Page 180 - CW E-Magazine (14-11-2023)
P. 180

Special Report


       Boosting alkaline H  evolution    the critical issue of poisoning caused  concentration of peroxocarbonate was
                           2
       reaction through water struc-     by insoluble S species formed during  64.7-mol/dm  with a current efficiency of
                                                                                     3
       ture manipulation                 the SOR. S-tolerant electrocatalysts are  19.2%. (Chem. Eng. Process – Process
                                         covered. Current challenges and future  Intensification, 2023, 191, Sep., 109468;
       Y. Jiao and Y. Zheng have referred to a   research are discussed. (Chem. Eng.  DOI: 10.1016/j.cep.2023.109468).
       recent breakthrough, which shows that   Jl., 2023, 469, 1 August, 143861; DOI:   Electrocatalysis as an efficient
       the performance can be improved by   10.1016/j.cej.2023143861).
       manipulating water structure at the elec-                          alternative to thermal catalysis
       trode-electrolyte interface using atomi-  Anodically-generated alkyl radi-  over PtRu bimetallic catalysts
       cally localised electric fields. IrRu Dizy-  cals derived from carboxylic  for hydrogenation of benzoic
       gotic Single-Atom Sites (DSAC) carries   acid as reactive intermediates  acid derivatives
                                         for addition to alkenes
                                                                          Y. Du et al have referred to the title pro-
                                         H. Ding and M. Orazov have reported   cess, which involves mild conditions for
                                         electrochemically driven C-C coupling.   ring hydrogenation. PtRu supported on
                                         Low anodic current density favours the   carbon paper was developed and this gave
                                         formation of the target product, but also   conversion of 92.9% and high selectivity
                                         leads to more solvent oxidation, which   of 100% and a high Faradaic efficiency
                                         can be suppressed by multiple methods
                                         to get high Faradaic efficiency of the
                                         targeted product with high selectivity.
                                         Thus, the reaction is CH (CH ) COOH
                                                            3
                                                                 2 n
       out the above work. Water dissociation  via Kolbe to CH (CH ) , reacting with
                                                      3
                                                          2 n
       kinetics was studied and an intricate  styrene, Ph-CH=CH , to give in methanol,
                                                        2
       examination of the interaction between  PhC(O-)[CH ) . Radical self-coupling
                                                   2 n
       water molecules and the catalyst surface  can be avoided. In the above reaction,
       was also studied. (Angew. Chem. Intl.  88% selectivity and 72% Faradaic effi-
       Ed.; DOI: 10.1002/abue.2023 07303).  ciency was realised. (ChemElectroChem   of 62.2% leading to cyclohexane carboxy-
                                         2023; DOI: 10.1002/cec.2022 01099).  lic acid in an acidic aqueous electrolyte
       Electrochemical H S splitting                                      without external H . The catalyst has
                          2
                                                                                          2
       [H S is extensively valorised via Claus   Peroxocarbonate production   outstanding stability. Theoretical calcu-
         2
       Process to make sulphur (S) and almost   by using a divided cylindrical   lations were done. (Green Chem., 2023;
       all S globally is recovered, rather than  electrochemical reactor  DOI: 10.1039/D3G 01540H).
       mined. Many attempts are being made
       to get H  + S from H S.]          O.  Gonzalez  and  J.M.  Bisang  have   Highly selective separation of
                                         reported the title reaction where a cati-
             2
                       2
                                                                             +
       K. Kim and C. Lee have referred to   onic exchange membrane is used and   Cs  from brines using an electro
                                                                          active layered composite of
       water splitting electrochemically, which   the anode was a Pt helical wire. The   vanadosilicate
       is severely impeded by the sluggish O    cathodic reaction was either O  reduction
                                                                2
                                      2
       evolution reaction (OER) occurring on   by using a rotating reticulated vitreous   Y. Bian et al have reported a green and
       the anode. By contrast, electrochemical   carbon or H  evolution at Ni or platinised   sustainable separation and recovery of
                                                  2
       sulphide oxidation reaction (SOR) has   Ti static electrodes. Best results were   Cs  from brine in a novel electrochemical
                                                                            +
                                                     3
       greater thermodynamic  and  kinetic    with 1-mol/dm  Na CO  solution in the   method. Here, layered vanadosilicate
                                                           3
                                                        2
       advantages. This combination of the   anodic compartment at a current density   composite was employed. In this method
                                                    2
                                                                                                       +
       SOR with H  evolution reaction (HER)   of 140 mA/cm  and 10°C. The maximum    the adsorption and desorption of Cs  on
                 2
       can well permit H S splitting to simulta-                          the electrode can be easily controlled
                     2
       neously generate green H  by lowering                              via the redox reactions of V. Thus, a
                           2
                                                                                                         +
       the energy input. These authors have                               good-to-excellent selectivity of Cs /K ,
                                                                                                      +
                                                                                    +/
                                                                                        2+
                                                                            +
       covered recent developments in this                                Cs /Ca , Cs Mg  can be realised with
                                                                                2+
       much desired process. Attention has                                separation factors of 11.7, 28.9 and 181.4,
       been given to strategies that can mitigate                         respectively. The coated electrode was
       180                                                                 Chemical Weekly  November 14, 2023
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