Assessing fuel cell vehicle innovation and the role of policy in Japan,Korea, and China

Despite intensive public and private research efforts into developing fuel cell vehicles (FCV), the global number of FCV remains small and they are unavailable for commercial purchase. We use an in-depth literature review, and bibliometric and patent analysis to analyse FCV technology within the conceptual framework of Rogers' innovation diffusion curve and suggest how the particular innovation systems and policies adopted in three key Asian car-manufacturing countries (Japan, Korea, and China) have influenced the development of FCV. Such analysis may capture trends not indicated by technical measures such as increases in efficiency or decreases in unit cost. Although Japan continues to lead in terms of number of patents and quality of academic research, Korea and China have been successful in developing fuel cell programs. Korean academics patent more frequently than their Japanese and Chinese peers, producing 18% of FC patents, with 16% of those filed also naming a private company. The 2008 financial crisis and ongoing economic uncertainty appears to have had some effect on patent activity whilst academic research appears unaffected. Diffusion curve analysis suggests that FCVs have not reached technological maturity.     

Fluoroalkylated silicon-containing surfaces-estimation of solid-surface energy

The design of robust omniphobic surfaces, which are not wetted by low-surface-tension liquids such as octane (γlv=21.6 mN/m) and methanol (γlv=22.7 mN/m), requires an appropriately chosen surface micro/nanotexture in addition to a low solid-surface energy (γsv). 1H,1H,2H,2H-Heptadecafluorodecyl polyhedral oligomeric silsesquioxane (fluorodecyl POSS) offers one of the lowest solid-surface energy values ever reported (γsv≈10 mN/m) and has become the molecule of choice for coating textured surfaces. In this work, we synthesize and evaluate a series of related molecules that either retain the POSS cage and differ in fluoroalkyl chain length or that retain the fluorodecyl chains surrounding a linear or cyclic molecular structure. The solid-surface energy (γsv) of these molecules was estimated using contact angle measurements on flat spin-coated silicon wafer surfaces. Zisman analysis was performed using a homologous series of n-alkanes (15.5≤γlv≤27.5 mN/m), whereas Girifalco-Good analysis was performed using a set of polar and nonpolar liquids with a wider range of liquid surface tension (15.5≤γlv≤72.1 mN/m). The hydrogen-bond-donating, hydrogen-bond-accepting, polar, and nonpolar (dispersion) contributions to the solid-surface energy of each compound were determined by probing the surfaces using a set of three liquid droplets of either acetone, chloroform, and dodecane or diiodomethane, dimethyl sulfoxide, and water.     

Life cycle assessment of the transmission network in Great Britain

Analysis of lower carbon power systems has tended to focus on the operational carbon dioxide (CO₂) emissions from power stations. However, to achieve the large cuts required it is necessary to understand the whole-life contribution of all sectors of the electricity industry. Here, a preliminary assessment of the life cycle carbon emissions of the transmission network in Great Britain is presented. Using a 40-year period and assuming a static generation mix it shows that the carbon equivalent emissions (or global warming potential) of the transmission network are around 11 gCO_2-eq/kWh of electricity transmitted and that almost 19 times more energy is transmitted by the network than is used in its construction and operation. Operational emissions account for 96% of this with transmission losses alone totalling 85% and sulphur hexafluoride (SF₆) emissions featuring significantly. However, the CO₂ embodied within the raw materials of the network infrastructure itself represents a modest 3%. Transmission investment decisions informed by whole-life cycle carbon assessments of network design could balance higher financial and carbon ‘capital’ costs of larger conductors with lower transmission losses and CO₂ emissions over the network lifetime. This will, however, necessitate new regulatory approaches to properly incentivise transmission companies.     

软件质量对于数字世界的重要意义

新冠肺炎疫情加快了数字化转型的步伐,软件在我们的工作、生活和学习中发挥了至关重要的作用.全球的数字化程度越来越高,人们对于数字产品的依赖也与日俱增,这一切都让软件质量成为了大众所关注的焦点. 当下,数字化转型的速度没有放缓的迹象,而基于软件的创新和发展仍将持续.据信息与软件质量联盟统计,软件质量问题在2020年给美国经...     

Changes in rumen bacterial and archaeal communities over the transition period in primiparous Holstein dairy cows

In the present study, we hypothesized that the rumen bacterial and archaeal communities would change significantly over the transition period of dairy cows, mainly as an adaptation to the classical use of low-grain prepartum and high-grain postpartum diets. Bacterial 16S rRNA gene amplicon sequencing of rumen samples from 10 primiparous Holstein dairy cows revealed no changes over the transition period in relative abundance of genera such as Ruminococcus, Butyrivibrio, Clostridium, Coprococcus, and Pseudobutyrivibrio. However, other dominant genus-level taxa, such as Prevotella, unclassified Ruminococcaceae, and unclassified Succinivibrionaceae, showed distinct changes in relative abundance from the prepartum to the postpartum period. Overall, we observed individual fluctuation patterns over the transition period for a range of bacterial taxa that, in some cases, were correlated with observed changes in the rumen short-chain fatty acids profile. Combined results from clone library and terminal-restriction fragment length polymorphism (T-RFLP) analyses, targeting the methyl-coenzyme M reductase α-subunit (mcrA) gene, revealed a methanogenic archaeal community dominated by the Methanobacteriales and Methanomassiliicoccales orders, particularly the genera Methanobrevibacter, Methanosphaera, and Methanomassiliicoccus. As observed for the bacterial community, the T-RFLP patterns showed significant shifts in methanogenic community composition over the transition period. Together, the composition of the rumen bacterial and archaeal communities exhibited changes in response to particularly the dietary changes of dairy cows over the transition period.     

Fostering active network management through SMEs’ practises

Managing the electricity network through ‘smart grid’ systems is a key strategy to address challenges of energy security, low carbon transitions and the replacement of ageing infrastructure networks in the UK. Small and medium enterprises (SMEs) have a significant role in shaping patterns of energy consumption. Understanding how their activities interrelate with changes in electricity systems is critical for active network management. A significant challenge for the transformation of electricity systems involves comprehending the complexity that stems from the variety of commercial activities and diversity of social and organizational practises among SMEs that interact with material infrastructures. We engage with SMEs to consider how smart grid interventions ‘fit’ into everyday operational activities. Drawing on analysis of empirical data on electricity use, smart metre data, surveys, interviews and ‘energy tours’ with SMEs to understand lighting, space heating and cooling, refrigeration and IT use, this paper argues for experimenting with the use of practise theory as a framework for bringing together technical and social aspects of energy use in SMEs. This approach reveals that material circumstances and temporal factors shape current energy demand among SMEs, with ‘connectedness’ an emergent factor.     

A simple route to form magnetic chitosan nanoparticles from coaxial-electrospun composite nanofibers

Composite non-woven mats of poly(vinyl pyrrolidone) (PVP), chitosan, and Fe₃O₄ were successfully fabricated using coaxial-electrospinning technique with PVP/chitosan as the shell and PVP/Fe₃O₄ as the core. Because of the templating and confinement properties of the nanofibers, magnetic chitosan nanoparticles (MCNPs) could be spontaneously formed through molecular self-assembly when the composite fibers were dissolved on treatment with acetum solution. By changing the weight ratio of Fe₃O₄:chitosan, the size of the MCNPs could be varied. The morphology, chemical composition, and magnetic characteristics of composite particles were characterized by means of scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and vibrating sample magnetometer. Experimental results indicated that the composite particles were super-paramagnetic with sizes in the range of 15–40 nm. This facile and new synthesis route comprises a convenient strategy to generate composite particles and should be broadly applicable to a wide range of systems, serving as a platform for the facile development of novel composite materials.     

Nitroxide Radicals@US‐Tubes: New Spin Labels for Biomedical Applications

The encapsulation of nitroxide radicals within ultrashort (ca. 50 nm) single‐walled carbon nanotubes (US‐tubes) is achieved. Tempo‐ and Iodo‐Tempo@US‐tubes are characterized by thermogravimetric analysis (TGA), X‐ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Electron paramagnetic resonance (EPR) spectra display characteristic signals due to the detection of the spin probes within the US‐tubes. Longitudinal proton relaxivities (r₁) of both nitroxide@US‐tubes samples are 7 to 13 times greater than the free nitroxide radicals in solution, giving relaxivities comparable to the clinical contrast agent (CA) Magnevist. In addition, transverse proton relaxivities (r₂) show unprecedented proton relaxation enhancement in comparison to any other reported nitroxide radical‐based system or the clinically approved T₂ CA, Resovist, under the same conditions. T₂‐weighted magnetic resonance imaging (MRI) phantom images show that the encapsulation of nitroxide radicals within the US‐tubes produces good contrast enhancement due to their high r₂ relaxivities. The nitroxide radicals@US‐tube agents are a new promising class of spin probes for MRI and electronic paramagnetic resonance imaging (EPRI) labeling, tracking, and diagnosis.     

Study of plant-air transfer of PCBs from an evergreen shrub: implications for mechanisms and modeling

The depuration of gas-phase polychlorinated biphenyls (PCBs) from a slow-growing evergreen shrub, Skimmia japonica Thunb., was studied to investigate the reversibility of uptake and the compartmentalization of PCB congeners within leaves with respect to air-plant exchange processes. Depuration of PCBs was monitored over periods of hours, days, and weeks. Equilibrium had not been attained between air and leaves during the uptake phase after many weeks. Depuration followed two-phase clearance kinetics, with phase 1 occurring over the order of hours and phase 2 continuing slowly over weeks. In phase 1, a substantial part (ca. 40%) of the PCB burden that the plants had accumulated over weeks was lost in 2-3 h. This observation is further evidence for the close dynamic coupling of air and vegetation compartments. In the second phase, very slow depuration over 28 d only removed a further approximately 25% of the accumulated PCB burden. Depuration rates in phase 2 varied between compounds and were not influenced by growth dilution. Depuration rates for both phases were not correlated with KOA, indicating that plant-air mass transfer coefficients were proportional to plant-air partition coefficients and, therefore, probably dominated by the plant-side resistance to diffusion. Photolysis and metabolism are unlikely to have influenced the rates of congener disappearance. Pathways into the leaf and possible storage locations within the plant are discussed with respect to the observed differences between uptake and clearance rates. Uptake and depuration are not mirror image processes, with a fraction of accumulated PCBs effectively stored in the leaves. This has important implications for terrestrial food chain transfer and global cycling with leaf concentrations remaining elevated long after a contamination event.     

PBDEs in European background soils: levels and factors controlling their distribution

Surface soils (0-5 cm) from remote/rural woodland (coniferous and deciduous) and grassland locations on a latitudinal transectthrough the United Kingdom and Norway were analyzed for polybrominated diphenyl ethers (PBDEs). Concentrations ranged between 65 and 12 000 sigma(ALL)PBDE ng kg(-1) dry weight. PBDE-47, -99, -100, -153, and -154-the major constituents of the penta-BDE technical product-dominated the average congener pattern of the soils. Indeed, the average congener composition and distribution measured in these European background soils closely matched that reported in the technical penta-BDE product. This is interpreted as evidence that transfer of the congeners present in penta-BDE-treated products from source-air-soil occurs with broadly similar efficiency, perhaps because there has been little weathering/degradation/alteration of the congener source pattern by processes operating during atmospheric transport or within the soil itself. BDE-183, a marker for the octa-BDE mix, was detected at concentrations ranging from <9 to 7000 (median approximately 50 ng kg(-1)). In most soils, it made a minor contribution to the sigma(ALL)PBDE concentration, but it was a major component in some samples from northern England. Forest soils tended to have higher concentrations than grasslands. Underlying the average soil composition, some differences in the congener pattern were observed. Notably, there was evidence of latitudinal fractionation, with the relative contribution of PBDE-47 and lighter congeners to the sigmaPBDE increasing northwards (with increasing distance from source areas), while the proportion of PBDE-99 and heavier congeners decreased. Plots of concentration against percentage soil organic matter had different slopes for different congeners. Higher slopes were generally seen for the lighter PBDEs (e.g., PBDE-47), indicating that they have undergone some air-surface exchange (hopping), while the slopes of heavier congeners (e.g., PBDE-153) were close to zero, indicating that they are retained more effectively by soils after deposition.