Gels | Special Issue : Physicochemical and Mechanical Properties of Polymer Gels

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14 pages, 662 KiB

Open AccessArticle

Molecular Simulation and Theoretical Analysis of Slide-Ring Gels under Biaxial Deformation

by Kotaro Tanahashi and Tsuyoshi Koga

Gels 2021, 7(3), 129; https://doi.org/10.3390/gels7030129 - 29 Aug 2021

Cited by 2 | Viewed by 2598

Abstract

Slide-ring (SR) gels, a new type of gels that have cross-links moving along the chains, are known to have unique mechanical characteristics. In the case of biaxial deformations, it has been experimentally shown that the stress–strain (S–S) relationships of SR gels can be [...] Read more.

Slide-ring (SR) gels, a new type of gels that have cross-links moving along the chains, are known to have unique mechanical characteristics. In the case of biaxial deformations, it has been experimentally shown that the stress–strain (S–S) relationships of SR gels can be well described by the neo-Hookean (NH) model. This behavior is quite different from that of conventional chemical gels, where the S–S curves deviate from the NH model. To understand the molecular mechanism of such peculiar elastic properties of SR gels, we studied the effects of movable cross-links by using molecular simulations and theoretical analysis. We calculate the S–S relationships in biaxial deformation for two types of models: slip model, where the cross-links can slide along chains representing SR gels, and non-slip model, which corresponds to conventional chemical gels. In the theoretical analysis, we calculate the S–S relationships by using the models with the Gaussian and the Langevin chains to investigate the nonlinear stretching effect of the chain in the slip and non-slip models. As a result, we found that the peculiar elastic behaviors of SR gels in biaxial deformations are well explained by the effect of movable cross-links suppressing the nonlinear stretching of the chain. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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7 pages, 1478 KiB

Open AccessArticle

Competition between Osmotic Squeezing versus Friction-Driven Swelling of Gels

by Miyu Seii, Tomoki Harano, Masao Doi and Yoshimi Tanaka

Gels 2021, 7(3), 94; https://doi.org/10.3390/gels7030094 - 14 Jul 2021

Viewed by 2022

Abstract

Some types of hydro-gels have almost the same equilibrium swelling volume in water and in ethylene glycol (EG), a highly viscous liquid completely miscible with water. Experiments showed that when a gel fully swollen with EG is immersed into a large amount of [...] Read more.

Some types of hydro-gels have almost the same equilibrium swelling volume in water and in ethylene glycol (EG), a highly viscous liquid completely miscible with water. Experiments showed that when a gel fully swollen with EG is immersed into a large amount of water, it temporarily swells up and then relaxes to the equilibrium volume in water. The temporary swelling is explained by the friction force exerted on the gel network from the outward EG flux In this paper, we experimentally show that the temporary swelling is suppressed by adding linear PEG (polyethylene glycol) in the outer water. Although the suppression seems to be explained by the osmotic pressure (i.e., by the same mechanism as the conventional osmotic squeezing), our theoretical analysis reveals that the effect of PEG is much stronger than that expected from the equilibrium osmotic pressure, implying that the PEG chains are condensed on the gel surface. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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12 pages, 2879 KiB

Open AccessArticle

Linear Dynamic Viscoelasticity of Dual Cross-Link Poly(Vinyl Alcohol) Hydrogel with Determined Borate Ion Concentration

by Takuro Taniguchi and Kenji Urayama

Gels 2021, 7(2), 71; https://doi.org/10.3390/gels7020071 - 14 Jun 2021

Cited by 2 | Viewed by 2962

Abstract

We investigated the linear dynamic viscoelasticity of dual cross-link (DC) poly(vinyl alcohol) (PVA) (DC-PVA) hydrogels with permanent and transient cross-links. The concentrations of incorporated borate ions to form transient cross-links in the DC-PVA hydrogels (C_B^IN) were determined by the [...] Read more.

We investigated the linear dynamic viscoelasticity of dual cross-link (DC) poly(vinyl alcohol) (PVA) (DC-PVA) hydrogels with permanent and transient cross-links. The concentrations of incorporated borate ions to form transient cross-links in the DC-PVA hydrogels (C_B^IN) were determined by the azomethine-H method. The dynamic viscoelasticity of the DC-PVA hydrogel cannot be described by a simple sum of the dynamic viscoelasticity of the PVA gel with the same permanent cross-link concentration and the PVA aqueous solution with the same borate ion concentration (C_B = C_B^IN) as in the DC-PVA gel. The DC-PVA hydrogel exhibited a considerably higher relaxation strength, indicating that the introduction of permanent cross-links into temporary networks increases the number of viscoelastic chains with finite relaxation times. In contrast, the relaxation frequency (ω_c) (given by the frequency at the maximum of loss modulus) for the DC-PVA hydrogel was slightly lower but comparable to that for a dilute PVA solution with the same C_B. This signifies that the relaxation dynamics of the DC-PVA hydrogels is essentially governed by the lifetime of an interchain transient cross-link (di-diol complex of boron). The effect of permanent cross-linking on the relaxation dynamics was observed in the finite broadening of the relaxation-time distribution in the long time region. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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10 pages, 20593 KiB

Open AccessArticle

Flowability of Gel-Matrix and Magnetorheological Response for Carrageenan Magnetic Hydrogels

by Junko Ikeda, Tomoki Kurihara, Keiju Ogura, Shota Akama, Mika Kawai and Tetsu Mitsumata

Gels 2021, 7(2), 56; https://doi.org/10.3390/gels7020056 - 6 May 2021

Cited by 5 | Viewed by 2312

Abstract

The relationship between rheological features in the absence of a magnetic field and magnetic response was investigated for κ-carrageenan magnetic hydrogels containing carbonyl iron particles. The concentration of carrageenan was varied from 1.0 to 5.0 wt%, while the concentration of carbonyl iron was [...] Read more.

The relationship between rheological features in the absence of a magnetic field and magnetic response was investigated for κ-carrageenan magnetic hydrogels containing carbonyl iron particles. The concentration of carrageenan was varied from 1.0 to 5.0 wt%, while the concentration of carbonyl iron was kept at 70 wt%. The magnetic response revealed that the change in storage modulus ΔG′ decreased inversely proportional to the carrageenan concentration. A characteristic strain γ₁ where G′ equals to G″ was seen in a strain range of 10⁻³. It was found that ΔG′ was inversely proportional to the characteristic stress at γ₁. Another characteristic strain γ₂ where the loss tangent significantly increased was also analyzed. Similar to the behavior of γ₁, ΔG′ was inversely proportional to γ₂. The characteristic stresses at γ₁ and γ₂ were distributed at 80–720 Pa and 40–310 Pa, respectively. It was revealed that a giant magnetorheology higher than 1 MPa can be observed when the characteristic stresses at γ₁ and γ₂ are below approximately 240 Pa and 110 Pa, respectively. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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14 pages, 3500 KiB

Open AccessEditor’s ChoiceArticle

Experimental Verification of the Balance between Elastic Pressure and Ionic Osmotic Pressure of Highly Swollen Charged Gels

by Tasuku Nakajima, Ken-ichi Hoshino, Honglei Guo, Takayuki Kurokawa and Jian Ping Gong

Gels 2021, 7(2), 39; https://doi.org/10.3390/gels7020039 - 1 Apr 2021

Cited by 10 | Viewed by 4809

Abstract

The equilibrium swelling degree of a highly swollen charged gel has been thought to be determined by the balance between its elastic pressure and ionic osmotic pressure. However, the full experimental verification of this balance has not previously been conducted. In this study, [...] Read more.

The equilibrium swelling degree of a highly swollen charged gel has been thought to be determined by the balance between its elastic pressure and ionic osmotic pressure. However, the full experimental verification of this balance has not previously been conducted. In this study, we verified the balance between the elastic pressure and ionic osmotic pressure of charged gels using purely experimental methods. We used tetra-PEG gels created using the molecular stent method (St-tetra-PEG gels) as the highly swollen charged gels to precisely and separately control their network structure and charge density. The elastic pressure of the gels was measured through the indentation test, whereas the ionic osmotic pressure was determined by electric potential measurement without any strong assumptions or fittings. We confirmed that the two experimentally determined pressures of the St-tetra-PEG gels were well balanced at their swelling equilibrium, suggesting the validity of the aforementioned relationship. Furthermore, from single-strand level analysis, we investigated the structural requirements of the highly swollen charged gels in which the elasticity and ionic osmosis are balanced at their swelling equilibrium. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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14 pages, 4222 KiB

Open AccessArticle

Effect of Nonlinear Elasticity on the Swelling Behaviors of Highly Swollen Polyelectrolyte Gels

by Jian Tang, Takuya Katashima, Xiang Li, Yoshiro Mitsukami, Yuki Yokoyama, Ung-il Chung, Mitsuhiro Shibayama and Takamasa Sakai

Gels 2021, 7(1), 25; https://doi.org/10.3390/gels7010025 - 1 Mar 2021

Cited by 8 | Viewed by 3499

Abstract

Polyelectrolyte gels exhibit swelling behaviors that are dependent on the external environment. The swelling behaviors of highly charged polyelectrolyte gels can be well explained using the Flory–Rehner model combined with the Gibbs–Donnan effect and Manning’s counterion condensation effect (the FRGDM model). This study [...] Read more.

Polyelectrolyte gels exhibit swelling behaviors that are dependent on the external environment. The swelling behaviors of highly charged polyelectrolyte gels can be well explained using the Flory–Rehner model combined with the Gibbs–Donnan effect and Manning’s counterion condensation effect (the FRGDM model). This study investigated the swelling properties of a series of model polyelectrolyte gels, namely tetra-polyacrylic acid-polyethylene glycol gels (Tetra-PAA-PEG gels), and determined the applicability of the FRGDM model. The swelling ratio (V_s/V₀) was well reproduced by the FRGDM model in the moderate swelling regime (V_s/V₀ < 10). However, in the high swelling regime (V_s/V₀ > 10), the FRGDM model is approx. 1.6 times larger than the experimental results. When we introduced the finite extensibility to the elastic free energy in the FRGDM model, the swelling behavior was successfully reproduced even in the high swelling regime. Our results reveal that finite extensibility is one of the factors determining the swelling equilibrium of highly charged polyelectrolyte gels. The modified FRGDM model reproduces well the swelling behavior of a wide range of polyelectrolyte gels. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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10 pages, 29132 KiB

Open AccessArticle

Fast and Large Shrinking of Thermoresponsive Hydrogels with Phase-Separated Structures

by Taehun Chung, Im Kyung Han, Jihoon Han, Kyojin Ahn and Youn Soo Kim

Gels 2021, 7(1), 18; https://doi.org/10.3390/gels7010018 - 16 Feb 2021

Cited by 12 | Viewed by 4750

Abstract

Thermoresponsive poly(N-isopropylacrylamide) (PNIPAAm) hydrogels have been attracting attention in a variety of functional materials, such as biomaterials, because they exhibit a volume phase transition phenomenon near physiological temperatures. However, the slow kinetics and small volume shrinkage of bulk PNIPAAm hydrogels upon [...] Read more.

Thermoresponsive poly(N-isopropylacrylamide) (PNIPAAm) hydrogels have been attracting attention in a variety of functional materials, such as biomaterials, because they exhibit a volume phase transition phenomenon near physiological temperatures. However, the slow kinetics and small volume shrinkage of bulk PNIPAAm hydrogels upon heating greatly limit their practical application. Here, we report PNIPAAm hydrogels with phase-separated structures that exhibited ultrafast shrinking upon heating. The phase separation into a PNIPAAm-rich phase and a water-rich phase was formed through aqueous polymerization in the presence of NaClO₄ salt. Through structural analysis of the hydrogels, a topologically heterogeneous and porous structure was observed, which was highly dependent on the NaClO₄ concentration in the polymerization step. Compared to conventional PNIPAAm hydrogels, the phase-separated hydrogels exhibited much faster and larger shrinkage upon heating. Simultaneously, the hydrogels quickly released a large amount of water owing to the effective water channels inside them. The present method can be widely applied to general hydrogels, and it can address the numerous limitations of hydrogels in terms of operating programmability and deformation efficiency. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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26 pages, 7966 KiB

Open AccessArticle

One-Shot Preparation of Polybasic Ternary Hybrid Cryogels Consisting of Halloysite Nanotubes and Tertiary Amine Functional Groups: An Efficient and Convenient Way by Freezing-Induced Gelation

by Nur Sena Okten Besli and Nermin Orakdogen

Gels 2021, 7(1), 16; https://doi.org/10.3390/gels7010016 - 5 Feb 2021

Cited by 3 | Viewed by 2687

Abstract

A convenient method for the preparation of polybasic ternary hybrid cryogels consisting of Halloysite nanotubes (HNTs) and tertiary amine functional groups by freezing-induced gelation is proposed. Ternary hybrid gels were produced via one-shot radical terpolymerization of 2-hydroxyethyl methacrylate (HEMA), 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS), [...] Read more.

A convenient method for the preparation of polybasic ternary hybrid cryogels consisting of Halloysite nanotubes (HNTs) and tertiary amine functional groups by freezing-induced gelation is proposed. Ternary hybrid gels were produced via one-shot radical terpolymerization of 2-hydroxyethyl methacrylate (HEMA), 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS), and DEAEMA in the presence of HNTs. The equilibrium swelling in various swelling media and the mechanical properties of the produced ternary hybrid gels were analyzed to investigate their network structure and determine their final performance. The swelling ratio of HNT-free gels was significantly higher than the ternary hybrid gels composed of high amount of HNTs. The addition of HNTs to terpolymer network did not suppress pH- and temperature-sensitive behavior. While DEAEMA groups were effective for pH-sensitive swelling, it was determined that both HEMA and DEAEMA groups were effective in temperature-sensitive swelling. Ternary hybrid gels simultaneously demonstrated both negative and positive temperature-responsive swelling behavior. The swelling ratio changed considerably according to swelling temperature. Both DEAEMA and HEMA monomers in terpolymer structure were dominant in temperature-sensitive swelling. Mechanical tests in compression of both as-prepared and swollen-state demonstrated that strength and modulus of hybrid cryogels significantly increased with addition of HNTs without significant loss of mechanical strength. Ultimately, the results of the current system can benefit characterization with analysis tools for the application of innovative materials. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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17 pages, 8308 KiB

Open AccessReview

Softness, Elasticity, and Toughness of Polymer Networks with Slide-Ring Cross-Links

by Koichi Mayumi, Chang Liu, Yusuke Yasuda and Kohzo Ito

Gels 2021, 7(3), 91; https://doi.org/10.3390/gels7030091 - 13 Jul 2021

Cited by 32 | Viewed by 6168

Abstract

Slide-ring (SR) gels cross-linked by ring molecules are characterized by softness (low Young’s modulus), elasticity (low hysteresis loss), and toughness (large fracture energy). In this article, the mechanical and fracture properties of SR gels are reviewed to clarify the physical understanding of the [...] Read more.

Slide-ring (SR) gels cross-linked by ring molecules are characterized by softness (low Young’s modulus), elasticity (low hysteresis loss), and toughness (large fracture energy). In this article, the mechanical and fracture properties of SR gels are reviewed to clarify the physical understanding of the relationship between the molecular-level sliding dynamics of the slide-ring cross-links and macroscopic properties of SR gels. The low Young’s modulus and large fracture energy of SR gels are expressed by simple equations as a function of the degree of sliding movement. The dynamic fracture behaviors of SR gels gives us the time scale of the sliding dynamics of the cross-links, which is at the micro-sec scale. The fast sliding motion of the cross-links leads to the elasticity of the SR gels. The SR concept can be applied to solvent-free elastomers and composite materials. Full article

(This article belongs to the Special Issue Physicochemical and Mechanical Properties of Polymer Gels)

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