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Journal of the Chilean Chemical Society

versión On-line ISSN 0717-9707

J. Chil. Chem. Soc. v.51 n.3 Concepción sep. 2006

http://dx.doi.org/10.4067/S0717-97072006000300007 

 

J. Chil. Chem. Soc., 51, N°.3 (2006), p.964-967

 

DETERMINATION OF NINE COMPONENTS IN BAYER LIQUORS BY HIGH PERFORMANCE ION CHROMATOGRAPHY WITH CONDUCTIVITY DETECTOR

 

JIAN BO XIAO*

College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, PR China


ABSTRACT

A High Performance Ion Chromatographic (HPIC) method for the determination of nine components in Bayer liquors was reported. Formic, acetic, propionic, oxalic, succinic, glutaric anion, F-, Cl-, and SO42- were separated and determined by High Performance Ion Chromatography with conductivity detector. The analytes were removed from Bayer liquor by using an ion-exchange resin column. The chromatographic separation was achieved with only one IonPac AS11-HC column thermostated at 30 °C. The precision results showed that the repeatability and reproducibility were <2.94 and <1.37%, respectively. The accuracy of the method was assessed by the recoveries ranging from 86.3 to 105.6 %. Under optimum conditions the detection limits ranged from 0.008 to 0.053 mg/l.

Keywords: Bayer liquors; High Performance Ion Chromatography; anions; determination


1. INTRODUCTION

The Bayer process can be summarized as the digestion of bauxite with caustic liquor and the subsequent precipitation of hydrated alumina [1]. Most bauxite contains organic matter in various amounts. The major source of organic matter introduced within the Bayer liquor comes from the bauxite in the form of humic substances. During the digestion, the organic matter is dissolved, degraded and oxidized with the results that the liquors darken, and notable amounts of oxalate and carbonate are formed.

Due to the acidic nature of the humic substances, more than 50% of the organic matter contained in the bauxite is extracted into the liquor. The principal degradation products are sodium oxalate and sodium carbonate. Depending upon the digestion conditions, typically 5-10% of the organic carbon is converted to sodium oxalate [2].

The process is cyclical and therefore concomitant impurities present in the raw materials or reagents may accumulate unless periodically removed [3, 4]. From an analytical chemistry perspective, Bayer liquor is a challenging matrix consisting of alumina, sodium hydroxide, sodium carbonate, sodium chloride, sodium sulphate, sodium oxalate as well as unknown organic acid anions all at varying concentrations [5–7]. The rapid and reliable determination of organic acids in Bayer liquor is of significant industrial importance because their presence is implicated in the formation of small particle size hydrated alumina [8].

A variety of techniques have been utilized for the identification and determination of sodium oxalate and humic substances in Bayer liquors; these have included titrimetry [9], ion chromatography [7, 10-11], capillary electrophoresis [7,11-15], flow injection analysis [16], high performance liquid chromatograph [17-21] and gas chromatography [22-24]. Any reports analyzing the humic acids by IC had been restricted to only oxalic acid analysis [10-11]. But the quantitative determination was not performed because the separation is inadequate. Oxalate was the main organic component in Bayer liquor. In many factories the oxalate was determined by titration with standard potassium permanganate solution. This method often resulted in low precision and accuracy. Furthermore, it takes much time and agents. The analysis of organic acids in Bayer liquors with IC systems is a difficult task due to high ionic strength and pH. Our particular interest concerns the development of a simple HPIC procedure for the determination of organic and inorganic anions levels in Bayer liquors. The method was successfully applied to analysis of Bayer liquor samples with high recoveries and precision.

2. EXPERIMENTAL

2.1. Materials and methods

2.1.1 Chemicals and standards

Analytical standard-grade formic, acetic, propionic, oxalic, succinic, glutaric acid, and sodium fluoride, sodium chloride, potassium sulfate were obtained from Sigma (St. Louis, MO, USA). Stock standard solutions were prepared by dissolution of acids in Milli-Q water; they were stored at 4 °C for 1 month. The Milli-Q water was purified by passage through a Compact Milli-RO and Milli-Q water system from Millipore (Milford, MA, USA). Working standard solutions were prepared daily by dilution with Milli-Q water. Potassium dihydrogenphosphate, sodium hydrogen carbonate, orthophosphoric and hydrochloric acid were analytical-reagent grade and supplied by Shanghai (Shanghai, China).

The samples were filtered through cellulose membrane filters Whatman (0.45 µm, Whatman, Clifton, NJ, USA). The eluent was filtered with membrane filters Phenomenex (0.45 µm, AFO-0504, CA, USA).

2.1.2. Apparatus

High Performance Ion Chromatographic analyses were carried out using a DIONEX Ion Chromatograph (USA) equipped with a DIONEX EG50 on-line degasser, a DIONEX EG50 GP50pump, and a ASRS-ULTRA?4-mm detection system (DIONEX). The detector signals were recorded on a chromatography data system Chromeleon 6.60. The column was an IonPac AS11-HC column (250 × 4.6 mm I.D., particle size 5 µm, Hanbon Science &Technology Co., Ltd). SPE column was an OnGuard H column (DIONEX). A PHS-3C pH meter (Shanghai, China) was also used.

2.1.3. Sample preparation

A 10 ml amount of Bayer liquor was diluted in 1000 ml of Milli-Q water. The pH was adjusted to approximately 7.50 using 8 mol/l HCl and the mixture was stirred for 15 min using a magnetic stirrer. The SPE procedure involved an ion-exchange cartridge (100 × 4.6 mmI.D., particle size 40 µm, Hanbon Science &Technology Co., Ltd), which was activated with 10 ml of sodium hydroxide solution 0.1 mol/l (percolation rate 3 ml /min). A 100-ml volume of solution diluted was passed through at a flow-rate of 0.5 ml/min. The cartridge was washed with 100 ml of water (3.0 ml/min) and organic acids and inorganic anions were eluted with 50 ml of hydrochloric acid 0.1 mol/l (1.0 ml/min). This solution was injected directly in the chromatograph after filtered.

2.1.4. Chromatographic conditions

The mobile phases used were water and potassium hydroxide. All procedures were carried out using a gradient elution program (Table 1). The flow-rate was 1.20 ml/min. The column was thermostated at 30 °C. Injection volume was 25 µl and all standards and Bayer liquor samples were filtered through a 0.45-µm membrane.

Table 1 Gradient profile used in Ion Chromatography

2.1.5. Calibration standards

The individual standards were dissolved in methanol and injected to determine individual retention times. Stock solutions of 100 µg/ml of all organic acids and inorganic anions were prepared by dissolving pure standards in methanol. The stock solutions and the six diluted standards were injected for linearity range and detection limit tests.

3. RESULTS AND DISCUSSION

3.1 Optimization studies of the chromatographic condition

3.1.1. Mobile phase

Solutions of acid or base, recommended in the literature [25-28] for determination of anions using High Performance Ion Chromatography, were tested. Solution of potassium hydroxide was selected because mobile phase consisting of acid produced interferences. Several concentrations of potassium hydroxide were tested and finally a gradient elution program was selected (Table 1).

3.1.2. Column temperature

The column was thermo stated at several different temperatures. The best results were obtained at a temperature of 30 °C.

3.1.3. Flow rate of mobile phase

Several mobile phase flow-rates (0.5-1.5 ml/min) were tested and finally a flow-rate of 1.20 ml/min was selected.

3.2 Chromatographic separation

Fig. 1 showed a chromatogram of these standard solutions. The chromatogram of sample is showed in Figs. 2. In this study gradient profiles were sufficient to separate six organic acids and three inorganic anions in a short time. Jackson compared the ion chromatography (IC) and capillary electrophoresis (CE) for determination of oxalate in Bayer liquors [11]. The eluent was complicated, which consisted of 1.6 mmol/l sodium tetraborate, 7.3 mmol/l boric acid, 1.6 mmol/l sodium gluconate, 5g/l glycerin, 120ml/l acetonitrile and 20 ml/l n-butanol at pH 8.5. Only oxalate, Cl-, and SO42- were analyzed. Xiao et al separated and determined six organic acids in Bayer liquors by RP-HPLC [21]. Oxalic, tartaric, acetic, succinic, glutaric and butene dicarboxylic acids were identified and quantified [21]. But tartaric and butene dicarboxylic acids were not found by High Performance Ion Chromatographic (HPIC) method. So the tailed peak between peaks 7 and 8 may be some components that can not be separated by HPIC method.

Fig. 1 IC-CD chromatogram of the standards.
1.F-, 2. acetic, 3 propionic, 4.formic, 5. Cl-, 6.glutaric, 7.succinic, 8. SO42-, 9.oxalic

Our particular interest concerns the development of a simple HPIC procedure for the determination of organic acids and inorganic anions levels in Bayer liquors. It is the first time that ion chromatography has been used to determine five organic acids (expect for oxalic acid) in Bayer liquor samples. A variety of techniques have been utilized for the determination of sodium oxalate in Bayer liquors. In contrast to these methods, the present method is simple, rapid and requires only extraction steps. A good separation can be achieved in a short separation time of 33 min.

Fig. 2. IC-CD chromatogram of sample
1. F-, 2. acetic, 3 propionic, 4.formic, 5. Cl-, 6.glutaric, 7.succinic, 8. SO42-, 9.oxalic

The levels of oxalic acid found in Bayer liquors by IC are in agreement with the volumetric analysis (VA): potassium permanganate titration. Deviation was 1.2%-2.4%. The oxalate levels determined by VA are always higher than the result of IC. We conclude that potassium permanganate is a versatile and powerful oxidant that can be used to determine many substances by direct or indirect titration. Some other compounds in Bayer liquors reacted with potassium permanganate.

3.3. Detection and quantification limits

Retention times of organic acids and inorganic anions analyzed were shown in the Table 2. The detection limit was calculated as sb+6s, where sb is the average signal of ten blank injections and s the standard deviation. The quantification limit was calculated as sb +10s, where sb is the average signal of ten blank injections and s the standard deviation. Table 3 shows detection and quantification limits of organic acids and inorganic anions analyzed. The detection limits ranged from 0.008 mg/l for F- to 0.053 mg/l for Cl- and the quantification limits ranged from 0.005 mg/l for F- to 1.00 mg/l for acetic acid.



3.4. Calibration curves

Calibration curves were determined for seven different concentrations of a mixture of organic acids and inorganic anions standard solutions. Each calibration sample was injected in triplicate. Calibration graphs for each compound were obtained by plotting concentration against peak area and applying the least squares method. Table 4 lists the parameters and correlation coefficients of the calibration plots. Each plot was linear over certain interval from the detection limit to at least 10 µg/ml for all organic acids and inorganic anions. The peak areas (y) and the theoretical concentrations of the calibration standards (x) were fit to the ln-quadratic function using the least squares regression in Microsoft Excel. The results of the regression analysis were then used to back-calculate the concentration results from the peak area data, and the back-calculated concentrations and appropriate summary statistics [mean, standard deviation (SD), and percent relative standard deviation (RSD)] were calculated and presented in tabular form.

Table 4 Parameters and correlation coefficients (r) of calibration plots for nine anions analyzed

Components a b r

F- 0.1850 -0.00100 0.9993
acetic 0.0332 0.0156 0.9995
propionic 0.0363 0.0029 0.9991
formic 0.0945 -0.00670 0.9996
Cl- 0.1319 -0.00850 0.9999
glutaric 0.0283 0.0004 0.9998
succinic 0.0328 0.0025 0.9999
SO42- 0.0955 0.0156 0.9999
oxalic 0.0800 0.0004 0.9999

Calibration plots are expressed as regression lines (y=ax+b), where y is the peak area and x is the amount of acid in mg/L Bayer liquor. The calibration test was repeated three times.

3.5. Precision

The precision study was comprised of repeatability and reproducibility studies. These were developed in three different Bayer liquors which contained low, medium and high organic acids and inorganic anions levels. The repeatability was established by injecting the Bayer liquor samples five times. The reproducibility was determined by analyzing each sample of Bayer liquors on 3 different days over about 1 month. The repeatability and the reproducibility are <2.94% and <1.37% (Table 5), respectively. These results indicate that the present method can be used for quantitative analyses of these nine anions in Bayer liquors.

Table 5 Repeatability and reproducibility of method

3.6. Recovery

To establish the accuracy of the method, this procedure was also performed on a mixture of organic acids and inorganic anions added to Bayer liquors. Table 6 shows the recoveries of these anions after applying the extraction procedure. It is not possible to compare to our results those of other workers because it is the first time that this study has been carried out to determine these nine components in Bayer liquors by Ion Chromatography.

Table 6 Recovery of nine anions added to sample after the extraction procedure

3.7. Nine nions contents in Bayer liquors analyzed

The organic acids and inorganic anions contents of sample were shown in Table 6. Cl- and SO42- concentration were very high in sample. Six organic acids (formic, acetic, propionic, oxalic, succinic, glutaric acid) and three inorganic anions (F-, Cl-, and SO42-) were separated and identified by the present ion chromatographic method.

4. CONCLUSION

The analysis of organic acids and inorganic anions in Bayer liquors with HPIC systems is a difficult task due to high ionic strength and pH. The present method allows the quantification of formic, acetic, propionic, oxalic, succinic, glutaric acid, F-, Cl-, and SO42- in Bayer liquors. The present method has the advantage of measuring organic acid in a single run, thus simplifying the analytical procedure.

 

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*Corresponding author. E-mail address: jnb_xiao@yahoo.com