Application Finder

Methanol, often present in spirits prepared with industrial solvents like wood alcohol, can lead to blindness and even death when ingested. After an incident involving methanol-laced alcohol in the Czech Republic, they adopted Raman spectroscopy as the preferred method for identifying and quantifying methanol in contaminated spirits, following an exhaustive study using various screening tools. This Application Note discusses the reasons why Raman spectroscopy is the ideal choice for this application and shows a real-world example of Raman analysis of methanol-laced rum.

The Restriction of Hazardous Substances (RoHS) Directive 2002/95/EC stipulates maximum limits for the hazardous metals cadmium, lead and mercury as well as the hexavalent chromium and the brominated flame retardants in electrical and electronic products. To ensure compliance, reliable analysis methods are required.This poster deals with the wet-chemical determination of trace concentrations of the six RoHS-restricted substances in a wide variety of materials including metals, electrotechnical components, plastics and wires. After sample preparation according to IEC 62321, the metals lead, cadmium and mercury are best determined by anodic stripping voltammetry (ASV) and the flame retardants PBB and PBDE are quantified by direct-injection ion chromatography (IC) using spectrophotometric detection. Chromium(VI) can be determined either by adsorptive stripping voltammetry (AdSV) or IC. Both methods are very sensitive and meet prescribed RoHS limits.

The presented IC system with inline sample preparation allows the determination of traces of lithium and sodium (ppt) in the presence of ppm quantities of ammonium and ethanolamine.

Non-enzymatic ethanol sensor based on a nanostructured disposable screen-printed electrode.

This method is applicable to all samples containing glycerin in the absence of other triols or other compounds that react with periodate to produce acidic products. Glycerin may be determined in the presence of glycols. A periodate solution reacts slowly with diols and triols in acidic aqueous media at room temperature. A quantitative amount of formic acid is generated from the reaction with glycerin (a triol). The reaction with diols produces neutral aldehydes. The amount of formic acid generated by this reaction is determined by titration against sodium hydroxide.

Determination of sodium, potassium, DMEA (dimethylethanolamine), calcium, choline, and magnesium in a saline solution using cation chromatography with direct conductivity detection.

Determination of mono-, di-, and trimethanolamine (MMA, DMA, TMA respectively), in the presence of lithium, sodium, ammonium, potassium, magnesium, cesium, calcium, and strontium using cation chromatography with direct conductivity detection.

Determination of traces of methylamine, isopropylamine diethylethanolamine, and diethylamine in the presence of lithium, sodium, ammonium, potassium, magnesium, and calcium using cation chromatography with direct conductivity detection.

Determination of choline in infant milk powder using cation chromatography with direct conductivity detection applying Metrohm Inline Dialysis.

Determination of hydroxylamine, ethanolamine, triethanolamine, and hydrazine using cation chromatography with direct conductivity detection.

Determination of monoethanolamine (MEA), diethanolamine (DEA), and triethanolamine (TEA) in the presence of lithium, sodium, ammonium, potassium, calcium, and magnesium using cation chromatography with direct conductivity detection.

Determination of monomethylamine (MMA), dimethylamine (DMA), trimethylamine (TMA), monoethanolamine (MEA), diethanolamine (DEA), and triethanolamine (TEA) using cation chromatography with direct conductivity detection.

Determination of lithium, sodium, ammonium, and monoethanolamine (MEA) using cation chromatography with direct conductivity detection and Metrohm Inline Preconcentration and Inline Calibration.

Water in steel-based cooling systems requires a pH value slightly above 7 to prevent corrosion. Often ammonium or organic amines are applied for pH adjustement. This application shows the separation of typical amines besides inorganic cations. Sample preconcentration applies combined Inline Preconcentration and Matrix Elimination (MiPCT-ME).

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.

In natural gas production, the removal of contaminants, and in particular acidic gases such as H2S and CO2, is exceptionally important. These acidic gases are removed in the amine wash through chemical treatment with amines or alkanol amines. This application shows a convenient and precise analysis with the separation of various amines and standard cations on a column of the Metrosep C 6 - 250/4.0 type with subsequent direct conductivity detection.

N-methyldiethanolamine and piperazine are used in scrubber solutions, e.g., in the natural gas process. Testing this type of samples by ion chromatography requires a good resolution and the separation of amines from standard cations. The separation is achieved on a Metrosep C 4 - 150/4.0 column applying direct conductivity detection.

Before the liquefaction process of the natural gas, carbonate and hydrogen sulfide need to be removed through a scrubber solution containing piperazine and N-methyl diethanolamine (MDEA). The concentration ratio of the two components is determined by ion chromatography on a Metrosep C 4 - 150/4.0 column applying direct conductivity detection.

Choline is important for the biosynthesis of numerous molecules, e.g., the neurotransmitter acetylcholine, and exists as an intermediate product in the human metabolism. Concentration determination takes place after microwave digestion. Separation is performed on the Metrosep C Supp 1 - 250/4.0 column following sequential suppression. Separation from the standard cations is outstanding.

Boiler feed water is a working medium in thermal power plant. To keep corrosion low, the pH value should be in the slightly alkali range, which is why amines are added to the feed water. This addition must be monitored regularly. Also important is the monitoring of the sodium concentration, because an increase of this indicates that cooling water is seeping into the condenser. Ion chromatography with conductivity detection following sequential suppression is the optimum system for monitoring, particularly in combination with intelligent Sample Preconcentration and Matrix Elimination.

This Application Note describes an NIR method for monitoring the esterification process in butyl acetate production. The developed NIR method shows excellent analytical performance equivalent to that obtainable with more time-consuming GC methods.

This Application Note describes the utilization possibilities of a new sensor design that permits, in combination with an NIRS XDS Process Analyzer, the determination of solvent residues in a High-Shear Granulator during the drying phase. This system configuration reduces the scattering of the density distribution of the powder samples so that it is possible, directly in the process, to model the water and solvent content precisely.

The purity of a recovered solvent (dichlormethane/methylene chloride) and two of its most important contaminants (methanol and water) are monitored with NIR spectroscopy.

Ink is a complex mixture that, along with numerous additives, is comprised mainly of solvent, dye, water and surfactant. Vis-NIR spectroscopy is outstandingly suitable for providing rapid and reliable determinations of constituents in the context of quality controls. This Application Note describes the determination of diethylene glycol (DEG), water, dye and surfactant.

This Application Note shows the determination of two important additives – butylglycol and propylheptyl alcohol – in water-soluble lacquers using Vis-NIR spectroscopy. Other lacquer constituents can also be determined in addition to the two additives.

This Application Note describes a fast, nondestructive, and reliable method for the determination of the chemical composition of alcohol mixtures exemplified by ethanol/isopropanol mixtures. With visible near infrared spectroscopy (VIS-NIRS), results are available in real-time, thus making NIRS highly suited for fast quality control.

Polyvinyl alcohol (PVA) is a linear polymer, used in a variety of medical products (e.g. eye drops). Here, the degree of alcoholysis is an important index for the water solubility, viscosity, and adhesion of the product. The degree of alcoholysis is defined as the percentage of hydroxyl functional groups compared to the total functional groups accessible in the molecule. Conventional alcoholysis determination can take up to six hours per sample. Compared to the primary method, analysis with near-infrared spectroscopy (NIRS) only takes one minute. The following application note describes the determination of the degree of alcoholysis by NIRS.

Safe and fast ethanol determination in hand sanitizers is possible with reagent-free near-infrared spectroscopy (NIRS). NIRS provides reliable results in a few seconds, quickly indicating when adjustments in formulation are necessary.

The production of biofuels from renewable feedstock has grown immensely in the past several years. Bioethanol is one of the most interesting alternatives for fossil fuels, since it can be produced from raw materials rich in sugars and starch. Ethanol fermentation is one of the oldest and most important fermentation processes used in the biotechnology industry. Although the process is well-known, there is a great potential for its improvement and a proportional reduction in production costs. Due to the seasonal variation of feedstock quality, ethanol producers to need to monitor the fermentation process to ensure the same quality product is achieved. Near-infrared spectroscopy (NIRS) offers rapid and reliable prediction of ethanol content, sugars, Brix, lactic acid, pH, and total solids at any stage of the fermentation process.

This application note presents near-infrared spectroscopy (NIRS) for the rapid and reliable simultaneous quantification of ethanol, glycerol, hydrogen peroxide, and water content in hand sanitizer formulations.

Determination of L-lactide, citrate, and lactate in an acetone solution using ion-exclusion chromatography with direct conductivity detection.

The determination of sugar and sugar alcohols is very important for food analysis. The Dose-in Gradient system extends the gradient capability of the standard IC system. The isocratic system is expanded to form a binary gradient system with just one 800 Dosino and one T-piece.

Glycol solutions act as antifreeze agents and are often used as such in motor vehicles. Due to the toxicity of (mono)ethylene glycol (MEG), use is being increasingly expanded to the non-toxic propylene glycol. This Application Note presents the separation and quantification of the two glycols. Separation is performed on the Metrosep Carb 2 - 250/4.0 column. Due to the absence of chromophores and the low conductivity of the glycols, pulsed amperometric detection (PAD) is used to facilitate determination.Key words: ethanediol, propanediol

Biodiesel or green diesel is manufactured from fats and vegetable oils through ester interchange of the triglycerides they contain, during which glycerin accumulates as byproducts in both free and bonded forms. These accelerate fuel ageing and lead to deposits and clogged filters, which is why maximum permissible highest concentrations have been established (in the US in ASTM D6751 and in the EU in EN 14214).The two specifications prescribe the ion chromatography determination of free and bonded glycerin. This Note describes the determination with the aid of the Metrosep Carb 2 - 150/4.0 column in accordance with ASTM D7591.

Propylene glycol, also called propane-1,2-diol, is a humectant and applied in topical solutions to increase the solubility of the active pharmaceutical ingredient (API) or the ability to penetrate the skin. In this application, propylene glycol is determined in a placebo and two topical solutions containing diclofenac as the API. The separation is achieved on a Hamilton RCX-30-250/4.0 column with subsequent pulsed amperometric detection (PAD).

Polyurethanes are a class of synthetic polymers formed by reacting liquid di/polyisocyanates and polyols with a catalyst and various additives in a reactor. Polymer properties are modified with stepwise additions of these chemicals at different points in time depending on whether the process has reached an equilibrium. NCO functional groups from unreacted isocyanates must be quenched at the end for a finished product, and this parameter must be known to determine the proper chemical mixing ratio. A fast, non-destructive real-time measurement of %NCO can be obtained by using NIR spectroscopy with a probe seated directly in the reactor.

This Process Application Note presents a way to closely monitor multiple parameters simultaneously during the dioctyl terephthalate production process with near-infrared spectroscopy.

Many fermentation quality parameters can be monitored simultaneously directly in the tank with inline near-infrared spectroscopy, such as the 2060 The NIR Analyzer.

This Application Note describes the rapid and non-destructive identification of conventional organic solvents using hand-held Raman spectrometers. Measurements with the handheld Raman spectrometer Mira M-1 require no sample preparation and provide immediate and unambiguous results.

This Application Note shows the rapid, non-destructive identification of isopropyl alcohol from two manufacturers using Raman spectroscopy following the creation of a suitable library. The measurements with the hand-held Raman spectrometer Mira M-1 require no sample preparation and provide immediate results that identify the samples unambiguously.

Determination of α-glycerophosphate and β-glycerophosphate in amino acids using anion chromatography with conductivity detection after chemical suppression.

Boehm titration is a quantitative analysis of functional groups on the surface of carbon materials based on their reactions with basic solutions of NaHCO3 (pKa = 6.4), Na2CO3 (pKa = 10.3), and NaOH (pKa = 15.7). This is a cost-efficient method that gives absolute values with high precision of the accessible, mainly oxygen-containing functional groups on the surface. Originally, Boehm titration was developed for carbon materials like conductive carbon black (CCB), activated carbon, porous carbon, and graphite. Modern carbon-based materials like graphene, graphene oxide (GO), or carbon nanotubes can also be analyzed this way.

Mannitol content determination is an important aspect of quality control in the pharmaceutical and food industries. Selective oxidative cleavage can be used to quantify the amount of 1,2-diol groups in the analyte. Determining the 1,2-diol content by iodometric titration can be fully automated for the most accurate results using an automated titrator and the dPt Titrode from Metrohm.

The determination of PBBE (tetrabromobisphenol A - TBBPA, octabromodiphenyl ether - OCTA and decabromodiphenyl ether - DECA) in a polymer sample was carried out with the Nucleosil EC - 250 mm column; for this purpose a methanol and phosphate buffer was used as an eluent and subjected to UV detection in accordance with the IEC 62321 method for RoHS testing.

Improve petrochemical quality control with NIRS. Fast, cost-effective, and no sample prep needed. Learn more in our eBook.

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

Ion chromatography is used as a high-performance analysis method in numerous applications. For complex analysis tasks, alternative detectors such as the amperometric detector or the UV/VIS detector are often also used in addition to the conductivity detector. This article describes the areas of utilization of the amperometric detector. Catchword: Antibiotics

More strict regulations paired with more complex products have increased testing complexity in the paint and coating industry. Therefore, producers ask for more powerful, safe and sustainable analytical methods. Testing by Vis-NIR spectroscopy is a sustainable and costefficient alternative to many wet chemical methods. This white paper describes how Vis-NIR spectroscopy improves testing procedures for various analyses during the formulation and production of paint and coatings in an economic and ecological way.Key words: testing, sustainable, VOC, paint, coating, binders, resins, additives, pigments, solvents

This white paper differentiates between methods for identification of unknowns and verification of known materials. The goal of this publication is, ultimately, to inform the user of the capabilities of the handheld Metrohm Raman Mira P system. Best practices for building robust training sets for materials verification with Mira P can also be found here.

An analytic chemist in your back pocket. A forensic laboratory in a suitcase. A HazMat team in the trunk of your car. First responders need all the help they can get when faced with potentially dangerous substances. Mira DS from Metrohm Raman is a sophisticated chemical analyzer that replaces the specialist with automation. The push of a button initiates proprietary Smart Acquire routines to optimize acquisition parameters and collect the highest quality spectra. These spectra are automatically subjected to library search and Mixture Matching routines capable of identifying up to three components of a mixture. When hazardous substances are detected, the user is alerted to immediate action with color-coded warnings.