A State-of-the-Art Review of Organic Polymer Modifiers for Slope Eco-Engineering
Abstract
:1. Introduction
2. The Technology of Ecological Slope Protection
3. Physicochemical Properties of Organic Polymer Modifiers
3.1. Synthetic Polymer Modifiers
3.2. Biopolymer Modifiers
4. Interaction Mechanism between Polymer Modifiers and Soil
4.1. Interaction Mechanism between Synthetic Polymer Modifiers and Soil
4.2. Interaction Mechanism between Biopolymer Modifiers and Soil
5. Engineering Properties of Polymer-Stabilized Slopes
5.1. Improvement of Mechanical Properties
5.2. Improvement of Permeability
5.3. Improvement of Erosion Resistance
5.4. Promotion of Vegetation Growth
6. Challenges and Future Prospects
- Organic polymer materials have the potential to replace traditional technologies used to protect highway slopes due to their renewable and sustainable nature. The cost of biopolymers has decreased by over 80% between 1990 and 2014, making large-scale production and application more cost-effective. In addition, incorporating biopolymer modifiers with a mass fraction between 0.2% and 0.5% in soil reinforcement and vegetation growth promotion processes can significantly reduce material costs compared to synthetic organic polymers. Although the biopolymer industry is still in its developmental stage, its economic feasibility is expected to improve over time.
- The preparation of biopolymer modifiers presents a significant challenge, particularly given the high purity standards required for use in the food and medical sectors. As a result, production costs are currently high. However, if purity standards were relaxed, production expenses could be halved. While biopolymers are primarily used in the food and medical sectors, there is a growing demand for their use in slope engineering, where technical requirements are lower. This increased demand is expected to drive improvements in biopolymer synthesis technology.
- The use of biopolymer modifiers in ecological slope restoration is crucial for mitigating climate change and promoting ecological health. Biopolymers, in particular, offer superior environmental properties and benefits compared to traditional curing materials. By reducing CO2 emissions from synthetic sources, biopolymers can address the negative impact of cement production on the environment. Currently, cement is the most commonly used curing agent for reinforced soils, but it generates approximately 1 ton of CO2 per ton of cement produced. By adopting biopolymers as an alternative, it can significantly reduce this environmental impact.
- There is a lack of research on the carbon sequestration potential of vegetation on roadside slopes, and there is a need for systematic and quantitative estimation studies. However, the ecological engineering of roadside slope vegetation can effectively utilize plant photosynthesis to absorb CO2 emitted by vehicle exhausts. The decarbonization of organic polymers is currently a priority in ecology, and further research should be conducted to explore the potential of decarbonization in both organic polymers and vegetation.
- Most previous research is conducted through laboratory macro- and micro-experiments. Future research on organic synthetic and biopolymer modifiers should be performed in complex natural environments. It is necessary to carry out large-scale slope ecological protection and outdoor tests using organic polymers. This is a prerequisite for the extensive application of these modifiers.
- Considering the rainfall in natural environments, whether the organic polymer modifier can maintain its effect under dry–wet cycles and continuous rainfall needs further study. The durability of organic polymer modifiers in a natural environment still needs to be tested to ensure that the vegetation has been established on the slope. Under the initial protection of organic polymer modifiers, a “protective cover” is provided for vegetation growth, and the slope surface is reinforced. The durability improvement can be accomplished by combining various types of polymers or by designing new polymers.
- A wide variety of polymer modifiers can promote plant growth, but few studies have considered the toxicity of these polymers or composite polymers. It is not clear whether these polymers pollute the surface soil and slope groundwater. Therefore, it is necessary to monitor polymers and plants to evaluate their environmental performance. Additionally, the current research on promoting plant growth is mostly a short-term (about one month) observation, while slope vegetation protection is a long-term task. Therefore, the growth status of vegetation should be continuously tracked and monitored in the future.
- The soil erosion model can estimate runoff and erosion levels at different points in a slope watershed. It considers factors leading to erosion and sediment yield, including rainfall, interception, surface water flow, and sediment transport. The erosion degree of soil solidified by polymer modifiers is mainly evaluated based on runoff, and the erosion mitigation mechanism of polymer modifiers is ignored. Furthermore, the new soil erosion model after polymer modifier solidification needs further investigation for more effective soil erosion control by polymer modifiers.
7. Conclusions
Author Contributions
Funding
Data Availability Statement
Conflicts of Interest
References
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Polymer Modifier Types | Composition | Basic Features | Reference |
---|---|---|---|
PAM | Synthesized from acrylamide subunits with straight chain or cross-linked conformation. | Cross-linked PAMs are water-absorbent and insoluble, but linear-chained PAMs are water-soluble. | [36] |
Linear-chained PAMs are suitable for soil reinforcement. | |||
PU | Composed of macromolecular polyols, polyisocyanates, etc. | The reaction products are stable, with good adhesion, heat resistance, and elasticity and short gelation time. | [37] |
Polyacrylate | Consists of monomers of acrylic acid and esters. | Easily polymerizes with other functional groups to form different polymers. | [38] |
Good hydrophilicity and high reactivity with vinyl and carboxyl groups. | |||
PVAc | Synthesis from vinyl acetate monomer. | Insoluble in water but soluble in benzene, acetone, etc. | [39] |
Good adhesion. | |||
PVA | Prepared by alcoholysis of poly (vinyl ester). | It has water solubility and is highly polar. | [40] |
MDI | Condensation of aniline with formaldehyde, followed by reaction with phosgene. | Its NCO group reacts easily with OH groups in water to form a mixture of diisocyanates and amines, and the solid mixture binds the soil particles together. | [41] |
Polymer Modifier Types | Source | Basic Features | Reference |
---|---|---|---|
Agar Gum | Rhodophyta (Red algae). | Belongs to reversible gels, i.e., it can be dissolved in boiling water and forms a gel after cooling at about 35 °C. | [48,49] |
Agar gels have rheological properties, hydrophilic. | |||
Guar Gum | Cyamopsis tetragonoloba (Leguminous shrub). | Rapid hydration in cold water, high-viscosity solutions can be formed even at low concentrations. | [50,51] |
Natural decomposition to monosaccharides and water by the action of microorganisms or enzymes, extreme pH, and temperature degradation. | |||
Persian gum | The trunk and branches of wild almond trees of Zagros forests in Iran. | Anionic polysaccharide, a plant exudate gel. | [52] |
Lignin | Vascular plant and algae. | Rich diversity of types and sources; it is a cross-linked complex phenolic polymer, soluble in strong alkaline and sulfite solutions. | [53] |
Starch | Seeds, grains, and roots of plants. | It can be used as a thickening agent, stabilizer, disintegrant, binder, etc. | [54] |
Xanthan Gum | Xanthomonas campestris (Bacteria). | High stability over a wide range of temperatures, pH, and electrolyte concentrations. | [51] |
Better viscosity for use in gels and suspensions. | |||
Gellan Gum | Sphingomonas elodea (Microbial fermentation). | Double helical chain form at low temperatures, presenting single helical chains at high temperatures. | [49,55,56] |
Temperature-dependent structure and viscosity transformation properties, i.e., thermal gelation. | |||
Good durability in dry and wet cycles. | |||
Dextran | Leuconostoc mesenteroides and Streptococcus mutans (Lactic acid bacteria). | A flexible biopolymer that forms a high density and low permeability in aqueous media. | [57] |
β-glucan | Cellulose, bran, and the cell walls of yeasts, fungi, and bacteria. | Water solubility, dispersibility, viscosity, and gelation properties. | [45] |
The natural β-glucan is electrostatically neutral and negatively charged when modified by hydroxyl groups (−OH). | |||
Curdlan | Agrobacterium biovars and Alcaligenes faecalis (Pathogenic bacteria). | Elastic but irreversible when heated. | [58] |
Being used as a water reducer in concrete mixtures to prevent the separation of cement aggregates. | |||
Scleroglucan | Sclerotium rolfsii (Fungus). | It has good water retention and thickening properties. | [59] |
Casein | Animal proteins. | Hydrophobic, capable of coagulating and forming suspended colloids. | [60] |
Gelatin | Animal bones, skin, and tendons. | Soluble in hot water, used as a gelling agent, stabilizer, emulsifier, and thickening agent. | [61,62] |
Polymer Modifier Types | Soil Types | Research Methods | Mechanism of Action | Reference |
---|---|---|---|---|
PAM | Expansive soil and clay | SEM | The gel structure is thin and lean, adhering to the surface of soil particles. | [80] |
Polyacrylate | Clay | SEM | Polymer functional groups with the −OH groups of the clay platelets via H-bonding. | [81] |
PVAc | Clay | SEM | Filling of voids. | [82] |
Long-chain macromolecules wrap around the surface of the aggregates and interconnect to form elastic and adhesive membrane structures. | ||||
PVA | Soft clay | SEM | Fill in the pores and form larger aggregates. | [74] |
PU | Sandy soil | SEM | Sand particles are tightly wrapped by a thin and tough polymer film, which forms a three-dimensional cross-linked network structure among the particles and plays a cementing role. | [18] |
MDI | Sand | SEM | Wrap the soil particles and fill the pores. | [78] |
Xanthan gum | Silt | SEM | Form sticky hydrogels to coat the soil particles and fill the pores. | [83] |
Form xanthan chains and a “honeycomb”-shaped pore structure. | ||||
Laterite | FESEM | The gel wraps the soil and forms an interlocking structure with the soil. | [84] | |
Gellan gum | Silt | SEM | Forming biofilms that produce network structures and gellan micelles that fill soil pores. | [83] |
Guar gum | Clay | SEM | Chemical bonding and wrapping bypass. | [85,86] |
Lignin | Silt and sandy soil | SEM, XRD, FTIR, and MIP | A flocculent soil structure is produced, and porosity is reduced. | [87,88] |
Cementing material covers the soil and binds and fills the pores | ||||
Persian gum | Kaolinite soil | SEM, SZM, BET, TGA, and PSA | Fill pores, compact structure; reacts with charged clay surfaces through hydrogen bonding and ion interactions. | [52] |
The carboxyl group crosslinks with the negatively charged surface of clay. | ||||
Forming sticky gels to aggregate soil particles. | ||||
Epoxy resin and aminoamide-based hardener mixtures | Kaolinite clay, bentonite, and cement | SEM and XRD | Epoxy resin provides a gel layer on top of the soil particles, and kaolinite clay does not react in any way with epoxy resin. | [89] |
XG-g-PAA | Laterite | FTIR, XRD, TGA, and SEM | The laterite nanoflakes flocculate and disperse homogeneously in the polymer matrix, forming a homogeneous composition. | [90] |
Solid sand specimens containing CSFA show dense contacts in the sand–sand grain transition region, where sand grains bond to each other through CSFA to form a bonding layer. | ||||
NaA is attached to the XG chain, and the -OH group of the laterite is involved in the polymerization reaction. | ||||
PAA hydrogel | Silty sand | 1H NMR relaxometry | Releasing gradually into the pores of the soil, the elastomeric gum acts as an adhesive agent. | [91] |
In arid environments, the cementation and friction among soil particles are intensified, thereby enhancing the overall structural stability of the soil. |
Polymer Modifier–Soil Interaction Patterns | Synthetic Polymer Modifiers | Biopolymer Modifiers |
---|---|---|
Filling and adsorption | Hydrophilic functional groups undergo ion-exchange reactions with soil particles, establishing hydrogen bonds and van der Waals forces. The surface layer of these aggregates is coated with long-chain macromolecules. | Modifiers present in the soil matrix undergo gelation, leading to encapsulation, adhesion, and pore-filling effects. Additionally, they exhibit electrostatic interactions that enable adsorption of soil particles. |
Pore structure | The formation of a three-dimensional adhesive network structure results in the flocculation of soil particles. | Refining the formation of biological chains and “honeycomb” pore structures within the soil. |
Membrane structure | The physical–chemical bond is established, and the modifier is linked to soil particles via chemical bonding, resulting in the formation of an elastic membrane structure. | The colloid–polymer bond is activated, resulting in the formation of a three-dimensional polymer membrane structure and stiffened polymer chains. |
Penetrating quality | The enhancement of bonding and reduction in particle spacing is contingent upon the uniform permeability of the modifier solution within the soil. | The infiltration of soil pores is restricted by high viscosity, cohesion, and surface tension. Moreover, the curing effect is significantly influenced by soil particle size. |
Polymer Modifier Types | Polymer Modifier Dosage | Soil Types | Plant Types | Vegetation Growth Properties | Reference |
---|---|---|---|---|---|
Acrylamide and potassium acrylate copolymer | 10% | Clay | Caragana korshinskii | Seed germination rate increased by approximately 244%. | [145] |
Hydrogel mixed with a peat-based | 1.5% | Clay | Quercus suber L. | Survival rate increased by over 20%. | [146] |
NBA mixed with SAR (ADNB) | NBA10 g/m2 and SAR60 g/m2 | Silty clay | Crotalaria pallida | Plant germination rate increased by 40%, plant height increased by 32.73%, and coverage rate increased by 553.85%. | [147] |
Xanthan gum | 0.5% | Silt | Ryegrass | 28% increase in height. | [83] |
Gellan gum | 0.5% | Silt | Ryegrass | 8% increase in height. | |
Guar gum | 0.5% | Silt | Ryegrass | 4% increase in height. | |
Starch | 0.5% | In situ soil (Seosan, Korea) and jumunjin sand | Ryegrass | The germination rate increases by about 5%, and the average root length after treatment increases. | [148] |
β-glucan | 0.5% | Korean red yellow soil | Oats | Increase seed germination rate by 6.6–10.8%. | [17] |
Xanthan gum | 0.5% | Korean red yellow soil | Oats | Increase seed germination rate by 1.9% to 5.5%. | |
M-CMC | 1.1% | Sand soil | Elymus | Plant biomass increased by 59.65%, plant lodging rate decreased by more than 60%, and drought resistance survival rate increased by more than 80%. | [149] |
FA and PAM | 10%FA and 0.1%PAM | Sand soil | A. splendens | The average height of plants increased by 145%, and the tillers number increased by 2.3 times. | [150] |
Potassium polyacrylate polymer | 0.08% | Sand soil | Festuca arundinacea ssp. | Aerial vegetation biomass doubled in size. | [151] |
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Wang, L.; Yao, Y.; Li, J.; Liu, K.; Wu, F. A State-of-the-Art Review of Organic Polymer Modifiers for Slope Eco-Engineering. Polymers 2023, 15, 2878. https://doi.org/10.3390/polym15132878
Wang L, Yao Y, Li J, Liu K, Wu F. A State-of-the-Art Review of Organic Polymer Modifiers for Slope Eco-Engineering. Polymers. 2023; 15(13):2878. https://doi.org/10.3390/polym15132878
Chicago/Turabian StyleWang, Lei, Yongsheng Yao, Jue Li, Kefei Liu, and Fei Wu. 2023. "A State-of-the-Art Review of Organic Polymer Modifiers for Slope Eco-Engineering" Polymers 15, no. 13: 2878. https://doi.org/10.3390/polym15132878
APA StyleWang, L., Yao, Y., Li, J., Liu, K., & Wu, F. (2023). A State-of-the-Art Review of Organic Polymer Modifiers for Slope Eco-Engineering. Polymers, 15(13), 2878. https://doi.org/10.3390/polym15132878