Furthermore, different well operations induce pH environments that change the clay mineral surface charge. This change results in adsorption prone surfaces and with reservoir rock made up of different minerals, and the effect of contacting minerals is critical as shown in our findings. This is due to the contacting mineral control wettability rather than the bulk mineralogy.The effect of sintering atmosphere (air and Ar) and temperature (1100, 1200, 1300 °C) on the microstructure, mechanical properties, and bioactivity of hydroxyapatite/tantalum (HA/Ta) composites were systematically investigated by pressureless sintering of the mixture of HA and Ta powders. It shows that the sintering atmosphere greatly impacts the phase composition and microstructure of the HA/Ta composites. The higher diffusion of atoms promotes shrinkage and causes deeper reaction fusion between the HA matrix and Ta, which improved the interfacial binding of the HA/Ta composites. The refined grain structure and improved interfacial binding obtained within the Ar atmosphere compared to the air atmosphere benefit the mechanical properties. The maximum bending strength and shrinkage observed for the composites sintered at 1300 °C in the Ar atmosphere are 27.24 MPa and 6.65%, respectively. The cell counting kit-8 (CCK-8) method was used to investigate the in vitro cytocompatibility of HA/Ta composites. The results revealed that the HA/Ta composites sintered with different conditions have no cytotoxicity. The simulated body fluid (SBF) soaking results showed that all of the studied composites possess desirable bioactivity, as demonstrated by their ability to form calcium-deficient carbonate apatite layer on the surfaces. For composites sintered at 1300 °C, the surface apatite layer coverage of the composites obtained in the Ar atmosphere was increased by 139.7% than the ones obtained in air, which confirmed an enhanced bioactive mineralization ability. The results indicated that the HA/Ta composites sintered at 1300 °C in Ar possess desirable mechanical properties and bioactivity. This work opens up the new possibility for preparing HA-based composites and is of great value in biomedical applications.Platycodon grandiflorum is a perennial plant that has been used for medicinal purposes. Specifically, it is widely used in Northern China and Korea for the treatment of various diseases. Terpenoids belong to a group called secondary metabolites and have attracted a wide range of interest. Here, we determined the expressed sequence tag (EST) library of the methyl jasmonate (MeJA)-treated hairy root of P. grandiflorum. AZ 960 concentration In total, 5760 ESTs were obtained, but after deleting the vector sequences and removing poor-quality sequences, a total of 2536 ESTs were attained. Of these, 811 contigs and 1725 singletons were annotated. The data were further analyzed with a focus on the gene families of the terpenoid biosynthetic pathway (TBP). We identified and characterized four TBP genes; among these were three full-length cDNAs encoding PgHMGS, PgMK, and PgMVD, whereas PgHMGR had a partial sequence based on the EST library database. Phylogenetic analysis and a pairwise identity matrix showed that these identified genes werlation occurred at 3 h after initial exposure for most of the genes. Meanwhile, triterpene saponin accumulation increased with the increase in the time of exposure, and at 48 h after initial exposure, the total saponin content was the highest recorded.Alginate materials with the advantages of being renewable, inexpensive, and environment-friendly have been considered promising fiber materials. However, they are prone to degrade under UV light, limiting their large-scale application in the textile field. Herein, the fracture of glycosidic bonds during the degradation process is revealed clearly by Fourier transform infrared (FT-IR) and 1H NMR. To effectively inhibit this process, functionalized multiwalled carbon nanotubes (MWCNTs) are chosen as dopants and used to interact with the sugar chain via hydrogen bonds. The results demonstrate that alginate materials with functionalized MWCNTs exhibit slower degradation rates. The intermolecular energy transfer between functionalized MWCNTs and sodium alginate (SA) is proposed for the antidegradation effect of functionalized MWCNTs, which is supported by the experiments. Moreover, SA/MWCNT fibers also show enhanced mechanical properties compared with pure alginate fibers. The appealing effect of the degradation inhibition feature makes the composite alginate materials very promising candidates for their future use in textile material development.The Mn x Ce y binary catalysts with a three-dimensional network structure were successfully prepared via a polymer-assisted deposition method using ethylenediaminetetraacetic acid and polyethyleneimine as complexing agents. The developed pore structure could facilitate the gas diffusion and accelerate the catalytic reaction for NH3 selective catalytic reduction (SCR). Moreover, the addition of Ce is beneficial for the exposure of active sites on the catalyst surface and increases the adsorption of the NH3 and NO species. Therefore, the Mn1Ce1 catalyst exhibits the best catalytic activity for NO x removal with a conversion rate of 97% at 180 °C, superior water resistance, and favorable stability. The SCR reaction over the Mn1Ce1 catalyst takes place through the E-R pathway, which is confirmed by the in situ diffuse reflectance Fourier transform analysis. This work explores a new strategy to fabricate multimetal catalysts and optimize the structure of catalysts.A functional N-halamine precursor with double bonds, 1-3-diallyl-s-triazine-2,4,6-trione (DTT), was synthesized and grafted onto polypropylene using dicumyl peroxide (DCP) as an initiator via melt blending at 200 °C. The DTT content grafted onto the polypropylene (PP) backbone was depended on both DTT and DCP concentrations in feed. The crystallization temperature of PP increased from 116 °C (neat PP) to 123 °C (10% DTT) with the increasing DTT content. Meanwhile, the crystallization rate and relative crystallinity of PP were significantly increased after introduction of the N-halamine precursor. Moreover, the incorporation of DTT had partial compensation for the decreasing mechanical properties of polypropylene, which resulted from degradation. When the amount of added DTT reached up to 5%, the chlorinated DTT-modified PP sheets were able to kill 105-6 cfu/mL Escherichia coli (CMCC 44103) and Staphylococcus aureus (ATCC 6538) within 10 min. The DTT-modified PP with the regenerating antibacterial property may have great potential for application in packaging, filters, and hygienic products.