Methanol Conversion to Hydrocarbons (MTH) Over H-ITQ-13 (ITH) Zeolite

Product flexibility is key to meeting fluctuating chemicals demands in the future. In this contribution, the methanol to hydrocarbons (MTH) reaction was investigated over two Ge-containing H-ITQ-13 samples, one with needle-like (H-ITQ-13(N), with (Si+Ge)/Al) = 42) and another with plate-like (H-ITQ-13(P), with (Si+Ge)/Al > 100) morphology. The samples were characterised using XRD, BET, SEM/EDS and FTIR spectroscopy, and their MTH performance was compared with the performance of H-ZSM-5 and H-ZSM-22. Similar specific surface areas (413 and 455 m² g^?1 for H-ITQ-13(N) and (P), respectively) and similar acid strength (Δν ~ ?327(?310) cm^?1) was observed for the two H-ITQ-13 samples. Testing of H-ITQ-13(N) at weight hourly space velocity (WHSV) = 2–8 h^?1 at 350–450 °C revealed that C₅₊ alkenes were the main products (35–45 % selectivity at 400 °C), followed by propene and butene. A low but significant selectivity for aromatic products was observed (6–8 % selectivity at 400 °C). Product selectivity was found to be independent of deactivation. The methanol conversion capacity of H-ITQ-13(N) was 120–150 g methanol g^?1 catalyst at 400 °C. Testing H-ITQ-13 at high (30 atm) and ambient pressure, respectively, at 350 °C showed that a high pressure led to enhanced C₅₊ selectivity, but close to a tenfold decrease in methanol conversion capacity. H-ITQ-13(P) was tested at 400 °C and 2 h^?1. It gave lower conversion than H-ITQ-13(N). Furthermore, when compared at the same conversion level, H-ITQ-13(P) gave higher C₅₊ alkene selectivity, lower aromatics selectivity, and a higher propene to ethene ratio than H-ITQ-13(N). The H-ITQ-13 samples yielded a product spectrum intermediate of H-ZSM-22 and H-ZSM-5. The effluent product cut-off of H-ITQ-13 was similar to that of H-ZSM-5 with tetramethylbenzene as the largest significant product, while H-ZSM-22 produced mainly linear and branched alkenes. The lifetime of H-ITQ-13(N) was clearly enhanced compared to H-ZSM-22, but inferior to H-ZSM-5.     

Temperature and electric field dependent hole mobility in a polyfluorene copolymer

Transport of holes in thin films of a low-bandgap alternating polyfluorene copolymer, APFO-Green5, was investigated by means of admittance spectroscopy as a function of field and temperature. The values of hole mobility were evaluated from the position of the maxima in the plots of the negative differential susceptance as a function of frequency. Hole mobility was found to be strongly field- and temperature-dependent. The charge transport parameters were extracted by analyzing the mobility data by the uncorrelated and the correlated Gaussian Disorder Models.     

“Virtual Design Studio”—Part 1: Interdisciplinary design processes

The “Virtual Design Studio (VDS)” is a software platform currently under development in support of an integrated, coordinated and optimized design of buildings and their energy and environmental systems. It is intended to assist collaborating architects, engineers and project management team members throughout from the early phases to the detailed building design development. The platform helps to facilitate the workflow and the processing of information in combination with appropriate, task-based performance simulation tools as further analyzed in Part 2 of this study (DOI: 10.1007/s12273-013-0111-1). The present paper summarizes how VDS relates to the building design process and its typical project stages, performance-based design considerations and respective performance optimization strategies. It outlines the methodology and scope for the organization, implementation and respective requirements for the VDS platform development based on the interdisciplinary design needs. Part 2 will present the methodology for the systems integration and software implementation of VDS.     

Solid-state photoelectrochemical device based on poly(3-hexylthiophene) and an ion conducting polymer electrolyte, amorphous poly(ethylene oxide) complexed with I3/I redox couple

The photoelectrochemical properties of a solid-state photoelectrochemical cell (PEC) based on poly(3-hexylthiophene), P3HT, and an ion-conducting polymer electrolyte, amorphous poly(ethylene oxide), POMOE, complexed with I₃⁻/I⁻ redox couple has been constructed and studied. The current–voltage characteristics in the dark and under white light illumination, transient photocurrent and photovoltage studies, photocurrent action spectra for front and back side illuminations and an open-circuit voltage and short-circuit current dependence on light intensity have been studied. An open-circuit voltage of 130 mV and a short-circuit current of 0.47 μA cm⁻² were obtained at light intensity of 100 mW/cm². IPCE% of 0.024% for front side illumination (ITO/PEDOT) and IPCE% of 0.003% for backside illumination (ITO/P3HT) were obtained.     

Photoelectrochemical solar energy conversion based on blend of poly(3-hexylthiophene) and fullerene

A solid-state photoelectrochemical solar energy conversion device based on blend of poly(3-hexylthiophene) (P3HT) and fullerene (C₆₀) has been constructed and characterized. The photoelectrochemical performance parameters of the device were compared with pure P3HT solid-state photoelectrochemical cell. The current–voltage characteristics in the dark and under white light illumination and photocurrent spectra for front- and backside illuminations have been studied. The following device parameters were obtained: an open-circuit voltage of 97.8 mV and a short-circuit current of 7.28 μA/cm² at light intensity of 100 mW/cm²; IPCE% of 0.43% for front side illumination (ITO/PEDOT) and IPCE% of 0.01% for backside illumination (ITO/P3HT:C₆₀). The dependence of the short-circuit current and an open-circuit voltage on the light intensity and time have also been studied.     

“Virtual Design Studio”—Part 2: Introduction to overall and software framework

The “Virtual Design Studio (VDS)” is a software platform for integrated, coordinated and optimized design of building energy and environmental systems. It is intended to assist management, architectural and systems design teams throughout the early to detailed building design stages as analyzed in Part 1 (DOI: 10.1007/s12273-013-0110-2). This paper presents an overview of the VDS design and method of software implementation, including system composition, architecture, graphical user interface (GUI), and simulation solver integration. A VDS user workflow is also illustrated with a simplified design example.     

Photoelectrochemical studies of the junction between poly[3-(4-octylphenyl)thiophene] and a redox polymer electrolyte

The photoelectrochemical properties of all-solid-state photoelectrochemical cell constructed from a conjugated polymer poly[3-(4-octylphenyl)thiophene] and an amorphous poly(ethylene oxide) complexed with iodide/triiodide redox couple were studied. In order to develop flexible photoelectrochemical cells, we have used a transparent polymeric metal, doped poly(3,4-ethylenedioxythiophene), as a counter electrode. It was shown that poly(3,4-ethylenedioxythiophene) improved the charge transfer between indium tin-oxide and iodide/triiodide redox couple. The spectral response, photocurrent time, and open-circuit voltage and short-circuit current dependence on light intensity have been studied. The photon to electron conversion efficiency obtained was low. The photocurrent and photovoltage dependence studies on light intensity indicate exciton recombination and/or traps as limiting factors.