Ion Concentration Research Articles

On the mechanism and energetics of electrochemical alloy formation between mercury and platinum for mercury removal from aqueous solutions

Mercury pollution is an acute global concern threatening the health of humans and wildlife. Thus, there is a need for new and improved techniques to reduce emissions and remove toxic mercury from aqueous environments. Electrochemical alloy formation, specifically between mercury ions in aqueous solution and a platinum electrode, emerges as a promising solution. Through analysis of reaction mechanisms and energetics related to the formation and dissolution of the PtHg4 alloy, this study aims to deepen our understanding of the underlying processes of effective electrochemical mercury removal. Potentiodynamic measurements indicate rapid alloy formation at a clean platinum surface, proceeding with only trace amounts of metallic mercury on the surface. However, once the electrode surface has sufficient mercury coverage with an alloy thickness of around 1.5 nm, clear evidence of metallic mercury on the surface is observed. Furthermore, the amount of absorbed mercury on the cathode increases linearly in time. The onset potential for the alloy formation is experimentally determined using electrochemical quartz crystal microbalance with dissipation monitoring to be approximately 0.64 V vs. SHE, and the alloy dissolution (oxidation) onset potential is found to be approximately 0.98 V vs. SHE, at a mercury ion concentration of 10 mg/L. Density functional theory calculations are used to provide a theoretical value for the reversible potential from a thermodynamics perspective, yielding a value of 0.78 V vs. SHE at a mercury ion concentration of 10 mg/L. This value is in excellent agreement with the experimental results, suggesting an overpotential of about 0.14 and 0.20 V for the alloy formation and oxidation, respectively. These findings provide important information on the reaction mechanisms and overpotentials of the PtHg4 alloy formation and dissolution, which are key factors for development of large-scale mercury removal based on this technique, as well as fundamental understanding of the electrochemical alloy formation between mercury ions and platinum.

Oxidative weathering of pyrite in acidic environments: Data-driven experimental evaluation coupled with Raman hyperspectral imaging

This study deals with the identification of the factors that affect pyrite oxidation in acid mine drainage conditions. For this scope, weathering experiments have been carried at laboratory scale based on the design of experiments methodology to evaluate the effect of factors such as major ion concentrations, crystal size, and humic acids presence over the amount of elemental sulfur produced due to the involved weathering reactions. In particular, metal and anionic concentrations in solution were quantified by inductively coupled plasma-atomic emission spectroscopy and ion-chromatography techniques, respectively, whereas the amount of elemental sulfur was quantified with a high-performance liquid chromatography with diode-array detection technique after proper extraction procedure. A partial least squares regression was calculated to establish a quantitative relationship between the considered factors and the amount of elemental sulfur. After evaluation of the model, ferric iron, crystal size and the presence of humic acids were identified as the relevant factors for pyrite oxidation under acidic conditions. In addition, the surface of the samples was characterized by Raman imaging spectroscopy and subsequently analyzed by explorative hyperspectral analysis methods to assess the spatial distribution of the elemental sulfur as the main weathering product, resulting in a homogenous distribution.

Development and application of a new macrocyclic ligand-functionalized mesoporous silica sorbent for selective separation of radiocesium from environmental wastewater

The growing reliance on nuclear energy and uncharacteristic accidents, such as those in Chornobyl and Fukushima, have emphasized the need for effective radiocesium (r-Cs: 137Cs) removal from environmental wastewater. This study presents the development of DFDB18C6@SBA-NH2, a novel solid-phase sorbent designed to remove r-Cs from aqueous environments selectively. The sorbent was synthesized by tethering a macrocyclic ligand, DFDB18C6 (di-formyl dibenzo-18-crown-6-ether), to amino-functionalized mesoporous SBA-15 (Santa Barbara Amorphous-15). The sorbent’s structure, thermal properties, and surface morphology were comprehensively characterized. Batch sorption experiments were performed to evaluate the influence of different operating factors on r-Cs sorption, including solution pH, contact duration, initial ion concentration, ambient temperature, and matrix ions contents. The sorption behavior was better explained with the pseudo-second-order kinetic and Langmuir isotherm models, which suggest a probable monolayer chemisorption process. The thermodynamic evaluation indicated the exothermic nature of the sorption process. The DFDB18C6@SBA-NH2 sorbent demonstrated significant 137Cs removal (approximately 85 %) from Fukushima-originated wastewater, with competing matrix ions such as Ca2+, Mg2+, Na+, and K+. These results highlight the potential of DFDB18C6@SBA-NH2 as a potential solid-phase sorbent for efficient and selective r-Cs decontamination in waste aqueous matrices.

Construction of MIL-100(Fe)-DMA material for efficient adsorption of Sr and Cs ions from radioactive wastewater

A novel metal-organic framework (MOF) material, MIL-100(Fe)-DMA, was synthesized using the solvothermal method. The structure of the MOF was characterized using scanning electron microscopy-energy dispersive X-ray spectroscopy, N2 adsorption–desorption isotherms, X-ray diffraction analysis, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and Mössbauer spectroscopy. Batch adsorption experiments were performed to investigate the effects of initial Sr2+ and Cs+ concentrations, adsorption time, pH, and coexisting cations on the adsorption performance of the material. The adsorption mechanism was further elucidated using adsorption kinetics and isotherm models. The results indicated that the adsorption of Sr2+ and Cs+ does not significantly affect the MOF material structure. As reaction time and initial ion concentration increased, the adsorption capacity of MIL-100(Fe)-DMA for Sr2+ and Cs+ increased rapidly and then gradually reached equilibrium. Optimal adsorption occurred under alkaline conditions, with maximum adsorption capacity observed at pH = 8. The adsorption process for Sr2+ and Cs+ was well described by the pseudo-second-order kinetic model, the Weber–Morris model, and the Langmuir adsorption isothermal model. The adsorption process was mainly identified as monolayer chemical adsorption, influenced by multiple factors. Characterization combined with density functional theory calculations revealed that the unsaturated carboxylic acid groups on the surface of the MOFs play a crucial role in the interaction with Sr2+ and Cs+.

The effect of magnesium impurities on the optical and spectral characteristics of calcium orthovanadate single crystals doped with chromium and manganese

The effect of magnesium co-doping on growth conditions, crystal composition, optical and spectral properties of manganese or chromium-doped Ca3(VO4)2 (CVO) crystal was studied. The single crystals were grown by the Czochralski method. Effective segregation coefficients of manganese and chromium in the CVO matrix with magnesium co-doping were calculated. A redistribution of the absorption lines intensities was observed in the absorption spectra of CVO:Mn:Mg and CVO:Cr:Mg. Low (15 K) temperature fluorescence measurements confirmed that co-doping CVO crystal with Mg ions leads to the redistribution of Mn ions concentration in different valence states, but does not cause changes in their spectral properties. In the presence of magnesium, additional annealing of the materials resulted in a slower reduction of the valence state of doping ions and a noticeable change in crystal coloration. All investigated impurities have practically no effect on the specific ferroelectric domain structure of CVO.

Heterogeneous reservoir seepage characterized by geophysical, hydrochemical, and hydrologic methods

Seepage characterization from reservoirs is challenging for various environmental and water resource applications. Nonintrusive geophysical methods can achieve excellent detection results, but they cannot provide a quantitative description of the amount of seepage. Integrating geophysical methods with traditional hydrochemical and hydrologic methods enables simultaneous localization and quantitative analysis of heterogeneous reservoir seepage. Ground and waterborne electrical resistivity tomography are used to scan a reservoir under a typical cutoff wall antiseepage system, and the measurements reveal the northern preferential infiltration area. The hydrochemical results reveal that the seepage bypass of the cutoff wall has led to evident ion concentration variations in groundwater near the dam. Based on the geologic stratum information, the typical cutoff wall antiseepage system is divided into three scenarios for numerical simulation to calculate the seepage. The total seepage of the reservoir over 15 months is approximately 7.15 × 106 m3, which is consistent with traditional water budget methods. However, in the northern part of the reservoir, only 27% of the entire dam contributes 77% of the total seepage. All methods have confirmed that the heterogeneous seepage is caused by the absence of an antiseepage seal in the northern region, which should be a primary focus for future monitoring and operational efforts. With the geophysical results undergoing extensive cross-validation, the results from the preceding methods are comprehensively leveraged, effectively lowering uncertainties and overcoming the limitations of geophysical methods in quantitatively characterizing seepage.

High sensitivity fiber optic SPR sensor for selenium ion concentration detection

Balance of selenium content is of great significance to human health, and there is a need for rapid and sensitive detection of selenium ion concentrations in the human body and food. This article proposes a highly sensitive fiber surface plasmon resonance (SPR) sensor for selenium ion concentration detection. By fabricating a fiber U-shaped ring composite structure and modifying Cu3VSe4 material, the sensitivity of the fiber SPR sensor is improved to 6826.82nm/RIU. Using 2,4-diamino-6phenyl-1,3,5-triazine to modify the surface of the sensor to achieve specific detection of selenium ion concentration. The experiment results indicate that the detection sensitivity of the sensor is 1.858nm/(lg(pg/ml)) with range of 100pg/ml-1μg/ml, and the LOD is 124.06pg/ml. The highly sensitive SPR sensor proposed in this article, without labeling, can achieve high sensitivity and rapid detection of selenium ions, providing a new approach for trace element content detection.

Comparative study of marine steel and welding joint in artificial seawater based on stress corrosion cracking and crack growth

In this work, the environmental fracture behavior of marine steel and its welding joint were compared in artificial seawater. The electrochemical measurement, slow strain rate tensile test, and low-frequency cyclic loading test were conducted. The results showed that the corrosion current density and stress corrosion cracking susceptibility of welding joints were higher than those of base metal, caused by high dislocation density and residual stress in the heat-affected zone. The acidification and ion concentration occurred at the crack tip of the welding joint and basic metal. pH value and Cl− concentration at the crack tip reached 4.1 and 3.8 mol/L, respectively. The crack growth rate of the welding joint was higher than that of base metal. The crack growth behavior was controlled by the mechano-electrochemical effect at the crack tip, and hydrogen embrittlement was the main factor.

Biological Evaluation of Lysionotin: a Novel Inhibitor of 5-Lipoxygenase for Anti-glioma.

To explore the potential mechanism of lysionotin in treating glioma. First, target prediction based on Bernoulli Naïve Bayes profiling and pathway enrichment was used to predict the biological activity of lysionotin. The binding between 5-lipoxygenase (5-LO) and lysionotin was detected by surface plasmon resonance (SPR) and molecular docking, and the inhibitory effects of lysionotin on 5-LO and proliferation of glioma were determined using enzyme inhibition assay in vitro and cell viability analysis, respectively. Furthermore, the pharmaceutical effect of lysionotin was explored by cell survival rate analysis and liquid chromatography with tandem mass spectrometry (LC-MS/MS). The protein expression, intracellular calcium ion concentration and cytoskeleton detection were revealed by Western blot, flow cytometry and fluorescence labeling, respectively. Target prediction and pathway enrichment revealed that lysionotin inhibited 5-LO, a key enzyme involved in the arachidonic acid metabolism pathway, to inhibit the proliferation of glioma. Molecular docking results demonstrated that 5-LO can be binding to lysionotin through hydrogen bonds, forming bonds with His600, Gln557, Asn554, and His372. SPR analysis further confirmed the interaction between 5-LO and lysionotin. Furthermore, enzyme inhibition assay in vitro and cell survival rate analysis revealed that 50% inhibition concentration of lysionotin and the median effective concentration of lysionotin were 90 and 16.58 µmol/L, respectively, and the results of LC-MS/MS showed that lysionotin inhibited the production of 5S-hydroperoxy-eicosatetraenoic acid (P<0.05), and moreover, the LC-MS/MS results indicated that lysionotin can enter glioma cells well (P<0.01) and inhibit their proliferation. Western blot analysis demonstrated that lysionotin can inhibit the expression of 5-LO (P<0.05) and downstream leukotriene B4 receptor (P<0.01). In addition, the results showed that lysionotin affected intracellular calcium ion concentration by inhibiting 5-LO to affect the cytoskeleton, as determined by flow cytometry and fluorescence labeling. Lysionotin binds to 5-LO could suppress glioma by inhibiting arachiodonic acid metabolism pathway.

Assessment of luminescent features on Sm3+ ions doped LiF assimilated lead-free borate glasses for visible photonic and optoelectronic applications

The distinctive set containing Sm3+ ions doped LiF incorporated Alkaline borate glasses have been synthesised via the melt quenching practice. 59B2O3+20LiF+(20–X)CaCO3+XBaCO3 +1Sm2O3 (where X = 5, 10, 15, 20 wt%) is the composition used for the glass preparation. The effect of samarium ions concentration dependency on the absorption and emission of barium and calcium oxide has been studied through several spectroscopic studies. The current set of glasses is ionic, determined by the bonding value. The hypersensitive absorption transition is found in the visible region of the absorption spectra, and the transition from 6H5/2 to 6P3/2 shows the highest oscillator strength of 14.87 × 10−6. The intensity parameters are denoted by Ωλ (where λ = 2,4,6) are assessed and discussed. The results indicate that Ω4 is higher when compared to the other two parameters. The lower Ω2 values further ensure the ionic nature of the glass samples. Moreover, the intensity parameters are utilised to predict some radiative properties for the lasing potential evaluation, which includes cross-sections of emission (σPE), probability of radiative transition (A), and experimental and radiative lifetime (τexp and τR). The decay profile was monitored for the 4G5/2 state, and consistently non-exponential behaviour was observed in all the glasses. Through the CIE colour chromaticity analysis, the CCT (colour-correlated temperature), dominant wavelength, colour, and purity of the emitted light have been evaluated. Concerning all aspects, the glass with 20 wt% of BaCO3 is found to be fit for photonic and optoelectronic applications.

Understanding the limits of binary diffusion for enhanced clay barrier design.

Waste containment and isolation strategies often utilize bentonite as a buffer material due to its swelling capacity, sealing efficiency, low permeability, and limited diffusive transport. However, previous experimental studies of ionic diffusion through bentonite have shown discrepancies with binary diffusion assumptions. Meticulous experiments and complementary analyses reveal that the migration of preexisting ions in the medium enables the differential flux of diffusing anions and cations, while maintaining local electroneutrality in all cases. The separation between the cationic and anionic fronts is electrically tied to the motion of the preexisting ions and reflects the interplay between valence, concentration, and self-diffusion coefficients of the ions involved. Imposing binary diffusion conditions forces the faster anions to diffuse at the same rate as cations. Therefore, effective barriers to mitigate both cation and anion transport should have low surface charge and low excess salts to minimize the preexisting ionic concentration.

Robust, transparent, self-healable, recyclable all-starch-based gel with thermoelectric capability for wearable sensor

Conventional all-starch-based (ASB) gels are weak and lack ductility. The preparation of a robust ASB gel with multi-functionalities e.g., self-healing, anti-freezing, conductivity, and so forth, is highly desirable but challenging. Herein, a new kind of ASB gel was prepared by gelatinizing starch in urea and choline chloride solution (UC) with the aid of water. Its tensile strength was up to 1.08 MPa with a tensile strain of 313 %, and this value hardly changed after 10 days ageing. A high healing efficiency of 98 % can be achieved after 1 h of healing at room temperature, and the healed tensile strength reaches up to ca. 1.06 MPa, which is almost the highest value for ASB gel. The resultant ASB gel can surfer from bending and twisting at −80 °C. Moreover, ASB gel also exhibits excellent biocompatibility and biodegradability. In addition, UC endowed the ASB gel with ion conductivity, allowing it to be used as a flexible strain sensor to monitor human movement. The ion-conductive ASB gel also exhibited thermoelectric ability with a Seebeck coefficient of 2.5 mV K−1, which can be further improved to 5 mV K−1 with a maximum output voltage of 252 mV by introducing a gradient of ionic concentration.

Comparison of Adsorption Capacity of Natural and Acid-activated Kaolinite Clay for Cesium ions from Aqueous Solution

Objectives : This study is to compare the removal efficiency of cesium ions in aqueous solutions by natural and acid-activated kaolinite clay.Methods : Natural kaolinite clay was acid-treated with H2SO4 (2M) at 80oC for 6 h under mechanical stirring. While activating natural kaolinite clay with acid, cations such as Al3+, Ca2+, Mg2+ and Fe3+ were partially eluted from the crystal lattice of natural kaolinite clay, and resulted in the increase in the surface area and the pore volume through the opening of crystal lattice. The surface area and the pore volume of acid-activated kaolinite clay were found to be roughly three times higher than natural kaolinite clay. The characteristics of natural and acid-activated kaolinite clay were observed by X-ray Fluorescence Spectroscopy, Energy Dispersive X-ray Spectroscopy, and BET Surface Area Analyzer.Results and Discussion : Generally, adsorption efficiency of Cs+ ion by acid-activated kaolinite clay showed much higher compared with natural kaolinite clay. At 50 mg L-1 of Cs+ ion concentration and the unit of dose in g L-1 , the adsorption efficiencies of Cs+ ion by natural and acid-activated kaolinite clay were 57.5% and 96.9%, respectively. The data obtained from this study were fitted to the adsorption isotherm and the kinetic models, respectively. It revealed that the Langmuir isotherm and the pseudo-second-order kinetic models described well the adsorption behavior of Cs+ ions on both natural and acid-activated kaolinite clay owing to their higher correlation coefficient R2. Based on the Langmuir isotherm coefficient Q, adsorption capacity of Cs+ ion by natural kaolinite clay and acid-activated kaolinite clay were 5.65 mg g-1 and 10.6 mg g-1, respectively.Conclusion : The results demonstrated that acid-activated kaolinite clay with acid treatment can be used as more effective adsorbent for the adsorption of Cs+ ions from aqueous solution than natural kaolinite clay.

Annealing effects on 100 keV silicon negative ions implanted SiO2 thin films

SiO2 thin film of thickness 300 nm grown on p-type silicon substrate was implanted with 100 keV silicon negative ions for the fluences of 1 × 1016, 5 × 1016, and 1 × 1017 ions cm−2. The implanted samples were investigated using an energy-dispersive X-ray (EDX) spectroscopic technique, and the samples were annealed at a temperature of 900 oC under N2 ambient. Ultraviolet–visible near infrared (UV-Vis-NIR) spectroscopy has been used to investigate the implanted SiO2 thin film samples before and after thermal annealing. EDX results revealed an increase in the atomic percentage and weight percentage of silicon ions as compared to oxygen ions in SiO2 thin film. This may be due to the increase in the concentration of silicon ions with the increase of implanted ion fluences within the SiO2 thin film. UV-Vis-NIR studies showed higher transmittance for thermally annealed samples as compared to non-annealed samples. This may be attributed to the creation of a new SiOx phase in the SiO2 matrix at higher temperatures. UV-Vis-NIR studies also exhibited an increase in the energy band gap value after thermal annealing. This effect may be related to the formation of silicon nanoclusters in SiO2 thin film.

Use of Activated and Modified Pumice Stone for Removal of Mercury (II) and Arsenic (III) Ions From Aqueous Solution

Removal of Hg (II) and As (III) ions from aqueous solutions using activated and modified pumice stone were investigated. The pH, temperature, initial metal ion concentration which are very important for removal studies, were investigated by batch method. The experiments demonstrated that the equilibrium adsorption data fit the Freundlich isotherm model well for Hg (II) and As (III) ions. The negative value of ΔH° = -199.92 kJ mol-1 and -78,15 kJ mol-1 for mercury (II) and arsenic (III) ions indicates that the adsorption process is exothermic. ΔS° were calculated as -267.85 J K-1 mol-1 for As (III) ions and the positive value of ΔS° = 0.69 kJ K-1 mol-1 for Hg (II) ions. The negative value of ΔG°=-405.14 kJ mol-1 for Hg (II) ions and -1.67 kJ mol-1 for As (III) ions indicates that adsorption is voluntary. EDTA has been found to be a good desorbent in desorption studies to recover arsenic and Hg ions. The experiments show that pumice stone can be used for Hg (II) and As (III) removal in aqueous solution.

Water deironing through the reagent and biosorption treatment and utilization of iron-rich sediments and biosornets in cement production

ABSTRACT The processes of reagent and sorption removal of iron ions from water were investigated and the efficiency of deironing was evaluated. Lime and biosorbents based on walnut shells were used through experiments. The range of iron ions concentrations from 2 to 100 mg/L was studied. The efficiency of deironing is reached maximum efficiency during biosorbtion. In order to create resource-efficient technologies, it is important to develop effective methods of sludge and spent sorbents utilisation. The sediments formed as a result of reagent and sorption purification of water from iron were utilised in the composition of cement with the consumption 3%. The effect of additives application in cement production was evaluated according to the following properties: normal density, coefficient of water separation, time of hardening, compressive strength at the age of 2 and 28 days.

Water Quality Assessment of the Euphrates River from Haditha to Al-Nasiriyah, Iraq

A comprehensive assessment of four gauging stations along the Euphrates River reach (Haditha, Al-Hindiya, Samawa, and Al-Nasiriyah) was conducted to assess the water quality deterioration spatially and temporarily for the period 2005-2021. The spotlight is on discharge rates and climate conditions, which mainly controlling water quality and availability. The mean monthly discharge rate was taken 2005–2021, in addition to the water quality parameters (TDS, pH, EC, Mg+2, Ca+2, Na+, SO4-2, Cl-, and HCO3-, BOD5, COD, FCB, and E. coli). The discharge rates showed a visible decrease downstream, causing the river salinity and all the ion concentrations to rise. The statistical package of social sciences revealed two groups of water pollution sources: The F1 reflects natural conditions produced from the dissolution of the basin rocks, with a percentage of 28.0% from the total variance; the eigenvalue is 4.4. F2 reflects the anthropogenic sources, contributing 14.5% and having an eigenvalue of 2.1. The total ionic salinity plot indicated less than 2000 mg/l at the Haditha and Al-Hindiya sites and between 3000 and 4000 mg/l at downstream sites (Samawa and Al-Nasiriyah). The transportation of dissolved loads is decreased downstream following the discharge rate as indicated by the rating curves, as follows: 781000, 542628.4, 443861, and 432950.4 tons/month for Haditha, Al-Hindiya, Samawa, and Al-Nasiriyah, respectively. Water type shows a notable downstream deterioration, from MgSO4 at Haditha and Na2SO4 at Al-Hindiya to NaCl at Samawa and Al-Nasiriyah sites.

Spesiasi dan Bioavailabilitas Merkuri dalam Sedimen Teluk Palu Pasca Gempa dan Tsunami dengan Metode Diffusive Gradient in Thin Film (DGT)

Speciation and bioavailability of mercury in the sediments of Palu Bay after the earthquake and tsunami were conducted using fractionation and Diffusion Gradient in Thin Films (DGT). This method has been conducted using sediment samples from the estuary of the Pondo River, Palu. Heavy metal speciation of mercury ions was conducted by looking at the distribution of mercury ions in various species by sequential extraction and heavy metal bioavailability of mercury ions. This method was conducted by looking at the migration of mercury ions from sediments into the seawaters using a Diffusive Gradient in Thin Films (DGT). The speciation of mercury ions concentration with sequential extraction as EFLE (easily, freely, leachable, exchangeable) fraction is about &lt; 0.0005 ppm, the oxidizable fraction is about &lt; 0.0005 ppm and the resistant fraction is between &lt; 0.0005 ppm to 0.0063 ppm. The results of DGT experiments to study the migration of mercury ions from sediments into the seawaters during 3 days of immersion is between 0.01003 ppm and 0.01748 ppm. The availability of mercury ions concentration in the sediments allows for the migration of mercury ions into water.

Oxidative transformation of methionine by pyridinium chlorochromate in aqueous DMF medium: A kinetic study

The Kinetics of Oxidative transformation of Methionine by pyridinium chlorochromate in aqueous DMF medium, containing perchloric acid has been studied. The rate of reaction was found to be of first order dependence on PCC, Methionine, and H+ ion Concentration. Michaelis–Menten type kinetics is observed respect to substrate. The increase in the rate of reaction with increase in acidity indicates the involvement of a protonated chromium(VI) species in the rate-determining step. The product of oxidation has been identified as methionine sulfoxide. The rate of reaction increased with increase in dielectric constant of the reaction medium. The plots of logkobs versus (D-1) / (2D+1) are non linear Indicating that there is an involvement of positive ion-dipole in the rate determining step. The activation parameters have been evaluated. On the basis of the experimental findings, a suitable mechanism and rate law has been proposed.

Greenhouse farming: Hydroponic vertical farming- Internet of Things (IOT) Technologies: An updated review

This review paper of literature highlights the importance of greenhouse urban farming technology, hydroponics, aeroponics, aquaponics, vertical farming and applications of Internet of Things (IOT) technologies. The greenhouse farming is a well known modern agriculture technology for optimal plant growth. Hydroponics, a soilless cultivation technique using nutrient solutions under controlled conditions, is used for growing vegetables, high-value crops, and flowers. Vertical farming is a popular trend in hydroponics that involves stacking multiple layers of plants in a vertical arrangement. This farming method saves space, reduces water usage, and increases yields per square foot of growing area. In comparison to conventional greenhouse cultivation, hydroponics requires less fertilizer, pesticides, and water due to the precise control over their distribution. The term “Internet of Things (IOT)” is a system of interconnected computing devices, sensors, objects, microcontrollers, and cloud servers that can transmit data across a network and control other devices remotely without human intervention. A better management of nutrient solution in hydroponic systems requires optimum pH, electrical conductivity (EC), or ions concentration. The three main greenhouse farming gases (GHGs) emissions in hydroponics hi-tech urban farming are nitrous oxide, methane and carbon dioxide (CO2). To measure the levels of CO2 in hydroponics, the more intermediate to advanced grower can use a CO2 monitoring and controllers system. Hydroponic vertical farming is in infancy in India. Although hydroponic vertical farming units for production of crops like strawberry, lettuce and other leafy vegetables, foliage and flowers are functioning in major metros of India. However, the organized hydroponic vertical farms for production of food crops are not available in India. Therefore, only a few successful hydroponic vertical farms have been built in India mainly due to the initial high price tag on construction and the cost of maintaining them afterwards. Another disadvantage is carbon footprint of hydroponic vertical farming is very high, and discourages its applications.