1,2-Propanediolizobutyl POSS as a co-flame retardant for rigid polyurethane foams
- 121 Downloads
Polyurethane (PU) foams physically modified by two additive phosphorous flame retardants (FR)—phenol isobutylenated phosphate or phenol isopropylated phosphate, and chemically reinforced by functionalized 1,2-propanediolizobutyl POSS (PHI-POSS) have been synthesized and investigated towards thermal and mechanical properties, as well as flammability behaviour. The foamed PU hybrid materials were prepared in a two-step process using a polyether polyol and polymeric 4,4′-diphenylmethane diisocyanate. On the basis of the obtained results of mechanical properties, thermal insulation, thermal stability and flammability investigations, the influence of the applied additives—including POSS nanoparticles, on the rigid polyurethane foams was determined. The analysis of thermogravimetric and microcalorimetry data revealed an improved resistance to burning of the PU foams containing hybrid reactive (POSS)/additive (phosphate) FR systems, as evidenced by reduced rate of heat release. Importantly, mechanical properties tests showed that incorporation of bulky silsesquioxane nanoparticles to polyurethane structure via covalent bonds strengthens the foam integrity.
KeywordsRigid polyurethane foam POSS Thermal stability Flammability
Polyurethanes (PU) are widely used materials, obtained in the reaction of isocyanates with compounds containing active hydrogen, most often polyols. PU are produced as foams, elastomers, as well as coatings and adhesives. Among the porous polyurethane materials, one can distinguish flexible and rigid polyurethane foams. Flexible polyurethane foams are used, among others, in the automotive and furniture industry, as fillings for mattresses and car seats, whereby rigid polyurethane foams find broad application as thermal insulation materials in, e.g. automotive and building sector [1, 2, 3, 4, 5, 6, 7].
One of the most important problems that is still not resolved is the polyurethane foams flammability—despite the very good thermal insulation properties, these materials do not often show the required values in the latest fire resistance tests . Different flame retardants, mostly containing nitrogen and phosphorous, are incorporated into the foam; however, a satisfactory effect is visible only after the modification with a large amount of flame retardants, which in turn may cause deterioration of thermal and mechanical properties of polyurethane foams [8, 9, 10, 11, 12, 13, 14, 15, 16]. This problem has been partially solved by modifying foams chemically through the formation of isocyanurate rings, which in turn improves the properties determined in the fire tests [17, 18].
Due to the wide use of rigid polyurethane foams in such industries as construction, automotive, furniture, the issue of flammability is extremely important. Foamed materials have a highly developed pore surface, and thus facilitate the access of oxygen to the material, resulting in easier combustion. The flammability of polyurethane systems is a threat to both material consistency and human health, so looking for suitable flame retardants or synthesis of inherently non-combustible material is still a serious challenge [19, 20, 21, 22, 23].
In order to meet the requirements for volatile organic compounds (VOC), flame retardant systems based on halogen-free phosphorus compounds are getting an increasing attention. These include, among others, phosphines and their oxides, phosphonates, phosphates and phosphites, characterized by low toxicity, lack of release of toxic gases and production of small amounts of fumes during combustion. Inorganic phosphorus compounds as well as red phosphorus are also used effectively. In addition, flame retardant has been used, which contain, in addition to the phosphorus atom, additionally nitrogen, expandable graphite, inorganic compounds or halogen, through the use of a synergistic effect of their action [24, 25, 26, 27, 28, 29, 30, 31, 32, 33].
Currently, the research attention is focused on reducing the flammability of foamed polyurethane materials by organic–inorganic hybrids . This type of compounds includes polyhedral oligomeric silsesquioxanes (POSS), which may exist in various structural forms and can be used as additive and reactive modifiers. POSS are three-dimensional Si–O cages of 1-3 nm diameter which can be functionalized with organic moieties to yield hybrid nanoparticles able to form covalent bonds with polymer backbone [35, 36, 37, 38, 39, 40, 41].
In this work, we present results of investigations on the application of 1,2-propanediolizobutyl POSS (PHI-POSS) as a reactive co-flame retardant for rigid polyurethane foams, which were modified by two additive phosphorous flame retardants (FR)—phenol isobutylenated phosphate (PIBP) or phenol isopropylated phosphate (PIPP).
Materials and methods
The rigid polyurethane foams (PUF) were manufactured using a two-step method—in the first step, the polyol premix (component A), containing a polyol (Rokopol RF-551from PCC Rokita), PHI-POSS, water and n-pentane as blowing agents, catalysts (Polycat-9 from Evonik), and surfactant (SR-321from Momentive) and selected phosphorus flame retardants (FR), was prepared by mechanical stirring. The PHI-POSS (1,2-propanediolizobutyl POSS) reactive additive was introduced into the polyol in an amount of 10 mass% of the polyol weight and dissolved in THF and dispersed by the ultrasonic homogenizer. Phenol isopropylated phosphate (Roflam F12 from PCC Rokita) and phenol isobutylenated phosphate (3:1) (Roflam B7 from PCC Rokita) in the amount of 0.25, 0.5 and 0.75 mass% based on the phosphorus content in the foam were used as additive phosphorus flame retardants.
In the second step, polymeric 4,4′-diphenylmethane diisocyanate (pMDI from Minova Ekochem) as component B was added to component A and the polyurethane system was mixed using a mechanical stirrer for 10 s. After this time, the mixture was poured into an open mould where free foaming occurred in the vertical direction.
Study of apparent density
The apparent density was determined according to PN-EN ISO 845 standard. From the obtained material, a rectangular prism of 200 × 200 × 25 mm3 was cut, which was measured to an accuracy of 0.01 mm, and then weighed with accuracy 0.01 g.
Heat conduction coefficient research
The heat conduction coefficient was measured in accordance with the PN-ISO 8301 standard using the Laser Comp Heat Flow Instrument Fox 200, 24 h after the material was obtained.
In this method, the value of the heat flux flowing through the foam with the dimensions of 200 × 200 × 25 mm3 is determined. According to Fourier’s law, if there is a temperature gradient along a given axis in the material, a certain amount of heat per unit of time flows through a unit of surface perpendicular to this axis, at a fixed heat flow. To provide a temperature gradient, the sample was placed in the apparatus between two plates at appropriate temperatures of 0 and 20 °C.
Compressive strength test
The compressive strength test was carried out in accordance with the PN-EN ISO 844 standard, using a Zwick Z005 TH Allround-Line device. The compressive stress (being the ratio of the maximum compressive force to the area of the cross-sectional area of the sample) at 10% deformation of the sample in the direction parallel (R) and perpendicular (P1, P2) to the direction of foam growth was measured.
Examination of the content of closed cells
The determination of the content of closed cells was made on the basis of the PN-EN ISO 4590 standard using apparatus for measuring the content of closed cells. Material samples with dimensions 25 × 25 × 100 mm3 were subjected to testing.
Thermogravimetric analysis was performed using a Netzsch TG 209 F1 Libra thermal analyser to determine the thermal stability of the obtained foams modified by PHI-POSS and two additive flame retardants. The samples (sample mass ca. 5 mg) were heated in an open corundum pan from 30 up to 800 °C at a heating rate of 10 °C min−1 under air atmosphere.
Microcalorimetry PCFC method
The analysis of the combustion process of flame retarded rigid polyurethane foams was carried out using a pyrolysis–combustion flow calorimeter (PCFC) manufactured by Fire Testing Technology Ltd. During the measurements, it was possible to register the amount of heat emitted (HRR), the rate of heat release by foam materials and the flash point. The samples tested had masses ranging from 1 to 3 mg.
Results and discussion
The best thermal insulation properties of systems containing PIBP as flame retardant had a system consisting of PHI-POSS and 0.25 mass% phosphorus content, which may be caused by the smallest apparent density of the obtained material (Fig. 1a).
In the case of systems with PIPP as a flame retardant and its mixture with PHI-POSS, similar dependencies as for systems containing PIBP as flame retardant were observed. Material comprising 0.25 mass% phosphorus and PHI-POSS had the lowest thermal conductivity coefficient, which is the result of the smallest apparent density of the obtained material (Fig. 1b).
For all compositions, an increase in apparent densities along with an increase in the amount of flame retardants introduced was observed. However, the introduction of PHI-POSS to rigid polyurethane foam systems resulted in an increase in the density of obtained materials, which is related to the increase in the viscosity of the initial compositions (Fig. 1).
However, the closest to 90% value had a composition based on the mixture of PIPP and PHI-POSS.
This effect may be caused by changing the initial viscosity of systems and the use of POSS and flame retardants, which may contribute to the opening of cells during the foaming process.
Due to the anisotropic nature of the obtained materials, compressive strength in the parallel and perpendicular direction was measured.
For systems in which PHI-POSS was added, an increase in mechanical parameters in each of the measured directions along with the amount of FR introduced (Fig. 3b) was found. Due to the changing apparent density of individual compositions, profiles compensating the influence of apparent density on this parameter have been presented (Fig. 3).
The addition of PHI-POSS to the rigid polyurethane foam system resulted in an improved compressive strength, especially in the direction perpendicular to the direction of growth.
The results of the mechanical properties tests clearly show the influence of PHI-POSS on the properties of the obtained materials—the reactive bulky silsesquioxane modifier incorporated into the structure of polyurethane strengthens its integrity.
The onset temperature and the maximum degradation rate temperatures of polyurethane foams modified by POSS and additive phosphorus flame retardants
However, an interesting change was observed for systems in which PHI-POSS was used. The addition of this modifier together with the PIBP flame retardant caused a significant reduction in the HRR peak, assuming the lowest value for 0.5 mass% of the FR PIBP content (Fig. 7).
PCFC micro-calorimeter results revealed an interesting synergy effect of a hybrid system consisting of a selected phosphoric additive flame retardants and PHI-POSS leading to the reduction of flammability of rigid polyurethane foams. This effect may be caused by the specific interactions of the applied modifiers in the rigid polyurethane foam, as well as through density changes of the porous structure. An increase in the apparent density may reduce the propagation of the smoking process due to the smaller surface development in the fabricated materials. One can also postulate the role of POSS as a charring agent; the layer formed at the PU surface may act as an insulating barrier which limits heat and mass transfer during combustion.
The obtained results have shown that the use of PHI-POSS with phosphorus additive flame retardants leads to the reduction of the rigid polyurethane foams flammability, without significant changes of the foams’ crucial mechanical and thermal conductivity properties.
The best thermal insulation properties showed PU/PHI-POSS systems containing an additive fire retardant in the amount of 0.25 mass% phosphorus as these materials have the lowest apparent density of all obtained materials.
Modified rigid polyurethane foam systems have adequate mechanical strength, that is especially visible for compositions containing PHI-POSS, which is probably the result of increasing the content of hard segments by incorporating a reactive modifier into the structure of the polyurethane backbone.
Flammability studies by micro-calorimeter pyrolysis and combustion revealed that hybrid reactive (POSS)/additive (phosphate) systems are characterized by improved resistance to burning. This effect may be linked with changed apparent density of the composite materials and more efficient formation of char barrier in the presence of POSS.
Importantly, the use of organic–inorganic hybrid systems with silsesquioxanes can provide perspectives in an effective protection of polyurethane materials against the fire.
This project was financed by the Polish National Science Centre under contract No. DEC-2011/02/A/ST8/00409.
- 3.Feng F, Qian L. The flame retardant behaviors and synergistic effect of expandable graphite and dimethyl methylphosphonate in rigid polyurethane foams. Polym Compos. 2014;35:301309.Google Scholar
- 5.Liang K, Mao A, Shi SQ. Incorporation of nanoparticles into soy-based polyurethane foams. NSTI-Nanotech. 2009;2:290–3.Google Scholar
- 9.Chen D, Zhao Y, Yan J, Chen L, Dong Z, Fu W. Preparation and properties of halogen-free flame retardant polyurethane foams. Adv Mater Res. 2012;418–420:540–3.Google Scholar
- 11.Wu D-H, Zhao P-H, Liu Y-Q, Liu X-Y, Wang X-F. Halogen free flame retardant rigid polyurethane foam with a novel phosphorus–nitrogen intumescent flame retardant. J Appl Polym Sci. 2014;131:39581.Google Scholar
- 12.Luo F, Wu K, Li Y, Zheng J, Guo H, Lu M. Reactive flame retardant with core-shell structure and its flame retardancy in rigid polyurethane foam. J Appl Polym Sci. 2015;132:42800.Google Scholar
- 20.Chen Y, Jia Z, Luo Y, Jia D, Li B. Environmentally friendly flame-retardant and its application in rigid polyurethane foam. Int J Polym Sci. 2014;2014:263716.Google Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.