126.5 GPa准静水压下的光谱学实验

 本文介绍了作者利用国内加工的金刚石压砧装置及组建的微区光谱系统进行100 GPa（百万大气压）准静水压光谱学实验的概况，证明压力产生装置和微区光谱系统的多功能性是充分可靠的。实验中遇到的压力产生能力超过压力测量能力的事实，反映了高压光谱学实验在压力范围扩大时所遇到的挑战。文中对高压下的拉曼、发射、吸收及反射光谱的实验原理和实验方法也作了概略的介绍。     

Experimental study on laser cleaning of paint layer on white marble surface北大核心CSCD

In order to effectively remove the surface paint of the cultural relic of white marble, the area extrapolation method and laser-induced plasma spectroscopy (LIPS) method were used to obtain the ablation threshold power of the gold, silver paint layer and white marble surface. On the basis of this, the optimal laser power for removing paint without damaging the white marble substrate was determined. The image processing method was used to study the cleaning degree and variation trend of cleaning rate of the gold and silver paint on the surface of 10 mm×10 mm white marble by laser cleaning, and the optimal laser spot overlap rate and the optimal cleaning times were obtained. Finally, the image processing method was used to evaluate the cleaning effect of laser cleaning of paint layer on the white marble surface. More than 93% of the cleaning degree shows that the synergistic use of the area extrapolation method, LIPS method and image processing method can effectively improve the laser cleaning efficiency of the paint layer on white marble surface. Copyright ©2022 Journal of Applied Optics. All rights reserved.     

覆盖型岩溶塌陷临界水位降幅模型试验研究

在考虑覆盖型岩溶塌陷各种影响因素的基础上,通过理论分析和室内模型试验,定量化的研究水位下降对岩溶塌陷的影响及其变化规律。结果表明,急剧的水位变化是影响覆盖型岩溶塌陷的重要因素,受覆盖层土体性质、溶洞内气压、溶洞开口大小等因素的影响。提出了水位下降过程中临界水位降幅公式;并以室内模型试验为例,对该公式进行验证评价,计算所得的塌陷临界水位降幅与实际情况符合较好。     

考虑客流量差异的区域公交车辆调度

考虑到公交客流时间分布非均衡以及公交区域调度的多条线路客流高峰时间、空间分布集中会导致总体客流的高低峰客流量差异进一步加大,提出在低平峰期允许部分公交车辆停运的抽停策略,从"部分车次被某辆车完成"的集合划分角度研究区域公交车辆调度问题,建立改进的区域公交车辆调度优化模型,并设计了最大最小蚁群算法进行求解.算例结果显示:与常规调度方案相比,车辆等待时间减少4034 min,等待时间在总工作时间中占比减少10%,驾驶员减少14个,证明了文中模型的有效性和实用性.     

侧链键合水杨醛型双齿席夫碱配基的功能化聚砜的合成及其稀土离子配合物的光致发光性能

通过氯甲基化聚砜(CMPSF)与4-羟基水杨醛(HSA)的亲核取代反应,将水杨醛(SA)基团键合在聚砜侧链,制得改性聚砜PSF-SA;再经PSF-SA的醛基分别与苯胺(AN)和环己胺(CA)发生席夫碱反应,获得了两种侧链键合了水杨醛型双齿席夫碱配基的功能化聚砜PSF-SAN和PSF-SCA,产物的结构由红外光谱和核磁共振氢谱表征。以两种功能化聚砜为大分子配体,与Tb(Ⅲ)离子及Eu(Ⅲ)离子分别配位,制得了二元高分子-稀土配合物,初步探索了配合物的光致发光性能。本文重点研究了功能化聚砜PSF-SAN和PSFSCA的制备反应,考察与分析了主要因素对CMPSF与HSA之间亲核取代反应的影响规律。结果表明,对于该亲核取代反应,适宜的溶剂为极性较强的N,N-二甲基乙酰胺,80℃为适宜的反应温度。大分子配体PSFSAN对Eu(Ⅲ)离子的荧光发射产生强烈的敏化作用,配合物PSF-(SAN)_3-Eu(Ⅲ)发射红光;大分子配体PSF-SCA对Tb(Ⅲ)离子的荧光发射也产生敏化作用,配合物PSF-(SCA)_3-Tb(Ⅲ)发射绿光。     

Purification and Characterization of a Urethanase from Penicillium variabile

Urethanase produced by Penicillium variabile was purified through ultrasonication, concentration by polyethylene glycol 20,000, and Superdex G-200 gel filtration chromatography. The molecular weight of urethanase was determined to be around 96 kDa by gel filtration. The purified enzyme showed a single band in SDS-PAGE with the molecular weight of ~13.7 kDa, which suggests that the enzyme has a multimeric structure composed of the same subunits. Peptide map fingerprinting analysis was then carried out by MALDI/TOF-TOF MS. Within the known sequences in NCBI, glucosamine-6-phosphate deaminase and 6-phosphogluconate dehydrogenase get high score as compared with urethanase. Sequence analysis informs that N-terminal sequence of urethanase is GTNTADNDAA. The Minchaelis constant (K _m) and maximum reaction rate (V _m) of urethanase are 27.2 mmol/L and 156.25 μmol/L min, respectively.     

Intermolecular H···O═C bonds induced 2D self‐assembly of thiophene based diketopyrrolopyrrole derivative

Compounds with diketopyrrolopyrrole (DPP) and thiophene moieties have attracted considerable attention because of their promising charge transport properties. The molecular conformation and self‐assembly of 2,5‐dihexadecyl‐3,6‐di(thiophen‐2‐yl)‐2,5‐dihydropyrrolo[3,4‐c]pyrrole‐1,4‐dione (TDPP‐C16) molecule have been investigated by scanning tunneling microscopy and density functional theory alculation. The TDPP‐C16 molecules adsorb with their optimized S‐shaped conformation and form a zipper‐like pattern on highly oriented pyrolytic graphite surface. R and S rotated structures are observed. The nanostructure is dominated by intermolecular double hydrogen bonds between C═O of the DPP units and hydrogen atom of thiophene rings in the neighboring molecules in each row. Atomic force microscopy and density functional theory calculation also display the existence of strong intermolecular hydrogen bonding. The results provide molecular evidence for the intermolecular interactions of the surface structure, which could benefit to the design of the organic semiconducting materials and understanding of underlying principle of charge transfer process. Copyright © 2017 John Wiley & Sons, Ltd.     

惠农政策执行中存在问题的成因与对策研究

近年来,各级党委、政府高度重视农村经济社会可持续发展,先后出台了一系列惠农政策,有力促进了农业的健康发展、农村面貌的变化、农民民生的改善,但也存在着一系列亟待解决的问题,影响了惠农政策预期目标的实现。认真分析惠农政策执行情况及存在问题,准确阐释其成因,以政策设计、政策执行和监督检查为重点,采取有针对性的对策措施,进而不断提高惠农政策执行的有效性和可持续性。     

RETRACTED ARTICLE: Microenvironment characterization for a novel biocompatible hybrid carbon-silicon material

The compatible carbon-silicon complex materials originated from precursor diglycerylsilane (DGS) and sugar-modified silane N-(3-triethoxysilylpropyl)gluconamide (GLS) have gained substantial popularity by demonstrating admirable properties to stabilize entrapped biomolecules. The microenvironment inside these materials, especially the distribution of sugar moieties inside the matrix, which is likely the most critical factor determining compatibility of these materials, still remains unclear. To deeply investigate the biocompatibility mechanism of these materials, we have adopted two different preparation routes for these materials by introducing GLS into the starting DGS sol stage, but things are different after the DGS gel is formed. A fluorescence probe rhodamine 6G is introduced herein in the DGS sol to monitor the distribution of GLS moieties, as well as the evolution of the microenvironment inside resulting materials. All in all, the findings demonstrated that the timing of GLS addition plays a critical role in controlling the evolution of the inner structure of materials, suggesting that this factor provides a promising route to tune the properties of the resulting materials. Supported by the National Natural Science Foundation of China (Grant No. 20876176), Scientific Research Foundation for the Returned Overseas Chinese Scholars by the State Education Ministry, Key Project of Chinese Ministry of Education (Grant No. 109100), Doctoral Project of Shandong Province (Grant No. 2008BS09013), Research Foundation of Key Laboratory of Carbon Materials, Institute of Coal Chemistry, CAS (Grant No. KFJJ0506), and Natural Science Foundation of Shandong Province (Grant No. Q2007B02)     

An online method combining a Gasbench II with continuous flow isotope ratio mass spectrometry to determine the content and isotopic compositions of minor amounts of carbonate in silicate rocks

An online method using continuous flow isotope ratio mass spectrometry (CF‐IRMS) interfaced with a Gasbench II device was established to analyze carbon and oxygen isotopic compositions and to estimate the content of minor amounts of carbonate in silicate rocks. The mixtures of standard materials and high‐purity quartz are firstly used to calibrate different quantities of carbonate in silicates. The results suggest that the accuracy and precision of the online analysis are both better than those obtained using an offline method. There is a positive correlation between the carbonate weight and the Mass44 ion beam intensity (or peak area). When the weight of carbonate in the mixtures is greater than 70 µg (equal to ～1800 mV Mass44 ion beam intensity), the δ¹³C and δ¹⁸O values of samples usually have accuracy and precision of ±0.1‰ and ±0.2‰ (1σ), respectively. If the weight is less than 70 µg, some limitations (e.g., not perfectly linear) are encountered that significantly reduce the accuracy and precision. The measured δ¹⁸O values are systematically lower than the true values by ?0.3 to ?0.7‰; the lower the carbonate content, the lower the measured δ¹⁸O value. For samples with lower carbonate content, the required phosphoric acid doses are higher and more oxygen isotope exchanges with the water in the phosphoric acid. To guarantee accurate results with high precision, multiple analyses of in‐house standards and an artificial MERCK sample with δ¹³C values from ?35.58 to 1.61‰ and δ¹⁸O from 6.04 to 18.96‰ were analyzed simultaneously with the unknown sample. This enables correction of the measured raw data for the natural sample based on multiple‐point normalization. The results indicate that the method can be successfully applied to a range of natural rocks. Copyright © 2010 John Wiley & Sons, Ltd.