Topography Structure and Scanning Tunneling Spectrum of Nickel( Ⅱ )-tetraphenylporphyrin Molecules on Au(111)

Scanning tunneling microscopy （STM） and scanning tunneling spectroscopy （STS） were performed on monolayer film of NiTPP supported on Au（111） under ultrahigh vacuum （UHV） conditions. The constant current STM images show remarkable bias dependence. High resolution STM data clearly show the individual NiTPP molecules and allow easy differentiation between NiTPP and CoTPP reported before. Scanning tunneling spectra, as a function of molecule-tip separation, were acquired over a range of tip motion of 0.42 nm. Spectra do not show the variation in band splitting with tip distance. It appears for molecules such as NiTPP that the average potential at the molecule is essentially the same at the same metal substrate. For molecules of the height of NiTPP, the scanning tunneling spectra should give reliable occupied and unoccupied orbital energies over a wide range of tip-molecule distances.

Graphene/Rh(111) Structure Studied Using In-Situ Scanning Tunneling Microscopy

Scanning tunnel microscopy （STM） is performed to verify if an Rh ＇nails＇ structure is formed accompanying the graphene growing during chemical vapor deposition. A structure of a graphene island in an Rh vacancy island is used as the start. While the graphene island is removed by oxygenation, the variations of the Rh vacancy island are imaged with an in-situ high-temperature STM. By fitting with our model and calculations, we conclude that the best fit is obtained for 0% Rh, i.e., for the complete absence of nails below graphene on Rh（111）. That is, when graphene is formed on Rh（111）, the substrate remains fiat and does not develop a SUPPorting nail structure.

Bacterial entombment by intratubular mineralization following orthograde mineral trioxide aggregate obturation: a scanning electron microscopy study

The time domain entombment of bacteria by intratubular mineralization following orthograde canal obturation with mineral trioxide aggregate（MTA） was studied by scanning electron microscopy（SEM）. Single-rooted human premolars（n560） were instrumented to an apical size #50/0.06 using ProF ile and treated as follows： Group 1（n510） was filled with phosphate buffered saline（PBS）; Group 2（n510） was incubated with Enterococcus faecalis for 3 weeks, and then filled with PBS; Group 3（n520） was obturated orthograde with a paste of OrthoM TA（BioM TA, Seoul, Korea） and PBS; and Group 4（n520） was incubated with E. faecalis for 3 weeks and then obturated with OrthoM TA–PBS paste. Following their treatments, the coronal openings were sealed with PBS-soaked cotton and intermediate restorative material（IRM）, and the roots were then stored in PBS for 1, 2, 4, 8 or 16 weeks. After each incubation period, the roots were split and their dentin/MTA interfaces examined in both longitudinal and horizontal directions by SEM. There appeared to be an increase in intratubular mineralization over time in the OrthoM TA-filled roots（Groups 3 and 4）. Furthermore, there was a gradual entombment of bacteria within the dentinal tubules in the E. faecalis inoculated MTA-filled roots（Group 4）. Therefore, the orthograde obturation of root canals with OrthoM TA mixed with PBS may create a favorable environment for bacterial entombment by intratubular mineralization.

Multiple characteristic structure fragments scans coupled to high-resolution mass spectrometry strategy for discovering unknown structural analogs of mycotoxins in food

The cereals and their products,which have been easily infected by fungi and contaminated with mycotoxins,are serious threat to both human and animals alike.And yet,detection of these unknown fungal infection and mycotoxins contaminates remains a great challenge.In this work,a holistic approach based on multiple characteristic structure fragments scans and high-resolution mass spectrometry(HRMS)was proposed for discovering unknown structural analogues of mycotoxins.The structural similarity of the same class of compounds provides a direction for the discovery and identification of unknown structural analogues of mycotoxins.The following steps were carried out:the fragmentation pathways of four types of mycotoxins were elucidated through comprehensive fragment analysis.By the combination of fragmentation pathways,the multiple characteristic structure fragments were screened out,with the common fragments were obtained by Veen diagram.Finally multiple characteristic structure fragments scans were carried out to find the unknown structural analogues of mycotoxins.The approach,first proposed by us,was proved to be effective in discovering and identifying 5 structural analogues of mycotoxins in real samples.It was proved to be a simple,fast and accurate method for early detection of fungal infection and mycotoxin contaminants,even for trace amounts of chemicals in complex matrix,and is of great significance to prevent hazardous substances infection from the food supply chains worldwide.

Morphology of Barium Hydrogen Phosphate Formation Induced by Phosphate-Mineralization Microbe

Phosphate-mineralization microbe was chosen to study the influences of bacterial mixture,filtrate,bacteria solution,bacterial body and bacterial secretion on barium hydrogen phosphate crystal formation.The chemical compositions and structures of samples were characterized with scanning electron microscopy（SEM）,transmission electron microscopy（TEM）,and X-ray diffraction techniques（XRD）,revealing that the crystal morphology of barium hydrogen phosphate was dumbbell-shaped pattern,nanoparticles via aggregate clusters,irregular sphere with different sizes.The results indicated that bacterial body and bacterial secretion could induce the formation of irregular quadrilateral and spheres,respectively.But the effect of bacterial secretion was stronger than that of bacterial body when induced barium hydrogen phosphate crystal in bacteria solution.However,the crystals form could be affected only in bacterial mixture,but filtrate could induce the formation of nanoparticles.As a result,the bacteria and metabolites play an important role in the process of crystal nucleation,growth,and accumulation of barium hydrogen phosphate.

Characterization of cake layer structure on the microfiltration membrane permeability by iron pre-coagulation

A cake layer is formed by coagulation aggregates under certain transmembrane pressure in the coagulation-microfiltration （MF） process. The characteristics of humic acid aggregates coagulated by different iron-based coagulants, such as charge, size, fractal dimension and compressibility, have an effect on the cake layer structure. At the optimum iron dose of 0.6 to 0.8 mmol/L for ferric chloride （FC） and polymer ferric sulfate （PFS） pre-coagulation, at the point of charge neutralization for near zero zeta potential, the aggregate particles produced possess the greatest size and highest fractal dimension, which contributes to the cake layer being most loose with high porosity and low compressibility. Thus the membrane filterability is better. At a low or high iron dose of FC and PFS, a high negative or positive zeta potential with high charge repulsion results in so many small aggregate particles and low fractal dimension that the cake layer is compact with low porosity and high compressibility. Therefore the membrane fouling is accelerated and MF permeability becomes worse. The variation of cake layer structure as measured by scanning electric microscopy corresponds with the fact that the smaller the coagulation flocs size and fractal dimension are, the lower the porosity and the tighter the cake layer conformation. This also explains the MF membrane flux variation visually and accurately.

On Test Data Compression Using Selective Don＇t-Care Identification

This paper proposes an effective method for reducing test data volume undermultiple scan chain designs. The proposed method is based on reduction of distinct scan vectorsusing selective don't-care identification. Selective don't-care identification is repeatedlyexecuted under condition that each bit of frequent scan vectors is fixed to binary values (0 or 1).Besides, a code extension technique is adopted for improving compression efficiency with keepingdecompressor circuits simple in the manner that the code length for infrequent scan vectors isdesigned as double of that for frequent ones. The effectiveness of the proposed method is shownthrough experiments for ISCAS'89 and ITC'99 benchmark circuits.

Soil Microbial Responses to Biochars Varying in Particle Size,Surface and Pore Properties

Biochars are known for their heterogeneity, especially in pore and surface structure associated with pyrolysis processes and sources of feedstocks. The surface area of biochar is likely to be an important determinant of the extent of soil microbial attachment, whereas the porous structure of biochar is expected to provide protection for soil microorganisms. Potential interactions between biochars from different sources and with different particle sizes were investigated in relation to soil microbial properties in a short-term incubation study. Three particle size （sieved） fractions （0.5-1.0, 1.0-2.0 and 2.0-4.0 mm） from three woody biochars produced from jarrah wood, jarrah and wandoo wood and Australian wattle branches, respectively, were incubated in soil at 25 ℃ for 56 d. Observation by scanning electron microscopy （SEM） and characterisation of pore and surface area showed that all three woody biochars provided potential habitats for soil microorganisms due to their high porosity and surface areas. The biochars were structurally heterogeneous, varying in porosity and surface structure both within and between the biochar sources. After the 56-d incubation, hyphal colonisation was observed on biochar surfaces and in larger biochar pores. Soil clumping occurred on biochar particles, cementing and covering exposed biochar pores. This may have altered surface area and pore availability for microbial colonisation. Transient changes in soil microbial biomass, without a consistent trend, were observed among biochars during the 56-d incubation.