Effect of surface modification of montmorillonite on the properties of rigid polyurethane foam composites

<正>This study investigated the influence of various organically modified montmorillonites(organoclays) on the structure and properties of rigid polyurethane foam(RPUF) nanocomposites.The organoclays were modified with cetyltrimethyl ammonium bromide(CTAB),methyl tallow bis(2-hydroxyethyl) quaternary ammonium chloride (MT2ETOH) and tris(hydroxymethyl)aminomethane(THMA) and denoted as CMMT,Cloisite 30B and OMMT, respectively.MT2ETOH and THMA contain hydroxyl groups,while THMA does not have long aliphatic tail in its molecule. X-ray diffraction and transmission electron microscopy show that OMMT and Cloisite 30B can be partially exfoliated in the RPUF nanocomposites because their intercalating agents MT2ETOH and THMA can react with isocyanate.However, CMMT modified with nonreactive CTAB is mainly intercalated in the RPUF matrices.At a relatively low filler content,the RPUF/CMMT composite foam has a higher specific compressive strength(the ratio of compressive strength against the apparent density of the foams),while at relatively high filler contents,RPUF/Cloisite 30B and RPUF/OMMT composites have higher specific compressive strengths,higher modulus and more uniform pore size than the RPUF/CMMT composite.     

Flame‐retardant rigid polyurethane foam with a phosphorus‐nitrogen single intumescent flame retardant

A phosphorous‐nitrogen intumescent flame‐retardant, 2,2‐diethyl‐1,3‐propanediol phosphoryl melamine (DPPM), was synthesized and characterized by Fourier transform infrared spectroscopy and nuclear magnetic resonance. Flame‐retardant rigid polyurethane foams (RPUFs) with DPPM (DPPM‐RPUF) as fire‐retardant additive were prepared. Scanning electron microscope (SEM) and mechanical performance testing showed that DPPM exhibited a favorable compatibility with RPUF and negligibly negative influence on the mechanical properties of RPUF. The flame retardancy of DPPM on RPUF was investigated by the limiting oxygen index (LOI), vertical burning test and cone calorimeter. The LOI of DPPM‐RPUF could reach 29.5%, and a UL‐94 V‐0 rating was achieved, when the content of DPPM was 25 php. Furthermore, the DPPM‐RPUF exhibited an outstanding water resistance that it could still obtain a V‐0 rating after water soaking. Thermogravimetric analysis showed that the residual weight of RPUF was relatively low, while the charring ability of DPPM‐RPUF was improved greatly. Real‐time Fourier transform infrared spectroscopy was employed to study the thermo‐oxidative degradation reactions of DPPM‐RPUF. The results revealed that the flame‐retardancy mechanism of DPPM in RPUF was based on the surface charred layer acting as a physical barrier, which slowed down the decomposition of RPUF and prevented the heat and mass transfer between the gas and the condensed phases.     

Thermal and flame retardant properties of novel intumescent flame retardant polypropylene composites

Novel intumescent flame retardant polypropylene (PP) composites were prepared based on a char forming agent (CFA) and silica-gel microencapsulated ammonium polyphosphate (Si-MCAPP). The thermal and flame retardancy of flame retardant PP composites were investigated by limiting oxygen index, UL-94 test, cone calorimetry, thermogravimetric analysis, scanning electron micrograph, and water resistance test. The results of cone calorimetry show that the flame retardant properties of PP with 30 wt% novel intumescent flame retardants (CFA/Si-MCAPP = 1:3) improve greatly. The peak heat release rate and total heat release decrease, respectively, from 1,140.0 to 156.8 kW m^?2 and from 96.0 to 29.5 MJ m^?2. The PP composite with CFA/Si-MCAPP = 1:3 has the excellent water resistance, and it can still obtain a UL-94 V-0 rating after 168 h soaking in water.     

Synergistic effect of zeolite 4A on thermal,mechanical and flame retardant properties of intumescent flame retardant HDPE composites

The combination of synergistic agent with intumescent flame retardant (IFR) systems provides a promising way to prepare high performance IFR composites. In this study, the effects of the synthetic zeolite 4 A in combination with the IFR system consisting of ammonium polyphosphate (APP) and tris (2-hydroxyethyl) isocynurate (THEIC) on thermal degradation, mechanical properties, flame retardancy and char formation of high-density polyethylene composites were investigated by limiting oxygen index (LOI) measurement, cone calorimetry, scanning electron microscopy and laser Raman spectroscopy. The LOI value of HD/FR/Z-0.5 composite with an optimum content of 0.5 wt. % zeolite 4 A and 25 wt. % of total flame retardant reaches 26.3 %. A low loading of zeolite 4 A can improve the bench-scale combustion performance as determined by cone calorimetry, and promote the formation of more compact char residue with a highly graphitic structure. However, a low loading of zeolite in combination with the IFR system consisting of APP and THEIC produces no significant changes in mechanical performance.     

Halogen-free flame retardant PUF: Effect of melamine compounds on mechanical, thermal and flame retardant properties

Water blown rigid polyurethane foam (PUF) was prepared with melamine polyphosphate (MPP) and melamine cyanurate (MC) as fire retardant (FR) additives. The effect of these additives on the properties of rigid PUF such as physico-mechanical, morphological, thermo-oxidative stability, flame retardancy and smoke density properties were studied. The mechanical and thermo-oxidative stability of PUF filled with MC was found to be better than those of MPP filled PUF. The insulation property of both MPP and MC filled PUF was improved with respect to the neat PUF. The FR properties of these filled PUF were evaluated by cone calorimeter, limiting oxygen index (LOI), smoke density, rate of burning and char residue estimation. The FR property of MPP filled PUF was better than that of the MC filled PUF.     

Effect of blowing agent content on the structure and flame-retardant properties of rigid polyurethane foam/expanded graphite composites

Driven by global environmental issues, the development of green building materials has become an immediate focus. In this work, n-pentane was used as an environmentally friendly blowing agent to prepare flame-retardant rigid polyurethane foam (RPUF) with the addition of expandable graphite (EG) successfully, and the effect of n-pentane content on flame retardancy and compressive properties of RPUF/EG composites was investigated through limit oxygen index (LOI), vertical burning test (UL-94), scanning electron microscope (SEM), thermogravimetric analysis (TGA), and compressive properties test. SEM results show that the content of EG and n-pentane causes a change in the cell structure of RPUF. The change of the n-pentane content has also an obvious effect on the thermal stability, flame retardancy, and specific compressive strength of RPUF/EG composites. In addition, the cell structure of RPUF matrix has an obvious influence on the distribution of EG in the composites, which indirectly affects the flame-retardant efficiency of EG. This research explores the conditions for the application of environmentally friendly RPUF and expands its application prospects.     

Preparation of bio-based soybean oil polyol modified 3630 polyol-based rigid polyurethane foam and its improved thermal stability,flame retardant,and smoke suppression performances

Rigid polyurethane foam (RPUF) with 3630 polyol-based components was modified using bio-based soybean oil (SO) polyol. The effects of soybean oil polyol on the thermal stability, flame retardant and smoke suppression performances of the modified RPUFs were investigated by thermogravimetric analysis, integral programmed decomposition temperature (IPDT), pyrolysis kinetic analysis, limiting oxygen index, conical calorimetry and smoke toxicity analysis. The results indicated that the RPUF-SO2 (10 wt% soybean oil polyol) had the highest thermal decomposition rate temperature, initial thermogravimetric temperature, termination temperature, residual rate, IPDT and activation energy. Under various circumstances, the total heat release (THR) of RPUF-SO2 was 1.41, 1.61, and 2.51 MJ/m², respectively, and the peak heat release rate (PHRR) was lowered by 22.40%, 45.68%, and 19.86% in comparison to the original RPUF-0. In the meantime, RPUF-SO2 had the best light transmittance (57.20 and 60.60%), the lowest toxic gas emissions (0.31, 0.44, and 0.38 kg/s), and the lowest Ds (32.46 and 29.07). It also had an excellent smoke suppression effect. According to the current study, RPUF-SO2 performed better in terms of heat stability, flame retardancy and smoke suppression. This made it a good benchmark for further bio-based soybean oil polyol modified RPUFs.     

Thermal degradation and flame retardancy of rigid polyurethane foams containing a novel intumescent flame retardant

A novel cheap macromolecular intumescent flame retardants (MIFR) was synthesized, and its structure was a macromolecule containing phosphorus characterized by IR. Rigid polyurethane foam (PUF) filled with MIFR as fire retardant additive was prepared. The effects of MIFR on properties such as density, compressive strength, flame-retardant behavior, thermal stability, and morphology of char were studied. The compressive strength of the MIFR-filled PUF increased initially and then decreased with further increase of MIFR content while its density straightly increased. Its flammability and burning behavior were characterized by UL 94 and limiting oxygen index (LOI). Twenty five percent of MIFR was doped into PUF to get 24.5 of LOI and UL 94 V-0. Activation energy for the decomposition of samples was obtained using Kissinger equation. The resultant data show that for PUF containing MIFR, compared with PUF, the mass loss, thermal stability, and the decomposition activation energy decreased, the char yield increased, which shows that MIFR can catalyze decomposition and carbonization of PUF to form an effective charring layer to protect the underlying substrate.     

Flame retardant and thermal degradation properties of flame retardant thermoplastic polyurethane based on HGM@[EOOEMIm][BF4]

Journal of Thermal Analysis and Calorimetry - This article mainly studies the flame retardant and thermal degradation properties of thermoplastic polyurethane (TPU) composites based on...     

Thermal Degradation,Flame Retardance and Mechanical Properties of Thermoplastic Polyurethane Composites Based on AluminumHypophosphite简

Aluminum hypophosphite （AP） was used to prepare flame-retarded thermoplastic polyurethane （FR-TPU） composites, and their flame retardancy, thermal degradation and mechanical properties were investigated by limiting oxygen index （LOI）, vertical burning test （UL-94）, thermogravimetric analysis （TGA）, cone calorimeter （CC） test, Fourier transform infrared （FTIR） spectroscopy, scanning electron microscopy （SEM） and tensile test. TPU containing 30 wt% of AP could reach a V-0 rating in the UL-94 test, and its LOI value was 30.2. TGA tests revealed that AP enhanced the formation of residual chars at high temperatures, and slightly affected the thermal stability of TPU at high temperatures. The combustion tests indicated that AP affected the burning behavior of TPU. The peak of heat release rate （PHRR）, total heat release （THR） and mass loss rate （MLR） greatly reduced due to the incorporation of AP. The tensile test results showed that both the tensile strength and the elongation at break slightly decreased with the addition of AP. The digital photos and SEM micrographs vitrified that AP facilitated the formation of more compact intumescent char layer. Based on these results mentioned above, the flame-retarding mechanism of AP was discussed. Both the self-charring during the decomposing process of AP and its facilitation to the charring of TPU led to the great improvement in the flame retardancy of TPU.     

Effects of preparation conditions on properties of rigid polyurethane foam composites based on liquefied bagasse and jute fibre

Rigid polyurethane foams based on liquefied bagasse and reinforced with jute fibre were prepared. The effects of preparation conditions were investigated using a paper cup with a small horizontal section area as a mould. They were reflected in the foam height, which acted as a sensitive indicator. Density gradient existed in the foam rise direction and decreased from the bottom to top. Although the amount of blowing agent water was fixed, the foam height increased with stirring time after the addition of diphenyl methane diisocyanate, the isocyanate index and the catalyst content. This was partly due to the released heat that also contributed to the foam expansion. The relative intensity of the C─N stretching band at 1510 cm⁻¹ and the N─H out-of-plane bending band at 1527 cm⁻¹ in the FTIR spectrum reflected isocyanate reactions, which had a close relationship with the crosslink density. The normalized compressive strength was essentially attributed to the combined effects of the crosslink density and the thickness of cell walls and struts. Jute fibre enhanced the compressive strength only slightly due to poor interfacial adhesion between some fibres and the matrix.     

Mechanical properties,thermal stability,sound absorption,and flame retardancy of rigid PU foam composites containing a fire‐retarding agent: Effect of magnesium hydroxide and aluminum hydroxide

Isocyanate, polyether polyol, a flame retardant (10 wt%), and aluminum hydroxide/magnesium hydroxide (0, 5, 10, 15, and 20 wt%) are used to form the rigid polyurethane (PU) foam, while nylon nonwoven fabrics and a polyester aluminum foil are combined to serve as the panel. The rigid PU foam and panel are combined to form the rigid foam composites. The cell structure, compressive stress, combustion resistance, thermal stability, sound absorption, and electromagnetic interference shielding effectiveness (EMI SE) of the rigid foam composites are evaluated, examining the effects of using aluminum hydroxide and magnesium hydroxide. Compared with magnesium hydroxide, aluminum hydroxide exhibits superior performance to the rigid foam composites. When aluminum hydroxide is 20 wt%, the rigid foam composite has an optimal density of 0.153 g/cm³, an average cell size of 0.2466 mm, a maximum compressive stress of 546.44 Kpa, an optimal limiting oxygen index (LOI) of 29.5%, an optimal EMI SE of 40 dB, and excellent thermal stability and sound absorption.     

Thermal and flame retardant properties of novel intumescent flame retardant low-density polyethylene (LDPE) composites

A char-forming agent (CFA) and silica-gel-microencapsulated ammonium polyphosphate (MCAPP) were selected to form novel intumescent flame retardant system (IFRs), and then the influence of this novel IFRs on the thermal and flame retardant properties of low-density polyethylene (LDPE) were studied. The results of cone calorimetry show that the flame retardant properties of LDPE with 30?wt% novel IFR (CFA/MCAPP?=?1:3) improve remarkably. The heat release rate peak, total heat release (THR) decreases, respectively, from 1479.6 to 273.5?kW?m^?2 and from 108.0 to 80.5?MJ?m^?2. The LDPE composite with CFA/MCAPP?=?1:3 has the excellent water resistance, and it can still obtain a UL-94?V-0 rating after treated with water at 70?°C for 168?h.     

Effect of ethyl cellulose microencapsulated ammonium polyphosphate on flame retardancy,mechanical and thermal properties of flame retardant poly(butylene succinate) composites

Ethyl cellulose, a widely used bio-degradable shell material, microencapsulated ammonium polyphosphate (MAPP) was added to the bio-degradable poly(butylene succinate) (PBS) to improve its flame retardancy, compatibility, and thermal stability. The MAPP was well characterized by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy (SEM), water contact angle, and thermogravimetric (TG) analysis. The SEM results indicate the improved dispersion of MAPP into PBS matrix and the formation of the strong interfacial adhesion between MAPP and PBS than APP. With the incorporation of MAPP and char-forming agent into PBS, the limiting oxygen index of the composite was increased to 35.5 %, and the sample can pass the UL-94 V-0 rating, while the un-microencapsulated counterpart cannot reach the rating. The cone calorimeter test showed that the peak heat release rate was decreased by 46.7 % and the burning time was also prolonged compared to the pure PBS. The increased melt flow index and rheology test indicated the increase of viscosity and the improvement of anti-dripping properties. Moreover, the mechanical properties and thermal stability of MAPP composite were also obviously enhanced after the microencapsulation by mechanical, dynamical mechanical thermal analysis, and TG analysis.     

Preparation and mechanism of polyurethane prepolymer and boric acid co‐modified phenolic foam composite: Mechanical properties,thermal stability,and flame retardant properties

In this work, a new kind of co‐modified phenolic foam was synthesized with polyurethane prepolymer (PUP) and H₃BO₃ by a simple preparation method. Firstly, in order to determine the optimal amount of PUP, the effects of different PUP additions on the mechanical properties, foam microstructure, and pulverization rate of phenolic foam were investigated. Then H₃BO₃ was added to toughened phenolic foam, in order to reduce its fire hazard. The results showed that the mechanical properties of the PFPUP8 phenolic foam composite were the best when the PUP content was 8 wt%. It had a small and regular cell structure, and its pulverization ratio was reduced by 80% compared with that of pristine phenolic foam. Meanwhile, the flame retardant properties of PFPUP8 were improved in different degrees with an increase in the amount of H₃BO₃. Particularly, when the addition of H₃BO₃ was 10 wt%, the peak heat release rate, the total heat release, and the total smoke release values of PFPUP10B were decreased by 35.4%, 42.4%, and 45.2%, respectively, compared with those of PFPUP8. The value of the limit oxygen index was increased by 33.1%. Besides, the addition of H₃BO₃ had no adverse effect on the mechanical properties and pulverization ratio of PFPUP8. In addition, the specific mechanisms of toughening, flame retardant, and smoke suppression are also discussed in this paper on the basis of an investigation into the thermal properties of the toughened flame retardant foam composites by thermogravimetric analysis in N₂ atmosphere.     

Flame retardant properties and mechanism of an efficient intumescent flame retardant PLA composites

The charring agent (CNCA‐DA) containing triazine and benzene rings was combined with ammonium polyphosphate (APP) to form intumescent flame retardant (IFR), and it was occupied to modify polylactide (PLA). The flame retardant properties and mechanism of flame retardant PLA composites were investigated by the limited oxygen index (LOI), vertical burning test (UL‐94), thermogravimetric analysis, microscale combustion calorimetry, scanning electron microscopy, laser Raman spectroscopy analysis and X‐ray photoelectron spectroscopy. The analysis from LOI and UL‐94 presented that the IFR was very effective in flame retardancy of PLA. When the weight ratio of APP to CNCA‐DA was 3:1, and the IFR loading was 30%, the IFR showed the best effect, and the LOI value reached 45.6%. It was found that when 20 wt% IFR was loaded, the flame retardancy of PLA/IFR still passed UL‐94 V‐0 rating, and its LOI value reached 32.8%. The microscale combustion calorimetry results showed that PLA/IFR had lower heat release rate, total heat release, and heat release capacity than other composites, and there was an obvious synergistic effect between APP and CNCA‐DA for PLA. IFR containing APP/CNCA‐DA had good thermal stability and char‐forming ability with the char residue 29.3% at 800°C under N₂ atmosphere. Scanning electron microscopy observation further indicated that IFR could promote forming continuous and compact intumescent char layer. The laser Raman spectroscopy analysis and X‐ray photoelectron spectroscopy analysis results indicated that an appropriate graphitization degree of the residue char was formed, and more O and N were remained to form more cross‐linking structure. Copyright © 2016 John Wiley & Sons, Ltd.