Recent Progresses in Eco-Friendly Fabrication and Applications of Sustainable Aerogels from Various Waste Materials

Abstract

Tons of waste from residential, commercial and manufacturing activities are generated due to the growing population, urbanization and economic development, prompting the need for sustainable measures. Numerous ways of converting waste to aerogels, a novel class of ultra-light and ultra-porous materials, have been researched to tackle the issues of waste. This review provides an overview of the status of aerogels made from agricultural waste, municipal solid, and industrial waste focusing on the fabrication, properties, and applications of such aerogels. The review first introduced common methods to synthesize the aerogels from waste, including dispersion and drying techniques. Following that, numerous works related to aerogels from waste are summarized and compared, mainly focusing on the sustainability aspect of the processes involved and their contributions for environmental applications such as thermal insulation and oil absorption. Next, advantages, and disadvantages of the current approaches are analyzed. Finally, some prospective waste aerogels and its applications are proposed.

Graphic Abstract

Statement of Novelty

This review is undertaken to summarize, compare and evaluate several approaches to utilize different types of waste for the preparation of aerogels in terms of sustainability and engineering applications. Compared to previous works, this review focuses on the status and environmental impacts of wastes, and efforts from researchers worldwide to convert these wastes into aerogels for diverse applications through ecofriendly methods. Environmental aspects including impacts of synthesis procedures and solutions for environmental problems such as heat insulation and oil spill cleaning are highlighted. Our perspectives on the advantages and disadvantages of the mentioned approaches are presented in detail. Furthermore, we propose the prospects of the development of aerogels from waste as suggestions for future works. Hopefully, this review can inspire more studies to create high value materials from waste by ecofriendly fabrication methods to partly combat the increasing waste generation and offer solutions for engineering problems.

Introduction

Driven by a rapid growing population, urbanization and economic development, waste generation is significantly increasing all over the world. Primary waste sources include residential households, municipal services, treatment plants, and industrial and agricultural processes [1]. Municipal solid waste refers to waste generated in a community from households, offices, restaurants, schools, and other institutions. According to a report of the World Bank Group in 2018 [2], approximately 0.74 kg of municipal solid waste is produced per capita per day. This figure varies widely by country, ranging from 0.11 to 4.54 kg per capita per day. Waste generation is related to income levels. Despite only accounting for 16% of the world’s population, high-income nations produce around 34 percent, or 683 million tons annually, of the world’s waste. The global municipal solid waste is around 2.01 billion tons in 2016 and is projected to reach 3.40 billion tons by 2050.

However, municipal solid waste is only one of the waste sources that the world is facing. Figure 1 shows the amount of waste generated per capita per day worldwide by source. Industrial waste generation is much higher than that of municipal solid waste, of approximately 17.2 times higher. Statistics show that the industrial waste generation grows significantly with increase in income level. In high-income nations, the average amount of industrial waste is 42.62 kg/capita/day, while this figure is only 0.36 kg/capita/day in lower-middle income nations [2]. Therefore, a rapid industrialization seen in recent decades can exacerbate environmental problems without a proper waste management strategy. The number for agricultural waste generation is 3.35 kg/capita/day and can be higher in large agricultural producing countries. Construction and demolition waste accounts for 1.68 kg/capita/day, mainly emerged from demolition and rehabilitation of existing sites [3]. Although only making up a small fraction, hazardous, medical and electronic waste (e-waste) can severely damage the environment and human health if disposed improperly. Especially, the generation of e-waste is significantly increasing with the rapid development of technology that accompanies with modern urbanization.

Fig. 1.

Global average waste generation by source [2]

Due to the negative impacts of waste on the environment and community health, governments have put forth many efforts into waste management. Solid waste management accounts for more than 10% of municipal budgets in middle-income countries, and 4% in high-income countries [2]. According to the waste management hierarchy, waste should be managed in accordance with the following order of preference: prevention, reuse, recycling, treatment and disposal [4]. Despite not being the first priority, recycling offers numerous benefits such as saving energy, conserving natural resources, protecting the environment, and reducing waste amount to landfills and incinerators. Recycling is integral in converting a linear economy into circular economy to meet the sustainable development goals. Items such as papers, plastics, food, glass, metals, textiles and tires are recyclable. In 2019, Singapore recycled 99% of metal, 98% of slag and 94% of tires [5]. Moreover, waste can be recycled to high value materials such as activated carbon [6], graphene [7], building materials [8], membrane [9], and metals [10], adding more economic values.

Aerogels, a class of ultra-porous solid materials, are well-known for their low density (0.0011–0.5 g/cm³), high porosity (90–99%) and large surface area (10–2000 m²/g) [11]. The first aerogels were reported by Kistler in 1931 and followed by various aerogels from different precursors such as silica, cellulose, and organic compounds. The most commercially popular aerogels are silica aerogels, mainly used for thermal insulation. However, the main restriction of the wide use of aerogels is their high cost. One m² of a commercial aerogel for thermal insulation with a thermal conductivity of 15 mW/mK costs 280 USD, while it costs only 15 USD per m² for a conventional insulator with a thermal conductivity of 32 mW/mK and the same overall heat transfer coefficient [12]. A monolithic cylinder carbon aerogel for catalyst support with the size of 1 cm × 0.4 cm (diameter × height) costs 80 USD [13], while the same amount of silica gel with the same surface area costs approximately 3 USD [14]. One reason for this high cost is expensive starting materials, which limits the diversity of commercial aerogels. To obtain silica aerogels via supercritical drying, the precursor costs 95.4% and 42% of the production cost, when tetramethyl orthosilicate and sodium silicate are used, respectively. For carbon aerogels, the organic precursors cost makes up from 63% (phenolic-furfural) to 80% (resorcinol-formaldehyde) of the production cost [15]. Therefore, it is necessary to find low-cost precursors to reduce the cost of aerogel production.

Inspired by recycling, many approaches to aerogels from waste have been reported. These are advanced solutions for reducing the cost of starting materials and the amount of waste to landfills and incinerators. Researchers have mainly utilized municipal solid, agricultural and industrial wastes as precursors of aerogels due to their abundance. Many novel applications of aerogels besides thermal insulation have been discovered such as personal care products, medical devices, oil and organic solvents sorption, filtration, sound insulation, energy absorption, energy storage, bioelectronics, water treatment and catalyst, offering sustainable solutions for environmental and energy problems. Previous reviews mainly focused on a specific types of aerogel such as silica aerogel [16], cellulose aerogel [17], and carbon aerogel, [18] or on certain application such as acoustic insulation [19], photocatalyst [20] and biomedical applications [21]. However, taking advantage of wastes such as municipal solids, agricultural and industrial by-products to create high-value engineering aerogels has been a general trend in the world. This review will focus on analyzing the outstanding properties and applications of recycled aerogels from different wastes.

Fabrication of Aerogels from Waste

Common preparation methods of aerogels from waste are illustrated in Fig. 2. Generally, the fabrication of aerogels from waste is similar to that of conventional aerogels. The most well-known method for the synthesis of aerogels is sol-gel process, in which the precursor forms a colloid by hydrolysis and condensation reactions, and then turns into a gel by the formation of crosslinks. The resulting gel can be aged to strengthen the crosslinked network, and then solvents are replaced by air to obtain the aerogels. This is the approach using by Kistler et al. [22] for the synthesis of the first aerogel. In this work, the silicate precursor was hydrolyzed and condensed in an acidic condition. Since the evaporation of water would cause cracks and shrinkage to the gel due to the capillary force, solvent exchange was carried out to replace water by solvents with low critical point such as alcohol and propane. These solvents were then removed by drying over their critical point to avoid the liquid–vapor interface and achieve the aerogel with a reserved polymer network.

Fig. 2.

Schematic diagram of fabrication of aerogels using waste as raw materials

Gradually, more advanced gel drying techniques are introduced to modify the direct supercritical drying of Kistler, including supercritical CO₂ (scCO₂) drying, ambient pressure drying, and freeze-drying. The scCO₂ drying utilize the high solubility of scCO₂ to extract the solvent with no liquid–vapor interface, reserving the highly porous and textural structure of the liquid gel. One significant advantage of ScCO₂ is its low-temperature critical points (304 K, 7.4 MPa) compared to other solvents such as ethanol (517 K, 6.4 MPa) and hexane (507 K, 3.03 MPa), thus the scCO₂ is less energy-intensive [23]. In the ambient pressure drying, the surface of silica aerogel is hydrophobically modified to eliminate terminal silanol group (Si-

OH), and the solvent is exchanged into a low-surface-energy solvent such as hexane to minimize the shrinkage. Ambient pressure drying allows to considerably reduce the equipment and energy cost. However, scCO₂ drying and ambient pressure drying usually requires amounts of organic volatile solvents for solvent exchange steps, making these two techniques non-eco-friendly and time-consuming. This disadvantage can be avoided in the freeze-drying technique, in which the ice crystals in the frozen hydrogel are removed by sublimation at low pressure. Freeze-drying does not require solvent modifications; thus, no waste chemicals are generated. It is noted that generally the resultant gels that forms out of ambient pressure drying is termed xerogels while gels that are formed out of freeze-drying is termed cryogels [24]. However, in this review, the term aerogel will be used throughout as an indication to the porous material obtained from each of the gel drying method.

Compared to pure aerogel precursors, the composition of waste is complex and varied by sources. For example, cellulose from leaves and trees are usually found within a lignin shell, while cellulose from paper waste can be impure by sizing materials, fillers and pigments. The composition of the cellulose fibers in a specific species, such as pineapple, also depends on the maturity, the location and the fibers extraction conditions [25]. Therefore, pretreatment such as washing, grinding or thermal treating is usually conducted to remove the impurities and extract the desired components. Organic waste can be calcinated to serve as a source of carbon. Sometimes, solvent extraction is performed to obtain precursors such as sodium silicate from fly ash and rice husk ash.

After pretreatment, the precursor is dissolved into appropriate solvents to obtain a sol or dispersed with the support of binders to form a suspension. The former approach is the sol-gel process, which is mostly applicable for sodium silicate and metal powders. Polymeric materials are generally difficult to be dissolved in common solvents. For example, dissolving of cellulose requires the use of concentrated NaOH/urea solution or ionic liquid. In these cases, the latter approach using polymers as binders is more favorable. When dispersing solid precursors in a polymer solution, it is important to obtain a stable suspension. According to Stokes’ law, the settling velocity of the particle can be calculated by:

$$\mathrm{\omega }=\frac{\left({\mathrm{\rho }}_{\mathrm{p}},-,{\mathrm{\rho }}_{\mathrm{f}}\right){\mathrm{gd}}^2}{18\mathrm{\mu }},$$ 1

where $\mathrm{\omega }$ is the settling velocity; ${\mathrm{\rho }}_{\mathrm{p}}$, ${\mathrm{\rho }}_{\mathrm{f}}$ are the density of particle and fluid, respectively; d is the diameter of the particle; $\mathrm{\mu }$ is the velocity and g is the gravitational acceleration. To maintain a stable dispersion, the settling velocity should be kept minimum to prevent sedimentation. This is usually done by either increasing the viscosity of the polymer solution or reducing the size of raw materials. Anti-settling agents such as carboxymethyl cellulose (CMC) can be employed to facilitate this step. Subsequently, the sol or the suspension is transformed into a gel by the formation of crosslinks between polymer chains. The nature of the crosslinks can be chemical (mostly covalent bond), or physical (mostly hydrogen bond). Some hydrophilic polymers can be self-assembled to form a gel at appropriate temperature. Their self-crosslinking ability is due to the presence of hydrophilic functional groups such as hydroxyl or carboxylic acid, which form hydrogen bonds between polymer chains. To further strengthen the 3-dimension scaffold, chemical crosslinkers can be introduced, such as epichlohydrin [26] or Kymene [27] in the gelation of cellulose hydrogel.

The gel is then converted into the corresponding aerogels using the mentioned drying methods. It should be noted that supercritical drying and ambient pressure drying are accompanied by solvent exchange steps, and freeze-drying technique requires the gel to be frozen. Post-treatment such as hydrophobic coating, impregnation or carbonization can be conducted on the obtained aerogel to better serve for certain applications.

Aerogels from Municipal Solid Waste

Figure 3 describes main components of municipal solid waste, including food, green, paper, plastic, rags, metal, glass and other wastes. Food waste and green waste are dominant types of municipal solid waste, which accounts for 44% of the total. However, the utilization of food waste in advanced materials is limited due to its complex and unstable composition. In this review, various types of food waste such as coffee grounds, okara, sugarcane bagasse and banana peels are classified as agricultural waste and discussed their utilization to make aerogels in Sect. 4. Preparation, properties and applications of some aerogels from municipal solid waste are tabulated in Table 1.

Fig. 3.

Composition of municipal solid waste (%) [2]

Table 1.

Preparation and application of aerogels from municipal solid waste

No.	Waste materials	Type of aerogels	Fabrication process	Properties/applicationsa	References
1	Paper	Cellulose	Dispersion Gelation Solvent exchange Freeze-drying Silanization	Oil absorption: 24 g crude oil/g	[28]
2	Paper	Cellulose	Dispersion Gelation Solvent exchange Freeze-drying	Water absorption: 19 g/g Thermal insulation: 29–32 mW/mK	[29]
3	Paper	Cellulose	Dispersion Freeze-drying Crosslinking Silanization	Oil absorption: 95 g motor oil/g Thermal insulator	[27, 30]
4	Paper	Carbon	Dispersion Freeze-drying Pyrolysis	Oil and solvent absorption: 188 g pump oil/g; 70 g tetrachloromethane/g Emulsion separation Sensors and pressure-sensitive electronics	[31, 32]
5	Paper and cardboard	Cellulose	Mixing with flame retardant agent Dispersion Freeze-drying	Fire retardant	[33]
6	Cardboard	Cellulose/sodium alginate	Dispersion Crosslinking Freeze-drying Stearic acid modification	Oil and solvent absorption: 47 g tetrachloroethane/g; 34 g kerosene/g	[34]
7	Office paper	Cellulose/chitosan	Dispersion Freeze-drying	Metal ion adsorption:156.3 mg Cu2+/g	[35]
8	Newspaper	Cellulose	Ink and glue removal Dispersion Freeze-drying	Dye absorption	[36]
9	Newspaper	Cellulose	Ink and glue removal Dispersion Freeze-drying Silanization	Oil and solvent absorption: 44 g chloroform/g; 33 g kerosene/g Lampblack filtration	[37]
10	Plastic bottle	Polyethylene-terephthalate	Dispersion Freeze-drying	Thermal insulation: 35–38 mW/mK Acoustic insulation	[38]
11	Plastic bottle	Polyethylene-terephthalate	Dispersion Freeze-drying Silanization	Oil absorption: 79.4 g oil/g	[39]
12	Plastic bottle	Polyethylene-terephthalate/Silica	Dispersion Gelation Solvent exchange Silylation Ambient pressure drying	Thermal insulation: 37–47 mW/mK	[40]
13	Rubber tire	Rubber	Dispersion Freeze-drying Silanization	Thermal insulation: 35–49 mW/mK Acoustic insulation NRC = 0.41–0.56 Oil absorption: 19.3–25 g oil/g	[41–43]
14	Cotton fabrics	Cellulose	Dispersion Freeze-drying Crosslinking	Stopping liquid leakage	[44]
15	Cotton fabrics	Cellulose/Mg(OH)2	Dispersion Freeze-drying Crosslinking	Thermal insulation: 56–81 mW/mK	[45]
16	Cotton fabrics	Carbon/carbon oxide	Dispersion Dehydrating Drying Pyrolysis Oxidizing	Pollutant absorption: 1519 mg methylene blue/g Metal ion adsorption: 111.1 mg Pb2+/g	[46]
17	Denim	Cellulose	Dissolving in ionic liquid Regeneration Drying	Not mentioned	[47]
18	Cigarette filter	Carbon	Graphene oxide coating Ambient pressure drying Carbonization Polypyrrole coating Ambient pressure drying	Electromagnetic wave absorption	[48]
19	Bamboo chopstick	Carbon	Carbonization Dispersion Freeze-drying Pyrolysis	Oil and solvent adsorption: 129 g pump oil/g; 80 g chloroform/g	[49]
20	Aluminum foil	Aluminum hydroxide	Dispersion Precipitation Gelation Freeze-drying	Thermal insulation: 28–32 mW/mK	[50]

^aSpecifications to illustrate for applications: absorption capacity (for absorption), adsorption capacity (for adsorption), thermal conductivity (for thermal insulation)

Aerogel from Paper Waste

Paper and cardboard are the second most abundant types of municipal solid waste, making up 17% of the total. Approximately 419.7 million tons of paper and cardboard were produced in 2017, mainly for packaging and graphic usages [51]. Waste papers consist of approximately 40–80% of cellulose, 5–15% of hemicellulose and amounts of lignin and proteins [52]. In 2013, Nguyen et al. [28] introduced cellulose aerogels from paper waste. With an oil absorption capacity of 24 g/g and its biodegradability, the cellulose aerogel from used paper is a potential candidate for oil spill cleaning. However, the aerogel takes up to 7 days to prepare with many stages, including dispersion of the fibers in NaOH and urea, freeze gelation, coagulation in ethanol, solvent exchange to water, freeze-drying and hydrophobic coating. In 2014, Feng et al. [27] simplified the preparation of cellulose aerogels from paper by employing Kymene as a crosslinker. Compared to the NaOH/urea method, this new approach reduces the synthesis duration from 7 days to 3 days and eliminates toxic chemicals in the procedure. Moreover, the resulting aerogels have an oil absorption capacity of 95 g/g, 4 times higher than the previously reported cellulose aerogels [28]. The oil absorption of the fabricated aerogels exhibits pH insensitivity under different simulated conditions with a mixture of oil and water at pH 3, 5, 7, and 9. This is because the high porosity of the aerogels and oil viscosity are independent of the environmental pH values. It is witnessed that the aerogels absorb oil quickly in only 7 min when they are placed on the top of the oil-contaminated seawater (Fig. 4).

Fig. 4.

Oil absorption performance of paper aerogel in artificial seawater environment.

Reprinted from Feng et al. [30], Copyright (2015) with permission from Elsevier

Different types of paper are utilized in the fabrication of cellulose aerogels such as newspapers [36, 37], cardboards [33] and office papers [35] with various applications including fire retardant, oil and solvent absorption and pollutant removal. Besides, paper can replace toxic organic precursors to prepare carbon aerogels. Li et al. [32] reported elastically compressible and conductive carbon aerogels from waste paper using “oxidization–oven drying–carbonization” method, which is superior to the freeze-drying approach. In this work, waste paper pulp is oxidized by sodium chlorite, filtrated and oven dried to form the sodium chlorite/waste paper aerogels and pyrolyzed at 1000 °C to form carbon aerogels. These works show high potential of paper and cardboard waste for being used as a source of carbon and cellulose.

Aerogel from Plastic Waste

Plastic waste accounts for 12% of the total municipal solid waste. Over 300 million tons of plastic are produced annually, in which at least 8 million tons end up in water and deep-sea sediments [53]. It is not surprising that single-use plastics are one of the most common items found on beaches all over the world. Plastic production is expected to reach 8.3 billion tons by 2050 [54]. During the COVID-19 crisis in the first half of 2020, a growing reliance on food delivery services created a jump of plastic waste from 5,500 tons to 6,300 tons per day in Thailand [55]. However, recycling rates of plastic are relatively low, at around 30% in developed countries and close to 0% in developing countries [54]. Recycling plastic waste by remelting and reforming, downgrades the quality of plastics due to thermal degradation of polymer chains and thus low-grade and low-value secondary plastics are obtained. In 2018, recycled polyethylene terephthalate (rPET) aerogels from plastic bottles were introduced. The aerogel network is formed by hydrogen bonds between rPET fiber and poly(vinyl alcohol) (PVA), and acetal bonds between rPET fiber and glutaraldehyde [38]. The rPET aerogels show a hydrophobicity with water contact angles of 120.7°–149.8°, and a high elasticity with a low compressive Young’s modulus (1.16–2.87 kPa). They have a low thermal conductivity (35–38 mW/mK) and a high acoustic absorption with a noise reduction coefficient (NRC) of 0.45, higher than that of the commercial acoustic foam absorber with the same thickness. After coating with methyltrimethoxysilane (MTMS), the rPET aerogels can then be used as an oil and organic solvent absorber [39] (Fig. 5). The MTMS-coated rPET aerogel with 1.0 wt% rPET fiber and 0.10 wt% PVA has a high oil absorption capacity of 80 times of its weight and takes around 10 s to reach its maximum absorption capacity, demonstrating its potential use in oil spill cleaning applications. After being used for oil spill cleaning, the PET aerogel can release the absorbed oil by a simple squeezing method without any significant decrease in its absorption capacity after five absorption–recollection cycles. Recycling water bottles into PET aerogels not only encourages a circular economy, but also offers sustainable solutions for technical challenges such as heat and sound insulation and oil absorption.

Fig. 5.

Recycling of PET fibers into hydrophobic rPET aerogel for oil spill cleaning.

Reprinted from Le et al. [39], Copyright (2020) with permission from Elsevier

Aerogel from Rubber Waste

Due to the growing transport demand, over 1.7 billion new tires are produced per year. The figure for waste tires generated per year is over 1 billion, of which only 3–15% are recycled [56]. The car tires are mainly composed of synthetic polymers including nylon 6, nylon 6-6, dacron and rayon. The polymer contents in the car tires are difficult to dissolve with green solvents. One strategy to obtain the gel mixture of rubber is employing crosslinkers namely acetone, PVA and glutaraldehyde. Briefly, car tire fibers were dispersed into acetone/PVA/glutaraldehyde/water, followed by heat curing and freeze-drying to create durable aerogels as shown in Fig. 6 [41]. Functional groups on polymer chains of rubber are utilized to form crosslinks with acetone, PVA and glutaraldehyde via hydrogen bonds. The developed rubber aerogels are both flexible and durable with a high Young’s modulus up to 965.6 kPa, allowing them to spring back to their original shape instead of being deformed plastically after compression. The high elasticity of rubber aerogels is significantly useful compared to the brittleness of the conventional silica aerogels in terms of functioning in harsh environments with high mechanical impacts. Multiple applications of the rubber aerogels are demonstrated, such as thermal insulation (K = 35–47 mW/mK), sound insulation (NRC = 0.41) and oil absorption (up to 25.0 g/g). The rubber aerogels’ maximum oil absorption is approximately 1.7 and 2.8 times higher than that of commercial polypropylene mats and nonwoven polypropylene, respectively [56].

Fig. 6.

Fabrication and properties of rubber aerogels from car tire waste.

Reprinted from Thai et al. [41], Copyright (2019) with permission from Elsevier

Aerogel from Textile Waste

Recycled textiles are another abundant precursor for cellulose-based aerogels. With the rapid development of “fast fashion” involving the mass production of low-cost clothing with short lifetime, the global production of cotton reached 27.3 million tons in 2018 [57]. To utilize used clothing and leftover materials from textile industry, Han et al. [45] prepared hybrid cellulose/magnesium hydroxide nanoparticles aerogels from waste cotton fabric. The magnesium hydroxide nanoparticles are synthesized in situ in the gel structure, which enhance the flame retardancy of the composite aerogels. Duong et al. [44] developed compressed hybrid cotton aerogels from cotton and cellulose fibers using Kymene as a crosslinker. With the ability to volumetrically expand 16 times within 4.5 s, the aerogels possess potential applications in hemostatic devices, oil-spill cleaning and personal care. The better mechanical handleability of the cotton aerogels in contrast to aerogels from paper waste is attributed to the higher mechanical properties of cotton fibers compared to the delignificated wood fibers [58]. With good mechanical strength, high cellulose content and relatively long fibers, cotton fibers from fabric waste can be utilized to assemble aerogel scaffolds for multiple applications. Similar to the mentioned textile wastes, wool waste fibers were recycled into advanced aerogels to minimize their disposal and incineration. The aerogels were fabricated by using PVA to bind the wool waste fibers, freeze-drying and surface modification with methyltriethoxysilane. The prepared aerogels show a significantly high oil absorption capacity of 136.2 g/g that was 15 times greater than commercial polypropylene absorbents [59].

Aerogels from Agricultural Waste

Agricultural waste is defined as non-product outputs of the agricultural processing and production. They can be generated from cultivation activities, livestock production, aquaculture and food processing [60]. Conventionally, agricultural waste is managed by open burning or landfilling, resulting in harmful gases and organic substances released. Despite being considered low-value by-products, agricultural wastes are abundant sources of raw materials such as cellulose [61, 62], silica [63] and bioactive compounds [64]. Therefore, many works of utilizing agricultural waste as precursors for aerogels have been conducted.

Aerogels from Rice Husk Ash

Worldwide rice production is estimated to be 700 million tons in 2015, releasing approximately 140 million tons of rice husks during the milling process. Chemical composition of the rice husks includes cellulose (50%), lignin (25%–30%), silica (15%–20%), and moisture (10%–15%) [65]. Burning of rice husk results in rice husk ash containing around 90% of silica, which can be used as a precursor for silica aerogels [66]. Remarkably, Green Earth Aerogels Technologies (Spain) successfully produced commercial silica aerogels from rice husk ash [67]. Table 2 shows some approaches to silica aerogels with various morphologies from rice husk ash. Generally, rice husk ash is converted into sodium silicate by reacting with hot NaOH solution. The resulting mixture is gelated by an acid and aged to obtain a silica hydrogel. Subsequently, water in the gel is replaced by other volatile solvents. Finally, the aerogel is obtained by supercritical drying or ambient pressure drying. The density, pore volume, pore size and surface area of aerogels from rice husk ash are comparable to those of aerogels prepared by traditional methods [68]. As can be seen, the pore volume, pore size and surface area of the supercritical-dried silica aerogels are slightly larger than those of the ambient pressure dried ones [69]. It can be explained by the elimination of surface tension during supercritical drying, compared to the partial reduction of surface tension by silylation in ambient pressure drying technique.

Table 2.

Preparation and physical properties of silica aerogels from rice husk ash

No.	Type of silica aerogels	Fabrication process	Density (g/cm3)	Pore volume (cm3/g)	Pore size (nm)	Surface area (m2/g)	Referencess
1	Monolith	Silicate extraction Silylation by TMOS Gelation by acid Solvent exchange with ethanol Ambient drying	0.32–0.33	0.78–3.31	5–60	315–500	[70, 71]
2	Monolith	Silicate extraction Gelation by acid Solvent exchange with ethanol Silylation by TEOS Solvent exchange with n-hexane Ambient drying	0.67	3.1	10–40	273	[72]
3	Monolith	Silicate extraction Gelation by resin/acid Solvent exchange with ethanol ScCO2 drying	0.038–0.071	3.39–8.65	10–60	598–730	[73, 74]
4	Bead	Silicate extraction Gelation by acid Solvent exchange with ethanol Silylation Ambient pressure drying	0.055	N/A	N/A	773	[75]
5	Microsphere	Silicate extraction Emulsification with surfactants Settling Solvent exchange with ethanol ScCO2 drying	N/A	1.7	20	340	[76]

Aerogels from Fruit and Vegetable Waste

Fruit and vegetable harvesting and processing release various residues including pods, peel, pulp, stones, and seeds. These residues mainly contain soluble sugars, hydrolysable materials and fibers [77]. Common utilizations of fruit and vegetable waste are chemical production by extraction or fermentation and adsorption in waste water treatment [78]. Furthermore, fruit and vegetable waste have been utilized to prepare aerogels as shown in Table 3.

Table 3.

Preparation and application of aerogels from fruits and vegetables waste

No.	Waste materials	Type of aerogels	Fabrication process	Properties/applicationsa	References
1	Pineapple leaves	Cellulose	Dispersion Freeze-drying Silanization	Oil absorption: 37.9 g/g	[79]
2	Pineapple leaves	Cellulose	Dispersion Freeze-drying	Thermal insulation: 30–34 mW/mK Acoustic insulation	[80]
3	Pineapple leaves	Cellulose	Dispersion Gelation Freeze-drying	Gas adsorption: 1.08 mmol ethylene/g Metal ion adsorption: 0.835 mmol Ni2+/g	[81]
4	Sugarcane bagasse	Cellulose	Dispersion Freeze-drying Silanization	Oil absorption: 25 g/g Thermal insulation: 31–42 mW/mK	[82]
5	Coconut shell	Cellulose	Dispersion Solvent exchange to t-BuOH Gelation Freeze-drying Silanization	Oil and solvent adsorption: 669 g motor oil/g, 425 g t-BuOH/g	[83]
6	Durian shell	Carbon	Carbonization Freeze-drying Pyrolysis	Oil and solvent adsorption: 19.5 g sunflower oil/g, 18.6 g formic acid/g	[84]
7	Sugarcane bagasse	Carbon	Dispersion Freeze-drying Pyrolysis Activation	Energy storage	[85]
8	Cabbage leaves	Carbon	Carbonization Freeze-drying Pyrolysis	Energy storage Oil and solvent absorption: 202 g pump oil/g; 165 g cyclohexane/g	[86]
9	Banana peels	Carbon-Cellulose	Dispersion Freeze-drying Pyrolysis	Oil and solvent absorption: 115 g pump oil/g, 86 g chloroform/g Emulsion separation	[87]
10	Pomelo peels	Carbon	Carbonization Freeze-drying Pyrolysis	Oil and solvent absorption: 36 g sunflower oil/g, 31 g formic acid/g	[56]
11	Pomelo peels	Nitrogen/boron/ carbon	Carbonization Freeze-drying Impregnating Freeze-drying Pyrolysis	Energy storage	[88]
12	Sugarcane bagasse ash	Silica	Dissolving Silylation Dispersion Gelation Ambient pressure drying	Pore volume: 0.75–2.16 cm3/g Pore size: 3.39–7.38 nm Surface area: 450–1114 m2/g	[89]
13	Coffee grounds	Coffee-cellulose	Dispersion Freeze-drying Silanization	Thermal insulation: 37–45 mW/mK Oil absorption: 16 g oil/g	[90]
14	Jackfruit and durian	Carbon	Carbonization Freeze-drying Pyrolysis	Energy storage	[91]
15	Watermelon	Carbon	Carbonization Freeze-drying	Energy storage	[92]
16	Wheat straw and okara	Konjac glucomannan-based	Dispersion Freeze-drying	Filtration	[93]
17	Peanut hull	Peanut hull/graphene	Dispersion Carbonization Freeze-drying	Oil and solvent absorption: 58 g pump oil/g, 79 g chloroform/g Emulsion separation	[94]

^aSpecifications to illustrate for applications: Absorption capacity (for Absorption), Adsorption capacity (for Adsorption), Thermal conductivity (for Thermal insulation)

As seen, cellulose and carbon aerogels are the two most popular types of aerogels from these biomass residues. Cellulose aerogels can be obtained from pineapple leaves, sugarcane bagasse or coconut shells. Because of numerous hydroxyl groups on the cellulose chains of pineapple leaf fibers, PVA binder is used to create the hydrogen bonding between the fibers in the first pineapple aerogels developed by Luu et al. [95] and Do et al. [80] (Fig. 7a). The synthesized aerogels exhibit a low thermal conductivity (30–34 mW/mK) and can be used as fillers in thermal jackets to maintain the water temperature. The results show that the developed thermal jacket from pineapple aerogels can keep ice slurry from – 3 °C below 0 °C for 6 h, and hot water from 90 °C above 40 °C for 2.5 h, which is about three times better than a commercial product in terms of thermal insulation (Fig. 7b). Moreover, the 190-g thermal jacket shows the great potential to replace expensive and heavy 900-g vacuum thermos flasks. Functionalized pineapple leaf-derived aerogels with the presence of activated carbon show their ability in fruit preservation with ethylene gas adsorption capacity of 1.08 mmol/g at atmospheric pressure. The aerogels after coating with diethylenetriamine are also applied in treatment of contaminated wastewater with the maximum nickel ion adsorption uptake of 0.835 mmol/g [81]. Wan et al. [83] prepared cellulose aerogels from coconut shell for dealing with chemical leaks and oil spills. By surface modification with methyltrichlorosilane, the aerogels can adsorb solvents and oil of the amount as high as 296–669 times of their own weight, which is significantly higher than the oil absorption capacity of the hydrophobic pineapple aerogels (37.9 times) [79]. The high tensile strength and relatively long cellulose chains give plant fibers the ability to assemble into flexible aerogel sheets, which can be easily rolled up for transportation, storage, and usage in different situations.

Fig. 7.

a Fabrication of the pineapple fibers aerogel from pineapple leaves. Reprinted from Luu et al. [95]; b heat insulation performance of the thermal jacket made of pineapple aerogel. Reprinted from Do et al. [80], Copyright (2020) with permission from Elsevier

Organic substances from fruit and vegetable residues such as bagasse, peels and leaves can be used as inexpensive and abundant carbon sources for carbon aerogels. Zhu et al. [56] prepared carbon aerogels from pomelo peels via a three-step procedure including hydrothermal carbonization, freeze-drying and pyrolysis. The aerogels possess a high specific area of 466.0–759.7 m²/g and a high absorption capacity up to 36 times of their weight for various oil and organic solvents. Carbon aerogels from fruits and vegetables waste can be also designed for electronic devices such as capacitors and batteries. For instance, Cai et al. [86] reported carbon aerogels from cabbage leaves with a superior capacitance of 291 F/g and large capacitance retention of 96.76% over 10,000 cycles.

Interestingly, sugarcane bagasse can be processed in different pathways to obtain cellulose aerogels, carbon aerogels or silica aerogels. Dispersing sugarcane fibers in PVA, followed by freeze-drying and heat curing results in cellulose aerogels [82]. The aerogels after modification with MTMS have high hydrophobicity without affecting their porosity. A low thermal conductivity of 31–42 mW/mK and an oil absorption capacity of 25 g/g indicate potential applications of the aerogels in spill cleaning and heat insulation. Hao et al. prepared cellulose aerogels from bagasse via a freeze-drying approach, then pyrolyzed and activated the resulting aerogels to obtain carbon aerogels [85]. These carbon aerogels possess a comparable high specific capacitance of 142.1 F/g and an excellent capacitance retention of 93.9% over 5000 cycles, which are suitable for supercapacitor electrodes. Nazriati et al. utilized the bagasse ash in sugarcane factories as a silica source for the preparation of hydrophobic silica aerogels [89]. This approach involves surface modification of wet gels and ambient pressure drying. The surface area and pore volume achieved can be up to 1114 m²/g, and 2.16 cm³/g, respectively.

Aerogels from Industrial Waste

The amount of industrial waste generated per day is approximately 17 times higher than that of the municipal waste from our daily activities [2]. Industrial waste is usually generated in massive amounts and requires further treatment before releasing to the environment. There have been some works on utilizing industrial waste into construction materials such as concrete [96], cement [97], and for water treatment [98]. Studies of aerogels from industrial waste is currently restricted to some certain types of waste. It might be due to the presence of hazardous substances such as alkali, acid, fluoride, cyanide, arsenic and heavy metal ions, making the pretreatment of raw materials costly and complex [99]. Some types of aerogels from industrial waste are tabulated in Table 4.

Table 4.

Preparation and application of aerogels from industrial waste

No.	Waste materials	Type of aerogels	Fabrication process	Properties/applicationsa	References
1	Fly ash	Silica	Calcination Gelation Solvent exchange to ethanol Silylation Ambient pressure drying	Pore volume: 2.92–4.875 cm3/g Pore size: 4.875 nm Surface area: 362.2–907.9 m2/g	[100, 101]
3	Fly ash acid sludge	Silica	Dissolving Ion exchange Gelation Solvent exchange to ethanol Silylation Ambient pressure drying	Pore volume: 3.29–3.49 cm3/g Pore size: 10.7–12.6 nm Surface area: 700–850 m2/g	[102, 103]
4	Fly ash	Titan dioxide/Silica–Alumina	Calcination Gelation Solvent exchange to ethanol Silylation Ambient pressure drying TiO2 impregnation	Photocatalyst support	[104]
5	Fly ash	Fly ash	Dispersion Freeze-drying	Pore size: 2–5 nm Thermal insulation: 40–50 mW/mK Acoustic insulation	[105, 106]
6	Coal gangue	Silica	Calcination Gelation Solvent exchange to ethanol Silylation Ambient pressure drying	Pore size: 20–27.5 nm Pore volume: 4.81 cm3/g Surface area: 600–690 m2/g Thermal insulation: 20–26.5 mW/mK	[107, 108]
7	Dislodged sludge	Silica	Dissolving Ion exchange Gelation Solvent exchange to ethanol and hexane Silylation Ambient pressure drying	Pore volume: 1.53–3.56 cm3/g Surface area: 381–433 m2/g Pore size: 7.07–23.40 nm Thermal insulation: 30–32 mW/mK	[109]
8	Gold mine waste	Silica	Dissolving Silylation Dispersion Gelation Ambient pressure drying	Pore volume: 0.45 cm3/g Pore size: 2–100 nm Surface area: 284 m2/g	[110]
9	Wood fibers	Cellulose	Steam explosion Dispersion Freeze-drying Silanization	Oil absorption: 19.5 g/g	[111]
10	Red mud	Cellulose/red mud	Ball milling Dispersion Freeze-drying Crosslinking	Pollutant absorption: 30 g 2,4-dichlorophenol/g Thermal insulation: 17–23 W/mK Acoustic insulation	[112]
11	Animal skin trimmings	Collagen/polypyrrole	Dissolving Dispersion Polymerization Freeze-drying	Bioelectronics	[113]
12	Magnesium chips	Magnesium hydroxide	Dispersion Precipitation Gelation Freeze-drying	Thermal insulation: 30–42 mW/mK Acoustic insulation	[114]

^aSpecifications to illustrate for applications: absorption capacity, g/g (for absorption), adsorption capacity, mg/g (for adsorption), thermal conductivity, mW/mK (for thermal insulation)

Aerogels from Fly Ash

Released from factories and thermal power plants, fly ash is an abundant source of silica, alumina and other metal oxides. It is estimated that 800 million tons of fly ash are generated in the world annually [115]. Fly ash can be converted into sodium silicate by hydrothermal reaction and then used as a precursor for silica aerogels, which considerably increases the economic value of the fly ash. Based on this concept, many studies on silica aerogels from fly ash have been conducted. A typical synthesis of silica aerogel from fly ash begins when fly ash is hydrothermally reacted with an acid and then filtrated. The residue is dissolved in hot NaOH solution to obtain sodium silicate solution. From this resulting solution, silica gel is prepared by adjusting pH with an acid or an ion exchange resin. After aging, the gel is immersed in anhydrous ethanol for solvent exchange. The hydrophilic surface can be modified by silylation via the reaction of the gel with trimethylchlorosilane in hexane/ethanol. Finally, the gel is washed with hexane and dried at ambient pressure to achieve silica aerogels. The fly ash aerogels obtained via this approach possess a high water contact angle (140°–151°), a large surface area (850–900 m²/g) and a large pore size (12–24 nm), suggesting their potential applications in oil and organic pollutant removal. In addition, silica aerogels can also be prepared from coal gangue, dislodged sludge and gold mine waste. For instance, Zhu et al. [107] reported silica aerogels from coal gangue achieving a light weight (0.19 g/cm³), a high specific surface area (above 600 m²/g), a high porosity (> 90%) and a low thermal conductivity (20–25 mW/mK) as a potential candidate for thermal insulation. Duong et al. [105] developed a novel method to fabricate aerogels by using highly viscous and eco-friendly binders without the need for chemical pre-treatment on fly ash. A stable and porous structure is created via hydrogen bonds between oxide particles in fly ash and hydroxyl groups on PVA chains (Fig. 8). Because of the high molecular weight of 89,000–90,000 and viscosity of 11.6-15.4 cP (4% in H₂O at 20°C), PVA can prevent fly ash particles from settling and distribute them evenly in the aerogels.

Fig. 8.

Fabrication and binding mechanism of aerogels from fly ash.

Reprinted from Duong et al. [105], Copyright (2021) with permission from Elsevier

Another approach by Do et al. [106] was carried out by using a combination of industrial PVA with low viscosity and CMC as an anti-settlement agent to bind fly ash into a monolithic gel, followed by sublimation to obtain lightweight aerogels with porosity of 94.94–95.78%. Both fabricated fly ash aerogels exhibited heat insulation with poor thermal conductivity (40-50 mW/mK). Following the previous study, Do et al. [116] synthesized a multi-functional composite aerogel by consolidating two waste sources of fly ash and recycled plastic fibers. The novelty in this study is the use of xanthan gum at a low concentration of 0.4 wt% as a binder to adhere fly ash particles to the framework of plastic fibers and an anti-settling agent to avoid the sedimentation of fly ash. The as-fabricated composite aerogels are both excellent heat and sound insulation. Interestingly, although fly ash contains metal oxides, when it is converted into the composite aerogels, the heat conductivity of the materials is only from 34 to 39 mW/mK along with their ultra-lightweight properties proved by their density and porosity of 0.026–0.062 g/cm³ and 95.69–98.42%, respectively. The addition of rPET fibers is found to enhance the compressive strength of the aerogels. Compared to the previous fly ash-based aerogels [105, 106], the developed composite aerogels are 5 times lighter and 1.5 times better in heat insulation at ambient condition. Overall, these works represent green methods to utilize 100% of fly ash without any chemical treatment, increasing the atom efficiency of the process and thus reducing the amount of waste generated.

Aerogel from Leather Waste

Leather industry releases around 6 million tons of solid waste annually [117]. Processing one ton of raw hides and skins produces 50 kg of raw trimmings, which contains approximately 20% collagen [118]. Utilizing skin trimming wastes, Mekonnen et al. [113] fabricated collagen-polypyrrole hybrid aerogels. The skin trimmings are pretreated to yield hide powder, dissolved in acetic acid solution to form a collagen solution and mixed with pyrrole. The mixture is undergone an oxidative polymerization by FeCl₃ and sodium anthraquinone-2-sulfonate and then freeze-dried to obtain aerogels. The flexibility, brittleness, thermal stability, porosity, biocompatibility and electrical conductivity can be controlled by varying the concentration of polypyrrole in the aerogel matrix. It is suggested that the collagen-polypyrrole hybrid aerogels are potential candidates for various applications such as biosensor, tissue engineering, electrostatic discharge protection and electromagnetic interference shielding.

Aerogel from Metal Waste

Recycling metal waste into metal hydroxide aerogel is an advanced approach introducing by Yam et al. [114] (Fig. 9). Magnesium chips generated routinely in the machining process of casting are recycling into magnesium hydroxide aerogels. This fabrication employs PVA as a biodegradable binder and using freeze-drying method to obtain the aerogels. The Mg(OH)₂ particles are formed in situ through dissolving magnesium metal into hydrochloric acid (HCl) solution and reprecipitation by NaOH solution. The Mg(OH)₂ particles and the PVA chains are linked by hydrogen bonds. It is proved that the presence of the Mg(OH)₂ particles enhances the thermal stability and mechanical properties of the aerogels. The magnesium hydroxide aerogels can withstand up to 800 °C with approximately 50% of mass loss. Although 50% of mass loss is still relatively high, this work suggests a method to fabricate metal-based aerogels for high-temperature resistance. Most of the mass loss can be attributed to the thermal decomposition of the binders. Should binders with higher thermal stability be employed, the overall thermal stability of the aerogels will be significantly improved.

Fig. 9.

Appearance, SEM image and crosslinking mechanism of the magnesium hydroxide aerogels from magnesium chips.

Reprinted from Yam et al. [114], Copyright (2020) with permission from Elsevier

Discussion and Prospective

Various types of municipal solid, agricultural and industrial wastes have been converted into aerogels with a wide range of applications ranging from heat and sound insulation to energy storage. Remarkably, various multi-functional aerogels have been developed such as coffee grounds aerogels, cotton aerogels and red mud aerogels, which can serve different purposes. The properties of these aerogels, such as low thermal conductivity or high sorption capacity are comparable to the commercial materials, as shown in Fig. 10 [119–126]. By using low-cost, abundant starting materials, they can become sustainable choices for engineering applications such as thermal insulation or oil spill cleaning. For example, producing 1 m² of rubber aerogel with 1 cm of thickness from car tire costs less than 14 USD and takes less than 13 h, making the rubber aerogel competitive with the commercial insulators and sorbents [127].

Fig. 10.

a Thermal conductivity and b oil sorption capacity of aerogels from waste and other materials

Besides easing the burden on landfills and incinerators, these works also offer numerous green pathways to mitigate the waste and energy used in the fabrication. For example, Do et al. prepared cellulose aerogels from pineapple fibers without employing any organic solvents [79]. PVA as a biodegradable binder is being commonly consumed to fabricate a stable structure of aerogels from agricultural waste, making the obtained aerogels completely biodegradable. The cost-effective freeze-drying method has been frequently applied in numerous works to create a three-dimensional porous network of aerogels. Compared to scCO₂ drying, freeze-drying offers various advantages such as less operation time, lower equipment and operation cost, reducing solvent exchange steps in the synthesis procedure, and safer process because of non-requirement of high pressure gas [128]. Especially if environmental impacts are carefully considered, freeze-drying is probably the best choice. Moreover, the manufacturing cost of a freeze-dried aerogel is estimated at 42 USD/m² at laboratory scale, which is even competitive with the cost of the corresponding scCO₂-dried aerogel at industrial scale (21–70 USD/m²) [129]. Besides, conventional batch-wise freeze-drying has many disadvantages such as high time and energy consumption, uncontrolled freezing step, inefficient use if loading below maximum capacity, and sample-to-sample variation due to inhomogeneous energy distribution [130, 131]. These drawbacks can be overcome by using continuous freeze-drying. This approach has been investigated in pharmaceuticals production and found to improve the drying efficiency and the product uniformity [132]. Other promising techniques have been studied for the mass and continuous production of aerogels, such as nonwoven [133], continuous solvent exchange [134], fluidized bed drying [135] and continuous scCO₂ drying [136].

Waste, especially municipal waste, usually appears as a mixture with complex composition. If waste is not carefully classified from sources, the pretreatment process becomes extremely challenging. Pretreatment of raw materials comes with difficulties such as high cost in chemicals used, time-consuming process and release of toxic chemicals into the environment. For instance, the removal of ink and glue in newspapers to fabricate cellulose aerogels involves treating the waste newspapers with NaOH solution and acidified sodium chlorite (NaClO₂) solution, dispersing the mixture in 1-allyl-3-methylimidazolium chloride (AmimCl) and rinsing the mixture with ethanol at least six times [37]. Accordingly, alkali solutions, strong oxidants and organic solvents are released, requiring more cost for waste treatment and reducing the sustainability of the recycling process. Therefore, appropriate measures to pretreat the raw materials should be carefully chosen regarding to desired applications to minimize the detrimental effects of the fabrication to the environment and ecosystem.

With the rapidly development of technology, e-waste has attracted a great deal of attention. Technical innovations have shortened the lifespan of electrical devices, leading to the fast rate of e-waste generation. In 2018, 50 million tons of e-waste were generated worldwide. This figure may reach up to 120 million tons by 2050 [137]. Unlike other types of municipal electronic waste, e-waste contains both high value and hazardous materials such as polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCB), heavy metals and rare earth elements [138]. The mentioned work of Yam et al. [114] about metal-based aerogel from metal waste suggests a new way to recycle metals in e-waste into high-value aerogels. If utilized properly, e-waste can become a promising source of precursor for metal-based aerogels in the future.

With multiple extraordinary properties such as ultra-lightweight, ultralow thermal conductivity, high surface area and high modifiability, aerogels are able to fulfill stringent requirements of military and aerospace [139]. These fields involve situations that requires the insulators or sorbents to withstand extreme conditions, such as fire hazards or in polar regions. Through decades of development, the thermal and mechanical stability of the current aerogels are significantly improved than those of the first silica aerogels. However, to withstand such harsh environments, aerogels are expected to have a higher resistivity to environmental impacts. It is expected that advanced properties such as self-cleaning, self-healing, temperature resistance, and fire retardant will be focused to maintain the performance of aerogels under different working conditions. Inspired by the self-cleaning ability of lotus leaves, Cai et al. [140] prepared functionalized cellulose aerogels with a durable superhydrophobicity and anti-icing properties. The aerogels remain completely clean after pouring coffee, milk, and juice. Moreover, sand powders are easily removed from the aerogel surface by water rushing. This approach will reduce the cleaning and maintenance cost of aerogels insulators for building surfaces or pine line walls. To protect materials from damage and environmental conditions, making self-healable materials is an attractive approach. This class of materials can restore their original structure, properties and functionality after being damaged. There have been some works of self-healable aerogels such as chitosan/itaconic acid aerogels [141] and MXene−graphene composite aerogels [142], suggesting their potential applications in long-life insulators and devices. In addition, aerogels with ultralow or ultrahigh temperature resistivity are developed for both thermal insulation and oil absorption applications. Zhen et al. [143] synthesized the carbon nanofiber aerogels that can maintain high oil absorption capacity up to 139 g/g under a wide range of temperature, from liquid nitrogen temperature up to 400 °C, suggesting an absorbent for harsh scenarios such as oil spillage in Arctic. It is of worthy notice that conventional sorbents such as polyurethane or polyethylene cannot work above 200 °C while becoming brittle at low temperature. Feng et al. [144] developed carbon aerogels with a low thermal conductivity of 61 mW/mK at 2000 °C under 0.15 MPa argon, which is promising for space vehicles and military vehicles. Besides, fire-retardant aerogels have been concerned due to their ability to slow down the burning when fire occurs. Fire-retardant phenol-formaldehyde-resin/silica aerogels reported by Yu et al. [145] can resist up to 1300 ºC flame without disintegration and prevents the temperature on the non-exposed side to increase above 350 ºC. Similarly, graphene aerogels prepared by Wang et al. [146] can withstand an alcohol flame even heated to glowing. With a good fire-retardant ability, the applications of these aerogels can be extended to building protective layers or firefighter clothes. There have been few works about investigating these mentioned properties on the aerogels from waste. If these outstanding properties are successfully developed for the aerogels from waste, their values and potentials will be significantly improved.

Conclusions

The preparation of aerogels from waste has become a novel trend in material science and technology. Waste, with its low cost and abundance, has become a potential precursor for the sustainable syntheses of aerogels, encouraging the conversion of a linear economy to circular economy. Numerous types of municipal solid waste, agricultural waste and industrial waste are upcycled into aerogels with various applications. Those aerogels possess outstanding properties and can compete with commercially available materials in many diverse fields such as thermal insulation and oil spill cleaning. Noticeably, green fabrication methods such as eliminating organic solvents or using biodegradable binders have been more focused by researchers worldwide to create sustainable solutions for waste recycling. However, complex composition of waste, environmental impacts and scalability are current challenges for researchers to overcome. In the future, it is expected that more types of waste can be recycled into aerogels by more eco-friendly methods to create new value from waste and partially combat the increasing waste generation. Moreover, environmental resistivity of the aerogels should be developed to expand their applications in different conditions.

Declarations

Conflict of interest

There are no conflicts to declare.