We monitored the gas hydrate through low-field nuclear magnetic resonance measurement. An observed decrease of the relaxation time (T 2 ) intensity corresponds to the formation process, whereas an increase of the intensity corresponds to the dissociation process. The right domain of the spectrum with T 2 larger than 10 ms disappears gradually with the formation time, whereas the left domain with T 2 smaller than 1 ms remains invariant, indicating the gas hydrate forms preferentially in larger pores. In addition, the right domain increases rapidly with the dissociation time, revealing that the gas hydrate preferentially decomposes in large pores. The spectrum distributions move toward the fast relaxation domain with the growth of gas hydrate, because the generated gas hydrate occupies the large pore and accelerate the relaxation rate. There is no obvious relationship between the gas hydrate saturation and the porosity, whereas the volume and preliminary dissociation ratio are strongly correlated with the porosity.
The gut microbiome shapes local and systemic immunity. The liver is presumed to be a protected sterile site. As such, a hepatic microbiome has not been examined. Here, we showed a liver microbiome in mice and humans that is distinct from the gut and is enriched in Proteobacteria. It undergoes dynamic alterations with age and is influenced by the environment and host physiology. Fecal microbial transfer experiments revealed that the liver microbiome is populated from the gut in a highly selective manner. Hepatic immunity is dependent on the microbiome, specifically Bacteroidetes species. Targeting Bacteroidetes with oral antibiotics reduced hepatic immune cells by ~90%, prevented APC maturation, and mitigated adaptive immunity. Mechanistically, our findings are consistent with presentation of Bacteroidetes-derived glycosphingolipids to NKT cells promoting CCL5 signaling, which drives hepatic leukocyte expansion and activation, among other possible host-microbe interactions. Collectively, we reveal a microbialglycosphingolipid -NKT -CCL5 axis that underlies hepatic immunity.
Ceramics possess high temperature resistance, extreme hardness, high chemical inertness and a lower density compared to metals, but there is currently no technology that can produce satisfactory joints in ceramic parts and preserve the excellent properties of the material. The lack of suitable joining techniques for ceramics is thus a major road block for their wider applications. Herein we report a technology to weld ceramic nanowires, with the mechanical strength of the weld stronger than that of the pristine nanowires. Using an advanced aberration-corrected environmental transmission electron microscope (ETEM) under a CO2 environment, we achieved ceramic nanowelding through the chemical reaction MgO + CO2 → MgCO3 by using porous MgO as the solder. We conducted not only nanowelding on MgO, CuO, and V2O5 nanowires and successfully tested them in tension, but also macroscopic welding on a ceramic material such as SiO2, indicating the application potential of this technology in bottom-up ceramic tools and devices.
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