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FOOD HYDROCOLLOIDS · 2022 · IF 11.504

Modulation of viscosity, microstructure and lipolysis of W/O emulsions by cellulose ethers during in vitro digestion in the dynamic and semi-dynamic gastrointestinal models

Shahid Iqbal,Ping Zhang,Peng Wu,Quanyi Yin,Khemayanto Hidayat,Xiao Dong Chen

In this study, W/O emulsions incorporated with various proportions of two hydrocolloids , namely, methylcellulose (MC) and hydroxypropyl methylcellulose (HPMC), were prepared. The shear viscosity, microstructure, and lipolysis of the W/O emulsions before and during in vitro digestion in the dynamic (DIVHS) and semi-dynamic gastrointestinal models were evaluated and compared. The shear viscosity of both emulsions increased with the addition of MC and HPMC content up to a certain limit (0.5–2%), whereas it significantly decreased at a higher addition level (4%) due to the increased flocculation and coalescence in higher cellulose ethers. The HPMC emulsions (2 wt % in aqueous phases) showed higher viscosity and larger droplet size than the equivalent MC emulsions before and during simulated digestion, accompanied by the lower extent of lipolysis. These results are in line with the formation of a more compact and stronger gel structure in HPMC emulsions, which could retard lipase adsorption at the W–O interface. For both emulsions at the same concentration (40 wt%), a higher extent of free fatty acid (FFA) release was found during digestion in the dynamic system (HPMC ꞊ 62%, MC ꞊ 72%) compared to that in the semi-dynamic model (HPMC ꞊ 58%, MC ꞊ 70%). This behavior was supported by the smaller droplet size of emulsions digesta collected from the dynamic system having a larger surface area. Overall, the present study suggested that the dynamic DIVHS system was more effective in enzymatic hydrolysis of the W/O emulsions investigated than the semi-dynamic model under the current experimental conditions. This work had provided valuable insights into the modulation of the structural and digestive properties of W/O emulsions by the addition of MC and HPMC, which could be meaningful for the development of healthier emulsion-based food products ( e.g ., margarine and spreads) with reduced lipid digestibility.

CAS / MDL: 9004-65-3
研究领域: 食品科学 · 生物化学
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ACS Biomaterials Science & Engineering · 2023 · IF 5.8

Heparin-Mimetic Chitooligosaccharides-Based Monoliths Obtained from C/W Emulsions: Hemocompatibility and Toxin Removal Ability

Kaibo Xu,Liqin Cao,Zhouyu Wang,Liu-ping Chen

Hemoperfusion (HP) is one of the most prominent therapies for treating uremia, hyperbilirubinemia, and acute drug toxicity. The comprehensive performance of currently used porous HP adsorbents needs to be improved due to the impediment to their synthesis strategy. Herein, green carbon dioxide-in-water high internal phase emulsions (C/W HIPEs) were utilized and emulsified with poly(vinyl alcohol) (PVA) for the formation of a heparin-mimetic chitosan oligosaccharides/poly(acrylamide-co-sodium 4-styrenesulfonate) [COS/P(AM-co-SSS)] monolith, which exhibited good mechanical properties, stable swelling performance, hydrophilic properties, anticoagulant effect, and low hemolysis. It showed a strong toxin adsorption capacity (415.2 mg/g for creatinine, 199.3 mg/g for urea, 279.5 mg/g for bilirubin, and 160 mg/g for tetracycline). The adsorption process of porous COS/P(AM-co-SSS) followed the pseudo-second-order kinetic and Langmuir isotherm models. Moreover, the porous materials had a strong electrostatic force on creatinine. The removal of creatinine by simulated in vitro blood perfusion was 80.2% within 30 min. This work provides a green preparation strategy for developing novel HP materials, highlighting their potential application value in blood and environmental purification.

研究领域: 材料科学 · 生物医学工程 · 化学工程 · 环境科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 12 ·16577-16588 · IF 2.478

Co-W bimetallic carbides as sulfur host for high-performance lithium–sulfur batteries

Zhang Dongke,Huang Ting,Zhao Pengfei,Zhang Ze,Qi Xingtao,Yang Zhenyu,Cai Jianxin

Due to the low conductivity of sulfur and the dissolution of polysulfides, the application of lithium–sulfur (Li–S) batteries have encountered certain resistance. Increasing conductivity and introducing polarity into the sulfur host can effectively overcome these long-standing problems. Herein, we first prepared Co 3 W 3 C@ C@CNTs/S material and used it in the cathode of lithium–sulfur batteries. Carbon nanotubes treated with acidification have good dispersibility in aqueous solution, good adsorption on positively charged metal ions due to abundant oxygen-containing functional groups on the surface. After carbonization treatment, Co 3 W 3 C will be firmly anchored on the surface of carbon nanotubes, which is conducive to improving the electrical conductivity and stability of its own materials. Polar Co 3 W 3 C can form a strong interaction with polysulfide intermediates, effectively inhibiting its shuttle effect, improving the utilization of sulfur cathode electrodes, and keeping the capacity and cycle stability. The Co 3 W 3 C@C@CNTs/S electrode material has a capacity of 1093 mA h g −1 at 0.1 A g −1 and 482 mA h g −1 at 5 A g −1 . Even after 500 cycles of 2 A g −1 , the capacity of each cycle is only reduced by 0.08%. The excellent stability of this material can provide a new idea for the future development of lithium–sulfur batteries.

研究领域: 材料科学 · 能源存储技术
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RSC Advances · 2018 ·Vol. 8 ·期 20 ·10907-10913 · IF 2.936

Insight into the efficient catalytic conversion of biomass to EG and 1,2-PG over W–Ni bimetallic catalyst

Meng-Qing Li,Yu-Long Ma,Xiao-Xia Ma,Yong-Gang Sun,Zhi Song

In this work, a mesoporous silica microsphere (MSM) was selected as a support to prepare a bimetallic supported catalyst (15% W–5% Ni/MSM) by a co-impregnation method that was simple and easy to conduct. We wished to improve the capability of catalytic conversion of biomass into ethylene glycol (EG) and 1,2-propylene glycol (1,2-PG). 15% W–5% Ni/MSM was examined on microcrystalline cellulose (cellulose) and corn stalks in a one-pot catalytic process, and total yields of EG and 1,2-PG reached up to 82.40 wt% and 62.60 wt%, respectively. This remarkable catalytic performance of W–Ni/MSM catalyst could be attributed to the synergistic effect between the active sites of Ni and W and the unique structure of MSM, which was suitable for mass transfer and metal loading. Based on physicochemical characterizations, the metal component was well-distributed on the surface of the MSM, and the metallic Ni, W and WO3 of the fresh catalyst were converted mainly into NiWO4 during the catalytic conversion of cellulose. To shed light on the reaction mechanism of the catalyzed hydrogenation of biomass, a possible process involving the formation of HxWO3 homogeneous catalysts, cellulose hydrolysis, C–C cleavage and hydrogenation conversion to 1,2-PG and EG was illustrated. Furthermore, the reusability of W–Ni/MSM catalyst was tested and we explored the cause of decreased diols yields. In summary, this work provides important guidance to rationally design effective catalysts for biomass conversion.

研究领域: 催化 · 材料科学 · 化学工程 · 可再生能源
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Potential application of novel amphiphilic Janus-SiO2 nanoparticles stabilized O/W/O emulsion for enhanced oil recovery

Han Jia,Jiajun Dai,Lingchun Miao,Xin Wei,Hongtao Tang,Pan Huang,Haidong Jia,Juan He,Kaihe Lv,Dexin Liu

The Janus nanoparticles stabilized Pickering emulsions showed great application potential in various fields, including enhanced oil recovery (EOR). In this study, the amphiphilic Janus-SiO 2 nanoparticles (Janus-C12) are successfully synthesized by the Pickering emulsion method and characterized by Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), ζ-potential and contact angle measurements. The phase inversion from oil-in-water (O/W), multiple oil-in-water-oil (O/W/O) emulsion, to water-in-oil (W/O) emulsions was observed with the delicate control for the modification degrees of Janus-C12. The possible emulsification mechanisms for various Janus-C12 stabilized emulsions were proposed. The multiple O/W/O emulsion stability in harsh conditions and the influence factors (nanoparticles concentration, water/oil volume ratio and NaCl concentration) were studied systematically. Moreover, the Janus-C12–79% stabilized multiple O/W/O Pickering emulsions exhibited excellent EOR performance (additional oil recovery of 27.2%) in core flooding tests, and the possible EOR mechanism was explored via microscopic visualization experiments.

研究领域: 化学工程 · 材料科学 · 石油工程
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METALLURGICAL AND MATERIALS TRANSACTIONS A-PHYSICAL METALLURGY AND MATERIALS SCIENCE · 2022 ·Vol. 53 ·期 3 ·1085-1098 · IF 2.726

Fabrication and Characterization of Tungsten Heavy Alloys with High W Content by Powder Metallurgy

Li Zhi-Bo,Zhang He,Zhang Guo-Hua,Chou Kuo-Chih

In order to fabricate high-performance tungsten heavy alloys (97W–2.1Ni–0.9Fe (wt pct) and 99W–0.7Ni–0.3Fe) with higher W content and density by powder metallurgy technique, the ultrafine composite powder was synthesized through two-step reduction approach and used as the raw materials. Contrary to the expectations, it was found that a small amount of Ni has a great effect in activated pre-sintering, resulting in an undesired grain growth of W to micron size. Therefore, another simple and efficient method was developed to prepare high-purity, ultrafine and high-W-content composite powders. The sintering densification behavior of the prepared composite powders, as well as mechanical properties and corrosion resistance of as-sintered alloys were systematically investigated. The bending strength, compression strength, hardness, fracture toughness and anti-corrosion property of obtained 97W–2.1Ni–0.9Fe alloys are better than those of 99W–0.7Ni–0.3Fe alloys, attributed to the more homogeneous microstructure comprised of finer W grain and larger volume fraction of matrix phase.

研究领域: 材料科学 · 冶金工程
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2020 · IF 4.939

In situ W/O Co-doped hollow carbon nitride tubular structures with enhanced visible-light-driven photocatalytic performance for hydrogen evolution

Haoshan Wei,Yong Zhang,Guoao Zhang,Jiewu Cui,Yan Wang,Yongqiang Qin,Xueru Zhang,Hark Hoe Tan,Jiaqin Liu,Yucheng Wu

Heteroatom co-doping has been considered as an effective strategy to simultaneously overcome intrinsic shortcomings of g-C 3 N 4 to achieve enhanced photocatalytic properties, in which the involved dopants could play its role in altering electronic structure, optical absorption and charge separation of the catalyst. Herein, W/O co-doped hollow g-C 3 N 4 tubular structures are successfully obtained for the first time via a one-step thermal decomposition. By W/O co-doping, architecture of g-C 3 N 4 is able to be modulated with enhanced optical absorption towards visible region. In addition, narrowed band gap and restrained charge recombination are conducive for the excitation of electron-hole pairs and transportation. Photocatalytic water splitting tests indicate that the co-doped hollow tubular g-C 3 N 4 structures enable superior activity for generating hydrogen up to 403.57 μmol g −1  h −1 driven by visible light, nearly 2.5 times as high as that of pristine g-C 3 N 4 . This work presents a rational strategy to design co-doped g-C 3 N 4 as an efficient visible-light-driven photocatalyst .

CAS / MDL: 108-78-1
研究领域: 材料科学 · 化学 · 光催化 · 可再生能源
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Sulfonated P-W modified nitrogen-containing carbon-based solid acid catalysts for one-pot conversion of cellulose to ethyl levulinate under water-ethanol medium

Mingqiang Chen,Longyang Li,Yishuang Wang,Defang Liang,Zinan Zhou,Haosheng Xin,Chang Li,Gang Yuan,Jun Wang

Converting cellulose (Cel) into ethyl levulinate (EL) is one of the promising strategies for supplying liquid fuels. In this paper, the prepared sulfonated P-W-modified N-containing carbon-based solid acid catalyst (PWNCS), in which the Polyaniline (PANI) was employed as N and C precursors, successfully converted Cel into EL under the water-ethanol medium. The characterization results demonstrated that a tiny addition of P increased the Brønsted acid sites (BAS) content and defective WO 3 provided the Lewis acid sites (LAS), meanwhile, the sulfonation process did not change the fundamental structure but introduced the sulfonic groups to dramatically increase the acidic content. Therefore, under optimized reaction conditions, PWNCS realized about 100% Cel conversion and 71.61% of EL yield, furthermore, the selectivity of EL reached 89.14%. In addition, the effect of water on the reaction pathway of Cel to EL over PWNCS was proposed. The addition of water generally resulted in the hydration of defective WO 3 to reduce the LAS and increase BAS, which significantly inhibited the side reactions of retro-aldol condensation (RAC) and subsequent etherification reactions during Cel conversion and then improved the selectivity of EL.

研究领域: 催化 · 化学工程 · 可再生能源 · 生物化学
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Speeding up low-temperature SCR with reactants-coupling dual catalytic sites

Xiaolei Hu,Weiye Qu,Junxiao Chen,Dongrun Xu,Jing Liu,Yangyang Dong,Rui Liu,Zhen Ma,Xingfu Tang

Selective catalytic reduction (SCR) of NO x with NH 3 over V 2 O 5 -based catalysts has been widely used to control NO x emissions from power plants, but its application is largely limited in other industrial boilers because of insufficient catalytic efficiency at low temperatures. Here we resolve this problem by mechanistically designing a highly active Ce-W/TiO 2 catalyst with reactants-coupling dual catalytic sites. The results demonstrate that W and Ce are highly dispersed on the surfaces of Ce-W/TiO 2 to form dual catalytic sites, which act as acid-base pairs favorable for NH 3 and NO adsorption, respectively, thereby allowing the reaction of adsorbed NH 3 on the W site with oxidized NO species (NO 3 − ) adsorbed on the adjacent Ce site to proceed along a low-activation-energy pathway via Langmuir-Hinshelwood mechanism. Compared with Ce/TiO 2 , a W-Ce synergy gives rise to more abundant Ce 3+ on Ce-W/TiO 2 , which facilitates the activation of O 2 during SCR process, thus improving the low-temperature SCR performance. Therefore, the design of the dual catalytic sites based on the properties of reactants provides an alternative approach to developing highly active SCR catalysts.

CAS / MDL: 13463-67-7
研究领域: 环境科学 · 催化化学
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FOOD HYDROCOLLOIDS · 2022 · IF 11.504

Effects of different pH conditions on interfacial composition and protein-lipid co-oxidation of whey protein isolate-stabilised O/W emulsions

Jiaxin Chen,Xin Li,Chuanai Cao,Baohua Kong,Hui Wang,Hongwei Zhang,Qian Liu

The physical stability, interfacial composition and protein-lipid co-oxidation of O/W emulsions stabilised by whey protein isolate under different pH conditions (3.0, 5.0, 7.0 and 9.0) with fixed storage times were assessed in the present study. The results revealed that different pH conditions had distinct effects on the physical stability of the emulsions, as verified by the droplet size, ζ-potential and interfacial composition. Acidic conditions had an unnoticeable impact on protein-lipid co-oxidation. Remarkable physical barrier-like protection of the lipid core provided by adsorbed proteins (AP) was observed in the O/W emulsions under neutral conditions. However, alkaline conditions (pH 9.0) could induce the most severe protein-lipid co-oxidation when the storage time was extended, as indicated by the highest levels of protein and lipid oxidation products (carbonyl, N′-formyl- l -kynurenine, lipid hydroperoxides, thiobarbituric acid-reactive substances and volatile lipid oxidation products), in addition to the obvious molecular changes in unadsorbed proteins (UAP) or AP. Free radicals and metal ions could more easily react with highly unfolded and negatively charged AP under strong alkaline conditions. Our findings clearly revealed that the co-oxidation phenomenon of O/W emulsion systems were closely related to the synergistic effects between the transformation of interfacial composition and aggregation of oil droplets that occurred under different pH conditions.

研究领域: 食品科学 · 化学 · 生物物理学
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ACTA MATERIALIA · 2023 · IF 9.4

The effect of Ir and Sc on the emission capacity of W–Ir matrix scandate cathodes prepared via a novel in situ method

Junyan Gao,Peng Liu,Jinshu Wang,Ruimin Zhang,Yunfei Yang,Wenyuan Zhou,Hexiong Liu,Junhao Sun

The size and distribution of Sc 2 O 3 in the composite powder precursor has great effect on the emission property of scandate cathode. By one-step in-situ synthesis method, the composite powder exhibits the structure of quasi-spherical Sc 2 O 3 nanoparticles grown in situ on the surface of W/Ir grains, and the obtained W–Ir cathode with 3wt % Sc 2 O 3 could provide the emission current density of 83.43 A/cm 2 at 900 °C b , which is higher than other W–Ir mixed matrix scandate cathodes and W matrix scandate cathode. The XRD results showed that the high emission ability depended on the high content of active phase α-Ba 2 ScAlO 5 and low content of non-active phase BaAl 2 O 4 . In-situ TEM has been applied to observe the microstructure evolution of the cathode surface at high temperature for the first time. A serial change in the microstructural features of cathode surface and the migration of Ba, Sc and O on the substrate surface has been found, confirming the formation of Ba-Sc-O active layer. The first-principles calculations indicate that the active substances (Sc) are more stable (low adsorption energy of − 8.58 eV) on the IrW matrix cathode surface than on the tungsten matrix cathode surface, which is consistent with the low evaporation rate of the active substance detected by TFMS technique. Besides, the interaction between the active substance and the matrix was strengthened due to more electron transfer of Sc (1.88 e) and Ba (1.45 e), therefore lowering the work function . The feasible preparation technique makes such a cathode promising for applications in high-power microwave devices.

研究领域: 材料科学 · 电子工程 · 表面科学 · 纳米技术
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SENSORS AND ACTUATORS B-CHEMICAL · 2023 · IF 8.4

Al and W co-doped NiO nanoflowers with low crystallinity and rich oxygen vacancies for high stability and selective triethylamine detection

Lanlan Guo,Yanji Feng,Feng Shi,Wei Zhao,Hua Zeng,Tingyu Chen,Yingli Yang,Guodong Wang,Xiaolian Liu,Yan Wang,Xueli Yang

In this work, pure NiO, Al-doped NiO, W-doped NiO and a series of Al/W co-doped NiO nanoflowers were successfully prepared through a simple solvothermal method . Various characterization methods, such as XRD , SEM, TEM, HRTEM and XPS , were used to confirm the physical and chemical properties of the sensitive materials in terms of micro-nano structures, compositions and elemental distributions. The as-obtained Al/W co-doped NiO showed a nanoflower structure with an approximate size of ∼ 200 nm. What's more, among six sensors constructed from the sensitive materials, the sensor based on 3 at% Al 3+ /3 at% W 6+ co-doped NiO (3Al3W-NiO) achieved the highest response (R g /R a =112) toward 100 ppm triethylamine with a low detection limit (1 ppm) at 325 ℃. Besides, this sensor also exhibited excellent response/recovery characteristics and long-term stability. These favorable sensing performances of the 3Al/3 W co-doped NiO sensor are not only modulated by the initial resistance (R a ), but are also closely related to the large specific surface area , porous structures , low crystallinity , rich oxygen vacancies and high Ni 3+ /Ni 2+ ratio in the composite nanomaterials.

研究领域: 材料科学 · 纳米技术 · 化学传感器 · 气体传感
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