Search

Methyl acetate (MA) has a wide range of applications as an important industrial chemical. Traditional MOR zeolite for carbonylation of DME to MA accumulated carbon easily because of a 12-membered ring (12 MR) channel. In this work, we innovatively developed the method of recrystallization ferrierite (FER) zeolite using special chelating ligand sodium oleate which can affect ions other than alkali metals. The characterization results of N 2 adsorption, transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FT-IR) show that hydrothermal recrystallization of ferrierite using sodium oleate resulted in a higher Si/Al ratio, a bigger specific surface area and a larger number of Brønsted acid sites in the eight MR channels, which was more efficient in the reaction of carbonylation of dimethyl ether than ordinary alkali treatment.

Enhancing the stability of the resin-dentin bonding interface via simultaneously improving the antibacterial, mechanical, and adhesive properties of a dental adhesive is the key to prolonging the longevity of dental restoration for caries treatment. Herein, we present the stabilization effect of Ag + - and Zn 2+ -exchanged zeolite A (denoted as Ag-A and Zn-A, respectively) on the resin-dentin bonding interface. Ag-A and Zn-A zeolites exhibited sustained ion release capability, outstanding biocompatibility to L929 cells (<2 mg/mL), and excellent antibacterial ability to Streptococcus mutans (minimum inhibitory concentration: 100 μg/mL for Ag-A and 200 μg/mL for Zn-A). One-step self-etching adhesives modified by Ag-A, Zn-A, or Ag-/Zn-A (1/1 in weight) zeolites with an ultralow loading of 0.2 wt % exhibited favorable antibacterial activity with the inhibition of biofilm formation by 70.33, 56.47, and 62.54%, respectively. Compared to the control group, Zn-A- and Ag-/Zn-A-modified adhesives significantly increased the wettability properties of the adhesive and the long-term resin-dentin bond strength (by ∼25%) after 5000 thermocycles of aging. The current data demonstrated that the introduction of 0.2 wt % Zn-A or Ag-/Zn-A into the adhesive remarkably enhanced the stability of the resin-dentin bonding interface. Our findings provide a new strategy to modify the dental adhesive for further optimizing the longevity of dental restorations for caries.

Cu‐exchanged low‐silica CHA zeolites (Si/Al≤4) synthesized without organic templates are promising candidate catalysts for ammonia selective catalytic reduction of nitrogen oxides (NH3‐SCR), but their practical application is restricted due to the low hydrothermal stability. Here, inspired by the transcription from duplex DNA to RNA, we synthesized Al pairs enriched low‐silica CHA zeolite (CHA‐SPAEI, Si/Al=3.7) by using silicoaluminophosphate (SAPO) featured by strict alternation of −Al−O−P(Si)−O−Al−O− tetrahedra as seed. The proportion of Al pairs in CHA−SPAEI is 78 %, which is much higher than that in the conventional low‐silica CHA (CHA‐LS, 52 %). After hydrothermal ageing at 800 °C for 6 h, Cu‐exchanged CHA‐SPAEI shows NO conversion above 90 % within 225–500 °C under a gas hourly space velocity of 200,000 h−1, which is much better than that of Cu‐exchanged CHA‐LS. The spatial close proximity of Al pairs in CHA‐SPAEI is confirmed by the 27Al double‐quantum single‐quantum two‐dimensional NMR analyses. The strict −P(Si)−O−Al−O−P(Si)−O‐ sequence in the fragments from the dissolution of SAPO seed promotes the Al pairs with the −Al−O−Si−O−Al−O− sequence via a transcription process. The utilization of aluminophosphate‐based zeolites as seeds opens up a new avenue for the regulation of the Al distribution in zeolites. [ABSTRACT FROM AUTHOR]

Zeolites are one of the most important heterogeneous catalysts, with a high number of large‐scale industrial applications. While the synthesis of new zeolites remain rather limited, introduction of germanium has substantially increased our ability to not only direct the synthesis of zeolites but also to convert them into new materials post‐synthetically. The smaller Ge‐O‐Ge angles (vs. Si‐O‐Si) and lability of the Ge−O bonds in aqueous solutions account for this behaviour. This Minireview discusses critical aspects of germanosilicate synthesis and their post‐synthesis transformations to porous materials. [ABSTRACT FROM AUTHOR]