Skip to main content
Scientific Reports logoLink to Scientific Reports
. 2019 Feb 7;9:1601. doi: 10.1038/s41598-018-38317-5

Effects of zinc chloride–silicone oil treatment on wood dimensional stability, chemical components, thermal decomposition and its mechanism

Zhengbin He 1,2,, Lijie Qu 1, Zhenyu Wang 1, Jing Qian 1, Songlin Yi 1,
PMCID: PMC6367429  PMID: 30733516

Abstract

The hygroexpansion and anisotropy of wood limit its application in construction and wood products industry. Zinc chloride–silicone oil was use to decrease the hygroscopicity and improve the dimensional stability of wood at 80 °C, 140 °C, 160 °C and 180 °C. The effects of the treatment on the dimensional stability, chemical structure, thermal degradation, morphology of wood were evaluated, and the mechanism was determined. Results indicated that the zinc chloride–silicone oil treatment at 80 °C improved the dimensional stability and decreased the hygroscopicity of wood. The tangential, radial, and volumetric swelling coefficients of the treated wood decreased by 9.7%, 33.5%, and 18.2%, respectively, relative to those of the untreated wood. Zinc chloride–silicone oil treatment also changed the chemical structure of wood by degrading the wood components and decreasing the moisture absorption groups. Moreover, zinc chloride–silicone oil treatment significantly influenced the thermal degradation of wood, as samples treated with zinc chloride–silicone oil at 140 °C, 160 °C and 180 °C presented sharp peaks around 511 °C, 501 °C and 473 °C. The control group exhibited a more common derivative thermogravimetric curve with a sharp peak at 375 °C. In addition, the silicone oil could impregnate wood, occlude moisture passage, and prevent the movement of moisture in wood. This method can be applied in building and wood industries to expand the applications of wood products.

Introduction

Wood is a natural and renewable lignocellulosic material characterized by a high strength-to-weight ratio, low energy cost for processing, environmental sustainability13, natural degradation, and regulation of air temperature and humidity4. Wood has thus been used for construction, building, furniture, decoration5,6, and other applications in recent years. However, as a natural material containing cellulose, hemicellulose, and lignin, wood is also prone to hygroexpansion and anisotropy7,8, it shrinks and swells when equilibrium moisture content (EMC), which is controlled by environmental temperature and humidity, changes with the environmental conditions. Then, wood defects, such as cracks, transformation, and decay generated9, and markedly shortening the service life and value of wood products, thus limiting their wide application.

Thermal treatment of wood is an environmentally friendly method to improve the dimensional stability, weathering ability, and other characteristics of wood1013. This method has been widely employed in various settings. However, while this approach is suitable for improving wood quality, it consumes substantial energy based on the scheduling requirement of high temperature and high investment cost; equipment must be heat-preserved and decay-resistant14. Therefore, a low-temperature heat treatment schedule should be applied to reduce energy costs.

Wood thermal treatment can potentially increase the dimensional stability of wood and other characteristics primarily because wood components undergo degradation under high-temperature conditions1517. Zinc chloride solution is also weakly acidic and can be used as a catalyst to promote wood hemicellulose and cellulose degradation at reduced temperatures and decrease moisture absorption18. Therefore, zinc chloride was used as the catalyst, and silicone oil was used as the heating medium in the treatment of wood samples to determine the optimal schedule for zinc chloride–silicone oil treatment. The effects of zinc chloride–silicone oil treatment on the dimensional stability, chemical components, and thermal decomposition behavior of wood were evaluated to broaden the application of wood.

Results and Discussion

Dimensional stability of wood

The dimensional stability of wood is one of the most important parameters for wood applications. Wood with low dimensional stability can shrink or swell when the EMC in the surrounding environment decreases or increases13. Wood moisture also changes with variations in environmental temperature and humidity, leading to defects19. Therefore, the dimensional stability of wood significantly affects the quality and application of wood product. Moreover, the swelling coefficients in the tangential and radial directions are the most significant factors for estimating the dimensional stability of wood7,13. The samples were evaluated after treatment, and the results indicated that the samples treated at 140 °C, 160 °C and 180 °C were so degraded that its surface was carbonized, the sample failed to retain its original shape, and its structure was broken by the catalyst of zinc chloride at high temperature; meanwhile the samples treated at 80 °C in a silicone oil bath retain its intact structure. Figure 1 shows the effects of zinc chloride treatment in a silicone oil bath at 80 °C on the tangential swelling (TS), radial swelling (RS) and volumetric swelling (VS) coefficients of wood. TS coefficient varied from 2.36% to 2.13%, reflecting a decrease of 9.7%. RS coefficient decreased from 2.15% to 1.43%, reflecting a decrease of 33.5%. VS coefficient decreased from 4.82% to 3.94%, indicating a reduction of 18.2%. Thus, the zinc chloride-silicon oil treatment reduced the TS, RS, and VS coefficients of the wood, thus increasing its dimensional stability. This improvement in dimensional stability may be attributed to the following: (i) low acidity of the zinc chloride solution at a certain temperature, leading to hemicellulose degradation in wood18,2022, and (ii) water repellency of the silicone oil, reducing the hygroscopicity of wood6,23.

Figure 1.

Figure 1

Effects of zinc chloride–silicone oil treatment on wood swelling.

Fourier Transform Infrared (FTIR) Spectroscopy analysis

The hygroscopicity of wood is directly influenced by the hygroscopic group, such as hydroxyl; variations in the chemical groups of wood can affect its dimensional stability2428. FTIR spectroscopy is a suitable technique for measuring variations in chemical structure of treated samples2932. The FTIR spectra of the samples treated with zinc chloride in silicone oil bath are presented in Fig. 2. Wood impregnated with zinc chloride and treated in silicone oil substantially influenced the chemical structures of the wood. The band intensity at 3423 cm−1 corresponding to -OH stretching33 and the band intensity at 2905 cm−1 corresponding to –CH stretching34 generally decreased relative to those of the control group. This result may be attributed to the degradation of hemicellulose and other components in the wood cell wall, which has free hydroxyl and can absorb moisture3538. Thus, the dimensional stability of the wood increased39,40. Moreover, the band intensities at 2970 cm−1 corresponding to –CH2 stretching4143 increased relative those of the control because of silicone oil impregnation. The samples impregnated with zinc chloride and treated in silicone oil exhibited markedly increased band intensities at 1263 cm−1 corresponding to Si-CH3 stretching in silicone oil. In addition, 800 cm−1 was assigned to the Si-C, Si-O, and Si-O-CH3 groups44, indicating that silicone oil was impregnated into wood. Therefore, hemicellulose and other hygroscopic groups in the cell wall of the wood impregnated with zinc chloride could be degraded, and water-repellent silicone oil was absorbed by wood, thereby reducing the hygroscopicity and improving dimensional stability of wood.

Figure 2.

Figure 2

FTIR spectra of samples treated with zinc chloride in silicone oil bath.

Thermal decomposition by thermogravimetric (TG) and derivative thermogravimetric (DTG)

To evaluate the effects of zinc chloride–silicone oil treatment on the thermal characteristics of wood, the thermogravimetric (TG) and derivative thermogravimetric (DTG) curves of treated and untreated samples are presented in Fig. 3. Significant differences between the treated and untreated samples were observed. A small weight loss (approximately 1.1–3.7 wt%) was observed from the TG curve during the first stage (from 28 to 100 °C), which was the dehydration stage; no significant degradation of wood components was exhibited29,30. The weight loss decreased with an increase in treatment temperature because the wood immersed in the silicone oil and heated to a certain temperature underwent drying, and the rate of moisture loss increased with temperature. Residual moisture was also low in the treated samples. The temperature varied from 100 °C to 200 °C during the second stage under which some wood components might be degraded, and some complex structures could break their bonds4548. The largest mass loss occurred during the third stage with temperatures ranging from 200 to 580 °C. During this stage, all structural components, including hemicellulose, cellulose, and lignin (66–81% of total mass) in the samples were thermally degraded28,49. Three peaks were observed for all samples. The samples impregnated with zinc chloride at 80 °C showed three peaks around 278 °C, 346 °C, and 525 °C; those treated at 140 °C showed three peaks at 278 °C, 354 °C, and 511 °C; those treated at 160 °C showed peaks at 278 °C, 355 °C, and 501 °C; and those treated at 180 °C showed peaks at 281 °C, 473 °C, and 557 °C. During the higher-temperature stage, the samples treated at 80 °C, 140 °C, 160 °C, and 180 °C showed peaks at 527 °C, 511 °C, 501 °C, and 473 °C, respectively, which might be the reason that more complex structures could break their bonds during silicone oil treatment. Consequently, samples are easily during the TG analysis. Moreover, the treated samples appeared different from the untreated samples. The control group showed a more common DTG curve with a sharp peak at 375 °C, which was attributed to cellulose, hemicellulose or lignin decomposition50. These differences could be attributed to zinc chloride being acidic in water, thus promoting wood degradation during treatment. Most wood components were degraded when the temperature increased to 180 °C21. During the fourth stage, the gradual mass loss was observed in the samples. The content of residual material varied between the control group and the treated group, which could be attributed to the incomplete degradation of the impregnated zinc chloride and silicone oil during thermal degradation.

Figure 3.

Figure 3

TG and DTG curves for the treated and untreated wood.

Morphology and mechanism

Morphological analysis by Scanning Electron Microscopy (SEM)

Figure 4 presents the morphology of the untreated (left) and treated (right) samples. The samples impregnated with zinc chloride and treated at 80 °C significantly influenced the morphology of the wood. Most porosity (e.g., pits) of the treated samples was occluded, and the internal surface of the wood was smoother than that of the control group. Some components were degraded during treatment process, thereby occluding the internal water passage in wood and decreasing numbers of the hygroscopic group. These features improve the dimensional ability of wood, reduce its hygroscopicity, and expand its applications in buildings and furniture.

Figure 4.

Figure 4

SEM micrographs (800×) for the control group (left) and the group treated at 80 °C (right).

Mechanism

On the basis of the aforementioned results, wood impregnated with zinc chloride and treated in silicone oil exhibits increased dimensional stability, reduced hydroxy content, and lowered hygroscopicity. Zinc chloride is hydrolyzed in water and generates acid and zinc ion. The impregnation of wood with solution might have increased the degradation of moisture absorption groups. A tentative mechanism is presented in Fig. 5. Hemicellulose, one of the components in wood, contains moisture-absorbing groups (i.e., hydroxy), and most of the hydroxyl on its branched chain can absorb or lose moisture, along with variations in temperature and humidity3537. These factors can generate defects, affect the quality of wood, and limit its applications. The branched chain in the hemicellulose is degraded in a weak acid environment at certain temperatures, with zinc chloride as the catalyst20,21. Consequently, some branched chain degraded from the hemicellulose is dissolved in the solution; simultaneously, the distances between some hydroxyl on the hemicellulose branched chain is close, and the hydrogen bond was established. Thus the free hydroxyl, which could absorb the moisture in the hemicellulose, decreased, thereby reducing the amount of water that could be absorbed by wood18,22. Thus, a decrease in hygroscopic group improved the wood dimensional stability and reduced the hygroscopicity of wood during application.

Figure 5.

Figure 5

Mechanism of wood degradation during treatment.

Conclusions

The zinc chloride–silicone oil treatment can improve the dimensional stability and decrease the hygroscopicity of wood. The method can also reduce the swelling coefficient of wood at 80 °C. The TS, RS and VS coefficients of the treated wood decreased by 9.7%, 33.5%, and 18.2%, respectively, relative to those of the control group. The treatment conducted at certain temperatures also affected the chemical structure, degraded the hemicellulose, and decreased the hydroxyl content and other components of wood. Moreover, the zinc chloride–silicone oil treatment largely influenced the thermal degradation of wood. The thermal degradation generally includes four stages, revealing significant differences between the treated and untreated samples during the third stage (200–580 °C), with approximately 66–81% of total mass degraded. Three peaks were observed for all samples. At high temperature stages, the peaks of the samples treated at 80 °C, 140 °C, 160 °C and 180 °C were observed around 527 °C, 511 °C, 501 °C and 473 °C; meanwhile, the control group demonstrated a more commonly observed DTG curve with a sharp peak at 375 °C. In addition, the samples impregnated with zinc chloride and treated at 80 °C significantly influenced the wood morphology. Thus, silicone oil impregnated the wood and occluded water passage (e.g., pits). Several internal components of wood could thus degrade and potentially decrease the hygroscopicity and increase the dimensional stability of wood. The zinc chloride–silicone oil treatment can improve the dimensional stability and decrease the hygroscopicity of wood because zinc chloride generates weak acids and the catalyst of zinc chloride can promote hemicellulose degradation and decrease moisture absorption in wood. In addition, silicone oil can occlude water passage and prevent the migration of moisture into the internal wood.

Materials and Methods

Materials

Chinese fir (Cunninghamia lanceolata (Lamb.) Hook), a type of fast-growing wood planted across large areas of China, was taken as the experimental material. It was obtained from Sichuan Province, China. The dimension of the test specimens was 20 mm (tangential) × 20 mm (radial) × 20 mm (longitudinal) with an initial moisture content of (80 ± 5) % according to GB/T 1931–2009 standard51.

Wood heat treatment

Impregnation with zinc chloride

In this study, 120 wood samples with a moisture content of 80% were immersed in a zinc chloride solution at 2% w/w and then treated in a vacuum chamber at 0.005 MPa for 1.0 h. Pressure was then recovered to atmospheric pressure, and vacuuming and the reverse process were performed thrice to impregnate the samples with zinc chloride.

Heat treatment

After impregnation with zinc chloride, the 120 wood samples were divided into four groups, each of which was immersed into a silicone oil bath at room temperature and then treated at 80 °C, 140 °C, 160 °C, and 180 °C with a heating rate of 15 °C/min. The samples were then treated for 2 h when the temperature of the silicone oil reached target temperature.

Dimensional stability of wood

A total of 20 wood samples were used to measure the dimensional stability of wood, and swelling tests were performed in accordance with the GB/T 1931–2009 standard48. The treated and control groups were oven-dried and subsequently stored in a climate-controlled chamber at 20 °C and 65% humidity to reach the EMC. The dimensions were measured before and after conditioning. The swelling coefficients were determined using Eq. (1):

a=lwl0l0×100% 1

where a is the swelling coefficient (radial, tangential, and volumetric), (%); l0 denotes the initial dimension of the samples (mm); and lw represents the dimension after conditioning (mm).

Chemical structure analysis

FTIR was used to analyze the chemical structure of the wood with the use of a standard FTIR spectroscope (Tensor 27; Bruker, Germany). A total of 32 scans were conducted for each sample, recorded in 4000–500 cm−1 range at a resolution of 2 cm−1 in the transmission mode.

Thermogravimetric analysis (TGA)

TGA was used to compare the degradation characteristics of the treated and untreated samples. The thermal stability of each sample (6.56 mg) was determined using a thermogravimetric analyzer (Netzsch STA449F3; Germany) at a heating rate of 10 °C/min and final temperature of 900 °C in a nitrogen environment with a flow rate of 60 mL/min.

Morphological characteristics

The surface shape of the samples was assessed based on morphological by SEM (Hitachi S-3400N II; Tokyo, Japan) to investigate potential variations in physical structure.

Acknowledgements

This paper was supported by the National Key R&D Program of China (2018YFD0600305), the Fundamental Research Funds for the Central Universities of China (2015ZCQ-CL-01), the Hot Tracking Project in Beijing Forestry University-Wood Solar Synergistic Energy-Saving Drying Technology (2017BLRD04), and the China Scholarship Council (CSC) scholarship.

Author Contributions

Z.H. and S.Y. designed the experiments. L.Q., Z.W. and J.Q. carried out the experiments. Z.H. and L.Q. analyzed the data and wrote this manuscript. S.Y. gave valuable suggestions on the experiments and manuscript. Z.H., L.Q., Z.W. and J.Q. modified the manuscript in detail. All authors read and approved the final manuscript.

Competing Interests

The authors declare no competing interests.

Footnotes

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Zhengbin He, Email: hzbcailiao@bjfu.edu.cn.

Songlin Yi, Email: ysonglin@bjfu.edu.cn.

References

  • 1.Popescu CM, Popescu MC. A near infrared spectroscopic study of the structural modifications of lime (Tilia cordata Mill.) wood during hydro-thermal treatment. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2013;115:227–233. doi: 10.1016/j.saa.2013.06.002. [DOI] [PubMed] [Google Scholar]
  • 2.Li T, Cheng DL, Avramidis S, Wålinder MEP, Zhou DG. Response of hygroscopicity to heat treatment and its relation to durability of thermally modified wood. Construction and Building Materials. 2017;144:671–676. doi: 10.1016/j.conbuildmat.2017.03.218. [DOI] [Google Scholar]
  • 3.Liu L, et al. Morphology, composition, and mixing state of primary particles from combustion sources - crop residue, wood, and solid waste. Sci Rep. 2017;7:5047. doi: 10.1038/s41598-017-05357-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Kržišnik D, Lesar B, Thaler N, Humar M. Micro and material climate monitoring in wooden buildings in sub-Alpine environments. Construction and Building Materials. 2018;166:188–195. doi: 10.1016/j.conbuildmat.2018.01.118. [DOI] [Google Scholar]
  • 5.Wang Y, Zhang Z, Fan H, Wang J. Wood carbonization as a protective treatment on resistance to wood destroying fungi. International Biodeterioration & Biodegradation. 2018;129:42–49. doi: 10.1016/j.ibiod.2018.01.003. [DOI] [Google Scholar]
  • 6.Okon KE, Lin F, Chen Y, Huang B. Effect of silicone oil heat treatment on the chemical composition, cellulose crystalline structure and contact angle of Chinese parasol wood. Carbohydrate Polymers. 2017;164:179–185. doi: 10.1016/j.carbpol.2017.01.076. [DOI] [PubMed] [Google Scholar]
  • 7.Skaar, C. Wood water relations. (Springer Verlag, 1988).
  • 8.He, Z. B. & Yi, S. L. Wood drying theory. (China Forestry Press, 2016).
  • 9.Rostand MP, Dubois F, Sauvat N, Fournely E. Strain analysis in dried green wood: Experimentation and modelling approaches. Engineering Fracture Mechanics. 2013;105:182–199. doi: 10.1016/j.engfracmech.2013.04.002. [DOI] [Google Scholar]
  • 10.Croitoru C, et al. Surface properties of thermally treated composite wood panels. Applied Surface Science. 2018;438:114–126. doi: 10.1016/j.apsusc.2017.08.193. [DOI] [Google Scholar]
  • 11.Kocaefe D, Younsi R, Poncsak S, Kocaefe Y. Comparison of different models for the high-temperature heat-treatment of wood. International Journal of Thermal Sciences. 2007;46:707–716. doi: 10.1016/j.ijthermalsci.2006.09.001. [DOI] [Google Scholar]
  • 12.Shen H, Zhang S, Cao J, Jiang J, Wang W. Improving anti-weathering performance of thermally modified wood by TiO2 sol or/and paraffin emulsion. Construction and Building Materials. 2018;169:372–378. doi: 10.1016/j.conbuildmat.2018.03.036. [DOI] [Google Scholar]
  • 13.Wood D, Vailati C, Menges A, Rüggeberg M. Hygroscopically actuated wood elements for weather responsive and self-forming building parts – Facilitating upscaling and complex shape changes. Construction and Building Materials. 2018;165:782–791. doi: 10.1016/j.conbuildmat.2017.12.134. [DOI] [Google Scholar]
  • 14.Association, F. T. Thermowood handbook, https://www.thermowood.fi (2003).
  • 15.Cui W, Zhang NN, Xu M, Cai LP. Combined effects of ZnO particle deposition and heat treatment on dimensional stability and mechanical properties of poplar wood. Sci Rep. 2017;7:9961. doi: 10.1038/s41598-017-10606-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Rowell RM, Ibach RE, McSweeny J, Nilsson T. Understanding decay resistance, dimensional stability and strength changes in heat-treated and acetylated wood. Wood Material Science & Engineering. 2009;4:14–22. doi: 10.1080/17480270903261339. [DOI] [Google Scholar]
  • 17.Wang W, Zhu Y, Cao J, Guo X. Thermal modification of Southern pine combined with wax emulsion preimpregnation: Effect on hydrophobicity and dimensional stability. Holzforschung. 2015;69:405–413. doi: 10.1515/hf-2014-0106. [DOI] [Google Scholar]
  • 18.Sun YC, Cheng J. Hydrolysis of lignocellulosic materials for ethanol production: a review. Bioresour. Technol. 2002;83:1–11. doi: 10.1016/S0960-8524(01)00212-7. [DOI] [PubMed] [Google Scholar]
  • 19.Arends T, Pel L, Smeulders D. Moisture penetration in oak during sinusoidal humidity fluctuations studied by NMR. Construction and Building Materials. 2018;166:196–203. doi: 10.1016/j.conbuildmat.2018.01.133. [DOI] [Google Scholar]
  • 20.Rowell, R. M. Handbook of wood chemistry and wood composites. (CRC press, 2012).
  • 21.Yang, S. H. Plant fiber chemistry. (China Light Industry Press, 2010).
  • 22.Gatenholm, P. Hemicelluloses: Science and Technology. (American Chemical Society, 2003).
  • 23.Moretto, H. H., Schulze, M. & Wagner, G. Ullmann’s encyclopedia of industrial chemistry. (Wiley-VCH publishers, 2005).
  • 24.Mitani A, Barboutis I. Changes caused by heat treatment in colour and dimensional stability of beech (Fagus sylvatica L.) wood. Drvna Ind. 2014;65:225–232. doi: 10.5552/drind.2014.1250. [DOI] [Google Scholar]
  • 25.Petr P, Aleš D. Moisture absorption and dimensional stability of poplar wood impregnated with sucrose and sodium chloride. Maderas. Ciencia y tecnología. 2014;16:299–311. [Google Scholar]
  • 26.Rouco MCA, Muñoz GR. Influence of blue stain on density and dimensional stability of Pinus radiata timber from northern Galicia (Spain) Holzforschung. 2015;69:97–102. doi: 10.1515/hf-2014-0014. [DOI] [Google Scholar]
  • 27.Jiang J, Li J, Gao Q. Effect of flame retardant treatment on dimensional stability and thermal degradation of wood. Construction and Building Materials. 2015;75:74–81. doi: 10.1016/j.conbuildmat.2014.10.037. [DOI] [Google Scholar]
  • 28.Guo J, Song K, Salmén L, Yin Y. Changes of wood cell walls in response to hygro-mechanical steam treatment. Carbohydrate Polymers. 2015;115:207–214. doi: 10.1016/j.carbpol.2014.08.040. [DOI] [PubMed] [Google Scholar]
  • 29.Chen W, et al. Individualization of cellulose nanofibers from wood using high-intensity ultrasonication combined with chemical pretreatments. Carbohydrate Polymers. 2011;83:1804–1811. doi: 10.1016/j.carbpol.2010.10.040. [DOI] [Google Scholar]
  • 30.He Z, et al. Influence of ultrasound pretreatment on wood physiochemical structure. Ultrasonics Sonochemistry. 2017;34:136–141. doi: 10.1016/j.ultsonch.2016.05.035. [DOI] [PubMed] [Google Scholar]
  • 31.Naron DR, Collard FX, Tyhoda L, Görgens JF. Characterisation of lignins from different sources by appropriate analytical methods: Introducing thermogravimetric analysis-thermal desorption-gas chromatography–mass spectroscopy. Industrial Crops and Products. 2017;101:61–74. doi: 10.1016/j.indcrop.2017.02.041. [DOI] [Google Scholar]
  • 32.Basso MC, et al. MALDI-TOF, 13C NMR and FTIR analysis of the cross-linking reaction of condensed tannins by triethyl phosphate. Industrial Crops and Products. 2017;95:621–631. doi: 10.1016/j.indcrop.2016.11.031. [DOI] [Google Scholar]
  • 33.Wang HW, et al. New Insight on Promoted thermostability of poplar wood modified by MnFe2O4 nanoparticles through the pyrolysis behaviors and kinetic study. Sci Rep. 2017;7:1418. doi: 10.1038/s41598-017-01597-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Popescu MC, Froidevaux J, Navi P, Popescu CM. Structural modifications of Tilia cordata wood during heat treatment investigated by FT-IR and 2D IR correlation spectroscopy. Journal of Molecular Structure. 2013;1033:176–186. doi: 10.1016/j.molstruc.2012.08.035. [DOI] [Google Scholar]
  • 35.Liu, Y. X. & Zhao, G. J. Wood science. (China Forestry Press, 2012).
  • 36.Nishimura H, Kamiya A, Nagata T, Katahira M, Watanabe T. Direct evidence for alpha ether linkage between lignin and carbohydrates in wood cell walls. Sci Rep. 2018;8:6538. doi: 10.1038/s41598-018-24328-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Ruhlandt A, Toperwien M, Krenkel M, Mokso R, Salditt T. Four dimensional material movies: High speed phase-contrast tomography by backprojection along dynamically curved paths. Sci Rep. 2017;7:6487. doi: 10.1038/s41598-017-06333-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Esteves B, Velez Marques A, Domingos I, Pereira H. Chemical changes of heat treated pine and eucalypt wood monitored by FTIR. Maderas. Ciencia y tecnología. 2013;15:245–258. [Google Scholar]
  • 39.Çetinkol ÖP, et al. Understanding the impact of ionic liquid pretreatment on eucalyptus. Biofuels. 2010;1:33–46. doi: 10.4155/bfs.09.5. [DOI] [Google Scholar]
  • 40.Kumar R, Mago G, Balan V, Wyman CE. Physical and chemical characterizations of corn stover and poplar solids resulting from leading pretreatment technologies. Bioresource Technology. 2009;100:3948–3962. doi: 10.1016/j.biortech.2009.01.075. [DOI] [PubMed] [Google Scholar]
  • 41.Huang X, Kocaefe D, Kocaefe Y, Boluk Y, Pichette A. A spectrocolorimetric and chemical study on color modification of heat-treated wood during artificial weathering. Applied Surface Science. 2012;258:5360–5369. doi: 10.1016/j.apsusc.2012.02.005. [DOI] [Google Scholar]
  • 42.Tjeerdsma BF, Militz H. Chemical changes in hydrothermal treated wood: FTIR analysis of combined hydrothermal and dry heat-treated wood. Holz als Roh- und Werkstoff. 2005;63:102–111. doi: 10.1007/s00107-004-0532-8. [DOI] [Google Scholar]
  • 43.Gu Y, Shou G, Zhang W, Zhao D. Application of near infrared spectroscopy for discrimination of similar rare woods in the Chinese market. Journal of Near Infrared Spectroscopy. 2014;22:423. doi: 10.1255/jnirs.1136. [DOI] [Google Scholar]
  • 44.Selamoglu N, Mucha JA, Ibbotson DE, Flamm DL. Silicon oxide deposition from tetraethoxysilane in a radio frequency downstream reactor: Mechanisms and step coverage. Journal of Vacuum Science & Technology B Microelectronics & Nanometer Structures. 1989;7:1345–1351. doi: 10.1116/1.584536. [DOI] [Google Scholar]
  • 45.Esteves BM, Pereira HM. Wood modification by heat treatment: A review. Bioresources. 2009;4:370–404. [Google Scholar]
  • 46.Cademartori PHG, dos Santos PSB, Serrano L, Labidi J, Gatto DA. Effect of thermal treatment on physicochemical properties of Gympie messmate wood. Industrial Crops and Products. 2013;45:360–366. doi: 10.1016/j.indcrop.2012.12.048. [DOI] [Google Scholar]
  • 47.Lin BJ, et al. Thermal degradation and compositional changes of wood treated in a semi-industrial scale reactor in vacuum. Journal of Analytical and Applied Pyrolysis. 2018;130:8–18. doi: 10.1016/j.jaap.2018.02.005. [DOI] [Google Scholar]
  • 48.Kesik HI, Korkut S, Hiziroglu S, Sevik H. An evaluation of properties of four heat treated wood species. Industrial Crops and Products. 2014;60:60–65. doi: 10.1016/j.indcrop.2014.06.001. [DOI] [Google Scholar]
  • 49.Kluska J, Ronewicz K, Kardaś D. Thermal characteristics of single wood particle pyrolysis using particle image velocimetry. Int J Therm Sci. 2019;135:276–284. doi: 10.1016/j.ijthermalsci.2018.09.020. [DOI] [Google Scholar]
  • 50.Giuntoli J, et al. Quantitative and kinetic TG-FTIR study of biomass residue pyrolysis: dry distiller’s grains with solubles (DDGS) and chicken manure. Journal of Analytical & Applied Pyrolysis. 2009;85:301–312. doi: 10.1016/j.jaap.2008.12.007. [DOI] [Google Scholar]
  • 51.Zhao, R. J. et al. Wood moisture content measuring method. Wood-determination of moisture content for physical and mechanical test, MOD, CN-GB, GB/T 1931–2009 (2009).

Articles from Scientific Reports are provided here courtesy of Nature Publishing Group

RESOURCES