Chlorine and caustic soda are two of the most produced chemical substances globally. They are used to manufacture numerous intermediate chemicals, which in turn, are important feedstock materials for several industries (e.g., pulp and paper, petrochemical, and pharmaceutical). The chlor-alkali process is responsible for the majority of chlorine and caustic soda production.
The chlor-alkali process creates these two products together in similar proportions via electrolysis of sodium (or potassium) chloride brine. For the process to be as efficient as possible, the brine must be free of impurities (e.g., alkaline earth metals), otherwise the expensive membranes can become fouled which results in unexpected high maintenance costs.
Metrohm Process Analyzers can be used in several stages of this process—from monitoring impurities in raw to ultra-purified brine. This Process Application Note describes a method to determine the strontium and barium concentration in brine as early detectors of membrane fouling via online process ion chromatography. Using this multiparameter analytical technique can help reduce the risk of premature membrane fouling and avoid unexpected maintenance and high utility costs with 24/7 automated analysis.
Different methods can be used to create chlorine and caustic soda (NaOH) from brine, but the most applied electrolysis technique in Europe is the membrane cell technique, since it does not include mercury and asbestos like the other options.
Figure 1 depicts an illustration of the membrane cell technique for chlorine production from saturated brine feedstock. For the chlor-alkali membrane cell technique, the anode and cathode are separated by a selective ion-exchange membrane. This allows only the positively charged Na ions to penetrate the cathode half-cell. Purified brine is pumped into the anode half-cell as an electrolyte. Then, the negatively charged Cl ions from the brine are oxidized at the anode, converting them into chlorine gas (Cl2). At the side of the cathode half-cell, water is reduced to hydrogen gas (H2), leaving the resulting hydroxide ions (OH-) to react with Na+ that has migrated through the membrane, ultimately forming NaOH.
For this process to be as efficient as possible and to avoid premature membrane fouling, the brine feedstock must be free of impurities. This makes chemical analysis of the brine indispensable.
Depending on the origin of the brine, the ionic impurities can vary. Calcium and magnesium (hardness) are the most common ionic impurities here. Monitoring these substances provides important information about the efficiency of the impurity removal prior to the electrolysis step (Figure 2). However, strontium and barium can also be present and are just as harmful to the membranes even in trace amounts. Typically, Sr2+ and Ba2+ are the first multivalent ions to break through the ion-exchange membrane, which makes them excellent parameters to monitor the life of the ion exchangers. By monitoring trace levels of strontium and barium in the purified brine, a breakthrough can be detected earlier before calcium and magnesium can foul the membrane. The desired measuring range for both of these contaminants is 10–100 μg/L.
The most frequently applied analytical techniques for the determination of strontium and barium in brine are ion chromatography (IC), inductively coupled plasma mass spectrometry (ICP-MS), and ICP optical emission spectrometry (ICP-OES). Although ICP is a multiparameter technique covering large analytical ranges, it is also expensive, cannot easily be implemented online, and requires knowledgeable staff. Furthermore, the detection limit of strontium and barium is not low enough with ICP compared to IC analysis, and the operational costs for ICP are higher because of the use of large amounts of high purity argon.
Metrohm Process Analytics offers a solution for monitoring strontium and barium in brine: the 2060 Ion Chromatograph (IC) Process Analyzer featuring combined Inline Preconcentration and Inline Matrix Elimination. With one injection, the 2060 IC Process Analyzer is able to quantify strontium and barium. The analysis system is fed directly and continuously with samples via a bypass in the process stream.
Automatic calibration guarantees excellent detection limits as well as high reproducibility and recovery. Additionally, the 2060 IC Process Analyzer provides alarms if pre-set warning or intervention concentration limits are reached, helping to save costs by preventing premature membrane fouling.
The analysis is carried out fully automatically using Inline Preconcentration (Metrosep Chel PCC 1 VHC/4.0.) combined with Inline Matrix Elimination. The detection of trace levels of strontium and barium is done through a conductivity detector. This combination of techniques enables the possibility to measure very low amounts of strontium and barium in highly concentrated brine (Figure 3), achieving a measuring range of 12–120 μg/L for both analytes.
The many intelligent sample preconditioning techniques offered by Metrohm ion chromatography (e.g., preconcentration and matrix elimination) make the analysis of cationic impurities in brine solutions simple and easy to perform in an online capacity. Integration of a built-in eluent production module and optional PURELAB® flex 5/6 from ELGA® for continuous pressureless ultrapure water supply allows easy autonomous online operation around the clock.
|Strontium||12–120 μg/L||12 μg/L|
|Barium||30–120 μg/L||30 μg/L|
The Metrohm Process Analytics 2060 IC Process Analyzer can reliably measure trace amounts of strontium and barium in industrial brines commonly used in the chlor-alkali industry. This analysis method used in the analyzer allows chlor-alkali producers to prevent the premature fouling of expensive ion exchange membranes used in the process as well as the significant costs for replacement and maintenance.
- Low utility and maintenance costs by preventing premature membrane fouling
- Stable baseline and 24/7 operation due to Inline eluent preparation
- Safe working environment due to automated sampling
- Excellent detection limits, high reproducibility, and superior recovery rates owing to automated sampling and calibration
- High precision analyses for a wide spectrum of analytes with multiple detector options