Automated H2O2 monitoring during photo-Fenton processes using an Arduino self-assembled automatic system.

A cheap and easy to use Arduino self-assembled automatic system was employed to continuously monitor the hydrogen peroxide consumption during the photo-Fenton degradation of caffeine, selected as model target compound. The automatic system made it possible to measure the H2O2 concentration in the reaction cell via a colorimetric reaction and to take samples for HPLC analysis minimising the operator manual intervention and exposure to UV radiation. The obtained results were compared in terms of LOD and LOQ with H2O2 measurements manually performed using UV-Vis spectrophotometry, evidencing better analytical performance when using the automatic system; LOD and LOQ were respectively 0.032 mM and 0.106 mM for the automatic system against 0.064 mM and 0.213 mM for UV-Vis spectrophotometry. Furthermore, the photo-Fenton treatment was optimised by means of a Design of Experiments (DoE) investigating the effect of added H2O2 concentration, iron concentration and caffeine initial concentration on system performances. The use of the automatic device for such monitoring provided several advantages: automation (with consequent reduction of the workload), measurement increased precision, reduced reagents consumption and waste production in agreement with the principles of Green Analytical Chemistry.

A smartphone image-based method for the colorimetric characterization of historical pigments in mural paintings.

In this article, the detailed description of a smartphone-based analytical method to turn a smartphone into a colorimeter is described and applied to mural painting replicas. The method consists of a camera characterization process, to estimate CIELAB values from RGB camera responses, correcting for potential experimental interferences, like the effect of the lighting/capture geometry or software for color modification and enhancement. Next, the estimated CIELAB descriptors were used to build a chemometric Support Vector Classifier to objectively distinguish among the colors of the different pigments. The method was validated in terms of color reproduction and classification performance.•A smartphone-based method is described to capture mural painting color.•A color gamut-specific camera characterization procedure is developed and the performance of the smartphone-based colorimeter is compared with a spectrophotometer.•A classification method based on the estimated CIELAB descriptors is validated in terms of classification performance.

Unveiling origins, composition, and appearance of ancient Islamic gold coins through elemental and smartphone-based colorimetric studies.

In this article, the Islamic gold coins collections of the University of Valencia is studied for the first time for its elemental composition and colorimetric properties. To that end, non-destructive elemental analysis using energy-dispersive X-ray fluorescence is applied to obtain the coins' elemental profile. Additionally, the colour of the coins is assessed using smartphone-based colorimetry as an innovative non-invasive method. Results indicate that the Islamic coins could be attributed to Almoravids, and the gold origin could be the famous Sudanese gold, an ore which was valued all over the world. Also, the text found in the coins was translated and allowed to objectively identify the mint and year. Based on these results, it can be seen that the earliest coins struck in the Iberian Peninsula are characterised by slightly lower gold concentrations than the ones struck in the northern part of Africa, pointing towards a potential recycling of coins which already circulated in the area. In conclusion, this work provides new analytical insights into a peculiar and unique type of samples, allowing to draw some conclusions in terms of their origins and materials, and for the first time allows to characterise the chromatic coordinates of this type of samples.

Smartphone-based procedure to determine content of single synthetic dyes in food using the Arata-Possetto extraction method.

The use of additives, including dyes, is common in the preparation of food products. The analytical control of artificial food dye content is relevant since some, such as azo dyes, may produce cancer and attention deficit disorders and hyperactivity in children. Consequently, the maximum permitted concentration of azo dyes in food is regulated by current legislation. Therefore, it is of interest to find simple and fast procedures for the control of these compounds. The aim of this study is to determine the concentration of azo dyes in food samples by the Arata-Possetto method - based on the extraction of azo dyes employing natural wool -, followed by the analysis of an image captured by a smartphone camera. After experimentally determining the optimal extraction conditions, the calibration curves for standard solutions of different food dyes and the color of the dyed wool were obtained. Results from dyed wool image processing were compared with the absorbance spectra of the solutions before extraction as measured by a diode array spectrophotometer. The spectrophotometric and the image processing procedures were employed to obtain the calibration curves for different food dyes, which were subsequently employed to analyze food samples. Statistical treatment shows that the results of both methods are comparable.

The casts of Pompeii: Post-depositional methodological insights.

The casts of Pompeii bear witness to the people who died during the Vesuvius 79 AD eruption. However, studies on the cause of death of these victims have not been conclusive. A previous important step is the understanding of the post-depositional processes and the impact of the plaster in bones, two issues that have not been previously evaluated. Here we report on the anthropological and the first chemical data obtained from the study of six casts from Porta Nola area and one from Terme Suburbane. A non-invasive chemical analysis by portable X-ray fluorescence was employed for the first time on these casts of Pompeii to determine the elemental composition of the bones and the plaster. Elemental profiles were determined providing important data that cross-referenced with anthropological and stratigraphic results, are clearly helpful in the reconstruction of the perimortem and post-mortem events concerning the history of these individuals. The comparative analyses carried out on the bone casts and other collections from burned bones of the necropolis of Porta Nola in Pompeii and Rome Sepolcreto Ostiense, and buried bones from Valencia (Spain), reveal the extent of high temperature alteration and post-depositional plaster contamination. These factors make bioarchaeological analyses difficult but still allow us to support asphyxia as the likely cause of death.

Development of an automated colorimeter controlled by Raspberry Pi4.

A low-cost new instrument to carry out automated colorimetric analysis has been developed. The device consists of a carousel sampler, built by a 3D-printer, and a Raspberry Pi4-controlled signal measurement module based on the RGBC (red, green, blue and clear) responses of a TCS34725 color light-to-digital converter with IR filter. The device has been tested with calibration standards of different food dyes (Tartrazine, Red Allure AC and Brilliant Blue FCF) and three food samples containing one of each food dye. The new device provides R2 > 0.995 and a LOD of 1.1, 1.4 and 0.1 µmol L-1 for each food dye, respectively. The results are statistically comparable to those obtained with a conventional benchtop spectrophotometer. The proposed device achieves a reduction in sample and waste volume and in analysis time, minimizes the use of energy, and allows in situ measurements, being an automated method it is safer for operators in comparison to the reference method, yielding similar analytical results and following the principles of green analytical chemistry.

Smartphone-based colorimetric study of adulterated tuna samples.

In this work, a colorimetric analysis of adulterated tuna samples is carried out using both a spectroradiometer and a smartphone as capture devices. Yellowfin tuna (Thunnus albacares) slices were treated with nitrate and nitrite salts, as well as with two different vegetable extracts (beetroot and radish), and the resulting NO2- and NO3- concentration was analysed using HPLC-DAD. The results indicate that both nitrite and beetroot treatments work properly as colouring agents in tuna, being nitrate also effective. When assessing the effect of radish, the final flesh had a more whitish colour. Overall, this approach allows to obtain colorimetric data which can distinguish among the different adulterating agents.

Sequential spectrofluorimetric determination of free and total glycerol in biodiesel in a multicommuted flow system.

A new procedure for spectrofluorimetric determination of free and total glycerol in biodiesel samples is presented. It is based on the oxidation of glycerol by periodate, forming formaldehyde, which reacts with acetylacetone, producing the luminescent 3,5-diacetyl-1,4-dihydrolutidine. A flow system with solenoid micro-pumps is proposed for solution handling. Free glycerol was extracted off-line from biodiesel samples with water, and total glycerol was converted to free glycerol by saponification with sodium ethylate under sonication. For free glycerol, a linear response was observed from 5 to 70 mg L(-1) with a detection limit of 0.5 mg L(-1), which corresponds to 2 mg kg(-1) in biodiesel. The coefficient of variation was 0.9% (20 mg L(-1), n = 10). For total glycerol, samples were diluted on-line, and the linear response range was 25 to 300 mg L(-1). The detection limit was 1.4 mg L(-1) (2.8 mg kg(-1) in biodiesel) with a coefficient of variation of 1.4% (200 mg L(-1), n = 10). The sampling rate was ca. 35 samples h(-1) and the procedure was applied to determination of free and total glycerol in biodiesel samples from soybean, cottonseed, and castor beans.

A multicommuted stop-flow system employing LEDs-based photometer for the sequential determination of anionic and cationic surfactants in water.

It has been developed an automatic stop-flow procedure for sequential photometric determination of anionic and cationic surfactants in a same sample of water. The flow system was based on multicommutation process that was designed employing two solenoid micro-pumps and six solenoid pinch valves, which under microcomputer control carry out fluid propelling and reagent solutions handling. A homemade photometer using a photodiode as detector and two light emitting diodes (LEDs) with emission at 470 nm (blue) and 650 nm (red) as radiation sources, which was tailored to allow the determination of anionic and cationic surfactants in waters. The procedure for anionic surfactant determination was based on the substitution reaction of methyl orange (MO) by the anionic surfactant sodium dodecylbenzene sulfonate (DBS) to form an ion-pair with the cetyl pyridine chloride (CPC). Features such as a linear response ranging from 0.35 to 10.5 mg L(-1) DBS (R=0.999), a detection limit of 0.06 mg L(-1) DBS and a relative standard deviation of 0.6% (n=11) were achieved. For cationic surfactant determination, the procedure was based on the ternary complex formation between cationic surfactant, Fe(III) and chromazurol S (CAS) using CPC as reference standard solution. A linear response range between 0.34 and 10.2 mg L(-1) CPC (R=0.999), a detection limit of 0.05 mg L(-1) CPC and a relative standard deviation of 0.5% (n=11) were obtained. In both cases, the sampling throughput was 60 determinations per hour. Reagents consumption of 7.8 microg MO, 8.2 microg CPC, 37.2 microg CAS and 21.6 microg Fe(III) per determination were achieved. Analyzing river water samples and applying t-test between the results found and those obtained using reference procedures for both surfactant types provide no significant differences at 95% confidence level.

Monitoring of the smoking process by multicommutation Fourier transform infrared spectroscopy.

Nicotine was selected as the target molecule for monitoring of the smoking process by multicommutation Fourier Transform Infrared spectroscopy (FTIR). The method involved the use of CHCl3 for on-line extraction of nicotine from tobacco, cigarette filters and tobacco ash from NH4OH alkalinized samples, and absorbance measurement of the characteristic band at 1316 cm(-1) in the stopped-flow mode, by obtaining the peak area in the range between 1334 and 1300 cm(-1). Under the best operational conditions, the procedure developed provided a detection limit of 0.05 mg mL(-1) nicotine, corresponding to 0.5 mg g(-1) in the solid sample, a relative standard deviation less than 2.5%, and a sampling frequency of 12 determinations h(-1). It can be concluded that nicotine migrates in the smoke mainstream towards the filter during the smoking process. The smoking of cigarettes and cigars is different. Nicotine is retained weakly by both tobacco and filter in the case of cigarettes, and strongly by the unburned tobacco in cigars. The incomplete smoking of cigars and cigarettes reduces nicotine intake and thus reduces the additive effect.

Speciation of chromium in natural waters by micropumping multicommutated light emitting diode photometry.

A simple and sensitive multicommutated flow procedure, implemented by employing a homemade light emitting diode (LED) based photometer, has been developed for the determination of chromium (VI) and total chromium in water. The flow system comprised a set of four solenoid micro-pumps, which were assembled to work as fluid propelling and as commutating devices. The core of the detection unit comprised a green LED source, a photodiode and a homemade flow cell of 100mm length and 2mm inner diameter. The photometric procedure for the speciation of chromium in natural waters was based on the reaction of Cr (VI) with 1,5-diphenylcarbazide. Cr (III) was previously oxidized to Cr (VI) and determined as the difference between total Cr and Cr (VI). After carrying out the assays to select the best operational conditions the features of the method included: a linear response ranging from 10 to 200mugl(-1) Cr (III) and Cr (VI) (r=0.999, n=7); limits of detection of 2.05 and 1.0mugl(-1) for Cr (III) and Cr (VI), respectively; a relative standard deviation lower than 2.0% (n=20) for a typical solution containing 50mugl(-1) Cr; a sampling throughput of 67 and 105 determinations per hour for total Cr and Cr (VI), respectively, and recovery values within the range of 93-108% for spiked concentrations of the order of 50mugl(-1).

Micropumping multicommutation turbidimetric analysis of waters.

A micropumping multicommutation manifold to perform turbidity determinations in waters is described. The procedure is based on the use of a combination of hydrazine sulfate and hexamethylenetetramine, to obtain an external standard of nephelometric turbidity units (NTU), which could compare the absorbance measurements at high wavelengths for samples with a calibration line obtained from a concentrated formazine standard diluted on-line. To minimize sample and reagent consumption and waste generation, the flow system was designed with two solenoid micro-pumps, one of them for the alternative introduction of the formazine standard and samples and the other one for the water carrier. The multicommutation approach makes possible the on-line dilution of a single standard to obtain the external calibration. The linear response was ranged up to 160NTU. The coefficient of variation was estimated as 1.6 and 3.2% for 10 and 100mm flow cell, respectively, for solutions containing 40NTU (n=10). Approximately, 60 determinations can be carried out per hour with limit of detection values of 1 and 0.1NTU, consuming only 160 or 240muL formazine solution and generating 1.8 or 2.0mL waste per determination, using measurement cells of 10 and 100mm optical pathlength, respectively. The procedure was successfully applied to 11 different water samples. Recovery studies were carried out and results obtained were between 97.5+/-0.2 and 100+/-1%. The development of a homebuilt light emitting diode (LED)-based portable flow analysis instrument was checked for in situ turbidimetric measurements, providing this equipment a LOD value of 0.09NTU working with a blue LED at 464nm and a LOD value of 0.1NTU working with an IR LED.

Evaluation of a multicommuted flow system for photometric environmental measurements.

A portable flow analysis instrument is described for in situ photometric measurements. This system is based on light-emitting diodes (LEDs) and a photodiode detector, coupled to a multipumping flow system. The whole equipment presents dimensions of 25 cm x 22 cm x 10 cm, weighs circa 3 kg, and costs 650 euro. System performance was evaluated for different chemistries without changing hardware configuration for determinations of (i) Fe(3+) with SCN(-), (ii) iodometric nitrite determination, (iii) phenol with sodium nitroprusside, and (iv) 1-naphthol-N-methylcarbamate (carbaryl) with p-aminophenol. The detection limits were estimated as 22, 60, 25, and 60 ng mL (-1) for iron, nitrite, phenol, and carbaryl at the 99.7% confidence level with RSD of 2.3, 1.0, 1.8, and 0.8%, respectively. Reagent and waste volumes were lower than those obtained by flow systems with continuous reagent addition. Sampling rates of 100, 110, 65, and 72 determinations per hour were achieved for iron, nitrite, phenol, and carbaryl determinations.

Multicommutation-NIR determination of Hexythiazox in pesticide formulations.

A multicommutated flow-system was designed in order to increase analytical throughput and for controlling thermal effects on the NIR spectra for determination of Hexythiazox in pesticide formulations. An on-line standard addition was carried out showing the versatility and repeatability of multicommutation for the on-line mixing and dilution of solutions. Results obtained for commercial samples were statistically comparable with those obtained by an HPLC-reference method. Multicommutation-NIR allows the analysis of 52 samples per hour, in front of the 30 samples per hour analyzed by the NIR-batch procedure and the 7 samples per hour analyzed by HPLC-reference method.

Sample preparation improvement in polycyclic aromatic hydrocarbons determination in olive oils by gel permeation chromatography and liquid chromatography with fluorescence detection.

The determination of 15 polycyclic aromatic hydrocarbons (PAHs) in olive oil samples has been improved in order to obtain a fast methodology with a low limit of detection through the combination of liquid-liquid extraction with acetonitrile and preparative gel permeation chromatography (GPC) prior to the injection of purified extracts into a C18 column. Acetonitrile-water was used as the mobile phase with a gradient from 50 to 95%, w/w, acetonitrile in 30 min. The oven temperature was maintained at 15 degrees C, and fluorometric detection was made at a fixed excitation wavelength of 264 nm and variable, optimal emission wavelength for each analyte ranging from 352 nm for 11-H-benzo(b)fluorene to 500 nm for indeno(1,2,3-cd)pyrene. Recovery for all the compounds studied varied from 75 to 111%, and limit of detection values from 0.05 ng/g for benzo(k)fluoranthene to 0.48 ng/g for indeno(1,2,3-cd)pyrene, corresponding to 0.09 ng/g benzo(a)pyrene. Results were compared with those obtained by liquid-liquid extraction followed by a cleanup on silica and a direct GPC treatment of oil samples diluted in dichloromethane, 2 other methodologies that are appropriate for quantifying PAHs in olive oils. However, the proposed method improves the determination limits, reduces the time of analysis, and provides a highly stable baseline for sample chromatograms.

Determination of phenols in waters using micro-pumped multicommutation and spectrophotometric detection: an automated alternative to the standard procedure.

An automated and greener spectrophotometric procedure has been developed for the determination of phenol in water at 700 nm. The method uses the reaction between phenol, sodium nitroprusside, and hydroxylamine hydrochloride in a buffered medium at pH 12.3. The flow manifold comprises four solenoid micro-pumps employed for sample and reagent introduction into the reaction coil and to transport the colored product formed to the detector. The linear dynamic range was 50-3,500 ng mL(-1) (R = 0.99997; n = 6) and the method provided a limit of detection (3sigma) of 13 ng mL(-1). The sampling throughput was estimated to be 65 measurements per hour and the coefficient of variation was 0.5% (n = 10) for a 1.0 microg mL(-1) phenol concentration. Recoveries of 92-105% were obtained for phenol determination in spiked water samples at concentration levels from 50 to 5,000 ng mL(-1). The use of multicommutation reduced the reagent consumption 25-fold, the sample consumption 225-fold, and the waste generation 30-fold compared with the batch procedure. The proposed method is an environmentally friendly alternative to the official 4-aminoantipyrine method since it avoids the use of chloroform.

Micro-pumping flow system for spectrophotometric determination of anionic surfactants in water.

A novel procedure has been developed for spectrophotometric determination of anionic surfactants in water using a solenoid micro-pump as fluid-propulsion device. The proposed method is based on substitution of methyl orange (MO) by anionic surfactants in the formation of an ion-pair with the cetyl pyridine ion (CPC+) at pH 5.0. The flow network comprised four solenoid micro-pumps which, under microcomputer control, enabled sample and reagent introduction, and homogenisation in the reaction zone. The system is flexible and simple to operate and control, and sensitive and precise. The analytical plot for the anionic surfactant was linear between 1.43x10(-6) and 1.43x10(-5) mol L(-1) (0.5 to 5.0 mg L(-1); R=0.997, n=5). The relative standard deviation was 0.8% (n=11) for a sample containing 5.74x10(-6) mol L(-1) (2 mg L(-1)) surfactant. The limit of detection was 9.76x10(-8) mol L(-1) (0.034 mg L(-1)) and the sampling throughput was 60 determinations per hour. The results obtained for washing-water samples were comparable with those obtained by use of the reference method, and no significant differences at the 95% confidence level were observed.

An environmentally friendly multicommutated alternative to the reference method for anionic surfactant determination in water.

It has been developed a fully mechanized procedure for the spectrophotometric determination of anionic surfactants in water expressed in terms of SDS concentration. The reference method, based on the reaction of SDS with methylene blue (MB) followed by extraction in chloroform, was mechanized in order to reduce the consumption of organic solvents. The system was based on the multicommutation approach and provided a 35 times reduction of the waste production without sacrificing the figures of merit of the method in terms of sensitivity and repeatability, for a dynamic linear range from 0.2 to 1.7mgl(-1). Results obtained for washing water samples were comparable with those obtained using the reference method and no significant differences, at 95% confidence level, were observed. Other useful characteristics are a solvent consumption of 0.7ml per determination, a sampling throughput of 40 determinations per hour, a relative standard deviation of 5.9% (n=10) for a sample containing 2x10(-6)moll(-1) (576mugl(-1)) surfactant and a limit of detection of 6.1x10(-9)moll(-1) (1.7mugl(-1)).

A portable and low cost equipment for flow injection chemiluminescence measurements.

A compact, reliable and low cost flow injection chemiluminescence system is described. The flow system consists of a set of solenoid micro-pumps that can dispense reproductive micro-volumes of solutions. The luminometer was based on a coiled cell constructed from polyethylene tubing that was sandwiched between two large area photodiodes. The whole equipment costs about US$ 750 and weights ca. 3 kg. Equipment performance was evaluated by measuring low concentrations of hydrogen peroxide by oxidation of luminol and for the determination of ammonium, based on its inhibition of the luminescence provided by the reaction of luminol and sodium hypochlorite. Linear responses were achieved within 1.0-80 micromol L(-1) H(2)O(2) and 0.6-60 micromol L(-1) NH(4)(+) with detection limits estimated as 400 nmol L(-1) H(2)O(2) and 60 nmol L(-1) NH(4)(+) at the 99.7% confidence level. Coefficients of variation were 1.0 and 1.8%, estimated for 20 micromol L(-1) H(2)O(2) and 15 micromol L(-1) NH(4)(+) (n=20), respectively. Reagent consumption of 55 microg luminol, effluent volume of 950 microL per determination and sampling rate of 120 samples per hour were also achieved.

A multicommutated flow system for determination of bismuth in milk shakes by hydride generation atomic fluorescence spectrometry incorporating on-line neutralization of waste effluent.

A highly sensitive method was developed for determination of bismuth in milk shakes by multicommutation hydride generation atomic fluorescence spectrometry (HG-AFS) based on off-line sonication for 10 min with aqua regia 8% (v/v) and on-line waste treatment. The instrumentation and chemistry variables were studied in order to provide the best performance. The limit of detection in the original samples, established for a probability level of 99.6% (k = 3), was 1.67 ng/g Bi. The method provides a fast alternative in control analysis with a sampling throughput of 72 h as compared with 31 h obtained by the classical continuous measurement. Additionally, multicommutation reduces waste generation by a factor of 2.6. The consumption of sample, reductant, and blank, as compared with continuous mode HG-AFS, was reduced 9.6, 4.5, and 13.3 times, respectively. To confirm the accuracy of the method, recovery studies were performed, and excellent agreement between multicommutation and continuous measurement-based values was obtained. Application of the developed methodology for bismuth determination in milk shake samples from the Spanish market provided concentrations ranging from 4.2 to 15.0 ng/mL, and good comparability with data obtained by continuous measurements after microwave-assisted total digestion of samples for a 95% probability level and 12 degrees of freedom was found.