Solid State NMR Spectroscopy a Valuable Technique for Structural Insights of Advanced Thin Film Materials: A Review

Solid-state NMR has proven to be a versatile technique for studying the chemical structure, 3D structure and dynamics of all sorts of chemical compounds. In nanotechnology and particularly in thin films, the study of chemical modification, molecular packing, end chain motion, distance determination and solvent-matrix interactions is essential for controlling the final product properties and applications. Despite its atomic-level research capabilities and recent technical advancements, solid-state NMR is still lacking behind other spectroscopic techniques in the field of thin films due to the underestimation of NMR capabilities, availability, great variety of nuclei and pulse sequences, lack of sensitivity for quadrupole nuclei and time-consuming experiments. This article will comprehensively and critically review the work done by solid-state NMR on different types of thin films and the most advanced NMR strategies, which are beyond conventional, and the hardware design used to overcome the technical issues in thin-film research

Design and synthesis of novel di‐ and triblock amphiphilic polyelectrolytes:Improving salt‐induced viscosity reduction of water solutions for potential application in enhanced oil recovery

In the present study, three different block copolymers based on styrene, tert‐butyl methacrylate, and glycidyl methacrylate (GMA) were synthesized via sequential atom transfer radical polymerization. The addition of the GMA block was found to be best performed at 60°C. The polymers were then hydrolyzed and neutralized, to afford amphiphilic block copolymers, and the rheological properties of their aqueous solutions were measured, in order to investigate solution properties relevant for enhanced oil recovery, as a function of the polymer structure. It was observed that these polymers behave as thickening agents with shear thinning behavior. As expected, the polymers were sensitive to the presence of salt, as lower viscosities were recorded in saline water. However, the viscosity is less affected by high salinity, when compared to previously studied analogous diblock systems. In the best case, the viscosity only decreased by a factor of 1.8 upon salt addition whereas it decreased by a factor of 10 in previously reported non‐GMA containing polymers. Finally, thermo‐responsive behavior was found for one of the synthesized polymers. In particular, a hydrolyzed triblock poly[styrene‐b‐tert‐butyl methacrylate‐b‐glycidyl methacrylate], which synthesis is reported here for the first time, showed a thermothickening behavior, promising for the intended application in oil recovery

Initiated Chemical Vapor Deposition (iCVD) of Bio-Based Poly(tulipalin A) Coatings:Structure and Material Properties

A solvent-free route of initiated chemical vapor deposition (iCVD) was used to synthesize a bio-renewable poly(α-Methylene-γ-butyrolactone) (PMBL) polymer. α-MBL, also known as tulipalin A, is a bio-based monomer that can be a sustainable alternative to produce polymer coatings with interesting material properties. The produced polymers were deposited as thin films on three different types of substrates—polycarbonate (PC) sheets, microscopic glass, and silicon wafers—and characterized via an array of characterization techniques, including Fourier-transform infrared (FTIR), proton nuclear magnetic resonance spectroscopy ((1)H NMR), ultraviolet visible spectroscopy (UV–vis), differential scanning calorimetry (DSC), size-exclusion chromatography (SEC), and thermogravimetric analysis (TGA). Optically transparent thin films and coatings of PMBL were found to have high thermal stability up to 310 °C. The resulting PMBL films also displayed good optical characteristics, and a high glass transition temperature (T(g)~164 °C), higher than the T(g) of its structurally resembling fossil-based linear analogue-poly(methyl methacrylate). The effect of monomer partial pressure to monomer saturation vapor pressure (P(m)/P(sat)) on the deposition rate was investigated in this study. Both the deposition rate and molar masses increased linearly with Pm/Psat following the normal iCVD mechanism and kinetics that have been reported in literature

RAFT Polymerization of a Biorenewable/Sustainable Monomer via a Green Process

A biorenewable polymer is synthesized via a green process using the RAFT principle for the first time in supercritical CO2 at 300 bar and 80 °C. α-Methylene-γ-butyrolactone polymers of various chain lengths and molecular weights are obtained. The molecular weights vary from 10 000 up to 20 000 with low polydispersity indexes (PDI <1.5). Furthermore, the monomer conversion in supercritical CO2 is substantially higher, respectively 85% for ScCO2 compared to ≈65% for polymerizations conducted in dimethyl formamide (DMF) solvent. Chain extensions are carried out to confirm the livingness of the formed polymers in ScCO2. This opens up future possibilities of the formation of different polymer architectures in ScCO2. The polymers synthesized in ScCO2 have glass transition temperature (Tg) values ranging from 155 up to 190 °C. However, the presence of residual monomer encapsulated inside the formed polymer matrix affects the glass transition of the polymer that is lowered by increasing monomer concentrations. Hence, additional research is required to eliminate the remaining monomer concentration in the polymer matrix in order to arrive at the optimal Tg

Proton Nuclear Magnetic Resonance (1H-NMR) Methodology for Monolefin Analysis:Application to Aquaprocessing-Upgraded Bitumen

Olefins are problematic components of petroleum products responsible for gum formation, polymers, and solid deposition in oil facilities. This work presents a methodology developed for monolefin analysis of whole oils, diluted bitumen, and partially upgraded heavy oils. A proton nuclear magnetic resonance (1H-NMR) technique calibrated with naphtha fractions of known monolefin contents is proposed. Internal standard addition (IS, dioxane) makes the method independent of the sample C/H atomic ratios (i.e., paraffin/aromatic hydrocarbon ratios). The developed method was applied for monolefin determination of partially upgraded whole bitumen processed under mild catalytic steam cracking (CSC) conditions and is also identified as aquaprocessing (AQP). Large viscosity reductions for AQP-upgraded products (up to 99%) were determined with associated monolefin contents <1.2 wt %

Adsorption of Algerian Asphaltenes onto Synthesized Maghemite Iron Oxide Nanoparticles

In this study, the adsorption of Algerian asphaltene sample extracted from Hassi Messaoud oil field is conducted for the first time. The adsorption process was performed using novel synthesized iron oxide nanoparticles (γ-Fe2O3). γ-Fe2O3 Nanoparticles were in-house synthesized and characterized by an array of techniques using, Brunauer-Emmett-Teller (BET), high-resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD). The results showed that the synthesized nanoparticles have an average crystalline domain size around 10 nm and a specific surface area of 120 m2/g. The adsorption process of the Algerian asphaltenes took place in a batch mode by dissolving the asphaltenes in toluene at 25°C. Different initial concentrations of asphaltene solutions were used in this study, namely 100, 500, and 1000 ppm. During this adsorption, both isotherm and kinetic studies were investigated. The results showed that the synthesized iron oxide nanoparticles are promising nano-adsorbents that have a high affinity to remove the asphaltenes and the equilibrium was recorded after 15 min. The Solid-Liquid-Equilibrium (SLE) model was used to correlate the adsorption experimental data

A study on the characteristics of Algerian Hassi-Messaoud asphaltenes:Algerian Hassi-Messaoud asphaltenes: solubility and precipitation

This study focuses on detailed characterizations of asphaltene fractions extracted from the Algerian Hassi-Messaoud oil field. It was found that the extracted asphaltenes are not completely soluble in toluene, instead two fractions of asphaltenes were obtained upon solubilizing the heptane-precipitated neat asphaltenes in toluene. Extensive characterizations of the toluene-soluble and insoluble fractions were carried out using elemental analysis, Fourier transform infrared (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD) and solid-state nuclear magnetic resonance (ssNMR). It was suggested that the high oxygen content and uneven compositional structures are the main contributors to asphaltene instability. The toluene-insoluble fractions were found to have higher polarity and aromaticity as well as more oxygen content than the neat asphaltenes and toluene-soluble fractions

A Comparative Review of Binder-Containing Extrusion and Alternative Shaping Techniques for Structuring of Zeolites into Different Geometrical Bodies

Zeolites are crystalline metallosilicates displaying unique physicochemical properties with widespread applications in catalysis, adsorption, and separation. They are generally obtained by a multi-step process that starts with primary mixture aging, followed by hydrothermal crystallization, washing, drying, and, finally, a calcination step. However, the zeolites obtained are in the powder form and because of generating a pressure drop in industrial fixed bed reactors, not applicable for industrial purposes. To overcome such drawbacks, zeolites are shaped into appropriate geometries and desired size (a few centimeters) using extrusion, where zeolite powders are mixed with binders (e.g., mineral clays or inorganic oxides). The presence of binders provides good mechanical strength against crushing in shaped zeolites, but binders may have adverse impacts on zeolite catalytic and sorption properties, such as active site dilution and pore blockage. The latter is more pronounced when the binder has a smaller particle size, which makes the zeolite internal active sites mainly inaccessible. In addition to the shaping requirements, a hierarchical structure with different levels of porosity (micro-, meso-, and macropores) and an interconnected network are essential to decrease the diffusion limitation inside the zeolite micropores as well as to increase the mass transfer because of the presence of larger auxiliary pores. Thus, the generation of hierarchical structure and its preservation during the shaping step is of great importance. The aim of this review is to provide a comprehensive survey and detailed overview on the binder-containing extrusion technique compared to alternative shaping technologies with improved mass transfer properties. An emphasis is allocated to those techniques that have been less discussed in detail in the literature.</p

Binder-free zeolite Beta beads with hierarchical porosity:Synthesis and application as heterogeneous catalysts for anisole acylation

Three zeolites (H-Beta, H-ZSM-5 and H-Y) were synthesized in the form of binder-free macroscopic beads (350-800 µm) using a hydrothermal method employing anion-exchange resin beads as hard template. The beads obtained after removal of the hard template by calcination consisted of crystalline zeolite domains connected with each other to form a hierarchical porous network in which the zeolitic micropores are accessible through meso- and macropores, as proven by characterization with XRD, N2 physisorption, SEM, and TEM. The composition, the nature and amount of acid sites and the degree of hydrophobicity of these beads were investigated by means of XRF, solid-state NMR, pyridine-FTIR and TGA. The zeolite beads were tested as heterogeneous catalysts in the Friedel-Crafts acylation of anisole with acetic anhydride to produce para-methoxyacetophenone. H-Beta-Beads displayed the best catalytic performance with 95% conversion of acetic anhydride and 76% yield of para-methoxyacetophenone in a batch reactor test (90 °C, 6 h). Next, the catalytic performance of H-Beta-Beads was compared in both batch and continuous-flow mode to extrudates prepared by mixing zeolite Beta powder with either kaolin or bentonite binders. H-Beta-Beads outperformed the extrudates in batch-mode reactions and could be reused in multiple runs without discernible loss of activity. In the continuous-flow test, H-Beta-Beads demonstrated higher average activity but deactivated more rapidly than the extrudates

Synergistic Catalytic Effects of Alloys of Noble Metal Nanoparticles Supported on Two Different Supports:Crystalline Zeolite Sn-Beta and Carbon Nanotubes for Glycerol Conversion to Methyl Lactate

Two multifunctional catalytic systems comprising Sn-based/doped crystalline zeolite Beta were synthesized, and they were employed as heterogeneous catalysts in the selective conversion of glycerol to methyl lactate. The first catalytic system, named Au-Pd-Sn-deAl-7.2-Beta-DP, was created through the post-synthesis dealumination of the parent zeolite Beta (Si/Al = 10) using 7.2 M HNO3. Subsequently, it was grafted with 27 mmol of SnCl4, resulting in Sn-deAl-7.2-Beta. Following this, Au and Pd nanoparticles were supported on this catalyst using the deposition–precipitation (DP) method. The second catalytic system was a physical mixture of Au and Pd nanoparticles supported on functionalized carbon nanotubes (Au-Pd-F-CNTs) and Sn-containing zeolite Beta (Sn-deAl-7.2-Beta). Both catalytic systems were employed in glycerol partial oxidation to methyl lactate under the following conditions: 140 °C for 4.5 h under an air pressure of 30 bar. The Au-Pd-Sn-deAl-7.2-Beta-DP catalytic system demonstrated 34% conversion of glycerol with a 76% selectivity for methyl lactate. In contrast, the physical mixture of Au-Pd-F-CNTs and Sn-deAl-7.2-Beta exhibited higher activity, achieving 58% glycerol conversion and a nearly identical selectivity for methyl lactate (77%). The catalytic results and catalyst structure were further analyzed using various characterization techniques, such as X-ray diffraction (XRD), N2 physisorption, scanning electron microscopy (SEM), X-ray fluorescence (XRF), transmission electron microscopy (TEM), UV-vis spectroscopy, and pyridine Fourier transform infrared (FTIR). These analyses emphasized the significance of adjusting the quantity of active sites, particle size, and active sites proximity under the chosen reaction conditions.</p