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16Journal of Siberian Federal University. Chemistry 3 (2013 6) 221-229
УДК 547.313.4 : 542.943-92'7.002.67
Products ofHomogeneous Two-Stage Oxidation of 1-Butene to Butanone with O2 Over the Catalyst Pd + Heteropoly Acid
Viktor F. Odyakov and Elena G. Zhizhina*
Boreskov Institute of Catalysis, 5 Lavrentieva, Novosibirsk, 630090 Russia
Received 27.04.2013, received in re-vised form 18.06.2013, accepted 24.0Si.2013
Oxidation of 1-butene to butanone in the presence of homogeneous catalyst Pd + HPA (H12P3Mo18V7O85) followed by regeneration off the catalyst with O2 proceeds with selectivity 9)7.5%. ¡Side products of the process are ace tic acid (1.4 %) and condensed compounds C7H1202, C8hi14Ct2, C6H602, and C8H10O2 (total 1.1 %). In the course of the catalyst rogeneration at 170 °C under O2 pressure, the compounds C6-C8 are completely/ oxidiucd to CO2 and acetic acid. n-Butanal is absent in the re action products, that permits readily to separate butanone as a water aueotrope from the reduced catalyst.
Keywords: Oxidation of 1-butene to butanone, homogeneous catalyst Pd + HPA, reaction products.
Introduction
The processes of oxidation of lower tlkenes C2-C4 to carbonyl compounds witli dioxygen by reaction (1) arerf gneat practical importance:
CH2=CHR + h/2 O2 ——— OH3OOR. (1)
Here R = H, CH3, or C2H5. Io thee late i950s the Wacker company had nuggested for such processes a homogeneous catalyse, which whs ate aqueous sotution of PdCl2 + CuCl2 [1, U], CuCl2 here is a reversible oxidant, which reduced form is readily oxidized with dioxygen. Such catalyst had a high concentration of chlorides (up to 2 M), that led to formation of toxic chloroorganic side products. Their amount strongly increased in the series C2 (ca. 2 % [3]) < C3 (ca. 4 %) < C4 (> 6 %) [2, 4]. Amount of chloroorganics strongly increased also at elevated temperature [4] but decreased after dehydrochlorination (see later). Besides, various amounts of aldehydes, RCH2CHO, were formed together with ketones, CH3COR. When propene or 1-butene were oxidized, yield of RCH2CHO varied from 3 to 18 % [2, 5]. Only in oxidation of 2-butene, butanone was the single reaction product [1]. Now
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* Corresponding author E-mail address: [email protected]
only the oxidation of C2H4 to CH3CHO is implemented with the Wacker catalyst on industrial scale [6].
To eliminate formation of chlorinated products in oxidation of lower alkenes Ce-C4 wieh dioxygen in the presence of any Pd-containing catalysts, in tir mid-19P0s Matveev and co-aurhors suggested chloride-free Pd + heteropoly acid catalysts. In th(s case, aqueous solutions of the Keggin type Mo-V-P heteropoly acids, H3+xPMo12-xVxO40 (HPA-x, 2 < x < 6), weee rtvarsible oxidants [7]. The reversibility of oxidative properties oJT the HPA-x solutions favorably distinguishes them from non^eveasible oxidants, such as CrO3, KMnO4, or NaIO4. To provide maxamal celectivaty aad nonexplosiveness, processes (1) in the presence of such catalysts are carried out in two steps (2) + (3) in separate reactors:
m/2 CH2=CH-R + HPA-x + m/2 H20 Pd" > ln/2 CH3COR + HmHPA-x, (2)
HmHPti-x P iy"4 r+2 -2 HPA-x P m"2 H20. (3)
At oxidation of lower alke nes, the target products of reaction (2), CH3COR, ane oasily separated from the reduced Pd + HmHPA-x catalyst (ry evaporatioa. At step (33), that is common for sll processes (1), the catalyst is regenerated at 130-145°C under O2 or air pressure [8].
The chloride-free Pd + HPA-x catalysts were highly selective (97-99 %) in oxidation of alkenes C2-C4 to CH3COR [7]. In particular, the selectivity of 1-butene oxidation to butanone exceeded 97 %. However, it was later found that thermostability of the aqueous solutions of Keggin-type HPA-x was not high. So, the often used 0.2 M HPA-4 solution gradually evolved vanadium-containing deposits during operations at t > 140 °C [9]. For oxidation of 1-butene to butanone, later we have developed catalysts Pd + HPA-x' based on modified non-Keggin HPA-x' solutions, HaPzMoyVxOb (HPA-x', 1 < z < 3; 8 < y < 16; 4 < x' < 12; a = 2b-6y-5(x' + z); 40 < b < 89). Certain solutions from this series had high concentration of vanadium (2.0-2.2 M) and improved thermostability [10]. Among them, 0.25 M solution of total composition H12P3Mo18V7O85 (HPA-7') was the most promising. It was recommended by us as a main components of the homogeneous Pd + HPA-7' catalyst for the 1-butene oxidation to butanone [10].
Selectivity of this process over the Pd + HPA-7 ' catalyst is as high as that over Pd + HPA-x catalysts. At that, high concentration of vanadium in the new catalyst provides a 3 -fold higher productivity in the total process (1). High thermostability of the Pd + HPA-7' catalyst allows us readily to regenerate this catalyst by reaction (3) at higher temperature (160-170 °C) [11]. This also increases efficiency of the catalyst. We have demonstrated that the Pd + HPA-7' catalyst is capable of stable operation for at least several months of continuous work.
Kinetics of the 1-butene oxidation to butanone in the presence of the Pd + HPA-x and Pd + HPA-x' catalysts was reported in our previous works [11, 12]. Physicochemical properties of the HPA-x' solutions were thoroughly discussed in [13]. In the present work, we give detailed information on products of the 1-butene oxidation over the new Pd + HPA-7' catalyst.
Experimental
The 0.25 M solution of H12P3Mo18V7O85 (HPA-7') was synthesized by the method described elsewhere [14]. Palladium was introduced into the HPA-7' solution as PdSO4 to obtain the concentration [Pd] = 6x103 M.
For oxidation reaction (2), we used 99.6 % 1-butene from Budyonnovsk Chemical Plant (Russia) having only 2-butenes and n-butane as admixtures. 1-Butene used in our work contains no butadiene or acetylenes that hinder oxidation of alkenes in the presence of Pd. The oxidation of 1-butene was performed in a shaken thermostated reactor at 30-70°C for 15-17 min to the complete reduction of the catalyst solution [12]. The resulting butanone was evaporated from the reduced catalyst as a water azeotrope containing 89 % of butanone and boiling at 73.4°C [15]. Degree of the butanone evaporation (ca. 97 %) was controlled by the GLC method (see later). Regeneration of the catalyst with dioxygen by reaction (3) was carried out for 20 min in a stainless steel autoclave at 170°C and PO = 4 atm [8].
The reaction products were analyzed by the GLC method using a Tsvet 500 chromatograph with glass capillary column (40 m x 0.25 mm) and flame-ionization detector. Methyl silicone rubber SE-30 was used as a stationary phase, and helium as a carrier gas. The analysis was made via thermoprogrammed heating from 60 to 160 °C with a ramp rate of 20°/min. The chromatograms were recorded and analyzed using a Mul'tikhrom computer system. In the study, we have analyzed: a) the reduced Pd + HmHPA-7' catalyst solution containing products of reaction (2); b) the condensate of the products evaporated from this catalyst; c) the Pd + HPA-7' catalyst solution oxidized by reaction (3).
For identification, the reaction products were analyzed also by GC-MS method using a capillary quartz column (30 m x 0.25 mm) in the temperature range of 50-200 °C. Non-polar methylpolysiloxane CP-SIL 8 (Chrompack) was used as a stationary phase intended for chromato-mass spectrometers.
Results and Discussion
The composition of products of the 1-butene oxidation in reaction (2) in the presence of the tested chloride-free Pd + HPA-7' catalyst is presented in Table 1. For comparison, Table 1 shows also products of oxidation of butene-butane fractions in the presence of other catalysts. In the presence of the Wacker PdCl2 + CuCl2 catalyst, content of the side chlorine-containing organics was > 6 % [2, 4]. In the presence of the Catalytica' s catalyst PdCl2 + NaxHPA-x containing acidic salts of HPA-x (x = 3-6) and small amount of HCl, yield of chlorinated products was only 0.15 % [18]. However, even so small amount of chloroorganics hampered purification butanone from by-product, n-butanal (see later).
With our chlorine-free Pd + HPA-7' catalyst, no chloroorganics is produced, and selectivity of butanone formation attained 97.5 %, with the total amount of side products not exceeding 2.5 %. However, composition of side products significantly differs from composition of them in the presence of other catalysts.
In our case, the main side product of the 1-butene oxidation is acetic acid (HOAc), its content attains to 1.4 %. Other side products, accounting for ca. 1.1 %, are C7H1202 (I, 0.3 %), C8H1402 (II, 0.1 %), C6H602 (III, 0.3 %), and a mixture of C8HW02 isomers (IV, 0.4 %). Note that n-butanal (n-C3^CHO) is not found among these products, thus indicating that its content in the products mixture does not exceed 0.05 %.
It is known that HOAc is formed at oxidation of butanone with vanadium(V) compounds in strongly acidic media [19]. Our catalyst based on the HPA-7' solution is characterized indeed by high acidity and has pH0 < 0. Acidity of our catalyst is comparable with acidity of concentrated solutions of heteropoly acids as H3PW12O40 and H4SiW12O40 [20], and far exceeds acidity of other catalysts intended for oxidation of n-butene fractions with dioxygen. For comparison, pH values of the Pd-containing catalysts based on NaxHPA-x [21] or CuCl2 [2] varied from 0.4 to 1.0.
Table 1. Composition of products of w-butene fractions oxidation in the presence of various homogeneous Pd-containing catalysts
Patent holder Catalyst composition Total w-butenes part in C4 fraction, % " Selectivity on butanone, % Side products, % Refs.
Wacker-Chemie, BRD PdCl2 + CuCl2 + HC1; 94 111 85-88 w-butanal: 2-4; 3-chloro- and 3,3-dichlo- [2]
[CI ] = 1.2-2.0 M ro-2-butanone: 4-6; diacetyl 6 and other
Cl-free compounds: 2-3.5
BashNIIPN, USSR PdCl2 + CuCl2 + Cu(OAc)2 + 1202 70-90 acetone; 3-chloro- and 3,3-dichloro-2-buta- [16]c
HOAc; none; diacetyl6; fert-butanol11
[CI ] = 0.6-0.75 M
Catalytica of Mountain View, PdCl2 + HC1 + NaxHPA-x; 68 ^ 93.4 AcOH: 2.9; w-butanal: 0.63; [18]
USA [CI ] = 0.035 M C2H5CHO + AcH: 0.57; Cl-derivatives: 0.15;
1- and 2-butanols: 0.23; other ketones:
0.09; nonvolatile compounds: ~2.0
Institute of Catalysis, SB PdS04 + HPA-x'; gg g m, a4 97.5 AcOH: 1.4; 3-methyl-2,4-hexanedione (I): 0.3; the pre-
RAS, Russia [CI ] = 0 3-methy 1-2,4-heptanedione (II): 0.1; C6H<A sent work
(III): 0.3; isomers of C8H10O2 (IV): 0.4
" All C4 fractions contain other components: al n-butane; a2 «-butane, ¿so-butane, and ¿so-butene (ca. 10 %) [17]; «-butane, ¿so-butane, trace amounts of C3, butadiene, and C5. '"Including 99.6 % of 1-butene and 0.2 % of 2-butenes. 6 Product of 3,3-dichloro-2-butanone hydrolysis.
' In [16], only qualitative composition of side oxidation products was reported. " It was formed through hydration of ¿so-butene presented in the C4 fraction.
As for other side products, compound II with high probability is 3-methylheptane-2,4-dione (C8), and compound I is 3-methylhexane-2,4-dione (C7). Then, isomers IV, being hydrogen-poorer in comparison with ß -diketone II, can be interpreted as products of dehydrogenation or dehydrocyclization of the diketone. In that case, compound III is the product of ß-diketone C6H10O2 dehydrogenation or dehydrocyclization. But this ß-diketone is not detected in our study, probably due to its low concentration. Note that ß-diketone C6H10O2 is a lower homologue of ß-diketones II (C7H1202) and I (C8H1402),
We believe that products of the 1-butene oxidation had initially contained also «-butanal, which further turned into compounds II, I, IV, and III according to Fig. 1. Earlier, when C4 fractions contained 1-butene were oxidized in the presence of other catalysts such as Pd + NaxHPA-x or PdCl2 + CuCl2, «-butanal was always detected in products of oxidation. Thus, in the presence of the PdCl2 + NaxHPA-x catalyst, products of oxidation of the fraction with ratio 1-butene : 2-butenes ~ 0.5 contained 0.63 % of «-butanal and no ß-diketones I and II [18]. Taking into account the chemical properties of «-butanal
n-<C,H7CH0
V
O OH
-2H
[o]
O (II)
C2H5CHO
V
O OH
- 2H
[o]
( I)
CH3CH0
V
O OH
- 2H
Pd r*
[*]
-2H
a o >d:'
Pd+ [*] -2H+
a o .Pd''
[O] [**]
[O] [**]
CgHioO (IV )
C6H602 (III)
Fig. 1. Formation of side products in reaction (2): [*] The Pd11 complex is in equilibrium with P-diketone and contains two P-ketoenol ligands. (Only one ligand is shown in the Sclieme). Every ligand detaches H+ at the complex formation with Pd11. [**] Every ligand loses 3 H atoms at the oxidative decomposition of the Pd11 complex
0
0
0
and composition of the observed products of reaction (2), we think that a part of «-butanal, «-C3H7CHO, is subjected to partial oxidative degradation [22, 23] yielding C2H5CHO and CH3CHO (Fig. 1). Further each of the three aldehydes condenses with butanone [24, 25] forming ß-hydroxyketones ('aldols') with composition CH3COCH(CH3)CH(OH)R, where R = «-C3H7, C2H5, or CH3. These 'aldols' contain the secondary alcohol group -CH(OH)-.
As was shown in [26], secondary alcohols are readily oxidized to ketones in the presence of the catalytic system Pd + HPA-x. Hence, the system Pd+HPA-7' would certainly oxidize ß-hydroxyketones to ß-diketones CH3COCH(CH3)COR. It is known that various metal ions, in particular Pd2+, form complexes with enolic forms of ß-diketones, for example, with enol form of well-known acetylacetone, CH3COCH2COCH3, i.e. with CH3C(OH)=CHCOCH3 [27]. However, as the enol forms of ß-diketones shown in Fig. 1 are weak acids, their complexation with Pd2+ in strongly acidic media is reversible. This feature offers to explain why GLC analysis of products of the 1-butene oxidation reveals not all ß-diketones, but only those from them which complexes with Pd2+ are less stable. In turn, ß-diketones are partially dehydrocyclized to form non-identified compounds of type III or IV with a lower content of hydrogen.
In strongly acidic media, the oxidative transformations of «-butanal into lower aldehydes, 'aldols' and ß-diketones shown in Fig. 1 are rather readily. The dehydrocyclization of ß-diketones into compounds III and IV proceeds more slowly. This is the reason why «-butanal, which supposedly was among initial side products of the 1-butene oxidation in the presence of the Pd + HPA-7' catalyst, was not detected in our products of reaction (2).
The C6-C8 compounds from Fig. 1, being less volatile as compared to butanone, are evaporated not completely with butanone. The remaining part of these compounds goes further to the reactor for catalyst regeneration. At ca. 170°C under the O2 pressure, these compounds are gradually oxidized to HOAc and CO2.
Thus, the interaction of the reduced Pd + HmHPA-7' catalyst at step (3) with O2 at high temperature results in its regeneration with simultaneous oxidation of all side products except HOAc. As was revealed earlier, small amounts of HOAc (up to 10 %) do not hinder the 1-butene oxidation at step (2) in the presence of the Pd + HPA-x catalyst. On the contrary, HOAc increases rate of this reaction due to improved solubility of 1-butene in the catalyst [28].
During the long-term cyclic testing via reactions (2) + (3), the amount of HOAc in the solution of catalyst Pd + HPA-7' gradually increases to 8-10 % and then remains at a stationary level, because HOAc begins to evaporate from the reduced catalyst together with butanone. Note also that the real absence of «-butanal in the products of the 1-butene oxidation strongly facilitates separation of butanone from the reaction products. It is known that «-butanal forms an azeotrope with water that boils at 68.0°C and is difficultly separable from the (butanone + water) azeotrope boiling at 73.4°C [15]. Thus, if «-butanal was really formed at the oxidation of «-butenes in the presence of the Pd + NaxHPA-x catalyst, then there was a need to reduce it to «-butanol in a separate reactor [18]. At that, the reduction of «-butanal was accompanied by a partial reduction of butanone to sec-butanol, that indeed decreased total selectivity of the Catalytica butanone process [21].
The use of the Wacker chloride catalyst gave even a more complicated mixture of products of the «-butenes oxidation. The mixture was also treated with dihydrogen in a separate reactor, where both reduction of «-butanal to «-butanol and dehydrochlorination of side 3-chloro- and 3,3-dichloro-
2-butanone to butanone occurred [2]. Since at our 1-butene oxidation over the Pd + HPA-7' catalyst, n-butanal is really absent in the reaction products, there is no necessity of its reduction. This significantly simplifies process (1) of butanone production over the Pd + HPA-7' catalyst developed in our work.
Conclusion
Selectivity of butanone formation at the 1-butene oxidation with dioxygen over the homogeneous Pd + HPA-7' catalyst attains 97.5 %. Side products of this oxidation are acetic acid (1.4 %) and the condensed compounds of C6-C8 series (1.1 %) that are formed in the strongly acidic medium. During regeneration of the catalyst at 170°C and P0 = 4 atm, the C6-C8 compounds are almost completely oxidized to CO2 and HOAc. Small amounts of HOAc in the catalyst solution do not hinder the 1-butene oxidation, since they increase solubility of 1-butene in the catalyst. An important advantage of the Pd+HPA-7' catalyst is the absence of n-butanal in products of the 1-butene oxidation. This considerably facilitates separation of butanone from the reduced catalyst without decrease of total productivity of process (1).
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Продукты гомогенного двухстадийного окисления бутена-1 в бутанон кислородом в присутствии катализатора Pd + гетерополикислота
В.Ф. Одяков, Е.Г. Жижина
Институт катализа им. Г.К. Борескова Сибирского отделения РАН Россия 630090, Новосибирск-90, пр. Академика Лаврентьева, 5
Окисление бутена-1 в бутанон в присутствии гомогенного катализатора Pd + ГПК (Н12Р3Мо18У7085) с последующей регенерацией катализатора кислородом протекает с селективностью 97,5 %. Побочными продуктами процесса являются уксусная кислота (1,4 %) и продукты конденсации С7Н12О2, С8Н14О2, С6Н6О2 и С8Н10О2 (в сумме 1,1 %). В ходе регенерации катализатора при 170 °C под давлением O2 соединения C6-C8 полностью окисляются до CO2 и уксусной кислоты. В продуктах реакции н-бутаналь отсутствует, и это позволяет легко отделить от восстановленного катализатора бутанон в виде азеотропа с водой.
Ключевые слова: окисление бутена-1 в бутанон, гомогенный катализатор Pd + гетерополикислота, продукты реакции.
