2 % for Na+. The introduction of nitrogen functional groups increased the electrical conductivity and layer spacing of MXene, thereby improving the pseudocapacitive adsorption performance in the presence of Pb(II). The complexation function of the TiOH group on nitrogen-doped Ti3C2Tx surface increased and contributed to the selective adsorption of Pb(II). The removal efficiency of Pb(II) increased with increasing solution pH and cell voltage, reaching the maximum value at pH 5.0 and 1.5 V, respectively. The effect of supporting electrolyte type on the removal of Pb(II) was negligible. In addition, the removal efficiency for mixed heavy metal ion solutions, including Cu(II), Ni(II), and Pb(II), exceeded 79.0 %. It exhibited the highest removal efficiency for Pb(II) at 97.9 %. After five cycles of electrochemical adsorption–desorption, the nitrogen-doped Ti3C2Tx maintained a stable Pb(II) removal efficiency of 97.0 %. This work provides a promising material for the electrochemical removal of low-concentration heavy metal ions from wastewaters.

Soilless Production of Lettuce (Lactuca sativa) in the Atacama Desert Using Fog Water: Water Quality and Produce Mineral Composition

Soilless vegetable production in the Atacama Desert of Northern Chile is spreading since it is perceived as an alternative that requires much less water than open field soil production. However, strong competition between mining and urban use for human population consumption exists, forcing growers to use alternative water sources. Fog is commonly present in the coastal areas of Northern Chile; however, little information exists with regards to its chemical composition and the effect on nutrient quality of the produce. To address this knowledge gap, a set of experiments was carried out in Chañaral, a small town located in the Atacama Desert of Northern Chile. There, a 200 m2 greenhouse equipped with twenty deep flow pools was used in two consecutive growing cycles. Water for the mixing of the nutrient solution was collected from the fog using fog-catchers and later stored in 2000-L tanks. Fog water quality (electrical conductivity, pH and mineral content) was monitored directly from the storage tanks. Two types of lettuce, green butterhead and red oak leaf, were compared on their yield and accumulation of nutrients and heavy metals. The results indicate that fog water is of good quality for soilless production, with an electrical conductivity value of 0.65 ± 0.18 and low content of heavy metals. Plants’ heavy metal accumulation is below the recommendation of Food and Agriculture Organization and World Health Organization. Fog water presents as a viable water source for soilless production in Northern Chile.

Chemometric evaluation, source apportionment, and health risk analysis of natural spring water in Murree, outer Himalayas

IntroductionContamination of water is a critical threat to human health at a global level. Water pollutants, such as heavy metals, can have adverse effects on the well-being of humans, animals, and the natural ecosystem of a region. Study AreaMurree is the most visited tourist destination in Pakistan. The rural population of Murree uses natural spring water for drinking, household use, and irrigation. MethodsThis study assessed the elemental concentration of water from 20 natural springs in Murree using Inductively Coupled Plasma Optical Emission Spectroscopy. Source apportionment and spatial distribution of heavy metals were assessed using statistical approaches such as Pearson's correlation coefficient, principal component analysis, and interpolation. The study assessed the quality of water for drinking and irrigation in Murree's natural spring water using the metal index, sodium absorption ratio, magnesium absorption ratio, percentage sodium, Kelly's ratio, and salinity hazard. The health risks associated with heavy metals were assessed by computing Average daily dose, Hazard quotient, Hazard Index, and Cancer Risk. ResultsThe mean concentration of metals in mgL-1 varied in the following order: Ca (51.23) > Na (22.3) > Mg (16.26) > Si (6.51) > K (1.59) > Se (1.17) > Sr (0.48) > Ba (0.209) > Al (0.060) > Li (0.015) > Zn (0.005) > Fe (0.0033) > Ni (0.0032) > Cr (0.001). Metal index was calculated for Al (0.3), Ba (0.29), Cr (0.024), Ni (0.14), Fe (0.004), Zn (0.002), Sr (0.07), Mg (0.32), and Ca (0.25), revealing low levels of metal pollution. The geology of the study area was identified as the primary source of heavy metals in the water. The estimated values of health hazards showed that ingestion is the primary exposure pathway, with children having a higher risk. The health hazards posed by the heavy metal contact from the waters of Murree are not alarming. Quality indices show that the irrigation water sourced from the natural springs is of satisfactory quality. ConclusionThe study concluded that the spring water of Murree has low concentrations of heavy metals; their concentration is dependent upon the geology of the study area and is good for drinking and irrigation.

Spatial and seasonal dynamics of zooplankton functional groups and their relationship with environmental factors in urban rivers in Haikou City, China

The urban rivers, including Changwang, Meishe, and Wuyuan in Haikou City, China, are vital water resources. Despite the rivers experiencing anthropogenic impacts, limited studies have investigated their water quality and ecological community structure. This study assessed zooplankton functional groups' spatial and seasonal dynamics relative to environmental factors in the three urban rivers. The samples were collected and analyzed seasonally between March and December 2019. The environmental factors varied significantly at spatial and seasonal scales (p < 0.05). Meishe and Wuyuan Rivers had higher electrical conductivity, salinity, TN, and TP than Changwang, which had low turbidity. Seasonally, higher TP, TN, NH3-N, and CODMn levels were found in the spring, while summer and autumn experienced high temperatures. Additionally, spring and summer had high Chl-a levels. Likewise, spring had the lowest heavy metal concentrations, while nearly all metals were elevated in winter and summer. Generally, the average metal content followed the order of Mn > Zn > Cu > Ni > As > Cr > Co > Pb > Cd. The environmental parameters were within class III of the China standard for surface waters (GB 3838–2002), suggesting negligible pollution. This study identified 159 zooplankton species, including 62 Rotifers, 50 Protozoans, 31 Cladocerans, and 16 Copepods. They were classified into 11 functional groups, dominated by Rotifers filter feeders (RF), Rotifers carnivores (RC), and small copepods and cladocerans filter feeders (SCF), followed by Middle copepods and cladocera carnivores (MCC) and Middle copepods and cladocerans filter feeders (MCF). Analysis of similarity (ANOSIM) revealed seasonal differences (p < 0.001) in zooplankton functional groups, with RF and RC most dominant in summer, autumn, and winter, while SCF, MCF, and MCC were dominant in spring. Hence, the redundancy analysis (RDA) and Pearson Correlation analysis revealed that temperature, Chl-a, TP, salinity, CODMn, NH3-N, TN, As, Co, and Cd were the main environmental factors influencing zooplankton functional groups. This study helps understand urban rivers' water quality and ecological community structure, bridging the knowledge gap. The findings are essential for water quality monitoring and management.

Eco-friendly thiol-functionalized magnetic oxygenous carbon nitride nanocomposites for effective elimination of heavy metals

The increased pollution of water resources by toxic heavy metals poses a huge threat to the aqueous ecosystem. Since the low concentrations of heavy metals are often highly toxic but difficult to remove, novel efficient adsorbents still need to be explored. Herein, the superparamagnetic thiol-functionalized oxygenous carbon nitride nanocomposite (CNO/Fe3O4-SH) with multifunctional groups such as –NH2, –OH, –SH, and –COOH was fabricated by a simple and eco-friendly method. The maximum adsorption capacities of Pb2+, As3+, and Cd2+ ions on CNO/Fe3O4-SH at pH = 6 were 80.79, 71.78 and 66.19 mg/g, respectively, when their equilibrium concentrations were 20 mg/L. Under the equilibrium concentration below 0.01 mg/L, the adsorption capacities of these heavy metals over CNO/Fe3O4-SH were much higher than those of other adsorbents. The competitive adsorption investigations showed that the adsorption order in polymetallic solutions was Pb2+ > As3+ > Cd2+. Adsorption kinetics and isotherms studies indicated that the adsorption of Pb2+, As3+ and Cd2+ by CNO/Fe3O4-SH was attributed to monolayer adsorption and the adsorption process was controlled by chemical adsorption. The thermodynamic experiments showed that the adsorption processes were spontaneous and endothermic. After six adsorption/desorption cycles, CNO/Fe3O4-SH maintained its original morphology and adsorption ability, indicating its excellent regeneration performance, which had significant potential application in the decontamination of trace heavy metal ions in water.

Promoting microalgal biofilm formation by crushed oyster shell-hydroxyapatite layer on micropatterned aluminum coating for heavy metal ions removal

Microalgal biomass has shown inspiring potential for the heavy metal removal from wastewater, and forming microalgal biofilm is one of the sustainable methods for the microalgal biomass production. Here we report the formation of microalgal biofilm by accelerated colonization of typical algae Chlorella on thermal sprayed aluminum (Al) coatings with biologically modified surfaces. Micro-patterning surface treatment of the Al coatings promotes the attachment of Chlorella from 6.31 % to 17.51 %. Further enhanced algae attachment is achieved through liquid flame spraying a bioactive crushed oyster shell-hydroxyapatite (CaCO3-HA) composite top layer on the micropatterned coating, reaching 46.03–49.62 % of Chlorella attachment ratio after soaking in Chlorella suspension for 5 days. The rapidly formed microalgal biofilm shows an adsorption ratio of 95.43 % and 85.23 % for low concentration Zn2+ and Cu2+ in artificial seawater respectively within 3 days. Quick interaction has been realized between heavy metal ions and the negatively-charged extracellular polymeric substances (EPS) matrix existing in the biofilm. Fourier transform infrared spectroscopy (FTIR) results indicate that both carboxyl and phosphoryl groups of biofilms are crucial in the adsorption of Cu2+ and the adsorption of Zn2+ is due to the hydroxyl and phosphate groups. Meanwhile, the biofilm could act as a barrier to protect Chlorella against the attack of the heavy metal ions with relatively low concentrations in aqueous solution. The route of quick cultivating microalgal biofilm on marine structures through constructing biological layer on their surfaces would give insight into developing new techniques for removing low concentration heavy metal ions from water for environmental bioremediation.

Ecological risk assessment of heavy metals in surface sediments and their impact on macrobenthos in Asan Bay, South Korea

Bay ecosystems with unique economic and ecological value are more vulnerable to heavy metal pollution than other marine ecosystems. In South Korea, rapid economic development has exacerbated heavy metal pollution in bay environments. This study analyzed concentrations of seven heavy metals and the structure of macrobenthic community in Asan Bay. Five heavy metal indices (PLI, Pn, RI, TRI, and MERMQ) were used to assess ecological risk. Additionally, spearman correlation, biota–environment matching (BIO-ENV), and redundancy analysis (RDA) were utilized to determine the influence of heavy metals on macrobenthic communities. Although average concentrations of seven heavy metals were below sediment quality guidelines (SQGs), the average concentration of Cd was close to the threshold effects level (TEL). The nemerow pollution index (Pn) and the potential ecological risk index (RI) indicated that Cd was the primary heavy metal contributing to ecological risk. Spearman correlation, BIO-ENV, and RDA indicated that heavy metals were the main environmental factors influencing macrobenthic communities in Asan Bay. However, five heavy metal indices (PLI, Pn, RI, TRI, and MERMQ) did not show a response to the macrobenthic communities. Overall, low concentrations of heavy metals have a certain negative impact on macrobenthic communities in Asan Bay. This study can serve as an important reference for marine environmental protection and policy-making in Asan Bay.

Life cycle assessment of rice residue as the lightweight biocomposites for structural ceiling: A critical review

The research focuses on the sustainable utilization of rice residue for lightweight biocomposites, emphasizing the importance of pre-treatment methods like NaOH interventions on cellulose, hemicellulose, and lignin in rice residue. The balance in pre-treatment timing is crucial for maintaining the structural integrity of these components. Rice Husk Ash (RHA) stands out for its low heavy metal content and high refractoriness, making it versatile for various applications. Rice straw (RS), another component of rice residue, offers abundant cellulose and low lignin, making it suitable for biocomposite matrices. The study delves into extracting cellulose and CNCs from RS for eco-friendly packaging, targeted drug delivery, and high-quality composites. It also explores how advanced farming practices can reduce waste and enhance crop yields.

Engineering properties as a supplement cementitious material of ground copper reduction slag extracted valuable metal from Cu slag

We have examined whether the copper reduction slag (CRS) generated after recovering valuable metals from copper slag (CS) by reduction process can be used as supplementary cementitious materials (SCMs). According to the test results, the Cu secondary slag with low Fe, Cu, and heavy metal contents had a suitable oxide composition for using as a SCM. CRS showed better grinding efficiency than that of ground blast furnace slag (GGBS). Ground CRS contributed to the formation of tobermorite under autoclaved curing conditions. The compressive strength of CRS mortar replacing 50 % of OPC generated 93 % of that of the OPC mortar. Based on the results of this study, we found that the CRS has highly appropriate engineering characteristics for using as SCMs for concrete. In addition, it is judged that the method of using secondary slag as a material for precast concrete produced under hydrothermal conditions can greatly contribute to the construction process of buildings by securing mechanical performance.

Comparison of Phosphogypsum-Steel Slag-Based cement and Portland cement for stabilization of heavy metals in oil-based drillings cuttings

This research compared Portland cement and Phosphogypsum-Steel Slag-Based (PSSB) cement in terms of their capabilities to stabilize heavy metals (specifically lead and nickel) in Oil-Based Drill Cuttings (OBDC). In the experimental section, the qualitative analysis of heavy metal constituents in OBDC was captured by X-ray Photoelectron Spectroscopy (XPS). Additionally, an acetic acid leaching test was implemented for the heavy metal leaching concentration to evaluate the ceramsite stabilization effect on OBDC. In the simulation phase, cement models, heavy metal ion models, and stabilization models were constructed to explore the stabilization mechanism of heavy metals. Results demonstrated that PSSB cement exhibits superior stabilization effects on OBDC compared to Portland cement. Flame Atomic Absorption Spectrophotometry (FAAS) tests showed that PSSB cement reduced Ni and Pb leaching by 21.87 % and 47.32 %, respectively, compared to Portland cement. In PSSB cement, the diffusion coefficients for Ni and Pb ions were observed to decrease by 42.92 % and 79.63 %, respectively, as revealed through Mean Square Displacement (MSD) analysis. The cohesive energy of PSSB cement was 76.73 % lower than that of Portland cement, and its interaction energies for stabilizing Ni and Pb ions were 59.43 % and 76.22 % lower, respectively, demonstrating greater stability and efficiency in metal stabilization. PSSB cement exhibited lower heavy metal concentration and better structural stability than Portland cement.

Analysis of 18 elements in Alpine goat milk in the first third of lactation

The research objective was to examine the influence of the first third of the lactation stage on 18 mineral elements in Alpine goat milk. The research was carried out on 20 goats of the French-Alpine breed, which were on average 5 years old and in the fourth lactation. The goats were monitored on the 30th and the 90th day of lactation. Their milk was analysed for chemical composition by the infrared spectroscopy. By means of inductively coupled plasma (ICP), a total of 18 minerals were analysed (Ca, P, K, Na, K, Mg, Fe, Zn, Cu, Se, Mn, Mo, Co, Cr, Ni, Cd, Pb, As and Hg). The period of milk sampling in the first third of lactation significantly influenced the changes in concentrations of Na, Se, Mo, Cr, Ni and As. Significantly higher concentrations of Na and As were determined in milk sampled on the 90th day, while lower concentrations of Se, Mo, Cr and Ni were determined in milk sampled on the 30th day of the first third of lactation. Analysis of the correlation coefficients between the investigated trace elements and the selected toxic elements in Alpine goat milk showed a significantly positive correlation between Ca:Mg, Ca:P, Ca:Co, Ca:Ni, Ca:Mo; Mg:P, Fe:As, Pb:Cd and P:Ni. In the first third of lactation, Alpine goat milk contained a very low concentration of heavy metals. The described changes indicate that Alpine goat milk is rich in essential elements, while the concentration of toxic elements is very low in the first third of lactation.

115 years of sediment deposition in a reservoir in Central Europe: Effects of the industrial history and environmental protection on heavy metals and microplastic

AbstractHumans have considerably influenced accumulation rates and sediment composition in lake deposits. Due to near‐continuous accumulation, lakes and reservoirs are an excellent archive of these anthropogenic influences. The Urft Reservoir in the Eifel Mountains, western Germany, provides a unique record of the human influence on the landscape for the past 115 years. In 2020 and 2021, 24 cores and 23 surface samples were obtained from the bottom of the, by that time drained, reservoir. Grain size, heavy metals, weathering signatures and microplastic were analysed. For the chronology, caesium‐137 and microplastic were used. Using the first occurrence of microplastic as well as different plastic types for dating was not successful. However, a distinct layer with a high number of microplastic particles could be traced back to a fire in 1991 and was used as an additional stratigraphic marker in the age‐depth model. A period of relatively high accumulation rates in the reservoir occurred in the mid‐1950s and was related to enhanced construction works in the local valleys. Analysis of heavy metal content in the reservoir sediments shows a strong connection to historical changes in ore industry in the valley of the Urft. Stricter environmental protection laws and the decline of the metal processing industry resulted in a reduced input of lead, copper and zinc in the reservoir until the mid‐1980s. Since then, heavy metal content has remained relatively constant. A major flooding event in July 2021 did not lead to the remobilisation of older contaminated deposits as indicated by low heavy metal content in flood deposits. Accordingly, also the microplastic content is not increasing following the extreme event. Due to the degree of weathering of the flood deposits, it is argued that mainly hillslope material was transported into the Urft and subsequently into the Urft Reservoir during this event.

Soil–water contamination assessment due to dumpsite-impacted leachates in a metamorphic environment

Environmental contamination is a complex issue that significantly impacts human health and ecological systems, especially in developing countries like Nigeria. This study explores the interplay between surface-subsurface soil-rock resistivity and subsurface geotechnical properties, along with multiple soil-water pollution indices at and around the Old Owo-Ikare road (OOIR) dumpsite in southwestern Nigeria. Water samples from five wells and one stream were collected and analyzed, alongside twelve soil samples from four trial pits at varied depths for geoenvironmental assessment. Analyzed hydrogeochemical parameters include Na, Ca, Mg, K, Cr, Pb, Zn, Ni, Mn, Fe, and cations (NO, SO4, Cl) in the water samples. Nine dipole-dipole electrical resistivity tomography (ERT) profiles and six Schlumberger vertical electrical sounding (VES) points were used to determine surface–subsurface resistivity distribution. Water analysis results showed elevated levels of K, Ni, Cr, and Pb concentrations. Geotechnical tests indicated that most dumpsite soil meets good landfill material criteria with low permeability (5.92×10−6 to 1.49×10−4cm/s). ERT and VES inverted models revealed four lithologic layers with two main curve types (HA and QA). Elevated heavy metal levels in the dumpsite soil and inverted resistivity models suggested leachate contamination in the topsoil and weathered bedrock units. Despite relatively lower heavy metal concentrations compared to other Nigerian and Ghanaian dumpsites, multi-pollution indices indicated significant contamination in both water and soil samples, posing moderate to very high environmental risks based on World Health Organisation standards. Additionally, human health risk assessment suggested a risk of cancer and non-cancer-related diseases from prolonged well water consumption. Therefore, ongoing monitoring and remediation efforts are essential to forestall imminent pollution in uncovered areas.

Molybdenum tailings calcination for phase composition of Si-Ca-K-Mg fertilizers: Modification of phase transformation and its effects on plant growth

The high value and comprehensive utilization of molybdenum tailings for the production of fertilizer of calcium silicon magnesium potassium (Si-Ca-K-Mg fertilizer) was investigated, considering the abundant potassium feldspar (K-feldspar) content in the tailings. The effects of calcination temperatures, times, and additives (CaCO3 and CaSO4) on reaction degree, final product type, and phase transition process were studied. The results indicated that at 1200 °C, calcination time of 120 min and m(molybdenum tailings):m(CaCO3):m(CaSO4) = 1:0.7:0.2, the final product met Type I product requirements according to Chinese national standards GB/T36207-2018 as well as extremely low heavy metal contents. In the calcination process, CaO resulted from CaCO3 absorbs the liquid phase produced during K-feldspar decomposition to form CaSiO3, facilitating the K-feldspar decomposes into KAlSiO4. Simultaneously, the Ca2+ in CaSO4 replaces undecomposed K-feldspar’s K+. Additionally, CaO reacts with Al2O3, MgO, and SiO2 to produce gehlenite (Ca2Al2SiO7) and akermanite (Ca2MgSi2O7), providing plants with Ca, Mg, and Si elements. The nutrients of the fertilizer were readily assimilated by plants, improving acidic soil without causing any harm to the soil or vegetation. This work offers new ideas for large-scale and high-value utilization of molybdenum tailings as well as addressing the shortage of soluble potassium resource in China.

Ionic liquid catalyzed low-temperature hydrothermal carbonization of sewage sludge to produce hydrochar with low heavy metal content and positive energy recovery

An ionic liquid (IL, [DMAPA]HSO4) was prepared to facilitate the removal of heavy metals by hydrothermal carbonization (HTC) in sewage sludge (SS) and to obtain a positive energy recovery (ER, (Energyoutput/Energyinput − 1) > 0). The results found that the removal efficiencies of the Fe, Mn, Zn, Co, and Cd from SS exceeded 75 % with positive ER (6 %) at 20 wt% IL dosage (IL:SS). IL promoted the HTC reactions of proteins and polysaccharides to produce fixed carbon and small molecule polymers. The process mainly relies on IL to catalyze the dehydration and graphitization of SS and to destroy the heavy metal binding sites such as carboxyl and hydroxyl groups. Additionally, IL aids in constructing the macropore structures in hydrochar, thereby facilitating the release of heavy metals and water during the HTC process. This discovery holds promise for removing heavy metals from SS by one-pot HTC processes with positive energy recovery.

Temporal and spatial evolution of different heavy metal fractions and correlation with environmental factors after prolonged acid mine drainage irrigation: A column experiment

Acid mine drainage (AMD) has global significance due to its low pH and elevated heavy metal content, which have received widespread attention. After AMD irrigation in mining areas, heavy metals are distributed among soil layers, but the influencing factors and mechanisms remain unclear. AMD contamination of surrounding soil is primarily attributed to surface runoff and irrigation and causes significant environmental degradation. A laboratory soil column experiment was conducted to investigate the temporal and spatial distribution of the heavy metals Cd and Cu, as well as the impact of key environmental factors on the migration and transformation of these heavy metals following long-term soil pollution by AMD. After AMD addition, the soil exhibited a significant increase in acidity, accompanied by notable alterations in various environmental parameters, including soil pH, Eh, Fe(II) content, and iron oxide content. Over time, Cd and Cu in the soil mainly existed in the exchangeable and carbonate-bound fractions. In spatial terms, exchangeable Cu increased with increasing depth. Pearson correlation analysis indicated significant negative correlations between pH and Cu, Cd, and Eh in pore water, as well as negative correlations between pH and the exchangeable fraction of Cd (F1), carbonate-bound fraction of Cd (F2), and exchangeable fraction of Cu (F1) in the solid phase. Additionally, a positive correlation was observed between pH and the residual fraction of Cu (F5). Furthermore, the soil total Cd content exhibited a positive correlation with pyrophosphate-Fe (Fep) and dithionite-Fe (Fed), while CdF1, CdF2, total Cu, and CuF1 displayed positive correlations with Fep. Our findings indicate that the presence of AMD in soil leads to alterations in the chemical fractions of Cd and Cu, resulting in enhanced bioavailability. These results offer valuable insights for developing effective remediation strategies for soils near mining sites.

Evaluating hydrothermal liquefaction hydrochar from sewage sludge as a phosphorus resource through struvite production

Hydrothermal liquefaction (HTL) has attracted considerable attention for valorizing sewage sludge to biofuels while the solid residue, hydrochar, has received little attention for its final application. In the current work hydrochar recovered from hot separation in a pilot-scale HTL plant is evaluated for its nutrient value, in particular as a sustainable Phosphorus (P) resource. Following thorough characterization of the hydrochar, P recovery as struvite (NH4MgPO4·6H2O) is investigated to produce a fertilizer with a lower heavy metal content that could be used in current agricultural practices. P extraction using inorganic (hydrochloric and sulphuric) and organic (citric) acids is evaluated by applying 0.1–1 mol/L of acids for 1–12 h with a liquid/solid ratio of 10 mL/g. A second-order polynomial model was established by response surface methodology (RSM) to predict the P extraction with different acids. The optimum operating conditions for maximum P extraction (94 %) are suggested as 0.7 M of acid strength (H2SO4) and 6.5 h of extraction time. Addition of citric acid (CA) during the struvite precipitation from acid-leached P solution was found to improve the struvite purity from 36.6 % to 54 % with a reduction in heavy metal content. Furthermore, morphological analysis validated the formation of struvite. Upon comparison with the regulations, hydrochar was found to exceed some of the heavy metal limits but was low in polyaromatic hydrocarbons (PAHs), per- and polyfluorinated substances (PFAS) and showed low toxicity to Aliivibrio fischeri. P extraction and struvite precipitation are shown to reduce heavy metal contents below regulatory limits with P recoveries from 40 % to 67 %. Thus, as an alternative to direct land application of hydrochar, harvested struvite from hydrochar could be applied as a fertilizer with no apparent environmental risk.

Microbial Application in Heavy Metal Removal from Pharmacological Industrial Effluent

In industrial effluents, significant amounts of metallic cations such as zinc, copper, iron, manganese, lead, nickel, and cadmium are present. Long-term irrigation with these effluents increases the amount of organic carbon and heavy metals in the soil, increasing the likelihood that they will enter the food chain and, eventually, result in significant bioaccumulation. Many techniques for the treatment and disposal of metal-containing wastes, such as ion exchange, reverse osmosis, in flotation, and evaporation, have been developed in order to reduce metal pollution issues. The main disadvantages of conventional treatments are low efficiency at low concentrations of heavy metals, expensive handling, and safe disposal of toxic sludge. In light of this, an effort has been made to investigate how tannery affects the growth of green gram.

Investigating the potential of mineral precipitation in co-pyrolysis biochar: Development of a novel Cd (II) adsorption material utilizing dual solid waste

Ionic cadmium (Cd (II)) in water is a significant threat to ecosystems, the environment, and human health. Research is currently focused on developing efficient adsorption materials to combat Cd (II) pollution in water. One promising solution involves co-pyrolyzing solid residue from anaerobic digestion of food waste with oil-based drill cuttings pyrolysis residue to create a biochar with high organic matter content. This biochar has a lower heavy metal content and leaching toxicity compared to China's national standards, making it both safe and resourceful. It exhibits a high adsorption capacity for Cd (II) in water, reaching up to 47.80 ± 0.37 mg/g. Raising the pyrolysis temperature above 600 °C and increasing the amount of pyrolysis residue beyond 30 % enhances the biochar's adsorption capacity. The adsorption process is primarily driven by mineral precipitation, offering a promising approach for dual waste resource management and reducing heavy metal pollution.

Treatment of electroplating wastewater using electrocoagulation and integrated membrane.

Electroplating wastewater contains heavy metal ions and organic matter. These contaminants not only endanger the environment but also pose risks to human health. Despite the development of various treatment processes such as chemical precipitation MBR, electrocoagulation (EC) ceramic membrane (CM), coagulation ultrafiltration (UF) reverse osmosis (RO), and CM RO. These methods are only effective for low concentrations of heavy metals and struggle with high concentrations. To address the challenge of treating electroplating wastewater with high heavy metal content, this study focuses on the wastewater from Dongfang Aviation Machinery Processing Plant. It introduces an EC and integrated membrane (IM) treatment process for electroplating wastewater. The IM comprises microfiltration (MF) membrane, nanofiltration (NF) membrane, and RO membrane. Results indicated that under specific conditions, such as a pH of 8, current density of 5 A/dm2, electrode plate spacing of 2 cm, 35 min of electrolysis time, and influent pH of 10 for the IM, removal rates of Zn2+, Cu2+, Ni2+, and TCr in the wastewater exceeded 99%. The removal rates of chemical oxygen demand (COD), suspended solids (SS), total phosphorus (TP), total nitrogen (TN), and petroleum in wastewater exceed 97%. Following a continuous cleaning process, the membrane flux can consistently recover to over 94.3%.