Reaction Of NaBH4 Research Articles

High-Efficiency and Fast Hydrogen Production from Sodium Borohydride: The Role of Adipic Acid in Hydrolysis, Methanolysis and Ethanolysis Reactions.

In this study, hydrogen production through the hydrolysis, ethanolysis, and methanolysis reactions of NaBH4 using adipic acid as a catalyst was investigated for the first time. Adipic acid solutions were prepared with methanol and ethanol at concentrations of 0.1, 0.2, 0.3, 0.4, and 0.5 M. In these reactions, NaBH4-MR (methanolysis) and NaBH4-ER (ethanolysis) reactions were carried out at 30, 40, and 50 °C with NaBH4 concentrations of 1.25%, 2.5%, and 5%. Hydrolysis reactions (NaBH4-HR) were conducted at 0.1 M under the same conditions. In the ethanolysis and methanolysis reactions at 30 °C, total hydrogen conversion was achieved at 0.3 M, 0.4 M, and 0.5 M. However, in the hydrolysis reactions, total hydrogen production was only obtained at 50 °C. It was observed that in the NaBH4-MR and NaBH4-ER reactions, total hydrogen conversion could be achieved within 4-5 s. The utilization of adipic acid as a catalyst for hydrogen production from NaBH4 through ethanolysis and methanolysis reactions is proposed as a highly efficient and fast method, characterized by impressive conversion rates.

Ruthenium nanoparticle immobilised on ionic liquid polymer as efficient catalyst for the hydrolysis of NaBH4

Development of heterogeneous catalyst is significant key for achieving high performance of NaBH4 hydrolysis to produce hydrogen. The stability of sodium borohydride in the presence of suitable catalyst is the efficient method to generate hydrogen. In this work, styrene-imid PIILP, polymer 1 decorated styrene, imidazolium ionic liquid, and cross-coupling is successfully synthesised by AIBN initiated radical polymerisation, then precipitation with 3,3′,3″phosphinetriyltribenzene sulfonate with ratio (1:0.3) to isolate the first styrene-imid- sulphonated PIILP, polymer 2. RuNP@styrene-imid-sulphonated PIILP, RuNPs catalyst 3 was synthesised by impregnation with RuCl3, then reduction by NaBH4. Moreover, several analytical techniques such as, 31P, 1H, 13C solid-state NMR, CHN, IR, XPS, TEM, TGA-DTA, and SEM were examined to explore the obtained catalyst 3. The hydrogen generation from NaBH4 utilizing catalyst 3 was exhibited the catalytic behaviour studying several parameters such as, temperature, catalytic loading, and NaBH4 concentrations this work was deducted the activation energy (30.32 kJmol-1), and the turnover frequency (TOF) reached up 134.9, 112.77, and 98.38 moleH2.molcat−1.min−1 at 40, 35 and 30 °C. The effectiveness of Ruthenium nanoparticle catalyst 3 for the hydrolysis reaction of NaBH4 was examined in H2O and D2O resulting kinetic isotope effect (KIE) kH/kD = 3. In addition, RuNPs demonstrated a promising efficient for reuse catalyst 3 after five cycles for the catalytic hydrolysis.

Application of Platinum Nanoparticles Decorating Mesoporous Carbon Derived from Sustainable Source for Hydrogen Evolution Reaction

The perpetually fluctuating economic and environmental climate significantly increases the demand for alternative fuel sources. The utilization of hydrogen gas is a viable option for such a fuel source. Hydrogen is one of the most energy-dense known substances; however, it is unfortunately also highly volatile, especially in the diatomic gaseous state most commonly used to store it. The utilization of a hydrogen feedstock material such as sodium borohydride (NaBH4) may prove to mitigate this danger. When NaBH4 reacts with water, hydrogen stored within its chemical structure is released. However, the rate of hydrogen release is slow and thus necessitates a catalyst. Platinum nanoparticles were chosen to act as a catalyst for the reaction, and to prevent them from conglomerating, they were embedded in a backbone of mesoporous carbon material (MCM) derived from a sustainable corn starch source. The nanocomposite (Pt-MCM) was characterized via transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). Pt-MCM underwent catalytic testing, revealing that the catalytic activity of the Pt-MCM composite catalysts increased with increasing quantities of sodium borohydride, lower pH levels, and higher temperatures. The activation energy of the catalyzed reaction was found to be 37.7 kJ mol−1. Reusability experiments showed an initial drop off in hydrogen production after the first trial but subsequent stability. This Pt-MCM catalyst’s competitive activation energy and sustainable MCM backbone derived from readily available corn starch make it a promising option for optimizing the hydrogen generation reaction of NaBH4.

One-pot two-step reduction of CO2 with amines and NaBH4 to N-substituted compounds at atmospheric pressure

In this paper, the reductive N-formylation, methylation and cyclization of amines with carbon dioxide (CO2) using sodium borohydride (NaBH4) at atmospheric pressure, via a one-pot two-step procedure, is presented. Formato borohydride (NaBHn(OCHO)4-n), in situ formed in the reaction of NaBH4 with CO2, as an efficient agent to promote the corresponding reaction, and the mechanism is proposed on the basis of experiments. This wide substrate scope and simple operational methodology also facilitates the effective synthesis of formamides, methylamines, benzimidazoles and other heterocyclic compounds avoiding high temperature and pressure.

Hydrogen generation from sodium borohydride hydrolysis using a heterogeneous biocatalyst prepared with Zabrus tenebrionides Goeze 1777 (Coleoptera: Carabidae) chitin

Co–B/Chi, which is made up of highly distributed Co–B particles, was synthesized by impregnation and chemical reduction methods. Scanning electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, Brunauer–Emmett–Teller adsorption and Fourier transform infrared spectroscopy analyses were used to describe the morphology and microstructure of Co–B/Chi. The synthesized catalyst showed high catalytic activity in the hydrolysis reaction of NaBH4. The unsupported Co–B samples were compared with the chitin-supported Co–B catalyst, and the result showed that higher catalytic activity and good cycling stability for NaBH4 hydrolysis were obtained with the chitin-supported catalyst. The reaction conditions were investigated to achieve high hydrogen production. The maximum rate of hydrogen production was obtained at 40 °C and 20 mg catalyst amount. At ideal conditions, the hydrolysis reaction’s activation energy was determined to be 51.65 kJ mol−1. It is indicate that Co–B/Chi is a viable low-cost catalyst for the hydrolysis of NaBH4 for hydrogen production.

A Co-Fe/calcium phosphate catalyst improves the release of hydrogen from NaBH4

In this study, catalysts for hydrogen release via either hydrolysis or methanolysis were developed with a focus on solid-state hydrogen storage. The catalyst and supports were produced and deposited concurrently during an electrochemical process. The goals of this study include the electrochemical syntheses of Co-Fe/calcium-phosphate catalysts and an assessment of their performance in the release of hydrogen during the hydrolysis and methanolysis of NaBH4. Catalyst synthesis was accomplished via an electrochemical method that uses an electrochemical cell with two chambers separated by a bipolar membrane. The catalyst particles are formed in the cathode chamber. The duration of electrolysis influences the calcium-phosphate phase. The pH is low at the beginning of electrolysis; brushite is formed. Hydroxyapatite is produced when the electrolyte solution is electrolyzed for a longer time, and the pH of the solution becomes high. The pH of the solution impacts both the calcium phosphate phase and the amount of metal catalyst in a solution. A higher metal catalyst content (Co and Fe) makes the hydrogen release rate more significant. Hydrogen was released at a rate of 7173 mL per minute per gram of Fe-Co during the hydrolysis reaction of NaBH4. Between 81,000 and 98,000 mL of hydrogen was produced per gram of Fe-Co each minute during the methanolysis reaction with NaBH4.

Reaction of NaBH4 and NaB(OH)4 as a way to increase the yield of hydrogen in catalytic hydrolysis of sodium borohydride by water

In this work, sodium tetrahydroxoborate (NaB(OH)4) that is the main product of the hydrolysis reaction of NaBH4 with a relatively small excess of water is studied in the reaction with sodium borohydride in the presence of a catalyst and without it. It was found, that mixtures consisting of NaB(OH)4 and NaBH4 begin to melt at 70 °C with the formation of a liquid phase without destroying the close coordination environment for both types of boron atoms. When a cobalt-based catalyst is added to mixtures, significant hydrogen evolution is observed. The resulting products are hydrogen and amorphous borates with a gross composition close to [NaBO2·0.75H2O].Carrying out the catalytic hydrolysis of borohydride in the system of initial composition H2O:NaBH4:catalyst under the conditions same to that the catalytic reaction of NaBH4 and NaB(OH)4 was observed is a promising way to produce H2 since it provides a high yield of hydrogen at small amounts of catalyst and atmospheric pressure. Catalytic hydrolysis carried out in the temperature range 80–120 °C with initial molar ratios H2O:NaBH4 = 3 and 2.7, and atmospheric pressure demonstrates a hydrogen yield of 8.3 wt% and NaBH4 conversion of 96 % at only 2.3 wt% of CoCl2 as catalyst. Since the resulting final composition of borates is close to [NaBO2·0.66H2O], the potential mass yield of hydrogen in this process can reach 9.3 wt%.

Silver-Nanoparticle-Decorated Fused Carbon Sphere Composite as a Catalyst for Hydrogen Generation

The dwindling supply of fossil fuels has resulted in a search for an efficient alternative energy source. Hydrogen gas offers an abundant, clean-burning supply of energy that can be readily produced over time via the water-splitting reaction of sodium borohydride (NaBH4). This study explored the synthesis of a novel catalyst comprised of silver nanoparticles supported on fused carbon spheres (AgNP-FCS). This composite catalyst was then tested for its ability to optimize the hydrolysis reaction of NaBH4. The fused carbon spheres (FCS) were synthesized via a sustainable source, namely a dextrose solution. The synthesized AgNP-FCS catalyst was characterized using transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The average diameter of silver nanoparticles on the catalyst was found to be 30 nm with 3.7% loading. This catalyst was tested under various reaction conditions, including temperatures, doses of NaBH4, and solution pHs. The activation energy of the reaction as catalyzed by AgNP-FCS was determined to be 37.0 kJ mol−1, which was competitive when compared to similar catalysts for this reaction. A study of the reusability of this catalyst suggests that the catalyst can be used multiple times consecutively with no loss in hydrogen generated. This material presents an opportunity for a sustainable catalyst to optimize the amount of hydrogen generated via the hydrolysis of NaBH4.

The catalytic activity of halloysite-supported Ru nanoparticles in the methanolysis of sodium borohydride for hydrogen production

Finding environmentally friendly new energy sources is very urgent for a sustainable and clean energy future. It is vital to reach clean energy sources such as hydrogen, which does not create a polluting by-product when burned with oxygen. In this study, for a livable clean universe, hydrogen production studies were carried out from sodium borohydride (NaBH4), which is a very good hydrogen storage material, in a methanolysis environment, over ruthenium nanoparticles (Ru (0) NPs) impregnated on halloysite (Hall) support material (Ru (0)@Hall) at room conditions. The catalytic performance of the newly synthesized Ru (0)@Hall nanocatalyst was tested in the NaBH4 methanolysis reaction for hydrogen production. It was determined that Ru (0)/Hall nanocatalyst showed excellent activity (initial turn-over frequency (TOFinitial) = 1882 h−1; 31.37 min−1) and reusability (at the end of the 5th cycle, it retained 90% of its initial activity) performance in the catalytic methanolysis of NaBH4. The analyzes of the Ru (0)@Hall nanocatalyst, both fresh and at the end of the 5th catalytic cycle, were made with advanced analytical methods (ICP-OES, XRD, XPS, SEM, HRTEM, TEM, TEM-EDX, BET) and the nature of the catalytic material was clarified. The results showed the homogeneous distribution of Ru (0) NPs on the Hall surface (mean size = 1.53 ± 0.17 nm). Kinetic studies of hydrogen production from catalytic methanolysis reaction of NaBH4 were performed based on nanocatalyst [Ru (0)@Hall], substrate [NaBH4] concentrations, and temperature (298–318 K). From the kinetic data, the kinetic parameters (Ea, ΔH≠, and ΔS≠) were calculated and the rate equation was determined.

Enhanced photocatalytic performance of auto-combusted nanoparticles for photocatalytic degradation of azo dye under sunlight illumination and hydrogen fuel production

In this study, an innovative nanomaterial was synthesized for hydrogen production from methanolysis on sodium borohydride (NaBH4) in order to be a solution for future energy problems. The nanocomposite containing FeCo, which does not contain noble metals, and whose support material is Polyvinylpyrrolidone (PVP), was synthesized by means of a thermal method. TEM, XRD and FTIR characterization methods were used for the analysis of the morphological and chemical structure of the nanocomposite. Nanocomposite particle size was found to be 2.59 nm according to XRD analysis, and 5.45 nm according to TEM analysis for scale of 50 nm. For catalytic properties of nanomaterial in the methanolysis reaction of NaBH4, temperature, catalyst, substrate, and reusability experiments were carried out and kinetic calculations were obtained. Among the activation parameters of FeCo@PVP nanoparticles, turnover frequency, enthalpy, entropy and activation energy were calculated as 3858.9 min−1, 29.39 kJ/mol, −139.7 J/mol.K, and 31.93 kJ/mol, respectively. As a result of the reusability test of the obtained FeCo@PVP nanoparticles catalysts, which was carried out for 4 cycles, the catalytic activity was 77%. Catalytic activity results are given in comparison with the literature. In addition, the photocatalytic activity of FeCo@PVP NPs was evaluated against MB azo dye under solar light irradiation for 75 min and was found to be as 94%.

Poly(2-aminoethyl methacrylate) based microgels catalyst system to be used in hydrolysis and methanolysis of NaBH4 for H2 generation

The poly(2-aminoethyl methacrylate) (p(AEM)) microgels were synthesized by microemulsion polymerization technique and used for in situ metal nanoparticle preparation to render as p(AEM)-M (M: Co or Ni) microgel composites and were used in p(AEM) based poly ionic liquid (PIL) microgels. Next, these p(AEM)) based microgel materials were used as catalysts for hydrogen (H2) production from both hydrolysis and methanolysis reactions of sodium borohydride (NaBH4). It was found that the catalytic hydrolysis of the NaBH4 reaction, catalyzed by p(AEM)-Co microgel composite was completed in 140 min, whereas the methanolysis of NaBH4 methanolysis catalyzed by the PIL of p(AEM)+Cl− microgels was completed in 5 min both with 250 ± 2 mL H2 production. Furthermore, p(AEM)-Co microgel composite catalysts maintained 80% catalytic activity after 5 consecutive uses in NaBH4 hydrolysis. On the other hand, p(AEM)+Cl− microgels were found to afford more than 50% catalytic activity even after 20 repetitive use in NaBH4 methanolysis due to superior regeneration ability. Moreover, activation energy values for p(AEM)-Co microgel composites catalyzed NaBH4 hydrolysis reaction were calculated as 38.9 kJ/mol in comparison to 37.3 kJ/mol activation energy of p(AEM)+Cl− microgel catalyzed methanolysis reaction.

Bacillus thuringiensis Based Ruthenium/Nickel Co-Doped Zinc as a Green Nanocatalyst: Enhanced Photocatalytic Activity, Mechanism, and Efficient H2 Production from Sodium Borohydride Methanolysis

Today, the development of green nanocatalysts is among the popular topics due to the need for energy production and the cleaning of organic pollutants. In this approach, Bacillus thuringiensis, a bacterium, was used as a biosupport of ruthenium/nickel co-doped zinc nanoparticles (btRNZn NPs) to release hydrogen from the methanolysis of sodium borohydride (NaBH4). In addition, their photocatalytic activity was reported against Methyl Orange (MO) organic dye. This study focused on the preparation, characterization, and catalytic and photocatalytic activity of the btRNZn biocatalyst for the release of hydrogen from the methanolysis of NaBH4 and removal of MO dye. According to TEM analysis, the average size of btRNZn NPs was found to be 11.78 nm; in addition, btRNZn NPs showed a photodegradation effect of 68.2% against MO dye at 90 min, and its photocatalytic mechanism was discussed. The effects of the catalyst, substrate, and temperature in the methanolysis reaction of NaBH4 in the presence of the catalyst were investigated extensively. The reaction kinetics was calculated, and TOF, activation energy, and enthalpy energy were measured as 2497.14 h–1, 14.89 kJ/mol, and 12.35 kJ/mol, respectively. It was observed that the methanolysis process is a first-order reaction based on the amount of the catalyst and substrate. This study aimed to synthesize a nanobiocatalyst (btRNZn NPs) by a biological method, and it will be used as a great photocatalyst to prevent wastewater pollution; also, it can be an excellent catalyst to produce hydrogen from NaBH4 methanolysis. The application of btRNZn NPs in solar photocatalysis to prevent wastewater pollution and to research it for energy production through hydrogen creation are both made clear by these studies.

α-MoB2 Nanosheets for Hydrogen Evolution in Alkaline and Acidic Media

α-MoB2 is recognized as the most efficient molybdenum boride for electrocatalytic hydrogen evolution reaction (HER). However, the convenient synthesis of single phase α-MoB2 is still challenging, and its HER activity in alkaline electrolytes remains unclear. Herein, we report the first successful synthesis of the α-MoB2 nanosheets by a simple and facile molten salt method through the MoCl5 and NaBH4 reaction at 850 °C. The α-MoB2 nanosheets exhibit a remarkable HER performance in alkaline electrolytes, delivering a low overpotential of 124 mV at a current density of 10 mA/cm2. In acidic electrolytes, an improved performance was found in comparison to that of the bulk and nano α-MoB2 with an overpotential as low as 141 mV at 10 mA/cm2. Such HER performance arises from the nanosheet structure that allows more active planes to be exposed. In addition, the α-MoB2 nanosheets possess an outstanding stability in both acidic and alkaline media, showing negligible current density drop even after 3000 cycles and more than 24 h of potentiostatic operation.

Boric acid versus boron trioxide as catalysts for green energy source H2 production from sodium borohydride methanolysis

Here, boric acid (H3BO3) and its dewatered form, boron trioxide (B2O3) were tested as catalysts for hydrogen (H2) evolution in the methanolysis of sodium borohydride (NaBH4) in methanol. Parameters such as catalyst types and their amounts, NaBH4 concentration, and the reaction temperature affecting the hydrogen generation rate (HGR) were studied. It has been found that H3BO3 and B2O3 catalyzed methanolysis reaction of NaBH4 follow up first-order kinetics relative to the concentration of NaBH4. Furthermore, the conversion and activity of these catalysts were examined to determine their performance in ten consecutive use. Interestingly, H3BO3 and B2O3 have demonstrated superior catalytic performances in methanolysis of NaBH4 comparing to the studies published in literature with the activation energy of respectively 22.08 kJ.mol-1, and 23.30 kJ.mol-1 in H2 production. The HGR was calculated as 6481 mL.min-1.g-1 and 5163 mL.min-1.g-1 for H3BO3 and B2O3 catalyst, respectively for 50 mg catalyst at 298 K. These results are comparably better than most metal nanoparticle catalysts used for H2 production in addition to the naturally occurring boron-based environmentally friendliness of these materials.

Mechanistic implications of the solvent kinetic isotope effect in the hydrolysis of NaBH4

The sodium borohydride, NaBH4, hydrolysis mechanism is studied via the H2O/D2O kinetic isotope effect (KIE). This reaction is of importance as NaBH4 is considered as a hydrogen storage material. Nowadays, hydrogen is thought to be one of the most promising and efficient clean energy carriers. In order to control the rate of the hydrogen evolution reaction (HER), one has to understand the mechanism of its production. The H2O/D2O KIE of the reactions of NaBH4 and NaBD4 with water was studied in solutions containing a ratio of H2O/D2O = 1.00. The separation factor, α, of both reactions is α = 5.0 ± 1.0. The rate of the hydrolysis of BD4− in H2O is faster than that of BH4−. The results point out that the rate-determining step in all hydrolysis stages is the H–OH bond scission.

SiO2 PARTICLE EMBEDDED SILICA AEROGELS: ENVIRONMENTAL AND ENERGY APPLICATIONS

The purpose of the study is the preparation of silica aerogels by using the hydro(solvo)thermal synthesis assisted sol-gel method, the preparation of SiO2 particle-added silica aerogels, and the investigation of their potential use in the environment and energy fields. It has been observed that the prepared silica aerogels can be used as an adsorbent for organic contaminant removal applications. It has been observed that silica aerogels progressed rapidly in the reaction of NaBH4 with methanol as SiO2 particle embedded silica aerogel.

Investigation of hydrogen production from sodium borohydride by carbon nanotube‐graphenesupportedPdRubimetallic catalyst forPEMfuel cell application

In this study, hydrogen (H2) generation from the hydrolysis of sodium borohydride (NaBH4) catalyzed by bimetallic Palladium-Ruthenium (PdRu) supported on multiwalled carbon nanotube-graphene (MWCNT-GNP) hybrid material is investigated. The effect of various parameters such as temperature, NaBH4 concentration, and catalyst loading and effect of base concentration are examined to observed optimum operating conditions. Experimental results show that the PdRu/MWCNT-GNP bimetallic catalyst has high catalytic activity on NaBH4 hydrolysis reaction. It has been found that PdRu/MWCNT-GNP catalyst shows low activation energy of 22.33 kJ/mol for hydrolysis reaction of NaBH4. The PdRu/MWCNT-GNP catalyst also exhibits H2 generation rate of 79.2 mmol/min·gcat at 45°C. It shows good cycle stability in the catalyst reusability test and retained 89% of its initial catalytic activity after fifth use. The high catalytic activity of the PdRu/MWCNT-GNP catalyst makes it promising in H2 generation from NaBH4 hydrolysis for commercial proton exchange membrane fuel cell (PEMFC) applications.

Static observation of the interphase between NaBH4 and LiI during the conversion reaction

To determine the synthesis conditions for NaI–NaBH4–LiI solid solutions in a single phase, the conversion reaction of NaBH4 ​+ ​LiI → NaI ​+ ​LiBH4 was investigated by preparing mixed pellets of NaBH4/LiI. The extent of the reaction was investigated under different reaction temperatures and pressures. Although it was not possible to completely suppress the conversion reaction in this study, the low temperature and high-pressure conditions were shown to be favorable to avoid the presence of LiBH4. A significant point is that the conversion reaction was investigated in a static condition in the form of pellets, whereas most of the metal borohydride-halide composites have been fabricated by ball-milling. The microstructure of NaBH4/LiI mixed pellets at different ageing times was observed by scanning electron microscope (SEM), Auger electron spectroscopy (AES), wavelength dispersive X-ray spectroscopy (WDS) and time of flight secondary ion mass spectroscopy (ToF-SIMS). The analysis revealed that the reaction interphase between NaBH4 and LiI occurs in the order of LiI/NaI/LiBH4/NaBH4. It was clearly confirmed that the growth of the NaI layer continued with time even at room temperature. In conjunction with the array of the interphase, the diffusion of Na+ in LiBH4 appears to be a necessary condition for the growth of the NaI layer. The present results suggest that a detailed investigation of the conversion reaction between other metal borohydrides and halides (for example, CeCl3/LiBH4, ZrCl4/KBH4, etc.) in the static condition would likely reveal the diffusion of the new ions in the existing compounds.

Synthesis of Ni-B/Hydroxyapatite by Electrochemical Method and Its Application as Catalyst on NaBH<sub>4</sub> Hydrolysis

The result of burning hydrogen which is environmentally friendly makes hydrogen as a very attractive fuel. Hydrogen storage is interesting research material. One alternative to hydrogen storage is a metal-hydride as NaBH4. In this paper, the catalyst for hydrogen production from storage, namely The result of burning hydrogen, which is environmentally friendly, makes hydrogen a desirable fuel. Hydrogen storage is exciting research material. One alternative to hydrogen storage is a metal-hydride as NaBH4. In this paper, the catalyst for hydrogen production from storage, namely NaBH4, was synthesized by electrochemical. Ni-B catalyst with hydroxyapatite as catalyst support was prepared by electrochemical. Ni-B/HA catalyst was synthesized at various current densities (namely 67, 133, and 200 mA/cm2) and various electrolysis times (namely 30, 60, and 90 minutes). The resulting catalysts were analyzed by XRD and used as the catalyst for hydrogen production from the hydrolysis reaction of NaBH4. The fastest hydrogen production was obtained using a catalyst generated at 133 mA/cm2 and an electrolysis time of 60 minutes. The reaction rate equation for the hydrolysis of NaBH4 has a first-order reaction to the concentration of NaBH4. The resulting reaction rate constant ranged from 233.33 mL/g/min to 861.11 mL/g/min. The relationship between reaction temperature and reaction rate constant can be expressed by the equation k = 2.2x106exp (5534/T).

RELEASING HYDROGEN FROM NABH4 VIA HYDROGEL BASED CoF2 CATALYST

In this paper, the dehydrogenation reaction of NaBH4 was performed in the presence of Co-ion loaded hydrogel catalyst. The reactions took place within 27, 18 and 9 hours at 25, 35 and 45 °C, respectively. In addition, the relation between the initial concentration of NaBH4 and released hydrogen was investigated at 45°C. A linear relationship between initial borohydride concentration and produced H2 was determined. Also, differential method was used to determine reaction rate constants and rate order. Hence, first-order-kinetics was proved by using experimental data. After that, the activation energy was found as 58.26 kJ/mol by means of the slope of the graph of lnk versus 1/T for the dehydrogenation reaction. This value is nearly equal to 50kJ/mol, which was expected in literature for the studies of the catalytic dehydrogenation. As the hydrophilic and macroporous structure of the prepared poly(acrylamide-co-acrylic acid) (p(AAm-co-AAc)-Co) hydrogel catalyst allowed inlet of NaBH4 solution up to its interior and release of produced H2, effect of pore diffusion limitation was neglected. Dehydrogenation index of NaBH4 was calculated as 2526.31 mL H2/g NaBH4 according to the amount of NaBH4 in the aqueous solution