Isopropanol Research Articles

Influence of WO3 Content in Phosphated Tungsten-Zirconium Oxide Catalysts on the Catalytic Pathways of Glycerol Transformation.

The catalytic performance of phosphate-stabilized WOx-ZrO2 compositions in gas-phase glycerol dehydration has been investigated. Results show that varying WO3 concentrations direct the process towards either acrolein or allyl alcohol formation. Catalysts with low WOx content exhibit strong Lewis acid sites (Zr4+ and W6+), where these metal ions likely function as redox sites, facilitating glycerol hydrogenolysis to produce allyl alcohol. Higher WO3 concentrations (exceeding 20 wt.%) lead to the shielding of some W6+ and Zr4+ sites by polytungstate surface complexes, which are strong Brønsted acid sites. This alteration promotes glycerol dehydration through the removal of two water molecules, thereby shifting the selectivity towards acrolein formation.

Ruthenium-Catalyzed Synthesis of 2-Pyrazolines via Acceptorless Dehydrogenative Coupling of Allylic Alcohols with Hydrazines.

Described herein is the synthesis of 2-pyrazolines via acceptorless dehydrogenative coupling of allylic alcohols with hydrazines based on a Ru3(CO)12/NHC-phosphine-phosphine ligand L catalytic system. The reaction not only exhibits low catalyst loading (only 0.3 mol %), wide substrate scope, good to excellent yields, and high selectivity but also omits the use of sacrificial hydrogen acceptor with only H2 and H2O as byproducts, making the reaction green and atom-economical.

Enantioselective Synthesis of Axially Chiral Allylic Nitriles via Nickel-Catalyzed Desymmetric Cyanation of Biaryl Diallylic Alcohols.

Axially chiral nitriles are common motifs in organic photoelectric materials, biological compounds, and agrochemicals. Unfortunately, the limited synthetic approaches to axially chiral nitriles have impeded their availability. Herein, we report the first nickel-catalyzed desymmetric allylic cyanation of biaryl allylic alcohols for the synthesis of axially chiral nitrile structures in high yields with excellent enantioselectivities (up to 90% yield and >99% ee). This process enables the synthesis of a diverse range of axially chiral allylic nitriles bearing β,γ-unsaturated alcohol moieties. Leveraging the allylic alcohol and cyano groups as versatile functionalization handles allow for further derivatization of these axially chiral frameworks. Density functional theory (DFT) calculations suggest that both steric and electronic interactions play crucial roles in determining the enantioselectivity of this transformation. Moreover, this mild and facile protocol is also applicable for gram-scale preparation of the chiral nitriles.

Enantioselective Synthesis of Axially Chiral Allylic Nitriles via Nickel‐Catalyzed Desymmetric Cyanation of Biaryl Diallylic Alcohols

Axially chiral nitriles are common motifs in organic photoelectric materials, biological compounds, and agrochemicals. Unfortunately, the limited synthetic approaches to axially chiral nitriles have impeded their availability. Herein, we report the first nickel‐catalyzed desymmetric allylic cyanation of biaryl allylic alcohols for the synthesis of axially chiral nitrile structures in high yields with excellent enantioselectivities (up to 90% yield and >99% ee). This process enables the synthesis of a diverse range of axially chiral allylic nitriles bearing β,γ‐unsaturated alcohol moieties. Leveraging the allylic alcohol and cyano groups as versatile functionalization handles allow for further derivatization of these axially chiral frameworks. Density functional theory (DFT) calculations suggest that both steric and electronic interactions play crucial roles in determining the enantioselectivity of this transformation. Moreover, this mild and facile protocol is also applicable for gram‐scale preparation of the chiral nitriles.

Morphology and elemental composition of titanium powders for additive machines obtained by electrospark dispersion of OT4 alloy metal waste in propyl alcohol

Morphology and elemental composition of titanium powders for additive machines obtained by electrospark dispersion of OT4 alloy metal waste in propyl alcohol

PTFE layer formation during brush electroplating of nickel

Brush electrodeposition of Ni/PTFE composite coatings was explored using a nickel high speed solution and polytetrafluoroethylene (PTFE) particles 6–9 μm in diameter. A novel bilayer-like, partially intercalated structure was produced, consisting of a rough nickel sublayer covered by an outer, compact, smooth PTFE layer. The study of the coating growth revealed that the PTFE particles bind together on the nickel coating valleys and grow until all the surface is covered by a polymer layer without the need of a baking stage. The resulting coating presents a hydrophobic surface with a low coefficient of friction (0.10) and higher corrosion resistance to salt spray testing than the nodular nickel coating. The coatings were produced using an aqueous nickel plating solution, where the hydrophobic PTFE particles were suspended using different substances: cetrimonium bromide (CTAB) cationic surfactant, isopropyl alcohol premixed with the particles, and ethanol premixed with the particles. High concentrations of the suspending products were detrimental for the deposition process, but optimal values of 0.1 g/l, 3 ml/l and 3 ml/l respectively were found. All compounds successfully suspended the PTFE particles and both alcohols produced the Ni/PTFE coating described before, but the CTAB failed to co-deposit the polymer.

Preparation and performance evaluation of CNF‐enhanced polyether‐modified polysiloxane defoamer

AbstractIn this article, polyether‐modified polysiloxanes were synthesized by the reaction of poly(methyl hydrogen siloxane) (PMHS) with Allyl alcohol polyether B‐400. FT‐IR, laser particle size analysis, hydrophilic–lipophilic balance (HLB) value test, and surface tension measurements were used to characterize its structures and properties. The results show that the control law for the HLB value of polyether‐modified polysiloxanes was obtained as follow: the HLB value increases with increasing hydrogen content of PMHS. When the polyether‐modified polysiloxanes were used to emulsify the polysiloxane, at the HLB value of 10.5, the average particle size of the emulsion was about 0.23 μm with a narrow particle size distribution. The emulsion has good emulsifying and dispersing properties, as well as excellent foam elimination and foam inhibition performance. When the cellulose nanofibrils (CNF) was used as a protective agent for the preparing of the polysiloxane defoamer, the stability of the emulsion does not affect, but its foam elimination and foam inhibition of emulsion can be further improved at the presence of CNF. The lowest surface tension of CNF‐enhanced polyether‐modified polysiloxane defoamer is about 22.4 mN m−1, which has good surface property. When the concentration of CNF‐enhanced polyether‐modified polysiloxane defoamer was 0.1 g L−1, the foam elimination time and foam inhibition time were 5.8 s and 38 min, respectively, at the temperature (80°C) and alkali environment (pH 13).

Energy-efficient heat pump-assisted pre-concentration integrated with sequential [EMIM][BF4] and ethylene glycol-based extractive distillation for enhanced recovery of ethanol and isopropyl alcohol from wastewater

Recovering ethanol and isopropyl alcohol (IPA) from wastewater offers significant economic and environmental advantages. In this work, 1-ethyl-3-methylimidazolium tetrafluoroborate ([EMIM][BF4]) and ethylene glycol (EG) are proposed as double entrainers for separating IPA/ethanol/water mixtures. The novel process sequentially uses [EMIM][BF4] to separate ethanol/water and IPA/water azeotropes, followed by EG for near-boiling mixture of ethanol/IPA. Energy-economic comparisons of extractive distillation process using single and double entrainers are performed. To address the issue of high water content in mixtures, the heat pump-assisted pre-concentration (HPP) integrated with extractive distillation processes are proposed. Subsequently, the effect of water content in the mixtures on process performances are analyzed. The results indicate that compared to using a single entrainer [EMIM][BF4] or EG process, the double entrainers process reduces energy cost and total annual cost (TAC) by 19.9% to 45.3% and 18.6% to 52.7%, respectively. The HPP scheme effectively reduces the mole fraction of water from 60% to 26.05%, further decreasing energy costs by 4.2% to 22.2%. The energy cost and TAC of the double entrainers process decreases by 4.8% to 50%, and 2.8% to 52.1% compared with the single entrainer process under HPP schemes. The double entrainers [EMIM][BF4]-EG process shows promising prospects from energy and economic perspectives.

Ni(II)-catalyzed asymmetric alkenylation and arylation of aryl ketones with organoborons via 1,5-metalate shift

Chiral tertiary alcohols are an important structural motif, however, the general and efficient methodologies for their synthesis are less reported. Herein, we report a Ni(ІІ)-catalyzed asymmetric alkenylation and arylation of aryl ketones with organoborons under air via a 1,5-metalate shift strategy to obtain chiral tertiary allylic alcohols and diaryl alcohols. The reaction demonstrates good functional group tolerance and delivers chiral tertiary alcohols with good to excellent results. Furthermore, this method can be applied to the late-stage modification of drugs and the efficient synthesis of natural products. Notably, the reaction proceeds through an outer-sphere mechanism. The Ni(II) complex functions both as a Lewis acid to activate the ketone and create a chiral environment, and as coordination bridge linking the ketone and the organoboron-derived “ate” complex, facilitating the 1,5-metalate shift without forming a C-Ni bond. This approach contrasts with traditional transition metal-catalyzed nucleophilic addition reactions that involve carbon-metal bond formation.

Roles of modified additives in the repair of damaged SiC-ZrB2/SiC coating of carbon/carbon composites

Damaged SiC-ZrB2/SiC (SZS) coatings of carbon/carbon (C/C) composites were repaired using polysiloxane (PSO)-based repair agents. SiC-ZrB2 powder was used as an inert filler, and Al2O3 and isopropyl alcohol (IPA) were introduced as modified additives. The effects of each component of the repair agents on the chemical composition, microstructure, and oxidation behavior of the repaired coatings were investigated, and the repair mechanism was clarified. The repaired area was dense and smooth, showed good compatibility with the original coating, and remained intact after oxidation at 1500 ℃ for 360 min. The addition of Al2O3 promoted the pyrolysis of PSO and formation of β-SiC, which was beneficial to the densification and oxidation resistance of the repaired coatings. The introduction of IPA improved the fluidity of the repair agents, and the repair agents infiltrated the coated C/C composites through the micropores on the damaged surface under capillary action, thereby enhancing the interfacial bonding strength. The weight loss of the damaged coating after oxidation decreased from 21.16 % to 0.48 % after repair. This work offers an approach for optimizing the repair of Si-based ceramic coatings.

Multifunctional Polymer Synthesis via Sequential Postpolymerization Modification Using a Single Aldehyde Repeat Unit: Allylation and Orthogonal Esterification and Thiol-ene Reaction.

Herein, we present a highly efficient method for synthesizing multifunctional polymers. This method involves the sequential postpolymerization modification (PPM) of a highly reactive aldehyde polymer. We introduce an allylic alcohol functionality into the polymer backbone via Barbier-type allylation, a process facilitated by easy-to-handle indium(0) powder. This step enables the formation of orthogonal pendants, secondary alcohol, and terminal alkene, which can be further functionalized through esterification and thiol-ene click reactions. All of these processes are carried out under mild conditions, ensuring high efficiency and a wide range of functional groups. Our study underscores PPM's operational simplicity and versatility in developing advanced polymer materials and expanding the scope of multifunctional polymer design.

Fabrication and Performance Evaluation of a Directly Immersed Photovoltaic-Thermal Concentrator for Building Integration

A novel concentrating photovoltaic-thermal solar collector was designed, fabricated and experimentally investigated at the University of Lleida, in Spain. Two designs based on two dielectric liquids, isopropyl alcohol (IPA) and deionised water (DIW), were developed. In both cases, the solar cells were directly liquid-immersed. The study includes experiments and numerical simulations. The proposed concentrator was incorporated into a testing unit to examine its potential as a façade by controlling light and thermal flux transmitted into a building. The results show promising electrical performance and acceptable thermal performance, with thermal losses ranging from 14 to 20 W °C−1m−2. The optical efficiency was around 73% in the case of the concentrator with DIW and about 76% for the one with IPA. Regarding electrical performance, the fill factors for IPA and DIW configurations are as follows: 62.8% and 61.7%, respectively. The comparison results reveal striking differences between the testing unit with and without solar concentrators, with the concentrator-equipped unit showing around four times lower illuminance and a 50% reduction in maximum heat fluxes and interior temperature. Generally speaking, it can be said that these energy-generating façades show satisfactory behaviour and offer interesting possibilities for building-integrated applications.

Development and Manufacturing Method of Electrodes for a High Temperature Oxygen Sensor

The article discusses the use of zirconium dioxide stabilized with yttria as an electrolyte for the formation of a high-temperature ceramic oxygen concentration sensor. The fundamental possibility of using such a material is due to the high electrical conductivity caused by the mobility of oxygen ions in the vacancies of the solid electrolyte. The operating principle of such a sensor as an electrochemical concentration element is discussed. It has been shown that the use of such sensors is relevant for various industries (including chemical, metallurgical, oil and gas, energy and others). Options for forming electrodes of an electrochemical sensor using various materials and deposition methods are considered. A method for forming a platinum coating using a chemical method using isopropyl alcohol and subsequent pyrolysis was tested. It has been experimentally shown that the chemical method is applicable for the formation of electrodes of an electrochemical sensor. The electrical characteristics of the resulting coatings were measured. The optimal composition of the reaction mixture and the required number of layers to create a stable operating electrochemical sensor have been determined. The dependence of the potential of the formed electrochemical sensor from stabilized zirconium oxide on oxygen concentration in a wide temperature range has been studied. It has been shown that when using a scheme of sequential transformations, hydrolysis of platinum tetrachloride - deposition on a substrate - reductive pyrolysis, it is possible to obtain a high-quality conductive coating for the formation of gas sensor electrodes. The optimal composition of the reaction mixture for the formation of platinum electrodes has been selected. The optimal number of layers was determined to ensure the required level of electrical conductivity of the electrodes. It has been shown that an electrochemical element based on zirconium dioxide and platinum electrodes, formed according to the scheme developed in this work, can be used as a high-temperature oxygen sensor.

Investigation on oxygen vacancy regulation mechanism of ZnO gas sensors under temperature modulation mode to distinguish alcohol homologue gases

Homologous gases are difficult to be detected due to their similar chemical properties, especially for metal oxide semiconductor gas sensors whose selectivity has always been a significant challenge. Dynamic temperature modulation method with periodically changing operating temperature was used to detect alcohol homologous gases. However, there are still problems with the deviceization of heating control circuits. In this paper, dynamic temperature modulated method which needs a simple heating circuit is used to distinguish alcohol homologous gases in combination with oxygen vacancy modulation of ZnO gas sensors. Ethyl alcohol, n-propyl alcohol, isopropyl alcohol and n-butyl alcohol were measured by ZnO gas sensors with different oxygen vacancies content ratios under rectangular wave with a voltage range of 2–6 V. It was found that the greatest difference among the response curves when the material calcined at 600°C which has the largest oxygen vacancies content ratio. Finally, the recognition of the four homologue gases measured by ZnO-600 sensor was achieved by dynamic time warping and the recognition accuracy is 99.33 %.

Pre-procedural Topical Antisepsis in the Neonate: A Systematic Review Evaluating Risk Factors for Skin Injury.

Pre-procedural antisepsis is a critical component of hospital-acquired infection prevention in the neonatal intensive care unit (NICU). However, broadly utilized topical antiseptic agents pose an elevated risk of disruption to neonatal skin integrity, and evidence-based guidelines are lacking. This systematic review of the literature sought to assess and characterize the predisposing risk factors for and types of neonatal skin injury from topical antiseptic agents. A systematic search of Medline Ovid, Embase, Web of Science, CINAHL, and Cochrane Library was conducted, including academic literature providing data on neonatal skin injuries related to topical antisepsis in the NICU. A total of 19 articles (99 patients) met the inclusion criteria. Of the available data, most reported skin injuries were described in extremely preterm (98.1%) and very low birth weight (98.4%) infants. The majority of reported adverse cutaneous events were attributed to chlorhexidine preparations (74.8%), followed by octenidine (18.2%), povidone-iodine (6.1%), and isopropyl alcohol (2.0%). Erythema (40.1%), skin breakdown (23.4%), and chemical burns (17.5%) were the skin reactions reported most frequently, followed by skin irritation (8.3%), and skin necrosis (2.8%). Our findings indicate that both extremely preterm and very low birth weight infants are particularly susceptible to skin toxicities from pre-procedural antiseptic preparations. These data underscore the need for future research to support the development of guidelines which minimize iatrogenic cutaneous injuries in the neonatal population, specifically for the care of infants under 2 months of age, for whom current recommendations are lacking due to a paucity of data.

Effect of Allyl and Propargyl Alcohols on the Equilibrium Conditions of Methane Hydrate Formation

Effect of Allyl and Propargyl Alcohols on the Equilibrium Conditions of Methane Hydrate Formation

Coordination Compounds of Cobalt(II) Nitrate and Perchlorate with Acetamide and Carbamide: Precursors for the Synthesis of Catalytically Active Tricobalt Tetraoxide

The reactions of cobalt(II) nitrate or perchloride with acetamide (AA) or carbamide (Ur) in an aqueous medium produce coordination compounds [Co(Ur)4](NO3)2 (I), [Co(Ur)6](NO3)2 (II), [Co(AA)4(H2O)2](NO3)2 (III), [Co(AA)4(H2O)2](NO3)2 ∙ 2AA (IV), [Co(Ur)6](ClO4)2, (V), [Co(AA)4(H2O)2](ClO4)2 (VI), and [Co(AA)6](ClO4)2 (VII). The compositions of the isolated complexes are determined by physicochemical methods, and the crystal and molecular structures of compounds II, V, VI, and VII are solved. Specific features of the thermal behavior of all synthesized compounds in a wide temperature range are studied in detail. These compounds are shown to be used as precursors in the preparation of nanosized Co3O4 using self-propagating high-temperature synthesis. The catalytic activity of thus synthesized Co3O4 in the model epoxidation of allyl alcohol is studied.

1,2-bis(triethoxysilyl)methane (BTESM)-derived organic–inorganic membranes with controlled sol particle size: Preparation and pervaporation dehydration performance of isopropanol aqueous solutions

1,2-bis(triethoxysilyl)methane (BTESM) is a bridged-type organoalkoxysilane, which was utilized for organic–inorganic membranes preparation via a sol–gel method to achieve high permselectivity, thus are promising for dehydration and purification of organic solvents. However, the particle size of the derived sol is crucial for membrane preparation during sol–gel processing, significantly influencing the membrane’s performance. Herein, we reported a novel strategy of controlling the sol particle size by adjusting the pH during the preparation process. BTESM-derived membranes were prepared by BTESM-H+ sol and BTESM-swing sol, which were subsequently employed for the dehydration of isopropanol (IPA) through pervaporation (PV). Compared with the BTESM-H+ sol, the particle size of the BTESM-swing sol prepared by the pH-swing method was increased from 1.3 nm to 32.7 nm. The larger particle size could hinder the permeation into the intermediate layer. Meanwhile, the dense arrangement of silica particles could efficiently retain IPA molecules, thereby substantially enhancing the rejection rate of IPA. The average particle size of the BTESM-swing sol was 18.7 nm at an acid-base ratio of 1.2 and acid-silicon ratio of 0.55, resulting a permeate flux of 1.04 kg·m−2·h−1 and separation factor of 521, while IPA rejection rate was 97.84 %. This work has shown that adjusting the pH during the process is a useful strategy of controlling the sol size for the preparation of organic–inorganic membranes. Hence, the control of sol particle size to achieve a high-performing membrane layer offers a novel approach to producing diverse membrane materials.

Charge regulated pH/NIR dual responsive nanoplatforms centered on cuproptosis for enhanced cancer theranostics

Multifunctional nanoplatforms capable of simultaneously executing multimodal therapy and imaging functions are of great potentials for cancer theranostics. We present an elegantly designed, easy-to-fabricate poly(acrylic acid)/mesoporous calcium phosphate/mesoporous copper phosphate nanosphere (PAA/mCaP/mCuP NS) with outstanding pH/NIR-sensitive multimodal-synergic anti-tumor effects. Optimal porous PAA NS scaffolds were prepared at room temperature by balancing the intra-PAA polymer and polymer-solvents Lennard-Jones potentials in a water:isopropyl alcohol (IPA) mix-solvent. Subsequent sponging of Ca2+ and Cu2+, and adsorption of PO43− to the PAA template were achieved through exquisite electrostatic interactions among ions and the ionizable PAA side-chain in an aqueous environment. This forms the basis for the tumor microenvironment pH-triggered release of Cu2+ to induce cuproptosis, as well as the photothermal effect originating from CuP, while Ca2+ can enhance the nanoplatform's biocompatibility and can damage mitochondria when overloaded. Lastly, PAA/mCaP/mCuP NSs still exhibit high drug loading efficiency for doxorubicin (DOX), enabling chemotherapy. Satisfactory anti-tumor effects of these modalities, along with their synergistic effects, were verified both in vitro and in vivo, with the NSs demonstrating good biodegradation in the latter. The fabricated NS itself holds great promise as an anti-tumor nanomedicine, and the thorough mechanical insights into NS formation may inspire the design of next-generation multifunctional nanoplatforms.

Enantioselective Separation and Pharmacokinetics of a Chiral 1,4-Dihydropyrimidine Derivative in Rats: A Combined Chromatography and Docking Approach.

Chirality in 1,4-Dihydropyrimidines influences their pharmacological properties and synthetic strategies. Enantiomers of chiral drugs often exhibit different pharmacokinetic profiles. Therefore, separating and studying individual enantiomers is crucial to optimize drug efficacy and safety. Enantiomeric separation of ±4-(4-chlorophenyl)-6-methyl-2-oxo-N-(O-toyl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide (DP-1), which is a 1,4-Dihydropyrimidine derivative is achieved on CHIRALCEL® OD-H column (particle size: 5 μm, inner diameter: 4.6 mm, length:150 mm), following by investigating the kinetic properties of (R) and (S) enantiomers. The separation was achieved with a mobile phase composed of 70% (v/v) isopropyl alcohol and 30% (v/v) n-hexane. For the bioanalytical study, acetonitrile was used to precipitate the rat plasma samples and validated the method according to USFDA guidelines. The validated bioanalytical method was then successfully applied to determine the pharmacokinetic parameters of the drug in biological samples. Molecular modeling techniques, specifically docking simulations, were employed to predict the elution order of DP-1 enantiomers. The docking results revealed moderate binding interactions between the enantiomers and the chiral stationary phase (CSP), which aligns with the theoretical expectation that stronger interactions lead to longer retention times on the column.