Wet Digestion Research Articles

Simple Method for Calcium Determination in Crude Oil Emulsion Using Digital Image Colorimetry

A portable device for digital image colorimetry (DIC) is reported for the determination of Ca in crude oil emulsions. ASTM D4807 was used for sample preparation for the isolation of saline species containing Ca. DIC was evaluated based on the complexation reactions with Ca using calcein, murexide, and calcon. Partial least squares (PLS) provided the best determination coefficients (higher than 0.990) for all complexing reagents. Significant interference of Mg was observed for the determination of Ca using calcein. PLS models with the lowest root mean square error of cross validation (RMSECV) values were obtained for murexide and calcon for a concentration of 0.250 mmol L−1 at pH of 13. The best conditions for camera focal length were 11 and 2 mm for murexide and calcon. For light intensity, the optimized conditions for murexide and calcon was 180 lux. Stabilities of color complexes over the time were 30 and 15 min for murexide and calcon, respectively. DIC/murexide provided the lowest root mean square error of prediction (RMSEP) and a linear response was observed from 0.5 to 10 mg L−1 Ca and the relative standard deviation (RSD) was lower than 10%. Significant differences were not observed between the results obtained by DIC/murexide and those obtained by microwave-assisted wet digestion (MAWD) with determination by inductively coupled plasma-optical emission spectrometry (ICP-OES). A limit of quantification of 0.50 mg kg−1 Ca were obtained using DIC/murexide. This approach is an alternative and useful method for the determination of Ca in crude oil samples, with advantages of miniaturization, low cost, and ease of operation.

Accurate Boron Determination in Tourmaline by Inductively Coupled Plasma Mass Spectrometry: An Insight into the Boron-Mannitol Complex-Based Wet Acid Digestion Method.

Tourmaline, a boron-bearing mineral, has been extensively applied as a geothermometer, provenance indicator, and fluid-composition recorder in geological studies. In this paper, the decomposition capability of an HF-HNO3-mannitol mixture for a tourmaline sample was investigated in detail for the first time, and a wet acid digestion method based on the boron-mannitol complex for accurate boron determination in tourmaline by inductively coupled plasma mass spectrometry (ICP-MS) was proposed. With a digestion temperature of 140 °C, tourmaline samples of 25 mg (±0.5 mg) can be completely decomposed by a ternary mixture, which consisted of 0.6 mL of HF, 0.6 mL of HNO3, and 0.7 mL of 2% mannitol (wt.), via a continuous heating treatment of 36 h. Following gentle evaporation at 100 °C, the sample residues were re-dissolved using 2 mL of 40% HNO3 solution (wt.) and diluted to about 2.0 × 105-fold by a two-step method using 2% HNO3 solution (wt.). The boron contents in a batch of parallel tourmaline samples were then determined by ICP-MS, and results showed that the boron concentration levels were in a range of 3.20-3.44% with determination RSDs less than 4.0% (n = 5). It was found that the boron concentrations obtained at the mass of 10B were comparable with results from the measurements at the mass of 11B. This revealed that the usage of 2% mannitol with a quantity as high as 0.7 mL in this developed approach did not exhibit significant effect on the quantification accuracy of boron at the mass of 11B. It was also found that the processes including fluoride-forming prevention and fluoride decomposition deteriorated the boron-reserving efficiency of mannitol for tourmaline, causing the averaged boron contents to vary from 2.25% to 3.57% (n = 5). Furthermore, the stability of the boron-mannitol complex under 185 °C by applying the laboratory high pressure-closed digestion method was evaluated, which showed that there existed a 60.36% loss of boron compared to that under 140 °C by using this proposed approach. For this ternary mixture, the tourmaline decomposing efficiency was found to be weakened prominently using 100 °C as the digestion temperature, and tourmaline powders can be observed even after 72 h of continuous heating with B contents within 1.09-1.23% (n = 5). To assess the accuracy of this developed method, the boron recovery of anhydrous lithium tetraborate was studied. It was found that the boron recoveries were within 96.59-102.12% (RSD < 1%, n = 5), demonstrating the accuracy and reliability of this proposed method, which exhibits advantages of high B preserving efficiency, and giving concentration information of both B and trace elements simultaneously. By applying such a boron-mannitol complex-based wet acid digestion method, the chemical composition of boron and trace elements in three tourmaline samples from different pegmatites were quantified, which provided valuable information to distinguish regional deposits and the associated evolution stages.

Two-step extraction for the evaluation of metal-organic framework impregnated materials.

Metal-organic frameworks (MOFs) are widely used for gas adsorption, separation, and sensing materials. In most cases, MOFs are not used in their crystal form but as impregnated materials because the fine crystals result in high-pressure drops. One key characteristic of MOF-impregnated materials is the amount of MOF in the material. This is evaluated using the wet digestion method; however, it is limited to determining only the metal content. Moreover, some metal, denoted as free metal, will not react with ligands to form MOFs. Additionally, it is crucial to determine the ligand amount, which cannot be determined using wet digestion. In the present study, a two-step extraction method for copper (II) benzene-1,3,5-tricarboxylate (Cu-BTC MOF) impregnated materials was developed to determine the MOF formed and free metals and ligands. Various solvents were applied to evaluate the extraction efficiencies. The results led to the selection of ethanol (EtOH) for extracting free Cu2+ and BTC, while 0.3M HNO3 was chosen to extract MOF-formed Cu2+ and BTC. The MOF-impregnated sample material was first extracted using EtOH and then 0.3M HNO3. The Cu2+ and BTC in the obtained extract solutions, as well as EtOH and HNO3, were analyzed using flame atomic absorption spectroscopy and high-performance liquid chromatography, respectively. In standard addition tests, free and MOF-formed Cu2+ and BTC were quantitatively extracted from MOF-impregnated materials. The developed two-step analysis method was successfully applied to Cu-BTC-impregnated materials used in gas sensing.

The analytical assessment of metal contamination in industrial soils of Saudi Arabia using the inductively coupled plasma technology

Abstract In response to significant demand for evaluating the presence of heavy elements in diverse industrial areas of Saudi Arabia, the study sought to analyze the concentration ratios of 16 elements across 11 different artificial soil types in the industrial zones situated in Riyadh, Sudair, and Al-Ahsa. To achieve this objective, the research utilized the wet digestion technique and employed an ICPE-9000 spectrophotometer for quantifying element concentrations. The study had a dual focus: initially, it sought to gauge the pollution attributed to heavy metals arising from enrichment processes, and second, it evaluated the geographical accumulation of pollutants in the soil. The results revealed varying concentration levels of heavy metals across the industrial areas under study. Specifically, the soil in the Yanbu region exhibited the highest concentration values for iron, manganese, zinc, chromium, nickel, copper, cobalt, cadmium, and beryllium. In contrast, the soil in the industrial area of Riyadh had the highest concentration values for lead, mercury (Hg), molybdenum (Mo), selenium (Se), and arsenic (As). Furthermore, the highest concentration of Cd was recorded in the soil of the Jubail region. Conversely, the soil in the Al-Ahsa region displayed the lowest concentration levels for these heavy metals. The conductivity of the synthetic soil ranged from 0.47 to 6.07 μS·cm−1, accompanied by a pH range of 6.6–8.6. The results emphasized the fluctuations in element concentrations, indicating significant implications for both environmental and human health. Notably, around 20% of the gathered samples showed concentrations of heavy elements like Mo, As, Hg, and Se that surpassed the allowable limits.

Health Risk Assessment of Potentially Toxic Elements Contamination of Commonly Consumed Fruits in Bahir Dar Town, Northwest Ethiopia.

Excess accumulation of potentially toxic elements in frequently consumed fruits is a serious threat to human health. The aim of this study was to determine the levels of cadmium (Cd), chromium (Cr), copper (Cu), and lead (Pb) and to estimate the noncarcinogenic and carcinogenic health risks associated with their daily intake in commonly consumed fruits in Bahir Dar town, northwest Ethiopia. Three types of fruits (mango, banana, and orange) were collected using a simple random sampling method from open markets in Bahir Dar town. Wet digestion was used, and the concentration of potentially toxic elements was analyzed in the edible portion of the fruits. The average daily intake (ADI), hazard quotient (HQ), hazard index (HI), and target cancer risk (TCR) were estimated to assess the human health risks posed by the intake of those potentially toxic elements from the consumption of the studied fruits. The concentrations of Cr and Cu were lower than the maximum limit of normal values in mango, banana, and orange. However, the Pb and Cd concentrations (mg kg-1) in mango were 0.576 and 1.771, respectively, which exceeded the FAO/WHO recommended permissible limits of 0.3 mg kg-1 and 0.2 mg kg-1, respectively. The ADI of potentially toxic elements was found to be lower than the maximum permitted tolerable daily intake in the studied fruits, and the HI values (mgday-1 kg-1) of all studied potentially toxic elements were lower than one in banana and orange, except mango (3.69). The TCR values for Pb, Cd, and Cr in banana and orange were 7.16 × 10-4 and 7.15 × 10-4, respectively, which exceeded the recommended threshold risk limit (>1 × 10-4), but in mango (1.71 × 10-3), the level was above the moderate risk limit (>1 × 10-3). However, the TCR value in all the studied fruits was above the recommended safe limit (ILCR < 1 × 10-6) set by the United States Environmental Protection Agency (US-EPA). The study revealed that the consumption of mango fruit in the studied areas may pose noncarcinogenic and carcinogenic adverse health effects.

Development of a wet digestion method for the analysis of metal soap in fat, oil, and grease deposits using the Taguchi method

Conventional methods for evaluating lipid-based metal salts in fats, oils and grease (FOG) deposits often fall short in assessing the efficiency of grease interceptors for food service establishment wastewater, primarily due to their inadequate specificity for fatty acid (FA) metal soaps. To address this issue, this study introduces a wet acid digestion method developed for the accurate analysis of metal soap content in FOG samples. The Taguchi experimental design method was used to determine the optimal conditions for digestion including temperature, contact time, solid/liquid ratio and type of acid mixture with the aim of more accurately quantifying metal salt concentrations. This work focused on identifying the most effective acid combinations for digesting FOG to enable analysis of commonly found metals. Extensive comparisons revealed that HNO3:H2SO4:H2O2 (1:2:1) and HNO3:H2O2 (1:3) were particularly effective at 180°C for 16 h due to their significant oxidation potential. The HNO3:H2O2 (1:3) mixture yielded the highest concentrations of Ca, Mg, Na, and K of 296.38±0.66, 54.95±1.01, 247.65±2.27, and 46.09±3.44 mg/g, respectively, aligning with the stringent optimisation principles of the Taguchi method. A one-way ANOVA test validated significant variances in metal contents (p < 0.005), and a t-test indicated a notably higher concentration of Ca compared to other metals. The study presents a sophisticated approach to evaluating the FA metal soap content of FOG ensuring enhanced accuracy and precision compared to established methods.

Some biological activities and element levels of Lycoperdon pratense

Mushrooms are natural products with many biological activities. In this study, antioxidant, antimicrobial, anticholinesterase activities and element levels of Lycoperdon pratense Pers. were determined. In this context, the mushroom was extracted with ethanol in a soxhlet device. Antioxidant potential was determined using Rel assay kits. Antimicrobial activity was determined using the agar dilution method. Antialzheimer activity was determined by acetyl- (AChE) and butyrylcholinesterase (BChE) potentials. The levels of elements accumulated in the mushroom were scanned using the wet digestion method. As a result of the analysis, the TAS value of the mushroom was measured as 2.589 ± 0.118 mmol Trolox equiv./L, the TOS value was 10.360 ± 0.197 µmol H2O2 equiv./L and the OSI value was 0.401±0.013. The mushroom extract was found to have high activity against bacteria. It was determined that the extract had an effect against microorganisms at concentrations between 50-400 μg/mL. It was determined that the anti-AChE IC50 value of the mushroom extract was 14.48 ± 0.80 μg/mL and the anti-BChE IC50 value was 23.10±1.21 μg/mL. It is also thought that it can be used as an indicator in terms of element levels within the mushroom. As a result, it was determined that the mushroom has antioxidant, antimicrobial and antiallergic potential.

Comparative Analysis of Soil Phosphorus Determination Methods and Their Correlation with Plant Phosphorus in Standing Wheat Crops

This study compared the accuracy of various soil phosphorus assessment methods to measure the soil's ability to supply plants with phosphorus over a brief period in the field. Twenty individual soil samples were collected from a standing wheat (Triticum aestivum L) crop at depths ranging from zero to twenty centimeters. An equivalent plant spike sample was also procured from the soil sampling fields. In comparison to the wet acid digestion method used to detect phosphorus in plants, several methods were utilized to assess phosphorus in the soil, including resin extractable phosphorus, AB-DTPA extractable phosphorus, NaHCO3 extractable phosphorus, water-soluble phosphorus in suspension, and paste. The levels of variation and deficiency of phosphorus, which were found by different methods followed different patterns as shown by the fact that, AB-DTPA method finds phosphorus deficiency in 20% of samples while on the other hand, Olsen method finds phosphorus deficiency in 80% of samples. Even with such a small sampling area, none of the procedures showed a significant correlation with any other method that might account for uneven variation among the samples when determined by distinct procedures. However, corrections were observed to a certain degree between ammonium bicarbonate-diethylenetriaminepentaacetic acid (AB-DTPA) extractable and resin, as well as between other procedures and the plant P scale. Both resin and ammonium bicarbonate-diethylenetriaminepentaacetic acid (AB-DTPA) had a strong relationship with plant phosphorus, with the former showing a significant correlation of 0.48 and 0.21, respectively. Hence Resin and AB-DTPA methods are recommended for the determination of phosphorus under certain soil and plant conditions.

Health Risk Assessment Of Potentially Toxic Element Concentrations In Fish And Vegetables Obtained From Six Selected Dams In Osun State, Nigeria

This study aimed to assess the levels of certain heavy metals in tilapia fish (Oreochromis niloticus), as well as vegetables, and to evaluate the potential health risks associated with the presence of toxic elements from Dec. 2019 to June 2023. A total of 60 tilapia fish, 12 okra (Abelmoschus esculentus) and 12 bitter leaf (Vernonia amygdalina) from six major dams in Osun State were prepared for analysis using wet digestion with aqua-regia. The concentrations of heavy metals were measured using an Atomic Absorption Spectrophotometer (Shimadzu AA-630). The health risk associated with fish consumption was estimated using various parameters. Statistical analysis was conducted using the Statistical Package for Social Sciences (SPSS) version 16.0. The concentrations of micro elements followed the order of Fe &gt; Zn &gt; Cu &gt; Mn in decreasing concentrations. These concentrations exceeded the permissible limits set by the World Health Organization (WHO) for Ni, Cd, Pb, and Cr, which are 0.6, 0.3, 0.3, and 0.7 mg L-1, respectively. The results obtained for okra and bitter leaf were within the limits established by the World Health Organization (WHO). Therefore, the presence of these metals indicates the need for close environmental monitoring of the six selected dams.

Analysis of heavy metals in barley dust and health risk assessment in Malt Factory, Ethiopia

ABSTRACT The recent rapid industrialisation in Ethiopia has become a critical concern from pollution of the environment, including contamination by heavy metals. The purpose of this study was to determine heavy metals in barley dust and evaluate the health risks associated with workers in Gondar Malt Factory, Ethiopia. For this, the concentrations of some potentially toxic heavy metals (Cu, Ni, Cd, Cr, Pb, Zn and Fe) were determined in samples from four different production lines (barley receiving, aspiration, grading, and final product dispatch lines). Prior to metal analysis by flame atomic absorption spectroscopy, a 1 g barley dust was subjected to an optimised wet digestion procedure using 8 mL HNO3, 4 mL HClO4 heated for 4 h at 250°C. The average concentration (mg/kg) of the metals was found to be in the range of 3.3‒4.8 Cu, 4.7‒9 Cd, 9.5‒11.5 Pb, 3063‒3463 Fe, 17.7‒24.7 Ni and 148‒180 Zn. Chromium was below the detection limit of the method in all the samples. The results showed that the barley dust contained significant concentration of the heavy metals. However, the study has found the absence of non-carcinogenic risk, from the analysed heavy metals in the barley dust, through both dermal contact and inhalation routes of exposure. Similarly, no carcinogenic risk was associated with the analysed heavy metals in the barley dust, except for Pb. Hence, proper management control system needs to be implemented to minimise chronic health risks from exposure to Pb.

Stormwater runoff microplastics: Polymer types, particle size, and factors controlling loading rates

Stormwater runoff is a pathway of entry for microplastics (MPs, plastics <5 mm) into aquatic ecosystems. The objectives of this study were to determine MP size, morphology, chemical composition, and loading across urban storm events. Particles were extracted from stormwater samples collected at outfall locations using wet peroxide oxidation and cellulose digestion followed by analysis via attenuated total reflectance (ATR) FTIR. Concentrations observed were 0.99 ± 1.10 MP/L for 500–1000 μm and 0.41 ± 0.30 MP/L for the 1000–5000 μm size ranges. Seventeen different polymer types were observed. MP particle sizes measured using a FTIR-microscope camera indicated non-target size particles based on sieve-size classification, highlighting a potential source of error in studies reporting concentration by size class. A maximum MP load of 38.3 MP/m2 of upstream catchment was calculated. MP loadings had moderate correlations with both rainfall accumulation and intensity (Kendall τ = 0.54 and 0.42, respectively, both p ≤ 0.005). First flush (i.e. rapid wash-off of pollutants from watershed surfaces during rainfall early stages) was not always observed, and antecedent dry days were not correlated with MP abundance, likely due to the short dry periods between sampling events. Overall, the results presented provide data for risk assessment and mitigation strategies.

From grass to gas and beyond: Anaerobic digestion as a key enabling technology for a residual grass biorefinery

Roadside grass clippings hold potential as a sustainable source of bioenergy as they do not compete with crops for land use, and are only partially utilized for low-value applications. In this study, we proposed using roadside grass as a sole feedstock for anaerobic digestion (AD) in three different settings, and assessed the potential of producing biomaterials and fertilizers from grass-based digestate. Wet continuous digestion at pilot scale and dry batch digestion at pilot and large scales resulted in biogas yields up to 700 Nm3.t−1 DOM with a methane content of 49–55 %. Despite promising results, wet AD had operational problems such as clogging and poor mixing; once upscaled, the dry digestion initially also presented an operational problem with acidification, which was overcome by the second trial. Digested grass fibers from the pilot dry AD were processed into biomaterials and performed similarly or better than the undigested fibers, while around 20 % performance reduction was observed when compared to reference wood fibers. A mass balance indicated reduced fiber recovery when higher biogas production was obtained. The liquid fraction from the pilot dry AD was characterized for its nutrient content and used as a biofertilizer in another study. In contrast, the leachate collected from the large-scale dry AD had a low nitrogen content and high chloride content that could hinder its further use. Finally, a regional market analysis was conducted showing that the biocomposites produced with the available grass fibers could substitute at least half of the current European market based on our results.

The Impact of Raw and Composted Food Waste Anaerobic Digestates on Soil Organic Carbon Management: A Pot Study

PurposeEver increasing food waste production has promoted anaerobic digestion and composting for its proper management, producing a relevant amount of recycled organic waste (OW) for possible agricultural uses. However, little is known regarding soil carbon management using this type of OW.MethodsIn this study, an anaerobic digestate from the wet digestion of food waste (WETD), and one from the dry-batch process (DRYD), along with their respective composts (WETC and DRYC), were utilized in a pot test over two growing cycles (84 + 84 days), with and without mineral nitrogen (N) fertilization, and were compared with a bio-waste compost (BWC) and a chemical reference (Chem). At the end of the two growth cycles (days 84 and 168), the ryegrass dry biomass (DW) and the N uptake were assessed.ResultsThe pot soil was analyzed for soil organic carbon (SOC) and the potassium permanganate (KMnO4) oxidizable fraction (CL) as well as δ13C and Δ13C. At day 84, the SOC (g kg− 1) was the highest in DRYD and DRYC (8.53) > WETD and WETC (7.71) = BWC (7.86) > Chem (6.68), and performed similarly at day 168. At day 84, the carbon management index (CMI) was > 100% in all the organic treatments in comparison with Chem, except for WETD. At day 168, a + 30% CMI was registered in WETD and WETC> BWC> DRYD and DRYC> Chem.ConclusionThis pattern was related to a generally marked δ13C depletion being confirmed by Δ13C, thus indicating the conservation of the carbon form compost, this very likely being related to the preferential lignin accumulation.

Potential Toxic Metal Concentration and Risk Assessment in Agricultural Soil and Lentil Crop (Lens culinaris Medik) in Dawunt Woreda, Northwest Wollo, Ethiopia.

Health implications for the population due to consuming contaminated crops have been a great concern worldwide. This study aimed to measure the levels of potential toxic elements in lentils and their growing soil in Dawunt Woreda, Ethiopia. Accordingly, 15 soil samples along with the lentil samples were collected to measure the level of potential toxic elements, including chromium (Cr), manganese (Mn), iron (Fe), lead (Pb), cadmium (Cd), copper (Cu), and cobalt (Co), by using an inductively coupled plasma optical emission spectrometer and for assessing the potential ecological and human health risk. The wet digestion method using aqua regia (HCl/HNO3 3 : 1) was employed for soil and lentil sample preparation. The mean concentrations of Fe, Mn, Co, Cu, Cd, Pb, and Cr in the lentil sample were 60.4, 9.68, 0.75, 5.7, 0.25, 0.9, and 1.15 mg/kg, respectively. In soil, the mean concentrations of Fe, Mn, Co, Cu, Cd, Pb, and Cr were 649, 19.9, 3.32, 40.0, 15.2, 1.83, and 69.1 mg/kg, respectively. All of the potential toxic metals in agricultural soil and lentil samples were found to be below the reference level set by the World Health Organization, except Cd, in the soil samples. Five single metal and three cumulative pollution index parameters were employed for the data and results showed that Fe, Cu, and Cr moderately pollute the soil and are highly contaminated by Cd. The cumulative pollution indices also confirmed that the extent of soil pollution varied from highly contaminated to moderate contamination. The possible health risks at various exposure routes have also been estimated. The single-metal and cumulative-metals health risks (cancer and noncancer) of adults and children due to chronic exposure to soil and consumption of lentils were estimated using the health quotient and health index values as per the United States Environmental Protection Agency guidelines. Thus, the results revealed no significant adverse health risks (cancer and noncancer) for adults and children. Therefore, the inhabitants in the study area have no significant health impacts due to either the consumption of lentil crops or exposure to agricultural soil particles.

Occurrence and abundance of microplastics and plasticizers in landfill leachate from open dumpsites in Sri Lanka

This is the first attempt that investigate the abundance of plasticizers in leachate sediment in the scientific literature, alongside the debut effort to explore the abundance of microplastics and plasticizers in landfill leachate and sediment in Sri Lanka. Microplastics in sizes ranging from ≥2.0–5.0, ≥1.0–2.0, and ≥ 0.5–1.0 mm were extracted from the leachate draining from ten municipal solid waste open dump sites and sediment samples covering seven districts. Microplastics were extracted by density separation (Saturated ZnCl2) followed by wet peroxide digestion and the chemical identification was conducted by Fourier Transform Infrared spectroscopy. Plasticizers were extracted to hexane and analyzed by high-performance liquid chromatography. The total mean microplastic abundance in leachate was 2.06 ± 0.62 mg/L whereas it was 363 ± 111 mg/kg for leachate sediments. The most frequently found polymer type was polyethylene (>50%), and white color was dominant. The average concentration of bisphenol A (BPA), benzophenone (BP) and diethyl-hydrogen phthalate (DHEP) in leachate was 158 ± 84.4, 0.75 ± 0.16 and 170 ± 85.8 μg/L respectively. Furthermore, BP and DHEP in leachate sediment was 100 ± 68.3 and 1034 ± 455 μg/kg respectively. As landfill leachate is directly discharged into nearby surface and groundwater bodies that serve as sources of drinking water, the study highlights the potential concerns of microplastic and plasticizer exposure to the surrounding Sri Lankan community through consumption of contaminated drinking water. Therefore, there is a timely need of develop the effective waste management and pollution control measures to minimize the possible threats to both the environment and human health.

A Clinico-epidemiological Study to Evaluate the Status of Iodine Deficiency Disorder in North 24 Pargana District of West Bengal

Background: Iodine deficiency disorders (IDD) being major public health problems in India, including WestBengal needs to be continuously monitored through recommended methods and indicators.Present study is aiming to assess the total goiter rate, urinary iodine excretion, iodine content of salts at households’ level among primary school children and to find association with the socio-demographic characteristics of the study population.Method: A school-based, cross-sectional study was conducted during March 2019 to August 2019 among 540schoolchildren of class three and four. Goiter was assessed by standard palpation technique, urinary iodineexcretion (UIE) was analyzed by wet digestion method and salt samples were tested by spot iodine testing kits.The total goiter rate (TGR) was 10.56 %. About 97.22 % of the salt samples tested were adequately iodized. Though consumption of iodized salt was adequate irrespective of socio demographic characteristics; goiter prevalence was significantly different with respect to mother’s education level. Median urinary iodine excretion was found to be with in normal range. Lastly, a comparison is made between indicators of IDD over years which showed significant fall of TGR % of North 24 Pgs and a significant increase of adequately iodized salt consumption from 2004 to 2019.Conclucion: 2019 resurvey of North 24 parganas indicates that the district achieved close to the goal of NIDDCP i.e. prevalence of IDD should be below 10%. It also proved that universal salt iodinization program has increased the household’s iodine consumption above national goal of 91.2%. Goiter prevalence is found to be less in children whose mother attend the education up to 12th standard and beyond.

Particle Size of Calcium Hydroxide Prepared by Wet Digestion: Influencing Factors and Mechanism

AbstractThe wet dissolution process of lime is an effective approach for synthesizing calcium hydroxide. Process parameters and additives exert influence on the product particle. Among the process parameters, lime particle size, reaction temperature, and time have a significant impact on product particle size, followed by liquid‐solid ratio and stirring speed. The experiment proved that reaction time affects product particle size by affecting the crystal growth, while other process parameters affect the particle size by affecting the ion diffusion behavior. In terms of inorganic additives, Ca(OH)2 has minimal effect on product particle size; however, NaOH and CaCl2 can significantly enhance it with a greater dose leading to a larger increase. The experiment proved that Ca(OH)2, NaOH, and CaCl2 influence particle size through their impact on ion diffusion behavior. Regarding organic additives, soluble starch exhibits the greatest effect on product size followed by triethanolamine and polyvinylpyrrolidone K30. The experiment proved that soluble starch, triethanolamine, and polyvinylpyrrolidone K30 affect product particle size by influencing its crystallization position. Finally, an ultrafine slurry of calcium hydroxide was prepared using the lime wet digestion method based on the aforementioned research, with particle size distribution characterized by D10, D50, and D90 values of 0.303, 1.750, and 4.534 µm respectively.

Comparisons of Different Digestion Methods for Heavy Metal Analysis from Fruits

Fruit juices are produced in home or industrially from horticultural crops by pressing the liquid part. They are rich in sugar, vitamins, and minerals like iron, copper, potassium, folate minerals, and vitamins A, B, and C which are essential for giving the body the nutrients it needs to stay healthy since fruits contain vital mineral components like copper (Cu), iron (Fe), and manganese (Mn), which is necessary for human growth and respiration. However, they may have heavy metals which may poison health risk and toxic even the presence is in little amount. Since fruit juices doesn’t pass through different processes, except extracting the liquid from the fruits of vegetables contamination and heavy metals affect human health. Before determination of heavy metals different procedures are applied for analysis. Digestion is the key component for determination of heavy metals from different samples. In this paper we are concerned on wet digestion methods for analysis. Closed system wet digestion is preferred since it lower the risk of contamination. There are different wet digestion types. Some of them are conventional wet digestion, ultraviolet digestion, ultrasound-assisted acid decomposition, conventional heating, microwave-assisted wet digestion etc. From thus, microwave digestion procedure was preferred for the digestion of samples for determination of heavy metals due to its ability to oxidize almost all of the organic samples.

Microwave-induced combustion for further determination of potentially toxic elements in honey by ICP-MS.

Microwave-induced combustion (MIC) was proposed in this study for honey decomposition aiming for As, Cd, Hg, and Pb determination by inductively coupled plasma mass spectrometry (ICP-MS). Sample mass (up to 1.0g), absorbing solution (0.5 to 14.4mol L-1 HNO3, and H2O), heating program, and combustion aids were evaluated. The Eurachem guidelines were used for method validation. The proposed method enabled combustion of a high sample mass (0.8g of honey, with 0.4g of microcrystalline cellulose and 100 µL of 6mol L-1 NH4NO3) using 6mL of an absorbing solution consisting of 1mol L-1 HNO3, which resulted in low residual carbon in solution (< 25mg L-1). Honey samples from different geographical origins were analyzed. Results showed no significant difference in comparison to other two microwave decomposition methods, based on microwave-assisted wet digestion with single reaction chamber (MAWD-SRC) and microwave-assisted wet digestion (MAWD). Standard addition experiments resulted in recoveries higher than 98%. The limits of detection ranged from 1.10 (As) to 4.60ngg-1 (Pb). In addition to using only diluted reagents and resulting in digests virtually free of interferences, the proposed method was faster (< 30min) than most of those presented in the literature.

Characterization of mineral composition of leaves and flowers of wild-growing Sambucus nigra.

The objective of this study was to determine the mineral content in the leaves and flowers of wild-grown Sambucus nigra collected from eleven different locations in Kosovo. The samples were digested in a microwave system using the wet digestion method. The minerals were determined by the application of inductively coupled plasma-atomic emission spectrometry (ICP-AES) and inductively coupled plasma-mass spectrometry (ICP-MS). A total of 31 elements were determined, 15 elements by the ICP-AES method (Al, B, Ba, Ca, Cr, Cu, Fe, K, Mg, Mn, Na, P, Sr, V, and Zn) and 16 elements by the ICP-MS method (Ag, As, Be, Bi, Cd, Co, Cs, Ga, Hg, In, Li, Ni, Pb, Rb, Tl, and U). The leaves of S. nigra show a higher content of minerals compared to the flowers, except for the flower of the sample SN-FL10, which is characterized by a high concentration of Fe, Al, Pb, Be, and Tl. The concentration of heavy metals and toxic elements (Pb, Cd, and Hg) was within the permissible concentrations according to Eur. Ph.