PROPELLANTS EXPLOSIVES PYROTECHNICS
·
2023
·Vol. 48
·期 4
·e202200154
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IF 1.8
Chengcheng Zeng,Zongwei Yang,Jiahui Liu,Ling Ding,Shilong Hao,Feiyan Gong,Zhijian Yang
Low melting point compound MTNP was usually adopt to form co-crystal explosive with CL-20 to reduce sensitivity, and the co-crystal may have the potential of green engineering application. Improving mechanical properties of co-crystals explosive is one of the effective ways to broaden its practical application. In this work, CL-20/MTNP energetic co-crystal was selected to be coated by polydopamine (PDA) and neutral bonding agent (NBA), with enhanced mechanical properties and developed interfacial strength between crystal and binder. The TG-DSC curve showed that thermal decomposition of co-crystal explosives divided into two steps, and the melting point delayed to 210 °C compared with that of MTNP. After surface modification, the storage modulus of PBX was increased by more than 20 % at the temperature range of (25–120) °C, and creep strain was also effectively reduced. The Brazilian and compressive strength of PDA coating samples increased by 69.89 % and 210.53 % respectively, as well as improved elongation, leading to increased fracture toughness. Here, the highlighted modification on the surface of CL-20/MTNP co-crystal can be used as a reference insight to improve the mechanical properties of new explosives.
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JOURNAL OF SOLID STATE ELECTROCHEMISTRY
·
2022
·Vol. 27
·期 3
·679-694
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IF 2.747
Tai Xiaoming,Liu Cansen,Chen Wanlin,Mai Yongjin,Zhang Liuyan,Wu Xinghua,Jie Xiaohua
Rubber tires, as an important part of automobiles, are produced by molding operation under molten temperature and high pressure. However, mold fouling during the vulcanization process is a rock-ribbed problem that not only leads to the loss in productivity and degradation of product quality but also results in severe accidents and enormous economic losses. In this work, a promising Co-Mo/CeO 2 composite coating was electroplated and investigated to solve the mold fouling problem. The effect of CeO 2 content on the surface morphology, microstructure, hardness, tribological and electrochemical behavior is systematically studied. With an addition of 10 g/L CeO 2 , the Co-Mo/CeO 2 composite coating not only possesses the highest microhardness, the best wear and corrosion resistance but also features hydrophobicity and remarkable mold antifouling performance. This study offers a new strategy for producing composite coatings with excellent performance to reduce mold fouling in practical tire industry applications. Graphical Abstract
Co-Mo/CeO 2 composite coatings with excellent corrosion and wear resistance as well as low surface energy were simply electrodeposited and applicated for antifouling in tire mold for the first time.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2023
·
IF 22.1
Baoyu Wang,Mingrui Li,Songdang Zhang,Hongguo Wu,Yuhe Liao,Hu Li
Finite size effect is closely correlated with heterogeneous catalytic activity and selectivity as reducing the metal to a few nanometers, but may suffer from deficient active sites for cascade reactions. Here, a type of dual-size heterogeneous N-doped cobalt catalysts (Co SAs-NPs /NC(n)) with the coexistence of Co single-atoms (Co-SAs) and Co nanoparticles (Co-NPs) were prepared for efficient synthesis of benzimidazoles (up to 91% yield) from 2-nitroanilines and bio-based alcohols via cascade hydrogen transfer-dehydrogenative cyclization. Experimental results and density functional theory calculations suggested that the bio-alcohol dehydrogenation mainly occurs at Co-SAs sites, while Co-NPs sites remarkably facilitate the subsequent reduction of nitro species, indicating the synergistic effect between Co-SAs and Co-NPs in the coupled hydrogen transfer process. The Co SAs-NPs /NC(0.25) catalyst can be recycled and applied to a wide range of substrates (28 examples). This catalytic approach based on the metal size effect opens a new route for the direct upgrading of biomass feedstocks involving multiple reactions.
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JOURNAL OF LUMINESCENCE
·
2023
·
IF 3.6
Renping Cao,Caiping Chen,Fangrui Cheng,Ting Chen,Bang Lan,Lan Li,Ru Liu,Jing Wang
In this work, we synthesize Ca 3 Bi(PO 4 ) 3 :Dy 3+ , Ca 3 Bi(PO 4 ) 3 :Eu 3+ , and Ca 3 Bi(PO 4 ) 3 :Eu 3+ , Dy 3+ . The crystal structure, phase purity, and the luminescence properties of samples are investigated, respectively. Ca 3 Bi(PO 4 ) 3 :Dy 3+ under excitation at 350 nm shows yellow emission because of the 4 F 9/2 → 6 H 15/2 , 6 H 13/2 , 6 H 11/2 , and 6 H 9/2 transitions of Dy 3+ . Ca 3 Bi(PO 4 ) 3 :Eu 3+ with excitation at 394 nm emits red-orange emission due to the 5 D 0 → 7 F 1 , 7 F 2 , 7 F 3 , and 7 F 4 transitions of Eu 3+ ion. Ca 3 Bi(PO 4 ) 3 :Dy 3+ , Eu 3+ with excitation at 394 nm mainly shows the emission of Eu 3+ , however, that with excitation at 350 nm mainly derive from Dy 3+ ion. We investigate the effects of the ratio between Dy 3+ and Eu 3+ in Ca 3 Bi(PO 4 ) 3 :Eu 3+ , Dy 3+ on the luminescence properties. The energy transfer from Dy 3+ to Eu 3+ in Ca 3 Bi(PO 4 ) 3 :Eu 3+ , Dy 3+ is found. We analyze the luminous mechanism of samples by energy level diagrams of Dy 3+ and Eu 3+ ions. The results are helpful for the research of other Dy 3+ and Eu 3+ co-doped luminescence materials.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2023
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IF 7.2
Xiaodi Zhang,Jiming Wang,Guojie Zhang,Jun Liu,Ying Wang,Yuqing Zhao,Guoqiang Li
To improve the DRM reaction performance of the catalysts, a series of Co–Ni/WC-AC catalysts are prepared by impregnation using WC-AC as the support. The structural features of the fresh and spent catalysts are characterized by BET, XRD , H 2 -TPR, XPS and TG . The results show that the introduction of Ni in the 20Co/WC-AC catalyst promotes the conversion of W species to WC. Further, WC enhances the interaction between the active metal and the support. Thus, the activity and sintering resistance of Co–Ni/WC-AC catalysts are improved. It is also found that the introduction of different ratios of Ni has a significant effect on the chemical environment (oxygen environment) on the catalyst surface.10Co–10Ni/WC-AC catalysts showed high surface O α and O β contents of 26% and 53%, respectively. The catalyst shows excellent catalytic performance. The conversion of CH 4 and CO 2 is stable at about 84% and 85% at 800 °C.
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CHEMISTRY OF MATERIALS
·
2023
·
IF 8.6
Shan Ye,Wenjing Ma,Guodong Fu
The bilayer hydrogel actuators have attracted extensive attention for their unique stimulus-responsive properties. Most of the current research studies only focused on changing the constituent materials of two layers in the fixed bilayer structure to enhance the responsive deformability of bilayer hydrogels without involving the exploration on a structural level, which limited its further development. In this study, we proposed a novel bilayer-co-gradient structure constructed via a simple and low-cost structural programming strategy, which was self-assembled by introducing an embedded gradient structure into a single bilayer structure with the assistance of gradient-dissolved oxygen in nature. This multistructure endowed the hydrogel with a faster bending response than a single bilayer structure due to the synergistic asymmetry of the simple bilayer structure and the embedded gradient structure. It was found that the prepared hydrogels exhibited significantly anisotropic electrical conductivity and swelling properties. Moreover, the stimulus-responsive shape deformation exhibited superior temperature- and pH-based deformation programmability. Additionally, this hydrogel could serve as a hydrogel gripper to perform grasping behavior, which demonstrated that our study opens up a new route for designing and fabricating smart actuators.
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Polymers
·
2023
·Vol. 15
·期 2
·356
·
IF 5
Fengfeng Zhao,Hui Quan,Shijun Zhang,Yihui Xu,Zheng Zhou,Guangxin Chen,Qifang Li
Graphene conductive inks have attracted significant attention in recent years due to their high conductivity, corrosion resistance, and environmentally friendly nature. However, the dispersion of graphene in aqueous solution is still challenging. In this work, we synthesized an amphiphilic graft copolymer, polyvinyl alcohol-g-polyaniline (PVA-g-PANI), and studied the graphene dispersion prepared with the graft copolymer by high-speed shear dispersion. The amphiphilic graft copolymer can be used as a stabilizer and adhesive agent in graphene dispersion. Given the steric hindrance of the graft copolymer, the stability of graphene dispersion is improved by decreasing the probability of π–π stacking. PVA-g-PANI has a better stability on graphene dispersion than carboxymethylcellulose sodium (CMC-Na) and a mixture of PVA and PANI. The graft copolymer has only a slight effect on the conductivity of graphene dispersion due to the existence of conductive PANI, which is beneficial for preparing the graphene dispersion with good conductivity and adhesion. Graphene dispersion is well-adapted to screen printing and is very stable with regard to the sheet resistance bending cycle.Keywords:graphene;conductive inks;graft copolymer;aqueous solution
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PubMed
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DIAMOND AND RELATED MATERIALS
·
2023
·
IF 4.1
Jiying Shi,Linlin Zang,Long Zhang,Jingzhen Wang,Qing Xu,Yanhong Zhang,Liguo Sun
Porous carbon supported metal nanoparticles as supercapacitor electrode materials have attracted extensive attention. In this paper, cobalt nitrate/polystyrene microspheres/chitosan(Co(NO 3 ) 2 /PS/CS) balls were fabricated by emulsion encapsulation and self-assembly process. After carbonization, Co nanoparticles (NPs) loaded on porous ball-in-ball N-doped carbon (Co/BNC) were prepared. Co/BNCs with high surface area profit formation of sufficient active sites and facilitate ion transport due to the interconnected and interpenetrating porous carbon structure. The electrochemical performances of Co/BNCs are affected by Co NPs content and the Co/BNC with the optimal Co NPs content (Co/BNC-2) possesses a commendable specific capacitance of 1120 F g −1 at 1 A g −1 . Moreover, the capacitance retention of the asymmetric supercapacitors assembled by Co/BNC-2 and activated carbon is about 85.38 % after 5000 cycles. Remarkably, the device exhibits a maximum energy density of 60.9 Wh kg −1 at 764 W kg −1 and maintains 37.8 Wh kg −1 at 7878 W kg −1 . Co/BNCs mentioned here have the potential to be candidates for high-performance supercapacitor electrode materials.
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CHEMOSPHERE
·
2022
·
IF 8.943
Qingyi Zeng,Jing Tan,Beibei Gao,Tao Cai,Qingyan Zhang,Yi-Lin Liu,Sheng Chang,Shuaifei Zhao,Suqing Wu
A cobalt (Co)-doped perovskite molybdenum trioxide (α-MoO 3 ) catalyst (Co-MO) was synthesized by a facile pyrolysis strategy and used for degrading various organic contaminants via peroxymonosulfate (PMS) activation. The doped Co was inserted in the inter space between the octahedron [MoO 6 ], facilitating the growth of the α-MoO 3 crystal on the [010] direction. This unique structure accelerated the activation of PMS as the Co-MO could function as a carrier for electron transfer to facilitate the Co(II)/Co(III) cycle in the Co-MO/PMS system. As a result, the Co-MO/PMS system showed noticeable activity for removing 100% bisphenol A (BPA) under a broad conditions within 30 min. The radical quenching test and electron paramagnetic resonance analysis revealed that singlet oxygen ( 1 O 2 ) was the main active species for BPA degradation in the Co-MO/PMS system, while free radicals, such as O 2 •- , SO 4 •- and •OH, were also produced as the intermediate species. Furthermore, the carrier mechanism may enable the Co-MO/PMS system maintain relatively high performance during repeat use, and also excellent adaptability was revealed by the well function in various water matrices and high activity in degrading various refractory organic pollutants. Our findings pave a useful avenue for the rational design of novel cobalt-doped catalysts with high catalytic performance toward wide environmental applications.
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Arabian Journal of Chemistry
·
2022
·
IF 6.212
Lusheng Shi,Pengquan Yan,Zhihua Gao,Wei Huang
Due to the complexity of the structure–activity relationship of the CuAl 2 O 4 spinel catalyst, optimization of the catalyst structure is a great challenge. In this paper, three different CuAl 2 O 4 spinel catalysts were prepared by the solid-phase method using copper hydroxide, copper nitrate, and copper oxide as the copper source, respectively, to study the difference in the structure of CuAl 2 O 4 spinel catalysts induced by the raw materials and the catalytic behavior for CO hydrogenation. The structure of CuAl 2 O 4 spinel catalyst was characterized by XRD, BET, SEM, TEM, H 2 -TPR and XPS. The activity of CO hydrogenation over the CuAl 2 O 4 spinel catalyst without pre-reduction was evaluated in the slurry reactor. The results demonstrated that different copper sources had obvious influence on the CuAl 2 O 4 spinel texture properties, surface enrichment degree, as well as decomposition and reduction ability, which further regulated the ratio of Cu + /Cu 0 and thus affected the catalytic performance, especially the alcohol distribution. The CuAl 2 O 4 spinel, employing copper hydroxide as the copper source, showed better selectivity of C 2+ OH, which was assigned to a higher ratio of Cu + /Cu 0 , along with larger pore size and pore volume. Moreover, the synergistic effect between Cu 0 and γ-Al 2 O 3 improved the selectivity of dimethyl ether.
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ChemNanoMat
·
2023
·Vol. 9
·期 3
·e202200521
·
IF 3.8
Xinjie Guo,Xingyu Gan,Yun Wang,Xiaoxia Lv,Fengxiang Wang,Shuxin Wang,Shan Peng
Graphical A Co/CoO@NC/CNT-10 catalyst was effectively synthesized using melamine-assisted pyrolysis with Co-MOF as the precursor. With the synergistic effect of metal species, oxygen defects and N-doped carbon nanotubes, the intrinsic activity and electron transfer ability of the catalysts were greatly improved, showing excellent electrocatalytic oxygen reduction performance. Low-cost and high-efficiency oxygen reduction reaction (ORR) electrocatalysts are the basis for large-scale applications of electrochemical energy storage and conversion technologies such as fuel cells and metal-air batteries. Herein, cobalt and oxygen vacancy-rich cobalt oxide encapsulated in nitrogen-doped carbon and carbon nanotubes (Co/CoO@NC-CNTs) have been prepared by direct solid-state pyrolysis of Co-MOF. The carbon morphology, oxygen vacancy content and type of nitrogen can be finely tuned by mixing Co-MOF with proper amounts of melamine. The optimized material has an interwoven CNT structure with abundant micro- and mesopores, suitable nitrogen type and certain number of oxygen vacancies and exhibiting outstanding ORR electrocatalytic performance in alkaline media with an onset potential of 0.96 V and a half-wave potential of 0.88 V vs RHE, which is higher than 20 wt% Pt/C, as well as being highly stable and well resistant to methanol.
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ACS Catalysis
·
2022
·
IF 13.7
Yongjun Ji,Shaomian Liu,Shaojia Song,Wenqing Xu,Liang Li,Yu Zhang,Wenxing Chen,Huifang Li,Jingang Jiang,Tingyu Zhu,Zhenxing Li,Ziyi Zhong,Dingsheng Wang,Guangwen Xu,Fabing Su
Pt-based catalysts are promising for the selective catalytic reduction of NOx by CO (CO-SCR), but some technical issues hinder their practical application, including the high Pt loading needed, high reduction temperature, and the low tolerance toward SO2. Here, we report a novel Pt catalyst for CO-SCR, which has negatively charged single-atom Pt embedded on CuO squares, and the latter is supported on CoAlO nanosheets. This Pt–CuO/CoAlO catalyst with an ultra-low Pt loading (0.02 wt %) exhibited 91% NO conversion and 80% N2 selectivity in 3% O2 at 200 °C. More importantly, it showed almost no activity loss in 200 ppm SO2 over a 15 h test. The theoretical calculations reveal that the negatively charged Pt has a stronger NO adsorption ability than the positively charged Pt, and Cu serves as the CO adsorption site. The much-weakened SO2 adsorption on Pt–CuO/CoAlO relative to the NO and CO adsorption effectively avoids the catalyst poisoning by SO2.
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