基于孔压静力触探(CPTU)测试的连云港海相粘土前期固结压力确定方法研究

首先回顾了基于孔压静力触探(CPTU)测试确定前期固结压力的方法,通过连云港海相粘土场地进行的CPTU试验资料,以室内固结试验得到的前期固结压力作为参考值评估了经验方法预测前期固结压力的有效性。最简单的方法是直接建立前期固结压力和净锥尖阻力的关系,同时也是最有效的方法。     

Separation and concentration of sulfonylurea herbicides in milk by ionic‐liquid‐based foam flotation solid‐phase extraction

The ultrasound‐assisted ionic liquid foam flotation solid‐phase extraction of sulfonylurea herbicides in milk was developed and validated. The proteins and lipids were isolated from the sample matrix by adding salt and adjusting the pH value. The target analytes eluted from the solid‐phase extraction cartridge were determined by high‐performance liquid chromatography. Some experimental parameters, including the pH value of sample solution, amount of NaCl, ionic liquid type, extraction time, flow rate of carrier gas, flotation time, and solid‐phase extraction cartridge type were investigated and optimized. Under the optimized experimental conditions, the limits of detection for metsulfuron, pyrazosulfuron, chlorimuron‐ethyl, and nicosulfuron were 1.3, 0.6, 0.7, and 1.1 μg/L, respectively. When the present method was applied to the analysis of milk samples the recoveries of the analytes ranged from 84.3 to 105.2% and relative standard deviations were >5.7%.     

孔压静力触探(CPTU)测试成果影响因素及原始数据修正方法探讨

孔压静力触探(CPTU)是20世纪80年代在国际上兴起的新型原位测试技术,因其诸多优点,目前在欧美诸国已得到广泛应用。由于探头规格、技术标准和操作程序的差异,影响CPTU测试成果的因素很多,而且其影响程度也各不相同。根据前人的研究成果,对CPTU测试成果的影响因素进行了分析总结,以期在CPTU资料整理和应用中引起重视。最后,简要论述了考虑诸多影响因素的原始数据修正方法。     

基于安卓电视机芯智能升级的应用研究

对比了目前几种安卓电视智能升级方案,提出了一种在现有电视技术条件下,通过一个自定义接口完成安卓电视机芯智能升级的方案。该方法具有电视整机机芯升级简单、便捷、成本低、原有整机利用率高的优点。并以50个管脚的自定义接口为例,具体阐述了安卓电视机芯升级的软件、硬件解决方案。     

Use of a tree‐structured hierarchical model for estimation of location and uncertainty in multivariate spatial data

Analysis and modeling of spatial data are of considerable interest in many applications. However, the prediction of geographical features from a set of chemical measurements on a set of geographically distinct samples has never been explored. We report a new, tree‐structured hierarchical model for the estimation of geographical location of spatially distributed samples from their chemical measurements. The tree‐structured hierarchical modeling used in this study involves a set of geographic regions stored in a hierarchical tree structure, with each nonterminal node representing a classifier and each terminal node representing a regression model. Once the tree‐structured model is constructed, given a sample with only chemical measurements available, the predicted regional location of the sample is gradually restricted as it is passed through a series of classification steps. The geographic location of the sample can be predicted using a regression model within the terminal subregion. We show that the tree‐structured modeling approach provides reasonable estimates of geographical region and geographic location for surface water samples taken across the entire USA. Further, the location uncertainty, an estimate of a probability that a test sample could be located within a pre‐estimated, joint prediction interval that is much smaller than the terminal subregion, can also be assessed. Copyright © 2014 John Wiley & Sons, Ltd.     

pH manipulation: a facile method for lowering oxidation state and keeping good yield of poly(m-phenylenediamine) and its powerful Ag+ adsorption ability

A method of pH manipulation has been used to improve chemically oxidative polymerization of m-phenylenediamine (mPD) through concurrent addition of NaOH when adding oxidant (NH(4))(2)S(2)O(8). pH detection and open-circuit potential technique were adopted to monitor the polymerization process of mPD and to explain the oxidation state-pH and yield-pH relationships. Results from Fourier transformed infrared (FTIR) and X-ray photoelectron (XPS) spectroscopies indicate that a low oxidation state is under control by regulating NaOH concentration. At 2.5 M NaOH, the oxidation state of poly(m-phenylenediamine) (PmPD) is 64.7 mol % (measured by molar content of quinoid imine from XPS), while the yield is 84%. The synthesized PmPD possesses better Ag(+) adsorption performance when lowering its oxidation state. Moreover, the Ag(+) adsorbance of PmPD can reach 1693 mg g(-1). Meanwhile, Ag(+) adsorption mechanism was studied by pH tracking, X-ray diffraction (XRD) patterns, and X-ray photoelectron spectroscopy. The adsorption process includes redox reaction, chelation, and physical adsorption.     

Production and Characterization of Polyclonal and Monoclonal Abs Against the RNA-Binding Protein QKI

RNA-binding protein QKI, a member of the Signal Transduction and Activation of RNA family, is found to be essential in the blood vessel development and postnatal myelination in central nervous system (Woo et al., Oncogene 28:1176–1186, 2009; Lu et al., Nucleic Acids Res 31(15):4616–4624, 2003; Bohnsack et al., Genesis 44(2):93–104, 2006). However, its wide expression pattern suggests other fundamental roles in vivo (Kondo et al., Mamm Genome 10(7):662–669, 1999). To facilitate the understanding of QKI function in various systems, we prepared the polyclonal and monoclonal antibodies against QKI. To obtain the antigen, recombinant His-tagged QKI was expressed in Escherichia coli and highly purified by Ni²⁺-chelated column combined with hydrophobic and ion exchange methods. Following three types of immunizations with different adjuvants, including Freund’s, PAGE gel, and nitrocellulose membrane, only the antiserum produced with Freund’s adjuvant is effective for Western blot detection. Several McAb clones are able to recognize both endogenous and over-expressed QKI with high affinity in Western blot and immunofluorescence. The specificity of Ab was validated as weakening, and no specific signals were observed in cells with QKI knocking down. Immunohistochemistry analysis further showed positive staining of QKI in kidney where QKI mRNA was abundantly expressed, ensuring the wide applications of the QKI Abs in the ongoing mechanistic studies.     

Fabrication of carbon nanofiber by pyrolysis of freeze-dried cellulose nanofiber

The possibility of fabricating carbon nanofibers from cellulose nanofibers was investigated. Cellulose nanofiber of ~50 nm in diameter was produced using ball milling in an eco-friendly manner. The effect of the drying techniques of cellulose nanofibers on the morphology of carbon residue was studied. After pyrolysis of freeze-dried cellulose nanofibers below 600 °C, amorphous carbon fibers of ~20 nm in diameter were obtained. The pyrolysis of oven-dried precursors resulted in the loss of original fibrous structures. The different results arising from the two drying techniques are attributed to the difference in the spatial distance between cellulose nanofiber precursors.     

Zirconium oxide aerogel for effective enrichment of phosphopeptides with high binding capacity

In this study, zirconium oxide (ZrO₂) aerogel was synthesized via a green sol–gel approach, with zirconium oxychloride, instead of the commonly used alkoxide with high toxicity, as the precursor. With such material, phosphopeptides from the digests of 4 pmol of β-casein with the coexistence of 100 times (mol ratio) BSA could be selectively captured, and identified by MALDI-TOF MS. Due to the large surface area (416.0 m² g⁻¹) and the mesoporous structure (the average pore size of 10.2 nm) of ZrO₂ aerogel, a 20-fold higher loading capacity for phosphopeptide, YKVPQLEIVPN[pS]AEER (MW 1952.12), was obtained compared to that of commercial ZrO₂ microspheres (341.5 vs. 17.87 mg g⁻¹). The metal oxide aerogel was further applied in the enrichment of phosphopeptides from 100 ng nonfat milk, and 17 phosphopeptides were positively identified, with a 1.5-fold improvement in phosphopeptide detection compared with previously reported results. These results demonstrate that ZrO₂ aerogel can be a powerful enrichment material for phosphoproteome study.     

Vibrational and orientational dynamics of water in aqueous hydroxide solutions

We report the vibrational and orientational dynamics of water molecules in isotopically diluted NaOH and NaOD solutions using polarization-resolved femtosecond vibrational spectroscopy and terahertz time-domain dielectric relaxation measurements. We observe a speed-up of the vibrational relaxation of the O-D stretching vibration of HDO molecules outside the first hydration shell of OH(-) from 1.7 ± 0.2 ps for neat water to 1.0 ± 0.2 ps for a solution of 5 M NaOH in HDO:H(2)O. For the O-H vibration of HDO molecules outside the first hydration shell of OD(-), we observe a similar speed-up from 750 ± 50 fs to 600 ± 50 fs for a solution of 6 M NaOD in HDO:D(2)O. The acceleration of the decay is assigned to fluctuations in the energy levels of the HDO molecules due to charge transfer events and charge fluctuations. The reorientation dynamics of water molecules outside the first hydration shell are observed to show the same time constant of 2.5 ± 0.2 ps as in bulk liquid water, indicating that there is no long range effect of the hydroxide ion on the hydrogen-bond structure of liquid water. The terahertz dielectric relaxation experiments show that the transfer of the hydroxide ion through liquid water involves the simultaneous motion of ~7 surrounding water molecules, considerably less than previously reported for the proton.