A Global Community of Courts? Modelling the Use of Persuasive Authority as a Complex Network

There is a growing discussion in the legal literature of an emerging global community of courts composed of a network of increasing judicial dialogue across national borders. We investigate the use of foreign persuasive authority in common law countries by analyzing the network of citations to case law in a corpus of over 1.5 million judgments given by the senior courts of twenty-six common law countries. Our corpus of judgments is derived from data available in the vLex Justis database. In this paper we aim to quantify the flow of jurisprudence across the countries in our corpus and to explore the factors that may influence a judge’s selection of foreign jurisprudence. Utilization of foreign case law varies across the countries in our data, with the courts of some countries presenting higher engagement with foreign jurisprudence than others. Our analysis shows that there has been an upward trend in the use of foreign case law over time, with a marked increase in citations across national borders from the 1990s onward, potentially indicating that increased digital access to foreign judgments has served to facilitate and promote comparative analysis. Not only has the use of foreign case law generally increased over time, the factors that may influence the selection of case law have also evolved, with judges gradually casting their research beyond the most influential and well-known foreign authorities. Notwithstanding that judgments emanating from the United Kingdom (chiefly from the courts of England and Wales) constitute the most frequently consulted body of jurisprudence, we find evidence that domestic courts favor citing the case law of countries that are geographically proximal

New thermoplastic polyurethane elastomers based on sulfur-containing chain extenders

New thermoplastic polyurethane elastomers (TPUs) were synthesized by a one-step melt polyaddition from poly(oxytetramethylene) diol of M¯n = 2000 g/mol as the soft segment, 1,1’-methanediylbis(4-isocyanatocyclohexane) (HMDI, Desmodur W®), and 2,2’-[methanediylbis(benzene-4,1-diylmethanediylsulfanediyl)]diethanol (diol E) or 6,6’-[methanediylbis(benzene-4,1-diylmethanediylsulfanediyl)]dihexane-1-ol (diol H) as unconventional chain extenders. The effects of the kind and amount of the polymer diol and chain extender used on the structure and properties of the polymers were studied. The polymers were examined by Fourier transform infrared spectroscopy, gel permeation chromatography, thermogravimetric analysis, differential scanning calorimetry, Shore hardness and tensile testing. Both the adhesive and optical properties were determinated for a selected polymer. The obtained TPUs were amorphous, colorless, high-molar-mass materials. It was observed that the polymers with the diol E showed higher hardness and tensile strengths but smaller elongations at break than diol H-based ones. All of the polymers exhibited a relatively good thermal stability. Their temperatures of 5% mass loss were in the range 312-338°C

New thermoplastic poly(carbonate-urethane) elastomers

Two series of novel thermoplastic poly(carbonate-urethane) elastomers, with different hard-segment content (30 - 60 wt %), were synthesized by melt polymerization from poly(hexane-1,6-diyl carbonate) diol of Mn = 2000 as a soft segment, 4,4'-diphenylmethane diisocyanate (MDI) or hexane-1,6-diyl diisocyanate (HDI) and 6,6'-[methylenebis(1,4-phenylenemethylenethio)]dihexan-1-ol as a chain extender. The structure and basic properties of the polymers were examined by Fourier transform infrared spectroscopy, X-ray diffraction analysis, atomic force microscopy, differential scanning calorimetry, thermogravimetric analysis, Shore hardness and tensile tests. The resulting TPUs were colorless polymers, showing almost amorphous structures. The MDI-based TPUs showed higher tensile strengths (up to 21.3 MPa vs. 15.8 MPa) and elongations at break (up to 550% vs. 425%), but poorer low-temperature properties than the HDI-based analogs

New thermoplastic poly(carbonate-urethane) elastomers

Two series of novel thermoplastic poly(carbonate-urethane) elastomers, with different hard-segment content (30 - 60 wt %), were synthesized by melt polymerization from poly(hexane-1,6-diyl carbonate) diol of Mn = 2000 as a soft segment, 4,4'-diphenylmethane diisocyanate (MDI) or hexane-1,6-diyl diisocyanate (HDI) and 6,6'-[methylenebis(1,4-phenylenemethylenethio)]dihexan-1-ol as a chain extender. The structure and basic properties of the polymers were examined by Fourier transform infrared spectroscopy, X-ray diffraction analysis, atomic force microscopy, differential scanning calorimetry, thermogravimetric analysis, Shore hardness and tensile tests. The resulting TPUs were colorless polymers, showing almost amorphous structures. The MDI-based TPUs showed higher tensile strengths (up to 21.3 MPa vs. 15.8 MPa) and elongations at break (up to 550% vs. 425%), but poorer low-temperature properties than the HDI-based analogs