Cost-effective formaldehyde assay platform for multi-sample analysis in one run based on pervaporation coupled with a biodegradable sensor and a simple heat control unit.

A novel, cost-effective platform using a biodegradable sensor and a simple heat control unit was proposed for multi-sample formaldehyde (FA) assay in one run based on pervaporation. The biodegradable sensor was a composite starch gel attached to paper and immobilized with a mixture of color agents of modified 4-amino-3-hydrazino-5-mercapto-1,2,4-triazol (AHMT). The sensor was situated on the cap of a vial that served for pervaporation. Two types of heat control units were specially designed using the concepts of aluminum block and water bath heating. With these two designs, multi-sample assays together with standard calibration could be performed in the same run under the same conditions. An FA solution was placed in the vial of the pervaporation unit. After a heating period, FA vapor would change the color of the sensor to purple due to the reaction between AHMT and FA. As a result, the color intensity was proportional to the FA concentration. The change of the color (green or G intensity) was monitored using a smartphone camera and image processing software. Factors affecting the sensitivity of the assay, pervaporation time, pervaporation temperature, FA solution volume, and humidity, were studied. Under the chosen condition, the developed procedure, with a calibration of G intensity = 7.93[FA] + 198, R2 = 0.98, was applied to analyze real samples of seafood and mushrooms available in local markets in Thailand. As there were 24 pervaporation units in the proposed platform, 5 working standards and 9 samples with duplicates could be included in a 1-run assay either in the laboratory or on-site. The developed assay offers green chemical analysis with a simple, cost-effective approach. This serves the UN-SDGs of #2, #3, #7, #10, and #12.

Green Downscaling of Solvent Extractive Determination Employing Coconut Oil as Natural Solvent with Smartphone Colorimetric Detection: Demonstrating the Concept via Cu(II) Assay Using 1,5-Diphenylcarbazide.

Coconut oil as a natural solvent is proposed for green downscaling solvent extractive determination. Determination of Cu(II) using 1,5-Diphenylcarbazide (DPC) was selected as a model for the investigation. Cu(II)-DPC complexes in aqueous solution were transferred into coconut oil phase. The change of the color due to Cu(II)-DPC complexes in coconut oil was followed by using a smartphone and image processing. A single standard concept was used for a series of Cu(II) standard solutions. A downscaling procedure using a 2 mL vial provided a calibration: color intensity = -142 [Cu(II)] + 222, (R2 = 0.98), 10% RSD. Using a well plate, a calibration was: color intensity = 61 [Cu(II)] + 68 (R2 = 0.91), 15% RSD. Both were for the range of 0-1 ppm Cu(II). Application of the developed procedure to water samples was demonstrated. The developed procedures provided a new approach of green chemical analysis.

Modified Natural Rubber as a Simple Chemical Sensor with Smartphone Detection for Formaldehyde Content in a Seafood Sample.

A new biodegradable platform-based sensor for formaldehyde assay is proposed. Natural rubber latex was modified to polylactic acid-chloroacetated natural rubber polymer blend sheets. The polymer blend sheet was grafted using a water-based system with amine monomers as a platform, with a spot exhibiting positive polarity for immobilizing with anionic dye (Acid Red 27). The sensor was exposed to formaldehyde. The color intensity of the dye on the sensor spot would decrease. Using a smartphone with image processing (via ImageJ program), the color intensity change (∆B) could be followed. A linear calibration, ∆B intensity = 0.365 [FA] + 6.988, R2 = 0.997, was obtained for 10-150 mM FA with LOD and LOQ at 3 and 10 mM, respectively (linear regression method). The precision was lower than 20% RSD. Application to real seafood samples was demonstrated. The ready-to-use sensor with the proposed method was cost-effective, was portable for on-site analysis, and demonstrated green chemical analysis.

Lead Assays with Smartphone Detection Using a Monolithic Rod with 4-(2-Pyridylazo) Resorcinol.

A monolithic rod of polyurethane foam-[4-(2-pyridylazo) resorcinol] (PUF-PAR) as a simple chemical sensor for lead assays with smartphone detection and image processing was developed. With readily available simple apparatus such as a plastic cup and a stirrer rod, the monolithic PUF rod was synthesized in a glass tube. The monolithic PUF-PAR rod could be directly loaded by standard/sample solution without sample preparation. A one-shot image in G/B value from a profile plot in ImageJ for a sample with triplicate results via a single standard calibration approach was obtained. A linear single standard calibration was: [G/B value] = -0.038[µg Pb2+] + 2.827, R2 = 0.95 for 10-30 µg Pb2+ with a limit of quantitation (LOQ) of 33 µg L-1. The precision was lower than 15% RSD. The proposed method was tested by an assay for Pb2+ contents in drinking water samples from Bangkok. The results obtained by the proposed method agree with those of ICP-OES and with 100-120% recovery, demonstrating that the method is useful for screening on-site water monitoring.

Determination of Lead Employing Simple Flow Injection AAS with Monolithic Alginate-Polyurethane Composite Packed In-Valve Column.

A simple flow injection FlameAAS for lead determination with an alginate-polyurethane composite (ALG-PUC) monolithic in-valve column has been developed. The ALG-PUC monolithic rod was prepared by mixing methylene diphenyl diisocyanate with polyol and sodium alginate with the ratio of 2:1:1 by weight for a 5 min polymerization reaction. It was then put into a column (0.8 cm i.d × 11 cm length) situated in a switching valve for the FI set up. A single standard calibration could be obtained by plotting the loaded µg Pb2+ vs. FI response (absorbances). The loaded µg Pb2+ is calculated: µg Pb2+ = FRload × LT × CPb2+, where the FR load is the flow rate of the loading analyte solution (mL min-1), LT is the loading time (min), and CPb2+ is the Pb2+ concentration (µg mL-1). A linear calibration equation was obtained: FI response (absorbances) = 0.0018 [µg Pb2+] + 0.0032, R2 = 0.9927 for 1-150 µg Pb2+, and RSD of less than 20% was also obtained. Application of the developed procedure has been demonstrated in real samples.

Down-scaling Sample Preparation Using Polyurethane Foam and Colorimetric Technique for the Chromium Assay in Accessories.

A simple alternative colorimetric assay of chromium in accessories is proposed. A miniature part of a sample was dissolved by acid digestion. With dithiooxamide (DTO) complexes, metal interferences are retained in polyurethane foam synthesized in the lab, while chromium ions present in the eluate. A 100-µL volume of the eluate was measured for the absorbance using a handy spectrometer. The proposed method was successful for chromium assay and the results obtained agreed with the reference (FAAS) method. The amounts of chromium in accessories were found in the range of 100 to 390 mg g-1.

Green assay of anionic surfactant via ion-association with methylene blue sorbed on polyurethane foam monolithic rod and using a smartphone.

Anionic surfactant as sodium dodecyl sulfate (SDS) can be assayed by using methylene blue (MB). The ion-association of SDS-MB can be extracted solventless but sorbed on a specified polyurethane foam (PUF) monolithic rod, prepared in the lab by mixing polyether with methylene diphenyl diisocyanate (MDI). The blue product (the ion-association of SDS-MB) on the rod can be followed by a smartphone (iPhone 6S). With a set of conditions, a single standard calibration can be applied. The proposed green analytical procedure can be employed for on-site assay. Application to real water samples was demonstrated.

Removal of copper and iron by polyurethane foam column in FIA system for the determination of nickel in pierced ring.

Polyurethane foam (PUF) mini-column was used to eliminate copper and iron for the determination of nickel in pierced rings. The PUF mini-column was connected to FIA system for on-line sorption of copper and iron in complexes form of CuSCN(+) and FeSCN(2+). For this season, the acid solution containing a mixture of Ni(II), Fe(III), Cu(II) and SCN(-) ions was firstly flew into the PUF column. Then, the percolated solution which Fe(III) and Cu(II) ions is separated from analysis was injected into FIA system to react with 4-(2-pyridylazo) resorcinol (PAR) reagent in basic condition which this method is called pH gradient technique. The Ni-PAR complexes obtained were measured theirs absorbance at 500 nm by UV visible spectrophotometer. In this study, it was found that Cu(II) and Fe(III) were completely to form complexes with 400 mmol/L KSCN and entirely to eliminate in acidic condition at pH 3.0. In the optimum condition of these experiments, the method provided the linear relationship between absorbance and the concentration of Ni(II) in the range from 5.00 to 30.00 mg/L. Linear equation is y=0.0134x+0.0033 (R(2)=0.9948). Precision, assessed in the term of the relative standard deviation, RSD, and accuracy for multiple determinations obtained in values of 0.77-1.73% and 97.4%, respectively. The level of an average amount of Ni(II) in six piercing rings was evaluated to be 14.78 mg/g.