Excess Enthalpies Analysis of Biofuel Components: Sunflower Oil-Alcohols Systems.

This study addresses the pressing issues of energy production and consumption, in line with global sustainable development goals. Focusing on the potential of alcohols as "green" alternatives to traditional fossil fuels, especially in biofuel applications, we investigate the thermochemical properties of three alcohols (n-propanol, n-butanol, n-pentanol) blended with sunflower oil. The calorimetric analysis allows for the experimental determination of excess enthalpies in pseudo-binary mixtures at 303.15 K, revealing similarities in the trends of the curves (dependence on concentrations) but with different values for the excess enthalpies for each mixture. Despite the structural differences of the alcohols studied, the molar excess enthalpy values exhibit uniformity, suggesting consistent mixing behavior. The peak values of excess enthalpies for systems with sunflower oil and n-propanol, n-butanol and n-pentanol are, respectively, 3255.2 J/mole, 3297.4 J/mole and 3150.1 J/mole. Both the NRTL and Redlich-Kister equations show satisfactory agreement with the obtained values.

Some Remarks on the Boundary of Thermodynamic Stability.

In this paper, we have considered some elements of the classical phenomenological theory of thermodynamic stability, which seem controversial and ambiguous. The main focus is on the conditions of the stability boundary; a new version of the derivation of the relations defining the specified boundary is proposed. Although the final results, in general, coincide with the classical relations, the described approach, from our point of view, provides a clearer and more accurate idea of the stability conditions and their boundaries.

Excess Enthalpies for Binary Mixtures of the Reactive System Acetic Acid + n-Butanol + n-Butyl Acetate + Water: Brief Data Review and Results at 313.15 K and Atmospheric Pressure.

The data on molar excess enthalpies, HmE, for the binary mixtures acetic acid + n-butanol, acetic acid + n-butyl acetate and n-butanol + n-butyl acetate at 313.15 K and atmospheric pressure were obtained with use of the C80 isothermal mixing calorimeter (Setaram). The correlation of the data was carried out using the NRTL model and Redlich-Kister equation. A comparative analysis with the literature data on all available binary subsystems of the quaternary system was carried out. Other thermodynamic properties (Cp,mE, SmE, ΔmixSm, GmE and ΔmixGm) of the binary systems were estimated using literature data and well-known formulas of classical thermodynamics.

Comparative Atomic-Level Analysis of Sorption and Diffusion Properties of Membrane Materials on the Base of Polymer and Its Prepolymer: A Case Study of Polyheteroarylenes.

The sorption properties of polymers and the mobility of penetrants are the main factors which determine the trans-membrane processes. Other factors concern the membrane material structure and chemical nature. In this paper, we consider the case of polymers with similar structure units, namely a polymer and its pre-polymer (polybenzoxazinoneimide and imide-containing polyamic acid). The available experimental data show a great difference in the pervaporation process using these two polymeric membranes. Some explanation of this difference can be found at the atomic-level study. A comparative analysis of the diffusion of water and isopropanol molecules was carried out using the density functional theory and molecular dynamics simulations.

Geometric Analysis of a System with Chemical Interactions.

In this paper, we present some initial results aimed at defining a framework for the analysis of thermodynamic systems with additional restrictions imposed on the intensive parameters. Specifically, for the case of chemical reactions, we considered the states of constant affinity that form isoffine submanifolds of the thermodynamic phase space. Wer discuss the problem of extending the previously obtained stability conditions to the considered class of systems.

Toward Formal Analysis of Thermodynamic Stability: Le Chatelier-Brown Principle.

In this contribution, we carry on with the research program initiated in J. Math. Chem., 58(6), 2020. Using the methods from geometric thermodynamics, we formally derive and analyze different conditions for thermodynamic stability and determine the limits of their use. In particular, we study, in detail, several versions of the Le Chatelier-Brown principle and demonstrate their application to the analysis of thermodynamic stability.

Application of Polymer Membranes for a Purification of Fuel Oxygenated Additive. Methanol/Methyl Tert-butyl Ether (MTBE) Separation via Pervaporation: A Comprehensive Review.

Methyl Tert-butyl Ether (MTBE) remains the most popular fuel additive to improve fuel performance and reduce the emission of hazardous components. The most common method of MTBE production is a catalytic synthesis with a great excess of methanol to improve the reaction yield. The problems of obtaining pure MTBE from the final product have determined the search for new techniques; primarily membrane methods. Pervaporation as an optimal membrane process for highly selective separation of organic mixtures is of particular interest. This review is focused on analysis of the research works on the various polymer membranes and their efficiency for the separation of the azeotropic methanol/MTBE mixture. Currently the most popular materials with optimal transport properties are poly(vinyl alcohol), cellulose acetate and polyheteroarylenes. Mixed matrix membranes (MMM) are highly effective as well as they show overall operational stability.

Novel Polyester Amide Membranes Containing Biquinoline Units and Complex with Cu(I): Synthesis, Characterization, and Approbation for n-Heptane Isolation from Organic Mixtures.

The wide possibilities of designing a chemical structure and creating complexes with transition metals make polymers of heteroaromatic structure interesting objects, from both scientific and practical aspects. In this work, modern biquinoline-containing polymers, namely polyester amide (PEA) and its metal-polymer complex (PEA-Cu(I)), were synthesized and used to form dense flat membranes. A comparative study of their morphology, same physical properties (density, free volume, and contact angles), and thermomechanical characteristics was carried out. The transport properties of the modern membranes were studied during pervaporation, to solve a problem of n-heptane isolation from its binary mixtures with thiophene and methanol. It was shown that only the PEA membrane is selective for the separation of thiophene impurities from the mixture with n-heptane. In pervaporation of methanol/n-heptane mixture, the РЕА-Cu(I) membrane exhibits significantly higher pervaporation separation index, as compared with that of the РЕА membrane.

Asymmetric Membranes Based on Copolyheteroarylenes with Imide, Biquinoline, and Oxazinone Units: Formation and Characterization.

Modern ultrafiltration requires novel perfect membranes with narrow pore size, high porosity, and minimal pore tortuosity to achieve high separation performance. In this work, copolyamic acid (co-PAA) was synthesized and used for the preparation of asymmetric porous membranes by phase inversion technique. Several co-PAA membranes were heated up to 250 °C; during heating, they undergo solid-phase transformation into co-polybenzoxazinoneimide (co-PBOI) via dehydration and cyclization. Comparative characterization of both co-PAA and co-PBOI membranes was realized by scanning electron microscopy, mechanical testing, thermogravimetric analysis, and ultrafiltration experiments. Membrane calibration was carried out using a mixture of seven proteins with different molecular weights. During heat treatment, the molecular weight cut-off of the membranes decreased from 20 × 103 g/mol (co-PAA) to 3 × 103 g/mol (co-PBOI). Abnormally low dispersions of rejection (0.3 for co-PAA and 0.45 for co-PBOI) were observed for the studied membranes; this fact indicates that the membranes possess enhanced resolving power.

Plasticizing of chitosan films with deep eutectic mixture of malonic acid and choline chloride.

Chitosan (CS) films containing deep eutectic solvent (DES) based on malonic acid (MA) and choline chloride (ChCl) were successfully prepared by solution casting method by using DES content ranging from 0 to 82 wt%. A strong interaction of CS with the components of DES was demonstrated by analyses of water sorption isotherms, atomic force microscopy and FTIR results. The plasticizing effect of the MA and ChCl mixture on the CS matrix was shown by static bulk mechanical measurements, thermal analysis and quantitative nanomechanical mapping (QNM). Elongation at break increased from 3 to 62% at increase of DES content from 0 to 67 wt%, while further increase of DES content led to the decreasing of maximal elongation. Introduction of DES into CS films led to the appearance of glass transition temperature in the region +2 - -2.3 °C. QNM results indicated homogeneity of the films containing up to 75 wt% of DES.

Improved Hydrogen Separation Using Hybrid Membrane Composed of Nanodiamonds and P84 Copolyimide.

Membrane gas separation is a prospective technology for hydrogen separation from various refinery and petrochemical process streams. To improve efficiency of gas separation, a novel hybrid membrane consisting of nanodiamonds and P84 copolyimide is developed. The particularities of the hybrid membrane structure, physicochemical, and gas transport properties were studied by comparison with that of pure P84 membrane. The gas permeability of H2, CO2, and CH4 through the hybrid membrane is lower than through the unmodified membrane, whereas ideal selectivity in separation of H2/CO2, H2/CH4, and CO2/CH4 gas pairs is higher for the hybrid membrane. Correlation analysis of diffusion and solubility coefficients confirms the reliability of the gas permeability results. The position of P84/ND membrane is among the most selective membranes on the Robeson diagram for H2/CH4 gas pair.

Impact of Endometallofullerene on P84 Copolyimide Transport and Thermomechanical Properties.

Novel polymer composite materials, including unique nanoparticles, contribute to the progress of modern technologies. In this work, the endohedral fullerene C60 with incapsulated iron atom (endometallofullerene Fe@C60) is used for modification of P84 copolyimide. The impact of 0.1, 0.5, and 1 wt % endometallofullerene on the structure and physicochemical properties of polymer films is studied through scanning electron microscopy, thermogravimetric analysis, and thermomechanical tests. Transport properties are estimated through sorption and pervaporation techniques toward methanol and methyl acetate mixture. The inclusion of endometallofullerene into the copolyimide matrix improves membrane permeability and selectivity in the separation of methanol-methyl acetate mixtures. The maximal effect is achieved with a composite containing 0.5 wt % Fe@C60. The developed composites are effective for energy and resource saving purification of methyl acetate by pervaporation.

Effect of Domain Structure of Segmented Poly(urethane-imide) Membranes with Polycaprolactone Soft Blocks on Dehydration of n-Propanol via Pervaporation.

Segmented poly(urethane-imide)s (PUIs) were synthesized by polyaddition reaction and applied for preparation of membranes. Tolylene-2,4-diisocyanate, pyromellitic dianhydride, and m-phenylenediamine for chain extension were used to form hard aromatic blocks. Polycaprolactone diols with molecular weights equal to 530 and 2000 g mol-1 were chosen as soft segments. The effect of the length of soft segments on the structure, morphology, and transport properties of segmented poly(urethane-imide) membranes were studied using atomic force microscopy, small-angle and wide-angle X-ray scattering, and pervaporation experiments. It was found that a copolymer with a shorter soft segment (530 g mol-1) consists of soft domains in a hard matrix, while the introduction of polycaprolactone blocks with higher molecular weight (2000 g mol-1) leads to the formation of hard domains in a soft matrix. Additionally, the introduction of hard segments prevents crystallization of polycaprolactone. Transport properties of membranes based on segmented PUIs containing soft segments of different length were tested for pervaporation of a model mixture of propanol/water with 20 wt % H2O content. It was found that a membrane based on segmented PUIs containing longer soft segments demonstrates higher flux (8.8 kg µm m-2 h-1) and selectivity (179) toward water in comparison with results for pure polycaprolactone reported in literature. The membrane based on segmented PUIs with 530 g mol-1 soft segment has a lower flux (5.1 kg µm m-2 h-1) and higher selectivity (437).

Novel green PVA-fullerenol mixed matrix supported membranes for separating water-THF mixtures by pervaporation.

This study focuses first on the preparation of mixed matrix supported membranes of polyvinyl alcohol (PVA) and low-hydroxylated fullerenol C60(OH)12 used to create water selective membranes and then on their pervaporation properties for the separation of water-THF mixtures. These novel supported PVA membranes containing nano-carbon particles were prepared to reach high membrane performance for further integration in a dehydration process, such as distillation coupled to pervaporation. The separation of water-THF mixtures was performed with the supported membranes over a wide range of water concentrations in the feed mixture, i.e., from the azeotrope range up to 30 wt%, to evaluate the performance and stability of the thin active layer. SEM was used to visualize the internal morphology of the membrane. The influence of temperature on the transport properties was also investigated. All the membranes were highly water selective and stable up to 30 wt% water in the feed. The best compromise of transport properties was obtained for the C60(OH)12(5%)-PVA supported composite membrane: a permeate enrichment of 99.3 ± 0.3 wt% water and a flux of 0.25 ± 0.02 kg/(m2 h) for the separation of a mixture containing 5.7 wt% water and 94.3 wt% tetrahydrofuran (THF) at 30 °C. Considering its water stability, this supported membrane with a dense layer thinner than 2 µm appears promising for use in hybrid industrial processes to upgrade solvents with a smaller environmental footprint than conventional methods.

Structure of Composite Based on Polyheteroarylene Matrix and ZrO2 Nanostars Investigated by Quantitative Nanomechanical Mapping.

It is known that structure of the interface between inorganic nanoparticles and polymers significantly influences properties of a polymer⁻inorganic composite. At the same time, amount of experimental researches on the structure and properties of material near the inorganic-polymer interface is low. In this work, we report for the first time the investigation of nanomechanical properties and maps of adhesion of material near the inorganic-polymer interface for the polyheteroarylene nanocomposites based on semi-crystalline poly[4,4'-bis (4″-aminophenoxy)diphenyl]imide 1,3-bis (3',4-dicarboxyphenoxy) benzene, modified by ZrO2 nanostars. Experiments were conducted using quantitative nanomechanical mapping (QNM) mode of atomic force microscopy (AFM) at the surface areas where holes were formed after falling out of inorganic particles. It was found that adhesion of AFM cantilever to the polymer surface is higher inside the hole than outside. This can be attributed to the presence of polar groups near ZrO2 nanoparticle. QNM measurements revealed that polymer matrix has increased rigidity in the vicinity of the nanoparticles. Influence of ZrO2 nanoparticles on the structure and thermal properties of semi-crystalline polyheteroarylene matrix was studied with wide-angle X-ray scattering, scanning electron microscopy, and differential scanning calorimetry.

Aromatic Copolyamides with Anthrazoline Units in the Backbone: Synthesis, Characterization, Pervaporation Application.

Copolyamides with anthrazoline units in the backbone (coPA) were synthesized and dense nonporous films were prepared by solvent evaporation. Glass transition temperature, density, and fractional free volume were determined for the dense nonporous films composed of polyamide and two of its copolymers containing 20 and 30 mol % anthrazoline units in the backbone. Transport properties of the polymer films were estimated by sorption and pervaporation tests toward methanol, toluene, and their mixtures. An increase in anthrazoline fragments content leads to an increasing degree of methanol sorption but to a decreasing degree of toluene sorption. Pervaporation of a methanol⁻toluene mixture was studied over a wide range of feed concentration (10⁻90 wt % methanol). Maximal separation factor was observed for coPA-20 containing 20 mol % fragments with anthrazoline units; maximal total flux was observed for coPA-30 with the highest fractional free volume.

Structure and Transport Properties of Mixed-Matrix Membranes Based on Polyimides with ZrO2 Nanostars.

Mixed-matrix membranes based on amorphous and semi-crystalline polyimides with zirconium dioxide (ZrO2) nanostars were synthesized. Amorphous poly(4,4'-oxydiphenylenepyromellitimide) and semi-crystalline polyimide prepared from 1,4-bis(4-aminophenoxy)benzene and 4,4'-oxydiphthalic anhydride were used. The effect of ZrO2 nanostars on the structure and morphology of nanocomposite membranes was studied by wide-angle X-ray scattering, scanning electron microscopy, atomic force microscopy, and contact angle measurements. Thermal properties and stability were investigated by thermogravimetric analysis and differential scanning calorimetry. Transport properties of hybrid membranes containing 5 wt % ZrO2 were tested for pervaporation of a mixture of butanol⁻water with 10 wt % H2O content. It was found that a significant amount of the ZrO2 added to the semi-crystalline polyimide is encapsulated inside spherulites. Therefore, the beneficial influence of inorganic filler on the selectivity of mixed-matrix membrane with respect to water was hampered. Mixed-matrix membranes based on amorphous polymer demonstrated the best performance, because water molecules had higher access to inorganic particles.