A New Hollow-Fiber Adsorbent Material for Removing Arsenic from Groundwater

Lee, Sang Hyun; Kim, Sung Su

doi:https://doi.org/10.1155/2019/2715093

Journal of Chemistry

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Abstract Introduction Materials and Methods Results and Discussion Conclusions Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 2715093 | https://doi.org/10.1155/2019/2715093

A New Hollow-Fiber Adsorbent Material for Removing Arsenic from Groundwater

Sang Hyun Lee¹and Sung Su Kim¹

Academic Editor: Darren Sun

Received10 Jan 2019

Accepted22 Apr 2019

Published13 May 2019

Abstract

To optimize the arsenic-adsorption efficiency and the mechanical strength of a hollow-fiber-type adsorbent, the optimal condition of polymeric solution was determined as 32 wt.% TiO₂ and 17 wt.% polymer. A micropore-sponge form was developed at the slurry-extrusion speed of 2.500 ml/min and the internal coagulant-solution-extrusion speed of 1.250 ml/min, and the arsenic-adsorption efficiency improved. Given the result under conditions in natural groundwater containing various ions, the hollow-fiber-type adsorbent can be applied to real groundwater purification processes.

1. Introduction

Arsenic-contaminated groundwater is discovered continuously around the world. It has spread across Asia, including West Bengal, Taiwan, India, Bangladesh, and China, as well as throughout North America and South America, including the United States and Mexico, and also to European nations such as Germany. Arsenic has strong human toxicity, and it causes serious worldwide health problems, including acute symptoms such as skin diseases and neurotoxicity as well as chronic illnesses such as cancers of the lung, bladder, and skin [1].

Various methods and technologies have been reported for removing arsenic from drinking water including coagulation-flocculation [2, 3], oxidation [4, 5], ion exchange [6], adsorption [7–9], and membrane processes [10–12]. Investigators have indicated that adsorption is the most promising technology because of advantages including high removal efficiency, easy operation, and cost-effectiveness [13–16].

Arsenic adsorption is a processing technology that removes the dissolved substances from drinking water; specifically, the toxin adheres to the surface of the adsorbent, and the adsorbent determines its efficiency. Researchers have thus been investigating developing diverse adsorbents with improved efficiency including currently commercialized adsorbents, specifically, diverse metallic (hydr)oxides, such as aluminum oxide [17–19], iron (hydr)oxide [20–23], titanium dioxide [24, 25], zinc oxide [26], copper oxide [27], cerium hydr(oxide) [28], and zirconium oxide [29].

TiO₂ is being used widely as a nonorganic chemical for diverse materials such as synthetic textiles, paints, rubber, paper, and plastics, and researchers are studying using the chemical for purposes such as separating pollutants in gases and filtering groundwater. The authors have recently reported rapid increases in research on the TiO₂-based adsorption of arsenic [30] on forms such as TiO₂ nanoparticles [25, 31], titanate nanotubes [32], hydrous TiO₂ [33], granular TiO₂ [34, 35], and TiO₂-impregnated chitosan beads [36].

In this study, we produced a TiO₂-based polymeric hollow fiber using nonsolvent-induced phase separation (NIPS) and cut it small for use as an arsenic adsorbent. NIPS is a phase-transition phenomenon in which a polymer and a solvent are mixed uniformly to form a polymer solution; when the solvent that is contained in the polymer solution comes into contact with the nonsolvent (coagulant), the solvent in the polymer solution is exchanged with the nonsolvent via diffusion and convection, thereby separating the solvent into solid and liquid phases [37, 38]. The polymeric solution, which is a raw hollow-fiber material, is extruded through the mold and passes through the NIPS reaction twice, to react once with the internal and external coagulants. Through this process, the sponge (micro-) pore and the finger-form (macro- or meso-) pore are formed in the hollow fiber [39], and these greatly affect the diverse physiochemical characteristics of the fiber such as the nonsuperficial and flux characteristics. Hollow fiber can be tailored depending on the need by adjusting these characteristics, and therefore, research is important on developing hollow fiber for diverse uses such as in membranes for water treatment and gas separation [37, 38]. However, no researcher has yet reported on producing and applying a polymer-based hollow fiber as an adsorbent for arsenic removal. Thus, for this study, we conducted process optimization to produce a hollow fiber for arsenic adsorption by examining how these numerous pores remove arsenic across the wide specific surface areas and the cross sections of hollow fibers.

2. Materials and Methods

2.1. Preparation of Titanium Hollow-Fiber Adsorbents

We prepared the hollow-fiber adsorbent by NIPS using polysulfone from Solvay Co. (Brussels, Belgium) as the polymer and 1-methyl-2-pyrrolidone from Sigma-Aldrich (St. Louis, MO, USA) as the solvent. We used TiO₂ from Cristal Co. (Jeddah, Saudi Arabia) and polyvinylpyrrolidone (PVP) from Sigma-Aldrich as the pore-formation additive. First, the dried polysulfone was mixed with the N-methyl-2-pyrrolidone (NMP) solvent, and after the TiO₂ and the PVP were added, the polymeric solution was produced after 24 hr stirring. Then, the produced solution was degassed in a vacuum desiccator for 5 hr, placed in a syringe pump, connected to a spinneret, and finally extruded with an internal coagulant (Figure 1). The produced hollow fiber was subsequently maintained in an external coagulant for 6 hr and then cut to a length of 0.5 cm, kept in an oven at 105°C to eliminate the remaining moisture, and cooled in a desiccator.

2.2. Evaluating the Arsenic-Adsorption Efficiency in a Batch Reactor

We evaluated the arsenic-adsorption efficiency: the solution was first filtered. After that, we placed the adsorbent in the batch reactor; this was followed by arsenic adsorption at 20°C agitation temperature, agitation speed of 60 rpm, and less than 50 hr of agitation time; then, we measured the arsenic concentration. We produced the solution used in the arsenic-adsorption experiment using 99.0% sodium arsenite (NaAsO₂) obtained from Kanto Chemical (Tokyo, Japan) and conducted the experiment by setting the initial arsenic concentration to 0.2 mg/L in consideration of the actual concentrations in discharged groundwater.

We analyzed the arsenic using silver- (Ag-) diethyldithiocarbamate (DDTC), a colorimetric method. After we injected 36% hydrogen chloride (Sigma-Aldrich), we measured the potassium iodide and tin chloride concentrations in the sample; then, we injected granulated zinc (Sigma-Aldrich) that was captured from the Ag-DDTC solution into the sample to convert the arsenic into arsine (AsH₃) gas. The color of the solution changed according to the amount of AsH₃ that had been adsorbed in the wavelength of 520 nm.

2.3. Characterizing the Materials

To observe the surface of the adsorbent, we analyzed the samples fixed with the carbon tape using the Hitachi S-4800 (Hitachi Co., Japan) for scanning electron microscopy (SEM). To analyze the specific surface area and the pore size of the adsorbent, we used the Micromeritics ASAP 2010C analyzer (Micromeritics Co., Norcross, GA, USA) and obtained the specific surface area using the BET (Brunauer–Emmett–Teller) formula. We calculated the pore-size distribution according to the BJH (Barrett–Joyer–Hanlenda) method, which is used for calculating micropore size when the average liquid-meniscus radius according to the Kelvin formula and the thickness of the relative-pressure adsorption layer are known. After the gas was eliminated at room temperature (20°C) for 2 hr to prevent any high-temperature changes, we analyzed each sample, measuring material tensile strength using a universal testing machine. We applied weight continuously to calculate the tensile strength through the length to the sample rupture point.

2.4. Evaluating Arsenic-Adsorption Efficiency in a Continuous-Flow System Reactor

To evaluate the applicability of the continuous-flow process regarding the prepared adsorbent, we performed the experiment using an empty bed contact time (EBCT) column. We used the column-adsorption experiment to evaluate the breakthrough time and the pollutant-removal efficiency of the fixed-bed column, and for this study, set the point at which the discharge water exceeded the drinking-water standard of 0.01 mg/L as the reference breakthrough point. The column was made using an acrylic with the following specifications: 8 mm thick, 500 mm long, 20 mm horizontal width, and 20 mm vertical width. The column was designed to facilitate inflow and outflow provided by two 10 mm-diameter installations; one of these was located at the top of the column and the other at the bottom. The device was composed of a source water tank, a volume pump, and a column-connection tube. Water flowed in as the up flow through the controlled volume pump, and we measured the arsenic concentrations 24 hr after the EBCT was set differently according to the operating condition.

3. Results and Discussion

3.1. Optimizing the Hollow-Fiber Adsorbent Material

The diverse applications of TiO₂ include paints, photocatalysts, and catalyst supports. To evaluate its applicability as a source material of hollow-fiber adsorbent, we evaluated the adsorption efficiency of TiO₂ powder, as shown in Figure 2 and Table 1.

The Langmuir isotherm is expressed by the following equation:where q_e (μg/g) = amount of adsorbed adsorbate per unit mass of the adsorbent, C_e (μg/L) = unadsorbed adsorbent concentration in the solution at the equilibrium condition, q_m (μg/g) = maximum amount of adsorbate that was adsorbed per unit mass of the adsorbent to form a complete monolayer on the surface, and b (L/μg) = Langmuir constant.

Both the monolayer and multilayer adsorption processes can be studied using the following Freundlich adsorption isotherm, as it considers the adsorption of an adsorbate onto a heterogeneous adsorbent surface:where K_f and 1/n represent the number of adsorption sites and the adsorption strength, respectively; q_m is the maximum adsorption capacity of the adsorbent; and b is the Langmuir coefficient, which is between the adsorbent and the adsorbate. On isothermal adsorption analysis of the TiO₂ powder sample, both K_f and q_m were excellent.

For the hollow-fiber material, factors that affect pore formation are the solvent-dissolution rate, dispersant, metal oxide powder, and binder contents. Therefore, to determine the optimal slurry ratio, we measured the arsenic-adsorption efficiencies of the hollow-fiber adsorbents with different source contents (Table 2 and Figure 3).

The most important factor in determining the arsenic-adsorption efficiency of a hollow-fiber adsorbent is the content of the metal oxide, which is TiO₂ here. As shown in Table 2, we produced the adsorbent by reducing the amount of NMP proportional to the increase of the TiO₂ content under the following conditions: (THF_a∼THF_c). Furthermore, we reduced the polymer amount in the adsorbent of THF_d and THF_e conditions. The critical titanium content for optimal performance was 30%.

Because evaluating efficiency under specific conditions can distort the specific activity of the material, we performed isothermal adsorption tests (Freundlich and Langmuir) to verify the exact efficiency and mechanism; the results, shown in Tables 3 and 4, agreed with the findings in Figure 2.

The hollow fiber has a large pore in the form of a finger and a sponge-pore form that contains numerous micropores. According to the results in Table 5, THF_d and THF_e showed larger specific surface areas than the other fibers, indicating more involved micropores. The results further suggest that the sponge-like pore is more important than the finger-like structure in hollow-fiber adsorption.

In the real-world application of the adsorbent, exposing the adsorbent to high pressure, such as injecting a large amount of adsorbent or backwash, occurred frequently. Therefore, the adsorption efficiency and the mechanical strength are both very important. In terms of the Fe oxide-based commercial adsorbents in the actual process, the mechanical strength was relatively weak, and the coloring phenomenon that affects residential drinking water occurred during the backwash process. Therefore, it was necessary to verify the correlation between the mixing ratio and the mechanical strength and to determine the optimal condition by measuring the tensile strength of the hollow-fiber adsorbent that was produced by each mixing ratio (Table 6).

We confirmed that both Ti and polymer content can affect tensile strength. The tensile strength of silicone rubber, a ubiquitous material in daily life, ranges from 5.08 to 7.17 MPa [40], and the tensile strength of medium-strength concrete is 1.40–4.00 MPa [41]. Considering these facts together with the results of the present study, the tensile strength of the THF_e adsorbent with the lowest tensile strength is the same as that of concrete, and this tensile strength is sufficient for an adsorbent.

As presented in the introduction, the hollow-fiber adsorbent consists of far more micropores than the diverse adsorbents that are currently being used, and the micropores can be divided into finger-like and sponge-like structures according to the shape. In manufacturing hollow fibers using the NIPS method, the coagulation speed of the polymer is the important factor in determining the hollow-fiber pore structure [42], and the factors that influence the polymer’s coagulation speed are the slurry-extrusion speed and the extrusion speed of the internal-coagulant solution. Our analyses thus showed differences in the pore structures according to different variables that affect pore formation, and we also investigated correlations between the pore structure and the arsenic-adsorption efficiency. Chung et al. [43] reported that increasing the polymer-extrusion speed induces the polymer-chain orientation and promotes a more densely packed formation regarding the oriented polymer chain, eventually creating a dense skin layer. Therefore, we expected increased formation of the sponge-like pore structure with increased polymer-solution extrusion speed, with decreased formation of the large-diameter finger-like pores. In this study, we produced the hollow-fiber adsorbent by adjusting its extrusion speed, analyzed the pore structure with SEM, and measured the arsenic-adsorption efficiency of the adsorbent to determine the correlation of the pore structure to the adsorption efficiency. The micropore-structure observation results based on the slurry-extrusion speed are illustrated in Figure 4.

(a)

(b)

(c)

In the SEM analysis results, finger-like pores are clearly evident in the hollow fiber from the slurry extruded at the low speed of 0.312 ml/min; it is also clear that, in contrast, increasing the extrusion speed to 1.250 ml/min and then 2.500 ml/min increased the development of the sponge-like pores, and as these developed, the formation of the finger-like sponge was relatively restricted. Based on these results, we verified a correlation between hollow-fiber adsorbent pore structure and arsenic-adsorption efficiency (Figure 5).

In the arsenic-adsorption evaluation results of our above analyses, the hollow-fiber arsenic adsorbents extruded from slurry at extrusion speeds of 1.250 ml/min and 2.500 ml/min, with increased development of the sponge-like pores, showed excellent efficiency, and we concluded that this result was caused by the increased specific surface area from the considerable quantity of sponge-like pores.

Reuvers and Smolders [44] reported that, in general, if the exchange velocity of the hollow-fiber slurry and the nonsolvent is rapid, the large-diameter finger-like pores form, whereas a slow exchange velocity results in the formation of the sponge-like pores. The following two factors can adjust the exchange velocity of the slurry and the nonsolvent: the slurry extrusion speed and the flow rate of the internal-coagulant solution. We confirmed earlier in this paper that greater slurry-extrusion speed increases sponge-like-pore development, and based on these findings, we evaluated the pore-structure change by varying the internal-coagulant flow rate; the results are shown in Figure 6.

(a)

(b)

(c)

For the internal-coagulant solution, we produced the distilled water using a Puris water purification system (Miraest Co. Ltd., Gyeonggi-do, South Korea), and we produced the hollow-fiber adsorbent by adjusting the extrusion speed from 1.250 to 5.000 ml/min. We confirmed that the faster the flux of the internal-coagulant solution, the wider the distribution of the finger-like pores, whereas the slower the flux, the wider the distribution of the sponge-like pores. Decreasing the flux of the internal-coagulant solution decreased the exchange speed of the slurry and the nonsolvent, which means that the dissolution speed of the NMP in the internal coagulant decreased significantly. We determined that a considerable number of sponge-like pores were generated, which was confirmed by literature results [45].

As previously discussed, the slurry-mixing ratio and the extrusion speed contributed greatly to the change of the pore structure, and the arsenic-adsorption efficiency varied greatly according to the pore-structure change. The extrusion speed of the internal-coagulant solution affected the pore-structure change, leading to the conclusion that this process can change the efficiency; based on that conclusion, we measured the arsenic-adsorption efficiency of the adsorbents that were produced under each condition; these results are shown in Figure 7.

These evaluation results show that the adsorption efficiency was highest for the hollow-fiber adsorbent that was produced at an internal-coagulant solution extrusion speed of 1.250 ml/min. We also determined that increasing the extrusion speed decreased the adsorption efficiency. This result shows that arsenic-adsorption efficiency improves with more sponge-like pores, the micropores, in the fiber.

3.2. Evaluating the Hollow-Fiber Adsorbent Applicability in the Actual Process

We also tested the arsenic-adsorption efficiency of hollow-fiber adsorbents in groundwater that contained ions other than arsenic (Figure 8), primarily nitrate nitrogen, trihalomethane, hardness, free residual chlorine, and sulfate but also boron, chloroform, bromodichloromethane, chloral hydrate, dibromoacetonitrile, haloacetic acid, uranium, chemical oxygen demand, and evaporation residue. With the titanium-based hollow-fiber adsorbent, the difference in the arsenic-adsorption rate between the general synthetic wastewater and the actual groundwater was trivial. With the metal-oxide-based granular type of commercial adsorbent, however, the adsorption efficiency was greatly reduced.

Based on actual arsenic adsorption, we evaluated the adsorbent efficiency of the continuous-flow system we had designed at the lab scale for this study. We verified the efficiency by varying the setting of the EBCT, the influent per mass of the injected adsorbent [34, 45]; the corresponding results are shown in Figure 9.

In the experimental results in hollow-fiber-adsorbent mode 1 (EBCT: 3 min), the permeation results were converted into a concentration that was the same as the injected concentration within 11 days, and in mode 2 (EBCT: 5 min), the same concentration was reached at the breakthrough point. In mode 4 (EBCT: 25 min), the concentration of 0.01 mg/L, the drinking-water standard, was achieved within 35 days. The results of this study verified the applicability of the hollow-fiber adsorbent in the continuous-flow system, and they show that the hollow fiber can be applied when EBCT varies according to the influent condition.

4. Conclusions

In this study, we produced titanium-based polymeric hollow-fiber arsenic adsorbents with diverse pore structures and excellent specific surface area. To maximize the arsenic-adsorption efficiency and the mechanical strength of the adsorbents, we optimized the contents of NMP, polyurethane, metal oxide (TiO₂), and PVP, the raw materials. We confirmed that the optimal raw material for determining arsenic-adsorption efficiency was TiO₂ and the optimal substance for determining mechanical strength was polyurethane. Based on our findings and experimental results, the sample THF_d was optimal.

We examined the adsorption efficiency and the pore structure of the samples by adjusting the extrusion speed of the internal coagulant and hollow-fiber solutions. As the polymeric solutions’ extrusion speed increased and the extrusion speed of the internal coagulant solution decreased, more sponge-like, dense pores formed than finger-like pores. Additionally, arsenic-adsorption efficiency improved as the specific surface area increased.

We finally evaluated the arsenic-adsorption efficiency of the hollow-fiber adsorbents we produced in actual underground groundwater with ions other than arsenic. The adsorbents produced using titanium showed excellent efficiency even in the actual groundwater, in contrast with the granular type of commercial adsorbents manufactured using metal oxides. We also verified the efficiency of the adsorbent by manufacturing a lab-scale continuous-flow system, similar to the actual process. We observed that the effluent concentration varied according to EBCT, which is the case in the actual process.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this article.

Acknowledgments

This work was supported by Kyonggi University Research Grant 2016.

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Copyright © 2019 Sang Hyun Lee and Sung Su Kim. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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