In this paper, the influence of the various degradation conditions, on the molecular and supramolecular structure of polybutylene succinate (PBS) and polybutylene succinate adipate (PBSA) copolymer during degradation is described. The experiment was carried out by the use of injection molded samples and normalized conditions of biodegradation in soil, composting and artificial weathering. Materials were studied by size-exclusion chromatography (SEC) coupled with multiangle laser light scattering (MALLS) detection and wide-angle X-ray diffraction (WAXD). Additionally, the physical and mechanical properties of the samples were determined. The performed experiments clearly show difference impacts of the selected degradation conditions on the macroscopic, supramolecular and molecular parameters of the studied aliphatic polyesters. The structural changes in PBS and PBSA explain the observed changes in the physical and mechanical properties of the obtained injection molded samples.

In this paper, the influence of the molecular structure of polylactide (PLA)—characterised by its molar mass and content of d-lactide isomer—on the molecular ordering and α’–α form transition during fibre manufacturing by the wet spinning method is described. Fibres were studied by wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). Additionally, the physical and mechanical properties of the fibres were determined. This study also examines the preliminary molecular ordering and crystallisation of PLA fibres at various draw ratios. The performed experiments clearly show the dependence of the molecular ordering of PLA on the molar mass and d-lactide content during the wet spinning process. The fibres manufactured from PLA with the lowest content of d-lactide and the lowest molar mass were characterised by a higher tendency for crystallisation and a higher possibility to undergo the disorder-to-order phase transition (α’ to α form). The structural changes in PLA explain the observed changes in the physical and mechanical properties of the obtained fibres.

The degradation of bio-based plastic materials in field soil under natural conditions was investigated in this study. Three bio-based plastics materials, which contained polylactide (PLA) with polybutylene adipate terephthalate and additives (PLA_1), PLA-based polyester blend with mineral filler (PLA_2), and polybutylene succinate with mineral filler (PBS_1) in the form of the film, were subjected to soil burial biodegradation processes. The experiments were carried out in a climate with an average annual temperature of 9.4 °C, in winter and summer periods for one year. The degradation of the materials was evaluated by macro- and microscopic observations, weight loss, thermogravimetric analysis, and tensile test. Macroscopic observation indicated that changes in the color of film surface were visible for samples PBS_1 after 12 months of degradation. Using microscopic inspection the erosion of surface samples PLA_1 and PBS_1 after 12 months was observed. Mass loss of samples PLA_1 and PLA_2 after one year of degradation were below 0.6 %. Moreover, for PBS_1 sample, mass loss was equal to 4.3 %. Based on the obtained results of the mass loss, a description of the degradation kinetics was proposed, showing the changes in the thickness of the tested polymer over time. The thermal stability of the samples PLA_1 and PLA_2 decreased during the degradation process by 16.1 and 2.6 °C, respectively, and for PBS_1 increased by 1.7 °C. Tensile strength at break after 12 months of degradation decreased for sample PLA_1 and PLA_2 by 27.3 and 5.8 %, respectively, and increased for sample PBS_1 by 28.2 % compare to unexposed sample.

The unique properties of graphene, such as the high elasticity, mechanical strength, thermal conductivity, very high electrical conductivity and transparency, make them it an interesting material for stretchable electronic applications. In the work presented herein, the authors used graphene and carbon nanotubes to introduce chemical sensing properties into textile materials by means of a screen printing method. Carbon nanotubes and graphene pellets were dispersed in water and used as a printing paste in the screen printing process. Three printing paste compositions were prepared—0%, 1% and 3% graphene pellet content with a constant 3% carbon nanotube mass content. Commercially available materials were used in this process. As a substrate, a twill woven cotton fabric was utilized. It has been found that the addition of graphene to printing paste that contains carbon nanotubes significantly enhances the electrical conductivity and sensing properties of the final product.