The morphology and porosity of zeolite play a significant role in the activity and selectivity of catalytic reactions. It is a dream to optionally modulate zeolite morphology by regulating the crystallization process on the basis of comprehensively understanding the mechanisms. Herein, a series of MTW zeolite mesocrystals can be consciously fabricated with morphologies from a dense structure to a loose one of an oriented nanocrystallite aggregate by changing the H 2 O/SiO 2 ratio. Their intertwined classical/nonclassical crystallization processes are investigated comprehensively. The results indicate that the crystallization of MTW zeolite takes place by a chain of events, including the formation of wormlike particles (WLPs), their aggregation, and crystallization of aggregates. MTW with a loose structure mainly crystallizes by an internal reorganization after a fast aggregation of WLPs in a concentrated system. On the other hand, the dense structure of MTW is realized via the co-occurrence of a coalescence of the participating WLPs during its crystal growth with a slower rate in a dilute system. Moreover, the advantages of MTW with a loose structure are confirmed through cumene cracking and 1,2,4trimethylbenzene transformation. This method could pave the way for the synthesis of other zeolites with diverse morphologies and/or mesoporosities via subtle regulation of the crystallization pathway.

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A mobile atomic absolute gravimeter NIM-AGRb-1 based on light-pulse atom interferometer has been built, evaluated by the National Institute of Metrology (NIM) China, and participated in the pilot study of the International Comparison of Absolute Gravimeters (CCM.G-K2.2017) held at NIM Changping Beijing in October 2017. The sensitivity of the gravimeter is 44 µGal Hz −1/2 (1 µGal = 10 −8 m s −2 ≈ 10 −9 g) and its instability reaches as small as 0.2 µGal when averaged over 30 000 s. The instrumental and environmental effects were evaluated and corrected with a total uncertainty of 5.2 µGal. The absolute g measured by NIM-AGRb-1 was compared to that of a commercial FG5X-249 optical gravimeter with the two devices operating side by side in the same laboratory and their results agree within −0.2(6.3) µGal. NIM-AGRb-1 also demonstrated continuous operation over a period of more than 500 h.

Graphene-coated plastic substrates, such as polyethylene terephthalate (PET), are regularly used in flexible electronic devices. Here we demonstrate a new application of the graphene-coated nanoporous PET membrane for the selective separation of metal ions in an ion exchange manner. Irradiation with swift heavy ions is used to perforate graphene and PET substrate. This process could create graphene nanopores with carboxyl groups, thus forming conical holes in the PET after chemical etching to support graphene nanopores. Therefore, a monolayer nanoporous graphene membrane with a PET substrate is constructed successfully to investigate its ionic selective separation. We find that the permeation ratio of ions strongly depends on the temperature and H concentration in the driving solution. An electric field can increase the permeation ratio of ions through the graphene nanopores, but it inhibits the ion selective separation. Moreover, the structure of the graphene nanopore with carboxyl groups is resolved at the density functional theory level. The results show the asymmetric structure of the nanopore with carboxyl groups, and the analysis indicates that the ionic permeation can be attributed to the ion exchange between metal ions and protons on the two sides of graphene nanopores. These results would be beneficial to the design of membrane separation materials made from graphene with efficient online and offline bulk separation.