Activated aluminum for hydrogen generation from water

2021 ◽  
pp. 81-93
Author(s):  
F. Manilevich ◽  
◽  
Yu. Pirskyy ◽  
A. Kutsyi ◽  
V. Berezovets ◽  
...  

Al-based alloys and mechanochemically activated aluminum powders were prepared in this study, and the regularities of their hydrolysis reaction with water were studied. Aluminum alloys were prepared by melting aluminum with additions of Ga–In–Sn eutectic (5 wt.%), bismuth (3 wt.%), antimony (3 wt.%), or zinc (3 wt.%). The temperature-dependent kinetics of their hydrolysis in a temperature range 25–70 °C was studied by using a volumetric technique. The most efficient activation of the hydrolysis process was achieved for the Al–Ga– In–Sn-Zn alloy, particularly at low temperatures (5 and 25° C). The addition of bismuth to the Al–Ga–In–Sn alloy significantly decreases the hydrolysis rate, whereas the addition of antimony has only a weak effect on the process, despite the fact that the standard electrode potentials of bismuth and antimony have rather close values. Commercially available aluminum PA-4 and ASD-1 powders were mechanochemically activated by Ga–In–Sn or Ga–In–Sn–Zn eutectic alloys (5 wt.%) and graphite (1–3 wt.%) in a mixer type ball mill. Subsequently, they were pressed (P = 4 MPa) into the pellets, which were used to generate hydrogen from water via the hydrolysis process. X-ray diffraction study of the milled PA-4 powder revealed the presence of four phases, including aluminum, graphite, and two In–Sn intermetallic compounds (In3Sn and In1–xSnx, were x ≈ 0.04). The quantitative analysis by EDX showed a uniform distribution of the activating additives over the pellet surface, while the graphite was partly aggregated. Studies on the hydrolysis kinetics when utilizing Al-based pellets demonstrated that the process readily proceeds at temperatures ≥ 5° C. At the same time, the efficiency of hydrogen generation depends on the amount of the added graphite, particle size of aluminum powders, duration and medium of their mechanochemical treatment, and the hydrolysis temperature.

2010 ◽  
Vol 61 (4) ◽  
pp. 215-221 ◽  
Author(s):  
Ramanujam Sarathi ◽  
Binu Sankar ◽  
Satyanarayanan Chakravarthy

Influence of Nano Aluminium Powder Produced by Wire Explosion Process at Different Ambience on Hydrogen Generation Nano-aluminium particles are produced through the wire explosion process in different gas medium. The particles produced by wire explosion process, in helium medium are of smaller size compared to argon/nitrogen medium. The nano aluminium powder on reaction with water forms oxides having bayerite and boehmite structure. It is observed that nano aluminium on reaction with KOH solution at room temperature it forms bayerite. The results of the study were confirmed through Wide Angle X-ray diffraction (WAXD) and by Transmission Electron Microscope (TEM) studies. The reaction of nano aluminium powder with KOH solution/water indicates that the rate of hydrogen generation is high when nano aluminium powder reacts with KOH solution than with water. The rate of hydrogen generation gets reduced drastically when the nano aluminium powder which is exposed to air medium for some period is used for reaction with KOH/water. It is also observed that the rate of hydrogen generation is high with nano size aluminium particles compared with ultrafine particles.


1989 ◽  
Vol 4 (6) ◽  
pp. 1320-1325 ◽  
Author(s):  
Q. X. Jia ◽  
W. A. Anderson

Effects of hydrofluoric acid (HF) treatment on the properties of Y–Ba–Cu–O oxides were investigated. No obvious etching of bulk Y–Ba–Cu–O and no degradation of zero resistance temperature were observed even though the oxides were placed into 49% HF solution for up to 20 h. Surface passivation of Y–Ba–Cu–O due to HF immersion was verified by subsequent immersion of Y–Ba–Cu–O in water. A thin layer of amorphous fluoride formed on the surface of the Y–Ba–Cu–O during HF treatment, which limited further reaction between Y–Ba–Cu–O and HF, and later reaction with water. Thin film Y–Ba–Cu–O was passivated by HF vapors and showed no degradation in Tc-zero after 30 min immersion in water. The properties of the surface layer of Y–Ba–Cu–O oxide after HF treatment are reported from Auger electron spectroscopy, x-ray diffraction, and scanning electron microscopy studies.


2013 ◽  
Vol 741 ◽  
pp. 84-89 ◽  
Author(s):  
Sangworn Wantawee ◽  
Pacharee Krongkitsiri ◽  
Tippawan Saipin ◽  
Buagun Samran ◽  
Udom Tipparach

Titania nanotubes (TiO2NTs) working electrodes for hydrogen production by photoelectrocatalytic water splitting were synthesized by means of anodization method. The electrolytes were the mixtures of oxalic acid (H2C2O4), ammonium fluoride (NH4F), and sodium sulphate (VI) (Na2SO4) with different pHs. A constant dc power supply at 20 V was used as anodic voltage. The samples were annealed at 450 °C for 2 hrs. Scanning Electron Microscopy (SEM) and X-ray diffraction (XRD) were used to characterized TiO2NTs microstructure. TiO2NTs with diameter of 100 nm were obtained when pH 3 electrolyte consisting of 0.08 M oxalic acid, 0.5 wt% NH4F, and 1.0 wt% Na2SO4was used. Without external applied potential, the maximum photocurrent density was 2.8 mA/cm2under illumination of 100 mW/cm2. Hydrogen was generated at an overall photoconversion efficiency of 3.4 %.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Beata Zielińska ◽  
Ewa Mijowska ◽  
Ryszard J. Kalenczuk

K-Ta mixed oxides photocatalysts have been prepared by impregnation followed by calcination. The influence of the reaction temperature (450°C–900°C) on the phase formation, crystal morphology, and photocatalytic activity in hydrogen generation of the produced materials was investigated. The detailed analysis has revealed that all products exhibit high crystallinity and irregular structure. Moreover, two different crystal structures of potassium tantalates such as KTaO3and K2Ta4O11were obtained. It was also found that the sample composed of KTaO3and traces of unreacted Ta2O5(annealed at 600°C) exhibits the highest activity in the reaction of photocatalytic hydrogen generation. The crystallographic phases, optical and vibronic properties were examined by X-ray diffraction (XRD) and diffuse reflectance (DR) UV-vis and resonance Raman spectroscopic methods, respectively. Morphology and chemical composition of the produced samples were studied using a high-resolution transmission electron microscope (HR-TEM) and an energy dispersive X-ray spectrometer (EDX) as its mode.


2020 ◽  
Vol 73 (8) ◽  
pp. 794
Author(s):  
Aliyu M. Ja'o ◽  
Derek A. Wann ◽  
Conor D. Rankine ◽  
Matthew I. J. Polson ◽  
Sarah L. Masters

The molecular structure of morpholine borane complex has been studied in the solid state and gas phase using single-crystal X-ray diffraction, gas electron diffraction, and computational methods. Despite both the solid-state and gas-phase structures adopting the same conformation, a definite decrease in the B–N bond length of the solid-state structure was observed. Other structural variations in the different phases are presented and discussed. To explore the hydrogen storage potential of morpholine borane, the potential energy surface for the uncatalyzed and BH3-catalyzed pathways, as well as the thermochemistry for the hydrogen release reaction, were investigated using accurate quantum chemical methods. It was observed that both the catalyzed and uncatalyzed dehydrogenation pathways are favourable, with a barrier lower than the B–N bond dissociation energy, thus indicating a strong propensity for the complex to release a hydrogen molecule rather than dissociate along the B–N bond axis. A minimal energy requirement for the dehydrogenation reaction has been shown. The reaction is close to thermoneutral as demonstrated by the calculated dehydrogenation reaction energies, thus implying that this complex could demonstrate potential for future on-board hydrogen generation.


2011 ◽  
Vol 128-129 ◽  
pp. 882-885
Author(s):  
Rong Fu Zhou ◽  
Ding Xin Shuai ◽  
Yu Tang ◽  
Xue Tong Zhang

Hydrolysis process is the key part of sulfuric acid method’s production technology of titanium dioxide, it is also the most rigorous part of the process control, and precipitate out the white hydration precipitation TiO2 from the mother liquor, and separate from other soluble metal sundry ions, further purify the TiO2. The quality of hydrolysis product not only affects the normal operation of the follow-up, but also affects the quality of the final product directly. This article do some study and design to the hydrolysis automatic control, use computer,DCS and PLC control the hydrolysis operation process, temperature control, steam heating system, That means comprised monitoring station by the DCS,CRT, mouse and keyboard replace the simulates panel and operator, and use the fuzzy theory control the hydrolysis temperature rise process, improve the accuracy and precision of the operating, at the same time, reduce the labor intensity of the workers, realize the automatic control of the hydrolysis process, stabilize and improve the product quality effectively


2021 ◽  
pp. 38-52
Author(s):  
V. Berezovets ◽  
◽  
A. Kytsya ◽  
Yu. Verbovytskyy ◽  
I. Zavaliy ◽  
...  

Magnesium hydride (MgH2) has a high hydrogen storage capacity (7.6 wt%) and the Mg element is abundant on the earth. Due to its strong reduction ability, even at room temperature it can provide the hydrogen yield reaching 15.2 wt% H (1703 mL/g) when interacting with water, which makes it very attractive for the application in supplying hydrogen for autonomous H energy systems. However, the hydrolysis reaction is rapidly inhibited by the Mg(OH)2 passivation layer formed on the surface of MgH2. In order to remove the passivation film and improve the efficiency of the MgH2 hydrolysis process, several methods including alloying, ball milling, changing the aqueous solution, have been successfully utilized. In this paper the process of hydrolysis of magnesium hydride in aqueous solutions of MgCl2 used as a promotor of the interaction has been studied in detail. It was found that the initial hydrolysis rate, pH of the reaction mixture, and overall reaction yield are all linearly dependent of the logarithm of MgCl2 concentration. It has been shown that pH of the reaction mixture in the presence of MgCl2 is well described by considering a system “weak base and its salt with strong acid” type buffer solution. Reference data for this hydrolysis reaction were also carefully analyzed. The mechanism and the kinetic model of the process of MgH2 hydrolysis in water solutions involved passivation of the MgH2 surface by the formed Mg(OH)2 precipitate followed by its repassivation have been proposed. The obtained after the hydrolysis reactions precipitates were studied using XRD and EDS. It was found also that the final products of reaction consist of Mg(OH)2 (brucsite type) and remaining MgH2. This fact shows that the formation of solid species such as MgCl2 xMgO yH2O at the studied conditions is unlikely and decreasing of pH the reaction mixture has a different nature.


2020 ◽  
Vol 13 (06) ◽  
pp. 2051025
Author(s):  
Hongyan Liu ◽  
Qianyu Shi ◽  
Yumei Yang ◽  
Ya-Na Yu ◽  
Yan Zhang ◽  
...  

In this paper, CoO[Formula: see text]Co2P composite nanocatalysts as highly active catalysts were successfully prepared for catalytic hydrolysis of sodium borohydride (NaBH[Formula: see text] to generate hydrogen. For catalyst preparation, pre-synthesized Co(OH)2 nanosheets were uniformly mixed with sodium hypophosphite (NaH2PO[Formula: see text] and then treated through vapor-phase phosphorization process. For characterization, field-emission scanning electron microscopy (FE-SEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), N2 adsorption–desorption measurement and X-ray photoelectric spectroscopy (XPS) were carried out, and traditional water-displacement method was performed to measure the hydrogen generation rate (HGR). It was found that component and catalytic activity of the composites were greatly affected by the ratio of Co(OH)2 to NaH2PO2. When the ratio was 2:1, the obtained catalyst composed of CoO and Co2P presented the highest HGR up to 3.94[Formula: see text]L min[Formula: see text] g[Formula: see text] using a 2[Formula: see text]wt.% NaBH[Formula: see text][Formula: see text]wt.% NaOH solution at [Formula: see text]C, and the apparent activation energy was detected as low as 27.4[Formula: see text]kJ mol[Formula: see text]. Additionally, the optimum CoO[Formula: see text]Co2P catalyst still retains 60% of the initial activity after recycling four times.


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