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Welding technology may be considered as a promising processing method for the formation of packaging products from biopolymers. However, the welding processes used can change the properties of the polymer materials, especially in the region of the weld. In this contribution, the impact of the welding process on the structure and properties of biopolymer welds and their ability to undergo hydrolytic degradation will be discussed. Samples for the study were made from polylactide (PLA) and poly(3-hydroxyalkanoate) (PHA) biopolymers which were welded using two methods: ultrasonic and heated tool welding. Differential scanning calorimetry (DSC) analysis showed slight changes in the thermal properties of the samples resulting from the processing and welding method used. The results of hydrolytic degradation indicated that welds of selected biopolymers started to degrade faster than unwelded parts of the samples. The structure of degradation products at the molecular level was confirmed using mass spectrometry. It was found that hydrolysis of the PLA and PHA welds occurs via the random ester bond cleavage and leads to the formation of PLA and PHA oligomers terminated by hydroxyl and carboxyl end groups, similarly to as previously observed for unwelded PLA and PHA-based materials.

Excessive levels of plastic waste in our oceans and landfills indicate that there is an abundance of potential carbon sources with huge economic value being neglected. These waste plastics, through biological fermentation, could offer alternatives to traditional petrol-based plastics. Polyhydroxyalkanoates (PHAs) are a group of plastics produced by some strains of bacteria that could be part of a new generation of polyester materials that are biodegradable, biocompatible, and, most importantly, non-toxic if discarded. This study introduces the use of prodegraded high impact and general polystyrene (PS0). Polystyrene is commonly used in disposable cutlery, CD cases, trays, and packaging. Despite these applications, some forms of polystyrene PS remain financially and environmentally expensive to send to landfills. The prodegraded PS0 waste plastics used were broken down at varied high temperatures while exposed to ozone. These variables produced PS flakes (PS1&ndash, 3) and a powder (PS4) with individual acid numbers. Consequently, after fermentation, different PHAs and amounts of biomass were produced. The bacterial strain, Cupriavidus necator H16, was selected for this study due to its well-documented genetic profile, stability, robustness, and ability to produce PHAs at relatively low temperatures. The accumulation of PHAs varied from 39% for prodegraded PS0 in nitrogen rich media to 48% (w/w) of dry biomass with the treated PS. The polymers extracted from biomass were analyzed using nuclear magnetic resonance (NMR) and electrospray ionization tandem mass spectrometry (ESI-MS/MS) to assess their molecular structure and properties. In conclusion, the PS0&ndash, 3 specimens were shown to be the most promising carbon sources for PHA biosynthesis, with 3-hydroxybutyrate and up to 12 mol % of 3-hydroxyvalerate and 3-hydroxyhexanoate co-monomeric units generated.

Using conventional nondegradable and noncompostable polymers has a significant negative impact on the environment, so biodegradable polymers can attract much attention in regards to the current interest in the field of sustainable development, recycling, or environmental protection. Morphological and structural transformations resulting from the degradation of the material have a significant impact on the polymer material properties. Thus, evaluation and understanding of the structure, properties, and behavior of advanced materials for perspective food packaging applications is important to avoid degradation during storage. This review focuses on biodegradable polymer materials with approved or potential applications in food packaging. The major groups of biodegradable natural, microbial, and synthetic polymers will briefly be discussed with regard to properties required for packaging materials, like permeability, physical and mechanical properties, antioxidative and antimicrobial additives, plasticization, and biodegradability, based on studies reported in the literature as well as future trends.

The degradation of the advanced polymeric materials: blends of polylactide with poly[(R,S)-3-hydroxybutyrate] was studied in paraffin (an ingredient used in cosmetics) and compared with the degradation of pure poly[(R,S)-3-hydroxybutyrate]. The interaction between the polymeric materials studied and the paraffin was monitored during the degradation experiments, and the effects of this interaction were reported. Gel permeation chromatography, atomic force microscopy, electrospray mass spectrometry, nuclear magnetic resonance, differential scanning calorimetry and thermal gravimetric analysis revealed that degradation of the investigated materials occurs in the presence of paraffin. In the blends, poly[(R,S)-3-hydroxybutyrate] content was found to extend the disintegration time, and for the blends with good miscibility, reduced the degradation rate in the first step of degradation.

Degradation process of the rigid films prepared from polylactide (PLA) and its blend with poly[(R,S)-3-hydroxybutyrate] (PLA/a-PHB) in an industrial composting pile and in extracts from industrial compost was conducted. The significant changes in the number average molar mass (Mn) of the PLA and PLA/a-PHB samples without mass loss up to the 21 days of the experiment indicated that abiotic hydrolysis is the main process that occurs during the first weeks of the incubation of these samples in each environments studied. The observed progressive decrease in pH of sterile extract (SE) at invariable pH of the nonsterile extract (NSE) indicates that microbes present in compost can assimilate the products of abiotic hydrolysis of the incubated samples. The influence of microorganisms present in the compost on the (bio)degradation process of PLA and PLA/a-PHB was proved through 1H NMR and ESI-MS analysis of the compost extracts collected after specific degradation time periods.

The introduction of new, environmentally friendly and sustainable plastics in the packaging and end-user industry is a solution to the problem of waste management. The degradation of polyesters in different environments could result from an enzymatic attack or simple hydrolysis, or both. The degree of degradation of blends containing polylactide and poly(3-hydroxybutyrate-co-4-hydroxybutyrate), PLA/P(3HB-co-4HB), and its composites with 20 %wt of jute incubated in distilled water at 70 ℃ (abiotic conditions) under industrial composting conditions (system KNEER) was investigated using a Zeiss optical microscope, an atomic force microscope, gel permeation chromatography, differential scanning calorimetry and thermal gravimetric analysis. PLA/P(3HB-co-4HB) was tested under laboratory composting conditions in order to verify whether biodegradation of this material occurs under industrial composting conditions. The addition of jute fibres did significantly reduce the disintegration of the composites during degradation.

The semicrystalline poly(L-lactide) (PLLA) belongs to the materials with shape memory effect (SME) and as a bioresorbable and biocompatible polymer it have found many applications in medical and pharmaceutical field. Assessment of the SME impact on the polymer degradation profile plays crucial role in applications such as drug release systems or in regenerative medicine. Herein, the results of in vitro degradation studies of PLLA samples after SME full test cycle are presented. The samples were loaded and deformed in two manners: progressive and non-progressive. The performed experiments illustrate also influence of the material mechanical damages, caused e.g. during incorrect implantation of PLLA product, on hydrolytic degradation profile. Apparently, degradation profiles are significantly different for the material which was not subjected to the deformation and the deformed ones. The materials after deformation of 50% (in SME cycle) was characterized by non-reversible morphology changes. The effect was observed in deformed samples during the SME test which were carried out ten times.

The main aim of the present study was to determine the behavior of the specimens from Ecovio, in the form of dumbbell-shaped samples and films, during degradation in selected cosmetic ingredients such as water and paraffin. The (bio)degradation test of the prototype cosmetic package (sachet) made from a PBAT (poly[(1,4-butylene adipate)–co–(1,4-butylene terephthalate)]) and PLA (polylactide) blend was investigated under industrial composting conditions, and compared with the sample behavior during incubation in cosmetic media at 70 °C. During the degradation tests, the changes of the samples were evaluated using optical microscopy, 1H NMR (proton nuclear magnetic resonance) and GPC (gel permeation chromatography) techniques. The structures of the degradation products were investigated using ESI-MSn (mass spectrometry with electrospray ionization on positive and negative ions) analysis. The thermal properties of selected materials were determined by DSC (differential scanning calorimetry) and TGA (thermogravimetric analysis) analysis. It was concluded that the PBAT and PLA blend studied had a good stability during aging in cosmetic media, and could be recommended for long-shelf-life compostable packaging of cosmetics, especially with oily ingredients.

We report the synthesis and characterization of a novel polypyrrole material grafted with biodegradable oligo-3-hydroxybutyrate pendants. The polymer was prepared in a two-step process. Firstly, the potassium salt 1–(2-carboxyethyl)pyrrole was reacted with β-butyrolactone affording N-substituted macromonomer. Secondly, the macromonomer was oxidatively polymerised with FeCl3 Lewis acid. The reaction was carried out in solvents of assorted polarity: dimethylsulphoxide, acetonitrile, dimethylformamide and water. Obtained polymers have been characterised comprehensively using a suite of spectral techniques. The material was found to combine the well-known merits of 3-hydroxybutyrate polymers with the electrical conductivity imparted by polypyrrole units.

Knowledge of degradation and impairment phenomena of (bio)degradable polymeric materials under operating conditions, and thus the selection of test procedures and prediction of their behavior designates the scope and capabilities as well as possible limitations of both: the preparation of the final product and its durability. The main novelty and objective of this research was to determine the degradation pathways during testing of polylactide and polylactide/polyhydroxyalkanoate materials made with three-dimensional printing and the development of a new strategy for the comprehensive characterization of such complex systems including behavior during waste disposal. Prototype objects were subjected to tests for damage evolution performed under simulating operating conditions. The reference samples and the tested items were characterized by gel permeation chromatography and differential scanning calorimetry to determine changes in material properties. The studies showed that: polyhydroxyalkanoate component during accelerated aging and degradation in environments rich in microorganisms accelerated the degradation of the material, paraffin accelerates polylactide degradation and slows degradation of polyhydroxyalkanoate-based material, under the influence of an environment rich in enzymes, paraffin contamination accelerates biodegradation, under the influence of natural conditions, paraffin contamination slowed degradation, the processing conditions, in particular the printing orientation of individual parts of the container, influenced the material properties in its various regions, affecting the rate of degradation of individual parts.

The degree of degradation of pure poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)] and its composites with cork incubated under industrial and laboratory composting conditions was investigated. The materials were parallelly incubated in distilled water at 70 &deg, C as a reference experiment (abiotic condition). It was demonstrated that addition of the cork into polyester strongly affects the matrix crystallinity. It influences the composite degradation independently on the degradation environment. Moreover, the addition of the cork increases the thermal stability of the obtained composites, this was related to a smaller reduction in molar mass during processing. This phenomenon also had an influence on the composite degradation process. The obtained results suggest that the addition of cork as a natural filler in various mass ratios to the composites enables products with different life expectancies to be obtained.

The degradation process promotes physical and chemical changes in material properties, which can be characterised using thermal analysis techniques. The degree of polylactide film degradation in paraffin, glycerine and propylene glycol (as the thermal properties, crystallinity, thermal stability and decomposition kinetics changes) of the film during degradation at 70 °C, was investigated using dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). The changes in the thermal properties, crystallinity and thermal stability of the films during degradation indicate morphological and structural transformations, which result in the deterioration of the material properties for all of the investigated degradation media.

Poly( l -lactide), PLLA, belongs to the most widely used biodegradable polyesters. These polymers have attracted great attention in recent years due to their excellent material properties, which give a rise to potential applications in various commercial areas. Previously, PLLA reprocessing in a co-rotating twin-screw extruder was used as a model test for material recycling. It may be assumed basing on this study, that PLLA technological wastes may be suitable for reuse, for example, as an additive for neat PLLA. In order to verify such suitability of reprocessed PLLA its degradability under industrial composting conditions was studied at the static composting open-air pile. Incubation of this material in water at 70 °C (abiotic conditions) was also conducted. The progress of the degradation process was monitored by surface changes and measurements of sample weight loss and changes in the PLLA molecular weight. The molecular level structure of the water soluble degradation products of PLLA samples was determined by electrospray ionization multistage mass spectrometry (ESI-MS n ). Lactic acid and its oligomers terminated by hydroxyl and carboxyl end groups were identified as hydrolytic degradation products. The obtained results indicated that in selected environments (industrial composting and incubation under abiotic conditions) hydrolytic degradation via random ester bond scission occurs preferentially. It was demonstrated, that multi-reprocessing of PLLA did not significantly affect the rate of degradation and only slightly affected the disintegration progress of the PLLA samples.

Polyesters produced from renewable resources and susceptible to hydrolysis under the industrial composting conditions offer ecological advantages as compared to thermoplastics polymers and elastomers produced from fossil carbon sources. In this paper the degradation behaviour of polymer compositions of BTA, PLA and a-PHB in natural environment of industrial composting pile, consisting of leaves -40%, branches - 30% and grass - 30%, have been presented. The extend of degradation was monitored by macroscopic observations of sample surfaces, changes of molecular weight, polydispersity and composition of the tested materials and their weight loss.

This paper presents a forensic engineering study on the biodegradation behaviour of prototype packaging thermoformed from PLA-extruded film and plain PLA film under industrial composting conditions. Hydrolytic degradation in water was conducted for reference. The effects of composting duration on changes in molar mass, glass transition temperature and degree of crystallinity of the polymeric material were monitored using gel permeation chromatography (GPC) and differential scanning calorimetry (DSC). The chemical structure of water soluble degradation products of the polymeric material was determined using nuclear magnetic resonance (NMR) and electrospray ionization mass spectrometry (ESI-MS). The results show that the biodegradation process is less dependent on the thermoforming process of PLA and more dependent on the composting/degradation conditions that are applied. The increase in the dispersity index, leading to the bimodal molar mass distribution profile, suggests an autocatalytic hydrolysis effect at the early stage of the composting process, during which the bulk hydrolysis mechanism dominantly operates. Both the prototype PLA-packaging and PLA rigid film samples were shown to have a gradual increase in opacity due to an increase in the degree of crystallinity.

A preliminary study of the degradation of selected commercial packaging materials in compost and aqueous environments The paper presents the results of the degradation of two commercial packaging materials CONS-PET and BioPlaneta in the compost and distilled water at 70°C. The materials containing polylactide (PLA), CONS-PET 13% and BioPlaneta 20%, aliphatic-aromatic copolyester terephthalic acid/adipic acid/1,4-butanediol (BTA) and commercial additives degraded under the industrial composting conditions (composting pile or container) and in distilled water at 70°C in the laboratory holding oven. Distilled water provided the conditions for the hydrolytic (abiotic) degradation of the materials. Weight loss, changes of molecular weight, dispersity monitored via the GPC technique and the macroscopic surface changes of the tested materials were monitored during the experiments. The investigated systems show similar trends of degradation, however on the last day of the incubation the decrease of the molecular weight was higher in water than under the industrial composting conditions. The results indicate that commercial packaging materials can be degraded both while composting ((bio)degradation) and during the incubation in distilled water at 70°C (abiotic hydrolysis).

The results of the study on degradation of selected synthetic polyesters namely poly(L--lactide) (PLLA), poly[(DL)-lactide] (PLA) and aliphatic - aromatic co-polyester terephthalic acid/ adipic acid/1,4-butanediol (BTA) in the industrial compost heap, a compost containing activated sludge, standardized soil or dynamic sea water were presented. The course of degradation process was monitored by evaluation of changes of molecular weights of the samples by GPC method (Fig. 1, 3, 4 and 7), macroscopic changes of the surface (Fig. 2) and weight loss. It has been found that most significant decrease in molecular weight and clear disintegration of the materials investigated (particularly PLA samples) took place during the degradation under the industrial composting conditions. So this is the proper degradation environment for the tested compostable polymers, for their degradation processes in the other environments go much more slowly. The changes in the characteristic properties of the environments used were also evaluated during the process of polymers' degradation up to six-month time (Table 1, 2 and 5). Additionally, on the basis of the results of phytotoxicity test, no harmful effects of the degradation products of PLA and PLLA samples, incubated in the soil, on the growth and development of the plants seeds sown in the soil has been found (Fig. 5 and 6, Table 3 and 4).

The sustained release of multiple anti-cancer drugs using a single delivery carrier to achieve a synergistic antitumor effect remains challenging in biomaterials and pharmaceutics science. In this study, a supramolecular hydrogel based on the host–guest complexes between pH-responsive micelle derived poly(ethylene glycol) chains and α-cyclodextrin was designed for codelivery of two kinds of anti-cancer agents, hydrophilic 8-hydroxyquinoline glycoconjugate and hydrophobic doxorubicin. The host–guest interactions were characterized using X-ray diffraction and differential scanning calorimetry techniques. The resultant supramolecular hydrogel showed thixotropic properties, which are advantageous to drug delivery systems. In vitro release studies revealed that the supramolecular hydrogel exhibited faster drug release profiles in acidic conditions. The MTT assay demonstrated a synergistic cancer cell proliferation inhibition of DOX/8HQ-Glu mixture. In vitro cytotoxicity studies indicated excellent biocompatibility of the supramolecular hydrogel matrix, whereas the DOX/8HQ-Glu-loaded supramolecular hydrogel showed a sustained inhibition efficacy against cancer cells. The codelivery of hydrophobic anti-cancer drugs and hydrophilic anti-cancer drug glycoconjugates via a pH-responsive supramolecular hydrogel opens up new possibilities for the development of an effective cancer treatment based on the tumor-specific Warburg effect.