A Comparative Study of Features of Sorption of N-Buthylxanthate and Dibuthyldixanthogen Onto Metallic Supports and Rutile Using in situ Atomic Force Spectroscopy

被引:1
作者
Karacharov, Anton A. [1 ]
Likhatski, Maxim N. [1 ]
机构
[1] FRC Krasnoyarsk Sci Ctr SB RAS, Inst Chem & Chem Technol SB RAS, 50-24 Akademgorodok, Krasnoyarsk 660036, Russia
来源
JOURNAL OF SIBERIAN FEDERAL UNIVERSITY-CHEMISTRY | 2019年 / 12卷 / 03期
关键词
nanobubbles; surface; hydrophobic; sorption; potassium buthylxanthate; dibuthyldixanthogen; atomic force spectroscopy; contact angle; HYDROPHOBIC SURFACES; ISOELECTRIC POINTS; RANGE ATTRACTION; MICROSCOPE; ADSORPTION; ADHESION; BUBBLES; GAS;
D O I
10.17516/1998-2836-0131
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An interaction of potassium buthylxanthate and of dibuthyldixanthogen with metallic Ti, stainless steel and alpha-TiO2 surfaces was studied. Contact angle measurements by sessile drop technique showed that the treatment of initial substrate surfaces with potassium buthylxanthate aqueous solution or with dibuthyldixanthogen emulsion render them more hydrophobic. Using in situ atomic force spectroscopy, the sorption of surface active substances was shown to give rise to an increase in both adhesive force magnitude and the range within it acts at the approach of cantilever tip to the surface of both hydrophobic and hydrophilic samples. The maximum of both adhesive force and their range, up to 150 nm, took place in case of retract of cantilever tip from sample surface. Force curves are steeper, which related with the formation of nanobubbles on the surfaces of samples under study arising the long-range hydrophobic force of capillary origin. Dibuthyldixanthogen exhibited highly-active reagent properties inducing the formation of nanoscale gas structures on both hydrophobic and, in less extent, hydrophilic surfaces.
引用
收藏
页码:336 / 346
页数:11
相关论文
共 29 条
[1]   A History of Nanobubbles [J].
Alheshibri, Muidh ;
Qian, Jing ;
Jehannin, Marie ;
Craig, Vincent S. J. .
LANGMUIR, 2016, 32 (43) :11086-11100
[2]   Bridging bubbles between hydrophobic surfaces [J].
Attard, P .
LANGMUIR, 1996, 12 (06) :1693-1695
[3]   LONG-RANGE ATTRACTION BETWEEN HYDROPHOBIC SURFACES [J].
ATTARD, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (17) :6441-6444
[4]  
CHANTURIYA VA, 1993, ELECTROCHEMISTRY SUL
[5]   CAVITATION AND THE INTERACTION BETWEEN MACROSCOPIC HYDROPHOBIC SURFACES [J].
CHRISTENSON, HK ;
CLAESSON, PM .
SCIENCE, 1988, 239 (4838) :390-392
[6]   INTERACTIONS BETWEEN WATER-STABLE HYDROPHOBIC LANGMUIR-BLODGETT MONOLAYERS ON MICA [J].
CLAESSON, PM ;
BLOM, CE ;
HERDER, PC ;
NINHAM, BW .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1986, 114 (01) :234-242
[7]   Direct measurement of hydrophobic forces: A study of dissolved gas, approach rate, and neutron irradiation [J].
Craig, VSJ ;
Ninham, BW ;
Pashley, RM .
LANGMUIR, 1999, 15 (04) :1562-1569
[8]   A PHENOMENOLOGICAL THEORY OF LONG-RANGE HYDROPHOBIC ATTRACTION FORCES BASED ON A SQUARE-GRADIENT VARIATIONAL APPROACH [J].
ERIKSSON, JC ;
LJUNGGREN, S ;
CLAESSON, PM .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1989, 85 :163-176
[9]   CALIBRATION OF ATOMIC-FORCE MICROSCOPE TIPS [J].
HUTTER, JL ;
BECHHOEFER, J .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1993, 64 (07) :1868-1873
[10]   Nano bubbles on a hydrophobic surface in water observed by tapping-mode atomic force microscopy [J].
Ishida, N ;
Inoue, T ;
Miyahara, M ;
Higashitani, K .
LANGMUIR, 2000, 16 (16) :6377-6380