Equilibrium Swelling Research Articles

Preparation and properties of hydrogels loaded with phage endolysin Lys84

This study investigated the application of poly(N-isopropylacrylamide)-based interpenetrating network temperature-sensitive hydrogels (notation: IPNT) as the delivery vehicle for phage endolysin Lys84 and the potential of drug-loaded hydrogels as antimicrobial materials. Interpenetrating network temperature-sensitive hydrogels were prepared by free radical polymerization of sodium alginate and N-isopropylacrylamide. Drug-loaded hydrogels (IPNT-Lys84) were obtained by dry soaking method with the endolysin Lys84 of Staphylococcus aureus phage. The physical properties of the hydrogels with and without drug loading were characterized by infrared spectroscopy, scanning electron microscopy, and differential scanning calorimetry. The swelling and deswelling of the hydrogels as well as the release of endolysin Lys84 were investigated. Moreover, the antibacterial properties of IPNT-Lys84 hydrogels at different temperatures and concentrations of the drug solution were studied. The results showed that IPNT-Lys84 hydrogel had uniform pores and a low critical solubility temperature (LCST) of 32 ℃. The equilibrium swelling of the hydrogel was 30 g/g, and the water loss rate was 88% upon deswelling. The release rate of endolysin reached more than 70% within 6 h at 37 ℃. The bactericidal rate of IPNT-Lys84 hydrogel was over 99.9%. The research results showed the feasibility of using IPNT to deliver the endolysin Lys84, and IPNT-Lys84 hydrogel might be an effective antimicrobial material against multi-drug resistant Staphylococcus aureus.

Quince seed mucilage/β-cyclodextrin/Mmt-Na+-co-poly (methacrylate) based pH-sensitive polymeric carriers for controlled delivery of Capecitabine

In current work, quince seed mucilage and β-Cyclodextrin based pH regulated hydrogels were developed using aqueous free radical polymerization to sustain Capecitabine release patterns and to overcome its drawbacks, such as high dose frequency, short half-life, and low bioavailability. Developed networks were subjected to thermal analysis, Fourier transforms infrared spectroscopy, powder x-ray diffraction, elemental analysis, scanning electron microscopy, equilibrium swelling, and in-vitro release investigations to assess the network system's stability, complexation, morphology, and pH responsiveness. Thermally stable pH-responsive cross-linked networks were formed. Nanocomposite hydrogels were prepared by incorporating Capecitabine-containing clay into the swollen hydrogels. All the formulations exhibited equilibrium swelling ranging from 67.98 % to 92.98 % at pH 7.4. Optimum Capecitabine loading (88.17 %) was noted in the case of hydrogels, while it was 74.27 % in nanocomposite hydrogels. Excellent gel content (65.88 %–93.56 %) was noticed among developed formulations. Elemental analysis ensured the successful incorporation of Capecitabine.Nanocomposite hydrogels released 80.02 % longer than hydrogels after 30 h. NC hydrogels had higher t1/2 (10.57 h), AUC (121.52 μg.h/ml), and MRT (18.95 h) than hydrogels in oral pharmacokinetics. These findings imply that the pH-responsive carrier system may improve Capecitabine efficacy and reduce dosing frequency in cancer therapy. Toxicity profiling proved the system's safety, non-toxicity, and biocompatibility.

Synthesis of a polyacrylamide hydrogel modified with a reactive carbamate surfactant: Characterization, swelling behavior, and mathematical models

Hydrogels are polymeric materials that can absorb and retain large amounts of water. They have various applications in agriculture, horticulture, oil recovery, and water management. However, conventional hydrogels have limited swelling (Q), equilibrium swelling (Q∞), and water retention capacities (DQ) under different environmental conditions. In this study, we synthesized a series of hydrophobically associated hydrogels by the aqueous polymerization of acrylamide, acrylic acid, 2-acrylamide-2-methylpropanesulfonic acid, and a novel amphiphilic hydrophobic monomer (RCS-10). Further, we investigated the effects of the RCS-10 content on Q, the mechanical properties, and water retention capacity (DQ) of the hydrogels. We also examined the influence of temperature, pH, salt type and concentration, and urea concentration on Q, finding that an increase in the RCS-10 content decreased Q and increased the DQ of the hydrogels. The hydrogels exhibited high Q in distilled water, low-salt solutions, and low-urea (1 wt%) solutions. In the latter, the Q∞ was as high as 768.99 g/g. The hydrogels also showed excellent cyclic swelling performance and maintained high Q∞ (759.99 g/g) after six cycles. Crucially, the hydrophobic association hydrogels demonstrated superior swelling and water retention properties compared to conventional hydrogels. Thus, the hydrogels have applications in water management in various fields including agriculture and horticulture.

Tough, Stretchable, and Thermoresponsive Smart Hydrogels.

Self-healing, thermoresponsive hydrogels with a triple network (TN) were obtained by copolymerizing N-isopropyl acryl amide (NiPAAm) with polyvinyl alkohol (PVA) functionalized with methacrylic acid and N,N'-methylene bis(acryl amide) crosslinker in the presence of low amounts (<1 wt.%) of tannic acid (TA). The final gels were obtained by crystalizing the PVA in a freeze-thaw procedure. XRD, DCS, and SEM imaging indicate that the crystallinity is lower and the size of the PVA crystals is smaller at higher TA concentrations. A gel with 0.5 wt.% TA has an elongation at a break of 880% at a tension of 1.39 MPa. It has the best self-healing efficiency of 81% after cutting and losing the chemical network. Step-sweep strain experiments show that the gel has thixotropic properties, which are related to the TA/PVA part of the triple network. The low amount of TA leaves the gel with good thermal responsiveness (equilibrium swelling ratio of 13.3). Swelling-deswelling loop tests show enhanced dimensional robustness of the hydrogel, with a substantial constancy after two cycles.

Cross-Linking Characteristics, Morphology, Dynamics, and Mechanical and Thermal Properties of Polychloroprene/Polybutadiene/Nano-Zinc (CR/BR/nZn) Compositions with Reduced Fire Hazard.

The properties of unconventional blends of crystallizable and thermo-cross-linkable polychloroprene (CR) with polybutadiene (BR) were investigated in this study. The compositions were prepared using the method of reactive processing and cross-linking in the presence of nano-sized zinc (nZn). The purpose of the research was to assess the efficacy of nano-zinc as a curing agent of polychloroprene and polybutadiene (CR/BR) composites and to obtain rubber goods characterized by increased flame resistance. The blends were filled with nano-silica (aerosil) and fillers of natural origin (chalcedonite or silitin). The cross-linking process was characterized by determining the kinetics curves, the equilibrium swelling, and the Mooney-Rivlin elasticity constants. The morphology of the vulcanizate surface was specified by scanning electron microscopy (SEM). The dynamic and mechanical properties, flammability, and toxicity of gaseous substances involved in thermal decomposition were determined. Mass changes and thermal effects were studied using simultaneous thermal analysis (STA). It was confirmed that nano-zinc is an efficient curing agent for the polychloroprene and polybutadiene compositions, with a satisfactory degree of cross-linking (αc = 0.10, CRI = 4.11 min-1), good mechanical strength (TSb = 5 MPa), satisfactory tear resistance (Ts = 2.9 N/mm), and very high flame resistance (OI = 30%, HRRmax = 283 kW/m2). Filled products could be used as non-combustible materials, confirming the low fire hazard (1/tflashover = 3.5-6.4 kW/m2∙s). The most effective filler of the tested composites was nano-sized silica.

Improved Dual Network Model for Aging of Rubber Composites under Set Strains.

A new model is presented to predict rubber behavior during chemical aging at fixed strains. The model is validated using a carbon black-filled nitrile butadiene rubber aged in air at 125 °C. The model improves upon Tobolsky's dual network theory, designed for unfilled elastomers undergoing conventional aging but which has also often been used in rubber composites undergoing more complex aging scenarios. This work explores the shortcomings of the original model and demonstrates how the new model overcomes them. The model was validated using uniaxial tensile samples aged at 125 °C for 24-72 h at strains from 0-30%. The permanent set was measured, and the samples were tested on an Instron uniaxial test machine after aging. The cross-link density was estimated by equilibrium swelling. Results show that the new model more accurately models the stress-strain behavior to higher strains and provides more reliable estimates of chain scission and cross-linking after aging.

The Preparation and Characterization of N,N-Dimethyl Acrylamide-Diallyl Maleate Gel/Hydrogel in a Non-Aqueous Solution.

A few drugs need non-aqueous gels for release in the specific region of the intestine. The present work focuses on preparing N,N-Dimethyl acrylamide-Diallyl Maleate (DMAA-DAM) gel in Dimethyl sulfoxide (DMSO) solvent by applying different doses of gamma radiation and then characterization. The blend solution of 10%: 10%-DMAA: DAM was prepared in DMSO and irradiated at 2, 5, 10, 20, and 30 kGy doses from the Co-60 gamma source. After extraction, it was observed that all of the radiation doses yielded more than 95% gel content. The best gel content was found for 10 kGy dose, which was 97%. The equilibrium swelling was optimized 1800% of the dried gel for 5 kGy dose. Gel formation was confirmed by analyzing characteristic functional groups and the environment of protons in the gel structure by using FTIR and NMR spectroscopy. The thermal stability was tested using DSC and TGA which showed the glass transition temperature at 86.55 °C and the degradation started at 320 °C. The XRD pattern analysis revealed the semi-crystalline nature of the gel. Therefore, DMAA-DAM gels can be a good candidate for use in different fields of study, especially in drug delivery.

Modeling the swelling kinetics of preformed particle gels coated with a silicate layer

This study presented an organic–inorganic hybrid preformed particle gels (PPG) by coating a tetramethyl orthosilicate layer on acrylamide-based PPG to control the swelling rate of PPG in simulated aqueous media. The coated silicate layer on the PPG delayed the equilibrium swelling time by several hours. Furthermore, jump boundary conditions at interfaces were applied to develop a mathematical model for the swelling kinetics of hybrid PPG with three distinct regions and three moving boundaries. The proposed model results showed that the diffusion coefficient of distilled water and saltwater in the coated layer and its thickness control the swelling process of these hybrid gel particles. Furthermore, the error percentages of predictive results by the proposed mathematical model for experimental swelling kinetic measurements of coated PPG were less than 5.25%. The experimental results also showed that the silicate layer controlled PPG swelling kinetics and improved hybrid PPG's strength and thermal stability.

The Effect of Temperature on the Mechanical Properties of Alginate Gels in Water/Alcohol Solutions.

Alginate organohydrogels prepared in water/alcohol mixtures play an important role in electronic and superconductor applications in low-temperature environments. The study deals with the preparation of Ca-alginate organohydrogels and the analysis of their equilibrium swelling and mechanical properties at sub-zero temperatures. It is shown that the equilibrium degree of swelling at room temperature is noticeably affected by the concentration of co-solvents (methanol, ethanol, and 2-propanol) in the mixtures and the number of carbon atoms in the co-solvent molecules. Mechanical properties are studied in small-amplitude oscillatory tests. The data are fitted with a model that involves three material parameters. The influence of temperature is investigated in temperature-sweep oscillatory tests under a cooling-heating program, where a noticeable difference is observed between the storage and loss moduli under cooling and heating (the hysteresis curves). The hysteresis areas are affected by the cooling/heating rate and the number of carbon atoms in the co-solvents.

Mechanical Properties of Alginate Hydrogels Cross-Linked with Multivalent Cations.

Ionically, cross-linked alginate gels have a potential to be used in a wide range of biomedical, environmental and catalytic applications. The study deals with preparation of alginate hydrogels cross-linked with various cations and the analysis of their equilibrium swelling and mechanical properties. It is shown that the type of cations used in the cross-linking process affects the elastic moduli and the equilibrium degree of swelling of the gels. The experimental data in small-amplitude oscillatory tests are fitted with a model that involves two material parameters: the elastic modulus of a polymer network and a measure of its inhomogeneity. The influence of cations on these quantities is studied numerically. It is revealed that the dependence of the elastic modulus of ionically cross-linked alginate gels on their equilibrium degree of swelling differs from that predicted by the conventional theory for covalently cross-linked gels.

Hydrogels Based on Polyacrylamide and Calcium Alginate: Thermodynamic Compatibility of Interpenetrating Networks, Mechanical, and Electrical Properties.

The synthesis and physicochemical properties of hydrogels with interpenetrated physical and chemical networks were considered in relation to their prospective application as biomimetic materials in biomedicine and bioengineering. The study was focused on combined hydrogels based on natural polysaccharide-calcium alginate (CaAlg) and a synthetic polymer-polyacrylamide (PAAm). The series of hydrogels with varying proportions among alginate and polyacrylamide have been synthesized, and their water uptake has been characterized depending on their composition. The equilibrium swelling and re-swelling in water after drying were considered. The compatibility of alginate and polyacrylamide in the combined blend was studied by the thermodynamic approach. It showed a controversial combination of negative enthalpy of mixing among PAAm and CaAlg with positive Gibbs energy of mixing. Mechanical and electrical properties of the combined gels with double networking were studied as relevant for their prospective use as scaffolds for tissue regeneration and working bodies in actuators. The storage modulus and the loss modulus were determined in the oscillatory compression mode as a function of proportions among natural and synthetic polymers. Both moduli substantially increased with the content of CaAlg and PAAm. The electrical (Donnan) potential of hydrogels was measured using the capillary electrode technique. The Donnan potential was negative at all compositions of hydrogels, and its absolute values increased with the content of CaAlg and PAAm.

High biocompatible polyacrylamide hydrogels fabricated by surface mineralization for subchondral bone tissue engineering

The subchondral bone is an important part of cartilage which contains a large amount of hydroxyapatite. The mineral components of subchondral bone is the key factor which determines the biomechanical strength, and then affects the biological function of articular cartilage. Here, a mineralized polyacrylamide (PAM-Mineralized) hydrogel with good ALP activity, cell adhesion and biocompatibility was fabricated for subchondral bone tissue engineering. The micromorphology, composition and mechanical properties of PAM and PAM-Mineralized hydrogels were studied. The PAM hydrogels showed a porous structure, while the PAM-Mineralized hydrogels had well-distributed layers of hydroxyapatite mineralization on the surface. The XRD results show that the characteristic peak of hydroxyapatite (HA) was measured in PAM-Mineralized, indicating that the main component of the mineralized structure formed on the surface of the hydrogel after mineralization is HA. The formation of HA ectively decreased the rate of equilibrium swelling of the PAM hydrogel, with PAM-M reaching swelling equilibrium at 6 h. Meanwhile, compressive strength of PAM-Mineralized hydrogel (moisture state) reached 290 ± 30 kPa, compressive modulus reached 130 ± 4 kPa. PAM-Mineralized hydrogels did not affect the growth and proliferation of MC3T3-E1 cells. Surface mineralization of PAM hydrogel could significantly improve osteogenic differentiation of MC3T3-E1 cells. These results showed that PAM-Mineralized hydrogel could possess potential application in the field of subchondral bone tissue engineering.

Interelastomer Reactions Occurring during the Cross-Linking of Hydrogenated Acrylonitrile-Butadiene (HNBR) and Chloroprene (CR) Rubbers Blends in the Presence of Silver(I) Oxide (Ag2O) and Mechanical Properties of Cured Products.

The purpose of this paper was to examine the possibility of producing new blends of hydrogenated acrylonitrile-butadiene and chloroprene rubbers (HNBR/CR) unconventionally cross-linked with silver(I) oxide (Ag2O), and to investigate the physicomechanical properties of the obtained materials. From the obtained results, it can be concluded that HNBR/CR composites were effectively cured with Ag2O, which led to interelastomer reactions, and the degree of binding of HNBR with CR was in the range of 14-59%. The rheometric and equilibrium swelling studies revealed that the cross-linking progress depended on the weight proportion of both elastomers, and the degree of cross-linking was greater with more content of chloroprene rubber in the tested blends. Interelastomer reactions occurring between HNBR and CR improved the homogeneity and miscibility of the tested compositions, which was confirmed by differential scanning calorimetry (DSC) and scanning electron microscopy (SEM) analyses. The tensile strength and hardness of the obtained HNBR/CR/Ag2O vulcanizates proportionally increased with the content of CR, while the tear strength showed an inverse relationship. The obtained new, unconventional materials were characterized by significant resistance to thermo-oxidative factors, which was confirmed by the high aging factor.

Impact of composition and salinity on swelling and gel strength of poly (acrylamide-co-acrylic acid) preformed particle gel

The effects of various material compositions and reservoir environments on the ultimate strength and swelling kinetics of a commercial preformed particle gel (PPG) have been investigated. This study used different ratios of acrylamide and acrylic acid copolymers with a specific crosslinker concentration. Results have indicated that increasing the acrylic acid proportion enhances the PPGs’ ability to swell but weakens their network structure. In contrast, increasing the crosslinker content decreases the swelling ratio and increases the gel strength. The highest equilibrium swelling capacity among the six preformed particle gel samples was obtained for PPG2, which has the highest acrylic acid amount and the lowest crosslinker content, with a swelling ratio of 2400 g/g in deionized water and 59.8 g/g in brine 1 (67535.8 mg/l). On the contrary, PPG5, with the lowest acrylic acid and highest crosslinker content, has a swelling capacity of 239 g/g and more than 17 g/g in distilled and brine 1, respectively. Yet, PPG5 has the highest swollen gel strength of 615.5 Pa in deionized water and 3344 Pa in brine 1. The PPGs’ swelling ratios showed stepwise improvements along with increasing temperature, notably after 50 °C, yet, the storage modulus (G′) was negatively affected. The PPGs revealed the highest swelling behavior in pH 6–8, decreasing dramatically in more acidic and basic conditions. The swelling ratios of the PPGs in brine 1 at 50 °C were between 12 and 32 g/g, having strengths in the range of 566–5508 Pa, depending on the crosslinker ratio. The PPGs also demonstrated the ability to compete with other commercial PPGs as they have shown physical and thermal stability when aging at 50 °C, specifically those with high crosslinker content (PPG5).

Toughening Weak Polyampholyte Hydrogels with Weak Chain Entanglements via a Secondary Equilibrium Approach.

Polyampholyte (PA) hydrogels are randomly copolymerized from anionic and cationic monomers, showing good mechanical properties owing to the existence of numerous ionic bonds in the networks. However, relatively tough PA gels can be synthesized successfully only at high monomer concentrations (CM), where relatively strong chain entanglements exist to stabilize the primary supramolecular networks. This study aims to toughen weak PA gels with relatively weak primary topological entanglements (at relatively low CM) via a secondary equilibrium approach. According to this approach, an as-prepared PA gel is first dialyzed in a FeCl3 solution to reach a swelling equilibrium and then dialyzed in sufficient deionized water to remove excess free ions to achieve a new equilibrium, resulting in the modified PA gels. It is proved that the modified PA gels are eventually constructed by both ionic and metal coordination bonds, which could synergistically enhance the chain interactions and enable the network toughening. Systematic studies indicate that both CM and FeCl3 concentration (CFeCl3) influence the enhancement effectiveness of the modified PA gels, although all the gels could be dramatically enhanced. The mechanical properties of the modified PA gel could be optimized at CM = 2.0 M and CFeCl3 = 0.3 M, where the Young's modulus, tensile fracture strength, and work of tension are improved by 1800%, 600%, and 820%, respectively, comparing to these of the original PA gel. By selecting a different PA gel system and diverse metal ions (i.e., Al3+, Mg2+, Ca2+), we further prove that the proposed approach is generally appliable. A theoretical model is used to understand the toughening mechanism. This work well extends the simple yet general approach for the toughening of weak PA gels with relatively weak chain entanglements.

Insights into the effects of high‐temperature lubricating oils on the aging behavior and degradation mechanism of fluoroelastomers

AbstractThe aging behavior and degradation mechanism of fluoroelastomers (FKM) after exposure to thermal air, commercial lubricating oil, and the corresponding base oil at elevated temperatures were investigated. The FKMs immersed in oil and exposed to air are denoted by FKM‐O and FKM‐A, respectively. The crosslinking densities of the samples were determined by equilibrium swelling and dynamic mechanical analyses, and the results were different. Compared to the performances of FKM‐A, noticeable changes in the mechanical and swelling performances of FKM‐O were observed, attributed to the severe deterioration induced by both the lubricating oil and the high‐temperature. The FTIR results revealed that the dehydrofluorination induced by the oil caused the fracture of the CF bonds, and the degradation of the oil itself exerted negative impacts on the properties of the FKM. The findings of this study will facilitate the development of FKMs with degradation‐resistant properties for various applications.

The effects of degassing, neutralization, and dewatering on the CMC-g-poly (acrylic acid-co-methacrylic acid) hydrogel

CMC-g-poly (acrylic acid-co-methacrylic acid) hydrogel was prepared by free radical polymerization of acrylic acid (AA) and methacrylic acid (MAA) onto carboxymethyl cellulose (CMC) backbone using ammonium persulfate (APS) as an initiator and N, N′-methylene bisacrylamide (MBA) as a crosslinker. For investigating the effects of before and after treatments of the hydrogel on the swelling equilibrium, gel fraction, and weight loss, 3 sets of experiments with 5 samples were designed and the effect of degassing (using N2), neutralization with NaOH 1 M, and two stages of dewatering with acetone and ethanol was studied. The results confirmed the positive effects of all the after-treatment stages. The final data indicate that sample (v) with N2 as reaction atmosphere, one neutralization stage, and two dewatering stages exhibit a maximum swelling of 167 g/g, maximum gel fraction of 61.4%, and also maximum weight loss of 38.6%. These outcomes show that these treatments exhibit hydrogel with a good swelling ratio which is desirable in smart delivery systems, healthcare, and biomedical applications. The optimized sample was characterized by FT-IR, SEM, and TGA too.

Conceptualization and Investigation of Multicomponent Polymer Networks as Prospective Corticosteroid Carriers.

Dexamethasone (DXM) is a highly potent and long-acting synthetic glucocorticoid with anti-inflammatory, anti-allergic, and immunosuppressive effects. However, the systemic application of DXM can cause undesirable side effects: sleep disorders, nervousness, heart rhythm disorders, heart attack, and others. In the present study, multicomponent polymer networks were developed as potential new platforms for the dermal application of dexamethasone sodium phosphate (DSP). First, a copolymer network (CPN) comprising hydrophilic segments of different chemical structures was synthesized by applying redox polymerization of dimethyl acrylamide onto poly(ethylene glycol) in the presence of poly(ethylene glycol) diacrylate (PEGDA) as a crosslinker. On this basis, an interpenetrating polymer network structure (IPN) was obtained by introducing a second network of PEGDA-crosslinked poly(N-isopropylacrylamide). Multicomponent networks obtained were characterized by FTIR, TGA, and swelling kinetics in different solvents. Both CPN and IPN showed a high swelling degree in aqueous media (up to 1800 and 1200%, respectively), reaching the equilibrium swelling within 24 h. Additionally, IPN showed temperature-responsive swelling in an aqueous solution as the equilibrium swelling degree decreased considerably with an increase in the temperature. In order to evaluate the networks' potential as drug carriers, swelling in DSP aqueous solutions of varied concentration was investigated. It was established that the amount of encapsulated DSP could be easily controlled by the concentration of drug aqueous solution. In vitro DSP release was studied in buffer solution (BS) with pH 7.4 at 37 °C. The results obtained during DSP loading and release experiments proved the feasibility of the developed multicomponent hydrophilic polymer networks as effective platforms for potential dermal application.

Accelerated aging behavior and degradation mechanism of nitrile rubber in thermal air and hydraulic oil environments

AbstractThe aging behavior and degradation mechanism of nitrile rubber (NBR) under free and compression states were investigated in simulated air and hydraulic oil environments at various elevated temperatures. The variations in the crosslinking density, volatile components and the chemical structure of NBR during aging were studied using equilibrium swelling testing and dynamic mechanical analysis (DMA), pyrolysis‐gas chromatography–mass spectrometry and attenuated total reflection‐Fourier transform infrared spectroscopy. The migration of additives in different media and the crosslinking density of NBR aged in different conditions were compared. The tensile strength, DMA, and thermogravimetric analysis results were consistent with the changes in the crosslinking density of NBR and the migration of additives. Four effects of the simulated hydraulic system on the thermal aging of NBR were examined. Both the compression stress and the oil medium slowed the aging of NBR. The results can provide new insights into the use of NBR products in lubricating oil environments and NBR lifespan prediction in hydraulic working conditions.

Influence of crosslink on the formation of hydrophobic hydrogels

Recently invented hydrophobic hydrogel is a specific type of soft matter, which is composed of purely hydrophobic networks while maintaining ultra-high water content. Owing to their unique structures, hydrophobic hydrogels manifest various particularities for versatile applications. Therefore, it is essential to reveal the factors that determine the gels’ formation. Until now, the role played by the chemical crosslinks (e.g. crosslink ratio, structure) stays unclear. To figure out the mystery, herein we prepare a series of polyacrylate gels with different crosslinks at diverse crosslinker concentrations. Upon being soaked in water, the gels behave divergently in terms of dynamic swelling behavior. Unlike conventional gels, the maximum swelling degrees of three different hydrophobic hydrogels initially increase and then decrease with raising in crosslink ratio. Similarly, the swelling kinetics significantly vary with the crosslink ratio. From the data, a moderate crosslink ratio is required for the formation of hydrophobic hydrogels as it endows the polymer chain with high mobility and density. In addition, the chemical structure of crosslinks plays a less significant role in the formation of hydrophobic hydrogels but an important role in determining their swelling equilibrium states in water, which ultimately affects their mechanical performance. All these results may help us to uncover the formation mechanism of the hydrophobic hydrogels and establish a general standard for the preparation of such soft matter.