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Many pledges and laws are setting recycling targets without clearly defining quality of recycling. Striving to close this gap, this study presents an operational framework to quantify quality of recycling. The framework comprises three dimensions: the Virgin Displacement Potential (VDP); In-Use Stocks Lifetime (IUSL); and Environmental Impact (EI). The VDP indicates to what extent a secondary material can be used as a substitute for virgin material; the IUSL indicates how much of a certain material is still functional in society over a given time frame, and the EI is a measure of the environmental impact of a recycling process. The three dimensions are aggregated by plotting them in a distance-to-target graph. Two example calculations are included on poly(ethylene terephthalate) (PET) and glass. The results indicate that the recycling of bottle and container glass collected via a deposit–refund system has the lowest distance-to-target, at 1.05, and, thus, the highest quality of recycling. For PET bottles, the highest quality of recycling is achieved in closed-loop mechanical recycling of bottles (distance to optimal quality of 0.96). Furthermore, sensitivity analysis indicates that certain parameters, e.g., the collection rate for PET bottles, can reduce the distance-to-target to 0.75 when all bottles are collected for recycling.

Plastic packaging typically consists of a mixture of polymers and contains a whole range of components, such as paper, organic residue, halogens, and metals, which pose problems during recycling. Nevertheless, until today, limited detailed data are available on the full polymer composition of plastic packaging waste taking into account the separable packaging parts present in a certain waste stream, nor on their quantitative levels of (elemental) impurities. This paper therefore presents an unprecedented in-depth analysis of the polymer and elemental composition, including C, H, N, S, O, metals, and halogens, of commonly generated plastic packaging waste streams in European sorting facilities. Various analytical techniques are applied, including Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), polarized optical microscopy, ion chromatography, and inductively coupled plasma optical emission spectrometry (ICP-OES), on more than 100 different plastic packaging products, which are all separated into their different packaging subcomponents (e.g., a bottle into the bottle itself, the cap, and the label). Our results show that certain waste streams consist of mixtures of up to nine different polymers and contain various elements of the periodic table, in particular metals such as Ca, Al, Na, Zn, and Fe and halogens like Cl and F, occurring in concentrations between 1 and 3000 ppm. As discussed in the paper, both polymer and elemental impurities impede in many cases closed-loop recycling and require advanced pretreatment steps, increasing the overall recycling cost.

A simple method has been developed and validated for quantitative determination of lumefantrine in antimalarial finished pharmaceutical products using gas chromatography coupled to flame ionization detector. Lumefantrine was silylated with N,O–bis(trimethyl-silyl)trifluoro-acetamide at 70°C for 30 minutes, and chromatographic separation was conducted on a fused silica capillary (HP-5, 30 m length × 0.32 mm i.d., 0.25 μm film thickness) column. Evaluation of the method within analytical quality-by-design principles, including a central composite face-centered design for the sample derivatization process and Plackett–Burman robustness verification of the chromatographic conditions, indicated that the method has acceptable specificity toward excipients and degradants, accuracy [mean recovery = 99.5%, relative standard deviation (RSD) = 1.0%], linearity (=0.9986), precision (intraday = 96.1% of the label claim, RSD = 0.9%; interday = 96.3% label claim, RSD = 0.9%), and high sensitivity with detection limits of 0.01 μg/mL. The developed method was successfully applied to analyze the lumefantrine content of marketed fixed-dose combination antimalarial finished pharmaceutical products.

A diagnostic instrument comprising a combined assessment of core control and assurance activities and a microbial assessment instrument were used to measure the performance of current food safety management systems (FSMSs) of two poultry meat preparation companies. The high risk status of the company’s contextual factors, i.e., starting from raw materials (poultry carcasses) with possible high numbers and prevalence of pathogens such as Campylobacterspp., requires advanced core control and assurance activities in the FSMS to guarantee food safety. The level of the core FSMS activities differed between the companies, and this difference was reflected in overall microbial quality (mesophilic aerobic count), presence of hygiene indicators (Enterobacteriaceae, Staphylococcus aureus,and Escherichia coli), and contamination with pathogens such as Salmonella, Listeria monocytogenes,and Campylobacterspp. The food safety output expressed as a microbial safety profile was related to the variability in the prevalence and contamination levels of Campylobacterspp. in poultry meat preparations found in a Belgian nationwide study. Although a poultry meat processing company could have an advanced FSMS in place and a good microbial profile (i.e., lower prevalence of pathogens, lower microbial numbers, and less variability in microbial contamination), these positive factors might not guarantee pathogen-free products. Contamination could be attributed to the inability to apply effective interventions to reduce or eliminate pathogens in the production chain of (raw) poultry meat preparations.

A multi-residue method for the determination of 16 polycyclic aromatic hydrocarbons (PAHs), biocides diuron (DIU), octylisothiazolinone (OIT) and mecoprop (MCPP), and phthalates bis(2-ethylhexyl) phthalate (DEHP) and diisodecyl phthalate (DIDP) in material leachate and roof runoff is presented. The method aims to keep sample pretreatment as simple as possible, not only to minimize sample contamination and sample losses, but also to have an environmental friendly and cost efficient method with low solvent consumption, in line with the principles of Green Analytical Chemistry. Solid phase extraction (SPE, C18) in combination with GC-MS was used for this purpose. A good separation and accurate detection for the majority of included analytes was obtained, resulting in overall low detection limits ranging between 0.1 ng/L and 18 µg/L in aqueous matrices. Furthermore, the addition of a surrogate standard containing three deuterated PAHs prior to SPE extraction was found to increase the method's repeatability. For the higher molecular weighted PAHs and phthalates, recovery was affected by the concentration level as higher recoveries were observed at lower spiking levels. Furthermore, also the matrix was found to affect the recovery of these higher molecular weighted components as the recoveries in roof runoff and material leachate were higher in comparison to the ones found in bidest water. Water solubility and the affinity to adsorb onto particles were hypothesized to play an important role. The multi-residue SPE-GC-MS method was found to be suitable for the quick and reliable analysis of material leachates and roof runoff samples.