Eisenia fetida-driven vermitechnology for the eco-friendly transformation of steel waste slag into organic amendment: An insight through microbial diversity and multi-model approach.

The processing of steel waste slag from the black metallurgical sector seriously threatened the ecology. To counter these dangers, appropriate detoxification methods were required. Vermitechnology was one such strategy that could successfully convert this industrial waste into nutrient-rich products suitable for use in agriculture. This research primarily focuses on employing vermitechnology for the transformation of waste steel slag into vermicompost and to determine changes in microbial composition, nutrient cycling, and metal detoxification facilitated by earthworms (Eisenia fetida). Earthworm populations in steel waste vermibeds (sw-vermibeds) increased by 2.87-3.07 folds. T1(SW + CD-1:1) comparatively showed increased levels of nutrients such as nitrogen, phosphorus, and potassium. Microbial and enzymatic parameters were more pronounced in treatment T1. The findings of phospholipid fatty acid (PLFA) diversity demonstrate microbial diversity and fatty acid composition. Based on PLFA Sobol Sensitivity Analysis (SSA), PUFA and cyclo were the most sensitive inputs to the presence of heavy metal (HMs) concentrations in SW. In accordance with Taylor-based modelling, R-tree, and Mars were the most trusted regression models for predicting HMs toxicity on microbes. The bioavailable metal fractions of HMs (Fe, Ni, Cd, Cu, Pb, and Cr) decreased by 61-83%. The correlation was performed for 0 and 90 days for metal microbial interactions r (0 days), [BSR vs Fe, Cd, Cu, Ni = -0.99, -0.82, -0.43, -0.99] and r (90 days), [FDA vs Fe, Cu, Ni = -0.97, -0.47, -0.95]. Overall, the results indicated that T1(1:1 SW + CD) provided more favorable conditions for the development of microbes and Eisenia fetida. This research presents a new perspective to the world community on the transformation of harmful steel waste slag into advantageous biological resources by introducing a novel method of employing Eisenia fetida to remediate hazardous steel waste slag.

Aqueous mineral carbonation of three different industrial steel slags: Absorption capacities and product characterization.

Heavy carbon industries produce solid side stream materials that contain inorganic chemicals like Ca, Na, or Mg, and other metals such as Fe or Al. These inorganic compounds usually react efficiently with CO2 to form stable carbonates. Therefore, using these side streams instead of virgin chemicals to capture CO2 is an appealing approach to reduce CO2 emissions. Herein, we performed an experimental study of the mineral carbonation potential of three industrial steel slags via aqueous, direct carbonation. To this end, we studied the absorption capacities, reaction yields, and physicochemical characteristics of the carbonated samples. The absorption capacities and the reaction yields were analyzed through experiments carried out in a reactor specifically designed to work without external stirring. As for the physicochemical characterization, we used solid-state Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscope (SEM). Using this reactor, the absorption capacities were between 5.8 and 35.3 g/L and reaction yields were in the range of 81-211 kg CO2/ton of slag. The physicochemical characterization of the solid products with solid FTIR, XRD and SEM indicated the presence of CaCO3. This suggests that there is potential to use the carbonated products in commercial applications.

Exploring the potential of steel slag waste for carbon sequestration through mineral carbonation: A comparative study of blast-furnace slag and ladle slag.

Steel slag is a by-product of steelmaking which has emerged as a potential CO2 sequestration material due to its high reactivity and abundance. This research investigates the use of steel slag waste for the direct capture of carbon from air and its storage through mineral carbonation. Two abundant wastes, blast-furnace slag (BFS) and ladle slag (LS), were tested for their carbon sequestration potential, and the effects of operational parameters such as reaction time between CO2 and slag waste, temperature, liquid-solid ratio, and pressure on CO2 sequestration were determined. Quantitative and qualitative results reveal that much higher CO2 sequestration was achieved using LS compared to BFS after exposure to CO2 for 1 day at room temperature. By increasing the exposure time to four days, levels of CO2 sequestration increased gradually from 2.71% to 4.19% and 23.46%-28.21% for BFS and LS respectively. Increasing the temperature from 20 ± 2 °C to 90 ± 2 °C positively influenced CO2 sequestration in BFS, resulting in an enhancement from 3.45% to 13.21%. However, the impact on LS was insignificant, with sequestration levels rising from 27.72% to 29.90%. Moreover, better CO2 sequestration was observed for BFS than LS when the liquid-to-solid ratio increased from 3:1 to 4:1, whereupon the sequestration potential reached approximately 15% for BFS and 30% for LS at 90 ± 2 °C. Meanwhile, higher pressure reduced the sequestration potential of slag. The results of this study suggest that there is potential for scaling up the process to industrial applications and contributing to the reduction of CO2 emissions in the steelmaking industry.

Engineering properties optimization of dispersive soil by calcium silicate waste-The role of steel-making slag.

Steel slag (SS) is a byproduct that comes from the production of crude steel in alkaline oxidation furnaces. Resource utilization of steel slag, a calcium-silicon solid waste, is an urgent problem. This paper investigates a solid waste disposal method that applies different steel slag contents to modify dispersive soil. The engineering properties and modification mechanisms of dispersive soil specimens are studied and revealed by performing microstructure, mineral evolution, unconfined compressive strength (UCS), and tensile strength analysis. The pinhole test, mud ball crumb test (BCT), and mud cube crumb test (CCT) were carried out to determine the dispersivity of the soil specimens. Results show that when the steel slag content increases from 1% to 10%, the unconfined compressive strength and tensile strength increase by 176.05% and 75.40%, respectively. For soil specimens without curing time under 50 mm water head, the weight loss of the specimen with 10% steel slag content decreases by 72.03% compared to specimens with 1% steel slag content. Microstructural and mineralogical analyses indicate that the hydration reaction of steel slag changes the ionic composition of the soil and generates reaction products with effects such as filling and connection. To sum up, steel slag effectively improves water stability and mechanical properties of dispersive soil.

Nitrogen-doped activated carbon-based steel slag composite material as an accelerant for enhancing the resilience of flexible biogas production process against shock loads: Performance, mechanism and modified ADM1 modeling.

Anaerobic digestion for flexible biogas production can lead to digestion inhibition under high shock loads. While steel slag addition has shown promise in enhancing system buffering, its limitations necessitate innovation. This study synthesized the nitrogen-doped activated carbon composite from steel slag to mitigate intermediate product accumulation during flexible biogas production. Material characterization preceded experiments introducing the composite into anaerobic digestion systems, evaluating its impact on methane production efficiency under hydraulic and concentration sudden shocks. Mechanistic insights were derived from microbial community and metagenomic analyses, facilitating the construction of the modified Anaerobic Digestion Model No. 1 (ADM1) to quantitatively assess the material's effects. Results indicate superior resistance to concentration shocks with substantial increment of methane production rate up to 33.45% compared with control group, which is mediated by direct interspecies electron transfer, though diminishing with increasing shock intensity. This study contributes theoretical foundations for stable flexible biogas production and offers an effective predictive tool for conductor material reinforcement processes.

CuO nanosheets incorporated scrap steel slag coupled with persulfate catalysts for high-efficient degradation of sulfonamide from water.

A highly efficient and magnetically recoverable persulfate (PS) catalyst was prepared for the removal of sulfonamide (SMD) from wastewater, which is difficult to be degraded by the conventional biological treatment. In this study, the scrap steel slag (SSS) was used as supporting carrier and the CuO nanosheet was incorporated on the surface of SSS. The optimal conditions were determined as follows: the dosage of CuO/SSS was 1 g L-1, the PS concentration was 4 mM and the optimal initial pH was 6.85. Under the optimal conditions, the maximum SMD removal efficiency of 80.29% was achieved within 30 min by using CuO/SSS + PS. In addition, the CuO/SSS + PS system had a wide pH range (5-9) and more than 60% removal efficiency of SMD could be obtained with the pH between 3 and 11. The mechanism based on the phase transformation of Cu(I/II), Cu(II/III) and Fe(II/III) was elucidated by using different analytical techniques, such as SEM, XRD, XPS, BET, FTIR, VSM characterization and free radical analysis. This study provided a new pathway for the SSS resource utilization and the effective degradation of SMD from the refractory wastewater by using CuO/SSS catalyst coupled with PS system.

Desulfurization steel slag improves the saline-sodic soil quality by replacing sodium ions and affecting soil pore structure.

Flue gas desulfurization steel slag (DS), a solid waste produced by coal power plants and steelworks, was proposed as an amendment for the remediation of saline-sodic soil. A pot experiment including three dosages of DS alone (1%, 5%, 10% w/w) and their combination with fulvic acid (FA, 1%, w/w) was conducted to evaluate the potentials of DS as an amendment and to explore remediation mechanism of DS combined with FA on saline-sodic soil. The soil salinity, nutrition, pore structure, water retention, consistency, and desiccation cracking of DS and FA-amended soils were determined. Application of DS resulted in a significant reduction of pH, sodium adsorption ratio (SAR), and exchangeable sodium percentage (ESP) of saline-sodic soil. The DS amendment significantly increased the 6-15 µm pore volume of soil. The combination application of DS and FA showed better effect than the DS alone. The DS amendments at 5% and 10% significantly increased the field water capacity, permanent wilting point, and available water content of the soil, whereas significantly decreased the plastic limit, liquid limit, and plastic index. The DS alone and combined with FA could effectively control the development of desiccation cracking, reduced significantly the crack area density and average width of cracks of the soil. Consequently, the improvement of alkalinity and soil physical properties by DS amendment significantly increased the yield of alfalfa grown on saline-sodic soil. The remarkable improvement of physical properties of saline-sodic soil contributed to the decrease of SAR and ESP by the Ca2+ in DS replacing the Na + at soil colloid sites. Our results suggested that DS amendments alone or combined with fulvic acid have great potential as saline-alkali soil amendment.

Converting industrial waste into a value-added cement material through ambient pressure carbonation.

Converting industrial wastes into value-added building products in an environmental management strategy is a challenging yet vital component of the industrial process. Steel slag (SS), an industrial waste by-product from the steel-making process, is typically disposed of in landfill which consumes land resources and pollutes the environment. This paper explores the possibility of a closed-loop system to convert steel slag into a cement material through carbonation activation, thereby significantly reducing the amount of steel slag waste sent to landfills across Canada. The production of this cementing material can occur next to the steel mill, utilizing steel slag and carbon dioxide collected on-site to fabricate carbon-negative products. To save energy and allow production to be feasible on an industrial scale, ambient pressure (AP) carbonation is developed to reduce carbon emissions while improving their performance. High pressure (HP) carbonation curing and normal hydration (NH) references were also implemented at the same time to justify the application of AP carbonation in reducing CO2 emission. The results of this study found AP carbonation-activated SS compacts have comparable CO2 uptake (about 7.5 tons CO2/100 tons slag) and mechanically compressive strength values as those subjected to HP carbonation, suggesting that AP could be used to replace HP in carbonation curing to ensure a lower energy input. Additionally, AP seemed to possess as effective carbonation as HP. The studies investigated by multiple techniques including X-ray diffractometer (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopic analysis, and scanning electron microscopy (SEM) aim to identify the microstructure development of carbonated SS paste to assess carbonation results. Developed with life cycle assessment (LCA), environmental impact evaluation shows that AP presents a smaller global warming potential (GWP) value than HP. The comparable CO2 sequestration, satisfactory engineering properties, enhanced microstructure and lesser environmental impact in AP carbonation confirm the feasibility of replacing high pressure with extremely low pressure to cure concrete products. The use of AP carbonation for cement material created using steel slag reduces carbon emissions, energy usage, and natural resource consumption.

Lurgi-Thyssen dust catalytic thermal desorption remediation of di-(2-ethylhexyl) phthalate contaminated soils.

Fe2O3-assisted pyrolysis has been demonstrated to be a cost-effective thermal desorption (TD) technology. Lurgi-Thyssen dust (LTD) is a type of steel slag waste that contains a large amount of Fe2O3. In this study, to reduce energy consumption, LTD was added to contaminated soil to evaluate the feasibility of enhancing the TD removal efficiency of di-(2-ethylhexyl) phthalate (DEHP). The DEHP removal rate increased by 22.39% after adding 2% LTD at 200 °C for 20 min. Because of the catalytic pyrolysis of LTD, DEHP was pyrolyzed to form three types of short-chain esters: mono-(2-ethylhexyl) phthalate (MEHP), di (2-methylbutyl) ester, and methyl 2-ethylhexyl phthalate. The pyrolysis products of DEHP were less toxic and did not affect soil reuse. When the DEHP removal rate was 87.10%, LTD addition decreased the temperature and residence time of TD and alleviated the effect of TD on the soil physicochemical properties. Additionally, the desorption of DEHP from soil fitted the pseudo-second-order kinetic model well. Thus, the addition of LTD to contaminated soil enhanced the efficiency of TD remediation. Moreover, this study could provide a practical and economical strategy for LTD reuse.

Effective removal of phosphorus from high phosphorus steel slag using carbonized rice husk.

High phosphorus steel slag and carbonized rice husk are two common wastes characterized by high generation and low secondary use values. Through the reduction of high phosphorus steel slag by biomass, both wastes were fully utilized, thus reducing the negative impact on the environment. In this study, variables such as temperature, time, and amount of reactants were changed to determine the optimal conditions for the reaction of steel slag with carbonized rice husk at high temperatures. The actual amount of reducing agent consumed during the reduction was significantly greater than that predicted by theoretical calculations. Adding three carbon equivalent of carbonized rice husk and maintaining at 1500°C for 30 min could remove 79.25% of P2O5 in the slag. By modeling the material cycle in which high phosphorus steel slag was treated with biomass, the product could be used for crop growth. Meanwhile, the reduced iron and residual steel slag can be used to make steel again, thereby leading to a sharp reduction in fossil fuel usage and greenhouse gas emissions in this process.

Heavy metal pollution risk of desulfurized steel slag as a soil amendment in cycling use of solid wastes.

The by-product of wet flue gas desulfurization, desulfurized steel slag (DS), had chemical characteristics like natural gypsum that can be used to improve saline-sodic soil. However, contamination risk of heavy metals for cycling utilization of DS in agriculture was concerned mostly. Both pot and field experiments were conducted for evaluating the potential pollution risk of DS as the amendment of saline-sodic soil. Results showed that application of DS decreased the contents of Cd, Cu, Zn, and Pb, while significantly increasing chromium (Cr) content in DS-amended soils. The field experiment demonstrated that the migration of heavy metals (Cd, Zn, Cu, and Pb) in the soil profile was negligible. The application of DS at the dosage of 22.5-225 tons/ha significantly increased the Cr content in alfalfa (Medicago sativa L.) but lower than the national standard for feed in China (GB 13078-2017). DS altered the chemical fraction of heavy metals (Zn, Cu, and Pb), transferred exchangeable, reducible into oxidizable and residual forms in DS-amended soil. Application of DS combined with fulvic acid (FA) could effectively reduce the movement of heavy metals in soil and the accumulation of Cr in alfalfa. Based on our results, DS was a safe and feasible material for agricultural use and presented relatively little pollution risk of heavy metals. However, the results also showed that DS to a certain extent had a potential environmental risk of Cr if larger dosages of DS were used.

Removal of p-Nitrophenol from simulated sewage using steel slag: Capability and mechanism.

The steel slag was investigated for the removal of p-nitrophenol (4-NP) from simulated sewage by batch adsorption and fixed-bed column absorption experiments. The results showed that the maximum adsorption capacity was 109.66 mg/g at 298 K, pH of 7, initial concentration 100 mg/L, and dose 0.8 g/L. The adsorption process fitted the Langmuir isothermal adsorption model and followed pseudo-second-order kinetic models, the activation energy of adsorption (Ea) was 10.78 kJ/mol, which indicated that the adsorption was single-molecule layer physical adsorption. The regeneration efficiency was still maintained at 84.20% after five adsorption-desorption cycles. The column adsorption experiments showed that the adsorption capacity of the Thomas model reached 13.69 mg/g and the semi-penetrating time of the Yoon-Nelson model was 205 min at 298 K. Fe3O4 was identified as the main adsorption site by adsorption energy calculation, XRD and XPS analysis. The FT-IR, Zeta potential, and ionic strength analysis indicated that the adsorption mechanism was hydrogen bonding interaction and electrostatic interaction. This work proved that steel slag could be utilized as a potential adsorbent for phenol-containing wastewater treatment.

Flame-Retarded Rigid Polyurethane Foam Composites with the Incorporation of Steel Slag/Dimelamine Pyrophosphate System: A New Strategy for Utilizing Metallurgical Solid Waste.

Rigid polyurethane (RPUF) was widely used in external wall insulation materials due to its good thermal insulation performance. In this study, a series of RPUF and RPUF-R composites were prepared using steel slag (SS) and dimelamine pyrophosphate (DMPY) as flame retardants. The RPUF composites were characterized by thermogravimetric (TG), limiting oxygen index (LOI), cone calorimetry (CCT), and thermogravimetric infrared coupling (TG-FTIR). The results showed that the LOI of the RPUF-R composites with DMPY/SS loading all reached the combustible material level (22.0 vol%~27.0 vol%) and passed UL-94 V0. RPUF-3 with DMPY/SS system loading exhibited the lowest pHRR and THR values of 134.9 kW/m2 and 16.16 MJ/m2, which were 54.5% and 42.7% lower than those of unmodified RPUF, respectively. Additionally, PO· and PO2· free radicals produced by pyrolysis of DMPY could capture high energy free radicals, such as H·, O·, and OH·, produced by degradation of RPUF matrix, effectively blocking the free radical chain reaction of composite materials. The metal oxides in SS reacted with the polymetaphosphoric acid produced by the pyrolysis of DMPY in combustion. It covered the surface of the carbon layer, significantly insulating heat and mass transport in the combustion area, endowing RPUF composites with excellent fire performance. This work not only provides a novel strategy for the fabrication of high-performance RPUF composites, but also elucidates a method of utilizing metallurgical solid waste.

Recycling of crushed concrete and steel slag in drainage structures of geotechnical works and road pavements.

A crushed concrete aggregate, processed from construction and demolition waste and a siderurgical aggregate, processed from electric arc furnace steel slag, were selected based on their very high availability worldwide and known technical feasibility to be used in construction works. Given the association of their presence to the possibility of reducing the drainage capacity of unbound granular layers of road pavements and drainage structures which they may be associated with, there are studies and regulations that do not recommend their use. The causes that are at the origin of restrictions are mainly the possibility of formation of tufa and recementation phenomena. This behaviour has also hampered their recycling in drainage structures of geotechnical works. Therefore, it was considered that it would be relevant to investigate the drainage capacity of those recycled aggregates, using a leachate produced in a municipal solid waste landfill and tap water. To reference their behaviour, two natural aggregates, a basalt and a limestone, were also studied under identical test conditions. The results obtained showed no reduction in the drainage capacity of the recycled aggregates, similarly to what was observed with the natural aggregates. The possibility of building drainage structures with the tested aggregates is verified.

Application of Bacillus mucilaginosus in the carbonation of steel slag.

The stacking of steel slag has detrimental effects mainly for the waste of resources and the pollution of environment. In this study, a novel method based on microbially induced calcium precipitation (MICP) was proposed by utilizing a type of microorganism named Bacillus mucilaginosus, which could secrete carbonic anhydrase (CA) through the metabolism process, accelerating the hydration of carbon dioxide (CO2) and thus facilitating the formation of carbonate ions (CO32-). First, comparing the biologically deposited calcium carbonate with the chemically deposited one, it was found that the crystallinity and crystal size of the biological deposition was lower, leading to its cementitious properties. Under the condition of 1 wt. (weight) % dosage, the carbonation degree increased from 66.34 to 86.25% and the compressive strength improved greatly from 7.4 to 11.2 MPa as well. The weight gain rate of biologically carbonated specimens was also twice as much as the directly carbonated ones. This work strongly demonstrated that biological carbonation technology could not only improve the CO2 sequestration potential of steel slag but also enhance the mechanical properties and durability of steel slag products. KEY POINTS: • Bacillus mucilaginosus could resuscitate and proliferate in the steel slag environment. • B. mucilaginosus secreted carbon anhydrase, which could accelerate the hydration of CO2 and facilitate the precipitation of calcium carbonate. • Biologically carbonated steel slag had greater mechanical performance than directly carbonated one.

Characteristics of the immobilization process of arsenic depending on the size fraction released from excavated rock/sediment after the addition of immobilization materials.

Chemical immobilization is an effective technique to suppress the release of arsenic from naturally arsenic-containing excavated rock/sediment. For designing the chemical immobilization technique, it is important to understand that the immobilization of arsenic depends on the sizes of ionic arsenic and arsenic retained on the colloids and suspended particles that are released from the excavated rock/sediment. Tests on the size fractionation of the arsenic released and the subsequent immobilization were conducted. The total amount of the size fraction of arsenic released from six excavated rock/sediment ranged from 0.16 to 0.75 mg kg-1. The distributions of size fraction of arsenic released were categorized into three types: the dominant fraction was suspended particle fraction (SP-F) and ionic fraction (I-F), and a compatible amount of SP-F and I-F was included. Steel slag, calcium oxide, and ferrihydrite, which can effectively and stably immobilize ionic arsenic with different mechanisms, decreased the total amounts of the size fraction of arsenic released at 28%-84%, 59%-83%, and 57%-84%, respectively. Ferrihydrite and calcium oxide greatly reduced the I-F and the small and large colloid fractions. The steel slag was effective in reducing the SP-F at >86 %. In most arsenic fractions, the immobilized arsenic was not re-released at <7 %. This study provides the first experimental evidence of the variation in the released arsenic size depending on the excavated rock/sediment. In addition, the size fraction of the arsenic that could be immobilized depended on the immobilizing material. Thus, it is suggested that the combined application of immobilization materials would present a useful approach for immobilizing various released arsenic phases and preventing immobilized arsenic from re-release.

The application of steel slag in a multistage pond constructed wetland to purify low-phosphorus polluted river water.

To investigate the effect of a constructed wetland (CW) with steel slag as the filler on water contaminated by low phosphorus levels, a multistage pond CW system was designed in this study. Low-phosphorus polluted river water was used as the research object. This study explored the effects of using steel slag as a CW filler on phosphorus removal and the total phosphorus (TP) purification effect of the wetland system. The results showed that the TP removal rates in the ecological pond, oxidation pond, surface flow wetlands and submerged plant pond were 5.17%, 8.02%, 21.56%, and 16.31%, respectively. Intermittent increases in phosphorus concentration were observed in the reactors and were caused by the decay of plant tissues, which released pollutants. Because steel slag was added to the filler, the TP concentrations in the effluent of the first- and second-level horizontal subsurface CWs increased by 151.13% and 16.29%, respectively, compared to the influent concentration. The 20th to 40th days of the test run was a period of rapid phosphorus release of the system. The use of steel slag has a potential risk of phosphorus release when applied in CWs used to purify low-phosphorus contaminated water bodies.

Fracture Behavior of Permeable Asphalt Mixtures with Steel Slag under Low Temperature Based on Acoustic Emission Technique.

Acoustic emission (AE), as a nondestructive testing (NDT) and real-time monitoring technique, could characterize the damage evolution and fracture behavior of materials. The primary objective of this paper was to investigate the improvement mechanism of steel slag on the low-temperature fracture behavior of permeable asphalt mixtures (PAM). Firstly, steel slag coarse aggregates were used to replace basalt coarse aggregates with equal volume at different levels (0%, 25%, 50%, 75%, and 100%). Then, the low-temperature splitting test with slow loading was used to obtain steady crack growth, and the crack initiation and propagation of specimens were monitored by AE technique in real time. From the low-temperature splitting test results, SS-100 (permeable asphalt mixtures with 100% steel slag) has the optimal low-temperature cracking resistance. Therefore, the difference of fracture behavior between the control group (permeable asphalt mixtures without steel slag) and SS-100 was mainly discussed. From the AE test results, a slight bottom-up trend of sentinel function was founded in the 0.6-0.9 displacement level for SS-100, which is different from the control group. Furthermore, the fracture stages of the control group and SS-100 could be divided based on cumulative RA and cumulative AF curves. The incorporation of 100% steel slag reduced the shear events and restrained the growth of shear cracking of the specimen in the macro-crack stage. Finally, the considerable drops of three kinds of b-values in the final phase were found in the control group, but significant repeated fluctuations in SS-100. In short, the fracture behavior of PAM under low temperature was significantly improved after adding 100% steel slag.

Investigation of Biofilms Formed on Steelmaking Slags in Marine Environments for Water Depuration.

Steelmaking slags are a promising resource as artificial seaweed beds for the reconstitution of marine environments. To grow seaweed well, the formation of biofilms is an essential process in biofouling. This study focused on the formation of initial biofilms on steelmaking slag samples and analyzed the resulting bacterial communities using the next-generation sequencing technique. Three types of steelmaking slag were submerged in an area of Ise Bay in Mie Prefecture, Japan, for 3 and 7 days in the summer and winter seasons to allow the formation of biofilms. The bacterial communities of these biofilms were richer in sulfur-oxidizing bacteria compared to the biofilms formed on polyurethane sponges. It was found that Helicobacteraceae dominantly grew on the biofilms formed on the slag samples. This shows that steelmaking slags have potential to be used as artificial seaweed beds and marine water purifiers.

Removal of zinc from submerged arc furnace flue gas wash water using steel slag with polyacrylamide.

The aim of this research was to investigate zinc removal from submerged arc furnace flue gas wash water with steel slag and polymer treatment. The current treatment for the submerged arc furnace flue gas wash water is treatment with polymer only which aids in the settling of particulate zinc. However, in this research enhanced removal of zinc by also precipitating soluble zinc using steel slag was studied. The zinc removal results were compared with the results using commercial neutralizing agents NaOH, Mg(OH)2, and Ca(OH)2 together with polymer. The precipitation conditions were simulated with MINEQL + software and the calculated results were compared with the results from laboratory jar test experiments. Zinc was removed to less than the target concentration 2 mg/l with steel slag and polymer treatment at pH 9. Additionally, turbidity of the treated water decreased to 20 NTU compared to the initial 860 NTU. However, the amount of steel slag needed in the treatment was significantly higher than the amounts of NaOH and Ca(OH)2. The main zinc removal mechanism of steel slag was precipitation as zinc oxide. Calculated zinc removal was higher than the experimental which indicates that equilibrium was not reached in the precipitation experiments which could be due to relatively short contact time chosen to simulate the actual process conditions at the plant.