DIAMOND AND RELATED MATERIALS
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2023
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IF 4.1
Xinyu Cheng,Yi He,Yi Fan,Liping Yan,Huilian Zhou,Jiamin Zhong,Zhiyuan Li,Jinxue Song
PDA-functionalized h-BN nanomaterials (Ph-BN) were used to reinforce the electrodeposited Ni W coatings. Compared with the h-BN nanomaterial, Ph-BN has better dispersion in the plating solution, which can effectively improve the mechanical and corrosion resistance of the coating. Compared with the Ni W coating, the microhardness value of the Ni-W/Ph-BN coating (662.8 Hv) was increased by 33.47 % and the friction coefficient (0.382) was reduced by 41.86 %. This is due to the special ceramic composite layered structure of Ph-BN namely the combination of flexible unit PDA structure and rigid unit h-BN structure, which will synergistically hinder the shedding of the coating during the friction process and help to improve the wear resistance of the coating. The R ct value of Ni-W/Ph-BN is 34,500 Ω•cm 2 , which is 105.36 % higher compared to Ni W coating. Ni-W/Ph-BN also has the smallest corrosion rate (0.0465 mm•a −1 ), which is 45.74 % lower relative to Ni W coating. The uniformly dispersed Ph-BN nanosheets in the coating prolong the corrosion path for corrosive ions. Besides, the PDA has the effect of anchoring Fe 2+ / Fe 3+ , which will be beneficial for the composite coating corrosion resistance improvement.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2020
·
IF 16.683
Jinzhu Ma,Yingfa Chen,Guangzhi He,Hong He
Numerous catalytic reaction systems take oxygen vacancy as the active site to initiate the redox cycle. However, the oxygen vacancy is easily occupied by various oxygen-containing species (e.g., water or other intermediates), resulting in catalyst deactivation . Here, we demonstrate that the layered double hydroxide (LDH) catalysts fundamentally solve the deactivation of oxygen vacancy frequently encountered with metal oxide catalyst systems, which simultaneously realizes the superior reactivity and durability for catalyzing ozone decomposition. First-principles calculations reveal that the ubiquitous surface hydroxyls on the layered hydroxide serve as the reactive sites and the redox cycle is achieved by a robust H-transfer mechanism in the 2D confined LDH systems, which are responsible for the extraordinary activity and resistance of LDH catalysts.
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SENSORS AND ACTUATORS B-CHEMICAL
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2020
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IF 7.1
Kaiwu Zhang,Xuan Wang,Caicheng Long,Jin Xu,Zixin Jiang,Bo Feng,Peng Zhang,Junjie Fei,Taiping Qing
DNA templated fluorescent copper nanoclusters (DNA-CuNCs) have demonstrated enormous potential for biochemical analysis. However, most of them are focused on DNA-related sensing. Here, we designed a hairpin DNA/RNA chimeric chain for the formation of fluorescent CuNCs and further applied it to detect reverse transcription-associated ribonuclease H (RNase H). The DNA/RNA chimera templated copper nanoclusters (DNA/RNA-CuNCs) exhibited similar spectral properties with DNA-CuNCs. In the presence of RNase H, the RNA segment in chimera is hydrolyzed and release short oligonucleotides, which fail to synthsize fluorescent CuNCs. The capabilities for RNase H detection from complex samples and screening of inhibitors were verified. This strategy exhibited high sensitivity for RNase H with a detectable minimum concentration of 5.5 × 10 −4 U mL -1 , which is lower than the developed fluorescent methods. This work will open up new thoughts to design new template for metal nanoclusters and broaden their application in RNA-related sensing.
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ACS Sustainable Chemistry & Engineering
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2020
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IF 7.632
Tian Ma,Zhensheng Shen,Huan Li,An Li,Qian Feng,Yingqiang Sun,Shuguang Deng
Brønsted acid ionic liquids (BAILs) are effective to biodiesel production of in situ transesterification of wet algae due to their dual role as both solvents of cellulose and catalysts of transesterification. The cellulose solubilities of BAILs are depending on H-bonding of BAILs-cellulose in varied solvent conditions, which subsequently affect the biodiesel productions. For this reason, the effects of H-bonding between BAILs including [Bmim][H2PO4], [Bmim]2[HPO4], [Bmim][HSO4], and cellulose under different methanol and water conditions on cellulose extractions are experimentally and theoretically investigated. The cellulose extractions in BAILs are decreasing as [Bmim][H2PO4] > [Bmim]2[HPO4] > [Bmim][HSO4], contrary to the variation of their thermal stabilities and crystallinities caused by varied H-bonding of BAILs-cellulose. Increasing methanol is positive to cellulose extractions in [Bmim][HSO4], while negative to those in [Bmim][H2PO4] and [Bmim]2[HPO4], due to the solvent effect of methanol confirmed by cyclic voltammetry (CV) measurements. The effect of water on H-bonding of BAILs-cellobiose is contrary to the effect of methanol. It is confirmed via the bonding interaction of BAILs-cellobiose through the density functional theory (DFT) computational method. However, the biodiesel yields are varied differently due to the competition of H-bonding of BAILs-cellobiose and deprotonation of BAILs under different methanol and water conditions. This study might pave the way to neutralize the negative effect of water on in situ transesterification via enhancing the cellulose extractions of BAILs.
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RSC Advances
·
2020
·Vol. 10
·期 17
·10006-10016
·
IF 3.119
Ruimin Li,Shiyong Xing,Shuai Zhang,Minghan Han
H-beta zeolites of 100–200 nm (named BEA-L) and 20–30 nm (named BEA-S) were treated by chemical liquid deposition (CLD) of tetraethyl orthosilicate (TEOS) to improve the selectivity of 2-phenyl linear alkylbenzene (2-LAB) from benzene alkylation with 1-dodecene. The results indicate that H-beta zeolite with a smaller crystal size has a longer lifetime due to shorter channels and less diffusion limitation. The deposited SiO2 layers passivated the external surface acid sites of the zeolite and made the pores narrower. BEA-L lost more external Brønsted acid sites than BEA-S with the same added amount of TEOS, which was due to the severe aggregation of BEA-S grains. This increased passivation gave BEA-L increased 2-LAB selectivity. And when the added amount of SiO2 was 7.20 wt% of the parent zeolite, the selectivity of 2-LAB over BEA-L significantly increased from 41.9% to 54.7% while that of BEA-S only increased by 2%.
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JOURNAL OF LUMINESCENCE
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2019
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IF 2.961
Zhihai Wu,Pan Wang,Jun Wu,Jiao Wei,Yanni Sun,Nengping Wang,Zhenfu Zhao
Recently, all-inorganic perovskite (CsPbX 3 (X = Cl, Br, I)) nanocrystals (NCs) have caused extensive attention due to their high photoluminescence quantum yield (PL QY), high color purity, and narrow full width at half maximum (FWHM). Although the excellent optical properties of perovskite NCs (PNCs) endow them good application prospects, their inherent instability severely limits the commercialization process. In this paper, highly-luminescence and ultra-stable phosphor were obtained by loading PNCs onto the surface of amino modified hexagonal boron-nitride (h-BN) white graphene (PNCs-BNWG), This structural design can effectively suppress the attenuation of photoluminescence (PL) intensity and enhance thermal stability, thereby realizing the high stability and brightness white LEDs. The synthesis process is simple and can be finished in a few minutes to ensure scalable production. Compared with bare PNCs, it can maintain excellent optical properties. The high PL QY and thermal stability mainly stem from the isolation effect that separates PNCs from each other on the surface of BNWG and their superior high transparency as well as thermal conductivity . In addition, multi-color inks are produced by dispersing PNCs-BNWG nanocomposites in PDMS to form a multicolor painting demonstrating high PL QY and wide color gamut.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2019
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IF 3.375
Junjie Zhu,Linbo Wu,Zhiyang Bu,Suyun Jie,Bo-Geng Li
Searching for highly efficient and robust CO2 adsorbents is very important for CO2 capture, utilization, and storage. In this study, new polyethylenimine-grafted metal–organic framework (MOF)–polymer composites, abbreviated as PEI@PGD-H, were synthesized via high internal phase emulsion (HIPE) template polymerization of divinylbenzene and glycidyl methacrylate, followed by in situ generation of HKUST-type MOF in the presence of hydrophobic-modified CuO nanoparticles via the reaction of CuO with 1,3,5-benzenetricarboxylic acid and then polyethylenimine (PEI) functionalization via epoxy–amine reaction and amine–metal sites interaction. The coexistence of the hierarchical interconnected porous skeleton of poly(glycidyl methacrylate–divinylbenzene) (PGD), high specific surface area of MOF, and chemical CO2 adsorption of PEI endows PEI@PGD-H with high CO2 adsorption capacity, rate, and selectivity. PEI70@PGD-H shows a CO2/N2 separation factor as high as 76 and CO2 adsorption capacities of 4.3, 3.0, and 1.8 mmol of CO2/g from pure CO2, simulated flue gas, and air, respectively. After 20 CO2 adsorption–desorption cycles, the adsorbent still retained a high and stable CO2 capture capacity over 2.8 mmol of CO2/g for simulated flue gas. The adsorbent also displays reasonably good thermal stability, excellent water endurance, low desorption energy, and easy shaping. The desorption heat is as low as 48 kJ/mol of CO2. These features make PEI@PGD-H highly efficient, robust, and low-energy CO2 adsorbents for practical application in CO2 capture.
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ACS Applied Materials & Interfaces
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2019
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IF 8.456
Haiyan Qiao,Pengfei Qi,Xiaohui Zhang,Linan Wang,Yeqiang Tan,Zhaohui Luan,Yanzhi Xia,Yanhui Li,Kunyan Sui
Herein, we demonstrate a ternary ionic hydrogel sensor consisting of tannic acid, sodium alginate, and covalent cross-linked polyacrylamide as skin-mountable and wearable sensors. Based on the multiple weak H-bonds and synergistic effects between the three components, the as-prepared hybrid hydrogel exhibits ultrastretchability with high elasticity, good self-healing, excellent conformability, and high self-adhesiveness to diverse substrates both in air and underwater. More importantly, the ternary hydrogel exhibits high strain sensitivity especially under subtle strains with a gauge factor of 2.0, which is close to the theoretical value of the ionic hydrogel sensors; an extremely large workable range of strain (0.05–2100%); and a low operating voltage 0.07 V. Consequently, the sensor demonstrates superior sensing performance for real-time monitoring of the large and subtle human motions, including limb motions, swallowing, smiling, and wrist pulse. Therefore, it is believed that the STP hydrogel has great potential applications in health monitoring, smart wearable devices, and soft robots.
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Molecular Catalysis
·
2019
·
IF 2.938
Haibin Wang,Shaodong Liu,Tingting Sun,Zhanao Lv,Zhen Zhan,Guochuan Yin,Zhuqi Chen
In catalytic double bond migration reaction, E -configuration olefins were normally generated as the dominant product because E -configuration was thermodynamically favored. However, Z-configuration products are sometimes desired in pharmaceutical chemistry owing to the structure-activity relationship. In this paper, we have demonstrated a new strategy that Lewis acid promoted an widely employed and convenient ruthenium(II) complex for the catalytic isomerization of O-allylethers, leading to thermodynamic-unfavored Z-product under mild conditions. The model substrate of allyl phenyl ether can be simply scaled up to 20 mmol to produce Z-product with TON of 2453 and TOF of 13,430 h −1 at 40–60 °C. The system of Ru(II)/Lewis Acid catalysts was suitable for various substituted O -allylethers and other types of substrates. Through mechanism study including kinetic study, ligand inhibition effect and molecular spectroscopy, the dissociation of PPh 3 ligand by the addition of Lewis acid, and the formation a five-membered Ru complex from anchimeric assistance were both recognized as essential steps to improve the reactivity and to control the stereoselectivity of catalytic double bond migration reaction through metal hydride addition-elimination mechanism. This new strategy may provide a new opportunity to produce thermodynamic-unfavored product in heterocyclic compounds for pharmaceutical chemistry.
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RSC Advances
·
2018
·Vol. 8
·期 31
·17389-17398
·
IF 2.936
Yunquan Zheng,Qisheng Pan,Liuda Mo,Wenyi Zhang,Yunjian Duan,Chengqun Chen,Haijun Chen,Yanghao Guo,Xianai Shi,Jianmin Yang
Alzheimer's disease (AD) is an extremely complex disease, characterized by several pathological features including oxidative stress and amyloid-β (Aβ) aggregation. Blockage of Aβ-induced injury has emerged as a potential therapeutic approach for AD. Our previous efforts resulted in the discovery of Monascus pigment rubropunctatin derivative FZU-H with potential neuroprotective effects. This novel lead compound significantly diminishes toxicity induced by Aβ(1-42) in Neuro-2A cells. Our further mechanism investigation revealed that FZU-H inhibited Aβ(1-42)-induced caspase-3 protein activation and the loss of mitochondrial membrane potential. In addition, treatment of FZU-H was proven to attenuate Aβ(1-42)-induced cell redox imbalance and Tau hyperphosphorylation which caused by okadaic acid in Neuro-2A cells. These results indicated that FZU-H shows promising neuroprotective effects for AD.
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JOURNAL OF HAZARDOUS MATERIALS
·
2018
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IF 6.434
Jing Zhang,Juncong Li,Huiyu Su,Ying Zhao,Xiang Zeng,Maohua Hu,Wei Xiao,Xuhui Mao
In this study, the effect of oxyanions on the photodegradation of sulfonamides by graphitic carbon nitride (g-C 3 N 4 ) was investigated. The results showed that the presence of disilicate (DS) could substantially improve the photodegradation of sulfamethazine (SMZ) in g-C 3 N 4 aqueous suspension. The primary mechanism for the enhancing effect of DS was hydrogen bonding (H-bonding) interaction. The hydroxyl groups ( OH) and bridging oxygen (Si O Si) of DS can form H-bonds with the amine groups of g-C 3 N 4 particles and sulfonamides, therefore soluble DS can act as a bridge to enhance the transfer and adsorption of SMZ onto the surface of g-C 3 N 4 particles. The presence of DS did not change the mechanism of photodegradation, but there was an optimal concentration for DS to achieve the strongest enhancing effect. H-bonding effect was also found for other oxyanions derived from weak acids, such as silicate, dihydrogen phosphate and borate ions, because the partial ionization of these oxyanions allowed the existence of hydroxyl groups to form H-bonds. The present study not only deepens our understanding of the interface process of the photodegradation of sulfonamides in g-C 3 N 4 aqueous suspension, but also provides a potential method to enhance the photocatalytic degradation of antibiotics in wastewater streams.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2019
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IF 4.084
Tingwei Zhang,Yijuan Lu,Wenzhi Li,Mingxue Su,Tao Yang,Ajibola Ogunbiyi,Yongcan Jin
In order to efficiently produce γ-valerolactone (GVL) from furfural , a Zr-graphitic carbon nitride/H-β composite (Zr CN/H-β) had been simply prepared via an impregnation-calcination protocol. The morphology and structure, elemental information, and total acid and base properties of the Zr CN/H-β and related catalysts (H-β, CN/H-β, and Zr/H-β) were determined by SEM, TEM , X-ray photoelectron spectroscopy (XPS), and temperature-programmed desorption (TPD-NH 3 , CO 2 ) characterizations. The effects of reaction temperature and time, and the furfural dosage on GVL production as well as the recyclability of Zr CN/H-β were investigated. With a catalyst/furfural dosage of 0.1/0.22 g, the Zr CN/H-β produced a remarkable 76.5% of GVL yield at 160 °C in 18 h using isopropanol as the solvent. The results of NH 3 , CO 2 -TPD experiments indicated that the simultaneous introduction of Zr species and carbon nitride onto H-β formed new types of acid and base, which should be responsible for the high efficient conversion of furfural to GVL. Additionally, the recyclability of Zr CN/H-β was reasonable.
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