Dehydration Mechanism Research Articles

Theoretical prediction of the dehydration mechanism of 1, 3-butanediol as a potential biofuel surrogate

Theoretical prediction of the dehydration mechanism of 1, 3-butanediol as a potential biofuel surrogate

Kinetic study of the double dehydration of sorbitol into isosorbide over commercial sulfonic acid resin

Biomass-derived chemicals show great promise as an alternative resource for the replacement of fossil fuel-derived chemicals. The double dehydration of sorbitol produces isosorbide, which is an important chemical building platform and a component in food, pharmaceuticals, and plasticizers. Homogeneous catalysts are used to perform this reaction due to their good performance, but they also exhibit some drawbacks. Therefore, in this study, the sulfonic acid resin Purolite CT269 was used as a heterogeneous catalyst to study isosorbide production. The reaction was carried out with a 4.43 wt.% catalyst loading, reaction temperature of 151 °C, and reaction time of 4 h under a vacuum. 100 % conversion of sorbitol was observed within 2 h, and an isosorbide yield of about 78 % was achieved after 4 h. The kinetics of the reaction were evaluated, the rate law followed a first-order reaction model, and the reaction rate depended on the concentration of reactant. The Langmuir–Hinshelwood–Hougen–Watson (LHHW) model was used to determine that the first dehydration was the rate-determining step of this reaction. The study also examined the deactivation of the catalyst using FE-SEM, N2 adsorption/desorption, DSC, TGA, and XPS, confirming that changes to the catalytic properties after the reaction negatively impacted the performance of the sorbitol dehydration reaction. The catalytic performance and kinetic analysis were used to explain the mechanism of the double dehydration of sorbitol into isosorbide, providing essential information for catalyst and isosorbide production process design.

Effect of trehalose dehydration on crystal morphology and food caking during post-treatment

Morphological changes of trehalose crystals during drying and reprocessing lead to a series of post-processing problems, which result in a significant investment in production costs. In this work, the mechanism of drying temperature on the morphology and caking behavior of trehalose was investigated. When the drying temperature was too high (≥393.15 K), a large number of pores, cracks and burrs appeared on the surface of crystals. These lead to crystal fragmentation during agitated drying process. The dehydration kinetics showed that the rearrangement of the new structure after dehydration and the change of the dehydration mechanism were the reasons for the morphological changes of trehalose crystals. Caking experiments showed that the dried product exhibited higher hygroscopicity and tendency to caking. Compared with trehalose dihydrate, the product flowability decreased by 30.0 %, critical caking period decreased by 82.1 %, and caking strength increased by 13 times after high-temperature drying (413.15 K).

Synergistic Effects of Nonthermal Plasma and Solid Acid Catalysts in Thermo-Catalytic Glycerol Dehydration

To enhance the bio-based synthesis of acrolein from glycerol, a hybrid approach combining in situ nonthermal plasma (NTP) with thermo-catalytic dehydration was employed. This study investigated the impact of the reaction temperature and NTP discharge field strength on glycerol conversion, acrolein selectivity, byproduct formation, and coke deposition using two catalysts of silicotungstic acid supported on mesoporous alumina and silica. The results revealed that, while the reaction temperature and NTP field strength exhibited complex interactions, the in situ application of NTP markedly improved both glycerol conversion and acrolein selectivity when optimized for specific temperature–NTP field strength combinations. Additionally, the reaction mechanisms of glycerol dehydration with the two catalysts, in the presence and absence of NTP, were systematically analyzed and discussed based on the experimental data.

A Review on In Vivo Research Dehydration Models and Application of Rehydration Strategies

Background: Dehydration, a common condition where the amount water lost from the body exceeds intake, disrupts metabolic processes and negatively impacts health and performance. Rehydration, the process of restoring body fluids and electrolytes to normal levels, is crucial for maintaining physiological health. In vivo dehydration models are experimental systems used to study the effects of dehydration on living organisms. However, a comprehensive summary of in vivo models and the application of human rehydration strategies is lacking. Methods: This review provides a comprehensive overview of various in vivo models and rehydration strategies. Results: In vivo models, stimulated by fluid restriction, exercise, thermal exposure, and chemicals, have been used to study dehydration. Importantly, the principles, characteristics, and limitations of the in vivo models are also discussed, along with rehydration administration methods, including oral, intestinal, intravenous, subcutaneous, and intraperitoneal routes. Additionally, rehydration strategies and the application for managing different dehydration conditions both in daily life and clinical settings have been summarized. Conclusions: Overall, this review aims to enhance the understanding of the conditions in which in vivo dehydration models and rehydration strategies are applicable, thereby advancing research into the physiological and pathological mechanisms of dehydration and supporting the development of effective rehydration therapies.

Performances and Mechanisms of Dehydration of Levoglucosan to Levoglucosenone over Cesium Heterpolyacid Salts

Performances and Mechanisms of Dehydration of Levoglucosan to Levoglucosenone over Cesium Heterpolyacid Salts

Effect and Mechanism of Zirconium Crosslinker on Retarding Degradation of HPAM/PEI Gel System in Medium-Salinity Reservoirs

Summary The objective of this paper is to investigate the effect of the addition of zirconium crosslinker on retarding the degradation of the partially hydrolyzed polyacrylamide/polyethyleneimine (HPAM/PEI) gel system. Dehydration and degradation under salinity conditions pose serious challenges to the effectiveness of the HPAM/PEI system used for water control treatment in heterogeneous reservoirs. In this study, rheological tests, Fourier transform infrared (FTIR) spectroscopy, and 13C nuclear magnetic resonance (NMR) spectroscopy are used to elucidate the characteristics and mechanisms of dehydration and degradation of HPAM/PEI gel in medium-salinity conditions. The effects of three types of zirconium crosslinkers on the gelation performance of the HPAM/PEI system are evaluated. Furthermore, the mechanism by which an organic zirconium complex (ZrOr complex) with triethanolamine (TEA) and lactic acid (LA) as ligands improves the stability of the HPAM/PEI system under medium-salinity conditions is revealed. The results indicate that ZrOr complex notably retards the degradation of the HPAM/PEI system under medium-salinity conditions (50 g/L) for more than 60 days while improving its gel strength. TEA and LA as ligands have a positive effect on crosslinking of HPAM with the organic Zr4+ complex by modulating the availability of Zr4+ and the homogeneity of the crosslinking reaction. Specifically, our data suggest that TEA stabilized Zr4+ and retarded its release through its chelating effect, while LA improved the efficiency and effectiveness of the crosslinking reaction by increasing the solubility of Zr4+ and providing additional carboxyl groups. The synergistic effect of the two ligands significantly improved the properties of the final crosslinked product. Evidence from FTIR, 13C NMR, and microstructural tests supports the conclusion that the retardation of degradation and enhancement of gelation performance in the HPAM/PEI system by ZrOr complex are associated with its crosslinking with carboxyl groups produced by HPAM hydrolysis, leading to the formation of a more uniform and compact network structure. A field trial conducted in the Beiyao Block demonstrated the potential of the ZrOr complex to extend the treatment lifetime of the HPAM/PEI gel system in medium-salinity reservoirs.

Structural Basis of the Dehydratase Module (hDH) of Human Fatty Acid Synthase.

The human fatty acid synthase (hFASN) produces fatty acids for cellar membrane construction, energy storage, biomolecule modifications and signal transduction. Abnormal expression and functions of hFASN highly associate with numerous human diseases such as obesity, diabetes, and cancers, and thereby it has been considered as a valuable potential drug target. So far, the structural and catalytic mechanisms of most of the hFASN enzymatic modules have been extensively studied, except the key dehydratase module (hDH). Here we presented the enzymatic characterization and the high-resolution crystal structure of hDH. We demonstrated that the hDH preferentially catalyzes the acyl substrates with short lengths between 4 to 8-carbons, and exhibits much lower enzymatic activity on longer substrates. Subsequent structural study showed that hDH displays a pseudo-dimeric organization with a single L-shaped composite hydrophobic catalytic tunnel as well as an atypical ACP binding site nearby, indicating that hDH achieves distinct substrate recognition and dehydration mechanisms compared to the conventional bacterial fatty acid dehydratases identified. Our findings laid the foundation for understanding the biological and pathogenic functions of hFASN, and may facilitate therapeutical drug development against diseases with abnormal functionality of hFASN.

Low temperature carbonization and synergistic flame retardancy of cotton fabric coated by phosphorus‑nitrogen flame retardants

To solve the problems of flammability and smoldering of cotton fabric, its flame-retardant finishing was executed with biomass wool keratin (WK) and cyclic phosphate ester (CPE) through the soaking and baking process. The synergistic mechanism of WK low-temperature melting and CPE catalytic dehydration prompted the formation of protective carbonization layer on cotton fabric surface, and this protective layer reduced its pyrolysis rate, inhibited the production of combustible materials and improved its flame retardancy. The results of synchronous thermal analysis indicate that the initial decomposition temperature of WK and CPE is lower than that of cotton fabric, and they precede the endothermic degradation before fabric main body. This effectively promotes the low-temperature carbonization of cotton fabric and inhibits its pyrolysis. The initial decomposition temperature of WK/CPE treated fabrics advances by 47.9 °C–97.8 °C, presenting significant low-temperature carbonization trend. Moreover, they form 3.0 %–20.0 % aromatic structural char before the pyrolysis of cotton cellulose due to the low-temperature dehydration and carbonization reactions. The damage length after vertical burning is only 4.0 cm for treated fabric with five layers, its after-flame and smoldering disappear, and its limiting oxygen index value increases to 28.7 %. This research provides an effective idea for the flammability and smoldering problems of cotton fabric.

Colored Radiative Cooling and Flame-Retardant Polyurethane-Based Coatings: Selective Absorption/Reflection in Solar Waveband.

The aesthetic demand has become an imperative challenge to advance the practical and commercial application of daytime radiative cooling technology toward mitigating climate change. Meanwhile, the application of radiative cooling materials usually focuses on the building surface, related tightly to fire safety. Herein, the absorption and reflection spectra of organic and inorganic colorants are first compared in solar waveband, finding that iron oxides have higher reflectivity in NIR region. Second, three kinds of iron oxides-based colorants are selected to combine porous structure and silicon-modified ammonium polyphosphate (Si-APP) to engineer colored polyurethane-based (PU) coating, thus enhancing the reflectivity and flame retardancy. Together with reflectivity of more than 90% in near-infrared waveband and infrared emissivity of ≈91%, average temperature drops of ≈5.7, ≈7.9, and ≈3.8°C are achieved in porous PU/Fe2O3/Si-APP, porous PU/Fe2O3·H2O/Si-APP, and porous PU/Fe3O4·H2O/Si-APP, compared with dense control samples. The catalysis effect of iron oxides in the cross-linking reaction of pyrolysis products and dehydration mechanism of Si-APP enable PU coating to produce an intumescent and protective char residue. Consequently, PU composite coatings demonstrate desirable fire safety. The ingenious choice of colorants effectively minimizes the solar heating effect and trades off the daytime radiative cooling and aesthetic appearance requirement.

Mathematical modeling of the effects of thickness and temperature on thin-layer drying kinetics of oven-dried cooking bananas (Musa spp., sub. grp. ABB) slices

Cooking bananas is a major beneficial food in developing countries that is involved in improving human well-being and health. However, owing to its high moisture content, it quickly deteriorates. Understanding the dehydration mechanism of raw banana slices is important for subsequent processing, preservation, transportation, and product quality. Thus, this study investigates the influence of slice thickness (5, 10, and 15 mm) at varying temperatures (45, 55, and 65 °C) in a convective oven dryer on thin-layer drying kinetics and extrapolates their effect on the drying kinetics of cooking banana slices. As the temperature and slice thickness increased, the drying time also increased. Midilli’s model was found to be the best for explaining the experimental data. The effective moisture diffusivity ranged from 1.393 × 10 −8 to 8.889 10 −8 m2/s. The dependence of moisture diffusivity on temperature was described by an Arrhenius-type equation, and the activation energies were found to be 23.599, 24.804, and 24.223 kJ/mol for thicknesses of 5, 10, and 15 mm, respectively.

Multiple Stabilization Effects of Benzylhydrazine on Scalable Perovskite Precursor Inks for Improved Perovskite Solar Cell Production

AbstractPerovskite precursor inks suffer various forms of degradation, such as iodide anion oxidation and organic cation breakdown, hindering reliable perovskite solar cell manufacturing. Here we report that benzylhydrazine hydrochloride (BHC) not only retards the buildup of iodine as previously reported but also prevents the breakdown of organic cations. Through investigating BHC and iodine chemical reactions, we elucidate protonation and dehydration mechanisms, converting BHC to harmless volatile compounds, thus preserving perovskite film crystallization and solar cell performance. This inhibition effect lasts nearly a month with minimal BHC, contrasting control inks without BHC where organic cations fully react in less than a week. This enhanced understanding, from additive stabilization to end products, promises improved perovskite solar cell production reliability.

Multiple Stabilization Effects of Benzylhydrazine on Scalable Perovskite Precursor Inks for Improved Perovskite Solar Cell Production.

Perovskite precursor inks suffer various forms of degradation, such as iodide anion oxidation and organic cation breakdown, hindering reliable perovskite solar cell manufacturing. Here we report that benzylhydrazine hydrochloride (BHC) not only retards the buildup of iodine as previously reported but also prevents the breakdown of organic cations. Through investigating BHC and iodine chemical reactions, we elucidate protonation and dehydration mechanisms, converting BHC to harmless volatile compounds, thus preserving perovskite film crystallization and solar cell performance. This inhibition effect lasts nearly a month with minimal BHC, contrasting control inks without BHC where organic cations fully react in less than a week. This enhanced understanding, from additive stabilization to end products, promises improved perovskite solar cell production reliability.

Pervaporation Dehydration Mechanism and Performance of High-Aluminum ZSM-5 Zeolite Membranes for Organic Solvents.

Membrane-based pervaporation (PV) for organic solvent dehydration is of great significance in the chemical and petrochemical industries. In this work, high-aluminum ZSM-5 zeolite membranes were synthesized by a fluoride-assisted secondary growth on α-alumina tubular supports using mordenite framework inverted (MFI) nanoseeds (~110 nm) and a template-free synthesis solution with a low Si/Al ratio of 10. Characterization by XRD, EDX, and SEM revealed that the prepared membrane was a pure-phase ZSM-5 zeolite membrane with a Si/Al ratio of 3.8 and a thickness of 2.8 µm. Subsequently, two categories of PV performance parameters (i.e., flux versus separation factor and permeance versus selectivity) were used to systematically examine the effects of operating conditions on the PV dehydration performance of different organic solvents (methanol, ethanol, n-propanol, and isopropanol), and their PV mechanisms were explored. Employing permeance and selectivity effectively disentangles the influence of operating conditions on PV performance, thereby elucidating the inherent contribution of membranes to separation performance. The results show that the mass transfer during PV dehydration of organic solvents was mainly dominated by the adsorption-diffusion mechanism. Furthermore, the diffusion of highly polar water and methanol molecules within membrane pores had a strong mutual slowing-down effect, resulting in significantly lower permeance than other binary systems. However, the mass transfer process for water/low-polar organic solvent (ethanol, n-propanol, and isopropanol) mixtures was mainly controlled by competitive adsorption caused by affinity differences. In addition, the high-aluminum ZSM-5 zeolite membrane exhibited superior PV dehydration performance for water/isopropanol mixtures.

Selective recovery of vanadium from chloride titanium dioxide effluent and preparation of high-purity thermotropic vanadium dioxide(M): An ammonia-free process

Vanadium recovery is critical for the hazard-free treatment and resourceful utilization of chloride titanium dioxide effluent (CTDE). Traditional ammonia precipitation vanadium recovery process from chloride titanium dioxide effluent suffered issues of the long process, high cost, and severe ammonia pollution risk. To solve these issues, an ammonia-free method consisting of V extraction from chloride titanium dioxide effluent by D2EHPA, direct VO2+ hydrolysis precipitation, and vacuum calcination was designed to produce VO2(M). The effect of conditions on V recovery, impurities behaviors, and vacuum dehydration mechanisms in each step was systematically investigated. Experimental results demonstrated that over 96.50% of vanadium was precipitated in the form of VO2∙xH2O by mixing CaO powder at 25 °C for 5 min until pH reached 4.20. And then, high purity VO2(M) (VO2 >99.50%) was prepared by vacuum calcined at 500 °C for 2 h in the tube furnace. Further characterizations revealed that the crystal structure of the calcined product was a monoclinic crystal structure with the space group of P21/c (VO2(M)), and the phase transition temperature was 57.8 °C. This demonstrated that the produced VO2(M) had met the established market standards and exhibited stable thermotropic degeneration, making it suitable for use in thermistors and other related fields. Compared with the conventional ammonia precipitation V recovery process, the proposed process exhibits a promising industrial application due to the short flow, near-zero wastes, higher economic efficiency, and superior product performance. In conclusion, it provides a clean and efficient vanadium recovery strategy from chloride titanium dioxide effluent.

The studies on dehydration reaction mechanism of irradiated solid acid - nanostructured sodium - bentonite clay

Research findings can offer data and a theoretical framework for a quantitative examination of the bentonite dehydration mechanism. The reasons for changes in pore’ water under the influence of gamma rays in vacuum and in the presence of oxygen was discussed using TGA and DTA, FT-IR spectroscopy. It was revealed that dehydration and pore characteristics are mutually dependent. A question about the associated evolution of dehydration pore‘s water in nanostructured sodium – bentonite clay under the influence of ionizing rays with and without oxygen has been comparatively studied. The article is devoted to a discussion of how ionizing radiation, passing through nanoclays, produces, or rather begins to produce, chemical effects. It was used Infrared spectroscopy as the method for determining structural responses of natural clay from the Alpoid deposit in the Republic of Azerbaijan, to gamma rays exposure. It was found that under influence of ionizing rays in vacuum obtained hydrogen peroxide. It is of great interest for the study of the dehydration reaction mechanism and its role in formation of H2 under gamma irradiation.

Characterizing dehydration in short-term spaceflight using evidence from Project Mercury

Short-term spaceflight is commonly perceived as posing minimal risk to human health and performance. However, despite their duration, short-term flights potentially induce acute physiological changes that create risk to crews. One such change is dehydration (primarily body water loss) due to a heat-stressed environment. Such loss, if severe and prolonged, can lead to decrements in performance as well as increase the risk of more serious medical conditions. Though the general mechanisms of dehydration are broadly understood, the rate and extent of dehydration in short-term spaceflight has not been characterized. Combining data from the six spaceflights of the US Mercury program with a causal diagram illustrating the mechanisms of dehydration, we fit a path model to estimate the causal effects for all pathways in the causal model. Results demonstrate that Mercury astronauts experienced some degree of dehydration across the range of suited time and that the relationship between suited time and dehydration appears to be logarithmic. We discuss causal interpretations of the results and how the results from this and similar analyses can inform countermeasure development for short-term spaceflight.

Combustion Behavior of Cellulose Ester Fibrous Bundles from Used Cigarette Filters: Kinetic Analysis Study.

This study is focused on the detailed examination of the combustion properties and kinetic analysis of a cellulose acetate fibrous bundle (CAFB), separated from used cigarette filters. It was shown that the faster rate of CAFB heating allows a large amount of heat to be supplied to a combustion system in the initial stages, where the increase in heating rate has a positive response to ignition behavior. The best combustion stability of CAFB is achieved at the lowest heating rate. Through the use of different kinetic methods, it was shown that combustion takes place through two series of consecutive reaction steps and one independent single-step reaction. By optimizing the kinetic parameters within the proposed reaction models, it was found that the steps related to the generation of levoglucosenone (LGO) (by catalytic dehydration of levoglucosan (LG)) and acrolein (by breakdown of glycerol during CAFB burning-which was carried out through glycerol adsorption on a TiO2 surface in a the developed dehydration mechanism) represent rate-controlling steps, which are strongly controlled by applied heating rate. Isothermal predictions have shown that CAFB manifests very good long-term stability at 60 °C (which corresponds to storage in a sea shipping container), while at 200 °C, it shows a sudden loss in thermal stability, which is related to the physical properties of the sample.

Investigation on the Initial Stage of the Dehydration Process in Mg(OH)2 by Density Functional Theory Calculations.

Mg(OH)2/MgO has been attracting considerable interest as a viable candidate for thermochemical heat storage materials, particularly within the temperature range of 200-400 °C. Nonetheless, the typical dehydration temperature of Mg(OH)2, which occurs within the 300-400 °C range, needs to be reduced to enhance its effectiveness in various applications for thermal energy storage. While several studies have shown that heterospecies doping can lower the dehydration temperature, the fundamental mechanism underlying this effect still remains unclear. Here, we employed density functional theory calculations to elucidate the dehydration mechanism of Mg(OH)2, with a particular focus on the initial stage of the dehydration that determines the temperature beginning the reaction. Our findings indicate that the formation of water molecules on the (001) surface is critical in the early stages of the dehydration. This discovery provides a comprehensive explanation for the role of dopants (Na, Li, or LiCl) in reducing the dehydration temperature by decreasing the formation energy of paired H and OH defects and the migration barrier of H on the surface. The present study will significantly advance the development of novel dopants for Mg(OH)2, facilitating a lower dehydration temperature and, thereby, increasing its suitability for heat storage applications.

Multistep kinetics in self-induced sol–gel process of amorphous anhydride formation during thermal dehydration of potassium tetraborate tetrahydrate

AbstractThe physico-geometrical mechanism and kinetics of the multistep thermal dehydration of potassium tetraborate tetrahydrate was investigated as a model reaction to produce amorphous anhydrate via the self-induced sol–gel process. The thermal dehydration is composed of three consecutive dehydration steps: (1) a surface reaction in the solid-state accompanied by crack formation; (2) a rapid mass loss process accompanied by liquefaction to form the aggregate of the gel powders; and (3) the dehydration of gel powder aggregate to form a glassy anhydride. The changes in the contribution of the individual dehydration steps to the overall process according to the sample particle size and the heating rate (β) were identified as specific features of the multistep dehydration, which was characterized quantitatively using mathematical deconvolution analysis with log-normal four-parameter functions. The difficulty in determining the apparent activation energy (Ea) of the individual dehydration steps using isoconversional analysis due to the changes in the contribution depending on β values was addressed using modulated temperature thermogravimetry. Using the contributions and the apparent Ea of the individual dehydration steps as initial values, the kinetic description of the multistep thermal dehydration was refined through a kinetic deconvolution analysis using the cumulative kinetic equation. As a result, the individual dehydration steps were kinetically characterized as: (1) a surface reaction described by the first-order rate law with Ea,1 of approximately 68 kJ mol−1; (2) a reaction accompanied by liquefaction controlled by an autocatalytic rate behavior with Ea,2 of approximately 123 kJ mol−1; (3) a diffusion-controlled dehydration of gel powder with Ea,3 of approximately 82 kJ mol−1.