Rapid Detection of Mercury Ions Using Sustainable Natural Gum-Based Silver Nanoparticles

: Fabrication of metal nanostructures using natural products has attracted scientists and researchers due to its renewable and environmentally benign availability. This work has prepared an eco-friendly, low-cost, and rapid colorimetric sensor of silver nanoparticles using tree gum as a reducing and stabilizing agent. Several characterization techniques have been exploited to describe the synthesized nanosensor morphology and optical properties. Ultraviolet − Visible (UV − Vis) spectroscopy has been used for monitoring the localized plasmon surface area. High-resolution transmission electron microscopy (HR-TEM) illustrated the size and shape of silver nanoparticles. X-ray diffraction spectra showed the crystallography and purity of the product. Silver nanoparticles decorated with almond gum molecules (AgNPs@AG) demonstrated high sensitivity and colorimetric detection of mercury ions in water samples. The method is based on the aggregation of AgNPs and the disappearing yellow color of AgNPs via a spectrophotometer. The detection limit of this method was reported to be 0.5 mg/L. This work aimed to synthesize a rapid, easy-preparation, eco-friendly, and efﬁcient naked-eye colorimetric sensor to detect toxic pollutants in aqueous samples.


Introduction
Population growth worldwide has led to increased demand for drinking water in recent years. However, water resources have suffered from pollution due to industrial sectors' discharging various kinds of pollutants and harmful substances. Many kinds of pollutants, such as herbicides, pesticides, dyes, plastics, oil derivatives, and heavy metals [1][2][3][4], have been found in water effluents, which is the main reason behind the development of health issues among people. Mercury and its compounds are among the most harmful species reported and adversely affect human health [5]. Mercury affects the central nervous system, liver, and kidney. Further, it can disturb the immune system due to impaired hearing, vision, paralysis, and emotional instability. Many analytical techniques are employed for detecting mercury ions, such as inductively coupled plasma atomic emission and mass spectroscopy, cold vapor atomic absorption spectroscopy, cold vapor atomic fluorescence spectroscopy, and high-performance liquid chromatography with UV−Vis detection [6]. However, these techniques suffer from several limitations, for instance, time consumption, harmful solvents, equipment costs, and complex procedures [7]. Therefore, developing new approaches to detecting and determining mercury ions becomes crucial and an urgent need.
Metal nanoparticles possess several unique optical, photothermal, and electrical properties. These distinctive characteristics make scientists more curious to investigate and uncover the potential applications of metal nanoparticles [8]. Gold, silver, and copper nanoparticles have been used widely in many fields such as medicine, industry, agriculture,

Fabrication of AgNPs@AG
Nanotechnology's essence is synthesizing nanoparticles according to simple, easy, inexpensive, and environmentally friendly steps, including the use of green natural resources. However, validating the principle of the synthesis of nanoparticles using bio-waste extracts, including plants, is considered to be of paramount importance in the scientific and research community. Over the past years, many green metallic nanoparticles, including copper, selenium, titanium, and silver, have been synthesized according to the green reduction mechanism through active biological components operating in plants. Most of the plant body comprises multiple vital compounds, such as proteins, carboxylic acids, flavonoids, glycosides, and polysaccharides, in addition to a percentage of metals and hydrating compounds. Due to its high biosignificance, the gum contents have been investigated by Hossein and Ali's group using HPLC and FTIR analysis [21]. The HPLC analysis revealed that the gum contains an excellent ratio of many active chemical compounds, such as proteins, polysaccharides, uronic acid, fats, and ash.
In contrast, the FTIR study for these compounds showed that their structures consist of various active functional groups such as C=O, CO 2 H, OH, and NH 2 . According to the analysis, the high value of the almond gum return to the polysaccharide, which involve several monosaccharides such as rhamnose, mannose, glucose, xylose, arabinose, and galactose existing in the branched chain of structure. However, due to the foundation of hydroxy−flavonoid structure in these saccharides containing a high OH groups ratio, it is responsible for reducing many metal ions to nanoparticles. Therefore, the formation of AgNPs@AG can be attributed to the poly-and monosaccharides molecules, which are considered active chelating compounds because they possess multiple hydroxyl groups located at carbon atoms of the flavone rings (Scheme 1). This hypothesis has been confirmed by several published reports on reducing various metal ions, such as Cu 2+ , Se 2+ , Ti 4+ Fe 3+ , and Zn 2+ , using plant extracts [22]. analysis revealed that the gum contains an excellent ratio of many active chemical compounds, such as proteins, polysaccharides, uronic acid, fats, and ash. In contrast, the FTIR study for these compounds showed that their structures consist of various active functional groups such as C=O, CO2H, OH, and NH2. According to the analysis, the high value of the almond gum return to the polysaccharide, which involve several monosaccharides such as rhamnose, mannose, glucose, xylose, arabinose, and galactose existing in the branched chain of structure. However, due to the foundation of hydroxy−flavonoid structure in these saccharides containing a high OH groups ratio, it is responsible for reducing many metal ions to nanoparticles. Therefore, the formation of AgNPs@AG can be attributed to the poly-and monosaccharides molecules, which are considered active chelating compounds because they possess multiple hydroxyl groups located at carbon atoms of the flavone rings (Scheme 1). This hypothesis has been confirmed by several published reports on reducing various metal ions, such as Cu 2+ , Se 2+ , Ti 4+ Fe 3+ , and Zn 2+ , using plant extracts [22]. Scheme 1. The supposed mechanism for the fabrication of AgNPs@AG by an almond gum extract.

UV−Vis Analysis Measurement
Employing ultra violet-visible spectroscopy to identify nanoparticles is a powerful and valuable method for the preliminary diagnosis of bio-fabricated AgNPs@AG. However, after mixing the required colorless components for the preparation of the AgNPs@AG catalyst, dark brown color was formed. The formation of this color was an initial confirmation of the synthesis of AgNPs@AG. Nevertheless, for more support, the observed color value of the catalyst was read on a nanodrop 2000/2000c spectrophotometer at the scale of 250−700 nm, where a robust and broad curve at 410 nm was recorded on the formation of nanoparticles with LSPR properties. The appearance of this result is a confirmation point on the formation of NPs in nanosizes, which agrees with a previous Scheme 1. The supposed mechanism for the fabrication of AgNPs@AG by an almond gum extract.

UV−Vis Analysis Measurement
Employing ultra violet-visible spectroscopy to identify nanoparticles is a powerful and valuable method for the preliminary diagnosis of bio-fabricated AgNPs@AG. However, after mixing the required colorless components for the preparation of the AgNPs@AG catalyst, dark brown color was formed. The formation of this color was an initial confirmation of the synthesis of AgNPs@AG. Nevertheless, for more support, the observed color value of the catalyst was read on a nanodrop 2000/2000c spectrophotometer at the scale of 250−700 nm, where a robust and broad curve at 410 nm was recorded on the formation of nanoparticles with LSPR properties. The appearance of this result is a confirmation point on the formation of NPs in nanosizes, which agrees with a previous published report' data [23]. The brown−yellow color formation was returned to the reduction process between the Ag + ions and active functional groups present in the gum extract components and eventually formed Ag 0 . Moreover, it was due to the excitation of the surface plasmon resonance (SPR) vibrations of electrons in AgNPs (Figure 1-red line). The valence band and the conduction band of the AgNPs were very close, making a good reason for electrons moving freely, giving a sharp SPR absorption band at 410 nm [24]. In contrast, this band was monitored after adding a brown−yellow sensor solution to the mercury ions sample (Figure 1-blue line). The analysis revealed excellent suppression for the sensor color to be colorless during 13 seconds at ambient conditions. Furthermore, this color's disappearance and formation of a colorless phase were approved on the well unit of Ag with Hg ions to form a Ag−Hg phase in the aqueous solution. This result has been proven in many literature and research works [25].
published report' data [23]. The brown−yellow color formation was returned to the reduction process between the Ag + ions and active functional groups present in the gum extract components and eventually formed Ag 0 . Moreover, it was due to the excitation of the surface plasmon resonance (SPR) vibrations of electrons in AgNPs (Figure 1-red line). The valence band and the conduction band of the AgNPs were very close, making a good reason for electrons moving freely, giving a sharp SPR absorption band at 410 nm [24]. In contrast, this band was monitored after adding a brown−yellow sensor solution to the mercury ions sample (Figure 1-blue line). The analysis revealed excellent suppression for the sensor color to be colorless during 13 seconds at ambient conditions. Furthermore, this color's disappearance and formation of a colorless phase were approved on the well unit of Ag with Hg ions to form a Ag−Hg phase in the aqueous solution. This result has been proven in many literature and research works [25].

Surface Morphology Diagnosis
Investigation of the oxidation states and nature of the surface of the prepared nanomaterials is crucial and widely needed in multiple applications and fields. For this requirement, XPs analysis was utilized to diagnose the orbitals type formed for AG surfaces and encapsulated AgNps as well as the reaction mixture sample (AgNPS−Hg or Ag−Hg) as shown in Figure 2a,b. For the AG extract ( Figure 2a-blue line), the XPS analysis chart showed two firm peaks located at binding energies of 283 and 539 eV, returning to the carbon atom (C 1s) and an oxygen atom (O 1s), respectively. However, the appearance of these atoms (i.e., C and O) are generally back to the presence of multi-organic compounds in gum bio content such as flavones, phenols, and carboxylic acids, which especially possess multi-functional groups in their structures such as C−C, C−O−C, C=O, OH, and COOH. The presence of these active groups came from the existence of hydroxyl and carbonyl groups that built the polymeric structure of polysaccharides. Additionally, these single bands (C 1s and O 1s) were extensive supports and evidence of the stability of cyclic C−C atoms of ketonic polysaccharides rings in the resin structure. The measured results of previous works strongly confirm the recorded data in this regard [26]. In contrast, after encapsulating the AG−Ag NPs by resin, the analysis survey of XPs (Figure 2a-black line) showed excellent three satellite peaks located at 288, 400, and 533 eV, respectively, which

Surface Morphology Diagnosis
Investigation of the oxidation states and nature of the surface of the prepared nanomaterials is crucial and widely needed in multiple applications and fields. For this requirement, XPs analysis was utilized to diagnose the orbitals type formed for AG surfaces and encapsulated AgNps as well as the reaction mixture sample (AgNPS−Hg or Ag−Hg) as shown in Figure 2a,b. For the AG extract ( Figure 2a-blue line), the XPS analysis chart showed two firm peaks located at binding energies of 283 and 539 eV, returning to the carbon atom (C 1s) and an oxygen atom (O 1s), respectively. However, the appearance of these atoms (i.e., C and O) are generally back to the presence of multi-organic compounds in gum bio content such as flavones, phenols, and carboxylic acids, which especially possess multi-functional groups in their structures such as C−C, C−O−C, C=O, OH, and COOH. The presence of these active groups came from the existence of hydroxyl and carbonyl groups that built the polymeric structure of polysaccharides. Additionally, these single bands (C 1s and O 1s) were extensive supports and evidence of the stability of cyclic C−C atoms of ketonic polysaccharides rings in the resin structure. The measured results of previous works strongly confirm the recorded data in this regard [26]. In contrast, after encapsulating the AG−Ag NPs by resin, the analysis survey of XPs (Figure 2a-black line) showed excellent three satellite peaks located at 288, 400, and 533 eV, respectively, which are attributed to the core levels of C 1s, Ag 3d, and O 1s, respectively. Noticing and recording these orbitals is a good indication of the coating of synthesized NPs by gum components. This diagnosis corresponds well with the previously published reports for the fabrication of a zerovalent silver state [27]. No presence or appearance of other elements in the spectrum analysis is a well proof of the use of almond gum as a sustainable reducing and stabilizing agent for designing silver nanosensors. However, the sensor activity for the prepared AgNPs@AG was tested, and XPs analysis survey was applied to show the sensor efficiency in detecting Hg ions to prove the reaction process between AgNPs and Hg ions. XPs diagnosis for the mixture (Figure 2b-brown line) revealed significant photoelectron peaks values at 100 and 120 eV, which returned to the orbital states of Ag 3d5/2 and Hg 4f, respectively. These types of orbitals were formed due to the adsorption of mercury ions on the gum surface. The redox process by the transition of electrons between the Ag 0 and Hg 2+ ions occurred, thus forming the Ag−Hg state. These obtained results agree with the previous literature in forming the Ag−Hg phase [28]. The stability and contacting effects for each AgNPs@AG and formatted Ag−Hg solutions with ambient conditions were evaluated for more support. The process was performed by opening the bottle head at different times (24 to 240 h), as shown in Figure 2b (black line). The fabricated sensor recorded no notable change in color or their stability to produce another state, indicating the perfect role of the gum in protecting the silver nanoparticles and using it for long periods.
are attributed to the core levels of C 1s, Ag 3d, and O 1s, respectively. Noticing and recording these orbitals is a good indication of the coating of synthesized NPs by gum components. This diagnosis corresponds well with the previously published reports for the fabrication of a zerovalent silver state [27]. No presence or appearance of other elements in the spectrum analysis is a well proof of the use of almond gum as a sustainable reducing and stabilizing agent for designing silver nanosensors. However, the sensor activity for the prepared AgNPs@AG was tested, and XPs analysis survey was applied to show the sensor efficiency in detecting Hg ions to prove the reaction process between AgNPs and Hg ions. XPs diagnosis for the mixture (Figure 2b-brown line) revealed significant photoelectron peaks values at 100 and 120 eV, which returned to the orbital states of Ag 3d5/2 and Hg 4f, respectively. These types of orbitals were formed due to the adsorption of mercury ions on the gum surface. The redox process by the transition of electrons between the Ag 0 and Hg 2+ ions occurred, thus forming the Ag−Hg state. These obtained results agree with the previous literature in forming the Ag−Hg phase [28]. The stability and contacting effects for each AgNPs@AG and formatted Ag−Hg solutions with ambient conditions were evaluated for more support. The process was performed by opening the bottle head at different times (24 to 240 h), as shown in Figure 2b (black line). The fabricated sensor recorded no notable change in color or their stability to produce another state, indicating the perfect role of the gum in protecting the silver nanoparticles and using it for long periods.

XRD Measurement
XRD is a unique tool used to determine the crystalline structure of the fabricated materials at different scales. However, XRD analysis has been applied for each AG, AgNPs@AG, and Ag−Hg. The spectrum line pattern of AG (black line) revealed a signifi-

XRD Measurement
XRD is a unique tool used to determine the crystalline structure of the fabricated materials at different scales. However, XRD analysis has been applied for each AG, AgNPs@AG, and Ag−Hg. The spectrum line pattern of AG (black line) revealed a significant broad peak located at 2θ, 20 • , which assumed back to the polysaccharide present in the gum composition [29]. This value was recorded besides the formation of AgNPs, after they encapsulated the AgNPs, where the analysis spectrum of AgNPs@AG (brown line) revealed excellent four peaks localized at 2θ values of 38.27 • , 44.48 • , 64.59 • , and 77.46 • , respectively, which had the corresponding planes (hkl) (111), (200), (220), and (311), respectively, as shown in Figure 3. The recorded results confirmed that the prepared AgNPs@AG possessed face-centered cubic lattices [15]. The appearance of sharp peaks in the X-ray spectrum at the base level strongly indicated that the synthesized AgNPs were prepared in a good form. The average size (D) for the as-prepared AgNPs@AG was calculated by employing the Scherrer equation (D = [0.9λ/ βcosθ]), where λ and β represent the wavelength source and the breadth of the diffraction line at its half intensity maximum recorded in XRD spectrum, respectively. The calculations showed that the average size of the prepared AgNPs@AG crystalline was found to be 19 nm. However, after treating the prepared sensor with the sample of mercury ions, the XRD spectrum pattern (blue line) recorded the absence of AgNPs@AG peaks with the appearance of new interesting sharp peaks at locations 25.79 • , 32.51 • , 56.26 • , and 66.11 • , which returned to the formation of the Ag−Hg status. These measured values agree with the previous work's results [30].

FESEM and HR-TEM Photograph Analysis
The external and internal structures of the prepared nanoparticles has been explored and determined by FESEM and HR-TEM microanalysis. It is essential for its contribution to characterizing the particle type involved in the colorimetric response process. The analysis of FE-SEM photos (Figure 4a) revealed that AgNPs@AG formed in tiny and nonagglomerated spherical shapes due to the oily biomass nature of the gum extract. In addition, the image analysis (Figure 4b) revealed that the AgNPs@AG particles formed with perfect sizes ranging from 15 to 17 nm, which indicated the efficiency of the bio fabrication method. However, after adding these small nanosize AgNPs to the Hg ions sample, FESEM images showed excellent aggregation of precipitate, attributed to the formation of Ag−Hg (Figure 4c). The formation of the mercury−silver state occurred through the adsorption of mercury ions on the active surface of the AgNPs. Further, it could be due to its adhesion to the resin covering the AgNPs surface, which then interacted with the active AgNPs. There was a consistent parallel agreement between the images acquired from the HR-TEM and the data collected from the FESEM regarding the formation of small nanosphere particles. (Figure 4d). In contrast, Figure 4e proved the good trapping of mercury ions by the sensor with perfect aggregation. XRD and XPs have confirmed this hypothesis analysis results, in addition to the results and explanations of the published research.

EDS and EDC Identification
Synthesizing and producing good, clean, cheap, and sustainable sensors using green methods for colorimetric response is considered one of the most important challenges for researchers. For this purpose, the purity of fabricated AgNPs@AG was evaluated by determining their components using elements distribution spectroscopy (EDS) supported by elements spread diagram (ESD). The EDS spectrum (Figure 5a) revealed good weights ratios of elements for silver (Ag = 34.2%), oxygen (O = 17.5%), and carbon (C = 47.4%). No emergence or recording of other elements in the EDS chart is strong evidence of the clean methodology for this process. However, this advantage was exploited for the detection of Hg ions by the prepared sensor, where the analysis revealed the excellent formation of the Ag−Hg compound with ratios of 45, 67, 77, and 98, which belonged to the Ag, O, C and Hg, respectively (Figure 5b). EDS analysis clearly supported the XRD, XPs, FESEM, and HR-TEM analysis results, as it proved that the agglomeration of components and the formation of the Ag−Hg structure were due to the role of the bio-active surface of AgNPs and their resin coating that acted as a linking and reducing agent.

Factors
Affecting the Sensing Process 2.7.1. Effect of pH on the Reaction Medium It was recorded that the pH of AgNPs@AG was slightly acidic (6.1). This could promote that the as-prepared silver nanosensor was coated with proton donor functional groups such as hydroxyl, carboxyl, and carbonyl groups, which remarkably exist in carbohydrate molecules mentioned in almond gum constituents [31]. However, by examining the impact of acidity and basicity on the medium of the reaction, we observed that the absorbance value of the mixture was increased. This could be attributed to the formation of turbidity. Moreover, the assumed reason we expected was the presence of a small percentage of protein participating in the capping process of silver nanoparticles. However, the optimum pH of the mixture was assigned at 6.1, as shown in Figure 6.  methodology for this process. However, this advantage was exploited for the detection of Hg ions by the prepared sensor, where the analysis revealed the excellent formation of the Ag−Hg compound with ratios of 45, 67, 77, and 98, which belonged to the Ag, O, C and Hg, respectively (Figure 5b). EDS analysis clearly supported the XRD, XPs, FESEM, and HR-TEM analysis results, as it proved that the agglomeration of components and the formation of the Ag−Hg structure were due to the role of the bio-active surface of AgNPs and their resin coating that acted as a linking and reducing agent.

Effect of pH on the Reaction Medium
It was recorded that the pH of AgNPs@AG was slightly acidic (6.1). This could promote that the as-prepared silver nanosensor was coated with proton donor functional groups such as hydroxyl, carboxyl, and carbonyl groups, which remarkably exist in carbohydrate molecules mentioned in almond gum constituents [31]. However, by examining the impact of acidity and basicity on the medium of the reaction, we observed that the absorbance value of the mixture was increased. This could be attributed to the formation of turbidity. Moreover, the assumed reason we expected was the presence of a small percentage of protein participating in the capping process of silver nanoparticles. However, the optimum pH of the mixture was assigned at 6.1, as shown in Figure 6.

Calibration Curve of the Method
The validity of the method was examined after standardizing the optimum conditions. The change in ∆A value of AgNPs@AG was monitored at 410 nm (Figure 7a) upon mixing the silver nanosensor with Hg 2+ ions. The method observed good linearity achieved over a concentration range of 10-180 mg/L (see Figure 7b) by plotting the absorbance values against Hg 2+ concentrations. Further, the correlation of determination (R 2 ) was 0.989. Therefore, the limit of detection (LOD) was 0.5 mg/L, and the limit of quantification (LOQ) was calculated to be 1.69 mg/L. The limit of detection (LOD) and the limit of quantification (LOQ) were determined from the equation (3 ∂/slope) and (10 ∂/slope), respectively.

Effect of Time on the Sensing Process
The time effect was studied by monitoring the color change of AgNPs@AG from yellow color to colorless. Further, the sensing behavior was tracked using a spectrophotometer following the decreasing absorbance value against blank. It was shown that the sensing of mercury ions in an aqueous medium by silver nanoparticles was very rapid and the yellow color of AgNPs@AG disappeared instantly after the addition of silver nanoparticles with Hg 2+ ions. The recorded time for this action was 30 s, indicating that the sensing process was swift and efficient.

Comparative Study between AgNPs@AG and Other Catalysts in Hg Detection
Comparing and evaluating the preparation approach, ease of conduct, and activity of any newly prepared catalyst with previously synthesized catalysts is crucial to achieving the same purpose. Here, the activity and efficiency of our fabricated sensor based on the LSPR of AgNPs@AG to detect Hg 2+ ions were compared with those obtained by previous methods and works (Table 1). Furthermore, the prepared catalyst was compared with many different nano metallic sensors for detecting Hg 2+ ions. The comparison table shows that our novel fabricated AgNPs@AG revealed good results for Hg 2+ ions detection compared to the different synthesized green sensors and chemically synthesized ones. The good benefits of AgNPs@AG sensor are represented in the quick sensing of Hg 2+ ion with the color change and noticing it with the naked eye in a short time. This result confirmed that the surface of our catalyst had excellent activity. In addition, it had high efficiency with low cost and was environment-friendly. Another advantage was that our procedure for estimating Hg 2+ ions was compared with the different approaches. The recorded data for our work principle proved that it is easy to perform, sensitive, and cheap without needing any further enhancement or using large complex apparatuses or relatively complex detection steps that need a long time.

Evaluation of the Sensor Selectivity
The performance sensitivity, selectivity, and the naked eye noticeable for AgNPs@AG sensor against groups of different anions and cations were evaluated. The test was performed with the same optimum conditions (a mixture of 3 mL Hg 2+ and 50 µL of Ag-NPs@AG) against several cations and anions. The recommended method was tracked to evaluate the effect of the interferences on determining the Hg 2+ ions. However, interferences for I − , Cl − , Na + , and Li + were at 1000 ppm and those for Mg 2+ , Ba 2+ , and NO3 − were at 250 ppm, whereas interferences for Zn 2+ , Fe 2+ and Co 2+ were at 50 ppm. For adequate consideration, an error of 5% in concentration was recorded. The sensor behavior against mercury ions revealed excellent yellow color with a clear naked eye seen (Figure 8a). In contrast, the foreign ions did not overlap with the required ion (Hg ions) during the sensing process, even with the high concentrations, with no color change. However, based on the monitoring process of the reaction mixture by the naked eye (Figure 8a), no change in the yellow color solution was observed in less than 13 seconds and even 10 minutes for the common ions of Zn 2+ , Co 2+ , Fe 2+ , Mg 2+ , Ba 2+ , Na + , K + , I − , Cl − , and NO 3 − even at concentrations 500 times higher than for mercury. UV−Vis analysis supported this behavior more (Figure 8b,c). The variation detail of UV−Vis measurements revealed that the sensor's selectivity worked only with mercury ions with a significant change in the absorbance curve, ranging from 0 to 0.19 nm. In contrast, the analysis revealed low absorbance changes with the other ions (Zn 2+ , Co 2+ , Fe 2+ , Mg 2+ , Ba 2+ , Na + , Li + , I − , Cl − , and NO 3 − for the ranges of 0.01, 0.03, 0.02, 0.04, 0.04, 0.04, 0.02, 0.04, 0.04, and 0.05 nm, respectively). The results confirmed that this novel sensor had excellent detection performance for mercury ions in the effluent.

Performance of the AgNPs@AG Sensor in Tap Water Samples
In this part, the performance of the developed AgNPs@AG sensor was evaluated by utilizing it with collected actual water samples for the detection and determination of mercury ions. Water samples (home drinking water) were collected from different places in Shekan area in Duhok city and in Kurdistan region in Iraq during different times. This test was performed to prove the reliability of the efficient colorimetric detection response method of the AgNPs@AG sensor in practical applications. First, the principle of pretreatment for water samples was applied according to the protocol of Section 2.4. According to the obtained data in Table 2, it was reported that the sensor behavior revealed no color transformation with the samples of tap water (i.e., before dealing it with mercury ions) even with high addition concentrations of the sensor. Furthermore, it indicated no mercury ions in tap water samples or overlapping water total contents with the sensor solution. In contrast, after the treatment of the same water samples with mercury ions, the recovery experiments for mercury ions were carried out, and the results were recorded as shown in Table 2. The recovery process results revealed that the prepared silver catalyst had good recovery activity for mercury ions and with ratios of 91.5-101.7% at different concentrations (10-50 ppm), which proved that the presented method is feasible for the mercury ions detection in real environmental water samples.

Assumed Colorimetric Response of AgNPs@AG against Hg 2+ Ions
The proposed mechanism for the response of the as-prepared nano silver catalyst (AgNPs@AG) against sensing and detection of mercury ions [Hg 2+ ] is predicted, as the illustrated pathway (Scheme 2): firstly, mercury ion [Hg 2+ ] coordinates with almond gum by hydroxyl [−OH] and carboxylic [−CO2H] groups, as confirmed and proved by the XPs study, leading to the formation of Hg-almond gum complex. Furthermore, during an increase in Hg 2+ ion concentration, Hg 2+ ions quickly adsorb on the active surface of the AgNPs, after the redox reaction between Ag0 and Hg 2+ and production of Ag + and Hg + . After that, the state of Ag 0 is changed to the Ag + state through the electron transfer process from almond gum to Ag + , thus initializing the process between both Ag + and Hg + to form of the Ag−Hg phase. Therefore, in this process, almond gum plays a significant role in reducing, stabilizing, and being a good electron donor in preparation for each AgNP and Ag−Hg state. Furthermore, the electron transmission from almond gum to Ag + gains support from the suggested synthetic procedure without additional reducing agents used during the AgNPs fabrication [30]. The fabrication of AgNPs@AG and the formation of Ag-Hg were confirmed and supported by UV−Vis measurement, XRD study, XPs analysis, and an increase in the nanoparticles' sizes for both silver nanoparticles and the amalgamate that appeared by the FESEM and HR-TEM images analysis. The increase in nanoparticle size was due to the well-active surface of the prepared NPs, causing perfect agglomeration and a "swelling effect" that occurs, which is attributed to the diffusion of Hg atoms, thus increasing the total nanoparticle sizes. Another vital piece of evidence, the high decrease in the wavelength value of AgNPs@AG at a constant position (410 nm) at the addition of mercury ions, could be attributed to the displacement of almond gum on the AgNPs surface by mercury ions due to the higher affinity of Ag toward the Hg ions. Hence, this leads to the fabrication of Ag−Hg with the aqueous phase.
A healthy almond gum was collected from Charboot village, Zeebar district in Akre and Duhok−Kurdistan region of Iraq in August 2021. A mercury chloride stock solution (100 mg/L) was prepared daily due to dissolving a certain weight of mercury chloride salt in distilled water. The stock solution of mercury chloride was then stored in a dark container in a cool place for the subsequent experiments. All experiments were performed in Scheme 2. Assumed colorimetric response of AgNPs@AG against Hg 2+ ions.
A healthy almond gum was collected from Charboot village, Zeebar district in Akre and Duhok−Kurdistan region of Iraq in August 2021. A mercury chloride stock solution (100 mg/L) was prepared daily due to dissolving a certain weight of mercury chloride salt in distilled water. The stock solution of mercury chloride was then stored in a dark container in a cool place for the subsequent experiments. All experiments were performed in the laboratory under ambient conditions.

Preparation of the Almond Gum Solution
The solution of 1% almond gum was prepared following these steps. First, the solid particles of almond gum were crushed to a fine powder by a mortar. Next, 1 g of the gum powder was transferred to a conical flask, dissolved with 100 mL distilled water and stirred vigorously at 50 • C for 30 min. Finally, the mixture was filtered with a gauze and a filter paper to separate insoluble solid fractions and stored in a refrigerator at 2 • C to be used for the reduction process of silver ions.

Fabrication of Silver Nanoparticles (AgNPs@AG)
The synthesis process included mixing 3 mL of a 0.1 M AgNO3 solution with 25 µL of 0.3 M NaOH. The mixture was stirred at 70 • C for 20 min. Afterwards, 2 mL of 1% almond gum solution were added to the mixture, followed by stirring for 45 min. A yellow−brown color appeared 15 min after the addition of the almond gum solution. The yellow−brown color continuously developed, until the whole mixture became brown, indicating the reduction process of silver ions and the formation of silver nanoparticles.

Detection of Hg 2+ Ions by AgNPs@AG
An easy and short procedure was conducted to investigate the efficiency of Ag-NPs@AG as a rapid colorimetric sensor to detect mercury ions in an aqueous solution. A group of 5 mL glass vials was arranged and filled with 3 mL of different concentrations of mercury ions (10,20,30,40,50,60,70,80,90, and 100 mg/L). It was shown that the yellow color of AgNPs@AG disappeared rapidly after each addition of silver nanoparticles to the mercury solution, indicating that AG@NPs worked as an efficient probe against mercury ions in an aqueous solution. The procedure was monitored by a UV−Vis device to follow the decrease in absorbance at 410 nm to confirm the sensing process.

Detection of Mercury Ions in Real Water Samples
Various drinking water samples were collected from different locations in Shekhan District and Duhok in Iraq. The sensing of mercury ions in real water samples was conducted according to the optimum conditions of the procedure.

Diagnosis Techniques Used
The synthesized AgNPs@AG sensor was diagnosed with several techniques, including using an ultraviolet−visible (UV-Vis) spectrophotometer (nanodrop 2000/2000 c) to record the predicted LSPR band for the brown−yellow solution of AgNPs. X-ray diffraction (XRD) measurement was performed for AgNPs@AG by a PAN analytical X'PERT PRO model X-ray diffractometer operated at 30 kV and 45 mA, to reveal the crystalline nature of AgNPs@AG. The chemical surface nature of AgNPs@AG was diagnosed with an X-ray photoelectron spectroscopy (XPS) tool (PHI 5000 Versa Prob II: Supplier Model, japan), supported with an Al anode set at 140 W and operated at a pass energy of 50 eV. Fieldemission scanning electron microscopy (FESEM) analysis (SEM-ZEISS-Singapore, Malaysia) with an accelerating voltage of 20 kV, supported with energy-dispersive spectroscopy (EDS) measurement, was used to predict the shape nature of the prepared nanoparticles. Highresolution-transmission electron microscopy (HR-TEM) measurements were carried out for AgNPs@AG by a JOEL apparatus (model 1200 EX; Cu grid), with an accelerating voltage of 40 kV, supported with a elements spread diagram (ESD) using (ZEISS-TEM instrument), operating at a 200 magnification.

Conclusions
In this study, silver nanoparticles have been synthesized employing a green strategy at ambient conditions. Natural exudate (almond gum) has been used as a reducing and stabilizing agent in order to produce a stable silver nanostructure. The distinctive optical properties and sensing behaviors of the as-prepared silver nanoparticles were observed due to reaction with mercury ions (Hg 2+ ) in an aqueous solution. Rapid and high sensitivity have been reported when mixing the silver nanosensor with a proper quantity of the target ions. In addition, it has been shown that the synthesized silver nanoparticles were stable and lasted for two months and no decolorization was observed.