Difference in polypropylene fragmentation mechanism between marine and terrestrial regions

Two kinds of marine polypropylene (M1-PP and M2-PP) and one land PP (L-PP) samples were collected from two beaches and land in Japan, respectively, to study the fragmentation mechanisms. Delamination was observed on both M1-PP and M2-PP surfaces. Moreover, there was no delamination but an abrasion patch structure on the surface of L-PP. The delamination was studied using an advanced oxidation process-degraded PP as the marine PP model. The number and shape of cracks varied with an increase in degradation time. The fluctuations in the values and ratios of the carbonyl index as well as the weight change ratio were due to repeated oxidation and delamination. We found that the delamination behavior depends on the oxidation state. Poly(oxyethylene)8 octylphenyl ether (POE8) surfactant treatment caused the delamination to speed up, which is a typical characteristic of polyolefin environmental stress cracking (ESC). These results reveal that delamination is based on ESC.Article Highlights Two kinds of marine and one land polypropylene (PP) samples were collected from two beaches and land, respectively, to study the fragmentation mechanisms. Delamination was observed on both of marine PP surfaces. Moreover, there was no delamination but an abrasion patch structure on the land PP surface. We found that the delamination was based on environmental stress cracking mechanism by employing a marine PP model.

Formation of ZrC–SiC Composites from the Molecular Scale through the Synthesis of Multielement Polymers

In the field of non-oxide ceramic composites, and by using the polymer-derived ceramic route, understanding the relationship between the thermal behaviour of the preceramic polymers and their structure, leading to the mechanisms involved, is crucial. To investigate the role of Zr on the fabrication of ZrC–SiC composites, linear or hyperbranched polycarbosilanes and polyzirconocarbosilanes were synthesised through either “click-chemistry” or hydrosilylation reactions. Then, the thermal behaviours of these polymeric structures were considered, notably to understand the impact of Zr on the thermal path going to the composites. The inorganic materials were characterised by thermogravimetry-mass spectrometry (TG-MS), X-ray diffraction (XRD), and scanning electron microscopy (SEM). To link the macromolecular structure to the organisation involved during the ceramisation process, eight temperature domains were highlighted on the TG analyses, and a four-step mechanism was proposed for the polymers synthesised by a hydrosilylation reaction, as they displayed better ceramic yields. Globally, the introduction of Zr in the polymer had several effects on the temperature fragmentation mechanisms of the organometallic polymeric structures: (i) instead of stepwise mass losses, continuous fragment release prevailed; (ii) the stability of preceramic polymers was impacted, with relatively good ceramic yields; (iii) it modulated the chemical composition of the generated composites as it led, inter alia, to the consumption of free carbon.

Mass spectral and theoretical investigations of the transient proton-bound dimers on the cleavage processes of the peptide GHK and its analogues

Fragmentation mechanisms of the singly protonated peptides GHK, GHKH and HGHK have been investigated by mass spectrometry and theoretical calculations.

Electron-induced fragmentation mechanisms in organic monomers and their implications for photoresist optimization for EUV lithography

The electron-induced fragmentation mechanisms of two important EUV-photoresist monomers methyl isobutyrate and methacrylic acid are investigated in the film and gas-phases.

The mass spectrometric fragmentation mechanisms of catenulane and isocatenulane diterpenes

The EI-MS fragmentation mechanisms of three diterpenes from Catenulispora acidiphila and two semisynthetic derivatives were studied in extensive 13C-labelling experiments.