Recent progress in engineering near-infrared persistent luminescence nanoprobes for time-resolved biosensing/bioimaging

Persistent luminescence nanoprobes (PLNPs) can remain luminescent after ceasing excitation. Due to the ultra-long decay time of persistent luminescence (PersL), autofluorescence interference can be efficiently eliminated by collecting PersL signal after autofluorescence decays completely, thus the imaging contrast and sensing sensitivity can be significantly improved. Since near-infrared (NIR) light shows reduced scattering and absorption coefficient in penetrating biological organs or tissues, near-infrared persistent luminescence nanoprobes (NIR PLNPs) possess deep tissue penetration and offer a bright prospect in the areas of in vivo biosensing/bioimaging. In this review, we firstly summarize the design of different types of NIR PLNPs for biosensing/bioimaging, such as transition metal ions-doped NIR PLNPs, lanthanide ions-doped NIR PLNPs, organic molecules-based NIR PLNPs, and semiconducting polymer self-assembled NIR PLNPs. Notably, organic molecules-based NIR PLNPs and semiconductor self-assembled NIR PLNPs, for the first time, were introduced to the review of PLNPs. Secondly, the effects of different types of charge carriers on NIR PersL and luminescence decay of NIR PLNPs are significantly emphasized so as to build up an in-depth understanding of their luminescence mechanism. It includes the regulation of valence band and conduction band of different host materials, alteration of defect types, depth and concentration changes caused by ion doping, effective radiation transitions and energy transfer generated by different luminescence centers. Given the design and potential of NIR PLNPs as long-lived luminescent materials, the current challenges and future perspective in this rapidly growing field are also discussed.

     

酸性服役管线管BNS力学及耐腐蚀性能研究

文章介绍了包钢钢管公司酸性服役管线管BNS成分设计要求,对材料的拉伸性能、冲击性能、组织以及耐腐蚀性能进行了检测和分析,正火处理后,材料具有良好的力学性能和抗腐蚀性能.试验结果表明,设计的BNS完全能满足酸性服役条件下管线管性能要求.     

Two‐Photon Up‐Conversion Photoluminescence Realized through Spatially Extended Gap States in Quasi‐2D Perovskite Films

A new approach to generate a two‐photon up‐conversion photoluminescence (PL) by directly exciting the gap states with continuous‐wave (CW) infrared photoexcitation in solution‐processing quasi‐2D perovskite films [(PEA)₂(MA)₄Pb₅Br₁₆ with n = 5] is reported. Specifically, a visible PL peaked at 520 nm is observed with the quadratic power dependence by exciting the gap states with CW 980 nm laser excitation, indicating a two‐photon up‐conversion PL occurring in quasi‐2D perovskite films. Decreasing the gap states by reducing the n value leads to a dramatic decrease in the two‐photon up‐conversion PL signal. This confirms that the gap states are indeed responsible for generating the two‐photon up‐conversion PL in quasi‐2D perovskites. Furthermore, mechanical scratching indicates that the different‐n‐value nanoplates are essentially uniformly formed in the quasi‐2D perovskite films toward generating multi‐photon up‐conversion light emission. More importantly, the two‐photon up‐conversion PL is found to be sensitive to an external magnetic field, indicating that the gap states are essentially formed as spatially extended states ready for multi‐photon excitation. Polarization‐dependent up‐conversion PL studies reveal that the gap states experience the orbit–orbit interaction through Coulomb polarization to form spatially extended states toward developing multi‐photon up‐conversion light emission in quasi‐2D perovskites.     

白云岩与砂岩致密储集体质量的差异性

白云岩与砂岩致密储集体质量参数为随机分布的连续谱系，孔隙结构、物理参数复杂多变，表征难度较大。基于铸体薄片、压汞、核磁共振、孔隙度和渗透率等测试技术，结合大量天然气勘探开发实际资料，采用统计分析对比方法，重点讨论了储层质量宏观与微观参数特征。结果表明，白云岩与砂岩致密储集体质量参数具有正态分布特征，是一种金字塔数据结构，常规储层比例一般为15%~20%，是砂岩或白云岩致密储层的“甜点”；致密砂岩储层微观孔隙发育，孔、喉连通性较好，分布比较均匀，储层孔、渗关系较好，表现为相对高孔和低渗；白云岩致密储层质量尽管具有孔、喉连通性差和孔、渗关系较差的不利因素，但也具有相对高渗、低束缚水饱和度、低排驱压力及裂缝网络发育等有利因素，天然气渗流能力较好，勘探开发潜力较大。我国发育碳酸盐岩沉积，应加强致密白云岩气藏成藏条件研究与勘探。     

Key Role of Microtubule and Its Acetylation in a Zinc Oxide Nanoparticle–Mediated Lysosome–Autophagy System

Autophagy is a biological process that has attracted considerable attention as a target for novel therapeutics. Recently, nanomaterials (NMs) have been reported to modulate autophagy, which makes them potential agents for the treatment of autophagy‐related diseases. In this study, zinc oxide nanoparticles (ZNPs) are utilized to evaluate NM‐induced autophagy and debate the mechanisms involved. It is found that ZNPs undergo pH‐dependent ion shedding and that intracellular zinc ions (Zn²⁺) play a crucial role in autophagy. Autophagy is activated with ZNPs treatment, which is inhibited after Zn²⁺ sequestration via ethylenediamine tetra‐acetic acid. Lysosome‐based autophagic degradation is halted after ZNPs treatment for more than 3 h and is accompanied by blockage of lysophagy, which renews impaired lysosomes. Furthermore, the microtubule (MT) system participates in ZNP‐induced lysosome–autophagy system changes, especially in the fusion between autophagosomes and lysosomes. MT acetylation is helpful for protecting from ZNP‐induced MT disruption, and it promotes the autophagic degradation process. In conclusion, this study provides valuable information on NM‐induced lysosome–autophagy system changes, particularly with respect to the role of lysophagy and the MT system, which point to some attractive targets for the design of engineered nanoparticles.     

电磁搅拌对大圆坯结晶器冶金行为影响的探讨

 为了探究结晶器电磁搅拌(M EMS)对大圆坯结晶器内综合冶金行为的影响。以大断面圆坯连铸结晶器冶金行为为研究对象，基于电磁热流体与凝固传输理论建立三维耦合数值模型。揭示大圆坯连铸常用五孔水口浇注条件下结晶器内电磁场、流场、传热与凝固等综合冶金行为，提出电磁搅拌对结晶器冶金性能影响的多参量评价方法。以中碳铬钼齿轮钢650 mm大圆坯连铸为例，指出结晶器电磁搅拌存在最佳搅拌电流，可获得相对较好的综合冶金效果。具体表现为弯月面保持一定的切向速度和过热度，有利于保护渣的熔化和夹杂物的上浮去除；液面波动幅度在控制范围内，可避免卷渣、改善表面质量；结晶器内钢液过热得到有效耗散，有利于等轴晶形核改善铸坯内部质量；侧孔出流钢液速度得到有效控制，可抑制注流对初凝坯壳的冲刷，提高了初生坯壳生长的均匀性。此外，电磁搅拌产生的水平旋流强度也可得到有效控制，有利于避免常见的皮下白亮带现象。     

基于图形处理器的形态学重建系统

形态学重建是医学图像处理中非常基础和重要的操作。它根据掩膜图像的特征对标记图像反复进行膨胀操作，直到标记图像中的像素值不再变化为止。对于传统基于中央处理器（CPU）的形态学重建系统计算效率不高的问题，提出了使用图形处理器（GPU）来加速形态学重建。首先，设计了适合GPU处理的数据结构：并行堆集群；然后，基于并行堆集群，设计和实现了一套基于GPU的形态学重建系统。实验结果表明，相比传统基于CPU的形态学重建系统，基于GPU的形态学重建系统可以获取超过20倍的加速比。基于GPU的形态学重建系统展示了如何把基于复杂数据结构的软件系统高效地移植到GPU上。     

基于EDEM和Fluent的废电路板颗粒气流静电分选仿真研究

为了提高废电路板破碎料的分选效率,选用铜颗粒和玻璃颗粒作为研究对象,利用静电气流复合分选技术在EDEM和Fluent耦合仿真下寻求最佳的分选参数。并在Fluent中添加风,对风速进行优化。结果表明:施加在两极板上的库仑力在±1.7×10~5nC之间时,粒径为3mm的颗粒综合分选效率最优,在此基础上,当风速达到35m/s时,综合分选效率都优于静电分选效率。     

Fabrication and Thermal Dissipation Properties of Carbon Nanofibers Derived from Electrospun Poly(Amic Acid) Carboxylate Salt Nanofibers

Polyimides (PIs) possess excellent mechanical properties, thermal stability, and chemical resistance and can be converted to carbon materials by thermal carbonization. The preparation of carbon nanomaterials by carbonizing PI‐based nanomaterials, however, has been less studied. In this work, the fabrication of PI nanofibers is investigated using electrospinning and their transformation to carbon nanofibers. Poly(amic acid) carboxylate salts (PAASs) solutions are first electrospun to form PAAS nanofibers. After the imidization and carbonization processes, PI and carbon nanofibers can then be obtained, respectively. The Raman spectra reveal that the carbon nanofibers are partially graphitized by the carbonization process. The diameters of the PI nanofibers are observed to be smaller than those of the PAAS nanofibers because of the formation of the more densely packed structures after the imidization processes; the diameters of the carbon nanofibers remain similar to those of the PI nanofibers after the carbonization process. The thermal dissipation behaviors of the PI and carbon nanofibers are also examined. The infrared images indicate that the transfer rates of thermal energy for the carbon nanofibers are higher than those for the PI nanofibers, due to the better thermal conductivity of carbon caused by the covalent sp² bonding between carbon atoms.     

Utilization of bio‐sourced myrcene for efficient preparation of highly cis‐1,4 regular elastomer via a neodymium catalyzed copolymerization strategy

The depletion of fossil based chemicals and the associated pollution have presented huge challenges to sustainability. In this study, we report on bio‐available myrcene participating in copolymerization with isoprene and butadiene by using neodymium catalysts without disruption of the pristine polymer's properties. Efficient incorporation of myrcene into the copolymer was achieved with slightly retarded reactivity compared to the reactivities of butadiene and isoprene. Copolymerization of myrcene with hydroxyl myrcene still remained compatible with the catalyst systems when the cocatalyst was fed in excess, resulting in a novel type of full myrcene based functional elastomer. The high cis‐1,4 selectivity of the system maintained the same level as the homopolymerization. Significant affinity to polar substances was deduced from the remarkably reduced water contact angle, a strong indication of good compatibility with reinforcing fillers. All copolymers displayed over 93.2% cis‐1,4 regularity and high molecular weight with narrow ?. Good resistance to low temperature was also achieved as indicated by the low glass transition temperature for all copolymers. This study verified that myrcene can be used as a sustainable monomer substituent for general diene based elastomer preparation. © 2020 Society of Chemical Industry