<p>Thermal modification of <i>Salix tetrasperma</i> wood was conducted at temperatures ranging from 60 to 200&#xa0;°C for durations of 2, 4, and 6&#xa0;h to evaluate changes in its chemical and mechanical properties. The treatment induced notable alterations in extractives and structural components. Peak values for cold-water (7.44%) and hot-water (11.56%) soluble extractives were recorded at 140&#xa0;°C and 120&#xa0;°C, respectively, while the lowest values (5.17% and 8.76%) occurred at 200&#xa0;°C. Alcohol-benzene extractives and lignin content increased with temperature, reaching maxima of 13.61% and 24.77% at 200&#xa0;°C, compared to 9.03% and 16.49% in the untreated control. Conversely, holocellulose content showed a declining trend with heat, dropping from 79.18% in the control to 70.89% at 200&#xa0;°C. Mechanically, tensile strength peaked at 0.059&#xa0;kN/mm<sup>2</sup> at 140&#xa0;°C and declined to 0.040&#xa0;kN/mm<sup>2</sup> at 200&#xa0;°C. Bending strength was highest in the control (0.010&#xa0;kN/mm<sup>2</sup>) and lowest (0.007&#xa0;kN/mm<sup>2</sup>) at 180&#xa0;°C and 200&#xa0;°C. Compression strength parallel to grain reached its maximum at 160&#xa0;°C (0.037&#xa0;kN/mm<sup>2</sup>), whereas perpendicular compression was highest in the control (0.031&#xa0;kN/mm<sup>2</sup>). Minimum compression values were noted at 200&#xa0;°C. These results underscore the potential of thermal modification to strategically tailor the physico-chemical properties of <i>Salix tetrasperma</i> wood, improving its dimensional stability, durability, and overall performance for industrial and structural applications.</p>

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Enhanced strength and chemical stability of Salix tetrasperma wood through thermal modification

  • Sufiya Shabir,
  • Bhupender Dutt,
  • Rajneesh Kumar,
  • Dinesh Sharma,
  • Irtizah Mushtaq

摘要

Thermal modification of Salix tetrasperma wood was conducted at temperatures ranging from 60 to 200 °C for durations of 2, 4, and 6 h to evaluate changes in its chemical and mechanical properties. The treatment induced notable alterations in extractives and structural components. Peak values for cold-water (7.44%) and hot-water (11.56%) soluble extractives were recorded at 140 °C and 120 °C, respectively, while the lowest values (5.17% and 8.76%) occurred at 200 °C. Alcohol-benzene extractives and lignin content increased with temperature, reaching maxima of 13.61% and 24.77% at 200 °C, compared to 9.03% and 16.49% in the untreated control. Conversely, holocellulose content showed a declining trend with heat, dropping from 79.18% in the control to 70.89% at 200 °C. Mechanically, tensile strength peaked at 0.059 kN/mm2 at 140 °C and declined to 0.040 kN/mm2 at 200 °C. Bending strength was highest in the control (0.010 kN/mm2) and lowest (0.007 kN/mm2) at 180 °C and 200 °C. Compression strength parallel to grain reached its maximum at 160 °C (0.037 kN/mm2), whereas perpendicular compression was highest in the control (0.031 kN/mm2). Minimum compression values were noted at 200 °C. These results underscore the potential of thermal modification to strategically tailor the physico-chemical properties of Salix tetrasperma wood, improving its dimensional stability, durability, and overall performance for industrial and structural applications.