It is shown by angle-resolved x-ray photoelectron spectroscopy that cavitands derived from resorcin[4]arenes provided with four dialkylsulfide chains form stable monolayers on gold surfaces that are well organized by self-assembly. The cavitand headgroups at the surface of the resorcin[4]arene monolayer act as molecular recognition sites for small organic molecules with remarkable selectivity for perchloroethylene (C ₂ Cl ₄ ). Comparative thermal desorption experiments indicate binding sites with high interaction energies of C ₂ Cl ₄ at the surface of the resorcin[4]arene monolayers. Fast and reversible "host-guest" interactions were found by the monitoring of extremely small mass changes (in the nanogram range) with a quartz microbalance oscillator provided with gold electrodes coated by resorcin[4]arene monolayers.

The Dutch post-consumer plastic packaging recycling network has been described in detail (both on the level of packaging types and of materials) from the household potential to the polymeric composition of the recycled milled goods. The compositional analyses of 173 different samples of post-consumer plastic packaging from different locations in the network were combined to indicatively describe the complete network with material flow analysis, data reconciliation techniques and process technological parameters. The derived potential of post-consumer plastic packages in the Netherlands in 2014 amounted to 341 Gg net (or 20.2 kg net.cap-1.a-1). The complete recycling network produced 75.2 Gg milled goods, 28.1 Gg side products and 16.7 Gg process waste. Hence the net recycling chain yield for post-consumer plastic packages equalled 30%. The end-of-life fates for 35 different plastic packaging types were resolved. Additionally, the polymeric compositions of the milled goods and the recovered masses were derived with this model. These compositions were compared with experimentally determined polymeric compositions of recycled milled goods, which confirmed that the model predicts these compositions reasonably well. Also the modelled recovered masses corresponded reasonably well with those measured experimentally. The model clarified the origin of polymeric contaminants in recycled plastics, either sorting faults or packaging components, which gives directions for future improvement measures.

The presence of contaminants in polyethylene terephthalate (PET) bottles and derived materials from the various steps in the recycling loop is studied. Based on these measurements, a model is proposed to generically describe the accumulation of these contaminants within closed‐loop recycling schemes for PET bottles. The measured levels of particle contamination and chlorine content of PET bottles, pellets, and intermediate recycling products are used to derive the modelling parameters. Previously determined relations between these measured parameters and critical bottle properties are used to model the effect of the accumulation of the contaminants on the bottle properties. The measurements reveal that the type of collection system influences the accumulation of contaminants in PET bottles greatly. PET bottles in mono‐collection systems accumulate less contaminants than PET bottles in co‐collection systems do. Therefore, PET bottles within recycling schemes using mono‐collection systems can contain more recycled content than those from co‐collection systems, without exceeding acceptation limits on critical bottle properties such as haziness, yellowing, and migration.

The effect of recycled content and type of recycled poly (ethylene terephthalate) (rPET) on the haziness; colour parameters L*, a*, and b*; total colour change; ultraviolet‐visual spectrum (UV‐VIS) absorption; and environmental stress cracking (ESC) of PET bottles was studied. Three series of PET bottles were made at a small scale production facility with same type of virgin PET and three different types of rPET with recycled contents of 25%, 50%, 75%, and 100%. Also, the particle contamination of the produced PET bottles was studied by dissolving bottle fragments and counting the insoluble particles. A linear relationship was found between the haziness of PET bottles and the particle contamination, with a coefficient of determination of 0.96. Linear relationships were also found between the colour parameters L* and b* and the particle contamination of the PET bottles, but the slope differed for each type of rPET. The origin of rPET (mono‐collection or cocollection) seems to be the crucial factor determining particle contamination and colour of the produced bottles. No correlation was found between the recycled content and the incidence of ESC. However, PET bottles in which high intrinsic viscosity (IV) values were measured showed lower chances of ESC than PET bottles with low IV values