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2D nanodendrites (NDs) and nanosheets (NSs) have been regarded as efficient nanocatalysts for enhancing the electrocatalytic performance due to their low coordinated sites and abundant electrocatalytic centers. Nevertheless, it remains challenging to construct advanced NDs and NSs in a single reaction system. Herein, by tuning the volume ratios of mixed solvents, the reduction and diffusion rate of Sn2+ on Pd NSs template was rationally controlled to prepare PdSn NDs and PdSn NSs. Ascribed to the open 2D nanostructure, high specific surface area, and robust synergistic effect, the as-prepared PdSn NDs and PdSn NSs exhibited distinguished electrocatalytic activities for ethylene glycol oxidation reaction (EGOR) and ethanol oxidation reaction (EOR), as well as commendable electrocatalytic durability, which were far superior to the Pd NSs and commercial Pd/C. In addition, the PdSn NDs exhibited enhanced reaction kinetics because the characteristic branch structure exposed a high density of active sites. This work may provide significant guidance for preparing excellent nanocatalysts with various morphological features by simply optimizing the content of the coexisting solvents.
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Exploring highly effective bifunctional electrocatalysts with surface structural advantages and synergistic optimization effects among multimetals is greatly important for overall water splitting. Herein, we successfully synthesized Pt-loaded NiFe-metal-organic framework nanosheet arrays grown on nickel foam (Pt-NiFe-MOF/NF) via a facile hydrothermal-electrodeposition process. Benefiting from large exposed specific surface, optimal electrical conductivity and efficient metal-support interaction endow Pt-NiFe-MOF/NF with highly catalytic performance, exhibiting small overpotential of 261 mV toward oxygen evolution reaction and 125 mV toward hydrogen evolution reaction at a current density of 100 mA cm-2 in alkaline medium. More significantly, the assembled water electrolyzer comprising the Pt-NiFe-MOF/NF//Pt-NiFe-MOF/NF couple demands a low cell voltage of 1.45 V to reach 10 mA cm-2. This work renders a viable approach to design dual-functional electrocatalysts with exceptional electrocatalytic activity and stability at high current density, showing the great prospect of water electrolysis for commercial application.
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The development of efficient and stable Pd-based electrocatalysts is extremely important to facilitate the development of catalysts for polyol oxidation reactions. To synthesize Pd-based catalysts with excellent catalytic performance, a series of PdAg porous nanowires (PdAg PNWs) with different elemental ratios was constructed by facile synthesis using a seed-mediated method. The synthesized PdAg PNWs have a rough surface and a porous one-dimensional structure, which optimize the specific surface area and surface area of catalysts, thereby providing more active sites for catalysts. PdAg PNWs benefited from the geometric effect of porous nanowires and the synergy between Pd and Ag, showing excellent catalysis (8243.0 and 4137.0 mA mgPd-1) for the ethylene glycol oxidation reaction (EGOR) and glycerol oxidation reaction (GOR). Among them, the optimal Pd62Ag38 PNWs show the highest catalytic activity (6.0 times and 3.9 times higher than Pd/C) and stability compared with Pd57Ag43 PNWs, Pd51Ag49 PNWs, and Pd/C for EGOR and GOR. At the same time, this porous one-dimensional structure also endows PdAg PNWs with faster electron transfer capabilities than Pd/C. This work will likely provide an effective strategy for constructing cost-effective catalysts.
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Myeloid phagocytes, neutrophils in particular, are easily consumed when they fight against a large number of invading microbes. Hence, they require efficient and constant replenishment from their progenitors via the well-orchestrated emergency myelopoiesis in the hematopoietic organs. The cellular and molecular details of the danger-sensing and warning processes to activate the emergency myelopoiesis are still under debate. In this study, we set up a systemic infection model in zebrafish (Danio rerio) larvae via circulative administration of LPS. We focused on the cross-talk of macrophages with myeloid progenitors in the caudal hematopoietic tissue. We revealed that macrophages first detected LPS and sent out the emergency message via il1ß The myeloid progenitors, rather than hematopoietic stem and progenitor cells, responded and fulfilled the demand to adapt myeloid expansion through the synergistic cooperation of NF-κB and C/ebpß. Our study unveiled a critical role of macrophages as the early "whistle blowers" to initiate emergency myelopoiesis.
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Infecciones Bacterianas/inmunología , Interleucina-1beta/metabolismo , Mielopoyesis/inmunología , Proteínas de Pez Cebra/metabolismo , Animales , Animales Modificados Genéticamente , Proteína beta Potenciadora de Unión a CCAAT/genética , Proteína beta Potenciadora de Unión a CCAAT/metabolismo , Modelos Animales de Enfermedad , Embrión no Mamífero , Humanos , Interleucina-1beta/genética , Lipopolisacáridos/inmunología , Macrófagos/enzimología , Macrófagos/metabolismo , Factor de Transcripción ReIA/genética , Factor de Transcripción ReIA/metabolismo , Pez Cebra , Proteínas de Pez Cebra/genéticaRESUMEN
The core@shell structure dimension of the Pd-based nanocrystals deeply impacts their catalytic properties for C1 and C2 alcohol oxidation reactions. However, the precise simultaneous control on the synthesis of core@shell nanocrystals with different shell dimensions is difficult, and most synthesis on Pd-based core@shell nanocatalysts involves the surfactants participation by multiple steps, thus leads to limited catalytic properties. Herein, for the first time, a facile one-step surfactant-free strategy is developed for shell dimension reconstruction of PdAu@Pd core@shell nanocrystals by altering volume ratios of mixed solvents. The Pd-based sunflower-like (SL) and coral grass-like (CGL) nanocrystals are obtained with different 2D hexagonal nanosheet assembles and 3D network shells, respectively. Benefitting from the clean surface shell of 2D ultrathin nanosheets structure, high atom utilization efficiency, and robust electronic effect. The PdAu@Pd SL achieves the ascendant methanol/ethanol/ethylene glycol oxidation reaction (MOR/EOR/EGOR) activities, much higher than Pd/C catalysts, as well as the improved antipoisoning ability. Notably, this one-step construction shell dimension of PdAu@Pd core@shell catalysts not only provide a significant reference for the improvement of surfactant-free synthetic routes, but also shed light on the advanced engineering on shell dimensions in core@shell nanostructures for electrocatalysis and so forth.
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Nanopartículas , Paladio , Catálisis , Etanol , SolventesRESUMEN
Ring-opening copolymerization (ROCP) of benzylsulfonyl macroheterocyclosiloxane (BSM) and five different cyclosiloxanes was systematically investigated. A general approach for the synthesis of benzylsulfonyl-containing silicone copolymers with various substituents, including methyl, vinyl, ethyl, and phenyl, was developed herein. A series of copolymers with variable incorporation (from 6 % to 82 %) of BSM were obtained by modifying the comonomer feed ratio and using KOH as the catalyst in a mixed solvent of dimethylformamide and toluene. The obtained copolymers exhibited various composition-dependent properties and unique viscoelasticity. Notably, the surface and fluorescent characteristics as well as the glass transition temperatures of the copolymers could be tailored by varying the amount of BSM. Unlike typical sulfone-containing polymers, such as poly(olefin sulfone)s, the prepared copolymers displayed excellent thermal and hydrolytic stability. The universal strategy developed in the present study provides a platform for the design of innovative silicone copolymers with adjustable structures and performance.
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Pt-based catalysts with core@shell structures are widely used in alcohol oxidations due to their excellent catalytic performance. In this work, we synthesized a series of core@shell PtAuAg@PtAg hollow nanodendrites (HNDs) with different compositions by a simple seed-mediated method. The PtAuAg@PtAg HNDs with a hollow core and dendritic shell exhibit excellent catalytic performance for ethylene glycol oxidation reaction (EGOR) and methanol oxidation reaction (MOR). Among these, Pt38Au29Ag33 HNDs have the highest mass activity (12364.0 mA mgPt-1/3278.0 mA mgPt-1) for EGOR and MOR, which is 4.2 times and 5.3 times higher than that of commercial Pt/C (2941.0 mA mgPt-1/617.6 mA mgPt-1), respectively. More importantly, after successive cyclic voltammetry tests, the retained mass activities of Pt38Au29Ag33 HNDs are 3913.8 mA mgPt-1 and 348.3 mA mgPt-1, which are much higher than that of commercial Pt/C as well. The excellent catalytic performance of PtAuAg@PtAg HNDs can be attributed to the structure of HNDs, which can greatly increase the surface area and active sites, as well as the electronic and synergistic effects among Pt, Au, and Ag. This research may provide new ideas for the development of high-efficiency hollow catalytic materials for EGOR and MOR.
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OBJECTIVE: The available content of mercury (Hg) in farmland soil is directly related to the safety of agricultural products. Meanwhile, humans may accumulate high concentrations of Hg through the food chain, resulting in health damage. Regarding the remediation technologies of Hg-contaminated soil, research and development is mainly concentrated on the immobilisation of Hg in soil and efficient extraction by accumulators. Therefore, in this work, the highly Hg-tolerant strain Pseudomonas alkylphenolica KL28 was used to study the removal effect of Hg in a solution, immobilization effect of Hg in soil, and its effect on growth, Hg accumulation and photosynthetic characteristics of Brassica campestris L. RESULTS: KL28 could effectively remove Hg2+ in the solution, with the removal ratio of 96.0% at 24 h. This strain could reduce decreases in shoots' and roots' dry weights by 31% and 16%, respectively, at a Hg concentration of 20 mg/L. The available Hg in the soil decreased to 4.7-9.4% in 8 days treated with KL28 bacterial solution at a dosage of 100 L/hm2. Meanwhile, with increases in Hg concentrations, Fv/Fm, Y(II), Y(I) and Y(NPQ) in the leaves of B. campestris showed a downward trend while Y(ND) and Y(NO) displayed an upward trend. Under the stress of 20 mg/L Hg2+, KL28 could reduce the Fv/Fm from 11.2 to 6.1%. CONCLUSIONS: KL28 could effectively remove Hg in the solution, immobilize Hg in soil, promote growth, decrease Hg accumulation and affect photosynthetic characteristics of B. campestris, indicating its potential use in Hg contaminated soils.
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Brassica/química , Mercurio , Pseudomonas , Contaminantes del Suelo , Biodegradación Ambiental , Brassica/crecimiento & desarrollo , Brassica/microbiología , Mercurio/aislamiento & purificación , Mercurio/metabolismo , Fotosíntesis , Hojas de la Planta/química , Hojas de la Planta/crecimiento & desarrollo , Hojas de la Planta/microbiología , Raíces de Plantas/química , Raíces de Plantas/crecimiento & desarrollo , Raíces de Plantas/microbiología , Pseudomonas/química , Pseudomonas/metabolismo , Contaminantes del Suelo/aislamiento & purificación , Contaminantes del Suelo/metabolismoRESUMEN
BACKGROUND AND PURPOSE: Carboplatin is a platinum-containing compound with efficacy against various malignancies. The physico-chemical stability of carboplatin in dextrose 5% water (D5W) has been thoroughly studied; however, there is a paucity of stability data in clinically relevant 0.9% sodium chloride infusion solutions. The manufacturer's limited stability data in sodium chloride solutions hampers the flexibility of carboplatin usage in oncology patients. Hence, the purpose of this study is to determine the physical and chemical stability of carboplatin-sodium chloride intravenous solutions under different storage conditions. METHODS: The physico-chemical stability of 0.5 mg/mL, 2.0 mg/mL, and 4.0 mg/mL carboplatin-sodium chloride solutions prepared in polyvinyl chloride bags was determined following storage at room temperature under ambient fluorescent light and under refrigeration in the dark. Concentrations of carboplatin were measured at predetermined time points up to seven days using a stability-indicating high-performance liquid chromatography method. RESULTS: All tested solutions were found physically stable for at least seven days. The greatest chemical stability was observed under refrigerated storage conditions. At 4â, all tested solutions were found chemically stable for at least seven days, with nominal losses of ≤6%. Following storage at room temperature exposed to normal fluorescent light, the chemical stability of 0.5 mg/mL, 2.0 mg/mL, and 4.0 mg/mL solutions was three days, five days, and seven days, respectively. CONCLUSION: The extended physico-chemical stability of carboplatin prepared in sodium chloride reported herein permits advance preparation of these admixtures, facilitating pharmacy utility and operations. Since no antibacterial preservative is contained within these carboplatin solutions, we recommend storage, when prepared under specified aseptic conditions, no greater than 24 h at room temperature or three days under refrigeration.
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Carboplatino/química , Estabilidad de Medicamentos , Soluciones Farmacéuticas/química , Cloruro de Polivinilo/química , Cloruro de Sodio/química , Embalaje de Medicamentos/métodos , Almacenaje de Medicamentos/métodos , Infusiones Intravenosas/métodos , Refrigeración/métodos , TemperaturaRESUMEN
Zeolitic imidazolate frameworks (ZIFs), a class of promising metal organic frameworks (MOFs) material, display high porosity and chemical/thermal stability. However, there are problems such as few active sites and restricted exposed active areas, which limit the oxygen evolution reaction (OER) performance of catalysts. Here, starting from zeolitic imidazolate framework-67 (ZIF-67), we have successfully synthesized Pt-doped CoFe layered double hydroxide (Pt/CoFe LDH) catalysts for efficient OER catalysis. The obtained Pt/CoFe LDH-4 catalysts provides large surface areas and abundant active sites, which further improves the OER performance. In detail, the Pt/CoFe LDH-4 exhibits a lower overpotential of 263 mV at a current density of 40 mA cm-2, in 1 M KOH solution, the stability of the catalyst exceeds 120 h at this current density, far superior to commercial catalyst RuO2. This study describes a new design idea for synthesis of LDH catalytic materials with low noble metal doping, which broadens the way to the synthesis of robust OER catalysts derived from ZIF-67.
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Two-dimensional (2D) Pd-based nanostructures with a high active surface area and a large number of active sites are commonly used in alcohol oxidation research, whereas the less explored ring structure made of nanosheets with large pores is of interest. In this study, we detail the fabrication of PdCu nanorings (NRs) featuring hollow interiors and low coordinated sites using a straightforward solvothermal approach. Due to increased exposure of active sites and the synergistic effects of bimetallics, the PdCu NRs exhibited superior catalytic performance in both the ethanol oxidation reaction (EOR) and the ethylene glycol oxidation reaction (EGOR). The mass activities of PdCu NRs for EOR and EGOR were measured at 7.05 A/mg and 8.12 A/mg, respectively, surpassing those of commercial Pd/C. Furthermore, the PdCu NRs demonstrated enhanced catalytic stability, maintaining higher mass activity levels compared to other catalysts during stability testing. This research offers valuable insights for the development of efficient catalysts for alcohol oxidation.
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Hydroponic cultivation of lettuce is an increasingly popular sustainable agricultural technique. However, Escherichia coli, a prevalent bacterium, poses significant concerns for the quality and safety of hydroponically grown lettuce. This study aimed to develop a growth model for E. coli and background microflora in hydroponically grown lettuce. The experiment involved inoculating hydroponically grown lettuce with E. coli and incubated at 4, 10, 15, 25, 30, 36 °C. Growth models for E. coli and background microflora were then developed using Origin 2022 (9.9) and IPMP 2013 software and validated at 5 °C and 20 °C by calculating root mean square errors (RMSEs). The result showed that E. coli was unable to grow at 4 °C and the SGompertz model was determined as the most appropriate primary model. From this primary model, the Ratkowsky square root model and polynomial model were derived as secondary models for E. coli-R168 and background microflora, respectively. These secondary models determined that the minimum temperature (Tmin) required for the growth of E. coli and background microflora in hydroponically grown lettuce was 6.1 °C and 8.7 °C, respectively. Moreover, the RMSE values ranged from 0.11 to 0.24 CFU/g, indicating that the models and their associated kinetic parameters accurately represented the proliferation of E. coli and background microflora in hydroponically grown lettuce.
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Objective: This study aimed to identify the risk factors for subchorionic hematoma (SCH) in the first trimester of in vitro fertilization (IVF) twin pregnancies and investigate the impact of SCH on pregnancy outcomes. Study design: A prospective cohort study was conducted at Chengdu Women and Children's Central Hospital. The study recruited patients who were identified with twin pregnancies in the first trimester, undergoing IVF treatment from January 2020 to May 2021. The demographic characteristics and pregnancy outcomes were compared between the SCH and the non-SCH groups. A logistic regression analysis was used to determine the risk factors for SCH and adverse pregnancy outcomes. Results: In the first trimester, 38% of patients developed SCH. The independent risk factors for SCH included male factor, hydrosalpinx, polycystic ovary syndrome (PCOS), previous miscarriage, and adenomyosis. With respect to the pregnancy outcomes, only the rate of twin pregnancy loss before 20 gestational weeks was significantly higher in the SCH group than in the non-SCH group. After adjusting for the confounding factors, the presence of SCH diminished the ovarian reserve, and previous miscarriage was independently related to twin pregnancy loss before 20 gestational weeks. Conclusion: This may be the first study to evaluate the risk factors of SCH in twin pregnancies who underwent IVF-ET/FET treatment, which may provide some theoretical basis for clinical practice in the future. Furthermore, it was found that the occurrence of SCH was associated with the loss of both pregnancies before 20 gestational weeks. Therefore, these patients should be offered increased surveillance and timely treatment.
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Porous nanospheres (PNSs) have great development prospects in the electrocatalysis field because of their structural characteristics, such as a large specific surface area. However, it is still a challenge to find a simple and energy-saving method for the controllable synthesis of PNS nanocatalysts. In this paper, a one-pot CTAC-assisted strategy was developed for the successful formation of PdPtAg PNSs with high porosity at room temperature. Benefitting from the unique structures, optimized composition, acceleration of charge transfer and enhanced resistance to CO poisoning, the PdPtAg PNSs displayed considerably improved electrocatalytic performance with high mass activity and stability toward the ethylene glycol oxidation reaction (EGOR) and glycerol oxidation reaction (GOR). The EGOR and GOR mass activities of PdPtAg were 5.00 A mgmetal-1 and 3.06 A mgmetal-1, which are 6.22 and 1.91 times that of commercial Pd/C, respectively. This work is expected to offer a new path for improving catalytic performance by simple design and adjustment of morphology.
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Bimetallic two-dimensional (2D) nanomaterials are widely used in electrocatalysis owing to their unique physicochemical properties, while trimetallic 2D materials of porous structures with large surface area are rarely reported. In this paper, a one-pot hydrothermal synthesis of ternary ultra-thin PdPtNi nanosheets is developed. By adjusting the volume ratio of the mixed solvents, PdPtNi with porous nanosheets (PNSs) and ultrathin nanosheets (UNSs) was prepared. The growth mechanism of PNSs was investigated through a series of control experiments. Notably, thanks to the high atom utilization efficiency and fast electron transfer, the PdPtNi PNSs have remarkable activity of methanol oxidation reaction (MOR) and ethanol oxidation reaction (EOR). The mass activities of the well-tuned PdPtNi PNSs for MOR and EOR were 6.21 A mg-1 and 5.12 A mg-1, respectively, much higher than those of commercial Pt/C and Pd/C. In addition, after durability test, the PdPtNi PNSs exhibited desirable stability with the highest retained current density. Therefore, this work provides a significant guidance for designing and synthesizing a new 2D material with excellent catalytic performance toward direct fuel cells applications.
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The study aimed to evaluate the clinical significance of thyroid hormone-responsive (THRSP) and explore its relevant pathways in thyroid carcinoma (THCA). The gene expression data of THRSP were obtained and the prognostic significance of THRSP in THCA was analyzed through various bioinformatics databases. Then, the factors influencing THRSP mRNA expression were explored, and the function of THRSP in predicting the lymph node metastasis (LNM) stage was determined. We further performed the enrichment analysis and constructed a protein-protein interaction (PPI) network to examine potential regulatory pathways associated with THRSP. THRSP gene expression was significantly increased in THCA compared with the normal tissues. High THRSP mRNA expression had a favorable overall survival (OS) in THCA patients (P < .05). Additionally, the mRNA expression of THRSP was related to stage, histological subtype, and methylation among THCA patients (all P < .05). Besides, THRSP served as a potent predictor in discriminating the LNM stage of thyroid cancer patients. According to Kyoto Encyclopedia of Genes and Genomes (KEGG) and gene set enrichment analysis (GSEA) on THRSP-associated genes, THRSP was positively related to metabolic pathways. The upregulation of THRSP predicted a good OS in THCA patients. Furthermore, THRSP might inhibit THCA progression through positive regulation of metabolism-associated pathways.
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Neoplasias de la Tiroides , Biología Computacional , Humanos , Metástasis Linfática , Mapas de Interacción de Proteínas , ARN Mensajero/metabolismo , Hormonas Tiroideas/metabolismo , Neoplasias de la Tiroides/tratamiento farmacológico , Neoplasias de la Tiroides/genéticaRESUMEN
Low-dimensional noble-metal materials (LDNMs) with different structural advantages have been considered as the high-performance catalysts for C2 alcohol electrooxidation. However, it is still a great challenging to precisely construct nanomaterials with low-dimensional composite structure thus to take advantages of various dimension, especial without the surfactant participation. Most studies focus on the modulation of the single dimensional nanocatalysts, the correlation between electrocatalytic performances and low-dimension composite have been rarely reported. Herein, we engineered a simple one-step approach to design multi-low-dimensional PdPt nanomaterials by using different Pd precursors. The low-dimensional PdPt nanocrystals (NCs) composed of zero dimension (0D) dendrite-like nanoparticles and two dimension (2D) nanosheets were obtained by using Pd(OAc)2, and meanwhile the 2D PdPt nanosheet assemblies (NAs) were synthesized by the introduction of NaPdCl4. Specifically, benefitting from the unique low-dimension structures with fast electron/mass transfer, and optimized electronic and synergistic effect, the multi-low-dimensional 0D-2D PdPt NCs showed the highest ethanol oxidation reaction (EOR)/ethylene glycol oxidation reaction (EGOR) mass activities, which were much higher than 2D PdPt NAs. The 0D-2D PdPt NCs also exhibited the highest structural stability. Generally, this work could inspire more advanced designs for surfactant-free synthesis and promote the fundamental engineering on nanocatalysts with low-dimension composite structure for electrocatalytic fields.
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OBJECTIVE: To investigate the clinical outcomes and prognostic factors of refractory/relapsed acute myeloid leukemia (AML) patients who received allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS: The clinical data of 80 refractory/relapsed AML patients who received allo-HSCT from December 2013 to June 2020 were retrospectively analyzed, including the overall survival (OS) rate, disease-free survival (DFS) rate, relapse rate, incidence of transplant-related mortality (TRM), and the related risk factors were explored. RESULTS: Hematopoietic reconstitution was obtained in all 80 patients after transplantation, the 3-year OS and DFS rates were (48.8±6.3)% and (40.8±6.7)%, respectively. The 3-year cumulative incidence of relapse and TRM were 33.8% (95%CI: 0.254-0.449) and 15.0%(95%CI: 0.114-0.198), respectively. Univariate analysis showed that non-remission (NR) status before transplantation, DNMT3A R882 mutations and grade II-IV acute graft-versus-host disease (aGVHD) had negative effects on OS and DFS. Multivariate analysis indicated that the DNMT3A R882 mutations and grade II-IV aGVHD were independent risk factors for OS (HR=0.253, 95%CI: 0.092-0.695, P=0.008; HR=5.681, 95%CI: 2.101-15.361, P=0.001) and DFS (HR=0.200, 95%CI: 0.071-0.569, P=0.003; HR=7.117, 95%CI: 2.556-19.818, P<0.001). The 3-year cumulative incidence of relapse was 71.4%(95%CI: 0.610-0.836) in genetic high-risk group, which was higher than 23.3%(95%CI: 0.147-0.370) in intermediate-risk group and 23.5%(95%CI: 0.127-0.437) in favorable-risk group (P=0.006). CONCLUSION: Allo-HSCT is an effective and safe choice for refractory/relapsed AML patients. DNMT3A R882 mutations and grade II-IV aGVHD are negative prognostic factors of allo-HSCT for refractory/relapsed AML patients.
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Enfermedad Injerto contra Huésped , Trasplante de Células Madre Hematopoyéticas , Leucemia Mieloide Aguda , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Humanos , Leucemia Mieloide Aguda/genética , Leucemia Mieloide Aguda/terapia , Pronóstico , Recurrencia , Estudios Retrospectivos , Trasplante Homólogo/efectos adversosRESUMEN
The application of graphite carbon nitride photocatalysts is hampered by their low specific surface areas, few active sites, and low photogenerated electron-hole transfer rates. Here, we report a green and controllable strategy for synthesizing kelp-like carbon nitride nanosheets through self-assembled materials prepared from melamine and trithiocyanuric acid using sonochemistry. The prepared carbon nitride nanosheets showed superior and long-lasting photocatalytic activity in hydrogen evolution and the degradation of tetracycline hydrochloride. The significantly enhanced photocatalytic performance of carbon nitride nanosheets is attributed to the curled porous nanosheet structure and the appropriate amount of O-doping. This work provides a new design strategy for preparing shape-controlled carbon nitride catalysts via a green, fast, sonochemically mediated self-assembly approach.
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Grafito , Kelp , Grafito/química , Hidrógeno , Nitrilos , TetraciclinaRESUMEN
Salting and rehydration of myofibrils can be interfered with free radical diffusion process. This study investigated the effects of salt content (0, 1, 3 and 5%) and H2O2/ascorbate-based hydroxyl radical (OH)-generating system (1, 10, 20 mM H2O2) on the oxidation, conformation, aggregation, and thermal stability of porcine myofibrillar proteins (MPs). Results showed that 5% of salt inhibited carbonylation of MPs with intensive sulfhydryl loss and tryptophan quenching. Fourier transform infrared (FTIR), laser light scattering, and scanning electron microscopy (SEM) suggested that 20 mM H2O2 transformed more α-helix into ß-sheet of MPs, favoring larger aggregates being selectively exposed towards solvent during salt-induced fiber swelling. Oxidized MPs brined with ≤1% salt underwent partial unfolding with higher flexibility, while up to 5% of salt greatly hampered their hydration potential and weakened inter-fibrillar hydrogen bond with an improved protein solubility. Micro-rheology revealed that 1% of salt and 10 mM H2O2 rendered a denser structure of heat-set MPs gels.