Effect of pH and Molecular Length on the Structure and Dynamics of Short Poly(acrylic acid) in Dilute Solution: Detailed Molecular Dynamics Study

被引:51
作者
Mintis, Dimitris G. [1 ,2 ]
Mavrantzas, Vlasis G. [1 ,2 ,3 ]
机构
[1] Univ Patras, Dept Chem Engn, GR-26504 Patras, Greece
[2] FORTH ICE HT, GR-26504 Patras, Greece
[3] Swiss Fed Inst Technol, Dept Mech & Proc Engn, Particle Technol Lab, CH-8092 Zurich, Switzerland
关键词
POLYION COMPLEX VESICLES; DERIVING ATOMIC CHARGES; FORCE-FIELD; POLYACRYLIC-ACID; PHASE-BEHAVIOR; POLY(DIALLYLDIMETHYLAMMONIUM CHLORIDE); EFFICIENT GENERATION; AQUEOUS-SOLUTION; HYALURONIC-ACID; AM1-BCC MODEL;
D O I
10.1021/acs.jpcb.9b01696
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Long MD simulations are carried out using a detailed all-atom force field to investigate the effect of pH or, equivalently, degree of ionization alpha(-) (= 0, 50, 100%) and degree of polymerization N (= 20, 23, 46, 70, and 110) on the structure and dynamics of poly(acrylic acid) (PAA) at infinite dilution. To ensure the validity and add to the reliability of our research conclusions, a systematic validation of several molecular mechanics force fields is performed. It is observed that the generalized AMBER force field in combination with the RESP charge fitting method best describes both the structural and dynamical behavior of PAA in comparison to experimentally obtained data. It is found that < R-g(2)>(0.5) changes with N as < R(2)g > similar to N-nu, with nu = 0.27 at alpha(-) = 0% degree of ionization (acidic conditions), nu = 0.94 at alpha(-) = 50% degree of ionization (neutral conditions), and nu = 0.87 at alpha(-) = 100% degree of ionization (basic conditions), which is in perfect agreement with theory. The global shape of the PAA chain in the solution is quantified in terms of the three eigenvalues of the average radius-of-gyration tensor, the relative shape anisotropy kappa(2), and the asphericity parameter b. It is revealed that at alpha(-) = 0%, the chain adopts a spherelike conformation, while at alpha(-) = 50 and 100%, its conformation is flattened and flexible. In addition, it is revealed that as the degree of ionization increases, the persistence length L-p increases, which suggests that PAA chains become stiffer with increasing pH. The global and local conformational changes of the PAA chain with the degree of ionization are found to be highly related to the solvation of the polymer. Finally, it is revealed that the diffusion coefficient D of the center of mass of PAA also exhibits a power law scaling with N, D similar to N-nu, with nu = 0.25 at alpha(-) = 0% degree of ionization, nu = 0.46 at alpha(-) = 50% degree of ionization (neutral conditions), and nu = 0.44 at alpha(-) = 100% degree of ionization (basic conditions), in excellent agreement with recent experimental data and theoretical predictions.
引用
收藏
页码:4204 / 4219
页数:16
相关论文
共 115 条
  • [1] Gromacs: High performance molecular simulations through multi-level parallelism from laptops to supercomputers
    Abraham, Mark James
    Murtola, Teemu
    Schulz, Roland
    Páll, Szilárd
    Smith, Jeremy C.
    Hess, Berk
    Lindah, Erik
    [J]. SoftwareX, 2015, 1-2 : 19 - 25
  • [2] Nutrient removal and sludge production in the coagulation-flocculation process
    Aguilar, MI
    Sáez, J
    Lloréns, M
    Soler, A
    Ortuño, JF
    [J]. WATER RESEARCH, 2002, 36 (11) : 2910 - 2919
  • [3] Study of the multilayer assembly and complex formation of poly(diallyldimethylammonium chloride) (PDADMAC) and poly(acrylic acid) (PAA) as a function of pH
    Alonso, T.
    Irigoyen, J.
    Iturri, J. J.
    Larena, I. L.
    Moya, S. E.
    [J]. SOFT MATTER, 2013, 9 (06) : 1920 - 1928
  • [4] [Anonymous], 2017, COMPUTER SIMULATION
  • [5] Spontaneous Formation of Nanosized Unilamellar Polyion Complex Vesicles with Tunable Size and Properties
    Anraku, Yasutaka
    Kishimura, Akihiro
    Oba, Makoto
    Yamasaki, Yuichi
    Kataoka, Kazunori
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (05) : 1631 - 1636
  • [6] Gyration tensor based analysis of the shapes of polymer chains in an attractive spherical cage
    Arkin, Handan
    Janke, Wolfhard
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2013, 138 (05)
  • [7] Atkins P., 2011, PHYS CHEM LIFE SCI
  • [8] Hydrogen-bond dynamics near a micellar surface: Origin of the universal slow relaxation at complex aqueous interfaces
    Balasubramanian, S
    Pal, S
    Bagchi, B
    [J]. PHYSICAL REVIEW LETTERS, 2002, 89 (11) : 1 - 115505
  • [9] A WELL-BEHAVED ELECTROSTATIC POTENTIAL BASED METHOD USING CHARGE RESTRAINTS FOR DERIVING ATOMIC CHARGES - THE RESP MODEL
    BAYLY, CI
    CIEPLAK, P
    CORNELL, WD
    KOLLMAN, PA
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (40) : 10269 - 10280
  • [10] Berendsen HJC, 1981, INTERMOLECULAR FORCE, P331, DOI DOI 10.1007/978-94-015-7658-1_21