Netzsch STA 449

Nanomaterials are increasingly valued tools in drug delivery research as they offer enhanced stability, controlled release and more effective drug encapsulation. Though yet to be introduced in clinical trial, mesoporous silica nanoparticles are promising delivery systems, due to their high chemical and mechanical stability while remaining biodegradable. This work provides proof of concept for particle based vaccines as cost-effective alternatives for dendritic cell immunotherapy. Synthesis and surface chemistry of the nanoparticles are optimized for protein conjugation and nanoparticles are characterized for their physicochemical properties and biodegradation. Ovalbumin is used as a model protein to load nanoparticles to produce a nanovaccine. The vaccine is tested in vitro on dendritic cultures to verify particle and vaccine uptake, toxicity, maturation effects and explicitly ovalbumin cross-presentation on MHC class I molecules. The optimized synthesis protocol renders reproducible mesoporous silica nanoparticles, resistant against agglomeration, within the required size range and have carboxylic surface functionalization necessary for protein conjugation. They are biodegradable over a time span of 1 week. This period is adjustable by changing synthesis parameters. UV sterilization of the particles does not induce quality loss, nor does it have toxic effects on cells. Treatment with mesoporous silica nanoparticles increases expression of MHC and costimulatory molecules of dendritic cells, indicating an adjuvant effect of nanoparticles on the adaptive immune system. Nanovaccine uptake and cross-presentation of ovalbumin are observed and the latter is increased when delivered by nanoparticles as compared to control conditions. This confirms the large potential of mesoporous silica nanoparticle based vaccines to replace dendritic-based active specific immunotherapy, offering a more standardized production process and higher efficacy.

Stephanie Seré, Ulrique Vounckx, Jin Won Seo, Ilse Lenaerts, Stefaan Van Gool, Jean-Pierre Locquet. Frontiers in Nanotechnology, 2, 2020.

The rational design of cost-effective and highly efficient catalysts for the oxygen evolution reaction (OER) is vastly desirable for advanced renewable energy conversion and storage systems. Tailoring the composition and architecture of electrocatalysts is a reliable approach for improving their catalytic performance. Herein, we developed hierarchical ultra-thin Co nanosheets coupled with N-doped carbon plate (Co-NS@NCP) as an efficient OER catalyst through a feasible and easily scalable NaCl template method. The rapid dissolution-recrystallization-carbonization synthesis process allows Co nanosheets to self-assemble into plenty of secondary building units and to distribute uniformly on N-doped carbon plate. Benefitting from the vertically aligned Co nanosheet arrays and hierarchical architecture, the obtained Co-NS@NCP possess an extremely high specific surface area up to 446.49 m² g⁻¹, which provides sufficient exposed active sites, excellent structure stability, and multidimensional mass transfer channels. Thus, the Co-NS@NCP affords remarkable electrocatalytic performance for OER in an alkaline medium with a low overpotential of only 278 mV at 10 mA cm⁻², a small Tafel slope, as well as robust electrocatalytic stability for long-term electrolysis operation. The present findings here emphasize a rational and promising perspective for designing high-efficiency non-precious electrocatalysts for the OER process and sustainable energy storage and conversion system.

Yue Wang, Meng Li, Qixing Zhou, Qin Wang, Xingyuan Zhang, Dongmei Sun, Yawen Tang. Frontiers in Nanotechnology, 3, 2021.

Magnesium hydride (MgH₂) is a promising solid-state hydrogen source with high storage capacity (7.6 wt%). Although it is recently established that MgH₂ has potential applications in medicine because it sustainably supplies hydrogen gas (H₂), the biological functions of MgH₂ in plants have not been observed yet. Also, the slow reaction kinetics restricts its practical applications. In this report, MgH₂ (98% purity; 0.5–25 μm size) was firstly used as a hydrogen generation source for postharvest preservation of flowers. Compared with the direct hydrolysis of MgH₂ in water, the efficiency of hydrogen production from MgH₂ hydrolysis could be greatly improved when the citrate buffer solution is introduced. These results were further confirmed in the flower vase experiment by showing higher efficiency in increasing the production and the residence time of H₂ in solution, compared with hydrogen-rich water. Mimicking the response of hydrogen-rich water and sodium hydrosulfide (a hydrogen sulfide donor), subsequent experiments discovered that MgH₂-citrate buffer solution not only stimulated hydrogen sulfide (H₂S) synthesis but also significantly prolonged the vase life of cut carnation flowers. Meanwhile, redox homeostasis was reestablished, and the increased transcripts of representative senescence-associated genes, including DcbGal and DcGST1, were partly abolished. By contrast, the discussed responses were obviously blocked by the inhibition of endogenous H₂S with hypotaurine, an H₂S scavenger. These results clearly revealed that MgH₂-supplying H₂ could prolong the vase life of cut carnation flowers via H₂S signaling, and our results, therefore, open a new window for the possible application of hydrogen-releasing materials in agriculture.

Longna Li, Yuhao Liu, Shu Wang, Jianxin Zou, Wenjiang Ding, Wenbiao Shen. Frontiers in Plant Science, 11, 2020.

Cell-encapsulated bioscaffold is a promising and novel method to allow fabrication of live functional organs for tissue engineering and regenerative medicine. However, traditional fabrication methods of 3D scaffolds and cell-laden hydrogels still face many difficulties and challenges. This study uses a newer 3D fabrication technique and the concept of recycling of an unutilized resource to fabricate a novel scaffold for bone tissue engineering. In this study, fish-extracted gelatin was incorporated with bioactive ceramic for bone tissue engineering, and with this we successfully fabricated a novel fish gelatin methacrylate (FG) polymer hydrogel mixed with strontium-doped calcium silicate powder (FGSr) 3D scaffold via photo-crosslinking. Our results indicated that the tensile strength of FGSr was almost 2.5-fold higher as compared to FG thus making it a better candidate for future clinical applications. The in-vitro assays illustrated that the FGSr scaffolds showed good biocompatibility with human Wharton jelly-derived mesenchymal stem cells (WJMSC), as well as enhancing the osteogenesis differentiation of WJMSC. The WJMSC-laden FGSr 3D scaffolds expressed a higher degree of alkaline phosphatase activity than those on cell-laden FG 3D scaffolds and this result was further proven with the subsequent calcium deposition results. Therefore, these results showed that 3D-printed cell-laden FGSr scaffolds had enhanced mechanical property and osteogenic-related behavior that made for a more suitable candidate for future clinical applications.

Chun-Ta Yu, Fu-Ming Wang, Yen-Ting Liu, Alvin Kai-Xing Lee, Tsung-Li Lin, Yi-Wen Chen. Applied Sciences, 10 (6), 2168, 2020.

In view of the current and urgent environmental protection needs, the use of industrial solid waste in China’s Ningdong is becoming more and more important. In this paper, NaP zeolite with good physical properties is synthesized by using coal gasification coarse slag (CGCS) as the raw material, without the addition of a silicon and aluminum source, without the addition of a template agent, and without high-temperature calcination. Add a small amount of NaOH and deionized water to the CGCS to adjust the molar ratio to SiO2:Al2O3:Na2O:H2O = 5.2:1.0:5.0:100. The effects of aging time, crystallization temperature, and crystallization time parameters on synthetic zeolite were studied. The raw materials and the obtained zeolite were tested by XRF, XRD, SEM, FT-IR, TG-DSC, BET, and other technologies. The results show that the specific surface area of the synthesized NaP zeolite can reach 161.06 m2/g, which has the characteristics of large specific surface area, regular morphology, and high crystallinity. We obtained NaP zeolite through a simple and low-cost synthesis method. The synthesized NaP zeolite was used to simulate the removal of ammonia nitrogen in wastewater, and the optimal removal rate was 92.67%. Among them, Na+ plays an important role in the synthesis of NaP zeolite and ion exchange with NH4+. Our research provides new ideas for solving the large-scale accumulation of CGCS and treating ammonia nitrogen in industrial wastewater. Thus, it is a promising green environmental protection and “treating waste by waste” route.

Wenxin Ji, Shiyue Zhang, Pengde Zhao, Shasha Zhang, Ning Feng, Liping Lan, Xiaoguang Zhang, Yonggang Sun, Yuanyuan Li, Yulong Ma. Applied Sciences, 10 (8), 2694, 2020.

The major challenge in the production of xylene from benzene alkylation with methanol is to avoid the side reaction of methanol with olefins, and this leads to the low utilization efficiency of methanol and the generation of byproduct ethylbenzene. Hierarchical porous Ti-ZSM-5 with appropriate acidity was achieved by substituting part of Al by Ti in the synthesis process, which exhibited the high utilization efficiency of methanol and high suppression of the ethylbenzene formation by the efficient suppression of methanol to olefins.

Jie Cen, Ning Zhang, Hualei Hu, Nan Yao, Zhengjia Li, Linyan Yang, Feng Feng, Chunshan Lu, Xiaonian Li. Catalysts, 10 (6), 693, 2020.

In this work, a novel route is discussed to produce in one step ZnO/Burkeite powders by the modified solution combustion method. The ZnO particles enhance the photocatalytic activity in the degradation of Rhodamine B, in which Burkeite mineral acts as a support due to the pH-dependent morphology of the particle aggregates of the as-synthesized powders. The X-ray diffraction (XRD) characterization shows the presence of a heterostructure: ZnO/Burkeite. The Scanning Electron Microscopy (SEM) image shows a morphological dependence with the pH of the solution used for the synthesis. The results show that the system with the highest degradation (92.4%) corresponds to the case in which ZnO/Burkeite heterostructure was synthesized with a pH 11.

A. Luna-Flores, M.A. Morales, R. Agustín-Serrano, R. Portillo, J.A. Luna-López, G.F. Pérez-Sánchez, A.D. Hernández-de la Luz, N. Tepale. Catalysts, 9 (10), 817, 2019.

TiO2/g-C3N4 (GNT) fibers with 1%, 2.5% and 5% (wt%) ratios have been synthesized via one-step electrospinning using polyvinylpyrrolidone (PVP) polymer. Results showed mesoporous fibrous catalysts consisted of anatase (80.0–85.1%) and rutile phase (14.9–20.0%), with diameter between 200–300 nm and band gap lower than 3.0 eV confirming the absorption shift to visible-light region. The formation of •OH radicals and methylene blue dye degradation increases as the g-C3N4 doping percent also increases, following the trend ΤiO2 < GNT1% ≈ GNT2.5% < GNT5%. A z-scheme mechanism is attributed to the photocatalytic performance confirming the potential for green chemistry and environmental technology applications.

Feidias Bairamis, Ioannis Konstantinou, Dimitrios Petrakis, Tiverios Vaimakis. Catalysts, 9 (11), 880, 2019.

Herein, we report on the growth of Cr4+–Li2CaGeO4 crystals by the flux growth method from the flux of LiCl, as well as on the effect of doping Li2CaGeO4 with Cr4+ ions on the NIR region spectral properties and crystal structure. The results quantified the occupancy of Cr4+ in Ge4+ sites. The emission spectrum presented broad bands in the NIR region, i.e., 1000–1500 nm excited by 980 nm, with maximum peaks at 1200 nm at room temperature caused by the transition of 3T2→3A2 in Cr4+ ions. The lifetime decreased with the Cr4+ ion doping concentration, specifically from 14.038 to 12.224 ms. The chemical composition and the valence state of chromium in Li2CaGeO4 were analyzed using X-ray photoelectron spectroscopy, which showed that the chromium in Li2CaGeO4 was tetravalent and no trivalent chromium was found. Therefore, the Cr4+–Li2CaGeO4 crystal has a great potential and future in optical applications.

Dongmei Wang, Xiaowei Zhang, Xinyu Wang, Zhuang Leng, Qianqian Yang, Wen Ji, Hai Lin, Fanming Zeng, Chun Li, Zhongmin Su. Crystals, 10 (11), 1019, 2020.

Using renewable H2 for CO2 hydrogenation to methane not only achieves CO2 utilization, but also mitigates the greenhouse effect. In this work, several Ni-based catalysts with V species using 3D-mesoporous KIT-6 (Korea Advanced Institute of Science and Technology, KIT) as support were prepared at different contents of NiO and V2O5. Small Ni nanoparticles with high dispersibility on 20Ni-0.5V/KIT-6 were identified by X-ray diffraction (XRD), TEM and hydrogen temperature-programmed desorption (H2-TPD) analysis, which promoted the production of more Ni active sites for enhancing catalytic activity for CO2 methanation. Moreover, TEM and hydrogen temperature-programmed reduction (H2-TPR) characterizations confirmed that a proper amount of Ni and V species was favorable to preserve the 3D-mesoporous structure and strengthen the interaction between active Ni and KIT-6. The synergistic effect between Ni and V could strengthen surface basicity to elevate the ability of CO2 activity on the 20Ni-0.5V/KIT-6. In addition, a strong interaction with the 3D-mesoporous structure allowed active Ni to be firmly anchored onto the catalyst surface, which was accountable for improving catalytic activity and stability. These results revealed that 20Ni-0.5V/KIT-6 was a catalyst with superior catalytic activity and stability, which was considered as a promising candidate for CO2 hydrogenation to methane.

Hongxia Cao, Wenyuan Wang, Tianlei Cui, Hongyan Wang, Guang Zhu, Xiangkun Ren. Energies, 13 (9), 2235, 2020.

Depending on the application of bismuth telluride thermoelectric materials in cooling, waste heat recovery, or wearable electronics, their material properties, and geometrical dimensions should be designed to optimize their performance. Recently, thermoelectric materials have gained a lot of interest in wearable electronic devices for body heat harvesting and cooling purposes. For efficient wearable electronic devices, thermoelectric materials with optimum properties, i.e., low thermal conductivity, high Seebeck coefficient, and high thermoelectric figure-of-merit (zT) at room temperature, are demanded. In this paper, we investigate the effect of glass inclusion, microwave processing, and annealing on the synthesis of high-performance p-type (BixSb1−x)2Te3 nanocomposites, optimized specially for body heat harvesting and body cooling applications. Our results show that glass inclusion could enhance the room temperature Seebeck coefficient by more than 10% while maintaining zT the same. Moreover, the combination of microwave radiation and post-annealing enables a 25% enhancement of zT at room temperature. A thermoelectric generator wristband, made of the developed materials, generates 300 μW power and 323 mV voltage when connected to the human body. Consequently, MW processing provides a new and effective way of synthesizing p-type (BixSb1−x)2Te3 alloys with optimum transport properties.

Amin Nozariasbmarz, Daryoosh Vashaee. Energies, 13 (17), 4524, 2020.

Alkaloids, typical nitrogen compounds, were found to be abundant in tobacco waste. The recovery of alkaloids from tobacco waste for biological pesticides could reduce the use of traditional chemical pesticides and avoid the pollution of farmland by the leaching of alkaloids from tobacco waste. Considering the fact that alkaloids can easily volatilize, thermal treatment is expected to be a potential technology to achieve the release and recovery of alkaloids from tobacco waste. For better understanding of conversion behavior of nitrogen-containing compounds in tobacco waste during thermal treatment, purge/trap-GC/MS (gas chromatography mass spectrometry), PY-GC/MS (pyrolysis-gas chromatography mass spectrometry), and fixed-bed/ATD-GC/MS (auto-thermal desorption gas chromatography mass spectrometry) were adopted to detect the ingredients and concentration of nitrogen-containing compounds in tobacco waste and/or volatiles. The results of purge/trap-GC/MS showed that nitrogen-containing compounds in tobacco waste could be effectively evaporated at 180 °C in the forms of N-benzyl-N-ethyl-P-isopropyl benzamide, 2-Amino-4-methylphenol, or N-butyl-tert-butylamine. Specifically, N-benzyl-N-ethyl-P-isopropyl benzamide was the main nitrogenous compound in the volatiles of tobacco wastes accordingly. (S)-3-(1-Methyl-2-pyrrolidinyl) pyridine was dominant in N-compounds in pyrolysis condition according to the results of Py-GC/MS. In air atmosphere, with the heating temperature increasing, the concentration of main (S)-3-(1-Methyl-2-pyrrolidinyl) pyridine was firstly increased and then decreased. Besides, the interactions between the released volatiles could be accelerated at a high temperature. Accordingly, these findings suggested that pyrolysis under proper conditions could effectively promote the extraction of alkaloids from tobacco waste.

Min Wei, Fu Yang, Xuyan Song, Ran Li, Xi Pan, Qiang Gao, Yunlu He, Mingqiao Ye, Hongyun Hu. Energies, 13 (18), 4619, 2020.

The condensation-collection and quantitative analysis of bio-oil limit its component investigation and utilization. In order to find a convenient method for the analysis of bio-oil, the present study conducted an attempt for bio-oil quantitative analysis with the addition of internal standards before pyrolysis. Based on their good thermal stability, phenethyl acetate and naphthalene were selected as standards in the study and experiments were carried out to compare the effects of two added modes (adding into the biowaste before pyrolysis or adding into bio-oil after pyrolysis) on the bio-oil analysis. The results showed that both phenethyl acetate and naphthalene were mainly volatilized under testing conditions, which could be transferred into the oil with the volatile matters during biowaste pyrolysis. Through the co-pyrolysis experiments of the internal standards with lignin and cellulose, almost no interactions were found between the internal standards and such components. Furthermore, adding these standards before pyrolysis hardly affected the properties of noncondensable gas and biochar from the used biowaste samples (tobacco and sawdust waste). Compared with the bio-oil analysis results via traditional methods by adding standards into the bio-oil after pyrolysis, the results regarding the component distribution characteristics of the bio-oil were similar using the proposed method through the addition of standards before pyrolysis. Considering adequate mixing of the added standards (before pyrolysis) in the generated bio-oil, the proposed method could partly help to avoid inaccurate analysis of bio-oil components caused by incomplete collection of the pyrolytic volatiles.

Xuyan Song, Min Wei, Qiang Gao, Xi Pan, Junpeng Yang, Fan Wu, Hongyun Hu. Energies, 13 (23), 6202, 2020.