INSTALLATION INSTRUCTIONS and TROUBLESHOOTING GUIDE. for the OnGuard- CARTRIDGE

Transcription

1 INSTALLATION INSTRUCTIONS and TROUBLESHOOTING GUIDE for the OnGuard- CARTRIDGE (OnGuard-RP, P/N ) (OnGuard-H, P/N ) (OnGuard-P, P/N ) (OnGuard-Ag, P/N ) (OnGuard-A, P/N ) (OnGuard-Ba, P/N ) QUICKSTART STEPS AND LINKS Click blue text below to get started. 1. See Section 2.2, "OnGuard-H" for use instructions. 2. See Section 2.3, "OnGuard-Ag" for use instructions. 3. See Section 2.4, "OnGuard-P" for use instructions. 4. See Section 2.5, "OnGuard-RP" for use instructions. 5. See Section 2.6, "OnGuard-A" for use instructions. 6. See Section 2.7, "OnGuard-Ba" for use instructions. DIONEX Corporation, 1997, 1998, 2001 Document No Revision June 2001

2 Page 2 of 11 OnGuard I Manual Doc. No TABLE OF CONTENTS SECTION 1 - INTRODUCTION... 3 SECTION 2 - CARTRIDGE USAGE Pretreatment Procedures for the Cartridges ONGUARD-H RECOVERY DATA REMOVAL OF CARBONATE ONGUARD-Ag RECOVERY DATA ONGUARD-P RECOVERY DATA ONGUARD-RP RECOVERY DATA REMOVAL OF SURFACTANTS ONGUARD-A RECOVERY DATA ONGUARD-BA OPTIMIZED REMOVAL OF SULFATE RECOVERY DATA TRACE LEVEL BROMATE ANALYSIS... 11

3 Page 3 of 11 OnGuard I Manual Doc. No SECTION 1 - INTRODUCTION The DIONEX line of sample pretreatment cartridges, consisting of the OnGuard-RP (P/N ), the OnGuard-H (P/N ), the OnGuard-P (P/N ), the OnGuard-Ag (P/N ), the OnGuard-A (P/N ) and the OnGuard-Ba (P/N ) is designed for sample clean up or matrix elimination, including removal of both column-fouling substances and interfering ions, where at least 4 mls of sample is available. This document describes recommended manual pretreatment procedures for the cartridges and provides examples of how to use each type of cartridge. In manual pretreatment, the luer-compatible cartridge housing is connected directly to the luer fitting on the injection port of an Ion Chromatograph (IC). If semiautomated sample pretreatment with DIONEX Automated Sampler vials is preferred, the cartridges can be connected to the luer tapers on the OnGuard Sample Preparation Workstation (P/N ). Even if the actual sample injection will be made manually, the workstation is convenient for prewashing cartridges. For complete installation and operating instructions, refer to the operator s manual for the workstation (Document No ).

4 Page 4 of 11 OnGuard I Manual Doc. No SECTION 2 - CARTRIDGE USAGE 2.1 PRETREATMENT PROCEDURES FOR THE CARTRIDGES For optimum results with the OnGuard cartridges, always observe the following basic principles of usage. 1. To provide the necessary pressure on the cartridges in manual pretreatment of samples, use a 5-mL syringe, especially when using an OnGuard-P cartridge. Back pressure in this cartridge is higher than in the other types of OnGuard cartridges. 2. Before using a cartridge, flush it with the volume of deionized water or solvent recommended in Table 1, "Recommended Cartridge Preparation Procedures", Columns 3, to remove trace ionic contaminants from the cartridge and condition the packing. EXAMPLE: Before application of the sample, flush the OnGuard-RP cartridge first with 5 ml of methanol and then with 10 ml of deionized water. When doing low level analyses (e.g., 100 ppb to 1 ppm chloride with loop injections), flush the cartridge as directed in Table 1, "Recommended Cartridge Preparation Procedures", Columns 3. Afterwards, treat the cartridge with an additional 2 ml of deionized water and inject into the Ion Chromatograph to determine a blank level. If the cleaning was inadequate, flush the cartridge with additional water and then recheck. 3. To maximize loading on the cartridge bed, put the sample through at the recommended flow rate (Table 1, "Recommended Cartridge Preparation Procedures", Column 4). The most efficient use of the cartridge beds is obtained at sample flow rates less than 4.0 ml/min for sorption-based processes and less than 2.0 ml/min for ion exchange processes. Higher flow rates are practical if less than maximum loading is acceptable. 4. Always discard the recommended initial effluent volume (Table 1, "Recommended Cartridge Preparation Procedures", Column 5) when treating a sample or standard. EXAMPLE: After filling a 5-mL syringe with sample, push the first 3 ml into a waste container. Collect the next 2 ml for injection into the Ion Chromatograph. 5. If the substance to be removed by the cartridge is colored or otherwise visible in the cartridge (e.g., AgCl precipitate), use the cartridge until the visible band extends about three-fourths of the way to the cartridge outlet. For absolute determination of loading capacity for a specific application, aliquots of sample can be put through the cartridge and tested by the appropriate detection method (e.g., UV, ph, conductivity, or precipitation) until a breakthrough is observed. EXAMPLE: To test Cl - breakthrough on the OnGuard-Ag cartridge, push ml aliquots of sample through the cartridge into several small beakers containing 5-10 ml of 0.1 N AgNO 3. Breakthrough occurs when a AgCl precipitate is first observed in one of the beakers. 6. Optimum performance is achieved when the cartridges are used in a vertical direction.

5 Page 5 of 11 OnGuard I Manual Doc. No Table 1 Recommended Cartridge Preparation Procedures Maximum Initial Sample Flushing Volume Flow Rate Volume to discard Cartridge Solvent (ml) (ml/min) (ml) OnGuard-RP 1. Methanol DI water 10 for anion ion-pair applications, continue with: M TMAOH 4 4. DI water 10 OnGuard-H DI water OnGuard-P* DI water OnGuard-Ag DI water OnGuard-A DI water OnGuard-Ba DI water * The OnGuard-P cartridge may not appear full when received, but the bed will swell when flushed. 2.2 ONGUARD-H The OnGuard-H cartridge (P/N ) contains sytrene-based, strong acid resin in the H + form. The resin has a very high selectivity for multivalent cations such as calcium and the transition metals. The cartridge is designed primarily for the removal of high levels of alkaline earths and transition metals from sample matrices, for the neutralization of caustic samples, and for the removal of carbonate. The cation exchange capacity is meq/ cartridge on a water-swollen basis. Resin capacity is 5.0 meq/g (dry). With one cartridge, 10 ml of 0.2 M NaOH may be neutralized before analysis. The resin is stable over a ph range of RECOVERY DATA When using the OnGuard-H, recoveries of a group of carboxylic acids that included acetic, valeric, benzoic, succinic, and tartaric acids were greater than 98% at ph 4 or above, except for aromatic acids such as benzoic acid, where recoveries were greater than 95% at over ph 5. NOTE Adding a small amount of an organic solvent such as 2% isopropanol or acetonitrile to the sample improves recovery of aromatic acids REMOVAL OF CARBONATE OnGuard-H, in combination with nitrogen or helium sparging, is effective for removing carbonate from samples. The sample is passed through the cartridge in the standard way (See Table 1, "Recommended Cartridge Preparation Procedures"). This process acidifies the carbonate to carbonic acid. The carbonic acid is then removed by sparging the sample for 5 min. More than 400 ppm carbonate can be removed from more than 10 mls of sample, depending on the concentrations of other cations also present in the sample.

6 Page 6 of 11 OnGuard I Manual Doc. No ONGUARD-AG The OnGuard-Ag cartridge (P/N ) contains a silver form, high capacity, strong acid cation exchange resin. Except for the ionic form, it is very similar to the OnGuard-H packing. The OnGuard-Ag cartridge removes Cl -, Br -, I -, AsO 4 3-, CrO 4, CN -, MoO 4, PO 4 3-, SeO 3, SeCN -, SO 3-, S, SCN - and WO 4 by precipitation. Recoveries for analytes of interest should be confirmed. Recovery of nitrite may be low in acidic samples, depending on the sample ph and the quantity applied to the cartridge. The cartridge has a capacity of meq/cartridge on a water-swollen basis. For example, approximately 9 ml of 1% NaCl may be treated with one OnGuard-Ag cartridge. The OnGuard-Ag is often followed by an OnGuard-H cartridge. The OnGuard-H traps any silver ion that may breakthrough, thus protecting the analytical column. NOTE Samples with ph greater than 7 will form a black silver oxide precipitate in the cartridge RECOVERY DATA Recoveries of 2 ppm fluoride, 10 ppm nitrate, and 15 ppm sulfate are greater than 98%. When phosphate is an analyte in a matrix passed through the OnGuard-Ag cartridge, the recovery of phosphate should be determined for the matrix. Phosphate may precipitate with Ag depending on the matrix composition. Phosphate recoveries should be determined by standard addition to the matrix. 2.4 ONGUARD-P The OnGuard-P cartridge (P/N ) contains a polyvinylpyrrolidone (PVP) polymer with a very high selectivity for phenolics, azo containing compounds, aromatic carboxylic acids, and aromatic aldehydes. PVP also has a very high selectivity for triiodide. The cartridge is recommended for removing the phenolic fraction of humic acids, tannic acids, lignins, anthocyanins, and azo dyes from samples prior to either anion or cation analyses. These substances are all known foulants of anion exchange resins. The OnGuard-P can successfully treat these samples because the cartridge packing does not contain anion or cation exchange functionality. A major application for OnGuard-P cartridges is the removal of phenolics from sample matrices. Loading capacities for phenolics on OnGuard-P are maximized at a sample ph of 4. Lignin sulfonate, ph adjusted to ph 3.7, can be removed from aqueous samples at a capacity of about 6 meq/cartridge RECOVERY DATA Recoveries of 2 ppm fluoride, 3 ppm chloride, 10 ppm nitrate, 15 phosphate, and 15 ppm sulfate are greater than 98%. Recovery of nitrate at the 1 ppm level is greater than 95%. Table 2, "Recovery Data for OnGuard-P", shows the results of recovery experiments for some carboxylic acids. Selectivity of the OnGuard-P packing for protonated aliphatic carboxylic acids is slight compared to that for phenolics, azo-containing compounds, aromatic carboxylic acids, and aromatic aldehydes. When using the cartridge for an organic acid analysis, recovery determinations should be made for accurate results.

7 Page 7 of 11 OnGuard I Manual Doc. No Table 2 Recovery Data for OnGuard-P ph 4.5 ph 6.1 Acetic acid, 5 ppm 100% 100% Valeric acid, 20 ppm 94.5% 98.5% Benzoic acid, 10 ppm 63.9% 100% Succinic acid, 10 ppm 94.3% 98.1% Tartaric acid, 10 ppm 99.2% 100.5% NOTE: Results are accurate to within + 5%. 2.5 ONGUARD-RP The OnGuard-RP cartridge (P/N ) contains a macroporous divinylbenzene reversed phase packing. This resin has a very high selectivity for hydrophobic substances, especially unsaturated or aromatic substances. It is compatible with all HPLC solvents. The resin is stable over a ph range of OnGuard-RP can replace C-18 bonded phases for many applications, especially where sample ph is extreme. OnGuard-RP is recommended for removing the following types of substances from sample matrices: aromatic dyes, hydrocarbons, surfactants, and some carboxylic acids. It is also useful for trace enrichment, a technique in which substances are isolated and concentrated on the cartridge from sample matrices and then eluted from the cartridge in a clean minimum volume solvent. Since the packing contains no anion or cation exchange sites, the OnGuard-RP cartridge may be used prior to ion exchange analysis to remove hydrophobic contaminants. In a reversed phase mode, the divinylbenzene resin functions as a hydrophobic substrate. Before using the cartridge with aqueous samples, treat it with methanol (see Table 1, "Recommended Cartridge Preparation Procedures") to wet the packing and promote the most efficient use of the resin surface. Consider the following experimental results: two OnGuard-RP cartridges were treated with 5 ml of 1000 ppm aqueous sodium lauryl sulfate (SLS) at 4.0 ml/min. One cartridge was pretreated with methanol; the other was not. The eluate from the pretreated cartridge contained 24 ppm of SLS, while the eluate from the untreated, semi-dry cartridge contained 979 ppm of SLS. Very little of this anionic surfactant was retained on the untreated cartridge RECOVERY DATA Recovery of carboxylic acids is ph dependent. At an acidic ph, where the carboxylic acids are protonated, significant losses occur. Table 3, "Recovery Data for OnGuard-RP", summarizes the data generated for a group of carboxylic acids that included monovalents, an aromatic, and divalents. The initial 3 ml of sample from the cartridge was discarded (see Table 1, "Recommended Cartridge Preparation Procedures") and the data was calculated on the following 2 ml. As indicated in Table 3, "Recovery Data for OnGuard-RP", the addition of a small amount of isopropanol or other organic solvent aids recovery of the more hydrophobic acids.

8 Page 8 of 11 OnGuard I Manual Doc. No Table 3 Recovery Data for OnGuard-RP ph 2.5 ph 4.5 ph 4.5 ph 6 Cartridge (aq) (aq) (2% IPA) (aq) Acetic acid, 5 ppm 50% 81% 100% 100% Valeric acid, 20 ppm 0% 0% 10% 3% Benzoic acid, 10 ppm 0% 3% 14% 8% Succinic acid, 10 ppm 50% 100% 100% 98% Tartaric acid, 10 ppm 100% 101% 100% 100% NOTE: Results are accurate to within + 5% REMOVAL OF SURFACTANTS In addition to use in a reversed phase mode, OnGuard-RP can also be used in an ion pairing mode to remove ionic substances. The recommended ion pairing reagent is tetramethylammonium hydroxide (see Table 1, "Recommended Cartridge Preparation Procedures", for use conditions). Significant losses of the inorganic anions occur when quaternary ammonium type ion pairing reagents larger than tetramethyl (e.g., tetraethyl and tetrapropyl) are used. Any substance that can be retained by MPIC using NH 4 OH or TMAOH reagents can be removed from a matrix on OnGuard-RP in the ion pairing mode. In general, higher loading capacities for anionic surfactants can be obtained in the ion pairing mode than in the reversed phase mode: about 20 mg/cartridge of sodium lauryl sulfate (SLS) can be removed in the reversed phase mode, while 90 mg/cartridge can be removed in the ion pairing mode with TMAOH reagent. Recoveries of fluoride, chloride, phosphate, nitrate, and sulfate are greater than 98% in the reversed phase mode. Recoveries for these anions in the ion pairing mode, using TMAOH reagent, are greater than 96%. 2.6 ONGUARD-A The OnGuard-A Cartridge (P/N ) contains styrene-based, strong base anion exchange resin in the HCO 3 - form. The resin is selective for anionic species and is designed primarily for the removal of anionic contaminants in sample matrices or neutralization of acidic samples. The OnGuard-A cartridge is also very useful in removing anionic amino acids, peptides, proteins and other contaminants from glycoproteins, hydrolysates or carbohydrate samples. The anion exchange capacity is about 0.7 meq/cartridge on a water-swollen basis. The resin is stable over a ph range of RECOVERY DATA Recoveries of 5 ppm lithium, 20 ppm sodium, 20 ppm potassium, 20 ppm magnesium and 100 ppm calcium are greater than 98%. 2.7 ONGUARD-BA The OnGuard-Ba cartridge (P/N ) contains a barium-form, high capacity, strong acid cation exchange resin. The cation exchange capacity is meq/cartridge on a water-swollen basis. Resin capacity is 5.0 meq/g (dry). When used properly, the OnGuard-Ba cartridge removes sulfate and chromate by precipitation. Recoveries for analytes of interest should be confirmed.

9 Page 9 of 11 OnGuard I Manual Doc. No Precipitation of sulfate by barium-form resin is dependent on the elution of barium ion from the resin by sample matrix cations. Results therefore can be highly variable. OnGuard-Ba will reduce sulfate from a 100 ppm sodium sulfate sample to about 15 ppm. If the spiking technique described in is used, the sulfate from a 100 ppm sodium sulfate sample is reduced to about 0.5 ppm OPTIMIZED REMOVAL OF SULFATE NOTE This technique uses several types of OnGuard Cartridges. Please check that your analytes of interest are not removed by any of the cartridges. DIONEX has developed a technique* for assuring optimum removal of sulfate by OnGuard-Ba that is independent of sample matrix composition. In this method, samples are spiked with a divalent displacing cation, such as Ca 2+ or Mg 2+ in order to ensure that Ba 2+ is available for precipitation with SO 4 from the sample. Co-precipitation of various analyte anions with BaSO 4 is minimized by spiking the sample with CO 3. Low recovery of some oxyanions can be significantly improved by the addition of CO 3 to the samples prior to pretreatment with the barium-form device. The chloride salt of the displacing cation is used because the Cl - counterion can be trapped on the silver-form resin. Carbonate can be removed by acidifying through H-form resin and sparging. Low recoveries of anions in the presence of barium sulfate may be due to co-precipitation. The addition of carbonate improves recoveries to varying degrees depending on the analyte (see Table 4, "Recovery of Oxyanions from Ba 2+ -form Resin"). Recoveries of analytes of interest should always be determined in the sample matrix. In this technique, as in any other for sample pretreatment, the recovery for the analytes of interest must be determined for each sample type. Lower concentrations of Ca 2+ may be used if less than maximum sulfate removal is required. The Ca 2+ is effective in eluting the Ba 2+ from the resin so that it can precipitate with sulfate. OnGuard-Ba is followed by OnGuard-Ag in order to remove the chloride contributed to the sample by the calcium chloride as well as the other ions indicated in Section 2.3, "OnGuard-Ag". This technique is outlined below. Materials Needed: 1. OnGuard-Ba 2. OnGuard-Ag 3. OnGuard-H (or in-line MetPac CC-1 for Ag + trapping only if removal of carbonate is not needed) 4. Extra-pure calcium chloride Procedure: A. Prepare OnGuard-Ba, OnGuard-Ag and OnGuard-H as described in Table 1, "Recommended Cartridge Preparation Procedures". B. Connect these cartridges in order of Ba-Ag- H. See Figure 1, "Manual Use of Multiple OnGuard Cartridges for Sulfate Removal". C. Prepare a 0.5 M CaCl 2 solution from extrapure calcium chloride. D. Spike the sample to 100 mg/l Ca 2+ or Mg 2+ using chloride salts. Spike with CO 3 if oxyanions are the analytes of interest. E. Apply spiked sample to the cartridge train at less than 2 ml/min. Follow the manual protocol i.e., discard the first 3 mls. 1. Deliver Sample at < 2 ml/min with luer-lock syringe 2. OnGuard-Ba removes sulfate 3. OnGuard-Ag removes chloride 4. OnGuard-H removes soluble silver and carbonate 5. Sparge with helium gas at 5 psi for 5 min to remove carbonate Figure 1 Manual Use of Multiple OnGuard Cartridges for Sulfate Removal

10 Page 10 of 11 OnGuard I Manual Doc. No RECOVERY DATA Table 4 Recovery of Oxyanions from Ba 2+ -form Resin (Following Figure 1, "Manual Use of Multiple OnGuard Cartridges for Sulfate Removal") Sample Matrix Composition (in meq/l) Matrix SO 4 Cl - Na + Ca 2+ CO 3 Comments Matrix without CO 3 but with Ca Matrix with both CO 3 and Ca 2+ Sample Matrix Composition 1 2 Added Recovered Added Recovered Analytes ng % ng % NO BrO SeO ClO SeO AsO PO 4 3-* 20 0 na * Samples in a matrix of 1 mm Na 2 SO 4 (without Ca 2+ ) show a 42 % recovery of phosphate. A paper entitled "Approaches to Sample Preparation for Ion Chromatography - Sulfate Precipitation on Barium-form Ion Exchangers" by R. W. Slingsby and C. A. Pohl is available from DIONEX Corporation and has been submitted to J. Chromatography, IC Symposium 1995 edition.

11 Page 11 of 11 OnGuard I Manual Doc. No TRACE LEVEL BROMATE ANALYSIS Complete details for this method can be found in Application Note 101, "Trace Level Determination of Bromate in Ozonated Drinking Water by Ion Chromatography". The following is a summary of the procedure. A. Set up a 3-cartridge OnGuard train as described in Section 2.7.1, "Optimized Removal of Sulfate". B. Prepare 0.5 M MgCl 2 7H 2 O C. Prepare M Na 2 CO 3 D. Spike 9.8 mls of sample with 100 µls of the magnesium chloride solution and 100 µls of the sodium carbonate solution. This produces a sample with M Mg 2+ and 100 mg/l CO 3. The addition of carbonate to the sample aids bromate recovery. Mg 2+ is used rather than Ca 2+ because MgCO 3 is soluble at this level, as compared to CaCO 3. E. Apply sample as in Figure 1, "Manual Use of Multiple OnGuard Cartridges for Sulfate Removal", including sparging to remove the carbonate prior to ion chromatographic analysis.