Application Finder

This Application Note describes the digestion of a cement sample and the photometric determination of iron in accordance with DIN EN 196-2 by means of Optrode at 610 nm. Sulfosalicylic acid is used as the indicator and EDTA as the titrant for the determination.

This Application Note is devoted to the photometric determination of magnesium in cement using the Optrode (610 nm). After digestion of a sample aliquot, the magnesium content is determined using EDTA titration.

This Application Note treats the photometric titration of nickel using the Optrode (520 nm). Murexide was used as the indicator and EDTA as the titrant.

This Application Note details the photometric determination of chondroitin sulfate with 1-hexadecylpyridinium chloride as titrant and with the Optrode (660 nm). The method is in compliance with the Ph. Eur. and the USP.

ASTM D8192 describes the photometric titration of the total hardness, calcium hardness, and magnesium hardness in water with an optical sensor for objective endpoint indication, increasing precision and reliability. The method is suitable for both colored and colorless samples such as groundwater, surface water, wastewater, and drinking water. Using a fully automated OMNIS system equipped with an Optrode ensures that the sample preparation and analysis are repeatable.

This Application Note describes the photometric determination of sulfate using the Optrode (610 nm). Sulfate is titrated with a lead nitrate solution; dithizone is used as indicator.

Vitamin C, also known as ascorbic acid or L-ascorbic acid, is an essential nutrient involved in the repair of tissues and the enzymatic production of certain neurotransmitters. It is required for the functioning of several enzymes and immune performance, and is also an important antioxidant. This nutrient is found in many foods and is often used as a dietary supplement.This Application Note describes the photometric determination of ascorbic acid according to the standard ISO 6557-2. To increase the objectivity on the determined equivalence point and the reproducibility of the results, an autotitrator equipped with a photometric sensor, the Optrode, is used. The titrant 2,6-Dichlorophenol-indophenol (DCIP or DPIP) simultaneously serves as titrant and indicator.

The carboxyl end groups (CEG) in polymers, such as polyethylene terephthalate (PET), are a measure of the number of unreacted carboxylic acid groups at each end of a polymer chain. The number of CEGs may influence the hydrolysis resistance of geosynthetics, such as geogrids and geotextiles. The lower the CEG value the higher is the hydrolysis resistance of geosynthetics, which in turn increases their stability.This Application Note describes the photometric titration of carboxyl end groups in PET pellets using the Metrohm Optrode. The acidic end groups of the polymer are titrated with an ethanolic KOH solution using bromophenol blue as indicator.

This Application Note describes the photometric determination of bismuth nitrate using the Optrode (520 nm). The sample is titrated with EDTA solution past the endpoint; xylene-orange is used as the indicator. The method for bismuth nitrate fulfills the directives defined in the Ph. Eur. and the USP.

This Application Note looks at the photometric determination of manganese sulfate using the Optrode (610 nm). Manganese is titrated with EDTA; Eriochrome Black T is used as indicator. The method complies with Ph. Eur. and the USP.

This Application Note describes the photometric determination of zinc sulfate using the Optrode at a wavelength of 610 nm. Complexometric titration of zinc requires EDTA as titrant and Eriochrome Black T as indicator. The method fully complies with Ph. Eur. and USP.

This Application Note describes the determination of total content of Ba, Ca, Mg, Pb and Zn in unused lubricating oil by means of the Optrode (610 nm). An excess of EDTA is first added to the metals. Afterwards, the excess EDTA is titrated back with magnesium chloride solution up to the end point of the indicator Eriochrome Black T.

The acid number (AN) of insulating, transformer, and turbine oils is crucial to ensure safe operation, operating equipment control, and corrosion prevention. These oils generally have low AN specifications and their AN determination by manual color-indicator titration is difficult, especially when analyzing colored samples.Using a Titrator with a photometric sensor to detect the end point ensures that the titrations are always carried out under the same conditions. This greatly increases the precision and reliability of the results, which in turn results in improved monitoring for your operations.

Basic additives are added to petroleum products to inhibit corrosion as they have a neutralizing effect on acidic compounds, which are formed as a result of degradation processes. Total base number (TBN) indicates the amount of basic additives present and thus can be used as a measure for the degradation of the petroleum product.Using an automated titration system with a photometric sensor to detect the end point ensures that the titrations are always carried out under the same conditions. This improves the precision and reliability of the results.This Application Notes describes the fully automated photometric determination of TBN in used engine oil using the Metrohm Optrode for the indication of the methyl orange endpoint (at 520 nm).

Fresh as well as used petroleum products may contain acidic components as additives or degradation products. The acid number (AN) is a measure for the relative amount of acids present expressed as mg KOH per g sample. Moreover, AN is used as a quality parameter of lubricating oils both for assessing the quality of new formulations and as an indicator for the degradation of such formulations during service. The use of a pH electrode suitable for non-aqueous titrations ensures the reliable determination of the equivalence point. A flexible sleeve diaphragm facilitates its cleaning especially after use in heavily contaminated samples, such as in used engine oils. Using the correct electrode greatly increases the precision and reliability of the results. This Application Note describes the potentiometric determination of the acid number according to ASTM D664 and IP 177 using the pH electrode Solvotrode easyClean.

Basic chemicals are added to petroleum products to prevent corrosion as they neutralize acidic components that form during the use and aging of these products. The base number (BN) gives an indication regarding the amount of these basic additives present, and it can be used as a measure for the degradation of the petroleum product.This Application Note describes the potentiometric determination of the base number according to ISO 3771, ASTM D2896, and IP 276 using the Metrohm Solvotrode easyClean and a fully automated OMNIS system.

The present Application Note describes an automated system with which the acidity can be determined in a wide variety of juice samples. The high degree of automation (e.g., automated calibration and titer determination) reduces errors to a minimum and offers outstanding reproducibility.

Acid copper baths are mainly used for the copper deposition on semiconductor wafers. Small amounts of chloride increase the speed of deposition and reduce anode polarization. However, higher concentrations are undesired, as this will decrease the quality of the copper deposition. Therefore, it is quite important to monitor the amount of chloride to have an effective, yet high-quality copper deposition process.In this Application Note, a fully automated solution based on titration is presented. In comparison to ion chromatography, titration offers the benefit that no dilution of the sample is necessary, and the hardware is comparatively low-priced. Furthermore, the fully automated solution allows users to minimize handling errors, to reduce workloads, and to guarantee outstanding reproducibility.

This Application Note describes an automated system with which the chloride content in various water samples can be determined. The high degree of automation (e.g., automated addition of acid and titer determination) reduces errors to a minimum and ensures outstanding reproducibility.

In many countries, the aluminum concentration in water is limited to 0.2 mg/L. This application note shows how the analysis of aluminum in water can be done fully automatically by complexometric titration with EDTA.

In this Application Note, the determination of calcium in milk is shown with the copper ion-selective electrode which is less sensitive to contamination from proteins.

This Application Note describes the fully automated complexometric determination of total iron in cement with a copper ion-selective electrode.

This Application Note describes the fully automated complexometric determination of zinc(II) in aqueous solutions with a copper ion-selective electrode.

The hydroxyl number (HN) is an important sum parameter for quantifying the presence of hydroxyl groups in chemicals. As a key quality parameter, it is determined in various substances. For pharmaceutical samples, USP chapter <401> and Ph. Eur. Chapter 2.5.3 describe the determination. However these methods either use toxic pyridine and require refluxing or have long reaction times.In this Application Note, an alternative method according to ASTM E1899 is presented. This method is pyridine-free and does not require refluxing or long reaction times. The determination is performed at room temperature with only a small sample size. The analysis including all preparation steps is performed with a fully automatic OMNIS system. This allows parallel analysis of multiple samples, increasing productivity in the laboratory by 50%.

This Application Note describes the iodometric, bivoltametric determination of ascorbic acid in orange juice using the Double Pt-sheet electrode.

This Application Note describes the bivoltametric titration of ascorbic acid in orange juice. 2,6-dichlorophenol indophenol (DPIP) is used as titrant; endpoint determination takes place using the Double Pt-sheet electrode.

This Application Note describes automatic sulfate determination using a combined ion-selective calcium electrode. Sulfate is precipitated with an excess of barium chloride solution. Excess barium is subsequently back-titrated with a standard EGTA solution.

This Application Note describes an automated system with which the chloride content in bouillon can be determined. The high degree of automation (e.g., automatic addition of acid and titer determination) reduces errors to a minimum and ensures outstanding reproducibility.

This application note shows the use of an ion-selective copper electrode to measure the indium concentration in an aqueous solution.

Zirconium can be analyzed quickly and easily in slightly acidic solutions with back titration. The ion-selective copper electrode is used in this Application Note to determine zirconium in aqueous solution.

Water hardness is often determined photometrically using two different indicators and while performing the determination at two different pH values. Additionally, the determination itself is subjective, as the color change is determined by the analyst and not by an analytical device.This application note introduces a more robust option to easily assess calcium, magnesium, and total hardness in water by using the Cu-ISE and two different titrants. Sample preparation is identical for both analyses and can therefore be automated without any issues.

The titratable acidity gives an indication of the freshness of milk and yogurt as well as other fermented milk products. The determined titratable acidity in milk is mainly given through the absorption of hydroxyl ions by milk proteins and milk salts. The acidity increases with bacterial acidification and with enzymatic lipolysis. The titratable acidity corresponds to the amount of sodium hydroxide required to titrate 100 g sample to a pH value of 8.30.In this Application Note, an easy and accurate method to determine the titratable acidity in milk according to DIN 10316 and in yogurt according to ISO/TS 11869 and IDF/RM 150 is demonstrated.

In order to maintain product quality, the sodium chloride content in dairy products must be monitored and not exceed the limits defined by the respective public health authorities. The chloride content in food correlates with the salt content, its determination is therefore described in various norms and standards. However, preparation of such samples is time consuming, as it includes a chloride extraction with warm water. Whole milk powders in particular are difficult to handle as an inhomogeneous dispersion of fat in the titration suspension occurs.In order to reduce the workload, increase sample throughput, and eliminate the matrix challenges posed by high fat products, this Application Note presents a fully automatic potentiometric titration of chloride with silver nitrate in milk and milk powder based on ISO 21422, IDF 242, AOAC 2015.07, AOAC 2015.08 and AOAC 2016.03

The salt content in food is a critical parameter, given that the WHO recommends a maximum daily intake of 5 g for an adult. In butter with a salt content exceeding 0.1%, it can be determined by a precipitation titration of chloride with silver nitrate. However, during manual titration the operator cannot leave the system unattended because he has to exchange the sample beakers manually which is time consuming and prone to errors.This Application Note describes the automated determination of chloride in salted butter in accordance with ISO 15648, ISO 21422, IDF 179 and IDF 242. If automated according to the norms and standards, salt determination can be performed completely unattended with superior reproducibility of results increasing efficiency in the laboratory.

The WHO recommends a maximum daily intake of 5 g salt for an adult. The chloride content in food correlates with the salt content, its determination is therefore described by various standards. In cheese and cheese products with a chloride content higher than 0.2%, chloride is usually determined by a precipitation titration with silver nitrate. However, time-consuming sample preparation is required, as the cheese has to be homogenized and the chloride extracted with hot water.This Application Note describes the fully automatic determination of chloride in cheese according to EN ISO 5943, ISO 21422, IDF 242 and IDF 88 including sample preparation with a Polytron homogenizer. This increases productivity due to a higher sample throughput and lower work load for the operator.

This Application Note describes the nonaqueous acid-base titration of ketoconazole in accordance with the European Pharmacopoeia. The Solvotrode easyClean was used as the electrode.

Potentiometric titration with silver nitrate can be used for the determination of mercaptans in refinery products. This Application Note describes their automatic determination in a middle distillate sample (gas oil).

The alpha acid level (AA%) in hops plays a major role in the bitterness they can impart to beer. The AA% can vary between 1% up to 20% in hops. During boiling in the brewing process, alpha acids transform into iso-alpha acids which make the beer bitter. For this reason, it is important for brewers to know the exact AA value of the hops they use. The determination of AA% in hops with conductometric titration according to the EBC method 7.4 is shown in this Application Note.

The basicity and the CPR (controlled polymerization rate) are very important parameters for the quality of polyols used in polyurethane production. The knowledge of these values is crucial to prevent gelation during handling in the production. In this Application Note their determination by automated, potentiometric titration according to ISO 14899 is described.

Acrylic acid dimerizes spontaneously. Determining the dimer content is, therefore, a key part of the quality control for acrylic acid. One quality control parameter for the dimerization is the acid number. This Application Note describes its determination by automated, potentiometric titration.

The composition of salts with laxative and expectorant effects must be determined precisely in medications. The sulfate content is determined using automatic potentiometric titration with EGTA as titrant in accordance with Ph. Eur. 8.0.

The partial acid number (also partial acid value) describes the quantity of potassium hydroxide that is required for neutralizing all carboxyl-terminated groups and free acids plus half the anhydride groups in an unsaturated polyesterresin (UPR). This Application Note describes the determination of the partial acid value by automatic, potentiometric titration according to EN ISO 2114 using KOH in ethanol as titrant.

The total acid number (TAN) indicates the amount of potassium hydroxide required for neutralizing all carboxyl-terminated groups and free acids plus the free anhydride groups in an unsaturated polyester resin (UPR). In this Application Note the TAN determination using automated, potentiometric titration according to EN ISO 2114 using KOH in ethanol as titrant is described.

The hydroxyl number indicates the amount of potassium hydroxide in milligrams required to neutralize the acetic acid taken up on acetylation of 1 g of an unsaturated polyester resin (UPR) containing free hydroxyl groups. In this Application Note the determination of the hydroxyl number by automated, potentiometric titration according to EN ISO 2554 using KOH in methanol as titrant is described.

Polyurethane (PU) is a class of very important polymers due to its flexibility and insulating properties. It is used in various industries such as the automobile industry, in building construction, as well as in the production of synthetic fibers. PU is mostly produced via a chemical reaction between polyisocyanates and polyols.The isocyanate (NCO) content in the raw material is crucial to control its properties. This Application Note shows an easy and straightforward way to determine the NCO content in polyurethane raw materials using a fully automated titration system from Metrohm.

The pHe is a measure of acid strength in alcohol fuels and in ethanol. It can be used as predictor of the corrosion potential of an ethanol-based fuel. The determination of the pHe is preferred over the total acidity, because total acidity overestimates the contribution of weak acids (e.g., carbonic acid) and underestimates the contribution of strong acids (e.g., sulfuric acid). Furthermore, the acid strength is an important parameter to determine in order to reduce the risk of failing motors.This Application Note describes the determination of the pHe value using the 913 pH Meter and the EtOH Trode according to ASTM D6423, which covers denatured fuel ethanol and ethanol fuel blends.

Nicotine is a nitrogenous alkaloid that is hazardous to health and is characterized by a very high potential for addiction. The nicotine content in tobacco products must be determined and specified precisely. This Application Note exhibits an easy and straightforward method for nicotine determination in tobacco by non-aqueous titration.Results determined by GC and IC are given as a comparison. In comparison to chromatographic methods, titration is an «absolute method», meaning it is not necessary to calibrate the system prior to the analyses.

The iodine adsorption number (IAN) of carbon black is related to the surface area and can therefore be used for the characterization of carbon black. The presence of volatiles, surface porosity, or extractables will influence the iodine adsorption number. In this Application Note, the fully automated determination of the iodine adsorption number including sample preparation is described.

The hydroxyl number is an important sum parameter for quantifying the presence of hydroxyl groups in a chemical substance. As a key quality parameter, it is regularly determined in various polymers like resins, paints, polyesterols, fats, and solvents. Unlike other standards, EN 4629-2 works pyridine-free and without refluxing at elevated temperatures for a longer time. The determination is based on the catalytic acetylation of the hydroxyl group. It is performed at room temperature, requires only a small sample volumen, and can be fully automated.This Application Note describes the potentiometric determination of the hydroxyl number in 1-octanol and polyethylene glycol according to EN 4629-2. Using the OMNIS DIS-Cover technique, all sample preparation steps can be fully automated. Furthermore, the use of an OMNIS Sample Robot allows parallel analysis of multiple samples. The average time per analysis for one sample is thus reduced from approximately 49 min to 25 min., considerably increasing productivity in the laboratory.

The hydroxyl number is an important sum parameter for quantifying the presence of hydroxyl groups in a chemical substance. As a key quality parameter, it is regularly determined in various polymers like resins, paints, polyesterols, fats and solvents. Unlinke other standards, ASTM E1899 works pyridine-free and without refluxing at elevated temperatures for a longer time. It is performed at room temperature, requires only a small sample size, is applicable to extremely low hydroxyl numbers (<1 mg KOH/g sample) and can be performed fully automatically. This Application Note describes the potentiometric determination of the hydroxyl number in 1-octanol and polyethylene glycol according to ASTM E1899, EN 15168 and DIN 53240-3. Using the OMNIS DIS-Cover technique all sample preparation steps can be fully automated. Moreover, the use of an OMNIS Sample Robot allows parallel analysis of multiple samples. The average time per analysis for one sample is thus reduced from approximately 24 min to 12 min., increasing productivity in the laboratory considerably.

Lithium is a soft metal which is used for many applications, such as production of high-temperature lubricants or heat-resistant glass. Furthermore, lithium is used in large quantities in for battery production. It is obtained from brines and high-grade lithium ores. Depending on the lithium concentration, extraction may or may not be economically viable.This Application Note demonstrates a method to determine the lithium concentration in brines by potentiometric titration. Lithium and fluoride precipitate in ethanol as insoluble lithium fluoride. Using ammonium fluoride as the titrant and a fluoride ion-selective electrode (ISE), determination via potentiometric titration is possible. This method is more reliable, faster, and less expensive than the determination of lithium in brine by other more sophisticated techniques such as atomic absorption spectroscopy (AAS).

The bromine number is an important parameter for the determination of aliphatic C=C double bonds in petroleum products. The bromine number is usually determined using electrochemical titration at 5 °C, where the bromine is generated in situ from a bromide/bromate solution. For the titration, a solvent mixture of glacial acetic acid, methanol, and chloroform is used. In this Application Note, the toxic chloroform was replaced with diethyl carbonate.

The pHe value is an indicator for the acid strength and shows the presence of strong acids or bases in ethanol. In Europe, ethanol is used as a blending component in gasoline and needs to have a pHe value between 6.5 and 9.0.This Application Note describes a fast and accurate determination of the pHe value using the EtOH-Trode.

Metformin is one the most commonly used drugs for diabetes type 2 belonging to the group of biguanides. This Application Note describes the determination of metformin hydrochloride assay according to USP using acetic anhydride as solvent.

Quaternary ammonium salts are the active ingredients in fabric softener and require accurate determination to assess the cost and the performance of the fabric softener. This Application Note describes the determination of diamidoamine-based quaternary ammonium salts by potentiometric titration.

Quaternary ammonium salts are the active ingredients in fabric softener and require accurate determination to assess the cost and the performance of the fabric softener. This Application Note describes the determination of dialkyl dimethyl quaternary ammonium salts by back titration.

The bromine number indicates the degree of unsaturation and relies on the simple addition of bromine to the double bonds of alkenes. One mole of bromine is consumed for each mole of carbon-carbon double (C=C) bond present in a substance. In petroleum products, the bromine number corresponds to the olefin content.Normally, chlorinated solvents are used for the determination of the bromine number. In this Application Note they have been replaced by toluene. This makes the determination more ecological. The titration is performed automatically on an OMNIS system in combination with a double Pt-wire electrode. With this setup, a fast and accurate determination by potentiometric titration can be realized.

The knowledge of the exact silver content of silver allows used for jewelry is very important to ensure the quality of jewelry. Therefore, the determination procedure is regulated internationally and nationally. A common approach is the titration with potassium bromide after an acidic digestion of the silver using a silver electrode for indication.

This Application Note details the determination of acid-neutralizing capacity (ANC) in several pharmaceutical samples in compliance with USP<301> standards.

Kjeldahl method is used to determine the nitrogen content in organic and inorganic samples. Kjeldahl consists of three steps: digestion, distillation, and titration. During the catalytic digestion step, organic nitrogen is converted into ammonium. Sodium hydroxide is added just before the distillation step for converting ammonium into ammonia. Through steam distillation the latter is transferred into the receiver vessel containing an absorbing agent (e.g., boric acid). Finally, the separated ammonia is titrated against sulfuric acid. Protein content in samples can also be determined from the nitrogen content obtained by Kjeldahl setup. USP describes the titration method to determine nitrogen content in organic products using Kjeldahl nitrogen setup. This Application Note illustrates nitrogen determination in heparin sodium.

Vitamin C, also known as ascorbic acid or L-ascorbic acid, is an essential nutrient involved in the repair of tissues and the enzymatic production of certain neurotransmitters. It is required for the functioning of several enzymes and immune performance, and is also an important antioxidant. This nutrient is found in many foods and is often used as a dietary supplement.USP general chapter <580> describes a titration technique to determine the assay of Vitamin C as ascorbic acid, sodium ascorbate, and calcium ascorbate dehydrate, or their mixture in finished dosage forms as capsules, tablets, and oral suspensions. This Application Note demonstrates the Vitamin C determination in water-soluble vitamin tablets. The methodology can also be applied for oil-soluble vitamin or mineral tablets, as well as oil- and water-soluble vitamin or mineral capsules.

Denatured fuel ethanol may contain additives such as corrosion inhibitors and detergents as well as contaminants from manufacturing that can affect the acidity of produced ethanol fuel. An increased acid content in solvents could lead to a variety of problems like a shorter storage stability or chemical corrosion.Using the dSolvotrode for indication, the acidity is determined as acetic acid by titration with sodium hydroxide as titrant.

Corrosion of metallic components is an inherent problem for engines, because metals naturally tend to oxidize in the presence of water and/or acids. Increased acid content is indicated by a low pH value, and could lead to a variety of problems like a shorter storage life (stability) or a reduced buffer capacity of the used engine coolant or antirust.In this Application Note, engine coolants or antirust samples are dissolved in water, and the pH measurement using the Profitrode is carried out according to ASTM D1287.

Corrosion of metallic components is an inherent problem for engines, because metals naturally tend to oxidize in the presence of water and/or low pH value. The reserve alkalinity of engine coolants and antirusts is a measure of the buffering ability to absorb acidity. The reserve alkalinity is frequently used for quality control during production and often listed in the specifications of the coolants. A fast and accurate determination is therefore important.This Application Note describes the straightforward determination of reserve alkalinity according to ASTM D1121. Using a fully automated system allows an accurate and reliable determination due to the reduction of human errors. Furthermore, the operator is free to carry out other tasks increasing the efficiency of the laboratory.

The presence of acidic components in volatile solvents could be a result of contamination, decomposition during storage, distribution or manufacture. An increased acid content in solvents could lead to a variety of problems like shorter storage stability or chemical corrosion. Using the Optrode for indication, the acidity is determined by photometric titration with sodium hydroxide as titrant and phenolphthalein as indicator. If the volatile solvent is water soluble, it is dissolved in deionized water, if not, it is dissolved in carbon-dioxide free ethanol.

The permanganate index (PMI) is a sum parameter that indicates the total load of oxidizable organic and inorganic matter in water. The substances concerned are mainly humic materials/acids that are primarily formed when dead organic material present in soil is further broken down and released into water sources. As it is an indicator of the water quality, testing of the PMI for drinking water is obligatory in many countries.For the determination, it is necessary to heat the stabilized water sample to 95 °C and higher for a stipulated time. Afterwards, the amount of permanganate that has remained after the reaction with the sample is determined titrimetrically. This sample preparation step requires considerable manual effort.In this Application Note, a fully automated procedure for the determination of the PMI according to GB/T 11892 is described, including all sample preparation steps. The gains in productivity because of a reduced manual workload are considerable.

The bromine index is an important parameter for the determination of aliphatic C=C double bonds in petroleum hydrocarbons. For the titration, a solvent mixture of glacial acetic acid, methanol, and dichloromethane is usually used.In this Application Note, the chlorinated solvent in the solvent mixture was replaced with toluene, resulting in a more environmentally beneficial method in comparison to ASTM D2710 and IP 299.

The vaping and electronic cigarette industries have grown impressively in the past decade. The mixtures used in these products are usually called «e-liquid», «e-fluid», or «e-juice». To ensure the quality of these e-liquids, testing the most important quality parameters, such as nicotine content, is required. Nicotine in tobacco is usually determined by gas chromatography or liquid chromatography. Aqueous acid base titration is a much more affordable alternative for this determination. As e-liquids do not contain other components which might interfere with the titration, the aqueous acid base titration presented in this Application Note can be applied for nicotine determination. This method is an affordable and reliable way to determine the nicotine content in e-liquids and their nicotine starting material, ensuring the quality of these products.

This Application Note presents a potentiometric titration method for a potassium bicarbonate and potassium carbonate assay meeting all USP General Chapter <1225> requirements.

The FOS/TAC value, sometimes referred to as VFA/TA, is a meaningful parameter for assessing both the current condition and the development of anaerobic digestion processes in a digester of a biogas plant. Knowledge of this value can help decrease the risk of acidification problems, which can result in a costly crash of the entire digestion process. Therefore, an accurate and reliable determination of the FOS/TAC value is important for both efficient and cost-effective production operations. This value is determined by an acid-base titration. Using the Eco Titrator from Metrohm equipped with an Ecotrode plus electrode, a reproducible and accurate determination of the FOS/TAC value is possible.

Water treatment with ozone (O3) is a common procedure for the disinfection of swimming pools. It is important that a sufficient but not excessive amount of O3 is produced to disinfect the water. Otherwise, the remaining ozone could enter the swimming water, which could irritate the respiratory system or the skin of bathers.Ozone is also used in drinking and waste water treatment because it is significantly more effective than chlorine at inactivating or killing viruses and bacteria. This application note describes a method to determine the ozone concentration in water by potentiometric titration according to DIN 38408-3.

Nitrogen-based compounds are widely distributed in the environment and are essential growth nutrients for photosynthetic organisms. Therefore, it is important to monitor and control the amount of nitrogen compounds which are released into the environment.In this Application Note, a method to determine the nitrogen content in water by Kjeldahl digestion and distillation followed by a photometric or potentiometric titration according to ASTM D3590 is presented. The universality, precision, and reproducibility of the Kjeldahl method have made it the internationally recognized method for e.g. estimating the protein content in many matrices and it is the standard method to which all other methods are judged against.

Lithium salts (e.g., lithium carbonate and lithium hydroxide) are used in myriad applications. Lithium hydroxide is used for the production of lithium stearate, an important engine lubricant. In addition, it is utilized as an air purifier due to its ability to bind carbon dioxide. While the majority of lithium carbonate is used for aluminum production, it is also used for the glass and ceramic industry. It lowers the melting point of these materials, lowering the associated electricity costs and making it cheaper to produce them.For all of these applications, it is important to know the quality of the pure lithium salts used in the various production processes. This Application Note presents an easy method for the assay of lithium hydroxide and lithium carbonate on an automated OMNIS system.

Lithium nitrate is an oxidizing agent used in the manufacture of red-colored fireworks and flares. In addition, the lithium nitrate trihydrate compound absorbs heat well and can be used for thermal energy storage. Since lithium nitrate is a hygroscopic substance, its purity must first be verified before it is used for synthesis or other applications. The purity assay is done by a fully automated precipitation titration between lithium and fluoride in an ethanolic solution. The benefit of titration is that the lithium nitrate does not need to be diluted after dissolving in ethanol as with other techniques such as ICP-MS.

Sodium hypochlorite and sodium chloride can be effectively use as disinfectant for water and surfaces. The World Health Organization (WHO) recommends, depending on the application, concentrations in disinfectants of 1000 mg/L to 5000 mg/L NaOCl and up to 200 g/L NaCl.This Application Note demonstrates a reliable method to determine the hypochlorite and sodium chloride content in disinfectants by two subsequent argentometric titrations in the range recommended by the WHO.

The lithium-ion battery market is continuously growing due to the tremendous demand for battery powered consumer products. So-called «NCMs», a mixture of nickel, cobalt, and manganese oxides, have been gathering interest as cathode materials, replacing traditional compounds like cobalt oxides.Quality analysis of the post-sintered materials or recycled batteries can be performed by titration, as demonstrated in this Application Note. A fully automated analysis of the corresponding metals can be performed with OMNIS and its pipetting equipment.

In order to consistently manufacture high quality baked goods, it is critical to measure the pH value and acidity content in the raw materials and during the production steps. These factors have a major influence on the taste and storage lifetime of the final product. Consistent product quality is only possible with precise measurements during the process.This Application Note describes the measurement of pH value and the total titratable acidity in flour, dough, and bread using the Eco Titrator from Metrohm.

If consumed in excess, sodium may damage the cardiovascular system. It is therefore in the interest of food manufacturers to reduce the salt content and while preserving the flavor of the food.To ensure consistent quality, it is critical to know the exact salt content in the raw materials and the final products. This is only possible by performing precise measurements during the production process.This Application Note explains the determination of sodium chloride in dough and bread quickly according to AOAC 971.27 with the Eco Titrator equipped with an Ag Titrode.

Coagulation and flocculation are an essential part of treating both drinking water and wastewater. Aluminum salts such as aluminum sulfate and polyaluminum chloride (PAC) are often used for this purpose. For the precise application and exact dosage of the flocculant, it is important to accurately determine its aluminum content. In this Application Note, the aluminum content is accurately and reliably analyzed based on ABNT NBR 11176 using the 859 Titrotherm equipped with a Thermoprobe HF and sodium fluoride as titrant.

Many of the key factors that influence coffee taste correlate with chemical properties that can be measured. These include pH, titratable acidity, refractive index, and caffeine. Historically, many of these analyses have included long, manual sample preparation processes using the time-consuming, liquid chromatography (LC) technique. This Application Note looks at a faster, simpler, alternative method for analysis of key quality parameters in coffee using a single titration platform: OMNIS.

Sodium lactate is a salt form of lactic acid used in many regulated industries—therefore an accurate determination of the lactate content is required and is already covered in several norms. One such monograph by the US Pharmacopoeia (USP) results in high accuracies and well-defined titration curves but uses titrants and solvents that are more costly than necessary. In comparison, the presented modified method from Metrohm requires a 1:1 mixture of water and acetone and uses aqueous hydrochloric acid as titrant, resulting in an estimated cost reduction of 40% per titration compared to the USP method (USP–NF 2021, Issue 2). Furthermore, the time needed for each analysis is reduced to just 12% of the USP method (excluding blank determination). This Application Note presents both methods to determine lactate content and shows the results obtained on an OMNIS system.

This Application Note presents a complementary method that allows a consecutive determination after the sample preparation (digestion) of both metal ions in one beaker with an optical sensor and xylenol orange as an indicator.

About 20% of our sugar comes from sugar beet crops, mostly grown in Europe and the U.S. where the climate is temperate, whereas the other 80% is produced from sugar cane in tropical areas. Lime salts and pH are very important factors which are controlled during the sugar manufacturing process. Complexometric titration is often used to determine the concentration of lime salts in such kinds of samples. This Application Note presents a more robust method for determining calcium compounds in sugar beet juice. Subjectivity of color change determination is eliminated by using an ion selective electrode (ISE).

This Application Note compares the OMNIS Titrator and 888 Titrando for determinations of nitric acid, phosphoric acid, and acetic acid in an aluminum etching bath, as well as the determination of tetramethylammonium hydroxide (TMAH). Identical analysis parameters were used, showing that OMNIS delivers results on par or even better than with other established titration systems.

The pH value in carbon black, an essential additive in modern lithium-ion batteries, is accurately and reliably analyzed in this Application Note by using the 913 pH Meter equipped with a Unitrode easyClean according to ASTM D1512 as well as ISO 787-9 and GB/T 1717-1986.

Hydrochloric acid is a strong, inorganic mineral acid with great significance in the chemical industry. The potentiometric titration of hydrochloric acid with sodium hydroxide is one of the most important and also most frequent analyses performed in the laboratory. In this Application Note, an acid-base titration is presented where the concentration of HCl is determined with NaOH using a pH electrode with an integrated Pt1000 temperature senor for the most accurate results

Phosphoric acid is a triprotic inorganic acid used for many purposes: as a raw material for the production of phosphate fertilizers, detergents, as an electrolyte in phosphoric acid fuel cells, rust removers, and for the passivation of iron and zinc to protect against corrosion. This Application Note presents an acid-base titration where the concentration of phosphoric acid is determined over all three of its dissociable protons by titrating it with sodium hydroxide.

Alkalinity defines the acid-binding capacity of natural water. A distinction is made between total alkalinity (m-value) and carbonate alkalinity (p-value). This Application Note presents the determination of pH and alkalinity in water with a titration method conforming to EPA 310.1, Standard Methods 2320 B (Titration Method), ASTM D1067, EN ISO 9963-1, and EN ISO 9963-2.

The amine value is an important parameter and quality indicator to determine in chemical processes and pharmaceuticals. This Application Note presents the nonaqueous perchloric acid titration of triethanolamine.

The total acid number (TAN) is an important parameter for assessing the acidity of oils and fuels. This Application Note determines TAN using conductometric titration.

This application presents the fully automated determination of acidity in jet fuel as per ASTM D3242 via photometric titration with an automatic titrator and the Optrode.

Rare earth elements (REEs) are critical materials whose deposit viability and processing streams require accurate mass-fraction determination during ore dissolution and purification. This Application Note describes a rapid potentiometric back-titration using a copper ion-selective electrode (Cu-ISE) that enables selective quantification and partial separation of REEs in complex matrices with near-quantitative recovery. As an absolute, flexible, and cost-effective method with ICP-compatible sample preparation, back-titration is well suited both as a reference technique and for rapid on-site analysis.

Lithium carbonate is a key cathode material for lithium-ion batteries, and accurate carbonate content determination is essential for assessing purity and ensuring consistent battery performance, stability, and safety. This Application Note describes the automated determination of carbonate in lithium carbonate using the OMNIS Titrator and OMNIS Sample Robot with Dis-Cover lids according to the draft ISO 10662 standard. The OMNIS system provides fast, reliable purity analysis and can be readily expanded to support additional titration applications.

The determination of amino acid is an important task in pharmaceutical and biochemical applications. A binary gradient separates in this example 17 amino acids of a commercially available standard solution. The post-column reaction with ninhydrin requires a temperature of 120 °C, while the samples need to be cooled for stability.

Potassium bromate is used as a flour improver. The determination of the carcinogen bromate in flour requires extraction and additional sample preparation. In this application, Inline Dialysis is used after sonication and centrifugation of the extraction mixture. Bromate is detected by conductivity following suppression and UV/VIS detection and post-column reaction.

Ion chromatography trace analysis of anions in seawater is difficult, due to the high chloride concentrations. In contrast to chloride, nitrite, bromide and nitrate absorb UV radiation in the low wavelength range, thus enabling a UV detection of these three anions. This Application Note describes the separation on a column of the Metrosep Carb 2 - 100/4.0 type with a sodium chloride eluent. This minimizes the influence of the surplus chloride and enables low detection limits.

Nitrite in tobacco facilitates the release of tobacco-specific nitrosamines. Most of these nitrosamines are carcinogenic. Therefore, the determination of nitrite in tobacco is required. This application describes the determination of nitrite and nitrate in acetic acid extracts of tobacco. The ion chromatographic separation is followed by UV/VIS detection after sequential suppression.

This Application Note demonstrates the analysis of Cr(VI) in drinking water samples using IC-PCR in accordance with the procedure outlined in Appendix C, Section C.4 of EN ISO 18724.

Lead is commonly used as stabilizer in electroless nickel plating processes. The regular and precise determination of the electrochemically active Pb(II) concentration is essential to keep the plating process running optimally under stable conditions. Differential pulse anodic stripping voltammetry can be used to determine the active lead content after dilution. The voltammetric determination has been established as a straightforward, sensitive, selective, and interference-free method for this application.

Determination (after digestion) of zinc, cadmium, lead, copper, nickel, and cobalt in fabrication powder of vitamin tablets.

Determination of manganese, iron, and molybdenum (after digestion) in fabrication powder of vitamin tablets.

Ti is determined in polyethylene terephthalate (PET) after digestion in sulfuric acid and hydrogen peroxide. Adsorptive stripping voltammetry (AdSV) with mandelic acid as complexing agent is used for this application.

Co is determined in polyethylene terephthalate (PET) after digestion in sulfuric acid and hydrogen peroxide. The application is carried out with adsorptive stripping voltammetry (AdSV) in ammonia buffer with dimethylglyoxime (DMG) as complexing agent.

Sb is determined in polyethylene terephthalate (PET) after digestion in sulfuric acid and hydrogen peroxide. The application is carried out with anodic stripping voltammetry (ASV) in hydrochloric acid.

Aluminum can be determined in drinking water by adsorptive stripping voltammetry at the HMDE using alizarin red S (DASA) as complexing agent. The method is linear up to 35 μg/L. The detection limit for this method is β(Al) = 1 μg/L, the limit of quantification is β(Al) = 3 μg/L. The sensitivity of the method cannot be increased by deposition.

This Application Note describes the polarograhic determination of copper in electroplating baths used in the production of thin-film copper indium gallium diselenide solar cells (CIGS cells). The CIGS absorber layer is electrodeposited on a molybdenum-coated substrate.Copper analysis is carried out after dilution of the sample with sulfuric acid as supporting electrolyte.

This Application Note describes the polarographic determination of indium in electroplating baths used in the production of copper indium gallium diselenide thin-film solar cells (CIGS cells). The CIGS absorber layer is electrodeposited on the molybdenum-coated substrate. Indium analysis is carried out after dilution of the bath sample with sulfuric acid as supporting electrolyte.

This Application Note describes the determination of gallium in electroplating baths used in the production of copper indium gallium diselenide thin-film solar cells (CIGS cells). The CIGS absorber layer is electrodeposited on a molybdenum-coated substrate. Gallium analysis using anodic stripping voltammetry (ASV) is carried out after dilution of the sample with sulfuric acid as supporting electrolyte.

This Application Note describes the polarographic determination of selenite in electroplating baths used in the production of copper indium gallium diselenide thin-film solar cells (CIGS cells). The CIGS absorber layer is electrodeposited on a molybdenum-coated substrate. Selenite analysis is carried out after dilution of the sample with sulfuric acid as supporting electrolyte.

This Application Note describes the polarographic determination of cadmium in electroplating baths used in the production of copper indium gallium diselenide (CIGS) or copper indium diselenide thin-film solar cells (CIS). Cadmium sulfide (CdS) from the electrolyte solution is deposited as a thin film on the CIS or CIGS absorber layer via chemical bath deposition (CBD).

This Application Note describes the polarographic determination of thiourea in electroplating baths used in the production of copper indium gallium diselenide (CIGS) or copper indium diselenide thin-film solar cells (CIS). Cadmium sulfide (CdS) from the electrolyte solution is deposited as a thin film on the CIS or CIGS absorber layer via chemical bath deposition (CBD).

The presence of iron in drinking water can lead to an unpleasant taste, stains, or even growth of «iron bacteria» that can clog plumbing and cause an offensive odor. Over a longer period, the formation of insoluble iron deposits is problematic in many industrial and agricultural applications. To avoid these problems, the U.S. Environmental Protection Agency (EPA) defines the Secondary Maximum Contaminant Level (SMCL) for water treatment and processing plants as 0.3 mg/L Fe in drinking water.The voltammetric determination of the iron triethanolamine complex on the non-toxic Bi drop electrode allows both the detection at very low levels (limit of detection of 0.005 mg/L) and measurements in a wide range of concentrations up to 0.5 mg/L.

The main sources of nickel pollution are electroplating, metallurgical operations, or leaching from pipes and fittings. Catalysts for the petroleum and chemical industries are major application fields for cobalt. In both cases, the metal is either released directly, or via the waste water-river pathway into the drinking water system. Therefore in the EU the legislation specifies 20 µg/L as the limit value for the Ni concentration in drinking water.The simultaneous and straightforward determination of nickel and cobalt is based on adsorptive stripping voltammetry (AdSV). The unique properties of the non-toxic Bi drop electrode combined with AdSV results in an excellent performance in terms of sensitivity.

The total iron content as well as the distribution of Fe(II) and Fe(III) are critical quality attributes for iron citrate. Conventional techniques such as ICP and mass spectrometry do not directly distinguish iron species without additional sample preparation. This study shows how voltammetry enables direct, selective quantification of Fe(II) and Fe(III) in citrate matrices, while standard addition compensates for matrix effects to ensure reliable results.

brightRC enables reliable CVS (or CPVS) brightener quantification without repeated standard additions, especially for additive systems with nonlinear signal behavior. By using external response curve (RC) calibration and flexible regression, it avoids systematic errors inherent to linear standard addition methods and significantly reduces analysis time. This makes brightRC ideal for high throughput routine control in stable copper plating baths.

Today's Raman instrumentation is faster, more rugged, and less expensive than in the past and the advances in component miniaturization have led to the design of portable devices with extremely high performance designed for field-based investigations. This study focuses on the use of handheld Raman spectroscopy for the characterization and identification of samples encountered in various application areas related to forensic science.

Small, fast high-performance Raman spectrometers are now readily available. Three real-life Raman quantitative and semi-quantitative analysis applications are discussed. These applications showcase the versatility of Raman spectroscopy and the potential impact that it can make in various industries such as security, pharmaceutical, and plastics and polymers.

Allowing non-destructive chemical identification through opaque materials, award-winning STRam represents an evolution in Raman technology.

This e-book explains how Raman and near-infrared (NIR) spectroscopy enable rapid, nondestructive polymer analysis, ensuring high quality while reducing costs and waste.

This Metrohm White Paper presents the important role of electrochemistry in the environmental sciences. The applications have to do with basic research for the fuel cell that yields energy from wastewater, the electrical clean-up of contaminated soil and electrochemical CO2 reduction of greenhouse gases for isolating chemical raw materials.

The coupling of ion chromatography and inductively coupled plasma mass spectrometry (ICP/MS) leads to a high-performance measurement system that masters several particularly challenging analyses. It enables for example reliable determination of element compositions, oxidation states and chemical bonds. This information is used, for example, for assessing the toxicity of medications, environmental and water samples as well as foods and beverages.

Metrohm Raman presents a unique handheld materials identification system designed to meet the needs of defense and security professionals. Meet Mira DS, the most adaptable Raman analyzer available today. Mira DS was developed directly in response to requests from first responders in the field for a small, rugged, automated materialsidentification system that ensures the safety of the user in any situation.

Near-Infrared spectroscopy (NIRS) is a widely used analytical technique for quantitative analysis of various products in research and industrial applications. This white paper summarizes the workflow of the development of quantitative methods according to ASTM E1655.

Near-infrared spectroscopy (NIRS) is a widely used analytical technique for qualitative and quantitative analysis of various products in research and industrial applications. Because of different reasons it might be necessary to transfer analytical methods from one NIR analyzer to another one. This white paper summarizes the workflow of such method transfer.

A person suspected of possessing a narcotic can be charged with a crime only after the identity of the illicit substanceis confirmed. This confirmation is typically provided by analytical chemists in forensic laboratories and requires highly technical separation and detection methods. Unfortunately, such labs often have deep caseloads that lead to delays in testing. Handheld Raman analyzers bring the reliability and accuracy of lab analysis to first responders in the field, allowing for rapid and accurate identification of street drugs with a white powder appearance. With such tools, demand for forensic analysis can be reduced and enforcement agencies can enforce drug policies with greater safety, speed, and precision.

Propylene oxide (PO) is a major industrial product used in assorted industrial applications, mainly for the production of polyols (the building blocks for polyurethane plastics). Several production methods exist, with and without co-products. This white paper lays out opportunities to optimize PO production for safer and more efficient processes, higher quality products, and substantial time savings by using online process analysis instead of laboratory measurements.

«Dissolved oxygen» describes the amount of oxygen molecules (O2) which are dissolved in a liquid phase under certain conditions. In this white paper, two different methods for the analysis of dissolved oxygen, titration and direct measurement, are compared and contrasted to help analysts determine which method is more suitable for their specific applications. Here, we primarily focus on the determination of dissolved O2 in water. However, the same principle applies for other liquid phases such as non-alcoholic or alcoholic beverages.

Rancidity of oils and fats is a factor which can immediately reduce the sale price of these products to customers in the food and cosmetics industries. Oils which remain stable over longer periods of time are more highly valued as they lead to a higher quality end product. Rancidity is a natural process which occurs as fats and oils age and oxidize, and can be delayed or even stopped by addition of antioxidants at the right time.Determination of rancidity is possible in several ways (e.g., measuring the acid number or peroxide value), though these tests only give information about the current state of the product, with no indication about the remaining shelf life. One analytical method that can measure this time span until spoilage is the Rancimat method, which artificially ages the samples to determine whether antioxidants may be needed to help manufacturers get the full value from their oils.

This White Paper presents four different «green» sensors: the scTRACE Gold, screen-printed electrodes, the glassy carbon electrode, and the Bi drop electrode from Metrohm that can be used to determine low concentrations of heavy metals in different sample matrices, such as boiler feed water, drinking water, and sea water.

This White Paper compares automated Inline Ultrafiltration and Inline Dialysis to the traditional Carrez clarification procedure for the analysis of milk samples by ion chromatography (IC). A continuous test series over approximately six months proved Inline Dialysis to be a reliable and valuable alternative to treat dairy products prior to IC analysis.

This White Paper discusses the concept and benefits of NIR spectroscopy and outlines several real-life laboratory application examples with the use of OMNIS NIRS, the cutting-edge NIR spectrometer from Metrohm.

Due to its price and wide availability, the anionic surfactant sodium lauryl sulfate (SLS; SDS) can be found in many detergents as an emulsifier or as a fat solvent e.g., in cleaning or cosmetic products. To avoid causing severe dry skin and hair, and thus skin irritation, regulations in many countries have restricted the sodium lauryl sulfate concentration in ready-to-use products to a range between 0.05–2.5% SLS. To control the concentration of SLS in different products, a titration is carried out with TEGO® trant A100 and the Optrode. The evaluation is done automatically by means of a software, leading to reliable and reproducible results.

Forensic institutes examine terrorist attacks and warfare agents via trace detection analysis of the used explosives and their residuals. Of particular importance is the acquisition of «chemical fingerprints» for criminal investigation departments and governmental security agencies. Institutes for public health and environmental protection analyze such compounds that can contaminate the underlying soil and infiltrate ground water.Forensic investigation with ion chromatography (IC) using suppressed conductivity detection allows a sensitive and robust determination of anionic contaminants such as chlorate, thiosulfate, thiocyanate, and perchlorate next to the common inorganic anions over a broad concentration range.

Measures to monitor or prevent corrosion are crucial in nuclear power plants, where significant risks to health and safety can occur if corrosion is left unchecked. Anions corrode metals under high temperature and pressure, therefore their concentrations must be monitored at all times. The analytical challenge in the primary circuit is detection of anions in the μg/L range alongside gram quantities of boric acid and lithium hydroxide. Precise, reliable trace analysis requires the method to be automated as much as possible. The 2060 IC Process Analyzer from Metrohm Process Analytics can measure several anions from a single injection, with combined Inline Preconcentration and Inline Matrix Elimination to measure low anion concentrations precisely and reliably time after time.

Purity of rare earth elements (REEs) can be determined by absolute complexometric titration with xylenol orange (ISO 23597). This approach achieves around 100% recovery, eliminates the need for calibration, and offers higher accuracy and reproducibility than techniques such as AAS (atomic absorption spectroscopy). Photometric titration with the Optrode M2 offers adjustable wavelength detection, providing a fast, precise, and cost-effective alternative to other conventional methods.

As an alternative to flame photometry, ion chromatography with non-suppressed conductivity detection has been approved by the USP as a validated method to quantify potassium and sodium content in potassium and sodium bicarbonates and citric acid effervescent tablets for oral solution. The present IC method has been validated according to USP General Chapter <621>.

As an alternative to flame photometry, ion chromatography with non-suppressed conductivity detection has been approved by the USP as a validated method to quantify potassium content in potassium bicarbonate and potassium chloride effervescent tablets for oral solution. The Metrosep C 6 - 150/4.0 column (L76) provides the required separation of potassium and magnesium. The present IC method has been validated according to USP General Chapter <621>.

Drinking water which has been disinfected via the ozonation process can contain undesirable levels of bromate, a carcinogen, via oxidation of bromide in the raw water. Already several agencies including the World Health Organization have recommended concentration limits for bromate set in place to limit its risks to our health. Ion chromatography is mentioned in several analytical standards for the determination of disinfection byproducts (DBP) including bromate, such as EPA 300.1, 317.0, 321.8, 326.0, ASTM D6581, ISO 11206, and ISO 15061. Monitoring trace levels of bromate online means higher throughput and less time spent performing manual laboratory tests, and ensures quality drinking water is produced.

Boric acid requires precise monitoring in the primary circuit to control nuclear reactor reactivity. The 2060 TI Process Analyzer monitors boric acid online in near-real time.

In this article portable Raman spectroscopy as an effective tool for at-line characterization of carbon black is presented. Raman spectroscopic analysis can be an effective test to characterize carbon black material, including the structural order.

The benefits of a TE-cooled spectrometer in Raman systems are discussed to deliver lower system noise over longer integration times, resulting in lower limits of detection.

Handheld Raman is used for raw material testing of different sample types and forms. The use of optimized sampling accessories enhances the utility of handheld Raman without compromising data quality or complicating testing.

The TacticID®-GP Plus has multiple measurement modes to support safety and security users. A-Mode allows the user to create library Raman or SERS spectra customizable for spectral search range and hit quality index (HQI) threshold. A-mode is of beneficial use to forensics laboratories that would like to utilize expansion of SERS detection of designer drugs specific to their geographical regions or for food safety in perspective markets. In this example, A-Mode is used to create a SERS library of melamine to easily detect the presence of melamine in infant formula using a single indicator peak.

Although the process of building, validating and using a method is well-defined through software, the robustness of the method is dependent on proper practice of sampling, validation, and method maintenance. In this document, we will detail the recommended practices for using the multivariate method with NanoRam-1064. These practices are recommended for end users who are in the pharmaceutical environment, and can expand to other industries as well. This document aims to serve as a general reference for NanoRam-1064 users who would like to build an SOP for method development, validation and implementation.

The simultaneous ion chromatographic determination of trace-levels of lanthanides (or lanthanoides) was achieved by using either direct non-suppressed conductivity detection or UV/VIS detection after post-column reaction (PCR) with arsenazo III at 655 nm. Conductivity detection under isocratic conditions resulted in an overall analysis time of approx. 70 minutes. In contrast, the determination of the lanthanides via gradient elution and subsequent spectrophotometric detection of the arsenazo III-lanthanide(III) complexes was performed within 22 minutes. Besides the outstanding analysis time, UV/VIS detection excelled by its enhanced selectivity and sensitivity and did not suffer from interferences by ubiquitous non-lanthanide impurities such as iron(III) or other transition metals. For both conductivity and spectrophotometric detection, the inclusion of sample preconcentration steps lowered the limit of detection (LOD) to the sub-ppb range.

Metrohm's iColumns are the first IC columns that are equipped with a data chip that stores freely definable data, fixed column data as well as data entered by the MagIC NetTM software. Any relevant information such as column type, standard parameters, maximum pressure, etc. can be called up at any time. Analysis data continuously entered by the MagIC NetTM software guarantees a complete column and GLP-compliant surveillance irrespective of the IC system in which the column is operated. The MagIC NetTM software surveys the critical column data and indicates any infringement of limits.

Available sample size, mass sensitivity, efficiency and the detector type are important criteria in the selection of separation column dimensions. Compared to conventional 4 mm i.d. columns, microbore columns excel, above all, by their low eluent consumption. Once an eluent is prepared, it can be used for a long time. Additionally, the lower flow rates of microbore columns facilitate the hyphenation to mass spectrometers due to the improved ionization efficiency in the ion source.With the same injected sample amount, a halved column diameter involves a lower eluent flow and results in an approximate four-fold sensitivity increase. In a converse conclusion, this means that with less sample amount, microbore columns achieve the same chromatographic sensitivity and resolution than normal bore columns. This makes them ideally suited for samples of limited availability.

Metrohm`s intelligent Preconcentration Technique with Matrix Elimination (MiPCT-ME) excels in its capacity to perform automatic ion chromatographic determinations over 6 orders of magnitude. Crucial requirements for this are the system`s intelligence and the exact measurement of the sample volume. While the intelligence allows to compare results and take decisions, the dosing device takes over the high-precision liquid handling of even single-digit microliter volumes to the preconcentration column. By using only one analytical setup and without additional rinsing, samples containing both ultratraces and high concentrations can be analyzed.As the other Metrohm Inline Techniques, the MiPCT-ME technique presented reduces the workload, ensures complete traceability, is free of carryover effects and significantly improves accuracy and reproducibility of the results.

It is essential to know before starting the sample analysis if the electrode is in a good state or not. A well workingelectrode will increase the quality of your results, as the accuracy and precision will be increased. Furthermore, tedious error tracking can be omitted and no sample is wasted due to a defect or old electrode. There exist several ways how to check metal electrodes, e.g., measurement of redox potentials, potentiometric titration or bivoltammetric titration. This bulletin describes the best methods for the various by Metrohm available metal electrodes.

It is a comparatively easy matter to coat platinum electrodes with platinum black by electrolytic deposition of the metal from a platinizing solution.

This bulletin contains two parts. The first part gives a short theoretical overview while more details are offered in the Metrohm Monograph Conductometry. The second, practice-oriented part deals with the following subjects:Conductivity measurements in general; Determination of the cell constant; Determination of the temperature coefficient; Conductivity measurement in water samples; TDS – Total Dissolved Solids; Conductometric titrations;

The sample preparation for ion chromatography is divided into steps which should generally be implemented to preserve the column and into steps which should be performed to obtain an improved chromatogram. The goal is to have the test substance in ionic form in solution without the presence of interfering substances.

This Bulletin describes the determination by ion chromatography of anions, particularly fluoride, chloride, nitrite, bromide, nitrate, and sulfate using the Hamilton PRPX100 IC anion column without chemical suppression.

In titration, the titrant reacts with the analyte either exothermically (gives off heat) or endothermically (absorbs heat). The Thermoprobe measures the temperature change during titration. When all of the analyte has reacted with the titrant, the temperature of the solution will change, and the endpoint of the titration is indicated by an inflection in the temperature curve. Catalytically enhanced titrations using paraformaldehyde as catalyst are based on the endothermic hydrolysis of the paraformaldehyde in the presence of excess hydroxide ions. Edible oils are dissolved in a mixture of toluene and 2-propanol (1:1) and titrated with standardized TBAH (0.01 mol/L) in 2-propanol to a catalytically enhanced endpoint.

Automatic sample handling and analysis is very convenient for routine measurements on large number of samples. Metrohm offers a wide range of high performance liquid handling devices that can be combined with the Autolab product range and can be directly controlled by the NOVA software.

The Metrohm 800 Dosino is the workhorse of any automated liquid handling setup. This instrument can be conveniently used in combination with the NOVA software and integrated conveniently with electrochemical measurements performed with the Autolab systems.

The Metrohm 858 Professional Sample Processor is a robotic liquid handling system capable of handling large series of samples automatically. This instrument provides a platform that can be directly controlled by the NOVA software and combined with the Autolab potentiostat/galvanostat for automated high-throughput electrochemical measurements.

The use of an appropriate full scale together with the zero function of the 732 IC Detector minimizes baseline noise dramatically. Much lower detection limits are achieved.

Fast IC means short run times and a high sample throughput on columns with a relatively high flow rate and the standard eluent. Mono-, di- and tri-ethanolamine are separated with the Metrosep C 4 - 150/2.0 within 2.5 minutes.

Fast IC means short run times and a high sample throughput on columns with a relatively high flow rate and the standard eluent. Mono-, di- and trimethylamine are separated with the Metrosep C 4 - 150/2.0 within four minutes.

Automatic dilution reduces manual work and improves the reproducibility and accuracy of the results. So far, the Inline Dilution Technique (MIDT) has been tested in a range of max. 1:100. Using a dedicated sample needle this range is enlarged significantly. This AN shows the performance of an Inline Dilution with a factor of 1:2000 as well as a comparison of manual and inline dilution for a dilution factor of 1:1000.

The ASTM standard G100 is an electrochemical method to test localized corrosion of aluminum 3003-H14 and other alloys. A cyclic galvanostatic staircase polarization (galvanostaircase) is composed of an upward and a downward scan. The potential values at the end of each step are collected and linearly fitted, and the potential values at zero current are found.

The ASTM B825 is used to determine the corrosion and tarnish film on metal surfaces. This is achieved by using the so-called cathodic reduction method. With the help of a Metrohm Autolab PGSTAT302N and a Metrohm Autolab 1 L corrosion cell, a procedure to replicate the ASTM B825 is shown.

The mass transport characteristics of the diffusion controlled oxidation and reduction of the ferri/ferro cyanide couple was studied using the Autolab RDE with a low noise liquid Hg contact.

This document describes a very simple procedure that can be used to produce small deposits of platinum on a goldsubstrate. This simple procedure is based on an electrochemical process known as displacement deposition, during which the deposition of a noble metal occurs by the oxidation of a precursor metal adlayer deposited on the substrate, at open circuit potential (OCP).

The TSC SW Closed and TSC Battery cells are compact systems designed for measurements on air or moisture-sensitive materials, such as those used in batteries. In this document, two testing procedures are explained. The first procedure is withpotentiostatic cyclic voltammetry (CV), while the second is via electrochemical impedance spectroscopy (EIS).

In order to calculate the conductivity of an electrolyte, the cell constant of the cell must be known. The combination of the Metrohm Autolab PGSTAT204 equipped with the FRA32M module in combination with the Autolab Microcell HC setup was used for the determination of the conductivity cell constants of TSC1600 temperature controlled electrochemical cell.

The kinetic and mass transfer parameters of the electro-oxidation reaction of TEMPO were measured using the TSC Surface measuring cell for the Autolab Microcell HC system. The cell allows the study of electrochemical processes in liquid electrolytes in a three electrode configuration under temperature control.

A fuel cell is an electrochemical energy conversion device that produces electricity and heat by electrochemically combining a fuel (typically hydrogen) and an oxidant (typically oxygen). The higher efficiency also results in much lower carbon dioxide emissions and negligible amounts of SOx and NOx (when reformed fuel is used) compared with fossil fuel-based technologies for the same power output.

The use of impedance measurements on fuel cells under load makes it possible to study the influence of the different fuel cell elements on the behavior and (if detectable) on the ageing of the fuel cell. To perform high current density measurements, the Autolab systems can be connected to a third party electronic load. This extends the measurable range of the instrument by several current decades.

The operational behavior of a fuel cell stack is usually evaluated by determining the polarization and power density curves of the cell. These curves provide a quick characterization of the stack performance and an assessment of its optimal operating conditions (temperature, humidity, electrocatalyst, ion-exchange membrane).

Standardisation of sodium tetraphenylborate (NaTPB) solution for the determination of potassium and for nonionicsurfactants.

Standardization of 0.1 mol/L ammonium ferrous sulfate solution for use in thermometric titration of Cr(VI) solutions.

Determination of free fatty acids (FFA) in oils.

Standardization of copper back-titrant using standard tetrasodium EDTA titrant in the determination of metals.

Standardization of disodium dimethylglyoximate by thermometric titration with standard Ni(II) solution.

Standardization of barium acetate titrant used in the determination of sulfate in phosphoric acid. The same procedure is applied if barium chloride is chosen as the titrant.

Standardization of sodium fluoride titrant for determination of aluminum.

Standardization of 0.1mol/L perchloric acid in glacial acetic acid by catalyzed endpoint thermometric titration.

Standardization of titrant for direct determination of sodium.

The determination of the total base number (TBN) in motor oils is accomplished by means of titration with a standard solution made up of trifluoromethanesulfonic acid in glacial acetic acid and isobutyl vinyl ether as reagent for improved end point identification.

Determination of bicarbonate and carbonate in a mixture by sequential thermometric titrations.

Standardization of ~1mol/L tetrasodium EDTA solutions for thermometric complexometric analysis.

Standardization of 1 mol/L tetrasodium EDTA (Na4EDTA) solutions by titration with standard magnesium solution.

Even in low concentration, sulfide ions cause odor and corrosion problems in ground water and waste water. They can release hydrogen sulfide in acidified water, which is toxic in even minuscule amounts. This Application Note describes the determination of sulfide concentration in water via direct measurement with the Ag/S-ISE in accordance with ASTM D4658.

Bromide is ubiquitous in sea water, where it is present in concentrations of around 65 mg/L. By contrast, the maximum bromide concentration in drinking and ground water is usually less than 0.5 mg/L. A higher bromide content may indicate a contamination of the water caused by fertilizer, road salt or industrial waste water. This Application Note describes the determination of the bromide content in water via direct measurement with a Br ion-selective electrode in accordance with ASTM D1246.

Determination of anions in a Schoeniger absorption solution of a test mixture without decomposition of the H2O2 using anion chromatography with direct conductivity detection.

Determination of cyanide using anion chromatography with amperometric detection at the silver electrode.

Determination of chromate using anion chromatography with post-column reaction and UV/VIS detection.

Determination of borate and silicate in ultrapure water using anion chromatography with direct conductivity detection.

Near-infrared spectroscopy (NIRS) was used as an analysis method for quality control of soap noodles. Quantitative models for the determination of Total Fatty Matter, Iodine Number, and C8–C14 were developed, enabling fast and reliable quality control.

Determination of lauric acid, myristic acid, palmitic acid, and stearic acid using ion-pair chromatography with direct conductivity detection.

Determination of organic acids and phosphate using ion-exclusion chromatography with direct conductivity detection.

Determination of gluconic acid and glycolic acid using ion-exclusion chromatography with direct conductivity detection.

Determination of formate, acetate, propionate, butyrate, valerate, and capronate in an aqueous absorption solution using ion-exclusion chromatography with conductivity detection after chemical suppression.

Determination of lactate, formate, acetate, propionate, butyrate, isobutyrate, valerate,and isovalerate in a standard solution using ion-exclusion chromatography with conductivity detection after chemical suppression.

Determination of glycolic acid, formic acid, glutaric acid, acetic acid, propionic acid, and butyric acid in a standard solution using ion-exclusion chromatography with suppressed and non-suppressed conductivity detection.

Determination of carbonate in an aqueous ammonia solution using ion-exclusion chromatography with suppressed conductivity detection.

Determination of formate, acetate, propionate, isobutyrate, butyrate, isovalerate, valerate, and capronate added to tap water using anion chromatography with conductivity detection after suppression. The MCS is placed upstream of the chemical suppressor to remove interfering CO2.

Determination of sulfite, nitrite, nitrate, sulfate, imidodisulfonate, and peroxodisulfate using ion-pair chromatography with conductivity detection after suppression.