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Page 1: Modification & Application of Borate Zirconia Catalyst

05 May 2006 MTech IIT KGP 1

MODIFICATION & APPLICATION OF BORATE ZIRCONIA CATALYST

Ranjeet Kumar04CH6022

Under the guidance of

Dr. Sonali SenguptaDepartment of Chemical engineering

IIT Kharagpur

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Contents….

IntroductionLiterature surveyExperimentsMesoporous borate zirconiaCharacterizationConclusionReferences

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Contents….

IntroductionLiterature surveyExperimentsMesoporous borate zirconiaCharacterizationConclusionReferences

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• Overall catalyst market is around $10 bn.• And revenue generated by processes using catalysts exceeds the catalyst market probably by factor between 100 and 1000, i.e. is somewhere between $1.000 and 10.000 billion

Fig: 1. Catalyst market total around $10 bn and its division into different application

Slight improvement in catalyst performance can lead to big saving in RM & energy.

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Importance of Alkylation Reactions

Used in• Pharmaceuticals, Agrochemicals,

• Resins, Additives,

• Polymerization inhibitors, Antioxidants

• Petroleum refining

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• Heavy environment pollution

• Troublesome product recovery & purification

• Catalysts cannot be reused

• Lower stability at higher temperature.

• Poor selectivity

• Use of expensive acid-resistant MOC

Alkylation reaction with solid catalysts are becoming emerging field in catalysis

Problems with Friedel-Craft alkylation---

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Objective:- To search an environmental friendly process to produce ortho-alkylates

with high selectivity

>> OPTIONS ARE:-

ZEOLITES

CATION EXCHANGE REGINS

» unstable at higher temperature

ZIRCONIA CATALYST

» its high acidity favors C-alkylation.

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Borate zirconia

• B2O3/ZrO2 catalyst (30mol% B) is reported as a superacid catalyst

suitable for isomerization of butane & pentanes.

• AlCl3 and borate zirconia had shown comparable performance for

Friedel-Craft acylation & beckman rearrangement of cyclohexanone

oxime.

• Comparable performance with heterogeneous catalysts like zeolite

H-beta and sulphated zirconia.

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Contents….

IntroductionLiterature surveyExperimentsMesoporous borate zirconiaCharacterizationConclusionReferences

IntroductionLiterature survey

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Literatures on BZ

• No literature is available for preparation of ortho-xylene

using heterogeneous catalysts

• Activity & selectivity of zirconia based catalysts are very

sensitive to the method of preparation & heat treatments.

• Most of the studies have been carried out using large

quantities of the catalyst, and the effect of parameters

need to be addressed.

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Contents….

IntroductionLiterature surveyExperimentsMesoporous borate zirconiaCharacterizationConclusionReferences

IntroductionLiterature survey

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ZrOCl2 + H2O. . ..

8 ZrOCl2 clear solution

Addition of NH3

8

Till pH = 10

Precipitate ofZr(OH)4

Zirconium hydroxide was filtered Washed with hot water

Zr(OH)4 was then dried

Immersed in boric acid solution Heated to dryness Calcined

Preparation of BZ

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ZrOCl2 + H2O. . ..

8 ZrOCl2 clear solution

Addition of NH3

8

Till pH = 10

Precipitate ofZr(OH)4

Zirconium hydroxide was filtered Washed with hot water

Zr(OH)4 was then dried

Immersed in sulfuric acid solution filtered Dried Calcined

Preparation of SZ

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Reactants Reaction hr. Catalyst % conversion of MeOH

Phenol +methanol

4 hours BZ 2.205

Phenol +methanol

8 hours BZ 14.186

Toluene +methanol

4 hours BZ 5.577

Two different systems of reactions were investigated in batch reactor :-1) Phenol + MeOH –

2) Toluene + MeOH –

Reaction temp was 250°C

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Maximum temp attainable in this reactor is 300°C

Reactor set-up

Fig.- 1, reactor and controller

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Fig.-2, stirrer & vessel

Reactor set-up…

Capacity of the vessel is 260 ml

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• Alkylated product may increase by modifying reaction

conditions.

• Max temp is main constraint, reacton time may be

increased to get good result.

• Catalyst may be unsuitable for the desired reaction.

• Catalysts prepared above were microporous and may be

unsuitable for large molecule like benzene or phenol.

Microporous materials – pore size less than 2 nm (20 A°)

Reasons for low conversion may be

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Mesoporous catalyst with wider opening may be more suitable for alkylation of phenol & toluene.

Forward path >>>

Pore size Type of material

< 2 nm microporous

>2 nm & < 50 nm mesoporous

>50 nm macroporous

Table - 2,IUPAC definition for materials on the basis of pore size

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Contents….

IntroductionLiterature surveyExperimentsMesoporous borate zirconiaCharacterizationConclusionReferences

IntroductionLiterature survey

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Literatures on Mesoporous zirconia catalyst

• No literature is available on mesoporous borate zirconia.

• Mesoporous sulphated zirconia and other mesoporous catalysts are

reported and are useful for alkylation reactions. [7], [8], [9], [11].

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Contents….

IntroductionLiterature surveyExperimentsMesoporous borate zirconiaCharacterizationConclusionReferences

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Preparation of Mesoporous BZ

• Co-operative nucleation of molecular inorganic solution (I), with

surfactant molecules (S).

• Two different surfactants were selected for searching/standardizing

the preparation method ---

1) sodium lauryl sulfate (C12H25NaO4S) (SLS)

2) tetradecyltrimethylammonium bromide (C17H38BrN)

(TTBr or Cetrimide)Acid percolation in mesoporous materials, neutral templating are other methods for mesoporous catalyst preparation

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In this case I = Zirconium Oxychloride + Water + Borax S = SLS / TTBr + Water

Steps of preparation: - a) preparation of solution

b) aging

c) filtration

d) washing

e) calcinations/extraction

More the hours of aging better is the catalyst

Preparation of Mesoporous BZ

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Trials for standardizing the preparation method

Zr : SLS : B : H2O SA m2/g

1 0.3 0.05 500 75.53

1 0.3 0.05 750 NA

1 0.3 0.05 1000 83.26

1 0.3 0.05 1250 NA

1 0.3 0.05 1500 86.70

Trial 1:-

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Zr : SLS : B : H2O SA m2/g

1 0.2 0.05 500 37.00

1 0.2 0.05 750 43.80

1 0.2 0.05 1000 NA

1 0.2 0.05 1250 NA

1 0.2 0.05 1500 85.53

Trial 2 :-

Since the range of surface area was not so wide so Zr : Sufactant : B : H2O :: 1 : 0.3 : 0.05 : 1000 was taken as base for further trials.

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• Trials were done by changing surfactant, instead of SLS,

cetrimide was used.

• Instead of calcinations extraction of aged precipitate with

ethanol plus sodium acetate solution was done.

• Aging hours were increased from 72 hours to 120 hours.

• Instead of making one solution of S & I, two separate

solutions were prepared and mixed drop wise.

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Contents…

IntroductionLiterature surveyExperimentsMesoporous borate zirconiaCharacterizationConclusionReferences

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Elemental analysis of prepared catalyst

Energy Dispersive X-Ray Spectrometer (EDS) was done in CRF lab –

>>Test confirmed the presence of Zr, O.

It failed to detect the presence of B.

>>> Presence of B was confirmed by Atomic Absorption Spectrometry

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XRD

XRD of MBZ

0

50

100

150

200

250

0 1 2 3 4 5 6 7 8 9 10

2 theta

Fig.:- XRD pattern of MBZ shows a peak at 3°.

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pore dia, nm Pore vol, ml/g % Pore vol, ml/g %

Under 6 0.02806 41.89 0.02301 37.91

6-8 0.00561 8.37 0,00559 9.21

8-10 0.00308 4.60 0.00318 5.24

10-12 0.00347 5.18 0.00274 4.51

12-16 0.00379 5.66 0.00368 6.06

16-20 0.00384 5.73 0.00424 6.98

20-80 0.01455 21.72 0.01484 24.45

Above 80 0.00459 6.85 0.00342 5.64

TOTAL 0.06699 100 0.06069 100

Adsorption

Reading from pore size analyzer

Desorption

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Adsorption isotherm

The adsorption isotherm is type IV IUPAC classification with hysteresis, which Indicate a mesoporous material.

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Surface area & pore size distribution

Apparatus used was – Coulter’s SA3100 for SA & pore size

analysis.

SMARTSORB-90 for SA

Mesoporous Microporous

SA – 310 m2/g 85-115 m2/g

Pore volume – 0.23 cm3/g 0.09-0.12 cm3/g>>> An excellent surface area (310 m2/g) was obtained by using separate

solution of S ( Cetrimide ) & I, 72 hr aging, and extraction.

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• Reaction was carried out in a flow reactor at 450°C over MBZ

catalyst, reactants were toluene and methanol.

• Reaction mixture was analyzed in GC, retention time of

product confirmed presence of o-xylene.

•Conversion of methanol was about 30%.

Reaction with MBZ

.>>>>

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Flow reactor

>>>>>

preheater

reactor

condenser

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conclusions

• Surface area of prepared catalyst is 310 m2/g, it is highest among

mesoporous zirconia catalysts.

• Conversion of methanol is about 30% which may be increased by

searching optimum reaction conditions.

• Large pores will allow the use of bulky oxidants in fine chemical

preparation.

• Catalyst has shown its activity in alkylation reaction.

• It may open a path to produce many fine chemicals.

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[1] Sonali Sengupta, G. D. Yadav, Yogeeta B. Jadhav (2003), “Novelties of kinetics and mechanism of liquid–liquid phase transfer catalysed reduction of p-nitroanisole to p-anisidine”, Chemical Engineering Science, vol 58 , p 2681-1689.

[2] Sonali Sengupta, G. D. Yadav, Yogeeta B. Jadhav, (2003), “Selectivity engineered phase transfer catalysis in the synthesis of fine chemicals: reactions of p-chloro- nitrobenzene with sodium sulphide”, Journal of molecular Catalysis A: Chemical, vol 200, p 117-129.

[3] Kusum M. Malshe, Pratap T. Patil, Shubhangi B. Umbarkar, Mohan K. Dongare (2004), “Selective C-methylation of phenol with methanol over borate zirconia solid catalyst”, Journal of Molecular Catalysis A : Chemical, vol 212, p 337–344.

[4] Ullman’s Encyclopedia of Industrial chemistry, vol. A 19, fifth ed.,(1989), p313.[5] S. Velu, C.S. Swamy, (1996), “Selective C-alkylation of phenol with methanol over

catalysts derived from copper-aluminium hydrotalacite”, Applied Catalysis A : General, vol 145, p 141-154.

[6] Takako Funamoto, Takamasa Nakagawa, Kohichi Segawa, (2005), “Isomerization of n-butane over sulfated zirconia catalyst under supercritical conditions”, Applied Catalysis A:General, vol 286, p 79-84.

[7] Yin-Yan Huang, Timothy J. McCarthy, Wolfgang M.H. Sachtler(1996),”Preparation and catalytic testing of mesoporous sulfated zirconium dioxide with partially tetragonal wall structure” Applied Catalysis A:General, vol 148 (1996) p 135-154.

References

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[8] Yinyong Sun, Lina Yuan , Shengqian Ma, Yu Han, Lan Zhao, Wei Wang, Chang-Lin Chen, Feng-Shou Xiao(2004), Improved catalytic activity and stability of mesostructured sulfated zirconia by Al promoter, Applied Catalysis A: General, vol 268, p 17-24[9] Cornelia Breitkopf , Arnd Garsuch, Helmut Papp (2005), “Structure– activity relationships for sulfated zirconias — comparison of mesoporous samples based on organic precursors”, Applied Catalysis. A: General, vol 296, p 148-156.[10] Huiyuan Gao, Jerry Y. S. Lin, Baoquan Zhang (2005), “Electroless plating synthesis, characterization & permeation of Pd-Cu membranes supported on ZrO2 modified porous stainless steel”, Journal of Membrane Science, Vol 265, Issues 1-2, p 142-152[11] Yinyong Sun, Lei Zhu, Huijuan Lu, Runwei Wang, Sen Lin, Dazheng Jiang, Feng-Shou Xiao (2002), “Sulfated zirconia supported in mesoporous materials”, Applied Catalysis. A: General,vol 237 p 21–31.[12] Daniela Terribile, Alessandro Trovarelli,*, Jordi Llorc, Carla de Leitenburg, Giuliano Dolcetti (1998) “The preparation of high surface area CeO2±ZrO2 mixed oxides by a surfactant- assisted approach”, Catalysis Today, vol 43, p 79-88.[13] G. Pacheco , E. Zhao , E. Diaz Valdes, A. Garcia, J.J. Fripia (1999), “Microporous zirconia from anionic and neutral surfactants”, Microporous and Mesoporous Materials, vol 32 p 175–188.[14] Debra J. McIntosh, Ronald A. Kydd(2000), “Tailoring the pore size of mesoporous sulfated Zirconia” Microporous and Mesoporous Materials, vol 37, p 281–289

References…..

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Thanks


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