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European Journal of Wood and Wood Products

Open Access 03.05.2024 | Original Article

Enhancing the fire resistance properties of thermally modified Robinia pseudoacacia wood with natural and synthetic flame retardants: chemical characterisation and fire behaviour

verfasst von: Salvio Marino, Milan Gaff, Anil Kumar Sethy, Gourav Kamboj, Fatemeh Rezaei, František Kačík, S. Behnam Hosseini, Haitao Li, David Hui

Erschienen in: European Journal of Wood and Wood Products

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Abstract

The increasing demand for wood with enhanced flame retardant characteristics in construction applications necessitates strategic interventions. This study explores the fire behaviour and chemical characterisation of Robinia pseudoacacia wood subjected to thermal modification and flame retardant treatments. Thermal modification was carried out at three different temperatures (160 °C, 180 °C and 240 °C). The fire properties of wood coated with Flame Gard (F), a commercial flame retardant, arabinogalactan (A), a natural flame retardant, melamine adhesive (MF) with ammonium polyphosphate (AP), nanosilica (NS), nanoclay (NC) (MF-AP-NS and MF-AP-NC) and arabinogalactan with AP, NS and NC (A-AP-NS and A-AP-NC), were assessed using cone calorimetry in terms of the weight loss rate, ignition time and heat release rate. The commercial flame retardant Flame Gard outperformed the natural and fortified flame retardants in terms of the weight loss rate, heat release rate (HRR) and ignition time (t_ig). Unmodified samples exhibited superior fire properties in terms of t_ig and HRR compared to thermally modified samples. The peak heat release rate (kW.m^− 2) and time to peak heat release rate (s) showed a moderate degree of dependency on the chemical constituents of the wood.

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HRR₁₈₀

Heat release rate (180 s)

HRR₃₀₀

Heat release rate (300 s)

pHRR

Peak heat release rate

tpHRR

Time taken to peak HRR

THR

Total heat release

t_ig

Time to flame initiation

Mass of residue after measurement

m´´10–90%

Rate of weight loss per unit area in the main combustion phase

Δm

Weight loss

MARHE

Maximum average energy release rate

EHC

Efficient combustion heat

No flame retardant

Natural flame retardant (arabinogalactan)

Synthetic flame retardant

MF-AP-NC

Mixture of melamine formaldehyde, ammonium phosphate, and nanoclay

MF-AP-NS

Mixture of melamine formaldehyde, ammonium phosphate, nanosilica

A-AP-NC

Mixture of arabinogalactan, ammonium phosphate, and nanoclay

A-AP-NS

Mixture of arabinogalactan, ammonium phosphate, and nanosilica

1 Introduction

Wood, as a sustainable raw material, plays a significant role in climate change mitigation by sequestering atmospheric carbon dioxide and storing it until its use. Wood plays an important role in indoor and outdoor structures. Despite its advantages in strength, versatility and high insulation rating, wood naturally has low resistance to biological attack, moisture, and fire. This is why there is high demand for tropical wood species, which are known for their natural durability. Robinia pseudoacacia L., originally from North America but cultivated in Europe for over 400 years, is considered to be a promising substitute for tropical hardwoods. Black locust wood is highly valued in multiple industries due to its desirable characteristics and its ability to grow rapidly (Dünisch et al. 2010; Kačík et al. 2022).

For long-lasting outdoor applications, the heartwood of black locust is highly recommended. To mitigate the limitations of low durability, the wood is often treated thermally and chemically. The gradual heating of wood at high temperatures leads to physical and chemical changes, which in turn impacts its polymeric components (Kim et al. 2006).

Thermal modification (150–240 °C) improves the natural durability of wood (Čermák et al. 2015; Hao et al. 2018). The improvement in the fire resistance of wood after thermal modification is attributed to the reduction in hemicellulose and extractives. Despite these benefits, flame retardants are commonly applied to further enhance fire resistance. The fire safety issues associated with wood pose a disadvantage for its use as a building material. In comparison to many other inorganic materials, wood is widely recognized for its low thermal stability (Jiang et al. 2010; Hirata et al. 1991; Rowell 2005).

Various coatings, both organic and inorganic, have been used to enhance the performance and appearance of wood in order to achieve desired objectives. However, the use of certain coatings can pose significant safety risks due to the release of toxic gases. Fire resistance coatings are the preferred choice for fire protection, but their widespread application is limited due to their high cost (Gong et al. 2021). Alum and vinegar were historically used as flame retardant treatments, with inorganic salt being the most commonly used flame retardant for wood treatments (Gong et al. 2021; Lowden and Hull 2013).

Flame retardants can affect the ignition of solid materials through four mechanisms (Friedman 1998); first, they promote the formation of char, which reduces the formation of flammable gases; second, they release gases that contribute to slowing down the gaseous combustion reaction; third, they undergo endothermic decomposition, reducing the heat necessary for the combustion of the substance, and fourth, they form an insulating char layer on the surface of the combustible material. Two basic methods for improving the flame retardance of wood-based material involve impregnating them with flame retardants, or applying flame retardants as a coating (Moon and Emrick 2013; Isitman and Kaynak 2010; Naumann et al. 2012; Wang and Yang 2010). Substances such as ammonium phosphate, ammonium sulphate, zinc chloride, sodium tetra borate and boric acid are the most commonly used flame retardants. These substances aim to improve the fire properties of wood, namely to reduce weight loss, burning rate and maximum burning rate, while maintaining acceptable hygroscopicity, strength and tack of the treated wood surface (LeVan and Winandy 1990; Kol et al. 2010; Bekhta et al. 2016).

However, it should be noted that certain agents accelerate the deterioration of the wood surface; for instance, water leaching of chemicals is a crucial factor affecting the performance of retardants. Additionally, while thermal modification can improve the properties of wood, it can make also the wood more hydrophobic and affect its mechanical properties (Winandy 2013; Tribulová et al. 2017). There are various approaches to enhancing the flame retardance of wood, including the use of hybrid organic/inorganic retardants, nanoparticle suspensions and additives in commercial products. Some natural substances, such as arabinogalactan, have also demonstrated good flame retardant activity (Merk et al. 2015; Gaff et al. 2019; Popescu and Pfriem 2020). The perfect flame retardant for wood would possess several desirable attributes, including high efficiency, low toxicity, low environmental impact, durability, chemical and dimensional stability post treatment, no adverse effects on the physical and mechanical characteristics of the wood, affordability, ready availability and ease of use (Fu et al. 2017).

Many potential flame retardants can be harmful to both humans and the environment, and these products may leach from wood and lose their effectiveness. Researchers are exploring the use of carbon-based material in flame retardants to improve performance while minimising toxicity. Pre-treatment of wood can also enhance the effectiveness of flame retardants. A thermal analysis and flammability assessment are two common approaches to evaluate the efficiency of a flame retardant on a small scale. Techniques such as differential thermal analysis, thermogravimetric analysis (TGA), cone calorimetry, lateral ignition flame spread test (LIFT), and large-scale calorimetry, are frequently employed for these purposes (Lowden and Hull 2013). While cone calorimetry provides a range of measurable flammability parameters, it is only suitable for well-ventilated fire scenarios. The flame spread on the material surface also needs to be considered when assessing fire propagation. As a result, it can be challenging to attribute the outcomes specifically to post-flashover fires or under-ventilated fires.

In recent years, thermally modified wood has gained attention due to its improved properties such as high dimensional stability, durability, and decay resistance. However, it is important to consider how thermal modification can potentially affect the fire resistance properties of wood. This study aims to examine the effect of natural and synthetic fire retardants on the combustion and chemical properties of thermally treated Robinia pseudoacacia wood. Although Robinia pseudoacacia is a highly durable wood and may not require any modification, its high shrinkage value (Pollet et al. 2012) can be a deterrent in many specialised applications. Thermal modification can certainly improve its dimensional stability besides adding to its decay resistance.

This study provides information on the burning properties, thermal degradation, and chemical composition of treated and untreated wood samples. The findings should contribute to an understanding of the potential advantages of using flame retardants to enhance the fire resistance properties of thermally modified wood products modified at different temperatures (160, 180, and 210 ºC).

2 Experimental procedure

2.1 Material

2.1.1 Wood

100 × 100 × 20 mm (in the axial × radial × tangential direction) Robinia pseudoacacia samples were conditioned in a chamber at a relative humidity of 65 ± 3% and temperature of 20 ± 2 °C until they reached a moisture content of about 12%. After conditioning, the test samples were divided into three groups based on the type of retardant used: natural retardants, synthetic retardants, and reference samples without any retardant treatment. Ten replicate samples were used for each treatment. The samples were thermally modified at three different temperatures (160, 180, and 210 °C). Unmodified samples were also taken as control samples.

2.1.2 Thermal modification

The ThermoWood® process was used to thermally modify the wood samples. The thermal modification was conducted in a heat chamber (S400/03) manufactured by L.A.C, Rajhrad, Czech Republic. The process consists of three main phases. The parameters of the thermal modification and a description of each phase for the different thermal treatment temperatures (160, 180, and 210 °C) are shown in Table 1. The average density values for the specimens of Robinia pseudoacacia wood are shown in Table 2.

Table 1

Thermal modification parameters

Parameters	Temperature (°C)
Parameters	160	180	210
Application of heat (hours)	9.9	13.1	15.5
Thermal modification (hours)	3	3	3
Application of cooling (hours)	5.8	10.5	11
Total modification time (hours)	18.7	26.6	29.5

Table 2

Average moisture and density of Robinia pseudoacacia wood

Specimens	Unmodified (reference)	160	180	210 °C
Mass per unit volume (kg/m³)	765 (5.1)	690 (2.0)	660 (6.4)	497 (5.5)
Moisture content (%)	12%

Note Variation coefficients (CV) in percentages are shown in parentheses alongside the values

2.1.3 Flame retardants

2.1.3.1 Naturally occurring flame retardant

Many flame retardants currently used contain compounds that are harmful to health and release toxic gases when burnt. Recently, extensive research has focused on the potential of biomacromolecules (e.g. DNA, proteins, and polysaccharides) as alternative flame retardants because of their biodegradable and non-toxic nature. Hemicelluloses are the second most abundant component of terrestrial lignocellulosic biomass, and they have applications in the manufacturing of various materials because of their abundance, renewability, and biodegradability. Their combination (e.g. arabinoxylan, galactomannan) with inorganic substances (e.g. nanoclay, bentonite) can provide products with excellent mechanical, fire-retardant, and barrier properties (Huang et al. 2019; Leong et al. 2021; Hosseinashrafi et al. 2023). Due to its unique structure including a high degree of branching and an unusually high content of terminating 4-O-methyl-glucuronic acid (4-OMe GlcA) residues, arabinogalactan is a promising polysaccharide in the development of flame retardants. Arabinogalactan is a highly branched biopolymer consisting of arabinose and galactose monosaccharide units, often found attached to proteins, which are found on plasma membranes and in cell walls. Arabinogalactans AGs) form two main groups based on their structure: the arabino-4-galactans (1,4-β-D-galactans decorated with α-L-arabinose, α-L-Ara) are classified as type I AG and the arabino-3,6-galactans (1,3-β-D-galactan:1,6-β-D-galactan decorated with α-L-Ara) are classified as type II AG (D’Adamo 1996; Pfeifer et al. 2020; Ghosh et al. 2023; Ma and Johnson 2023).

2.1.3.2 Synthetic flame retardant

Flame Gard (Rovinka, Slovakia) is a viscous coating that dries to a transparent finish with a light-yellow tint, allowing the original wood pattern to remain visible. During combustion, the flame retardant coating undergoes thermal degradation on the protected surface, resulting in the formation of a dense, non-flammable foam layer that acts as thermal insulation. These foam layers effectively prevent fire and the transfer of heat, thereby enhancing the fire resistance properties of the wood. The fire-retardant coating is suitable for indoor applications with a relative humidity (RH) of 80% and a moisture content (MC) of 20% (Gaff et al. 2019).

In addition to Flame Gard, other chemicals such as ammonium phosphate (AP), nanosilica (NS) and nanoclay (NC) were also used as flame retardants. Four different flame retardant coating formulations, two with melamine adhesive and two with arabinogalactan were also tested for their fire performance. Melamine adhesive from M/s Akzo Nobel, Netherlands, with a viscosity ranging from 1,500 to 9,000 mPas and a solid content of 65%, was used. The details of the formulations are as follows:

Melamine adhesive + 15% AP + 5% NC (MF-AP-NC).
Melamine adhesive + 15% AP + 5% NS (MF-AP-NS).
Arabinogalactan (50% in water) + 15% AP + 5% NC (A-AP-NC).
Arabinogalactan (50% in water) + 15% AP + 5% NS (A-AP-NS).

3 Methods

3.1 Physical properties

The density of the wood and the moisture content were evaluated according to ISO 13061-2 (2014) and ISO 13061-1 (2014), respectively.

3.2 Chemical analyses

For the chemical analysis, a 0.5–1.0 mm specimen was extracted with an ethanol-toluene mixture according to ASTM D1107-96 (2013). The acid-insoluble lignin content was determined using the ASTM D1106-96 (2013) method. The holocellulose content was determined with the method described by Wise (1946), while the cellulose content was determined using the Seifert (1956) method.

3.3 Measurement methodology - cone calorimeter

Measurements were conducted with cone calorimetry (Fig. 1) in accordance with ISO 5660-1. The samples had a square shape with dimensions of 100 × 100 mm and a thickness of 20 mm. Prior to the measurement, the samples were wrapped in aluminium foil on the sides and bottom. Thermal insulation made of mineral fibers served as a base. The suction speed or airflow rate was set to 0.024 m³·s^-1. The measurement was performed in a horizontal position with the emitter positioned above the sample. An external heat of 25 kW·m^-2 was applied to the samples. The oxygen content in the flue gas was recorded by the computer at 5 s intervals. The burning characteristics of the treated samples obtained by the cone calorimeter include TTI, HRR, pHRR, T_pHRR and weight loss.

4 Results and discussion

Lignin is the most thermally stable wood component, and its yield increases during thermal treatment. This phenomenon is due to the formation of pseudo-lignin in condensation reactions of degradation products of lignin and polysaccharides (Hu et al. 2012; Shinde et al. 2018). Cellulose is more thermally stable than hemicelluloses because of its crystalline structure. Cellulose degradation occurs at a higher temperature than that of hemicelluloses and begins in its amorphous regions. Due to the faster degradation of hemicelluloses, the relative amount of cellulose increased up to a temperature of 240 °C. However, a significant decrease was observed above 260 °C, indicating cellulose degradation (Missio et al. 2015). Table 3 shows the average values of the chemical components of wood.

Table 3

Chemical analysis without modification and after thermal modification of black locust wood

Temperature (°C)	Extractives (%)	Lignin (%)	Holocellulose (%)	Cellulose (%)	Hemicelluloses (%)
Without modification (reference)	9.29 (0.82)	25.31 (0.55)	68.46 (0.60)	40.50 (0.53)	27.96 (0.70)
160	8.71 (3.32)	23.94 (2.14)	67.35 (0.29)	44.88 (0.18)	22.47 (1.10)
180	8.38 (2.03)	25.23 (0.54)	63.97 (0.25)	47.63 (0.42)	16.33 (2.10)
210	7.64 (1.93)	28.82 (0.25)	59.30 (0.28)	54.45 (0.51)	4.85 (4.44)

The results show the mean % of oven dry weight, coefficients of variation in %, n = 4

The cone calorimetric results of fire resistance coating on unmodified and thermally modified wood at an external heat flow of 25 kW·m^-2 were analyzed in terms of TTI, HRR, PHRR, (T_PHRR) and THR, and they are shown in Table 4. The results show a higher HRR at 180 and 300 kW·m², P_HRR, EHC, THR, t_PHRR and MARHE, and weight loss is greater in unmodified wood and thermally modified wood coated with a natural fire retardant than in wood samples coated with a synthetic flame retardant.

Table 4 presents the mean values of the burning parameter and coefficient of variation (CV).

Table 4

Burning properties of wood with and without modification

Variables		Burning properties
Flame retardant	Thermal modification (°C)	t_ig(s)	HRR₁₈₀(kW·m^-2)	HRR₃₀₀(kW·m^-2)	pHRR (kW·m^-2)	t_pHRR (s)	THR (MJ·m^-2)
No flame retardant	Unmodified (reference)	73.8 (7.8)	32.5 (34.5)	61.4 (14.8)	124.5 (7.1)	1304.2 (35.4)	163.6 (4.0)
	160	74.0 (6.1)	31.5 (35.7)	57.9 (19.2)	145.8 (6.4)	1319.0 (26.4)	185.0 (6.5)
	180	72.8 (1.5)	51.4 (37.1)	71.0 (7.2)	113.5 (26.0)	1010.2 (54.6)	144.4 (27.1)
	210	71.6 (2.1)	48.2 (16.0)	78.2 (13.0)	132.7 (15.0)	954.4 (42.5)	176.6 (11.2)
Synthetic flame retardant	Unmodified (reference)	52.2 (7.6)	23.0 (33.5)	42.6 (13.6)	88.1 (7.3)	925.2 (36.0)	114.2 (3.6)
	160	51.9 (6.8)	22.0 (35.3)	40.7 (19.5)	102.9 (7.2)	928.7 (28.4)	131.0 (6.7)
	180	50.8 (2.9)	35.9 (38.2)	50.1 (7.3)	78.9 (25.0)	713.9 (54.8)	100.4 (26.1)
	210	50.0 (2.6)	33.6 (16.8)	54.9 (13.1)	94.1 (15.3)	663.4 (42.9)	122.8 (11.5)
Natural flame retardant	Unmodified (reference)	67.0 (7.6)	29.5 (33.7)	55.7 (14.9)	112.5 (7.1)	1169.9 (34.9)	147.6 (4.8)
	160	66.7 (6.5)	28.3 (35.3)	53.4 (19.1)	134.4 (7.5)	1192.5 (27.9)	166.9 (7.8)
	180	68.2 (4.0)	47.8 (34.3)	65.0 (6.4)	104.4 (27.7)	916.6 (54.6)	129.8 (25.4)
	210	64.3 (2.4)	43.3 (16.6)	70.9 (13.0)	120.4 (13.9)	889.6 (46.6)	158.7 (12.0)
Variables		Burning properties
Flame retardant	Thermal modification (°C)	Weight on permanent flame g)	m_r(g)	m´´_10-90%(g.m^-2·s^-1)	m´´ (g.m^-2·s^-1)	Δm (g·m^-2)	MARHE (kW·m^-2)	EHC (MJ·kg^-1)
No flame retardant	Unmodified (reference)	151.2 (4.8)	55.0 (11.5)	6.0 (5.2)	5.7 (5.8)	9868.8 (5.8)	91.0 (4.0)	16.6 (4.7)
	160	143.3 (1.7)	54.5 (1.9)	6.2 (3.3)	5.8 (2.7)	10054.2 (2.6)	102.9 (6.5)	18.4 (4.8)
	180	125.7 (15.4)	58.0 (6.8)	5.5 (5.4)	5.2 (5.5)	7655.6 (26.2)	80.3 (27.0)	18.8 (3.6)
	210	130.6 (10.9)	49.4 (11.8)	5.7 (10.0)	5.3 (10.2)	9183.4 (10.5)	98.3 (11.1)	19.2 (3.1)
Synthetic flame retardant	Unmodified (reference)	105.1 (4.5)	38.5 (13.0)	4.2 (5.9)	4.0 (5.4)	6927.4 (7.2)	64.4 (4.1)	11.8 (5.5)
	160	100.1 (2.8)	38.5 (2.6)	4.4 (3.8)	4.1 (4.0)	7023.1 (3.8)	72.3 (6.3)	12.9 (6.7)
	180	87.4 (15.9)	40.4 (6.9)	3.9 (3.6)	3.6 (5.0)	5292.4 (25.0)	56.0 (28.2)	13.1 (4.5)
	210	90.8 (11.0)	34.5 (12.6)	4.1 (10.1)	3.7 (11.0)	6433.9 (12.2)	68.5 (11.0)	13.4 (4.0)
Natural flame retardant	Unmodified (reference)	136.8 (3.4)	49.9 (11.1)	5.4 (7.3)	5.2 (6.3)	8866.9 (7.9)	80.7 (4.1)	14.7 (6.3)
	160	129.3 (1.4)	49.1 (1.3)	5.5 (4.9)	5.3 (6.3)	9142.1 (2.9)	93.2 (6.5)	16.5 (6.2)
	180	115.8 (17.5)	54.3 (6.9)	5.0 (4.6)	4.9 (9.4)	6917.5 (26.8)	75.9 (30.9)	17.3 (7.8)
	210	117.3 (11.6)	44.4 (12.4)	5.2 (10.7)	4.8 (11.6)	8387.5 (11.1)	87.2 (11.2)	17.0 (6.1)

Coefficients of variation (CV)% values are in parentheses

Table 5 presents the results of statistical analysis assessing the influence of thermally modified wood and flame retardants on various burning properties. This includes parameters such as test time, heat release rate (HRR₁₈₀ and HRR₃₀₀), peak heat release rate (pHRR), times to peak heat release rate (tpHRR), total heat release rate (THR), weight on permanent flame, mass loss rate (mr), change in mass per unit area (Δm) and effective heat of combustion (EHC). P values (Table 5) show that the flame retardant has a significant effect on the fire properties of wood.

Table 5

Statistical analysis of the influence of thermal modification and flame retardants on burning properties

Significance level P
	Intercept	Temperature (°C)	Flame retardant	Temperature (°C) *Flame retardant
Test time (s)	***	NS	***	NS
HRR₁₈₀ (kW·m^-2)	***	***	***	NS
HRR₃₀₀ (kW·m^-2)	***	***	***	NS
pHRR (kW·m^-2)	***	***	***	NS
t_pHRR (s)	***	NS	***	NS
THR (MJ·m^-2)	***	***	***	NS
Weight on permanent flame (g)	***	***	***	NS
m_r (g)	***	***	***	NS
Δm (g·m^-2)	***	***	***	NS
m´´ (g.m^-2·s^-1)	***	***	***	NS
m´´_10-90% (g.m^-2·s^-1)	***	***	***	NS
MARHE (kW·m^-2)	***	***	***	NS
EHC (MJ·kg^-1)	***	***	***	NS

NS – not significant, *** - significant, the level of significance was set at P < 0.05

Figure 2a shows the rate of weight loss in thermally modified wood with (arabinogalactan-A and Flame Gard-F) and with no flame retardant. The weight loss of natural untreated wood was consistently 6 to 13% higher compared to wood modified at 160, 180, and 210 ºC. However, with the exception of samples modified at 180 º (p value = 0.008), no significant variation was observed in the rate of weight loss in thermally modified samples compared to unmodified samples. The weight loss rate with a natural flame retardant (arabinogalactan-A) was almost comparable to that of thermally modified wood, indicating that natural flame retardant has no significant effect on the rate of weight loss. Poor adhesion of arabinogalactan to the wood surface and imperfect layer formation led to rapid wood surface burning in the experiment, yielding similar results to untreated wood samples (Gaff et al. 2019). However, it is striking that the commercial flame retardant Flame Gard (F) outperformed the thermally modified wood and samples coated with arabinogalactan in terms of weight loss rate (Gašparík et al. 2017). The improvement in the weight loss rate after application of Flame Gard was significantly higher (p value ≤ 0.02).

Even though there is variability in the quality of natural products, the demand for improvement with potential natural products is growing; it was in this endeavor that we attempted to improve the properties of arabinogalactan by incorporating a traditional flame retardant such as ammonium phosphate and nanoparticles of silica and clay. A similar combination with melamine adhesive was also tested, as melamine adhesive is a good binder, and it also adds to the nitrogen content of the flame retardant, which has proven flame retardant properties. Figure 2b shows the effectiveness of the retardant (MF-AP-NC and MF-AP-NS) coating. The performance of both nanosilica (NS) and nanoclay mixture with melamine formaldehyde (MF) and ammonium phosphate (AP) was almost the same, with the exception of wood modified at 160 ºC, where NC outperformed NS. When the values of melamine-based formulations were compared to the values of only thermally modified samples (N) and samples coated with arabinogalactan (Fig. 2a), all the values were comparable, with the exception of wood thermally modified at 210 ºC; the weight loss rate was significantly reduced in samples coated with a melamine-based formulation. When compared to Flame Gard, all the melamine-based formulations were still inferior, with the exception of wood thermally modified at 210 ºC and coated with an NS-based melamine formulation, where the values were comparable (p value = 0.22). The results pertaining to the arabinogalactan formulation (A-AP-NC and A-AP-NS) are shown in Fig. 2c. A-AP-NC coating only significantly improved unmodified samples (p value = 0.002), whereas the values were comparable in other samples. The performance of Flame Gard was once again significantly better than that of A-AP-NC and A-AP-NS. Between melamine and arabinogalactan formulations, the performance of the melamine-based formulation was comparatively superior in terms of the weight loss rate; this can be attributed to the presence of nitrogen in the melamine molecule.

Figure 3 shows the effect of thermal modification and flame retardant coatings on the ignition time (t_ig). The ignition time of Flame Gard was significantly better (p value < 0.002), and its performance on unmodified wood was the best compared to only thermally modified samples (N) and samples coated with arabinogalactan (Fig. 3a). The ignition times of Flame Gard-coated samples were about 1.8–2.3 times higher than in thermally modified samples (N) and samples coated with arabinogalactan. Figure 3b and c shows the performance of melamine-based and arabinogalactan-based formulations on the t_ig, respectively. No significant difference was observed in either of these formulations in terms of improvement in the t_ig. It should be noted that the t_ig in unmodified samples with all types of treatment was comparatively better than that of thermally modified wood; this can be attributed to the higher equilibrium moisture content of unmodified wood compared to thermally modified wood. Higher moisture content consumes more energy for evaporation, thereby leaving less energy for ignition, and this in turn delays the ignition time.

The cone calorimetry test employs the principle of O₂ combustion, evaluating the material performance. Among the crucial parameters measured, the heat release rate (HRR) is the most important, as it signifies the intensity of the fire (Fig. 4). Figure 4a illustrates the effect of thermal modification and a flame retardant coating on the heat release rate (kW/m²) after 180 s. A visual analysis showed that Flame Gard (F) significantly reduces the HRR in comparison to the only thermally modified wood (N) and wood coated with arabinogalactan (A). The average HRR of Flame Gard-coated samples was in the range of 19–37 kW/m², depending on the modification temperature, while in samples only thermally modified and samples coated with arabinogalactan it was in the range of 70–93 kW/m². The HRR of Flame Gard-coated samples was about 2.5–3.7 times lower than that of thermally modified samples (N) and samples coated with arabinogalactan. As in the case of ignition time, the HRR of unmodified samples, irrespective of treatment, was the lowest compared to thermally modified samples; this is due to the higher equilibrium moisture content of unmodified wood. Figure 4b and c show the performance of melamine-based and arabinogalactan-based formulations on the HRR, respectively. No significant difference was observed in either of these formulations in terms of improvement in the HRR. The results are in line with the results reported in the literature (Lowden and Hull 2013; Marney et al. 2008; Jiang et al. 2014).

Figure 5 shows the effect of thermal modification and flame retardant coating on the heat release rate (kW/m²) after 300s. The HRR results after 300 s were similar to those observed after 180s. Flame Gard (F) significantly reduced the HRR (Fig. 4a) in comparison to thermally modified samples (N) and samples coated with arabinogalactan (A). The average HRR of Flame Gard-coated samples was in the range of 18–37 kW/m², depending on the modification temperature, whereas in thermally modified samples and samples coated with arabinogalactan, it ranged between 60 and 84 kW/m². The HRR of Flame Gard-coated samples was about 2.3–3.3 times lower than that of thermally modified samples (N) and samples coated with arabinogalactan. Figure 5b and c show the performance of melamine-based and arabinogalactan-based formulations on the HRR after 300s, respectively. No significant difference was found in either of these formulations in terms of improvement in the HRR.

The results of the Spearman correlation indicate the extent of the relationship between the fire properties and chemical components of wood (Table 6). The peak heat release rate, pHRR (kW.m^-2) and time to peak heat release rate, tpHRR (s) showed a moderate degree of dependence ranging from − 52 to 47%, whereas there was no significant correlation between chemical components for other fire characteristics.

Table 6

Correlation analysis evaluating the interaction between chemical components and reaction to fire characteristics and flammability

	Extractives (%)	Lignin (%)	Holocellulose (%)	Cellulose (%)	Hemicelluloses (%)
t_ig (s)	10	-8	9	-9	9
HRR₁₈₀ (kW.m^− 2)	-39	34	-46	42	-44
HRR₃₀₀ (kW.m^− 2)	-46	47	-52	46	-49
pHRR (kW.m^− 2)	3	-6	6	1	2
t_pHRR (s)	38	-26	34	-30	32
THR (MJ.m^− 2)	0	2	1	4	-2
Weight at flame (g)	35	-19	32	-32	32
m_r (g)	21	-27	21	-21	21
Δm (g.m^− 2)	23	-8	22	-18	20
m´´ (g.m^− 2s^− 1)	21	-18	23	-20	21
m´´_10−90% (g.m^− 2s^− 1)	14	-10	16	-13	15
MARHE (kW.m^− 2)	0	1	1	4	-2
EHC (MJ.kg^− 1)	-30	13	-27	29	-28

5 Conclusion

This study investigated the efficacy of natural (arabinogalactan) and synthetic flame retardants, Flame Gard (F), melamine adhesive with ammonium polyphosphate, nanosilica (MF-AP-NS and MF-AP-NC) and arabinogalactan with ammonium polyphosphate and nanosilica (A-AP-NS and A-AP-NC) on the burning characteristics of Robinia pseudoacacia wood thermally modified at temperatures of 160, 180, and 210 ºC. The salient findings of this study are as follows:

Commercial flame retardant Flame Gard (F) outperformed thermally modified samples and samples coated with arabinogalactan in terms of the weight loss rate, ignition time and heat release rate.
The performance of Flame Gard was significantly better than that of A-AP-NC and A-AP-NS in terms of the weight loss rate, ignition time heat release rate.
Melamine-based formulations were still inferior, with the exception of wood thermally modified at 210 ºC and coated with an NS-based melamine formulation, where the values were comparable to those of Flame Gard-coated samples.
Between melamine and arabinogalactan formulations, the performance of melamine-based formulations was comparatively superior in terms of the weight loss rate.
The ignition time and heat release rate of unmodified samples with all types of treatments were comparatively better than in thermally modified wood.

Acknowledgements

The authors would like to express their gratitude for the support of ‘Advanced research supporting the forestry and wood-processing sector´s adaptation to global change and the 4th industrial revolution’ No CZ.02.1.01/0.0/0.0/16_019/0000803 financed by OP RDE”, and they are also grateful for the support of the University-wide Internal Grant Agency (CIGA) of the Faculty of Forestry and Wood Sciences, project No 2016–4309 as well as the support of the Slovak Research and Development Agency, project No APVV-16-0326.

Declarations

Competing interests

The authors declare no competing interests.

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ASTM D1107-96 (2013) Standard Test Method for Ethanol-Toluene Solubility of Wood. ASTM International. West Conshohocken. PA. https://doi.org/10.1520/D1107

ASTM D1106-96 (2013) Standard Test Method for Acid-Insoluble Lignin in Wood. ASTM International. West Conshohocken. PA. https://doi.org/10.1520/D1106

Bekhta P, Bryn O, Sedliacik J, Novák I (2016) Effect of different fire retardants on birch plywood properties. Acta Facultatis Xylologiae Zvolen res Publica Slovaca 58(1):59. https://doi.org/10.17423/afx.2016.58.1.07CrossRef

Čermák P, Rautkari L, Horáček P, Saake B, Rademacher P, Sablík P (2015) Analysis of dimensional stability of thermally modified wood affected by re-wetting cycles. BioResources 10(2):3242–3253. https://doi.org/10.15376/biores.10.2.3242-3253CrossRef

D’Adamo P (1996) Larch Arabinogalactan. J Naturopathic Med 6(1):33–37

Dünisch O, Richter HG, Koch G (2010) Wood properties of juvenile and mature heartwood in Robinia pseudoacacia L. Wood Sci Technol 44(2):301–313. https://doi.org/10.1007/s00226-009-0275-0CrossRef

Friedman R (1998) Principles of fire protection chemistry and physics. Jones & Bartlett Learning

Fu F, Lin L, Xu E (2017) Functional pretreatments of natural raw materials. In Advanced high strength natural fibre composites in construction 87–114. Woodhead Publishing. https://doi.org/10.1016/B978-0-08-100411-1.00004-2

Gaff M, Kačík F, Gašparík M, Todaro L, Jones D, Corleto R, Osvaldová LM, Čekovská H (2019) The effect of synthetic and natural fire-retardants on burning and chemical characteristics of thermally modified teak (Tectona grandis L. f.) wood. Constr Build Mater 200:551–558. https://doi.org/10.1016/j.conbuildmat.2018.12.106CrossRef

Gašparík M, Osvaldová LM, Čekovská H, Potůček D (2017) Flammability characteristics of thermally modified oak wood treated with a fire retardant. BioResources 12(4):8451–8467CrossRef

Ghosh K, Takahashi D, Kotake T (2023) Plant type II arabinogalactan: structural features and modification to increase functionality. Carbohydr Res 108828. https://doi.org/10.1016/j.carres.2023.108828

Gong J, Zhai C, Wang Z (2021) Pyrolysis and autoignition behaviors of beech wood coated with an acrylic-based waterborne layer. Fuel 306:121724. https://doi.org/10.1016/j.fuel.2021.121724CrossRef

Hao Y, Pan Y, Du R, Wang Y, Chen Z, Zhang X, Wang X (2018) The influence of a thermal treatment on the decay resistance of wood via FTIR analysis. Adv Mater Sci Eng 2018:1–7. https://doi.org/10.1155/2018/8461407CrossRef

Hirata T, Kawamoto S, Nishimoto T (1991) Thermogravimetry of wood treated with water-insoluble retardants and a proposal for development of fire‐retardant wood materials. Fire Mater 15(1):27–36. https://doi.org/10.1002/fam.810150106CrossRef

Hosseinashrafi SK, Hosseinihashemi SK, Gorji P, Akhtari M (2023) Environment-friendly waterborne fire retardants for protection of wood and bark against fire flames. BioResources 18(4):7681–7699. https://doi.org/10.15376/biores.18.4.7681-7699CrossRef

Hu C, Jiang G, Xiao M, Zhou J, Yi Z (2012) Effects of heat treatment on water-soluble extractives and color changes of merbau heartwood. J Wood Sci 58:465–469. https://doi.org/10.1007/s10086-012-1265-7CrossRef

Huang C, Fang G, Tao Y, Meng X, Lin Y, Bhagia S, Ragauskas AJ (2019) Nacre-inspired hemicelluloses paper with fire retardant and gas barrier properties by self-assembly with bentonite nanosheets. Carbohydr Polym 225:115219. https://doi.org/10.1016/j.carbpol.2019.115219CrossRefPubMed

Isitman NA, Kaynak C (2010) Nanoclay and carbon nanotubes as potential synergists of an organophosphorus flame-retardant in poly (methyl methacrylate). Polym Degrad Stab 95(9):1523–1532. https://doi.org/10.1016/j.polymdegradstab.2010.06.013CrossRef

ISO 13061-1 (2014) Wood-determination of moisture content for physical and mechanical tests. International Organization for Standardization. Geneva. Switzerland

ISO 13061-2 (2014) Wood-determination of density for physical and mechanical tests. International Organization for Standardization. Geneva. Switzerland

Jiang J, Li J, Hu J, Fan D (2010) Effect of nitrogen phosphorus flame retardants on thermal degradation of wood. Constr Build Mater 24(12):2633–2637. https://doi.org/10.1016/j.conbuildmat.2010.04.064CrossRef

Jiang T, Feng X, Wang Q, Xiao Z, Wang F, Xie Y (2014) Fire performance of oak wood modified with N-methylol resin and methylolated guanylurea phosphate/boric acid-based fire retardant. Constr Build Mater 72:1–6. https://doi.org/10.1016/j.conbuildmat.2014.09.004CrossRef

Kačík F, Kubovský I, Bouček J, Hrčka R, Gaff M, Kačíková D (2022) Colour and Chemical Changes of Black Locust Wood during Heat Treatment. Forests 14(1):73. https://doi.org/10.3390/f14010073CrossRef

Kim HS, Kim S, Kim HJ, Yang HS (2006) Thermal properties of bio-flour-filled polyolefin composites with different compatibilizing agent type and content. Thermochimica Acta 451(1–2):181–188. https://doi.org/10.1016/j.tca.2006.09.013CrossRef

Kol HS, Ozbay G, Köse L, Kurt S (2010) Effects of some impregnation chemicals on combustion characteristics of laminated veneer lumber (LVL) produced with oak and poplar veneers. BioResources 5(1):70–80CrossRef

Leong WI, Lo OLI, Cheng FT, Cheong WM, Seak LC, U (2021) Using recombinant adhesive proteins as durable and green flame-retardant coatings. Synth Syst Biotechnol 6(4):369–376. https://doi.org/10.1016/j.synbio.2021.10.005CrossRefPubMedPubMedCentral

LeVan SL, Winandy JE (1990) Effects of fire-retardant treatments on wood strength: a review. Wood Fiber Sci 113–131

Lowden LA, Hull TR (2013) Flammability behavior of wood and a review of the methods for its reduction. Fire Sci Rev 2:1–19. https://doi.org/10.1186/2193-0414-2-4CrossRef

Ma Y, Johnson K (2023) Arabinogalactan proteins–multifunctional glycoproteins of the plant cell wall. Cell Surf 9:100102. https://doi.org/10.1016/j.tcsw.2023.100102CrossRefPubMedPubMedCentral

Marney DC, Russell LJ, Mann R (2008) Fire performance of wood (Pinus radiata) treated with fire retardants and a wood preservative. Fire Mater 32(6):357–370. https://doi.org/10.1002/fam.973CrossRef

Merk V, Chanana M, Keplinger T, Gaan S, Burgert I (2015) Hybrid wood materials with improved fire retardance by bio-inspired mineralisation on the nano-and submicron level. Green Chem 17(3):1423–1428. https://doi.org/10.1039/C4GC01862ACrossRef

Missio AL, Mattos BD, de Cademartori PH, Pertuzzatti A, Conte B, Gatto DA (2015) Thermochemical and physical properties of two fast-growing eucalypt woods subjected to two-step freeze–heat treatments. Thermochimica Acta 615:15–22. https://doi.org/10.1016/j.tca.2015.07.005CrossRef

Moon S, Emrick T (2013) High flame resistant and strong electrospun polyacrylonitrile–carbon nanotubes–ochre nanofibers. Polymer 54(7):1813–1819. https://doi.org/10.1016/j.polymer.2013.01.053CrossRef

Naumann A, Seefeldt H, Stephan I, Braun U, Noll M (2012) Material resistance of flame retarded wood-plastic composites against fire and fungal decay. Polym Degrad Stab 97(7):1189–1196. https://doi.org/10.1016/j.polymdegradstab.2012.03.031CrossRef

Pfeifer L, Shafee T, Johnson KL, Bacic A, Classen B (2020) Arabinogalactan-proteins of Zostera marina L. contain unique glycan structures and provide insight into adaption processes to saline environments. Sci Rep 10(1):8232. https://doi.org/10.1038/s41598-020-65135-5CrossRefPubMedPubMedCentral

Pollet C, Verheyen C, Hebert J, Jourez B (2012) Physical and mechanical properties of black Locust (Robinia pseudoacacia) wood grown in Belgium. Can J for Res 42(5):831–840. https://doi.org/10.1139/x2012-037CrossRef

Popescu CM, Pfriem A (2020) Treatments and modification to improve the reaction to fire of wood and wood-based products—An overview. Fire Mater 44(1):100–111. https://doi.org/10.1002/fam.2779CrossRef

Rowell RM (2005) Handbook of wood chemistry and wood composites. CRC. https://doi.org/10.1201/9780203492437

Seifert VK (1956) Über Ein neues verfahren Zur Schnellbestimmung Der rein-cellulose. Papier 10:301–306

Shinde SD, Meng X, Kumar R, Ragauskas AJ (2018) Recent advances in understanding the pseudo-lignin formation in a lignocellulosic biorefinery. Green Chem 20(10):2192–2205. https://doi.org/10.1039/C8GC00353JCrossRef

Tribulová T, Kačík F, Evtuguin DV (2017) Impacts of inorganic chemicals used for wood protection: a review. Acta Facultatis Xylologiae Zvolen res Publica Slovaca 59(2):5–22. https://doi.org/10.17423/afx.2017.59.2.01CrossRef

Wang G, Yang J (2010) Influences of expandable graphite modified by polyethylene glycol on fire protection of waterborne intumescent fire resistive coating. Surf Coat Technol 204(21–22):3599–3605. https://doi.org/10.1016/j.surfcoat.2010.04.029CrossRef

Winandy JE (2013) State of the art paper: effects of fire-retardant treatments on chemistry and engineering properties of wood. Wood Fiber Sci 15:131–148

Wise LE (1946) Chlorite holocellulose, its fractionation and bearing on summative wood analysis and on studies on the hemicelluloses. Paper Trade J 122:35–43

Titel: Enhancing the fire resistance properties of thermally modified Robinia pseudoacacia wood with natural and synthetic flame retardants: chemical characterisation and fire behaviour
verfasst von: Salvio Marino
Milan Gaff
Anil Kumar Sethy
Gourav Kamboj
Fatemeh Rezaei
František Kačík
S. Behnam Hosseini
Haitao Li
David Hui
Publikationsdatum: 03.05.2024
Verlag: Springer Berlin Heidelberg
Erschienen in: European Journal of Wood and Wood Products
Print ISSN: 0018-3768
Elektronische ISSN: 1436-736X
DOI: https://doi.org/10.1007/s00107-024-02079-x

Springer Professional

Abstract

Publisher’s Note

1 Introduction

2 Experimental procedure

2.1 Material

2.1.1 Wood

2.1.2 Thermal modification

2.1.3 Flame retardants

2.1.3.1 Naturally occurring flame retardant

2.1.3.2 Synthetic flame retardant

3 Methods

3.1 Physical properties

3.2 Chemical analyses

3.3 Measurement methodology - cone calorimeter

4 Results and discussion

5 Conclusion

Acknowledgements

Declarations

Competing interests

Publisher’s Note