PC/PET/EPDM共混体系的结晶与熔融行为

本文用解偏振光法与DSC法分别测定并研究了PC/PET/EPDM共混体系的结晶速度、结晶度、Avrami指数(n)和熔融温度及其影响因素,共混物中PET的结晶速度、结晶度均随PC含量增加而下降;EPDM用量不超过10%时,可提高PET的结晶速度,但不影响结晶度和成核与增长方式,n值不变。当EPDM为5%时,结晶速度呈现极大值。经退火处理的共混物呈现熔融双峰,PC量增加,高温熔融峰略移向高温方向;热处理温度升高或时间延长,则低温熔融峰移向高温方向。     

毛细管色谱柱定量分析的研究

用毛细管色谱柱进行定量分析,必须测定正确的"定量校正值"。本文提出了用标准的二元混合物测定这种校正值的方法;并探讨了不同的操作条件对定量校正值的影响。     

SEQUENCES OF POWERS OF TOEPLITZ OPERATORS ON THE BERGMAN SPACE

We consider Toeplitz operators Tu with symbol u on the Bergman space of the unit ball,and then study the convergences and summability for the sequences of power...     

Effect of carbon doping on corrosion resistance and conductivity of CrMoN-coated 316L stainless steel bipolar plates

Journal of Solid State Electrochemistry - CrMoCN coatings with different carbon contents are prepared on 316L stainless steel substrates by closed-field unbalanced magnetron sputtering. The...     

Metal Organic Framework Glasses: A New Platform for Electrocatalysis?

Metal organic framework (MOF) glasses are a coordination network of metal nodes and organic ligands as an undercooled frozen-in liquid, and have therefore broadened the potential of MOF materials in the fundamental research and application scenarios. On the road to deploying MOF glasses as electrocatalysts, it remains several basic scientific hurdles although MOF glasses not only inherit the structural merits of MOFs but also endow with active catalytic features including concentrated defects, metal centers and disorder structure etc. The research on the ionic conductivity, catalytic stability and reactivity of MOF glasses has yielded scientific insights towards its electrocatalytic applications. Here, we first comb the history, definition and basic properties of MOF glasses. Then, we identify the main synthetic methods and characterization techniques. Finally, we advance the potentials and challenges of MOF glasses as electrocatalysts in furthering the understanding of these themes.     

Synthesis of Sequence-specific Poly(ester-carbonate) Copolymers via Chemoselective Terpolymerization Controlled by the Stoichiometric Ratio of Phosphazene/Triethylborane

Chemoselective terpolymerization can produce polymer materials with diverse compositions and sequential structures, and thus have attracted considerable attention in the field of polymer synthesis. However, the intrinsic complexity of three-component system also brings great chanllenge, in regard to the reactivity and selectivity of different monomers. Herein, we report the terpolymerization of CO₂/epoxide/anhydride by a binary organocatalytic C₃N₃-Py-P₃/TEB (triethylborane) system. Both the activity and chemoselectivity were highly dependent upon the molar ratio of C₃N₃-Py-P₃ to TEB, and sequence-controlled poly(ester-carbonate) copolymers were readily synthesized through one-pot/one-step methodology by tuning the stoichiometric ratio of phosphazene/TEB. In particular, C₃N₃-Py-P₃/TEB with a molar ratio of 1/0.5 exhibited an unprecedentedly high chemoselectivity for ring-opening alternating copolymerization (ROAC) of cyclohexene oxide (CHO) and phthalic anhydride (PA) first and then ROAC of CO₂/CHO. Thus, well-defined triblock polycarbonate-b-polyester-b-polycarbonate copolymers can be produced from the mixture of CO₂, CHO and PA using a bifunctional initiator. With C₃N₃-Py-P₃/TEB=1/1, tapered copolymers were obtained, while random copolymers with high content of polycarbonate (PC) were synthesized with further increasing the amount of TEB. The mechanism of the unexpected chemoselectivity was further investigated by DFT calculations.     

ATP-Responsive Nanoparticles Covered with Biomolecular Machine “Chaperonin GroEL”

Herein, we report an ATP-responsive nanoparticle (^GroELNP) whose surface is fully covered with the biomolecular machine “chaperonin protein GroEL”. ^GroELNP was synthesized by DNA hybridization between a gold NP with DNA strands on its surface and GroEL carrying complementary DNA strands at its apical domains. The unique structure of ^GroELNP was visualized by transmission electron microscopy including under cryogenic conditions. The immobilized GroEL units retain their machine-like function and enable ^GroELNP to capture denatured green fluorescent protein and release it in response to ATP. Interestingly, the ATPase activity of ^GroELNP per GroEL was 4.8 and 4.0 times greater than those of precursor ^cysGroEL and its DNA-functionalized analogue, respectively. Finally, we confirmed that ^GroELNP could be iteratively extended to double-layered NP.     

Mechanochemical Release of Fluorophores from a “Flex-activated” Mechanophore

Optical force probes that can release force-dependent and visualized signals with minimal changes in the polymer main chains under mechanical load are highly sought after but currently limited. In this study, we introduce a flex-activated mechanophore (FA) based on the Diels–Alder adduct of anthracene and dimethyl acetylenedicarboxylatea that exhibits turn-on mechanofluorescence. We demonstrate that when FA is incorporated into polymer networks or in its crystalline state, it can release fluorescent anthracenes through a retro-Diels–Alder mechanochemical reaction under compression or hydrostatic high pressure, respectively. The flex-activated mechanism of FA is successfully confirmed. Furthermore, we systematically modulate the force delivered to the mechanophore by varying the crosslinking density of the networks and the applied macroscopic pressures. This modulation leads to incremental increases in mechanophore activation, successive release of anthracenes, and quantitative enhancement of fluorescence intensity. The exceptional potential of FA as a sensitive force probe in different bulk states is highlighted, benefiting from its unique flex-activated mode with highly emissive fluorophore releasing. Overall, this report enriches our understanding of the structures and functions of flex-activated mechanophores and polymeric materials.