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Rapporten bringer indlæg og referater af diskussionerne på et kollokvium afholdt som led i samarbejdet inden for FN's økonomiske kommission for Europa (ECE) i marts 1980. Hovedemnerne er energipolitik, regionale energi-scenarier, varmeplanlægning og transport. Rapporten er på engelsk.

Abstract Stand-alone graphene-based films were prepared from graphene oxide (GO) nanoplatelets and their use as counter-electrodes (CEs) in dye-sensitized solar cells (DSCs) was investigated. The graphene-based CEs were produced by spray deposition of GO and chemically reduced GO, followed by thermal annealing under an inert atmosphere. These GO-based CEs were shown to have similar transparency as a reference CE made of Pt. Consistent with impedance data from symmetrical half-cells, DSCs assembled with such GO-based CEs exhibited relative efficiencies of ca. 75% comparatively to the reference Pt CE. The possibility of obtaining transparent (transmittance higher than 80%) and reasonable catalytic films for DSCs (energy conversion efficiency of 2.64%) from GO nanoplatelets was demonstrated. The need for reduction of the graphene oxide nanoplatelets prior to deposition was not observed, allowing for a simplified CE manufacturing process. However, further work is still needed to equal or surpass the performance of Pt CEs.

Adsorption of randomly branched polyelectrolytes, "hairy" particles and internally structured macromolecules, collectively denoted as heterogeneously charged nanoparticles, on charged surfaces is important in many technological and natural processes. In this paper, we will focus on (1) the charge regulation of both the nanoparticle and the surface and (2) the surface complexation between the particle functional groups and the surface sites and will theoretically study the adsorption using the extended surface complexation approach. The model explicitly considers the electrochemical potential of a nanoparticle with an average (smeared-out) structure and charge both in bulk solution and on the surface to obtain the equilibrium adsorption. The chemical heterogeneity of the particle is described by a distribution of the protonation constant. Detailed analysis of the chemical potential of the adsorbed nanoparticle reveals that the pH and salt dependence of the adsorption can be largely explained by the balance between an energy gain resulting from the particle and surface charge regulation and the surface complexation and an energy loss from the unfavorable interparticle electrostatic repulsion close to the surface. This conclusion is also supported by the strong impacts that the chemical heterogeneity of the particle functional groups, the magnitude of the surface complexation, the number of the functional groups, and the size of the particle have on the adsorption.

Abstract The biodiesel production from white mustard (Sinapis alba L.) seed oil (WMSO) by transesterification with methanol over the quicklime powder was investigated in a batch stirred reactor. Two independent first-order models with respect to triacylglycerols (TAGs) or a more complex model that combined the changing mechanism and the first-order rate law with respect to TAGs and fatty acid methyl esters (FAMEs), respectively described successfully the kinetics of this transesterification reaction. Besides that, the response surface methodology coupled with a full factorial design with replication was applied to model and optimize esters content with methanol-to-WMSO molar ratio, catalyst amount and reaction time (X1, X2 and X3, respectively). The analysis of variance indicated that all individual process factors, the interactions X1–X2 and X2–X3 and the quadratic term X 2 2 influenced significantly FAME content at the 95% confidence level. According to the reduced quadratic model, complete conversion could be achieved with the catalyst loading of 9.8%–10% and the methanol-to-WMSO molar ratio in the range between 6.1:1 and 11.6:1 in 50 min. WMSO was transesterified even faster than sunflower oil in the presence of both quicklime and KOH, due to higher total content of unsaturated fatty acids.

A better understanding of the genetics of seedling characteristics in rice could be helpful in improving rice varieties. Zhenshan 97 and Minghui 63, the parents of Shanyou 63, an elite hybrid developed during the last decade in China, vary greatly with respect to their physiological and morphological traits at the seedling growth stage. In this study, we used a population of 240 recombinant inbred lines derived from a cross between Zhenshan 97 and Minghui 63 to identify quantitative trait loci (QTL) for seedling characteristics. All plant material was grown in hydroponic culture. Data for the following characters were collected at 30 days and 40 days post-sowing: plant height, shoot dry matter weight (SDW), maximum root length, root dry weight (RDW), total dry weight, and root-shoot ratio (the ratio of SDW to RDW). Analysis using composite interval mapping detected 16 QTL for the six traits in 30-day-old seedlings. Of these 16 QTL, Minghui 63 alleles increased trait values at only two of them. The QTL in the vicinity of R3166 on chromosome 5 simultaneously influenced PH, SDW, MRL, RDW, and TDW in the same direction. Twenty QTL were detected for the same traits in the 40-day-old seedlings. However, at this stage Minghui 63 alleles increased trait values at eight QTL. The QTL linked to R3166 also affected PH, SDW, MRL, RDW, and TDW. Only four QTL were common to the two stages. These results clearly indicate that different genes (QTL) control the same traits during different time intervals. Zhenshan 97 alleles had positive effects during the first 30 days of seedling growth, but thereafter the positive effects of Minghui 63 alleles on seedling growth gradually became more pronounced.

This chapter discusses the present scenario and market trend of some important natural plant fibers such as cotton, flax, jute, and hemp. Production, processing, and applications of these fibers are discussed. The factors influencing the sustainability of these natural plant fibers are presented and various lifecycle assessment studies performed on these fibers to evaluate their environmental impacts and sustainability are discussed.

Abstract A numerical and experimental study was conducted, with the purpose of inferring the influence of the CO2 concentration ( x CO 2 ) for different equivalence ratios ( ϕ ) on CH4/CO2/air (biogas) flames chemiluminescence. A thorough analysis on the signals of OH∗, CH∗, C 2 ∗ and CO 2 ∗ was performed. Typical biogas compositions were tested under laminar atmospheric flame conditions, within the unburned equivalence ratio of 0.9 and 1.14 with CO2 concentrations up to 40% in the blend. Experimental measurements of chemiluminescence were done using spectroscopy in the UV–visible region of the spectra. Simulations were performed with the GRI-Mech 3.0 mechanism without accounting for the nitrogen chemistry, extended with a chemiluminescence kinetics of OH∗, CH∗, C 2 ∗ and CO 2 ∗ , in a burner-stabilized frame in CANTERA. Experimental measurements and numerical simulations are compared and generally are in good agreement. It was verified that CO2 dilution leads to a regular decrease in the emission intensities of OH∗, CH∗, C 2 ∗ and CO 2 ∗ . Relations between chemiluminescence intensity ratios and x CO 2 and ϕ were found. It was shown that OH∗/ CO 2 ∗ and C 2 ∗ / CO 2 ∗ have the potential predict x CO 2 in CH4/CO2/air flames. Moreover, it was verified that OH∗/CH∗, OH∗/ C 2 ∗ and CH∗/ C 2 ∗ are well suited to infer ϕ for the blends tested. It was verified that x CO 2 does not cause relevant changes in the chemiluminescence ratios when inferring ϕ .

The high power density, ease of transportation and storage and many years of development of internal combustion engine technologies have put liquid hydrocarbon fuels at a privileged position in our energy mix. Therefore processes that use renewable energy sources to produce liquid hydrocarbon fuels from H2O and CO2 are of crucial importance. Concentrated Solar Power (CSP) can be employed as the only energy source for the renewable production of hydrogen from water either indirectly, e.g. by supplying the electricity for electrolysis, or directly by supplying the necessary heat for thermochemically producing hydrogen. Among the various thermochemical cycles tested so far for CSP-driven hydrogen production via water splitting (WS), those based on redox-pair oxide systems, are directly adaptable to carbon dioxide splitting (CDS) and/or combined CO2/H2O splitting for the production of CO or syngas, respectively. The acknowledgement of this fact has recently revived the interest of the scientific community on such technologies. The current article presents the development, evolution and current status of CSP-aided syngas production via such redox-pair-based thermochemical cycles. At first the various redox oxide material compositions tested for water/carbon dioxide splitting are presented and their redox chemistries are discussed. Then the selection of suitable solar reactors is addressed in conjunction with the boundary conditions imposed by the redox systems as well as the heat demands, technical peculiarities and requirements of the cycle steps. The various solar reactor concepts proposed and employed for such reactions and their current status of development are presented. Finally, topics where further work is needed for commercialization of the technology are identified and discussed.