Ultrasonic study of molecular association of poly(vinyl chloride) solution in tetrahydrofuran

Ultrasonic absorption, velocity, adiabatic compressibility, relaxation time and relaxation amplitude measurements are reported on poly(vinyl chloride) (PVC) solution in tetrahydrofuran (THF) using pulsed ultrasonic apparatus operating at 2 MHz and 313 K. Results show a linear increase of velocity. density, viscosity, absorption coefficient, relaxation time and relaxation amplitude values with the increase of PVC concentration in THF. In contrast the compressibility decreases with increasing PVC concentration. This suggests interaction between PVC and THF molecules.     

Synthesis and photovoltaic properties of an alternating phenylenevinylene copolymer with substituted-triphenylamine units along the backbone for bulk heterojunction and dye-sensitized solar cells

We have fabricated bulk heterojunction (BHJ) photovoltaic devices based on the as cast and thermally annealed P:[6,6]-phenyl-C-61-butyric acid methyl ester (PCBM) blends and found that these devices gave power conversion efficiency (PCE) of about 1.15 and 1.60% respectively. P is a novel alternating phenylenevinylene copolymer which contains 2-cyano-3-(4-(diphenylamino)phenyl)acrylic acid units along the backbone and was synthesized by Heck coupling. This copolymer was soluble in common organic solvents and showed long-wavelength absorption maximum at 390-420 nm with optical band gap of 1.94 eV. The improvement of PCE after thermal annealing of the device based on the P:PCBM blend was attributed to the increase in hole mobility due to the enhanced crystallinity of P induced by thermal treatment. In addition, we have fabricated BHJ photovoltaic devices based on the as cast and thermally annealed PB:P:PCBM ternary blend. PB is a low band gap alternating phenylenevinylene copolymer with BF₂-azopyrrole complex units, which has been previously synthesized in our laboratory. We found that the device based on this ternary blend exhibited higher PCE (2.56%) as compared to either P:PCBM (1.15%) or PB:PCBM (1.57%) blend. This feature was associated with the well energy level alignment of P, PB and PCBM, the higher donor-acceptor interfaces for the exciton dissociation and the improved light harvesting property of the ternary blend. The further increase in the PCE with thermally annealed ternary blend (3.48%) has been correlated with the increase in the crystallinity of both P and PB. Finally, we used copolymer P as sensitizer for quasi solid state dye-sensitized solar cell and we achieved PCE of approximately 3.78%.     

Preparation of PZT Thin Films by Liquid-Source MOCVD Using of Cyclohexane Solvent

Pb(Zr, Ti)O₃ thin films were grown on 8-inch Ir(111)/SiO₂/Si substrate by a MOCVD system aiming at application utilizing high-density ferroelectric memory (FRAM). Two types of solvents, THF and cyclohexane were used for liquid source delivery. It was found that the ferroelectric properties of the MOCVD-PZT films using cyclohexane solvent were better than them using THF solvent. By choosing cyclohexane as solvent, the MOCVD-PZT thin films showed strong ?111? preferred orientation and the Pt/PZT/Ir capacitors exhibited promising ferroelectric performances, for instance, large switching charge (Qsw) of 56.4 uC/cm².     

Biodiesel Feedstock from Emulsions Produced by Aqueous Processing of Yellow Mustard

The multi-stage treatment of stable oil-in-water emulsions produced during non-enzymatic aqueous processing of dehulled yellow mustard flour with cyclic ethers [tetrahydrofuran (THF) and 1,4-dioxane] was investigated to produce a single-phase oil-solvent-water miscella suitable for biodiesel production. While the single-stage treatment of yellow mustard emulsion recovered 97 % and 95 % of the oil by using 4:1 THF:oil and 9:1 dioxane:oil weight ratios, respectively, miscella phases containing more than 7 % water formed, which made them unsuitable as biodiesel feedstock. Multi-stage treatments of the emulsion using lower THF:oil and dioxane:oil weight ratios were further developed to produce oil-solvent-water miscella phases with low water content. While three-stage extraction of emulsions using 0.5:1, 1:1, 1.5:1, and 2:1 dioxane:oil weight ratios did not destabilize the emulsion, three-stage extraction using 0.5:1 and 0.75:1 THF:oil weight ratios effectively recovered over 97 % of the oil, resulting in the production of oil-rich miscella phases containing only 1 % and 1.5 % water, respectively. These miscella phases were analyzed for free fatty acid and phosphorus contents and proved to be excellent feedstocks for the preparation of high-purity methyl esters through single-phase base-catalyzed transmethylation.     

对异丙基氯化镁格氏试剂制备方法的研究

用镁和氯代异丙烷为原料,四氢呋喃作溶剂,在一定条件下合成了格氏试剂,格氏试剂的收率达90%以上。探讨了各种因素对合成格氏试剂的影响。     

Solid fraction modelling for CO2 and CO2–THF hydrate slurries used as secondary refrigerants

In the present paper, the suitability of hydrate slurries in secondary refrigeration was investigated by the means of a new hydrate solid-fraction model. Considering the high melting enthalpy of CO₂-containing hydrates, slurries presenting high hydrate solid fractions can carry sufficient latent heat to be useful for a two-phase secondary-refrigerant application. The model presented in this paper allowed to calculate the solid fraction of CO₂ and CO₂–THF hydrate from thermodynamic conditions of pressure and temperature. Contrary to a previous work on single CO₂ hydrates in a closed system, the present model can take into account hydrate mixture and is well adapted to additional CO₂ injections (opened system). By relying on the hydrate-conversion model results, the study of hydrates in suspension in a carrying liquid was also studied in an experimental loop and was based on a formation process by CO₂ injection in a cooled aqueous solution.     

活性炭对THF水合物储氢特性影响的实验研究

该实验利用高压水合物实验研究装置,在恒容条件下,研究了温度为1℃、压力分别为6.4 MPa、7.4MPa和8.4 MPa、四氢呋喃(简称THF)摩尔浓度为5.0％时,活性炭对THF水合物储氢特性的影响.研究结果表明,不加活性炭时的平均诱导时间为333 min,加活性炭时的平均诱导时间为250 min,所以活性炭可以在高...     

In situ injection of THF to trigger gas hydrate crystallization: Application to the evaluation of a kinetic hydrate promoter

This paper investigates an original method to efficiently trigger gas hydrate crystallization. This method consists of an in situ injection of a small amount of THF into an aqueous phase in contact with a gas-hydrate-former phase at pressure and temperature conditions inside the hydrate metastable zone. In the presence of a CO₂–CH₄ gas mixture, our results show that the THF injection induces immediate crystallization of a first hydrate containing THF. This triggers the formation of the CO₂–CH₄ binary hydrate as proven by the pressure and temperature reached at equilibrium. This experimental method, which “cancels out” the stochasticity of the hydrate crystallization, was used to evaluate the effect of the anionic surfactant SDS at different concentrations, on the formation kinetics of the CO₂–CH₄ hydrate. The results are discussed and compared with those published in a recent article (Ricaurte et al., 2013), where THF was not injected but present in the aqueous phase from the beginning and at much higher concentrations.