Dibutyl Ether Research Articles

Ternary Liquid-Liquid Equilibria in a Few Nonaqueous Two-Phase Systems

AbstractThe composition of coexisting phases for liquid-liquid and solid-liquid-liquid equilibria were measured at 298.2 and 313.2 K and under atmospheric pressure for the following systems: {sodium bromide + formamide + ethyl acetate}, {sodium thiocyanate + ethanol + (R)-limonene}, and {sodium thiocyanate + methanol + dibutyl ether}. These concentrations were determined mainly by chromatography and, for the first system, with the help of argentometric titration. The standard uncertainties in mole fractions varied between 0.001 and 0.008. The tie-line data were reproduced by the NRTL model with medium accuracy. Several empirical equations were used and tested to correlate binodal curves. The rational form of the equation, based on the liquid–liquid–solid tie-line, turned out to be the most adequate.

Experimental Study on Pressure Oscillation Characteristics of Di-N-Butyl Ether in a Constant Volume Vessel

ABSTRACT This paper conducted experimental research on spontaneous pressure oscillation characteristics of di-n-butyl ether (DBE). Based on a constant volume vessel (CVV) with 210 mm in length and 180 mm in diameter, the initial pressure, temperature, and equivalence ratio ranges of 0.05–0.3 MPa, 373–453 K, and 0.7–1.6. The experimental data of combustion pressure, CVV vibration and sound pressure were analyzed. The results indicate that DBE exhibits the strongest pressure oscillation at high pressures, moderate temperatures and equivalence ratios. The highest oscillation intensity is achieved at 0.3 MPa, 433 K, equivalence ratio of 1.4. The vibration and sound pressure signals exhibit the same patterns as combustion pressure signals. Spectrum analysis is conducted by Fast Fourier Transform of pressure signals, it shows that the amplitude of the characteristic frequency increases with the increase of oscillation intensity. In addition, to further reveal the influence of combustion instability on oscillation intensity, the dimensionless parameter Peclet number and critical radius are compared, it shows that the combustion instability has strong effect on pressure oscillation, and diffusive-thermal instability is the key factor that influences pressure oscillation. This study is believed to be beneficial for organizing better combustion for internal combustion engines.

Thermophysical study for Binary mixtures of Dimethyl carbonate with Anisole, Butyl vinyl ether, Diisopropyl ether and Dibutyl ether at 303.15, 308.15 and 313.15 K

Ultrasonic velocity, density and viscosity have been determined for the binary compositions of dimethyl carbonate+ butyl vinyl ether, + diisopropyl ether, + anisole and + dibutyl ether at T= 303.15, 308.15 and 313.15 K. The inventive data is applied to assess the excess molar volume VmE, deviation in viscosity Δη and the acoustical parameters namely isentropic compressibility (Ks), free volume (Vf ), free length (Lf ) and internal pressure (πi). The excess or deviation properties are contoured to the Redlich-Kister polynomials and the outcomes are elucidated in terms of molecular interactions present in compositions.

Measurements and Correlation of Isobaric Vapor–Liquid Equilibria and the Isothermal Surface Tension of the Methyl Butyrate + Dibutyl Ether Binary Mixture

Measurements and Correlation of Isobaric Vapor–Liquid Equilibria and the Isothermal Surface Tension of the Methyl Butyrate + Dibutyl Ether Binary Mixture

Thermophysical and Excess Properties of Binary Mixtures of Dibutyl Ether and Components of Biodiesel

Thermophysical and Excess Properties of Binary Mixtures of Dibutyl Ether and Components of Biodiesel

Exploring alternative fuel solutions: lemon grass oil biodiesel blend with dibutyl ether additive for VCR diesel engines - an experimental analysis

There has been an intense surge in interest in the search for alternative sources of petroleum fuels in the modern world as a result of the inflation of fuel prices and the historic supply gap. When compared to petroleum fuels, biodiesel is becoming an increasingly valuable option due to the fact that it produces less emissions and provides the almost same amount of energy. In point of fact, the prime aim of this work is to explore the possibility of utilizing biodiesel derived from lemongrass oil and including dibutyl ether as an additive for the test diesel engine operating on varied compression ratios. The findings showed that the best operating settings are a 17.5 compression ratio with a blend of 30% biodiesel and 70% diesel fuel. At greater loads, brake thermal efficiency is lower than that of diesel engines. Lower loads result in lower specific fuel usage. Mechanical efficiency at higher loads is highest in the B30 blend, but emission metrics such as CO, CO2, HC, and NOx were reduced with the inclusion of an additive, though HC rose with higher loads of lemongrass oil biodiesel blends. When compared to the B30 biodiesel blend with various composition additives, the B30 + 4% additive has the highest efficiency at the fourth load in terms of both brake power and mechanical efficiency.

Active site requirements for bio-alcohol dehydration: Effect of chemical structure and site proximity

Synthesis-structure-activity relations are reported, describing how interzeolite conversion (IZC) allows synthesis of ZSM-5 (MFI framework) with fixed physicochemical properties, except the variable local acid site (Al) arrangement, by variation of the synthesis time. Local confinement and acidity effects are probed by applying both H-ZSM-5 and Na-ZSM-5 samples in alcohol dehydration. Pyridine and divalent cobalt ion probing are used to quantify the amount of accessible acid sites and of Al in close proximity. Al in close proximity shows a strong influence on n-butanol dehydration turnover rates. The turnover rates are also strongly dependent on local confinement: in Na-form, ZSM-5 synthesized with more Al present as isolated species is a factor of 3–7 times more active than Na-ZSM-5 with fewer isolated Al. However if the zeolites are in proton form, ZSM-5 with more proximate sites show a higher activity compared to ZSM-5 with more isolated sites. Linear butene selectivity increases in Na-ZSM-5 compared to H-ZSM-5, caused by a suppressed dibutyl ether formation. The selectivity towards 1-butene is enhanced to a greater extent on proximate sites, likely due to a local/steric constraint at the active site. Decomposition of DBE over Na-ZSM-5 is more active compared to n-butanol dehydration, independent of acid site proximity. Also for 2-propanol dehydration, Na-ZSM-5 is less active than H-ZSM-5, yet the activity difference is attenuated compared to n-butanol dehydration. Essentially, due to the intrinsic higher reactivity of 2-propanol, the acid site requirement is less stringent. These findings highlight the importance of local confinement and Al proximity in acid-catalyzed conversion of oxygenated compounds.

Lightweight Electrolyte Design for Li/Sulfurized Polyacrylonitrile (SPAN) Batteries.

Sulfurized polyacrylonitrile (SPAN) recently emergesas a promising cathode for high-energy lithium (Li) metal batteries owing to its high capacity, extended cycle life, and liberty from costly transition metals. As the high capacities of both Li metal and SPAN lead to relatively small electrode weights, the weight and specific energy density of Li/SPAN batteries are particularly sensitive to electrolyte weight, highlighting the importance of minimizing electrolyte density. Besides, the large volume changes of Li metal anode and SPAN cathode require inorganic-rich interphases that can guarantee intactness and protectivity throughout long cycles. This work addresses these crucial aspects with an electrolyte design where lightweight dibutyl ether (DBE) is used as adiluent for concentrated lithium bis(fluorosulfonyl)imide(LiFSI)-triethyl phosphate (TEP) solution. The designed electrolyte (d = 1.04g mL-1) is 40%-50% lighter than conventional localized high-concentration electrolytes (LHCEs), leading to 12%-20% extra energy density at the cell level. Besides, the use of DBE introduces substantial solvent-diluent affinity, resulting in a unique solvation structure with strengthened capability to form favorable anion-derived inorganic-rich interphases, minimize electrolyte consumption, and improve cell cyclability. The electrolyte also exhibits low volatility and offers good protection to both Li metal anode and SPAN cathode under thermal abuse.

Green-solvent-processed lead-free perovskite solar cells

Tin-based perovskite has been considered as one of the most potential candidates for lead-based perovskite. The solution proceed method was widely utilized in fabricating tin perovskite solar cells. So far, all fabrication processes for tin perovskite solar cells involved toxic organic solvents, which is contrary to the development of environmentally friendly perovskite solar cells. In this study, we report for the first time, by using a mixed green solvent N-diethyl formamide and green 1,3-dimethyl-3,4,5,6-Tetrahydro-2 (1H)-pyrimidinone as precursor solvent, and a green solvent dibutyl ether as antisolvent, a high-quality FA0.75MA0.25SnI3 film was achieved. The optical band gap of the prepared perovskite layer was 1.36 eV, which was close to the ideal band gap. The green-solution-proceed perovskite films showed reduced defect density. As a consequence, the champion green-solution-proceed photovoltaic device achieved a power conversion efficiency of 4.4%. Moreover, it still maintains 80% of the initial efficiency after 600 h of storage in a nitrogen atmosphere. This work would promote the perovskite solar cells from a ‘new’ technique to a ‘new and green’ technique.

The influence of molecular structure on the oxidation reactivity of long-chain ethers: Experimental observation and theoretical analysis

Long-chain ethers have been proposed as promising biofuels for advanced combustion methods, yet their low-temperature oxidation (LTO) characteristics remain poorly understood. In this study, the LTO reactivities of n-heptane and five long-chain ethers with different structures, including dibutyl ether (DBE), diethylene glycol dimethyl ether (DGM), polyoxymethylene dimethyl ethers (PODE), 1,2-dimethoxyethane (1,2-DME), and dipropyleneglycol dimethyl ether (DPGDE) are investigated using a cooperative fuel research (CFR) engine, which is closer to the actual internal combustion engine operating environment. Products formed from LTO of ethers and n-heptane are investigated over a wide range of compress ratios (CRs), and their relationship to the global oxidation reactivity is suggested based on the quantum chemistry calculation. The presence of oxygen atoms in long-chain ethers significantly enhances oxidation reactivity, with the global oxidation reactivity ranking as follows: DGM > DPGDE > 1,2-DME > DBE > PODE > n-heptane. The key intermediate species generated during the LTO of n-heptane include aldehydes, ketones, and cyclic ethers, while oxygen atoms in ethers facilitate the formation of acids. The species pathway analysis and quantum chemistry calculations reveal that (1,5) and (1,6) H-transfers of alkylperoxy radical (ROȮ) are critical chain-propagation channels, playing pivotal roles in the LTO process. The impact of oxygen on oxidation reactivity can be attributed to two primary factors: accelerating the H-abstraction of ȮH and H-transfer of ROȮ by weakening the neighboring C-H bonds, and enhancing the branching ratio of H-transfer of ROȮ. The arrangement of two oxygen atoms between every two carbon atoms (–OCH2CH2O–) is optimal for oxidation reactivity, while the arrangement of oxygen and carbon (–OCH2OCH2–) weakens the oxidation activity due to fewer available hydrogens for H-transfer. The methyl group in branching-chain, exhibit reduced oxidation reactivity due to the strength of C-H bonds. Additionally, for ethers with the same structure, a longer carbon chain allows for more available hydrogens, resulting in stronger oxidation reactivity.

Enhancing the catalytic performance of H-ZSM-5 in bio n-butanol dehydration by zeolite crystal engineering

NH4F etching is used as an unbiased chemical etching technique to hierarchize commercially available nano-sized ZSM-5 crystals. A structure-function relationship is reported, describing how the introduction of mesoporosity in a microporous ZSM-5 zeolite significantly increases its catalytic performance in (aqueous) n-butanol dehydration. Three parent samples are etched under two severity modes: mild (5 minutes of etching) and harsh (40 minutes of etching). Intrinsic features of the parent ZSM-5’s, such as their silanol populations, influence the outcome of the etching procedure. For all materials, crystallinity is unaffected, total pore volume increases while micropore volume is almost constant, and active site accessibility increases. For all materials, etching increases the catalytic activity for n-butanol dehydration. Cofeeding water to n-butanol further increases the stability of all catalysts. Microkinetic modeling reveals that the increased activity is related to a decreased stability of dibutyl ether (DBE), the most abundant surface intermediate. A decreased DBE adsorption energy, due to the increased accessibility of the acid sites, facilitates its desorption. NH4F etching, a flexible and easy technique to engineer zeolites' textural properties, does not affect the intrinsic nature and quantity of their active sites, leading to superior catalytic performances. Our results highlight the possibility to further increase the efficiency of zeolite catalysis in biomass conversion processes.

Investigation of the effect of ether oxygenated additives on diesel engine performance, combustion, and exhaust emissions - An experimental approach

Conventional energy sources, including diesel and petrol, are decreasing day by day, while their reserves are limited. However, it is difficult to find alternative fuels to replace them. Hence, to fulfill the growing energy demand and reduce environmental emissions, it is vital to find a wide variety of oxygenated compounds to conventional diesel fuels that show low emission potential from transport engines. In this research, we investigated diesel engine performance, combustion, and exhaust emissions with the addition of 10 %, 15 %, 25 %, and 30 % of three different oxygenated blends, including Diethylene Glycol Dimethyl ether (DGM), Di-n-Butyl Ether (DBE), and Tripropylene-Glycol Monomethyl ether (TPGM). This paper presents the brake-specific fuel consumption (BSFC), Brake Thermal Efficiency (BTE), Brake Mean Effective Pressure (BMEP), and Brake Specific Energy Consumption (BSEC) for these fuel blends. The generated emissions of carbon dioxide (CO2), Carbon Monoxide (CO), and nitrogen oxide (NO) were quantified for four different engine speeds of 1500, 1800, 2000, and 2400 rpm for neat (100 %) oxygenated blends. This research also shows the in-cylinder pressure and heat release rate (HRR) of these three oxygenated blends. The outcome of this paper will help future researchers to develop automobiles and vehicles for oxygenated blends with conventional fuels.

Investigating the potential of a higher reactivity fuel to achieve faster heat-up of aftertreatment systems

Shortening the aftertreatment system heat-up period will be crucial to meet upcoming emissions regulations, which mandate significant reductions in tail-pipe emissions for on-road heavy-duty vehicles. This work studies the impact of increasing fuel reactivity on the combustion of post injections during the expansion stroke. The work demonstrates an operating strategy using a blend of di-butyl ether (a potential low-carbon biofuel component) and #2 diesel that achieves higher exhaust enthalpy, while maintaining similar engine-out emissions (NOx and combustion efficiency) in comparison to the baseline #2 diesel fuel (cetane number 41). On average, a 12% increase in exhaust enthalpy was observed for the blend (cetane number 60) relative to the baseline fuel. The ability to operate the higher reactivity fuel at a more retarded post-injection timing, where combustion with #2 diesel was found to be more unstable, and less complete was key to achieving higher exhaust enthalpy. However, a small fuel penalty (∼ 3%–5%) was also associated with the higher reactivity fuel with this operating strategy. The formation of fuel lean regions, due to the long ignition delays at late injection conditions, was predicted to be the leading contributor to the increased emissions of products of partial combustion. Chemical kinetic simulations using surrogates for the fuels used in the experiments, demonstrated the ability of a higher cetane fuel to outperform the baseline fuel under fuel lean conditions with equivalence ratios less than 0.7.

Anion‐Reinforced Solvation Structure Enables Stable Operation of Ether‐Based Electrolyte in High‐Voltage Potassium Metal Batteries

AbstractElectrolytes with anion‐dominated solvation are promising candidates to achieve dendrite‐free and high‐voltage potassium metal batteries. However, it's challenging to form anion‐reinforced solvates at low salt concentrations. Herein, we construct an anion‐reinforced solvation structure at a moderate concentration of 1.5 M with weakly coordinated cosolvent ethylene glycol dibutyl ether. The unique solvation structure accelerates the desolvation of K+, strengthens the oxidative stability to 4.94 V and facilitates the formation of inorganic‐rich and stable electrode‐electrolyte interface. These enable stable plating/stripping of K metal anode over 2200 h, high capacity retention of 83.0 % after 150 cycles with a high cut‐off voltage of 4.5 V in K0.67MnO2//K cells, and even 91.5 % after 30 cycles under 4.7 V. This work provides insight into weakly coordinated cosolvent and opens new avenues for designing ether‐based high‐voltage electrolytes.

Anion-Reinforced Solvation Structure Enables Stable Operation of Ether-Based Electrolyte in High-Voltage Potassium Metal Batteries.

Electrolytes with anion-dominated solvation are promising candidates to achieve dendrite-free and high-voltage potassium metal batteries. However, it's challenging to form anion-reinforced solvates at low salt concentrations. Herein, we construct an anion-reinforced solvation structure at a moderate concentration of 1.5 M with weakly coordinated cosolvent ethylene glycol dibutyl ether. The unique solvation structure accelerates the desolvation of K+, strengthens the oxidative stability to 4.94 V and facilitates the formation of inorganic-rich and stable electrode-electrolyte interface. These enable stable plating/stripping of K metal anode over 2200 h, high capacity retention of 83.0 % after 150 cycles with a high cut-off voltage of 4.5 V in K0.67MnO2//K cells, and even 91.5 % after 30 cycles under 4.7 V. This work provides insight into weakly coordinated cosolvent and opens new avenues for designing ether-based high-voltage electrolytes.

Molecular Interaction Studies of Binary Mixtures of Diethyl Oxalate With Butyl Vinyl Ether, Diisopropyl Ether, Anisole and Dibutyl Ether in Terms of Thermodynamic, Transport and Acoustic Properties

Viscosity, the speeds of sound and density were measured in the binary mixtures of diethyl oxalate with butyl vinyl ether, diisopropyl ether, anisole and dibutyl ether at T = 303.15, 308.15 and 313.15 K. The experimental data were used to calculate the excess molar volume ,deviation in viscosity Δη and the acoustical parameters, namely isentropic compressibility (KS), free volume (Vf ), free length (Lf ) and internal pressure (πi). The excess or deviation properties were fitted to the Redlich-Kister polynomials and the results interpreted in terms of the molecular interactions present in mixtures. Theoretical viscosities were calculated using the Grunberg-Nissan, Lobe and Krishnan-Laddha models before their merits were studied in terms of interaction parameters.

Fabricating Planar Perovskite Solar Cells through a Greener Approach.

High-quality perovskite thin films are typically produced via solvent engineering, which results in efficient perovskite solar cells (PSCs). Nevertheless, the use of hazardous solvents like precursor solvents (N-Methyl-2-pyrrolidone (NMP), dimethyl sulfoxide (DMSO), dimethylformamide (DMF), gamma-butyrolactone (GBL)) and antisolvents (chlorobenzene (CB), dibutyl ether (DEE), diethyl ether (Et2O), etc.) is crucial to the preparation of perovskite solutions and the control of perovskite thin film crystallization. The consumption of hazardous solvents poses an imminent threat to both the health of manufacturers and the environment. Consequently, before PSCs are commercialized, the current concerns about the toxicity of solvents must be addressed. In this study, we fabricated highly efficient planar PSCs using a novel, environmentally friendly method. Initially, we employed a greener solvent engineering approach that substituted the hazardous precursor solvents with an environmentally friendly solvent called triethyl phosphate (TEP). In the following stage, we fabricated perovskite thin films without the use of an antisolvent by employing a two-step procedure. Of all the greener techniques used to fabricate PSCs, the FTO/SnO2/MAFAPbI3/spiro-OMeTAD planar device configuration yielded the highest PCE of 20.98%. Therefore, this work addresses the toxicity of the solvents used in the perovskite film fabrication procedure and provides a promising universal method for producing PSCs with high efficiency. The aforementioned environmentally friendly approach might allow for PSC fabrication on an industrial scale in the future under sustainable conditions.

Experimental and Simulation Insights into the Thermophysical Properties of Dibutyl Ether Mixed with n-Heptane and n-Octane

Experimental and Simulation Insights into the Thermophysical Properties of Dibutyl Ether Mixed with n-Heptane and n-Octane

Ether‐Based Electrolyte for High‐Temperature and High‐Voltage Lithium Metal Batteries

AbstractThe compatibility of lithium metal with organic solvents is the most crucial for lithium metal batteries (LMBs). Even though ether solvents show excellent compatibility toward lithium metal, the reactivity of the ether solvents at elevated temperatures and high voltages hinders their utilization in lithium metal battery systems. In this study, a high‐temperature ether electrolyte is designed comprising lithium oxalyldifluoroborate (LiODFB), diethylene glycol dibutyl ether (DGDE), 3‐methoxypropionitrile (MPN), and fluorinated ethylene carbonate (FEC), which is abbreviated as MDF electrolyte. The presence of MPN in the electrolyte changes the solvation structure, thereby facilitating increased redox reactions of ODFB− and synergizing with FEC to build a robust solid electrolyte interface (SEI), effectively inhibiting lithium dendrites growth and solvent decomposition. Consequently, the MDF electrolyte exhibits not only long cyclic stability and high coulombic efficiency in Li||Cu and Li||Li cells but also excellent cyclic characteristics in both Li||LiFePO4 (LFP) and Li||LiNi0.8Co0.1Mn0.1O2 (NCM811) cells. Remarkably, these cells demonstrate stable operation even when exposed to higher temperatures of up to 80 °C, while the Li||NCM811 cell maintains consistent cyclic stability at an elevated voltage level of 4.5 V.

Antisolvent effects in green solvent engineering of FA-based quasi-2D Ruddlesden–Popper perovskite films for efficient solar cells

We investigate the proper green solvents for fabricating the high performance formamidinium (FA)-based quasi-2D perovskites solar cells. We find the petroleum ether is a more suitable antisolvent for quasi-2D perovskite crystallization than the traditional used antisolvent dibutyl ether.