半序集的碰撞数与分层深度贪婪算法

设Ｐ＝（Ｘ，≤）是一个半序集，本文在关于碰撞数的深度贪婪算法的基础上，直接证明了对任意的Ｐ存在一个最优的ＤＬＧ扩张，给出了ＤＬＧ半序集的定义，并证明了半序集Ｐ是ＤＬＧ半序集的一个充分条件，最后给出了ＤＬＧ扩张算法。     

On lower bounds for a class of quadratic 0, 1 programs

We present a new method of obtaining lower bounds for a class of quadratic 0, 1 programs that includes the quadratic assignment problem. The method generates a monotonic sequence of lower bounds and may be interpreted as a Lagrangean dual ascent procedure. We report on a computational comparison of our bounds with earlier work in [2] based on subgradient techniques.     

Preparation of metal‐organic framework UiO‐66‐incorporated polymer monolith for the extraction of trace levels of fungicides in environmental water and soil samples

A zirconium terephthalate metal‐organic framework‐incorporated poly(N‐vinylcarbazole‐co‐divinylbenzene) monolith was fabricated in a capillary by a thermal polymerization method. The optimized monolith had a homogeneous structure, good permeability, and stability. The monolith could be used for the effective enrichment of fungicides through π‐π interactions, electrostatic forces, and hydrogen bonds. The potential factors that affect the extraction efficiency, including ionic strength, solution pH, sample volume, and eluent volume, were investigated in detail. The monolith‐based in‐tube solid‐phase microextraction coupled with ultra‐high‐performance liquid chromatography and high‐resolution Orbitrap mass spectrometry was performed for the analysis of five fungicides (pyrimethanil, tebuconazole, hexaconazole, diniconazole, and flutriafol) in environmental samples. Under the optimized conditions, the linear ranges were 0.005–5 ng/mL for pyrimethanil, 0.01–5 ng/mL for flutriafol, and 0.05–5 ng/mL for other fungicides, respectively, with coefficients of determination ≥0.9911. The limits of detection were 1.34–14.8 ng/L. The columns showed good repeatability (relative standard deviations ≤9.3%, n = 5) and desirable column‐to‐column reproducibility (relative standard deviations 5.3–9.4%, n = 5). The proposed method was successfully applied for the simultaneous detection of five fungicides in water and soil samples, with recoveries of 90.4–97.5 and 84.0–95.3%, respectively.     

Discovering Credit Cardholders’ Behavior by Multiple Criteria Linear Programming

In credit card portfolio management, predicting the cardholder’s spending behavior is a key to reduce the risk of bankruptcy. Given a set of attributes for major aspects of credit cardholders and predefined classes for spending behaviors, this paper proposes a classification model by using multiple criteria linear programming to discover behavior patterns of credit cardholders. It shows a general classification model that can theoretically handle any class-size. Then, it focuses on a typical case where the cardholders’ behaviors are predefined as four classes. A dataset from a major US bank is used to demonstrate the applicability of the proposed method.     

Jump number and width

The maximum jump number of ordered sets having width w and tower number t, denoted by s(w, t), satisfies $$c_l tw\lg w \leqslant s\left( {w,t} \right) \leqslant tw\lg w$$ for some positive constants c ₁ and c ₂. Specifically, we can obtain c ₁=1/8 and c ₂<11/10. When w and t are sufficiently large and w is a power of 2, then $$\left( {\frac{1}{2} - \varepsilon } \right)tw\lg w \leqslant s\left( {w,t} \right) < \frac{7}{{10}}tw\lg w$$ This gives an answer to a problem posed by W. T. Trotter ([3], Problem 15).     

蒙古查干苏布尔加(Tsagaan Suvarga)大型斑岩型铜钼矿床含矿蚀变岩常量、微量和稀土元素地球化学特征及意义

蒙古Tsagaan Suvarga大型斑岩型铜钼矿床围岩蚀变类型主要有网脉状硅化、泥化、石英-绢云母化、钾硅酸岩化和青盘岩化。从热液成矿中心向外的矿化蚀变分带特征为含铜网脉状硅化蚀变带→含铜泥化带→含铜钼石英-绢云母化带→含铜钼钾硅酸岩化带→青盘岩化带。早期为钾硅酸岩化带,中期为石英-绢云母化和硅化,晚期为泥化带和碳酸盐化(方解石)。含矿蚀变岩明显受不同级次构造-裂隙带控制,北东向和北西向裂隙带可能是斑岩成矿热液体系的运移通道。随着接近循环热液成矿体系的成矿中心和硅化不断增强,REE,LREE和HREE含量降低,轻和重稀土元素之间分异程度增强;轻和重稀土元素之间分异程度与硅化-钾硅酸盐化之间关系具有指数关系。随着(Na2O K2O)含量逐渐增高,从负Eu异常→无Eu异常→正Eu异常→明显正Eu异常,说明Eu异常受循环热液成矿体系的碱交代程度控制明显,因此,正Eu异常、轻和重稀土元素之间分异程度明显及其相关围岩蚀变特征是寻找与蒙古Tsagaan Suvarga斑岩型铜钼矿床类似的找矿预测指标。     

Highly active Pd(II) catalysts with pyridylbenzoimidazole ligands for the Heck reaction

The air-, and thermo-stable palladium(II) complexes C1-C10 are prepared by the reaction of PdCl₂(CH₃CN)₂ with pyridylbenzoimidazole. With various substituents on the pyridine ring, palladium atom was coordinated by two pyridylbenzoimidazole molecules via nitrogen atoms of benzoimidazole. The structure of complexes C3, C4, C6, and C7 has been confirmed by X-ray diffraction analysis. Without substituents on the pyridine ring, palladium atom was directly coordinated with two nitrogen atoms of pyridine and benzoimidazole nitrogen via intramolecular chelation (C10). These complexes performed the Heck olefination of aryl bromides in a good to high yield under phosphine-free conditions.     

Organic Additive-derived Films on Cu Electrodes Promote Electrochemical CO2 Reduction to C2+ Products Under Strongly Acidic Conditions

Electrochemical CO₂ reduction (CO₂R) at low pH is desired for high CO₂ utilization; the competing hydrogen evolution reaction (HER) remains a challenge. High alkali cation concentration at a high operating current density has recently been used to promote electrochemical CO₂R at low pH. Herein we report an alternative approach to selective CO₂R (>70 % Faradaic efficiency for C₂₊ products, FE_C2+) at low pH (pH 2; H₃PO₄/KH₂PO₄) and low potassium concentration ([K⁺]=0.1 M) using organic film-modified polycrystalline copper (Modified-Cu). Such an electrode effectively mitigates HER due to attenuated proton transport. Modified-Cu still achieves high FE_C2+ (45 % with Cu foil /55 % with Cu GDE) under 1.0 M H₃PO₄ (pH≈1) at low [K⁺] (0.1 M), even at low operating current, conditions where HER can otherwise dominate.     

Systematic and site-specific analysis of N-sialoglycosylated proteins on the cell surface by integrating click chemistry and MS-based proteomics

Glycoproteins on the cell surface are ubiquitous and essential for cells to interact with the extracellular matrix, communicate with other cells, and respond to environmental cues. Although surface sialoglycoproteins can dramatically impact cell properties and represent different cellular statuses, global and site-specific analysis of sialoglycoproteins only on the cell surface is extraordinarily challenging. An effective method integrating metabolic labeling, copper-free click chemistry and mass spectrometry-based proteomics was developed to globally and site-specifically analyze surface N-sialoglycoproteins. Surface sialoglycoproteins metabolically labeled with a functional group were specifically tagged through copper-free click chemistry, which is ideal because it is quick, specific and occurs under physiological conditions. Sequentially tagged sialoglycoproteins were enriched for site-specific identification by mass spectrometry. Systematic and quantitative analysis of the surface N-sialoglycoproteome in cancer cells with distinctive invasiveness demonstrated many N-sialoglycoproteins up-regulated in invasive cells, the majority of which contained cell adhesion-related domains. This method is very effective to globally and site-specifically analyze N-sialoglycoproteins on the cell surface, and will have extensive applications in the biological and biomedical research communities. Site-specific information regarding surface sialoglycoproteins can serve as biomarkers for disease detection, targets for vaccine development and drug treatment.     

气相色谱-质谱法同时检测动物组织中多种激素类兽药的残留量

建立了不同动物基质(肌肉、肝脏、肾脏)中己烷雌酚、己烯雌酚、己二烯雌酚、还原尿睾酮、表睾酮、雌酮、雌二醇、炔雌醇和雌三醇激素残留量的气相色谱-质谱联用(GC-MS)检测方法。以乙腈为提取溶剂,固相萃取柱净化,微波辅助衍生化,用双(三甲基硅烷基)三氟乙酰胺(BSTFA)与甲基氯硅烷(TMCS)(体积比为99 :1)的硅烷化试剂在吡啶存在下进行衍生化反应。实验结果表明,9种激素的检出限为0.1～1 μg/kg。3种动物基质中9种激素的平均回收率为68.8%～93.1%,实验室内相对标准偏差(RSD)为4.1%～22.3%,实验室间RSD为3.1%～17.9%。方法的技术指标满足动物组织中激素类兽药残留分析的要求。