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Study on the use of oxidant scrubbers for elimination of interferences due to nitrogen dioxide in analysis of atmospheric dimethylsulfide

Abstracts

In this work, oxidant scrubbers were evaluated for their ability to prevent sampling losses of dimethylsulfide caused by reactions with nitrogen dioxide. Various compounds and mixtures were used in the preparation of the oxidant scrubbers. An automatic flow analysis device was used to compare scrubbing efficiency for nitrogen dioxide. Among the scrubbers tested, the best were shown to be the one made with filter paper or glass wool coated with iron (II) sulfate, sulfuric acid and pyrogallic acid, and the one made from with paper coated with triethanolamine. The results obtained under laboratory conditions, using dimethylsulfide standard gas, and in field experiments confirmed that these scrubbers are suitable for the prevention of oxidation during sampling.

dimethylsulfide; atmospheric trace gases; sampling technique; nitrogen dioxide scavenger


Neste trabalho foi avaliado o desempenho de filtros para dióxido de nitrogênio, buscando evitar perdas durante a amostragem de sulfetos orgânicos, provocadas por oxidantes atmosféricos. Diferentes compostos e misturas foram usadas para recobrir superfícies sólidas empregadas na preparação destes filtros. Um sistema automatizado de análise em fluxo foi utilizado para comparar a eficiência de retenção de dióxido de nitrogênio pelos filtros. Entre os materiais testados na preparação dos filtros, as melhores escolhas foram papel ou lã de vidro impregnados com a mistura de sulfato de ferro (II), ácido sulfúrico e ácido pirogalico e ainda os filtros feitos de papel impregnados com trietanolamina. Os resultados obtidos em laboratório com mistura de gás padrão de dimetilsulfeto e experimentos em campo confirmaram a qualidade dos filtros e indicaram que eles podem ser utilizados para evitar a oxidação de sulfetos orgânicos durante a sua amostragem.


Article

Study on the use of oxidant scrubbers for elimination of interferences due to nitrogen dioxide in analysis of atmospheric dimethylsulfide

Beatriz A. Rodrigues, Luís R.M. Pitombo, Arnaldo A. Cardoso*

Departamento de Química Analítica, Universidade Estadual Paulista, CP 355, 14800-900, Araraquara - SP, Brazil

Neste trabalho foi avaliado o desempenho de filtros para dióxido de nitrogênio, buscando evitar perdas durante a amostragem de sulfetos orgânicos, provocadas por oxidantes atmosféricos. Diferentes compostos e misturas foram usadas para recobrir superfícies sólidas empregadas na preparação destes filtros. Um sistema automatizado de análise em fluxo foi utilizado para comparar a eficiência de retenção de dióxido de nitrogênio pelos filtros. Entre os materiais testados na preparação dos filtros, as melhores escolhas foram papel ou lã de vidro impregnados com a mistura de sulfato de ferro (II), ácido sulfúrico e ácido pirogalico e ainda os filtros feitos de papel impregnados com trietanolamina. Os resultados obtidos em laboratório com mistura de gás padrão de dimetilsulfeto e experimentos em campo confirmaram a qualidade dos filtros e indicaram que eles podem ser utilizados para evitar a oxidação de sulfetos orgânicos durante a sua amostragem.

In this work, oxidant scrubbers were evaluated for their ability to prevent sampling losses of dimethylsulfide caused by reactions with nitrogen dioxide. Various compounds and mixtures were used in the preparation of the oxidant scrubbers. An automatic flow analysis device was used to compare scrubbing efficiency for nitrogen dioxide. Among the scrubbers tested, the best were shown to be the one made with filter paper or glass wool coated with iron (II) sulfate, sulfuric acid and pyrogallic acid, and the one made from with paper coated with triethanolamine. The results obtained under laboratory conditions, using dimethylsulfide standard gas, and in field experiments confirmed that these scrubbers are suitable for the prevention of oxidation during sampling.

Keywords: dimethylsulfide, atmospheric trace gases, sampling technique, nitrogen dioxide scavenger.

Introduction

Sulfur gases and their reaction products play an important role in the chemistry of the global troposphere and in the biogeochemical sulfur cycle1-5. Sulfur compounds are released into the atmosphere by various natural and anthropogenic sources. A substantial increase in anthropogenic sulfur emission has taken place in the last century. It is responsible for malodorous odor in sewage systems, in pulp and paper industry6-8. In petrochemical processes sulfur compounds can be emitted and cause air pollution during oil prospecting, refining and when fuel is burned7,9,10. A few decades ago, biogenic H2S was believed to be the dominant form in which gaseous sulfur was released to the atmosphere. The importance of H2S emission has been continually revised ever since3-5,11. Current thought attributes an increasing role to dimethylsulfide (CH3)2S (DMS).

Although knowledge of the chemistry of sulfur compounds in the environment has much improved, there is evidence to suggest that determination of reduced sulfur compounds may often be subject to significant inaccuracies11. The main source of uncertainty associated with these data occurs during the collection step. Frequently, the analysis of these compounds requires a cryogenic preconcentration step to enhance low atmospheric concentrations. The cotrapping of water has been a complex problem: the ice may limit sample volumes and water may be injected into columns12 . However, the main problem is the destruction of sulfur compounds by oxidizing species11-15. The species commonly present in the atmosphere, which may cause sampling losses, include ozone (O3), nitrogen dioxide (NO2) and hydrogen peroxide (H2O2).

Several types of oxidant scrubbers have been suggested to remove oxidants during cryogenic preconcentration. Braman and co-workers16 used glass pearl coated with Na2CO3, Barnard co-workers17 and Andreae and Raemdonck18 used packed tubes containing Na2CO3/chromasorb as sulfur dioxide scrubbers, Bates and Johnson19 used glass fiber filters coated with NaOH. A KOH filter scrubber presented rapid loss of efficiency compared to carbonate-based Anakrom scrubbers20. Hofmann co-workers12 used a Nafion drier in combination with cotton wadding as an oxidant scavenger. Davison and Allen13 investigated in-line scrubbers utilizing Na2CO3, FeSO4.7H2O, KI or KBr, either pure or coated onto a chromatographic support, which they found to be ineffective for oxidant removal in moderately polluted air. The KI scrubbers were, however, effective when used in clean remote marine air. Comparing the various oxidant scrubbers, Kittler co-workers14 found the KI/glycerol/Vitrex filter to be superior to the scrubbers using KOH, NaOH, MnO2 and Na2CO3. Other methods have included neutral aqueous potassium iodide21, ferrous sulfate22 and 100% cotton wadding in combination with a Nafion drier23. Although much work has been done on the analysis of organic sulfides, the nature of the oxidant interference remains largely unknown. The development and use of new scrubbers is an empirical process11 . So far there is no consensus about the use of oxidant scrubbers in the analysis of reduced sulfides.

The present work describes the development of oxidant scrubbers for organic sulfide analysis in air. The oxidant scrubbers were made out of solid supports coated with reactive species, to remove the oxidants before the collection of organic sulfide. Comparative data on the scrubbers was obtained by automated flow analysis. Dimethylsulfide, the commonest organic sulfide found in the air, and nitrogen dioxide, the most common oxidant found in the air, were used in the development of this work.

Experimental

Method of sampling and analysis of organic sulfides

The method used to sample and analyze organic sulfides is non-cryogenic and has already been reported24,25. Glass wool coated with sodium tetrachloropalladate (II) was shown to be very efficient for the collection of dimethylsulfide (DMS). The resulting complex ([Pd(DMS)2Cl2]) is only slightly soluble in water, but readily soluble in organic solvents. The solutions showed a well-defined absorption peak in the near UV region (e=17.05 x103 l mol-1 cm-1 at 303 nm) and the absorbance values were proportional to the amount of DMS present. Gases such as H2S, CO, CS2, COS, NH3 and SO2 did not cause interference because they neither react with sodium tetrachloropalladate (II) nor produce compounds soluble in the solvents used to extract the [Pd(DMS)2Cl2](s). Oxidants such as nitrogen dioxide react with complexed DMS, interfering in subsequent DMS estimation.

The sodium tetrachloropalladate (II) solution was prepared by dissolving 0.6 mmol PdCl2 and 5.1 mmol NaCl in 55 mL of 0.1 mol L hydrochloric acid. This solution was used to coat 1.0 g of glass wool. The coating procedure was that recommended in the previous paper24 .

Sampling and analysis followed the protocol: a) a sorbent tube containing substarte was connected to the stream of the DMS gas mixture; b) after collection of DMS, the packing substrate was transferred to an extraction tube; c) the contents of the extraction tube were shaken with toluene until dissolution of [Pd(DMS)2Cl2] was complete; d) the solution was transferred to a 5.0 mL volumetric flask and the volume was adjusted; e) a photometric measurement was made at 303 nm with a Varian-Cary 219 spectrophotometer, using quartz cuvettes of 10.0 mm optical path length.

Gas generation

The experimental arrangement is shown in Figure 1. The pumped air was purified in a column containing, in sequence, silica gel, soda lime and activated carbon. The air stream was maintained at a steady temperature by a coil and flowed into a glass chamber containing a permeation tube. The air flow was controlled at 430 mLmin-1 using a critical orifice. For the DMS standard gas mixture, a permeation tube emitting 519 ngDMS min-1 at 30ºC (VICI Metronics, Santa Clara, CA) was used. For the NO2 standard gas mixture, the permeation tube described by Teckentrup and Klockow26, filled with condensed NO2 gas was used. The permeation rate of NO2 was evaluated by the oxidation of an iodine solution, according to the procedure described by Littman and Benoliel27.The permeation rate measured was 1.2µg NO2 min-1 at 27ºC.


Oxidant scrubber materials

Initially, solid substrates were prepared coated with substances known to react with nitrogen dioxide. Glycerol was used in some cases because of its humectant property, which should enhance the reactions with nitrogen dioxide. At first, 24 different compositions were tested. The supporting material was prepared from Whatman qualitative filter paper cut into small discs of 5mm diameter. The filter paper was soaked in solution, using 50 mLof aqueous solution per 2.5 g. of filter paper. The filters were dried at 60ºC in an stove with air circulation, producing the oxidant scrubber materials, which were stored in a desiccator in the dark.

Use of packed scrubbers

A glass tube with flow connections as in Figure 2 (1.5 cm internal diameter, 10 cm length) was filled with 3 g impregnated filter discs and closed with a Teflon stopper. The scrubber discs were retained in the tube with silanized wool glass. Kittler and co-workers14 proposed visual indication of the oxidation of iodide solution to measure the capacity of substrates for retention of oxidant. The blue/purple coloration of a starch-based iodine indicator was used to compare of several scrubbing systems. This visual comparison of the filters showed a discrepancy of up 24% among replicates. With the purpose of improving this evaluation standard, the measurement of the iodine formed by oxidation was adapted for automated flow analysis (Figure 3). The solution was prepared as suggested by Littman and Benoliel27 and contained about 200g potassium iodide, 36g disodium phosphate dodecahydrate, and 14g potassium dihydrogen phosphate per liter of solution. The solution of iodine in 20% potassium iodide and starch exhibits a blue color with a characteristic absorption spectrum and an intense maximum at 477 nm. In this procedure, the scrubber was connected to the stream of air containing nitrogen dioxide. The air, after passing through the scrubber, readily oxidized the iodide to iodine by any nitrogen dioxide remaining. The absorbance of the iodine solution was continuously measured and recorded. The fast formation of iodine was a signal of scrubber breakthrough.



Results and Discussion

Interference of nitrogen dioxide

The reaction of nitrogen dioxide with the dimethylsulfide collected as [Pd(DMS)2Cl2](s) was evaluated. The procedure involved two steps: first the Na2PdCl4(s) sorbent tube was connected up to the stream of DMS gas mixture standard for 30 min; in the second step, air containing nitrogen dioxide was passed through the sorbent tube in different periods of time. The absorption spectra of the products formed are shown in Figure 4. The absorption spectra of compounds formed by reaction of nitrogen dioxide with the [Pd(DMS)2Cl2](s) showed the transformation of this compound.


Efficiency of oxidant scrubbers

In air sampling, suitable flow rate and duration of sampling are two parameters which must be determined for a specific analytical method applied to the compound of interest. If, as here, a sampling time of 30 min at flow rate 430 mL min-1 is chosen for organic sulfide in air, then the oxidant scrubber should remain effective during this period. As a parameter for evaluating the efficiency of oxidant scrubbers for 30 min of sampling, the capacity of a mixture of NO2 and air to oxidize the iodide was first measured. When the air containing nitrogen dioxide was passed directly through the iodide solution at 430 ml min-1, the absorbance of the solution increased linearly (Figure 5), and after 30 min, the signal measured was 0.330 (absorbance units), corresponding to the iodine formed by reaction of 36 mg of NO2. In sequence, each one of the scrubbers was connected to the system upstream of the iodide solution and the absorbance of the solution measured. The oxidation of iodide depended on the quantity of NO2 not retained by the scrubber. To evaluate the efficiency of each oxidant scrubber with respect to retention of NO2 during a 30 min sampling interval, the following equation was used:

where e is the efficiency in percentage of an oxidant scrubber in retention of NO2 after 30 min; 0.330 is the absorbance of the iodide solution after containing nitrogen dioxide was passed through the solution for 30 min; and A30 is the absorbance of the iodide solution after scrubbed air contained nitrogen dioxide had been passed through the solution for 30 min. Table 1 lists scrubber performance for the 24 different compositions of coating solution studied. The results showed a discrepancy of up to 5% among replicates.


Effects of reduction of the amount of oxidant scrubber material

In order to design a scrubber that was more compact and easier to handle, the amounts of sorbent materials were reduced and the efficiency of scrubbers re-evaluated. Some sorbent were not tested because their preparation is more laborious. These experiments were carried out using a Teflon tube (0.3 cm internal diameter and 7.5 cm length) fitted with connectors on each end. The packing substrates, about 0.3 g, were held inside the Teflon tube by silanized glass wool. The results showed that the scrubbers maintained a good retention capacity for nitrogen dioxide (Table 2). These scrubbers were then evaluated during collection of DMS onto sampling tubes located downstream of the scrubbers.

Recovery of DMS using different oxidant scrubbers

It is important that the oxidant scrubbers should neither react with DMS, nor adsorb DMS present in the sample air stream. Tests were conducted to measure possible losses of analyte. The DMS standard gas was passed through the oxidant scrubber, and it was collected in the sampling tube over 30 min intervals. Table 3 shows the results of these experiments. The best coating solutions used were: a) 25% (m/v) ferrous ammonium sulfate, 1% (v/v) sulfuric acid and 5% pyrogallic acid; b) 25% triethanolamine. These solutions were also used to coat different supporting materials including: glass wool (fiber medium), silica gel (1-4 mm), and glass pearl (3 mm diameter). Scrubbers containing these materials were tested with the DMS standard gas using the same procedure. Only the solution of 25% (m/v) ferrous ammonium sulfate, 1% (v/v) sulfuric acid and 5% (v/v) pyrogallic acid coated on glass wool was shown to be inert towards DMS.

Studies of preservation DMS collected in sampling tube

The stability of DMS collected as [Pd(DMS)2Cl2](s) was assessed. DMS (15.6 µg) was initially collected in the sampling tube, after which the air/nitrogen dioxide mixture, scrubbed by passage through one of three devices, was passed through the sampling tube for 2 h (about 144 µg NO2). The results show (Table 4) that the scrubbers employed can be used successfully for retention of NO2, and hence preservation of DMS collected. It should be noted that the NO2 concentration used in this experiment was many times higher than typical NO2 concentrations found in the polluted ambient atmosphere.

Test of oxidant scrubbers in field sampling

The analytical method reported here in was used to measure atmospheric DMS levels in the environment. The basic system for sampling comprised an air pump, a gasmeter, a sampling tube (glass wool coated with Na2PdCl4) and a scrubber. A dust filter made from silanized glass wool was placed in front of the filter pack. The oxidant scrubber made from the solution of 25% (m/v) ferrous ammonium sulfate, 1% (v/v) sulfuric acid and 5% (v/v) pyrogallic acid coated on to filter paper was used because it was easier to handle than the other filters. All samples were collected for 3 h because the levels of DMS were unknown. The sampling was conducted at the Chemistry Institute (Araraquara SP Brasil), July 1995. This site is an urban area and the trace gas compositions may have been affected by the presence of an automobile traffic highway within 500 m, and emissions from anaerobic wastewater treatment 2 Km distant. In the winter (June and July), periodic episodes of odor pollution have been noted at this site. Measurements carried out on polluted days resulted that the level of DMS varied from 3.8-12.4 mg m3. Figure 6 shows the absorption spectra of solutions resulting from field sampling with and without scrubbers. When the scrubber was used, the organic solution obtained from the sampling tube, showed a well-defined absorption peak, with the maximum absorbance at 303 nm characteristic of unoxidized [Pd(DMS)2Cl2]. On the other hand, when the filter pack was removed during sampling, the absorption spectrum of the solution obtained showed the existence of oxidized [Pd(DMS)2Cl2].


Conclusion

Direct analysis of DMS is generally impossible due to their low concentrations in air, which are frequently below the direct quantification limits of the current methods. Determination of atmospheric DMS employing preconcentration can result in very large sampling losses unless potential oxidants in the air sample are removed prior to the concentration step. Although much work has been done on the analysis of DMS in air, the nature of the oxidant interference remains largely unknown. The gas phase reaction of DMS with atmospheric oxidants such as ozone or NO2 is extremely slow28,29. In the preconcentration procedure it is possible that the through surface sorption the concentration of both oxidant and sulfur compound are increased such that the reaction proceeds more rapidly than in the gas phase11.

Oxidant scrubbers were evaluated for their ability to prevent sampling losses of DMS. The comparison of the filters showed a discrepancy of up to 5% among replicates. Scrubbers utilizing either (a) a mixture of 25% ferrous ammonium sulfate, 1% H2SO4 and 5% pyrogallic acid or (b) 25% triethanolamine possess efficient retention capacity for NO2.The scrubbers are easy to prepare and to store. The results showed that these scrubbers are suitable for the preservation of dimethylsulfide collected during atmospheric sampling. Furthermore, the technique employing such scrubbers, combined with the Na2PdCl4 sorbent used for preconcentration and analysis of DMS in ambient air, requires minimal sample handling and instrumentation. Results obtained under laboratory conditions and during the course of a small field experiment confirm that the use of a scrubber in combination with a Na2PdCl4 sorbent is suitable for measurements of DMS. Therefore, the described method offers a useful alternative for the determination of DMS in ambient air. In addition, use of the scrubbers described could probably be adapted to other analytical techniques of precocentration such as cryogenic trapping or adsoption on a solid support.

Acknowledgments

This work was abstracted from the PhD thesis submitted by B. A Rodrigues to the Instituto de Química de Araraquara, State University of São Paulo, Brazil (UNESP).

The authors wish to acknowledge the financial support of the Coordenação do Aperfeiçoamento de Pessoal de Nïvel Superior (CAPES) and Conselho Nacional do Desenvolvimento Científico e Tecnológico (CNPq), Brazil.

Received: August 31, 1999.

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Publication Dates

  • Publication in this collection
    01 June 2000
  • Date of issue
    Feb 2000

History

  • Received
    31 Aug 1999
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