Determination Of Iodine Research Articles

A selective resonance Rayleigh scattering method for determination of iodine by graphene oxide surface molecularly imprinted polyacrylamide probe

A new graphene oxide nanosurface molecularly imprinted polymer (GO@MIP) probe was synthesized by microwave irradiation, using graphene oxide (GO) as the carrier, iodine as the template molecule, acrylamide as the functional monomer, ethylene glycol dimethacrylate (EGDMA) as the crosslinking agent, azodiisobutyronitrile (AIBN) as the initiator, and acetonitrile as the pore forming agent. The nanoprobe recognizes the iodine, and exhibits significant resonance Rayleigh scattering energy transfer (RRS-ET) effect between iodine as the acceptor and the nanoprobe as donor. When iodine concentration was in the linear range of 0.02–0.5 mmol/L, the decreased RRS intensity was linear to the concentration. And it was used for the determination of iodine in water samples and iodate ions in salt samples.

Electroanalysis with Carbon Paste Electrodes: A Look Behind the Scientific-Research Activities of the Electroanalytical Group in Pardubice

In this article, a retrospective view of the research activities of the electroanalytical group at the University in Pardubice (UPCE) is presented, offering a concise overview on the development, continuing work, and significant achievements in electrochemical measurements with carbon paste electrodes (CPEs). At the very beginning, a brief history of the field is provided and the state-of-the-art in a global view outlined. Second, research activities with CPEs and related configurations in the former Czechoslovakia and the succeeding Czech Republic are also summarised and the respective publications cited. The introductory section ends with a historical survey of the activities of the electroanalytical group at the UPCE, characterising the individual time periods with CPEs from the mid-1980s up until now and highlighting the most important achievements and the corresponding publications. The pivotal part of the text then gathers five various examples representing some of the truly key-themes that have made electroanalysis at UPCE well-known and, at the same, distinctive. Namely, overviewed, commented, and illustrated in selected figures are (i) carbon paste mixtures with atypical binders from liquid esters, (ii) extractive pre-concentration onto the carbon paste bulk and determination of iodine, (iii) method for determination of Ag(I) ions at a CPE with extraordinary analytical performance, (iv) carbon pastes as substrates for mercury, gold, bismuth, and antimony films, and (v) recent applications of CPEs prepared from carbonaceous materials of natural origin.

Method development for multielement determination of halogens and sulfur in teas

Abstract Microwave-induced combustion was evaluated as a sample preparation method for several types of tea (black, green, lemon balm, boldo, and mint) for further determination of bromine, chlorine, fluorine, iodine, and sulfur by ion chromatography. Parameters such as the sample mass efficiently decomposed and the most suitable absorbing solution (ultrapure water and 25, 50, 100, and 150 mmol L−1 NH4OH) were evaluated, considering the characteristics of the analytes and the determination technique used. The maximum sample mass possible to be decomposed was 900 mg of milled tea in the form of pellets, and the absorbing solution chosen was 100 mmol L−1 NH4OH, which provided suitable stabilization of the analytes (recoveries between 95 % and 103 %). To assess the accuracy of the proposed method, a certified reference material (BCR 060, aquatic plant) was analyzed. Agreements with the certified values ranged from 101 % to 107 %. The proposed method was used to analyze tea samples and the concentrations ranged from 549 to 2,549 mg kg−1 for chlorine, 223 to 828 mg kg−1 for fluorine, and 786 to 4,023 mg kg−1 for sulfur; bromine and iodine concentrations were below the limits of quantification (42 and 80 mg kg−1, respectively) in all evaluated samples.

Introduction of a spectrophotometric method for salivary iodine determination on microplate based on Sandell-Kolthoff reaction.

Iodine is an essential element for the synthesis of thyroid hormones. Therefore, a reliable marker of iodine supply is important. Iodine is predominantly excreted via kidneys, but also via salivary glands. Our aim was to introduce a new and simple method for determination of salivary iodine concentration (SLIC). Self-prepared chemicals and standards for Sandell-Kolthoff reaction on microplate with ammonium peroxydisulfate (AP) in the range 0-400 µg/L were used. Suitability of water-based standards (WBS) and artificial saliva-based standards (ASS) for standard curve were tested. We followed standards for method validation, defined concentration of used AP and compared our results with Inductively Coupled Plasma Mass Spectrometry (ICP-MS). WBS gave more reliable results than ASS as an underestimation of iodine concentration was found for ASS. LoB was 6.5 µg/L, LoD 12.0 µg/L, therefore analytical range was 12-400 µg/L. Intra- and inter-assay imprecisions at iodine concentrations, namely 20, 100, 165, and 350 µg/L were 18.4, 5.1, 5.7, and 2.8%, respectively, and 20.7, 6.7, 5.1, and 4.3%, respectively. Suitable molarity of AP was 1.0 mol/L and showed no difference to 1.5 mol/L (P values for samples with concentration 40, 100, and 150 µg/L, were 0.761, 0.085, and 0.275, respectively), whereas there was a significant change using 0.5 mol/L (P<0.001). Saliva samples could be diluted up to 1:8. There was no interference of thiocyanate and caffeine up to 193.5 mg/L. Our original method was comparable to ICP-MS. Spaerman coefficient was 0.989 (95% CI: 0.984-0.993). The new method for SLIC determination is in excellent agreement with ICP-MS and easy-to-use.

Quantitative analysis of iodine and bromine in soil using an energy-dispersive X-ray fluorescence spectrometer with three-dimensional polarized optics.

A nondestructive and simple method for the determination of bromine and iodine in soil was investigated using an energy-dispersive X-ray fluorescence spectrometer equipped with three-dimensional polarized optics. Using a gadolinium X-ray tube and Mo and Al2O3 as optimal secondary target materials, K-lines were detected for bromine and iodine. The minimum detection limits for bromine and iodine were calculated using JSAC0411, a certified reference material of soil for metal composition analysis, and were 0.77mg/kg for bromine and 2.3mg/kg for iodine at a measurement time of 600s. The results of the determination of bromine and iodine in soil samples by the standard addition method were 256 ± 8mg/kg for iodine and 67.9 ± 1.3mg/kg for bromine with JSAC0411, which were in close agreement with the results measured by inductively coupled plasma mass spectrometry (ICP-MS) after alkaline extraction with tetramethylammonium hydroxide (TMAH) solution. The method developed in this study is an excellent technique for direct analysis of soil by X-ray fluorescence analysis without any pretreatment such as alkaline extraction. It is expected to be a practical analytical method for elucidating the dynamics of bromine and iodine in agricultural land and soil.

Improvement and Study on the Determination of Iodine in Geochemical Samples by Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

Improvement and Study on the Determination of Iodine in Geochemical Samples by Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

Collaborative Study for Iodine Monitoring in Mandatory Direct-Iodized Sauce in Thailand.

Direct iodization in fish sauce, soy sauce, and seasoning sauces plays a crucial role in optimizing the iodine intake of Thailand's people. However, determining the iodine content to ensure that these sauces meet the standard of Thailand's Food and Drug Administration (FDA) is challenging. In this study, all local laboratories equipped with inductively coupled plasma-mass spectrometry (ICP-MS) and with experience in iodine analysis by any analytical method were invited to participate in a hands-on training workshop and two rounds of interlaboratory comparison. The aim was to improve laboratory performance and assess the potential for iodine monitoring for mandatory direct-iodized sauces. All target laboratories participated in this study. The hands-on training workshop harmonized the analytical method and increased the capacity of participating laboratories. Most laboratories (7/8) achieved satisfactory performance for six test samples based on interlaboratory comparison. Samples were extracted by tetramethylammonium hydroxide (TMAH), with the presence of 6% 2-propanol, 0.01% triton X-100, internal standard, and iodine determination in direct-iodized sauces by ICP-MS. The reproducibility standard deviation (SL), after the removal of outlier results for iodine content, was 7-22% iodine at a level of 0.03-4.81 mg/L. Moreover, the Thai FDA's judgment range for official control activities should expand the range of 2-3 mg per 1 L (ppm) by at least 22%.

Examining the influence of desalinated water on iodine concentration in tap water in Israel

IntroductionIn Israel, desalinated water is a major source of drinking water. Previous studies have suggested that the levels of iodine in water provided by authorities may not accurately reflect the levels reaching end-users. Materials and MethodsWe analyzed 21 tap water samples collected from different localities across Israel, 13 post-treated desalinated water samples from three of the largest Israeli desalination plants, and several natural water samples. An improved method of ICP-MS developed in our laboratory was used to analyze the content of iodine and other macro-elements, and determination of iodine was performed in alkaline media. ResultsOur results showed that it is possible to distinguish between sample groups based on iodine concentration, water hardness, and Ca/Mg ratio. The median iodine concentrations for four groups of tap water samples ranged from 0.3 to 12.3 µg/L, which is lower than the concentrations previously reported by other researchers in Israel. Based on typical consumption, the water samples can provide no more than 3.39% of the recommended dietary allowance level for iodine. The analysis of post-treated desalinated water samples indicated that these waters comply with industrial specifications but contain only trace concentrations of iodine and much less magnesium than recommended by different public health authorities for public consumption of drinking water. ConclusionThe total iodine concentrations found were lower than several observations reported in previous years in the literature. There are currently no strict regulations regarding iodine and magnesium levels in drinking and/or softened (desalinated) water, but the intensive desalination plant application is already exhibiting a negative impact on public health. Further investigations are needed, but the present study provides useful insights for developing an effective policy to ensure adequate iodine supply for the population of Israel through drinking water.

4-Aminobenzoic acid, 2-phenoxyethanol and iodine used as tracers in a short-term in vivo-kinetics study for tattoo ink ingredients: Mass spectrometry method development and validation

Tattoos have been gaining popularity in recent years, leading to a growing interest in researching tattoo inks and the tattooing process itself. Since the exposure to soluble tattoo ink ingredients has not yet been investigated, we here present the method validation for a short-term biokinetics study on soluble tattoo ink ingredients. The three tracers 4-aminobenzoic acid (PABA), 2-phenoxyethanol (PEtOH) and iodine will be added to commercially available tattoo inks, which will subsequently be used on healthy study participants. Following the tattooing process, blood and urine will be sampled at specific time points and analysed for these tracers. For this purpose, a method using liquid chromatography separation coupled to a quadrupole time-of-flight mass spectrometer (LC-QTOF-MS) in positive and negative ESI mode for the quantification of PABA, PEtOH and selected metabolites and an inductively-coupled plasma (ICP)-MS method for the determination of iodine were developed and validated. For LC-QTOF-MS analysis, the most applicable additives for LC eluents (0.01 % formic acid for positive and 0.005 % acetic acid for negative mode) were identified. Protein precipitation with acetonitrile was chosen for sample preparation. The methods were validated for selectivity, specificity, carryover, linearity, limit of detection (LOD) and quantification (LOQ), matrix effects, accuracy and precision, stability under different conditions and dilution integrity according to national and international guidelines with an allowed maximum variation of ±15 %. The LC-QTOF-MS method met the imposed guideline criteria for most parameters, however, some metabolites showed strong matrix effects. Validation of the ICP-MS method revealed that the KED-H2 collision mode is superior to the standard analysis mode due to enhanced method accuracy. The methods were validated for the relevant matrices plasma, urine, tattoo ink and tattoo consumables and proved to be applicable for the main target substances in the short-term biokinetics study. A proof-of-concept study showed successful quantification of iodine and PABA metabolites. The PEtOH metabolite was also quantified, but showed strong matrix effects in urine. Therefore standard addition was selected as an alternative quantification method.

Methods for determining iodine in urine

Iodine deficiency remains a serious threat to public health worldwide, especially in children and pregnant women. Despite the apparent ease of iodine deficiency elimination with the help of a simple and highly effective strategy of compulsory salt iodization, the problem of iodine deficiency and iodine deficiency disorders remains urgent for public health in the Russian Federation. The most effective and informative way to study iodine status at population level is determination of iodine concentration in urine in epidemiological studies. This article presents a review of urinary iodine determination methods, as well as methodological recommendations for iodine determination, developed and adopted in National Medical Research Center for Endocrinology.

Determination of the Elemental Iodine in Human Breast Milk by Inductively Coupled Plasma mass Spectrometry.

Adequate iodine status in lactating women is defined by a maternal median urinary iodine concentration (UIC) ≧ 100µg/L. However, the above-mentioned criterion does not account for the secretion of iodine into breast milk and could not truly reflect the amount of iodine delivered to the infants. Measuring breast milk median iodine concentration (BMIC) is crucial, but the method to measure BMIC has not been developed and validated in Taiwan. We adopted the ammonia dilution method without prior sample digestion to measure BMIC by inductively coupled plasma mass spectrometry (ICP-MS). Samples and iodate calibrators were prepared into an aqueous solution containing Triton X-100, 0.5% ammonia solution, and tellurium (128Te) as the internal standard. Precision, accuracy, serial dilution, and recovery tests were performed for method validation. The range of intra-assay and inter-assay coefficient of variation for the four human breast milk samples with different iodine concentrations were 3.2-4.7% and 2.3-5.5%, respectively. The standard NIST 1549 milk powder was prepared into three different concentrations of 50µg/L, 100µg/L, and 200µg/L to assess the accuracy; the bias was < 5%. A recovery of 95-105% was achieved for four human breast milk samples spiked with sodium iodide solution. The serial dilution test confirmed linearity up to 0.998. The limit for detection and quantification was 0.78µg/L and 2.34µg/L, respectively. The results of the current study confirmed that this ICP-MS method is accurate and reliable in measuring BMIC.

Determination of bromine, iodine, and other components in northern Hainan island soil

The emergence of the integrated wavelength-dispersive and energy-dispersive Zetium X-ray fluorescence spectrometer technique offered new chances to analyze elemental distribution with minimal sample preparation in complex matrix geological samples-northern Hainan island soils. Wavelength-dispersive X-ray fluorescence was applied for the measurement of bromine in the northern Hainan island soil. To reduce the fluctuations of the low-bromine-content measurement results, a two-channel measurement of bromine was designed, and the average value of the two-channel measurements was used as the final result. The soil samples in northern Hainan Island were rich in iodine, with a content range of a few µg/g to more than 100 µg/g, and these were particularly suitable to be analyzed by energy-dispersive X-ray fluorescence spectrometer. The geological samples in northern Hainan Island were brown, purple, and brown-red soil containing kaolinite, ilmenite, rutile, anatase, and goethite. These soil samples were rich in titanium, aluminum, and iron. The titanium concentration in the northern Hainan Island soil was anomalously high (up to 15.05%), far exceeding the content range of the calibration curve. Owing to the empirical coefficient matrix correction method, unreliable or even unreasonable results were obtained for some elements. By systematically mitigating matrix effects through the development of custom reference materials and building matrix-matched measurement and calibration routines, the quantification of Vanadium, Barium, and major components in northern Hainan Island soil samples was optimized. The efficacy of the X-ray fluorescence spectrometer method was confirmed by comparison with inductively coupled plasma–optical emission spectroscopy analysis. This work demonstrates the capability of the integrated wavelength-dispersive and energy-dispersive Zetium X-ray fluorescence spectrometer technique for reliable quantitative elemental analysis of complex matrix geological samples.

Iodine intake assessment in the staff of a Porto region university (Portugal): the iMC Salt trial

PurposeIodine deficiency disorder (IDD) is an ongoing worldwide recognized problem with over two billion individuals having insufficient iodine intake. School-aged children and pregnant women are often target groups for epidemiological studies, but there is a lack of knowledge on the general adult population. The aim of this study was to assess the iodine status among a Portuguese public university staff as a proxy for the adult working population.MethodsThe population study covered 103 adults within the iMC Salt randomized clinical trial, aged 24–69 years. Urinary iodine concentration was measured spectrophotometrically using the Sandell–Kolthoff reaction. Iodine food intake was assessed using a 24-h dietary recall. The contribution of discretionary salt to the iodine daily intake was assessed through 24-h urinary sodium excretion (UIE) and potentiometric iodine determination of household salt.ResultsThe mean urine volume in 24 h was 1.5 L. The median daily iodine intake estimated from 24-h UIE was 113 µg/day, being lower among women (p < 0.05). Only 22% of participants showed iodine intake above the WHO-recommended cutoff (150 µg/day). The median daily iodine intake estimated from the 24-h dietary recall was 58 µg/day (51 and 68 µg/day in women and men, respectively). Dairy, including yoghurt and milk products, were the primary dietary iodine source (55%). Iodine intake estimated from 24-h UIE and 24-h dietary recall was moderately correlated (Spearman rank correlation coefficient r = 0.34, p < 0.05). The average iodine concentration in household salt was 14 mg I/kg, with 45% of the samples below the minimum threshold preconized by WHO (15 mg I/kg). The contribution of discretionary salt to the daily iodine intake was around 38%.ConclusionThis study contributes new knowledge about iodine status in Portuguese working adults. The results revealed moderate iodine deficiency, particularly in women. Public health strategies and monitoring programs are needed to ensure iodine adequacy in all population groups.

Use of ionic liquids for extraction separation and concentration of iodide ions in brine samples.

Iodine in natural salt waters such as iodine-rich underground brine generally exists as iodide ions, and to extract iodide ions, it is necessary to oxidize them to nonpolar iodine molecules. In this study, we report that iodide ions in natural brine containing high concentrations of chloride ions can be quantitatively extracted without oxidation by extraction using ionic liquids. Extraction with the ionic liquids trihexyltetradecylphosphonium chloride and trioctyl ammonium chloride was found to be able to enrich trace amounts of iodide in brine samples up to 40- and 100-fold, respectively. The selectivity coefficients for I- over Cl- determined in this study clearly show that the ionic liquids have much higher I-/Cl- selectivity than typical strongly basic anion exchangers. Extraction with trihexyltetradecylphosphonium chloride was applicable as a preconcentration method for iodine determination by XRF analysis. Iodide ions extracted with trioctyl ammonium chloride were quantitatively stripped with an aqueous alkaline solution. These results indicate that ionic liquid extraction is useful for the separation and concentration of iodide from brines.

Relationship between iodine knowledge and dietary iodine intake in pregnant and lactating women: a cross-sectional study.

This study assessed the iodine knowledge of pregnant and lactating women and the relationship to dietary iodine intake and iodine status. The factors influencing iodine intake were analysed. Basic information and iodine knowledge were collected via a questionnaire. A FFQ assessed dietary iodine intake. The urinary iodine concentration (UIC) was measured using the arsenic-cerium catalytic spectrophotometric determination of iodine in urine (WS/T 107 -2016). A cross-sectional study involving pregnant and lactating women in Xinjiang, China was conducted. A total of 1181 pregnant women and 504 lactating women were enrolled in the study. The median UIC for pregnant and lactating women was 179·27 and 192·81 µg/l, respectively, and the dietary iodine intake was 407·16 and 356·89 µg/d, respectively. Of the pregnant and lactating women, 73·4 % and 82·5 % had medium iodine knowledge, respectively. In pregnant women, iodine knowledge and dietary iodine intake were positively correlated. High iodine knowledge and iodine education were shown to be protective factors for excessive iodine intake in pregnant women. This study demonstrated that the iodine nutritional status of women in Xinjiang was appropriate, and iodine knowledge was at a medium level, but there was confusion about iodine nutrition. Public education is needed to improve iodine knowledge and active iodine supplementation awareness among these populations of women.

ANALYSIS OF METHODS FOR DETERMINATION OF CHLORINE DIOXIDE, CHLORITE AND CHLORATE ANIONS IN DRINKING WATER

The analysis shows that the primary measure for the purification of drinking water is its reliable disinfection with oxidants, which are chlorine and its compounds, chlorine dioxide, ozone. The aim of the article is to analyze the existing methods for determination of chlorine dioxide, chlorite, hypochlorite and chlorate anions in drinking water. To analyze the chlorine dioxide strength solutions (to control the generator performance) the iodometric method (determination of chlorine dioxide concentration, concentration of free chlorine, chlorite and chlorate anions; relative error ≤ 5%) and the method of direct absorption at 445 nm (determination of chlorine dioxide concentration in the range of concentrations of 100-700 mg / l; relative error ≤ 2%) were used. To analyze the residual concentrations of chlorine dioxide, chlorite and hypochlorite anions in their joint presence the titrimetric and photometric methods with N,N-діетил-1,4-фенилендіамінсульфатом (DFD) (error of determination is of 0.05 mg/l) were used as well as iodometric method with photometric determination of iodine at 350 nm in the concentration range 0.01-0.5 mg/l. To analyze the residual concentrations of chlorine dioxide (selective methods), such methods were used: the photometric method with chlorophenol red in the concentration range of 0.02-0.7 mg/l; relative error ≤ 5%; photometric method with chromic violet acid in the concentration range of 0.1-1.5 mg/l. The method of ion chromatography was used to analyze the residual concentrations of chlorite and chlorate anions. Given the necessity for harmonization of domestic regulatory and guidance documentation with European one, it should be considered as necessary to control chlorites and chlorates in drinking water by method of ion chromatography. It is appropriate to conduct research on the approbation of ion chromatography method for the simultaneous determination of chlorites and chlorates in samples of water after its disinfection by various oxidants (sodium hypochlorite, ozone, chlorine dioxide).

Multi-Techniques for Iodine Determination and Dose Uniformity Assays in Iodized Mineral Dietary Supplements

The determination of iodine in iodized mineral dietary supplements is considered a challenge, especially in view of the variety in the sample composition and the analyte concentration. Thus, in this work, microwave-induced combustion (MIC) was combined with ion chromatography (IC) and ion-selective electrode potentiometry (ISE) for iodine determination and dose uniformity assays in mineral dietary supplements. Sample masses up to 800 mg were efficiently digested and only a diluted alkaline solution (200 mmol L-1 NH4OH) was necessary to absorb the analyte for further determination step. The final digest was fully compatible with multi-technique detection usually available in routine analysis laboratories. Recoveries ranging from 94% to 106% was achieved and relative standard deviations for repeatability and intermediate precision were always lower than 8%. Limits of quantification were 4 µg g-1 and 10 µg g-1, respectively, by using IC and ISE. The analytical method was applied for iodine determination in mineral dietary supplements from four brands with different iodine dosages (from 100 to 1250 μg g-1, according to the manufacturers) and for uniformity assay evaluation using individual tablets/capsules of mineral dietary supplements. Non-compliance regarding label information for some samples was reported, drawing the attention of supervisory institutions. The analytical strategies presented in the present study can be successfully used in routine analysis of the quality control of mineral dietary supplements.

Определение содержания йода, йодидов и йодатов в пищевых продуктах

Currently iodine deficiency diseases are one of the most important medical and social problems. In this regard, the purpose of the study is to determine the content of iodine, iodides, iodates in iodized salt, drinking and mineral water, seaweed, to determine the stability of the iodine content in salt. For the qualitative determination of iodides and iodates ions in salts and molecular iodine in seaweed, an iodine starch reaction has been carried out. The presence of iodide ions in iodized water has been determined by reaction with silver nitrate and chlorine water, the iodine released has been extracted with chloroform. Quantitative determination of iodine in salt has been carried out by the titrimetric method, in water – by colorimetric method, in seaweed – by gravimetric method with subsequent titration. The study has found that iodized salt contains iodine in the form of potassium iodate, in an amount of 18.65 μg / g of elemental iodine, kelp contains molecular iodine in the amount of 8.12 μg / g of elemental iodine, and iodized water contains potassium iodide in the amount of 0.327 μg / ml of elemental iodine. The study has proved that over time, the amount of iodine in the salt iodized with potassium iodate decreases after a month by 5.6 times. In order to comply with the daily rate of iodine intake, it is necessary to include in your diet about 9.7 g of iodized salt, which exceeds the daily norm of its consumption in 5 g. In this regard, it is recommended to use iodized salt (not more than 5 g) or iodized water (0.7 L of water) or kelp (18.47 g) as a prevention of iodine deficiency.

A New Method for the Determination of Phosphorus and Iodine in Phosphate Rock by Ion Chromatography After Continuous Acid Digestion and Distillation

A New Method for the Determination of Phosphorus and Iodine in Phosphate Rock by Ion Chromatography After Continuous Acid Digestion and Distillation

Development of a simple and fast ultrasound-assisted extraction method for iodine determination in phosphate rock and phosphogypsum by-product using titrimetric method

ABSTRACT Phosphate rocks, as well as their derivatives and by-products, are complex minerals that make elemental analysis very complicated. Iodine is commonly found in these matrices, and its concentration must be controlled. The present work describes the development of a novel rapid digestion protocol based on ultrasonic-assisted acid digestion for the determination of iodine in phosphate rock and phosphogybsum samples by Iodometric titration. The developed method occurs at low digestion temperature and uses a dilute nitric acid 5% (v/v) solution instead of concentrated acid. The investigated parameters influencing UAD, were completely optimised using experiments design methodology (DOE). Iodine recoveries from dilute nitric acid digestion without sonication were generally lower overall when compared to UAD results, illustrating the effect of ultrasound on iodine dissolution. This technique effectively addresses iodine volatilisation and sample losses problem encountered while using classical digestions. Method validation included: defining the detection and quantification limit of iodine using this method were about 2.2 and 8 mg.kg−1, respectively, and it's suitable for the proposed application. Moreover, the repeatability and reproducibility, expressed as RSD for phosphogybsum sample was 7%, 8.3% respectively, while for phosphate samples is tacked as the mean of relative standard deviation 3.4%, 3.8%. Additionally, accuracy of the method was assessed by analysing a certified reference material and the iodine concentration was found to be in good agreement with the indicative values for this CRM. Thus, the mean recoveries in fortified sample were between 96% and 107%.The developed method is fast, accurate, and it is applicable to the monitoring of iodine in the phosphate industries.