Speeds of sound and isentropic compressibilities of (2-ethoxyethanol + ethylene glycol, diethylene glycol, triethylene glycol, and tetraethylene glycol) binary mixtures at 298.15 K

The speed of sound (u) has been obtained at a frequency of 8.3 MHz in {CH₃CH₂OCH₂CH₂OH + HOCH₂CH₂(OCH₂CH₂)_nOH}for n = 0, 1, 2, and 3 over the whole composition range of studied binary liquid mixtures, at T = 298.15 K. The speed of sound values were combined with those of our previous results for densities and viscosities to obtain isentropic compressibility (κ_s), free volume (V_f), and intermolecular free length (L_f). From all these data excess isentropic compressibility (κ_s^E), excess free volume (V_f^E) and excess intermolecular free length (L_f^E) as well as the deviations of the speed of sound (Δu) were obtained. The results are interpreted in terms of molecular interactions occurring in the solutions.     

Preparation and characterization of SnS nanocrystals by a triethanolamine-assisted diethylene glycol solution synthesis

Stoichiometric, phase-controllable SnS nanocrystals (NCs) were prepared by a solution chemical synthesis using triethanolamine-assisted diethylene glycol solvent, tin(II) chloride and thioacetamide as precursors at injection temperature of 180-220 °C. The influences of triethanolamine adding amounts, injection temperature, refluxing time on crystal phase, growth morphology and optical property of the synthesized SnS NCs were investigated. The results showed that both orthorhombic (OR) and zinc-blende (ZB) phase of SnS NCs could be formed by altering triethanolamine amounts.     

Samarium(III) picrate tetraethylene glycol complex: Photoluminescence study and active material in monolayer electroluminescent

A mononuclear Sm(III) complex involving Pic and EO4 (where Pic=picrate anion and EO4=tetraethylene glycol) has been studied. It shows a bright-orange emission when used as active material in a monolayer electroluminescent device of ITO/EO4-Sm-Pic/Al. The crystal structure of the complex consists of [Sm(Pic)₂(H₂O)(EO4)]⁺ cation and [Pic]⁻ anion. The Sm(III) ion is coordinated with nine oxygen atoms from one EO4 ligand in a pentadentate mode, two Pic anions each in bidentate and monodentate modes, and one water molecule. Both the terminal alcohol groups of the acyclic EO4 ligand were involved in the O-H…O hydrogen bonding by infinite one-dimensional (1D) chain within a symmetry direction [0 1 0]. The photoluminescence (PL) spectrum of the thin film shows the typical spectral features of the Sm(III) ion (⁴G_5/2→⁶H_7/2 transitions). The root-mean-square (rms) of the roughness of thin film is 30.605 nm and indicates that the formation of the monolayer electroluminescent device is not uniform and retains a high crystallinity. Typical semiconductor current-voltage (I-V) property was also observed in this device with threshold and turn voltages of 2.8 and 6.2 V, respectively. The [Sm(Pic)₂(H₂O)(EO4)](Pic)·H₂O complex can be applied as a luminescent center in OLED for bright-orange emission.     

Molecular interactions and structural effects on mixing pentanol in polyethylene glycol diacrylate and polyethylene glycol dimethacrylate

To understand the intermolecular interactions in binary mixtures of pentanol with polyethylene glycol diacrylate and polyethylene glycol dimethacrylate respectively, absolute viscosity and refractive index have been measured over the whole composition range, at 298.15 K, 303.15 K and 313.15 K, under atmospheric pressure. Molar refraction and interaction parameter have been calculated. The experimental data have been used to evaluate deviation in viscosity, deviation in refractive index and excess Gibb's free energy of activation for viscous flow, and the results have been fitted to Redlich-Kister polynomial equation.     

Study of optical properties and molecular structure of plasma polymerized diethylene glycol dimethyl ether

This paper deals with plasma polymerization processes of diethylene glycol dimethyl ether. Plasmas were produced at 150 mtorr in the range of 10 W to 40 W of RF power. Films were grown on silicon and quartz substrates. Molecular structure of plasma polymerized films and their optical properties were analyzed by Fourier transform infrared spectroscopy (FTIR) and ultraviolet-visible spectroscopy. The IR spectra show C–H stretching at 3000–2900 cm^-1, C=O stretching at 1730–1650 cm^-1, C–H bending at 1440–1380 cm^-1, C–O and C–O–C stretching at 1200–1000 cm^-1. The concentrations of C–H, C–O and C–O–C were investigated for different values of RF power. It can be seen that the C–H concentration increases from 0.55 to 1.0 au (arbitrary unit) with the increase of RF power from 10 to 40 W. The concentration of C–O and C–O–C decreases from 1.0 to 0.5 au in the same range of RF power. The refraction index increased from 1.47 to 1.61 with the increase of RF power. The optical gap calculated from absorption coefficient decreased from 5.15 to 3.35 eV with the increase of power. Due to its optical and hydrophilic characteristics these films can be applied, for instance, as glass lens coatings for ophthalmic applications.     

Shear elasticity and strength of the liquid structure by an example of diethylene glycol

Experimental data for the dependence of the low-frequency (10⁵ Hz) shear elasticity of diethylene glycol on the shear deformation angle have been presented. At small shear angles, the range of linear elasticity has been observed, which narrows with rising strain. The effective viscosity behaves similarly.     

二乙二醇单甲醚液相导热系数的实验研究

利用钽丝作为热线的瞬态双热线系统对温度区间233－373K、压力区间为0．1—30 MPa的液相二乙二醇单甲醚（diethylene glycol monom ethylether,DGMME）的导热系数进行了实验研究,并将实验数据拟合为温度和压力的关联式。实验数据与导热系数关联式计算结果的标准偏差和最大偏差分别为0．...     

Proton tracks and the formation of pores in poly[diethylene glycol bis-(allyl carbonate)

Modern dosimetry needs efficient detectors for registering light ions, especially light ions having energies of up to 10 MeV/amu. That is why this research pays attention to the development of materials for such a task. In this work, a CR-39 detector, which is the most efficient detector, was used. It was irradiated with low-energy protons. Using sensitive electrolytic etching and electron scanning microscopy, a complete analysis was carried out of the process of the formation of a pore starting from its opening to the final stage of its formation. The process of sequential track breakthroughs was observed. The data obtained on the shape of the pore and the parameters of its formation allow simulation of the process of etching. The etch rates and sensitivity of etching are determined. The influence of energy losses on the geometry of the pore is considered.     

Density, viscosity, and excess properties of the binary mixture of diethylene glycol monomethyl ether + water at T = (293.15, 303.15, 313.15, 323.15, 333.15) K under atmospheric pressure

Densities and viscosities have been measured as a function of composition for the binary liquid mixture of diethylene glycol monomethyl ether CH₃O(CH₂)₂O(CH₂)₂OH + water at T = (293.15, 303.15, 313.15, 323.15, 333.15) K under atmospheric pressure. Densities were determined using a capillary pycnometer. Viscosities were measured with Ubbelohde capillary viscometer. From the experimental data, the excess molar volumes V^E, and viscosity deviations δη, and the excess energies of activation for viscous flow ΔG^*E were calculated. These data have been correlated by the Redlich–Kister type equations to obtain their coefficients and standard deviations. The results suggest that molecular interaction between diethylene glycol monomethyl ether and water is strong.     

Parameters of viscous flow in dilute solutions of polyalkyl glycol ethers in secondary alcohols

Densities and viscosities were measured for the binary dilute mixtures of triethylene glycol monomethyl ether (TRIEGMME) in 2-alcohols (2-propanol (2-PR), 2-butanol (2-BU), and 2-pentanol (2-PE)) and tetraethylene glycol dimethyl ether (TEGDME) in 2-pentanol, at temperatures from 288.15 K to 318.15 K and in 0 ≤ x₂ ≤ 0.10 mol fraction range of the polyalkyl glycol ethers. The values of the dynamic viscosity in the TRIEGMME + 2-PR systems are more viscous than pure solvent at the work temperatures. The Jones-Dole B coefficients and β_G interaction parameters for viscous flow values were calculated and explain the behavior observed. The partial molar volumes at infinite dilution of solute in 2-alkanols were calculated by the parameters of viscous flow obtained in dilute solutions polyalkyl glycol ethers in 2-alkanols. The values have been compared with the values of partial molar volume at infinite dilution obtained by density measurement for both solutes in the 2-propanol, 2-butanol, and 2-pentanol.     

Controlling synthesis of Fe nanoparticles with polyethylene glycol

This study looks at the synthesis of Fe nanoparticles using a borohydride reduction of metal salts in the presence of carboxyl and methoxyl terminated polyethylene glycol (PEG). As the PEG concentration is varied, there is a corresponding increase in the Fe content of samples as determined by Mossbauer spectroscopy. Particle sizes are between 70 and 300 nm as indicated by transmission electron microscopy. As the polymer concentration is increased the overall saturation magnetization of the coated nanoparticles initially increases due to the increased iron content with a maximum of 70 emu/g for nanoparticles with the largest Fe content. The magnetization then begins to decrease as the polymer concentration begins to contribute to a significant volume fraction of the sample. All samples are magnetically soft with high remanence as indicated by SQUID magnetometry measurements.     

Experimental study on correlation between sound velocity and solute molecular weight in polyethylene glycol solution

In this study,ultrasound grating was used to measure the sound velocity in solutions of ethylene glycol and polyethylene glycol with molecular weights of 200,600,2000,and 10000.We found Parthasarathy empirical rule,that is,sound velocity is higher in the solution of larger molecules,is invalid in the case of polyethylene glycol solution. We tried to provide a tentative explanation using the Flory-Krigbaum's chained block cloud model.     

Use of polyethylene glycol coatings for optical fibre humidity sensing

Humidity induced change in the refractive index and thickness of the polyethylene glycol (PEG) coatings are in situ investigated for a range from 10 to 95%, using an optical waveguide spectroscopic technique. It is experimentally demonstrated that, upon humidity change, the optical and swelling characteristics of the PEG coatings can be employed to build a plastic fibre optic humidity sensor. The sensing mechanism is based on the humidity induced change in the refractive index of the PEG film, which is directly coated onto a polished segment of a plastic optical fibre with dip-coating method. It is observed that PEG, which is a highly hydrophilic material, shows no monotonic linear response to humidity but gives different characteristics for various ranges of humidity levels both in index of refraction and in thickness. It undergoes a physical phase change from a semi-crystalline structure to a gel one at around 80% relative humidity. At this phase change point, a drastic decrease occurs in the index of refraction as well as a drastic increase in the swelling of the PEG film. In addition, PEG coatings are hydrogenated in a vacuum chamber. It is observed that the hydrogen has a preventing effect on the humidity induced phase change in PEG coatings. Finally, the possibility of using PEG coatings in construction of a real plastic fibre optic humidity sensor is discussed.     

A detailed chemical kinetic model of high-temperature ethylene glycol gasification

In recent experimental investigations, ethylene glycol is used as a model substance for biomass-based pyrolysis oil in an entrained flow gasifier. In order to gain a deeper insight into process sequences and to conduct parametric analysis, this study describes the development and validation of a detailed chemical kinetic model of high-temperature ethylene glycol gasification. A detailed reaction mechanism based on elementary reactions has been developed considering 80 species and 1243 reactions for application in CFD software. In addition to mechanism validation based on ignition delay times, laminar flame speeds and concentration profiles, simulation results are compared to experimental data of ethylene glycol gasification under complex turbulent reactive flow conditions.     

Effect of oligoethylene glycol moieties in porous silicon surface functionalisation on protein adsorption and cell attachment

We report on the synthesis of two carboxy-functional alkene compounds as modifiers of porous silicon (pSi) surface chemistry by means of thermal hydrosilylation. Both alkene compounds have hydrophobic, aliphatic carbon segments, with terminal carboxylic acid functionality appended through a thioether linkage. In one of the alkene linkers, we incorporated a short oligoethylene glycol (OEG) moiety to explore its low-fouling properties when attached to porous silicon. We examined surface stability of the surface-modified porous silicon in aqueous milieu. Albumin and fibronectin were adsorbed and, using carbodiimide chemistry, covalently immobilised to linker-modified porous silicon, and the propensity for mammalian cells to attach to these surfaces investigated. Surface chemistry was characterised by infrared spectroscopy and the stability of porous silicon in an aqueous milieu was investigated by interferometric reflectance spectroscopy (IRS). Surfaces functionalised with the alkene linker containing OEG displayed greater resistance to the adsorption of albumin. This linker also facilitated higher levels of covalent protein immobilisation to the functionalised pSi surface. Higher levels of cell attachment were observed on pSi surfaces with fibronectin covalently immobilised onto the OEG linker, than for fibronectin covalently immobilised on the non-OEG linker.     

Tunable monoenergy positron annihilation spectroscopy of polyethylene glycol thin films

Doppler broadening and coincidence Doppler broadening of annihilation radiation experiments have been performed in three kinds of polyethylene glycol(PEG) membrane formed with different average molecular weight using the tunable monoenergy slow positron probe as a function of implantion energy. The obtained positron annihilation parameters are interpreted from two aspects: surface effect and differences in micro-structure or chemical environment of positron annihilation. The experimental results show that the regulation of densification of PEG molecular packing and distribution uniformity from the near surface layer to the bulk region in the film forming process can be well realized by changing its molecular weight. Combining a variable monoenergetic slow positron beam and these two positron annihilation spectroscopy methods is a powerful tool to study positron annihilation characteristics and for polymeric thin-film fine structure analysis.     

定向结晶条件下聚乙二醇6000的强动力学效应

在单向温度场条件下, 采用不同抽拉速度实现了聚乙二醇6000的定向生长、界面形貌的实时观测及界面温度的测量, 进而揭示了其生长机制. 实验结果表明, 随着抽拉速度的增大, 界面的温度逐渐减小, 过冷度逐渐增大. 运用高聚物结晶的次级形核理论模型, 对实验数据进行了计算, 得到在界面过冷度为13.5 K左右时, 生长机制发生了由区域Ⅱ向区域Ⅲ的转变. 实验数据与等温结晶数据的比较发现等温结晶方法中获得过冷度相对较大, 是因为其包含了热过冷. 聚乙二醇6000定向结晶过程中需要的最大动力学过冷度为20 K, 说明由于高聚物的二维形核, 其生长主要由界面动力学控制, 具有较强的动力学效应.     

A comparative study of non-polar solvents effect on dielectric relaxation and dipole moment of binary mixtures of mono alkyl ethers of ethylene glycol and of diethylene glycol with ethyl alcohol

Dielectric relaxation and dipole moment of binary mixtures of homologous series of mono alkyl ethers of ethylene glycol and of diethylene glycol, i.e., mono methyl, mono ethyl and mono butyl ethers of ethylene glycol (ROCH₂CH₂OH) and mono methyl, mono ethyl and mono butyl ethers of diethylene glycol (ROCH₂CH₂OCH₂CH₂OH) with ethyl alcohol (C₂H₅OH) of different concentrations were studied in dilute solutions of benzene, dioxane and carbon tetrachloride at 35 °C. Permittivity (ε′) and loss (ε″) at 10.1 GHz, static dielectric constant ε_o at 1 MHz and high frequency limiting dielectric constant ε_∞ = n_D² at optical frequency of these molecules and their binary mixtures at different concentration were measured in dilute solutions of non-polar solvents. The average relaxation time τ_o, relaxation times corresponding to overall molecular reorientation τ₁ and group rotations τ₂ were determined using Higasi's single frequency measurement equations for dilute solutions. The evaluated values of relaxation times and free energy of activation ΔF were used to explore the solvent effect on molecular dynamics of these polar binary systems in non-polar solvents. The excess inverse relaxation time and excess free energy of activation were determined to confirm the existence of hydrogen-bonded heterogeneous cooperative domains of the ethers and alcohol molecules at different concentration their binary mixtures in non-polar solvents. The dipole moment of the binary mixtures was evaluated using Higasi's and Guggenheim's equation for dilute solutions. The evaluated values of dipole moments and computed dipole moment values using a simple mixing equation of the polar molecules binary mixture were used to explore the effect of non-polar solvent environment on heterogeneous molecular interactions between ethers and alcohol molecules. The effect of number of carbon atoms in the molecular structure of these homologous series molecules was also considered for the interpretation of various evaluated dielectric parameters.     

Colloidal stability measurements of graphene nanoplatelets covalently functionalized with tetrahydrofurfuryl polyethylene glycol in different organic solvents

In this study, a facile, efficient, and cost-effective method was proposed for mass-production of tetrahydrofurfuryl polyethylene glycol-functionalized graphene nanoplatelets (TFPEG-treated GNPs) with improved colloidal stability in water and different organic solvents. In this method, zirconium(IV) oxychloride octahydrate was used as catalyst to covalently functionalize GNPs with TFPEG via direct esterification of carboxylic acid on the GNPs with the hydroxyl chains of TFPEG. Covalent functionalization was verified by Fourier transform infrared spectroscopy, Raman spectroscopy, and thermogravimetric analysis. Further, the morphology of the TFPEG-treated GNPs was determined via a high-resolution transmission electron microscopy. The stability of the treated GNPs in colloidal form was examined by dispersing 0.01 wt% of the solid sample into different organic solvents namely distilled water, methanol, ethanol, ethylene glycol, and 1-hexanol. It was found that the sedimentation rate of TFPEG-treated GNPs in distilled water, methanol, ethanol, ethylene glycol, and 1-hexanol was at 11, 25, 36, 18, and 47%, respectively, recorded after 15 days. Viscosity and thermal conductivity of water-based TFPEG-treated GNP nanofluids were also measured at different concentrations (0.100, 0.075, 0.050, and 0.025 wt%). The results suggest that these nanofluids have great potential for use as working fluids in industrial heat transfer systems.