Measuring knowledge transfer between fields of science

In this paper we report on the results of an exploratory study of knowledge exchange between disciplines and subfields of science, based on bibliometric methods. The goal of this analysis is twofold. Firstly, we consider knowledge exchange between disciplines at a global level, by analysing cross-disciplinary citations in journal articles, based on the world publication output in 1999. Among others a central position of the Basic Life Sciences within the Life Sciences and of Physics within the Exact Sciences is shown. Limitations of analyses of interdisciplinary impact at the journal level are discussed. A second topic is a discussion of measures which may be used to quantify the rate of knowledge transfer between fields and the importance of work in a given field or for other disciplines. Two measures are applied, which appear to be proper indicators of impact of research on other fields. These indicators of interdisciplinary impact may be applied at other institutional levels as well. This revised version was published online in August 2006 with corrections to the Cover Date.     

Electrochemical oxidation by square-wave potential pulses in the imitation of oxidative drug metabolism

Electrochemistry combined with mass spectrometry (EC-MS) is an emerging analytical technique in the imitation of oxidative drug metabolism at the early stages of new drug development. Here, we present the benefits of electrochemical oxidation by square-wave potential pulses for the oxidation of lidocaine, a test drug compound, on a platinum electrode. Lidocaine was oxidized at constant potential and by square-wave potential pulses with different cycle times, and the reaction products were analyzed by liquid chromatography-mass spectrometry [LC-MS(/MS)]. Application of constant potentials of up to +5.0 V resulted in relatively low yields of N-dealkylation and 4-hydroxylation products, while oxidation by square-wave potential pulses generated up to 50 times more of the 4-hydroxylation product at cycle times between 0.2 and 12 s (estimated yield of 10%). The highest yield of the N-dealkylation product was obtained at cycle times shorter than 0.2 s. Tuning of the cycle time is thus an important parameter to modulate the selectivity of electrochemical oxidation reactions. The N-oxidation product was only obtained by electrochemical oxidation under air atmosphere due to reaction with electrogenerated hydrogen peroxide. Square-wave potential pulses may also be applicable to modulate the selectivity of electrochemical reactions with other drug compounds in order to generate oxidation products with greater selectivity and higher yield based on the optimization of cycle times and potentials. This considerably widens the scope of direct electrochemistry-based oxidation reactions for the imitation of in vivo oxidative drug metabolism.     

Spatial distribution of the gain and temperature across the flow in a slit-nozzle supersonic chemical oxygen-iodine laser with transonic and supersonic schemes of iodine injection

Spatial distributions of the gain and temperature across the flow were studied for transonic and supersonic schemes of the iodine injection in a slit-nozzle supersonic chemical oxygen-iodine laser as a function of the iodine and secondary nitrogen flow rate, jet penetration parameter, and gas pumping rate. The mixing efficiency for supersonic injection of iodine (/spl sim/0.85) is much larger than for transonic injection (/spl sim/0.5), the maximum values of the gain being /spl sim/0.65%/cm for both injection schemes. Measurements of the gain distribution as a function of the iodine molar flow rate nI/sub 2/ were carried out. For transonic injection, the optimal value of nI/sub 2/ at the now centerline is smaller than that at off axis locations. The temperature is distributed homogeneously across the flow, increasing only in the narrow boundary layers near the walls. Opening a leak downstream of the cavity in order to decrease the Mach number results in a much larger mixing efficiency (/spl sim/0.8) than for a closed leak.     

Synergy between bio‐based industry and the feed industry through biorefinery

Processing biomass into multi‐functional components can contribute to the increasing demand for raw materials for feed and bio‐based non‐food products. This contribution aims to demonstrate synergy between the bio‐based industry and the feed industry through biorefinery of currently used feed ingredients. Illustrating the biorefinery concept, rapeseed was selected as a low priced feed ingredient based on market prices versus crude protein, crude fat and apparent ileal digestible lysine content. In addition it is already used as an alternative protein source in diets and can be cultivated in European climate zones. Furthermore, inclusion level of rapeseed meal in pig diet is limited because of its nutritionally active factors. A conceptual process was developed to improve rapeseeds nutritional value and producing other bio‐based building blocks simultaneously. Based on the correlation between market prices of feed ingredients and its protein and fat content, the value of refined products was estimated. Finally, a sensitivity analysis, under two profit scenario, shows that the process is economically feasible. This study demonstrates that using biorefinery processes on feed ingredients can improve feed quality. In conjunction, it produces building blocks for a bio‐based industry and creates synergy between bio‐based and feed industry for more efficient use of biomass. © 2015 Society of Chemical Industry     

Citation delay in interdisciplinary knowledge exchange

As part of a larger project to investigate knowledge flows between fields of science, westudied the differences in speed of knowledge transfer within and across disciplines. The agedistribution of references in three selections of articles was analysed, including almost 800.000references in journal publications of the United Kingdom in 1992, 700.000 references inpublications of Germany in 1992, and more than 11 million references in the world total ofpublications in 1998.The rate of citing documented knowledge from other disciplines appears to differ sharplyamong disciplines. For most of the disciplines the same ratio's are found in the three data sets.Exceptions show interesting differences in the interdisciplinary nature of a field in a country. Wefind a general tendency of a citation delay in case of knowledge transfer between different fieldsof science: citations to work of the own discipline show less of a time lag than citations to work ina foreign discipline. Between disciplines typical differences in the speed of incorporatingknowledge from other disciplines are observed, which appear to be relatively independent of timeand place: for each discipline the same pattern is found in the three data sets. The disciplinespecific characteristics found in the speed of interdisciplinary knowledge transfer may be point ofdeparture for further investigations. Results may contribute to explanations of differences incitation rates of interdisciplinary research.     

Layered distributed operating system

The improved efficiency of microelectronics and the development of digital transmission systems have allowed experimentation with distributed computing architectures. The requirements of a distributed operating system are outlined, and the principles and architecture used in the system are explained. A method is described of managing the system directories, and an analysis is given of the results obtained.     

Characterization of a synthetic 37-residue fragment of a monoclonal antibody against herpes virus by capillary electrophoresis/electrospray (ionspray) mass spectrometry and 252Cf plasma desorption mass spectrometry

A peptide comprising 37 amino acids of the antigen binding site of a monoclonal antibody directed against glycoprotein D of herpes simplex virus was synthesized. The synthetic peptide and the impurities formed in the synthesis were characterized by capillary electrophoresis/ionspray mass spectrometry and by 252Cf plasma desorption-time of flight mass spectrometry. The measured average molecular mass of the synthetic peptide was 4627.16 Da, which was only 0.08 Da higher than the calculated value (4627.08 Da). The plasma desorption mass spectrum of the synthetic peptide showed a protonated molecule at m/z 4624.1, which was 4 Da lower than the calculated one (4628.09 Da). The amino acid sequence of the peptide was confirmed in part by electrospray (ionspray) mass spectrometry using a high nozzle skimmer voltage difference. Five impurities were separated and identified by capillary electrophoresis/mass spectrometry and two of them also appeared in the plasma desorption mass spectrum.