Sample preparation of polymers for halogen determination requires special attention because they are difficult to bring into solution and due to the risk of analyte losses when using acid digestion. A method using microwave-induced combustion (MIC) was optimized for accurate determination of halogens in polymeric parts obtained in waste of electrical and electronic equipment. Results were compared with those by using microwave-assisted extraction (MAE) with alkaline solution and microwave-assisted wet digestion (MAWD) using concentrated nitric acid, which are common choices for sample preparation. In this particular case, the MAE method was not suitable and underestimated results were obtained, showing the necessity for the complete digestion. Even with the use of MAWD under high temperature and pressure, incomplete digestion and high acid content were obtained, which were unsuitable for analysis and resulted in poor recovery. Only by using MIC (diluted ammonia as absorbing solution) acceptable recoveries (95 to 104%) and agreement with certified values for the certified reference materials (CRMs) of polymers were obtained. Thus, a suitable method for all halogen to be determined by ion chromatography (IC) or inductively coupled plasma mass spectrometry (ICP-MS), with the exception of F, was obtained in agreement with the requirements by the Restriction of the Use of Certain Hazardous Substances (RoHS) European directive.

In this paper, a feasible method was proposed for the chlorine and fluorine determination in eye-pencil samples using ion chromatography (IC). The microwave-induced combustion (MIC) was used to digest up to 200 mg of a sample, with 50 mg of microcrystalline cellulose as a combustion aid and only water for analytes absorption. Cl and F recoveries were 105 ± 1 and 93 ± 5%, respectively, when standard solutions were used in the recovery tests. Certified reference materials (CRM) were also digested mixed to the sample, and no significant difference between the obtained results and the certified values was observed. Precision was assessed in terms of repeatability and intermediate precision, with relative standard deviations (RSD) lower than 9%. Limits of detection (LOD) for Cl and F were 37 and 4 mg kg-1, respectively. Ultrasound-assisted extraction (UEA) was also evaluated; however, the results were not satisfactory. The proposed method was suitable for Cl and F determination in eye-pencil because it proved to be accurate, precise and safe, and also minimized waste generation and had high throughput.

A method for determining low levels of As and Cd by dispersive liquid-liquid microextraction (DLLME) and inductively coupled plasma mass spectrometry (ICP-MS) was proposed. The following parameters that affect extraction efficiency were investigated: type and volume of extraction solvent (1000 µL acetone), type and volume of dispersive solvent (75 µL carbon tetrachloride), amount of ammonium pyrrolidinedithiocarbamate and sodium diethyldithiocarbamate as chelating agents, sample mass (0.5 g in 10 mL ultrapure water), pH of sample solution (2.0) and number of washing steps (one). Accuracy was evaluated by analytes determination in sugar samples by ICP-MS after digestion by microwave-induced combustion (MIC). No significant difference was observed between results of the proposed DLLME method and MIC in the case of both analytes. Instrument calibration was performed by the standard addition method and good linearity was achieved. Limits of quantification (LOQs) were 0.7 and 0.2 ng g-1 for As and Cd, respectively. The main advantages of this method are relatively high sample mass, low dilution, suitable preconcentration factors and significantly low LOQs (ng g-1 range). When the proposed method was used for determining As and Cd in four sugar samples, their concentrations ranged from 1.13 to 2.95 ng g-1 and from 0.31 to 0.43 ng g-1, respectively.

Dry ashing, dissolution in aqueous medium or wet digestion methods were evaluated for sample preparation of shampoo for the subsequent indirect determination of sulfur by UV-Vis spectrophotometry. Among the sample preparation methods evaluated, microwave-assisted wet digestion using 7 mol L-1 HNO3 was the most suitable method for this purpose. Accuracy of the proposed method was evaluated by recovery test using standard solution, and the recovery was about 96%. Moreover, for comparison of results, S (as SO42-) was also determined by ion chromatography, after microwave-assisted wet digestion using concentrated HNO3, and no significant difference was observed between the obtained results (according to the t-test for a 95% confidence level, p = 0.288). Relative standard deviations were always lower than 10% and the limit of detection was 0.007% w/v. Finally, the proposed method was applied for analysis of sixteen shampoos used to many types of hair, from different brands produced in Brazil, and the concentration of S ranged from 0.78 to 2.82% w/v.

In this work, a method using microwave-induced combustion (MIC) was optimized in order to obtain a fast, simple, efficient and greener sample preparation method for coal digestion and further determination of sulfur by inductively coupled plasma optical emission spectrometry (ICP OES). Accuracy was evaluated by comparison of the results with those obtained using elemental analysis by UV-fluorescence, microwave-assisted acid digestion with determination by ICP OES and by analysis of certified reference materials of coal. Some parameters that influence MIC method, such as the type and concentration of absorbing solution, the necessity of using a reflux step as well as the cooling time were carefully optimized. No statistical difference was observed for combustion without reflux followed by 5 min of cooling, in comparison to the reference values obtained by elemental analysis. Complete digestion was obtained with this fast and simple method (total digestion program required only 6 min) and using a diluted acid solution for quantitative recovery. The feasibility of digests for sulfur determination as sulfate by ion chromatography (IC) with conductivity detection was also demonstrated. The possibility of determining other elements, commonly monitored in coals, is another advantage of this high-efficiency digestion method (MIC) combined with the multielemental capacity of ICP OES or IC instruments.

A combustão iniciada com micro-ondas (MIC) foi aplicada para decomposição de amostras de tabaco de cigarro e subsequente determinação de bromo e cloro por espectrometria de emissão óptica com plasma indutivamente acoplado (ICP OES). Massas de amostra de até 500 mg foram decompostas em frascos fechados e pressurizados com 20 bar de oxigênio. A combustão foi completada em menos de 30 s e os analitos foram absorvidos em solução diluída de (NH4)2CO3. A exatidão foi avaliada usando materiais de referência certificados e mediante a determinação utilizando ICP-MS. A concordância foi melhor do que 98% usando 50 mmol L-1 de (NH4)2CO3 como solução absorvedora e 5 min de refluxo. A temperatura durante a combustão foi superior a 1400 ºC e o conteúdo de carbono residual nos digeridos após MIC foi menor que 1%. Até oito amostras podem ser decompostas simultaneamente. Limites de quantificação utilizando MIC e determinação por ICP OES foram de 12 e 6 µg g-1 para Br e Cl, respectivamente

The microwave-induced combustion (MIC) was applied for cigarette tobacco samples digestion and further determination of bromine and chlorine by inductively coupled plasma optical emission spectrometry (ICP OES). Samples masses up to 500 mg were combusted in closed vessels using 20 bar of oxygen. Combustion was complete in less than 30 s and analytes were absorbed in diluted (NH4)2CO3 solution. Accuracy was evaluated using certified reference materials with similar matrix composition and comparison with results obtained using ICP-MS. The agreement was better than 98% using 50 mmol L-1 (NH4)2CO3 as absorbing solution and 5 min of reflux. Temperature during combustion was higher than 1400 ºC and the residual carbon content in digest obtained after MIC was lower than 1%. Up to eight samples could be processed simultaneously and a single absorbing solution was suitable for both Br and Cl. Limit of quantification by MIC and further ICP OES determination was 12 and 6 µg g-1 for Br and Cl, respectively.