Table 3.
Chemical Treatment | Name of the Fiber | Chemical Reagents Used | Method | Structure Improvement | Application | References |
---|---|---|---|---|---|---|
Alkaline | Hemp | NaOH | Treated fiber with NaOH at 20 °C for 48 h and washed using distilled water and acetic acid to neutralize the excess of NaOH. | Better fiber-matrix adhesion led to an increase in interfacial energy and thus enhancing the thermal and mechanical properties of the composites | Polymer reinforcements | [69,94] |
Jute, | [69,94] | |||||
Sisal | [69,94] | |||||
Kapok | [69,94] | |||||
Kenaf | NaOH | Treated kenaf fiber with 6% of NaOH solution for 24 h. Then, kenaf fibers were rinsed and immersed into a solution that contained distilled water and 1% acetic acid to neutralize the remaining NaOH. After washing, the kenaf short fibers were dried in an oven for 24 h. | Better physical, morphological, and mechanical properties because of the compatibility of kenaf with polypropylene composites | Automotive | [69,95] | |
Napier grass | NaOH | Napier grass fibers were treated with 2% and 5% of NaOH at room temperature for 30 min. The fibers were washed with tap water and distilled water many times and dried at 100 °C. | enhanced tensile properties | Reinforcement for composites | [69,96] | |
Carica papaya | NaOH | Carica papaya fibers were treated with 5% NaOH for 60 at 25 °C. Then, the fibers were washed many times using HCI solution and deionized water. Then, the fibers were dried at 100 °C in an oven for moisture removal. | Better performance in mechanical properties, thermal stability, and good interfacial bonding between cellulosic fiber and the matrix. | Light weight industrial | [69,97] | |
Saline | Sugar palm | Saline | Sugar palm fibers were immersed with 2% saline for 3 h. Then, the fibers were immersed in a mixture of methanol–water (90/10 w/w) for 3 h hydrolysis under agitation. The fibers were thoroughly rinsed with distilled water and then oven-dried at 60 °C for 72 h. | Improve properties of sugar palm fiber and enhance fiber-matrix bonding sugar palm fiber–thermoplastic polyurethane composites. | Industrial application | [69,98] |
Acetylation | Dombeya buettnerri | Acetyl anhydride | The fibers were soaked with 2% up to 6% of acetyl anhydride for 3 h at room temperature. Then, the fibers were washed with tap water and repeatedly rinsed with distilled water until all excess acid had been removed. Then, the fibers were dried for 2 h at 105 °C. | Enhanced surface morphology and mechanical properties. | Engineering materials applications | [69,99] |
Combretum racemosum | ||||||
Banana (Musa parasidica) | ||||||
Alkaline hydrogen peroxide | Citrus fibers | Hydrogen peroxide | The citrus fibers were immersed in hydrogen peroxide for 4 h at 60 °C. Then, the fibers were adjusted to pH 6 with acid hydrochloric (1.0 M) at 25 °C. The mixture was centrifuged at 6000× g for 15 min; the residue was then collected and washed in pure ethanol and dried via oven at 60 °C for 7 h. | High water holding and swelling capacities could be used as emulsifiers in juice and jam. It also has better thermal stability and viscosity properties. | Application in food industry | [100] |
Benzoylation | Sisal fiber, |
Benzoyl chloride | Increase strength of composite and thermal stability, decrease water absorption | Industrial application | [101] | |
Sugar palm | Soaked with a mixture solution of 1% NaOH and 5 mL of C7H5ClO with respective soaking times. Then, fibers were washed and soaked in absolute ethanol for 1 h, washed again until pH became neutral, and dried overnight at 50 °C. | Improvement in tensile strength | Furniture and components inside vehicle | [102] | ||
Acrylation and Acrylonitrile Grafting | Flax-fiber | Acrylic acid solution | Flax fibers were immersed in NaOH solution for 0.5 h and then soaked in acrylic acid solution at 50 °C for 1 h, washed with distilled water, and dried. | Improving the physical and mechanical properties | Plastic, automobile, and packaging industries | [103] |
Maleated Coupling Gents | Jute fiber | Maleic anhydride- polypropylene (MAPP) | The fibers were immersed in MAPP solution in toluene at 100 °C. | Increase in mechanical strength | Industrial applications with offer cost-effective and value-added composite material | [104] |
Permanganate Treatment | Sisal fiber | Potassium permanganate KmnO4 |
Sisal fibers were soaked carefully in a solution of KmnO4/acetone with a concentration of 0.02% for 3 min. After that, the fibers were taken out, washed many times with distilled water, and dried | Improve fiber strength and fiber-matrix adhesion | Industrial application | [101] |
Peroxide Treatment | Sisal fibers | Benzoyl peroxide from acetone solution | Fibers were coated with benzoyl peroxide from acetone solution after alkali pre-treatment. A saturated solution of the peroxide in acetone was used. Fibers were then dried. | Enhance in tensile properties | Substitute the wood | [105] |
Isocyanate Treatment |
Pineapple leaf fiber | toluene solution containing poly(methylene)-poly(phenyl)isocyanate |
Fibers were dipped in toluene solution containing PMPPIC (5 wt% of fiber) for half an hour at 50 °C. The fibers were then decanted and dried in an air oven at 70 °C for 2 h. Later these were mixed with polyethylene using toluene as the solvent containing PMPPIC (6 wt% of fiber) at a temperature of 120 °C. | Enhance mechanical properties | Structural and non-structural application | [106] |
Ionic Liquid | Chitin fiber | 1-ethyl-3-methylimidazolium acetate | Chitin derived from shrimp shell biomass that has been thermally pretreated, pressed, and ground. Chitin was isolated using a microwave-assisted dissolution of [C2mim][OAc], followed by water coagulation, washing, and oven drying. | Improve the mechanical strength of chitin fibers | High-performance chitinous sorbents for applications such as metal recovery from seawater |
[107] |
Thermal decomposition kinetic | Wood, bamboo, agricultural residue, and bast fibers |
Phosphonium ionic liquids | All raw materials were washed with water to remove impurities before being dried in an oven at 75 degrees Celsius for 12 h. The dried materials were then ground and screened using a Wiley mill. For testing, samples with particle sizes ranging from 20 to 28 meshes were collected. Various degradation models, including the Kissinger, Friedman, Flynn–Wall–Ozawa, and modified Coats–Redfern methods to determine the apparent activation energy of these fibers. |
Improve the thermal stability of the fibers | Renewable biomass energy/natural fuels and forest fire propagation control, practical engineering applications. | [108] |