A theoretical and experimental study of phosphate ester inhibitors for AISI 1018 in carbon dioxide-saturated 3.5 wt% NaCl solution

Phosphate ester was investigated as a corrosion inhibitor for AISI 1018 carbon steel in carbon dioxide-saturated chloride solutions at different temperatures and pressures. The corrosion tests were realized by electrochemical techniques, weight loss measurements, bubble tests, and a high-pressure/high-temperature autoclave system. The corrosion tests demonstrated that the investigated molecule is an excellent corrosion inhibitor. The inhibiting effect is even bigger at high pressure and temperature than at atmospheric pressure and room temperature. The thermodynamic parameters were calculated and determined to obey the Langmuir isotherm. Polarization studies revealed that the evaluated inhibitor is a mixed type.     

Group and group-interaction contribution method for estimating the melting temperatures of deep eutectic solvents

Deep eutectic solvents (DESs) are mixtures of two or more components that have lower melting temperatures compared to their constituting components. DESs possess many advantages, for example, low volatility, low flammability, and low toxicity, which make them promising alternatives to traditional organic solvents. The melting temperature, one of the important physical properties, is of essential importance for industrial applications. In this work, a group and group-interaction contribution method was proposed to estimate the melting temperatures of DESs using an extensive database (1528 DESs, 1541 data points). The average absolute relative deviation (%AARD) between the estimated and experimental values of the melting temperature was 5.67% for binary DESs. Subsequently, this method was also extended to estimate the melting temperature of ternary DESs, with the AARD of 6.13%. The results indicate the high accuracy and broad applicability of the method and pave the way for the rational design of task-specific DESs.     

LiAlH4–ZrCl4 mixtures for hydrogen release at near room temperature

The dehydrogenation temperature of LiAlH₄ was significantly reduced by the production of mixtures with ZrCl₄. Stoichiometric 4:1, and 5 mol % mixtures of LiAlH₄ and ZrCl₄ were produced by ball milling at room temperature and ?196 °C, and tested for dehydrogenation at low temperature. Cryogenic ball-milling resulted in an effective way to produce reactive mixtures for hydrogen release; because of achieving small aggregates size (5–20 μm) in 10 min of cryomilling while preventing substantial decomposition during preparation. Dehydrogenation reaction in the mixtures LiAlH₄/ZrCl₄ started around 31–47 °C under different heating rates. Partial dehydrogenation was proved at 70 °C: 4.4 wt % for the 5 mol% ZrCl₄–LiAlH₄ mixture, and 3.4 wt % for the best 4:1 stoichiometric mixture. Complete dehydrogenation up to 250 °C released 6.4 wt% and 4.1 wt%, respectively. Dehydrogenation reactions are exothermic, and the LiAlH₄/ZrCl₄ mixtures are unstable and difficult to handle. The activation energy of the exothermic reactions was estimated as 113.5 ± 9.8 kJ/mol and 40.6 ± 6.6 kJ/mol for 4LiAlH₄+ZrCl₄ and 5%mol ZrCl₄+LiAlH₄ samples milled in cryogenic conditions, respectively. The dehydrogenation pathway was changed in the LiAlH₄/ZrCl₄ mixtures as compared to pure LiAlH₄. Dehydrogenation reaction is proposed to form Al, LiCl, Zr, and H₂ as main products. Modification of the dehydrogenation reaction of LiAlH₄ was achieved at the cost of reducing the total hydrogen release capacity.     

The influence of inner material with different average thermal conductivity on the performance of whole insulation system for liquid hydrogen on orbit storage

At present, several composite insulation systems were proposed that can be used for passive insulation systems, including foam-variable density multilayer insulation (VDMLI), aerogel-VDMLI and hollow glass microspheres (HGMs)-VDMLI. The passive insulation systems with different inner material (IM) showed different performances. However, the relationship between the average thermal conductivity of IM and the insulation performance of the whole system has rarely been investigated. It is of great significance for efficient configuration and matching of the passive insulation system. In this paper, a series of average thermal conductivity of IM were assumed to predict the insulation performance of the whole system at 20 K–300 K and high vacuum. In order to further illustrate the relationship between IM and MLI/VDMLI, the foam was replaced by the HGMs as 5 mm a unit forming a series of HGMs-foam-MLI/VDMLI insulation systems. The performance of the systems was investigated. After the foam was completely replaced by the HGMs, the performance of MLI and VDMLI systems was improved 33% and 13%, respectively. Moreover, each mode of heat transfer including solid conduction, radiation, and gas conduction for foam-MLI/VDMLI and HGMs-MLI/VDMLI insulation systems were calculated and analyzed.     

Research and development of liquid hydrogen (LH2) temperature monitoring system for marine applications

Monitoring the temperature in liquid hydrogen (LH₂) storage tanks on ships is important for the safety of maritime navigation. In addition, accurate temperature measurement is also required for commercial transactions. Temperature and pressure define the density of liquid hydrogen, which is directly linked to trading interests. In this study, we developed and tested a liquid hydrogen temperature monitoring system that uses platinum resistance sensors with a nominal electrical resistance of approximately 1000 Ω at room temperature, PT-1000, for marine applications. The temperature measurements were carried out using a newly developed temperature monitoring system under different pressure conditions. The measured values are compared with a calibrated reference PT-1000 resistance thermometer. We confirm a measurement accuracy of ±50 mK in a pressure range of 0.1 MPa–0.5 MPa.     

Enhancement effect of zero-valent iron nanoparticle and iron oxide nanoparticles on dark fermentative hydrogen production from molasses-based distillery wastewater

This study investigates the effect of two different iron compounds (zero-valent iron nanoparticle: nZVI and iron oxide nanoparticles: nIO) and pH on fermentative biohydrogen production from molasses-based distillery wastewater. The nZVI and nIO of optimum particle sizes of 50 nm and 55 nm respectively were synthesized and applied for fermentative hydrogen (H₂) production. The addition of nIO & nZVI at (0.7 g/L, pH: 6) resulted in the highest H₂ yield, H₂ production rate, H₂ content and COD reduction. Moreover, the kinetic parameters of H₂ production potential (P) and H₂ production rate (R_m) increased to 387 mL, and 22.2 mL/h, respectively for nZVI, these values were 363 mL and 21.8 mL/h for nIO. The results obtained indicated the positive effect of nZVI and nIO addition on enhanced fermentative H₂ production. The addition of nZVI & nIO resulted in 71% and 69.4% enhancement in biohydrogen production respectively.     

The role of Al2O3, MgO and CeO2 addition on steam iron process stability to produce pure and renewable hydrogen

Steam iron process represents a technology for H₂ production based on iron redox cycles. Fe_xO_y are reduced by syngas/carbon to iron, which is subsequently oxidized by steam to produce pure H₂. However, the system shows low stability.In this work, the effect of promoters (Al₂O₃, MgO and CeO₂) on Fe_xO_y stability is investigated (10 consecutive redox cycles). Bioethanol is used as a reducing agent. The particles are synthesized by coprecipitation method, analysed by BET, XRD, SEM and tested in a fixed bed reactor (675 °C, 1 bar). Pure H₂ is obtained controlling the Fe_xO_y reduction degree feeding different amounts of ethanol (4.56–1.14 mmol) until no CO is detected in oxidation. The results show that the promoters not only improve the thermal stability of Fe_xO_y but also affect its redox activity and react with iron forming spinel structures. MgO led to the highest activity and cyclability (H₂ = 0.15 NL; E = 35%).     

Novel composite membrane based on zirconium phosphate-ionic liquids for high temperature PEM fuel cells

Composite membranes composed of zirconium phosphate (ZrP) and imidazolium-based ionic liquids (IL), supported on polytetrafluoroethylene (PTFE) were prepared and evaluated for their application in proton exchange membrane fuel cells (PEM) operating at 200 °C. The experimental results reported here demonstrate that the synthesized membrane has a high proton conductivity of 0.07 S cm^?1, i.e, 70% of that reported for Nafion. Furthermore, the composite membranes possess a very high proton conductivity of 0.06 S cm^?1 when processed at 200 °C under completely anhydrous conditions. Scanning electron microscopy (SEM) images indicate the formation of very small particles, with diameters in the range of 100–300 nm, within the confined pores of PTFE. Thermogravimetric analysis (TGA) reveals a maximum of 20% weight loss up to 500 °C for the synthesized membrane. The increase in proton conductivity is attributed to the creation of multiple proton conducting paths within the membrane matrix. The IL component is acting as a proton bridge. Therefore, these membranes have potential for use in PEM fuel cells operating at temperatures around 200 °C.     

Improved photon management in a photoelectrochemical cell with Nd-modified TiO2 thin film photoanode

Photon management involving particularly an up-conversion process is proposed as a relatively novel strategy for improving the efficiency of hydrogen generation in photoelectrochemical cells (PEC) with wide-band gap photoanodes. Optically active photoanode has been constructed by electrodeposition of titanium dioxide nanopowders containing Nd³⁺ ions, synthesized via a sol-gel method, onto ITO/TiO₂(thin film) substrates. Thin films of TiO₂ have been deposited by means of RF magnetron sputtering in an ultra-high-vacuum system. X-ray diffraction, scanning electron microscopy, UV-VIS-NIR spectrophotometry, and photoluminescence have been applied to assess the properties of photoanodes. In experiments involving photon-assisted water splitting, an external up-converter containing Yb³⁺/Er³⁺ rare-earth ions has been used. Photocurrent as a function of voltage (V_B) under illumination with white light is relatively high (280 μA at V_B = 0 V) for pure TiO₂ thin films and it is not affected by the electrodeposition of TiO₂:Nd³⁺ powders. NIR-driven up-conversion with laser excitation at λ = 980 nm has been found responsible for a 13-fold increase in photocurrent at V_B = 0 V in the modified PEC configuration.