Metal Removal Research Articles

Mechanistic Insights into Micelle-Enhanced Nanofiltration for Heavy Metal Removal: Transformation of Ion Transport and Fouling Phenomena.

Toxic heavy metals are widely present in typical scenarios, such as mines and electroplating wastewater, presenting significant risks to biological and environmental safety. Membrane processes encounter a challenge in effectively intercepting heavy metals due to their small hydration radius. This research showcases the high efficiency of micelle-enhanced nanofiltration (MENF) in removing heavy metals. At the critical micelle concentration, sodium dodecyl sulfate demonstrated a high removal of Cu2+, Ni2+, Zn2+, and Cd2+ while maintaining substantial potential for complexation of heavy metals. The formation of micelles and the bonding of heavy metals with surfactants bolstered the resistance of heavy metal ions to transmembrane transport. The presence of heavy metals in ionic form in wastewater facilitated their complexation with surfactants or micelles. Notably, the valence state and concentration of interfering ions in the environment could slightly influence the removal of heavy metals by MENF. Additionally, MENF displayed remarkable antifouling properties. The loose gel layer created by surfactant molecules and the micelle enhanced the membrane permeability and reduced the scaling tendency of heavy metals. This study contributes to an improved understanding of the mechanisms involved in heavy metal rejection by using MENF.

Biosorption of Cd(II), Co(II), and Cu(II) onto Microalgae under Acidic and Neutral Conditions

The biosorption of Cd, Co, and Cu onto three microalgae species (Chlorella vulgaris, Scenedesmus sp., and Spirulina platensis) was compared to determine the microalgae’s capability for heavy metal adsorption in acidic and neutral environments. The Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models were used to characterize the adsorption of the heavy metals onto microalgae. The maximum adsorption capacity (qmax) determined using the Langmuir and D-R model showed results in the order of Cu > Co > Cd in both acidic and neutral conditions. A shift from acidic to neutral conditions increased the microalgae’s adsorption affinity for heavy metals, as determined using the Freundlich parameter (KF). The adsorption affinity of the biomass for Cd and Co was in the order S. platensis > C. vulgaris > Scenedesmus sp. while that of Cu was in the order C. vulgaris > Scenedesmus sp. > S. platensis. In addition, it was found that the adsorption of Cd and Co enhanced the production of Dissolved Organic Content (DOC) as a byproduct of biosorption, whereas the adsorption of Cu appeared to suppress the generation of DOC. The mean adsorption energy (E) values computed by the D-R model were less than 8 (kJ/mol), indicating that physisorption was the primary force of sorption in both acidic and neutral settings. The findings of this study suggest that microalgae may be used as a low-cost adsorbent for metal removal from industrial effluent.

Adsorption mechanism of Cd2+ on solid waste–based PRB composite filler and pore structure dynamic evolution laws

In this study, a composite granular filler (CGF) was prepared primarily using steel slag, fly ash, and desulphurization gypsum to remedy the default of expensive, passivation, and ease of failure for the traditional permeable reactive barrier (PRB). The adsorption characteristics of the CGF on Cd2+ were investigated by the static adsorption, and the strength loss and scatter ratio were clarified with an immersion test. Dynamic adsorption and visualization modeling were used to determine the primary factors influencing adsorption and the evolution laws of material corrosion and pore clogging. Various characterization methods were used to research the adsorption mechanism. The results showed that the CGF fit with the pseudo-second-order kinetic model and Langmuir model, and the optimal adsorption capacity reached 8.64 mg/g; the minimum ratio of scatter and strength loss were 4.95% and 6.16%, respectively. The pump speed greatly influenced the breakthrough curves. The maximum dynamic adsorption capacity reached 1.81 mg/g, and the Thomas model described the adsorption behavior well. After adsorption, the porosity increased by 7.79%, and clogging in the middle of the column was not serious. The connected pores still accounted for 99.48%, and the pore network model (PNM) maintained excellent connectivity. Hydration products generated in the CGF ensured strength and durability, and they also benefited the adsorption of Cd2+ through ion exchange, co-precipitation, and surface adsorption. This research provides a new solid-waste resource utilization method for heavy metal removal in groundwater and a theoretical basis for the long-term purification of PRB with good potential for application and economic benefits.

Deep-sea microorganisms-driven V5+ and Cd2+ removal from vanadium smelting wastewater: Bacterial screening, performance and mechanism

The disorderly discharge of industrial wastewater containing heavy metals has caused serious water pollution and ecological environmental risks, ultimately threatening human life and health. Biological treatment methods have obvious advantages, but the existing microorganisms exhibit issues such as poor resistance, adaptability, colonization ability, and low activity. However, a wide variety of microorganisms in deep-sea hydrothermal vent areas are tolerant to heavy metals, possessing the potential for efficient treatment of heavy metal wastewater. Based on this, the study obtained a group of deep-sea microbial communities dominated by Burkholderia-Caballeronia-Paraburkholderia through shake flask experiments from the sediments of deep-sea hydrothermal vents, which can simultaneously achieve the synchronous removal of vanadium and cadmium heavy metals through bioreduction, biosorption, and biomineralization. Through SEM-EDS, XRD, XPS, and FT-IR analyses, it was found that V(V) was reduced to V(IV) through a reduction process and subsequently precipitated. Glucose oxidation accelerated this process. Cd(II) underwent biomineralization to form precipitates such as cadmium hydroxide and cadmium carbonate. Functional groups on the microbial cell surface, such as -CH2, C=O, N-H, -COOH, phosphate groups, amino groups, and M-O moieties, participated in the bioadsorption processes of V(V) and Cd(II) heavy metals. Under optimal conditions, namely a temperature of 40 °C, pH value of 7.5, inoculation amount of 10%, salinity of 4%, COD concentration of 600 mg/L, V5+ concentration of 300 mg/L, and Cd2+ concentration of 40 mg/L, the OD600 can reach its highest at 72 h, with the removal efficiency of V5+, Cd2+, and COD in simulated vanadium smelting wastewater reaching 86.32%, 59.13%, and 61.63%, respectively. This study provides theoretical insights and practical evidence for understanding the dynamic changes in microbial community structure under heavy metal stress, as well as the resistance mechanisms of microbial treatment of industrial heavy metal wastewater.

Mixed-matrix membrane designed with water channels and sieving effect for effective removal of heavy metals

The challenge of eliminating heavy metal ions from water has been addressed using Polysulfone (PSf) membranes, which have demonstrated significant potential in treating contaminated solutions. This research aimed to improve the permeability and separation performance of PSf membranes by incorporating Al2SiO6 into their structure. The introduction of Al2SiO6 into the membrane matrix was achieved through the nonsolvent-induced phase separation (NIPS). The resulting mixed-matrix membrane (MMM) exhibited improved efficiency in water filtration. The inclusion of Al2SiO6 led to desirable changes in membrane properties such as hydrophilicity, contact angle and porosity, thereby enhancing the performance of heavy metal ion removal capability. Under a pressure of 2 bar, the mixed matrix membranes achieved rejections exceeding 95 % for lead and 70 % for arsenic. Furthermore, the occurrence of Al2SiO6 enhanced the anti-fouling assets of the PSf membrane by increasing its hydrophilic nature and facilitating the development of a hydration layer, which tends to prevent the interactions between the membrane surface and foulant. These properties make these membranes suitable candidates for separating toxic ions from water.

Feasibility of intimately coupled CaO-catalytic-ozonation and bio-contact oxidation reactor for heavy metal and color removal and deep mineralization of refractory organics in actual coking wastewater

Considering the challenges for both single and traditional two-stage treatments, advanced oxidation and biodegradation, in the treatment of actual coking wastewater, an intimately coupled catalytic ozonation and biodegradation (ICOB) reactor was developed. In this study, ICOB treatment significantly enhanced the removal of Cu2+, Fe3+, and color by 39 %, 45 %, and 52 %, respectively, outperforming biodegradation. Catalytic ozonation effectively breaking down unsaturated organic substances and high-molecular-weight dissolved organic matter into smaller, more biodegradable molecules. Compared with biodegradation, the ICOB system significantly increased the abundances of Pseudomonas, Sphingopyxis, and Brevundimonas by ∼ 96 %, ∼67 %, and ∼ 85 %, respectively. These microorganisms, possessing genes for degrading phenol, aromatic compounds, polycyclic aromatics, and sulfur metabolism, further enhanced the mineralization of intermediates. Consequently, the ICOB system outperformed biodegradation and catalytic ozonation treatments, exhibiting chemical oxygen demand removal rate of ∼ 58 % and toxicity reduction of ∼ 47 %. Overall, the ICOB treatment showcases promise for practical engineering applications in coking wastewater treatment.

Heavy metal removal by porous asphalt in cyclical wetting and drying

Porous asphalt pavement (PAP) is subjected to wetting and drying cycles involving storms of varying intensity and inter-event drying periods to study the impact of continuous weather systems on heavy metal removal in runoff. Four physical models: a complete PAP system, a PAP surface, a geotextile fabric and a reservoir of cobblestone aggregate, were created at the lab-scale and tested with stormwater contaminated with dissolved Mn(Ⅱ), Zn(Ⅱ), Cu(Ⅱ), and Cr(Ⅵ). The models were exposed to repeated wetting and drying cycles spanning over 27 days in triplicate. Wetting involved light, moderate and heavy rainfall intensities. All pavement material designs performed well at removing Cu(Ⅱ) and Cr(Ⅵ). The PAP system had an overall better performance at removing Mn(Ⅱ), Zn(Ⅱ), Cu(Ⅱ), and Cr(Ⅵ) than any of the individual pavement materials but was unable to remove all of the heavy metals simultaneously to sufficiently high levels. The materials used in the filter layer and reservoir structure and their adsorption and desorption capacities should be assessed for potential contamination (leaching) of Zn(Ⅱ) and Mn(Ⅱ), respectively, prior to construction. Wetting and drying cycles had the greatest impacts on the reservoir structure’s performance versus any of the other layers. Leaching of Mn(II) observed from cobblestone aggregate was affected by the solution composition and pH. Removal of selected heavy metals was rapid in first flush and fluctuated with storm event intensity.

Simultaneous removal of heavy metals and electricity generation from wastewater in constructed wetland-microbial fuel cells

Constructed wetlands (CWs) are environmentally friendly and cost-effective methods for wastewater treatment. Recently, there have been innumerable efforts to integrate CWs with microbial fuel cells (MFCs) to enhance the removal of pollutants while generating electricity. Constructed Wetland-Microbial Fuel Cells (CW-MFCs) are engineered systems incorporating physical, chemical, and biological processes for wastewater treatment. However, the application of CW-MFCs to remove multiple heavy metals from wastewater is still an active area of research. The present study explores for the first time the utilization of different types of CW-MFCs, including CW-MFC-planted, CW-MFC-unplanted, and CW-sand-filter for simultaneous removal of different concentrations of organic pollutants and multiple heavy metals such as zinc (Zn), cadmium (Cd), copper (Cu), and lead (Pb) from wastewater while generating electricity. The study employed nine CW-MFC microcosms, some of which were planted with Phragmites australis. The initial concentrations of Cu, Pb, Zn, and Cd were maintained at 2, 10, and 30 mg/l, respectively, while initial COD concentrations were 120, 500, and 1000 mg/l. Remarkably, the maximum removal rates achieved were 98.83 %, 95.74 %, 92.91 %, and 90.75 % for Cu, Pb, Zn, and Cd, respectively, and the maximum removal rate of COD was 97.96 % at 10 mg/l of Cu, Pb, Zn, Cd, and 500 mg/l of COD in CW-MFC-planted. The attained highest voltage, current, and power densities reached 687 mV, 4000 mA/m3, and 785.86 mW/m3, respectively, in CW-MFC-planted. This study demonstrates the significant impact of CW-MFC-planted systems on wastewater treatment and electricity generation.

Autocatalytic degradation of Cu-EDTA in the Calcite/PMS system: Singlet oxygen and Cu(III)

The simultaneous removal of heavy metal complexes (HMCs) and heavy metal ions presents a significant challenge in treating wastewater. To address this, we propose a Calcite/Peroxymonosulfate (Calcite/PMS) system aimed at simultaneously decomplexing Cu-EDTA and removing Cu ions. Calcite/PMS system could achieve 99.5 % Cu-EDTA decomplexation and 61.9 % Cu ions removal within 60 min under initial conditions of Cu-EDTA (10 mg/L), Calcite (3 g/L), and PMS (2 mM). Singlet oxygen (1O2) emerged as the predominant reactive species responsible for Cu-EDTA decomplexation, which selectively targeted the N-C bonds in the Cu-EDTA structure to produce intermediates with lower biotoxicity than EDTA. Interestingly, solid phase Cu(III) (≡Cu(III)) promoted the generation of superoxide radicals (O2•−) with a contribution of up to 72.8 %. Subsequently, nascent ≡Cu(III) and O2•− accelerated the degradation of intermediates. Besides, coexisting organic substances inhibited Cu-EDTA decomplexation, whereas inorganic ions had a weak impact. After five cycles of use, the Calcite/PMS system retained 99.3 % efficiency in decomplexing Cu-EDTA. This investigation provides valuable insights into using calcite to remove HMCs and enhances our comprehension of the decomplexation intermediates accelerating HMCs degradation.

Use of feed additive Actigen in the production of compound feed for pregnant sows

The introduction of various innovative technologies in diff erent branches of animal husbandry involves the use of various non-traditional feed additives in animal diets, which contribute not only to the disclosure of genetic potential, but also to the removal of heavy metals from the body of animals, bees and poultry. The purpose of the research was to use the Actigen feed additive in the production of compound feed for pregnant sows. Scientifi c and economic experiment in improving the production technology of compound feed for pregnant sows was carried outunder the conditions of a compound feed plant at Agrofi rm Ariant LLC. The object of the study was compound feed, as well as pregnant sows. For the research, 2 groups of pregnant sows (control and experimental) were formed per 10 heads in each according to the principle of pairs-analogues. The sows of control group compound feed without the Actigen feed additive was given, and the sows of experimental group it was with Actigen additive. The Actigen feed additive was used at a dose of 0.5 kg per 1 ton of compound feed. The results of the experiment showed that the experimental group produced by 9 live piglets more than the control group, and the average weight of one piglet in the experimental group was0.15 kg more than in the control group. There were 4 stillborn piglets in the control group, which was 1 head or 33.3 % more than in the experimental group. The average live weight of one piglet at weaning in the experimental group was 6.00 kg, which was 0.80 kg more than in the control group. The weight of the litter at weaning in the control group was 54.08 kg, and in the experimental groupit was 69.60 kg, which was 15.52 kg more than in the control group. Thus, the Actigen feed additive at the dose of 0.5 kg per 1 ton of compound feed had a positive infl uence on the reproductive traits of sows.

Effective removal of chromium, copper, and nickel heavy metal ions from industrial electroplating wastewater by in situ oxidative adsorption using sodium hypochlorite as oxidant and sodium trititanate nanorod as adsorbent

Sodium hypochlorite and synthesized sodium trititanate nanorods (Na2Ti3O7, 186 × 1270 nm) were used as the oxidant and adsorbents for in situ oxidative adsorption treatment of actual electroplating wastewaters containing Cr(VI) (2.6‒5.2 mg∙L‒1), Cu2+ (2.7‒5.4 mg∙L‒1), and Ni2+ (0.2705‒0.541 mg∙L‒1) ions at pH of 8.8‒9.1 and 20‒60 °C. The as-synthesized sodium trititanate nanorods were characterized by XRD, HRTEM, N2 adsorption/desorption, SEM, EDX, and Zeta potential techniques. The concentrations of heavy metal ions in wastewaters were analyzed by ICP technique. After in situ oxidative adsorption treatment under the concentrations of 25 g∙L‒1 for sodium hypochlorite and 125 mg∙L‒1 for sodium trititanate nanorods at 60 °C for 5 h, the heavy metal ion concentrations could be reduced from initial value of 2.6 to final value of 1.92 mg∙L‒1 for Cr(VI), 3.6 to 0.17 mg∙L‒1 for Cu2+, and from 0.2705 to 0.097 mg∙L‒1 for Ni2+, respectively. Cr(VI), Cu2+, and Ni2+ ions could be effectively removed by the in situ oxidative adsorption method. The in situ oxidative adsorption processes of Cr(VI), Cu2+, and Ni2+ ions are satisfactorily simulated by the pseudo-second order adsorption kinetics and Langmuir adsorption isotherm, respectively. Adsorption thermodynamics analyses reveal that the oxidative adsorption processes of Cr(VI), Cu2+, and Ni2+ ions are spontaneous and endothermic. The oxidation degree of metal-contained complexes influences the values of thermodynamics functions.

Revisiting the role of algal biocathodes in microbial fuel cells for bioremediation and value-addition

Algal-microbial fuel cells (A-MFC) offers a sustainable solution for wastewater treatment and energy recovery. The performance of a typical MFC is affected by the oxidative-reductive reactions occurring in it. The cathodic reduction is facilitated by electron acceptors such as oxygen and ferricyanide. However, higher operational cost is incurred from their application. Algae owing to its phototrophic metabolism, oxygenates the cathode photosynthetically and acts as a mediator for cathodic electron transfer. Mixotrophic metabolism of algae enable their adaptation and growth in pollutant-rich toxic environments, making them suitable for wastewater treatment and remediation. A-MFCs enable the generation of algal biomass, a rich source of carbohydrates, lipids, proteins, pigments, and many more for commercial applications. Algal-based CO2 sequestration, nutrient and heavy metal removal via assimilation and carbon capture pathways make A-MFC systems a promising approach for bioenergy generation and wastewater remediation. Hence, this review offers an overview on the principles and applications of A-MFC and their relevance in developing a waste-centered-circular economy.

Multicomponent Equilibrium Isotherms and Kinetics Study of Heavy Metals Removal from Aqueous Solutions Using Electrocoagulation Combined with Mordenite Zeolite and Ultrasonication

Multicomponent Equilibrium Isotherms and Kinetics Study of Heavy Metals Removal from Aqueous Solutions Using Electrocoagulation Combined with Mordenite Zeolite and Ultrasonication

Adsorption of heavy metal ions by carbon-based adsorbent using magnetic nitrogen-doped carbon and graphene oxide

ABSTRACT The adsorption of weighty metal particles from contaminated water sources has garnered significant attention due to its critical role in environmental remediation and ensuring safe drinking water. Heavy metal ions can be removed from water using conventional adsorbents such as activated zeolites; however, these materials have low absorption and slow kinetics. To solve these issues, carbon-based adsorbents that exhibit easy synthesis, high porosity, design ability, and stability have been proposed. In this review, a carbon-based adsorbent, named M-NC, and graphene oxide were created for the particular evacuation of weighty metal particles. To increase the potential for Heavy Metals (HM) immobilization, sulfide-modified biochar was created via a process called synchronous carbon layer epitome. A hypothetical physicochemical and thermodynamic examination of the adsorption of weighty metals Zn2+, Cd2+, Ni2+, Ag2+, Pb2+ and Cu2+ on carbon-based adsorbents was done with factual material science fundaments. The biochar with large surface areas is utilized to eliminate weighty metal particles, quite possibly the most significant heavy metal pollutants, from aqueous solutions. The limit of the adsorbent for eliminating weighty metal ions was concentrated on utilizing Langmuir adsorption isotherm under ultrasound-helped conditions. The Mesoporous Silica Nanoparticles (MNCs) can be applied to the Langmuir model and pseudo-second-order kinetics. It is possible to use the Langmuir and second-order kinetic equations to accurately explain the adsorption method. Thermodynamic limitations were also envisioned because sorption is exothermic when it happens spontaneously. A homogeneous measurable physical science adsorption typically was utilized to describe and analyze the experimental heavy metal removal isotherms at 30°C and pH5 utilizing adsorbents produced by pyrolysis of biomasses (broccoli stalks). The experimental results were investigated in terms of Langmuir and pseudo-2nd-order kinetic equations, Freundlich and isotherm models. The outcome of pH, initial heavy metal ion concentration, contact time, and adsorbent dosage regarding the adsorption capacity and removal efficiency of Pb2+ and Cd2+ on the hydrogel was examined. This study contributes to the advancement of information in the ground of environmentally friendly heavy metal removal techniques, specifically focusing on the usage of biomass-based adsorbents. These findings have the potential to address the need for effective solutions in water purification and environmental cleanup efforts.

Influence of Electrolyte Concentration on Metal Removal Rate and Surface Finish Quality in Electrochemical Machining Masking

Electrochemical machining (ECM) is a specialized and precise manufacturing technique involving selective metal removal to achieve the desired shape or form. This article’s primary focus is examining the technical facets associated with the procedure. The elements mentioned encompass the system’s design and optimization, the electrolyte solution’s careful selection, and the precise control of the etching parameters. When considering the overall framework, it is essential to consider important factors such as the concentration of electrolytes, the operational voltage, and the value of the current flowing through the system. The main objective of this study is to evaluate the influence of different concentrations of sodium chloride electrolyte on the metal removal rate (MRR). This will be achieved by utilizing a direct current power supply. The present investigation used aluminum, steel, and stainless steel materials as the substrate for experimentation. These materials were selected to have identical dimensions for the anode and cathode. The main objective of this study is to evaluate the influence of varying concentrations (0.5, 1, 1.5, and 2 mole/liter) of sodium chloride electrolyte on the material removal rate and surface roughness. The findings have been disclosed, revealing the utmost removal rate for aluminum, steel, and stainless-steel materials across all levels of electrolyte concentration. The experimental information is currently presented, related to the rates of metal removal at various electrolyte concentrations of 2 moles per liter. The rates of mass loss observed in aluminum are comparatively higher when compared to those surveyed in steel and stainless steel. The roughness of a machined surface is inversely proportional to the concentration of the electrolyte.

Chelating Cellulose for Removal of Heavy Metals

Chelating Cellulose for Removal of Heavy Metals

Effects of metal ion removal from Antarctic krill oil on its qualities and stabilities of colour and oxidation

Effects of metal ion removal from Antarctic krill oil on its qualities and stabilities of colour and oxidation

Post-Synthetic Modification of Calix[4]arene Framework by Iridium-Mediated Alkyne Insertion into an Inert C-C Bond: A Novel Strategy for Unsymmetrical Macrocycles.

As a novel synthetic method for unsymmetrical macrocycles, we herein developed a post-synthetic modification of calix[4]arenes by insertion of a terminal alkyne into an inert C(methylene)-C(aryl) bond of the macrocyclic framework. In this transformation, C-iridated calix[4]arenes, readily synthesized through C-H bond activation of the parent calix[4]arene, undergoes C(methylene)-C(aryl) bond cleavage followed by insertion of an alkyne to provide a ring-expanded calix[4]arene complex. Removal of the iridium metal from the resulting complex was readily accomplished by a simple treatment with an acid. The developed sequential method affords novel unsymmetrical, monofunctionalized macrocyclic compounds via 3 steps from the parent calix[4]arene in good yield. The unique unsymmetrical structures of the alkyne-inserted macrocycles were evaluated by X-ray single crystal analyses. On the basis of theoretical calculations, we propose a reaction mechanism involving an uncommon C-C bond cleavage step through δ-carbon elimination for the ring enlargement process.

Montmorillonite-coupled microbially induced carbonate precipitation (MICP) enhanced contaminant removal and carbon capture in cyanide tailings

Microbial induced carbonate precipitation (MICP) technology is an effective method for immobilization of heavy metals in tailings. However, how to sustainably improve the removal of contaminants and the carbon capture capacity of tailings is a current concern. In this study, montmorillonite-coupled MICP (Mt-MICP) process is proposed to solidify cyanide tailings by improving mineralization properties, heavy metal and cyanide removal, and carbon capture. The results showed that Mt -MICP increased the amount of mineralized precipitation by 0.16–1.33 times; Total cyanide (T-CN) and free cyanide (F-CN) concentrations were reduced by 82.00 and 97.14 %, respectively; Cr, Zn, Cu and Pb leaching concentrations were reduced by 87.18, 42.85, 60.56 and 88.79 %, respectively. Characterizations results such as X-computed tomography (X-CT) confirmed that Mt enhanced the uniformity of the bio-cementation. Furthermore, the Mt-MICP process increased CO2 capture from tailings by 27.15∼34.55 %. Density Functional Theory (DFT) and thermogravimetry (TG) showed that Mt increased the adsorption energy of tailings for CO2 and was converted to CaCO3 by urea catalysis. This work provided new insights into the harmless treatment of CT and microbial carbon capture.

Surgical techniques for optimal lens management of posterior segment metallic intraocular foreign body removal: a case series.

We describe three different approaches for lens management in cases of metallic IOFBs involving the posterior segment. All consecutive posterior segment metallic IOFB cases from 2012 to 2023 at a single institution were included in this retrospective case series. Surgical outcomes and surgical videos are presented. A total of 25 metallic IOFB cases were included. In 9 cases, there was no significant lens involvement, therefore not requiring lens extraction at the time of IOFB removal. In 8 cases with traumatic cataract, lens extraction sparing the anterior lens capsule was performed with IOFB removal. In 8 cases, both lens extraction and lens capsule removal were required at the time of IOFB removal. We demonstrate our algorithm to capsular management in patients who present with IOFB with good visual outcomes in follow-up.