Alcoholic Solvents Research Articles

Improved Molecular Packing of Self-Assembled Monolayer Charge Injectors for Perovskite Light-Emitting Diodes.

Self-assembled monolayers (SAMs) have shown great potential as hole injection materials for perovskite light-emitting diodes due to their low parasitic absorption and ability to adjust energy level alignment. However, the head and anchoring groups on SAM molecules with significant differences in polarity can lead to the formation of micelles in the commonly used alcoholic processing solvent, inhibiting the formation of an intact SAM. In this work, the introduction of methyl groups on carbazole in the phosphonic-acid-based SAM materials is found to facilitate energy level alignment and promote the formation of compact SAMs. The alternative molecular structure also enhances the solvent resistance of poly(9-vinylcarbazole), suppressing interfacial defect densities and nonradiative recombination processes in the emissive perovskites. PeLEDs based on the methyl-containing SAMs exhibit ∼30% enhancement in efficiency. These findings contribute to a better understanding of the design of SAM materials for PeLED applications.

Green HPLC Enantioseparation of Chemopreventive Chiral Isothiocyanates Homologs on an Immobilized Chiral Stationary Phase Based on Amylose tris-[(S)-α-Methylbenzylcarbamate

Sulforaphane is a chiral phytochemical with chemopreventive properties. The presence of a stereogenic sulfur atom is responsible for the chirality of the natural isothiocyanate. The key role of sulfur chirality in biological activity is underscored by studies of the efficacy of individual enantiomers as chemoprotective agents. The predominant native (R) enantiomer is active, whereas the (S) antipode is inactive or has little or no biological activity. Here we provide an enantioselective high-performance liquid chromatography (HPLC) protocol for the direct and complete resolution of sulforaphane and its chiral natural homologs with different aliphatic chain lengths between the sulfinyl sulfur and isothiocyanate group, namely iberin, alyssin, and hesperin. The chromatographic separations were carried out on the immobilized-type CHIRALPAK IH-3 chiral stationary phase with amylose tris-[(S)-methylbenzylcarbamate] as a chiral selector. The effects of different mobile phases consisting of pure alcoholic solvents and hydroalcoholic mixtures on enantiomer retention and enantioselectivity were carefully investigated. Simple and environmentally friendly enantioselective conditions for the resolution of all chiral ITCs were found. In particular, pure ethanol and highly aqueous mobile phases gave excellent enantioseparations. The retention factors of the enantiomers were recorded as the water content in the aqueous-organic modifier (methanol, ethanol, or acetonitrile) mobile phases progressively varied. U-shaped retention maps were generated, indicating a dual and competitive hydrophilic interaction liquid chromatography (HILIC) and reversed-phase liquid chromatography retention mechanism on the CHIRALPAK IH-3 chiral stationary phase. Finally, experimental chiroptical studies performed in ethanol solution showed that the (R) enantiomers were eluted before the (S) counterpart under all eluent conditions investigated.

Highly efficient and selective hydrogenation of furfural to furfuryl alcohol and cyclopentanone over Cu-Ni bimetallic Catalysts: The crucial role of CuNi alloys and Cu+ species

The selective hydrogenation of furfural derived from biomass is of significant importance in the synthesis of valuable chemical compounds. In this work, Cu-Ni bimetallic catalysts with varying metal ratios were effectively synthesized using the urea deposition method and employed in catalytic hydrogenation of furfural (FA) to furfuryl alcohol (FOL) and cyclopentanone (CPO) in different solvents. The study revealed that the synergistic interaction between Cu and Ni favors the formation of CuNi alloys, thereby facilitating the reduction of CuO and NiO and resulting in larger amount of metallic species (Cu0/+ and Ni0), and promoting the formation of highly dispersed nanoparticles. Moreover, the formed Cu+ species can serve as Lewis acid sites and improve the adsorption of polarized C = O, thus significantly enhancing the selectivity to FOL. More importantly, the cooperation between Cu+ species and water can promote the aqueous-phase hydrogenation-rearrangement (AP-HR) of FA to CPO. Also, in-situ/on-line DRIFTS shows that Cu3Ni1/SiO2 preferentially adsorbs and activates C = O and prefers to form 4-hydroxy-2-cyclopentenone (HCP), which is the key intermediate to form CPO. DFT calculations agree with the in-situ/on-line DRIFTS, showing that Cu3Ni1 (111) crystal surface with the lowest d-band center and the strongest electronic effects presents the highest adsorption energies of H2, H2O, and FA, the lowest adsorption energies of H*, FOL, and CPO, and the lowest energy barriers of Piancatelli rearrangement of FOL to HCP. Under the optimum conditions, Cu3Ni1/SiO2 gives 99.9 % yield to FOL at 333 K in isopropanol and 96.7 % yield to CPO at 413 K in water. The low cost and high activity of Cu3Ni1/SiO2 make it a potential catalyst for the green production of FOL and CPO in industry.

Unveiling the dissolution behavior of letrozole in fourteen pure solvents: Insights from experiments and molecular simulations

The dissolution behavior of an active pharmaceutical ingredient (API) in different solvents is of great importance for the design and optimization of its crystallization process. In this study, the solubility of letrozole in fourteen pure solvents was determined using a gravimetric method within the temperature range of 283.15–323.15 K at atmospheric pressure. The results demonstrate a significant correlation between letrozole’s dissolution behavior and the molecular structure (carbon chain length and presence of branched chains) and properties (dielectric constant and cohesive energy density) of the solvent. Solubility analysis and simple crystallization experiments suggest that acetonitrile may serve as a suitable solvent for the cooling crystallization of letrozole. To enhance the applicability of solubility data, five mathematical models were employed for data fitting. In addition, the Van’t Hoff equation was utilized to calculate the apparent thermodynamic properties of the letrozole dissolution process. Furthermore, molecular simulations were conducted to investigate the dissolution behavior of letrozole in different solvents, revealing distinct patterns of interaction between solute and solvent molecules. Specifically, in alcohol solvents, alcohol ether solvents, and acetonitrile, solute molecules interact with solvent molecules primarily as hydrogen bond acceptors, whereas the opposite behavior is observed in ester solvents and acetone. Binding energy, radial distribution function (RDF), and coordination number (CN) analyses effectively elucidate the dissolution behavior of letrozole in solvents of the same category, indicating that stronger solute–solvent interactions result in higher solubility. A comprehensive examination of solute–solvent and solvent–solvent interactions offers a rational explanation for letrozole’s dissolution behavior in solvents of different categories, highlighting the decisive impact of solvent–solvent interactions, particularly in alcohol solvents and acetone.

Deep-eutectic-solvent modulation of self-assembled multi-responsive films based on polyvinyl alcohol/cellulose nanocrystal and grape skin red for highly sensitive food monitoring

To enhance the mechanics performance, sensitivity and response range of multi-responsive photonic films, herein, a facile method for fabricating multi-responsive films is demonstrated using the evaporative self-assembly of a mixture of grape skin red (GSR), cellulose nanocrystal (CNC), polyvinyl alcohol (PVA) and deep eutectic solvent (DES). The prepared materials exhibited excellent thermal stability, strain properties, solvent resistance, ultraviolet (UV) resistance and antioxidant activity. Compared to a pure PVA film, the presence of GSR strengthened the antioxidant property of the film by 240.1 % and provided excellent UV barrier capability. The additional cross-linking of DES and CNC promoted more efficient phase fusion, yielding a film strain of 41.5 %. The addition of hydrophilic compound GSR, wetting and swelling due to the DES and the surface inhomogeneity of the films rendered the multi-responsive films high sensitivity, wide response range and multi-cyclic stability in environments with varying pH and humidity. A sample application showed that a PVA/CNC/DES film has the potential to differentiate between fresh, sub-fresh and fully spoiled shrimps. The above results help in designing intelligent thin film materials that integrate antioxidant properties, which help in monitoring the changes in food freshness and food packaging.

Efficiency enhancement of non-fullerene organic solar cells using PEDOT:PSS diluted with alcohol solvents as the hole transport layer

The poly3,4-ethylenedioxythiophene) poly(styrene sulfonate) (PEDOT:PSS) hole transport layer (HTL) has always played a crucial role in achieving high-efficiency organic solar cells (OSCs) owing to its unique advantages of suitable energy levels and high optical transparency. However, the inherent insulation and easy aggregation property of PSS results in relatively low conductivity and high surface roughness of the PEDOT:PSS film, which is unfavorable for charge transport and the morphology of the top layer. To address these problems, we use PEDOT:PSS diluted in a series of alcoholic solvents and evaluate them on the PM6:Y6 system. Among these, the PM6:Y6 devices using PEDOT:PSS modified with ethanol as the HTL demonstrate the best vertical phase segregation and carrier extraction. In addition, the PEDOT:PSS film with added ethanol also has the smoothest surface compared to those diluted in the other alcoholic solvents. Finally, a high power conversion efficiency of 18.13% was obtained with the PM6:Y6 devices based on PEDOT:PSS modified by ethanol. This work provides a sufficient reference for the alcoholic modification of PEDOT:PSS and also proposes a feasible solution for high-efficiency OSCs.

Ti3AlC2 MAX Phase Modified Screen-Printed Electrode for the Fabrication of Hydrazine Sensor.

Hydrazine is considered a powerful reducing agent and catalyst, showing diverse applications in agricultural industries, toxic degradation research, and wastewater management. Additionally, hydrazine can trigger some specific reactions when combined with suitable oxidants. Due to its highly polar nature, hydrazine can easily dissolve in alcohol, water, and various other polar solvents. Therefore, it can be extensively utilized in different areas of application and industries such as rocketry and various chemical applications. Despite its beneficial properties, hydrazine is unstable, posing significant risk due to its highly toxic nature. It is extremely hazardous to both human health and the environment. It can cause various illnesses and symptoms such as dizziness, temporary blindness, damage to the central nervous system, and even death when inhaled in sufficient quantities. Therefore, it is highly important to monitor the level of hydrazine to prevent its toxic and hazardous effects on human beings and the environment. In the present study, we discuss the simple fabrication of a disposable cost-effective and eco-friendly hydrazine sensor. We used a screen-printed carbon electrode, i.e., SPCE, as a base for the construction of a hydrazine sensor. The Ti3AlC2 MAX has been used as a suitable and efficient electrode material for the fabrication of disposable hydrazine sensors. We modified the active surface of the SPCE using a drop-casting approach. The resulting Ti3AlC2 MAX modified SPCE (Ti3AlC2@SPCE) has been utilized as an efficient and low-cost hydrazine sensor. Cyclic voltammetry, i.e., CV, and linear sweep voltammetry, viz., LSV, was employed as a sensing technique in this study. The optimization of pH and electrode material loading was conducted. The Ti3AlC2@SPCE exhibited excellent sensing performance toward hydrazine oxidation. A reasonable detection limit (0.01 µM) was achieved for hydrazine sensing. The fabricated sensor also demonstrated a reasonable linear range of 1-50 µM. This work provides the design and fabrication of simple disposable Ti3AlC2@SPCE as a suitable electrode for the determination of hydrazine using LSV technology.

Experimental and Theoretical Rotational Diffusion Studies of 7DM4M1M1,8, N-2(1H)-one and 7A4T2H1B-2-one in Series of Alcohol Solvents: Stoke's-Einstein-Debye and Alavi-Waldeck Models.

Rotational diffusion studies of two solutes 7-(dimethylamino)-4-methoxy-1-methyl-1,8-naphthyridin-2(1H)-one (7DM4M1M1,8, N-2(1H)-one) and 7-amino-4-(trifluoromethyl)-2H-1-benzopyran-2-one (7A4T2H1B-2-one) having equal volumes but different chemical natures are studied in series of alcohol solvents at 303K using steady-state methods. HOMO-LUMO, Electron density, Molecular electrostatic potential (MEP), etc., are obtained from computational calculations using Gaussian 09 software. Rotational reorientation times of 7DM4M1M1,8, N-2(1H)-one solute molecule is found to be less than 7A4T2H1B-2-one solute molecule indicates it rotates slowly in chosen solvents. Stoke's-Einstein-Debye (SED) model with stick boundary conditions for the 7A4T2H1B-2-one solute molecule is modeled to describe mechanical friction. Polar solutes along with mechanical friction also experience dielectric friction. Both these frictions being non-separable, the Alavi-Waldeck (AW) model is studied for dielectric friction contribution to the total friction solute experiences in solvents. AW model effectively explains the observed dielectric friction in alcohol solvents.

Synthesis and pyrolysis of polyacrylate-supported flavor precursors

Herein we present a novel ‘polymerization strategy’ aimed at synthesizing flavor precursors, with a focus on enhancing their thermal stability and release properties. Three volatile flavors, menthol, methyl cyclopentenolone, and ethyl maltol, are reacted with acryloyl chloride to produce corresponding vinyl monomers. These monomers undergo radical polymerization to form homopolymers (P1−P3). To improve solubility in alcohol solvents, a hydrophilic oligoethylene glycol monomer is introduced, copolymerized with the flavor containing monomers, resulting in copolymers (P4−P6). An important advantage of these polymers lies in their significantly enhanced thermal stability, exhibiting an increase of approximately 100 to 200 °°C compared to small molecular flavors. Furthermore, our methodology enables efficient release of the target flavors upon heating, as evidenced by online analyses of volatiles from pyrolysis using fixed-bed reactor combined with single photoionization mass spectrometry (FBR-SPIMS) and pyrolysis-gas chromatography-mass spectrometry (Py-GC–MS). This work represents a practical and innovative approach to improving the thermal stability of volatile flavors and elevating their release temperature, offering promising applications in high-temperature food processing and tobacco industries.

Tuning Mechanical Characteristics and Permeability of Alginate Hydrogel by Polyvinyl Alcohol and Deep Eutectic Solvent Addition.

Alginate-based hydrogels are widely utilized for various applications, including enzyme immobilization and the development of drug delivery systems, owing to their advantageous characteristics, such as low toxicity, high availability and cost-effectiveness. However, the broad applicability of alginate hydrogels is hindered by their limited mechanical and chemical stability, as well as their poor permeability to hydrophobic molecules. In this study, we addressed the mechanical properties and chemical resistance of alginate hydrogels in a high-pKa environment by the copolymerization of alginate with polyvinyl alcohol (PVA). The addition of PVA resulted in a threefold improvement in the shear modulus of the copolymeric hydrogel, as well as enhanced chemical resistance to (S)-α-methylbenzylamine, a model molecule with a high pKa value. Furthermore, we addressed the permeability challenge by introducing a betaine-propylene glycol deep eutectic solvent (DES) into the PVA-alginate copolymer. This led to an increased permeability for ethyl 3-oxobutanoate, a model molecule used for bioreduction to chiral alcohols. Moreover, the addition of the DES resulted in a notable improvement of the shear modulus of the resulting hydrogel. This dual effect highlights the role of the DES in achieving the desired improvement of the hydrogel as an immobilization carrier.

Study on the molecular interactions of binary mixtures of allyl alcohol and amino-alcohol solvents through thermodynamic properties and FT-IR spectra and correlation with the Jouyban–Acree model

ABSTRACT Densities (ρ), speeds of sound (u), and viscosities (η) for three binary mixtures of allyl alcohol with 3-amino-propan-1-ol, 2-amino-2-methyl-propan-1-ol (aminomethyl propanol), and 1-amino propan-2-ol (isopropanol amine) were calculated at temperatures ranging from 303.15 to 313.15K and at atmospheric pressure over the entire composition range. Experimental measurements were used to calculate the excess molar volume, excess isentropic compressibility, deviation in viscosity, and excess Gibbs free energy of the activation of viscous flow. Partial molar properties and partialmolar properties at infinite dilution are also calculated. The Prigogine–Flory–Patterson (PFP) theory is applied to identify the predominant molecular interaction. The results of the Jouyban–Acree model are discussed in terms of the mean relative deviation (MRDs) and individual relative deviation (IRD) between the calculated and experimental parameters as an accuracy criterion. FTIR studies have also been added to confirm the experimental findings of the investigated mixtures.

Modification of ramie fibre with a mixture of NaOH solution and iso-propanol solvent for enhancing its dyeing performance

Deep shade dyeing of ramie fibre is challenging due to its high degree of polymerisation, orientation, and crystallinity. The present work involved pre-treating ramie fibre with a solution containing a mixture of NaOH and alcohol in order to improve its dyeing ability. Based on the first screening results, it has been shown that iso-propanol is the optimal alcohol solvent for modifying ramie fibres with a mixture of NaOH solution, resulting in greater levels of dye exhaustion (E%), dye fixation rate (F%), total dye fixation efficiency (T%), and K/S values. Subsequently, the orthogonal array experimental technique (L16) was utilised to optimise the treatment conditions, and it was determined at a temperature of 25 °C, using a NaOH solution with a concentration of 140 g/L, a liquid ratio of 1:2 for the volume ratio of NaOH solution to iso-propanol solvent, and a treating period of 3 min. The treated samples were subjected to a range of analytical techniques, including XRD, FTIR, TGA, and SEM; these analyses conclusively verified that the samples' properties were altered due to the optimal combination treatment. The combination solution-treated samples had significantly higher barium values compared to the other samples, suggesting an ideal mercerisation treatment. The colourfastness to washing values exhibited satisfactory results for the treated samples. Besides, a handle assessment of raw ramie fabric and treated ramie fabric was conducted to enhance the practical application feasibility.

Shape-controllable preparation of covalent organic frameworks and their application in efficient removal of aromatic organic pollutants

Covalent organic frameworks (COFs), as well-ordered porous materials, have garnered considerable attention in the adsorption of environmental contaminants due to their long-range ordered crystal structure, great specific surface area, etc. In this work, alcoholic solvents were used as the reaction media to successfully synthesize three COFs with regular crystalline structures under nearly ambient conditions, whereas conventional synthetic techniques have not been documented for the synthesis of TAPB-TFPT COFs. Inspired by the excellent physical and chemical properties of the generated rod-like TAPB-DHTP COFs, which can be served as an ideal solid adsorbent for aromatic organic pollutant adsorption and removal. It is worth mentioning that TAPB-DHTP COFs showed fast adsorption kinetic rates (within 40 min) and high adsorption capacities (288 mg/g, 87.7 mg/g and 105 mg/g) for naphthalene, 2-naphthol and 2-naphthylamine, superior to most reported adsorbents. The effective removal of aromatic organic pollutants is ascribed to numerous non-covalent interactions between targets and TAPB-DHTP COFs, including π-π interactions and hydrogen bonding. Thus, this research might present a promising route to the green preparation of COFs and their prospective application in environmental restoration.

Improving the dyeability of ramie fibre by sequential alkaline and alcohol pretreatments

The high crystallinity of ramie fibre poses challenges in achieving optimal dyeing performance, such as reduced dye exhaustion. To enhance the dyeing capabilities of ramie fibre, several alterations were experimented with, such as caustic mercerization using a NaOH solution. However, because of the high NaOH concentration, removing the NaOH residue from inside the fibre becomes challenging. Herein, the present research aims to enhance the dyeing efficiency of ramie fibre by using sequential alkaline and alcohol pretreatment methods to reduce NaOH usage, accordingly relieving the wash process stress. The preliminary screening findings have revealed that iso-butanol is the most suitable alcohol solvent for modifying ramie fibres after treating it with NaOH solution since it leads to higher dye exhaustion (E%, 95.7%), dye fixation rate (F%, 88.2%), total dye fixation efficiency (T%, 84.4%), and K/S values (41.4). After that, the orthogonal array experimental scheme (L16) was applied to optimize dyeing performance. The NaOH usage was decreased to 160 g/L, the treating time was reduced to 3 min, and the dyeing performance of ramie fibre treated under the optimum conditions was better than that of a caustically mercerized one. It was determined that the NaOH concentration factor had the most contribution, accounting for 75.34% of the observed effects. The NaOH solution temperature factor followed closely behind, contributing 22.69%. Additionally, using analytical methods such as XRD, FTIR, TG, and SEM confirmed that the sequential treatment with the optimum conditions altered the structural behaviour of the original ramie fibre, which performances were similar to the mercerized ramie fibre. The barium value of sequentially iso butanol solvent treated fibre showed a greater level (213) compared to caustic mercerized fibre (179), indicating a significant advantage of mercerization performance was achieved. This advantage may be linked to improved colourfastness and handling qualities. Furthermore, the breaking force of both ramie fabrics was increased after the alkaline treatment and the sequential alkaline and iso-butanol treatment.

Promotion of Water as Solvent in Amination of 4-Chloropyrrolopyrimidines and Related Heterocycles under Acidic Conditions.

A switch of reaction medium from organic solvents to water can improve the safety and lower the cost of production processes. Hydrochloric acid-promoted amination of fused pyrimidines has been studied using 4-chloro-7H-pyrrolo[2,3-d]pyrimidine and aniline as model compounds. Higher rate was observed in water than in four alcoholic solvents and DMF. An important aspect is that the amount of acid should be kept low to minimize the competing solvolysis. The substrate scope for the amination in water was evaluated by reacting 4-chloro-7H-pyrrolo[2,3-d]pyrimidine with 20 aniline derivatives with variance in steric and electronic properties. Preparative useful reactions were seen for 14 of the 20 derivatives. Unsuited nucleophiles are ortho-substituted anilines with a pKa below 1. Amination of the corresponding quinazoline, thienopyrimidine, and purine also proceeded well in water. Highly lipophilic and crystalline compounds are more efficiently aminated in 2-propanol. Aliphatic and benzylic amines react poorly under acidic conditions, but these aminations can be done in water without acid.

Role of oxophilic metal ions (Mo, Zr, Ti) impregnated Ni/γ-Al2O3 catalysts for hydrothermal liquefaction of kraft lignin

In this study, the effect of oxophilic metal ions (Mo, Zr, and Ti) loaded Ni/γ-Al2O3 (Al) catalysts was explored for the first time for the hydrothermal liquefaction of kraft lignin using IPA for 30 min/280 °C. The liquefaction of lignin was noticed to be 65.4 wt% with 10 wt% loaded Ni/Al with an 81.3% total conversion. The performance of Ni/Al was enhanced remarkably by using the oxophilic metal ions as promoters owing to an increase in the Lewis character of the catalyst's surface. The bio-oil yield was a maximum of 72 wt% with a 91.5% conversion using 3 wt% loaded Ti–10Ni/Al. The different alcoholic solvents such as methanol, ethanol, and IPA were also examined for the same. However, the best liquefaction was noticed with IPA owing to better H-donor tendency. Additionally, a series of IPA-water co-solvent examinations attributed to a significant improvement in the liquefaction to 74.8 wt% (50:50) IPA-water system. The optimum catalyst 10Ni–3Ti/Al was tested for four catalytic cycles, which indicated a slight loss in the catalytic activity because of blockage of the catalytic active site by char deposition. The GC-MS investigation of optimum catalytic bio-oil showed the highest selectivity of acetosyringone (68.5%) and 2-methoxy-phenol (22.8%), which was observed to be only 30.1 and 5.1% for non-catalytic bio-oil. The 1H NMR and FT-IR investigation of raw lignin and bio-oil proved the breakage of lignin's 3D structure into respective G-and S-type monomeric compounds. Additionally, catalysts were characterized using the XRD, BET, and XPS analysis.

Changing absorption intensity ratios for methylene violet Bernthsen in normal alcohols and at different temperatures

Absorption spectra of methylene violet Bernthsen (MVB) are reported, obtained in normal alcohols, methanol through 1-octanol, and at different temperatures, 15 °C to 75 °C. Two distinct absorption intensities are apparent. The 565 nm intensity increases relative to the 598 nm intensity as alcohol chain length increases. For each solvent, increasing temperature causes similar intensity ratio effects. Computational spectra of MVB in methanol indicates a decrease in hydrogen-bonding as temperature increases with a corresponding loss of intensity in the low energy peak consistent with the experimental observations. Hydrogen-bonding is indicated as playing a role in the alcoholic solvent effects.

Ligand effects, solvent cooperation, and large kinetic solvent deuterium isotope effects in gold(I)-catalyzed intramolecular alkene hydroamination.

Kinetic studies on the intramolecular hydroamination of protected variants of 2,2-diphenylpent-4-en-1-amine were carried out under a variety of conditions with cationic gold catalysts supported by phosphine ligands. The impact of ligand on gold, protecting group on nitrogen, and solvent and additive on reaction rates was determined. The most effective reactions utilized more Lewis basic ureas, and more electron-withdrawing phosphines. A DCM/alcohol cooperative effect was quantified, and a continuum of isotope effects was measured with low KIE's in the absence of deuterated alcoholic solvent, increasing to large solvent KIE's when comparing reactions in pure MeOH to those in pure MeOH-d4. The effects are interpreted both within the context of a classic gold π-activation/protodeauration mechanism and a general acid-catalyzed mechanism without intermediate gold alkyls.

Hydrophilic sol-gel TiO2 coating on procaine-loaded injector needle for painless clinical treatments

Titanium dioxide (TiO2) coatings are demanded in clinical applications due to their biocompatible, porosity, and semiconducting properties. Drug release studies take advantage of these unique aspects of TiO2 for painless injection for those who have to take medicine through the injection frequently. In this study, TiO2 was prepared via the sol-gel method with Titanium tetra isopropoxide (TTIP) precursor in alcohol solvent for pH 3, 4, and 5 values. The prepared solution was coated on stainless steel substrates and injectors via dip coating. Following these steps, samples were calcinated at various temperatures (100°C, 300°C, 500°C, 700°C). The structural, physical, and chemical composition, chemical bond, wettability, and drug-release properties of coated samples were researched. Contact angle values affirmed that high temperatures and ultraviolet (UV)-light irradiation made samples more hydrophilic (26°±5° at 700°C for pH 4). Procaine, a short-time period local anaesthetic, was chosen as a model drug. Increased calcination temperature and raised hydrophilicity led to improve the released drug amount. Drug release studies were carried out using Franz diffusion cells at 36.5°C. Samples at 500°C calcinated released the highest amount of drug (90%) for 45 sec injection time. This study shed light on how TiO2 coating can be successfully utilized for clinical applications in the future.

Solvothermal synthesis of bismuth-based halide perovskites: Investigating the influence of alcohol solvents on photocatalytic performance

Our study explores the effect of different solvents on the synthesis of bismuth-based halide perovskite (BHP) crystals with distinct morphologies. BHP crystals were successfully synthesized using various alcohol solvents, including ethanol (EtOH), butanol (BuOH), ethylene glycol (EG), glycerol (GL), and without the use of alcohol solvents. The choice of solvent acted a crucial role in shaping the nucleation and growth of BHP crystals, as it affected key solvent characteristics, including dielectric constant, ion-coordination, and atomic chain length. The resulting BHP crystals exhibited varying geometrical and structural features, which, in turn, significantly impacted their photophysical properties and photocatalytic activity for the degradation of organic pollutants under visible light irradiation. The introduction of EtOH into the synthesis process led to larger crystallite sizes and an increased adsorption of oxygen molecules on BHP, thereby enhancing the separation of photo-excited electrons and holes. Consequently, the photodegradation efficiency of rhodamine B achieved an impressive 99.6% after 30 min of irradiation. The degradation rate of tetracycline hydrochloride over BHP photocalysts followed this order: mesoporous structure with strong agglomeration of particles (EtOH) > irregular agglomerates composed of spherical particles (BuOH) > irregular clusters of sheets (EG) > thick plates (GL) > flower-like agglomerates (without the use of an alcohol solvent). Our evaluation considered changes in morphological characteristics, surface properties, and photon absorption capacities of the BHP crystalline structures. This study provides valuable insights into the role of various alcohol solvents in tailoring the structure and improving the photocatalytic performance of BHP photocatalyst synthesized through the solvothermal route.