Comparison of precious metal oxide/titanium monolith catalysts in wet oxidation of wastewaters
[Display omitted] ► Ru/Ir oxide/Ti monolith catalysts showed remarkable catalytic activity in WO. ► Good catalytic activity is tied to the uniform distribution of the two oxides. ► Beneficial was the fragmented structure of Ru and Ir oxides. ► Commercial mesh was most stable among the condition of w...
Saved in:
Published in | Applied catalysis. B, Environmental Vol. 127; pp. 99 - 104 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier B.V
30.10.2012
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | [Display omitted]
► Ru/Ir oxide/Ti monolith catalysts showed remarkable catalytic activity in WO. ► Good catalytic activity is tied to the uniform distribution of the two oxides. ► Beneficial was the fragmented structure of Ru and Ir oxides. ► Commercial mesh was most stable among the condition of wastewater wet oxidation. ► Loss of precious metal content was observed during longer usage.
CWO (catalytic wet oxidation) of a process wastewater and phenolate solution was carried out at 230°C, 200°C and total pressure of 50bar, with oxygen, in a stainless steel autoclave. Monolith Ti mesh supported precious metal oxide catalysts were characterized with XPS, ICP-MS, SEM and their activity compared in oxidation of model and real wastewaters.
The Ru/Ir oxide coated Ti monolith catalysts showed remarkable catalytic activity in wet oxidation both in the overall oxidation expressed by COD (chemical oxygen demand) decrease and in the carbon mineralization expressed by TOC (total organic carbon) decrease. This was valid for the real pharmaceutical wastewater as well as for a phenolate solution too. Meshes containing Ru, Pd and Ir oxide alone were less active than Ru/Ir together on Ti. This observation is in accordance with the electrochemical properties of the same mesh used in hypochlorite production.
The commercial mesh was most stable under the conditions of wet oxidation, however the loss of its precious metal content was observed during longer usage. The Ru/Ir monolith catalysts prepared in our laboratories had similar initial activity but they were less stable, the leaching and/or abrasion of the surface precious metal oxide layer was faster, independently of that their had fragmented or continuous structure, resulting from the preparation methods.
The loss of activity during longer usage can be the result of deposition of iron and silicon oxides too, as showed by SEM (scanning electron microscopy) analysis.
An important feature of the good catalytic activity of the Ru/Ir oxide coated Ti mesh can be the uniform distribution of the two oxides showed by LA–ICPMS (laser ablation–inductive coupled plasma mass spectrometry). According to XPS (X-ray photoelectron spectroscopy) results, the upper surface layer of the catalysts is covered by a mixture of Ru–Ir–Ti oxide of approximately 0.1:0.02:1 atomic ratio for commercial catalyst, and an 0.5:0.7:1.0 atomic ratio for catalysts prepared in our laboratories. We suppose that such mixture of oxides with uniform distribution are the carrier of the good catalytic activity. |
---|---|
AbstractList | CWO (catalytic wet oxidation) of a process wastewater and phenolate solution was carried out at 230 degree C, 200 degree C and total pressure of 50 bar, with oxygen, in a stainless steel autoclave. Monolith Ti mesh supported precious metal oxide catalysts were characterized with XPS, ICP-MS, SEM and their activity compared in oxidation of model and real wastewaters. CWO (catalytic wet oxidation) of a process wastewater and phenolate solution was carried out at 230 degree C, 200 degree C and total pressure of 50 bar, with oxygen, in a stainless steel autoclave. Monolith Ti mesh supported precious metal oxide catalysts were characterized with XPS, ICP-MS, SEM and their activity compared in oxidation of model and real wastewaters. The Ru/Ir oxide coated Ti monolith catalysts showed remarkable catalytic activity in wet oxidation both in the overall oxidation expressed by COD (chemical oxygen demand) decrease and in the carbon mineralization expressed by TOC (total organic carbon) decrease. This was valid for the real pharmaceutical wastewater as well as for a phenolate solution too. Meshes containing Ru, Pd and Ir oxide alone were less active than Ru/Ir together on Ti. This observation is in accordance with the electrochemical properties of the same mesh used in hypochlorite production. The commercial mesh was most stable under the conditions of wet oxidation, however the loss of its precious metal content was observed during longer usage. The Ru/Ir monolith catalysts prepared in our laboratories had similar initial activity but they were less stable, the leaching and/or abrasion of the surface precious metal oxide layer was faster, independently of that their had fragmented or continuous structure, resulting from the preparation methods. The loss of activity during longer usage can be the result of deposition of iron and silicon oxides too, as showed by SEM (scanning electron microscopy) analysis. [Display omitted] ► Ru/Ir oxide/Ti monolith catalysts showed remarkable catalytic activity in WO. ► Good catalytic activity is tied to the uniform distribution of the two oxides. ► Beneficial was the fragmented structure of Ru and Ir oxides. ► Commercial mesh was most stable among the condition of wastewater wet oxidation. ► Loss of precious metal content was observed during longer usage. CWO (catalytic wet oxidation) of a process wastewater and phenolate solution was carried out at 230°C, 200°C and total pressure of 50bar, with oxygen, in a stainless steel autoclave. Monolith Ti mesh supported precious metal oxide catalysts were characterized with XPS, ICP-MS, SEM and their activity compared in oxidation of model and real wastewaters. The Ru/Ir oxide coated Ti monolith catalysts showed remarkable catalytic activity in wet oxidation both in the overall oxidation expressed by COD (chemical oxygen demand) decrease and in the carbon mineralization expressed by TOC (total organic carbon) decrease. This was valid for the real pharmaceutical wastewater as well as for a phenolate solution too. Meshes containing Ru, Pd and Ir oxide alone were less active than Ru/Ir together on Ti. This observation is in accordance with the electrochemical properties of the same mesh used in hypochlorite production. The commercial mesh was most stable under the conditions of wet oxidation, however the loss of its precious metal content was observed during longer usage. The Ru/Ir monolith catalysts prepared in our laboratories had similar initial activity but they were less stable, the leaching and/or abrasion of the surface precious metal oxide layer was faster, independently of that their had fragmented or continuous structure, resulting from the preparation methods. The loss of activity during longer usage can be the result of deposition of iron and silicon oxides too, as showed by SEM (scanning electron microscopy) analysis. An important feature of the good catalytic activity of the Ru/Ir oxide coated Ti mesh can be the uniform distribution of the two oxides showed by LA–ICPMS (laser ablation–inductive coupled plasma mass spectrometry). According to XPS (X-ray photoelectron spectroscopy) results, the upper surface layer of the catalysts is covered by a mixture of Ru–Ir–Ti oxide of approximately 0.1:0.02:1 atomic ratio for commercial catalyst, and an 0.5:0.7:1.0 atomic ratio for catalysts prepared in our laboratories. We suppose that such mixture of oxides with uniform distribution are the carrier of the good catalytic activity. |
Author | Széles, Éva Szabó, Sándor Tungler, Antal Kristóf, János Hosseini, Arezoo M. Szentmiklósi, László Schay, Zoltán |
Author_xml | – sequence: 1 givenname: Arezoo M. surname: Hosseini fullname: Hosseini, Arezoo M. organization: Hungarian Academy of Sciences Centre for Energy Research, Konkoly Thege Miklós út 29-33, Budapest 1121, Hungary – sequence: 2 givenname: Antal surname: Tungler fullname: Tungler, Antal email: antal.tungler@energia.mta.hu, atungler@iki.kfki.hu organization: Hungarian Academy of Sciences Centre for Energy Research, Konkoly Thege Miklós út 29-33, Budapest 1121, Hungary – sequence: 3 givenname: Zoltán surname: Schay fullname: Schay, Zoltán organization: Hungarian Academy of Sciences Centre for Energy Research, Konkoly Thege Miklós út 29-33, Budapest 1121, Hungary – sequence: 4 givenname: Sándor surname: Szabó fullname: Szabó, Sándor organization: Research Center for Natural Sciences of HAS, Pusztaszeri út 59-67, Budapest 1025, Hungary – sequence: 5 givenname: János surname: Kristóf fullname: Kristóf, János organization: Pannon University, Egyetem u. 10, Veszprém 8200, Hungary – sequence: 6 givenname: Éva surname: Széles fullname: Széles, Éva organization: Hungarian Academy of Sciences Centre for Energy Research, Konkoly Thege Miklós út 29-33, Budapest 1121, Hungary – sequence: 7 givenname: László surname: Szentmiklósi fullname: Szentmiklósi, László organization: Hungarian Academy of Sciences Centre for Energy Research, Konkoly Thege Miklós út 29-33, Budapest 1121, Hungary |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26493893$$DView record in Pascal Francis |
BookMark | eNqNkUmP1DAQhS00SPQs_4BDLkhckikv8XJBQi02aSQuzBXLcRzhVmIH200z_x73ZMSR4VSXr96rV-8SXYQYHEKvMXQYML89dGa1pgwdAUw6kB0Ae4F2WAraUinpBdqBIrylVNBX6DLnAwAQSuQOfd_HZTXJ5xiaODVrctbHY24WV8zcxN9-dLfFFxP8cWmWGOLsy4-mmpn5IZfc-NCcXHkETfGbyMnk4k6muJSv0cvJzNndPM0rdP_xw7f95_bu66cv-_d3rWVclpZYzs_Hjf0w9CMXPZaqnwQmMEhGxGQsIQPBrqcEjJIY7NhLSocJuFBjz-gVervprin-PLpc9OKzdfNsgqtxNOZC1sxU8f9BhRJMcnge7QljQAnpn0cpUzWqkqqibENtijknN-k1-cWkB41Bn_vUB731qc99apC69lnX3jw5mGzNPCUTrM9_dwlnilb1yr3bOFf__cu7pLP1Llg3-lpu0WP0_zb6AydXuHI |
CitedBy_id | crossref_primary_10_1007_s11144_015_0894_4 crossref_primary_10_1016_j_jiec_2016_11_005 crossref_primary_10_1007_s11244_018_1029_8 crossref_primary_10_1016_j_jece_2017_07_061 crossref_primary_10_1016_j_jiec_2015_12_019 crossref_primary_10_1016_j_matchemphys_2015_02_034 crossref_primary_10_1016_j_jwpe_2021_102482 crossref_primary_10_1007_s10967_016_4774_9 crossref_primary_10_1039_C5CY01083G crossref_primary_10_1016_j_jenvman_2018_09_003 |
Cites_doi | 10.1021/ie060906z 10.1007/s10967-010-0765-4 10.1016/j.apcatb.2003.08.005 10.3311/pp.ch.2011-2.02 10.1007/s11144-011-0315-2 10.1021/ie051059n 10.1016/j.chemosphere.2006.09.035 10.3311/pp.ch.2011-1.01 10.1016/j.cattod.2007.03.035 10.1016/S0920-5861(99)00112-1 10.1595/147106705X45640 |
ContentType | Journal Article |
Copyright | 2012 Elsevier B.V. 2015 INIST-CNRS |
Copyright_xml | – notice: 2012 Elsevier B.V. – notice: 2015 INIST-CNRS |
DBID | IQODW AAYXX CITATION 7ST C1K SOI 7SR 7SU 7U5 8BQ 8FD FR3 JG9 KR7 L7M |
DOI | 10.1016/j.apcatb.2012.08.004 |
DatabaseName | Pascal-Francis CrossRef Environment Abstracts Environmental Sciences and Pollution Management Environment Abstracts Engineered Materials Abstracts Environmental Engineering Abstracts Solid State and Superconductivity Abstracts METADEX Technology Research Database Engineering Research Database Materials Research Database Civil Engineering Abstracts Advanced Technologies Database with Aerospace |
DatabaseTitle | CrossRef Environment Abstracts Environmental Sciences and Pollution Management Materials Research Database Civil Engineering Abstracts Engineered Materials Abstracts Technology Research Database Environmental Engineering Abstracts Solid State and Superconductivity Abstracts Engineering Research Database Advanced Technologies Database with Aerospace METADEX |
DatabaseTitleList | Environment Abstracts Materials Research Database Environment Abstracts Materials Research Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Engineering Chemistry Environmental Sciences |
EISSN | 1873-3883 |
EndPage | 104 |
ExternalDocumentID | 10_1016_j_apcatb_2012_08_004 26493893 S0926337312003487 |
GroupedDBID | --K --M -~X .~1 0R~ 1B1 1~. 1~5 23M 4.4 457 4G. 53G 5GY 5VS 7-5 71M 8P~ 9JN AABNK AACTN AAEDT AAEDW AAIAV AAIKJ AAKOC AALRI AAOAW AAQFI AAXUO ABFNM ABMAC ABNUV ABXDB ABYKQ ACDAQ ACGFS ACIWK ACRLP ADBBV ADEWK ADEZE ADMUD AEBSH AEKER AFKWA AFRAH AFTJW AGHFR AGUBO AGYEJ AHPOS AIEXJ AIKHN AITUG AJBFU AJOXV AKURH ALMA_UNASSIGNED_HOLDINGS AMFUW AMRAJ AXJTR BKOJK BLXMC CS3 EBS EFJIC EFLBG ENUVR EO8 EO9 EP2 EP3 F5P FDB FIRID FNPLU FYGXN G-Q GBLVA HZ~ IHE J1W KOM LX7 M41 MO0 N9A O-L O9- OAUVE OZT P-8 P-9 P2P PC. Q38 RIG ROL RPZ SDF SDG SES SPC SPD SSG SSZ T5K ~02 ~G- AAPBV AAQXK ABPIF ABPTK AHHHB AI. ASPBG AVWKF AZFZN BBWZM EJD FEDTE FGOYB HLY IQODW NDZJH R2- SCE SEW VH1 WUQ XFK XPP AAXKI AAYXX AKRWK CITATION HVGLF 7ST C1K SOI 7SR 7SU 7U5 8BQ 8FD FR3 JG9 KR7 L7M |
ID | FETCH-LOGICAL-c468t-2c663373d5bb5d6751895f7120b8427fac22b21e5320a9810cd5833bf0679d543 |
IEDL.DBID | AIKHN |
ISSN | 0926-3373 |
IngestDate | Fri Oct 25 04:23:57 EDT 2024 Fri Oct 25 09:19:03 EDT 2024 Fri Oct 25 01:09:36 EDT 2024 Fri Oct 25 07:49:16 EDT 2024 Thu Sep 12 17:41:00 EDT 2024 Sun Oct 22 16:05:38 EDT 2023 Sat Mar 02 16:00:59 EST 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | Ti mixture of oxides Wet oxidation Ru Ti mesh Ir Monolith catalyst Wastewater Plasma Iron oxide Support Oxides X ray Laboratory Fragment Waste water Mineralization Titanium Photoelectron spectrometry Oxidation Silicon Structure Deposition Scanning electron microscopy Oxygen Catalytic reaction Oxide layer Transition metal Carbon Heterogeneous catalysis Electrochemical properties Stainless steel Preparation Laser Models Mass spectrometry Catalyst Environmental protection |
Language | English |
License | CC BY 4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c468t-2c663373d5bb5d6751895f7120b8427fac22b21e5320a9810cd5833bf0679d543 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
PQID | 1349468989 |
PQPubID | 23462 |
PageCount | 6 |
ParticipantIDs | proquest_miscellaneous_1678000396 proquest_miscellaneous_1677974860 proquest_miscellaneous_1524403225 proquest_miscellaneous_1349468989 crossref_primary_10_1016_j_apcatb_2012_08_004 pascalfrancis_primary_26493893 elsevier_sciencedirect_doi_10_1016_j_apcatb_2012_08_004 |
PublicationCentury | 2000 |
PublicationDate | 2012-10-30 |
PublicationDateYYYYMMDD | 2012-10-30 |
PublicationDate_xml | – month: 10 year: 2012 text: 2012-10-30 day: 30 |
PublicationDecade | 2010 |
PublicationPlace | Kidlington |
PublicationPlace_xml | – name: Kidlington |
PublicationTitle | Applied catalysis. B, Environmental |
PublicationYear | 2012 |
Publisher | Elsevier B.V Elsevier |
Publisher_xml | – name: Elsevier B.V – name: Elsevier |
References | Yang, Feng, Wan, Lin, Zhu, Jiang (bib0025) 2005; 17 Szentmiklósi, Belgya, Révay, Kis (bib0080) 2010; 286 Hosseini, Tungler, Horváth, Schay, Széles (bib0065) 2011; 55 Heponiemi, Rahikka, Lassi, Kuokkanen (bib0030) 2009; 17 Cybulski (bib0040) 2007; 46 Hosseini, Bakos, Jobbágy, Tardy, Mizsey, Makó, Tungler (bib0060) 2011; 55 Révay, Belgya, Molnár (bib0085) 2005; 265 A. Heponiemi, L. Rahikka, U. Lassi, T. Kuokkanen, Chemical Engineering Transactions 17 (2009), 9th International Conference on Chemical and Process Engineering, 10–13 May, 2009, Rome, Italy. Luck (bib0010) 1999; 53 Pintar, Gorazd, Besson, Gallezot (bib0015) 2004; 47 Révay, Belgya (bib0075) 2004 Révay (bib0090) 2009; 81 Eugenia Suarez-Ojeda, Guisalsola, Baeza, Fabregat, Stuber, Fortuny, Carrera (bib0005) 2007; 66 Levec, Pintar (bib0045) 2007; 124 Bhargava, Tardio, Prasad, Föger, Akolekar, Grocott (bib0035) 2006; 45 Tunay, Kabdasli, Arslan-Alaton, Olmez-Hanci (bib0050) 2010 Hosseini, Tungler, Bakos (bib0070) 2011; 103 Lei, Zhang, He, Wu, Yang (bib0020) 2005; 49 Cybulski (10.1016/j.apcatb.2012.08.004_bib0040) 2007; 46 Pintar (10.1016/j.apcatb.2012.08.004_bib0015) 2004; 47 Lei (10.1016/j.apcatb.2012.08.004_bib0020) 2005; 49 Tunay (10.1016/j.apcatb.2012.08.004_bib0050) 2010 Révay (10.1016/j.apcatb.2012.08.004_bib0090) 2009; 81 Révay (10.1016/j.apcatb.2012.08.004_bib0075) 2004 10.1016/j.apcatb.2012.08.004_bib0055 Szentmiklósi (10.1016/j.apcatb.2012.08.004_bib0080) 2010; 286 Eugenia Suarez-Ojeda (10.1016/j.apcatb.2012.08.004_bib0005) 2007; 66 Hosseini (10.1016/j.apcatb.2012.08.004_bib0060) 2011; 55 Yang (10.1016/j.apcatb.2012.08.004_bib0025) 2005; 17 Hosseini (10.1016/j.apcatb.2012.08.004_bib0065) 2011; 55 Luck (10.1016/j.apcatb.2012.08.004_bib0010) 1999; 53 Levec (10.1016/j.apcatb.2012.08.004_bib0045) 2007; 124 Bhargava (10.1016/j.apcatb.2012.08.004_bib0035) 2006; 45 Heponiemi (10.1016/j.apcatb.2012.08.004_bib0030) 2009; 17 Hosseini (10.1016/j.apcatb.2012.08.004_bib0070) 2011; 103 Révay (10.1016/j.apcatb.2012.08.004_bib0085) 2005; 265 |
References_xml | – volume: 17 year: 2009 ident: bib0030 publication-title: Chemical Engineering Transactions contributor: fullname: Kuokkanen – start-page: 1 year: 2004 end-page: 30 ident: bib0075 publication-title: Handbook of Prompt Gamma Activation Analysis with Neutron Beams contributor: fullname: Belgya – volume: 53 start-page: 81 year: 1999 end-page: 91 ident: bib0010 publication-title: Catalysis Today contributor: fullname: Luck – volume: 49 start-page: 91 year: 2005 end-page: 97 ident: bib0020 publication-title: Platinum Metals Review contributor: fullname: Yang – volume: 47 start-page: 143 year: 2004 end-page: 152 ident: bib0015 publication-title: Applied Catalysis B contributor: fullname: Gallezot – volume: 286 start-page: 501 year: 2010 end-page: 505 ident: bib0080 publication-title: Journal of Radioanalytical and Nuclear Chemistry contributor: fullname: Kis – volume: 55 start-page: 3 year: 2011 end-page: 10 ident: bib0060 publication-title: Periodica Polytechnica Chemical Engineering contributor: fullname: Tungler – volume: 45 start-page: 1221 year: 2006 end-page: 1258 ident: bib0035 publication-title: Industrial and Engineering Chemistry Research contributor: fullname: Grocott – volume: 17 start-page: 623 year: 2005 end-page: 626 ident: bib0025 publication-title: Journal of Environmental Sciences contributor: fullname: Jiang – volume: 46 start-page: 4007 year: 2007 end-page: 4033 ident: bib0040 publication-title: Industrial and Engineering Chemistry Research contributor: fullname: Cybulski – volume: 265 start-page: 261 year: 2005 end-page: 265 ident: bib0085 publication-title: Journal of Radioanalytical and Nuclear Chemistry contributor: fullname: Molnár – volume: 55 start-page: 49 year: 2011 end-page: 59 ident: bib0065 publication-title: Periodica Polytechnica Chemical Engineering contributor: fullname: Széles – volume: 103 start-page: 251 year: 2011 end-page: 260 ident: bib0070 publication-title: Reaction Kinetics Mechanism and Catalysis contributor: fullname: Bakos – volume: 124 start-page: 172 year: 2007 end-page: 184 ident: bib0045 publication-title: Catalysis Today contributor: fullname: Pintar – volume: 81 start-page: 6851 year: 2009 end-page: 6859 ident: bib0090 publication-title: Analytical Chemistry contributor: fullname: Révay – year: 2010 ident: bib0050 article-title: Chemical Oxidation, Applications for Industrial Wastewaters contributor: fullname: Olmez-Hanci – volume: 66 start-page: 2096 year: 2007 end-page: 2105 ident: bib0005 publication-title: Chemosphere contributor: fullname: Carrera – volume: 46 start-page: 4007 year: 2007 ident: 10.1016/j.apcatb.2012.08.004_bib0040 publication-title: Industrial and Engineering Chemistry Research doi: 10.1021/ie060906z contributor: fullname: Cybulski – volume: 286 start-page: 501 year: 2010 ident: 10.1016/j.apcatb.2012.08.004_bib0080 publication-title: Journal of Radioanalytical and Nuclear Chemistry doi: 10.1007/s10967-010-0765-4 contributor: fullname: Szentmiklósi – volume: 47 start-page: 143 issue: 3 year: 2004 ident: 10.1016/j.apcatb.2012.08.004_bib0015 publication-title: Applied Catalysis B doi: 10.1016/j.apcatb.2003.08.005 contributor: fullname: Pintar – volume: 81 start-page: 6851 year: 2009 ident: 10.1016/j.apcatb.2012.08.004_bib0090 publication-title: Analytical Chemistry doi: 10.3311/pp.ch.2011-2.02 contributor: fullname: Révay – ident: 10.1016/j.apcatb.2012.08.004_bib0055 – volume: 103 start-page: 251 issue: 2 year: 2011 ident: 10.1016/j.apcatb.2012.08.004_bib0070 publication-title: Reaction Kinetics Mechanism and Catalysis doi: 10.1007/s11144-011-0315-2 contributor: fullname: Hosseini – volume: 45 start-page: 1221 year: 2006 ident: 10.1016/j.apcatb.2012.08.004_bib0035 publication-title: Industrial and Engineering Chemistry Research doi: 10.1021/ie051059n contributor: fullname: Bhargava – volume: 66 start-page: 2096 year: 2007 ident: 10.1016/j.apcatb.2012.08.004_bib0005 publication-title: Chemosphere doi: 10.1016/j.chemosphere.2006.09.035 contributor: fullname: Eugenia Suarez-Ojeda – volume: 55 start-page: 49 issue: 2 year: 2011 ident: 10.1016/j.apcatb.2012.08.004_bib0065 publication-title: Periodica Polytechnica Chemical Engineering doi: 10.3311/pp.ch.2011-2.02 contributor: fullname: Hosseini – volume: 265 start-page: 261 year: 2005 ident: 10.1016/j.apcatb.2012.08.004_bib0085 publication-title: Journal of Radioanalytical and Nuclear Chemistry doi: 10.3311/pp.ch.2011-1.01 contributor: fullname: Révay – volume: 17 start-page: 623 issue: 4 year: 2005 ident: 10.1016/j.apcatb.2012.08.004_bib0025 publication-title: Journal of Environmental Sciences contributor: fullname: Yang – volume: 124 start-page: 172 issue: 3–4 year: 2007 ident: 10.1016/j.apcatb.2012.08.004_bib0045 publication-title: Catalysis Today doi: 10.1016/j.cattod.2007.03.035 contributor: fullname: Levec – volume: 55 start-page: 3 issue: 1 year: 2011 ident: 10.1016/j.apcatb.2012.08.004_bib0060 publication-title: Periodica Polytechnica Chemical Engineering doi: 10.3311/pp.ch.2011-1.01 contributor: fullname: Hosseini – start-page: 1 year: 2004 ident: 10.1016/j.apcatb.2012.08.004_bib0075 contributor: fullname: Révay – year: 2010 ident: 10.1016/j.apcatb.2012.08.004_bib0050 contributor: fullname: Tunay – volume: 53 start-page: 81 year: 1999 ident: 10.1016/j.apcatb.2012.08.004_bib0010 publication-title: Catalysis Today doi: 10.1016/S0920-5861(99)00112-1 contributor: fullname: Luck – volume: 49 start-page: 91 issue: 2 year: 2005 ident: 10.1016/j.apcatb.2012.08.004_bib0020 publication-title: Platinum Metals Review doi: 10.1595/147106705X45640 contributor: fullname: Lei – volume: 17 year: 2009 ident: 10.1016/j.apcatb.2012.08.004_bib0030 publication-title: Chemical Engineering Transactions contributor: fullname: Heponiemi |
SSID | ssj0002328 |
Score | 2.1716418 |
Snippet | [Display omitted]
► Ru/Ir oxide/Ti monolith catalysts showed remarkable catalytic activity in WO. ► Good catalytic activity is tied to the uniform distribution... CWO (catalytic wet oxidation) of a process wastewater and phenolate solution was carried out at 230 degree C, 200 degree C and total pressure of 50 bar, with... |
SourceID | proquest crossref pascalfrancis elsevier |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 99 |
SubjectTerms | Abrasion Abrasion resistance Catalysis Catalysts Chemistry Exact sciences and technology General and physical chemistry Monolith catalyst Oxides Precious metals Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry Ti mesh Ti mixture of oxides Titanium Waste water Wastewater Wet oxidation X-ray photoelectron spectroscopy |
Title | Comparison of precious metal oxide/titanium monolith catalysts in wet oxidation of wastewaters |
URI | https://dx.doi.org/10.1016/j.apcatb.2012.08.004 https://search.proquest.com/docview/1349468989 https://search.proquest.com/docview/1524403225 https://search.proquest.com/docview/1677974860 https://search.proquest.com/docview/1678000396 |
Volume | 127 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fS9xAEB70fGhFSnut9LQ9ttDX7SWbZLN5lEM5W_DFCj51ySYbmoK50ORQX_zbndkkp6JcoY8Js_kxs5n5sjszH8DXoMAgjpGAU9UnD6UX8MTGhmd5oDA6ZIXMXZbvmVxchN8vo8stmA-1MJRW2fv-zqc7b92fmfXanNVlOTv3EiGDIA58yq9C3L0NOxiOhBrBztHpj8XZ2iEjaHAOGeU5DRgq6FyaV1pnaWsox0u4Xp49Y9sLEWqvThvUW9ERXjzz3S4gnbyFNz2SZEfdw76DLVuN4dV8IHAbw-6jXoNj2D9-KGnDYf033byHX_M1FSFbFqymdhfLVcOuLMktb8rcEkdSWpWrK4aTlhLmfjO37HPbtA0rK3ZtWyforEwXuU4bWpSjzp0f4OLk-Od8wXvWBZ6FUrVcZNKpNY-MiXJJ2zJJVMSoZaNCERdpJoQRviVGiTRRvpflVLllClqSyqMw2IdRtazsR2CZkgkCEmG93IS-NUogvkTrB4hSVaHMBPigaV13zTX0kHX2R3eW0WQZTVSZXjiBeDCHfjJJNPr_f4ycPrHe-naIBxPCbBP4MphTo5lo1yStLGpbU_9GVEyikg0yEaIkj3zjBhkZx_jzpqS3UUa5cml58N-vegiv6cjFV-8TjNq_K_sZgVNrprD97c6f9p_HPYoMF8A |
link.rule.ids | 315,783,787,4509,24128,27936,27937,45597,45691 |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB6V9lCqqoKFii1QjMTV2qyTOPaxWrXa0rIXWqknrDhxRCo1G5GsWv49M06yUFEtEtdknMd88cwXex4An8ICnTh6Ak5ZnzySQci1SyzP8lChd8gKmfso34WcX0efb-KbLZgNuTAUVtnb_s6me2vdH5n02pzUZTn5GmghwzAJpxRfhbz7GewgG9A4O3dOzi_mi7VBRtLgDTLKcxowZND5MK-0ztLWUoyX8LU8-45tT3io_TptUG9F1_DiL9vtHdLZCzjomSQ76R72JWy5agS7s6GB2wj2_qg1OILD098pbTisn9PNK_g2W7ciZMuC1VTuYrlq2J0jueVDmTvqkZRW5eqO4UdLAXPfmV_2-dm0DSsrdu9aL-hRpovcpw0tylHlztdwfXZ6NZvzvusCzyKpWi4y6dWax9bGuaRtGR0XCWrZqkgkRZoJYcXUUUeJVKtpkOWUuWULWpLK4yg8hO1qWbk3wDIlNRIS4YLcRlNnlUB-ieiHyFJVoewY-KBpU3fFNcwQdXZrOmQMIWOoVWYQjSEZ4DCPPhKD9v8fI48fobe-HfJBTZxtDB8HOA3CRLsmaeVQ24bqN6JitNIbZGJkSQHZxg0yMknw503JYKOM8unS8ui_X_UD7M6vvlyay_PFxVt4Tme8rw3ewXb7Y-XeI4lq7XE_SX4BS04ZtA |
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=Comparison+of+precious+metal+oxide%2Ftitanium+monolith+catalysts+in+wet+oxidation+of+wastewaters&rft.jtitle=Applied+catalysis.+B%2C+Environmental&rft.au=Hosseini%2C+Arezoo+M&rft.au=Tungler%2C+Antal&rft.au=Schay%2C+Zoltan&rft.au=Szabo%2C+Sandor&rft.date=2012-10-30&rft.issn=0926-3373&rft.volume=127&rft.spage=99&rft.epage=104&rft_id=info:doi/10.1016%2Fj.apcatb.2012.08.004&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0926-3373&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0926-3373&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0926-3373&client=summon |