Abstract
Silica gel was prepared and treated thermally and hydrothermally and was characterized as solid stationary phase in gas chromatography. The characteristics have been evaluated in terms of polarity, selectivity, and separation efficiencies. These parameters were used to assess the outer silica surface contributions and the degree of surface deactivation brought about by different treatment techniques. The parent silica elutes the paraffinic hydrocarbons with high efficiency of separation and elutes aromatic hydrocarbons with nearly good separation and has bad separation of alcohols. The calcined silica at 500°C and 1000°C has a pronounced effect on the separation of aromatic hydrocarbons compared with the parent silica and hydrothermal treatment of silica. With respect to alcohols separation, the obtained bad separations using treated and untreated silica reflect the little effect of the thermal and hydrothermal treatment on the silica surface deactivation.
1. Introduction
Gas chromatography (GC) is now widely used to examine the physicochemical characteristics of many solid and liquid materials. Carefully selected test solutes are injected into the flow of carrier gas and transported over the surface of stationary phase such as silica or others. The retention time and the peak elution profiles of standard solutes affected by interactions between the solutes and stationary phase are used to estimate those interactions [1, 2].
GC can be used for studying the behavior of stationary phase through investigating the interactions between these stationary phases and some solutes from different families [3–5].
Silica gels have long attracted attention since they are widely used and as stationary phase in chromatography, catalyst, extract, filter surface properties covering a wide range of acidity surface reactivity and pore structure [6–8]. The surface of silica gel can be modified easily by physical or chemical treatments leading in each case to different adsorptive properties. These treatments may include calcinations [9], hydrothermal treatment [10], silylation [11–13], and incorporation of organic and inorganic salts or organic compounds [14–17].
Usually, the separation of the mixture requires selective stationary phase, so there are many thousands of these phases, and the novelty of this approach is the silica gel preparation and its treatment with different methods in order to obtain different silica surfaces to cover most chromatographic problems. The purpose of this work is the synthesis and modification of silica gel through thermal and hydrothermal treatment to produce various silica surface modifiers as solid stationary phases in gas chromatography and their application to separate polar and nonpolar organic petroleum compounds.
2. Experimental
2.1. Preparation of Silica Gel
Wide porous silica gel as a parent material was prepared by a conventional precipitation method according to the De Boer method [18]. The prepared silica gel was crushed and sieved using an automatic mechanical sieve. The portion from 60–80 mesh was selected, washed by 6 mol HCl, and stored for different physical and chemical treatments.
2.2. Thermal and Hydrothermal Treatments of Silica Gel
The acid-washed silica gel (60–80 mesh) was subjected to various treatments, namely, thermal treatment and hydrothermal treatment, with the aim of producing different surface-modified silica gels. Thermal treatments were carried out by calcinations in air for 5 h at 1000°C. Hydrothermal treatments were carried out by reaction with liquid water at 220°C and 15 atm for 24 h in an autoclave. In addition, silica gels were obtained by a combination of two modifications in order to improve their properties as solid gas chromatographic stationary phases. The studied silica samples obtained using thermal and hydrothermal treatments are listed in Table 1.
2.3. Gas Chromatography
The untreated silica and surface-modified silica gels were subjected to an inverse gas chromatography with the aim of investigating their performance as solid stationary phases. The solid material was packed in a stainless steel column (1/8 inch and 7 feet) by charging under vacuum. The packed column was activated at 200°C for 24 h in a stream of pure nitrogen gas at a flow rate of 15 mL min.
The gas chromatograph used was an AT Unicam-610 equipped with FID. Nitrogen gas was used as a carrier at a flow rate of 25 mL min−1. The analysis was carried out at different temperatures depending on the column efficiency resulting in the optimum separation of the studied solutes. Different solutes, namely, mixtures of n-paraffins, aromatic and polyaromatic hydrocarbons, ketones, acetates, ethers, and n-alcohols were used as probes for the chromatographic characterization.
3. Results and Discussion
3.1. Rohrschneider Scheme
Characterization of silica modified stationary phases according to Rohrschneider’s method is based on the determination of retention indices for five solutes, namely, benzene, ethanol, methyl ethyl ketone, nitro methane, and pyridine on SE-30 (nonpolar stationary phase) and then on the solid stationary phases to be characterized. The retention index differences () at 100°C can be calculated and then the so-called Rohrschneider constants X (Benzene), Y (Ethanol), Z (Methyl ethyl ketone), U (Nitro methane), and S (Pyridine) are obtained in Table 2. The elution order of the Rohrschneider probes is the same for all the studied silica-modified samples. The polarity of the chromatographic columns depends not only on the solid stationary phases under study but also on the solutes to be analyzed. Thus, each solute of the five solutes selected for this scheme of characterization may refer to a certain type of interaction between stationary phases and solutes.
The retention indices of the modified silica (SiC500, Sith, and SiCth) are given in Table 2, it has been found that of all modified silica below that of the untreated silica sample except the case of using ethanol and methyl ethyl ketone as props. The higher polarity of these excepted silica columns was focused, suggesting that the hydrothermal treatment of both untreated and calcined silica is nonselective stationary phases for polar compounds like alcohols and ketones. The ordered classification of stationary phases with numerical data is very valuable for comparison of columns for a particular type of analysis. The characterization reflects the deactivation degree of silica gel after modifications and the selectivity of these silica samples toward separation of solutes from different families.
3.2. Separation Efficiencies
The efficiency of gas chromatographic separation for the studied silica samples can be evaluated in terms of resolution and separation factor; and given in Table 3. The selected solutes represent their corresponding families; the solute pairs were chosen as test samples for evaluation of the selectivity of the untreated and treated silica gels as solid stationary phases in GC. The resolution and separation factor of SiC500 and Si columns show the highest values than the other columns using normal paraffins and aromatic hydrocarbons as props. This increases their separation efficiency and selectivity toward this type of analysis as shown in Figures 1–3.
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For separation of alcohols, the parent and all modification techniques unsuccessful in this type of analysis and their resolution and separation factor are not available. These reflected on the alcohol separation giving bad elution accompanied with overlap and tailing peaks.
3.3. Selectivity and Applications
The selectivity of the studied silica samples can be verified by using the uniformity criterion () for model systems comprising normal paraffines, aromatic and polyaromatic hydrocarbons, ethers, ketones, acetate, and alcohols. Consider where is the number of peaks on the chromatogram, is the base width of the narrowest peak keff is the separation factor for the worst separated pair of components, and is the duration of analysis. From Table 4 and in Figures 1, 2, and 3, it has been found that all modifications differ in their separation efficiency according to the separated solutes. The saturated hydrocarbons can be separated as shown in Figures 1 and 2 with high efficiency by the parent and calcined silica at 500°C ( and , resp., for paraffins) compared with the calcined silica at 1000°C and hydrothermal treatment of silica.
Also, the calcined silica at 500°C () is the most efficient column for separation of aromatic hydrocarbons followed by the parent silica () as shown in Figure 3.
For separation of alcohols, the parent and modified silica stationary phases failed in eluting alcohols which may be due to the fact that these treatment are not enough for deactivating the silica surface to a degree enough to separate the alcohol compounds as shown in Figure 4.
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4. Conclusions
(1)The resolution and separation factor of SiC500 and Si columns show the highest values compared other columns using normal paraffines and aromatic hydrocarbons as props. This increases their separation efficiency and selectivity toward this type of analysis. These were reflected by the highest average Rohrschneider props on parent silica than the other treatments. (2)The untreated silica gives suitable surface enough for eluting paraffinic hydrocarbons as previous works. The calcined silica at 500°C exhibits higher resolution values 3.918 for normal paraffins, which was confirmed with good separation of paraffines (Figure 1) giving symmetric and sharp peaks. (3)The aromatic hydrocarbons give nearly the same behavior of paraffines. The resolution of aromatic hydrocarbons on calcined silica at 500°C and Si columns shows higher values than the other columns.(4)The parent and treated silica gels failed in the separation of alcohols; this may be due to the fact that these treatments have little effect on the silica surface deactivation. (5)All studied parameters of characterization of silica gels via gas chromatography may be used in interpreting the reactivity of silica surfaces and factors controlling the adsorption of solutes.