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本文在无生命、物质和科学三个限制的前提下讨论“信息”到底是什么.依次论证:(1)自然科学没有能力度量信息的“质”,只能讨论信息的“量”;(2)“信息熵”只是度量信息“量”的概念;(3)在无生命的物质科学领域内,信息熵完全等价于Boltzmann熵,对应于实验中的热熵;(4)运用Occam剃刀原理,信息熵和Boltzmann熵两个名词只能留下其中的任意一个;(5)“熵”取决于体系的微观状态总数,即最终取决于热运动引起的分子核骨架的动态变化.于是,在无生命、物质和科学三个限制的领域内“信息”只是望文生义的产物. 相似文献
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采用INDO方法计算了{Fe[P(OMe)_3]_3(C_8H_(13))}~+的简化离子[Fe(PH_3)_3(C_8H_(13))]~+,将正则分子轨道用Edmiston-Ruedenberg定域化方法变换为定域分子轨道,结果表明:在对应C_1-H_(1A)键的定域分子轨道中,明显包含有铁原子轨道成分(7.8%),Fe-H_(1A)和Fe—C_1键级分别为0.190和0.302。指出C_1-H_(1A)键是以一对成键σ电子配位到铁原子上的。C_8H_(13)环以包含三个碳原子的η~4—共轭体系与铁原子相互作用。铁以二价(d~6-Fe(Ⅱ)的形式存在于该离子中。C_1-H_(1A)键的配位满足了文献[15]提出的Fe(Ⅱ)的共价12价。 相似文献
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Chen Chen Xiangheng Niu Yan Chai Hongli Zhao Minbo Lan Yonggang Zhu Gang Wei 《Electroanalysis》2013,25(6):1446-1452
This work presents a disposable bismuth‐antimony film electrode fabricated on screen‐printed electrode (SPE) substrates for lead(II) determination. This bismuth‐antimony film screen‐printed electrode (Bi‐SbSPE) is simply prepared by simultaneously in situ depositing bismuth(III) and antimony(III) with analytes on the homemade SPE. The Bi‐SbSPE can provide an enhanced electrochemical stripping signal for lead(II) compared to bismuth film screen‐printed electrodes (BiSPE), antimony film screen‐printed electrodes (SbSPE) and bismuth‐antimony film glassy carbon electrodes (Bi‐SbGC). Under optimized conditions, the Bi‐SbSPE exhibits attractive linear responses towards lead(II) with a detection limit of 0.07 µg/L. The Bi‐SbSPE has been demonstrated successfully to detect lead in river water sample. 相似文献
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Dr. Xiangheng Niu Prof. Dr. Minbo Lan Dr. Hongli Zhao Dr. Chen Chen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(29):9534-9541
The investigation of highly efficient catalysts for the electrochemical oxidation of glucose is the most critical challenge to commercialize nonenzymatic glucose sensors, which display a few attractive superiorities including the sufficient stability of their properties and the desired reproducibility of results over enzyme electrodes. Herein we propose a new and very promising catalyst: Pt cubes well‐dispersed on the porous Cu foam, for the the electrochemical oxidation reaction of glucose in neutral media. The catalyst is fabricated in situ on a homemade screen‐printed carbon electrode (SPCE) substrate through initially synthesizing the three‐dimensional (3D) porous Cu foam using a hydrogen evolution assisted electrodeposition strategy, followed by electrochemically reducing the platinic precursor simply and conveniently. Field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) proofs demonstrate that Pt cubes, with an average size (the distance of opposite faces) of 185.1 nm, highly dispersed on the macro/nanopore integrated Cu foam support can be reproducibly obtained. The results of electrochemical tests indicate that the cubic Pt‐based catalyst exhibits significant enhancement on the catalytic activity towards the electrooxidation of glucose in the presence of chloride ions, providing a specific activity 6.7 times and a mass activity 5.3 times those of commercial Pt/C catalysts at ?0.4 V (vs. Ag/AgCl). In addition, the proposed catalyst shows excellent stability of performance, with only a 2.8 % loss of electrocatalytic activity after 100 repetitive measurements. 相似文献
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Bin Ran Chaozhan Chen Bo Liu Minbo Lan Huaying Chen Yonggang Zhu 《Electrophoresis》2022,43(20):2033-2043
The detection of cancer biomarkers is of great significance for the early screening of cancer. Detecting the content of sarcosine in blood or urine has been considered to provide a basis for the diagnosis of prostate cancer. However, it still lacks simple, high-precision and wide-ranging sarcosine detection methods. In this work, a Ti3C2TX/Pt–Pd nanocomposite with high stability and excellent electrochemical performance has been synthesized by a facile one-step alcohol reduction and then used on a glassy carbon electrode (GCE) with sarcosine oxidase (SOx) to form a sarcosine biosensor (GCE/Ti3C2TX/Pt–Pd/SOx). The prominent electrocatalytic activity and biocompatibility of Ti3C2TX/Pt–Pd enable the SOx to be highly active and sensitive to sarcosine. Under the optimized conditions, the prepared biosensor has a wide linear detection range to sarcosine from 1 to 1000 µM with a low limit of detection of 0.16 µM (S/N = 3) and a sensitivity of 84.1 µA/mM cm2. Besides, the reliable response in serum samples shows its potential in the early diagnosis of prostate cancer. More importantly, the successful construction and application of the amperometric biosensor based on Ti3C2TX/Pt–Pd will provide a meaningful reference for detecting other cancer biomarkers. 相似文献
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He Yanfang Niu Xiangheng Shi Libo Zhao Hongli Li Xin Zhang Wenchi Pan Jianming Zhang Xifeng Yan Yongsheng Lan Minbo 《Mikrochimica acta》2017,184(7):2181-2189
Microchimica Acta - The authors describe a photometric method for the determination of free cholesterol based on the oxidation of cholesterol by the catalytic action of the enzyme... 相似文献
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Li Y Shi L Qin LX Qu LL Jing C Lan M James TD Long YT 《Chemical communications (Cambridge, England)》2011,47(15):4361-4363
A green fluorescent protein chromophore inspired chemosenor for Zn(2+) was designed and synthesized. A Zn(2+) specific fluorescence enhancement was observed due to restricted rotation between the 1,10-phenanthroline and imidazolone moieties. 相似文献
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Synthesis and evaluation of a maltose‐bonded silica gel stationary phase for hydrophilic interaction chromatography and its application in Ginkgo Biloba extract separation in two‐dimensional systems 下载免费PDF全文
Qianying Sheng Kaiya Yang Yanxiong Ke Xinmiao Liang Minbo Lan 《Journal of separation science》2016,39(17):3339-3347
Maltose covalently bonded to silica was prepared by using carbonyl diimidazole as a cross‐linker and employed as a stationary phase for hydrophilic interaction liquid chromatography. The column efficiency and the effect of water content, buffer concentration, and pH value influenced on retention were investigated. The separation or enrichment selectivity was also studied with nucleosides, saccharides, amino acids, peptides, and glycopeptides. The results indicated that the stationary phase processed good separation efficiency and separation selectivity in hydrophilic interaction liquid chromatography mode. Moreover, a two‐dimensional hydrophilic interaction liquid chromatography× reversed‐phase liquid chromatography method with high orthogonality was developed to analyze the Ginkgo Biloba extract fractions. The development of this two‐dimensional chromatographic system would be an effective tool for the separation of complex samples of different polarities and contents. 相似文献