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学者姓名：郑玉婴
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Abstract ：
Antistatic nylon-6 (PA6) composites have attracted considerable attention due to their tailored properties for electronics, textiles, and automotive applications. In this paper, the antistatic PA6 composites comprising with polypropylene (PP), aminated multi-walled carbon nanotubes (MWCNTs-NH2) and aminated carbon black (CB-NH2) were prepared by melt blending and compression molding. In the composite system, PP was used as the co-matrix to assist the phase separation of PA6. MWCNTs-NH2 and CB-NH2 were introduced as conductive fillers. All composites showed good thermal stability with the T5 % higher than 376 degrees C and the composites containing fillers showed higher residues after thermal degradation due to the good thermal stability of MWCNTs-NH2 and CB-NH2. The DSC and XRD results indicated that the crystallization properties of the composite materials were determined by PA6 and PP rather the conductive fillers. In general, the introduction of conductive fillers decreased the mechanical properties but effectively improved the conductivity of the composites and then the antistatic properties. Besides, the antistatic analysis and mechanical test denoted that MWCNTs-NH2 and CB-NH2 showed synergistic effect on improving the antistatic and mechanical properties of the composites, which was more evident at high MWCNTs-NH2 quantity. The micromorphologies obtained by SEM first confirmed the ductile fracture of these composites, and then disclosed a two-phase structure of PA6 and PP polymer matrix, where the conductive fillers were found in the PA6 phase. Considering both mechanical and antistatic properties, the composite (PCNB-3) containing both 3 phr MWCNTs-NH2 and CB-NH2 was proposed for the antistatic PA6 composite.
Keyword ：
Antistatic composites Antistatic composites Carbon nanomaterials Carbon nanomaterials Hybrid conductive fillers Hybrid conductive fillers PA6 PA6 Phase separation Phase separation
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| GB/T 7714 | Liu, Xuelian , Li, Qian , Zheng, Yuying et al. Polypropylene assisted phase separation nylon-6 antistatic composites: MWCNTs-NH2 and CB-NH2 as hybrid conductive nanofillers [J]. | POLYMER , 2025 , 328 . |
| MLA | Liu, Xuelian et al. "Polypropylene assisted phase separation nylon-6 antistatic composites: MWCNTs-NH2 and CB-NH2 as hybrid conductive nanofillers" . | POLYMER 328 (2025) . |
| APA | Liu, Xuelian , Li, Qian , Zheng, Yuying , Zheng, Weijie . Polypropylene assisted phase separation nylon-6 antistatic composites: MWCNTs-NH2 and CB-NH2 as hybrid conductive nanofillers . | POLYMER , 2025 , 328 . |
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Slow rebound polyurethane foam (SPUF) has developed rapidly because of its excellent performance in sound insulation, energy absorption, and tactile sensation. However, the friction-induced electrostatic charge accumulation occurs easily due to its high resistivity. In this paper, dimethyl octadecyl hydroxy ethyl ammonium nitrate (SN) intercalated reduced graphene oxide (SN-RGO) were prepared as the conductive agent. The antistatic slow rebound polyurethane foam (ASR-PUF) was prepared with SN-RGO/carbon black as antistatic system and silicone-modified polyethylene glycol (Si-APEG) as low temperature resistant agent. The structures of SN-RGO were investigated by Fourier transform infrared spectra (FT-IR), wide-angle X-ray diffraction (WAXD), and scanning electron microscope (SEM), respectively. The effects SN-RGO on the structures, mechanical properties, low-temperature resistance, and antistatic property of ASR-PUF were studied. It was found that SN-RGO acts as heterogeneous cell nucleating agent, which slightly increases the apparent core density and slightly decreases the porosity of ASR-PUF. The addition of SN-RGO increases both the tensile strength and elongation at break of ASR-PUF, and has little effect on the temperature sensitive index. The surface resistance of ASR-PUF decreases to 1.1 x 108 Omega with a SN-RGO content of 4 wt%, thereby achieving an antistatic effect.Highlights SN-RGO acts as heterogeneous cell nucleating agent in PU foaming. SN-RGO/carbon black provide good antistatic property and mechanical properties without affecting the low-temperature resistance of ASR-PUF. ASR-PUF with an appropriate content of SN-RGO exhibits excellent comprehensive performance.
Keyword ：
antistatic antistatic intercalated reduced graphene oxide intercalated reduced graphene oxide low-temperature resistance low-temperature resistance polyurethane foam polyurethane foam
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| GB/T 7714 | Cao, Jing , Wang, Li , Zheng, Yuying . Preparation of antistatic slow rebound polyurethane foam based on dimethyl octadecyl hydroxy ethyl ammonium nitrate intercalated reduced graphene oxide/carbon black antistatic system [J]. | POLYMER ENGINEERING AND SCIENCE , 2025 , 65 (5) : 2192-2202 . |
| MLA | Cao, Jing et al. "Preparation of antistatic slow rebound polyurethane foam based on dimethyl octadecyl hydroxy ethyl ammonium nitrate intercalated reduced graphene oxide/carbon black antistatic system" . | POLYMER ENGINEERING AND SCIENCE 65 . 5 (2025) : 2192-2202 . |
| APA | Cao, Jing , Wang, Li , Zheng, Yuying . Preparation of antistatic slow rebound polyurethane foam based on dimethyl octadecyl hydroxy ethyl ammonium nitrate intercalated reduced graphene oxide/carbon black antistatic system . | POLYMER ENGINEERING AND SCIENCE , 2025 , 65 (5) , 2192-2202 . |
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Poly (butylene adipate-co-terephthalate) (PBAT) and polylactic acid (PLA) as a biodegradable thermoplastic material have been expected to replace traditional undegradable plastics. However, PBAT resins are highly flammable and have poor thermal stability and lower compressive strength performance. For enhancing PBAT compressive strength, thermal stability, and flame retardancy performance, polylactic acid (PLA) resin was used to mix with the PBAT matrix. Meanwhile, a biomass additive (PA@CS) was prepared through phytic acid (PA) solution as the grinding medium modifying cellulose (CS) particles by the ball milling process. As the PBAT/10PLA/PA@CS foam presented, PA@CS implanted into pore walls which supported the structure integrity of foams and presented the lowest surface temperature when heating at 170 °C for 180 s. The compressive strength of PBAT/10PLA/PA@CS foam with 5 wt% of PA@CS addition reached 1.05 MPa at 20 % strain. During the combustion process, PA@CS, as flame retardants, demonstrated excellent suppressing heat dispassion and fire-resistance performance. For instance, 5 wt% of PA@CS presented the highest ultimate oxygen index (LOI) (27.9 %), and UL-94 V-0 rating. In detail, 5 wt% of PA@CS also reduced the peak of heat release rate (PHRR) from 851.47 kW m−2 to 524.45 kW m−2 by 38 %, total heat release (THR) from 84.34 MJ m−2 to 66.45 MJ m−2 by 21 %. In this work, PA@CS as an efficient biomass flame retardant provided technical support for the development of high-performance compressive strength, thermal insulation, and flame retardancy PBAT/PLA foams. © 2024 Kingfa Scientific and Technological Co. Ltd.
Keyword ：
Catalytic cracking Catalytic cracking Cellophane Cellophane Elastomers Elastomers Foams Foams Premixed flames Premixed flames Reinforced plastics Reinforced plastics Sintering Sintering Supercritical fluid extraction Supercritical fluid extraction
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| GB/T 7714 | Hong, Xiansheng , Li, Yunlong , Zheng, Yuying et al. Constructing a biomass flame retardant for fire-safe, thermal management, and compressive strength application of polybutylene adipate terephthalate/ polylactic acid foams [J]. | Advanced Industrial and Engineering Polymer Research , 2025 , 8 (2) : 251-263 . |
| MLA | Hong, Xiansheng et al. "Constructing a biomass flame retardant for fire-safe, thermal management, and compressive strength application of polybutylene adipate terephthalate/ polylactic acid foams" . | Advanced Industrial and Engineering Polymer Research 8 . 2 (2025) : 251-263 . |
| APA | Hong, Xiansheng , Li, Yunlong , Zheng, Yuying , Li, Qian . Constructing a biomass flame retardant for fire-safe, thermal management, and compressive strength application of polybutylene adipate terephthalate/ polylactic acid foams . | Advanced Industrial and Engineering Polymer Research , 2025 , 8 (2) , 251-263 . |
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A series of boron-doped graphene-supported nanoflower-catalysts (nf-MnOx/BG) were synthesized using an in- situ method to boost intrinsic catalytic performance. The regulation of catalyst structure, morphology, and active sites was systematically researched to explore the promoting factors of catalytic activity. The prepared nf-MnOx/ BG-3 catalyst achieves superior NH3-SCR performance throughout the test process (>= 90% NOx conversion at the temperature ranging from 140 to 280 degrees C), comparable to the current mainstream graphene-based catalyst. The ratios of O alpha/(O alpha + O beta) and Mn4+/Mn3+are effectively increased by boron atom doping, which is strongly associated with excellent catalytic deNOx efficiency. Meanwhile, the boron sites with unpaired electronic structures accelerate the reaction of fast-SCR by promoting oxidation and adsorption of nitrogen oxide species. Interestingly, the boron sites can be used as an additional Lewis acid and adsorbed NO2 site to participate in the low-temperature SCR reaction and effectively improve the low-temperature activity.
Keyword ：
Boron-doped Boron-doped deNO x efficiency deNO x efficiency Fast-SCR Fast-SCR In-situ method In-situ method Nanoflower-catalysts Nanoflower-catalysts
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| GB/T 7714 | Zheng, Weijie , Zhang, Zhiwei , Hong, Xiansheng et al. Boron-doped graphene-based nanoflower-catalyst promoting low temperature NH3-SCR performance: An interesting site [J]. | ENVIRONMENTAL RESEARCH , 2025 , 274 . |
| MLA | Zheng, Weijie et al. "Boron-doped graphene-based nanoflower-catalyst promoting low temperature NH3-SCR performance: An interesting site" . | ENVIRONMENTAL RESEARCH 274 (2025) . |
| APA | Zheng, Weijie , Zhang, Zhiwei , Hong, Xiansheng , Zheng, Yuying . Boron-doped graphene-based nanoflower-catalyst promoting low temperature NH3-SCR performance: An interesting site . | ENVIRONMENTAL RESEARCH , 2025 , 274 . |
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The poor resistance of high-density polyethylene (HDPE) to thermal-oxidative aging and ultraviolet (UV) degradation significantly limits its service life. In this study, the nanocomposite ZnO-AO was synthesized using gamma-glycidoxypropyltrimethoxysilane (GPTMS) as a bridging agent, which facilitated the loading of a significant quantity of the hindered phenolic antioxidant (AO) onto the surface of ZnO nanoparticles, and the HDPE/ZnOAO composites were subsequently prepared by melt blending. The results indicated that the combination of ZnO and AO was synergistic, and the more optimized para-substituent structure of AO significantly reduced the hydroxyl bond dissociation energy (BDE) of the hindered phenols, thereby enhancing antioxidant activity. Additionally, the hydroxyl groups on the surface of ZnO were substituted with AO, which improved the particle dispersion. After 400 h of UV aging, HDPE/ZnO-AO retained 78.36 % and 95.92 % of its elongation at break and impact strength, respectively, compared to only 2.25 % and 6.17 % for pure HDPE. After 28 days of thermal- oxidative aging, the carbonyl index of HDPE/ZnO-AO increased by only 0.18, significantly lower than that of HDPE (0.43). Accordingly, the ZnO and AO, covalently linked by GPTMS, demonstrated enhanced performance compared to individual original capabilities, successfully integrating efficient thermal-oxidative stability and UV protection. This study provides a promising approach for the development of long-lasting HDPE composites.
Keyword ：
High-density polyethylene High-density polyethylene Hindered phenolic Hindered phenolic Thermal oxidation stability Thermal oxidation stability Ultraviolet irradiation stability Ultraviolet irradiation stability Zinc oxide Zinc oxide
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| GB/T 7714 | Ai, Jianglai , Zheng, Yuying , Zhang, Jie . Enhanced stabilisation performance of HDPE via siloxane bonded ZnO with phenolic antioxidants [J]. | POLYMER DEGRADATION AND STABILITY , 2025 , 236 . |
| MLA | Ai, Jianglai et al. "Enhanced stabilisation performance of HDPE via siloxane bonded ZnO with phenolic antioxidants" . | POLYMER DEGRADATION AND STABILITY 236 (2025) . |
| APA | Ai, Jianglai , Zheng, Yuying , Zhang, Jie . Enhanced stabilisation performance of HDPE via siloxane bonded ZnO with phenolic antioxidants . | POLYMER DEGRADATION AND STABILITY , 2025 , 236 . |
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The gradual permeation of corrosive mediums, external mechanical damage, and ultraviolet (UV) radiationinduced aging are critical factors contributing to the rapid deterioration of the anticorrosive functionality of polymer coatings. In this study, a two-dimensional anticorrosive enhancement material, fluorinated graphene loaded with zinc oxide nanoparticles (FG@ZnO), was synthesized via the heterogeneous nucleation growth method. This material was then embedded into a polyurethane coating to modify the coating matrix, and a biomimetic lotus leaf-like fine micro-nanostructure was fabricated on the coating surface employing a templating approach. Through this internal-external dual modification strategy, an FG@ZnO/SPU composite coating with multiple protective functions was constructed to offer enduring corrosion protection to the steel substrate. Experimental findings reveal that the composite coating exhibits excellent superhydrophobicity, with a water contact angle as high as 152 degrees. Even after immersion in a 3.5 % NaCl solution for 80 days, the composite coating maintains an exceptionally high low-frequency impedance modulus of 1.332 x 1010 Omega cm2, demonstrating exceptional long-term anticorrosive performance. In instances of coating damage, FG@ZnO markedly relieves the corrosion reaction between the corrosive medium and the steel substrate while suppressing galvanic corrosion. Furthermore, the composite coating demonstrates effective resistance against UV radiation-induced aging effects. These exceptional multiple protective properties are attributed to the internal-external dual modification effect of embedded FG@ZnO and biomimetic lotus leaf hydrophobic modification. This study provides an attractive strategy for preparing polymer composite coatings with multiple protective functions for enduring corrosion protection of metals.
Keyword ：
Barrier properties Barrier properties Corrosion inhibition Corrosion inhibition Internal -external dual modification Internal -external dual modification Multiple protective functions Multiple protective functions Superhydrophobicity Superhydrophobicity UV aging resistance UV aging resistance
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| GB/T 7714 | Zhang, Jie , Zheng, Yuying . Constructing multi-protective functional polyurethane composite coating via internal-external dual modification: Achieving superhydrophobicity, enhanced barrier, corrosion inhibition, and UV aging resistance properties [J]. | PROGRESS IN ORGANIC COATINGS , 2024 , 194 . |
| MLA | Zhang, Jie et al. "Constructing multi-protective functional polyurethane composite coating via internal-external dual modification: Achieving superhydrophobicity, enhanced barrier, corrosion inhibition, and UV aging resistance properties" . | PROGRESS IN ORGANIC COATINGS 194 (2024) . |
| APA | Zhang, Jie , Zheng, Yuying . Constructing multi-protective functional polyurethane composite coating via internal-external dual modification: Achieving superhydrophobicity, enhanced barrier, corrosion inhibition, and UV aging resistance properties . | PROGRESS IN ORGANIC COATINGS , 2024 , 194 . |
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In recent years, loading antioxidants onto inorganic nanoparticles has attracted increasing interest. However, the existing studies not only have low antioxidant loading efficiency, but also ignore the relationship between structural changes and antioxidant properties before and after antioxidant modification, greatly limiting the improvement of the antioxidant properties of composites and their application scope. In this work, we successfully prepared bis-hindered phenolic antioxidants containing silica hydroxyl groups (Bis-mAO) and loaded them onto silicon dioxide (SiO 2 ) to get the nanocomposites (Bis-mAO-SiO 2 ). The melt blending method further prepared the corresponding polyphenylene sulfide (PPS)/Bis-mAO-SiO 2 composites. The results showed that the higher antioxidant loading and more suitable antioxidant structure made Bis-mAO-SiO 2 possess excellent antioxidant properties. The prepared PPS/Bis-mAO-SiO 2 composites remained stable under high temperatures and oxygen environments. Impressively, the maximum weight loss rate temperature of PPS/Bis-mAO-SiO 2 was increased by 11.60 degrees C compared to that of PPS, and after accelerated thermal oxidation at 220 degrees C for 24 h, the relative intensity ratio between O and C of PPS/Bis-mAO-SiO 2 only increased to 0.086, much lower than 0.132 for PPS. Moreover, the viscosity of PPS/Bis-mAO-SiO 2 only increased by 29.05 % and 88.75 % after accelerated thermal oxidation at 220 degrees C for 12, 24 h. Compared, PPS ' s viscosity increased substantially by 79.22 % and 250.3 %, respectively. This meant that the Bis-mAO-SiO 2 successfully achieved a synergistic integration of high antioxidant properties and thermal stability, implying that the work offered a strategy for fabricating hightemperature resistant antioxidant composites.
Keyword ：
Hindered phenolic Hindered phenolic Polyphenylene sulfide Polyphenylene sulfide Rheological properties Rheological properties Silicon dioxide Silicon dioxide Thermal oxidation stability Thermal oxidation stability
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| GB/T 7714 | Cai, Weilong , You, Jian , Wang, Wei et al. Double-hindered phenolic SiO 2 composites with excellent oxidation resistance and thermal stability for enhanced thermal oxidation stability of PPS [J]. | CHEMICAL ENGINEERING JOURNAL , 2024 , 487 . |
| MLA | Cai, Weilong et al. "Double-hindered phenolic SiO 2 composites with excellent oxidation resistance and thermal stability for enhanced thermal oxidation stability of PPS" . | CHEMICAL ENGINEERING JOURNAL 487 (2024) . |
| APA | Cai, Weilong , You, Jian , Wang, Wei , Chen, Huaiyin , Liu, Longmin , Ma, Yuhan et al. Double-hindered phenolic SiO 2 composites with excellent oxidation resistance and thermal stability for enhanced thermal oxidation stability of PPS . | CHEMICAL ENGINEERING JOURNAL , 2024 , 487 . |
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The rapid progress in miniaturization and integration of semiconductor power devices has made heat dissipation a critical concern in the development of high-performance semiconductor devices, thereby increasing the demands for the heat transfer efficiency of polymer composites. To address this issue, an efficient three-dimensional (3D) heat conduction network structure is constructed in the polymer matrix by leveraging the mutual reaction of amino and epoxy groups on the surface of the filler treated by coupling during the melt mixing process, this approach leads to an enhancement in the thermal conductivity of the composites. First, the inert surfaces of graphene nanosheets (EX-G) and carbon fibers (CF) are coated with polydopamine (PDA) to form active sites. Subsequently, the graphene (EX-G), alumina (Al2O3), and carbon fiber (CF) are treated with an amine coupling agent (KH550) and epoxy coupling agent (KH560), respectively. Notably, at a filler content of 25 wt%, the thermal conductivity (TC) of the composites increases by approximately 282% compared to pure nylon 6. This research contributes novel insights into the field of thermally conductive polymer composites.Highlights The surface of the EX-G and CF covered by PDA generates active sites. Fillers reduce the interface thermal resistance through chemical bonds. Fillers surface reaction builds a 3D thermal conductive network. 3D network structure can significantly improve the TC of composites. Only 25 wt% of hybrid fillers in a 282% increased TC of composites. Schematic illustration of heat flow conduction through a 3D thermally conductive structure in a composites. image
Keyword ：
composites composites coupling agent coupling agent non-covalent functionalization non-covalent functionalization thermal conductivity thermal conductivity three-dimensional structural network three-dimensional structural network
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| GB/T 7714 | Li, Qian , Rao, Ranyi , Hong, Xiansheng et al. Thermal conductive nylon 6 composites using hybrid fillers to construct a three-dimensional thermal conductive network [J]. | POLYMER COMPOSITES , 2024 , 45 (7) : 6169-6183 . |
| MLA | Li, Qian et al. "Thermal conductive nylon 6 composites using hybrid fillers to construct a three-dimensional thermal conductive network" . | POLYMER COMPOSITES 45 . 7 (2024) : 6169-6183 . |
| APA | Li, Qian , Rao, Ranyi , Hong, Xiansheng , Hu, Hanwen , Li, Yu , Gong, Ziyu et al. Thermal conductive nylon 6 composites using hybrid fillers to construct a three-dimensional thermal conductive network . | POLYMER COMPOSITES , 2024 , 45 (7) , 6169-6183 . |
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Cleanup of oil spills has become one of the most challenging tasks in recent years, as marine oil spills have had a great negative impact on human health and the ecological environment. This also urgently requires the development of new materials and methods with superhydrophobic properties for oil-water separation. As new porous materials, metal-organic frameworks (MOFs) have attracted much attention due to their unique structures and fascinating properties. However, powdered MOF materials are difficult to recycle, and therefore, suitable substrates need to be selected to construct superhydrophobic composites. The surface hydroxyl groups of cellulose fibers offer great possibilities for their superhydrophobic preparation. In this paper, HDTMS-UiO-66@CFs composites with superhydrophobicity were strategically synthesized by in-situ growth of Zr(IV)-based MOFs linked to hexadecyltrimethoxysilane (HDTMS) on cellulosic fibers (cotton fabric) by using a hydrothermal synthesis method. The HDTMS-UiO-66@CFs composites have a water contact angle of 172 degrees and the absorption capacity of light oil and heavy oil is more than 1100%, and the oil-water separation efficiency is as high as 96%. Due to the in-situ growth of the HDTMS-UiO-66 material on cotton fibers, which makes the material more resistant and stable, the material can still maintain its superhydrophobic properties in various harsh environments and after repeated use. Therefore, the newly developed HDTMS-UiO-66@CFs composites have a high potential as novel adsorbent materials for cleaning up offshore oil spills and other applications.Highlights In-situ growth of superhydrophobic metal-organic frameworks (MOF) particles on cellulose fibers. The porous structure of hexadecyltrimethoxysilane (HDTMS)-UiO66 plays a key role in hydrophobicity. HDTMS-UiO66@CFs are chemically stable and have long-term durability. Schematic diagram of the preparation process and properties of superhydrophobic zirconium-based metal-organic framework/cellulose fiber composites. image
Keyword ：
cotton fabrics cotton fabrics hydrophobicity hydrophobicity oil-water separation oil-water separation zirconium-based metal-organic framework zirconium-based metal-organic framework
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| GB/T 7714 | Hu, Hanwen , Li, Yu , Hong, Xiansheng et al. A superhydrophobic zirconium-based metal-organic framework/cellulose fiber composite material [J]. | POLYMER ENGINEERING AND SCIENCE , 2024 , 64 (5) : 1981-1992 . |
| MLA | Hu, Hanwen et al. "A superhydrophobic zirconium-based metal-organic framework/cellulose fiber composite material" . | POLYMER ENGINEERING AND SCIENCE 64 . 5 (2024) : 1981-1992 . |
| APA | Hu, Hanwen , Li, Yu , Hong, Xiansheng , Li, Qian , Rao, Ranyi , Gong, Ziyu et al. A superhydrophobic zirconium-based metal-organic framework/cellulose fiber composite material . | POLYMER ENGINEERING AND SCIENCE , 2024 , 64 (5) , 1981-1992 . |
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A thermal conductive structural adhesive (TCSA) plays a crucial role in battery performance and safety. TCSA made of polyurethane (PU) has not only a good thermal conductivity but also good mechanical strength and substrate bonding strength. However, it has to be cost-effective and easy to be prepared. This work aims to synthesize a series of castor oil-based PU TCSAs with different amounts of thermal conductive powder using commercially available castor oil polyols, isocyanates, Al2O3, and additives. The shear strength of the TCSA containing 88% thermally conductivity powder reached 5.6 MPa, which was similar to that without the thermal conductivity fillers, but its toughness significantly decreased. Its thermal conductivity was as high as 1.8 W/mK, and it was thermally stable below 270 degrees C. Preparation process of castor oil based TCSA and application scenarios in new energy batteries. image
Keyword ：
adhesives adhesives biodegradable biodegradable coatings coatings conducting polymers conducting polymers polyurethane polyurethane
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| GB/T 7714 | Ding, Ao , Liu, Guang , Xu, Pingfan et al. Design of castor oil-based polyurethane thermal conductive structural adhesive for new energy batteries [J]. | JOURNAL OF APPLIED POLYMER SCIENCE , 2024 , 141 (24) . |
| MLA | Ding, Ao et al. "Design of castor oil-based polyurethane thermal conductive structural adhesive for new energy batteries" . | JOURNAL OF APPLIED POLYMER SCIENCE 141 . 24 (2024) . |
| APA | Ding, Ao , Liu, Guang , Xu, Pingfan , Wang, Yixin , Zheng, Yuying , Luo, Yaofa et al. Design of castor oil-based polyurethane thermal conductive structural adhesive for new energy batteries . | JOURNAL OF APPLIED POLYMER SCIENCE , 2024 , 141 (24) . |
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