alexa
Reach Us +441414719275
Study of Loading SO<sub>4</sub> <sup>2-</sup> on Sb-SnO<sub>2</sub> Nanocrystal and its Calcination Temperature to Make Solid Superacid SO<sub>4</sub> <sup>and#8853;</sup>/Sb-SnO<sub>2</sub>
ISSN: 2329-6798
Modern Chemistry & Applications
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Study of Loading SO4 2- on Sb-SnO2 Nanocrystal and its Calcination Temperature to Make Solid Superacid SO4 /Sb-SnO2

Xuejun Zhang1,2*, Xiao-Ning Zhang2, Qin-Qin Ran1, Han-Mei Ouyang1, Hui Zhong2 and Han Tao1,2
1Guizhou Province Key Laboratory of Fermentation Engineering and Biological Pharmacy, Guizhou University, Guiyang, China
2School of Brewing and Food Engineering, Guizhou University, Guiyang 550025, China
Corresponding Author : Xuejun Zhang
Guizhou Province Key Laboratory of Fermentation Engineering and Biological Pharmacy
Guizhou University, Guiyang, 550003, China
Tel: 86-851-473-3086
E-mail: [email protected]
Received July 26, 2014; Accepted September 18, 2014; Published September 23, 2014
Citation: Zhang X, Zhang XN, Ran QQ, Ouyang HM, Zhong H, et al. (2014) Study of Loading SO4 2- on Sb-SnO2 Nanocrystal and its Calcination Temperature to Make Solid Superacid SO4 /Sb-SnO2. Mod Chem appl 2:135. doi: 10.4172/2329-6798.1000135
Copyright: © 2014 Zhang X, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Related article at
DownloadPubmed DownloadScholar Google

Visit for more related articles at Modern Chemistry & Applications

Abstract

SO4 2-/SnO2 were reported to be a solid superacid with an acid strength equal to that of SO4 2-/ZrO2. But papers concerning the SO4 2-/SnO2 catalyst have been quite few, because of difficulty in preparation of the oxide gels from its salts SnCl4. A highly dispersed light yellow powder, Sb-SnO2 nanocrystal, was obtained by the synthesis method of “P-CNAIE” and the drying method of “AD-IAA”. The Sb doping made the energy gap of nano-crystalline SnO2 narrower. A saturated solution of ammonium sulfate was dropped into organic solutions containing a fixed amount of Sb-SnO2 nano-powders in different ratio in order to load Sb-SnO2 powder with ammonium sulfate. This method has an outstanding advantage that is the loading ratio of (NH4)2SO4 to Sb-SnO2 can come to very high and no free water causes the aggregation of Sb-SnO2 nano powder. The methods of Differential Scanning Calorimetry (DSC) and Thermogravimetric analysis (TG) demonstrated that the working ratio of Sb-SnO2 to (NH4)2SO4 was 1:1.4 to 1:1.6 wt% and the most favorable calcination temperature for the generation of superficially sulfated groups of Sb-SnO2 particles should fall between 380°C and 400°C. The adsorption reaction of indicator reveals that the solid acid, calcined Sb- SnO2 with a bluish color had a H0 ≤ -14.5 at least.

Keywords
Solid superacid; Stannic oxide; Nanocrystal; Impregnation; Ammonium sulfate; Calcination temperature
Introduction
Acid catalysts, especially superacid catalysts, play a vital role in the chemical industry of our time. Many organic reactions such as esterification, condensation, cracking, alkylation, saturated hydrocarbon isomerization, can be economically and effectively accomplished with the presence of acid catalysts.
In 1979, Hino et al. [1] indicated, for the first time, that the acid strength of the SO4 2−/ZrO2 catalyst is estimated to be H0 (Hammett indicator) ≥ -14.52, one of the strongest solid superacids. Sulfated zirconia (SO4 2/ZrO2) is a typical solid superacid and exhibits a high catalytic activity for the skeletal isomerization of saturated hydrocarbons and other reactions [2-6]. Sulfated tin oxide (SO4 2−/SnO2) was later reported by Matsuhashi et al. [4] to be one of the candidates with the strongest acidity, acid strength of which is almost equal to that of SO4 2−/ ZrO2 at least [7-9]. And SnO2 is more readily available and cheaper than ZrO2 [10].
Matsuhashi et al. [11] concluded in 2001 that the preparation of many solid superacids of sulfated metal oxides commonly underwent three steps: (i) preparation of amorphous metal oxide gels as precursors; (ii) treatment of the gels with sulfate ion by exposure to a H2SO4 solution or by impregnation with (NH4)2SO4; and (iii) calcination of the sulfated materials at a high temperature in air. For the synthesis of solid superacid SO4 2−/SnO2, however, it is difficult to prepare the tin oxide gel precursors from the SnCl4 salts. [11] Hence, the synthesis and application of SO4 2−/SnO2 catalysts are seldom reported.
Herein we propose a novel three-step method for the preparation of solid superacid SO4 2−/SnO2. In contrast to the three-step process proposed by Matsuhashi et al., the present method uses metal oxide crystals, instead of metal oxide gels, as precursors. Specifically, this method includes: (i) preparation of high purity nanometer metal oxide crystal with a lot of superficial hydroxyls; (ii) treatment of the gels with sulfate ions, where the as-prepared Sb-SnO2 nanoparticles were dispersed in organic solvent and then impregnated with saturated ammonium sulfate solution to associate with (NH4)2SO4 by water molecule adsorbed on (NH4)2SO4; (iii) calcination [12] of the impregnated nano-powders. A coupling reaction of superficial hydroxyls with (NH4)2SO4 by losing NH3 and H2O undergoes at a proper temperature.
After calcination, the obtained solid powder has been firmly bonded with a group =SO4 on its surface, which means that SO4 2− is by no means a sulphate radical attached to nano particle any more. In virtue of Bronsted’s and Lewis’ acid-base theory, the attached SO4 2− should be a base but an acid since its negative charge. Our experiments, however, demonstrated such calcined nano particles were a superacid. So we believed that the molecular structure of solid superacid should be noted as SO4 /SnO2 but SO4 2−/SnO2, the latter written form of solid superacid, including SO4 2−/ZrO2, is being widely and incorrectly adopted.
Matsuhashi et al. [11] further indicated that papers concerning the SO4 2−/SnO2 catalyst have been quite few, because of difficulty in preparation, compared with the relative ease of preparation of the SO4 2−/ZrO2 material, in particular owing to the difficulty in preparation of the oxide gels from its salts SnCl4.
Experiments
The synthesis of the precursor, antimony doped stannic oxide
The Sb-SnO2 nanocrystals were synthesized using the method “precipitation–condensation with non-aqueous ion exchange (P-CNAIE)” and dried with the assistance of the Iso-Amyl Acetate (AD-IAA). These two methods were developed in our lab and reported in the published literatures [13-15]. A typical procedure includes the following steps. In an airtight flask containing 200 mL anion-exchange resin, 100 mL alcohol, and 10 mL of ammonia water, 200 mL ethanol solution containing SnCl4·5H2O (18.0%, w/v) and SbCl3 (0.665%, w/v) were added dropwise with fast stirring. At the same time, NH3 gas was aerated in the reaction solution. The reaction solution was held close to neutral pH by adjusting the speed of addition. After the addition was complete, the reaction solution was separated from the ion-exchange resin particle through a glass-sand funnel and reacted repeatedly with fresh anion-exchange resin on a shaker. The final chlorine-free colloid solution was held idle on a bench to allow the stratification of the turbid liquid. The upper lightly turbid solution was removed and kept aside for final recovery of all solid content, and the lower dense precipitated slurry was added ~80 mL of iso-amyl acetated to make a co-boiling system. The pale-yellow dispersive fine powders were obtained by codistilling off water absorbed on the colloid and solvents.
All the exchanged ion-exchange resins were collected and repeatedly washed with fresh solvent to collect any residual precipitate on the surface of the resins. The washed solvent were applied to a short column of ion exchange to remove any remaining chlorine, and were combined with the upper lightly turbid solution, in which the resulting dried powders were added and dispersed on a shaker. In succession, the combined solution was distilled and left behind a fine light-yellow powder of Sb-SnO2. In this way, all of the metal hydrolysate can be recovered and an exact doping as experimenter desires was achieved.
The impregnation with (NH4)2SO4
The sulfated Sb-doped SnO2 crystals were prepared in our study as follows. 2 g of Sb-doped SnO2 powder obtained in the synthesis of the precursor, antimony doped stannic oxide was placed in a 50 mL plastic centrifuge tube containing 45 mL of methanol. After the powders were dispersed on a shaker, 3.0 mL of saturated ammonium sulfate, equal to ~2 g of (NH4)2SO4, was added in methanol solution, and then the tube continued to be shaken on a shaker violently as the saturated solution was dropped in methanol, when very tiny (NH4)2SO4 precipitate was separated in solution. The Sb-doped SnO2 powders loaded with (NH4)2SO4 were separated by centrifugation and further washed in anhydrous alcohol. The process was repeated for three times and finally centrifuged at 4000 r/min. The final sediment was dried under an infrared ray lamp and a dispersed powder was obtained.
The coupling reaction of superficial hydroxyls with (NH4)2SO4
The mixed powders obtained in the impregnation with (NH4)2SO4 were transferred on a corundum plate, and then calcinated in a muffle furnace. The calcination to couple “SO4” on superficial hydroxyls of Sb- SnO2 nanocrystals was carried out at 380°C for 2~3 h.
Results and Discussion
Through the synthesis method of “P-CNAIE” and the drying method of “AD-IAA”, highly dispersed pale yellow powders were obtained. Based on our observation, without doping of the antimony, the colloidal solution of stannic chloride and finally dried powders always presented white colour, which implicates that the yellow color of as-prepared powders is caused by doping antimony or, more exactly, by Sb doping into crystal lattice of stannic oxides, because yellow is caused by the formation of crystal with variation of band gap, instead by cluster or hydrolysate that has a forbidden band.
Figure 1 shows TEM images and electron diffraction pattern of nano-meter sized material synthesized in the experiment section. The electro diffraction pattern, the middle image, indicates that the obtained nano material has a determinate crystal structure, which is also confirmed by the TEM image B, from which a layer lattice structure can be distinctly identified. The TEM image A shows the size of as-prepared powders is significantly less than 20 nm. In addition, XRD pattern in Figure 2 illustrates the degree of crystallization and the size of nano particle. Diffraction peaks and their position in the pattern indicate the nano material is stannic oxide crystal, and broad and weak peaks suggest that crystals are nano-meter sized. The positions of peaks are consistent with the standard one that showed in the X-Ray Powder Diffraction Standards of SnO2, PDF No. 41-1445 from Jade 5.0, see the red bar in Figure 2.
Crystal structure is of course important because the structure endows the material with some special properties, such as optical, semiconductor and electrical properties. On the other hand, superficial hydroxyl is, however, critical for the surface modification of nanomaterials, and for hybrid nano-composites to mix with polymers.
In the calcination, it was found that superficial hydroxyl on Sb-SnO2 nanoparticles had significant effect on the sulfating and roasting of Sb-SnO2 nanocrystal, which had been demonstrated by Differential Scanning Calorimetry and Thermogravimetric analysis (DSC-TG). The fewer the number of superficial hydroxyl exist, the fewer the sulfated groups exist on the surface of Sb-SnO2 nanocrystals. The thermogravimetric analysis (Figure 3) and differential scanning calorimetry (Figure 4) on the as-prepared powders support this view of point. Compared with curves 1 (Sb-SnO2) and 8 ((NH4)2SO4), curves 2 to 7 (Sb-SnO2 + (NH4)2SO4) have an additional segment from a to b in Figure 3. It is easy to understand that this segment probably implies the generation of superficially sulfated groups. Curves 2 to 7 are thermogravimetric curves of Sb-SnO2 nanocrystals that were pretreated at different temperatures, from 25°C to 550°C, for 3 h and then impregnated with a given amount of (NH4)2SO4 before thermogravimetric analysis. It can be seen that the higher the preprocessing temperatures is, the shorter the line segments from a to b, thus the fewer the amount of sulfated group is. As the preprocessing temperature increases, especially at/over 320°C (Figure 3), the weight losses of Sb-SnO2 nanocrystals are heavier, resulting from the dehydration between hydroxyls and leading to the decrease of the quantity of the superficial hydroxyls. The decrease in amount of superficial hydroxyls brought about the decline of the quantity of superficially sulfated groups, and the decrease of acid strength or catalytic activities of nanoparticles.
Figure 4 is Differential Scanning Calorimetry (DSC) curves, which more clearly showed the variation of and the difference between samples 1 to 8 due to the distinct images of endothermic peaks and exothermic peaks. The red line has a clear exothermic peak that was caused by the crystallization of superficial hydroxyls of Sb-SnO2 nanoparticles at ~ 376°C. And the blue one is the differential thermal curve of (NH4)2SO4 with two glaring endothermic peaks. The two endothermic peaks are associated with the decomposition of (NH4)2SO4 into NH3, H2O and SO3, corresponding to the chemical reaction on following equations:
(NH4)2SO42 NH3↑+ H2SO4 (1)
H2SO4H2O↑ + SO3↑ (2)
It should be pointed out that as the reaction of (NH4)2SO4 with superficial hydroxyls of Sb-SnO2 nanoparticles progressed, the amount of free (NH4)2SO4 decreased and the decomposition temperature of H2SO4 decreased as well, see the peak B on curve 5 in Figure 4.Nevertheless, it is noted that a third endothermic peak appeared in differential thermal curves of samples 7 to 2. The third endothermic peak only appeared in the curves of Sb-SnO2 plus (NH4)2SO4 and become more obvious as the pretreatment temperatures of Sb-SnO2 decreased. The appearance of the third peak suggests the cleavage of a chemical bond. As compared with differential thermal curves of Sb- SnO2 and (NH4)2SO4, the third peaks on curves 6 to 2 suggests a bonding reaction took place between superficial hydroxyl and (NH4)2SO4, or more exactly, between superficial hydroxyl and H2SO4. Therefore, the breaking of bonds represented by the third peak should belong to superficially sulfated groups, which were newly generated groups in the calcination process. We speculate the breaking of bonds contributing to the absorption of heat might follow the cracking reaction as equations (3) and (4) show.
(3)
(4)
Based on the above discussed, a summary is drawn in Figure 5, which simply and clearly illustrates the three endothermic peaks. It can be easily understood that the third endothermic peak on the blue curve in Figure 5 should belong to the splitting action of a new group. This new group generated in the calcination process by “=SO4” bonding to Sb-SnO2 nano-particle against the endothermic peaks on black curve of (NH4)2SO4. In other words, the calcination did make “=SO4” group loaded on the Sb-SnO2 nanoparticles forming a solid superacid with a stable “=SO4” group.
According to the data shown in Figures 3-5, we proposed that the most favorable temperature for the generation of superficially sulfated groups of Sb-SnO2 particles should fall between 380°C and 400°C, before the decomposition temperature of H2SO4 and after the crystallization temperature of Sb-SnO2. To illustrate the generation of solid superacid of Sb-SnO2, the authors here proposed that a series of chemical reaction such as Figure 6 shows might occur on the surface of Sb-SnO2 as the preparation of solid superacid of Sb-SnO2 underwent.
According to the proposed, group “=SO4” is absolutely impossible to attach to Sb-SnO2 nano-particle in the form of SO4 2−. It should be a group bonded on Sb-SnO2 particle since the dissociation temperature of bonded “=SO4” is up to 470°C.
The relative acid strength of the calcined Sb-SnO2 powders was measured by the adsorption reaction of indicator. The powders (ca. 0.5 g) were calcined at 380°C ~ 390°C in air for 3 h and then placed in a glass vacuum desiccator as the powder was hot. After the sample was pretreated in a vacuum for 2 h and cooled down to room temperature, some cyclohexane solution containing 5% of Hammett indicator was sucked into the vacuum desiccator. The desiccator was heated to 60°C by placing it in a constant water bath, which resulted in the exposure of powder to the indicator vapor. The present powder sample was gradually colored by indicator and changed distinctly the colorless basic form of p-nitrotoluene (pKa or H0=-11.4), m-nitrotoluene (-12.0), m-nitrochlorobenzene (-13.2), 2,4-dinitrotoluene (-13.8) and 2,4-dinitrofluorobenzene (-14.5) to the yellow conjugate acid form, that is to say, the acid strength of the solid acid is estimated at least to be Ho < -14.5. All of the measurements convincingly demonstrated the calcined Sb-SnO2 was a solid acid, more exactly solid superacid (Figure 7).
As an acid, the sulfated Sb-SnO2 should be able to release hydrogen proton or have electron pair acceptors to accept molecules bearing electron pair or negative ions in term of Bronsted’s proton theory or in the light of Lewis theory of acids and bases. According to the molecular structural forms put forward by Hino et al [1]. however, SO4 2-/ZrO2 and SO4 2-/SnO2 are absolutely impossible to show any acidity because group SO4 2− is a conjugate base of H2SO4. Based on the derivation of a series of chemical reaction in calcination and through analysis of the possible structures of Sb-SnO2 solid acid, a more reasonable structure is proposed in Figure 7.
Because the calcination had the group “SO4” bonded on Sb- SnO2 nanoparticles and become a stable group “=SO4” of Sb-SnO2 but an attached acid radical “SO4 2−”, authors believed that the great enhancement of acidity of sulfated Sb-SnO2 resulted from a number of dangling bonds around group=SO4. The both oxygen and tin with dangling bond are electron deficient groups and have electronwithdrawing effects, which leads to the transfer of negative charge from=SO4 to dangling bonds and make =SO4 a positive group with acidity. So, we proposed the solid superacid of Sb-SnO2 should be noted as SO4 ⊕/SnO2 that, as a Lewis’ acid, owns a great affinity for molecules bearing electron pair or negative ions.
Some further experiments concerning the impregnation of Sb-SnO2 with ammonium sulfate were conducted using methods of Differential Scanning Calorimetry (DSC) and Thermogravimetry (TG) to study an optimal impregnation ratio of ammonium sulfate to Sb-SnO2.
The nano-crystalline Sb-SnO2 powders had to be dispersed in organic solvent since it could not be recovered if it scattered in water.The ammonium sulfate, however, had to be dissolved in water for its solubility in organic solvent is very low. In the impregnation of Sb-SnO2 powders with ammonium sulfate, a saturated solution of ammonium sulfate was dropped into organic solutions containing a fixed amount of Sb-SnO2 nano-powder in different ratio. The ammonium sulfate precipitated as it dropped into organic solvent and Sb-SnO2 nanoparticles coupled the precipitate via water molecules that adsorbed on (NH4)2SO4 fine particles. Without free water, for all water molecules were adsorbed on (NH4)2SO4 fine particles. The dried powder was a uniform dispersion of powder of (NH4)2SO4 fine particles and Sb-SnO2 nano-particles. The outstanding advantage of the method presented here, that is the impregnation of Sb-SnO2 powder with saturated ammonium sulfate, is that the impregnation ratio of (NH4)2SO4 to Sb-SnO2 can come to very high and no free water that will cause the aggregation of Sb-SnO2 nano powder.
To obtain an optimal impregnation ratio of ammonium sulfate to Sb-SnO2, a series of Sb-SnO2 nano-powder impregnated with (NH4)2SO4 in different ratio were studied on the Simultaneous TG-DSC Apparatus, STA 409PC, NETZSCH, Germany. The resulted analysis diagrams are showed in Figure 8. Here the Sb-SnO2 nano-powder did not undergo any heat treatment and just impregnated with (NH4)2SO4 directly in organic solvent. It can be simply and clearly identified the endothermic peaks and their height from the Thermo gravimetric (TG) and Differential Scanning Calorimetry (DSC) profiles of Sb- SnO2 impregnated with different amount of (NH4)2SO4. The height of peaks told us if there were excessive or deficient (NH4)2SO4, by which an optimal impregnation ratio of ammonium sulfate to Sb-SnO2 was easily discovered. We have got the knowledge of what the peaks implied based on foregoing discussion, that is, the Peak A was an endothermic peak that caused by (NH4)2SO4 being resolved into NH3 and N2SO4, the Peak B an endothermic one which resulted from the decomposition of H2SO4, and the Peak C, without a doubt, was brought about by the absorption of heat contributed by the dissociation of a newly generated group=SO4. The Peak A was always presented in curves of all samples since the decompositions of (NH4)2SO4 occurred for all samples but were different in their peak height due to different impregnation ratio, whereas, the Peak B only appeared as the amount of (NH4)2SO4, or exactly H2SO4, was excessive against superficial hydroxyl of Sb-SnO2 because only the H2SO4 that did not associate with superficial hydroxyl would decomposed.
Obviously, the optimal impregnation ratio should be located between curves 4 and 5 in Figure 8 because curve 5 has a large endothermic peak but curve 4 does not. To diagnose a more accurate optimum ratio of ammonium sulfate to Sb-SnO2, the authors carried out a series precise experiments in the small range of ratio of Sb-SnO2 to (NH4)2SO4 from 1:1.2 to 1:2.4 wt%. The quantitative analyses of the ratio were conducted by the methods of differentia scanning calorimetry and themogravimetry. The thermal analysis curves, especially DSC curves, in Figure 9, showed the ratio at 1:1.2 wt% did not have endothermic peak B, suggesting impregnated (NH4)2SO4 was not enough against the superficial hydroxyl, and the ratios at 1:1.6, 1:2.0 and 1:2.4 wt% all had projecting endothermic peaks at peak B, meaning impregnated (NH4)2SO4 were excessive.
In the preparation of solid superacid of Sb-SnO2 nanocrystal, the working ratio was selected at 1:1.4 to 1:1.6 wt%, a little excessive, in order to make full use of the superficial hydroxyl of Sb-SnO2 and get more superacid group=SO4.
Figure 10 is a picture of solid superacid of Sb-SnO2. The picture shows the deficiency (1:0.8 wt%) or excess (1:2.4 wt%) of impregnated (NH4)2SO4 would result in the blue solid superacid of Sb-SnO2 with little light yellow, while, a suitable or little excessive amount (1:1.4 and 1:1.6 wt%) of (NH4)2SO4 could get a solid superacid of Sb-SnO2 with an even blue after the calcination at 380°C. See the left one in Figure 10.
Conclusion
The nano-crystalline SnO2 doped with Sb (III) that was synthesized by method of “P-CNAIE” and the drying method of “AD-IAA” could be calcined to give a solid superacid after sulfated. It must be noted that a suitable amount of impregnated ammonium sulfate and a calcination temperature adapting to SnO2 are crucial to prepare the solid superacid of Sb-SnO2, which is written as SO4 /SnO2.
This paper proposed the impregnated ratio of Sb-SnO2 to (NH4)2SO4 should be between 1 g to 1.4 g and 1.6 g and the calcination temperature be 380°C to 400°C, and hence an even blue solid superacid powder was obtained. About the catalytic properties of Sb-SnO2 solid superacid will be discussed in another paper.
Acknowledgements
The authors would like to extremely thank the “Chun Hui” Project from the Ministry of Education of China for funding the researches.
References















Figures at a glance

image   image   image   image   image
Figure 1   Figure 2   Figure 3   Figure 4   Figure 5
image   image   image   image   image
Figure 6   Figure 7   Figure 8   Figure 9   Figure 10
Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Article Usage

  • Total views: 12609
  • [From(publication date):
    November-2014 - Jun 18, 2019]
  • Breakdown by view type
  • HTML page views : 8723
  • PDF downloads : 3886
Top