Ce and P123 modified layered double hydroxide (LDH) composite for the synthesis of polypropylene glycol monomethyl ether
The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO 2 /MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqu...
Saved in:
Published in | RSC advances Vol. 12; no. 36; pp. 23183 - 23192 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
16.08.2022
The Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO
2
/MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO
2
/MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO
2
/MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products.
The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. |
---|---|
AbstractList | The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO
/MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO
/MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO
/MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products. The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO2/MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO2/MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer–Emmett–Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO2/MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products. The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO 2 /MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO 2 /MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO 2 /MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products. The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO 2 /MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO 2 /MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer–Emmett–Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO 2 /MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products. The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO₂/MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO₂/MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer–Emmett–Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO₂/MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products. The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO2/MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO2/MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO2/MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products.The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green chemical industry. In this study, the CeO2/MgAl-LDH(P123) composite was prepared using a nucleation/crystallization isolation method and aqueous reconstruction method, and CeO2/MgAl-LDO(P123) solid base catalyst was prepared by calcination with it as precursor. Thereafter, the morphology, crystal structure, functional group, and thermal stability of the catalyst were characterized using scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller analysis, temperature-programmed desorption of carbon dioxide, thermogravimetry, and X-ray photoelectron spectroscopy. The results showed that the catalyst had a larger specific surface area, pore size and pore volume and more basic sites, providing sufficient catalytic activity for the polymerization process. The experimental results for the fabrication of MPPG using CeO2/MgAl-LDO(P123) as catalyst and methanol and propylene oxide as reaction raw materials showed that the conversion of propylene oxide reached 92.04% and the molecular weight of MPPG was 405 under the optimal reaction conditions. Moreover, the conversion of propylene oxide was maintained above 83.69% after the catalyst was reused six times. This study offers a new prospect for the green synthesis of MPPG products. |
Author | Cao, Xiaoyan Xu, Xiao Gu, Zhenggui Kong, Lingxin |
AuthorAffiliation | School of Chemistry and Materials Science Nanjing Normal Univesity Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control |
AuthorAffiliation_xml | – name: School of Chemistry and Materials Science – name: Nanjing Normal Univesity – name: Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control |
Author_xml | – sequence: 1 givenname: Xiaoyan surname: Cao fullname: Cao, Xiaoyan – sequence: 2 givenname: Lingxin surname: Kong fullname: Kong, Lingxin – sequence: 3 givenname: Zhenggui surname: Gu fullname: Gu, Zhenggui – sequence: 4 givenname: Xiao surname: Xu fullname: Xu, Xiao |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36090400$$D View this record in MEDLINE/PubMed |
BookMark | eNqNks9rFTEQx4NUbK29eFcCXqrwND_2Vy5Cea1WeKCInkM2mfSlZJM12ZXuf2_qa2stHswhM5DPfPlmZp6ivRADIPSckreUcPHOsKQIb2kDj9ABI1WzYqQRe_fyfXSU8yUpp6kpa-gTtM8bIkhFyAG6WgNWweAvlHE8ROOsA4O9WiCVaOLce8DbxaR45Qzg483p-Wus4zDG7CbANiY8bQHnJZSQXcbR4jH6ZUxxXDwEwBd-0dEX7RAHmLaLx-WG9Aw9tspnOLqJh-j7h7Nv6_PV5vPHT-uTzUpzQaeVNdYYDcQ2qvhvLe96K4ygtOJtr5XgtifADVeU00orbkVlqOlrqFnHOq75IXq_0x3nfoAiFaakvByTG1RaZFRO_v0S3FZexJ9S8I7UFS0CxzcCKf6YIU9ycFmD9ypAnLNkLe1K_0Vb_Q9akYYwzgr66gF6GecUSicKReoyoJp3hXp53_yd69v5FYDsAJ1izgms1G5Sk4vXf3FeUiKvt0Sesq8nv7fkrJS8eVByq_pP-MUOTlnfcX9Wjv8CoPDHMg |
CitedBy_id | crossref_primary_10_1039_D4NR00111G crossref_primary_10_1016_j_hazl_2024_100103 crossref_primary_10_1002_advs_202307094 crossref_primary_10_1016_j_heliyon_2025_e42072 crossref_primary_10_1016_j_jclepro_2023_140191 crossref_primary_10_1038_s41598_024_75724_3 crossref_primary_10_1016_j_surfcoat_2024_130943 crossref_primary_10_1021_acsaem_4c01984 |
Cites_doi | 10.1016/j.apcata.2007.06.031 10.1016/j.catcom.2011.01.027 10.1039/c1nr10628g 10.1007/s10562-020-03099-x 10.1007/s11144-020-01869-7 10.1016/j.clay.2006.06.010 10.1039/C5DT01479D 10.1016/j.jssc.2018.10.018 10.1016/j.jssc.2010.08.027 10.1016/j.jpcs.2009.12.018 10.1039/D1RA00227A 10.1016/S1381-1169(96)00371-8 10.1039/C7CS00318H 10.1002/sia.740180905 10.1039/C7DT03861E 10.1016/j.apcata.2019.117215 10.1081/CR-120001809 10.1039/C5CS00090D 10.1016/j.molcata.2004.12.025 10.1039/C6TA01668E 10.1016/j.ijhydene.2016.08.062 10.5650/jos.ess18177 10.1016/S1872-2067(14)60171-6 10.1039/C9CY01323G 10.1080/01614949608006464 10.1021/cr200434v 10.1007/s10934-019-00825-8 10.1016/j.jcat.2017.08.008 10.1016/j.jssc.2018.09.023 10.1016/0920-5861(91)80068-K 10.1039/C4CS00160E 10.1021/ie901114d 10.1002/pola.1991.080290502 10.1016/j.jcat.2019.02.028 10.1016/j.micromeso.2004.09.011 10.1016/j.cej.2019.03.048 |
ContentType | Journal Article |
Copyright | This journal is © The Royal Society of Chemistry. Copyright Royal Society of Chemistry 2022 This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry |
Copyright_xml | – notice: This journal is © The Royal Society of Chemistry. – notice: Copyright Royal Society of Chemistry 2022 – notice: This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry |
DBID | AAYXX CITATION NPM 7SR 8BQ 8FD JG9 7X8 7S9 L.6 5PM |
DOI | 10.1039/d2ra03716e |
DatabaseName | CrossRef PubMed Engineered Materials Abstracts METADEX Technology Research Database Materials Research Database MEDLINE - Academic AGRICOLA AGRICOLA - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef PubMed Materials Research Database Engineered Materials Abstracts Technology Research Database METADEX MEDLINE - Academic AGRICOLA AGRICOLA - Academic |
DatabaseTitleList | PubMed Materials Research Database CrossRef AGRICOLA MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 2046-2069 |
EndPage | 23192 |
ExternalDocumentID | PMC9380541 36090400 10_1039_D2RA03716E d2ra03716e |
Genre | Journal Article |
GrantInformation_xml | – fundername: ; grantid: J418013-3 – fundername: ; grantid: 21973045 |
GroupedDBID | 0-7 0R AAGNR AAIWI ABGFH ACGFS ADBBV ADMRA AENEX AFVBQ AGRSR AGSTE AGSWI ALMA_UNASSIGNED_HOLDINGS ANUXI ASKNT AUDPV BCNDV BLAPV BSQNT C6K EBS EE0 EF- GROUPED_DOAJ H13 HZ H~N J3I JG O9- OK1 R7C R7G RCNCU RPM RPMJG RRC RSCEA RVUXY SLH SMJ ZCN 0R~ 53G AAFWJ AAHBH AAJAE AARTK AAWGC AAXHV AAYXX ABEMK ABIQK ABPDG ABXOH AEFDR AESAV AFLYV AFPKN AGEGJ AHGCF AKBGW APEMP CITATION HZ~ M~E PGMZT NPM 7SR 8BQ 8FD JG9 7X8 7S9 L.6 5PM |
ID | FETCH-LOGICAL-c391t-fdfddce0f6a0067f38bf9d911437bca93fb0e3d3a1314ca3f94d1db5e528283c3 |
ISSN | 2046-2069 |
IngestDate | Thu Aug 21 14:07:16 EDT 2025 Thu Jul 10 22:43:50 EDT 2025 Fri Jul 11 07:41:16 EDT 2025 Mon Jun 30 06:53:39 EDT 2025 Mon Jul 21 06:04:31 EDT 2025 Tue Jul 01 04:20:18 EDT 2025 Thu Apr 24 23:05:55 EDT 2025 Wed Aug 24 10:45:25 EDT 2022 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 36 |
Language | English |
License | This journal is © The Royal Society of Chemistry. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c391t-fdfddce0f6a0067f38bf9d911437bca93fb0e3d3a1314ca3f94d1db5e528283c3 |
Notes | Electronic supplementary information (ESI) available. See https://doi.org/10.1039/d2ra03716e ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0003-4625-2281 0000-0003-1519-4904 |
OpenAccessLink | http://dx.doi.org/10.1039/d2ra03716e |
PMID | 36090400 |
PQID | 2705360538 |
PQPubID | 2047525 |
PageCount | 1 |
ParticipantIDs | proquest_miscellaneous_2714060232 pubmed_primary_36090400 pubmedcentral_primary_oai_pubmedcentral_nih_gov_9380541 crossref_citationtrail_10_1039_D2RA03716E crossref_primary_10_1039_D2RA03716E rsc_primary_d2ra03716e proquest_miscellaneous_2718371974 proquest_journals_2705360538 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2022-08-16 |
PublicationDateYYYYMMDD | 2022-08-16 |
PublicationDate_xml | – month: 08 year: 2022 text: 2022-08-16 day: 16 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: Cambridge |
PublicationTitle | RSC advances |
PublicationTitleAlternate | RSC Adv |
PublicationYear | 2022 |
Publisher | Royal Society of Chemistry The Royal Society of Chemistry |
Publisher_xml | – name: Royal Society of Chemistry – name: The Royal Society of Chemistry |
References | Manríquez (D2RA03716E/cit25/1) 2020; 131 Kwok (D2RA03716E/cit30/1) 2018; 47 Kuśtrowski (D2RA03716E/cit13/1) 2005; 78 Liu (D2RA03716E/cit35/1) 2019; 369 Wang (D2RA03716E/cit41/1) 2021; 11 Jiang (D2RA03716E/cit20/1) 2019; 9 Nayak (D2RA03716E/cit21/1) 2016; 41 Ingo (D2RA03716E/cit37/1) 2010; 18 Hu (D2RA03716E/cit38/1) 2011; 12 Tran (D2RA03716E/cit40/1) 2019; 372 Gu (D2RA03716E/cit1/1) 2009 Dan (D2RA03716E/cit31/1) 2018; 23 Nguyen (D2RA03716E/cit32/1) 2017; 23 Sels (D2RA03716E/cit9/1) 2001; 43 Pinthong (D2RA03716E/cit14/1) 2019; 68 Al-Aani (D2RA03716E/cit23/1) 2019; 586 Tan (D2RA03716E/cit16/1) 2014; 35 Wang (D2RA03716E/cit17/1) 2010; 183 Zhang (D2RA03716E/cit36/1) 2005; 231 Meis (D2RA03716E/cit29/1) 2010; 49 Martin (D2RA03716E/cit18/1) 1997; 118 Del Hoyo Martínez (D2RA03716E/cit12/1) 2007; 36 Sun (D2RA03716E/cit15/1) 2015; 44 Hong (D2RA03716E/cit28/1) 2011; 3 Feng (D2RA03716E/cit10/1) 2015; 46 Cabrera-Munguia (D2RA03716E/cit22/1) 2020; 150 Bukhtiyarova (D2RA03716E/cit7/1) 2019; 269 Faour (D2RA03716E/cit24/1) 2010; 71 Cavani (D2RA03716E/cit8/1) 1991; 11 Biedron (D2RA03716E/cit39/1) 1991; 29 Mohapatra (D2RA03716E/cit11/1) 2016; 4 Fan (D2RA03716E/cit4/1) 2014; 43 Trovarelli (D2RA03716E/cit19/1) 1996; 38 Wu (D2RA03716E/cit34/1) 2007; 329 Jing (D2RA03716E/cit42/1) Bing (D2RA03716E/cit2/1) 2019; 269 Wang (D2RA03716E/cit3/1) 2012; 112 Cosano (D2RA03716E/cit26/1) 2020; 27 Duan (D2RA03716E/cit6/1) 2006 Yu (D2RA03716E/cit5/1) 2017; 46 Marquez (D2RA03716E/cit33/1) 2017; 354 Wang (D2RA03716E/cit27/1) 2015; 44 |
References_xml | – doi: Jing Rong Dong Sun – issn: 2009 end-page: 2 doi: Gu Sheng Huang Chen – volume: 329 start-page: 106 year: 2007 ident: D2RA03716E/cit34/1 publication-title: Appl. Catal., A doi: 10.1016/j.apcata.2007.06.031 – volume: 12 start-page: 794 year: 2011 ident: D2RA03716E/cit38/1 publication-title: Catal. Commun. doi: 10.1016/j.catcom.2011.01.027 – volume: 3 start-page: 4655 year: 2011 ident: D2RA03716E/cit28/1 publication-title: Nanoscale doi: 10.1039/c1nr10628g – volume: 150 start-page: 1957 year: 2020 ident: D2RA03716E/cit22/1 publication-title: Catal. Lett. doi: 10.1007/s10562-020-03099-x – volume: 131 start-page: 1 year: 2020 ident: D2RA03716E/cit25/1 publication-title: React. Kinet., Mech. Catal. doi: 10.1007/s11144-020-01869-7 – volume: 46 start-page: 5291 year: 2015 ident: D2RA03716E/cit10/1 publication-title: ChemInform – volume: 36 start-page: 103 year: 2007 ident: D2RA03716E/cit12/1 publication-title: Appl. Clay Sci. doi: 10.1016/j.clay.2006.06.010 – volume: 44 start-page: 11223 year: 2015 ident: D2RA03716E/cit27/1 publication-title: Dalton Trans. doi: 10.1039/C5DT01479D – start-page: 193 year: 2006 ident: D2RA03716E/cit6/1 publication-title: Struct. Bonding – volume: 269 start-page: 494 year: 2019 ident: D2RA03716E/cit7/1 publication-title: J. Solid State Chem. doi: 10.1016/j.jssc.2018.10.018 – volume: 183 start-page: 2511 year: 2010 ident: D2RA03716E/cit17/1 publication-title: J. Solid State Chem. doi: 10.1016/j.jssc.2010.08.027 – volume: 71 start-page: 487 year: 2010 ident: D2RA03716E/cit24/1 publication-title: J. Phys. Chem. Solids doi: 10.1016/j.jpcs.2009.12.018 – volume: 11 start-page: 8375 year: 2021 ident: D2RA03716E/cit41/1 publication-title: RSC Adv. doi: 10.1039/D1RA00227A – volume: 118 start-page: 113 year: 1997 ident: D2RA03716E/cit18/1 publication-title: J. Mol. Catal. A: Chem. doi: 10.1016/S1381-1169(96)00371-8 – start-page: 2 year: 2009 ident: D2RA03716E/cit1/1 – volume: 46 start-page: 5950 year: 2017 ident: D2RA03716E/cit5/1 publication-title: Chem. Soc. Rev. doi: 10.1039/C7CS00318H – volume: 18 start-page: 661 year: 2010 ident: D2RA03716E/cit37/1 publication-title: Surf. Interface Anal. doi: 10.1002/sia.740180905 – volume: 47 start-page: 143 year: 2018 ident: D2RA03716E/cit30/1 publication-title: Dalton Trans. doi: 10.1039/C7DT03861E – volume: 23 start-page: 137 year: 2018 ident: D2RA03716E/cit31/1 publication-title: Chem.-Didact.-Ecol.-Metrol. – volume: 586 start-page: 117215 year: 2019 ident: D2RA03716E/cit23/1 publication-title: Appl. Catal., A doi: 10.1016/j.apcata.2019.117215 – volume: 43 start-page: 443 year: 2001 ident: D2RA03716E/cit9/1 publication-title: Catal. Rev. doi: 10.1081/CR-120001809 – volume: 44 start-page: 5092 year: 2015 ident: D2RA03716E/cit15/1 publication-title: Chem. Soc. Rev. doi: 10.1039/C5CS00090D – volume: 231 start-page: 83 year: 2005 ident: D2RA03716E/cit36/1 publication-title: J. Mol. Catal. A: Chem. doi: 10.1016/j.molcata.2004.12.025 – volume: 4 start-page: 10744 year: 2016 ident: D2RA03716E/cit11/1 publication-title: J. Mater. Chem. A doi: 10.1039/C6TA01668E – volume: 41 start-page: 21166 year: 2016 ident: D2RA03716E/cit21/1 publication-title: Int. J. Hydrogen Energy doi: 10.1016/j.ijhydene.2016.08.062 – volume: 68 start-page: 95 year: 2019 ident: D2RA03716E/cit14/1 publication-title: J. Oleo Sci. doi: 10.5650/jos.ess18177 – volume: 35 start-page: 1955 year: 2014 ident: D2RA03716E/cit16/1 publication-title: Chin. J. Catal. doi: 10.1016/S1872-2067(14)60171-6 – volume: 9 start-page: 6335 year: 2019 ident: D2RA03716E/cit20/1 publication-title: Catal. Sci. Technol. doi: 10.1039/C9CY01323G – volume: 38 start-page: 439 year: 1996 ident: D2RA03716E/cit19/1 publication-title: Catal. Rev. doi: 10.1080/01614949608006464 – volume: 112 start-page: 4124 year: 2012 ident: D2RA03716E/cit3/1 publication-title: Chem. Rev. doi: 10.1021/cr200434v – volume: 27 start-page: 441 year: 2020 ident: D2RA03716E/cit26/1 publication-title: J. Porous Mater. doi: 10.1007/s10934-019-00825-8 – volume: 354 start-page: 92 year: 2017 ident: D2RA03716E/cit33/1 publication-title: J. Catal. doi: 10.1016/j.jcat.2017.08.008 – volume: 269 start-page: 184 year: 2019 ident: D2RA03716E/cit2/1 publication-title: J. Solid State Chem. doi: 10.1016/j.jssc.2018.09.023 – volume: 11 start-page: 173 year: 1991 ident: D2RA03716E/cit8/1 publication-title: Catal. Today doi: 10.1016/0920-5861(91)80068-K – volume: 23 start-page: 1 year: 2017 ident: D2RA03716E/cit32/1 publication-title: J. Porous Mater. – ident: D2RA03716E/cit42/1 – volume: 43 start-page: 7040 year: 2014 ident: D2RA03716E/cit4/1 publication-title: Chem. Soc. Rev. doi: 10.1039/C4CS00160E – volume: 49 start-page: 1229 year: 2010 ident: D2RA03716E/cit29/1 publication-title: Ind. Eng. Chem. Res. doi: 10.1021/ie901114d – volume: 29 start-page: 619 year: 1991 ident: D2RA03716E/cit39/1 publication-title: J. Polym. Sci., Part A: Polym. Chem. doi: 10.1002/pola.1991.080290502 – volume: 372 start-page: 86 year: 2019 ident: D2RA03716E/cit40/1 publication-title: J. Catal. doi: 10.1016/j.jcat.2019.02.028 – volume: 78 start-page: 11 year: 2005 ident: D2RA03716E/cit13/1 publication-title: Microporous Mesoporous Mater. doi: 10.1016/j.micromeso.2004.09.011 – volume: 369 start-page: 205 year: 2019 ident: D2RA03716E/cit35/1 publication-title: Chem. Eng. J. doi: 10.1016/j.cej.2019.03.048 |
SSID | ssj0000651261 |
Score | 2.3993018 |
Snippet | The application of recyclable heterogeneous catalysts in the production of polypropylene glycol monomethyl ether (MPPG) is of great significance to the green... |
SourceID | pubmedcentral proquest pubmed crossref rsc |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 23183 |
SubjectTerms | Carbon dioxide Catalysts Catalytic activity Cerium oxides Chemical industry Chemistry Conversion Crystal structure Crystallization desorption electron microscopy Fourier transform infrared spectroscopy Fourier transforms Functional groups Hydroxides Infrared analysis Infrared spectroscopy isolation techniques methanol molecular weight Nucleation Photoelectrons polymerization Polypropylene glycol polypropylenes Pore size porosity Propylene oxide Raw materials Spectrum analysis surface area Thermal stability Thermogravimetry X ray photoelectron spectroscopy X-ray diffraction |
Title | Ce and P123 modified layered double hydroxide (LDH) composite for the synthesis of polypropylene glycol monomethyl ether |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36090400 https://www.proquest.com/docview/2705360538 https://www.proquest.com/docview/2714060232 https://www.proquest.com/docview/2718371974 https://pubmed.ncbi.nlm.nih.gov/PMC9380541 |
Volume | 12 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db5swELfW9mF7mbqPbmxd5Wl7WBXRBkwIfqxoumiLOilLJvaEANsJUgRRGqTQv35nAyZRo6nbC4mOk-NwP9-HOd8h9JnSnmcLl5gi7iUmKDzL9BLBTe7F3OWwnpwqQfbWHU6db0EvaNNt1emSdXyR3O89V_I_UgUayFWekv0HyepBgQDfQb5wBQnD9VEy9utkf7ALsqVNKqQ_uYhK2X-zw_JCnoqal2yVb1KmfMnR9VBuA8g8cpmsxXWS4V2ZwUddnGSZL-RBqGUJFol3ZosSwALjZ7lsN10uOuqM8LZXO_7pN8kE2kX3I7UJG6RRXrYI_F5nAEMIPNukmvy1UC9J5jybzYq0oQZFM8L23gSEtbJWrNuqMBuib5BY1Yzlgu-hNTrY3sIa2dGoUuns1fVdIkulMnsVybKDLm8tWvMW__ZHeDMdjcLJIJgcoCMbIglQhUfjX9Pgt96IAx_MslVdXT2zpowtoZft8LuOy4No5GFS7cGq6SGjfJXJMXpeBxn4qkLMC_SEZy_RU7_p7fcKbXyOATlYIgc3yME1cnCFHKyRg78Abs6xRg0G1GDAANaowbnAO6jBFWpwixqsUPMaTW8GE39o1j04zIRQa20KJhj8pa5wI-nYCOLFgjKwkA7px0lEiYi7nDASWcRykogI6jCLxT3ek7E8ScgJOszyjL9F2BaMQ7BNqJtwByKJyGNdGzgF0CmNmIHOmwccJnWBetknZRGqRAlCw2t7fKWEMTDQJ827rMqy7OU6beQU1sv2LrT7YHcgiCeegT7q2_D85ZuyKON5IXkscHTBnbX_yuPBr0A8bqA3lej1VGB8Kq2jgfo7oNAMsqj77p0snavi7pR4EEVZBjoB-Gj-FobvHjHp9-hZuxpP0eF6VfAP4Duv4zO153RWr4E_jnLKkA |
linkProvider | Royal Society of Chemistry |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Ce+and+P123+modified+layered+double+hydroxide+%28LDH%29+composite+for+the+synthesis+of+polypropylene+glycol+monomethyl+ether&rft.jtitle=RSC+advances&rft.au=Cao%2C+Xiaoyan&rft.au=Kong%2C+Lingxin&rft.au=Gu%2C+Zhenggui&rft.au=Xu%2C+Xiao&rft.date=2022-08-16&rft.issn=2046-2069&rft.eissn=2046-2069&rft.volume=12&rft.issue=36&rft.spage=23183&rft_id=info:doi/10.1039%2Fd2ra03716e&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2046-2069&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2046-2069&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2046-2069&client=summon |