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Because of the high specific surface area, excellent electronic conductivity, facile Li diffusion, and rich functional groups, Ti2C-based MXenes have been widely used to improve the electrochemical property of lithium-sulfur batteries. The complex surface functionalization (such as -OH, -S, -F, and -O) of MXenes boosts the performance but also causes controversies about the favorable functionalized surface in the electrochemical reaction during the charge and discharge process. In the present work, a theoretical study based on density functional theory has been carried out to clarify the favorable functionalized surface by comparing pristine Ti2C and -OH-, -S-, -F-, and -O-functionalized Ti2C surfaces from the aspects of adsorption ability, electronic conductivity, and kinetic conversion ability. It is found that compared with severe polysulfide deformation on pristine Ti2C and Ti2C(OH)2 surfaces, Ti2CO2, Ti2CS2, and Ti2CF2 have effective polysulfide adsorption. Ti2CO2 has the largest surface adsorption energy, followed by Ti2CS2, and Ti2CF2 is the weakest. Meanwhile, the narrow-band gap semiconductor property of Ti2CO2 during adsorption indicates worse electronic conductivity than metallic Ti2CS2 and Ti2CF2. In addition, for the kinetic conversion ability, the Ti2CS2 surface has the fastest polysulfide conversion and Li diffusion, followed by Ti2CF2, and Ti2CO2 represents the slowest conversion and diffusion. Accordingly, because of the medium binding energy, good electronic conductivity, and fast polysulfide conversion and Li diffusion, Ti2CS2 is revealed to be the favorable functionalized surface. More importantly, the origin for the Ti2CS2 surface with medium adsorption ability represents the fastest polysulfide conversion, and Li diffusion is further clarified. The great affinity of the Ti2CS2 surface to the product Li2S leads to facile polysulfide conversion. The uniform charge distribution on the Ti2CS2 surface contributes to the fast Li diffusion.During the process development of brigatinib, we have made an unusual observation about some impurities. Detailed investigation has led to the conclusion that impurity A is formed via the raw material 2 oxidation, impurity B is formed via the pyrolysis of DMF, impurity C is formed via raw material 4, and impurity D is formed via HCl-catalyzed decomposition of intermediate 3. The present work details a report of the journey toward the development of an efficient process for the commercial production of brigatinib substantially free from all the impurities.Accelerating the drainage of water in coal reservoirs can significantly improve the extraction efficiency of coalbed methane (CBM). find more The movement of water with different pH values in anthracite was tested and analyzed. The results showed that the electro-osmotic flow velocity increased first and then slightly decreased with the increase of time up to 120 h. The electro-osmotic flow was markedly strengthened under a strong acid (pH 2) or strong alkaline (pH 13) environment, and the direction of electro-osmosis was reversed at a pH of 3-4. The changes in zeta potential, surface groups, and minerals in anthracite were tested to analyze the mechanism of electro-osmotic characteristics. The results obtained from this work will provide a basis for the process of drainage and depressurization during the CBM extraction.Herein, colloidal dispersions of alkaline nanoparticles (NPs CaCO3 and Mg(OH)2) are stabilized by trimethylsilyl cellulose (TMSC) in hexamethyldisiloxane and employed to treat historical wood pulp paper by an effortless dip-coating technique. Both alkaline NPs exhibit high stability and no size and shape changes upon stabilization with the polymer, as shown by UV-vis spectroscopy and transmission electron microscopy. The long-term effect of NP/TMSC coatings is investigated in detail using accelerated aging. The results from the pH-test and back-titration of coated papers show a complete acid neutralization (pH ∼ 7.4) and introduction of adequate alkaline reserve even after prolonged accelerated aging. Scanning electron microscopy-energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and infrared and water contact angle measurements showed the introduction of a thin and smooth hydrophobic NP/TMSC coating on the paper fibers. Acid-catalyzed desilylation of TMSC was observed by declining C-Si infrared absorbance peaks upon aging. The CaCO3 coatings are superior to Mg(OH)2 with respect to a reduced yellowing and lower cellulose degradation upon aging as shown by colorimetric measurements and degree of polymerization analysis. The tensile strength and folding endurance of coated and aged papers are improved to 200-300 and 50-70% as illustrated by tensile strength and double folding endurance measurements.With the development of industry, the discharge of wastewater containing mercury ions posed a serious threat to human health. Using biomass waste as an adsorbent to treat wastewater containing mercury ions was a better way due to its positive impacts on the environment and resource saving. In this research, activated carbon (AC) was prepared from rice husk (RH) by the KOH chemical activation method. The characterization results of scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET), Fourier transform infrared (FTIR), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) showed that rice husk-activated carbon (RHAC) had good pore structure and oxygen-containing functional groups. The influences of contact time, initial concentration of Hg(II), adsorbent dosage, pH, and ionic strength on mercury ion removal were investigated. The Langmuir model was most suitable for the adsorption isotherm of RHAC, and its maximum adsorption capacity for Hg(II) was 55.87 mg/g. RHAC still had a high removal capacity for Hg(II) after five regeneration cycles. RHAC had excellent removal efficiency for mercury ion wastewater. At the same time, RH could be used as a nonpolluting and outstanding characteristic adsorbent material.Niemann-Pick type C1 (NPC1) is a large multidomain transmembrane protein essential for transporting cholesterol (CLR) from late endosomes and lysosomes to the endoplasmic reticulum and other cellular compartments. The lumen-facing N-terminal domain (NTD), involved in direct binding of CLR, is expected to have an optimum activity at acidic pH = 4.5. Here, we show that acidic pH is vital for the functionality of NPC1(NTD) and should be taken into account when studying the protein activity. We applied evolutionary, structural, and physicochemical analyses to decipher the consequences of a change in pH from acidic (pH = 4.5) to neutral (pH = 7.2) on the structural integrity of the NTD and its ability to bind CLR. We revealed that the change in pH from 4.5 to 7.2 increases the potential energy of the protein in both apo- and holo-states making the system less energetically favorable. At neutral pH, the flexibility of the protein in the apo-state is decreased caused by the alteration of specific interactions, which in turn might have a high impact on ligand recognition and binding.