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Bipolar Membrane Electrodialysis for LiOH Production

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Bipolar Membrane Electrodialysis for LiOH Production ( bipolar-membrane-electrodialysis-lioh-production )

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Membranes 2021, 11, 575 9 of 29 Membranes 2021, 11, x FOR PEER REVIEW 9 o Figure 4. LiOH production system by BMED. Figure 4. LiOH production system by BMED. Flow rate in each compartment was set between 1.0 and 1.5 cm·s−1 using peristaltic Experimental long-running tests of LiOH production were performed accordin pumps (Watson-Marlow 520SN/R2, Falmouth, UK), and a DC power supply (GW Instek the operating conditions shown in Table 5. Tests 1 and 2 compare the effects of two GPR-1810HD, New Taipei, Taiwan) was used to set the electric current. ferent cation-exchange membranes (CMX and CMB), while Tests 3 and 4 compare the Experimental long-running tests of LiOH production were performed according to fects of different bipolar membranes (Neosepta BP and Fumasep FBM). On the other ha the operating conditions shown in Table 5. Tests 1 and 2 compare the effects of two 14 wt% and 25 wt% LiCl concentration effects can be compared by Tests 1 and 3 at 1 different cation-exchange membranes (CMX and CMB), while Tests 3 and 4 compare the A∙m−2, while Tests 5 and 6 compare 14 wt% and 34 wt% LiCl concentrations at a curr effects of different bipolar membranes (Neosepta BP and Fumasep FBM). On the other density of 500 A∙m−2. In the latter case, to obtain comparable initial and final LiOH c hand, 14 wt% and 25 wt% LiCl concentration effects can be compared by Tests 1 and 3 centration ranges, the number of compartments was increased to four three-compartm at 1000 A·m−2, while Tests 5 and 6 compare 14 wt% and 34 wt% LiCl concentrations at cells. Equal initial−L2iOH and HCl concentrations of 0.5 wt% were used in all tests. a current density of 500 A·m . In the latter case, to obtain comparable initial and final initial LiCl concentration between 14 and 34 wt% was considered. Neosepta AMX LiOH concentration ranges, the number of compartments was increased to four three- used as an anionic membrane. The cation-exchange membranes and bipolar membra compartment cells. Equal initial LiOH and HCl concentrations of 0.5 wt% were used in were previously conditioned in a 0.5 M LiOH solution for 24 h, while the anion-excha all tests. An initial LiCl concentration between 14 and 34 wt% was considered. Neosepta membrane was conditioned in 0.5 M LiCl solution. AMX was used as an anionic membrane. The cation-exchange membranes and bipolar membranes were previously conditioned in a 0.5 M LiOH solution for 24 h, while the Table 5. Operating conditions of long-running tests of LiOH production according to different bipolar membranes, initial anion-exchange membrane was conditioned in 0.5 M LiCl solution. LiCl concentration, and current density. Table 5. Operating conditions of long-running tests of LiOH production according to different bipolar membranes, initial Test 123456 LiCl concentration, and current density. Cation membrane CMX CMB CMX CMX CMX CMX Bipolar membrane Neosepta BPNeosepta BPNeosepta BPFumasep FBMFumasep FBMFumasep F Test 123456 CMX CMX Number of three-compartment cells 2 2 2 2 4 4 4 Current density Cation membrane CMX Bipolar membrane (A∙m−2) Neosepta BP CMB CMX CMX Current density (A·m−2) 1000 LiCl initial concentration (wt%) Fumasep FBM LiCl initial concentration (wt%) 14 Time (min) 360 14 360 25 25 360 360 360 34 440 Time (min) 360 360 360 360 440 Number of three-compartment cells 2 1000 1000 1000 1000 500 500 Neosepta BP 1000 Neosepta BP 1000 1000 Fumasep FBM Fumasep FBM 500 14 14 4 14 34 2 2 2.5.3. SEC and  Calculation 14 25 25 360 2 500 2.5.3. SEC and φ Calculation + − Concentrations of different elements—such as Li , OH , and Cl —in the LiOH solu- Concentrations of different elements—such as Li+, OH−, and Cl−—in the LiOH so tion were measured at the end of each experiment. Lithium concentration was determined tion were measured at the end of each experiment. Lithium concentration was determi by atomic absorption spectrophotometry, chloride ion concentration was determined by an by atomic absorption spectrophotometry, chloride ion concentration was determined argentometric method, and hydroxide content was analyzed by acid–base volumetry. an argentometric method, and hydroxide content was analyzed by acid–base volumet − f g d n 0 e o e A w n n B n r

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