Related Experiment Video
Updated: Jul 5, 2025

Removal of Arsenic Using a Cationic Polymer Gel Impregnated with Iron Hydroxide
Published on: June 28, 2019
Recent advances in boron removal in aqueous media. An approach to the adsorption process and process optimization
Jéssica Carolaine Vieira de Azevedo1, Ana Paula Fonseca Maia de Urzedo1, Patrícia da Luz Mesquita1
1Chemical Engineering Department, Research Group On Waste Treatment and Management Processes, Federal University of Sao João Del Rei, São João Del Rei, MG, Brazil.
Abstract:
The numerous oxidation states of the element boron bring great challenges in containing its contamination in receptor bodies. This scenario increases significantly due to the widespread use of boron compounds in various industries in recent years. For this reason, the removal of this contaminant is receiving worldwide attention. Although adsorption is a promising method in boron removal, finding suitable adsorbents, that is, those with high efficiency, and feasible remains a constant challenge. Hence, this review presents the boron removal methods in comparison to costs of adsorbents, reaction mechanisms, economic viability, continuous bed application, and regeneration capacity. In addition, the approach of multivariate algorithms in the solution of multiobjective problems can enable the optimized conditions of dosage of adsorbents and coagulants, pH, and initial concentration of boron. Therefore, this review sought to comprehensively and critically demonstrate strategic issues that may guide the choice of method and adsorbent or coagulant material in future research for bench and industrial scale boron removal.
More Related Videos
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Extraction: Advanced Methods
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...

