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Special Report


       state NMR. Selectivity was over 90%.  the cost is an adverse factor. (ACS  as catalysts. Work was also done for C-7
       (ChemSusChem, 2024: DOI: 10.1002/  Omega, 2024: DOI: 10.1021/acso-  to C-12 primary alcohols. Hf(IV) and
       cssc.202400647).                  mega.3C04651).                   Ti(IV) trifl ates gave highest conversion
                                                                          with alkene yields of more than 70%, at
       Selective transformation of  Modifying of magnetic uio-            140-180°C. (Green Chem., 2024: DOI:
       5-hydroxymethylfurfural  66-nH  as a new nanosorbent               10.1039/D4GC01038H).
                                               2
       (HMF) to 3-hydroxymethyl- by thermo-alkaline-hydrolysis
       cyclopentanone (HMcP) over  technology for highly effi cient        2,3-Pentanedione (Pd) from
       ni catalysts                      enrichment of and determina-     lactic acid (LA)
                                         tion of quercetin in apple peel  N. Dhiman et al have reported the title
       M.V. Morales et al have discussed the                              conversion using ZrO  (Polymorphic)
                                                                                             2
       critical factors which affect the title  R. Chang et al have reported that mag-  as the catalyst. This catalyst exhibits
       transformation. Ni was supported on  netic UIO-66-NH -MH 0.05  has higher   high selectivity, activity and stability
                                                        2
       different carbon supports and metallic  adsorption than the title adsorbent and   for the title reaction. 95.5% selectivity
                                         has also signifi cantly higher magnetic   is reported at 325°C. (Green Chem.2024:
                                         properties. The maximum capacity was   DOI: 10.1039/D4GC02097A).
                                         65.30 mg per gm. Even after 7 cycles
                                         96.3% adsorption capacity was realised.   Selective hydrodeoxygenation
                                         (Sepn. Purfn. Technol., 2024: DOI:   of furfural (F) to 2-methylfuran
                                         10.1016/j.seppur.2024.128054, 353,   (MF)
                                         partA, Jan.2025, 128054).
                                                                          Y. Yao et al have worked on the title
       oxides with different structure and ac-  Sustainable upgrading of glyce-  process  which  involves  a  concerted
       id-base properties. Testing was done in   rol (G) into glycidol (Gd) and  combination of hydrogenation and
       a batch stirred reactor and competing   its derivatives under continu-  hydrogenolysis. Highly dispersed MoP
       reactions are discussed. It seems Ni/  ous-fl ow conditions         catalysts, supported on SiO , was used
                                                                                                 2
       ZrO catalyst gives a selectivity of 73%;                           and at full conversion of F, 96.3% selec-
          2
       Ni/HSAG-ox gives 87% selectivity.   A. Sivo et al have reported the title  tivity to MF was realised at 120°C, 1.0
       (ChemSusChem., 2024; DOI:10.1002/  process which can be easily integrated  MPa (20% MoP/SiO ) in a continuous
                                                                                           2
       cssc.202400559).                  with downstream synthetic steps to  fi xed bed reactor. (Ind. Eng. Chem. Res.,
                                                                          2023: DOI: 10.1021/acs.iecr.3C02804).
       orange mesocarp extract
       (oME) as a natural surfac-                                         upgradation of AquaSolv omni
       tant: Impact on fl uid-fl uid and                                    (AqSO) biorefi nery: access to
       fl uid-rock interactions during                                     highly ethoxylated lignins (ELs)
       chemical fl ooding                                                  in high yields through reactive
                                         produce value-added derivatives. Sus-  extraction
       A.A. Obuebite et al have referred to the  tainability of this process is discussed.
       use of surfactant fl ooding for secondary/  (Green Chem., 2024: DOI: 10.1039/  D. Rigo et al have worked on the title
       tertiary recovery of oil from depleted  D4GC01565G).               method  for  valorising lignins  (from
       fi elds. These authors have used OME as                            biomass) which involves simultaneous
       a potential green surface-active agent.  catalyst screening for dehydra-  functionalisation and extraction. Hydro-
       The extract is obtained from the orange  tion of primary alcohols from   thermally treated wood solids were
       mesocarp using alkaline water as solvent  renewable feedstocks under   refl uxed with EtOH : H O mixtures (70-
                                                                                             2
       and was characterised through FTIR.  formation of alkenes at energy-  99 v/v %) in the presence of catalytic
       Stability at 100°C and compatibility   saving mild reactions       amounts of H SO  (c=0.15 to 1.2 M).
                                                                                      2
                                                                                         4
       with divalent ions was checked. Micro-                             Ethoxylated Ls were obtained in 27-52 %
       emulsion system was characterised. An  A. Allahveroiyev et al have reported   yields; degree of substitution was up to
       additional oil is reported which shows  the conversion of 1-hexanol to 1-hexene,   40.8 ETO groups/100 Ar. (Green Chem.,
       its utility. Field testing was done, but  using Lewis acids such as metal trifl ates   2024: DOI: 10.1039/D3GC03776B).


       186                                                                    Chemical Weekly  August 13, 2024


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