Characterization of municipal solid waste residues for hydrothermal liquefaction into liquid transportation fuels.

This paper presents and evaluates a new method for characterising municipal solid waste residues for assessing the performance of thermochemical conversion technologies to produce fuels. The method combines information from three complementary analytical techniques to estimate the quantity of key organic waste fractions and was demonstrated using two commercial waste residues: 'BRDF' and 'Floc' produced from the mechanical processing of domestic waste. Cellulose content (mostly paper and textiles) is estimated using acid hydrolysis, while thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR) are combined to determine the plastics (LDPE and PET) and non-volatile fractions such as lignin of the wastes. High mass balance closures were achieved for both residues, although the nature of the non-volatile fraction was difficult to verify. Hydrothermal liquefaction (HTL) of cellulose rich BRDF (34.0% cellulose) produced much higher biooil yields than Floc (26.8% and 12.2%, respectively), with a cellulose content of only 22.4%. In both cases, most of the plastic and non-volatile waste fractions partitioned into the solid HTL product, representing a potential method for separating the plastic fractions from other waste components. Importantly, this combined waste characterization method can be used for characterization of any municipal waste residue using acid hydrolysis, TGA and FTIR data, providing accurate information about feedstock composition. It enables comparison between different waste valorisation studies of complex waste residues.

Microencapsulation of Salmonella-Specific Bacteriophage Felix O1 Using Spray-Drying in a pH-Responsive Formulation and Direct Compression Tableting of Powders into a Solid Oral Dosage Form.

The treatment of enteric bacterial infections using oral bacteriophage therapy can be challenging since the harsh acidic stomach environment renders phages inactive during transit through the gastrointestinal tract. Solid oral dosage forms allowing site-specific gastrointestinal delivery of high doses of phages, e.g., using a pH or enzymatic trigger, would be a game changer for the nascent industry trying to demonstrate the efficacy of phages, including engineered phages for gut microbiome modulation in expensive clinical trials. Spray-drying is a scalable, low-cost process for producing pharmaceutical agents in dry powder form. Encapsulation of a model Salmonella-specific phage (Myoviridae phage Felix O1) was carried out using the process of spray-drying, employing a commercially available Eudragit S100® pH-responsive anionic copolymer composed of methyl methacrylate-co-methacrylic acid formulated with trehalose. Formulation and processing conditions were optimised to improve the survival of phages during spray-drying, and their subsequent protection upon exposure to simulated gastric acidity was demonstrated. Addition of trehalose to the formulation was shown to protect phages from elevated temperatures and desiccation encountered during spray-drying. Direct compression of spray-dried encapsulated phages into tablets was shown to significantly improve phage protection upon exposure to simulated gastric fluid. The results reported here demonstrate the significant potential of spray-dried pH-responsive formulations for oral delivery of bacteriophages targeting gastrointestinal applications.