OP-II-3

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ABIEV RufatSt. Petersburg State Institute of Technology(Technical University)Moskowskii pr., 26190013 St. PetersburgRussiaTel: +7 812 494 9276E-mail: rufat.abiev@gmail.comAFANASENKO Vitaliy GennadyevichUfa State Petroleum Technical UniversityKosmonavtov str., 1450062 UfaRussiaE-mail: awirus@rambler.ruAGIRRE IonFaculty of Engineering of Bilbao(University of the Basque Country)Alameda Urquijo s/n48013 BilbaoSpainE-mail: ion.agirre@ehu.esAIOUACHE FaridQueen's University BelfastBT9 5AG BelfastUKE-mail: f.aiouache@qub.ac.ukALEKSEENKO Sergey VladimirovichInstitute of Thermophysics SB RASNovosibirskRussiaE-mail: aleks@itp.nsc.ruALTSHULER Heinrich NaumovichKemerovo Department of the Institute ofSolid State Chemistry andMechanochemistry SB RAS18, Sovetskii ave.650099 KemerovoRussiaTel: +7 384 2 36 3766Fax: +7 384 2 21 1838E-mail: sorbent@kemnet.ruAMARA MouradUniversité des Sciences et de la TechnologieHouari-boumedienneBP 32 El-Alia, Bab-Ezzouar16111 AlgiersAlgeriaTel: +213 21 24-7311Fax: +213 21 24 7311E-mail: mo_amara@yahoo.frLIST OF PARTICIPANTSAMINOVA GuzelKazan State Technological Universityul. Karla Marksa, 68420015 KazanRussiaTel: +7 843 23 14 292Fax: +7 843 23 14 211E-mail: a_guzel@mail.ruAMROUSSE RachidUniversity of PoitiersCNRS 6503 40 Avenue du Recteur Pineau F -86022 POITIERS CedexFranceE-mail: rachid.amrousse@univ-poitiers.frAMUTIO MaiderUniversidad del País Vasco48013 BilbaoSpainE-mail: maider.amutio@ehu.esANFIMOVA Natalya PetrovnaBoreskov Institute of Catalysis SB RASpr. Akademika Lavrentieva, 5630090 NovosibirskRussiaFax: +7 383 330 8056E-mail: anf@catalysis.ruANTAL Steven PeterInterphase Dynamics33 Rosemere12109 TroyUSATel: (518) 395 6985Fax: (518) 833 0219E-mail: antals@rpi.eduARABIOURRUTIA MiriamUniversidad del País Vasco480080 BilbaoSpainE-mail: miriam.arabiourrutia@ehu.esARACIL JoseUniversity of Complutense28040 MadridSpainE-mail: jam1@quim.ucm.esARJMAND MehdiRoyal Institute of Technology (KTH)Valhallavägen, 79SE-100 44 StockholmSwedenTel: +46 8 7906000Fax: +46 8 7906500E-mail: mehdiarjmand@yahoo.com596
ARKHIPOV Vladimir AfanasievichResearch Institute of Applied Mathematicsand Mechanics of Tomsk State UniversityLenina str., 36634050 TomskRussiaTel: +7 3822 529 547Fax: +7 3822 529 547E-mail: leva@niipmm.tsu.ruARPORNWICHAN<strong>OP</strong> AmornchaiChulalongkorn University10330 BangkokThailandE-mail: amornchai.a@chula.ac.thARUTYUNOV Vladimir SergeevichSemenov Institute of Chemical Physics RASKosygina str., 4119991 MoscowRussiaE-mail: arutyunov@center.chph.ras.ruAUTHAYANUN SuthidaChulalongkorn University10330 BangkokThailandE-mail: suthida_autt@hotmail.comAVETISOV Alexander KonstantinovichKarpov Institute of Physical ChemistryVorontsovo pole, 10105064 MoscowRussiaE-mail: avetisov@cc.nifhi.ac.ruAVGOUR<strong>OP</strong>OULOS GeorgeFoundation for Research and Technology-Hellas (FORTH),Institute of Chemical Engineering &High Temperature Chemical Processes(ICE-HT)P.O. Box: 1414, Stadiou Str., Platani-RioGR-26504 PatrasGreeceE-mail: geoavg@iceht.forth.grAVVAKUMOV Evgeny GrigorievichInstitute of Solid State Chemistry andMechanochemistry SB RASKutateladze str., 18630128 NovosibirskRussiaTel: +7 383 332 86 83Fax: +7383 332 28 47E-mail: avvakumov@solid.nsc.ruBABKIN Viatcheslav StepanovichInstitute of Chemical Kinetics andCombustion of SB RASInstitutskaya str., 3630090 NovosibirskRussiaTel: +7(383) 330 91 50Fax: +7(383) 330 73 50E-mail: babkin@kinetics.nsc.ruBACHURIKHIN Alexander LeonidovichN.D. Zelinsky Institute of OrganicChemistry RAS119991 MoscowRussiaE-mail: Shao-kahn@yandex.ruBANKOVIĆ PredragInstitute of Chemistry Technology andMetallurgy, Department of Catalysis andChemical EngineeringNjegoševa, 1211000 BelgradeSerbiaE-mail: predragb@nanosys.ihtm.bg.ac.rsBARAJAS Solano Andrés FernandoIndustrial University of SantanderCiudad Universitaria, Cra 27 calle 9AA678 BucaramangaColombiaTel: +57 7 634 4000Fax: +57 7 645 4697E-mail: andresfdobarajas@gmail.comBARCLAY DonaldAutoclave Engineers Division,Division of Snap-Tite Inc.8325 Hessinger Drive16509 CarnoustieUKTel: +1 814 869 5700Fax: +1 814 860 5811E-mail: donald_barclay@snap-tite.comBARRIO V. LauraUniversity of the Basque Country48013 BilbaoSpainE-mail: laura.barrio@ehu.esBASOV Nikolay LukichA.V. Topchiev Institute of PetrochemicalSynthesis RASLeninskiy pr., 29119991 MoscowRussiaTel: +7 (495) 954 4222Fax: +7 (495) 633 8520E-mail: basov@ips.ac.ruBAWOLAK KatarzynaTechnical University of Lodzul. Zeromskiego 11690-924 LodzPolandE-mail: kbawolak@p.lodz.plBEKSAEV SergeyNordbiochem Ltd.Kuuse 263303 PolvaEstoniaE-mail: sbeksaev@inbox.ru597
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Boreskov Institute of Catalysisof t
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INTERNATIONAL SCIENTIFIC COMMITTEEV
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SILVER SPONSORThe organizers expres
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PL-1HOW TO DESIGN OPTIMAL CATALYTIC
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MULTIFUNCTIONAL DEVICES FOR INTENSI
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PL-3DESIGN OF CATALYTIC PROCESSES F
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PL-3Indeed preparation and testing
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PL-4The second part of the lecture
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PL-5Reactor designs with intensifie
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PL-6MEMBRANE REACTORS: STATE OF THE
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KEY-NOTE PRESENTATIONS
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KN-1description, that can be charac
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KN-2selective catalytic reduction o
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KN-3Fig. 1. Experimental burner of
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KN-4~200°C. This is based on the H
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KN-5for addressing the quality of t
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KN-6reaction with ethanol and the b
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KN-7at temperature lower than 873K,
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REACTION KINETICS AND REACTION ENHA
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OP-I-2RELATION BETWEEN THE ACTIVATI
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COMPARISON OF CHEMICAL AND ENZYMATI
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OP-I-4NONLINEAR PHENOMENA DURING ME
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OP-I-5SPECIFICITY OF THE OSCILLATIO
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OP-I-6TRENDS IN BISTABILITY DOMAINS
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OP-I-7NON-STEADY-STATE CATALYST CHA
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OP-I-8TRANSIENT KINETIC STUDIES OF
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OP-I-9A REDOX KINETICS FOR THE PART
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OP-I-9500Flow of Air = 0.3 m 3 (STP
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OP-I-11ELUCIDATION OF THE REACTIVIT
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KINETIC MODELLING OF THE JOINT TRAN
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OP-I-13n-HEXANE SKELETAL ISOMERIZAT
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OP-I-14the slow branch of kinetic c
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OP-I-15The hydride palladium comple
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Energy Conservation (field j)∂∂
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OP-I-17Selectivity (mol. %)10099989
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OP-I-18According to GLC the main pr
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OP-I-19and slug dimensions, formati
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OP-I-20A RANS volume of fluids [1]
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OP-I-21the physical-chemical charac
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OP-I-22calculated values of pressur
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OP-I-23where L c - capillary length
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OP-I-24and diffuse transmission thr
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OP-I-25effect of bubble break-up wo
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OP-I-26strong influence on the soli
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OP-I-27wHCOOH=1+K2K1(1 + K3⋅ P⋅
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OP-I-28dimensional profiles detecte
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OP-I-29results. The results of the
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OP-I-30Fig. 1. Hydrodynamics and co
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OP-I-31Convection and diffusion wit
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TEMPERATURE RISE DURING REGENERATIO
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OP-II-2[4]. Similar temperature pro
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OP-II-3(Fig, 1 a, b) upon testing i
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OP-II-4In the second step optimizat
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OP-II-5membrane contactors were stu
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OP-II-6reaction over Cu/CeO 2-x cat
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OP-II-7is modelled by means of a tw
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OP-II-8the reactor [6]. However, th
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OP-II-9Figure 1. Computed volume fr
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OP-II-10assumes variables’ distri
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OP-II-11oxide support, it comes tha
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OP-II-12was connected to G.C. via s
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OP-II-13catalyst bed was 6 mm. Thre
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OP-II-14as coolant is an important
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OP-II-15Flow (L/h)7654321Bottoms ra
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OP-II-16(4) The gas recirculation r
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OP-II-17Catalytic reactions were ca
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OP-II-18At steady surface coverage
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OP-II-19gaimpulsegeneratorwateFig.
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OP-II-20examined (see Figure 1). Th
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OP-II-21References[1]. M.P. Dudukov
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OP-II-22of the hydrogen oxidation a
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OP-II-23TemperaturesensorsThe efflu
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OP-II-24of reactant conversions. Pa
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OP-II-25(surface) ‘wall-reaction
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OP-II-26It was found that the 10 wt
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OP-II-27non-flow type. During the M
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OP-III-A-1A NEW SIMPLE MICROCHANNEL
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BUBBLING FLUIDISED BED PYROLYSIS OF
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PINEWOOD PYROLYSIS UNDER VACUUM CON
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OP-III-A-5PYROLYSIS OF HDPE IN A CO
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OP-III-A-6REACTORS FOR THE GREEN TR
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DEHYDRATION OF GLYCEROL TO ACROLEIN
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OP-III-A-8LACTIC ACID BASED ON BIO
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RECOVERY OF ACETIC ACID FROM PYROLY
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OP-III-A-10LIPASE-CATALYZED REACTIO
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OP-III-A-11INVESTIGATION ON THERMOC
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OP-III-A-12SELECTIVE CATALYTIC DEOX
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ETHANOL STEAM REFORMING OVER COBALT
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OP-III-A-14HYDROTREATMENT CATALYSTS
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ORAL PRESENTATIONSSECTION IIIChemic
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OP-III-B-1Reactor parameters:Intern
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OP-III-B-2JOINT STEAM REFORMING OF
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OP-III-B-3LANDFILL BIOGAS PURIFICAT
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OP-III-B-4MODELING AND SIMULATION O
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OP-III-B-5DemonstratorThe medium-te
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OP-III-B-630/19.6 Nl/min (space vel
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OP-III-B-7mixed in the ratios: 94,8
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OP-III-B-8Table 1.Material balance
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OP-III-B-9Based on the results of t
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OP-III-B-10On this basis it can be
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OP-III-B-11Similar trends caused by
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OP-III-B-12(mol/s g cat)x108r4,6-DM
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OP-III-B-13carbon in Wyoming coal i
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OP-III-B-14MODELING PRODUCT DISTRIB
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OP-III-B-15COMBINED TECHNOLOGY OF U
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MATEMATICAL MODEL FOR DOWNDRAFT BIO
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OP-III-B-17CATALYTIC DEHYDRATION OF
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OP-III-B-18SYNGAS AND HYDROGEN PROD
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POSTER PRESENTATIONSSECTION I
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PP-I-1influence of the direction of
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PP-I-2At the agitation of the liqui
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PP-I-3NOLINEAR PHENOMENA IN CATALYT
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PP-I-4A NEW APPROACH TO KINETIC STU
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PP-I-5KINETICS OF PROX REACTION OVE
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PP-I-6PHENOMENA OF SUPERADIABATIC T
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ELECTROMAGNETIC REACTOR OF WATER TR
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PP-I-8DIRECT SYNTHESIS OF HYDROGEN
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PP-I-9DYNAMICS OF FIRST-ORDER PHASE
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PP-I-10ELECTROCHEMICAL OXIDATION OF
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PP-I-11CHEMPAK SOFTWARE PACKAGE: OP
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PP-I-12COMPUTER SIMULATION OF ENDOT
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PP-I-13MODELLING KINETICS OF PROCES
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PP-I-14THE INVESTIGATION OF REACTIO
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PP-I-15The qualitative picture of s
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Thus, knowing the composition of ra
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PP-I-17current density. Preliminary
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PP-I-18Hydrogenation kinetics was d
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PP-I-19the active mixing, amplitude
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PP-I-20where r, h indicate the radi
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PP-I-21model is very anisotropic be
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PP-I-22- Reduction of the number of
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PP-I-23oscillations of intermediate
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PP-I-25SYNTHESIS OF ETHYLENE OXIDE
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PP-I-26OPTIMUM KINETICS FOR POLYSTY
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PP-I-27TableSpecific surface area (
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PP-I-28γ-preirradiated sample), th
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PP-I-29commercial CFD solver FLUENT
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PP-I-30modulus, a considerable decr
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PP-I-31The destruction ways of CF 3
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PP-I-32[7]. Karoor S, Sirkar K. Gas
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PP-I-33above 750°. The catalytic p
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PP-I-35REVERSE FLOW REACTOR WITH FO
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FLOW-RECIRCULATION METHOD FOR INVES
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TO A PROBLEM OF OPTIMIZATION OF FUN
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PP-I-38THE INFLUENCE OF REACTION MI
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PP-I-39METHANOL OXIDATIVE STEAM REF
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PP-I-41CORRECT INVESTIGATION OF THE
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PP-I-42NEW APPROACH OF DEFINITION O
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PP-I-43STREAM HEAT EXCHANGE OF AERO
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PP-I-44HIGH TEMPERATURE OXYGEN TRAN
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PP-I-45KINETICS OF TRANSESTERIFICAT
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MATHEMATICAL MODELING AND OPTIMIZAT
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PP-I-47The basic side reaction is r
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PP-I-49EXPERIMENTAL STUDY OF THE HA
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PP-I-51ON THE KINETICS AND REGULARI
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PP-I-52DIFFERENTIAL THERMAL ANALYSI
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PP-I-53oxidation reaction demonstra
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PP-I-54of reaction. It is establish
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PP-I-55effects, are energetically c
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PP-I-56The experiments and simulati
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PP-I-57In the studied range of temp
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PP-I-58HeadingsAdvances in Chemical
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PP-I-59calculated. During the aroma
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PP-I-60with honeycomb catalyst) act
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Т - temperature, K, D eff - effect
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PP-I-62stirring rate were adopted u
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PP-I-63m 2 = (k 1 y 0 1 +k -1 +k 1
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POSTER PRESENTATIONSSECTION II
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PP-II-1values of operating paramete
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⎡⎛⎢⎜bF⎣⎝=2ab ⎞ 6+ ⎟
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PP-II-4HONEYCOMB MONOLITHIC CATALYS
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MATHEMATICAL MODELING OF THE ALUMIN
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PP-II-6MODELING OF VINYL ACETATE SY
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PP-II-7СENTRIFUGAL DISK REACTORAvv
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PP-II-83) An opportunity of operati
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PP-II-10UV-ACTIVATION OF METHANE CO
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PP-II-11COMBINED APPROACH (FMEA- HA
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PP-II-12Testing the pilot variant o
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PP-II-14NOVEL MICROREACTOR FOR THE
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PP-II-15of 1-2.5 lead to a decreasi
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PP-II-16stages. Kinetic parameters
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PP-II-17whiskers, which assure an a
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PP-II-18с m , с cat - density of
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PP-II-19decrease. So, the potential
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PP-II-20products became a mixture o
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PP-II-21A numerical algorithm and s
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PP-II-22motions at any external con
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PP-II-23One of the main technologic
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PP-II-24100 m x 250 μm x 0.5 μm,
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PP-II-25A model was developed to ca
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PP-II-26The results of calculations
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PP-II-27modes of reaction and two d
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PP-II-29OZONE-DESTRUCTION REACTOR B
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PP-II-30Fig. 1. Axial profile of me
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PP-II-31isobutylene in butene fract
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PP-II-322.5x10 -3 ( i )2.5x10 -3 (
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PP-II-33No olefinreadsorptionWith o
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PP-II-34using titania or Ag-doped t
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PP-II-35accidents, is condition dep
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PP-II-36be seen that at temperature
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PP-II-37the solid phase solute conc
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PP-II-38As shown in Table 1, the ca
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PP-II-39better to the obtained in t
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PP-II-40Hydrodynamic regime in the
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PP-II-41activity, relative unit1,21
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PP-II-42One of the major indicators
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PP-II-43These conditions are confor
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PP-II-44For the hepten, alpha-methy
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PP-II-46PARTIAL OXIDATION OF METHAN
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PP-II-47DEVELOPMENT OF VORTEX APPAR
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MODELING OF CFTALYTIC α-OLEFINS OL
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PP-II-49Hinselwood kinetic equation
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3) iterate concentrations at a cut
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PP-II-51data such flow sheet provid
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PP-II-53ON THE TECNOLOGY OF TECHNIC
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PP-II-54PROPYLENE POLYMERIZATION AN
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REACTOR FOR LIQUID-PHASE PROCESSES
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PP-II-56MODELING OF CATALYTIC MICRO
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PP-II-57MATHEMATICAL MODELING OF BE
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PP-II-58HONEYCOMB CATALYSTS WITH PO
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POSTER PRESENTATIONSSECTION IIISECT
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ReferencesPP-III-1[1]. A.N. Pestrya
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PP-III-2Table1. Percentages of diff
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PP-III-3conversion for the reaction
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PP-III-4900Reformer temperature (K)
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PP-III-5Catalytic performance of th
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PP-III-6optimization permit better
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PP-III-8DE-NO X SYSTEM BASED ON H 2
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PP-III-9SEPARATION BETWEEN CHLORIDE
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CONVERSION OF WASTE COTTON TO BIOET
Page 461 and 462:
PP-III-12THE METHOD OF GLYCERIC ACI
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NOx conversion vs. temperature is p
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PP-III-14intermetallic diffusion at
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PP-III-15The conversion of O 2 was
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PP-III-16H 2consumpition (a.u)(a)39
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PP-III-17the characteristic structu
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PP-III-18Figure 1. Influence of tem
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PP-III-19(a)(b)CH 4conversion, %100
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PP-III-20take into account own size
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PP-III-2110080CS-18CS-34CHZ30CHZ801
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EXPERIMENTALPP-III-22We synthesized
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PP-III-23Base composition component
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PP-III-25CO REMOVAL AT THE MICROSCA
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HYDROGEN PRODUCTION FROM METHANOL U
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PP-III-27NON CATALITIC PRODUCTION O
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PP-III-28Different reaction conditi
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PP-III-29followed by WGS reaction.
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PP-III-30As a solvent-coreactants w
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PP-III-31It was concluded that on t
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PP-III-32Hydrogenolysis of glycerol
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PP-III-331,6W 0, μmol Н 2/min1,20
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PP-III-34preparation (glass fiber f
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PP-III-35In the modification proces
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PP-III-36The kinetics of acid hydro
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PP-III-37reaction: i) C=O double bo
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PP-III-38methane and carbon monoxid
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PP-III-39from 25 to 60, which was d
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PP-III-401% w/w for Pd with respect
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PP-III-41material. Besides, the mol
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PP-III-43METHANOL AND DIMETHYL ETHE
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PP-III-44goal is attained by using
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OLIGOMERISATION OF TERTIARY AMINE L
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PP-III-47meter (Shimazu Co.; TOC-50
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PP-III-48the range of 29-87 kJ/mol
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PP-III-49determine the optimal type
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PP-III-50NEW CONCEPT FOR A SELF CLE
Page 533 and 534:
PP-III-51HYDROGEN PRODUCTION BY MET
Page 535 and 536:
PP-III-52CATALYTIC UPGRADING OF PRO
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PP-III-53CATALYTIC CONVERSION OF FI
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PROCESS FOR THE PRODUCTION OF BUTYL
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PP-III-55been previously fixed and
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PP-III-56The influence of reaction
Page 545 and 546: PP-III-57sample does not contain so
Page 547 and 548: PP-III-58The re-activation of the e
Page 549 and 550: PP-III-59The aim of this work is th
Page 551 and 552: PP-III-61BIODIESEL FROM MICROALGAE
Page 553 and 554: DEVELOPING MICROFLUIDIC DEVICE WITH
Page 555 and 556: THREE-PHASE DIRECT OILS HYDROGENATI
Page 557 and 558: Co-BASED CATALYSTS FOR THE HYDROLYS
Page 559 and 560: PP-III-65KINETIC STUDY OF THE CATAL
Page 561 and 562: PP-III-66PRODUCTION OF HYDROGEN AND
Page 563 and 564: PP-III-67ENHANCED GASIFICATION OF P
Page 565 and 566: PP-III-68INFLUENCE OF SPILLOVER ON
Page 567 and 568: PP-III-69AEROBIC OXIDATIVE COUPLING
Page 569 and 570: PP-III-70MECHANISMS FOR CHEMICAL RE
Page 571 and 572: PP-III-70SBS molecules and increase
Page 573 and 574: PP-III-71and as a resut, could enha
Page 575 and 576: PP-III-72conversion). Al 2 O 3 /PSS
Page 577 and 578: PP-III-73SBA50TiSBA% Transmittance5
Page 579 and 580: PP-III-74stove heating. Another par
Page 581 and 582: PP-III-75TG [%]0-10-20-30380°C400
Page 583 and 584: PP-III-76The elementary version of
Page 585 and 586: PP-III-77thermodynamically enhanced
Page 587 and 588: PP-III-78GFC textileStructuringmeta
Page 589 and 590: PP-III-79All the prepared spinel-ox
Page 591 and 592: PP-III-80Our new process is polluti
Page 593 and 594: PP-III-81Fig. 1. Scheme of the biog
Page 595: PP-III-82Pic. 1 Pic. 2Pic. 1. Schem
Page 599 and 600: CENTENO Felipe OrlandoNúcleo de Ex
Page 601 and 602: FLID Mark RafailovichScientific Res
Page 603 and 604: HOSEN Mohammad AnwarUniversity of M
Page 605 and 606: KOZLOVA EkaterinaBoreskov Institute
Page 607 and 608: MAKARSHIN Lev LvovichBoreskov Insti
Page 609 and 610: ONSAN Zeynep IlsenDepartment of Che
Page 611 and 612: REBOLLAR MoisesInstituto De Investi
Page 613 and 614: SHEIKH Munir AhmedTraining and Staf
Page 615 and 616: SULMAN Esfir MikhailovnaTver Techni
Page 617 and 618: ZHAPBASBYEV Uzak KairbekovichKazakh
Page 619 and 620: OP-I-3 Pécar D., Gorsek A.COMPARIS
Page 621 and 622: OP-II-3Kucherov A.V., Finashina E.D
Page 623 and 624: OP-III-A-9 Rasrendra C.B., Girisuta
Page 625 and 626: PP-I-9Bykov V., Tsybenova S.B.DYNAM
Page 627 and 628: PP-I-43 Pechenegov Y.Y., Kuzmina R.
Page 629 and 630: PP-II-10 Basov N.L., Oreshkin I., T
Page 631 and 632: PP-II-45 Stepanek J., Koci P., Kubi
Page 633 and 634: PP-III-19 Fedorova Z.A., Danilova M
Page 635 and 636: PP-III-53 Pölczmann G., Valyon J.,
Page 637: XIX International Conference on Che
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