4.7 Article

Strategic design unsaturated polyester resins composites with excellent flame retardancy and high tensile strength

Journal

POLYMER DEGRADATION AND STABILITY
Volume 206, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymdegradstab.2022.110190

Keywords

Unsaturated polyester resin; Flame retardancy; Mechanical performance; Flame-retarding mechanism

Funding

  1. National Natural Science Foundation of China
  2. [22105030]
  3. [U21A20103]

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A highly efficient flame retardant, MA-DOPO, was designed through a nucleophilic substitution reaction and showed promising improvement in tensile strength and flame retardancy of UPR composites. The flame-retarding mechanism involves the release of inert gas in the gas phase and catalytic carbonation in the condensed phase.
Unsaturated polyester resin (UPR) composites with excellent flame retardancy and high mechanical property is a great challenge to its widely application. In present work, a highly efficient flame retardant (MA-DOPO) con-taining nitrogen, sulfur and phosphorus elements was designed via a nucleophilic substitution reaction of amino and aldehyde groups. For the UPR/MA-DOPO15 composites, its tensile strength was 28.3 MPa, which was 19.9 % higher than that of neat UPR attributing to the formation of hydrogen bonds with UPR. It should be noted that tensile strength of UPR/MA-DOPO20 composites reached the highest 39.6 MPa, showing a growth trend with the enhancement of incorporation amount of MA-DOPO. Meanwhile, the UPR/MA-DOPO15composites passed the UL-94 V-0 rating with a LOI of 27.0%, and the peak heat release rate (PHRR) and total heat release rate (THR) were reduced by 35.1% and 41.6% in cone calorimeter (CC) test comparing to that of neat UPR respectively. Moreover, the detailed flame-retarding mechanism of MA-DOPO was investigated by the thermogravimetric infrared spectroscopy (TG-IR), Raman spectrum, X-ray photoelectron spectroscopy (XPS) and pyrolysis-gas chromatography/mass spectrometry (PY-GC/MS), in which the releasement of inert gas in gas-phase and the catalytic carbonation in condensed phase jointly taking effect.

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