Research Article  Open Access
Separate Determination of Borohydride, Borate, Hydroxide, and Carbonate in the Borohydride Fuel Cell by AcidBase and Iodometric Potentiometric Titration
Abstract
A methodology for quantitative chemical analysis of the complex “borohydrideboratehydroxidecarbonatewater” mixtures used as fuel in the borohydride fuel cell was developed and optimized. The methodology includes the combined usage of the acidbase and iodometric titration methods. The acidbase titration method, which simultaneously uses the technique of differentiation and computer simulation of titration curves, allows one to determine the contents of hydroxide (alkali), carbonate, and total “borate + borohydride” content. The iodometric titration method allows one to selectively determine borohydride, so the content of each of , , , and anions in the fuel becomes estimated. The average determination error depends on the number and ratio of compounds in a mixture. Specific details of the analysis of various fuel mixtures are discussed.
1. Introduction
The intense progress of electric vehicles, portable electronics, mobile communication tools, and other systems, which require independent power supply, stimulates the design of new chemical power sources [1, 2]. These sources have to possess highenergy specific characteristics but also they must be safe and comfortable in use. In this connection, the development of fuel cells (FC) in which chemical energy is directly converted into electrical one becomes most topical. Especially, direct borohydride fuel cells (DBFCs) are intensively evolved in which alkaline aqueous solutions of such salts as , , and are used as fuel [3–9]. In these systems, electrical energy is generated by means of hydrolysis and electrochemical oxidation of borohydrides into borates. In alkaline media, these are , , and [10–12] whose solubility essentially influences the power characteristics of FC [13–15]. The difficulty of the design of effective and sustainable anode electrocatalysts for the anodic oxidation of borohydride limits the efficiency and power density attainable in these devices [16–18].
The fuel of DBFCs is a multiple mixture whose specific characteristics directly depend on the ratio of its components [19–24]. It can be an aqueous solution of and in the initial state and an aqueous solution of , , and in the discharged (partially or fully) state. Besides, the fuel composition is changed due to side reaction; it can dry up or water out, and it also can be acidified and/or carbonated by chemical interaction with carbon dioxide from air. In this case, additional components will appear in the solution, such as carbonate and bicarbonate at deeper carbonization in accordance with the ionic reactions: I stage (carbonate formation) II stage (bicarbonate formation) These side reactions have high significance for the proper functioning of FC, since the salts and (as well as the corresponding lithium and potassium salts) poorly dissolve in aqueous alkaline solutions. These salts and their crystal hydrates are deposited in the porous structure of the electrodes to deteriorate them. So it is important, on the one hand, to preserve the fuel from contact with and, on the other hand, to control the carbonate concentration in it.
In this connection, for the development and maintenance of FCs, regular monitoring of the chemical composition of the fuel used is necessary. It requires control of the concentration of each dissolved component during the working process of FC, determination of the discharge degree of the fuel, and evaluation of the conformity of the current state of the fuel mixture to its theoretical composition calculated from material balance.
Earlier, a number of methods were proposed for quantitative determination of the total boron and boron compounds in analyzed samples [25–31]. To analyze borates and boric acid, the titrimetric [28–31], photometric [32], and fluorescent methods [33–35] have been suggested. It is also possible to carry out the selective determination of borohydrides by the hydrogen volumetric method [36, 37], titration [38–41] with permanganate [36], hypochlorite [42], iodate [10, 43], and the voltammetric [44–46] or potentiometric [47–49] titration methods. Titration of borohydride solutions with acid, in particular, HCl, was suggested in a few papers [36, 40, 50], where the reaction equation was written as In the case of potentiometric acid titration of aqueous solutions, it is pointed [36] that actually it is sodium borate formed as a result of hydrolysis which is titrated:
Thus, there is no unified method of quantitative analysis of boroncontaining compounds and other anions presented in the fuel solution of DBFC. For selective determination of each component, it is necessary to consecutively apply several techniques. In the present paper, we have developed a methodology for quantitative analysis of complex “borohydrideboratealkalicarbonatewater” mixtures based on the methods of acidbase and iodometric titration. The first method allows simultaneous estimation of the contents of hydroxide, carbonate, and the “borate + borohydride” total with their joint presence in the sample. The second method allows selective determining the borohydride content.
2. Experimental Section
The contents of hydroxide ions, carbonate ions, and total borate and borohydride ions were determined by the acidbase titration method with a 0.1 mol·L^{−1} HCl solution as the titrant. A fuel sample taken from FC for analysis is a highly alkaline medium. For acidbase titration, it was repeatedly diluted. A sample of a certain weight (0.1 to 0.5 g) was taken from the fuel analyzed, quantitatively transferred to a 250 mL glass for titration, and brought to 100.0 mL with distilled water. A homogeneous solution with pH ≈ 11–13 resulted. The analysis result was then recalculated in terms of the initial fuel in view of the dilution factor. A fixed initial volume of the titratable mixture = 100.0 mL is required to further correct modeling of the titration curve. Titration was started from some initial pH value and ended at pH ≈ 23. The positions of peaks were defined, and both titration curves (integral and differential) were saved in a data file for subsequent computer simulation. To analyze borohydride ions, the iodometric redox titration method was used. The analogous sample of the analyzed fuel (0.1 to 0.5 g) was quantitatively transferred into a 50 mL flask and brought to the mark with a 1 mol·L^{−1} solution. Then, a 5 mL aliquot was sampled, transferred to a glass for titration, and brought to 50 mL with a 1 mol·L^{−1} or solution with further titration with a 0.1 mol·L^{−1} standard iodine solution up to a preset potential value. An automatic ATP02 titrator (“Aquilon”, Russia) was applied. The software package of the titrator provides titration up to a preset electrode potential value or pH at an automatically changed rate of the titrant. A glass indicator electrode and a silverchloride reference electrode were used for acidbase titration; a platinum indicator electrode and a glass reference electrode were applied for iodometric titration. All analyses were carried out under thermostating at 25°C.
Chemically pure reagents (reagent grade) were used to prepare reference solutions of a desired composition for checking our analytical methodology. The chemicals used were (Vecton Corp, Russia, the analytical reagent content ); (Vecton Corp, the reagent content ), (Ecros Corp., Russia, the reagent content ; water content ), (Ecros Corp., the reagent content ; water content ), (Aviabor Corp, Russia, the reagent content ), (Aviabor Corp., the reagent content ), and distilled water without dissolved carbon dioxide. Every reagent had undergone common chemical analysis to analyze the basic substance, water content, and carbonate content. No analytically detectable carbonate impurity in the solid reagents was found. The exact composition of the solidstate reagents was taken into consideration at preparing reference solutions. The error of each controlled concentration of the reference solutions can be estimated less than 1.5%.
3. Results and Discussion
3.1. Determination of Borohydride, Borate, Hydroxide, and Carbonate by AcidBased Titration
The analyzed object was an aqueous solution containing a mixture of anions in a random ratio as highly soluble sodium and potassium salts. During the titration process by an aqueous solution of acid, the following reactions proceed: In the presence of , the first stage is the irreversible hydrolysis of catalyzed with acid which is not consumed. Protons are consumed at the second stage only (reaction (9)). As a result, the total boron () is titrated out at the acidbase titration.
Reactions (5)–(9) proceed concurrently. The predomination of this or that reaction is determined by the ratio of the corresponding dissociation constants of , , and water . This predomination changes as the titration curve goes with gradual change of pH from the initial pH value ≈ 11–13 to the final one ≈ 23. The values of the dissociation constants are such [51, 52] that at the addition of acid, the first reactions (5) and (6) occur, then the reactions (7) and (8) proceed, and the titration process is completed with reaction (9). It should be noted that the reaction (7) is written in a simplified form, as it is known about the existence of a number of borate anion forms but the final product of protolysis is orthoboric acid . This may be ignored within our pH range.
Borohydride hydrolysis reaction (6) takes place in aqueous alkaline solutions even at high pH but its rate is extremely low [21]. Table 1 comprises approximate rates of decomposition due to hydrolysis at 25°C. One can see that the hydrolysis of slowly proceeds at pH ≈ 11–13 in the solutions at acidbase titration, but this hydrolysis is part of the analytical procedure. Hydrolysis is sharply accelerated at pH ≈ 7–9 and the borate ions formed are further bound in reaction (7). No complex mechanism of the protolysis of ions [8, 21, 34] is reflected on the titration curve pH versus .

Let us assume that the initial aqueous solution has a volume , containing of alkali, of borohydride, of metaborate, and of carbonate. Hydrocarbonate cannot exist in the initial (highly alkaline) solution; that is, . The formation and consumption of very small amounts of water during the neutralization reaction are neglected but the dilution degree of the initial mixture titrant is taken into account. The titrant () is an aqueous solution with a concentration to be added into the mixture at the current time in the amount mL. Then, taking into account the titrantcaused dilution, the overall molar concentrations are Here is the total volume of the mixture at the current instant of titration. Unlike the overall concentrations , the current equilibrium values of the molar concentrations [], [], [], [], [], [], [], and [] are marked with symbols in square brackets and they are calculated from the equilibrium constants of the titration reactions.
An additional correction is taken into account for the average ionic activity coefficient. We used the 2nd approximation of DebyeHuckel’s theory as Gyuntelberg’s equation where the activity coefficient is only determined by the ionic strength of the solution and the squared ion charges [53]. Then, is the activity coefficient of all singlecharged ions, but in the equations containing the doublecharged carbonate ion concentration, the factor will appear. Gyuntelberg’s equation at 25°C looks like where is the ionic strength of the solution calculated by the formula in our case: Gyuntelberg’s equation has an advantage over other approximations of having no arbitrary parameters and describing well electrolyte solutions when , which is the case in our acidbase titration (the concentration of any ions in solution at different stages of titration did not exceed 0.1 mol·L^{−1}). The concentration of solutions was chosen so as not to blur steps on the titration curve and, at the same time, the correction to the activity coefficients should be small.
As a result, with the experimental data arrays , , , and using (10) and (11), we obtain the data arrays , , , and . The current values of the equilibrium concentrations at every titration point can be calculated from the conditions of chemical equilibrium and material balance by means of the appropriate formulae: where Here the ionic product of water (autoprotolysis constant) is at 25°C [52]; the dissociation constant of metaboric acid is ; the dissociation constant of carbonic acid at the first stage is at 25°C [52]; the dissociation constant of carbonic acid at the second stage is at 25°C [52]. Moreover, processing the titration curves of simple solutions of a fixed composition (e.g., 0.01 mol·L^{−1}) can be used for refinement of these dissociation constants.
Let us determine the calculated volume of the titrant from the material balance by acid, by boron, and by carbon, only considering the acid consumption by the titration reactions (5), (7)–(9). The material balance equation is thus written as (the initial content of acid in an alkaline solution mol·L^{−1} is ignored).
The calculated value of is estimated from the current pH value and (10) and (15). As a result, the calculated points of the titration curve of solutions containing a mixture of anions , , , and are determined by the equation where the current equilibrium values of molar concentrations are determined by (14) and (15). Equation (17) is very convenient for computer simulations. It allows calculating the dependence and plotting the whole calculated titration curve. By means of fitting the calculated curve to the experimental curve, we find the amounts of components in the sample: , , and . The concentration of borate is calculated by the difference of total boron minus borohydride; that is, . The amount of borohydride in the mixture is selectively determined by iodometric titration.
3.2. Determination of Borohydride in Solution by Iodometric Titration
As shown in [39], the quantification of in solution by direct iodometric titration is based on the reaction proceeding quantitatively in an alkaline medium: Usually, the direct titration is made in a low alkaline medium () because iodine interacts with hydroxide ions to form nonactive iodate ion in higher alkaline solution [34]:
However, borohydride ions are insufficiently stable at room temperature when pH < 11. Table 1 comprises approximate rates of decomposition due to hydrolysis. One can see that the fuel with alkalinity above 2 mol·L^{−1} is almost not subjected to hydrolysis at 25°C. The same applies to the iodometric redox titration method used by us, which requires a 1 mol·L^{−1} solution. In a 1 mol·L^{−1} alkaline solution, the addition of iodine to borohydride is also accompanied by extremely slight hydrogen release as a result of borohydride decomposition. Under these conditions, about 0.5–1% of ions is decomposed, while a negligible amount of iodate is formed by reaction (18) with iodine consumption of ~0.5–1%. Thus, any mistakes are compensated and direct iodometric titration allows one to obtain the result closest to the true value of borohydride concentration (the error not to exceed 0.05%).
3.3. Processing Titration Curves and Estimation of Accuracy
The titration curves versus and the appropriate dependences versus obtained by acidbase titration of aqueous solutions of various anion mixtures are shown in Figure 1 and the analogous curves obtained by iodometric titration are shown in Figure 2. The first distinct step presented (not always) on the iodometric titration curve reflects a complex mechanism of the chemical reaction (18) and is neglected. The determination of the amount of the titrant is carried out by the second sharp leap within the potential range 0 to 600 mV (Figure 2).
(a)
(b)
(c)
(d)
The titration curves were processed by two ways, namely, a simple method of differentiation and a more complex method of computer simulations. For the iodometric determination of borohydride it is enough to use the method of differentiation only, while for acidbase titration, the best results are obtained when both methods (differentiation and simulation) are used.
The method of differentiation is based on the equivalence points coinciding with the inflections on the pH versus curve and with appropriate maxima on the differential versus curve (Figure 1). The positions of the maximum points are fixed, the titrant volume consumed for titration of the th component is measured, and the amount of each component is calculated. However, in few complex cases, it is possible to state that an extreme point on the differential = 0 curve is close to an equivalence point at sharp changes of pH. If smoothed inflections with a small pH difference are observed or two points of inflection are near each other, a significant systematic error arises.
The method of simulation is based on the theory explained above. The program for calculating titration curves uses the appropriate theoretical equations (10)–(17) and combines the experimental pH versus curve with the calculated pH versus one. The variable parameters are the sought quantities of components in the aliquot , , and . The criterion of optimum is the minimum dispersion: Here is the number of points on the titration curve. Figure 1 shows the experimental and calculated titration curves for few solutions of various multicomponent mixtures. It is visible that the applied computational methods allow exact simulating experimental curves.
Error Analysis and Estimation of Accuracy. A number of reference solutions of a desired composition were prepared using , , , , , , and for validation of our analytical methodology (the concentration ranges of each analyzed ion in the considered samples are presented in Table 2). In order to detect systematic errors, the dependences of the “measured/weighted” ratios on the anionic fraction were plotted ( is the mole fraction of the th anion in the total amount of the analyzed anions; varies from 0 up to 1). The results are given in Figure 3. The average value of the “measured/weighted” ratio for each ion is presented in Table 3.


(a)
(b)
(c)
(d)
(e)
(f)
It is apparent from Table 3 that the simulation method also gives a systematic error. The causes can be simplification of the theory, the impossibility to consider all side processes, the inability to exactly calculate activity coefficients, and so forth, so the shape of the calculated curve may not completely coincide with the experimental curve. In particular, in the titration process of borate solutions, the formation of poliborates and their hydrated forms is possible. In the case of simulation, the lower branch of the titration curve should be limited when all equivalence points are passed over. Accelerated titration or cold solution may cause an additional error due to the inhibition of reaction (6) and the failure of chemical equilibrium.
The concentration of ions is estimated with an accuracy of 0.959 and 0.956 for the differentiation and simulation methods, respectively. The total of () is estimated with an accuracy of 1.023 and 1.012 for the differentiation and simulation methods, respectively (Table 3). Thus, for the system, the differentiation and simulation methods give similar results and have no advantages over each other, and the systematic error is small but naturally increases with decreasing share of the analyzed ion. The trend of the systematic error is shown in Figure 3(a) by means of solid lines. Both methods overestimate the content of boron in the sample and underestimate the content of alkali. For compensation of the systematic error, the following equations have been obtained for the method of differentiation: and for the method of simulation: After analysis and the determination of the components and , a correction procedure was carried out by multiplying the values found by the corresponding correction coefficients , calculated from formulae (21) or (22). Finally, the corrected amounts of the th component in the sample are Figure 3(b) shows the result of correction of the data given in Figure 3(a). The systematic error was totally compensated for all the variants of analysis (Table 3).
When the value of the anionic fraction , all points lie within the “measured/weighted” range 0.95–1.05; that is, the random error does not exceed 5%; all points lie within the range 0.88–1.12 when ; that is, the random error does not exceed 12%. It is only possible to perform semiquantitative analysis of any component at its very small content in the mixture (). On correction, the average accuracy parameter of the concentration is 1.000 for differentiation and 1.001 for simulation and the average accuracy parameter for the total is 1.008 for differentiation and 1.004 for simulation (Table 3).
The feature of titration of alkalinecarbonate solutions is the existence of three leaps on the titration curve (Figure 1(b)). The first leap belongs to alkali, while the second and third ones are due to carbonates. Correspondingly, when the quantities of components are determined by the location of peaks on the differential curve, the quantity of is included twice. The analysis of carbonate by means of the second peak gives a worse result than by the third one. At a very small content of carbonate, the second peak is not detected. The average “measured/weighted” value is 1.215 for ions by the second peak on the differential curve and 1.115 in the case of the third peak and the “measured/weighted” value is 1.089 for the method of simulation. The results of control determination of the alkali and carbonate contents in the reference solutions are shown in Figures 3(c) and 3(d) for the two methods as the dependence of the accuracy parameter on the anionic fractions . In all cases, the points of differentiation are more distant from the “correct” level than those of simulation. Consequently, the method of simulation gives more correct results for the system while the method of determination cannot be recommended because of its high systematic errors in carbonate analysis.
The systematic error naturally increases with decreasing fractions of the analyzed ions. In Figure 3(c), the trend of systematic errors is shown by means of solid lines for the method of simulation. The following equations have been suggested for compensation of this trend: After analysis and the determination of the and values, a correction procedure is carried out by formula (24). Figure 3(d) shows the result of such correction. The systematic error is completely compensated (Table 3). All points lie within the “measured/weighted” range 0.95–1.05 for the anionic fractions within ; that is, the random error does not exceed 5% and the random scattering does not exceed 12% when . If the fraction of carbonate is less than 0.15, the reliability of its analysis decreases because of the high random dispersion; therefore, it is required to increase the number of replicate samples. The direct titrimetric analysis of carbonate becomes impossible when .
A feature of titration of alkalineborohydrideboratecarbonate solutions is the existence of three weak leaps on the titration curve (Figure 1(d)). The first leap belongs to alkali, while the second belongs to the “” total, and the third one belongs to carbonate ions. Respectively, at the quantification of components by means of the position of peaks on the differential curve, the total content of boron can be only calculated after the determination and extraction of the carbonate quantity.
The results of our control determination of the anion contents in the mixtures by both methods are shown in Figure 3(e). The method of differentiation gives an unsatisfactory result for carbonate, underestimating its content significantly, the mean “measured/weighted” value being 0.615. The carbonate peak disappears when , which leads to incorrect determination of the total. Therefore, for the system (the highly carbonated and discharged fuel), the method of differentiation cannot be recommended because of its large systematic errors in carbonate analysis and the method of simulation is only suggested for use. The mean “measured/weighted” values are shown in Table 3. The determination accuracy is 0.874 for ions, 1.040 for the total, and 0.934 for ions. After correction, these parameters become 0.958, 0.992, and 1.008, respectively. The correcting coefficients are The systematic error is thus compensated; however, the random scattering of the points is higher than with more simple options. The random dispersion for alkali and boron does not exceed 15% (all points are within 0.85–1.15); however, it is only fair for carbonate when . If the carbonate content is less than 0.1, its semiquantitative analysis is only possible. But very small amounts of carbonate will not affect the functioning of DBFC and only higher concentrations of carbonate exceeding the solubility limit can be deposited in the electrode to hinder the functioning of DBFC.
4. Conclusions
The analytic technique presented in our paper includes taking a small fuel sample from DBFC and performing two types of titrations (acidbase and iodometric ones) which supplement each other. The necessity of exactly two techniques of titration is due to the fact that iodometric titration determines the quantity in the sample only, while the quantities of other fuel components are provided by acidbase titration (, , ). Therefore, the joint application of these titration techniques allows one to most fully quantify the current state of fuel in the process of DBFC functioning. The determination correctness of the technique has been shown on artificial mixtures with a wide variation of their composition. The average error depends on the number of components and their ratio in the mixture. The investigation results show that in the most complex case of highly carbonated and discharged fuel the maximal error of determination does not exceed 15%.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Acknowledgment
The authors would like to gratefully acknowledge the Russian Foundation for Basic Research for financial support (Project no. 120331802).
References
 J. B. Lakeman, A. Rose, K. D. Pointon et al., “The direct borohydride fuel cell for UUV propulsion power,” Journal of Power Sources, vol. 162, no. 2, pp. 765–772, 2006. View at: Publisher Site  Google Scholar
 C. P. de Leon, F. C. Walsh, D. Pletcher, D. J. Browning, and J. B. Lakeman, “Direct borohydride fuel cells,” Journal of Power Sources, vol. 155, no. 2, pp. 172–181, 2006. View at: Publisher Site  Google Scholar
 R. Aiello, J. H. Sharp, and M. A. Matthews, “Production of hydrogen from chemical hydrides via hydrolysis with steam,” International Journal of Hydrogen Energy, vol. 24, no. 12, pp. 1123–1130, 1999. View at: Publisher Site  Google Scholar
 S. C. Amendola, S. L. SharpGoldman, M. S. Janjua et al., “Safe, portable, hydrogen gas generator using aqueous borohydride solution and Ru catalyst,” International Journal of Hydrogen Energy, vol. 25, no. 10, pp. 969–975, 2000. View at: Publisher Site  Google Scholar
 H. I. Schlesinger, H. C. Brown, A. E. Finholt, J. R. Gilbreath, H. R. Hoekstra, and E. K. Hyde, “Sodium borohydride, its hydrolysis and its use as a reducing agent and in the generation of hydrogen,” Journal of the American Chemical Society, vol. 75, no. 1, pp. 215–219, 1953. View at: Google Scholar
 S. C. Amendola, P. Onnerud, M. T. Kelly, P. J. Petillo, S. L. SharpGoldman, and M. Binder, “Novel high power density borohydrideair cell,” Journal of Power Sources, vol. 84, no. 1, pp. 130–133, 1999. View at: Publisher Site  Google Scholar
 B. H. Liu and Z. P. Li, “Current status and progress of direct borohydride fuel cell technology development,” Journal of Power Sources, vol. 187, no. 2, pp. 291–297, 2009. View at: Publisher Site  Google Scholar
 B. H. Liu and Z. P. Li, “A review: hydrogen generation from borohydride hydrolysis reaction,” Journal of Power Sources, vol. 187, no. 2, pp. 527–534, 2009. View at: Publisher Site  Google Scholar
 B. Weng, Z. Wu, Z. Li, H. Yang, and H. Leng, “Hydrogen generation from noncatalytic hydrolysis of LiBH4/NH3BH3 mixture for fuel cell applications,” International Journal of Hydrogen Energy, vol. 36, no. 17, pp. 10870–10876, 2011. View at: Publisher Site  Google Scholar
 A. E. Sanli, I. Kayacan, B. Z. Uysal, and M. L. Aksu, “Recovery of borohydride from metaborate solution using a silver catalyst for application of direct rechargable borohydride/peroxide fuel cells,” Journal of Power Sources, vol. 195, no. 9, pp. 2604–2607, 2010. View at: Publisher Site  Google Scholar
 R. Jamard, J. Salomon, A. MartinentBeaumont, and C. Coutanceau, “Life time test in direct borohydride fuel cell system,” Journal of Power Sources, vol. 193, no. 2, pp. 779–787, 2009. View at: Publisher Site  Google Scholar
 J.H. Wee, “A comparison of sodium borohydride as a fuel for proton exchange membrane fuel cells and for direct borohydride fuel cells,” Journal of Power Sources, vol. 155, no. 2, pp. 329–339, 2006. View at: Publisher Site  Google Scholar
 A. V. Churikov, K. V. Zapsis, V. V. Khramkov, M. A. Churikov, M. P. Smotrov, and I. A. Kazarinov, “Phase diagrams of the ternary systems NaBH_{4} + NaOH + H_{2}O, KBH_{4} + KOH + H_{2}O, NaBO_{2} + NaOH + H_{2}O, and KBO_{2} + KOH + H_{2}O at −10°C,” Journal of Chemical and Engineering Data, vol. 56, no. 1, pp. 9–13, 2011. View at: Publisher Site  Google Scholar
 A. V. Churikov, K. V. Zapsis, V. V. Khramkov, M. A. Churikov, and I. M. Gamayunova, “Temperatureinduced transformation of the phase diagrams of ternary systems NaBO_{2} + NaOH + H_{2}O and KBO_{2} + KOH + H_{2}O,” Journal of Chemical and Engineering Data, vol. 56, no. 3, pp. 383–389, 2011. View at: Publisher Site  Google Scholar
 A. V. Churikov, K. V. Zapsis, A. V. Ivanishchev, and V. O. Sychova, “Temperatureinduced transformation of the phase diagrams of ternary systems NaBH_{4} + NaOH + H_{2}O and KBH_{4} + KOH + H_{2}O,” Journal of Chemical and Engineering Data, vol. 56, no. 5, pp. 2543–2552, 2011. View at: Publisher Site  Google Scholar
 G. Rostamikiaa and M. J. Janik, “Direct borohydride oxidation: mechanism determination and design of alloy catalysts guided by density functional theory,” Energy & Environmental Science, vol. 3, pp. 1262–1274, 2010. View at: Google Scholar
 B. Sljuki, J. Miliki, D. M. F. Santosa, and C. A. C. Sequeira, “Carbonsupported Pt_{0.75}M_{0.25} (M = Ni or Co) electrocatalysts for borohydride oxidation,” Electrochim Acta, vol. 107, pp. 577–583, 2013. View at: Publisher Site  Google Scholar
 B. H. Liu, J. Q. Yang, and Z. P. Li, “Concentration ratio of [OH^{−}]/[${\text{B}{\text{H}}_{4}}^{}$]: a controlling factor for the fuel efficiency of borohydride electrooxidation,” International Journal of Hydrogen Energy, vol. 34, no. 23, pp. 9436–9443, 2009. View at: Publisher Site  Google Scholar
 A. V. Churikov, A. V. Ivanishchev, I. M. Gamayunova, and A. V. Ushakov, “Density calculations for (Na, K)BH_{4} + (Na, K)BO_{2} + (Na, K)OH + H_{2}O solutions used in hydrogen power engineering,” Journal of Chemical and Engineering Data, vol. 56, no. 11, pp. 3984–3993, 2011. View at: Publisher Site  Google Scholar
 A. V. Churikov, V. O. Romanova, M. A. Churikov, and I. M. Gamayunova, “The model of fuel transformation at discharge of direct borohydride fuel cell,” International Review of Chemical Engineering, vol. 4, pp. 263–268, 2012. View at: Google Scholar
 A. V. Churikov, I. M. Gamayunova, K. V. Zapsis, M. A. Churikov, and A. V. Ivanishchev, “Influence of temperature and alkalinity on the hydrolysis rate of borohydride ions in aqueous solution,” International Journal of Hydrogen Energy, vol. 37, no. 1, pp. 335–344, 2012. View at: Publisher Site  Google Scholar
 Z. P. Li, B. H. Liu, K. Arai, and S. Suda, “A fuel cell development for using borohydrides as the fuel,” Journal of the Electrochemical Society, vol. 150, no. 7, pp. A868–A872, 2003. View at: Publisher Site  Google Scholar
 Y. Wang, P. Hea, and H. Zhou, “A novel direct borohydride fuel cell using an acidalkaline hybrid electrolyte,” Energy & Environmental Science, vol. 3, no. 10, pp. 1515–1518, 2010. View at: Publisher Site  Google Scholar
 J. Ma, N. A. Choudhury, and Y. Sahai, “A comprehensive review of direct borohydride fuel cells,” Renewable and Sustainable Energy Reviews, vol. 14, no. 1, pp. 183–199, 2010. View at: Publisher Site  Google Scholar
 R. Bruhlmann and L. Piatti, “An improved method for the titrimetric determination of boron in iron,” Chimia, vol. 11, p. 203, 1957. View at: Google Scholar
 A. Keshan and C. Bimba, “Cobaltpotassium and ammoniumcobalt dodecaborate,” Izvestiya Akademii Nauk Latvijskoj SSR, p. 115, 1954. View at: Google Scholar
 J. Czakow, T. Steciak, and O. Szczebinska, “The spectral determination of trace amounts of impurities in the solutions with the metal electrodes in the spark mode,” Analytical Chemistry, vol. 3, p. 745, 1958. View at: Google Scholar
 R. Rosotti, “A fast method for the determination of trace amounts of boron in the steel,” Analytical Chemistry, vol. 44, p. 208, 1962. View at: Google Scholar
 J. Varka and A. Sklaf, “Application of potentiometric titration. IV. Determination of B_{2}O_{3} in glass, enamels and boroncontaining raw materials,” Keramik, vol. 7, p. 12, 1957. View at: Google Scholar
 D. E. Williams and J. Vilamis, “Stability of the curcumin complex in boron determination,” Analytical Chemistry, vol. 33, pp. 1098–1100, 1961. View at: Publisher Site  Google Scholar
 S. Kertes and M. Lederer, “Paper chromatography of inorganic ions. Rf values in mixtures of butanol and Hbr,” Analytica Chimica Acta, vol. 15, no. C, pp. 543–547, 1956. View at: Google Scholar
 A. A. Nemodruk and Z. K. Karalova, The Analytical Chemistry of Boron, Nauka, 1964.
 C. A. Parker, “Raman spectra in spectrofluorimetry,” The Analyst, vol. 84, no. 1000, pp. 446–453, 1959. View at: Publisher Site  Google Scholar
 C. A. Parker and W. J. Barnes, “Fluorimetric determination of boron: application to silicon, sea water and steel,” The Analyst, vol. 85, no. 1016, pp. 828–838, 1960. View at: Publisher Site  Google Scholar
 M. V. Akhmanova, Methods of Determination and Analysis of Rear Elements, Izdat Akademija Nauk SSSR, 1961.
 E. H. Jensen, A Study on Sodium Borohydride, Nyt Nordisk Forlag Amold Busck, Copenhagen, Denmark, 1954.
 I. Fatt and M. Tashima, Alkali Metal Dispersions, D Van Nostrand Co Inc., Princeton, NJ, USA, 1961.
 D. A. Lyttle, E. H. Jensen, and W. A. Struck, “A simple volumetric assay for sodium borohydride,” Analytical Chemistry, vol. 24, no. 11, pp. 1843–1844, 1952. View at: Google Scholar
 P. K. Norkus, “Iodometric determination of borohydride,” Russian Journal of Analytical Chemistry, vol. 23, pp. 908–911, 1968. View at: Google Scholar
 N. N. Mal’ceva and V. S. Khain, Sodium Borohydride Properties and Application, Nauka, 1985.
 C. Harzdorf and O. Steinhauser, “Zur photometrisehen Titration von Fluorid mit Thoriumnitrat,” Fresenius' Zeitschrift für Analytische Chemie, vol. 210, no. 2, pp. 106–112, 1965. View at: Publisher Site  Google Scholar
 W. D. Davis, L. S. Mason, and G. Stegeman, “The heats of formation of sodium borohydride, lithium borohydride and lithium aluminum hydride,” Journal of the American Chemical Society, vol. 71, no. 8, pp. 2775–2781, 1949. View at: Google Scholar
 S. W. Chaikin, “Direct volumetric assay of sodium borohydride and potassium borohydride,” Analytical Chemistry, vol. 25, no. 5, pp. 831–832, 1953. View at: Google Scholar
 Ü. Ülkü and G. Somer, “Determination of trace borohydride in basic solutions using differential pulse polarography,” Turkish Journal of Chemistry, vol. 33, pp. 657–665, 2009. View at: Google Scholar
 H. Celikkan, H. Aydin, and M. L. Aksu, “The electroanalytical determination of sodium borohydride using a gold electrode,” Turkish Journal of Chemistry, vol. 29, pp. 519–524, 2005. View at: Google Scholar
 M. V. Mirkin and A. J. Bard, “Voltammetric method for the determination of borohydride concentration in alkaline aqueous solutions,” Analytical Chemistry, vol. 63, no. 5, pp. 532–533, 1991. View at: Google Scholar
 D. M. F. Santos and C. A. C. Sequeira, “Potentiometric monitoring of sodium borohydride in aqueous solutions,” Ciencia s Tecnologia dos Materials, vol. 20, no. 34, pp. 31–34, 2008. View at: Google Scholar
 D. M. F. Santos and C. A. C. Sequeira, “Sodium borohydride determination by measurement of open circuit potentials,” Journal of Electroanalytical Chemistry, vol. 627, pp. 1–8, 2009. View at: Google Scholar
 H. C. Brown and A. C. Boyd Jr., “Argentimetric procedure for borohydride determination,” Analytical Chemistry, vol. 27, no. 1, pp. 156–158, 1955. View at: Google Scholar
 V. B. Breicis, A. O. Berzina, and L. K. Lepin, “Potentiometric titration of water solutions of sodium borohydride by hydrochloric acid,” Scientific Short Letter of Riga Polytechnic Institute, vol. 15, pp. 179–188, 1965/1966. View at: Google Scholar
 U. U. Lurie, Handbook on Analytical Chemistry, Khimiya, 1979.
 R. A. Lidin, L. L. Andreeva, and V. A. Molochko, Handbook of Inorganic Chemistry Constants of Inorganic Substances, Khimiya, 1987.
 R. A. Robinson and R. H. Stokes, Electrolyte Solutions the Measurement and Interpretation of Conductance, Chemical Potential and Diffusion in Solutions of Simple Electrolytes, Butterworths, London, UK, 1959.
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