Sastri, M. V. C.

Varadarajan, T. K.

Viswanathan, B.

English

NOPR

Indian Journal of ChemistryVol. lCA, November 1976, pp. 851-854Dehydrogenation of Isopropyl Alcohol on Zinc Molybdate (ZnMo04)T. K. VARADARAJAN, B. VISWANATHAN & M. V. C. SASTRIDepartment of Chemistry, Indian Institute of Technology, Madras 600036Received 17 February 1976; accepted 1 May 1976The vapour phase decomposition of isopropyl alcohol on ZnMoO. and on ZnMoO. dopedwith various amounts of Li.O has been studied in the temperature range 300-350°at atmosphericpressure in a flow type reactor. From kinetic and electrical conductivity measurements andfrom studies of the effect of acetone, water and hydrogen separately to the feed, it is concludedthat the desorption of acetone (an acceptor step), is normally the rate-controlling step in thedehydrogenation reaction. However, on surfaces with a high Fermi level (e.g, pure ZnMoO.),the adsorption of alcohol by a donor mechanism becomes rate-determining in the same re-action.INtwo earlier papers--" studies on the catalyticdecomposition of isopropyl alcohol on defectzinc oxide and manganese molybdate werereported. It was shown that the dehydrogenationand dehydration reactions occurred independentlyof each other involving different types of surfacecharacteristics and that only the dehydrogenationreaction seemed to involve electron exchangesbetween the catalyst and the adsorbed substrate.The rate determining step of the dehydrogenationprocess also seemed to depend on the nature of thecatalyst. These conclusions receive further substan-tial support from the results of studies reported inthis paper on zinc molybdate.Materials and MethodsZinc hydroxide was precipitated from zinc nitrateby adding ammonia and the oven-dried precipitateheated for 48 hr at 150" to yield anhydrous ZnO.Molvbdic trioxide was obtained bv thermal de-composition of ammonium paramolybdate at 520°.Zinc molybdate was prepared by co-precipitationfrom a mixed solution of ammonium paramolybdateand zinc nitrate by dropwise addition of liquorammonia and heating the oven-dried precipitate for48 hr at 150° followed by 12 hr at 600°. The zinccontent in the final product was estimated by EDT Atitration. Its X-ray diffraction pattern conformedto that reported- for ZnMoO,. Its identity wasalso confirmed by IR spectrums,Doping of zinc molybdate with Li20 was carriedout by the addition of the calculated amount oflithium nitrate to a mixed solution of zinc nitrateand ammonium paramolybdate prior to co-pre-cipitation. The lithium content was estimatedindependently by analysis.The preparation of pure reagents and the proceduresfor carrying out the reaction studies in a flow-typeglass reactor and for making electrical measurements'[and adsorption measurements on the catalyst havealready been described'', The decomposition studieswere carried out on ZnO, ZnMoO~, and Li-dopedFig. 1 - Variation of electrical conductivity of zinc molyb-date with temperature in air and in hydrogenZnMoO, in the temperature range 300-350° and onMo03 in the range 230-275°.ResultsElectrical measurements - Seebeck coefficientmeasurement showed ZnMoO, to be an n-type semi-conductor. The variation of electrical conductivity(0") of ZnMoO, as a function of temperature in airand in hydrogen is shown in Fig. 1. The activationenergy for electrical conduction calculated from theseTABLE 1 - ELECTRICAL CONDUCTIVITY VALUES ATDIFFERENT TEMPERATURESTemp. ZnMoO.°Ca xl 08 (ohm"! crrr+) values ofZnMoO.+l·5 mole % ZnMoO.+3·0mole %Li:O Li.O299 2·044 0·662 0·638326 3·716 1-104 0·754348 7·059 1·813 1-160370 10·210 3·624 1·450392 15·340 6·304 2·786412 23·320 11·040 4·062432 30·590 18·120 6·094851INDIAN J. CHEM.• VOL. 14A. NOVEMBER 1976plots is 0·50 eV in hydrogen as against 0·62 eV in air,thus showing a rise in the Fermi level of the catalystas a result of hydrogen adsorption.The data in Table 1 show that the electricalconductivities of Li-doped samples at various tem-peratures are lower than those of the undopedmolybdate thus confirming the lowering of theFermi level of ZnMoOt as a result of doping withLi+ ions.Adsorption measurements - The adsorption iso-therms of isopropyl alcohol, acetone and water onZnMoOf,are shown in Figs. 2 and 3 and the Cla-peyron heats of adsorption deduced therefrom aregiven in Table 2. It is seen from Table 2 that thecomputed isosteric heats of adsorption of isopropylalcohol and acetone are less than the heats of vapori-zation at their boiling points but higher than theheats of vaporization reckoned at the temperaturesat which the reaction was studied.The surface acidity of the ZnMo04 catalyst wasestimated by measurement of ammonia adsorptionat 320° and 30 torr pressure. The fresh catalystadsorbed 1·51 mg NHa/g of the catalyst, whereasthe catalyst containing presorbed hydrogen (1·3 tug]g) took up ,....,2·4 mg NHa/g thus showing a markedincrease in acidity as a result of hydrogen adsorption.-- Acetone- - - lsopropy IAlcohol_ ~-l72'C,.(7",0,"""//jJ//I/IdIIZ0·3co!~to~ 0·2••1lIoFig. 2 - Adsorption isotherms of isopropyl alcohol andacetone on zinc molybdatei,!I_-,>-0- 3:}Q·C :IA.._-o...-·320·C!_____ -_~3.40"c50 60':0 30 40Pressure (torr)Fig. 3 - Adsorption isotherms of water on zinc molybdate10852TABLE 2 - HEAT OF ADSORPTION OF VARIOUS SUBSTRATESAdsorbate Temp. t:ili ~H:range [kcaljmole) (kcaljmole)(0C)Isopropyl alcohol 170-210 7·9 9·56 (82'3°)0·0 (238°)Acetone 280-370 4·7 7·2 (56·1°)6·5 (100°)0·0 (235°)Water 280-370 12·7 9·7 (100°)9·2 (140°)8·6 (180°)·Computed heat of vaporization values at various tempe-ratures. (Ref.: International critical Tables, Vol. V. p. 138).Decomposition kinetics: Studies on undoped ZnM 00 4and its component oxides - Zinc molybdate catalystwas found to be predominantly dehydrogenating,the selectivity for dehydrogenation being about 85%of the total decomposition. Of the componentoxides. Mo03 was predominantly dehydrating and7047·C60c: 50..'"o~~40:J:e! 30••o~202 3 4 5Contact time (see )Fig. 4 - Concentration-time plots for the dehydrogenation ofisopropyl alcohol on zinc molybdate'l25••20Lc: I~ r~ 15r~; lOri ~sf-%~~~1~~2:=~J~I-L-1.:~~~~Contact time (see )Fig. 5 - Concentration-time plots for the dehydration ofisopropyl alcohol on zinc molybdateVARADARAJAN et al.: DEHYDROGENATION OF ISOPROPYL ALCOHOLTABLE 3 - KINETIC PARAMETERSFOR THE DECOMPOSITIONOF ISOPROPYLALCOHOLCatalyst Dehydrogenation Dehydration SelectivityEapp(dehydrogenation)Ko Eapp Kokcaljmole min-l m-I kcaljmole mirr? m-IZnO 10·9 1·8 X 10' 1·00MoOa 27·0 8·5 X 1010 17-6 2·0 X 10' 0·30ZnMoO, 24·4 4·0 X 108 23·5 3·1 X 10' 0·85TABLE 4 - DECOMPOSITIONOF ISOPROPYLALCOHOLON PURE AND DOPED ZINC MOLYBDATEContact time ZnMoO. ZnMoO. + 0·5 mole % ZnMoO. + 1·0 mole % ZnMoO. + 1·5 mole %(see) Li20 LilO LilO% A 01 B/0% A %B %A %B %A %BTEMP.: 330o±2°0·5 15·0 2·5 22·5 21·5 20·0 18·5 18·5 19·01·0 25·0 4·0 33-0 35·0 29·0 30·0 26·0 33·01·5 35·0 6·0 37'S 41·0 29·0 36·0 31·0 43'52·0 42·0 8·0 38·5 42·0 33·0 38·0 35·0 50'0TEMP.: 350o±3°1·0 32·5 7'5 38·5 44·5 32·0 37·5 32·0 46·01·5 43·5 11·0 40·5 47·0 34·5 41·0 36·5 49'02·0 51·0 13-5 40·S 47·0 35·0 42·0 40·0 52,0(A) refers to dehydrogenation and (B) to dehydration.o with Aclttonltx with Nitrogltnb. with Hydro~n.a with WatltrN;;';(5c••e"'tJ,.,:I:~l"3 2['E'0 .ozFig. 6 - Effect of substrates on the dehydrogenatlOn ofisopropyl alcohol on zinc molybdateN~ 2.5r-----------~~~••2·0tlLe ',5a..o with Anton.x with Nitrogltnb. with Hydrogena with Watltr%~~0~.2~-O~·~4-L-OL.6-L-O~.~-"~~1.LO~Partial prnsur. of Isopropyl AlcoholFig. 7 - Effect of substrates on the dehydration of isopropylalcohol on zinc molybdateTABLE 5 - ACTIVATIONENERGY VALUES FOR DOPEDZnMoO. CATALYSTSMole % LilO dopedwith ZnMoO.Activation energy (kcalrmole)Dehydrogenation Dehydration0·51·01·53·014·316·512·417'024-119·617·230·5ZnO possessed almost exclusively dehydrogenatingactivity. The initial rates of the two reactions werederived from the plots of coneentration vs time(Figs. 4 and 5) and the values of apparent energiesof activation and frequency factors evaluated there-from are given in Table 3.The effects of addition of hydrogen, acetone andwater to the alcohol-feed and of varying the alcoholpartial pressure by dilution with nitrogen are shownin Figs. 6 and 7. It is seen that (i) addition ofacetone has no effect on either of the reactions,(ii) hydrogen enhances both, and (iii) addition ofwater decreases the dehydration rate preferentially.Studies on ZnMoO( doped with Li20 - Typicalvalues of the extents of dehydrogenation and de-hydration as a function of contact time and tem-perature are given in Table 4. The selectivity (fordehydrogenation) of the catalyst doped with 1·5moleper cent LisO was found to be almost 50% of thetotal decomposition as against 80% for pure ZnMoO(.The activation energy for dehydration reaction onLi-doped catalysts (Table 5) is 20± 3·0 kcaljmole853INDIAN J. CHEM., VOL. 14A, NOVEMBER 1976TABLE 6 - EFFECT OF SUBSTRATES ON THE DECOMPOSITION OF ISOPROPYL ALCOHOL ON ZINC MOLYBDATE DOPED WITH1·5 MOLE % LiaO(Temp.: 3300; contact time: 1·0 see)Partial pressureof alcohol(atm) Propylene HydrogenAmount of products formed in 1 hr (moles X 102)HydrogenIn presence of Ns0·50·70·80·92·433·173·433·712'653·103·924·26Propylene Hydrogen PropyleneIn presence of acetone In presence of HI2·323·073·593·882·212'493·253'274-145·205·494·534·765·22which is comparable with that obtained on pureZnMoO.. On the other hand, the value of theactivation energy for dehydrogenation reaction onLi-doped ZnMo04 (14·0 ± 2·0 kcal/mole) is consi-derably lower than that on pure ZnMo04 (24·5kcaljmole). This reveals a difference in the mecha-nism of dehydrogenation reaction on doped andundoped ZnMoO. catalysts.In order to understand this mechanistic difference,the decomposition of isopropyl alcohol was studiedin presence of acetone, hydrogen and nitrogen onzinc molybdate doped with 1·5 mole per cent Li20at 330°. It is seen from the values given in Table 6that as compared with undoped catalyst, additionof acetone decreases the dehydrogenation rate pre-ferentially and the presence of hydrogen enhancesboth dehydrogenation and dehydration rates.DiscussionMechanism of the dehydrogenation reaction - Theadsorption of alcoholby a donor mechanism and thedesorption of acetone by an acceptor processs-" areconsidered to be the two kinetically important stepsof the dehydrogenation reaction. Depending uponthe nature of the catalyst and the position of theFermi level, one or the other of these two steps canbe rate-controlling. From studies of the decom-position of isopropyl alcohol on ZnO catalyst, it hasbeen concluded that the adsorption of alcoholthrough oxygen of the hydroxyl group and thesubsequent rearrangements of adsorbed alcohol isthe rate-determining step", However, on MnMoO.catalyst, the desorption of acetone was found to bethe rate-controlling step. It is evident, therefore,that the rate-determining step is dependent on thenature of the catalyst surface under examination.854It was observed that 011 pure ZnMo04 the reactionwas not inhibited by addition of acetone to the feed.Further, the heat of adsorption of acetone (Table 2)being less than that of either alcohol or water, itfollows that on ZnMoO" the desorption of acetonecannot be rate-controlling in the overall reac-tion.Li-doped ZnMo04 samples have lower conductivityvalues than pure ZnMo04• It is known that addi-tion of monovalent oxides to n-type catalysts lowersthe Fermi level and decreases the concentration ofcharge carriers. Seebeck coefficient measurementshave confirmed this expectation. Consequently,the acceptor step of the reaction sequence (desorptionof acetone) is slowed down to become the rate-determining step of the dehydrogenation reaction.On Li-doped ZnMoO" the overall rate is inhibitedin the presence of acetone as shown by the resultsreported in Table 6. This observation supports theabove conclusion.I..References1. RAJARAM, P., SASTRY, M. V. c.. VISWANATHAN, B. &SRINIVASAN, V., Z. physik. Chem. (Neue Folge), 89(1974), 154.2. VISWANATHAN, B., SASTRI, M. V. C. & SRINIVASAN, V.,Z. pbysik, Chem. (Neue Folge), 79 (1972), 216.3. Low, M' J. D., SHIMIZU, M. & CUSUMANO, J., ]. pbys.Chem., 68 (1964), 1891.4. (a) BROWN, R. G., DENNING, J., HALLETTE, A. & Ross,S. D., Spectrochim. Acta, 26A (1970), 963. (b) CLARK,G. M. & DOYLE, W. P., Spectrochim. Acta, 22 (1966),1441.5. BIELANSKI, A., Catalysis and chemical kinetics (AcademicPress. New York), 1964, 115.6. ZHABROVA, G. M., Chem. Techn. (Berlin), 15 (1963),193.7. KRYLOV, O. V., J. phys. cu«; 39 (1965), 2911.

Dehydrogenation of Isopropyl Alcohol on Zinc Molybdate (ZnMoO4)

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Dehydrogenation of Isopropyl Alcohol on Zinc Molybdate (ZnMoO4)

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