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Special Report                                                                   Special Report


 Mn-pincer catalyst which retains the  mole  %) to give diethyl  terephthalate  conversion of alcohols into alde-  ZHSM-5 as the second oligomerisation
 high reactivity  and is recyclable  (5  and ethylene glycol exclusively at 98-  hydes or ketones. This method stands   catalyst by varying SiO /Al O  ratio.
                                3
                           2
                              2
 consecutive recycling was done). Turn-  99% at 160-180°C. FeCl  proved to be  out  for its  high  yields  and  that  too  at   Selectivity towards  C  hydrocarbons
                         9+
 3
 over number was  more than 230,000.  a better catalyst. Thus, textile waste can  room temperature, and broad sub-  was  assessed.  HZSM  –  5  gives  more
 (Angew. Chem. Intl.  Ed., 2025; DOI:  be valorised, and cotton waste is also  strates can be used. (Synthetic Com-  C  products with SiO /Al O  ratio of
                         2
        9+
                               3
                            2
 10.1002/anie.202423074).  recovered; cloth waste can be treated.  munications, 2025, 55, Issue 6;  DOI:   180.  Tandem catalysts are favoured.
 (Ind. Chem. Materials, 2025; DOI:  10.1080/00397911.2025.2461114).  (Ind. Eng. Chem. Res. 2025;  DOI:
 Chemical bonds containing   10.1039/D4.IM00081A).  10.1021/acs.iecr.4c 04755).
 hydrogen: Choices for   Co-conversion of toluene and
 hydrogen carriers and   Carbon shell-encapsulated   methanol  Hydrogen and carbon   Upcycling of polyethylene   (TS-1)  catalyst and abundant active
 catalysts  La-Ni composite catalyst   nanofi bre coproduction by   terephthalate (PET) to high-  Ti-VI species and hydration. The catalyst is
 for hydrogenolysis of   Y-Wu  et al have reported this title   CH  decomposition over Ni /   value aromatics via catalytic   bifunctional and has acidic sites. 99.8%
          4
 J. Cashel  et al have referred to com-  tetrahydrofurfuryl alcohol   co-conversion to  para-xylene (PX)   diatomite catalysts  pyrolysis over zeolites  selectivity of EG is reported (This TS-1
 pounds containing B-H, C-H, N-H, or  (THFA) to 1,5-pentanediol   and high olefi ns. Modifi ed ZSM-5 with   [This column has covered some papers   is a modifi ed version of the conventional
 O-H bonds with high H  content which  (PD)  precisely controlled deposition of silica   on the subject as  it gives H   without   L. Li  et al have studied the aromatic  TS-1) (Angew. Chem. Intl. Ed. 2025;
                               2
 2
 have been studied. Their performance   [This column has covered some papers   was used and the procedure is reported.   CO ;  there  is  a  modifi cation  to  pass   product distribution from thermal  and  DOI: 10.1002/anie.202502003).
         2
 is largely determined  by the nature   where the wonders of catalysis can be   The total selectivity of high olefi ns and   CO  on this carbon to make CO.]  catalytic  fast pyrolysis using Py-GC-
         2
 of these bonds, decomposition path-  witnessed as with the change of cata-  PX was 94% and PX in xylene isomer   D. Li et al have worked on reducing the   MS/FID.  Thermal pyrolysis at 550-  A platinum catalyst with
 ways, etc. CH OH, cyclohexane, and   lysts and operating conditions THFA   was at 99.5%; toluene conversion   cost of catalysts and new applications   800°C revealed that acetophenone  enhanced three-way catalytic
 3
 NH   off er  valuable  properties.  How-  can go to 1,2-; 1,4- and 1,5-PD.]  was maintained  at  43%. (ACS Cata-  of carbon. Natural diatomite has been   increases sharply with rising tempera-  activity supported on CeO
                                                                                                     2
 3
 ever,  there are many limitations  such   lysis, 2025, 15, No.5, 4147-4159; DOI:   used as a support for Ni catalysts. Ni   ture and becomes the dominant pro-  modifi ed with Al O  for
                                                                                           2
                                                                                              3
 as  high temperature for dehydrogena-  W. Liu et al have used the title catalyst   10.1021/acscatal.4c07812).  Phyllosilicates were synthesised on the   duct at 800°C. Catalytic pyrolysis with   natural gas vehicles
 tion,  slow  kinetics,  etc.  Modifi cations  for the transformation of THFA to PD.   surface of diatomite. At 500°C the CH    HZSM-5, H-Beta, and HY was studied.
 of catalysts are under study and recent  The method of preparing the catalyst is   Selective C2+ alcohol synthesis   conversion  was 30%. It  is  suggested   H-Beta yielded the highest benzene and  X. Wang et al have referred to Pt sup-
                                      4
 progress is covered. Innovations  are  reported. At 180°C and 3MPa a selec-  from syngas boosted by MnOx   that this can be added to natural rub-  naphthalene.  HY  signifi cantly  promo-  ported on CeO  as a potential three-way
                                                                                      2
 required for large scale adoption. (Angew.  tivity of 95% is reported. The catalyst  doped CoFe bimetallic alloy   ber as a fi ller and enhance its heat dis-  ted the  production  of acetophenone,  catalyst  (TWC) used for treatment  of
 Chem. Intl. Ed., 2025; DOI:  10.1002/  was  reused  fi ve  times.  (ACS Sustain- carbide catalysts  sipation properties. (ACS Sustainable   and mechanism is given. (ACS Sustain-  natural gas exhaust vehicle and this can
 anie.202423661).  able Chem. Eng., 2025; DOI: 10.1021/  [This column has covered many papers   Chem. Eng., 2025, DOI: 10.1021/acs-  able Chem. Eng., 2025; DOI: 10.1021/  have sintering of CeO  under harsh con-
                                                                                            2
 acssuschemeng.4c10905).  on Fischer-Tropsch Process, operated   suschemeng.4c09321).  acssuschemeng.5c00489).  ditions (say >600°C). To overcome this
 Depolymerisation of PET with   in petrochemical mode, to give olefi ns,   problem these authors have developed
 ethanol by homogeneous iron   Room-temperature aerobic   alcohols, etc.]  Selective hydrogenation   Green and effi  cient   a series of Pt/Al O -CeO  for modify-
                                                                                        2
                                                                                               2
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 catalyst for chemical recycling  oxidation of alcohols into   of dimethyl terephthalate   hydrogenation of   ing support for stability; 20 wt% Al O
                                                                                                         3
                                                                                                       2
 of cloth waste  carbonyl compounds using   Z. Li  et al have reported a series of   (DMT) to dimethyl   2-ethylhexenal to   improved the sintering resistance. This
 VO@GO catalyst  Mn-promoted catalysts  with regulated   1,4-cyclohexanedicarboxylate   2-ethylhexanol  catalyst gave good performance. (Ind.
 N.W.B. Awang et al have reported acid-,   proximity  between Mn and CoFe O .   (DMCHDC)  Eng. Chem. Res., 2025; DOI: 10.1021/
 2
 4
 base-free depolymerisation  of PET  S. Raju  et al have reported the title   A space-time  yield of higher alcohols   B. Cheng et al have used Ni/TiO  cata-  acs.iecr.4c04269).
                                                                   2
 –1
 with ethanol by FeCl , FeBr  (1.0-5.0  one-pot synthesis for the specific   of 137 mmol·g (Co+Fe) –1 ·h , with sta-  DMCHDC  is widely used in the syn-  lyst in isopropanol and have studied
 bility over 300 hours is reported. The
 3
 3
                                         the kinetics of the title reaction. Among  Stable Co-zeolite propane
 fraction of C2+ alcohols in total alco-  thesis of polyester resins, polyamides,   diff erent solvents, isopropanol gave the   dehydrogenation catalysts
       and plasticisers.
 hols is 94 wt%. (ACS Catal., 2025, 15,   highest performance. Conversion was   [Propane dehydrogenation is now
 No.5, 4069-4080; DOI; 10.1021/acs-  H. Han  et al have carried out the title   100% and the  selectivity  was 96.9%.   practiced  on a  grand scale  reaching
 catal.4c.7408).  hydrogenation using ZSM-5-25/50/100,   Catalyst  was  reused  fi ve  times.  (Ind.   750,000 tpa and even in India GAIL’s
       ZSM-35,  MOR,  and  β-supported  Ru   Eng. Chem. Res., 2025; DOI: 10.1021/  plant in Usar, Maharashtra, under exe-
 Tandem oligomerisation of   catalysts.  MoR-supported Ru gave   acs.iecr.4c03948).  cution is 500,000 tpa and the planned
 ethylene for production of jet   good performance, and the selectivity   unit of Petronet LNG  is 750,000 tpa.
 fuel over FER and MRI zeolites  was 95% and conversion 100%.  The   Ethylene to ethylene glycol   Here Pt based catalysts are used.]
       catalysts were fully characterised and   (EG) in one step
 F. Li et al have investigated three zeo-  Ru/MoR had higher Ru dispersion   Q. Liu et al have referred to Co-based
 lites  –  HFER,  HZSM-5,  and  HBeta  –   and stronger metal-support interac-  H. Tan  et al have reported  the title  catalysis as  promising substitutes for
 with diff erent pore technologies in the   tion. (Can. J. Chem. Eng., 2025; DOI:   one-step  synthesis using aq.H O  for  Pt- and Cr-based catalysts.  These
                                                                    2
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 fi rst oligomerisation step and assessed   10.1002/cjce.25625).  epoxidation with  Titanium silicalite-1  authors have adopted reaction-driven
 156  Chemical Weekly  May 27, 2025  Chemical Weekly  May 27, 2025                                     157
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