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Comment on merger proposal here in this section

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The Catalytic reformer, Catalytic reforming and Platforming articles cover exactly the same subject. They need to be merged into a single article ... by an expert who knows the subject from actual real-world experience, not just from reading reference publications or books. - mbeychok 06:27, 3 December 2006 (UTC)[reply]

I just completed the merger and major expansion of the the three articles. The merged article is named Catalytic reforming. ThePlatforming and Catalytic reformer articles now re-direct to Catalytic reforming. The Catalysts and Mechanisms section remains to be done and I will ask User:Smokefoot to write that section. Happy Holidays to all! - mbeychok 06:52, 16 December 2006 (UTC)[reply]

Help with Catalysts and Mechanisms section

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Smokefootwill be unable to help with the section on catalysts and mechanisms. Anyone having real, expert knowledge of catalytic reforming catalysts, please feel free to improve and/or expand this section. - mbeychok 04:01, 17 December 2006 (UTC)[reply]

It is a very good page, but it can be ameliorated. —Preceding unsigned comment added by 70.80.52.245 (talkcontribs) 11 April 2007 (UTC)

Why deletion by Arcenciel was deleted

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The stub article UOP LLC makes no mention at all about Catalytic Reforming ... one of UOP's major landmark proprietary processes. Until that article grows a bit and at least mentions Catalytic Reforming, I think that the sentence about UOP (that was deleted by Arcenciel) should remain here. mbeychok (talk) 04:18, 17 October 2008 (UTC)[reply]

"Catalytic reforming" doesn't include steam reforming or biomass reforming?

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The initial paragraph describes "catalytic reforming" as applied to napthas. The second paragraph, however, says that we are NOT talking about catalytic steam reforming, nor about catalytic reforming as applied to biomass-derived feedstocks.

Surely an article titled "Catalytic reforming" should cover ALL types of catalytic reforming, rather than covering one and explicitly ignoring others? -- Dan Griscom (talk) 19:26, 19 October 2008 (UTC)[reply]

hai can i get the module pcs of fabricated reformer

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Catalytic reforming uses Pt

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This long section, removed from the article, describes all manner of catalysts that could be used but mostly are not. The entire section was added by one editor. "

  1. Supported noble metals
  2. non-noble transition metal
CCR
Continuous Catalytic Reforming / platforming

The best [[Catalysis|catalyst]] for the synthesis of [[syngas]] utilising various procedures has been the subject of several research. [[Rhodium]],<ref>{{Cite journal |last1=Horn |first1=R |last2=Williams |first2=K |last3=Degenstein |first3=N |last4=Schmidt |first4=L |date=2006-08-15 |title=Syngas by catalytic partial oxidation of methane on rhodium: Mechanistic conclusions from spatially resolved measurements and numerical simulations |url=https://linkinghub.elsevier.com/retrieve/pii/S002195170600176X |journal=Journal of Catalysis |language=en |volume=242 |issue=1 |pages=92–102 |doi=10.1016/j.jcat.2006.05.008}}</ref><ref>{{Cite journal |last1=Salazar-Villalpando |first1=Maria D. |last2=Miller |first2=Adam C. |date=March 2011 |title=Catalytic partial oxidation of methane and isotopic oxygen exchange reactions over 18O labeled Rh/Gadolinium doped ceria |url=https://linkinghub.elsevier.com/retrieve/pii/S036031991002255X |journal=International Journal of Hydrogen Energy |language=en |volume=36 |issue=6 |pages=3880–3885 |doi=10.1016/j.ijhydene.2010.11.040}}</ref> [[ruthenium]],<ref>{{Cite journal |last1=Ishihara |first1=A |last2=Qian |first2=E |last3=Finahari |first3=I |last4=Sutrisna |first4=I |last5=Kabe |first5=T |date=2005-04-27 |title=Addition effect of ruthenium on nickel steam reforming catalysts |url=https://linkinghub.elsevier.com/retrieve/pii/S0016236105000852 |journal=Fuel |volume=84 |issue=12 |language=en |pages=1462–1468 |doi=10.1016/j.fuel.2005.03.006}}</ref><ref>{{Cite journal |last=Shamsi |first=Abolghasem |date=January 2009 |title=Partial oxidation of methane and the effect of sulfur on catalytic activity and selectivity |url=https://linkinghub.elsevier.com/retrieve/pii/S0920586108001430 |journal=Catalysis Today |language=en |volume=139 |issue=4 |pages=268–273 |doi=10.1016/j.cattod.2008.03.033}}</ref> and [[platinum]],<ref>{{Cite journal |last1=Souza |first1=Mariana M.V.M. |last2=Macedo Neto |first2=Octávio R. |last3=Schmal |first3=Martin |date=March 2006 |title=Synthesis Gas Production from Natural Gas on Supported Pt Catalysts |url=https://linkinghub.elsevier.com/retrieve/pii/S1003995306600030 |journal=Journal of Natural Gas Chemistry |language=en |volume=15 |issue=1 |pages=21–27 |doi=10.1016/S1003-9953(06)60003-0}}</ref><ref>{{Cite journal |last1=Salazar-Villalpando |first1=Maria D. |last2=Miller |first2=Adam C. |date=January 2011 |title=Hydrogen production by methane decomposition and catalytic partial oxidation of methane over Pt/CexGd1−xO2 and Pt/CexZr1−xO2 |url=https://linkinghub.elsevier.com/retrieve/pii/S1385894710011721 |journal=Chemical Engineering Journal |language=en |volume=166 |issue=2 |pages=738–743 |doi=10.1016/j.cej.2010.11.076}}</ref> as well as [[palladium]]<ref>{{Cite journal |last1=Ryu |first1=J |last2=Lee |first2=K |last3=Kim |first3=H |last4=Yang |first4=J |last5=Jung |first5=H |date=2008-05-08 |title=Promotion of palladium-based catalysts on metal monolith for partial oxidation of methane to syngas |url=https://linkinghub.elsevier.com/retrieve/pii/S0926337307003335 |journal=Applied Catalysis B: Environmental |language=en |volume=80 |issue=3–4 |pages=306–312 |doi=10.1016/j.apcatb.2007.10.010}}</ref> and [[iridium]]<ref>{{Cite journal |last1=Richardson |first1=J.T. |last2=Paripatyadar |first2=S.A. |date=May 1990 |title=Carbon dioxide reforming of methane with supported rhodium |url=https://linkinghub.elsevier.com/retrieve/pii/S0166983400821521 |journal=Applied Catalysis |language=en |volume=61 |issue=1 |pages=293–309 |doi=10.1016/S0166-9834(00)82152-1}}</ref> catalysts, have all been the subject of in-depth study on [[hydrogen production]], catalytic [[thermal decomposition]], and dry reforming catalysts.<ref>{{Cite journal |last=Barbero |first=J. |date=2003 |title=Support Effect in Supported Ni Catalysts on Their Performance for Methane Partial Oxidation |url=http://link.springer.com/10.1023/A:1023407609626 |journal=Catalysis Letters |volume=87 |issue=3/4 |pages=211–218 |doi=10.1023/A:1023407609626|s2cid=91889442 }}</ref> Noble metals-based catalysts are much more effective and often less susceptible to deactivation by carbon production or oxidation, but because they are more expensive (costing 100–150 times more than nickel catalysts), they are less frequently used.<ref>{{Cite journal |last1=Zeppieri |first1=M. |last2=Villa |first2=P.L. |last3=Verdone |first3=N. |last4=Scarsella |first4=M. |last5=De Filippis |first5=P. |date=2010-10-20 |title=Kinetic of methane steam reforming reaction over nickel- and rhodium-based catalysts |url=http://dx.doi.org/10.1016/j.apcata.2010.08.017 |journal=Applied Catalysis A: General |volume=387 |issue=1–2 |pages=147–154 |doi=10.1016/j.apcata.2010.08.017 |issn=0926-860X}}</ref> In [[Industrialisation|industrial uses]], catalysts depending on [[nickel]] are increasingly often utilised. However, due to [[carbon]] accumulation, their resilience is low. The most crucial issue for [[methane reforming]], particularly in dry reforming, is the suppression of carbon deposition for non-noble [[metal catalysts]]. Increasing the surface basicity of catalysts and regulating the [[particle size]]s of active ingredients are two techniques used to prevent carbon from depositing. The improvement of metal-support interaction, the creation of [[solid solutions]], and plasma processes are only a few of the strategies that have been developed to manage the metal particle sizes. The surface basicity of catalysts was increased by using basic [[Metal oxide adhesion|metal oxides]] as a support or [[Promoter activity|promoter]]. Increased catalysts and processes as a consequence of the work of several authors have improved overall [[efficiency]] and environmental performance.<ref>{{Cite book |url=http://doi.wiley.com/10.1002/9783527610044 |title=Handbook of Heterogeneous Catalysis: Online |date=2008-03-15 |publisher=Wiley-VCH Verlag GmbH & Co. KGaA |isbn=978-3-527-31241-2 |editor-last=Ertl |editor-first=Gerhard |location=Weinheim, Germany |language=en |doi=10.1002/9783527610044 |editor-last2=Knözinger |editor-first2=Helmut |editor-last3=Schüth |editor-first3=Ferdi |editor-last4=Weitkamp |editor-first4=Jens}}</ref><ref>{{Cite journal |last1=Molenbroek |first1=Alfons M. |last2=Helveg |first2=Stig |last3=Topsøe |first3=Henrik |last4=Clausen |first4=Bjerne S. |date=September 2009 |title=Nano-Particles in Heterogeneous Catalysis |url=http://link.springer.com/10.1007/s11244-009-9314-1 |journal=Topics in Catalysis |language=en |volume=52 |issue=10 |pages=1303–1311 |doi=10.1007/s11244-009-9314-1 |s2cid=95513283 |issn=1022-5528}}</ref>"