Shape-stabilized phase change material (SSPCM) is a promising thermal energy storage material in energy-saving buildings. However, its flammability leads to a fire risk. The conventional bulk addition method has a limited flame-retardant effect. Herein, a series of surface coatings with various flame retardants were introduced to improve flame retardance of SSPCM. The results showed that all of the coatings had flame-retardant effects on SSPCM; In particular, the EG coating performed the best: the horizontal burning time was the longest, the limiting oxygen index was above 30%, the V0 classification was obtained, the peak heat release rate was sharply decreased from 1137.0 to 392.5 kW/m² and the burning process was prolonged with the least total smoke production. The flame-retardant mechanism was discussed. As paraffin easily evaporated from the SSPCM at a moderate temperature, it caused flames. After being surface coated, the EG-based coatings first hindered the volatilization of paraffin at a moderate temperature, then expanded and formed thick porous carbon layers at a high temperature to block the transfer of combustibles, oxygen and heat between the bulk and the environment. Therefore, the surface coating strategy achieved a desirable flame-retardant level with fewer flame retardants.

To solve the pollution problems that result from polypropylene (PP), suitable biopolymers such as poly (lactic acid) (PLA) were selected to blend with PP. Since PP/PLA blends are often exposed to the natural environment, it is necessary to study the photodegradation behavior of PP/PLA blends. In this paper, PP/PLA blends with different compositions were prepared by extrusion and subjected to the accelerated laboratory weathering equipment. The effects of compatibilizers on the degradation behavior of PP/PLA blends were also studied. The weatherability of PP/PLA blends was studied through weight loss, optical microscope, Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The results revealed that PP is easy to degrade than PLA during accelerated laboratory weathering. PP/PLA blends are susceptible to the accelerated laboratory weathering process, and PP-rich and PLA-rich blends reduce the weathering resistance. Moreover, the results indicate that the initial degradation temperature, melting temperature, and crystallization temperature decrease after weathering related to the decreased thermal stability of PP/PLA blends. For instance, the initial degradation temperature of PP/PLA8.2 reduces from 332.2 °C to 320.2 °C. Moreover, the compatibilized sample is generally more resistant to weathering conditions than the uncompatibilized one due to the higher compatibility of PP and PLA.

During aging of polymers, oxidized species on macromolecular chains in solid state, volatile degradation products in liquid state and gaseous degradation products in gaseous state are often investigated separately. The conversion among these products is not especially concerned and biased results may be obtained based on the products in a single state. In this paper, photo-oxidative products of commercial polypropylene (PP) and unstabilized PP in solid, liquid and gaseous states were investigated by using Fourier transform infrared spectroscopy (FTIR), pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and gas chromatography (GC). By comparing the formation profiles, conversion among the photo-oxidative products in three states was traced. During photo-oxidative aging, the main chains of PP were first oxidized to form carbonyl species in solid state, or fractured to form volatile alkenes as liquid. With the proceeding of aging, the oxidized main chains fractured to form small molecules, resulting in the conversion of oxidized species from solid state to liquid and gaseous states. When the aging degree was extremely high, the accumulation of liquid oxidized products was limited due to migration and condensation. Therefore, both the carbonyl index (CI) and the concentrations of volatile oxidized products were increased first and then decreased, while the concentrations of gaseous products kept increasing all along.