Abstract An ultrasound pretreatment was used to increase anthocyanins content in blackberry juice. Whole fruits were inserted into a glass vessel without contact with any solvent, sonicated in an ultrasonic bath, and then pressed with a manual juicer. The experimental design showed that 7 min at 65% of ultrasound amplitude increased the anthocyanin content in juices from 31 to 56% for BRS Xingu, Guarani, and Xavante cultivars. Two major anthocyanins, cyanidin-3-glucoside and cyanidin-3-rutinoside were found in higher concentrations for sonicated fruits. Therefore, ultrasonic pretreatment of whole fruits increased the anthocyanins in blackberry juices using a simple, fast, and green approach.

Thermal infrared enthalpimetry (TIE) was used for hypochlorite determination in commercial hypochlorite-based bleaching solutions. Experimental parameters were evaluated for the reaction with a hydrogen peroxide solution. The most relevant conditions were 5% H2O2 (m/m) solution, stirring speed of 250 rpm, dispensing rate of 0.57 mL s-1, and 10 s after reaction for the simultaneous temperature readings of four replicates. Agreement to reference method NBR 9425 ranging from 98.2 to 103.2% was achieved, with a low variation among measurements (relative standard deviation < 3.5%). The number of analytical operations was reduced, and only H2O2 solution was required as a greener reagent. A low amount of residues was generated (2.4 and 152.8 mL for each replicate in TIE and official method, respectively), and the application of the green analytical procedure index (GAPI) showed the greenness of the proposed method.

A novel free PhotoMetrix UVC is proposed for both the operation of a universal serial bus video camera (UVC) and multivariate image analysis, allowing a full solution for point-of-use analysis. A UVC was placed in an open-source 3D-printed chamber illuminated by a white light-emitting diode (LED) with controlled intensity of light. The digital images captured were converted into red, green, and blue (RGB) histograms, and regression models were used within the app. As a proof-of-concept, four adulterants in raw milk samples were determined. The coefficient of determination (R2Cal) for all models was higher than 0.99, and no significant differences (p < 0.05) between the measured and predicted values were identified. The root mean square error of calibration (RMSEC) and root mean square error of cross validation (RMSECV) were satisfactory, with values less than 0.1 and 0.7 g L-1, respectively. The recoveries ranged from 90 to 120% in spiked milk samples, and partial least square (PLS) models showed root mean square error of prediction (RMSEP) of 0.28, 0.33, 0.48 and 0.39 g L-1 for chloride, hypochlorite, hydrogen peroxide and starch, respectively. The PhotoMetrix UVC app was feasible for the colorimetric chemical analysis using a smartphone improving the applicability, mobility, and usability.

The use of paper devices in chemical analysis has been increased due to their low cost, high surface area, portability, and biodegradability. A novel use of paper devices is proposed using thermal infrared enthalpimetry (TIE) for a rapid, green, and high throughput determination of wine acidities. The determination of total, fixed, and volatile acidities in red, white, and sparkling wine was carried out, and the results were compared with AOAC titration method. A multichannel pipette was used for reagent addition and an infrared camera for the temperature monitoring. The pipetting and temperature measurement conditions presented direct influence in the deviations among the measurements. The results obtained by TIE presented an agreement between 96 and 104% with the reference method (AOAC 962.12), for all samples. A high sample throughput was achieved reaching 480 samples h-1 for total acidity. A significant reduction in sample volume and reagent consumption was also obtained, with energy consumption up to 60 times lower in relation to the AOAC method. The association of TIE with a paper device provided a rapid, reliable and green method for the determination of acidities of wines.

Abstract In this work, a simple and fast method is proposed for the determination of ethanol in homeopathic medicines using thermal infrared enthalpimetry (TIE). Samples containing alcohol in a wide concentration range (from 5% to 95% v/v) were used. Purified water or absolute ethanol was added directly into homeopathic medicine and increase of temperature was monitored using an infrared camera. Total volume, stirring speed and dispensing rate of solutions were the most significant parameters studied for method optimization. A response surface methodology (RSM) was used for optimization of the experimental conditions. The method was validated in the following parameters: selectivity, linearity, linear range, precision (repeatability and intermediate precision), limit of detection and quantification, accuracy and robustness. Linear range was obtained from 4% to 55% (ethanol, v/v). The proposed method showed accuracy in agreement with the conventional one. The proposed method it was demonstrated a good alternative for determination of ethanol in homeopathic medicines, presenting low cost, fast analysis and agreement with the principles of green analytical chemistry.

Content uniformity (CU) is a parameter used to ensure the uniformity of the amount of active substances in pharmaceutical preparations. It is often evaluated in the quality control of pharmaceutical dosage forms, and a novel method was proposed for CU determination using thermal infrared enthalpimetry (TIE). Captopril tablets were dissolved in 24-well microplates and the heat released from the reaction of captopril and I2 was monitored with an infrared camera. Some experimental parameters were adjusted, as captopril/I2 ratio, stirring speed and dispensing rate, and the most suitable conditions were 1.00:1.00 (v/v), 250 rpm and 0.57 mL s-1, respectively. Interferences from tablet adjuvants (e.g., starch, cellulose and lactose) were not observed. The results obtained by TIE did not differ statistically (Student’s t-test, p > 0.05) from those from official method (UV spectrophotometry) described in pharmacopeia. The TIE method required 31 and 12 times less reagent and time, respectively. Therefore, the proposed method was suitable for routine analysis and agrees with the requirements of green analytical chemistry.

Oxidation using diluted HNO3 solution is dependent on reactions taking place in the gas phase, resulting in HNO3 regeneration, thus allowing sub stoichiometric reactions (16.7 mmol of C oxidized with 10.4 mmol of HNO3). Reactions for HNO3 regeneration are dependent on temperature gradient along reaction vessel. Thermographic images were obtained of external vessel wall after 2.5, 5 and 7.5 min of heating. Temperature inside reaction vessel was directly measured using a sapphire thermocouple in four different depth (3, 6, 12 and 16 cm). Reactions under inert atmosphere (7.5 bar Ar) were evaluated and normally presented higher temperature gradient than that performed with O2 pressure, since HNO3 regeneration reactions are exothermic. A better understanding of the regeneration of HNO3 and the dependence on the whole reaction vessel temperature in this system was possible combined to residual carbon content and residual acidity measurements to estimate the extent of organic matter oxidation.

In this work, solutions of oxidant salts were evaluated as alternative to nitrate solution for the ignition step in microwave-induced combustion (MIC) method. Aqueous solutions of KClO4, K2Cr2O7, KMnO4 and K2S2O8 in several concentrations were evaluated and it was observed that the ignition was dependent on the concentration and type of igniter solution. Moreover, it was possible to observe that ignition and combustion times are not related with sample mass, which was confirmed by evaluating sample masses ranging from 100 to 500 mg of whole milk powder. Certified reference materials were digested using K2Cr2O7 as igniter solution and digests analyzed by inductively coupled plasma optical emission spectrometry (ICP OES), with good agreement to certified values. The obtained results suggest that MIC can be performed using solutions of oxidants salts. In addition, the proposed study contributed to a better undestanding and explaining the ignition with microwaves.

A solid sampling electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP OES) method for determination of As, Cd, Cr, Cu, Mn, Mo, Ni, Pb, Pd, Pt, Rh, Ru and V in pharmaceuticals is proposed. Tricyclic pharmaceuticals were directly analyzed due to their difficult decomposition with acids. Pyrolysis and vaporization temperature, sample mass, and reaction gas (Freon) flow rate were evaluated. The effect of organic and inorganic compounds was evaluated for matrix matching. The limits of detection ranged from 0.04 µg g−1 (Cu) to 107 µg g−1 (As) and the relative standard deviation was lower than 10%. The investigated elements were not detected in the analyzed samples with the exception of Cr in cyclobenzaprine hydrochloride. Since there was no certified reference materials available for metals and metalloids in pharmaceuticals, the accuracy of the method was evaluated by an independent technique and by analyte recovery. Inductively coupled plasma mass spectrometry was employed for analyte determination after sample decomposition by microwave induced combustion. The agreement of the results found by both techniques was better than 87% and analyte recoveries ranged from 91 to 103%.

Um procedimento rápido para determinação de perda por dessecação (LOD) foi desenvolvido empregando aquecimento por radiação micro-ondas. Amostras de sacarídeos foram utilizadas e diferentes parâmetros foram avaliados, tais como a posição da amostra na cavidade do micro-ondas, massa de amostra e tempo de irradiação. Massas de amostra de 1 g e tempo de irradiação entre 15 e 25 min foram suficientes para a determinação da perda por dessecação de todos sacarídeos. Os resultados obtidos para perda por dessecação assistida por micro-ondas (MALOD) foram comparados com os resultados obtidos por LOD convencional em estufa e não apresentaram diferença significativa. O tempo de análise foi reduzido de 2,4 a 15 vezes, quando comparado ao sistema convencional de LOD e o desvio padrão relativo das medidas foi inferior a 1%. Até 16 amostras podem ser processadas simultaneamente, tornando o procedimento MALOD apropriado para análise de rotina

A fast procedure for loss on drying (LOD) determination was developed using microwave radiation. Samples of commercial saccharides were dried and the influence of sample position inside the microwave cavity, sample mass and irradiation time were evaluated. Sample mass of 1 g and irradiation time between 15 to 25 min were enough to LOD determination for all saccharides. Results obtained using the proposed microwave-assisted loss on drying (MALOD) procedure were compared with those obtained by conventional LOD determination using an oven and no statistical difference was found among results of these techniques. Using MALOD procedure the relative standard deviation was below 1%. The time for analysis was reduced from 2.4 to 15 times when compared to conventional LOD determination and up to 16 samples could be simultaneously processed making MALOD procedure suitable for routine analysis.

Um novo sistema para análise direta de amostras sólidas por espectrometria de absorção atômica com chama é proposto como alternativa para a determinação de elementos traço em carvão. Para a demonstração do potencial do procedimento a determinação de manganês foi investigada. Amostras de carvão foram moídas e pesadas diretamente em recipientes de polietileno e transportadas na forma de um aerossol seco até uma cela de quartzo posicionada entre o feixe óptico e a base do queimador. Sinais transientes foram totalmente integrados em 1 segundo. A influência das condições operacionais sobre os sinais foi estudada. Sinais de fundo foram sempre baixos e uma massa característica de 1,9 ng Mn foi encontrada. Os resultados foram considerados satisfatórios com respeito à exatidão (entre 97,5 e 103,2%) e precisão (RSD melhor que 6%). O sistema proposto é simples e pode ser facilmente adaptado a espectrômetros comerciais, permitindo a análise de mais de 80 amostras por hora.

A new device for the direct solid analysis by flame atomic absorption spectrometry was investigated as an alternative technique for the determination of trace elements in coal. The potential application of the proposed procedure for the determination of manganese was investigated. Ground coal test samples were weighed directly into polyethylene vials and carried as a dry aerosol to a slotted quartz vaporization cell placed between the flame burner and optical path. The transient signals obtained were totally integrated in 1 second. The effect of operating conditions on the analytical signal was investigated. Background signals were always low and a Mn characteristic mass of 1.9 ng was found. Results were considered satisfactory regarding to both accuracy (between 97.5 and 103.2%) and precision (RSD better than 6%). The proposed system is simple and can be easily adapted to any conventional atomic absorption spectrometers allowing the analysis of more than 80 test samples in an hour.