Hydrogel of HEMA, NVP, and Morpholine-Derivative Copolymer for Sulfate Ion Adsorption: Behaviors and Mechanisms.

SO42--containing compounds are widely present in wastewater generated from various industries and mining industries, such as slag leachate, pulp and paper wastewater, modified starch wastewater, etc. When the concentration of SO42- is too high, it will not only be corrosive to metal equipment but also accumulate in the environmental media. Based on this, a novel cationic hydrogel HNM was synthesized in this study by introducing morpholine groups into the conventional hydrogel HEMA-NVP system for the adsorption of SO42- in aqueous solutions. Characterizations by Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS) indicated that morpholine groups had been introduced into the as-synthesizedhydrogels. The scanning electron microscope (SEM) characterization results show that the introduction of morpholine groups changed the surface of the hydrogel from micron-scale wrinkles to nanoscale gaps, increasing the contact area with the solution. The results of static water contact angle (WCA), equilibrium water content (EWC), and SO42- adsorption capacity show that the introduction of morpholine groups not only further improved the equilibrium water content and hydrophilicity of the hydrogel but also greatly improved the SO42- adsorption capacity of the hydrogel, with the maximum SO42- adsorption amount of 21.59 mg/g, which was much higher than that of the hydrogel without morpholine groups of 5.15 mg/g. Further studies found that the adsorption of SO42- on the hydrogel HNM was pH-dependent, and acidic conditions were favorable for the adsorption. Therefore, the introduction of morpholine groups greatly enhanced the ability of conventional HEMA-NVP hydrogels to remove SO42- from aqueous solutions.

The effects of redox conditions on arsenic re-release from excavated marine sedimentary rock with naturally suppressed arsenic release.

Massive quantities of marine sedimentary rock are excavated from urban coastal areas. The excavated rock often releases arsenic with concurrent oxidation of framboidal pyrite, but the arsenic release is naturally suppressed with subsequent atmospheric exposure. The present study evaluated the re-release of arsenic from excavated rock in which arsenic release has been naturally suppressed by the atmospheric exposure in the presence of sulfate ions under various redox conditions using the biological reduction method. The atmospheric exposure and subsequent batch leaching test revealed that the amount of arsenic release that was naturally suppressed corresponded to 1.2% of the total arsenic content. The sequential extraction analysis also showed that the arsenic in the exposed rock was altered to insoluble phases. We observed a re-release of 6.0-18.2% of the total arsenic content under reductive conditions (< + 70 mV of Eh), exceeding the amount of arsenic that was naturally suppressed, even in the presence of sulfate ions. The correlation in the amount of arsenic and iron re-released demonstrates that arsenic re-release under reductive conditions is mainly regulated by the iron dissolution up to 10 mg kg-1 even in the presence of sulfate ion. Further reduction and dissolution of iron did not cause further increase in the arsenic re-release. Therefore, excavated marine sedimentary rock should be reused under redox conditions in which iron is not reduced. Otherwise, treatments such as chemical immobilization should be performed.

Efficient conversion to Cypridina luciferin from Cypridina luciferyl sulfate, coupled with enzymatic sulfation of acetic acid.

In Cypridina (Vargula) hilgendorfii, Cypridina luciferin is converted from Cypridina luciferyl sulfate by a sulfotransferase with adenosine 3', 5'-diphosphate (PAP), and is used for the luminescence reaction of Cypridina luciferase. We found that the luminescence activity of crude extracts of C. hilgendorfii was significantly stimulated by the addition of acetic acid. This stimulation may be explained by an efficient supply of PAP from 3'-phosphoadenosine 5'-phosphosulfate (PAPS) catalyzed by a sulfotransferase. Thus, acetic acid acts as a sulfate acceptor from PAPS, followed by forming acetyl sulfate and PAP. The structure of acetyl sulfate was identified using mass spectrometry and it spontaneously decomposed to acetic acid and free sulfate ion in aqueous solutions. This enzymatic conversion from Cypridina luciferyl sulfate to Cypridina luciferin could be coupled with acetic acid and PAPS by a sulfotransferase.

Effect of the cathode potential and sulfate ions on nitrate reduction in a microbial electrochemical denitrification system.

Recently, bioelectrochemical systems have been demonstrated as advantageous for denitrification. Here, we investigated the nitrate reduction rate and bacterial community on cathodes at different cathode potentials [-300, -500, -700, and -900 mV vs. standard hydrogen electrode (SHE)] in a two-chamber microbial electrochemical denitrification system and effects of sulfate, a common nitrate co-contaminant, on denitrification efficiency. The results indicated that the highest nitrate reduction rates (3.5 mg L(-1) days(-1)) were obtained at a cathode potential of -700 mV, regardless of sulfate presence, while a lower rate was observed at a more negative cathode potential (-900 mV). Notably, although sulfate ions generally inhibited nitrate reduction, this effect was absent at a cathode potential of -700 mV. Polymerase chain reaction-denaturing gradient gel electrophoresis revealed that bacterial communities on the graphite-felt cathode were significantly affected by the cathode potential change and sulfate presence. Shinella-like and Alicycliphilus-like bacterial species were exclusively observed on cathodes in reactors without sulfate. Ochrobactrum-like and Sinorhizobium-like bacterial species, which persisted at different cathode potentials irrespective of sulfate presence, were shown to contribute to bioelectrochemical denitrification. This study suggested that a cathode potential of around -700 mV versus SHE would ensure optimal nitrate reduction rate and counteract inhibitory effects of sulfate. Additionally, sulfate presence considerably affects denitrification efficiency and microbial community of microbial electrochemical denitrification systems.

Structure of Arabidopsis thaliana Rubisco activase.

The CO2-fixing enzyme ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) is inactivated by the formation of dead-end complexes with inhibitory sugar phosphates. In plants and green algae, the ATP-dependent motor protein Rubisco activase restores catalytic competence by facilitating conformational changes in Rubisco that promote the release of the inhibitory compounds from the active site. Here, the crystal structure of Rubisco activase from Arabidopsis thaliana is presented at 2.9 Šresolution. The structure reveals an AAA+ two-domain structure. More than 100 residues in the protein were not visible in the electron-density map owing to conformational disorder, but were verified to be present in the crystal by mass spectrometry. Two sulfate ions were found in the structure. One was bound in the loop formed by the Walker A motif at the interface of the domains. A second sulfate ion was bound at the N-terminal end of the first helix of the C-terminal domain. The protein packs in a helical fashion in the crystal, as observed previously for Rubisco activase, but differences in the helical pitch indicate flexibility in the packing of the protein.

Investigation of two novel approaches for detection of sulfate ion and methane dissolved in sediment pore water using Raman spectroscopy.

The levels of dissolved sulfate and methane are crucial indicators in the geochemical analysis of pore water. Compositional analysis of pore water samples obtained from sea trials was conducted using Raman spectroscopy. It was found that the concentration of SO42- in pore water samples decreases as the depth increases, while the expected Raman signal of methane has not been observed. A possible reason for this is that the methane escaped after sampling and the remaining concentration of methane is too low to be detected. To find more effective ways to analyze the composition of pore water, two novel approaches are proposed. One is based on Liquid Core Optical Fiber (LCOF) for detection of SO42-. The other one is an enrichment process for the detection of CH4. With the aid of LCOF, the Raman signal of SO42- is found to be enhanced over 10 times compared to that obtained by a conventional Raman setup. The enrichment process is also found to be effective in the investigation to the prepared sample of methane dissolved in water. By CCl4 extraction, methane at a concentration below 1.14 mmol/L has been detected by conventional Raman spectroscopy. All the obtained results suggest that the approach proposed in this paper has great potential to be developed as a sensor for SO42- and CH4 detection in pore water.

Electrically enhanced adsorption efficiency of aluminum nitride nanotube for sulfate ion removal from water.

Herein, the adsorption performance of sulfate ion in water on aluminum nitride nanotube(AlNNT) under the influence of an electric field was investigated using the density functional theory (DFT) calculation method. The model structure stability, adsorption energy, electronic and thermodynamic properties of sulfate ion adsorbed on the surface of AlNNT were studied. The calculation results indicate that sulfate ion reacts with multi-atoms on the surface of AlNNT, forming ionic bonds and undergoing chemical adsorption. As the electric field intensity increases, the adsorption energy and the transfer of electrons from sulfate ion to AlNNT increase, leading to a higher degree of hybridization of atomic orbitals and enhanced multi-atom interactions. Additionally, the thermodynamic data suggests that the adsorption between sulfate ion and AlNNT under electric field can occur spontaneously, the process of which is exothermic. The results of present study are expected to propose a novel method for separation and removal of sulfate pollutants from water.

Overlooked effect of ordinary inorganic ions on polyaluminum-chloride coagulation treatment.

Application of poly-aluminum chloride (PACl) coagulant is a popular mode of water treatment worldwide because of the high capacity of PACl to neutralize charge. The manufacture and use of PACls with various basicities in different regions around the world suggest that the characteristics of the raw water are important determinants of the efficacy of PACl application. However, attention has not been fully paid to the effects of water quality other than the substances to be removed. In this study, two typical PACls with different basicities were used to investigate why the performance of PACls depends on the characteristics of the raw water. We focused on the concentrations of inorganic ions in the raw water. Use of high-basicity PACl (HB-PACl) with a high content of polymeric-colloidal species (Alb+Alc) resulted in very slow floc formation and little turbidity removal in raw water with low concentrations of sulfate ions. The performance of the HB-PACl was inferior to that of normal-basicity PACl (NB-PACl), although the charge-neutralization capacity of the HB-PACl was higher. Rates of floc formation were strongly correlated with the rate of aluminum precipitation by hydrolysis reaction, which was identified as an indicator for evaluating the compatibility of raw water with PACl treatment. Among the common ions in natural water, the sulfate ion had the greatest ability to hydrolyze and precipitate PACl because of its divalency and tetrahedral structure. This conclusion followed from experimental results showing similar effects for selenate and chromate ions as for sulfate ions and somewhat smaller effects for thiosulfate ions. Bicarbonate ions and natural organic matter affected PACl hydrolysis-precipitation, but chloride ions, nitrate ions, and cations had little effect on PACl hydrolysis-precipitation. Interestingly, the abilities of sulfate ions to hydrolyze HB-PACl and NB-PACl were very similar, but bicarbonate ions were less effective in hydrolyzing HB-PACl than NB-PACl, and bicarbonate ions contributed little to the hydrolysis-precipitation of HB-PACl in raw water with normal alkalinity. Therefore, sufficient coagulation with HB-PACl therefore usually requires a certain concentration of sulfate ions in water to be treated. The implication is that which anions are most influential to the hydrolysis-precipitation of PACl, and thus to PACl's coagulation ability depends on the constituents of the PACl.

Sulfate ions diffusion in concrete under coupled effect of compression load and dry-wet circulation.

The diffusion of Sulfate ions in concrete is a complex process and affects the performance of concrete. Experiments on the time-dependent distribution of sulfate ions in concrete under the coupling of pressure load, dry-wet circulation, and sulfate attack, and the diffusion coefficient of sulfate ions with various parameters was tested. The applicability of the cellular automata (CA) theory to simulate the diffusion of sulfate ions was discussed. In this paper, a multiparameter cellular automata (MPCA) model was developed to simulate the impacts of load, immersion ways, and sulfate solution concentration for the diffusion of sulfate ions in concrete. The MPCA model was compared with experimental data, considering compressive stress, sulfate solution concentration, and other parameters. The numerical simulations verify the calculation results based on the MPCA model are in good agreement with the test data. Finally, the applicability of the established MPCA model was also discussed.

Renaturation of Myoglobin Denatured by Sodium Dodecyl Sulfate by Removal of Dodecyl Sulfate Ions Bound to the Protein Using Sodium Cholate.

The secondary and tertiary structures of myoglobin were disrupted by sodium dodecyl sulfate (SDS) but were hardly affected by the bile salt, sodium cholate (NaCho). This disruption was induced by the binding of dodecyl sulfate (DS) ions to the protein. In this study, the removal of DS ions bound to the protein was attempted using NaCho. The extent of removal of DS ions was estimated by the restoration of the secondary and tertiary structures of the protein disrupted by SDS. The secondary structural change was followed by monitoring mean residue ellipticity at 222 nm, [θ]222, which was frequently used as a measure of α-helical content. The tertiary structural change was followed by examining the Soret band absorbance of the protein. Evidently, the magnitude of [θ]222 of myoglobin in the SDS solution initially decreased and then increased back to almost its original value as the NaCho concentration increased. The initial decrease in [θ]222 indicated the cooperation of NaCho and SDS in disrupting the secondary structure at low concentrations of both surfactants. This cooperation was also observed in the tertiary structural change as a shift of the Soret band maximum wavelength, λmax, and a decrease in the molar absorption coefficient, εmax, at λmax. Above a certain NaCho concentration, the position of λmax and the magnitude of εmax were also restored to their original states. The secondary and tertiary structures were simultaneously restored by adding NaCho. These recoveries were attributed to removal of the DS ions bound to the protein. This removal might be due to the ability of cholate anions to strip DS ions bound to the protein. The stripped DS ions are more likely to form SDS-NaCho mixed micelles in bulk than SDS-NaCho mixed aggregates on the protein.

Nitrogen-doped carbon nanosheets with Fe-based nanoparticles for highly efficient degradation of antibiotics and sulfate ion enhancement effect.

Developing Fe-based catalysts with high-effective and environmentally friendly features in Fenton-like system for treating wastewater is still a challenge. Novel nitrogen-doped carbon nanosheets with Fe0/Fe3C nano-particles (Fe@NCS-900) were prepared through a simple solvent-free strategy by pyrolyzing the mixture of 2,6-diaminopyridine and ferric chloride hexahydrate under 900 °C. The Fe@NCS-900 possessed almost 100% removal efficiency and 66.5% mineralization rate for the degradation of CBZ in 10 min. Moreover, the Fe@NCS-900 exhibited an apparent first-order constant as high as 0.8809 min-1, which is 22 and 29 times higher than that of the commercial Fe0 and traditional Fenton system, respectively, which could be attribute to the high graphitization degree and rich nitrogen content. Besides, the results of the radical quenching experiments, electron paramagnetic resonance (EPR) and the probe experiments demonstrated that a large number of high valent iron species (Fe (IV)) besides singlet oxygen (1O2) and superoxide radicals (O2•-) existed and contributed to the CBZ degradation. More interestingly, the addition of coexisting anion SO42- in the reaction system could significantly boost the concentration of •OH and SO4•- by 28.3 times and 9.7 times, respectively, resulting in the increase of the apparent first-order constant by 5.9 times (5.1733 min-1), which was entirely different from previous reports that SO42- had no effect on the catalytic activity or even displayed slightly inhibitory effect. In addition, the catalyst exhibited broad pH adaptability in the pH range of 2-9. The intermediate products of CBZ degradation were investigated by liquid chromatography mass spectrometry (LC-MS) and the degradation pathway was proposed. This paper provides new insights for developing a promising Fe-based nitrogen-doped catalyst for practical wastewater treatment.

Development of polystyrene coated persulfate slow-release beads for the oxidation of targeted PAHs: Effects of sulfate and chloride ions.

In this study, we synthesized polystyrene coated persulfate polyacrylonitrile beads (PC-PSPANBs) to control persulfate (PS) release for targeted PAHs' degradation in a batch reactor. Initially, the persulfate release rate (ksr = 20.553 h-1) from PSPANBs was fast, but coating the PSPANBs with polystyrene controlled PS release rate (ksr= 2.841 h-1), nearly ten times slower than without coating. When Fe(II) activated PC-PSPANBs applied for 12 h degradation of acenaphthene (ACE), 2-methlynaphthalene (2-MN) and dibenzofuran (DBF), the optimum percent removal efficiencies (% R.Es) were as ACE (82.12%) > DBF (68.57%) > 2-MN (58.80%) and the optimum degradation rate constants (kobs) were found as ACE (11.348 h-1) > 2-MN (3.441 h-1) > DBF (1.101 h-1). The effect of SO42- and Cl- on ACE degradation showed that % R.E and kobs were enhanced with increasing anionic concentrations. The maximum % R.E was achieved for SO42- (76.24%) > Cl- (65.51%), but the highest kobs was in case of Cl- (1.536 h-1) > SO42- (0.510 h-1). The effectiveness of PS release longevity was also found because net degradations of ACE and DBF after first spiking were 12 mg L-1 and 16 mg L-1, while after second spiking were 18 mg L-1 and 10 mg L-1, respectively.

Shoot has important roles in strigolactone production of rice roots under sulfur deficiency.

Strigolactones (SLs) are a class of plant hormones that control plant architecture. SL levels in roots are determined by the nutrient conditions in the rhizosphere, especially the levels of nitrogen (N) and phosphorus (P). Our previous research showed that SL production is induced in response to deficiency of sulfur (S) as well as of N and P, and inhibits shoot branching, accelerates leaf senescence, and regulates lamina joint angle in rice. Here we show biomass, total S contents, and SL levels in rice under S-sufficient and S-deficient conditions using a split-root system. When one part of the root system was cultured in S-sufficient medium and the other in S-deficient medium (+S/-S), shoot fresh weight was unaffected relative to the +S/+S condition. The shoot weight significantly decreased in -S/-S condition. In contrast, there was no significant difference in root fresh weight between +S and -S conditions. In +S/-S condition, SL levels were systemically reduced in both parts, the shoot S content increased, but the root S content in S-deficient medium was unaffected relative to the -S/-S condition. These results suggest that shoots, not roots, recognize S deficiency, which induces SL production in roots.

Service Life Evaluation for RC Sewer Structure Repaired with Bacteria Mixed Coating: Through Probabilistic and Deterministic Method.

Since a concrete structure exposed to a sulfate environment is subject to surface ion ingress that yields cracking due to concrete swelling, its service life evaluation with an engineering modeling is very important. In this paper, cementitious repair materials containing bacteria, Rhodobacter capsulatus, and porous spores for immobilization were developed, and the service life of RC (Reinforced Concrete) structures with a developed bacteria-coating was evaluated through deterministic and probabilistic methods. Design parameters such protective coating thickness, diffusion coefficient, surface roughness, and exterior sulfate ion concentration were considered, and the service life was evaluated with the changing mean and coefficient of variation (COV) of each factor. From service life evaluation, more conservative results were evaluated with the probabilistic method than the deterministic method, and as a result of the analysis, coating thickness and surface roughness were derived as key design parameters for ensuring service life. In an environment exposed to an exterior sulfate concentration of 200 ppm, using the deterministic method, the service life was 17.3 years without repair, 19.7 years with normal repair mortar, and 29.6 years with the application of bacteria-coating. Additionally, when the probabilistic method is applied in the same environment, the service life was changed to 9.2-16.0 years, 10.5-18.2 years, and 15.4-27.4 years, respectively, depending on the variation of design parameters. The developed bacteria-coating technique showed a 1.47-1.50 times higher service life than the application of normal repair mortar, and the effect was much improved when it had a low COV of around 0.1.

Heterogeneous Fenton Degradation of Organic Pollutants in Water Enhanced by Combining Iron-type Layered Double Hydroxide and Sulfate.

Water pollution derived from organic pollutants is one of the global environmental problems. The Fenton reaction using Fe2+ as a homogeneous catalyst has been known as one of clean methods for oxidative degradation of organic pollutants. Here, a layered double hydroxide (Fe2+ Al3+ -LDH) containing Fe2+ and Al3+ in the structure was used to develop a "heterogeneous" Fenton catalyst capable of mineralizing organic pollutants. We found that sulfate ion (SO4 2- ) immobilized on the Fe2+ Al3+ -LDH significantly facilitated oxidative degradation (mineralization) of phenol as a model compound of water pollutants to carbon dioxide (CO2 ) in a heterogeneous Fenton process. The phenol conversion and mineralization efficiency to CO2 reached >99% and ca. 50%, respectively, even with a reaction time of only 60 min.

Adsorption of sulfate ion from water by zirconium oxide-modified biochar derived from pomelo peel.

Zirconium oxide-modified pomelo peel biochar (ZrBC) was synthesized for the adsorption of sulfate ion from aqueous solution. Zirconyl chloride octahydrate (ZCO) was used to modify pomelo peel biochar into ZrBC. The optimal dose of ZCO for modification is 0.5 mol/L, at which ZrBC shows the highest adsorption of sulfate ion. The adsorbents were characterized by the field emission scanning electron microscopy, X-ray photoelectron spectroscopy and surface area measurement. The results confirm that the presence of zirconium oxides and hydroxide groups on the ZrBC surface, and ZrBC has a porous structure and a higher specific surface area in comparison with pomelo peel biochar. ZrBC shows good affinity for sulfate ion with a maximum sulfate adsorption capacity of 35.21 mg/g, which is much higher than that of pomelo peel biochar (1.02 mg/g). The adsorption of sulfate on ZrBC is pH dependent, and acidic conditions favor the adsorption. The adsorption can reach near-equilibrium in approximately 120 min. The adsorption kinetics and isotherm follow the pseudo second-order equation and Langmuir adsorption model, respectively. Furthermore, nitrate and fluoride anions exhibit little influence on the adsorption of sulfate by ZrBC, whereas phosphate inhibits the adsorption under the same concentration conditions. ZrBC has the potential to be used for removal of sulfate from aqueous solution.

Removal of Dodecyl Sulfate Ions Bound to Human and Bovine Serum Albumins Using Sodium Cholate.

The secondary structures of human serum albumin (HSA) and bovine serum albumin (BSA) were disrupted in the solution of sodium dodecyl sulfate (SDS), while being hardly damaged in the solution of the bile salt, sodium cholate (NaCho). In the present work, the removal of dodecyl sulfate (DS) ions bound to these proteins was attempted by adding various amounts of NaCho. The extent of removal was estimated by the restoration of α-helical structure of each protein disrupted by SDS. Increases and decreases in α-helical structure were examined using the mean residue ellipticity at 222 nm, [θ]222, which was frequently used as a measure of α-helical structure content. The magnitudes of [θ]222 of HSA and BSA, weakened by SDS, were restrengthened upon the addition of NaCho. This indicated that the α-helical structures of HSA and BSA that were disrupted by the binding of DS ions were nearly reformed by the addition of NaCho. The NaCho concentration at which the maximum restoration of [θ]222 of each protein was attained increased nearly linearly with SDS concentration. These results indicated that most of the bound DS ions were removed from the proteins but the removal was incomplete. The removal of DS ions, examined by means of the equilibrium dialysis, was also incomplete. The α-helical structure restoration and the DS ion removal by NaCho were considered to be due to the ability of cholate anions to strip the surfactant ions bound to HSA and BSA. These stripped DS ions appeared to be more likely to form SDS-NaCho mixed micelles in bulk rather than SDS-NaCho mixed aggregates on the proteins.

Considerations on factors influencing the degradation of cellulose in alum-rosin sized paper.

In Europe, the use of aluminium(III) compounds, namely AlK(SO4)2·12H2O and later on Al2(SO4)3·18H2O for hardening gelatin sizes was recorded as early as the 16th century. This review is focused on the critical assessment of published data concerning the following chemical aspects of paper degradation: direct influence of H3O+ ions formed during hydrolysis of aluminium(III) species; influence of low-molecular organic acids formed within degradation processes; influence of pH variation on the redox potential of reactive oxygen species acting as oxidizing agent; consequences of the absorption of gaseous NO2 and SO2 present in the air for paper degradation; involvement of aluminium species in redox radical oxidation catalytic processes; possible effect of the coordination of Al(III) with small radius and high charge on oxygen atoms of cellulose carboxyl or hydroxyl groups. It is indicated how the understanding of the above mentioned effects can help slow down paper degradation.

Studies on effects of traffic tunnels on the migration of the contaminants under landfill sites.

Three landfills are located in the eastern part of the Chengdu City, and two traffic tunnels pass beneath the south portion of landfill-1. The landfills have a simple leachate collection system without any bottom liner and impermeable wall, which causes a severe corrosion of the traffic tunnels from 175 to 250 m in the test section. In order to explore how the traffic tunnels impact the transport path of contaminants infiltrating from landfills, a groundwater flow model and a solute transport model were established in the present study. It was found that, after 16 years of operation, the traffic tunnels will accelerate the vertical migration of sulfate ions in the area between the tunnels. Furthermore, 64 water samples along the traffic tunnels were collected to test the concentration of the contaminants. According to the distribution mechanism of the measured concentrations in the traffic tunnels, a preliminary treatment plan was proposed to control the further corrosion of the tunnels and the spread of the contaminants.

Quantitative Analytical Method for Single Rain Droplets via Crystal Formation in Photocrosslinking Polymer Gel.

Ion composition contained in individual rain droplets provides important information to investigate the chemistry in rain and clouds, but general rain sampling equipment temporally and spatially averages the information. Determination of the SO42- concentration in an individual rain droplet was achieved by precipitate production in synthesized acrylamide polymer gel. Concentration of the target ion was calculated from the droplet print diameter and precipitation area measured from digital microscope images. We investigated the effects of the interior electrolyte concentration in the polyacrylamide gel and UV irradiation time on the physical properties of the gel and precipitate formation. The precipitated components were identified by scanning electron microscopy with energy dispersive X-ray analysis. We also clarified the effects of coexisting ions on the reaction between the interior and exterior electrolytes. For actual rainwater, the SO42- concentration estimated by this method was in agreement with the results obtained by ion chromatography.