Selective Separation of Organic Electrolytes by Neutralization Dialysis with Grafted Polyethylene Films

The selective separation of organic electrolytes by neutralization dialysis was investigated with two kinds of grafted polyethylene (PE) films prepared through the photografting of 2-(dimethylamino) ethyl methacrylate (DMAEMA) onto the PE films and the subsequent quaternization and through the photografting of glycidyl methacrylate (GMA) and the subsequent sulfonation. The permeation flux of benzoic acid (BA) for the quarternized DMAEMA-grafted PE (PE-g-QPDMAEMA) films increased with an increase in the degree of quaternization, and the BA permeability had the maximum at the initial pH value of the permeate solution of 12.0. On the other hand, the sulfonation offered the phenylalaninol (Phl) permeability of the GMA-grafted PE (PE-g-PGMA) films. The selective separation for the binary BA/Phl or 2,5-dichlorobenzoic acid/Phl systems was successfully achieved by use of a pH difference between the feed and permeate solutions through the PE-g-QPDMAEMA and sulfonated PE-g-PGMA (PE-g-SPGMA) films. The maximum selective separation was obtained under the conditions that the initial pH values of the permeate solutions through the PE-g-QPDMAEMA and PE-g-SPGMA films were adjusted to 12.0 and 2.0, respectively. This procedure will be applied to separation and concentration of organic electrolytes and water purification.


Introduction
A variety of synthesized polymer membranes are involved in membrane-separation processes, such as energy saving, resources recovery [1], and environmental preservation mainly for removal of metal or inorganic ions such as K + , Ca 2+ , Mg 2+ , NO 3 , and SO4 2 [2][3][4] and organic electrolytes [5][6][7][8] and for desalination [9][10][11][12]. Most of these membranes are highly crosslinked in order to increase their mechanical stability and avoid excessive water swelling. However, since the increased closslinking may cause a decrease in the membrane permeability of organic ions with relatively high molecular weights, either the degree of crosslinking or the chain length of the crosslinking agent used is frequently adjusted in improving the membrane permeability [13].
On the other hand, a graft copolymer consists of a long sequence of monomer referred to as a backbone with branches of a long sequence of another monomer. Therefore, compatibilization of a pair of polymers with quite different characteristics can be achieved without any crosslinking agents. Various grafted polyethylene (PE) films have been prepared by the photografting of hydrophilic, ionic, or reactive monomers and the resultant grafted PE films were applied to membrane-separation processes in previous articles [14][15][16][17][18][19][20]. One end of each grafted polymer chain is covalently bonded to the PE substrate and the other end is not placed under restraint. Therefore, the membrane properties and permeation behavior can successfully respond to the change in the external stimuli such as the pH value [14], temperature [14], and electric field [15]. In addition, positively or negatively ionizable functional groups successively affixed to the grafted polymer chains can work as a fixed carrier to transport ionic species across the grafted PE films [18]. Here, since PE is insoluble in water and most organic solvents at ambient temperatures, the PE films photografted with ionic monomers such as methacrylic acid or Dialysis with Grafted Polyethylene Films 2-(dimethylamino) ethyl methacrylate (DMAEMA) possessed practical strength in the water-swollen state [14]. Negatively chargeable organic electrolytes were transported uphill by use of the pH difference [18] or through electrotransport [13] through the DMAEMA-grafted PE (PE-g-PDMAEMA) films.
We aimed at neutralization dialysis for the membrane separation of organic electrolytes. Neutralization dialysis has been mainly used for the selective separation of weakly acidic and basic compounds [21][22][23]. In this study, the application of the grafted PE films will be made to the selective separation of organic electrolytes through neutralization dialysis. The membranes for neutralization dialysis were prepared by the two-step process, or the photografting and functionalization. First, two different reactive functional monomers, DMAEMA and glycidyl methacrylate (GMA), were photografted onto the PE films [18][19][20]. Subsequently, functionalization of these grafted PE films, the quaternization of the PE-g-PDMAEMA films and sulfonation of GMA-grafted PE (PE-g-PGMA) films, was performed [24][25][26][27][28]. The permeability of the quaternized PE-g-PDMAEMA (PE-g-QPDMAEMA) and sulfonated PE-g-PGMA (PE-g-SPGMA) films to organic electrolytes was investigated by varying the initial pH value of the permeate solution, and then their selective permeation was estimated by use of the three-component type permeation cell.

Materials
A PE film (thickness, 30 µm; density, 0.924 g/cm 3 ) was supplied from Tamapoly Co. Ltd., (Tokyo, Japan) and used as a polymeric substrate for photografting. The PE films of 6 cm in length and 3 cm in width were washed with methanol and acetone, and then dried under reduced pressure. DMAEMA and GMA were purchased from Tokyo Chemical Industry Co. (Tokyo, Japan) and used without further purification. All other reagents were analytical grade or higher.

Photografting
The photografting of DMAEMA and GMA onto the PE films was performed in the same manner described in previous articles [16][17][18][19][20]. An aqueous DMAEMA solution was prepared at 1.0 M and the pH value was decreased to 8.0 with conc. HCl in order to increase the solubility of PDMAEMA [18,19]. A GMA monomer solution was prepared at 1.0 M in an aqueous 80 vol% ethanol solution because the solubility of GMA is very low in water [20,29]. The PE films were dipped in a 50 cm 3 acetone solution containing 0.25 g benzophenone (BP) as a sensitizer, and then acetone was evaporated at room temperature to coat their surfaces with BP. DMAEMA and GMA were photografted onto the BP-coated PE films at 60°C by applying UV rays emitted from a 400 W high-pressure mercury lamp to the monomer solutions in which the PE films were immersed. The resultant PE-g-PDMAEMA and PE-g-PGMA films were washed with acetone for 24 h to remove homopolymers formed, and then dried under reduced pressure. The grafted amounts inmmol/g were calculated from the weight increases of the PE films after photografting using eq. (1): where, Wg is the weight of a grafted PE film (g); W0, weight of an ungrafted PE film, andmM, (g/mol) molar mass of the monomer grafted (157.21 for DMAEMA and 142.15 for GMA).

Functionalization of Grafted PE Film and Their Membrane Properties
The quaternization of the PE-g-PDMAEMA films and sulfonation of the PE-g-PGMA films were performed as described below. The scheme of these reactions are illustrated in Figure 1. The PE-g-PDMAEMA films were immersed in dimethylsulfate ethanol solution at 60 wt% and the mixture was refluxed with moderate stirring for 3 hr at 70°C [28]. After the reaction, the PE-g-QPDMAEMA films were washed with 1 M HCl and acetone. On the other hand, the PE-g-PGMA films were immersed in an aqueous solution containing sodium sulfate at 10 vol% and 2-propanol at 15 vol%, and the reaction solution was heated at 70°C for 24 hr with moderate stirring [30]. After the reaction, the PE-g-SPGMA films were washed with acetone. The degree of functionalization (quaternization and sulfonation) was calculated from the weight increase of the PE-g-PDMAEMA and PE-g-PGMA films after the reaction. The amount of absorbed water was calculated from the weight increase of the PE-g-QPDMAEMA and PE-g-SPGMA films immersed in distilled water for 24 hr at 25°C. In addition, the nwater value, the number of water molecules assigned per monomer segment, was calculated from the amounts of grafted amount and of adsorbed water using eq. (3) in ref. 14.

Permeation Control of Organic Electrolytes by the pH Difference
The PE-g-QPDMAEMA or PE-g-SPGMA films swollen in water were fixed to the two-component type permeation cell [15,18]. First, the pH dependence of permeation of benzoic acid (BA, weak acid, pKa=4.2) and benzenesulfonic acid (BSA, strong acid) was investigated for the PE-g-QPDMAEMA films. An aqueous solution of BA (initial pH=3.2) or BSA (initial pH=2.1) at 10mM (100 cm 3 ) was put in one cell (feed side). An aqueous solution of HCl or NaOH at pH 2.0-12.0 (100 cm 3 ) was put in the other side (permeate side). Both solutions were mildly stirred at 25°C and the pH values of both solutions and the amounts of permeated BA or BSA were measured at the prescribed time intervals. The aliquots of 0.5 cm 3 were taken from the permeate solutions and diluted to 10 cm 3 with an aqueous HCl solution of pH 2.0.
The amounts of permeated BA and BSA were calculated from the absorbances at 229 nm for BA (log ε＝4.006 dm 3 /mol·cm) and 212.5 nm for BSA (log ε ＝ 4.141 dm 3 /mol·cm), respectively. The permeation flux (mmol/cm 2 ·hr) was calculated form the linear relationship of the permeated amounts, Qs, with the permeation time, ∆t, using eq (2) 14 where the quantity of 3.14 is the effective membrane area (cm 2 ) [34].
Phenylalaninol (Phl, pKb=6.2) as a weakly basic organic electrolyte was used for investigating the permeability of the PE-g-SPGMA films. The pH dependence of permeation of Phl was estimated by the above-mentioned procedure (log ε =3.918 dm 3 /mol·cm). In addition, the permeability of the PE-g-QPDMAEMA and PE-g-SPGMA films was measured as a function of the degree of functionalization and the grafted amount.

Selective Separation of Organic Electrolytes
The selective separation was investigated for the BA/Phl and 2,5-dichlorobenzoic acid (diClBA, pKa=0.96)/Phl systems by use of the pH difference through the PE-g-QPDMAEMA and PE-g-SPGMA films. The PE-g-QPDMAEMA and PE-g-SPGMA films swollen in water were fixed with a three-component type permeation cell. An aqueous binary equimolar mixture solution of BA/Phl or diClBA/Phl at 10mM was put in the central cell. An aqueous NaOH solution at pH 12.0 was put in the permeation cell across a PE-g-QPDMAEMA film and an aqueous HCl solution at pH 2.0 was put in the permeation cell across a PE-g-SPGMA film. Each solution was moderately stirred during the permeation experiments. The amounts of two organic electrolytes, designating one organic electrolyte as A and the other as B, permeated through the PE-g-QPDMAEMA and PE-g-SPGMA films from the binary feed solutions were determined by measuring the absorbances of the aliquots taken from the permeate solutions at two different wavelengths, λ1 and λ2, as shown in Figure 2. The absorbances, Abs1 and Abs2, were measured at one wavelength λ 1 at which the molar absorption coefficient of one organic electrolyte was the same as that of the other ( ε A 1 = ε B 1 ) and at the other wavelength λ 2 at which their molar absorption coefficients were quite different ( ε A 2 ≠ ε B 2 ). The amounts of permeated organic electrolytes were calculated using eqs. (3) and (4) [13,35].
Yuji Kimura and Kazunori Yamada: Selective Separation of Organic Electrolytes by Neutralization Dialysis with Grafted Polyethylene Films where C denotes the molar concentration of the organic electrolytes permeated, and L is the cell length (1 cm). In addition, separation factor was calculated using eq. (5): where X and Y denote the molar fraction of the organic electrolytes in the feed and permeate solutions, respectively [35].
The aliquots of 0.5 cm 3 taken from the permeate solutions were diluted to 10 cm 3 with an aqueous HCl solution at pH 2.0, and the absorbances were measured at 215.2 and 229.0 nm for the binary BA/Phl and diClBA/Phl systems. The concentration of the organic electrolytes was measured in the same manner described above. The PE-g-PDMAEMA films were quaternized with dimethylsulfate and the PE-g-PGMA films were sulfonated with sodium sulfate. Figure 3 shows the changes in (a) the degrees of quaternization for the PE-g-PDMAEMA films and (b) the degree of sulfonation for the PE-g-PGMA films with the grafted amount. The degree of quaternization decreased with an increase in the amount of grafted DMAEMA at the reaction time of 3 hr. Dimethylamino groups present in the inside of the PE-g-PDMAEMA films were not subject to the quaternization, although the PE-g-PDMAEMA films possessed a relatively high water absorptivity. Therefore, when the reaction time was prolonged to 5 hr at grafted amounts higher than 8mmol/g, the degree of quaternization further increased and went up to 70% at 10mmol/g.

Functionalization of PE-g-PDMAEMA and PE-g-PGMA Films
Here, the PE-g-PDMAEMA films can receive some damage at increased reaction times. In addition, since the photografting of DMAEMA progressed into the inside of the PE film at lower grafted amounts and the PE films were considerably expanded compared with the photografting of other hydrophilic monomers, such as methacrylic acid, acrylic acid, and methacrylamide, the PE-g-PDMAEMA films possessed higher water-absorptivity and a little lower strength in the water-swollen state than the other grafted PE films [14]. Therefore, the quaternization of PE-g-PDMAEMA films was carried out as brief a reaction time as possible. On the other hand, the degree of sulfonation of 97-100% was obtained irrespective of the grafted amount for the PE-g-PGMA films. Since PGMA was a water-insoluble polymer, the PE-g-PGMA had no solute permeability in the aqueous medium, sulfonation was considered to play an important role in conferring the water absorptivity and solute permeability to the PE-g-PGMA films. Figure 3 shows the typical XPS high-resolution spectra of C 1s , N 1s , O 1s , and S 2p for (a) PE-g-PDMAEMA, (b) PE-g-QPDMAEMA, (c) PE-PGMA, and (d) PE-g-SPGMA films. The XPS high-resolution C 1s spectrum for the PE-g-PDMAEMA film showed a peak at 289 eV assigned to -COO- [31] and a peak at 288 eV assigned to -CH2-N (CH3)2 and -N (CH3)2 groups in addition to a N 1s peak at 400 eV. After the quaternization, a new peak assigned to a quaternized ammonium group appeared at 402 eV in the N 1s spectrum. On the other hand, for the PE-g-PGMA films, an overlapped peak at 288 eV was enhanced and a new peak assigned to a sulfonate group appeared at 169 eV in the high-resolution S 2p spectrum by the sulfonation. These results indicate that the functionalization, that is the quaternization for PE-g-PDMAEMA films and the sulfonation for PE-g-PGMA films, was successfully performed.

Membrane Properties of PE-g-QPDMAEMA and PE-g-SPGMA Films
The water-absorptivity of the PE-g-QPDMAEMA and PE-g-SPGMA films were estimated as a function of the degree of functionalization. Figure 5 shows the changes in the amount of absorbed water with the degree of functionalization for the PE-g-QPDMAEMA film with the grafted amount of 7.5mmol/g and PE-g-SPGMA film with the grafted amount of 5.4mmol/g. The PE-g-PDMAEMA film possessed a relatively high water-absorptivity and an increase in quaternization led to a further increase in the water-absorptivity. Since the photografting of DMAEMA progresses in the inside of the PE films at lower grafted amounts, the PE film is subject to a little more expansion by water uptake [14]. On the other hand, sulfonation conferred the water absorptivity to the PE-g-PGMA films, which had little water absorptivity, and the amount of absorbed water linearly increased with an increase in the degree of sulfonation.   The water-absorptivity for the PE-g-QPDMAEMA and PE-g-SPGMA films was higher than PE films grafted with other hydrophilic monomers [17]. The membrane thickness in the water-swollen state also increased with the grafted amounts due to water uptake. The PE films expanded not only due to the photografting of DMAEMA and GMA and but also due to water uptake by the subsequent functionalizations. The expansion of PE films indicates that the internal grafting occurs simultaneously with the surface grafting for the photografting of DMAEMA and GMA on the PE films [14,17].

Permeability of PE-g-QPDMAEMA Films
The effects of the grafted amount, the degree of quaternization, and the initial pH values of the feed and permeate solutions on the BA and BSA permeation were investigated for PE-g-QPDMAEMA films. Figure 6   Here, no permeability of BA and BSA was observed at lower grafted amounts, since the ungrafted layer was left in the center of the PE film. The previous article reported that the ungrafted layer present the inside of the PE film disappeared at 5mmol/g for the photografting of DMAEMA [17]. On the other hand, the permeability to BA and BSA sharply decreased at further increased grafted amounts. The PE films became hydrophilic by the photografting of DMAEMA onto the PE films and the subsequent quaternization of the PE-g-PDMAREMA films. Therefore, the water absorptivity increased over the degree of quaternization as shown in Figure 5. A further increase in the water absorptivity by these two kinds of modification procedures had a favorable effect on the increase in permeation of BA and BSA. In particular, the conversion of weakly chargeable dimethylamino groups in strongly chargeable trimethylammonium groups and the increase in the amount of trimethylammonium groups effectively led to the increase in the BA and BSA permeability as explained in the next section. Here, the net amount of strongly basic trimethylammonium groups increased with an increase in the amount of grafted DMAEMA under the conditions that the PE-g-QPDMAEMA films had a constant degree of quaternization of 78-84%. It was found from a continuous increase in the nwater value as shown in Figure 6 that the water absorptivity increased over the grafted amount. However, the thickness of the PE-g-QPDMAEMA films also increased over the grafted amount in the water-swollen. Since the increase in the membrane thickness results in the increase in the membrane resistance, which would cause the decrease in the permeability of the PE-g-QPDMAEMA films. Since the permeation of BA and BSA through the PE-g-QPDMAEMA films decreased with an increase in the grafted amount in the range higher than 7.5mmol/g as shown in Figure 7, in this range the increase in the membrane thickness would be more highly influence on the membrane permeation than the increase in the water adsorptivity.  Figure 8 shows the change in the permeation flux of BA and BSA with the degree of quaternization for PE-g-QPDMAEMA films with the grafted amount of 6.1mmol/g. The initial pH values of the permeate solutions were adjusted to either 3.2 corresponding to the pH value of an aqueous BA solution at 10mM or 12.0. The permeation flux of BA and BSA was little independent of the degree of quaternization at the initial pH value of 3.2, and increased with an increase in the degree of quaternization at the initial pH value of 12.0. Since a dimethylamino group is a weakly chargeable functional group, a PDMAEMA chain carries no positive charges at pH 12 [18]. Therefore, the permeability to BA and BSA was low for PE-g-QPDMAEMA films with lower degrees of quaternization. On the other hand, BA and BSA anions can be ionically bonded to trimethylammonium groups affixed to the quaternized grafted PDMAEMA chains. BA and BSA anions can be released from the PE-g-QPDMAEMA films due to ion-exchange with hydroxyl ions present in the permeate solution [28,35]. These results indicate that ionically attractive interaction of BA or BSA anions with trimethylammonium groups affixed to the quaternized grafted PDMAEMA chains more successfully occurs due to an increase in the degree of quaternization. Figure 9 shows the permeation flux of BA and BSA with the initial pH value of the permeate solution for a PE-g-QPDMAEMA film with the grafted amount of 6.2mmol/g and the degree of quaternization of 86% and a PE-g-PDMAEMA film with the grafted amount of 6.2mmol/g. The BA and BSA permeabilities of the PE-g-QPDMAEMA and PE-g-PDMAEMA films were considerably low in the range of the initial pH values of 4.0 to 10.0. In these cases, the pH values of each permeate solution sharply decreased from the initial pH values to about 4 and the pH difference between the feed and permeate solutions across the PE-g-QPDMAEMA or PE-g-PDMAEMA films decreased in a short time. The PE-g-QPDMAEMA and PE-g-PDMAEMA films had relatively higher permeability to BA and BSA at the initial pH value of 2.0 than at the initial pH values of 4.0-10.0. A PDMAEMA chain has little positive charges in the pH range higher than 10 as shown in Figure 1 in the ref. 13. Therefore, the grafted PDMAEMA chains were contracted at pH 12.0, and the BA and BSA permeabilities of the PE-g-PDMAEMA film were lower than those of PE-g-QPDMAEMA films. On the other hand, more BA and BSA anions ionically complexed with trimethylammonium groups affixed to the grafted PDMAEMA chains and released into the permeate side through the ion exchange reaction with hydroxide ions at the interface facing to a permeate solution [36,37]. This behavior supports that the quaternization play a favorable role in the increase in the BA and BSA permeability. In addition, aqueous HCl solutions of pH 2.0 containing NaCl of different concentrations were put in the permeate side, and the BA permeability was measured to discuss a high BA permeability of the PE-g-QPDMAEMA film at pH 2.0. The permeation flux of BA for the PE-g-QPDMAEMA film gradually increased with an increase in the NaCl concentration from 11 at 0mM to 17mmol/cm 2 ･hr at 50mM (data not shown). The increase in the BA permeability is caused by contraction of quaternized grafted PDMAEMA chains. From this result, one of the reasons for the increase in the BA permeation at the initial pH value of 2.0 would be due to the screening effect by the addition of HCl. In addition, the isometrical contraction of the PE-g-QPDMAEMA film fixed between the permeation cells will also lead to an increase in the BA permeability [27,38]. It was found from the above experimental results that the PE-g-QPDMAEMA film had the maximum permeability to BA and BSA at the initial pH value of the permeate solution of 12.0.

Permeability of PE-g-SPGMA Films
The effects of the grafted amount, the degree of sulfonation, and the initial pH value of the permeate solution on the Phl permeation were investigated for the PE-g-SPGMA films. Figure 9 shows the variation in permeation flux of Phl with the grafted amount at the initial pH value of 2.0 for the PE-g-SPGMA films with the degree of sulfonation of 100%. Here, since the ungrafted layer was left in the center of the PE film in the range of the grafted amounts lower than 4 mol/g, the PE-g-SPGMA films had no Phl permeability [22]. The Phl permeability increased with an increase in the amount of grafted GMA and had the maximum value at 6.2mmol/g. For PE-g-SPGMA films with a constant degree of sulfonation, the increase in the grafted amount leads to the net amount of sulfonic groups as well as the amount of absorbed water as shown in Figure 5, indicating that sulfonation has a favorable influence on the increase in the Phl permeability. However, since the thickness of the PE-g-PGMA films increased over the grafted amount by the photografting of GMA and subsequent sulfonation. The increase in the thickness had a positive influence on the Phl permeability of PE-g-SPGMA films as is the case with PE-g-QPDMAEMA films. Subsequently, the Phl permeability of the PE-g-SPGMA films on the degree of sulfonation was investigated at 6.2mmol/g.  Figure 10 shows the change in the permeation flux of Phl with the degree of sulfonation for the PE-g-SPGMA films with the grafted amount of 6.2mmol/g at the initial pH value of the permeate solution of 2.0. No Phl permeation was observed through the PE-g-PGMA films because they had little water absorptivity. Since sulfonation offered hydrophilic properties to the PE-g-PGMA films, the Phl permeability increased with an increase in the sulfonation. In addition, the dependence of the Phl permeability on the initial pH value of the permeate solution was investigated for a PE-g-PSGMA film with the degree of sulfonation of 100%.  Figure 12 shows the variation in permeation flux of Phl with the initial pH value of the permeate solution for the PE-g-SPGMA film. Since the pH value of the permeate solution sharply increased to reach about 8.5 in the initial pH range between 4.0 and 8.0, the Phl permeability was considerably low. Here, the increase in the pH value of the permeate solution indicates that hydroxide ions sucessfully permeated through the PE-g-SPGMA films to the permeate solutions. The amount of permeated Phl gradually increased against the permeation time due to the concentration difference between the both solutions across the PE-g-SPGMA films at the initial pH values of 10.0 and 12.0. The PE-g-SPGMA film had a high permeability to Phl at the initial pH value of 2.0. Phl cations complexed with sulfonic groups appended to the sulfonated grafted PGMA chains are considered to be released into the permeate solution by the ionic exchange with hydrogen ions at the interface of the PE-g-SPGMA film. The maximum Phl permeability was obtained at the initial pH value of 2.0.

Selective Permeation of Organic Electrolytes
On the basis of the above-mentioned results, the selective separation was investigated for the BA/Phl system by using a PE-g-QPDMAEMA film with the grafted amount of 7.5mmol/g and the degree of quaternization of 86% and a PE-g-SPGMA film with the grafted amount of 6.2mmol/g and the degree of sulfonation of 100% in the three-component type permeation cell.
The pH values of the permeate solutions through the PE-g-QPDMAEMA and PE-g-SPGMA films were adjusted to 12.0 and 2.0, respectively. BA anions were selectively permeated through the PE-g-QPDMAEMA film. BA anions were complexed with trimethylammonium groups affixed to the quaternized grafted PDMAEMA chains, while Phl cations were repulsed against the quaternized grafted PDMAEMA chains. On the other hand, Phl cations were selectively permeated through the PE-g-SPGMA film because Phl cations were complexed with sulfonic groups affixed to the sulfonated grafted PGMA chains. Since it was found from these results that BA and Phl were selectively separated by use of the pH difference between the feed and permeate solutions through the PE-g-QPDMAEMA and PE-g-SPGMA films, the effect of the initial pH value of the BA/Phl mixture solutions on their selective separation was investigated. Figure 13 shows the effects of the initial pH value of the BA/Phl mixture solution on the separation factor. BA anions and Phl cations were selectively permeated through the PE-g-QPDMAEMA and PE-g-SPGMA films, respectively, irrespective of the initial pH value of the feed BA/Phl mixture solution. The BA permeability of the PE-g-QPDMAEMA film and the Phl permeability of the PE-g-SPGMA film had maximum values at pH 6.45 corresponding to the pH value of an equimolar BA/Phl mixture solution without pH adjustment.
Here, a decrease in the pH value of the BA/Phl mixture solution restrained the dissociation of BA. On the other hand, an increase in the pH value results in the decrease in the protonation of Phl. This behavior supports that as the initial pH value of the BA/Phl mixture solution departs from pH 6.45 by the addition of HCl or NaOH, the neutralization between protons and hydroxide ions more preferentially occurs. Therefore, as the pH value of the BA/Phl mixture solution departs from 6.45, the selective separation between BA and Phl decreased. Next, the selective separation was investigated in the diClBA/Phl system.  Figure 14 shows the effects of the initial pH value of the diClBA/Phl mixture solution on the separation factors. diClBA anions and Phl cations were selectively permeated through the PE-g-QPDMAEMA and PE-g-SPGMA films, respectively, irrespective of the initial pH value of the feed mixture solution. The permselectivity for the diClBA/Phl system had the maximum value at the initial pH value of 6.0 corresponding to the pH value of an equimolar diClBA/Phl mixture solution without pH adjustment. As the initial pH value of the diClBA/Phl mixture solution departed from 6.0, the permselectivity between the diClBA and Phl decreased. The addition of HCl or NaOH to the feed solution resulted in the decrease in the permselectivity for the diClBA/Phl system in the same manner as the BA/Phl system. The separation factor had the mixture values at the initial pH values of 6.5 and 6.0, which are the pH values of the equimolar BA/Phl and diClBA/Phl mixture solutions, respectively. The addition of HCl or NaOH for adjusting the pH values of the feed solutions increases in the concentration of coions (H + and Cl − ions for HCl and Na + and OH − for NaOH). Therefore, as shown in Figures 12 and 13, the increase in the permeation of coions added in the feed solution through the PE-g-QPDMAEMA and PE-g-SPGMA films will suppress the permeation of organic ions.

Conclusion
In this study, the permeation control and selective separation of organic electrolytes by use of the pH difference with the PE-g-QPDMAEMA and PE-g-SPGMA films were investigated and the following conclusions was obtained. The permeation flux of BA for the PE-g-QPDMAEMA film increased with an increase in the degree of quaternization, and the PE-g-QPDMAEMA film with the grafted amount of 7.5mmol/g had the maximum BA permeability at the initial pH value of the permeate solution of 12.0. In addition, the sulfonation offered the permeation of Phl to the pPE-g-PGMA films, and the PE-g-SPGMA film had the maximum Phl permeability at 6.2mmol/g. The selective separation for the binary BA/Phl and diClBA/Phl systems was achieved by use of the pH difference between the feed and permeate solutions through the PE-g-QPDMAEMA and PE-g-SPGMA films. The maximum permselectivity was obtained for the binary BA/Phl and diClBA/Phl systems under the experimental conditions that the initial pH values of the feed solutions through the PE-g-QPDMAEMA film and PE-g-SPGMA film were adjusted to 12.0 and 2.0, respectively and the equimolar organic electrolyte mixture solutions were put in the central feed without any pH adjustment. The above-mentioned results indicate that acidic and basic organic electrolytes are selectively separated by use of the pH difference through the PE-g-QPDMAEMA and PE-g-SPGMA films by neutralization dialysis technique. This procedure will be applied to separation and concentration of organic electrolytes and water purification.