Abstract: Network nodes and methods for control thereof for dynamic network slice selection. An AMF receives a UE request originating from the UE, the UE request being any one of a registration request and a session request. A network slice requester controls a transmitter to transmit a network slice selection request to a PC_NSS. A selection data manager of the PC_NSS determines selection data specifying one or more UE specific parameters affecting network slice selection. A network slice selector selects a network slice assignable for the UE, based on the selection data, determines network slice data and a corresponding network slice routing rule, and transmits them to the AMF. A network slice manager of the AMF controls assignment of a network slice to the UE in dependence on the received network slice data and network slice routing rule.

Abstract: A method performed by a first node (e.g., a network exposure function (NEF)) is provided. The method includes: the first node subscribing to an event for one or more user equipments (UEs) at a second node (e.g., a policy and control function (PCF)). Subscribing to the event comprises indicating one or more filters selected from the group of (i) a set of network identifiers (e.g., data network names (DNNs)) that the subscription applies to, (ii) a set of network slice identifiers (e.g., single network slice selection assistance information (S-NSSAIs)) that the subscription applies to, and (iii) a set of locations to which the subscription applies.

Abstract: The present invention provides a Molybdenum or Tungsten chalcogenide nanoobject having: (a) an object size comprised from 0.

Abstract: The present invention relates to the quantification of organic compounds originating from a chromatography system that does not involve the use of patterns, comprising the continuous conversion of the carbon of the compounds into carbon dioxide (CO2) involving a chemical reaction and the mixing of same, before or after separation, with a known, constant flow of a carbon compound, preferably CO2, with carbon isotope-13 (13C). The mixture is introduced into a mass spectrometer in which the isotopic ratio 12C/13C is continuously measured either in the carbon or in a characteristic ion originating from same. The isotope ratio is converted into a carbon mass flow measurement using on-line isotope dilution.