Abstract
Random copolymers of diallyldimethylammonium chloride (DADMAC) and carboxybetaine 2-(diallyl(methyl)ammonio) acetate (DAMA) with different compositions (10%/90%), (50%/50%) and (70%/30%), as well as poly(DAMA) and poly(DADMAC) homopolymers, were synthesized. Molecular characteristics of poly(DADMAC–co–DAMA) copolymers and homopolymers were determined in water solutions in the presence of 0.1 M NaOH and a low molecular weight salt (NaCl in various concentrations) by viscometery, dynamic and static light scattering. Dependences of several important conformational parameters, such as swelling coefficient α, the Huggins constant kH, and the second virial coefficient A2, on copolymer composition (charge asymmetry) and NaCl concentration in solution were analyzed. It was shown that growth of charge asymmetry leads to sharp increase in copolymer size.
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Introduction
In recent years, сationic polyelectrolyte poly(diallyldimethylammonium chloride) (poly (DADMAC)) has attracted increasing interest of researchers due to its unique chemical structure and a variety of current and possible applications [1,2,3,4,5]. The processes that allow for commercial production of poly(DADMAC) have been developed. The materials based on this polymer show high thermal stability and can function even under extreme environmental conditions [6, 7]. Polycarboxybetaine poly(2-(diallyl(methyl)ammonio)acetate (poly(DAMA)) is similar to poly(DADMAC) in chemical structure of the main chain. DAMA monomer contains a carboxylic group bonded to nitrogen through a methylene group. Carboxylic groups are ionizable in neutral and alkaline media, which allows obtaining negative charge within a single monomer unit, together with positive charge. Copolymerization of DADMAC with DAMA provides an opportunity to combine properties of polyelectrolyte (poly(DADAMAC)) and polybetaine (poly(DAMA)) in one macromolecule, and to control the effect of environment on polymer properties by varying the ratio of monomer units. It should be noted that the copolymer almost completely retains useful properties of these two homopolymers (such as solubility and thermal stability [8,9,10]).
It is rather difficult to provide quantitative theoretical description of properties of multiply charged macromolecular systems; moreover, such theories give only qualitative predictions for limiting cases. Therefore, it is most convenient to study influence of composition and environmental conditions on the properties of such macromolecules by experimental methods used in polymer physics.
Recently, we have obtained random poly(DADMAC-co-DAMA) copolymers containing 28% of cationic units and 72% of betaine units [11]. After dissociation, DADMAC units acquired positive charges, while DAMA units carried both positive and negative charges. Molar masses and hydrodynamic properties of the synthesized copolymers were studied in alkaline media of different ionic strengths. It was established that at insignificant concentrations of low molecular weight salt, the copolymer exhibits properties typical of polyelectrolyte, while at higher salt concentrations, intrinsic viscosity of the polymer practically does not depend on salt concentration (which is characteristic of polybetaines). Hence, varying copolymer composition makes it possible to change behavior of macromolecules in solution in the presence of a low molecular weight salt. To gain the detailed insight into this process, it is necessary to study a series of copolymers over a wider composition range.
In the present work, samples of poly(DADMAC-co-DAMA) copolymers of different compositions (10%/90%, 50%/50%, and 70%/30%), as well as samples of DAMA and DADMAC homopolymers, were synthesized. Molar masses and hydrodynamic characteristics of the synthesized copolymers and homopolymers were studied in water, in the presence of 0.1 M NaOH and low molecular weight salt NaCl (at various concentrations) using dynamic (DLS) and static (SLS) light scattering as well as viscometry.
Experimental
Materials
Polymers of DADMAC [12] and DAMA [13], as well as their copolymers [11], were prepared according to the conventional procedure (see Fig. 1). The monomers were polymerized in aqueous solution (C = 4.0 M) after removal of oxygen; 4,4′-azobis-(4-cyanovaleric acid) was used as an initiator; the polymerization proceeded at 60 °C for 4 h. The product was precipitated into propanol-2, purified by dialysis against deionized water in Spectra/Por 1 membrane, concentrated in vacuum and isolated by lyophilization.
Table 1 presents the percentage values of components in the synthesized copolymers. The obtained samples were denoted by two letters (pe = polyelectrolyte; pb = polybetaine; co = copolymer). For copolymers this letters are followed by a number in brackets that represents the percentage of DADMAC (x) monomer units in copolymer.
Methods
Dynamic (DLS) and static (SLS) light scattering experiments were carried out using a “PhotoCor-Complex” apparatus (Photocor Instruments Inc., Moscow, Russia) equipped with a real-time correlator (288 channels, minimal τ = 10 ns). Laser (λ = 405 nm) was used as an excitation source; the experiments were carried out at scattering angles (ϑ) ranging from 30° to 140° at a temperature of 25 ± 0.1 °C. Autocorrelation functions of scattered light intensity G(2)(t) = 〈I(t0)I(t0 + t)〉/〈I(t0)〉2 were processed using DynaLS software. It provides distributions I(τ) of scattered light intensities by relaxation times τ in accordance with the relation: G(1)(t) = ∫ I(τ) e−t/τdτ, where G(1)(t) is related to G(2)(t) by Siegert relation G(2)(t) = B + β|G(1)(t)|2, here B is base line, and β is coherence factor.
The distributions I(τ) of scattered light intensities by relaxation times τ contain two main peaks (see Fig. 2b, e, h). The first one corresponds to the diffusion of individual macromolecules; the second peak may be attributed to the presence of some number of high molar mass species in solutions. The nature of this species may be related to the presence of cross-linked polymers, appeared during storage or isolation of polymer, due to radical oxidation. Mass fractions of the high molar mass species, were estimated using relations from [14,15,16,17]. They do not exceed 1–2%, this makes impossible an observation of this fraction by NMR and viscometry. It should be noted that the presence of the slow mode in polyelectrolyte solutions is a famous problem, it was discussed particularly in [18, 19].
The dependence between 1/τ (where τ is the maximum position of I(τ) distribution) and the scattering vector squared q2 = (4πn/λ sin(ϑ/2))2 for all studied samples was a straight line passing through the origin, this indicating diffusional character of the observed processes [20,21,22]. Translational diffusion coefficients D at fixed concentrations were calculated from the slope of this line according to the following relationship: 1/τ = Dq2. The diffusion coefficients D0 were determined by extrapolation of D(c) dependence to infinite dilution in accordance with equation: D(c) = D0(1 + c2A2M).
Hydrodynamic radius Rh was calculated using the Stokes – Einstein equation [23].
Weight-average molar masses MW of the studied samples were determined from the static light scattering data according to the following equation:
where \( H=4{\pi}^2{n}_0^2{\left(\partial n/\partial c\right)}^2/\left({\lambda}^4{N}_A\right) \), Rϑ is the Rayleigh relationship, A2 is the second virial coefficient, \( \frac{\partial n}{\partial c} \) is the refractive index increment, and NA is the Avogadro number [24]. Rayleigh relationship was calculated from the equation \( {R}_{\vartheta }={\left(\frac{n_0}{n_T}\right)}^2\frac{I_s\left(\vartheta \right)-{I}_0\left(\vartheta \right)}{I_T\left(\vartheta \right)}\left({R}_T\bullet {I}_p\left(\vartheta \right)\right) \), where Is(ϑ), I0(ϑ), IT(ϑ) are scattered light intensities of studied solution, solvent and toluene at fixed angle, RT is toluene Rayleigh ratio, nT is toluene refractive index, Ip(ϑ) is an area of the peak on I(τ) distribution which corresponds to individual macromolecules [14, 15, 18].
Refractive indices of the solutions and the solvents were determined using an RM-40 automatic refractometer (Mettler Toledo, Switzerland). The following values of refractive indices were obtained: n0 = 1.3335 for aqueous solution of 0.1 M NaOH; n0 = 1.3346 for (0.1 M NaOH +0.1 M NaCl) solution, and n0 = 1.3433 in the case of (0.1 M NaOH +1 M NaCl) solution.
Viscosities of the investigated samples were measured with the use of a Lovis 2000 M rolling-ball microviscometer (Anton Paar, Austria) at 25 °C; the capillary inclination angle was varied from 55° to 35° at 5° intervals. The obtained values of dynamic viscosity of a solution η were averaged over a series of angles and used in calculations of reduced viscosity (ηr = (η − η0)/(η0c)), where c is the concentration of a solution. After extrapolation of reduced viscosity to infinite dilution, intrinsic viscosity [η] of the polymer under study was determined using the relationship ηr = [η] + ckH[η]2 [24]; here, kH is the dimensionless Huggins constant [25]. The kH constant, which characterizes a polymer - solvent system, depends on solvent quality. In θ-solvents, it is close to 0.4–0.7; in good solvents, kH = 0.2 − 0.4 [26]. The following solvent viscosity values η0 were obtained: η0 = 0.92 cP for aqueous solution of 0.1 M NaOH; η0 = 0.93 cP for (0.1 M NaOH +0.1 M NaCl) solution, and η0 = 1.01 cP in the case of (0.1 M NaOH +1 M NaCl) solution.
Density measurements were performed using a DM40 densitometer (Mettler Toledo, Switzerland).
Results and discussion
Molecular properties of DADMAC-co-DAMA copolymers
Concentration dependences of reduced viscosity and translation diffusion coefficient of copolymers are presented in Fig. 3. For all solvents and samples, these dependences were approximated by straight lines. The values of translation diffusion coefficients D0 and intrinsic viscosities [η] of the studied samples were determined by extrapolation of the above dependences to infinite dilution.
The values of weight average molar mass MW and the second virial coefficients A2 of copolymers were determined by static light scattering in three solvents: 0.1 M NaOH, (0.1 M NaOH +0.1 M NaCl) and (0.1 M NaOH +1 M NaCl) (see Table 2 and Fig. 3d, e, f).
The concentration dependence of the difference between refractive indices of solutions and solvents for all samples was a linear relationship (Fig. 4). The value of refractive index increment \( \left(\frac{\partial n}{\partial c}\right) \) was equal to 0.18 сm3/g for all the studied polymer solutions. Molecular characteristics of the studied copolymers are presented in Table 2.
Degree of polymerization Z of the studied samples was determined from the Z = MW/M0 ratio, where M0 is the molar mass of a monomer unit. It was calculated using the following equation: M0 = M0DADMACx + M0DAMA(1 − x) . Here M0DAMA and M0DADMAC are the molar masses of the DAMA and DADMAC monomer units correspondingly.
The values of equilibrium rigidity A for the investigated copolymers were estimated from the relationship:
where ADADMAC is the Kuhn segment length of the DADMAC macromolecule, and ADAMA is the Kuhn segment length of the DAMA macromolecule [11,12,13]. The values of equilibrium rigidity A obtained from Eq. (3) were equal to 4 nm for sample co(10), 4.7 nm for co(50), and 5.2 nm for co(70). Taking into account the length of the projection of a monomer unit on the direction of maximum elongation λ (that is equal to 0.28 nm [12, 13, 27] for polymers with DADMAC backbone), we calculated the amount of the Kuhn segments per macromolecule \( N=\frac{Z\bullet \lambda }{A} \) (see Table 2).
It can be concluded that all the studied samples consist of more than 20 Kuhn segments, and, therefore, draining effects do not make a decisive contribution into hydrodynamic behavior of macromolecules [23]. Note that kH and A2 demonstrate dependence on molar mass, although the A2 and kH values depend very slightly on molar mass of a sample [24, 28, 29] at fixed salt concentrations.
Dependence of conformational properties on charge asymmetry of DADMAC-co-DAMA copolymers
It was shown in [11, 13] that the decisive contribution into conformational changes of the DAMA macromolecules and the DADAMC-co-DAMA copolymer with 28% DADMAC units was made by interactions between the units widely separated along the chain. This fact, as well as relatively high degrees of polymerization of the samples under study, makes it possible to use the Flory ratio:
where Φ∞ is the Flory constant, \( \left\langle {h}_0^2\right\rangle \) is the mean square vector connecting ends of a chain in ideal conditions, α is the macromolecule swelling ratio, which is equal to the ratio of the coil size 〈h2〉1/2 to the coil size in θ-solvent \( {\left\langle {h}_0^2\right\rangle}^{1/2} \).
Figure 5a shows the dependence of the [η]/[η]0.1M NaOH + 1M NaCl ratio on concentration of the used low molecular weight salt (NaCl). The decrease in viscosity with increase in ionic strength of a medium is characteristic of all samples, but this effect is most pronounced in the case of copolymer with the maximum number of DADMAC units. When ionic strength of the medium changes by an order of magnitude (from 1M/L to 0.1 M/L), viscosities of solutions of this copolymer do not vary significantly. Sample co(10) exhibits noticeable swelling only if salt concentration remains below 0.1 M/L. This behavior agrees with the results obtained in [9].
The dependence between [η] of a sample and NaCl concentration may be caused by changes in hydrodynamic sizes of the macromolecules. This assumption is confirmed by the data of dynamic light scattering (Table 2). In addition, the values of the second virial coefficient A2 for samples co(50) and co(70) in the absence of NaCl significantly exceed the corresponding values obtained in 0.1 M and 1 M NaCl (Table 2). For sample co(10), increase in the second virial coefficient at decreasing salt concentration is less pronounced. This is most likely related to the fact that DAMA betaine units (that exhibit anti-polyelectrolyte behavior) predominate in this macromolecule. Sample pb showed typical anti-polyelectrolyte behavior (swelling of polymer coils) with increasing ionic strength of the medium. This phenomenon results from screening opposite charges along the chain, and hindering attraction between them. It will be recalled that this phenomenon is characteristic of carbobetaines in neutral environments and the media with pH approaching the alkaline values (i.e., when carboxyl groups are deprotonated [13, 30]).
It should be noted that all samples were studied under the conditions where polyelectrolyte effects do not manifest themselves explicitly (i.e., concentration dependences of reduced viscosity demonstrate the common linear character). In this case, conformation characteristics of the studied samples can be described in terms of volume effects [23]. Figure 5d shows dependences of the second virial coefficient A2 on percentage of DADMAC units in a copolymer in 0.1 M NaOH and 0.1 M NaOH+1 M NaCl solutions. In the case of 0.1 M NaOH solution, increase in the fraction of DADMAC units in a copolymer leads to a sharp increase in its A2 values. This indicates an increase in thermodynamic quality of the solvent. In the presence of 1 M NaCl, dependence between the second virial coefficient and the fraction of DADMAC units in samples is practically absent, which indicates screening of electrostatic attraction in the solution.
For the majority of samples, it was found that the Huggins constant decreases with decreasing concentration of a low molecular weight salt (NaCl), which also indicates rise in thermodynamic quality of solvent with decrease in the ionic strength of the medium. An exception is the pb sample that demonstrates the opposite behavior. The Huggins constant for this polymer in the absence of NaCl has a maximum value of 0.43. This is due to the fact that attraction between units of the polybetaine chain in the absence of NaCl is manifested as a decrease in thermodynamic quality of the solvent. The experimentally obtained dependences qualitatively agree with the theoretical results for conformational properties of polyampholytes and polyzwitterions in dilute solutions described in [31, 32]. Figure 5c shows dependences of the Huggins constants kH measured in 0.1 M NaOH and (0.1 M NaOH +1 M NaCl) on contents of DADMAC units in copolymer. It was established that in 0.1 M NaOH, a decrease in kH occurred with increasing percentage of DADMAC units. The obtained range of kH values corresponds to the kH values estimated for uncharged polymers in a good solvent [26], and thermodynamic quality of the solvent increases with increase in the fraction of DADMAC units in copolymer. In (0.1 M NaOH +1 M NaCl) solution, the dependence of kH on DADMAC fraction (x) was not been observed; the kH value averaged over all studied samples was close to 0.4, which corresponds to the kH values observed in solutions of flexible chains in θ-solvents [26].
According to Eq. (4), the equality \( \left[\eta \right]/{\left[\eta \right]}_{0.1 NaOH+1 NaCl}={\alpha}^3/{\alpha}_{0.1 NaOH+1 NaCl}^3 \) is true. The values of Φ∞, M are mutually reduced. Suggesting that in 0.1 M NaOH + 1 M NaCl all the studied compounds (except for pb) have the lowest sizes and electrostatic interactions are screened, we can introduce the value of apparent swelling coefficient \( {\alpha}_{app}^3={\alpha}^3/{\alpha}_{0.1 NaOH+1 NaCl}^3 \).
Figure 5b shows dependence of the \( {\alpha}_{app}^5-{\alpha}_{app}^3 \) difference on charge asymmetry in the studied macromolecules, and the inset in this figure shows the theoretical dependence obtained in [32]
Here f and g are the fractions of positive and negative charges in the chain, respectively, c0 is the concentration of low molecular weight salt (NaCl) in solution, and lb is the Bjerrum length. When plotting theoretical dependences, calculation of the equilibrium stiffness A in this relationship was carried out according to Eq. (3).
Note that there is qualitative agreement between theoretical and experimental data presented in Fig. 5b. In the absence of NaCl in solution, as well as in the presence of 0.1 M NaCl, an increase in the fraction of electrolyte units in the copolymer ultimately leads to an increase in the (α5 − α3) value. However, it should also be emphasized that, according to the experimental data obtained, low charge asymmetry leads to noticeable changes in the \( {\alpha}_{app}^5-{\alpha}_{app}^3 \) value, which were not observed in the theoretical dependence.
The effect of distribution of positively or negatively charged monomers along the chain on properties of polyampholytes was theoretically studied in [33]. It was found that alternating polyampholytes demonstrate higher solubility in comparison to random copolymers of the similar composition. In our case, every negative charge on the polymer chain is always accompanied by a positive charge in the DAMA monomer unit, that is, we are dealing with a partially ordered polyampholyte. Theoretical dependence for the α5 − α3 value was obtained in [32] for random polyampholytes, and, therefore, it may not correctly describe the behavior of a partially ordered polyampholyte.
It was shown in [11] that poly(DADMAC-co-DAMA) samples obtained by radical copolymerization of a mixture of the corresponding monomers are random copolymers. Consequently, DAMA and DADMAC monomers are distributed randomly along the chain. However, this system is peculiar, since one unit of DAMA monomer contains two opposite charges. One of important properties of the resulting macromolecule is that each negative charge on the chain is adjacent to a positive one. That is, no local area of the chain contains the prevailing amount of negative charges. Copolymerization of DAMA and DADMAC monomers at different molar ratios results in copolymers where, depending on the x ratio, positively charged monomers predominate to varying degrees. It was shown in [34] that block co-polyampholytes are capable of forming intramolecular complexes between two oppositely charged “blocks” of a chain due to electrostatic forces, since in one fragment of this chain, positive charges prevail, and the other part contains mostly negative charges. In the case studied in the present work, this situation cannot be realized, and any change in charge asymmetry leads only to an increase in copolymer size.
Conclusions
Copolymerization of DADMAC with carboxybetaine monomer DAMA allows preparation of random copolymers whose properties can be controlled by varying the ratio of monomer units. Dependences of thermodynamic parameters of the solution, such as the second virial coefficient A2 and the Huggins constant kH, on charge asymmetry of the copolymer, were obtained. It was established that an increase in charge asymmetry leads to an increase in thermodynamic quality of solvent (in the salt-free system). With increasing salt concentration in the solution, this dependence becomes less pronounced. Degree of sensitivity of the copolymer to environmental conditions can be changed by varying the DADMAC fraction in the copolymer. Thus, it was shown that varying composition of the copolymer may allow for fine adjustment of response of the resulting compound to environmental changes.
References
Kudaibergenov S, Nuraje N, Kudaibergenov SE, Nuraje N (2018) Intra- and Interpolyelectrolyte complexes of Polyampholytes. Polymers 10:1146. https://doi.org/10.3390/polym10101146
Wandrey C, Hernández-Barajas J, Hunkeler D (1999) Diallyldimethylammonium chloride and its polymers. Adv Polym Sci 145:125–182
Laschewsky A (2012) Recent trends in the synthesis of polyelectrolytes. Curr Opin Colloid Interface Sci 17:56–63
Abdollahi M, Ziaee F, Alamdari P, Koolivand H (2013) A comprehensive study on the kinetics of aqueous free-radical homo- and copolymerization of acrylamide and diallyldimethylammonium chloride by online 1H-NMR spectroscopy. J Polym Res 20:239. https://doi.org/10.1007/s10965-013-0239-9
Ali SA, Haladu SA, El-Sharif AMZ (2016) Synthesis and application of a cyclopolymer bearing a propylphosphonic acid and a propylcarboxylic acid pendants in the same repeating unit. J Polym Res 23:167. https://doi.org/10.1007/s10965-016-1006-5
Liang SJ, Zhu SP (2013) Fabrication of polyelectrolyte/TiO2 hybrid membrane via a simple method and characterization of its thermal behavior. Adv Mater Res 602-604:1484–1487. https://doi.org/10.4028/www.scientific.net/AMR.602-604.1484
Francis S, Varshney L, Sabharwal S (2007) Thermal degradation behavior of radiation synthesized polydiallyldimethylammonium chloride. Eur Polym J 43:2525–2531. https://doi.org/10.1016/j.eurpolymj.2007.03.009
Tsvetkov NV, Lezov AA, Vlasov PS, Gubarev AS, Lezova AA, Lebedeva EV, Polushina GE, Domnina NS (2017) Macromolecules of polycarboxybetaine poly(4-N,N-diallyl-N-methylammonio) butanoate: synthesis and molecular characteristics. Polymer 122:34–44. https://doi.org/10.1016/j.polymer.2017.06.030
Jaeger W, Bohrisch J, Laschewsky A (2010) Synthetic polymers with quaternary nitrogen atoms—synthesis and structure of the most used type of cationic polyelectrolytes. Prog Polym Sci 35:511–577. https://doi.org/10.1016/j.progpolymsci.2010.01.002
Jin F, Hu J, Yang M, Jin X, He W, Han H (2006) Determination of diallyldimethylammonium chloride in drinking water by reversed-phase ion-pair chromatography–electrospray ionization mass spectrometry. J Chromatogr A 1101:222–225. https://doi.org/10.1016/j.chroma.2005.10.012
Tsvetkov NV, Lezov AA, Vlasov PS, Lezova AA, Samokhvalova SA, Lebedeva EV, Polushina GE (2016) Copolymers of diallyldimethylammonium chloride and 2-(diallyl(methyl) ammonio) acetate: effect of composition and ionic strength on conformational properties. Eur Polym J 84:268–278. https://doi.org/10.1016/j.eurpolymj.2016.09.026
Lezov AV, Polushina GE, Lezov AA, Vlasov PS, Domnina NS (2011) Molecular properties of the copolymers of N,N-diallyl-N,N-dimethylammonium chloride and maleic acid. Polymer Science - Series A 53:93–101
Lezov AV, Vlasov PS, Lezov AA, Domnina NS, Polushina GE (2011) Molecular properties of poly(carboxybetaine) in solutions with different ionic strengths and pH values. Polymer Science - Series A 53:1012–1018
Wu C, Siddiq M, Woo KF (1995) Laser light-scattering characterization of a polymer mixture made of individual linear chains and clusters. Macromolecules 28:4914–4919. https://doi.org/10.1021/ma00118a019
Shibayama M, Karino T, Okabe S (2006) Distribution analyses of multi-modal dynamic light scattering data. Polymer 47:6446–6456. https://doi.org/10.1016/j.polymer.2006.06.060
Filippov SK, Lezov AV, Sergeeva OY, Olifirenko AS, Lesnichin SB, Domnina NS, Komarova EA, Almgren M, Karlsson G, Štepanek P (2008) Aggregation of dextran hydrophobically modified by sterically-hindered phenols in aqueous solutions: aggregates vs. single molecules. Eur Polym J 44:3361–3369. https://doi.org/10.1016/j.eurpolymj.2008.07.041
Litmanovich EA, Ivleva EM (2010) The problem of bimodal distributions in dynamic light scattering: theory and experiment. Polym Sci Ser A 52:671–678. https://doi.org/10.1134/S0965545X10060143
Sedlák M (1996) The ionic strength dependence of the structure and dynamics of polyelectrolyte solutions as seen by light scattering: the slow mode dilemma. J Chem Phys 105:10123–10133. https://doi.org/10.1063/1.472841
Sedlák M (1997) Dynamic light scattering from binary mixtures of polyelectrolytes. I. Influence of mixing on the fast and slow polyelectrolyte mode behavior. J Chem Phys 107:10799–10804. https://doi.org/10.1063/1.474196
Berne BJ, Pecora R (1976) Dynamic light scattering, with application to chemistry, biology and physics. John Wiley & Sons, New York
Pike ER (1974) Photon correlation and light beating spectroscopy1st edn. Springer US, New York
Mondal MH (2017) Study of autocorrelation function of polymer and polymer–nanocomposite solutions using dynamic light scattering method. J Polym Res 24:218. https://doi.org/10.1007/s10965-017-1368-3
Tsvetkov VN (1989) Rigid-chain polymers: hydrodynamic and optical properties in solution. Consultants Bureau
Tsvetkov VN, Eskin VE (1971) Structure of macromolecules in solution. National Lending Library for Science and technology
Huggins ML (1942) The viscosity of dilute solutions of long-chain molecules. IV. Dependence on concentration. J Am Chem Soc 64:2716–2718. https://doi.org/10.1021/ja01263a056
Pamies R, Hernández Cifre JG, del Carmen López Martínez M, García de la Torre J (2008) Determination of intrinsic viscosities of macromolecules and nanoparticles. Comparison of single-point and dilution procedures. Colloid Polym Sci 286:1223–1231
Lezov AA, Vlasov PS, Polushina GE, Lezov AV (2012) Effect of chemical structure and charge distribution on behavior of polyzwitterions in solution. Macromol Symp 316:17–24. https://doi.org/10.1002/masy.201250603
Yashiro J, Hagino R, Sato S, Norisuye T (2006) Chain stiffness and excluded-volume effects in polyelectrolyte solutions: characterization of sodium poly(2-acrylamido-2-methylpropanesulfonate) in aqueous sodium chloride. Polym J 38:57–63. https://doi.org/10.1295/polymj.38.57
Fisher LW, Sochor AR, Tan JS (1977) Chain characteristics of poly(2-acrylamido-2-methylpropanesulfonate) polymers. 1. Light-scattering and intrinsic-viscosity studies. Macromolecules 10:949–954. https://doi.org/10.1021/ma60059a012
Ali SA, Aal-e-Ali (2001) Synthesis and solution properties of a quaternary ammonium polyelectrolyte and its corresponding polyampholyte. Polymer 42:7961–7970. https://doi.org/10.1016/S0032-3861(01)00289-0
Kumar R, Fredrickson GH (2009) Theory of polyzwitterion conformations. J Chem Phys 131:104901
Higgs PG, Joanny J-F (1991) Theory of polyampholyte solutions. J Chem Phys 94:1543–1554
Wittmer J, Johner A, Joanny JF (1993) Random and alternating polyampholytes. EPL 24:263–268. https://doi.org/10.1209/0295-5075/24/4/005
Patrickios CS, Hertler WR, Abbott NL, Hatton TA (1994) Diblock, ABC triblock, and random methacrylic polyampholytes: synthesis by group transfer polymerization and solution behavior. Macromolecules 27:930–937. https://doi.org/10.1021/ma00082a008
Acknowledgements
The reported study was funded by Russian Foundation for Basic Research (RFBR), according to the research project No. 16-33-60104 mol_a_dk. Authors are grateful to the Center for Diagnostics of Functional Materials for Medicine, Pharmacology, and Nanoelectronics (St Petersburg State University).
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Lezov, A.A., Lezova, A.A., Vlasov, P.S. et al. Cationic electrolyte copolymers of diallyldimethylammonium chloride with carboxybetaine 2-(diallyl(methyl) ammonio) acetate of various compositions in water solutions of different ionic strengths. J Polym Res 26, 97 (2019). https://doi.org/10.1007/s10965-019-1755-z
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DOI: https://doi.org/10.1007/s10965-019-1755-z