Intake level and exposure assessment of fluoride in brick tea for herdsmen in Qinghai Province

ObjectiveTo evaluate the intake level of fluoride and potential health risks for herdsmen in Qinghai province.MethodsThe monitoring data of fluoride content in brick tea from 2019 to 2021 and the data of brick tea consumption by herdsmen in 2015 were used. Based on the deterministic assessment model， the daily intake of fluoride from brick tea by herdsmen was calculated.ResultsThe average fluorine content of brick tea was 464.32 mg/kg， the maximum was 1 206.00 mg/kg， and the over standard rate was 74.74% （213/285）， among which the over standard rate of Kang brick tea was the highest （100%， 12/12）. The average intake level of fluoride was 0.048 mg/kg BW per day， which was close to the tolerable upper intake levels （UL）. The daily fluoride intake of high-consumption group （P95） was 0.177 mg/ kg BW， which was 3.1 times that of UL. The average daily intake of fluoride from brick tea by female consumers was 1.3 times that of men.ConclusionThe concentration of fluoride in brick tea was high， and fluoride might cause health risk to tea drinkers especially for high-consumption groups. Some effective measures should be taken to solve this problem

Co2N nanoparticles embedded N-doped mesoporous carbon as efficient electrocatalysts for oxygen reduction reaction

Co-N-C electrocatalysts have attracted great attention in electrocatalytic ORR (oxygen reduction reaction) field. In this work, we propose to prepare Co 2 N nanoparticles embedded N-doped mesoporous carbon by a facile method including in situ copolymerization and pyrolysis under NH 3 atmosphere. The results show that more N atoms can be doped in carbon framework by NH 3 pyrolysis, it is also found that pyrolysis temperature and Co content can influence the ORR performance of samples. The sample prepared by adding Co precursor and pyrolysis at 700 °C has high N content (11.86 at.%) and relative large specific surface area (362 m 2 g −1 ), and it also exhibited superior electrocatalytic ORR performance in terms of E onset (−0.038 V vs. SCE), E 1/2 (−0.126 V vs. SCE) and large current density (5.22 mA cm −2 ). Additionally, the sample also shows better stability and resistance to methanol poisoning than Pt/C catalyst. The synergistic effect of Co-N active centers and hierarchical porous structures contribute the excellent electrocatalytic activity, which are considering as alternative catalysts for ORR in full cells

Stabilization of NaZn(BH4)3 via nanoconfinement in SBA-15 towards enhanced hydrogen release

In the present work, the decomposition behaviour of NaZn(BH4)3 nanoconfined in mesoporous SBA-15 has been investigated in detail and compared to bulk NaZn(BH4)3 that was ball milled with SBA-15, but not nanoconfined. The successful incorporation of nanoconfined NaZn(BH4)3 into mesopores of SBA-15 was confirmed by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, 11B nuclear magnetic resonance, nitrogen absorption/desorption isotherms, and Fourier transform infrared spectroscopy measurements. It is demonstrated that the dehydrogenation of the space-confined NaZn(BH4)3 is free of emission of boric by-products, and significantly improved hydrogen release kinetics is also achieved, with pure hydrogen release at temperatures ranging from 50 to 150 °C. By the Arrhenius method, the activation energy for the modified NaZn(BH4)3 was calculated to be only 38.9 kJ mol−1, a reduction of 5.3 kJ mol−1 compared to that of bulk NaZn(BH4)3. This work indicates that nanoconfinement within a mesoporous scaffold is a promising approach towards stabilizing unstable metal borohydrides to achieve hydrogen release with high purity

Stabilization of NaZn(BH4)3 via nanoconfinement in SBA-15 towards enhanced hydrogen release

In the present work, the decomposition behaviour of NaZn(BH4)3 nanoconfined in mesoporous SBA-15 has been investigated in detail and compared to bulk NaZn(BH4)3 that was ball milled with SBA-15, but not nanoconfined. The successful incorporation of nanoconfined NaZn(BH4)3 into mesopores of SBA-15 was confirmed by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, 11B nuclear magnetic resonance, nitrogen absorption/desorption isotherms, and Fourier transform infrared spectroscopy measurements. It is demonstrated that the dehydrogenation of the space-confined NaZn(BH4)3 is free of emission of boric by-products, and significantly improved hydrogen release kinetics is also achieved, with pure hydrogen release at temperatures ranging from 50 to 150 °C. By the Arrhenius method, the activation energy for the modified NaZn(BH4)3 was calculated to be only 38.9 kJ mol−1, a reduction of 5.3 kJ mol−1 compared to that of bulk NaZn(BH4)3. This work indicates that nanoconfinement within a mesoporous scaffold is a promising approach towards stabilizing unstable metal borohydrides to achieve hydrogen release with high purity

A combined hydrogen storage system of Mg(BH4)(2)-LiNH2 with favorable dehydrogenation

The decomposition properties of Mg(BH4)2−LiNH2 mixtures were investigated. Apparent NH3 release appeared from 50 to 300 °C for the Mg(BH4)2−LiNH2 mixtures with mole ratios of 1:1.5, 1:2, and 1:3, while only hydrogen release was detected for the mixture with a mole ratio of 1:1. In the case of the Mg(BH4)2−LiNH2 (1:1) sample, the onset of the first-step dehydrogenation starts at 160 °C, with a weight loss of 7.2 wt % at 300 °C, which is improved significantly compared to the pure Mg(BH4)2 alone. From Kissinger’s method, the activation energy, Ea, for the first and second step dehydrogenation in Mg(BH4)2−LiNH2 (1:1) was estimated to be about 121.7 and 236.6 kJ mol−1, respectively. The improved dehydrogenation in the combined system may be ascribed to a combination reaction between [BH4] and [NH2], resulting in the formation of Li−Mg alloy and amorphous B−N compound

General synthesis of transition metal oxide ultrafine nanoparticles embedded in hierarchically porous carbon nanofibers as advanced electrodes for lithium storage

A unique general, large-scale, simple, and cost-effective strategy, i.e., foaming-assisted electrospinning, for fabricating various transition metal oxides into ultrafine nanoparticles (TMOs UNPs) that are uniformly embedded in hierarchically porous carbon nanofibers (HPCNFs) has been developed. Taking advantage of the strong repulsive forces of metal azides as the pore generator during carbonization, the formation of uniform TMOs UNPs with homogeneous distribution and HPCNFs is simultaneously implemented. The combination of uniform ultrasmall TMOs UNPs with homogeneous distribution and hierarchically porous carbon nanofibers with interconnected nanostructure can effectively avoid the aggregation, dissolution, and pulverization of TMOs, promote the rapid 3D transport of both Li ions and electrons throughout the whole electrode, and enhance the electrical conductivity and structural integrity of the electrode. As a result, when evaluated as binder-free anode materials in Li-ion batteries, they displayed extraordinary electrochemical properties with outstanding reversible capacity, excellent capacity retention, high Coulombic efficiency, good rate capability, and superior cycling performance at high rates. More importantly, the present work opens up a wide horizon for the fabrication of a wide range of ultrasmall metal/metal oxides distributed in 1D porous carbon structures, leading to advanced performance and enabling their great potential for promising large-scale applications

Case Report: A novel heterozygous nonsense mutation in KRIT1 cause hereditary cerebral cavernous malformation

Cerebral cavernous malformation (CCM) is a vascular malformation of the central nervous system and mainly characterized by enlarged capillary cavities without intervening brain parenchyma. Genetic studies have identified three disease-causing genes (CCM1/KRIT1, CCM2/MGC4607 and CCM3/PDCD10) responsible for CCM. Here, we characterized a four-generation family diagnosed with CCM and identified a novel heterozygous mutation c.1159C>T, p.Q387X in KRIT1 gene by whole exome sequencing and Sanger sequencing. The Q387X mutation resulted in premature termination of KRIT1 protein, which was predicted to be deleterious by the ACMG/AMP 2015 guideline. Our results provide novel genetic evidence support that KRIT1 mutations cause CCM, and are helpful to the treatment and genetic diagnosis of CCM

Graphene-wrapped reversible reaction for advanced hydrogen storage

Here, we report the fabrication of a graphene-wrapped nanostructured reactive hydride composite, i.e., 2LiBH4-MgH2, made by adopting graphene-supported MgH2 nanoparticles (NPs) as the nanoreactor and heterogeneous nucleation sites. The porous structure, uniform distribution of MgH2 NPs, and the steric confinement by flexible graphene induced a homogeneous distribution of 2LiBH4-MgH2 nanocomposite on graphene with extremely high loading capacity (80 wt%) and energy density. The well-defined structural features, including even distribution, uniform particle size, excellent thermal stability, and robust architecture endow this composite with significant improvements in its hydrogen storage performance. For instance, at a temperature as low as 350 °C, a reversible storage capacity of up to 8.9 wt% H2, without degradation after 25 complete cycles, was achieved for the 2LiBH4-MgH2 anchored on graphene. The design of this three-dimensional architecture can offer a new concept for obtaining high performance materials in the energy storage field