Haku

This Application Note offers an easy way to determine the ammonia content in cacao nibs by using ion measurement, applying the standard addition technique in a reliable cost- and time-saving manner.

This Application Note covers the formation of calcium carbonate from solution.

Excess sodium intake increases the risk of health issues. Ion-selective electrodes (ISEs) offer a fast, accurate, and cost-effective method for measuring sodium in food.

Groundwater contains many minerals, but can be contaminated by sodium-rich leachate from landfills. Accurate Na determination in water is possible following AOAC 976.25 using the Na-ISE.

The water content of potassium chlorate is determined according to Karl Fischer using the oven method (300 °C).

The water content of methyl ethyl ketone peroxide is determined according to Karl Fischer using two-component reagents in order to prevent unwanted side reactions. (Separate solvent is used to ensure a high excess of sulphur dioxide and amine in the titration vessel.)

The water content of ammonium and potassium peroxodisulphate is determined according to Karl Fischer using two-component reagents. To prevent unwanted side reactions the determinations are carried out at -20 °C. Because the potassium salt is insoluble in the solvent, a high-frequency homogenizer is used to disintegrate the salt particles.

The water content of lyophilisates contained in vials is determined by Karl Fischer titration. Conditioned solvent (methanol) is injected into the vial to dissolve the sample and extract the water (ultrasonic bath). Afterwards the contents of the vial are transferred to the titration vessel to carry out the automatic determination.

Determination of water content in ink is possible with Karl Fischer titration, as shown in this Application Note.

The water content of ointments is determined according to Karl Fischer. Because of their high water and fat content, the samples are prediluted with a 1:1 mixture of chloroform and methanol.

The water content of yoghurt powder is determined according to Karl Fischer. Because of the relatively high water and fat content, the sample is prediluted with a 1:1 mixture of chloroform and methanol.

The water content of plastic chips is determined according to Karl Fischer. Because of the low water content of the sample, the oven method (200 °C) and coulometric titration have to be used.

The water content of explosive pellets is determined according to Karl Fischer after extraction with methanol.

The water content of coal dust is determined according to Karl Fischer. Because of the low water content of the voluminous sample, the oven method (nitrogen, 270 °C) and coulometric titration have to be used.

The water content of moisturising creams is determined according to Karl Fischer. Because of their high water content, the samples are first mixed and prediluted with dry methanol.

The water content of turbine oil is determined according to Karl Fischer. Because of the low water content of the sample, coulometric titration is used.

The water content of organic peroxides is determined according to Karl Fischer using two-component reagents. To prevent any unwanted side reactions, the determinations are carried out at -20 °C.

The water content of diesel fuel and petrol (gasoline) is determined according to Karl Fischer. Because of the low water content, the determinations are carried out by coulometric titration.

The water content of sweet liquorice is determined according to Karl Fischer. To dissolve the sample, a mixture of methanol and formamide is used as solvent and a high-frequency homogenizer as stirring device.

The water content of lemongrass oil is determined according to Karl Fischer. To prevent unwanted side reactions, special KF reagents for aldehydes and ketones are used and the determination is carried out at 0 ... 4 °C.

The presence of water in expandable polystyrene (EPS) can have a negative impact on the thermal insulation properties, as it increases thermal conductivity. If EPS is exposed to a high moisture environment, additional water may be absorbed, which can further affect thermal insulation.Direct analysis of the moisture content by Karl Fischer titration requires the water to be extracted from the EPS, which involves several time-consuming steps. Therefore, determination of the water content with an oven system is preferred. As EPS expands when heated, the use of sample boats, as required by ASTM D6869, is not possible, as the EPS will contaminate the oven system. This Application Note describes the determination of water content in EPS using an oven system with closed sample vials. A determination takes about 7 to 14 min depending on the water content of the sample and the sample size.

The water content of cyclopropyl methyl ketone is determined according to Karl Fischer by coulometric titration using special reagents for aldehydes and ketones.

In this application note, Karl Fischer titration is used to determine the water content of urea.

The water content of flour is determined according to Karl Fischer. To shorten the analysis times and to obtain more precise results, the determinations are carried out at 50 °C.

The water content of animal fat extract is determined according to Karl Fischer.

This Application Note describes the determination of water content in pesticides using Karl Fischer titration.

The water content of ethylene dichloride is determined according to Karl Fischer. As the sample may contain free chlorine, which interferes with the determination, separate KF reagents have to be used.

The water content of smoked salmon and smoked trout is determined according to Karl Fischer.

The water content of potato chips is determined according to Karl Fischer using the oven method (140 °C).

The water content of used lubricating oil is determined according to Karl Fischer by coulometric titration. To prevent unwanted side reactions special KF reagents are used.

The water content of lime is determined according to Karl Fischer using the oven method (150 °C).

The water content of color paste is determined according to Karl Fischer.

The water content of spices is determined according to Karl Fischer. To release the water from the cells, a high-frequency homogenizer has to be used.

The water content of bismuth subnitrate is determined according to Karl Fischer.

The water content of 2-methyl-1,3-butadiene and 2,5-norbornadiene is determined according to Karl Fischer using a special solvent mixture to prevent unwanted side reactions.

The water content of acetophenone and benzophenone is determined according to Karl Fischer using special KF reagents for ketones/aldehydes to prevent unwanted side reactions.

The water content of piperidine and piperazine is determined according to Karl Fischer using a buffered solvent mixture.

The water content of melamine is determined according to Karl Fischer in a buffered solvent mixture at 50 °C.

The water content of beta-caprolactam is determined according to Karl Fischer.

The water content of vinyl chloride is determined according to Karl Fischer.

The water content of 2-methyl-5-mercaptothiadiazole is determined according to Karl Fischer using a special solvent mixture to prevent unwanted side reactions.

Karl Fischer titration can be used to determine the water content in N-acetyl-L-cysteine. Special solvent mixtures can be used to prevent unwanted side reactions in the Karl Fischer titration. The water content of N-acetyl-L-cysteine can thus be determined quickly and accurately, as is shown in this Application Note.

This application note describes the water content determination in penicillin by using volumetric Karl Fischer titration. Unwanted side reactions can be avoided by using special solvent mixtures.

The water content of margarine is determined according to Karl Fischer.

Determination of the water content of liquid ammonia according to Karl Fischer after absorption of the water in ethylene glycol.

The water content of silicone oil is determined according to Karl Fischer by coulometric titration.

The water content of aniline is determined according to Karl Fischer in buffered solvent.

The water content in panthenol is determined according to Karl Fischer.

The water content in methylcyclohexane is determined by coulometric Karl Fischer titration.

The water content in Ca carbonate is determined by volumetric Karl Fischer titration.

This Application Note describes the determination of the water content in transformer oil using the oven technique.

Large sample sizes can lead to subtraction of too high blank values. This Application Note describes the calculation of a relative blank and thus helps to improve the accuracy of the method.

The water content, also called moisture content, of plastics is an important quality parameter, as it affects the properties and processability of some plastics. A high water content can lead to degradation of the plastic by hydrolysis or cause surface imperfections. Additionally, it can affect the physical properties of some plastics.For this analysis, the oven technique is used, as volatile compounds present in plastics will interfere, if the water content is directly determined by coulometric Karl Fischer titration. The water content determination in polycarbonate pellets, performed with the 885 Compact Oven Sample Changer and 899 Coulometer, is described in this Application Note.

This Application Note describes the determination of the water content in gelatine using the oven technique.

This Application Note describes the automated determination of the water content in liqueur (30% v/v) using volumetric Karl Fischer titration (MATi 10).

In this application note, Karl Fischer titration is used to determine water content in sodium acetate trihydrate. The MATi 10 allows this determination to be automated, saving users time in the laboratory.

This Application Note describes the automated determination of the water content in toothpaste using volumetric Karl Fischer titration (MATi 10).

This Application Note describes the determination of the water content in tablets using automated volumetric titration including sample preparation (MATi 11).

The bromine index indicates the degree of unsaturation and relies on the simple addition of bromine to the double bond of alkenes. One mole of bromine is consumed for each mol of carbon-carbon double bond. The bromine index indicates the olefin content in aromatic hydrocarbons. This Application Note describes the determination by coulometric titration according to ASTM D1492.

The water content determination by volumetric Karl Fischer titration is one of the most important analyses worldwide. Using an OMNIS system consisting of an OMNIS Titrator and an OMNIS Sample Robot, the fully automatic analysis of water content is possible in various products and matrices. The OMNIS Sample Robot is capable of running several different titrations in parallel. In this Application Note, we present the results of a volumetric Karl Fischer titration run in parallel to an aqueous acid-base titration on the same system. The water content is not influenced by the parallel running aqueous titration, allowing the combination of potentiometric titrations and Karl Fischer titrations on the same automated system.

The vaping and electronic cigarette industries are growing. The mixtures used in these products are usually called e-liquid, e-fluid, or e-juice. Toensure the quality of these e-liquids, testing the most important parameters is required. One important quality control parameter is water or moisture content.Water/moisture content determination by Karl Fischer titration (KFT) is an established and reliable procedure. Compared to other methods the advantages of KFT are its accuracy, speed, and selectivity. For high water content samples, such as e-liquids, volumetric KFT is the method of choice.In this Application Note a system for the fast and reliable determination of the water content in E-liquids is presented. This fully automated system performs the analysis including system preparation, blank, titer, and sample determination completely unattended. Hence, the workload of the operator is reduced to only weighing in the sample and placing the sealed sample vessels on the system.

Moisture in petroleum products causes several issues: corrosion and wear in pipelines and storage tanks, an increase in debris load resulting in diminished lubrication, blocked filters, or even harmful bacterial growth. As a result, increased water content can lead to infrastructure damage, higher maintenance costs, or even unwanted downtimes.Coulometric Karl Fischer titration is the method of choice for low water content in petroleum products. Using a Karl Fischer oven to vaporize the water present in the sample prior to titration not only greatly reduces matrix interferences, it can also be fully automated. This allows a reliable and cost-efficient analysis of the water content according to ASTM D6304 (Procedure B) in products such as diesel, hydraulic oil, lubricant, additive, turbine oil, and base oil.

Water content determination by volumetric Karl Fischer titration is one of the most important analyses worldwide, particularly when it comes to food quality. This parameter has a major influence on the growth of microorganisms, and thus indirectly affects the storability of the raw materials and final products. Consistent quality is only possible with precise measurements during the process. This measurement is performed with the Metrohm Eco KF Titrator for flour, dough, and baked goods.

Karl Fischer reagents contain buffer substances (usually imidazole) since the reaction constant is dependent on the pH value. A constant pH therefore ensures the most repeatable results. In 2015, imidazole was classified by European Union the as a CMR (carcinogenic, mutagenic or toxic) substance and the statement H360D was added, stating possible harm to fertility or a fetus. Meanwhile, other reagents free of imidazole are available for purchase. This Application Note summarizes test measurements with 34433 HYDRANAL™ NEXTGEN Coulomat AG-FI.

Test measurements on water standards are performed with an OMNIS KF Titrator and Karl Fischer reagents Aquagent® Complet 5 and Methanol Fast from Scharlau.

To determine water in crude oil, ASTM D4928 recommends coulometric Karl Fischer titration with the oven method, allowing full automation for high reproducibility.

Determination of acetic, propionic, butyric, valeric, and caproic acid in produced water using anion chromatography with conductivity and MS detection after post-column addition of ammonia for MS detection and inline sample preparation by dialysis.

Determination of chlorite, chlorate, and perchlorate in explosion residue using anion chromatography with conductivity and MS detection in tandem.

Determination of phosphate in produced water containing up to 100 g/L chloride as well as crude oil using anion chromatography with conductivity and MS detection after inline dialysis.

Determination of bromide and bromate in drinking water using anion chromatography with MS detection.

Determination of diethylamine and trimethylamine using cation chromatography with MS detection.

Urea is not a typical analyte for ion chromatography. In combination with MS, however, IC is the method of choice for the trace analysis of urea in ultrapure water. This Application Note shows the determination of urea concentrations in the ppb range using the Metrosep C 6 - 250/4.0 column.

Hexavalent chromium, also referred to as chromate or Cr(VI), is considered toxic and potentially carcinogenic, which is why its concentrations in drinking water should be kept as low as possible. Determination of Cr(VI) is performed by combining ion chromatography with ICP/MS. Separation takes place on the Metrosep A Supp 1 Guard/4.6.

Chromate (Cr(VI)) is considered toxic and potentially carcinogenic, which is why its concentrations in children's toys should be kept as low as possible. The EU directive 2009/48/EC defines limit values for the migration of chromate from children's toys. The hydrochloric-acid-containing migration solution is diluted with a buffer. 2000 μL of this solution are injected automatically using intelligent preconcentration technology and matrix elimination. Detection takes place via ICP/MS.

The maximum contaminant concentrations (Maximal Contaminant Level, MCL) of inorganic arsenic and selenium species in drinking water should not exceed 10 and 50 µg/L, respectively. Given that each of the two elements occurs in two oxidation levels – trivalent and pentavalent – a separation step is necessary prior to ICP/MS detection. This Application Note shows the simultaneous determination of the two arsenic (arsenite and arsenate) and selenium species (selenite and selenate). Separation takes place on the Metrosep Dual 3 - 100/4.0 column.

As a rule, soil contains small percentages of chromium that originate chiefly from rock weathering processes, although anthropogenic sources also exist. The speciation analysis of trivalent – Cr(III) – and hexavalent chromium – Cr(VI) – is important, because the former is a trace element and the latter is highly toxic. The two chromium species are separated as Cr(III)-EDTA-complex and chromate on the Metrosep A Supp 4 - 250/4.0 column. Mass spectrometric isotope dilution analysis (SIDMS) is used for quantification.

Speciation analysis of iron is important, given that its oxidation level has a great influence on environmental response, not only with respect to its absorption by organisms but also to the transport and the storage of the element. Iron(II) and Iron(III) are separated on the Metrosep A Supp 10 S-Guard/4.0 column. IC-ICP/MS with isotope dilution is used for quantification.

Differentiation between Cr(III) and Cr(VI) is possible following ISO 24384 guidelines by combining ion chromatography with inductively coupled plasma mass spectrometry.

Perchlorate contamination in drinking water may have different sources. Besides natural deposits, anthropogenic sources like fertilizers and rocket fuel residue add to hazardous water contamination. Perchlorate interferes with iodine uptake into the thyroid gland. Newborns and children are particularly vulnerable, affected as thyroid hormones are essential for growth. Besides ion chromatography (IC) followed conductivity detection, IC hyphenated with an MS detector can be used to measure perchlorate down to sub-µg/L levels. In this application IC is hyphenated with a triple-quadrupole MS (IC-MS/MS) for perchlorate determination in order to meet the requirements of EPA 332.0. This IC-MS/MS setup avoids the possible interference of sulfate.

Chlorinating drinking water can form carcinogenic byproducts. EPA Method 557 enables µg/L-level quantification of haloacetic acids using Metrohm IC-MS/MS technology.

During drinking water disinfection with chlorine, chloramine, or ozone, potentially toxic halogenated byproducts can be formed. The disinfectants can react with naturally occurring bromide and/or organic matter in the source water and form one of the most common and highly toxic disinfection byproducts (DBPs): haloacetic acids (HAAs). To protect human health, maximum tolerable levels of HAA in drinking waters are regulated (EPA 816-F-09-004). The EPA Method 557 specifies the analysis of HAAs beside bromate and dalapon by ion chromatography coupled to tandem mass spectroscopy (IC-MS/MS) with LODs varying from 0.02–0.11 µg/L. However, even with single MS, a high sensitivity is achieved to determine the current MCLs within an adequate accuracy. This Application Note describes the analysis of bromate, chlorite, monochloroacetic acid (MCAA), monobromoacetic acid (MBAA), bromochloroacetic acid (BCAA), bromodichloroacetic acid (BDCAA), dibromoacetic acid (DBAA), dichloroacetic acid (DCAA), tribromoacetic acid (TBAA), chlorodibromoacetic acid (CDBAA), and trichloroacetic acid (TCAA) with IC/MS. The Metrohm Driver 2.1 for EmpowerTM offers the analysis as a single software solution with EmpowerTM.

The new DIN draft standard 38407-53 outlines TFA analysis in water using direct injection LC-MS/MS, enabling quantification from 0.1–3.0 μg/L as shown in this Application Note.

Determination of NO3- and ClO4- in the presence of a large excess of HCl using anion chromatography with direct conductivity detection (using time program for full scale change after 18 min).

Determination of methylarsonic acid and dimethylarsinic acid using anion chromatography with direct conductivity detection.

Determination of anions in solder paste after alcoholic extraction using anion chromatography with direct conductivity detection.

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 silica (as silicate) in pure water with preconcentration using anion chromatography with direct conductivity detection (without any post-column reaction).

Determination of chloride, nitrate, phosphate, sulfate, and oxalate in dried potatoes using anion chromatography with direct conductometric detection.

Determination of acetate and methansulfonate in an organic salt using anion chromatography with direct conductivity detection.

Determination of acetate, formate, chloride, bromide, and sulfate in toluene using anion chromatography with direct conductivity detection.

Determination of carbonate in a solution of methyl-monoethanol-amine with anion chromatography with direct conductivity detection.

Determination of chloride, nitrate, phosphate and sulfate in plant leaf extracts using anion chromatography with direct conductometric detection.

Determination of chloride, bromide, and iodide in alkaline combustion solutions using anion chromatography with direct conductivity detection.

Determination of acetate, lactate, and chloride in electrolyte solutions using anion chromatography with direct conductivity detection.

Determination of chloride, nitrate, and sulphate in sugar-containing solutions without matrix elimination using anion chromatography with direct conductometric detection.

Determination of fluoride, chloride, nitrite, nitrate, and sulfate in an effluent sample using anion chromatography with direct conductometric detetction.

Determination of pyrophosphate, tripolyphosphate, and trimetaphosphate using anion chromatography with direct conductivity detection.

Determination of traces of iodide in HCl (25%) using anion chromatography with amperometric detection at a silver electrode.

Determination of traces of carbonate in urea using anion chromatography with direct conductivity detection.

Determination of traces of nitrite, thiosulfate, and iodide using anion chromatography with amperometric detection at the carbon paste electrode.

Determination of traces of bromide and iodide using anion chromatography with amperometric detection at the silver electrode.

Determination of traces of bromide in HCl (32%) using anion chromatography with amperometric detection at the silver electrode.

Determination of nitrate, sulfate, and thiocyanate in additives for building materials using anion chromatography with direct conductometric detection.

Determination of fluoride and chloride in gypsum using anion chromatography and subsequent direct conductometric detection.

Determination of sulfate in hydrochloric acid digest of gypsum using anion chromatography with direct conductometric detection.

Determination of perchlorate in process water using anion chromatography with direct conductivity detection.

Determination of traces of iodide in acetic acid using anion chromatography with amperometric detection at the carbon paste electrode.

Determination of iodide in wastewater (dye industry) using anion chromatography with amperometric detection at the silver electrode and dialysis for sample preparation.

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

Determination of silicate in tap water using anion chromatography with direct conductivity detection.

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

Determination of fosetyl-aluminum (aluminum tris(o-ethylphosphate)) using anion chromatography with direct conductivity detection.

Determination of carbonate in washing powder using anion chromatography with direct conductivity detection.

Determination of borate and silicate in washing powder using anion chromatography with direct conductivity detection.

Determination of acetate, chloride, citrate, and sulfate in a concentrate of an infusion solution using anion chromatography with direct conductivity detection. Non-suppressed IC is used to avoid interferences by the amino acids.

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

Determination of chloride and sulfate in a reactive dye using anion chromatography with direct conductivity detection. Suppressed IC does not work as the dye is hydrolyzed in alkaline solution and releases sulfate.

Determination of silicate and borate and their limits of determination (LOD) and quantification (LOQ) according to the EPA procedure for method detection limit (MDL) using anion chromatography with direct conductivity detection and Metrohm Inline Calibration.

Determination of acetate, chloride, and malate in an infusion solution using anion chromatography with direct conductivity detection.

Determination of acetate, phosphate, chloride, and citrate in an infusion solution using anion chromatography with direct conductivity detection.

Determination of nitrate in a nickel plating bath using anion chromatography with UV/VIS detection (205 nm).

Determination of sodium dodecylsulfate (SDS, sodium laurylsulfate) using anion chromatography with direct conductivity detection.

Determination of borate in a borate effluent using anion chromatography with direct conductivity detection.

Determination of phenol, m-cresol, 2,6-dimethylphenol and 2,3,6-trimethylphenol in tap water with amperometric detection using a glassy carbon electrode.

Determination of chloride and sulfate in effluent after Metrohm Inline Dialysis using anion chromatography with direct conductivity detection.

Determination of sulfide in an effluent sample using anion chromatography with amperometric detection.

Alendronate, also referred to as alendronic acid, is a biphosphonate used to treat osteoporosis. It is the main ingredient in the tablets and is determined in accordance with the Chinese Pharmacopoeia (2015). Separation takes place in the Metrosep A Supp 4 - 250/4.0 column; direct conductivity detection is used for quantification.

Pure sodium chloride contains much less iodide than e.g., table salt which usually is fortified with it. Trace determination of iodide is easily performed applying ion chromatography with amperometric detection. This detection mode is particularly selective and sensitive. The actual separation is achieved using a Metrosep A Supp 5 - 250/4.0 column. The detection happens at a silver working electrode. LOQ is at approximately 1.0 μg/L (in solution) and 50 μg/kg in the sample. The use of a shorter column might further improve the LOQ.

Two of the leading pain remedies, aspirin and acetaminophen, are compared with generic samples for content uniformity testing using near-infrared spectroscopy (NIRS). The method of standard addition is used for quantification. To reduce most of the effects that stem from particle size and packing differences, second derivative spectra are used.

This Application Note shows the potential of NIRS as a rapid (< 30 s) and nondestructive screening tool for solid dosage forms (e.g. tablets). NIRS requires neither sample preparation nor solvent use. Interferences that derive from scattering are minimized by converting to second derivative spectra.

This Application Note describes the determination of copolymer levels in polyethylene (PE) and polyvinylacetate (PVA) pellets using NIRS. The determination of the composition of the polymer blends takes less than 30 seconds and requires no sample preparation. The second derivative spectra are analyzed by means of the linear least-squares regression method.

This Application Note shows that NIR spectroscopy is an excellent tool for determining low concentrations of additives in finished polypropylene pellets. This is demonstrated by monitoring the UV stabilizer Tinuvin 770 and the antioxidant Irganox 225. The application of multiple linear regression (MLR) models minimizes interferences that originate from different coating thicknesses and interferences in the polymer pellets.

This Application Note demonstrates how NIR spectroscopy can be used to determine the content of coatings on nylon fibers, quickly and without requiring either sample preparation or the use of reagents. In order to suppress the effects arising from scattering on the surface coatings, one forms the second derivative spectra; the linear least-squares regression method is used to calculate the calibration function.

This Application Note describes how NIR spectroscopy can be used to determine residual lignin content in wood pulp. Using the major absorbance peaks of both lignin and cellulose in the second derivative spectra, the residual lignin content in wood pulp can be monitored during paper production.

Near-infrared spectroscopy (NIRS) is ideally suited to monitor the hardwood and softwood content in pulp and paper products.The herein described method bases on the fact that the changes in hardwood and softwood content are reflected in the intensity of the absorption bands of cellulose. A linear least-squares regression on second derivative spectra provide results that correspond very well with those of conventional laboratory determinations. With NIRS, an analytic method is available that provides results in real time.

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 demonstrates that a calibration model for caffeine and microcrystalline cellulose developed on the NIRS XDS Rapid Content Analyzer (RCA) is transferable to other NIRS XDS RCA. Due to the improved signal-to-noise ratio, reduced bandwidth and improved wavelength precision of the NIRS XDS, the transferability of the calibration model can be easily and efficiently performed.

This Application Note describes how the accuracy of your NIR measurements can be increased with instrument calibration.

This Application Note describes how the accuracy of your NIR measurements can be increased with reference standards.

Well-mixed active substances for medications are indispensable in the pharmaceutical industry. This applies not only to the pharmaceutical active ingredient but also for lubricants, binding agents, explosives, oxidants and dyes. Analysis of these active ingredients is expensive; they are also only rarely analyzed as a rule. The progress of the mixing procedures can be followed conveniently with NIR spectroscopy, on the one hand using visual comparisons and on the other by means of spectral algorithms. The progress of mixing processes can be predicted in real time with the help of the spectrum when the latter is used.

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.

This Application Note shows that NIR "predictive models" are optimally suitable for the non-destructive measurement of the release profiles of active ingredients from tablets. This is in accordance with the Process Analytical Technology (PAT) initiative of the FDA. The results demonstrate how NIRS considerably reduces the work involved for release studies in the laboratory.

This Application describes the determination of moisture, nitrogen, and fat in stool samples using near-infrared spectroscopy. These parameters are of great importance in medical diagnostics.

The determination of the water content of soft contact lenses using NIR spectroscopy is described in this Application. A liquid sample kit with gold diffuse reflector was used for measuring the lenses in transflexion mode. A PLS model was developed for predicting the water content.

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

In recent years, there has been a significant push to reduce the environmental impacts of fuels through improvements to fuel quality. The determination of key quality parameters of gasoline, namely research octane number (RON, ASTM D2699-19), motor octane number (MON, ASTM D2700-19), anti knock index (AKI), aromatic content (ASTM D5769-15), and density, conventionally requires several different analytical methods, which are laborious and need trained personnel. This application note demonstrates that the XDS RapidLiquid Analyzer, operating in the visible and near-infrared spectral region (Vis-NIR), provides a cost-efficient and fast solution for the multiparameter analysis of gasoline.

Determination of the diethylene glycol content, isophthalic acid content, intrinsic viscosity (ASTM D4603), and the acid number (AN) of polyethylene terephthalate (PET) is a lengthy and challenging process due to the sample’s limited solubility and the need to use different analytical methods. This application note demonstrates that the DS2500 Solid Analyzer operating in the visible and near-infrared spectral region (Vis-NIR) provides a cost-efficient and fast solution for a simultaneous determination of these parameters in PET. Vis-NIR spectroscopy allows for the analysis of PET in less than one minute without sample preparation or using any chemical reagents.

Pyrolysis gasoline (Pygas) is a by-product of ethylene production, which contains unwanted conjugated diolefins making it unsuitable as a motor fuel. To overcome this limitation, the olefin content needs to be reduced below 2 mg/g pygas in a selective hydrogenation unit (SHU). The diene value, or maleic anhydride value (MAV), is usually determined by the lengthy Diels-Alder wet chemical method (UOP326-17), requiring highly trained analysts. In contrast to the primary method, near-infrared spectroscopy (NIRS) is a cost-efficient and fast analytic solution for the determination of diene value in pyrolysis gasoline.

This Application Note describes the determination of various indices (mainly with ASTM and ISO conformance) for the characterization of kerosene as aviation turbine fuel using near-infrared spectroscopy. The following parameters were determined with the aid of an NIRS XDS Process Analyzer: degree of density in accordance with the American Petroleum Institute (API), aromatics content, Cetane Index, distillation characteristics pursuant to ASTM D86, flash point, freezing point, viscosity and hydrogen content. All of these parameters are determined quickly and easily with just a single measurement.

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 how, with the help of Vis-NIR spectroscopy and a special plant library, 46 different medicinal and aromatic plants, e.g., Organicum majoricum and Tilia cordata, can be conveniently identified on the basis of their spectrum. In comparison with alternative methods for the determination of plants, which are elaborate and require experienced scientists for their performance, the Vis-NIR method permits rapid and uncomplicated identification.

This Application Note shows the transfer of near-infrared spectroscopy analysis methods from the FOSS NIRSystems System II (5000/6500) Analyzer to the Metrohm NIRS XDS und DS2500 Analyzers. In addition, the advantages of the new NIRS XDS and DS2500 analyzers with extended spectral range and improved resolution are displayed, in particular with respect to the FOSS NIRSystems System II analyzer.

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 shows how the amine number and the solids content in electrophoretic lacquer coatings can be determined quickly and simply with Vis-NIR spectroscopy. Additional parameters can be determined reliably and conveniently with a single measurement.

This Application Note shows how purity, degree of substitution and water content of carboxymethyl celluloses (CMC) can be determined conveniently and rapidly in a single measurement with Vis-NIR spectroscopy.

This Application Note shows the determination of the ratio of cotton linter to pulp in cellulose samples with Vis-NIR spectroscopy. This linter-pulp ratio is an important characteristic in the paper industry which, unlike with elaborate wet-chemistry methods, can be determined quickly and conveniently with Vis-NIR spectroscopy.

This Application Note describes the simultaneous determination of the four most important analysis parameters of paint dryers – cobalt and solids contents, specific weight and viscosity – using a VIS-NIR analyzer. The visible range correlates with the metal content, while the NIR region provides the specific weight, viscosity and solids content.

This Application Note shows that near-infrared spectroscopy with its exceptionally short analysis times significantly accelerates quality monitoring of polymer granulates and raw materials. Polyethylene (PE) und polypropylene (PP) can be identified in parallel. PE density is also determined in the same measurement.

Polyols are widely used as polyurethane feedstocks, where tight quality control of parameters such as hydroxyl value, acid number, moisture, and viscosity is essential. Conventional titration methods are standardized but slow and costly due to hazardous chemicals and waste handling. Near-infrared spectroscopy (NIRS), recognized by ASTM for hydroxyl value determination, enables rapid, reagent-free, multiparameter analysis of polyols with significantly lower operating costs.

This Application Note shows the fast and parallel determination of water content and pH value in crude tall oil samples using near-infrared spectroscopy (NIRS). Crude tall oil is an important byproduct of pulp production in the power process. NIRS is an efficient alternative to conventional laboratory methods: It permits rapid raw material inspection, process monitoring and final product checking.

Sulfathiazoles are sulfonamides with antibiotic effect that occur in various polymorphous forms and that are often used in veterinary medicine. This Application Note shows the differentiation between commercial and sulfathiazole form I using near-infrared spectroscopy (NIRS) with the help of the overtone frequencies of N-H stretching vibration. Form I is the least stable polymorphous form. Crystallization and polymorphism must be monitored as part of quality controls. In this, NIRS is considerably more rapid and more reliable than conventional laboratory methods.

In this Application Note, Vis-NIR spectroscopy (Vis-NIRS) is used to determine six wood pulp properties in a single measurement: kappa number, applied density, freeness, breaking strength, buckling strength and tensile strength.

This Application Note describes the quantification of protein content in dietary supplements using Vis-NIR spectroscopy to reduce the workload of time-consuming and waste-generating primary methods, such as Kjeldahl digestion.

For lubricant analysis, determination of the Acid Number (ASTM D664), viscosity (ASTM D445), moisture content (ASTM D6304), and color number (ASTM D1500) require the use of multiple analytical technologies and, in part, large volumes of chemicals. This application note demonstrates that the XDS RapidLiquid Analyzer operating in the visible and near-infrared spectral region (Vis-NIR) provides a fast and cost-efficient alternative for the determination of the AN, viscosity, moisture content, and color number of lubricants. With no sample preparation or chemicals needed, Vis-NIR spectroscopy allows for multi parameter analysis of lubricants in less than one minute.

Heparin acts as an efficient anticoagulant and, in addition to direct injection, is also used as a lock-flush solution for rinsing catheters. Vis-NIR spectroscopy can be used to determine the strength of contaminated and purified heparin. This Application Note demonstrates that heparin strength can be determined reliably with Vis-NIR spectroscopy.

This Application Note demonstrates the data transfer from a Fourier transform to a dispersive NIR instrument, using quality control of lubricating oils as an example application. It is shown that FT-NIR instruments can be replaced by dispersive ones without time-consuming sample remeasurement and subsequent method development.

Determination of key quality parameters of palm oil, namely free fatty acids (FFA), iodine value (IV), moisture content, deterioration of bleachability index (DOBI), and carotene require the use of several different analytical methods, which are laborious and can lack in accuracy. This application note demonstrates that the XDS RapidLiquid Analyzer operating in the visible and near infrared spectral region (Vis-NIR) provides a cost-efficient and fast solution for the determination of these quality control parameters in palm oil. With no sample preparation or chemicals needed, Vis-NIR spectroscopy allows for the analysis of palm oil in less than a minute and can be used by anyone.

Vis-NIR spectroscopy is used to determine the droplet morphology in hair conditioner. This Application Note shows that near-infrared (NIR) spectroscopy can be used to distinguish between unprocessed and processed hair conditioner and to qualify quality parameters such as the droplet size.

Visible Near-infrared (Vis-NIR) spectroscopy is a valuable chemical analysis tool that can be used to determine quality parameters of hair creams. A qualitative method was developed in order to allow a fast out-of-spec analyses of an active antibacterial ingredient.

Near-infrared spectroscopy (NIRS) was used as an analysis method for quality control of hair spray samples. A model for an active ingredient within hair sprays was developed, enabling fast and reliable out-of-specification analyses.

Visible near-infrared (Vis-NIR) spectroscopy can be used as a fast and accurate analytical method for the quantification of different analytes and active ingredients in detergents, such as tetraacetylethylendiamin (TAED), sodium percarbonate (PCS), and enzymes. This Application Note shows how NIRS can be used for multi-constituent analyses in detergents in a single measurement.

Near-infrared spectroscopy (NIRS) was used in a preliminary study as a fast and accurate method for the quantification of different preservatives and active ingredients in liquid shampoo. This Application Note shows how this analytical method allows the simultaneous determination of several constituents in shampoo in a single measurement.

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.

Near-infrared spectroscopy (NIRS) was used as an analysis method for quality control of aqueous xanthan gum solutions. Quantitative models for the determination of optical density, glucose, and xanthan gum were developed, enabling fast and reliable quality control.

This Application Note shows that visible near-infrared spectroscopy (Vis-NIRS) can determine water content in ethanol-hydrocarbon blends. Vis-NIRS is a fast alternative to conventional lab methods: it accelerates raw material inspection, process monitoring, and final product control.

Determination of sodium laureth sulfate (SLES), cocamidopropyl betaine (CABP), cocamidopropylamine oxide (CAW), cocamide diethanolamine (DEA), and carbopol in shampoo is a cost- and time-intensive process due to the use of large volumes of chemicals per analysis. This application note demonstrates that the DS2500 Solid Analyzer operating in the visible and near-infrared spectral region (Vis-NIR) provides a cost-efficient and fast solution for a simultaneous determination these parameters in shampoo. With no sample preparation or chemicals needed, Vis-NIR spectroscopy allows for the complete analysis in less than a minute.

Near-infrared spectroscopy (NIRS) was used for quality control of skin creams. A model for the quantification of the water content was developed based on Karl Fischer titration (KF), enabling fast and reliable atline analysis and final product quality control.

This Application Note shows that visible near-infrared spectroscopy (Vis-NIRS) can be used for the quantification of five effective insecticide and herbicide components (Abamectin emulsifiable concentrate (EC), Emamectin EC, Cyhalothrin EC, Cypermethrin and Glyphosate) in pesticides. Vis-NIRS is an excellent alternative to conventional lab methods, saving both cost and time.

This Application Note shows that visible near-infrared spectroscopy (Vis-NIRS) can be used for the quantification of Baicalin content in herbal supplements. Vis-NIRS is a good alternative to the conventional lab method (HPLC) and can save both cost and time.

This Application Note shows that the visible range of the Metrohm Vis-NIR analyzer can be used to quantify the color intensity of dyes, providing comparable results to the reference analysis UV-Vis. The NIR region can be used in addition to distinguish between different dye types or different suppliers and can identify impurities in the undiluted dyes during raw material control. The combination of the visible and near-infrared wavelength ranges offer the benefit that only one analyzer is required to receive results on multiple parameters in a 30-seconds-scan results on both cost and time saving.

Functional group and viscosity analysis (ASTM D789) of polyamides can be a lengthy and challenging process due to the sample’s limited solubility. This application note demonstrates that the DS2500 Solid Analyzer operating in the visible and near-infrared spectral region (Vis-NIR) provides a cost-efficient and fast solution for a simultaneous determination of the intrinsic viscosity as well as the amine, carboxylic, and moisture content in polyamides. With no sample preparation or chemicals needed, Vis-NIR spectroscopy allows for the analysis of polyamides in less than a minute.

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.

This Application Note shows that visible near-infrared spectroscopy (Vis-NIRS) can determine the sun protection factor (SPF) of sunscreen products. Thanks to measurement durations of less than 30 seconds, NIR spectroscopy is ideally suited for rapid and reliable quality control.

Uniformity of dosage units must be tested for QC purposes in the pharma industry. NIRS gives results in seconds along with the quantification of APIs and excipients.

Specialty chemicals have to fulfill multiple quality requirements. One of these quality parameters, which can be found in almost all certificates of analysis and specifications, is the moisture content. The standard method for the determination of moisture content is Karl Fischer titration.This method requires reproducible sample preparation, chemicals, and waste disposal. Alternatively, near-infrared spectroscopy (NIR) can be used for the determination of moisture content. With this technique, samples can be analyzed without any preparation and without using any chemicals.

This Application Note presents Vis-NIR spectroscopy as a viable alternative to determine API content in cefixime tablets without sample preparation.

This Application Note demonstrates the feasibility of Vis-NIRS for the simultaneous determination of multiple chemical and physical parameters in epoxy resins. Vis-NIRS is a fast alternative to conventional lab methods: it accelerates raw material inspection, process monitoring, and final product control.

Control of NCO content in isocyanates is essential for polyurethane production. However, wet chemistry methods are slow, hazardous, and preparation intensive. Near-infrared spectroscopy (NIRS) offers a rapid, reagent-free alternative, determining NCO content in seconds without sample preparation. This makes NIRS a practical and environmentally compliant solution for routine quality control of isocyanate raw materials.

Rapid quality control for toothpaste is achieved by Metrohm`s Vis-NIR analyzers. Vis-NIR technology offers significant advantages compared to standard reference analysis. It is a cost effective and safe method because no hazardous chemicals are used.

This Application Note describes a fast method for the simultaneous quantification of nicotine and glycerin in liquid mixtures used for electronic cigarettes. With visible near infrared spectroscopy (VIS-NIRS), results are available without sample preparation, thus making VIS-NIRS highly suited for fast quality control.

Acid Number (AN) analysis of lubricants (ASTM D664) can be a lengthy and costly process due to usage of large amounts of chemicals and required cleaning steps of the analytical equipment between each measurement. This application note demonstrates that the XDS RapidLiquid Analyzer operating in the visible and near-infrared spectral region (Vis-NIR) provides a cost-efficient, fast alternative for the determination of the acid number of lubricants. With no sample preparation or chemicals needed, Vis-NIR spectroscopy allows for the analysis of AN in less than a minute.

Packaging has become an indispensable part in the food manufacturing process. To improve the appearance and properties of the packaging, a wide variety of coatings and inks are used. Different additives enhance rheological properties, control the wetting dispersion, or in the case of wax increase abrasion resistance. The regulations of these coatings in food packaging applications are very strict in some countries, creating the need for close monitoring of the production process.A fast, reliable, and simple to use solution for quantifying rheological additives and wax in such coatings is Visible-Near Infrared Spectroscopy (Vis-NIRS). Both parameters are determined simultaneously by Vis-NIRS in less than a minute.

Water activity is an important parameter to measure for non-sterile pharmaceutical quality and stability. The OMNIS NIR Analyzer provides this data within seconds.

This Application Note shows how NIRS is used for the multiparameter analysis of dry matter, pH value, viscosity, and surfactant content in liquid laundry detergent.

Naphtha is the first petroleum product during the distillation process of crude oil or coal tar. It is primarily used as a base material for the production of gasoline or as a solvent. Accidental spills occur regularly at many locations throughout the world, leading to soil contamination.Investigation of contaminated sites is usually performed using gas chromatography, for which the soil sample has to be frozen, grinded, and subsequently extracted prior to the analysis. Using Visible-Near Infrared Spectroscopy such sample preparation steps are not necessary at all, making this method a viable, fast, and simple to use alternative.

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.

Caprolactam is an important polymer used for the production of Nylon 6, which is the base material for industrial fibers. Due to its commercial significance, many different synthesis methods have been developed over the years. Caprolactam is hygroscopic and water soluble, therefore it is important to have a reliable analysis technique for water determination. Analyzing the water content by conventional methods requires each sample to be weighed, dissolved, heated, and titrated. Compared to the primary method, near-infrared spectroscopy (NIRS) offers unique advantages: it generates reliable results within seconds, but it does not need any sample preparation nor does it create chemical waste.

The quantification of residual moisture in lyophilized pharmaceutical peptides is an important measure for quality control in the pharmaceutical industry. For development purposes, such measurements are necessary and routinely performed during stability studies and to optimize the freeze-drying process (lyophilization). Currently, Karl Fischer titration is widely used for moisture determination in routine analysis. However, this method is time consuming and destroys the sample during analysis. This Application Note shows that near-infrared spectroscopy (NIRS) is a fast, reagentless, non-destructive method to determine moisture content in lyophilized pharmaceutical products.

Moisture content is one of the most commonly measured properties of fertilizers. Globally, regulations for different fertilizers vary, but local legal limits ensure that the maximum amount of water must not be exceeded. Next to gravimetric methods, Karl Fischer titration is often used for accurate moisture determination.Compared to these methods, near-infrared spectroscopy (NIRS) offers unique advantages: it generates reliable results within seconds, and at the same time does not create chemical waste. This Application Note explains how NIRS can offer fast, reagent-free analysis of moisture content in various fertilizer products.

The cetane index (ASTM D613), flash point (ASTM D56), cold filter plug point (CFPP) (ASTM D6371), D95 (ISO 3405), and viscosity at 40°C (ISO 3104) are key parameters to determine for diesel quality. The primary test methods are labor intensive and challenging due to the need to use different analytical methods. This application note demonstrates that the NIRS XDS RapidLiquid Analyzer provides a cost-efficient and fast solution (under 1 minute) for the simultaneous determination of these key parameters in diesel.