INTERNATIONAL JOURNAL OF PHARMACEUTICS
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2023
·
IF 5.8
Qiang Huang,Zhiren Zou,Xiaobo Li,Qinwen Xiao,Guang Liang,Wenqi Wu
The drug-amino acid co-amorphous systems and amorphous solid dispersions (ASDs) are promising methods to address the poor water solubility of poorly water-soluble drugs. However, some amino acids might not be perfect co-formers for co-amorphous systems, and the relatively low drug-loading of many ASDs is one of the main disadvantages of ASDs. Thus, poly- l -lysine and polyglutamic acid were selected as the co-formers, ball milled with basic mebendazole, neutral tadalafil and acidic valsartan at different weight ratios (from 3:1 to 1:3) to prepare poly (amino acid)-based ASDs, aiming to combine the advantages of co-amorphous systems (high drug-loading) and ASDs (relatively high T g and high physical stability). All the mixtures were converted into amorphous after milling. The powder dissolution studies showed that drug-poly (amino acid) ASDs improved the dissolution rate of the drug in different ways and to different degrees. Moreover, the two poly (amino acid)s enhanced the physical stability of amorphous drugs. It is worthy to mention that the salt formation between the drug and the poly (amino acid) does not necessarily mean better performance compared to non-salt forming systems, and salt formation is also not a prerequisite for the formation of promising drug-poly (amino acid) ASDs.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Shao-Bo Guo,Wei-Bin Zhang,Ze-Qin Yang,Shan-Shan Chai,Xian-Li Zhang,Xia Zhou,Xiong-Wei Han,Jianping Long
It has become a consensus to study transition metal phosphides with abundant earth reserves and good electrochemical properties as electrode materials for supercapacitors . Among them, cobalt phosphide is particularly attractive because of its good electrical conductivity and theoretical specific capacity. Therefore, cobalt phosphide composites were prepared by hydrothermal reaction and phosphating reaction in this paper. Due to the synergistic effect of different components and the interfacial effect between the components, the ion transport and charge transfer kinetics of the prepared Co/Co 2 P/CoP electrode are both improved, which exhibits excellent electrochemical performance. At the current density of 1 A g −1 , the prepared Co/Co 2 P/CoP electrode material has a specific capacitance of 193.3 mA h g −1 , after 6000 cycles of charge and discharge at the current density of 2 A g −1 , the specific capacitance maintains at 80 %. An asymmetric supercapacitor was assembled with the prepared material as the positive electrode and activated carbon as the negative electrode, which can provide an energy density of 37.87 W h kg −1 at a power density of 799.6 W kg −1 . At the current density of 1 A g −1 , the assembled supercapacitor can maintain 80 % of the initial specific capacitance after 5000 cycles. This provides ideas for future research on this type of energy storage materials .
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Membranes
·
2023
·Vol. 13
·期 2
·166
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IF 4.2
Jingfeng Li,Zeyu Cao,Bo Zhang,Xinai Zhang,Jinchao Li,Yaping Zhang,Hao Duan
CO is a significant product of electrochemical CO2reduction (ECR) which can be mixed with H2to synthesize numerous hydrocarbons. Membranes, as separators, can significantly influence the performance of ECR. Herein, a series of quaternized polybenzimidazole (QAPBI) anion exchange membranes with different quaternization degrees are prepared for application in ECR. Among all QAPBI membranes, the QAPBI-2 membrane exhibits optimized physico-chemical properties. In addition, the QAPBI-2 membrane shows higher a Faraday efficiency and CO partial current density compared with commercial Nafion 117 and FAA-3-PK-130 membranes, at −1.5 V (vs. RHE) in an H-type cell. Additionally, the QAPBI-2 membrane also has a higher Faraday efficiency and CO partial current density compared with Nafion 117 and FAA-3-PK-130 membranes, at −3.0 V in a membrane electrode assembly reactor. It is worth noting that the QAPBI-2 membrane also has excellent ECR stability, over 320 h in an H-type cell. This work illustrates a promising pathway to obtaining cost-effective membranes through a molecular structure regulation strategy for ECR application.
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International Journal of Polymeric Materials and Polymeric Biomaterials
·
2022
·
IF 3.221
Sahid Mehmood,Li Wang,Haojie Yu,Fazal Haq,Bilal-ul Amin,Md Alim Uddin,Shah Fahad,Muhammad Haroon,Di Shen,Zhipeng Ni
In this study, poly(cyclotriphosphazene-co-piperazine) p(HCCP-co-PIP) nanospheres were prepared. The successful preparation of the p(HCCP-co-PIP) nanospheres was confirmed by FT-IR, SEM, TEM, XRD, TGA and DLS, respectively. The prepared p(HCCP-co-PIP) nanospheres were used for drug delivery system. The model drug doxorubicin (DOX) was loaded in p(HCCP-co-PIP) nanospheres. The drug release properties of the p(HCCP-co-PIP) nanospheres were investigated in pH 4.0 and pH 7.4. The cumulative release was found to be 86.2% in pH 4.0 and 54.7% in pH 7.4 at 37 °C after 216 h. The obtained result suggested that the nanospheres could be used as drug carriers.
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SENSORS AND ACTUATORS B-CHEMICAL
·
2022
·
IF 9.221
Chaozhu Huang,Jingwei Zhao,Haichuan Guo,Ziqin Zhuang,Xiaohang Wang,Jiuyang Yu,Fengdong Qu,Minghui Yang
Gas sensing catalyst is the key to proton exchange membrane fuel cell type gas sensor. However, due to the limitations of Pt/C catalyst in an electronic structure and electrochemical stability, the sensing performance of the sensor inconformity the strict performance objectives, and new sensing materials are required. Here we demonstrate that a novel sensing catalyst, Pt/Ti 0.8 Mo 0.2 N, is a highly efficient CO sensing that outperforms the benchmark material Pt/TiN and Pt/C. Pt/Ti 0.8 Mo 0.2 N effectively reduces the cross-sensitivity of interfering gas and greatly improves the CO selectivity, sensitivity and long-term stability of the sensor. Simultaneously, profit by the design of a high humidity cathode sealing chamber, the relative humidity of the environment exhibits a slight impact on the sensor. Furthermore, we confirm that Pt/Ti 0.8 Mo 0.2 N exhibit the best gas sensing performance at low Pt loading of 15 wt%. This discovery points to the strategy of combining low-cost and high-performance electrode catalytic materials for new generation gas sensors.
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Catalysts
·
2022
·Vol. 12
·期 2
·236
·
IF 4.501
Xinlei Yu,Xun Tao,Yunfei Gao,Lu Ding,Yanqin Wang,Guangsuo Yu,Fuchen Wang
Compared to the Claus process, selective H2S catalytic oxidation to sulfur is a promising reaction, as it is not subject to thermodynamic limitations and could theoretically achieve ~100% H2S conversion to sulfur. In this study, we investigated the effects of Co and Fe co-doping in ABO3perovskite on H2S selective catalytic oxidation. A series of LaFexCo1−xO3(x = 0, 0.2, 0.4, 0.6, 0.8, 1.0) perovskites were synthesized by the sol-gel method. Compared to LaFeO3and LaCoO3, co-doped LaFexCo1−xO3significantly improved the H2S conversion and sulfur selectivity at a lower reaction temperature. Nearly 100% sulfur yield was achieved on LaFe0.4Co0.6O3under 220 °C with exceptional catalyst stability (above 95% sulfur yield after 77 h). The catalysts were characterized by XRD, BET, FTIR, XPS, and H2-TPR. The characterization results showed that the structure of LaFexCo1−xO3changed from the rhombic phase of LaCoO3to the cubic phase of LaFeO3with Fe substitution. Doping with appropriate iron (x = 0.4) facilitates the reduction of Co ions in the catalyst, thereby promoting the H2S selective oxidation. This study demonstrates a promising approach for low-temperature H2S combustion with ~100% sulfur yield.Keywords:hydrogen sulfide;selective oxidation;perovskite oxides;oxygen vacancy
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Liwei Yang,Yin Wei,Yaqi Peng,Yang Liu,Zhou Shu,Yansong Wang,Qingli Meng,Chuanliang Zhao,Hongmei Zhao,Fashan Yang,Bo Lai
Aiming at realizing heavy metal recycling and resource utilization, a carbon-based bimetallic material (Fe 1 Co 2 @C) was fabricated via calcining cationic resin exchanged with Fe and Co cations. It exhibited superior peroxymonosulfate (PMS) activation performance to degrade atrazine (ATZ) compared with the monometallic materials (Fe@C and Co@C). Fe 1 Co 2 @C/PMS performed high degradation of 5 mg/L ATZ with the reaction rate constant ( k obs ) of 0.0869 min −1 within 30 min of reaction time. The effects of catalyst loading, PMS dosage, initial pH, and the presence of inorganic ions (NO 3 − , SO 4 2− Cl − , and HCO 3 − ) and natural organic matters (NOMs) were also investigated in this work. According to the radical quenching experiments and electron paramagnetic resonance (EPR), hydroxyl radical ( • OH) and sulfate radical (SO 4 • − ) were identified to be the primary reactive oxygen species (ROS) responsible for the ATZ degradation, especially • OH. What’s more, reaction mechanism of Fe 1 Co 2 @C was demonstrated that −(C− SO 3 ) x − Co(II) and the synergy between Fe and Co on the surface could both promote the heterogeneous redox cycles of Co(II)/Co(III) and Fe(II)/Fe(III) to activate PMS. Based on the detection results of intermediates by LC-MS, possible degradation pathways of ATZ included dealkylation, dichlorination, hydroxylation, and deamination-hydroxylation processes were proposed. This research not only provides new insights of PMS activation by carbon-based bimetallic catalyst for water treatment, but also proposes a new way for reusing the waste saturated cation resin waste with heavy metal.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2022
·Vol. 33
·期 10
·8256-8269
·
IF 2.779
Kang Xiao-Ya,Ma Ying-Xia,Wang Jia-Wei,Shi Xiao-Feng,Chen Xin-Quan,Tian Hu,Ran Fen
The cobalt-based metal–organic framework (Co-MOF) as an electrode material with satisfied electrochemical performances has received much attention in energy storage field. Herein, a strip-like Co-MOF was fabricated by a simple one-step solvothermal strategy. In which, the strips are of distinct lengths and thicknesses, and haphazardly lap together to form a stable structure similar to a bird's nest that could provide more moderation space for the volume expansion of the Co-MOF as electrode material in charge and discharge process. The unique structure shows the characteristics of hierarchical pores, which could effectively improve the specific surface area of the Co-MOF material, thereby enhancing the storage of electrochemical energy. The strip-like Co-MOF is endowed with large specific surface area of 643.5 m 2 /g, high specific capacity of 135.1 C/g at a current density of 0.5 A/g, and good capacitance retention of 91.7% after 2000 cycles at 5 A/g. Moreover, the asymmetric supercapacitor device assembled by using the strip-like Co-MOF as cathode and commercial activated carbon (AC) as anode exhibits a specific capacitance of 58.3 F/g at the current density of 0.5 A/g in a voltage window of 1.55 V, and the maximum energy density is 19.5 Wh/kg at a power density of 389 W/kg. The novel strategy to construct unique microstructure MOF with good properties could be applied to prepare other MOF-based functional materials for various applications.
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COLORATION TECHNOLOGY
·
2022
·Vol. 139
·期 1
·57-67
·
IF 2.049
Fuchun Wang,Wei Ma,Bingtao Tang,Shufen Zhang
To obtain a new type of macromolecular reactive dye with high fixation and good light fastness, poly(styrene- co -maleic acid) was synthesised by co-polymerisation of styrene and maleic anhydride, then, through nitration, reduction, diazotisation and coupling reaction, novel macromolecular reactive dyes were prepared with a solubility greater than 60 g/L. The dyes were used to dye cotton fabrics; the results showed their fixation was more than 92%, and both the rub and wash fastness of the dyes were good. The light fastness of the red and blue dyes with the ethoxy group on melamine was grade 4, and for the yellow dye reached grade 5. The poly(styrene- co -maleic acid) macromolecular reactive dyes exhibit very good application prospects in practice.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
·
IF 5.518
Chengcheng Qi,Chongchao Zhang,Ziyin Yang
Defect engineering was considered as an effective strategy to regulate electrocatalytic activities of transition metal oxides . However, there are seldom reports about metal defects in electrochemical sensing. In this work, Co-defected Co 3 O 4 was synthesized via thermal treatment of glycerolatocobalt (CoGly) precursor for constructing a novel electrochemical nonenzymatic glucose sensor. The obtained nanomaterials were characterized by transmission electron microscopy (TEM), powder X-ray diffractometry (XRD), Raman spectra , X-ray photoelectron spectroscopy (XPS) and electrochemical techniques . The presence of Co defects regulated electronic structure of Co 3 O 4 , which not only speeds up electron transfer rate but also exposes more high-valent Co sites, thus improving electrocatalytic activities. Under optimized conditions, Co-defected Co 3 O 4 electrode exhibited excellent performance for glucose analysis with a wide linear range of 0.2 µM to 0.5 mM, a low detection limit of 0.16 µM. Importantly, an ultrahigh sensitivity of 2595.7 µA·mM −1 ·cm −2 was also obtained, which was about 10 times higher than that of conventional Co 3 O 4 . Therefore, engineering Co 3 O 4 with Co defects is an effective strategy to tailor electrocatalytic activity, which sheds light on the potential applications of metal defects in the field of electrochemical nonenzymatic sensing.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2022
·
IF 7.139
Songyin Yu,Fei Wang,Jianchun Jiang,Xinyi Luo,FeiFei Xing,Taotao He,Junfeng Feng,Xiaoxiang Jiang
The Co catalysts for lipid hydrotreatment into green diesel commonly has a poor dispersion of Co and big Co particle size due to metal agglomeration, limiting its catalytic performance. To solve this problem, three Co catalysts on activated carbon (AC), Al 2 O 3 , and nitrogen-doped carbon (NC) are prepared, among which the Co/NC is synthesized by using the Co metal-organic framework (MOF) as the precursor. In the hydrotreatment of oleic acid , the Co/NC catalyst attained 99.6% conversion and 99.6% alkane yield, much higher than Co/AC (76.8% and 14.9%) and Co/Al 2 O 3 (96.3% and 18.7%). From the characterizations of the catalyst, the excellent performance is ascribed to its lamellar structure , large specific surface area, and high dispersion of Co sites, providing massive Co-active sites for hydrotreatment reaction. Moreover, the catalytic performance of Co/NC under various hydrotreatment temperatures with different feedstocks is investigated.
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JOURNAL OF NANOBIOTECHNOLOGY
·
2022
·Vol. 20
·期 1
·1-11
·
IF 9.429
Chen Mo,Qiao Yingyu,Cao Jie,Ta La,Ci Tianyuan,Ke Xue
Background Acute myeloid leukemia (AML) showed limited clinical therapeutic efficiency with chemotherapy for its multi-distributed lesions and hard-to-kill leukemia cells deep in the bone marrow.Results Here, a biomimetic nanosystem (DR@PLip) based on platelet membrane (PM) coating and doxorubicin (DOX)/ginsenoside (Rg3) co-loading was developed to potentiate the local-to-systemic chemoimmunotherapy for AML. The PM was designed for long-term circulation and better leukemia cells targeting. The participation of Rg3 was proved to enhance the tumor sensitivity to DOX, thus initiating the anti-tumor immune activation and effectively combating the leukemia cells hiding in the bone marrow.Conclusion sIn conclusion, the strategy that combining immediate chemotherapy with long-term immunotherapy achieved improved therapeutic efficiency and prolonged survival, which provided a new perspective for the clinical treatment of AML.
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