Journal articles on the topic 'Surface free energy'

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1

Chibowski, Emil. "Apparent Surface Free Energy of Superhydrophobic Surfaces." Journal of Adhesion Science and Technology 25, no. 12 (January 2011): 1323–36. http://dx.doi.org/10.1163/016942411x555890.

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2

Ip, S. W., and J. M. Toguri. "The equivalency of surface tension, surface energy and surface free energy." Journal of Materials Science 29, no. 3 (February 1994): 688–92. http://dx.doi.org/10.1007/bf00445980.

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3

CHAUDHURY, M. K., and G. M. WHITESIDES. "Correlation Between Surface Free Energy and Surface Constitution." Science 255, no. 5049 (March 6, 1992): 1230–32. http://dx.doi.org/10.1126/science.255.5049.1230.

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4

Bachurová, Marcela, and Jakub Wiener. "Free Energy Balance of Polyamide, Polyester and Polypropylene Surfaces." Journal of Engineered Fibers and Fabrics 7, no. 4 (December 2012): 155892501200700. http://dx.doi.org/10.1177/155892501200700411.

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The wettability of a solid surface is often characterized by the contact angle of liquid on the solid surface. The wettability is pertinent to surface energy, which is an important parameter. The wettability can be affected, for example, by the roughness of the solid surface. In our work textiles are used as macroscopic roughness surfaces, and smooth plate surfaces are used as well to determine surface energies. For the calculation of surface energies it is fundamental to know the contact angle. The advancing and receding contact angles are measured, and the relation between the hysteresis and surface energy is monitored.
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5

Dourado, F., F. M. Gama, E. Chibowski, and M. Mota. "Characterization of cellulose surface free energy." Journal of Adhesion Science and Technology 12, no. 10 (January 1998): 1081–90. http://dx.doi.org/10.1163/156856198x00740.

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6

Scala, A., F. W. Starr, E. La Nave, H. E. Stanley, and F. Sciortino. "Free energy surface of supercooled water." Physical Review E 62, no. 6 (December 1, 2000): 8016–20. http://dx.doi.org/10.1103/physreve.62.8016.

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7

JANCZUK, BRONISLAW, and TOMASZ BIALOPIOTROWICZ. "Free surface energy of some polymers." Polimery 32, no. 07/08 (July 1987): 269–71. http://dx.doi.org/10.14314/polimery.1987.269.

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8

Gruebele, Martin. "Protein folding: the free energy surface." Current Opinion in Structural Biology 12, no. 2 (April 2002): 161–68. http://dx.doi.org/10.1016/s0959-440x(02)00304-4.

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9

Della Volpe, C., D. Maniglio, M. Brugnara, S. Siboni, and M. Morra. "The solid surface free energy calculation." Journal of Colloid and Interface Science 271, no. 2 (March 2004): 434–53. http://dx.doi.org/10.1016/j.jcis.2003.09.049.

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10

Siboni, S., C. Della Volpe, D. Maniglio, and M. Brugnara. "The solid surface free energy calculation." Journal of Colloid and Interface Science 271, no. 2 (March 2004): 454–72. http://dx.doi.org/10.1016/j.jcis.2003.09.050.

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11

Luangtana-Anan, M., and J. T. Fell. "Surface free energy determinations on powders." Powder Technology 52, no. 3 (October 1987): 215–18. http://dx.doi.org/10.1016/0032-5910(87)80107-9.

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12

Terpilowski, Konrad, Lucyna Holysz, and Emil Chibowski. "Surface free energy of sulfur—Revisited." Journal of Colloid and Interface Science 319, no. 2 (March 2008): 514–19. http://dx.doi.org/10.1016/j.jcis.2007.10.054.

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13

Chibowski, Emil, and Konrad Terpilowski. "Surface free energy of sulfur—Revisited." Journal of Colloid and Interface Science 319, no. 2 (March 2008): 505–13. http://dx.doi.org/10.1016/j.jcis.2007.10.059.

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14

Jańczuk, B., A. Zdziennicka, K. Jurkiewicz, and W. Wócik. "The surface free energy and free energy of adsorption of cetyltrimethylammonium bromide." Tenside Surfactants Detergents 35, no. 3 (May 1, 1998): 213–17. http://dx.doi.org/10.1515/tsd-1998-350315.

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15

Cantin, S., M. Bouteau, F. Benhabib, and F. Perrot. "Surface free energy evaluation of well-ordered Langmuir–Blodgett surfaces." Colloids and Surfaces A: Physicochemical and Engineering Aspects 276, no. 1-3 (March 2006): 107–15. http://dx.doi.org/10.1016/j.colsurfa.2005.10.025.

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16

Altay, Bilge Nazli, Ruoxi Ma, Paul D. Fleming, Michael J. Joyce, Adarsh Anand, Ting Chen, Bekir Keskin, et al. "Surface Free Energy Estimation: A New Methodology for Solid Surfaces." Advanced Materials Interfaces 7, no. 6 (January 24, 2020): 1901570. http://dx.doi.org/10.1002/admi.201901570.

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17

Ban, B. S., and Y. B. Kim. "Surface free energy and pretilt angle on rubbed polyimide surfaces." Journal of Applied Polymer Science 74, no. 2 (October 10, 1999): 267–71. http://dx.doi.org/10.1002/(sici)1097-4628(19991010)74:2<267::aid-app5>3.0.co;2-#.

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18

RUDAWSKA, ANNA, and STANISLAW ZAJCHOWSKI. "Surface free energy of polymer/wood composites." Polimery 52, no. 06 (June 2007): 453–55. http://dx.doi.org/10.14314/polimery.2007.453.

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19

Domińczuk, Jacek, and Anna Krawczuk. "Comparison of Surface Free Energy Calculation Methods." Applied Mechanics and Materials 791 (September 2015): 259–65. http://dx.doi.org/10.4028/www.scientific.net/amm.791.259.

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The paper presents the main methods of surface free energy calculation of solids based on the contact angle measurement. The basic of splitting the surface free energy into components as well as interactions at the solid-liquid boundary phase considered while developing calculation models were presented. Basing on test results of surface free energy of 0H18N9T stainless steel, the relation between the method of surface preparation and the surface free energy were shown. The analysis focuses on change of the polar part. Differences between methods were indicated and it was pointed that skipping the polar component in analysis of adhesive joints strength results in deterioration of prediction model.
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20

Álvarez Lugo, Allex E., and Silvia Caro Spinel. "Determining surface free energy for Colombian asphalts." Ingeniería e Investigación 29, no. 2 (May 1, 2009): 20–24. http://dx.doi.org/10.15446/ing.investig.v29n2.15156.

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The surface free energy (SFE) of a material is defined as being the energy required in vacuum to create a new surface unit. This property is directly related to a material’s fracture resistance and healing properties and to its capacity for creating strong bonds with other materials. The quality of the adhesion between asphalt binders and aggregates can also be assessed by computing these materials’ work of adhesion. This value can be used as an additional parameter for selecting and appropriately combining materials for hot mix asphalt as well as a component of micromechanical models for fracture and healing within these mixtures. This paper describes in detail a technique used for measuring the SFE of asphalts based on the Wilhelmy plate method and reports the first SFE measurements available for asphalts produced in the Colombian refineries of Barrancabermeja and Apiay. Corresponding results, along with the SFE for different aggregates, were used for analysing differences in the work of adhesion for different asphalt-aggregate combinations in dry conditions. Barrancabermeja asphalt produced the highest work of adhesion amongst the materials analysed here. The results also suggested that the effect of specific mineral filler on asphalt SFE is asphalt-dependent; such effect does not necessarily lead to increasing the SFE for the corresponding asphalt-mineral filler system.
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21

Eaton, Dean, Ivan Saika-Voivod, Richard K. Bowles, and Peter H. Poole. "Free energy surface of two-step nucleation." Journal of Chemical Physics 154, no. 23 (June 21, 2021): 234507. http://dx.doi.org/10.1063/5.0055877.

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22

Chibowski, Emil. "Determination of Surface Free Energy of Kaolinite." Clays and Clay Minerals 36, no. 5 (1988): 455–61. http://dx.doi.org/10.1346/ccmn.1988.0360511.

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23

Wu, Di. "The puckering free-energy surface of proline." AIP Advances 3, no. 3 (March 2013): 032141. http://dx.doi.org/10.1063/1.4799082.

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24

Heyraud, J. C., and J. J. Métois. "Surface free energy anisotropy measurement of indium." Surface Science Letters 177, no. 1 (November 1986): A596. http://dx.doi.org/10.1016/0167-2584(86)91085-6.

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25

Fllho, Fernando Costa e. Silva, Elvira Maria Breier Saraiva, Marcos André vannier Santos, and Wanderley de Souza. "The surface free energy ofLeishmania mexicana amazonensis." Cell Biophysics 17, no. 2 (October 1990): 137–51. http://dx.doi.org/10.1007/bf02990493.

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26

Pereni, C. I., Q. Zhao, Y. Liu, and E. Abel. "Surface free energy effect on bacterial retention." Colloids and Surfaces B: Biointerfaces 48, no. 2 (March 2006): 143–47. http://dx.doi.org/10.1016/j.colsurfb.2006.02.004.

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27

Rebbi, Claudio, and Jean Potvin. "The surface free energy in coexisting phases." Nuclear Physics B - Proceedings Supplements 9 (June 1989): 541–45. http://dx.doi.org/10.1016/0920-5632(89)90159-x.

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28

Heyraud, J. C., and J. J. Métois. "Surface free energy anisotropy measurement of indium." Surface Science 177, no. 1 (November 1986): 213–20. http://dx.doi.org/10.1016/0039-6028(86)90268-2.

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29

Tartaglino, U., D. Passerone, E. Tosatti, and F. Di Tolla. "Bent surface free energy differences from simulation." Surface Science 482-485 (June 2001): 1331–36. http://dx.doi.org/10.1016/s0039-6028(01)00709-9.

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30

Chibowski, E., and L. Holysz. "Surface Free Energy and Floatability of Minerals." Materials Science Forum 25-26 (January 1988): 521–24. http://dx.doi.org/10.4028/www.scientific.net/msf.25-26.521.

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31

McHale, Glen. "Surface free energy and microarray deposition technology." Analyst 132, no. 3 (2007): 192. http://dx.doi.org/10.1039/b617339j.

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32

Jańczuk, B., W. Wójcik, A. Zdziennicka, and F. González-Caballero. "Components of surface free energy of galena." Journal of Materials Science 27, no. 23 (May 20, 1992): 6447–51. http://dx.doi.org/10.1007/bf00576297.

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33

Kornblit, L., and A. Ignatiev. "The surface free energy of crystalline solids." Physica A: Statistical Mechanics and its Applications 141, no. 2-3 (March 1987): 466–74. http://dx.doi.org/10.1016/0378-4371(87)90175-0.

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34

Blank, Martin. "Protein Aggregation Reactions: Surface Free Energy Model." Journal of Theoretical Biology 169, no. 4 (August 1994): 323–26. http://dx.doi.org/10.1006/jtbi.1994.1154.

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35

Savvova, Oksana, Galina Shadrina, Olena Babich, and Оleksiy Fesenko. "Investigation of Surface Free Energy of the Glass Ceramic Coatings on Titanium for Medical Purposes." Chemistry & Chemical Technology 9, no. 3 (September 15, 2015): 349–54. http://dx.doi.org/10.23939/chcht09.03.349.

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36

Meng, Fan, and Noriyoshi Arai. "The Relationship between Nanostructured Bio-Inspired Material Surfaces and the Free Energy Barrier Using Coarse-Grained Molecular Dynamics." Biomimetics 8, no. 6 (September 25, 2023): 453. http://dx.doi.org/10.3390/biomimetics8060453.

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Bio-inspired (biomimetic) materials, which are inspired by living organisms, offer exciting opportunities for the development of advanced functionalities. Among them, bio-inspired superhydrophobic surfaces have attracted considerable interest due to their potential applications in self-cleaning surfaces and reducing fluid resistance. Although the mechanism of superhydrophobicity is understood to be the free energy barrier between the Cassie and Wenzel states, the solid-surface technology to control the free energy barrier is still unclear. Therefore, previous studies have fabricated solid surfaces with desired properties through trial and error by measuring contact angles. In contrast, our study directly evaluates the free energy barrier using molecular simulations and attempts to relate it to solid-surface parameters. Through a series of simulations, we explore the behavior of water droplets on surfaces with varying values of surface pillar spacing and surface pillar height. The results show that the free energy barrier increases significantly as the pillar spacing decreases and/or as the pillar height increases. Our study goes beyond traditional approaches by exploring the relationship between free energy barriers, surface parameters, and hydrophobicity, providing a more direct and quantified method to evaluate surface hydrophobicity. This knowledge contributes significantly to material design by providing valuable insights into the relationship between surface parameters, free energy barriers, and hydrophilicity/hydrophobicity.
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37

YIN, Zhen-Xing, Hui KONG, Hai-Chuan WANG, Jun ZHANG, Zhi-You LIAO, and Yuan LI. "Discussion on the Surface Tension and the Surface Free Energy." University Chemistry 31, no. 9 (2016): 77–82. http://dx.doi.org/10.3866/pku.dxhx201512011.

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38

Jańczuk, Bronisław, and Anna Zdziennicka. "Importance of surface layers in solid surface free energy determination." Surface Innovations 2, no. 3 (September 2014): 173–83. http://dx.doi.org/10.1680/si.13.00024.

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39

Demianenko, E. M., M. I. Terets, S. V. Zhuravskyi, Yu I. Sementsov, V. V. Lobanov, V. S. Kuts, A. G. Grebenyuk, and M. T. Kartel. "Theoretical simulation of the interaction of Fe2 cluster with A N, B, Si-containing carbon graphene-like plane." SURFACE 14(29) (December 30, 2022): 37–48. http://dx.doi.org/10.15407/surface.2022.14.037.

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Metal composites modified with various heteroatoms, such as N, B, Si, are used to obtain matrix composites with specified parameters with the strongest adhesive-cohesive bonds between metal atoms and a carbon nanoparticle. Such carbon nanoparticles functionalized with heteroatoms are promising for many metal composites. One of the interesting and promising metals as a matrix for such research work is iron. To predict the specifics of the interaction of iron with the surface of carbon nanomaterials supplemented with heteroatoms of different chemical structure, it is advisable to model such processes using quantum chemistry methods. The aim of the work was to find out the effect of temperature on the chemical interaction of iron clusters with native, boron-, silicon-, and nitrogen-containing graphene-like planes (GLP). The results of the calculations show that the highest value of the energy effect of the chemical interaction for the native graphene-like plane is +204.3 kJ/mol, in the case of calculations both by the B3LYP/6-31G(d,p) method and by the MP2/6-31G(d, p) (+370.7 kJ/mol). The lower value of the energy effect is found in the presence of nitrogen atoms in the composition of the graphene-like plane. This value is even lower for the interaction of iron dimers with a silicon-containing carbon nanocluster. The lowest values of the energy effect, calculated by both methods, are characteristic of the boron-containing graphene-like plane. In particular, for the B3LYP/6-31G(d,p) method, the value of the energy effect of the reaction is ‑210.5 kJ/mol, and for the MP2/6-31G(d,p) method this value is +16.6 kJ/mol. The presence of boron atoms in the composition of the nanocarbon matrix best contributes to the interaction with the iron nanocluster, regardless of the chosen research method. The dependence curves of the Gibbs free energy of the interaction of iron dimers with a graphene-like plane and its derivatives in all cases qualitatively correlate with similar energy effects. In addition, in all cases, the values of the Gibbs free energy increase with increasing temperature.
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40

Ansarifar, A., G. W. Critchlow, R. Guo, R. J. Ellis, Y. Haile-Meskel, and B. Doyle. "Assessing Effect of the Migration of A Paraffin Wax on the Surface Free Energy of Natural Rubber." Rubber Chemistry and Technology 82, no. 1 (March 1, 2009): 113–20. http://dx.doi.org/10.5254/1.3557001.

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Abstract The effect of the migration of paraffin wax on the surface free energy of natural rubber (NR) was investigated. The rubber was mixed with the wax and then stored at ambient temperature for up to 168 hrs before its surface free energy was measured using contact angle measurement. Static secondary ion mass spectrometry was also used to provide a chemical fingerprint of the rubber surfaces. The surface free energy decreased as a function of storage time because of the migration of the wax to the rubber surface. The highest rate of reduction was recorded up to 3 hrs and thereafter, the surface free energy decreased at a much slower rate, reaching a plateau after 48 hrs in storage. In total, the surface free energy reduced by approximately 46% as a result of the migration of the wax to the rubber surface. The reduction in surface free energy could adversely affect ability of the rubber to stick to itself and to other dissimilar elastomers.
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41

Fleurat-Lessard, Paul, and Tom Ziegler. "Tracing the minimum-energy path on the free-energy surface." Journal of Chemical Physics 123, no. 8 (August 22, 2005): 084101. http://dx.doi.org/10.1063/1.1948367.

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42

Ibrahim, Tarek, Farouk Hachem, Mohamad Ramadan, Jalal Faraj, Georges El Achkar, and Mahmoud Khaled. "Cooling PV panels by free and forced convections: Experiments and comparative study." AIMS Energy 11, no. 5 (2023): 774–94. http://dx.doi.org/10.3934/energy.2023038.

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<abstract> <p>This work concerns a comparative experimental study of cooling PV panels by free and forced convection and using finned plates. To this end, four prototypes are considered: the first one with a PV panel alone without cooling techniques, the second one consists of a PV panel with a rectangular finned plate attached to its rear surface and cooled by free convection, a third prototype consists of a PV panel cooled by forced convection by three axial-flow fans and a fourth prototype consists of a PV panel with a rectangular finned plate attached to its rear surface and cooled by forced convection by three axial-flow fans. Results showed an increase of 3.01% in the efficiency of the PV panel with finned plate under forced convection, an increase of 2.55% in the efficiency of the PV panel with finned plate under free convection and an increase of 2.10% in the efficiency of the PV panel under forced convection. Economic and environmental studies are also conducted and estimations of savings per year and amount of carbon dioxide emission reductions are provided.</p> </abstract>
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43

Sarkar, Pramit, and Balasubramanian Kandasubramanian. "Fluorine-free superhydrophobic characterized coatings: A mini review." Maritime Technology and Research 3, no. 4 (July 23, 2021): 365–76. http://dx.doi.org/10.33175/mtr.2021.251814.

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The scientific fraternity and coating companies have researched and developed coatings with superhydrophobic features for a wide range of applications, varying from automotive, oceanic, pharmaceutical, and thermal and power sectors, over the preceding few years. The self-cleaning features of superhydrophobic surfaces exhibit pronounced dust repelling and lower dust adhesiveness qualities, along with incomparable water repellence for maritime, automotive, and pharmaceutical applications. The advancement of super-hydrophobic surfaces for averting the accrual of impurities on surfaces is an active space of exploration globally. A lesser hysteresis of contact angle leads to drops of water sliding effortlessly on such surfaces. The solid surfaces’ surface energy can be weakened by fixing materials of lesser surface energy on the exterior, which can be performed by the following dual methods; either by fixing materials of reduced surface energy straight onto the exterior of a substrate in the form of a coating of that material, or by fixing materials of less surface energy on the exterior of nano-architectural structures and then dropping the coating of those nanoscale materials on the exterior of the substrate. The generation of nanoscale irregularities on substrates by dropping nanostructure layers on surfaces makes it an attractive option since, usually, nanomaterials have a minimum of one dimension, ranging from 1 - 100 nm. The nanostructures’ sizes unveil exceptional physical and chemical characteristics, principally owing to their greater specific surface area to volume quotient. This review encompasses the non-fluorinated superhydrophobic coatings developed to date.
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44

Krzywicka, Monika, Jolanta Szymańska, Szymon Tofil, Anna Malm, and Agnieszka Grzegorczyk. "Surface Properties of Ti6Al7Nb Alloy: Surface Free Energy and Bacteria Adhesion." Journal of Functional Biomaterials 13, no. 1 (March 7, 2022): 26. http://dx.doi.org/10.3390/jfb13010026.

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The laser micro-machining was carried out on a station equipped with a TruMicro 5325c laser emitting ultraviolet radiation (343 nm wavelength) in picosecond pulses. On the surface of the Ti6Al7Nb alloy, dimple texturing with a constant diameter of ~200 μm, different depths (from ~5 to ~78 μm) and density (from 10% to 50%) were produced. The value of surface free energy was determined with the Owens–Wendt method using two measuring liquids: distilled water and diodomethane. The Staphylococcus epidermidis strain was used to test the adhesion of bacteria. It was found that the surface free energy value is influenced by both of the texture parameters (density, depth). The density also affects the potential for biofilm formation. Based on the analysis, it was shown that with an increase in surface free energy, the number of adhering microorganisms increases exponentially. Moreover, the study shows that there is a correlation between the number of adhering microorganisms and surface free energy.
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45

ARIMA, Yusuke, Koichi KATO, and Katsuhiko NAKAMAE. "Slipperiness of Water Droplets on Polymer Surfaces : Effects of Surface Morphology and Surface Free Energy." Journal of the Japan Society of Colour Material 73, no. 10 (2000): 485–88. http://dx.doi.org/10.4011/shikizai1937.73.485.

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46

Wei, Yu, and Nobuo Maeda. "Critical Surface Tension and Specific Surface Free Energy of Clathrate Hydrate." Energy & Fuels 36, no. 1 (December 23, 2021): 407–14. http://dx.doi.org/10.1021/acs.energyfuels.1c03795.

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47

Hillert, M., and J. Ågren. "Effect of surface free energy and surface stress on phase equilibria." Acta Materialia 50, no. 9 (May 2002): 2429–41. http://dx.doi.org/10.1016/s1359-6454(02)00074-5.

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48

Attal, Jean-Pierre, Erik Asmussen, and Michel Degrange. "Effects of surface treatment on the free surface energy of dentin." Dental Materials 10, no. 4 (July 1994): 259–64. http://dx.doi.org/10.1016/0109-5641(94)90071-x.

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49

Park, Soo-Jin, and Marcel Brendle. "London Dispersive Component of the Surface Free Energy and Surface Enthalpy." Journal of Colloid and Interface Science 188, no. 2 (April 1997): 336–39. http://dx.doi.org/10.1006/jcis.1997.4763.

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50

Rojewska, M., A. Bartkowiak, B. Strzemiecka, A. Jamrozik, A. Voelkel, and K. Prochaska. "Surface properties and surface free energy of cellulosic etc mucoadhesive polymers." Carbohydrate Polymers 171 (September 2017): 152–62. http://dx.doi.org/10.1016/j.carbpol.2017.05.019.

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