アプリケーション検索（技術資料）

Several testing methods such as the determination of the acid and the iodine numbers in biodiesel as well as the quantification of sulfate and chloride in bioethanol are described.

A complete tap water analysis includes the determination of the pH value, the alkalinity and the total water hardness. Both the pH measurement and the pH titration by means of a standard pH electrode suffer from several drawbacks. First, the response time of several minutes is too long and, above all, the stirring rate significantly influences the measured pH value. Unlike these standard pH electrodes, the Aquatrode Plus with its special glass membrane guarantees rapid, correct and very precise pH measurements and pH titrations in solutions that have a low ionic strength or are weakly buffered. Total water hardness is ideally determined by a calcium ion-selective electrode (Ca ISE). In a complexometric titration, calcium and magnesium can be simultaneously determined up to a calcium/magnesium ratio of 10:1. Detection limits for both ions are in the range of 0.01 mmol/L.

Commercially available fuels are complex mixtures of hundreds of different hydrocarbons. For the calibration of the test engines or advanced experimental and computational research they are modeled by means of multicomponent surrogate mixtures that adequately represent the desired physical and chemical characteristics. By definition, every octane and cetane number corresponds to a specific mixing ratio of primary reference fuels (PRFs). Based on this information, the tiamoTM controlled automatic dosing device prepares the surrogate mixtures. The setup drastically minimizes time-consuming and error-prone manual preparation steps and the contact with hazardous solvents. Additionally, precise and accurate results are displayed on customizable reports that fully comply with all current GLP and GMP requirements.

Compared to the classical Epton titration, potentiometrically indicated two-phase titrations using organic-solvent-resistant Surfactrodes can be easily automated and require no toxic and environmentally hazardous chloroform. Even challenging matrices such as fats and oils in bath oils and hair conditioners or strong oxidizing agents in washing powder and industrial cleaners do not interfere with the titration of the ionic surfactants. Results obtained show excellent agreement to those of the Epton titration. Irrespective of the matrix, relative standard deviations of threefold determinations are all below 2.1%. While the Surfactrode Resistant is mainly used for oil-containing formulations, the Surfactrode Refill is ideal for washing powders and soaps. Both electrodes excel by their ruggedness and allow the rapid and precise determination of anionic and cationic surfactants.

Benzbromaron is one of the main uricosuric drugs currently used. In addition to sophisticated and expensive LC-MS and GC-MS methods, benzbromaron can be effectively determined by titration with sodium hydroxide solution using a straightforward, fully automated sample preparation method. A high-frequency homogenizer comminutes one or three tablets within 90 or 120 s respectively. The overall analysis time is 8 minutes. Ten-fold determinations with one and three tablets resulted in a benzbromaron content of 99.2 and 98.7 mg per tablet respectively. Increasing the number of tablets from one to three lowers the RSD from 1.36 to 0.88%. These results show an excellent agreement with the benzbromaron content indicated by the manufacturer (approx. 100 mg/tablet).Besides the presented Titrando/homogenizer combination, the other two members of the 815 Robotic Soliprep Sample Processor family offer comprehensive sample preparation possibilities within the fields of IC, HPLC, ICP or voltammetry.

This poster presents a highly reproducible procedure for the determination of the sodium contribution of acid-extractable organic species in Bayer process liquor. The precision of the method is estimated to be 0.2% RSD.

Hydroxyl is an important functional group and knowledge of its content is required in many intermediate and end-use products such as polyols, resins, lacquer raw materials and fats (petroleum industry). The test method to be described determines primary and secondary hydroxyl groups. The hydroxyl number is defined as the mg of KOH equivalent to the hydroxyl content of 1 g of sample.The most frequently described method for determining the hydroxyl number is the conversion with acetic anhydride in pyridine with subsequent titration of the acetic acid released: H3C-CO-O-CO-CH3 + R-OH -> R-O-CO-CH3 + CH3COOH. However, this method suffers from the following drawbacks: - The sample must be boiled under reflux for 1 h (long reaction time and laborious, expensive sample handling) - The method cannot be automated - Small hydroxyl numbers cannot be determined exactly - Pyridine has to be used, which is both toxic and foul-smellingBoth standards, ASTM E1899-08 and DIN 53240-2, offer alternative methods that do not require manual sample preparation and therefore can be fully automated: The method suggested in ASTM E1899-08 is based on the reaction of the hydroxyl groups attached to primary and secondary carbon atoms with excess toluene-4-sulfonyl-isocyanate (TSI) to form an acidic carbamate. The latter can then be titrated in a non-aqueous medium with the strong base tetrabutyl- ammonium hydroxide (TBAOH). The method suggested in DIN 53240-2 is based on the catalyzed acetylation of the hydroxyl group. After hydrolysis of the intermediate, the remaining acetic acid is titrated in a non-aqueous medium with alcoholic KOH solution. The present work demonstrates and discusses an easy way to determine the hydroxyl number according to ASTM E1899-08 or DIN 53240-2 with a fully automated titrimetric system for a great variety of industrial oil samples.

Sodium fluoride is used as a preservative in biological samples for alcohol analysis. All submitted blood samples, including those taken from vehicle drivers suspected of driving under the influence of liquor, have to be tested for adequate preservation prior to alcohol determination by gas chromatography. This is critical to ensure adequate sample preservation. Inadequate sample preservation may allow glycolysis and/or microorganism growth to produce ethanol.In the past this has been done by direct potentiometric measurement using a fluoride-selective electrode (F ISE), an ion meter and certified NaF standards. The sodium fluoride level was determined manually by dipping the electrode directly into the blood sample. Results were recorded manually. This poster describes two independent automated methods of analysis that allow the minimization of this tedious and time-consuming procedure.In the first one, the fluoride content in a blood aliquot is measured by direct potentiometric measurement after the addition of TISAB and deionized water. The second method employs the titration of the sample aliquot with La(NO3)3 after adding a buffer solution.

The thermometric titration method presented here permits a simple and direct determination of the total acid number (TAN) in petroleum products. It is an invaluable alternative to current manual and potentiometric methods. Thermometric titration uses a maintenance-free temperature sensor that does not require rehydration and is free of fouling and matrix effects. The procedure requires minimal sample preparation. Results agree closely with those from the potentiometric titrimetric procedure according to ASTM D664, but the thermometric titration method is far superior in terms of reproducibility and speed of analysis, with determinations being complete in approximately one minute.

このポスターで説明されている分析では、食料品中のナトリウムを簡単に測定するための有望なメソッドとしての TET について論じられています。ナトリウムのTETは、スープ、グレイビー、およびいくつかの塩味のスナックなどのような様々な食品サンプルマトリックスへの適用性が検証されました。エンタルピー変化は、高感度のデジタル温度計を用いて、溶液温度の変化としてモニタリングできます。ここで説明されているナトリウムの測定は、エルパソライト (NaK2AlF6) の発熱性沈殿物に依存しています。滴定試薬は、過剰なカリウムイオンを含むアルミニウム標準液です。滴定は食品サンプルの懸濁液にて直接実施され、2分以内に完了します。このメソッドは堅固で、完全自動で実施できる上に、再現性の高い高周波均質化によって様々な困難な食品マトリックス (ケチャップ、インスタントスープ、プレッツェルなど) に対応できます。このApplication Noteに加え、ナトリウムのTET測定に関するより詳しい情報は、YouTubeの弊社のアプリケーションビデオにてご覧いただけます:https://youtu.be/lnCp9jBxoEs

Thermometric titration can solve application problems that potentiometry cannot solve at all, or at least not satisfactorily.

AAPS会議にてUSPと共同で発表されたこのポスターは、炭酸水素カリウムの新たな電位差滴定のアッセイメソッド、および、選択肢を提供し、USPの総則の章< 1225>に従ったすべてのUSPメソッド検証の要求を満たす炭酸カリウムのアッセイを紹介するものです。電位差滴定に基づいたアッセイによる測定は、クロマトグラフィー技術に比べてより迅速で扱いやすく、簡単に自動化できるので、高いスループットのニーズを満たすことができます。適切な当量点検知メソッドと自動滴定の組み合わせは、手動によるミスを排除するだけではなく、データ完全性、および製薬におけるQA/QCのワークフローをより簡単にする21 CFR 11の要求を満たします。

外部フローセル搭載pHモジュールを使用した培養基のpHを測定するためのハイスループット自動システムが開発されました。カスタマーサンプルバイアルの形状とサイズを調整するため、カスタムのセプタム穿孔、通気針が開発されました。このアプリケーションには、精密かつ正確なpH測定が必要とされていました。この文書に記載されているデータは、顧客によってその検証プロセスの一部として収集され、その同意を得て使用するために提供されました。

アンチモン合金鉛ケーブル リード (約 1% Sb) に含まれるのアンチモンを測定するため、バイアンペロメトリック滴定で終点設定をおこなった自動滴定装置を使用して測定したアプリケーションです。0.01 mol/L KBrO3を滴定試薬として使用します。

Zinc, such as that occurring as a constituent of light alloys, can be determined by precipitation titration with potentiometric endpoint indication. The determination of zinc in the presence of cadmium is also possible.2 K4[Fe(CN)6] + 3 ZnCl2 → K2Zn3[Fe(CN)6]2 + 6 KCl

A potentiometric method for the determination of nickel in gold and silver electroplating baths is described. The titration is carried out with KCN. Gold and silver are removed before titration by a reduction process. It is also possible to determine nickel in steel alloys, etc. (see the literature reference).Ni2+ + 4 KCN + 2NH4+ → (NH4)2[Ni(CN)4] + 4 K+

A routine method for the determination of copper is described. After dissolving the sample and adding a KI/KCNS solution, the released iodine is back-titrated with thiosulfate. The endpoint indication is potentiometric.

A method for the potentiometric determination of CaCO3 in cement raw meal is described, in which the accurately weighed-out sample is treated with HCl, heated to boiling and the excess HCl is then back-titrated with NaOH.

This Bulletin describes the simultaneous determination of gold and copper by potentiometric titration using an Fe(II) solution as titrant. Fe(II) reduces Au(III) directly to the free metal, whereas Cu(II) does not react. By the addition of fluoride ions the Fe(III) is complexed and a shift of the redox potential is effected. Afterwards, potassium iodide is added, thus reducing the Cu(II) to Cu(I), and the free iodine is again titrated with the Fe(II) solution using a Pt Titrode.Chemical reactions:Au(III) + 3 Fe(II) → Au + 3 Fe(III)2 Cu(II) + 2 I- → 2 Cu(I) + I2I2 + 2 Fe(II) → 2 I- + 2 Fe(III)

Ag電極は、銀とハロゲン化物イオンまたは硫化物イオン間の沈殿滴定における電位差終点の指標として用いられます。銀リングのコーティングは電極の感度を向上させ、これにより検出限界を下げることができます。そのため、様々な種類のAg被覆電極が市販されています。この文書では、いかにAg電極の銀リングを電気分解にてAgCl、AgBr、AgIまたはAg2Sでコーティングできるかについて説明しています。

If chloride and bromide are present in approximately equal molar concentrations they can be titrated directly with silver nitrate solution after addition of barium acetate. If, however, the molar ratio n(Br-) : n(Cl-) changes from 1 : 1 to 1 : 5, 1 : 10, 5 : 1 or 10 : 1 then greater relative errors must be expected with this method. The Bulletin describes an additional titration method that allows bromide to be determined in the presence of a large excess of chloride. The determination of small chloride concentrations in the presence of a large excess of bromide is not possible by titration.

Two methods are described for the determination of chromium: a biamperometric titration and a polarographic analysis.

A potentiometric, nonaqueous method is described for analyzing nitrating acid using cyclohexylamine as titrant. Both sulfuric and nitric acid can be determined quantitatively.

カルボニル化合物 (CC) は、バイオオイル、燃料、環式および非環式溶媒、香料、鉱油などの多くの製品に存在しています。カルボニル化合物は、これらの製品の保管および加工中に不安定性の原因となることがあります。特に熱分解バイオオイルは、保管、ハンドリング、アップグレードの間、問題を起こすことで知られています。この Bulletin では、電位差滴定によるカルボニル化合物の測定のための水性および非水性分析滴定メソッドについて説明されています。

The determination of cyanide is very important not only in electroplating baths and when decontaminating wastewater but, due to its high toxicity, also in water samples in general. Concentrations of 0.05 mg/L CN- can already be lethal for fish.This Bulletin describes the determination of cyanide in samples of different concentrations by potentiometric titration.Chemical reactions:2 CN- + Ag+ → [Ag(CN)2]-[Ag(CN)2]- + Ag+ → 2 AgCN

サンプル分析の開始前に、電極が良い状態にあるかどうかを確かめることは不可欠です。正しく機能する電極は結果の質を高め、同様に正確性と精密性も向上することでしょう。その上、煩わしいエラートラッキングを省略でき、故障または電極の劣化が原因でサンプルを無駄にすることもありません。メタル電極のチェックには、酸化還元電位の測定、電位差滴定、またはバイボルタンメトリー滴定など、いくつかの方法があります。この文書では、メトローム社が提供する様々なメタル電極のための最適なメソッドが説明されています。

ケルダール窒素の電位差滴定は、最もよく用いられる分析法の1つです。この方法は、食品や飼料産業から下水や廃棄物の分析、また肥料産業にまで至る数多くの規格の実質となっています。原則的に、サンプルは濃縮硫酸に触媒を加えることで分解されます。発生した硫酸アンモニウムは、アルカリ溶液内でアンモニアとして蒸留し、吸収液に吸収して、そこで滴定します。本文書では、電量滴定 (蒸留なし) の可能性について議論する前に、消化溶液の蒸留後の電位差滴定における窒素の測定について詳しく説明しています。

銀は宝飾品と食器だけではなく、電気伝導体および電気接点においても重要な金属です。純銀、銀合金中の正確な銀含有量を知ることにより、宝飾品および銀食器の品質基準を満たしていることを保証することができます。めっき工業では、銀めっき浴槽中の銀の総量を知ることが、めっき浴を効率的に実施するために役立ちます。蛍光Ｘ線 (XRF) は、純銀と銀合金中の銀含有量を迅速に測定するための方法のひとつですが、これは金属の最も外側の部分の銀含有量しか測定できません。対照的に滴定は、サンプル全体について考慮すれば、厚めっきによる不正を防止する、より包括的なソリューションを提供します。このApplication Bulletinでは、EN ISO 11427、ISO 13756、GB/T 17823 および GB/T 18996に従った純銀、銀合金中の銀の、および銀めっき浴に含まれる銀の、それぞれ臭化カリウムまたは塩化カリウムでの滴定による電位差測定について説明しています

多くの品種のセメントがどれほど異なった特性を持とうとも、全てを同様に特徴づけているのが、カルシウム、マグネシウム、鉄、アルミニウム、ケイ素といった要素の成分です。カルシウム、マグネシウム、鉄、アルミニウムは、セメントサンプルを分解した後、610 nm の Oprode を使用した光度滴定によって、様々な指標により測定することができます。一方、ケイ素は重量滴定によって測定されます。

Boric acid is used in many primary circuits of nuclear power plants, in nickel plating baths, and in the production of optical glasses. Furthermore, boron compounds are found in washing powders and fertilizers. This bulletin describes the potentiometric and thermometric determination of boric acid. The determination also covers further boron compounds, when acidic digestion is applied.

Indication of the titration endpoint of the weakly alkaline or weakly acidic terminal groups in non-aqueous solution is frequently not easy. An improvement is possible by using a suitable titrant (TBAH = tetrabutylammonium hydroxide for terminal carboxyl groups; perchloric acid for terminal amino groups).An improvement in the evaluation can also be achieved by choosing benzyl alcohol as the solvent.The choice of electrode combination and the measuring setup is also important. Differential potentiometry using the three-electrode technique results in a great improvement in titrations in poorly conducting solutions. Noisy signals are eliminated.

The quality of egg-based pasta is primarily determined by its egg content. Also of importance, however, is the water content, which influences the storage life of the product, as well as the degree of acidity which, in the case of high values, indicates undesirable acidification during processing or drying. A check of the chloride content shows whether salt has been added to the pasta.

Halides interfere with most determinations of mercury or silver. However, if mercury or silver is titrated with sulfide ions, extremely insoluble sulfides are formed.A simple method is described that allows the direct titration of mercury(II) or silver(I) compounds in the presence of halides. The potentiometric titration takes place under alkaline conditions using thioacetamide as the titrant after formation of the EDTA complex.Organic compounds that are insoluble in alkaline EDTA can also be titrated after a Schoeniger digestion.

The quality of a vinegar depends on various factors. Since the contents of the individual components vary widely even from bottle to bottle, it is impossible to give average values. This Bulletin describes the determination of the following parameters in vinegar: pH value, total titratable acid, volatile, and non-volatile acid, free mineral acid as well as free and total sulfurous acid.

This Bulletin describes analysis methods for determining the following parameters: pH value, total titratable acid, ash alkalinity, formol number, total sulfurous acid, chloride, sulfate, calcium, and magnesium. These methods are suitable for the analysis of jams, fruit and vegetable juices, and their concentrates.

この技術資料では電位差自動滴定装置を使用した、DIN 10316、ISO/TS 11869、IDF/RM 150、ISO 6091、IDF 86準拠による牛乳とヨーグルトに含まれる酸の測定。EN ISO 5943、IDF 88、ISO 15648、IDF 179、ISO 21422、IDF 242準拠による牛乳、バター、チーズに含まれる塩化物含有量の測定について紹介しています。さらに、TETを用いた牛乳に含まれるナトリウム含有量の測定について紹介しています。AOCS Cd 12b-92、ISO 6886、GB/T 21121準拠によるバターの酸化安定性の測定、イオンクロマトグラフィによるラクトースフリーの牛乳中のラクトースの測定についても説明しています。

This Bulletin describes potentiometric titration methods for checking sulfuric acid and chromic acid anodizing baths. In addition to the main components aluminum, sulfuric acid, and chromic acid, chloride, oxalic acid, and sulfate are determined.

Potentiometric titration methods for the analysis of acid and alkaline tin plating baths are presented. The following methods are described: tin(II) / tin(IV) / total tin, free fluoroboric acid, or free sulfuric acid, chloride in acidic tin baths, free hydroxide, and carbonate in alkaline tin baths.

Methods are described for the potentiometric analysis of the following bath components:Brass plating bath: copper, zinc, free cyanide, ammonium, carbonate, and sulfite.Bronze plating bath: copper, tin, and free cyanide.

This Bulletin describes the potentiometric determination of lead, tin(II), and free fluoroboric acid.

This Bulletin describes titrimetric methods for the determination of cadmium, free sodium hydroxide, sodium carbonate, and total cyanide. The free cyanide can be calculated from the total cyanide and the Cd content.

In addition to its natural occurrence in fruit and vegetables, ascorbic acid (Vitamin C) is used as an antioxidant in foods and drinks. Ascorbic acid is furthermore also to be found in numerous drugs.Ascorbic acid and its salts and esters can be determined with titration or by using polarography, for which ascorbic acid is oxidized to form dehydroascorbic acid.Bi-voltammetric or photometric equivalence point indication can be used for titrimetric determination. It must be taken into account here that only bi-voltammetric indication is independent of the inherent color of the sample. Polarography is the most selective of the methods described, as other reducing or oxidizing substances are not recorded.

The potassium (or ammonium) ion is precipitated with sodium tetraphenyl borate, and the excess of this reagent back-titrated against the thallous(I) ion, using biamperometric endpoint detection. Ammonium can either be titrated together in an acid solution, or driven off by previous boiling in an alkaline solution. Methods are given for determining potassium in the presence of large excesses of sodium, ammonium, calcium, and magnesium.

この技術資料では金属イオンのキレート滴定、電位差滴定について記述します。滴定の終点検出には、銅イオン選択性電極を用います。電極はキレート物質と直接応答しないので、対応する銅錯体を溶液に添加します。この電極を用いれば、水の硬度を定量することや、電気めっき液や金属塩、鉱物、鉱石中の金属濃度を分析することが可能です。以下の金属イオンが定量できます：Al3+、Ba2+、Bi3+、Ca2+、Co2+、Fe3+、Mg2+、Ni2+、Pb2+、 Sr2+、Zn2+

Wine sometimes contains heavy metals which can be precipitated out by the addition of potassium ferrocyanide. Generally, these are quantities of iron ranging between 1 and 5 mg, and exceptionally up to 9 mg Fe/L. Zinc, copper, and lead – in descending order of content – may also be present. To estimate the quantity of potassium ferrocyanide necessary for the «décassage of the wine», only very complicated and relatively inaccurate methods have been described until now.This Bulletin permits accurate results to be obtained easily with a simple instrumentation. The results are available in a short time.

Bromide is removed from the sample as BrCN by distillation. The BrCN is absorbed in sodium hydroxide solution and decomposed with concentrated sulfuric acid, then the released bromide ions are determined by potentiometric titration with silver nitrate solution. Iodide does not interfere with the determination.Iodide is oxidized to iodate by hypobromite. After destruction of the excess hypobromite, the potentiometric titration (of the iodine released from iodate) is carried out with sodium thiosulfate solution. Bromide does not interfere, even in great excess.The described methods allow the determination of bromide and iodide in the presence of a large excess of chloride (e.g., in brine, seawater, sodium chloride, etc.).

This bulletin describes the determination of calcium, magnesium, and alkalinity in water by complexometric titration with EDTA as titrant. It is grouped into two parts, the potentiometric determination and the photometric determination.There are multiple definitions of the different types of water hardness. In this Application Bulletin, the following definitions are used: alkalinity, calcium hardness, magnesium hardness, total hardness, and permanent hardness. Explanations of these definitions and other expressions are provided in the Appendix.Determination of alkalinity during the photometric part is carried out in a separate acid-base titration before the complexometric titration of calcium and magnesium in water. Permanent hardness can be calculated from these values. The determination of calcium and magnesium in beverages (fruit and vegetable juices, wine) is also described.The photometric part includes the determinations of total and calcium hardness and thereby indirectly magnesium hardness using Eriochrome Black T and calconcarboxylic acid as indicators (in accordance with DIN 38406-3).

After acid digestion, the sample solution is neutralized with sodium hydroxide to form sodium dihydrogen phosphate. An excess of lanthanum nitrate is added and the released nitric acid is then titrated with sodium hydroxide solution.NaH2PO4 + La(NO3)3 → LaPO4 + 2 HNO3 + NaNO3This determination method is suitable for higher phosphate concentrations.

Besides acid-base titrations, the titrimetric determination of chloride is one of the most frequently used titrimetric methods of analysis. It is employed more or less frequently in practically every laboratory. This Bulletin shows you how to determine chloride in a wide range of concentrations using automatic titrators. Silver nitrate is normally used as titrant (for environmental reasons one should refrain from using mercury nitrate). The titrant concentration depends on the chloride content of the sample to be analyzed. It is crucial to choose the correct electrode for samples with low chloride contents.

This Bulletin describes the potentiometric determination of hydrogen sulfide, carbonyl sulfide, and mercaptans in gaseous and liquid products of the oil industry (natural gas, liquefied petroleum gas, used absorption solutions, distillate fuels, aviation gasoline, gasoline, kerosene, etc.). The samples are titrated with alcoholic silver nitrate solution using the Ag Titrode.