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A fully waterborne epoxy system was prepared from waterborne sorbitol-based epoxy resin cured with an alkylated polyalkylene polyamine hardener. The flame-retardant property was accomplished by the application of different additive phosphorous flame retardants (FRs). Phosphonate polyol and ethyl ethylene glycol phosphate which are in the liquid phase, and two FRs in the form of fine-grained particles; aluminium diethyl phosphinate (AlPi), ammonium polyphosphate (APP). The flame-retardant epoxy resin blends were prepared at the same levels of phosphorus content. The results are very promising as the self-extinguishing behaviour was observed at 3%P for all the investigated FRs and at 1%P in the case of APP. Limiting oxygen index (LOI) values were practically good for all FRs and extremely improved in the case of APP. LOI was 48% for the APP sample at 3%P content. Furthermore, this blend showed the best results in the forced flaming conditions as the total heat release in cone calorimetry measurements (THR) decreased by 43% and the peak of heat release rate (pHRR) decreased by 65% with more elongated burning compared to the reference SPE matrix. The efficient solid-phase FR effect of APP was confirmed by scanning electron microscopic (SEM) and attenuated total reflection-infrared spectrometry (ATR-IR) analysis of the residual char after cone calorimetry measurements. [ABSTRACT FROM AUTHOR]

Supercritical CO2-assisted extrusion technique was used to produce flame retarded foams from recycled poly(ethylene terephthalate) (rPET). Synergistic combination of aluminium-alkylphosphinate flame retardant (FR) and natural montmorillonite (MMT) was utilised to provide adequate flame retardancy at moderate loadings, i.e. with less than 9% of additives. Addition of FR was found to increase the rate of degradation during production (compounding and foam extrusion), which was effectively compensated by chain extender (CE) addition that ensured the melt strength required to obtain proper foam structure. The effects of the FR content and the CE addition on the viscosity of the rPET compounds and on the morphological, thermal, flammability and mechanical properties of the foam products were comprehensively investigated. When compared to injection moulded bulk materials of identical compositions, the highly porous structure of foams was found to increase flammability according to UL94 tests and LOI measurements but has not been shown to be detrimental to heat release rates as measured by cone calorimetry. It was concluded that with well-balanced composition, i.e. 8% FR + 1% MMT + 1% CE, low-density foams (with porosities higher than 70%) of uniform microcellular structure and prominent flame retardant characteristics (such as V0 rating according to UL94 standard, LOI of 28.5% and by 50% reduced peak of heat release rate and by 30% reduced total heat emission) can be manufactured even from rPET. [ABSTRACT FROM AUTHOR]

A water-soluble sorbitol polyglycidyl ether (SPE) epoxy monomer was cured with a waterborne polyamine hardener to prepare a fully waterborne epoxy system. Aluminum diethyl phosphinate (AlPi) and melamine cyanurate (MC) flame retardants (FRs) were utilized to develop the flame retardancy of this epoxy matrix. The effect of loading different weights of MC with only 1%P-content from AlPi was discussed to investigate the possible cooperative effect of these two FRs. The best results were obtained at 5% MC loading with 1%P of AlPi as the self-extinguishing behavior was observed with a good limiting oxygen index (LOI). Furthermore, under forced flaming conditions in cone calorimetry measurements, the peak of heat release rate (pHRR) decreased by 27.4%, and the total heat release (THR) decreased by 14.5% compared to the reference epoxy system. This enhancement of flame retardant properties might indicate the synergistic effect between MC and AlPi in a waterborne system. [ABSTRACT FROM AUTHOR]

Summary: Flame‐retarded sorbitol‐based bioepoxy resins cured with cycloaliphatic amine hardener and containing different commercially available additive‐type flame retardants (FRs) have been prepared. Three different oxidation states of phosphorus, aluminium diethyl phosphinate (AlPi) (+1), phosphonate polyol (+3), ethyl ethylene glycol phosphate and ammonium polyphosphate (APP) (+5), have been studied. The effect of using melamine cyanurate with APP and AlPi has been assessed. The self‐extinguishing V‐0 rating according to UL‐94 flammability standard tests and very good limiting oxygen index for combustion are displayed for most flame‐retarded samples at 3 wt% phosphorus content. The flame retardancy effect for the additives was confirmed using cone calorimetry. The samples containing MC with APP at 3%P content showed a dramatic reduction of the total heat release by 60% and reduction of the peak of heat release rate by 70% compared to the reference epoxy matrix. The addition of these FRs together did not decrease the glass transition temperature significantly. [ABSTRACT FROM AUTHOR]

As polypropylene (PP) has no charring ability on its own due to the lack of hydroxyl functional groups, the flame retardant system needs the addition of carbonizing agent in a relatively great amount. Ammonium-polyphosphate (APP), a conventional flame retardant additive was modified by microencapsulation with a sorbitol-based bioepoxy resin shell to create an intumescent flame retardant system with enhanced charring ability for PP. The flame retardant efficiency of the microencapsulated additive, which contains all the components needed in an effective intumescent flame retardant system, was evaluated in PP matrix at different loadings. When compared to the physical mixture of the component, the microencapsuated form of APP (MCAPP) was found to have improved flame retardant efficiency in PP. The LOI values of the MCAPP containing PP samples increased by 8–11 V/V% besides achieved V-0 classification according to the UL94 test. During cone calorimeter tests, the burning intensity was reduced (peak of heat release rate decreased by 20–35% and shifted in time), increased amount of charred residue was obtained, and based on the calculated Flame Retardancy Index (FRI) “Excellent” fire performance was achieved when MCAPP was used. The improved flame retardant performance is attributed to the effective interaction between the APP core and the readily available carbonizing shell, which promoted the formation of increased amount of char accompanied with improved heat protecting and barrier efficiency. [ABSTRACT FROM AUTHOR]

The flame retardancy of sorbitol-based epoxy resin is targeted. From the bioepoxy 3% phosphorus-containing matrix samples were prepared. Surprisingly, only HB classification of UL-94 test was reached with the application of ammonium polyphosphate (APP) and resorcinol bis(diphenylphosphate) (RDP). V-0 was reached in the case of red phosphorus (RP) and ammonium salt of DOPO (DXA), while the melamine salt resulted in HB rating, due to the lower P-content of the sample. In the meantime, the highest LOI value was reached in the case of APP. The V-0 red phosphorus composition, however, has an LOI of as low as 25 V/V%. In the case of the thermogravimetric analysis, the application of red phosphorus resulted in significantly increased thermal stability, but faster degradation than in the case of the reference. The RDP showed somewhat decreased stability, due to the less stable phosphorus ester bonds. The amount of the charred residues is increasing with the flame retardant content, but to different extents depending on the type of flame retardant. The highest values were reached with APP. Regarding the cone calorimeter results; the lowest heat release rate belongs to the APP-containing sample, while the V-0 compositions (RP and DXA) show poorer performance in this respect. [ABSTRACT FROM AUTHOR]

Ammonium-polyphosphate (APP) was modified by microencapsulation with a bio-based sorbitol polyglycidyl ether (SPE)-type epoxy resin and used as a flame retardant additive in polylactic acid (PLA) matrix. The bioresin-encapsulated APP (MCAPP) particles were characterized using Fourier transform infrared (FTIR) spectroscopy and Raman mapping, particle size distribution was determined by processing of scanning electron microscopic (SEM) images. Interaction between the APP core and the bioresin shell was revealed by combined thermogravimetric analysis (TGA)‑FTIR spectroscopy. The APP to SPE mass ratio of 10 to 2 was found to be optimal in terms of thermal, flammability, and mechanical properties of 15 wt% additive containing biocomposites. The bioresin shell effectively promotes the charring of the APP-loaded PLA composites, as found using TGA and cone calorimetry, and eliminates the flammable dripping of the specimens during the UL-94 vertical burning tests. Thus, the V-0 rating, the increased limiting oxygen index, and the 20% reduced peak of the heat release rate was reached compared to the effects of neat APP. Furthermore, better interfacial interaction of the MCAPP with PLA was indicated by differential scanning calorimetry and SEM observation. The stiff interphase resulted in increased modulus of these composites. Besides, microencapsulation provided improved water resistance to the flame retardant biopolymer system. [ABSTRACT FROM AUTHOR]

• Microfibrous structure of HPβCD promotes char formation in PLA/APP system. • Phosphorous silane treatment of HPβCD improves the flame retardant performance. • HPβCD contributes to enhanced physical and chemical interaction between the components. • Improved flame retardancy is provided by thermally stable char. Recently, the flame retardant effectiveness of a 2-hydroxypropyl-β-cyclodextrin (CD) type bio-based carbonising agent has been evinced to noticeably increase when used in a microfibrous form, as obtained by electrospinning method. In the present research, the flame retardant performance of the electrospun CD was further enhanced by reactive surface modification with a phosphorous silane (PSil) compound. Surface-treated and untreated CD-based carbonising agents were compared, both in powder and in microfibrous form, besides ammonium polyphosphate (APP) to form an intumescent flame retardant system for poly(lactic acid) (PLA). The Limiting Oxygen Index (LOI) of the flame-retarded PLA composites increased outstandingly, from 25.0% (corresponding to the 15 wt% APP containing PLA) to as high as 37.5%, as a result of adding only 3 wt% of PSil-treated microfibrous CD to the system. Also, the main combustion characteristics improved; compared to neat PLA, about 50% reduction in the peak heat release rate (pHRR) and 25% reduction in total heat release (THR) were achieved, accompanied by an increased amount of char residue after combustion. The beneficial effect of the PSil-treated CD microfibre relies mainly on its enhanced physical and chemical interaction with APP and its increased charring ability and thermal stability, which contribute to the formation of a fire protecting char of increased structural integrity. [ABSTRACT FROM AUTHOR]