Introduction

Aerospace technology has undergone tremendous development since the first flight by Wright Brothers in 1903, which has significantly improved the life quality of human beings and extended the capability of space explosion [1]. Nowadays, aerospace vehicles mainly include commercial/military airplanes, missiles, rockets, spaceships, and satellites, which are equipped with turbine, turbofan, ramjet, or rocket engines, and liquid hydrocarbon fuels are the main energy sources for propulsion [2]. Currently, the high-performance aircrafts are aiming for high thrust-to-weight ratio, high flight speed, and long flight distance. In this case, the energy density of fuels is critically important because it determines the flight range and payload of aircraft vehicles [3]. The mostly used jet fuels, like RP-3 (directly distilled from petroleum), have a relatively low density of 0.77–0.83 g/mL. Since 1950s, the high-energy-density (HED) fuels were synthesized, and considerable progress has been achieved later, especially in the past 20 years [4]. Herein, we will summarize the development of HED liquid fuels and propose the strategies to further increase their energy density.

Development of Liquid HED Fuel

For the volume-limited aircraft vehicles (especially for missiles), increasing energy density of the applied fuel helps to decrease the fuel tank volume to save more space for electronics and other components [5], or to extend the flight range and/or increase the payload without change of fuel tank [6]. The energy density of fuel is directly determined by the density and volumetric net heat of combustion (NHOC), and the latter is almost linearly positively correlated to the former (Fig. 1). Therefore, HED hydrocarbon fuel can also be named high-density fuel. The density of the widely used RP-3 is only 0.77–0.83 g/mL, while the density of synthetic HED fuels can reach 0.93 g/mL, such as JP-10 (America), T-10 (Russia), and HD-1 (China) (with their energy density increased by ca. 16%). Table 1 shows the composition and properties of typical HED fuels. These HED fuels all possess multi-cyclic molecule structures. The significant increase in fuel energy density can offset the slight decrease in gravimetric NHOC (caused by the decrease of hydrogen content), which is highly important to increase the flight distance of aircraft vehicles. Furthermore, liquid hydrocarbon fuels with density higher than 1.0 g/mL have also been developed, such as RJ-5 and RJ-7. However, RJ-5 has a very high freezing point (about 0 ℃) and RJ-7 shows high viscosity (> 400 mm2/s @ –40 ℃). When these fuels are applied in aircraft vehicles, the supercooled circumstances of high altitude may freeze the fuel or increase the viscosity suddenly, which will quickly cause the shutdown of engines. Therefore, the design and synthesis of HED fuel should not only consider the property of high density, but also make sure the high performance of other physicochemical properties, like cryogenic property, flash point, thermal oxidation stability, and so on.

Fig. 1
figure 1

Reproduced with permission from Ref. [5]. Copyright © 2020)

Volumetric NHOC of 64 kinds of hydrocarbon fuels vs. density (

Table 1 Composition and properties of typical HED fuels

Development of Liquid Fuels with High Energy and High Energy Density

For the weight-limited aircraft vehicles, their take-off weight is highly restricted, such as rocket and spacecraft. In this case, the specific impulse of liquid fuel is the key property, which highly depends on the gravimetric NHOC of fuel, the matching oxidant, and the composition of combustion products [7]. Normally, the increase in gravimetric NHOC can increase the specific impulse. For example, the specific impulses of the Syntin (Russia) and quadricyclane (QC) fuels are 5–6 s higher than those of rocket kerosene (RP-1 and RP-2, using O2 as the oxidant). Different from HED fuels, the above high-energy fuels all possess the stained molecule structure to provide more combustion heat. Meanwhile, the increase in density of high-energy fuel also benefits to save more space for aircraft vehicles or extend the flight range. So, liquid fuels with both high energy and high energy density are expected to meet the demand of volume-limited and weight-limited aircraft vehicles.

As shown in Fig. 2a, for the multi-cyclic fuels with five- or six-membered rings, the gravimetric NHOC increases linearly with (H/C)/M0.02 (M is molecule weight), while it decreases linearly with (H/C)/M0.02 for the strained fuels with three- or four-membered rings. From Fig. 2b, the density of all fuels decreases linearly with (H/C)/M0.19. The above results indicate that the multi-cyclic molecule structure with relatively low H/C ratio (high molecule weight) and more highly strained rings will show both high-energy and HED properties. For example, the typical strained QC (with one four-membered ring and two three-membered rings) shows 18% higher density and 5–6 s higher specific impulse than those of RP-1 and RP-2.

Fig. 2
figure 2

Reproduced with permission from Ref. [5]. Copyright © 2020)

a Gravimetric NHOC of 64 hydrocarbon fuels vs. (H/C)/M0.02 and b the densities (20 ℃) of 64 hydrocarbon fuels vs. (H/C)/M0.19 (

Recently, the hydrocarbon fuels with compact polycyclic molecule structures and strained three- or four-membered rings have been synthesized, and the typical fuels and their properties are shown in Fig. 3. Obviously, the introduction of three- or four-membered rings can obtain the highly strained fuels with both high density and specific impulse. These works provide the guidance for rational design and synthesis of fuels with high energy and high energy density, which are promising for the application in advanced rocket and rocket-based combined cycle engines.

Fig. 3
figure 3

Properties of typical strained hydrocarbon fuels. Note: the specific impulse was calculated using rocket propulsion analysis software (RPA v.2.3) with O2 (l) as the oxidants, and the chamber pressure, oxidizer excess coefficient and expansion pressure ratio were 7 MPa, 0.7 and 70, respectively

Energetic Nanofluid or Gelled Fuels

Until now, impressive progress has been made in the synthesis of HED liquid fuel (including the multi-cyclic and strained fuels, derived from petroleum, coal, biomass, and so on), via thermal polymerization, isomerization, photocatalysis, and hydrogenation processes [8,9,10,11,12]. However, with the limitation of inherent characteristics of hydrocarbon molecules, the increase extent of energy density for HED liquid fuel is less than 30% comparing with RP-3 jet fuel.

To break through the above bottleneck, the addition of energetic nanoparticles (NPs) (such as nano-sized Al or B) in HED fuels is a very promising approach, and this class of HED suspended fuel is denoted as nanofluid fuels. Al (density of 2.7 g/cm3, volumetric NHOC of 83.86 MJ/L) and B (density of 2.34 g/cm3, volumetric NHOC of 137.45 MJ/L) nanoparticles are the most used energetic materials to significantly increase the energy density of liquid hydrocarbon fuels [13]. Figure 4 shows the density range, gravimetric NHOC range, and volumetric NHOC range of multi-cyclic hydrocarbons, strained hydrocarbons, and nanofluid fuels. The 25 wt.% addition of nano-Al or nano-B in HD-01 or QC HED fuels can obtain the high-performance fuel with high density of 1.1–1.25 g/cm3 and high volumetric NHOC of 42.8–62.9 MJ/L. Moreover, adding Al or B nanoparticles can also shorten the ignition delay, increase the combustion efficiency and reduce the oxygen demand of fuel [14, 15]. The combustion result of rocket engine confirms that the ignition delay time of QC containing 15 wt.% Al NPs is 26 ms shorter than that of pristine QC, and the volumetric specific impulse is increased by ca. 3% [16]. Although the nanofluid fuels show very high energy density, there are still many problems that need to be solved for practical application.

Fig. 4
figure 4

a Density range, b gravimetric NHOC range, and c volumetric NHOC range of multi-cyclic hydrocarbon fuel, strained hydrocarbon fuel, and nanofluid/gelled fuels

The energetic particles are generally nanosized and easy to agglomerate and settle. Therefore, stabilizing the liquid hydrocarbon-solid NPs suspension becomes a big challenge for the synthesis, storage, and utilization of energetic nanofluid fuels. In order to obtain stable suspension nanofluid, the repulsive force among the NPs must be larger than their attractive force. Long-chain surfactant molecules can attach to the particle surface to form absorbed layer, and the overlap of the surfactant layer will produce repulsive force to overcome the van der Waals attraction, thus leading to high fuel stability. Using trioctylphosphineoxide (TOPO) as protecting ligands, the nanofluid containing 30 wt.% B NPs shows a good suspension property, with ca. 17% B NPs settlement from the nanofluid fuel in 3 d [17].

Even though, the long-term storage stability of nanofluid fuels is still far from the demand of their practical application. The development of the fuel with phase change ability, which is prepared as a solid state with the stable state for storage and can be quickly converted into liquid for usage under the condition of shearing or heating, seems to be a promising method, like the recent developed gelled fuel system [18].

Conclusions

HED fuels attract more and more attention to promote the performance of advanced aircraft vehicles, especially for space savings and flight range extension. Different from the normal jet fuels (RP-3), HED fuels are all synthesized with very good batch stability (like JP-10). The properties of HED fuels are directly determined by their molecule structures: the multi-cyclic structures with five- or six-membered rings show high energy density and are used for volume-limited aircraft vehicles, while multi-cyclic structures with three- or four-membered rings possess high energy and specific impulse and are used for the weight-limited aircraft vehicles. However, besides the density and NHOC properties, other performance of fuels should also be concerned, like freezing point, flashing point, viscosity, during the design and synthesis of new type of advanced fuels.

Adding energetic NPs in HED fuels is expected to greatly increase the energy density, but it is very difficult to stable the high-density NPs in liquid fuels (even the effective protecting ligands have been applied), which faces many problems during the practical application (i.e., storage, transportation, atomization, and combustion). Gelling the nanofluid fuels into the non-Newtonian fluid should be a good strategy to tackle these problems.