アプリケーション（技術資料）

この技術資料カタログは、半導体製造に関わる品質管理において、メトロームの分析機器を使用して分析可能なパラメータを一覧にまとめたものです。

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.

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

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+

銅の定量分析方法について説明します。試料を溶解し、KI/KCNS溶液を加えた後遊離したヨウ素をチオ硫酸で逆滴定します。終点検出は電位差滴定装置で行い ます。

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.

この技術資料では、Fe(II) 溶液を滴定液として使用し、電位差自動滴定装置で金と銅を同時に測定する方法について紹介しています。Fe(II) は Au(III) を直接還元して遊離金属にしますが、Cu(II) は反応しません。フッ化物イオンを加えると、Fe(III) は錯体を形成し、酸化還元電位がシフトします。その後、ヨウ化カリウムを加えて Cu(II) を Cu(I) に還元し、遊離ヨウ素を Pt ティトロード電極を使用して、Fe(II) 溶液で再度滴定します。

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。

シアン化物の測定は、電気めっき槽や廃水の浄化だけでなく、その高い毒性のため、一般的な水サンプルにおいても非常に重要です。0.05 mg/LのCN-濃度でも、魚類にとって致死的となる可能性があります。 この技術資料では、電位差滴定法を用いて、様々な濃度のサンプル中のシアン化物を測定する方法について紹介しています。

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。

核発電所の一次冷却系、ニッケルめっき浴、光学ガラス製造、洗剤、肥料などで使用されるホウ酸およびホウ素化合物の電位差滴定装置・温度滴定装置による定量法を紹介します。酸分解を行うことで他のホウ素化合物にも適用できます。

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。

この技術資料では、自動滴定装置を使用した硫酸およびクロム酸陽極酸化浴の検査法について解説します。主成分であるアルミニウム、硫酸、クロム酸に加え、塩化物、シュウ酸、硫酸塩も測定します。

このアプリケーションでは、酸性およびアルカリ性スズめっき浴の分析のための電位差滴定法を紹介します。 スズ(II) / スズ(IV) / 総スズ、遊離フッ化ホウ酸または遊離硫酸、酸性スズ浴中の塩化物、アルカリ性スズ浴中の遊離水酸化物および炭酸塩を測定しています。

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.

このアプリケーションでは、カドミウムめっき浴に含まれる、カドミウム、遊離水酸化ナトリウム、炭酸ナトリウム、および総シアン化物の滴定法について解説します。 遊離シアン化物は、総シアン化物とカドミウム含有量から算出できます。

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.

塩化物の滴定は、酸塩基滴定と共に、最も頻繁に用いられる滴定分析法の一つです。この技術資料では、自動滴定装置を用いて幅広い濃度の塩化物を測定する方法について解説しています。

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.

This Bulletin describes three potentiometric, one photometric, one thermometric and one conductometric titration method for sulfate determination. The question of which indication method is the most suitable depends primarily on the sample matrix.Method 1: Precipitation as barium sulfate and back titration of the Ba2+ surplus with EGTA. Use of the ion-selective calcium electrode as indicator electrode.Method 2: As with Method 1, although with the electrode combination tungsten/platinum.Method 3: Precipitation titration in semi-aqueous solution with lead nitrate in accordance with the European Pharmacopoeia using the ion-selective lead electrode as indicator electrode.Method 4: Photometric titration with lead nitrate, dithizone indicator and the Optrode 610 nm, particularly suitable for low concentrations (up to 5 mg SO42- in the sample solution).Method 5: Thermometric precipitation titration with Ba2+ in aqueous solution, particularly suitable for fertilizers.Method 6: Conductometric titration with barium acetate in accordance with DIN 53127

油脂に含まれる個々のグリセリドの正確な含有量の測定は困難かつ時間を要するものであるため、いくつかの油脂総パラメータまたは油脂指数は、油脂の特性評価と品質管理に用いられます。油脂は料理において重要なだけでなく、軟膏やクリームなどといった医薬品およびパーソナルケア製品のための重要な成分でもあります。したがって、いくつかの規格や基準では、最も重要な品質管理パラメータの測定について説明されています。このApplication Bulletinでは、以下の食用油脂における油脂パラメータのための8つの重要な分析メソッドについて説明されています:カールフィッシャーメソッドに準じた水分の測定; ランシマット法に準じた酸化安定性の測定; ヨウ素価; 過酸化物価; 鹸化価; 酸価、遊離脂肪酸 (FFA); 水酸基価; ポーラログラフィーを用いたニッケルの微量測定; これらのメソッドでは、塩素系溶剤を避けるために特別な措置が取られます。また、述べられたメソッドのうち出来る限り多くのものが自動化されます。

この Bulletin では、洗剤に含まれる大量の錯化剤の電位差滴定による測定について説明しています。銅イオン選択性電極（Cu-ISE）は、ここでは指示電極として使用されます。錯化剤の測定は、洗剤によく用いられているその他の成分によって妨げられることはありません。

臭素価および臭素指数は、石油製品中の脂肪族 C = C二重結合の測定において重要な品質管理パラメータです。いずれの指標からも、臭素と反応する物質の含有量に関する情報を知ることができます。両指標の違いは、臭素価はサンプル100gあたりの臭素の消費をグラムで、臭素指数は100gあたりの消費量をミリグラムで示すことです。このApplication Bulletinでは、ASTM D1159、ISO 3839、BS2000-130、IP 130、GB/T 11135 および DIN-51774-1に準じた臭素価の測定について説明されています。脂肪族炭化水素のための臭素指数測定は、ASTM D2710、IP 299、GB/T 11136 および DIN 51774-2に準じて説明されています。芳香族炭化水素のためには、臭素指数の測定はASTM D5776 および SH/T 1767に準じて説明されています。UOP 304は、その滴定溶媒に塩化第二水銀が含まれるため、臭素価または臭素指数の測定には推奨されません。

電気伝導度、pH値、p値およびm値 (アルカリ度)、塩化物含有量、カルシウムおよびマグネシウム硬度、総硬度、ならびにフッ化物含有量などといったか物理的および化学的パラメータの測定は、水質評価において必要不可欠です。この bulletin では、上記のパラメータを、一度の分析実行でいかに測定できるかが説明されています。水質分析においてさらに重要なパラメータは、過マンガン酸塩指数 (PMI) および化学的酸素要求量 (COD) です。そのため、この Bulletin では、EN ISO 8467に準じたPMIの完全自動測定、ならびにDIN 38409-44に準じたCODの測定についても説明しています。

The formol number represents a further parameter for the characterization of fruit and vegetable juices. As this is merely an index (the formalin number does not deal with the molecular size, nor with the quantity of amino acids), the conditions of the titration can be adapted to meet practical needs. This concerns mainly the pH value of the endpoint of the SET titration (pH = 8.5, pH = 9.0, pH = 9.2, etc.).

Mixtures of aluminum and magnesium ions can be analyzed automatically using potentiometric titration. The excess DCTA is back-titrated with copper(II) sulfate solution after the addition of 1,2-diaminocyclohexanetetraacetic acid (DCTA) and complex formation. The ion-selective copper electrode is used here as the indicator electrode. First, the aluminum is determined in acidic solution and then the magnesium in alkali solution.

このアプリケーションは、ニッケルめっき浴中の遊離ホウ酸および遊離テトラフルオロホウ酸の同時電位差滴定法について解説しています。

ポリウレタンは、最も一般的によく用いられるプラスチックの1種です。これは原料ポリオールのイソシアネートとの反応によって製造されます。この技術資料では、ASTM E1899 および DIN 53240-3に準じた測定について説明されています。

This Bulletin provides an overview of the potentiometric titer determination of current titrants. Many publications only describe methods with color indicators. However, the titration conditions chosen for the titer determination should resemble those used for the actual analysis as closely as possible. The tables contain suitable titrimetric standard substances and electrodes for selected titrants as well as additional information. Following this, an example is given to show what an SOP for a titer determination could look like.

この会報は、水分析の分野からの標準的な方法の調査を提供します。また、それぞれの決定に必要な分析機器と、対応するメトロームアプリケーション速報およびアプリケーションノートへの参照もあります。次のパラメータが処理されます：電気伝導率、pH値、フッ化物、アンモニウムおよびケルダール窒素、イオンクロマトグラフィーによる陰イオンおよび陽イオン、ボルタンメトリーによる重金属、化学酸素需要（COD）、水の硬度、遊離塩素も他のいくつかの水の成分として。

This Bulletin describes the fully automated determination of uranium according to the method of Davies and Gray: Uranium(VI) is reduced in concentrated phosphoric acid solution with iron(II) to form Uranium(IV). With molybdenum as a catalyst, the excess iron(II) is oxidized with nitric acid. The nitrous acid that is formed is destroyed with sulfamic acid before uranium(IV) is titrated with a potassium dichromate solution in the presence of a vanadium catalyst.

The Bulletin describes the determination of the following parameters in wine: pH value, total titratable acid, free sulfurous acid, total sulfurous acid as well as ascorbic acid (vitamin C) and other reductones.

The titrimetric determination of nonionic surfactants on the basis of polyoxyethylene adducts (POE adducts) is described in the Bulletin. The basis for the determination is the transfer of the nonionic surfactant into a pseudo-cation compound and its precipitation titration with sodium tetraphenylborate (Na-TPB). The NIO electrode is used for the indication of the potentiometric titration. This Bulletin describes determinations in raw products, formulations and wastewater and draws attention to special features, possibilities, limits and disruptions.

Anionic surfactants can be titrated with cationic surfactants and vice-versa. The Bulletin describes a multitude of substances that can be determined in this fashion and specifies the respective working conditions and parameters. In contrast to the classic two-phase titration in accordance with Epton, the titration with the anionic and cationic surfactants electrodes can be performed without chloroform. Furthermore, the equivalence point of the titration is difficult to determine in some cases with the Epton method and the titration cannot be automated.In many cases, a surfactant ISE is a remedy that is both environmentally friendly and suitable here. It was developed specially for application with potentiometrically indicated surfactant determinations.

This Bulletin describes a simple method for the determination of the calcium content in dairy products. The use of CuEGTA and the ion-selective copper electrode (Cu ISE) as indicator electrode allows the determination to be performed without time-consuming sample preparation. If the complexing agent EDTA is used as titrant instead of EGTA, the sum of calcium and magnesium is obtained. The magnesium content can then be calculated from the difference between the results of the two titrations.

塩素は、消毒目的で飲料水にしばしば添加されます。塩素の反応性および濃度によっては、その際に毒性のある消毒副生成物 (DBP) が放出されることがあります。そのため、飲料水の塩素濃度を厳しく管理する必要があります。この Application Bulletin では、DIN EN ISO 7939-1、APHA 4500-Cl メソッド B、および APHA 4500-Cl メソッド I の3つの標準メソッドに従ってどのように塩素濃度を測定するかが示されています。

The two potentiometric titration methods described here allow the determination of the content of commercial betaine solutions. Neither method is suitable for determining the betaine content of formulations. The possibilities and limits of both methods are described and distinctive features and possible sources of interference are mentioned. The Bulletin explains the most important theoretical principles and is intended to help users to develop their own product-specific titration methods.

このBulletinでは、電位差滴定を用いて測定できる数多くの界面活性剤および医薬品の概要をご覧いただけます。Metrohmは滴定の終点を示す5つの異なる界面活性剤電極、すなわちイオン界面活性剤電極、High Sense、Surfactrode Resistant、Surfactrode Refill、NIO界面活性剤電極を提供しています。それぞれの滴定試薬の製造およびそれらの試薬ファクター測定については、詳細に説明されています。 それに加え、このBulletinには、界面活性剤および医薬品分析の分野からの、170を超える数のテスト済みアプリケーションを表形式にした概要が含まれています。このガイドラインは、お客様を確実に目的地までご案内します: どの界面活性剤電極、および、どの滴定試薬がお客様の製品に最も適しているか、この表によって、ひと目でご覧いただけます。

On the basis of a multitude of practical examples, this Bulletin describes the potentiometric two-phase titration of ionic surfactants in raw materials and many other formulations.Two surfactant electrodes – the Surfactrode Resistant and the Surfactrode Refill – make it possible to perform this type of surfactant titration, analogous to the classic "Epton titration", with a high degree of automation. The achieved results correlate very well with those of Epton titration. The toxic, carcinogenic and environmentally hazardous chloroform can be replaced by other solvents such as methyl iosbutyl ketone or n-hexane.

Two-phase titration with potentiometric indication is a universal method for the determination of ionic surfactants in detergents. The results obtained are comparable to those with the classic two-phase titration in accordance with Epton (mixed indicator system disulfine blue / dimidium bromide). The present Bulletin addresses various parameters that could have an influence on potentiometric surfactant titration. The information provided makes it possible for the user to determine precisely the anionic surfactant content in practically all formulations.

In an acidic solution (containing NH4F * HF, Al(NO3)3 / KNO3) sodium forms NaK2AlF6 which precipitates in an exothermic solution, enabling analysis by thermometric titration. Several foods were analyzed, namely bouillon, gravy, tomato ketchup, corn chips, pretzel sticks as well as crackers. The reproducibility of the results was good. After weighing in and adding solutions, samples were crushed with a polytron to ensure homogeneity in the measuring solution. Relative standard deviations were between 0.08% and 3.75%. In addition to this application bulletin, you can find more information on thermometric sodium determination in foods in our application video available on YouTube:https://youtu.be/lnCp9jBxoEs

The presented Application Bulletin describes the apparatus and methods that are used for acid-base analysis of whole blood and blood plasma by Joergensen and Stirum. Evaluation of the measured data is performed with a software sold by Komstar AG.

この Application Bulletin では、界面活性剤の滴定に使用される界面活性剤測定用電極を検査するためのメソッドについて説明しています。イオン性界面活性剤の滴定のための界面活性剤測定用電極 (Ionic Surfactant electrodes イオン性界面活性剤電極) では、TEGO®trant を用いてドデシル硫酸ナトリウム (SDS または SLS) の測定がおこなわれます。陽イオン性界面活性剤の滴定に使用される界面活性剤測定用電極 (Cationic Surfactant electrodes 陽イオン性界面活性剤電極) では、逆に SDS を用いて TEGO®trant を滴定します。非イオン性界面活性剤の滴定用の電極 (NIO surfactant electrode 非イオン性界面活性剤電極) では、テトラフェニルホウ酸ナトリウム (sodium tetraphenylborate、STPB) を用いて PEG 1000 を滴定します。電極 Surfactrode Resistant および Surfactrode Refill を検査するためには、TEGOtrant を用いて SDS を滴定します。適切な検査基準は、ポテンシャルステップの高さと滴定曲線の形状です。キーワード: NaPh4B

Sulfate can be rapidly and easily titrated thermometrically using a standard solution of Ba2+ as titrant. In industry, the widespread procedure is applied to the determination of sulfate in wet-process phosphoric acid. This bulletin deals with the determination of sulfate in granular fertilizers such as MAP (monoammonium phosphate), DAP (diammonium phosphate) and TSP (triple superphosphate). Results are reported as percentage of elemental sulfur, %S.

Sulfate can be rapidly and easily titrated thermometrically using a standard solution of Ba2+ as titrant. In industry, the widespread procedure is applied to the determination of sulfate in wet-process phosphoric acid.

The determination of the total causticizer, sodium carbonate and aluminum oxide contents in (Bayer) process liquors can be accomplished with high precision and speed by using the 859 Titrotherm in a thermometric acid-base titration. A complete titration takes approximately 5 minutes.The procedure is an automated adaptation of the traditional Watts-Utley method, and is similar to the VanDalen-Ward thermometric titration method, but with the added advantage that the analysis can also be performed for the carbonate content of the liquor.

Phosphate can be rapidly and easily titrated thermometrically using a standard solution of Mg2+ as titrant. The phosphate-containing solution is basified and buffered with NH3/NH4Cl solution before titration. The formation of insoluble MgNH4PO4 is exothermic. The method is a titrimetric adaptation of a classical gravimetric procedure. This bulletin deals with the determination of phosphate in phosphoric acid and granular fertilizers such as MAP (monoammonium phosphate), DAP (diammonium phosphate) and TSP (triple superphosphate). Results are reported as percentage of P and P2O5.

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

The phosphoric acid content can be easily titrated with a standardized solution of 2 mol/L NaOH. The interfering calcium content in phosphoric fertilizer can be eliminated by adding a saturated oxalate solution.

ここで紹介する滴定システムは、ASTM E1899およびEN ISO 4629-2に準じたヒドロキシル価 (HN) の完全自動測定にも用いることができます。このメソッドにより、還流下の沸騰またはその他のサンプル前処理もなくポリオールおよびオキソ油を測定できるようになり、これにより多くのサンプルスループットに対処しなければならないラボにとって大きなメリットとなります。EN 15168およびDIN 53240-3規格は、ASTM E1899にあるのと同じ分析メソッドに引き継がれます。

This bulletin describes a procedure to determine the bromine index (BI) using coulometric titration. The bromine index is the fraction of reactive unsaturated compounds (mostly C=C double bonds) in hydrocarbons encountered in the petrochemical industry. The double bonds are split with the attachment addition of bromine.

This bulletin deals with the automated determination of calcium and magnesium in commercially available finished milk products using a 859 Titrotherm and a 814 USB Sample Processor. Calcium and magnesium in milk can be rapidly and easily titrated thermometrically using a standard solution of Na4EDTA as titrant.Thermometric titrations are conducted under conditions of constant titrant addition rate. The molarity of the titrant is computed automatically in tiamo (software) using the SLO command. Results are reported as mg Ca and Mg/100 mL.

This bulletin discusses automated determination of sodium in milk products available to the public using a 859 Titrotherm and a 814 USB Sample Processor. The sodium content of milk can be rapidly and easily titrated thermometrically with a standard solution of Al3+ as titrant. Thermometric titrations are conducted under conditions of constant titrant addition rate. The molarity of the titrant is computed automatically in tiamoTM (software) with the SLO command. Results are reported as mg Na/100 mL. In addition to this application bulletin, you can find more information on thermometric sodium determination in foods in our application video available on YouTube:https://youtu.be/lnCp9jBxoEs

This bulletin deals with the automated determination of mixtures of HNO3, HF and H2SiF6 in the range of approximately 200-600 g/L HNO3, 50-160 g/L HF, and 0-185 g/L H2SiF6 using thermometric titration.Etch acid mixtures containing HNO3, HF and H2SiF6 from the etching of silicon substrates can be analyzed in a sequence of two determinations using the 859 Titrotherm. The first determination involves a direct titration with standard c(NaOH) = 2 mol/L, followed by a back titration with c(HCl) = 2 mol/L. This determination yields the H2SiF6 content plus a value for the combined (HNO3+HF) contents. The second determination consists of a titration with c(Al3+) = 0.5 mol/L to determine the HF content. For freshly made up mixtures of HNO3 and HF containing no H2SiF6, a linked two-titration sequence is employed. Results from the two determinations are used by tiamoTM to yield individual results for HNO3, HF and H2SiF6.

全酸価 (TAN) の測定は、石油製品の分析において重要な役割を果たします。この 技術資料では、様々なタイプの滴定を使用した石油製品の全酸価の測定について説明しています。電位差測定は ASTM D664、分光光度測定は ASTM D974、そして温度滴定は ASTM D8045 に準じて解説しています。

This Application Bulletin shows the determination of the total base number in petroleum products by applying different titration types according to various standards.

This Application Bulletin describes the determination of the total acid number in various oil samples by catalytic thermometric titration as per ASTM D8045.

ジンクピリチオン (ZnPT)、銅ピリチオン (CuPT)、ナトリウムピリチオン (NaPT) などといったピリチオン錯体は、防カビ剤や殺菌剤として使用されます。ZnPTは、脂漏性皮膚炎またはフケといった皮膚症状の治療において使用されます。さらに、ZnPTは藻類やカビの生育を防ぐために塗料中で抗菌剤として使用されることもあります。CuPTは、主として水中に沈んでいる表面の生物付着を防ぐための殺生物剤として使用されます。一方、NaPTは水虫などの真菌症を治療するための抗真菌剤として使用されます。 様々なピリチオン錯体は、ヨウ素滴定で測定できます。この技術資料では、自動滴定装置によりPt Titrode電極を使用して、ピリチオン錯体のヨウ素滴定をおこなったアプリケーションを紹介しています。

Determination of Total Acid Number (TAN) values in mineral oils and similar fluids.

Determination of the sulfate content of wet process phosphoric acid.

Determination of fluoride in industrial solutions such as acid etching mixtures.

Determination of cuprous ions in the presence of ferrous ions in electrochemical copper leaching solutions.

Determination of a nonionic surfactant of the alkyl propylene oxide derivative type in commercial mixtures containing anionic surfactants.

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

Determination of soluble orthophosphate ions, for example soluble phosphate in fertilizers such as DAP.

Determination of the sulfate content of brines.

温度滴定装置を使用すると、油井やガス井で使用される掘削液などの総固形分含有量を数分以内で測定できます。

温度滴定法は、さまざまな掘削液中のカルシウム濃度を簡単、迅速、高い信頼性で測定できます。

Determination of ferrous ions in heat exchanger and vessel acid wash solutions, for measuring the effectiveness of acid inhibitors used in the solutions. Depending on the condition of the sample, the lower practical limit for the determination will vary from approximately 20-100mg/Kg Fe2+. Samples with high silicic acid contents require relatively large amounts of dilution water to render them mobile, and this limits the aliquot size and hence the amount of Fe2+ which can be analyzed.

Determination of water in moist particulate solids such as cobalt oxyhydroxide.

Determination of free acid in solutions containing metal ions, particularly Fe(III).

Determination of acetic anhydride in the presence of acetic acid in acylation mixtures.

Determination of mixtures of phosphoric, nitric, and acetic acids used in etching aluminum in the manufacture of semiconductor devices.

Determination of bromide and chloride in photographic developer solutions.

Determination of chloride in oil well drilling fluids.

Determination of chlorine in household bleaches.

Determination of chromium in leather waste solutions in the range between 1000 and 30,000 ppm.

Determination of free acid in copper refining solutions.

Determination of moisture in lubricating oils with TEOF (triethyl orthoformate).

Determination of nickel in the absence of cobalt and other interferences.

Determination of tar acids in coal tar products. This procedure may also be applied to the determination of a range of weakly acidic organic compounds such as carboxylic acids, hydroxy acids, phenols, phenolic acids, keto-enols, imides, and aromatic nitro compounds.11 Vaughan, G. A. Thermometric and Enthalpimetric Titrimetry. Van Nostrand Reinhold Co. Ltd (1973)

Determination of water in automotive lubricating oils.

This Application Note describes a method for the determination of causticizer, carbonate and aluminum oxide in used Bayer process liquors. The method is based on processes that were developed by Watts-Utley and VanDalen-Ward.

Determination of total basicity of extractable organic compounds of acidic character in Bayer process refinery liquors.

Standardization of 0.1 mol/L in propan-2-ol for use in applications for the determination of weakly acidic species in non-aqueous media.

Determination of chlorite by direct thermometric titration with standard sodium thiosulfate solution. The procedurewas applied originally to the determination of chlorite in hide treatment solutions.

Determination of low levels of sulfate (to approximately 20mg/L SO42-) by thermometric titration.

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

Determination of low levels of chloride (to approximately 5 mg/L Cl-) by thermometric titration.

Determination of calcium and magnesium in process solutions.

リンは植物の主要栄養素であり、エネルギーを要する多くの生物学的プロセスに関与するDNAおよびアデノシン三リン酸 (ATP) の構成成分です。植物に対して最も利用しやすいリンの形状はリン酸二水素であるように、肥料ではリンはリン酸塩という形態で存在します。リン含有量を知ることは、植物のための肥料を正しく選択するための助けとなります。伝統的に、リン酸塩は重量測定 (時間浪費の大きな方法) または分光測定 (高価な計測装置) にて測定されます。このApplication Noteでは、マグネシウムを用いた沈殿滴定にてリン酸塩を測定する代替メソッドが紹介されています。リン含有量 6.5～17% の様々な固形物および液体のNPK肥料が分析されました。TETによる分析では、液体NPK肥料の場合はサンプル前処理は不要、固形物NPK肥料の場合必要なのは最小限のサンプル前処理のみです。一回の測定におよそ5分かかります。

Determination of free fatty acids (FFA) in oils.

Determination of phosphate content in an acid etching bath.

Determination of sulfate and total acids in a nitrating mixture.

Determination of sodium lauryl ether sulfate surfactants.

Determination of low content of HCl (around 10 ppm) in silicone oil.

Standardization of cetyl pyridinium chloride solutions for use as a cationic surfactant titrant in the determination ofanionic surfactants such as sodium lauryl ether sulfate.

この技術資料では、温度滴定法で銅の定量にするチオ硫酸ナトリウムの標定試験の仕方について解説しています。

温度滴定法によるキレート滴定（錯滴定）では、 滴定試薬にEDTA・４NA（4NA 、エチレンジアミン四酢酸四ナトリウム）を使用して滴定を行います。この技術資料では、銅を使用して、EDTA・４NA滴定試薬を標定する方法について解説しています。

この技術資料では、マグネシウムを使用して、EDTA 四ナトリウム滴定液の評点試験方法について解説しています。

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

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

Determination of nickel in solution by titration with standard disodium dimethylglyoximate.

Determination of sodium, potassium, and silica values in sodium and potassium silicates.

Determination of sodium hypophosphite in electroless plating solutions.

Thermometric titration of nickel in electroless plating solution with disodium dimethylglyoximate.

Determination of aluminum in acidic, basic, and neutral solutions; including aluminum chloride, aluminum chlorohydrate (also in anti-perspirant formulations), alum, etching solutions, and aluminate solutions.

Determination of Na, P, and [Na]/[P] in precursor solutions and solids in the manufacture of sodium tripolyphosphate.

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

Standardization of sodium fluoride titrant for determination of aluminum.

Determination of sodium as chloride in ketchups, sauces and, similar food products.

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

Determination of sodium in salts, process solutions, and foods.

Standardization of titrant for direct determination of sodium.

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

Determination of sodium and potassium salts of carboxylic acids in aqueous media. May be used for analysis of reagent purity.

Determination of chloride in Bayer process liquor.

Determination of Fe3+ and Cu2+ in copper refining solutions by thermometric titration. It was found that the conventional approach of masking Fe3+ to permit the iodometric determination of Cu2+ is not possible in some copper refining solutions.

Determination of ammonium ions in ammonium salts and mixtures containing ammonium ion.

Determination of Total Acid Number (TAN) values in biodiesel to <0.05 mg KOH/g sample.

Determination of calcium and magnesium in seawater. The method is suitable for determining the effect of caustic soda and alumina refinery aluminate solutions on the calcium and magnesium content of seawater.

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

ヨウ素価 (IV) は、油脂に存在する二重結合の総数の尺度です。 「油脂100グラム中の二重結合と反応するヨウ素のグラム数」で表されます。 測定は、秤量したサンプルをシクロヘキサンなどの非極性溶媒に溶解し、氷酢酸を加えることによって行われます。 二重結合は、過剰の一塩化ヨウ素の氷酢酸溶液（「Wijs 溶液」）と反応します。 反応を促進するために水銀イオンが添加されます。 反応終了後、ヨウ化カリウム水溶液を加えて過剰の一塩化ヨウ素をヨウ素に分解し、標準チオ硫酸ナトリウム溶液で滴定します。

Determination of sodium in seawater and similar brines. This procedure is suitable for the analysis of sodium in seawater contaminated with sodium aluminate solutions emanating from alumina refineries, and seawater which has been used for the neutralization of alumina refinery waste («red mud») slurries.

Determination of total halides (Cl- + Br- +I-) in seawater and similar brines. This procedure is suitable for the analysis of total halides in seawater contaminated with sodium aluminate solutions emanating from alumina refineries, and seawater which has been used for the neutralization of alumina refinery waste («red mud») slurries. Given the small concentration of bromine andiodine in seawater, the total halide content approximates the chloride concentration.

Determination of free acid in sulfuric acid («acid shot») solutions employed in the removal of silicate scale in heat exchangers. This method is suitable for acid shot solutions where the silicic acid content is so high that the solutions have gelled.

Determination of the total sodium content of sodium aluminate liquors, such as Bayer Process liquor. This method is suitable for the analysis of all sodium aluminate solutions down to at least 1 g/L as Na2CO3. The determination may be automated by adding an 814 USB sample processor to an 859 Titrotherm.

Determination of phosphoric and nitric acids in liquors from the Nitrophos fertilizer manufacturing process.

この技術資料では、温度滴定法を利用してゼオライトの表面酸性を測定する方法について解説しています。

この技術資料では、ゼオライトの表面塩基度を温度滴定で測定する方法を紹介しています。

Determination of mixtures of sulfuric, phosphoric, and nitric acids. The procedure is suitable for automated analysis using an 814 Sample Processor.

不溶性の NaK2AlF6 を形成する、発熱反応を生じさせるための ~ pH 3 のフッ化水素アンモニウムの存在下におけるカリウムイオンの化学量論的超過を含むアルミニウムの標準液を用いたサンプルの無濾過の懸濁液の滴定。滴定試薬は、無水硫酸ナトリウムまたは炭酸ナトリウムから調合された溶液に対して標準化されます。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

Determination of hydrofluoric acid in mixed acid etchant solutions.

Automated determination of total acid number (TAN) in new and used lubricating oils and crude oils using the 814 USB Sample Processor. Dissolve oil sample in mixture of toluene and 2-propanol, add paraformaldehyde and titrate with 0.1 mol/L or 0.01 mol/L KOH in propan-2-ol. The endpoint is indicated by an endothermic response caused by the base-catalyzed depolymerization of paraformaldehyde.Reference: 1. M. J. D. Carneiro, M. A. Feres Júnior, and O. E. S. Godinho. Determination of the acidity of oils using paraformaldehyde as a thermometric end-point indicator. J. Braz. Chem. Soc. 13 (5) 692-694 (2002)

Automated determination of the H2SiF6 and HF contents of industrial grade hexafluorosilicic acid.

Automated thermometric titration of the nickel content of electroless nickel plating solutions. The determination is suitable for fully automated titration employing a 814 Sample Processor.

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

Automated determination of the zirconium content of zirconium acetate, as well as other zirconium compounds which can be rendered soluble as zirconium acetate.

Determination of boric acid in electroless plating solutions.

Determination of boron in ores of the element such as borax and ulexite.

Dissolution of urea in glacial acetic acid, and titration with standard 0.1 mol/L trifluoromethanesulfonic acid in acetic acid using isobutyl vinyl ether as a thermometric endpoint indicator.

Dissolution of oil in toluene, and titration with standard 0.1 mol/L trifluoromethanesulfonic acid in acetic acid using isobutyl vinyl ether as a thermometric endpoint indicator.

A measured amount of salt is titrated directly with a solution of 1 mol/L tetrasodium EDTA to thermometrically determined endpoints for Ca and Mg. Acetylacetone is added to alter the Ca and Mg EDTA stability constants for better endpoint sharpness.

酸エッチング溶液には、エッチング速度が高いためフッ化水素酸 (HF) が含まれることがよくあります。 この技術資料では、電位差滴定装置で使用する通常のガラス電極では測定が難しい、シリコンエッチング溶液中のフッ化物の測定を温度滴定法でおこなっている例を紹介しています。

Determination of the total acids concentration in mixtures of nitric-hydrofluoric acid intended for etching silicon substrates.

A sample of concentrated mineral acid is dissolved in anhydrous acetonitrile, and the water content titrated with a solution of TEOF in acetonitrile. The TEOF reacts exothermically with water in the presence of a strong acid (acting as a catalyst).

Hypochlorite ions react with bromide ions to form hypobromite ions, which in turn rapidly oxidize ammonium ions to nitrogen. Hypobromite reacts more rapidly with ammonium than hypochlorite, and is formed in situ (Vogel, 1961). The titration is carried out with in a solution containing bromide and bicarbonate.

A measured amount of milk is treated with trichloroacetic acid to coagulate milk solids and liberate calcium and magnesium as dissociated ion. The coagulated milk is filtered or centrifuged, and an aliquot of the clear serum is titrated with a standard solution of 1 mol/L tetra-sodium EDTA to thermometrically determined endpoints for Ca and Mg. Acetylacetone is added to alter the Ca- and Mg- EDTA stability constants for better endpoint sharpness.

A measured amount of acidic hydrometallurgical leach liquor is treated with potassium oxalate solution to mask potential interference from Fe(III) and other metal ions, and then titrated with standard 1 mol/L NaOH solution.

A measured amount of acidic hydrometallurgical leach liquor is first treated with hydrogen peroxide to oxidize Fe(II) to Fe(III), then with potassium pyrophosphate solution to mask interference from Fe(III) and other metal ions. Ammonium acetate solution is then added as a pH modifier, before being titrated with standardized disodium dimethylglyoximate to an exothermic endpoint.

A measured amount of acidic hydrometallurgical leach liquor is treated first with a complexing agent (sodium gluconate). It is then basified to ~pH 10.5 with a NH3 /NH4Cl buffer, prior to the addition of KCN solution to mask Fe(III). Caution! Do not add KCN to solutions of pH below 9! The Fe(III) is then reduced to Fe(II) by additon of ascorbic acid, prior to titrating the Mg content with standard Na4EDTA solution.

A measured amount of acidic hydrometallurgical leach liquor is further acidified with sulfuric acid, prior to being titrated with standard potassium dichromate solution to an exothermic endpoint. Thus, 1 mol K2Cr207 ≡ 6 mol Fe2+.

A measured amount of acidic hydrometallurgical leach liquor is pH modified with a small amount of glacial acetic acid, and the Fe(III) content reduced to Fe(II) with iodide ion. The liberated iodine is titrated with standard thiosulfate solution to an exothermic endpoint. Thus, 1 mol Fe3+= 1 mol S2O32-.

Results from three separate single endpoint titrations are used to calculate the results. The mixture of H2SO4, HF, and NH4F/HF contains H+ from H2SO4, HF, and NH4F/HF, SO42- from H2SO4, and F- from HF and NH4F/HF. Analysis of total H+ («total acids») by NaOH titration, F- by titrating with Al(NO3)3 («total fluoride») and SO42- by titrating with BaCl2 provides the information required to determine the composition of the mixture.

Sulfate is precipitated by reaction with an acidified barium chromate solution. The excess barium chromate is precipitated by basification with ammonia solution. Residual soluble chromate equivalent to the sulfate content of the sample is titrated with a solution of standard ferrous ion to a thermometrically determined endpoint.

Sulfate is precipitated as barium sulfate by reaction with an acidified barium chromate solution. The excess barium chromate is precipitated by basification with ammonia solution. Residual soluble chromate, equivalent to the sulfate content of the sample, is titrated with a solution of standard ferrous ion to a thermometrically determined endpoint.

Two separate titration sequences are required to analyze the mixture:- titration of the HF content with Al(NO3)3 (the «elpasolite» reaction)- titration of the H2SO4 with BaCl2 followed by titration with NaOH to determine the «total acids» contentThe HF, H2SO4, and «total acids» contents are converted to a HNO3 equivalent, with the HNO3 content found by subtracting the HF and H2SO4 from the «total acids» content.

A direct thermometric titration (TET) with 2 mol/L NaOH is used to determine the HF, NH4F, and maleic acid (C4H4O4) contents of acid cleaning solutions. Three endpoints (EPs) are obtained, which may be assigned as follows:EP1: C4H4O4 (pKa1 = 1.9), HF (pKa = 3.17)EP2: C4H4O4 (pKa2 = 6.07)EP2: NH4F (pKa = 8.2)The HF content is determined by subtracting the difference (EP2-EP1) from EP1.

This Application Note supplements AN-H-003 with the treatment of the standard addition of sulfate as sulfuric acid. This technique may be contemplated when either sulfate levels are too low for a satisfactory direct titration, or when the sample matrix hinders endpoint detection, leading to poor precision and accuracy.

This Application Note describes the determination of the free and total hydroxide and aluminum oxide content in Bayer process and other aluminate liquors. The method is not subject to interference by carbonate ions. An aliquot of sodium aluminate liquor is titrated with potassium hydrogen carbonate solution to yield the free hydroxide ion content of the liquor.

The presence of the hydrated ion [Fe(H2O)6]3+ can interfere with the determination of «free acid» due to the low pKa value (~2.2) of this ion. Ions of metals such as Fe, Cu, and Al can be masked effectively with fluoride, and permit the determination of the acid content by thermometric alkalimetric titration with good accuracy and precision.

This Application Note deals with the determination of ferric ion in acidic and copper-free solutions using thermometric titration. The ferric ion is reduced by iodide. The released iodine reacts exothermically when titrated with thiosulfate solution. The endpoint is determined through temperature plotting by the temperature sensor Thermoprobe.

This Application Note describes the determination of aluminum ion down to approximately 0.5 g/L in acidic solutions containing ferric, ferrous, and other ions whose hydroxides do not dissolve in strongly basic solutions.

This Application Note looks at the determination of ferrous ion in acidic solutions from approximately 0.25 g/L by thermometric titration with ceric titrant. The exothermic oxidation reaction shows a sharp endpoint that is detected using the Thermoprobe as a sensitive temperature sensor.

このApplication Noteでは、TET を用いた魚類缶詰製品におけるナトリウム総量の測定について説明しています。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

このApplication Noteでは、一部の国では「2分麺」とも呼ばれる即席麺におけるナトリウム総含有量の測定について説明しています。このような製品には、かなりの量のナトリウムが含まれており (1日当たりの推奨摂取量の少なくとも50％)、そのためナトリウム含有量の正確な分析が求められます。製品パッケージに挙げられた栄養素量は、塩化ナトリウム以外の添加ナトリウム塩の存在を記載しているため、(麺類に含まれるナトリウムは、添加された塩化ナトリウムにのみ起因すると仮定すると)、塩化物含有量の銀滴定は正確な測定には不向きです。TET により、迅速かつ直接的なナトリウムの測定が可能となります。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

このApplication Noteでは、マーガリンの製造で用いられる前駆体溶液中のナトリウム総濃度の測定について説明されています。前駆体溶液は、マーガリンを作るために食用の脂肪と油が混ぜ合わされたものです。微量の塩化ナトリウムおよびその他のナトリウム塩、ならびにカリウム塩は、この過程の途中で、通常は乳化剤、安定剤、酸化防止剤、ビタミン、着色料、化学調味料などの形でマーガリンに添加される場合があります。前駆体溶液中のナトリウム総含有量の分析は、後で最終製品においてナトリウム総含有量を分析するより、製造者にとって、効率と費用対効果がより高くなります。原則として、食料品のナトリウム含有量の間接的な測定には塩化物の銀滴定が用いられます。この方法は、塩化イオンがナトリウムイオンとのモル比 1:1 の分量で存在することが前提とされます。しかし、ナトリウムを含む食料品でよくあることですが、ナトリウムを含む添加化合物がマーガリンに存在する場合は、これは当てはまりません。いくつかの製法における塩化ナトリウムの部分的置き換えとしての塩化カリウムの使用は、誤差の更なる原因となります。温度終点滴定 (TET) によるナトリウムの直接滴定は、これらの問題を解決します。TET は、溶液中に存在するすべてのナトリウム含有量が考慮されるだけでなく、カリウムイオンの存在によって阻害されることもない直接的な測定メソッドです。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

This application note describes the determination of the total sodium content in soy milk products. The methodology may also be applied to the determination of sodium in milk products from cows, goats and sheep. A standard addition technique is employed to permit the accurate and precise determination of sodium at relatively low levels.

Silver and nitric acid are determined in silver electrolyte solutions by means of thermometric titration. The method provides accurate results in a short time and is ideally suited for routine process control.

このApplication Noteでは、温度滴定および滴定試薬としてEDTAを用いた二酸化ケイ素を含むサンプル中のアルミニウムの測定について説明しています。過剰なEDTAは、既知濃度のCu2+溶液を用いて滴定されます。初期の錯体化されていないCu2+イオンは　溶液中に存在するH2O 2と直ちに反応し、認識可能な急激な温度上昇を引き起こします。