Hot-pressing Process Research Articles

High-Performance Composite Membranes: Embedding Yttria-Stabilized Zirconia in Polyphenylene Sulfide Fabric for Enhanced Alkaline Water Electrolysis Efficiency.

Due to their excellent alkali resistance and chemical stability, polyphenylene sulfide (PPS) fabric membranes are widely used in alkaline water electrolysis (AWE) for hydrogen production. However, traditional PPS membranes suffer from poor hydrophilicity, low airtightness, and high area resistance, resulting in high energy consumption and reduced safety in industrial applications. This study addresses the aforementioned issues by coupling 3-(2,3-epoxy propoxy) propyl trimethoxy silane (KH560) via self-condensation to the PPS membrane and blending it with self-synthesized yttrium-stabilized zirconia nanoparticles (YSZNPs). The YSZNPs are loaded onto the modified PPS fiber surface through dip-coating and hot-pressing processes, forming a micro-mechanical interlocking structure that enhances the overall performance of the membrane in practical hydrogen production applications. The findings indicate that the developed composite membrane demonstrate outstanding hydrophilicity, minimal area resistance (0.21 Ω cm2), and elevated bubble point pressure (2.93224bar). Significantly, tests on gas purity indicate that the produced hydrogen and oxygen attain purities of 99.90% and 99.75%, respectively, when evaluated at a current density of 1.5 A cm-2. Moreover, after 500h of electrolysis testing in a simulated industrial environment, minimal decline in membrane performance is observed, highlighting the competitive edge of this composite membrane in the current AWE market.

Hot-Pressing Process of Flat-Pressed Wood-Polymer Composites: Theory and Experiment.

The objective of this research was to develop a mathematical model of the hot-pressing process for making flat-pressed wood-polymer composites (FPWPCs). This model was used to calculate and predict the temperature and time required for FPWPC pressing. The model's performance was analysed using the experimental results of hot pressing FPWPCs. It was found that an increase in the content of wood particles led to a rapid increase in the pressing time. The model and experiment showed that the core temperature of the wood-polymer mat remained nearly constant for the first 20-30 s of the hot-pressing process. After this period, this temperature increased rapidly until it reached 100 °C, after which the rate of increase began to decelerate sharply. This transition was more distinct in FPWPCs with a high wood-particle content, while in those with a high thermoplastic-polymer content, it was smoother. Increasing the pressing temperature contributed to a reduction in the time required to heat the FPWPC, as confirmed by both experimental data and the modelling of the hot-pressing process. A decrease in the predicted density of the FPWPC resulted in a directly proportional increase in the time required to heat the mat. Validation of the mathematical model revealed a mean absolute percentage error (MAPE) of only 2.5%, confirming its high precision and reliability. The developed mathematical model exhibited a high degree of accuracy and can be used for further calculations of the time required for FPWPC pressing, considering variable parameters such as pressing temperature, wood-polymer ratio, mat thickness, and density.

Mechanical properties and first-principle calculation investigation of ZrHfNbTa series refractory high entropy alloys prepared by a combined process

ABSTRACT Refractory high-entropy alloys (RHEAs) are widely used in aerospace engine, gas turbine high-temperature components, capacitors and catalysis. The study presents a combined process for preparing ZrHfNbTa series RHEAs. HEAs powders were prepared from metal oxide by molten salt electro-deoxidation process, and the bulk HEAs were prepared by vacuum hot-pressing sintering process. The study aimed to explore the alloying mechanism of mixed metal oxide in molten salt electro-deoxidation process to optimise the properties. The hardness and wear resistance of the bulk alloy were tested. The test results show that the hardness of ZrHfNbTa and VZrHfNbTa bulk RHEAs prepared by this process is 1251 and 1603 HV. According to the friction surface characterisation of bulk alloy, VZrHfNbTa HEA has better wear resistance than ZrHfNbTa. Based on the first-principle calculation results, the doping of V element produces a strong hybridisation of electron orbitals in RHEAs, which can effectively improve the mechanical properties of RHEAs.

Acetylation of wood: understanding the risk of de-acetylation during exposure to elevated temperature

Abstract Acetylation is a breakthrough in wood modification and has been established on industrial scale. However, concerns have been raised regarding the stability of acetylated wood under elevated temperatures, particularly during post hot-pressing processes to manufacture products such as laminated veneer lumber (LVL). At around 150 °C, the added acetyl groups might cleave off (“de-acetylation”) and by that release sorption sites for water. This would increase the moisture uptake of the modified wood. In this study, the impact of hot-pressing at 150 °C on the stability of acetylated beech veneers and LVL was investigated. Fourier transform infrared (FTIR) spectroscopy showed that the chemical composition of acetylated veneers seemed to be unaffected after the heat treatment. Dynamic vapor sorption (DVS) analysis and long-term storing over saturated salt-solutions in miniature climate chambers, indicated no de-acetylation on the basis of negligible changes in wood-water interactions. The number of hydroxyl groups of heat-treated acetylated samples was similar to that of not heat-treated ones, indicating the persistence of the effects of acetylation. By the present study, a certain resilience of acetylated wood towards elevated temperature, like it may occur during hot-pressing of acetylated veneers, became apparent and illustrated the thermal stability of this chemical modification approach.

Self-Repairable Carbon Fiber-Reinforced Epoxy Vitrimer Actuator with Multistimulus Responses and Programmable Morphing.

Smart shape-changing structures in aerospace applications are vulnerable to damage in harsh environments. Balancing high mechanical performance with self-repair capabilities poses a challenge due to inherent trade-offs between strength and flexibility. To address this challenge, an asymmetric bilayer-structured actuator was fabricated using commercially available continuous carbon fiber tows (CFs) as the passive layer and a dynamic cross-linked epoxy vitrimer as the active layer. The construction of the vitrimer-CF actuator involves a simple and scalable hot-pressing process, resulting in a tensile strength of 234 MPa and an interfacial bonding strength of 405 N·m-1. This actuator exhibits remarkable deformation capability (210°/7 s) and an efficient self-repair ability under various stimuli, including thermal (60-160 °C), light (0.4-1.0 W·cm-2), electric (2-4 V), and solvent (acetone). By adjustment of the orientation angle of CFs, complex left-handed and right-handed curling structures can be achieved. Leveraging the insights from photothermal/electrothermal actuation mechanisms, a quadruped crawling robot is developed capable of crawling 4 cm with a single light illumination. The actuator can lift objects 45 times its weight when subjected to light stimuli. Additionally, a flap actuator is constructed to achieve an angle change of 63° within 10 s under an electric stimulus, enabling remote control over the aircraft flight angle. These results demonstrate the potential of the vitrimer-CF actuator for advanced applications in intelligent aerospace structures.

Numerical Studies of Influencing Factors on the Homogeneity of the Powder Mixture during the Powder Spreading Process of Powder Bed Fusion–Laser Beam/Metal

Recent studies have focused on the alloying of nitrogen (N) in high‐alloy stainless steels by powder bed fusion–laser beam/metal (PBF‐LB/M). However, N‐induced pore formation remains a challenge. To overcome this, a combined PBF‐LB/M and hot isostatic pressing (HIP) process is developed. AISI 304L stainless steel powder was mixed with silicon nitride (Si3N4) powder and processed by PBF‐LB/M, allowing partial retention of Si3N4. This helps to maintain sufficient N content while reducing pore formation. The microstructure is then homogenised by HIP. A major challenge of this process is to maintain the homogeneity of the deposited powder mixture on the powder bed to ensure a consistent N content in the final products. This study combines experimental and numerical methods to address this issue: scanning electron microscopy is used to characterize the microstructure and map the local N content, while various numerical studies based on the discrete element method are carried out to investigate the effects of layer thickness, substrate surface roughness, and powder properties on the intermediate product. The numerical approach effectively predicts the N content distribution and homogeneity on the powder bed. The models are validated with experimental data and optimal process conditions for PBF‐LB/M are identified.

Tunning Pr to achieve ultra-high magnetic properties of anisotropic nanocrystalline (Sm,Pr)Co5 magnets

In this study, we reported on the bulk anisotropic nanocrystalline Sm1-xPrxCo5 (x = 0.2–0.6) magnets aimed at achieving excellent energy products. Through a combination of advanced processing techniques, including melt spinning, hot pressing, and hot deformation process, bulk magnets with a fine nanocrystalline structure were successfully synthesized. The results revealed that the substitution of Pr strengthened the c-axis texture and the saturation magnetization, facilitating the enhancement of remanence (Mr) and maximum magnetic energy product [(BH)max]. However, Pr substitution decreased the coercivity (Hci) due to the reduced magnetocrystalline anisotropy field. Excellent magnetic properties are obtained for Sm0.4Pr0.6Co5 magnets with the (BH)max of 23.2 MGOe and Hci of 11.8 kOe. The prepared (Sm,Pr)Co5 magnets with different Pr contents have essentially the same microstructure with RECo5 main phase grains of about 400 nm in diameter and fine dispersed rare earth-rich nanoprecipitates. Our findings can provide reliable reference for manufacturing nanocrystalline permanent magnet materials and promote the development of rare earth permanent magnet new materials.

Wave-transparent and eco-friendly flame-retardant phosphorus-based phthalonitrile/quartz composites by a synchronized self-curing strategy with cyano and alkynyl groups

The robust human–machine interaction systems of the aerospace industry necessitate the development of thermal resistant wave-transparent composites, with a pivotal focus on organic resin matrix. However, enhancing the heat resistance of such materials while preserving other critical attributes has been a formidable challenge. In this study, a novel designed strategy of a dual-curing functional phosphorus-based phthalonitrile monomer (P-ALK-PN) has been proposed. The optimized curing temperatures for intra- or intermolecular Diels-Alder reactions of alkynyl groups and polyaddition reaction of cyano groups resulted in a homogeneous and highly crosslinked N-enriched phthalonitrile system. After curing at 450 °C, the resin, namely P-ALK-PN-450 °C, demonstrated exceptional thermal stability (T5% = 644 °C), thermo-oxidative stability (T5% = 554 °C), and char yield at 800 °C (90.7 % in N2 and 67.5 % in air). Their quartz fiber reinforced composites (P-ALK-PN/QFs) were subsequently fabricated by the hot-pressing process. Upon post-curing at 420 °C, P-ALK-PN-420 °C/QF displayed elevated glass transition temperature (550 °C), flexural strength (319 MPa), and relatively low dielectric properties with a dielectric constant (Dk) of approximately 4.2 and a dissipation factor (Df) less than 0.02 across a wide temperature ranging from 25 °C to 600 °C. Especially, it exhibited excellent flame retardancy (only a 6.7 % weight loss at ambient temperatures exceeding 1300 °C for 200 s) as well, stemming from release of eco-friendly inert gases (NH3) and formation of a graphitized protective layer during pyrolysis. These promising results highlight the potential applications of P-ALK-PN resins in aerospace and high-performance engineering fields.

Study on the Thermal Condensation Mechanism of Dehydrogenated Polymer (DHP) and Glucuronic Acid.

The preparation of traditional wood-based panels mostly uses adhesives such as urea-formaldehyde resin and phenolic resin, which not only consumes petrochemical resources but also releases formaldehyde, posing potential health risks to the human body. Lignin, a natural adhesive in plant cells, is characterized by high reactivity, and it is expected to aid in the development of a new generation of green formaldehyde-free adhesives. However, current studies of lignin adhesives have revealed that while strides have been made in reducing formaldehyde emissions, its residual presence remains a concern, an issue which is compounded by inadequate water resistance. Dehydrogenated Polymer (DHP) has a lignin-like structure and good water resistance, offering a new option for the development of formaldehyde-free adhesives. In this paper, DHP and glucuronic acid were reacted with each other in a simulated hot-pressing environment to obtain DHP-glucuronic acid complex, and then the structure of the complex was characterized by infrared nuclear magnetic resonance to verify whether DHP can be efficiently connected with hemicellulose components under hot-pressing conditions. The results showed that the thermal condensation reaction of DHP and glucuronic acid can generate ester bonds at the Cα position in a simulated hot-pressing environment. This paper explores the thermal condensation mechanism of DHP and glucuronic acid, which is helpful for understanding the bonding process between adhesives and components of wood-based panels in the hot-pressing process, and provides key theoretical support for the design of more sustainable lignin adhesives.

Influence of hot-pressing temperature and density on the physical and mechanical properties of bamboo scrimber

Bamboo scrimber (BS) has been widely used as a high-performance engineering composite in construction and outdoor applications, typically employing a thermosetting adhesive that requires hot-pressing. Previous studies have focused on the effects of resin content and BS curing temperature, often overlooking the self-bonding of bamboo during the hot-pressing process. This study investigated the impact of hot-pressing temperature and density on the physical and mechanical properties of BS containing phenol–formaldehyde resin, with a particular focus on regulating BS self-bonding by adjusting these parameters. The study also examined the effects on the chemical composition and pore structure of BS. The results showed that increasing the hot-pressing temperature from 140 to 180 °C broke unstable bonds in the hemicellulose, cellulose, and lignin components of the BS, leading to new crosslinks through dehydration and thermal degradation reactions. This process enhanced self-bonding, improved water resistance, and resulted in different surface colors. Raising the density from 0.9 to 1.3 g/cm3 made the density distribution of BS more uniform and reduced the size and number of internal pores. These characteristics promoted interfacial bonding and impeded water flow through the material, thereby enhancing its water resistance and mechanical properties. This study elucidates the mechanism behind the performance enhancement of BS and offers insights for its low-cost and environmentally friendly production.

Improved mechanical properties and thermal conductivity of laser powder bed fused tungsten by using hot isostatic pressing

In this study, the microstructure evolution, mechanical properties and thermal conductivity of laser powder bed fused tungsten subjected to the subsequent hot isostatic pressing (HIP) processes with natural cooling (NC) and ultra-rapid quenching (URQ) were investigated. The results showed that the relative density was significantly improved after HIPping regardless of the cooling rates. The HIP-URQ treatment led to a near defect-free component with increased recrystallization and reduced dislocation density. The enhanced comprehensive mechanical properties, including the ultimate compressive strength of 1180 MPa without sacrificing microhardness was achieved for the HIP-URQ sample. Furthermore, the highest thermal conductivity of 168.6 W/(m·K) related to the densification behaviour and microstructure evolution during the HIP treatments was reported.

Tailoring the additional content of short carbon fiber in the reduced graphene oxide-Cu self-lubricating composites for enhanced mechanical and tribological performance

The reduced graphene oxide-Cu self-lubricating composites with short carbon fiber fillers were fabricated by powders wet-mixing combined with hot-pressed sintering process. The impacts of short carbon fiber content on microstructure, mechanical and tribological performance of reduced graphene oxide-Cu composites were characterized. The reduced graphene oxide/carbon fiber hybrid fillers were randomly distributed in the sintered bulk compacts. The hybrid filled composites achieved enhancement in mechanical and tribological properties. With increasing carbon fiber content, hardness and compressive yield strength of the prepared composites were increased, and both friction coefficient and wear rate showed a constant decrease trend under different loads. Owing to the synergy effect of reduced graphene oxide/carbon fiber hybrid lubricant fillers during sliding together with the greatly enhanced hardness and yield strength, up to 0.6 wt% carbon fiber incorporation resulted a lowest friction coefficient and decreased wear rate. Randomly distributed reduced graphene oxide/carbon fiber hybrid fillers provided the lubrication to reduce friction and wear for Cu matrix.

Microstructure evolution and property characteristics in hot-pressed Mo-W-Cu refractory functional alloys with varying tungsten content

Mo-W-Cu refractory functional alloys (RFAs), combining property advantages of MoCu and WCu alloys, have great application potential in microelectronics, aerospace technology, and military equipment due to their excellent electrical and thermal conductivity, low coefficient of thermal expansion, and high-temperature properties. W content in the alloy is a key factor influencing these properties. However, there is a lack of systematic investigation on the microstructure and properties of hot pressing (HP) processed Mo-W-Cu RFAs with different W contents these days. In this study, Mo-W-20Cu alloys with varying W content of 0–50 wt% RFAs are prepared by mechanical activation (MA) followed by hot pressing. The effect of W content on the microstructure and properties of the alloy is investigated in detail. The results show that all Mo-W-Cu RFAs mainly consist of Mo phase, W phase, and Cu phase after adding W. The microstructure observation shows that the Cu powder particles undergo a plastic deformation during the HP processing, resulting in the closure of the pores and the good metallurgical bonding with Mo phase and W phase at a relatively low temperature. Transmission electron microscopy (TEM) determination indicates that the MoCu phase interface and that of WCu both possess a semi-coherent structure. The property measurements demonstrate that the electrical and thermal conductivity properties of Mo-W-Cu RFAs continuously increase with W content rising while the relative densities of all the alloys are over 94 %. This study can provide a valuable theoretical and technological guidance for the investigation on preparation, microstructure, and properties of high-performance RFAs.

Functionalized cellulose-based adhesive with epoxy groups having high humidity resistance performance

Sustainable and environment friendly natural-based adhesive has been considered as an optimum alternative of industrial adhesive which is non-renewable and harmful to health. Cellulose is the most abundant natural polymer in nature and has potential applications in the field of adhesives. However, the inherent hydrophilic nature of cellulose-based adhesive significantly challenges its use in high humidity environments. In this paper, a highly hydrophobic and anti-swelling cellulose-based adhesive was prepared by epoxy modification of microcrystalline cellulose (MCC). The simultaneous enhancement of adhesive and cohesive properties is achieved through the reaction of epoxy groups with the hydroxyl groups from the wood and adhesive during the hot-pressing process. Prepared adhesive has excellent properties in extremely humid environments. The dry bonding strength of the prepared adhesive reached 6.02 ± 0.26 MPa, while the wet bonding strength was 4.78 ± 0.21 MPa after immersed in water at 63 °C for 3 h. Furthermore, the bonding strength remained largely stable in 90 % atmospheric humidity. The adhesive has a certain universality, which can bond to substrates such as aluminium, iron, and glass. This study presents an innovative approach to the manufacturing of cellulose-based adhesive with enhanced bonding performance and exceptional water resistance.

The Emission Characteristics of VOCs and Environmental Health Risk Assessment in the Plywood Manufacturing Industry: A Case Study in Shandong Province

The current emission characteristics of volatile organic compounds (VOCs) in the plywood manufacturing industry are not yet clearly understood, and their impact on occupational health warrants attention. This study examines VOC concentrations in adhesive-coating and hot-pressing workshops, aiming to discern the emission characteristics and evaluate the health risks to workers. The calculated VOC emission factors range from 1.5 to 3.6 g/m3 for plywood, and an average total VOC concentration of 954.17 μg/m3 is observed. Hot pressing (336.63 μg/m3) and adhesive coating (276.24 μg/m3) substantially contribute to organized and unorganized emissions, respectively. Oxygenated VOCs (OVOCs) (50.79%) predominate, followed by alkanes (16.22%) and halohydrocarbons (15.81%). Formaldehyde, acetone, and acetaldehyde are most prevalent in organized emissions, while dichloromethane, formaldehyde, and methyl methacrylate are dominant in unorganized emissions. Ozone formation potential (OFP) values range from 905.04 to 1822.35 μg/m3, with notable contributions from formaldehyde, methyl methacrylate, and acetaldehyde. Health risk assessments using the total lifetime cancer risk (T-LCR) values suggest potential cancer risks for identified VOCs, particularly formaldehyde in the hot-pressing process. These findings will contribute valuable insights for regional-scale VOC pollution control and offer guidance for minimizing environmental impact and improving occupational health and safety within the plywood manufacturing industry.

Influence of grain size and grain edge phase on the flexural strength of aluminum nitride ceramics with Y2O3 sintering additive

The necessity for efficient heat dissipation compels AlN packaging materials towards a thinner profile. In response to the ensuing concerns regarding the reliability of strength, the effects of the grain edge phases and grain size on flexural strength are investigated in this study. Different preparation processes, including (hot-pressed sintering, pressureless sintering, and annealing) are employed to prepare AlN ceramics with different grain edge phases and grain sizes. After classifying the morphology of the grain edge phases and fitting the Hall-Petch relationship, it is found that the grain edge phases had a more significant influence on the flexural strength. Depending on the morphology, the negative effects can be divided into three degrees. While the finer grain size proves advantageous for the flexural strength. Consequently, in the non-additive system, the flexural strength of AlN ceramic is 422 MPa, with an average grain size of 8.47 μm. For the additive-doped system, the maximum flexural strength can reach 532 MPa, which can be attributed to the limited average grain size resulting from the hot-pressed sintering process, approximately 1.32 μm. These results could potentially be employed in the microstructural design of high-strength AlN ceramics.

Conversion of Bamboo into Strong, Waterproof, and Biodegradable Thermosetting Plastic through Cell Wall Structure Directed Manipulation.

Reckoning with the global environmental challenge of plastic pollution, particularly in terms of recycling and biodegradation of thermosetting plastics, sustainable alternatives are imperative. The rapidly growing and eco-friendly material bamboo has great potential as a sustainable resource; however, it lacks the inherent self-bonding and plasticity characteristics found in plastics. This study presents a feasible approach to enhance the plasticity of bamboo by selectively removing part of its lignin and disrupting the crystalline structure of cellulose. Concurrently, this process selectively transforms hydroxyl groups into highly reactive dialdehyde groups to increase the reactivity of bamboo. The resulting activated bamboo units undergo a hot-pressing process to transform them into a type of thermosetting plastic (ABTP). The ABTP is highly moldable, and its color can be precisely regulated by adjusting the lignin content. Additionally, it exhibits exceptional solvent and water resistance, along with notable mechanical properties, including a tensile strength of 50 MPa, flexural strength of 80 MPa, flexural modulus of 5 GPa, and Shore D hardness approaching 90. Furthermore, the bamboo-derived plastic exhibits exceptional reusability and biodegradability, presenting feasible and environmentally friendly alternatives to conventional plastics while harnessing the sustainable development potential of bamboo.

A Comparative Study of Airbag Covers for Automotive Safety Using Coconut Shell Fiber/PP Composite Materials

In this study, we compared the physical properties of coconut fiber/polypropylene (PP) composite materials with coconut fiber as a reinforcing agent, produced through a hybrid injection molding process and a layered hot-pressing process. Through comparative experiments, the mechanical properties of both the hybrid injection-molded and layered hot-pressed materials were validated. The results indicated that, when using a coconut fiber content of 5%, the layered hot-pressed composite material exhibited optimal comprehensive performance. Specifically, its tensile strength reached 25.12 MPa, showing a 37.6% increase over that of pure PP materials of the same brand and batch. Its tensile modulus was 1.17 GPa, representing an 11.4% decrease. Additionally, its bending strength was 35.94 MPa, marking a 49.8% increase, and its bending modulus was 2.69 GPa, which is nearly double that of pure PP materials. Furthermore, through Creo modeling and an ANSYS simulation analysis, it was verified that this material could be applied to airbag covers in the field of automotive safety. This study confirmed that layered hot-pressed coconut fiber/PP composite materials exhibit superior mechanical properties to traditional materials and injection-molded composite materials, making them more suitable for airbag covers.

Waste ramie fiber/EVA composites with wideband sound-absorbing performance with mixing and foaming process

Increasing noise pollution and ramie fibers waste resource problems need to be solved urgently. In order to resolve the problems, the porous sound-absorbing composites with high sound-absorbing performance were prepared by using waste ramie fibers as reinforcement materials, vinyl acetate copolymer (EVA) as matrix materials, azodicarbonamide(AC) as foaming agent, ZnO as auxiliary foaming agent, and dicumyl peroxide (DCP) as cross-linking agent, which were mixed in a two-stick mixer according to a certain ratio and then hot-pressing process. The process conditions were optimized using single factor analysis. Under the optimal process conditions, the sound-absorbing composites had a maximum sound absorption coefficient (SAC) of 0.72, an average SAC of 0.37, and a noise reduction coefficient (NRC) of 0.41. The sound absorption performance grade reached level III, and the sound absorption performance was excellent in the frequency range of 600 ∼ 6300 Hz. The introduction of foaming agents made the composites with more pores, and the average SAC of foamed composites increased by 346 %(compared with the unfoamed composites). Then, the sound-absorbing mechanism was analyzed. This study presents a novel approach to the recycling and reusing of the waste ramie fibers. It also provides a theoretical and experimental basis for the development of sound-absorbing composites with wider sound absorption band, larger (sound absorption coefficient) SAC and wider application, which is of great significance for sound absorption in the building fields.

The influence of the hot-pressing process on the mechanical properties of continuous aramid fiber-reinforced PA12 composites

Abstract Hot-pressing post-treatment can effectively improve the mechanical properties of composite specimens. In order to improve the impact resistance of continuous aramid fiber-reinforced nylon 12 (CAF/PA12) composites, the effect of hot-pressing parameters on the interlaminar shear strength of the composite was studied. The effects of hot-pressing temperature, hot-pressing time, and hot-pressing pressure on the interlaminar shear strength of composite formed specimens were studied by single factor test. Based on the optimized parameters of hot-pressing, the influence of hot-pressing on low-speed impact performance was analyzed. The results shown that the interlaminar shear strength first increased and then decreased with the increase of hot-pressing temperature and pressure. With the extension of hot-pressing time, the interlaminar shear strength continued to increase. When the hot-pressing parameters were 170°C, 30 min, and 600 kPa, the shear strength and specimen quality were the best. Under this hot-pressing process, the low-speed impact performance was increased by 36.0%. In this paper, the research content of the hot-pressing process of composite materials was expanded, which provided a reference for the research of impact resistance of continuous aramid fiber-reinforced PA12 composite materials.