Cell surface activation of progelatinase A (proMMP-2) and cell migration

Gelatinase A (MMP-2) is considered to play a critical role in cell migration and invasion. The proteinase is secreted from the cell as an inactive zymogen. In vivo it is postulated that activation of progelationase A (proMMP-2) takes place on the cell surface mediated by membrane-type matrix metalloproteinases (MT-MMPs). Recent studies have demonstrated that proMMP-2 is recruited to the cell surface by interacting with tissue inhibitor of metalloproteinases-2 (TIMP-2) bound to MT1MMP by forming a ternary complex. bee MT1-MMP closely located to the ternary complex then activates proMMP-2 on the cell surface. MT1-MMP is found in cultured invasive cancer cells at the invadopodia. The MTMMP/TIMP-2/ MMP- 2 system t bus provides localized expression of proteolysis of the extracellular matrix required for cell migration.

The surface activation of boron to improve ignition and combustion characteristic

Boron is a very promising and highly attractive fuel because of high calorific value. However, the practical applications in explosives and propellants of boron have been limited by long ignition delay time and low combustion efficiency. Herein, nano-Al and graphene fluoride(GF) as surface activated materials are employed to coat boron(B) particles to improve ignition and combustion performance. The reaction heat of nano-Al coated B/KNO_(3)and GF coated B/KNO_(3)are 1116.83 J/g and 862.69 J/g, respectively, which are higher than that of pure B/KNO_(3)(823.39 J/g). The ignition delay time of B/KNO_(3)could be reduced through nano-Al coating. The shortest ignition delay time is only 75 ms for B coated with nano-Al of 8 wt%, which is much shorter than that of pure B/KNO_(3)(109 ms). However, the ignition delay time of B/KNOcoated with GF has been increased from 109 to 187 ms. B coated with GF and nano-Al shown significantly influence on the pressure output and flame structure of B/KNO_(3). Furthermore, the effects of B/O ratios on the pressure output and ignition delay time have been further fully studied. For B/KNO_(3)coated with nano-Al and GF, the highest pressures are 88 KPa and 59 KPa for B/O ratio of 4:6, and the minimum ignition delay time are 94 ms and 148 ms for B/O ratio of 7:3. Based on the above results, the reaction process of boron coated with GF and nano-Al has been proposed to understand combustion mechanism.

Surface Activation of Plane and Curved Automotive Polymer Surfaces by Using a Fittable Multi-Pin DBD Plasma Source

In this work, surface activation of automotive polymers using atmospheric pressure plasmas was investigated. The aim was to increase the polar fraction of the surface energy of both plane and convex polymer devices with a radius in the range of 30 mm. For this purpose, a fittable low temperature atmospheric pressure plasma source based on capacitively coupled multi-pin electrodes was set up and applied. Each single electrode generates a treatment spot of approximately 2 cm2 with a tunable power density of up to 1.4 W/cm2. The surface energy was evaluated by contact angle measurements. After treatment at a low energy density of 1.01 J/cm2, the polar fraction of the surface energy of the investigated polymers was increased by a factor of 3.3 to 132, depending on the polymer materials. It was shown that by applying the presented fittable plasma source, this effect is independent of the surface radius of the polymer sample.

Ab Initio Potential Surface in CH_4 Activation by PTCL_2

Ab initio potential surface of oxidative addition of CH4 to coordinatively unsaturated PtC12 is presented. The electron correlation has a big effect on the transition state and activation energy.

Mechanical and histological properties of an electrospun scaffold with a modified surface by plasma polymerization implanted in an in vivo model

This article presents the construction of scaffolds composed of polylactic acid(PLA)with different concentrations of hydroxyapatite(HA)by electrospinning,which were superficially modified with polypyrrole(PPy/I)by plasma polymerization.A preliminary study was conducted of the biological and mechanical behavior of the scaffolds when they were implanted in the back of rabbits for 30 days;bone cells differentiated from mesenchymal stem cells(MSCs)were used.The bone cell and scaffold structures were characterized by histological,immunohistochemical,and mechanical stress tests.Hematoxylin–eosin staining showed good tissue conformation.The immunohistochemical tests highlighted the presence of the main bone tissue proteins,such as collagen,osteocalcin,and osteopontin.The PLA/HA scaffolds were observed to exhibit cell adhesion and proliferation properties;however,the response was much better in the scaffolds that had a higher concentration of HA and that were coated with PPy/I.The results of the mechanical tests of the scaffolds indicated that the plasma treatment improved the adhesion and cell proliferation properties and contributed to the mechanical support,allowing the formation of neotissues with good viability of cell growth.

YAG laser welding with surface activating flux

YAG laser welding with surface activating flux has been investigated, and the influencing factors and mechanism are discussed. The results show that both surface activating flux and surface active element S have fantastic effects on the YAG laser weld shape, that is to obviously increase the weld penetration and D/W ratio in various welding conditions. The mechanism is thought to be the change of weld pool surface tension temperature coefficient, thus, the change of fluid flow pattern in weld pool due to the flux.

Effects of surface physicochemical properties on NH_3-SCR activity of MnO_2 catalysts with different crystal structures

α‐,β‐,δ‐,andγ‐MnO2nanocrystals are successfully prepared.We then evaluated the NH3selective catalytic reduction(SCR)performance of the MnO2catalysts with different phases.The NOx conversion efficiency decreased in the order:γ‐MnO2>α‐MnO2>δ‐MnO2>β‐MnO2.The NOx conversion with the use ofγ‐MnO2andα‐MnO2catalysts reached90%in the temperature range of140–200°C,while that based onβ‐MnO2reached only40%at200°C.Theγ‐MnO2andα‐MnO2nanowire crystal morphologies enabled good dispersion of the catalysts and resulted in a relatively high specific surface area.We found thatγ‐MnO2andα‐MnO2possessed stronger reducing abilities and more and stronger acidic sites than the other catalysts.In addition,more chemisorbed oxygen existed on the surface of theγ‐MnO2andα‐MnO2catalysts.Theγ‐MnO2andα‐MnO2catalysts showed excellent performance in the low‐temperature SCR of NO to N2with NH3.

Highly reversible lead-carbon battery anode with lead grafting on thecarbon surface

A novel C/Pb composite has been successfully prepared by electmless plating to reduce the hydrogenevolution and achieve the high reversibility of the anode of lead-carbon battery （LCB）. The depositedlead on the surface of C/Pb composite was found to be uniform and adherent to carbon surface. Becauselead has been stuck on the surface of C/Pb composite, the embedded structure suppresses the hydrogenevolution of lead-carbon anode and strengthens the connection between carbon additive and sponge lead.Compared with the blank anode, the lead-carbon anode with C/Pb composite displays excellent charge-discharge reversibility, which is attributed to the good connection between carbon additives and leadthat has been stuck on the surface of C/Pb composite during the preparation process. The addition of CIPb composite maintains a solid anode structure with high specific surface area and power volume, andthereby, it plays a significant role in the highly reversible lead-carbon anode.

Preparation and modification of activated carbon for benzene adsorption by steam activation in the presence of KOH

A series of activated carbons from Taixi anthracite were prepared by steam activation in the presence of KOH and then they were modified by different methods. The regulation of porosity and the modification of surface chemistry were carried out with the aim to improve the benzene adsorption capacity of activated carbon. The influences of KOH and activation process parameters including activation temperature, activation time and steam flow rate on porosity of activated carbon were evaluated, and the effect of modification methods on surface chemistry was investigated. Also, the relationship between benzene adsorption capacity and porosity and surface chemistry was analyzed. Results show that activation temperature is the dominant factor in the activation process; the introduction of KOH into the raw material can enhance the reactivity of char in activation process, meanwhile it shows a negative effect on the porosity development, especially on the mesopore development. Results of FTIR analysis indicate that anthracite-based activated carbon with condensed aromatics and chemically inert oxygen does not present the nature to be surface modified. Besides, benzene adsorption capacity has an approximate linear relationship with surface area and in our preparation, benzene adsorption capacity and surface area of activated carbon are up to 1210 m 2 /g and 423 mg/g, respectively.

Novel Zwitterionic Surfactants: Synthesis and Surface Active Properties of N-(3-Alkoxy-2-Hydroxypropyl)-N, N-Dimethyl glycine Betaines

Five new zwitterionic surfactants with long chain alkyl betaine structure incorporated with hydroxylpropyl group have been synthesized. Their structures were identified by elemental analysis, IR (HNMR)-H-1, and (CNMR)-C-13. Surface tension experiments showed that these surfactants have higher surface activity than those without hydroxypropyl group. The values of CMC and gamma(CMC) of these surfactants have been determined.

Effect of Anion Surface Active Agent on the Preparation of SrTiO_3 Nano-Crystals

SrTiO_3 nano-crystal samples with floccule or flake crystal morphology,which were indexed as a perovskite-type crystal structure based on the results of XRD and TEM,were successfully prepared by one-step liquid reaction method.And the growth mechanism of the SrTiO_3 nano-crystals under the liquid condition with/without adding the surface active agent was investigated.It was found that adding the surface active agent contributes to the processing in which the ions gathering bodies transit to a more stable phase through the chemical reaction and form the flake SrTiO_3 nano-crystals.

Effects of surface chemical properties of activated coke on selective catalytic reduction of NO with NH_3 over commercial coal-based activated coke

Surface chemical properties of typical commercial coal-based activated cokes were characterized by Xray photoelectron spectroscopy(XPS) and acid-base titration, and then the influence of surface chemical properties on catalytic performance of activated cokes of NO reduction with NH3 was investigated in a fixed-bed quartz micro reactor at 150 ℃. The results indicate that the selective catalytic reduction(SCR) activity of activated cokes with the increase of its surface acidic sites and oxygen content,obviously, a correlation between catalytic activity and surface acidic sites content by titration has higher linearity than catalytic activity and surface oxygen content by XPS. While basic sites content by acid-base titration have not correlation with SCR activity. It has been proposed that surface basic sites content measured by titration may not be on adjacent of acidic surface oxides and then cannot form of NO2-like species, thus the reaction of reduction of NO with NH3 have been retarded.

Magnetic Properties and Surface Activity Sites of Pt-Dy/γ-Al_2O_3 Catalysts

The magnetism and surface behaviour of Pt-Dy/γ-Al_2O_3 catalysts were studied respectively by means of a Faraday magnetic balance and the method of carbon disulfide.The ferromagnetic impurity in the support,γ-Al_2O_3,at low temperature was corrected for the first time.The magnetic susceptibilities of the cat- alysts follow the sequence in different stage of preparation:χ_(uncalcined)<χ_(calcined)<χ_(reduced). The magnetic susceptibilities of the catalysts decrease as they adsorb hydrogen,cyclohexane or benzene. There is a correlation between the aromatization yield of cyclohexane or heptane on these catalysts and the magnetic susceptibility of the catalysts.Since addition of Dy increases the number of adsorption sites and the relevant proportions of weak adsorption sites,the abilities of sulfur-resistance and cyclohexane dehydrogenation are improved.In Pt-Dy/γ-A:_2O_3 catalysts,Dy improves the aromatization activity and stability of the catalyst and plays the role of the electron promoter.

Investigation into the surface active groups of coal

The oxidation heat of coal is the direct reason leading to coal spontaneous combustion. When coal is exposed in oxygen atmosphere, the physical adsorption and chemisorption happened, and then which resulting chemical reaction followed heat between coal and oxygen. Owing to the complexity and uncertain of molecular structure of coal,it was only reduced that bridge bonds, side chains and O 2 containing functional groups in coal may be prone to oxidation in last year, but not to deeply investigate into the structures and the type of the active radicals. In this paper, according to the last achievements in coal structure research, the hypomethylether bond, hypoalkyl bond of α carbon atom with hydroxyl and α carbon atom with hypomethy side chain and hypomethyl bonds linking up two aromatic hydrocarbon in bridge bonds, and methoxy,aldehyde and alkyls of α carbon atom with hydroxy in side bonds are inferred to be free radical easily to lead to oxidize coal under the ambient temperature and pressure. The order from strong to weak of oxide activation of the seven surface active groups is aldehyde side chains, hypomethylether bonds, hypoalkyl bonds of α carbon atom with hydroxyl, hypoalkyl bonds of α carbon atom with hypomethyl, hypomethyl bonds linking up two aromatic hydrocarbon,methoxy, alkyls side chains of α carbon atom with hydroxyl. Because of the two unsaturated molecular tracks of O 2, unpaired electron clouds of the part of surface active groups of coal enter molecular tracks of O 2 to lead to chemisorb on the conjugate effect and induced effect of surface active groups, and then chemical reaction followed heat happens in them. On the basis of change of bond energy, weighted average method is adopted to count the reaction heat value of each mol CO,CO 2 and H 2O. The property of coal spontaneous combustion is different for the different number and oxidability of the active structure in the coal resulting in the different oxidation heat.

Imposing Active Sources during High-Frequency Passive Surface-Wave Measurement

Passive surface-wave utilization has been intensively studied as a means of compensating for the short-age of low-frequency information in active surface-wave measurement, In general, passive surface-wave methods cannot provide phase velocities up to several tens of hertz; thus, active surface-wave methods are often required in order to increase the frequency range, To reduce the amount of field work, we pro-pose a strategy for a high-frequency passive surface-wave survey that imposes active sources during con-tinuous passive surface-wave observation; we call our strategy ＂mixed-source surface-wave （MSW） measurement,＂ Short-duration （within 10 min） passive surface waves and mixed-source surface waves were recorded at three sites with different noise levels： namely, inside a school, along a road, and along a railway, Spectral analysis indicates that the high-frequency energy is improved by imposing active sources during continuous passive surface-wave observation, The spatial autocorrelation （SPAC） method and the multichannel analysis of passive surface waves （MAPS） method based on cross-correlations were performed on the recorded time sequences, The results demonstrate the flexibility and applicability of the proposed method for high-frequency phase velocity analysis, We suggest that it will be constructive to perform MSW measurement in a seismic investigation, rather than exclusively performing either active surface-wave measurement or passive surface-wave measurement,

STUDIES ON THE SURFACE MODIFICATION OF ANHYDRITE

The lack of the early phase gelation property has limited the application of anhydrite as building material products. The use of additives, however, activates the anhydrite surfaces and results in the occurrence of early phase gelation. Under different surface modification conditions,the solubility of anhydrite in water has been measured and it has indicated a correlation between the anhydrite surface activity and its solubility in water. This relationship can be utilized to further study the anhydrite surface activation.

Preparation and Unimolecular-Micellization Behavior of Homopolymer of Surface-Active Monomer AMC14AB

（2-acrylamido） ethyl tetradecyl dimethylammonium bromide （AMC14AB） was polymerized in aqueous solu- tion to form the homopolymer P（AMC14AB）. The physicochemical properties of P（AMC14AB） in aqueous solution were mainly studied with fluorescent probe method, surface tension measurement and conductom- etry. The experimental results show that the aggregation morphology of P（AMC14AB） in aqueous solution is unimolecular micelle as expected. Being different from conventional multimolecular micelle systems, the unimolecular micelle system of P（AMC14AB） not only shows critical micellar concentration （CMC=0）, （i.e. once added to pure water, the surface tension decreases immediately in spite how small the density is）, but also the surface tension stays almost the same with the concentration increasing. That is to say, there is no mutational point on the relationship curve between surface tension and concentration. Furthermore, the unimolecular micelle system of P（AMC14AB） has no Krafft temperature, i.e. at any temperature, so long as it is dissolved in water, the unimolecular micelles will form. Besides this, for the solubilization of hydrophobic organic substances, the unimolecular micelle system of P（AMC14AB） is obviously different from the common multimolecular micelle system, having no turning point on the relationship curve between toluene solubi- lizaion amount and P（AMC14AB） concentration, and the solubilizing ability of the unimolecular-micelle system of P（AMC14AB） for hydrophobic organic substances is much higher than that of the conventional multimolecular micelle solutions of common surfactants, such as centyl trimethyl ammonium bromide.

Surface activity of cancer cells:The fusion of two cell aggregates

A key feature that distinguishes cancer cells from all other cells is their capability to spread throughout the body.Although how cancer cells collectively migrate by following molecular rules which influence the state of cell-cell adhesion contacts has been comprehensively formulated,the impact of physical interactions on cell spreading remains less understood.Cumulative effects of physical interactions exist as the interplay between various physical parameters such as(1)tissue surface tension,(2)viscoelasticity caused by collective cell migration,and(3)solid stress accumulated in the cell aggregate core region.This review aims to point out the role of these physical parameters in cancer cell spreading by considering and comparing the rearrangement of various mono-cultured cancer and epithelial model systems such as the fusion of two cell aggregates.While epithelial cells undergo volumetric cell rearrangement driven by the tissue surface tension,which directs cell movement from the surface to the core region of two-aggregate systems,cancer cells rather perform surface cell rearrangement.Cancer cells migrate toward the surface of the two-aggregate system driven by the solid stress while the surface tension is significantly reduced.The solid stress,accumulated in the core region of the two-aggregate system,is capable of suppressing the movement of epithelial cells that can undergo the jamming state transition;however,this stress enhances the movement of cancer cells.We have focused here on the multi-scale rheological modeling approaches that aimed at reproducing and understanding these biological systems.

SYNIHESIS AND SURFACE ACTIVE PROPERTIES OF OXYETHYLENATED FATTY ALCOHOL 2-HYDROXYPROPYL SULFONATES

Synthesis and surface active properties of the oxyethylenated fatty alcohol 2-hydroxypropyl sulfonates were investigated.Of all surface active compounds studied,those with a 2-hydroxypropyl (HP) moiety in the molecule are more surface-active than the corresponding compounds without it.

Synthesis and Properties of Novel Surface Active Maleic Monomer Containing Phosphate Group

A novel surface active monomer （surfmer） containing poly（ethylene glycol） chain and terminated phosphate group was synthesized. The copolymerization of synthesized surfmer with NVP （N-vinylpyrrolidone） and with NVP and VEP （5-tert-butylperoxy-5-methyl-2-hexene-3-yne monomer） led to formation of corresponding surface-active copolymers. The capability of application of resulted copolymers as surface active macroinitiators of emulsion polymerization of styrene and as components of polymeric scaffolds was investigated.