Determination of total carbon and total organic carbon from volatile air pollutants. Part II

Summary The possibility of specific removal of carbon monoxide from a stream of air in the presence of vapours of volatile organic compounds was investigated. Weighed samples of oxalic acid were pyrolyzed to obtain standard mixtures of CO with air. Carbon monoxide present in the stream of air (at the flow rate of 700 cm³/ min) is quantitatively oxidized to CO₂ by a layer of the Körbl catalyst (diameter=12 mm, length=35 mm) heated to 90° C. The CO₂ formed can be specifically bound by a heated layer of ascarite⁴⁶. On the basis of model experiments it was concluded that under the conditions described in the paper the degree of oxidation of 16 various organic compounds ranged from 0.7 to 8.7%. Thus, the developed method can be applied as a mean of practically specific removal of CO from a stream of analyzed air in the course of determination of total organic carbon (TOC).

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Zusammenfassung Die Möglichkeit einer spezifischen Entfernung von Kohlenoxid neben Dämpfen flüchtiger, organischer Verbindungen aus dem Luftstrom wurde untersucht. Zur Herstellung von CO-Luftstandardgemischen dienten gewogene Mengen Oxalsäure, die thermisch zersetzt wurden. Das im Luftstrom (700 cm³/Minute) anwesende CO wird an einer auf 90° C erhitzten Körblkatalysatorschicht von 35 mm Länge und 12 mm Durchmesser quantitativ zu Kohlendioxid oxydiert, das dann an einer erhitzten Ascariteschicht⁴⁶ spezifisch gebunden wird. Bei Modellversuchen mit 16 verschiedenen organischen Verbindungen wurde festgestellt, daß der Oxydationsgrad unter den angegebenen Bedingungen 0,7–8,7% beträgt. Das entwickelte Verfahren kann somit zur praktisch spezifischen Entfernung von Kohlenoxid aus dem analysierten Luftstrom bei der Bestimmung des TOC-Gehaltes aus flüchtigen, organischen Verunreinigungen nach ihrer Oxydation Anwendung finden.

     

Determination of total carbon and total organic carbon from volatile air pollutants. Part III

Summary The possibility of selective oxidation of volatile organic compounds in the presence of methane was investigated. Thermal decomposition of a mixture of CH₃COONa and NaOH was used as the source of methane introduced into a stream of purified air. Oxidation of the methane present in a stream of air on a layer of the Körbl catalyst is only slight and does not exceed 10%, even in the case of simultaneous presence of acetic acid, which is completely oxidized under identical conditions. Other volatile organic compounds also undergo complete oxidation. It was found that the degree of oxidation of 16 organic compounds is 97.5%. The detection limit of the developed method depends primarily on the effective removal of the so-called carbon background of the air sample, resulting from the presence of CO₂, CO and CH₄. The developed method of selective oxidation can be used for specific elimination of the effect of methane on the results of determinations of TOC in volatile air pollutants.

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Zusammenfassung Die Möglichkeit einer selektiven Oxydation flüchtiger organischer Verbindungen neben Methan wurde untersucht. Methan wurde im gereinigten Luftstrom durch thermische Zersetzung eines Gemisches von CH₃COONa und NaOH hergestellt. Die Oxydation des Methans im Luftstrom an einer Körbl-Katalysatorschicht ist gering und überschreitet nicht 10%, sogar bei gleichzeitiger Anwesenheit von Essigsäure, welche unter diesen Bedingungen — wie andere flüchtige, organische Verbindungen — vollständig oxydiert wird. An 16 organischen Verbindungen wurde festgestellt, daß der Oxydationsgrad97,5% beträgt. Die Erfassungsgrenze der entwickelten Methode zur TOC-Bestimmung ist vor allem von einer effektiven Beseitigung des sogenannten Kohlenstoffblindwertes abhängig, der durch Anwesenheit von CO₂, CO und CH₄ in der Luftprobe verursacht wird. Das entwickelte, selektive Oxydationsverfahren kann somit zur spezifischen Eliminierung des Einflusses von Methan auf die Bestimmungsresultate des TOC-Gehaltes aus flüchtigen Luftverunreinigungen Anwendung finden.

     

Determination of total carbon and total organic carbon from volatile air pollutants

Summary The method developed based on the determination of TC and TOC in the form of the total amount of CO₂ requires application of the proper techniques for the final determination of CO₂. The possibility of using a stream of carrier gas at a convenient flow-rate for desorbing quantitatively CO₂ concentrated on a molecular sieve permits use of a wide variety of known analytical techniques for the final determination of CO₂. Various methods were compared on the basis of both absolute and calibration measurements. The absolute methods chosen were gravimetric (classical or an automated version based on application of a gravimetric automat and automatic recording balance), thermogravimetric analysis and coulometry. The calibration methods included thermal conductivity, the flame-ionization detector (after conversion of CO₂ into methane) and infrared absorption. Usefulness of the methods was evaluated on the basis of comparative statistical analysis of experimental data with respect to precision (Snedecor'sF-test and Bartlett'sU ²-test) and accuracy (Student'st-test).

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Zusammenfassung Das entwickelte Verfahren zur Bestimmung des TC- und TOC-Gehaltes in Form der gesamten Menge CO₂ erfordert die Anwendung geeigneter Analysentechniken zur Endbestimmung dieser Verbindung. Die Möglichkeit einer Desorption des am Molekularsieb angereicherten CO₂ in einem Gasstrom mit geeignetem Durchfluß erlaubt zur Endbestimmung von CO₂ die Anwendung einer Reihe verschiedener Analysenverfahren. Die Anwendbarkeit verschiedener, auf Absolutverfahren und auch auf relativen Messungen beruhender Methoden wurde vergleichend untersucht. Die folgenden Methoden zur CO₂-Bestimmung wurden gewählt: die Gravimetrie (klassische oder automatisierte unter Einsatz eines Wägeautomaten und einer registrierenden Waage), die Thermogravimetrie und die Coulometrie. Von den relativen Methoden wurden die Thermokonduktometrie, der Flammenionisationsdetektor (nach Umsetzung von CO₂ zu Methan) und das IR-Absorptionsmeßverfahren geprüft. Die Anwendbarkeit der Methoden wurde mit Hilfe statistischer Prüfverfahren beurteilt, wobei die Präzision (SnedecorsF-Test und BartlettsU ²-Test) und die Genauigkeit (Studentst-Test) der erhaltenen Analysenwerte verglichen wurden.

     

Determination of volatile organic compounds in ambient air. Comparison of methods

Two analytical methods for the determination of benzene vapour in ambient air are compared in this paper. The methods differ from each other in the sampling technique, type of sorbent, method of extraction and method of detection. The investigation of the methods using various techniques for sample analysing showed a significant influence of the way in which the analysis is carried out, on the final result of the analysis. Calculation of the standard deviations, relative standard deviations and confidence intervals allowed for assessment of the precision and repeatability of the methods. Of the two examined methods, that using an automated system of contaminant sampling and thermodesorption was more precise. This method has been applied to measurements of concentrations of benzene, toluene and xylenes in ambient air.     

Sorbent trapping of volatile organic compounds from air

The use of sorbents in trapping volatile organic compounds in air for subsequent analysis is reviewed. Sorbents are classified in accordance with the mechanism used to recover the trapped compounds, either solvent or thermal desorption. The use of sorbents is contrasted with other sampling procedures, such as collecting whole air samples using canisters. New developments such as solid-phase microextraction are described. In particular, emphasis is placed on a holistic approach to sampling and analysis, and communication is encouraged between those who take samples in the field, and those who perform the analysis.     

Capillary columns in series for GC analysis of volatile organic pollutants in atmospheric and alveolar air

Analysis of volatile organic compounds in air samples requires high resolution capillary gas chromatography. When the sample contains both polar and non-polar compounds, use of only one type of stationary phase can be unsuitable if it leads to the preferential separation of one kind of component having the same polarity at the expense of the separation of other classes of component. This paper describes the coupling of fused silica capillary columns of different polarity and length in order to achieve the separation of such complex mixtures. The combination is evaluated with a 42 component standard mixture and then applied to various atmospheric air samples and alveolar air of exposed subjects to demonstrate the capabilities of the complete sampling and separation technique.     

Determination of volatile organic compounds in contaminated air using semipermeable membrane devices

Semipermeable membrane devices (SPMDs) were evaluated as passive samplers for the determination of 26 volatile organic compounds (VOCs) in contaminated air of occupational environments. A direct methodology based on the use of head-space-gas chromatography-mass spectrometry (HS-GC-MS) was developed for VOCs determinations in SPMDs, without any sample pre-treatment and avoiding the use of solvents. A desorption temperature of 150 °C for 10 min was sufficient for a sensitive VOCs determination providing limits of detection in the range of 15 ng SPMD⁻¹ for 21 of 26 studied compounds. Linear and equilibrium uptake models were established for each VOC from compound isotherms. Highly volatile compounds were slightly absorbed and moderately volatile compounds were strongly absorbed by SPMDs. This study is the first precedent of the use of SPMDs for the simultaneous sampling of a wide number of VOCs. The use of SPMDs is a simple and low cost alternative to ordinary sampling devices such as Radiello^® diffusive samplers or badge-type solid-phase supports.     

Measurements of carbon dioxide with the air-gap electrode. Determination of the total inorganic and the total organic carbon contents in waters.

Ruthenium(II) reacts with 3-(2-pyridyl)-5.6-diphenyl-1,2.4-triazine (PDT) in water-alcohol solution at pH 5 to give a magenta-colored cationic complex having an absorption peak at 485 nm. The color is fully developed by heating at 85° C for 30 min. The system conforms to Beer's law; the optimal concentration range for measurement at 1.00-cm optical path is about 0.5–3.4 p.p.m. of ruthenium. The molar absorptivity is 2.1 · 10⁴ 1 mole^-1 cm^-1. The effects of reagent concentration, heating temperature and time, pH, and alcohol concentration have been studied. Common anions do not interfere. Separation from interfering cations is effected by distillation and recovery of ruthenium tetroxide. Spectrophotometric methods of continuous variations and of mole ratios, and elemental analysis of solid salts isolated from solution, indicate a ruthenium-to-PDT stoichiometry of 1:2, the PDT acting as a tridentate ligand.     

Determination of volatile organic compounds from truffles via SPME-GC-MS

Volatile organic compounds (VOCs) of nine Tuber species and two corresponding forms are identified via solid-phase microextraction-gas chromatography-mass spectrometry analysis. Seventy-five compounds are identified. The most abundant are dimethylsulphide, 2- and 3-methylbutanal, 2-methylpropanol, and butanone.     

Sorbent-based sampling methods for volatile and semi-volatile organic compounds in air. Part 2. Sorbent selection and other aspects of optimizing air monitoring methods

Sorbent tubes/traps are widely used in combination with gas chromatographic (GC) analytical methods to monitor the vapour-phase fraction of organic compounds in air. Applications range from atmospheric research and ambient air monitoring (indoor and outdoor) to occupational hygiene (personal exposure assessment) and measuring chemical emission levels. Part 1 of this paper reviewed the main sorbent-based air sampling strategies including active (pumped) tube monitoring, diffusive (passive) sampling onto sorbent tubes/cartridges plus sorbent trapping/focusing of whole air samples that are either collected in containers (such as canisters or bags) or monitored online. Options for subsequent extraction and transfer to GC(MS) analysis were also summarised and the trend to thermal desorption (TD)-based methods and away from solvent extraction was explained. As a result of this trend, demand for TD-compatible sorbents (alternatives to traditional charcoal) is growing. Part 2 of this paper therefore continues with a summary of TD-compatible sorbents, their respective advantages and limitations and considerations for sorbent selection. Other analytical considerations for optimizing sorbent-based air monitoring methods are also discussed together with recent technical developments and sampling accessories which have extended the application range of sorbent trapping technology generally.     

热解析-气相色谱法测定印刷品中总挥发性有机化合物释放量

建立用气袋法收集整册印刷品释放的挥发性有机化合物,热解析-气相色谱法检测总挥发性有机化合物(TVOC)的方法。将印刷品样品置入充满高纯氮气的密封PVF采样袋中,在35℃下放置12 h后,用采样器串联Tenax-TA采样管和采样袋,让袋内气体通过采样管,样品释放出的有机化合物被吸附到采样管的吸附剂上。用热解析-气相色谱法测试采样管中挥发性有机化合物的含量,其中苯、甲苯、邻二甲苯、间二甲苯、对二甲苯、乙苯、乙酸丁酯、苯乙烯和正十一烷按外标法定量,其它物质按甲苯标准曲线定量。该方法的加标回收率为74.4%~91.1%,测定结果的相对标准偏差不大于10%(n=9)。该方法的样品采集更贴近印刷品的实际生活场景,可以为评价印刷品挥发性有机物释放对人体健康的影响提供数据基础,为相关评价提供新思路。     

Determination of volatile organic compounds in urban and industrial air from Tarragona by thermal desorption and gas chromatography-mass spectrometry

This study describes the optimisation of an analytical method to determine 54 volatile organic compounds (VOCs) in air samples by active collection on multisorbent tubes, followed by thermal desorption and gas chromatography-mass spectrometry. Two multisorbent beds, Carbograph 1/Carboxen 1000 and Tenax/Carbograph 1TD, were tested. The latter gave better results, mainly in terms of the peaks that appeared in blank chromatograms. Temperatures, times and flow desorption were optimised. Recoveries were higher than 98.9%, except methylene dichloride, for which the recovery was 74.9%. The method's detection limits were between 0.01 and 1.25 μg m⁻³ for a volume sample of 1200 ml, and the repeatability on analysis of 100 ng of VOCs, expressed as relative standard deviation for n = 3, was lower than 4% for all compounds. Urban and industrial air samples from the Tarragona region were analysed. Benzene, toluene, ethylbenzene and xylenes (BTEX) were found to be the most abundant VOCs in urban air. Total VOCs in urban samples ranged between 18 and 307 μg m⁻³. Methylene chloride, 1,4-dichlorobenzene, chloroform and styrene were the most abundant VOCs in industrial samples, and total VOCs ranged between 19 and 85 μg m⁻³.     

Determination of complex mixtures of volatile organic compounds in ambient air: canister methodology

Canister methodology is applicable to 150 polar and nonpolar VOCs found in ambient air from parts-per-billion by volume (ppbv) to parts-per-million (ppmv) levels, and has been validated at parts-per-trillion (pptv) levels for a subset of these analytes. This article is a detailed review of techniques related to the collection of volatile organic compounds (VOCs) in evacuated Summa and fused-silica-lined canisters, and their analysis by gas chromatography/mass spectrometry (GC/MS). Emphasis is placed on canister cleaning, VOC stability in canisters, sample dilution, water management, and VOC cryogenic and sorbent preconcentration methods. A wide range of VOC preconcentration and water management methods are identified from the literature, and their relative merits and disadvantages are discussed. Examples of difficulties that commonly arise when processing canister samples are illustrated, and solutions to these problems are provided.     

Determination of complex mixtures of volatile organic compounds in ambient air: an overview

This article reviews developments in the sampling and analysis of volatile organic compounds (VOCs) in ambient air since the 1970s, particularly in the field of environmental monitoring. Global monitoring of biogenic and anthropogenic VOC emissions is briefly described. Approaches used for environmental monitoring of VOCs and industrial hygiene VOC exposure assessments are compared. The historical development of the sampling and analytical methods used is discussed, and the relative advantages and disadvantages of sorbent and canister methods are identified. Overall, there is considerable variability in the reliability of VOC estimates and inventories. In general, canister methods provide superior precision and accuracy and are particulary useful for the analysis of complex mixtures of VOCs. Details of canister methods are reviewed in a companion paper. C. C. Austin is an Invited Scientist of the National Research Council of Canada.     

Determination of oxygenated volatile organic compounds in ambient air using canister collection-gas chromatography/mass spectrometry.

This research attempts to establish a method to measure 11 kinds of oxygenated volatile organic compound (OVOC) in ambient air by using the canister collection-gas chromatography/mass spectrometry (GC/MS) method. Since several compounds such as acetone exhibited high blank concentrations due to their laboratory use, stringent quality control was conducted for the VOC-free added water and the VOC-free nitrogen gas. In order to prevent the decline of recovery rates due to lack of sufficient relative humidity, it is necessary to add VOC-free water when pressurizing and diluting the air samples. Thus, all the target compounds in ambient air were obtained from the canisters at high recovery rates without significant contamination. Furthermore, the canister collection-GC/MS method makes it possible to apply simultaneous air monitoring of OVOCs as well as volatile hazardous air pollutants without additional sampling.     

热脱附-气相色谱-质谱法测定环境空气中67种挥发性有机物

采用热脱附-气相色谱-质谱法,建立了同时分析环境空气中67种挥发性有机物的分析方法。对比了5种不同填充材料不锈钢吸附管对78种挥发性有机物的吸附能力。填充材料为Tenax TA和Carbograph 1TD的混合填料吸附管对分析物的捕集效果最好,在30 mL/min高纯He气持续吹脱45 min的情况下,未发生穿透（即穿透率小于10%）的化合物达67种,分析物的种类包括芳香烃、脂肪烃、卤代烃和含氧挥发性有机物等。优化了使用该吸附管测定67种目标物时的热脱附条件。在5~100 ng范围内,目标化合物的色谱响应值与其量间具有良好的线性关系,其相关系数（r）均在1.0000~0.9977之间。方法检出限为0.3~2.4 ng,以采样体积1 L计算,检出限为0.3~2.4 μg/m³。加标量为20 ng时,7次重复实验目标化合物回收率均在81.6%~114.9%之间,目标化合物的相对标准偏差为1.2%~10.1%。采用该方法对某车厢内空气进行了检测,检出了包括酯类、卤代烷烃、卤代烯烃以及芳香族化合物在内的19种目标化合物,其范围为1.1~84.1 μg/m³。该方法准确、可靠、灵敏度高,实现了对环境空气中67种目标污染物的准确定量。     

Multi-layer cartridges filled with multi-walled carbon nanotubes for the determination of volatile organic compounds in indoor air.

A kind of new multi-layer adsorbent including Tenax TA/multi-walled carbon nanotubes (MWCNTs)/Carboxen 564 was developed for collecting volatile organic compounds. The adsorption and desorption efficiencies of 11 kinds of adsorbents (including Activated charcoal, Tenax TA, Carboxen 564, Chromosorb 101, Chromosorb 102, Chromosorb 103, Chromosorb 105, Porapak Q, GDX 301, XAD-2, and MWCNTs) were compared. By combining the advantages of Tenax TA, MWCNTs, and Carboxen 564, new type of multi-layer adsorbents was developed. The adsorption and desorption efficiency, the sampling reproducibility, and the effect of water were improved using multi-layer adsorbents, Tenax TA/MWCNTs/Carboxen 564. New multi-layer adsorbents were successfully applied to the determination of volatile organic compounds (VOCs) in ambient air.     

Detection of volatile organic peroxides in indoor air

A supercritical fluid extraction cell filled with adsorbent (Carbotrap and Carbotrap C) was used directly as a sampling tube to enrich volatile organic compounds in air. After sampling, the analytes were extracted by supercritical fluid CO2 with methanol as modifier. Collected organic peroxides were then determined by a RP-HPLC method developed and validated previously using post-column derivatization and fluorescence detection. Some volatile organic peroxides were found in indoor air in a new car and a newly decorated kitchen in the lower microg m(-3) range. tert-Butyl perbenzoate, di-tert-butyl peroxide, and tert-butylcumyl peroxide could be identified.     

Direct screening and confirmation of priority volatile organic pollutants in drinking water

A screening tool was proposed for the rapid detection of eight priority volatile organic pollutants according to European standards in drinking water. The method is based on the direct coupling of a headspace sampler with a mass spectrometer, using a chromatographic column heated to 175 degrees C as an interface. The water sample was subjected to the headspace extraction process and the volatile fraction was introduced directly into the mass spectrometer, without prior chromatographic separation, achieving low detection limits (0.6-1.2 ng/ml) for all compounds. The mass spectrum resulting from the simultaneous ionization and fragmentation of the mixture of molecules constitutes the volatile profile of each sample. An appropriate chemometric treatment of these signals permitted them to be classified, on the basis of their volatile composition, as contaminated or uncontaminated with respect to the legally established concentration levels for these compounds in drinking water, and providing no false negatives. A conventional confirmation method was carried out to analyze positive water samples by using the same instrumental setup as in the screening method, but using an appropriate temperature program in the chromatographic column to separate, identify and quantify each analyte.     

Isolation of organic water pollutants by xad resins and carbon

The recovery efficiencies of XAD resins −2, −4, −7, and −8 and of resin mixtures were measured using distilled water samples containing 13 organic pollutants. An equal-weight mixture of XAD-4 and XAD-8 was most efficient. XAD-2 and XAD-4/8 were further terted and found effective using tapwater. Carbon was tested as a sorbent for materials not well retained by the resins. In-column solvent washing before sample sorption was found to be as effective as Soxhlet extraction for removing background impurities. Some compounds can be desorbed from carbon by in-column solvent elution; others require Soxhlet extraction. An XAD-4/8 column in series with a carbon column was used to sample 1000 1 of tapwater. Halomethanes, n-hydrocarbons, polynuclear aromatic compounds and dibenzofuran in the order of ng/l were identified using a gas chromatograph-mass spectrometer-computer system.