Solution Temperature Research Articles

Iron bed accelerator for discharging cylindrical NCA battery in salt solution

This study examines the iron bed accelerator for discharging cylindrical NCA batteries in salt solution. The use of Li-ion batteries has increased due to the rise of e-mobility in computers, cell phones, and electric vehicles. Recycling Li-ion batteries for raw material in lithium-ion battery production is increasingly important as the revolution unfolds. When disposing of, transporting, and recycling the battery, it is important to crush it to separate the black mass, plastic, and metal components. However, there is a potential explosion risk due to the remaining voltage in the battery. In recycling, the discharge step is significant. The research aimed to test a new method for discharging cylinder batteries using saltwater and an iron bed. Higher NaCl content increases pH and lowers electrochemical potential for water electrolysis. This unique combination enables the battery to discharge at a high rate. In 6 hours, the battery discharged in a 20 wt.% salt solution with 99.6% efficiency. The battery discharge efficiency decreased when exposed to 25 wt% and 30 wt% salt solutions, attributed to reduced water electrolysis intensity. According to the results of various experiments, it has been observed that as the temperature of the salt solution rises, there is a slight increase in the rate of battery discharge; however, no significant difference has been observed. This article talks about how batteries are discharged. It shows the electrochemical reaction using the Eh-pH diagram for Fe-Na-Cl. It also has a schematic diagram that shows the process and a chemical analysis of the precipitate that forms during the discharge test.

The development of undercut and bulge on a solidified surface

Abstract This study numerically investigates the development of undercuts and bulges parallel to the scanning direction on the surface solidified from a thermocapillary molten pool. The analysis considers various parameters, including power-off time, active solute concentration, beam power and radius, surface tension, liquid thermal conductivity, viscosity, and density. The formation and shapes of undercuts and bulges directly impact the yield, fatigue, fracture strength, and stress concentration in the solidified region. Unsteady two-dimensional fluid flow and heat transfer, which drive surface deformation in metals containing surface-active solutes (e.g., iron with sulfur), are solved using COMSOL Multiphase version 5.6. The development of the undercut, bulge, and molten pool is identified in six stages, based on whether the peak temperature is below the melting temperature, between the melting and critical temperatures, or above the critical temperature during heating and power-off periods. The critical temperature, determined as a function of solute content and temperature, leads to inward surface flow in the undercut near the pool edge, while the bulge in the central region can form due to either inward or outward surface flow. The predicted undercut depth and bulge height align well with previous scaling analyses and experimental data from laser polishing. These findings are relevant to various processes, including welding, additive manufacturing, polishing, melting, and solidification.

The combined leaching of copper, gold and uranium in chloride solutions. I. Chalcopyrite

In a study (Part II) aimed at the simultaneous heap leaching of copper (predominantly chalcopyrite), gold and uranium from an ore, it was found that this could be achieved using chlorate as the oxidant in chloride solutions. As a result, a more detailed study has been made using electrochemical and batch leach tests on pure chalcopyrite electrodes under typical heap leach conditions.The use of chlorate at moderately low concentrations has shown that enhanced rates of dissolution of chalcopyrite can be maintained over periods up to 4 days at ambient temperatures in acidic chloride solutions. The rate of dissolution is enhanced at higher acid concentrations. The rate in the presence of chlorate does not appear to depend on the iron(III) (and presumably the copper(II)) concentration.The observed rates are significantly greater than those predicted for oxidative dissolution from the electrochemistry and the mixed potential model. An alternative non-oxidative mechanism has been revisited to account for this difference.A preliminary measurement has been made of the kinetics of the oxidation of hydrogen sufide and iron(III) by low concentrations of chlorine produced by reaction of chlorate with chloride ions. These reactions are rapid, and theory shows that they would support the proposed non-oxidative mechanism.

A novel integrated hot forming with in-situ stress relaxation-aging for titanium alloy thin-walled components

The simultaneous achievement of high strength and precision in the fabrication of titanium alloy thin-walled components is a long-standing issue. This work proposes a novel integrated forming process, named Hot Forming with In-situ Stress Relaxation-Aging (short for HF-ISRA) to solve the special issue. In contrast to usual isothermal forming, the forming temperature in the proposed process is raised to the solution treatment temperature. Dies at a lower temperature realize in-situ stress relaxation-aging after hot forming. The role of the dies, in addition to forming, is also achieved post-forming heat treatment. This novel process comprises three main steps: solution heat treatment, rapid forming at solution temperature, and in-situ stress relaxation-aging. An experimental prototype of HF-ISRA was developed for V-bending test, in which a sheet blank was rapidly heated using electric current and the forming die was heated using heating rods. The process window of the proposed HF-ISRA was established based on the V-bending and uniaxial tensile tests of the TA15 titanium alloy. The results showed that compared with cold forming, the springback angle obtained using the optimized HF-ISRA decreased by 97.8 %, from 9°06′ to only 12′. The tensile strength at room temperature and 500 °C was improved by 4.4 % and 10.9 % compared with the as-received material, respectively. The relaxation mechanisms of αs were the precipitation, growth, and then globularization. The relaxation mechanism of αp was dislocation movements. The strength improvement in HF-ISRA was due to the formation of αs and dislocations strengthening. The stress-induced twinning in αs was also a contributor. The proposed novel process provides a new route for the fabrication of titanium alloy thin-walled components with high precision and strength.

In-situ monitoring of changes in temperature and microstrain during the chemical corrosion of stone cultural relics

Temperature changes during the chemical corrosion of stone cultural relics affect the condensation and evaporation of water and chemical reactions between soluble substances and corrosive solutions. This ultimately leads to changes in the internal structure and composition of the artifacts, which in turn lead to changes in the microstrain of cultural relics. To obtain in-situ real-time information on changes in the temperature and microstrain of stone cultural relics during chemical corrosion damage, a fiber Bragg grating (FBG) detection system was developed. The detection principle for the temperature and microstrain of sandstone was provided. Thermal field emission scanning electron microscopy, X-ray diffraction, and mercury intrusion porosimetry were used to characterize the surface morphology, composition, and pore structure of the sandstone samples, respectively. The temperature and microstrain changes of the sandstone samples under deionized water with different acidic/alkaline and salt solutions and at different temperatures were examined online in situ using the FBG measurement system. The results indicate that the dissolution of sandstone in the acidic solution (H2SO4 and NaHSO4) resulted in an exothermic chemical reaction as well as the dissolution of sandstone in the neutral salt solution (Na2SO4) and alkaline solution (NaOH and Na2CO3) led to material conversion and exothermic chemical reaction; the deionization reaction belongs to the dissolution reaction. The NaHSO4 solution caused the most serious corrosive disease on the sandstone surface. When the temperature of the NaHSO4 solution was 60 °C, the temperature and microstrain of the sandstone reached 63.9 °C and 253.6 με, respectively. The results of this study can support the research of revealing the corrosion mechanism of sandstone in different environments.

Phase-changing NIPAM-AM/ATO hydrogels for thermochromic smart windows with highly adaptive solar modulation

Improving the solar regulation and reducing the response temperature of thermochromic smart windows are pivotal importance for energy-saving buildings. However, these two strategies are challenging to be integrated into one window. Herein, a novel composite hydrogel based on N-isopropylacrylamide (NIPAM) doped with antimony-doped tin oxide (ATO) nanoparticles and acrylamide (AM) was developed for producing a high-performance smart window, which successfully achieved enhanced solar energy regulation and reduced response temperature. This smart window was fabricated by combining a reversible thermoresponsive hydrogel (TAH) that acted as a thermochromic material with a ATO multilayer film that performed as a transparent heater. The as-prepared smart window could modulate solar light over a range from ultraviolet (UV) to infrared (IR) radiation and achieved active responses to high-temperature weather. The smart window showed high luminous transmittance (Tlum, 82.92 %) together with an excellent solar modulation performance (ΔTlum = 73.31 %, ΔTIR = 38.26 %, and ΔTsol = 60.74 %), and a lower critical solution temperature of 32 °C. Even after 120 high- and low-temperature cyclic durability tests, the smart windows still exhibited a high solar modulation capability. In outdoor demonstrations, the as-prepared smart window exhibited a promising temperature regulation ability under strong solar irradiation. Therefore, the present universal modification framework provided some insights for the future design of energy-saving windows.

Tantalum in hydrothermal fluids

Understanding the behaviour of tantalum (Ta) in hydrothermal systems is pivotal for understanding its geochemical enrichment processes and economic extraction via hydrometallurgy. Yet, its behaviour in hydrothermal systems remains poorly characterised. This study investigates the coordination chemistry, speciation, and solubility of pentavalent Ta(V) in fluoride (F) − and chloride (Cl) −rich hydrothermal solutions up to 413 °C and 800 bar, utilising in-situ High Energy Resolution Fluorescence Detected X-ray Absorption Spectroscopy (HERFD-XAS). The results reveal the stability of high order fluoridotantalate complexes in fluoride-rich fluids solutions up to the highest investigated temperature, highlighting fluoride’s paramount role in enhancing Ta solubility through the formation of stable complexes in aqueous solutions. A transition from nonafluoridotantalate tetraanion (TaF94−) to heptafluoridotantalate dianion (TaF72−) complexes was observed as a function of temperature in solutions containing ≥1 m fluoride. Conversely, our findings indicate a negligible role for chloride in Ta complexation even in high Cl (∼6 m) aqueous solutions, suggesting that Ta chloride complexes do not contribute significantly to Ta transport in hydrothermal systems. Existing solubility data were reinterpreted based on an updated speciation model that integrates the in-situ XAS results. This confirms that Ta(OH)5(aq) predominates in solutions containing <0.02 m fluoride; oxyfluoridotantalate anions such as [TaF3(OH)3−] dominate in solutions containing intermediate fluoride concentrations (0.02–1 m), and the fluoridotantalate anions [TaF94− to TaF72−] occur in more concentrated fluoride solutions (>1 m) at hydrothermal conditions (∼100–400 °C). Derived thermodynamic data for these species enable better understanding and geochemical modelling of Ta transport in hydrothermal fluids, highlighting the potential of F-rich fluids to transport significant amounts of Ta.

Effect of discharge thermal action in ECDM on electrochemical behaviours of matrix material and its recast layer in glycol-based solution

The interaction between thermal and electrochemical corrosion in the ECDM process remains unclear. This study clarifies the effect of discharge thermal action on electrochemical corrosion. Real-time temperature curves indicate that the solution temperature in the electrochemical corrosion zone increased significantly due to discharge thermal action. The corrosion resistance of the recast layer’s passive film is superior to that of the matrix due to the enrichment of Cr2O3. As the electrolyte temperature rises, the passive film thickens but shows lower polarization resistances and poorer corrosion resistance due to a loose and weak structure. The matrix material and its recast layer dissolved uniformly, resulting in a considerably flat surface in a glycol-based solution, with enhanced levelling efficiency due to discharge thermal action.

PH- and temperature-dual responsive polymer emulsion for rapid release of drag reducer

Slick water fracturing fluid is widely used in major oil fields due to its low cost and high drag reduction. Polyacrylamide emulsions drag reducers play a decisive role in slick water fracturing. The dissolution rate of polymer emulsions drag reducers was increased by adding hydrophilic surfactants, but the stability of the emulsions is poor, which limits its wide application. In order to solve the contradiction between the stability of polymer emulsion and rapid release of drag reducer. Here, a P(AA-AM-AMPS) polymer emulsion drag reducer with dual stimulation response of pH and temperature was designed. Surfactant (D400/OA) with dual responses to pH and temperature is synthesized by using oleic acid (HOA) and polyether amine 400 (D400). D400/OA shows a remarkable pH- and temperature-responsive behavior due to the pH- and temperature-induced structural transformation of D400/OA. Interestingly, D400/OA-stabilized monomer emulsion exhibits an obvious pH- and temperature-induced structural transformation. Meanwhile, The D400/OA-stabilized monomer emulsion has remarkable stability, which benefits the inverse emulsion polymerization of P(AM-AA-AMPS) polymer. The obtained P(AM-AA-AMPS) polymer emulsion maintain stability whose particle size nearly unchanged by storing for 15 days. Interestingly, P(AM-AA-AMPS) polymer emulsion can be released completely by changing the pH or temperature of the aqueous solution. The apparent viscosity of P(AM-AA-AMPS) polymer, in either the alkaline (pH=10.31) solution of 25±2 °C or neutral (pH=7) solution of 70±2 °C, respectively required 40 s and 8 min to reached a maximum value of 96 mPa·s. The release rate of P(AM-AA-AMPS) polymer emulsion is further enhanced under the dual responsive of temperature (70±2 ℃) and pH (10.31) and it takes only 20 s, In addition, the drag reduction rate of P(AM-AA-AMPS) polymer emulsion is 72 % when completely released under the dual responsive of temperature and pH, showing a remarkable drag reduction property. The D400/OA-stabilized P(AM-AA-AMPS) polymer emulsion are expected to meet the demand for the production enhancement of the oil and gas reservoirs.

Optimization study of methylene blue dye adsorption on Chamaerops humilis fibers biosorption using a central composite design

This research explores the effectiveness of Chamaerops humilis (CH) fibers as a biosorbent for the adsorption of Methylene Blue (MB) dye from aqueous solutions. The fibers were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR). To optimize the dye removal process, a Design of Experiments methodology, specifically Central Composite Design (CCD), was applied. Factors such as solution pH, adsorbent dosage, contact time, and temperature were varied. The CCD analysis identified the optimal conditions for maximum removal efficiency (99.87 %) of a 10 mg/L MB solution, which were: 1.06 g/L of CH fiber dosage, pH 9.6, and a contact time of 60 min. The adsorption process aligned well with a pseudo-second-order kinetic model, and the maximum adsorption capacity of CH fibers was determined to be 9.422 mg/g. Thermodynamic parameters, including Gibbs free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) changes, were calculated, confirming that the adsorption is spontaneous and endothermic. The study highlights the potential of Chamaerops humilis fibers as an efficient and eco-friendly adsorbent for MB dye removal, offering a sustainable and cost-effective solution for wastewater treatment, particularly in industrial effluent management.

Membrane fouling in integrated forward osmosis and membrane distillation systems – A review

With the increase in water consumption, especially by the industrial and agricultural sectors, more strategies capable of increasing the recovery and reuse of water resources have been sought. An example of technology that assists in this challenge is membrane separation processes. However, systems that use this type of separation may be limited by the phenomenon of fouling. Integrated systems such as forward osmosis (FO) with membrane distillation (MD) have several advantages, such as obtaining a high-quality permeate from raw wastewater, the constant regeneration of the draw solution, which assists in continuous operation, and the possibility of association with biological tanks that enable nutrients recovery. However, these systems face limitations related to low flux values caused by membrane fouling. Therefore, the present review seeks to study fouling in integrated FO-MD systems to understand the main challenges of applying this technology and achieving higher permeate flux values. From the most recent studies, many strategies are being evaluated, such as different membrane materials, deposition of antifouling materials on membrane surface, feed temperature, draw solution substances, concentration and temperature, use of spacers and new modules configurations. That way, the low flux from those systems may be bypassed, enabling FO-MD systems scale up.

Phase behavior of aqueous two-phase systems formed with cholinium-based magnetic ionic liquids: Experimental insights and theoretical correlations

In this work, three cholinium-based MILs were synthesized, characterized and successfully applied to construct the magnetically responsive aqueous two-phase system (ATPs). This ATPs combined the advantages of ILs and magnetic responsiveness, and showed great potential in the field of extraction and separation. Phase behavior for the magnetic ionic liquid aqueous two-phase systems (MIL-ATPSs) containing [N 1 1n 2OH] [TEMPO-OSO3] + salts + water was investigated experimentally at different temperatures. Merchuk equation was adopted to fit the experimental binodal data with satisfactory correlation performances. The effects of the structure of MILs, temperature and types of salts on the phase behavior were evaluated. Investigation on the phase separation mechanism showed that the phase formation was affected by the structure and viscosity of MILs. The salting-out effect is recognized as the major force for phase separation, which is closely related to the Gibbs free energy of hydration (ΔhydG) and entropy of hydration (ΔhydS) of salts. In addition, a larger biphasic area was obtained by increasing the temperature, indicating the phase separation process was endothermic and entropically driven. The binodal curve at different temperature confirms that this MIL-ATPs has low critical solution temperature (LCST) phase transition behavior. All these experimentally measured data and the theoretical correlations can provide meaningful and valuable information that may promote further research and application.

Experimental setup for comprehensive study of non-stationary heat transfer in complex liquid media.

This paper presents a setup for studying non-stationary heat exchange in liquid media on a scale of small times and sizes at high heat flux densities created using a high-speed precision power controller. A platinum wire with a diameter of 20μm and a length from 0.5 to 1cm is used as a probe. The heating time ranged from 1 to 300ms, and the heat flux densities from 1 to 20 MW/m2 were achieved in the experiments. Strictly specified conditions for heat release in the probe are confirmed by maintaining a constant power in a series of pulses with an accuracy of 0.05%. Acquiring a primary electrical signal of thermograms is synchronized with high-speed video recording, allowing an accurate relationship between the applied thermal load and the mechanics of processes in the studied liquid. The setup capabilities were shown by comparing the boiling patterns of a simple substance, such as ethanol, and a solution with a lower critical solution temperature, a 30 vol.% solution of polypropylene glycol-425 in water, which have similar thermograms. As a result, a qualitative difference between the heating and boiling patterns observed using high-speed video and the presented setup fitting its purpose has been shown.

Impregnation, dehydration and crosslinking of responsive organoboron polymer to generate smart gating membrane for multimolecular gradient separation

Responsive materials have garnered increasing attention in the membrane separation field. However, fabricating smart gating membranes with tunable pore sizes to separate complex systems remains challenging. Herein, gating membranes with boroxine skeleton and temperature-tunable pores were successfully fabricated by fixing lower critical solution temperature (LCST)-type organoboron polymers (poly(N-isopropylacrylamide-co-glycidyl methacrylate/3-aminophenylboronic acid), PNG-APBA) onto the membrane surface via "impregnation-dehydration-crosslinking" strategy. The conformational behavior of the NIPAM-containing polymer chains (shrinking above LCST-stretching below LCST) serves as a functional gate, enabling the membranes to achieve reversibly tunable pore sizes and surface properties. The modified membranes exhibit gradient separation capabilities for small/medium/large molecules in complex polymer systems through temperature-tunable channels. The tunable pores also provided a potential tool for the high-selectivity separation of mixed proteins, such as lysozyme (LZM) and hemoglobin (Hb). Notably, the conformational behavior of the polymer chains endowed the membranes with excellent self-cleaning ability (FRR> 99.5%), while the boroxine network enhanced the grafting stability of the polymer chains, ensuring effective reversibility and repeatability of membranes.

A structural underpinning of the lower critical solution temperature (LCST) behavior behind temperature-switchable liquids

A structural underpinning of the lower critical solution temperature (LCST) behavior behind temperature-switchable liquids

Fe3O4/sugarcane bagasse magnetic composite: A low-cost and green adsorbent for enhanced adsorption of Rhodamine B from aqueous solutions

In this study, we have designed and synthesized an eco-friendly Fe3O4/sugarcane bagasse magnetic composite (Fe3O4/SCB). We investigated its application for efficiently removing Rhodamine B (RhB) from textile wastewater, a significant step towards addressing the environmental issue of textile dye pollution. The composite, made from sugarcane bagasse (SCB), a secondary product from the sugarcane industry, proved an effective adsorbent. The composite Fe3O4/SCB was characterized by PXRD, FT-IR, FE-SEM, VSM, BET N2 adsorption-desorption, and pHpzc. Results from batch adsorption studies show that the removal of RhB was 93.6 ± 1.16 % using a composite dose of 1 g/L, a RhB concentration of 10 mg/L, a contact period of 60 min, and a solution pH of 3 at 323 K of solution temperature. The kinetic studies indicate that the pseudo-second-order model most accurately describes the adsorption. Meanwhile, the equilibrium data is well-represented by the Freundlich isotherm. Further, the analysis of thermodynamic results, such as the changes in ∆Go, ∆So, and ΔHo, revealed that the adsorption was spontaneous, feasible, and endothermic. The adsorption mechanism involved chemisorption and physisorption, with significant roles played by electrostatic interactions and hydrogen bonding. Desorption studies identified 0.5 M NaOH as an effective desorbing agent, and the composite demonstrated excellent reusability over four adsorption-desorption cycles. Overall, the Fe3O4/SCB, with its easy preparation, abundance, cost-effectiveness, efficiency, and eco-friendly nature, presents a promising solution for effectively removing toxic RhB from aqueous solutions, inspiring further research and potential real-world applications.

Temperature-dependent behavior of poly(N-isopropylacrylamide) brushes via neutron reflectometry

Poly(N-isopropylacrylamide) (PNIPAAm)-modified interfaces are promising for various biomedical applications, however, the PNIPAAm brush structure must be investigated at various temperatures to enable the design of functional PNIPAAm interfaces. In this study, PNIPAAm brush structures with various densities and chain lengths are prepared via atom-transfer radical polymerization and analyzed using neutron reflectometry. The volume fraction of PNIPAAm exhibits temperature-dependent shrinkage; slight PNIPAAm shrinkage is observed below the lower critical solution temperature (LCST) of PNIPAAm, whereas large shrinkage occurs across the LCST of PNIPAAm. The volume of water in the PNIPAAm brush is 40% even when it is dehydrated at 37 °C and is slightly extended relative to its dry state. The dense PNIPAAm brush is thicker than the diluted PNIPAAm brush because the densely packed PNIPAAm chain tends to form an extended structure. A higher volume fraction of D2O is observed in the diluted PNIPAAm brush than in the dense PNIPAAm brush because the former can accommodate a larger volume of D2O. These results indicate that neutron reflectometry can provide essential information on the PNIPAAm brush configurations with various chain lengths and densities at different temperatures. These findings are applicable to the design of further functional PNIPAAm brush interfaces for biomedical applications.

An orthogonal analytical platform for determining critical material attributes for in situ formation of thermosensitive hyaluronic acid-poly(N-isopropylacrylamide) copolymers

The developability assessment of the in situ formation of thermosensitive injectables requires the unequivocal determination of their lower critical solution temperatures (LCSTs). Herein, we established a standardized threshold for LCST detection by harmonizing and cross-validating the orthogonal methods using techniques such as nuclear magnetic resonance spectroscopy, light scattering, turbidimetry, backgrounded membrane imaging, and rheology. The selected techniques were in agreement and promptly disclosed unique features and instrumental biases of otherwise difficult interpretations in the characterization of thermosensitive polymers. Thus, various hyaluronic acid–poly(N-isopropylacrylamide) copolymers were synthesized via strain-promoted azide–alkyne cycloaddition to understand their critical material attributes. Structure–function relationships and behaviors of the copolymers were tested under in vitro-simulated in vivo conditions.

Effects of solution treatment on microstructure and properties of Ti-5.7Al-3.9Sn-0.91Mo-3.4Zr-0.40Si-0.38Nb-0.95Ta titanium alloy

This study investigated the effects of solution treatments under various conditions on the matrix and silicides microstructure and their impact on the mechanical properties of high-temperature Ti60 (Ti-5.7Al-3.9Sn-0.91Mo-3.4Zr-0.40Si-0.38Nb-0.95Ta) titanium alloy. The microstructure evolution during solution treatments was characterized, and the tensile properties at 600 °C and room temperature (RT) were investigated. The results show that the fraction and grain size of martensite and silicides can be tailored through solution treatments. With increasing solution temperature, the fraction of primary α (αp) phase and silicides decreases, while that of the transformed β (βt) microstructure increases. After solution treatment at 1025 °C, the yield strength (YS) and ultimate tensile strength (UTS) reach 685.0 MPa and 900.8 MPa, respectively, at 600 °C, increasing by 18.0% and 27.0%, respectively, compared to the initial state. The elongation (EL) remains at 16.2%. The strengthening mechanisms of Ti60 alloy include grain boundary strengthening of the αp phase and martensite formed during rapid cooling, as well as precipitation strengthening of the silicides. With increasing solution temperature from 950 °C to 1025 °C, the fraction of martensite strengthening increases from 38.4% to 89.3%, while the fraction of precipitation strengthening of silicides decreases from 3.63% to 1.17%.

Microalgae aggregation induced by thermoresponsive polymers

Algal biomass harvesting is one of key technical hurdles impeding the commercialization of algae-based biorefinery. The goal of this work is to develop an innovative technology for algae cell harvesting. Thermoresponsive polymers (TRPs) such as poly(N-isopropylacrylamide) (PNIPAM) and its derivatives were studied on their properties and potential applications for microalgae harvesting. Various PNIPAM was synthesized, and the effects of charge, molecular weight (MW), amine content, and polymer concentration on the polymer phase transition temperature, the degree of phase separation, and the harvesting of microalgae (Chlorella vulgaris) were investigated. The lower critical solution temperature (LCST) of PNIPAM decreased with the increase of polymer concentration, while the decline rate reduced under high MW. The amine content didn’t significantly affect the LCST of TRPs. Approx. 92 % of algae cells were harvested by PNIPAM-300 kDa. Modified TRPs showed few benefits in enhancing algae harvesting. TRPs are a promising class of polymers for microalgae harvesting.