Modification of Rigid Polyurethane Foams with the Addition of Nano-SiO2 or Lignocellulosic Biomass.

Many achievements have been made on the research of composite polyurethane foams to improve their structure and mechanical properties, and the composite foams have been widely utilized in building insulation and furniture. In this work, rigid polyurethane foams (RPUFs) with the addition of different fillers (nano-SiO2, peanut shell, pine bark) were prepared through the one-step method. The effects of inorganic nano-SiO2 and organic biomass on foam properties were evaluated by means of physical and chemical characterization. The characterization results indicate that the compressive strength values of prepared foams could fully meet the specification requirement for the building insulation materials. The inorganic and organic fillers have no effect on the hydrogen bonding states in composite RPUFs. Furthermore, compared to the biomass fillers, the addition of nano-SiO2 greatly influenced the final residual content of the fabricated foam. All composite foams exhibit closed-cell structure with smaller cell size in comparison with the parent foam. The prepared composite foams have the potential for utilization in building insulation.

1. Introduction

In order to achieve high-quality development for current society, energy efficiency and green economy have been sustainably developing [1,2,3,4]. The construction industry is an important link to sustainable development [5]. The use of environment-friendly materials in modern buildings cannot only greatly reduce construction waste but also avoid excessive use of natural resources [6]. In view of this, the utilization of biomass, especially crop wastes, is an effective way to save energy and protect the environment in the building industry [7,8]. Furthermore, the estimated amounts of tremendous crop wastes in China covered a large scale from 620 to 940 tons every year. Therefore, the utilization of biomass resources will significantly reduce excessive CO2 emissions [9]. Rigid polyurethane foams (RPUFs) are the most commonly used polymer materials in the field of building for thermal insulation and sound absorption because of their preferable thermal stability; fire-, heat-, impact-, and crack-resistance; etc. [10,11,12,13,14,15]. Therefore, the research on the preparation of bio-based RPUFs or composite RPUFs with the addition of biomass fillers is necessary in future studies.

As for bio-based RPUFs, bio-based polyols, which could be produced from vegetable oils [16,17,18] and plant fibers [19,20,21] are usually served as raw materials due to the existence of abundant hydroxyl groups or double bonds in these polyols. However, chemical modification for vegetable oils or liquefaction for plant fibers is always needed to transform them into bio-based polyols, and extra energy consumption is necessary for pretreating those biomass feedstocks. Compared to bio-based RPUFs, the direct addition of biomass fillers into RPUFs has also gained much more attention. The fillers, such as nanoparticles, insulating glass microspheres, and carbon fibers, have been used to improve the functionality of polyurethane in many studies [22,23,24,25,26]. As previously reported, composite polyurethane foam with tea-leaf fibers as filler could improve sound absorption performance [27]. The electrically conductive polymer material prepared by using multiwall carbon nanotubes had a promising application in sensors and intelligent sandwich composite cores [28]. The flame-retardant property of RPUF could be enhanced by adding expanded graphite, fly ash, etc. [29,30,31,32,33]. However, many researches are still focusing on functionalization rather than sustainable development. The utilization of biomass as filler, especially crop wastes, is an effective way to fabricate RPUFs for the purpose of saving energy and protecting the environment in the construction industry to support sustainable development

The aim of this work was to synthesize the RPUFs composited with inorganic filler (nano-SiO2) or organic fillers (peanut shell and pine bark). Their compressive strength, hydrogen bonding states, thermal behavior, and morphology were characterized. The effects of different fillers on those physical and chemical properties of RPUFs were intensively evaluated.

2. Experimental

2.1. Materials

Polyethylene glycol 400 (PEG 400) was purchased from Tianjin Damao Chemical Co., Ltd., Tianjin, China. Polymeric methylene-4,4′-diphenyl diisocyanate (PM-200, 32.0 wt % of isocyanate group) was obtained from Wanhua Chemical Group Co., Ltd., Yantai, China. Triethylene diamine (A-33), stannous octoate (T-9), and silicone-based surfactant (L-580) were purchased from Air Products and Chemicals, Inc., Allentown, PA, USA. The hydrophilic nano-SiO2 with the specific surface area of 200 m2·g−1 was purchased from Aladdin biochemical technology co., Ltd., Shanghai, China. Pine bark (PB) and peanut shell (PS) were respectively obtained from Rizhao and Qingdao, China. They were dried to constant weight and then ground under the speed of 10,000 rpm. The obtained powders with the size of ≤250 μm were collected for further utilization.

2.2. Synthesis of Polyurethane Foam

RPUFs were synthesized via a one-step procedure. The content of all the additives was a relative weight percent to the PEG 400. Firstly, the PEG 400 (100 wt %), foaming agent (deionized water, 2.5 wt %), foam stabilizer (L-580, 2.0 wt %), catalysts (T-9 of 0.3 wt % and A-33 of 1.0 wt %), and auxiliary filler (nano-SiO2, PB or PS) were mixed in a 500 mL plastic beaker with stirring of 800 rpm for 5 min. Then the pre-weighted PM-200 (equivalent ratio of isocyanate group to hydroxyl group = 1/1) was quickly fed into the beaker under constant stirring. Finally, the RPUFs were demolded from beaker after 24 h curing, and then they were post-cured at room temperature for 72 h before the characterization tests. The foams composited with nano-SiO2, PS, and PB as filler are denoted as RPUF/SiO2, RPUF/PS and RPUF/PB.

2.3. Foams Characterization

Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectra of RPUFs were analyzed on the Bruker VERTEX 70 (Bruker Optik GmbH, Ettlingen, Germany) with 32 scans under the frequency range of 4000–400 cm−1 and a resolution of 2 cm−1. The thermogravimetry (TG) scans were collected on a Netzsch Simultaneous Thermal Analyzer STA 449F5 Jupiter (Netzsch, Selb, Germany) from 30 to 800 °C at the heating rate of 10 °C·min−1 under the nitrogen atmosphere. The apparent densities of RPUFs were measured according to GB/T 6343-2009. The compressive strength was tested according to GB/T 8813-2008 on an electronic universal testing machine of H10KS (Hounsfield Test Equipment Ltd., Redhill, Surrey City, UK) at a loading speed of 5 mm·min−1. The foam cell structure was observed through a cold-field emission scanning electron microscope of Hitachi S-4800 (Hitachi High-Technologies Corp., Tokyo, Japan).

3. Result and Discussion

3.1. Compressive Strength

Compressive strength, which depends greatly on the foam density, is the crucial parameter to evaluate the compression properties of RPUFs. The specific compressive strength (the ratio of compressive strength to density) was used in this study for characterizing the compression properties of the prepared composite forms [34]. It can be seen from Figure 1 that the apparent density increases with the increase in nano-SiO2 content (up to 4 wt %), then almost reaches a plateau. However, when the addition amount of nano-SiO2 was >7 wt %, the viscosity of blends experiences a sharp increase, resulting in the shutdown of the foaming reaction [35]. In the case of the addition of lignocellulosic biomass into the RPUF foaming process, the density of obtained foams decreases with the elevated content of PS or PB. The lignocellulosic biomass filler could act as the nucleating agent for promoting foam growing process to rapidly form a low-density foam.

Figure 1

The apparent density of prepared composite RPUFs.

As illustrated in Figure 2, the compressive strength has the same change tendency as the specific compressive strength of prepared composite RPUFs. Their values increase with the increase of nano-SiO2 content in the RPUF/SiO2 samples. The presence of nano-SiO2 would lead to the formation of thick and dense pore walls, thus could improve the compressive strength of RPUF/SiO2 samples. However, the compressive strength and specific compressive strength of RPUF/PS or RPUF/PB samples represent a rapid decrease with the addition of PS or PB (≤2%), then varies slightly with further increase in PS or PB content. This could be attributed to the loose pores arrangement and relatively thin pore walls in those foams, which would be also discussed in the following discussion of the morphology investigation. These results indicated that the type and the addition content of fillers could significantly tune the physical properties of the fabricated RPUFs as compared to the previous reports [36,37]. According to GB/T 21558-2008, the compressive strength value of RPUFs used as the building insulation materials should be higher than 80 kPa. Therefore, the compressive strength of the above composite RPUFs meets the requirement for external wall insulation in building fields.

Figure 2

The compressive strength and specific compressive strength curves of prepared composite RPUFs under the deformation degree of 10%.

3.2. Hydrogen Bonding States from ATR-FTIR

The ATR-FTIR is generally used for characterizing the hydrogen bonding (H-bonding) states in polyurethanes. Figure 3 shows the integrated (a) and partial (b) ATR-FTIR spectra of RPUFs with and without the addition of fillers. It can be seen from Figure 3a that all the prepared RPUFs exhibit the similar spectra, and there is no stretching vibration peak at around 2275 cm−1 for isocyanate (N=C=O) group, demonstrating that the isocyanate groups have reacted completely with polyols and water during polymerization [38]. Furthermore, two principal vibration regions for N–H stretching and C=O stretching band, with free (non-H-bonding), ordered (strongly H-bonding) and disordered (amorphous) states, can be observed in Figure 3b. Apparently, the ordered and disordered N–H stretching vibrations appear at around 3363 cm−1 and 3295 cm−1, respectively. The free N–H stretching vibration is present at 3496 cm−1 as a shoulder peak on the side of those bands [39]. The hydrogen bonding of N–H with ether oxygen (N−H−EO) is responsible for the absorbance peak at 3220 cm−1. Moreover, the characteristic absorbance peaks of H-bonding C=O groups generally appear at lower wavenumbers [40]. The stretching vibration peaks located at 1721 cm−1, 1705 cm−1, and 1657 cm−1 could be ascribed to the free, disordered and ordered hydrogen bonding state in the C=O groups, respectively [41,42]. These results imply that the organic or inorganic fillers have no effect on the hydrogen bonding states in composite RPUFs in comparison with the parent RPUF. The fillers did not react with the ingredients in the foaming process, but participated as inert materials to only change the physical properties of the prepared composite RPUFs.

Figure 3

The ATR-FTIR spectra of RPUFs with and without fillers: integrated curves (a) and partially enlarged curves (b).

3.3. Thermal Behavior

The thermal stability of polyurethanes is related to the intrinsic nature as well as the equivalent ratio of functional groups of the hard and soft segment. Moreover, the degree of phase separation between the hard and soft segments also plays a considerable role in determining the thermal stability of polyurethanes [43]. The thermal behavior of the prepared RPUFs was characterized by thermogravimetry (TG) and the corresponding differential thermogravimetry (DTG), as depicted in Figure 4. Compared to parent RPUF, there are no obvious changes in TG curve shape after the addition of nano-SiO2, PS or PB. The substantial degradation stage above 200 °C is attributed to the urethane bond decomposition through the breakdown of isocyanate and polyols [44], forming the primary amines and terminal olefinic group on the polyester chain [45], and the maximum weight loss rate can be observed at around 320–330 °C from DTG curves. Moreover, a weak weight loss peak can be found at the higher temperature (430–550 °C), probably resulting from the C–C bond cleavage [46], and the final residual content for RPUF, RPUF/SiO2, RPUF/PS and RPUF/PB is 16.4%, 20.0%, 18.0%, and 17.1%, respectively. The thermal stability of RPUFs is improved by the addition of the fillers, especially the inorganic one. The organic fillers could be decomposed when heated, while the inorganic nano-SiO2 filler remained stable, thus leading to the high residual content of the RPUF/SiO2.

Figure 4

The TG and DTG curves of (a) RPUF, (b) RPUF/SiO2 (7 wt %), (c) RPUF/PS (10 wt %), and (d) RPUF/PB (10 wt %).

3.4. Morphology Investigation

The camera pictures and SEM images of prepared RPUFs are shown in Figure 5 and Figure 6, respectively, to investigate the foam structure such as pore size, cell walls, and wall joints. Morphology changes of RPUFs mainly depend on the preparation condition of samples. It can be seen from Figure 5 that the cell size of RPUF/SiO2 is smaller than that of the RPUF/PS and RPUF/PB, which is consistent with the results of the apparent density analysis (Figure 1). RPUFs samples for SEM observation were cut from the perpendicular orientation to the foam growth direction. It can be observed from Figure 6 that all prepared RPUFs possess the closed-cell structure with many windows, and the cell size of composite RPUFs with the addition of fillers is much smaller than that of the parent foam. The closed-cell structure of the prepared composite RPUFs could be beneficial for the application of acoustical and thermal insulation.

Figure 5

Camera pictures of (a) RPUF/SiO2 (7 wt %), (b) RPUF/PS (10 wt %), and (c) RPUF/PB (10 wt %).

Figure 6

The SEM images of (a) RPUF, (b) RPUF/SiO2 (7 wt %), (c) RPUF/PS (10 wt %), and (d) RPUF/PB (10 wt %).

4. Conclusions

In this work, the effects of inorganic and organic fillers on compressive strength, density, thermal behavior, and morphology of rigid polyurethane foams were investigated. The results indicated the density of RPUF/SiO2 increased with the increase in the filler content while the density of RPUF/PS and RPUF/PB experienced the opposite trend. The compressive strength values of prepared RPUFs could fully meet the specification requirement for the building insulation materials. Moreover, the organic or inorganic fillers have no effect on the hydrogen bonding states in composite RPUFs in comparison with the parent RPUF. The addition of inorganic nano-SiO2 filler could bring relatively higher residual content in the corresponding RPUF/SiO2, while the organic fillers could be easily decomposed when heated, leading to the lower residual content of the RPUF/PS and RPUF/PB. The close-cell structure and appropriate compressive strength make the composite RPUFs suitable for serving as building insulation materials.