Poly Aspartic Acid Research Articles

Amperometric sensor based on carbon nanotube, ionic liquid, and polyaspartic acid for ascorbic acid determination

AbstractAn amperometric sensor for ascorbic acid determination has been developed by modifying the surface of a glassy carbon electrode (GCE) with polyaspartic acid (PolyAsp), carboxylated multi‐walled carbon nanotube (c‐MWCNT), and ionic liquid (IL, 1‐butyl‐3‐methylimidazolium hexafluorophosphate). The amount of each modification material on the surface was optimized in order to achieve good analytical performance. The operating conditions of c‐MWCNT−IL/PolyAsp/GCE were optimized. The performance characteristics of c‐MWCNT−IL/PolyAsp/GCE were investigated at optimum pH (8.0) and optimum potential (+0.20 V), and the sensor responded linearly to ascorbic acid between 5.3–2766.3 μM with a sensitivity of 19.64 μA mM−1 and detection limit of 3.0 μM. Determination of ascorbic acid in vitamin C tablet, vitamin C injection solution, and orange juice was successfully performed with the presented sensor and the recovery values were found between 98.9% and 101.6%.

Calcium phosphate nanoclusters modify periodontium remodeling and minimize orthodontic relapse.

Orthodontic relapse is one of the most prevalent concerns of orthodontic therapy. Relapse results in patients' teeth reverting towards their pretreatment positions, which increases the susceptibility to functional problems, dental disease, and substantially increases the financial burden for retreatment. This phenomenon is thought to be induced by rapid remodeling of the periodontal ligament (PDL) in the early stages and poor bone quality in the later stages. Current therapies, including fixed or removable retainers and fiberotomies, have limitations with patient compliance and invasiveness. Approaches using biocompatible biomaterials, such as calcium phosphate polymer-induced liquid precursors (PILP), is an ideal translational approach for minimizing orthodontic relapse. Here, post-orthodontic relapse is reduced after a single injection of high concentration PILP (HC-PILP) nanoclusters by altering PDL remodeling in the early stage of relapse and improving trabecular bone quality in the later phase. HC-PILP nanoclusters are achieved by using high molecular weight poly aspartic acid (PASP, 14 kDa) and poly acrylic acid (PAA, 450 kDa), which resulted in a stable solution of high calcium and phosphate concentrations without premature precipitation. In vitro results show that HC-PILP nanoclusters prevented collagen type-I mineralization, which is essential for the tooth-periodontal ligament (PDL)-bone interphase. In vivo experiments show that the PILP nanoclusters minimize relapse and improve the trabecular bone quality in the late stages of relapse. Interestingly, PILP nanoclusters also altered the remodeling of the PDL collagen during the early stages of relapse. Further in vitro experiments showed that PILP nanoclusters alter the fibrillogenesis of collagen type-I by impacting the protein secondary structure. These findings propose a novel approach for treating orthodontic relapse and provide additional insight into the PILP nanocluster's structure and properties on collagenous structure repair.

Effects of N, N-bis (carboxymethyl)-L-glutamic acid and polyaspartic acid on the phytoremediation of cadmium in contaminated soil at the presence of pyrene: Biochemical properties and transcriptome analysis

Chelator-assisted phytoremediation is an efficacious method for promoting the removal efficiency of heavy metals (HMs). The effects of N, N-bis(carboxymethyl)-L-glutamic acid (GLDA) and polyaspartic acid (PASP) on Cd uptake and pyrene removal by Solanum nigrum L. (S. nigrum) were compared in this study. Using GLDA or PASP, the removal efficiency of pyrene was over 98%. And PASP observably raised the accumulation and transport of Cd by S. nigrum compared with GLDA. Meanwhile, both GLDA and PASP markedly increased soil dehydrogenase activities (DHA) and microbial activities. DHA and microbial activities in the PASP treatment group were 1.05 and 1.06 folds of those in the GLDA treatment group, respectively. Transcriptome analysis revealed that 1206 and 1684 differentially expressed genes (DEGs) were recognized in the GLDA treatment group and PASP treatment group, respectively. Most of the DEGs found in the PASP treatment group were involved in the metabolism of carbohydrates, the biosynthesis of brassinosteroid and flavonoid, and they were up-regulated. The DEGs related to Cd transport were screened, and ABCG3, ABCC4, ABCG9 and Nramp5 were found to be relevant with the reduction of Cd stress in S. nigrum by PASP. Furthermore, with PASP treated, transcription factors (TFs) related to HMs such as WRKY, bHLH, AP2/ERF, MYB were down-regulated, while more MYB and bZIP TFs were up-regulated. These TFs associated with plant stress resistance would work together to induce oxidative stress. The above results indicated that PASP was more conducive for phytoremediation of Cd-pyrene co-contaminated soil than GLDA.

Natural Chelating Agent-Treated Electron Transfer Layer for Friendly Environmental and Efficient Perovskite Solar Cells.

In perovskite solar cells (PSCs), the electron transfer layer (ETL) characteristics have significant effects on the photoelectric conversion efficiency (PCE) of the devices. Herein, a natural chelating agent polymer polyaspartic acid (PASP) is doped into the SnO2 precursor solution attributed to a strong interaction between PASP molecules and SnO2, which strengthens the interface contact and passivates the vacancy oxygen trap of the obtained SnO2 ETL, thus promoting the transfer of electrons. In addition, PASP can also regulate the growth of perovskite crystals, leading to an improved crystal quality of the perovskite films. Meanwhile, there is an excellent chelate anchoring of PASP to uncoordinated Pb2+, facilitating the reduction of trap defects at the interface, improving the stability of device, and suppressing the leakage of toxic Pb. Finally, the photovoltaic performance of the optimized device was greatly improved, and the PCE was increased from 21.22 to 23.49%, with outstanding environmental stability. This work provides an inexpensive and efficient treatment strategy that improves the performance and stability of friendly environmental PSCs.

With Blue Light against Biofilms: Berberine as Natural Photosensitizer for Photodynamic Inactivation of Human Pathogens

Evolving antibiotic resistance of bacteria is a prevailing global challenge in health care and requires the development of safe and efficient alternatives to classic antibiotics. Photodynamic Inactivation (PDI) has proven to be a promising alternative for treatment of a broad range of microorganisms. Photodynamic Inactivation uses photoactive molecules that generate reactive oxygen species (ROS) upon illumination and in the presence of oxygen, which immediately kill pathogenic target organisms. Relevant photoactive properties are provided by berberine. Originally extracted from Barberry (Berberis vulgaris), it is a natural compound widely used in Traditional Chinese Medicine for its antimicrobial and anti-inflammatory effects. With this study, we demonstrated the potential of berberine chloride hydrate (Ber) as a photosensitizer for PDI of important human pathogens, Gram(+) Staphylococcus capitis subsp. capitis, Gram(+) Staphylococcus aureus, and Gram(−) Escherichia coli. In vitro experiments on planktonic and biofilm cultures were conducted focusing on Ber activated with visible light in the blue wavelength range. The number of planktonic S. capitis cells was reduced by 7 log10 steps using 100 µM Ber (5 min incubation, illumination with 435 nm LED array, radiant exposure 25 J/cm2). For an antibacterial effect of 4 log10 steps, static S. capitis biofilms required 1 mM Ber, a drug-to-light interval of 60 min, and illumination with 100 J/cm2. Almost all planktonic cells of Staphylococcus aureus could be photokilled using 100 µM Ber (drug-to-light interval of 30 min, radiant exposure 25 J/cm2). Biofilms of S. aureus could be phototreated (3 log10 steps inactivation) when using 1 mM Ber incubated for 5 min and photoactivated with 100 J/cm2. The study is highlighted by the proof that PDI treatment using Ber showed an antibacterial effect on Gram(−) E. coli. Planktonic cells could be reduced by 3 log10 steps with 100 µM Ber (5 min incubation, 435 nm, 25 J/cm2). With 5 mM ethylenediamine tetraacetic acid disodium salt dihydrate (Na2EDTA) or 1.2% polyaspartic acid (PASA) in addition, a relative inactivation of 4 log10 steps and 7 log10 steps, respectively, was detectable. Furthermore, we showed that an antibacterial effect of 3.4 log10 towards E. coli biofilms was given when using 1 mM Ber (5 min incubation, 435 nm, 100 J/cm2). These results underscore the significance of PDI-treatment with Ber as a natural compound in combination with blue light as valuable antimicrobial application.

Effects of biodegradable dispersants on the separation flotation of chalcopyrite and serpentine

The presence of serpentine slime coating on the chalcopyrite surfaces severely affects the chalcopyrite floatability. In this study, three biodegradable polymers, namely polyaspartic acid (PASP), polyepoxy succinic acid (PESA), and hydrolyzed polymaleic (HPMA) were used as dispersants to disperse the chalcopyrite and serpentine particles. The micro-flotation experiments demonstrated that the application of dispersants in the flotation effectively reduced the negative impact of serpentine over a wide pH range, restoring the recovery rate of chalcopyrite to about 85%. The XPS analysis revealed that the dispersants could be adsorbed onto the mineral surfaces through the binding of carboxyl groups with the magnesium or copper sites. As a result, the surface potentials of serpentine changed from positive to negative, while that of the chalcopyrite became even more negative, resulting in a strong electrostatic repulsion between them, which effectively eliminated the covering of the serpentine on the chalcopyrite surface. The AFM force measurements indicate a weak interaction of the polycarboxylic acids dispersants with the surface of chalcopyrite. Consequently, the adsorption of dispersants on the chalcopyrite surface has an insignificant impact on the subsequent adsorption of collectors, which is further supported by the adhesion force measurements between the air bubble and mineral surfaces. Therefore, the application of polycarboxylic acid dispersants in the flotation significantly enhanced the floatability of chalcopyrite in the presence of the serpentine fines.

NMR Immunosensor Based on a Targeted Gadolinium Nanoprobe for Detecting Salmonella in Milk.

Detecting harmful pathogens in food is not only a crucial aspect of food quality management but also an effective way to ensure public health. In this paper, a complete nuclear magnetic resonance biosensor based on a novel gadolinium (Gd)-targeting molecular probe was developed for the detection of Salmonella in milk. First, streptavidin was conjugated to the activated macromolecular polyaspartic acid (PASP) via an amide reaction to generate SA-PASP. Subsequently, the strong chelating and adsorption properties of PASP toward the lanthanide metal gadolinium ions were exploited to generate the magnetic complex (SA-PASP-Gd). Finally, the magnetic complex was linked to biotinylated antibodies to obtain the bioprobe and achieve the capture of Salmonella. Under optimal experimental conditions, the sensor we have constructed can achieve a rapid detection of Salmonella within 1.5 h, with a detection limit of 7.1 × 103 cfu mL-1.

Synthesis and Performance Evaluation of Modified Polyaspartic-Acid-Based Scale Inhibitor

This paper focuses on the selection and application of scale inhibitor by studying the problem of pipeline scaling in geothermal well development. Adding scale inhibitor can effectively reduce the treatment cost and achieve a good scale resistance effect, but the commonly used polyaspartic acid scale inhibitor has problems such as poor scale inhibition effect and large use limitations. Therefore, a new modified polyaspartic acid scale inhibitor (His-Tyr-SA-PASP) was prepared using polysuccinimide (PSI) as the raw material and histidine (His), tyrosine (Tyr), and sulfonic acid (SA) as the modification reagent. When the dosage of His-Tyr-SA-PASP was 8 mg/L, the scale inhibition rate of CaCO3 was 94.40%. In addition, the scale inhibition effect of His-Tyr-SA-PASP on CaCO3 was better than that of PASP. At the same time, under the condition of a static experiment at 75 °C, according to the ion concentration of water samples in different scale zones, this paper also identified the ratio of four composite scale inhibitors. When the dosage of compound scale inhibitor was 100 mg/L, Sodium of Polyaspartic Acid–Diethylene Triamine Penta (Methylene Phosphonic Acid)–2-Phosphonobutane-1,2,4-Tricarboxylic Acid–Amino Trimethylene Phosphonic Acid–Copolymer of Maleic and Acrylic Acid = (10:10:5:1:9), (15:10:5:2.5:2.5), (12.5:5:10:1:6.5), and (15:5:10:4:1) and the scale inhibition rate was more than 95%. Under the condition of a dynamic experiment, the optimized composite scale inhibitor still showed a scale inhibition rate of more than 90%. It provides a useful reference for the practical application of water treatment in geothermal wells and has the prospect of industrial application.

Enhancing cell cryopreservation with acidic polyamino acids integrated liquid marbles

Cryopreservation is highly desired for long-term maintenance of the viability of living biosamples, while effective cell cryopreservation still relies heavily on the addition of dimethyl sulfoxide (DMSO) and fetal bovine serum (FBS). However, the intrinsic toxicity of DMSO is still a bottleneck, which could not only cause the clinical side effect but also induce cell genetic variants. In the meantime, the addition of FBS may bring potentially the risk of pathogenic microorganism contamination. The liquid marbles (LMs), a novel biotechnology tool for cell cryopreservation, which not only have a small volume system that facilitated recovery, but the hydrophobic shell also resisted the harm to cells caused by adverse environments. Previous LM-based cell cryopreservation relied heavily on the addition of FBS. In this work, we introduced acidic polyaspartic acid and polyglutamic acid as cryoprotectants to construct LM systems. LMs could burst in an instant to facilitate and achieve ultrarapid recovery process, and the hydrophilic carboxyl groups of the cryoprotectants could form hydrogen bonds with water molecules and further inhibit ice growth/formation to protect cells from cryoinjuries. The L929 cells could be well cryopreserved by acidic polyamino acid-based LMs. This new biotechnology platform is expected to be widely used for cell cryopreservation, which has the potential to propel LMs for the preservation of various functional cells in the future.

Module-combinatorial design and screening of multifunctional polymers based on polyaspartic acid for DNA delivery

It is crucial to develop non-viral gene vectors that can efficiently and safely transfect plasmid DNA into cells. Low transfection efficiency and high cytotoxicity of cationic polymers hinder their application as gene carriers. Modification of cationic polymers has emerged as an attractive strategy for efficient and safe nucleic acids delivery. In this study, a simple and rapid method is developed to synthesize a series of multifunctional polymers by utilizing biodegradable polyaspartic acid as the backbone and modifying it with three modules. This one-component polymer possesses capabilities for nucleic acid condensation, cellular uptake, and endosomal escape. Polymers containing imidazole, triazole, or pyridine group exhibited promising transfection activity. Substituted with dodecylamine or 2-hexyldecan-1-amine enhance cellular uptake and subsequent transfection. Furthermore, the influence of ionizable amine side chains on gene delivery is investigated. Two optimal polymers, combined with the avian encephalomyelitis virus (AEV) plasmid vaccine, induced robust specific antibody responses and cellular immune responses in mice and chickens. Through module-combination design and screening of polyaspartamide polymers, this study presents a paradigm for the development of gene delivery vectors.

A new approach to scale inhibitor detection: Application and analysis of a novel modified membrane enrichment method

Scaling of reverse osmosis (RO) is an important factor affecting its permeability. Various types of scale inhibitors are widely used to reduce scale formation on membrane surfaces. In particular, polyaspartic acid (PASP) is increasingly used due to its environmental benefits. However, efficient detection of PASP during application remains a challenge. Here, we report method for enrichment and determination of PASP using dodecyl dimethyl benzyl ammonium chloride (DDBAC)-modified membranes. The DDBAC-PES membrane detection method improved detection accuracy by 45 % compared to the conventional method. This is due to DDBAC binding to PASP, causing small molecules to combine into larger ones. Additionally, DDBAC reduced the electronegativity of the PES membrane surface, resulting in a PASP retention rate increase from 90 % to 97 %. The experimental result was explained and demonstrated in DFT calculations. The binding energy of DDBAC to PASP was calculated to be −2.774 eV. In addition，the DDBAC-PES membrane maintained good stability of the PASP assay after two months of storage. It also demonstrated the validity and practicality of detection using the new module. Theoretical calculations also give the same results as the experimental ones.

Mechanism of polyaspartic acid as acid-base regulation depressant in reverse flotation separation of molybdenite and talc

The separation of talc and molybdenite through flotation has become a significant issue. The current inorganic and organic depressants demonstrate inadequate selectivity and limited efficacy in both positive flotation and reverse flotation of molybdenite. In this study, the utilization of the highly efficient green agent polyaspartic acid (PASP) as a molybdenite depressant was explored to investigate its pH-dependent acid-base depression mechanism. In the case of pH 4.0, molybdenite exhibited effective depression, talc was floated, PASP was desorbed at pH 10.0, and molybdenite was activated. In this study, the impact of electrostatic force on the adsorption process of PASP and examined the mechanism of PASP on molybdenite surface were studied by means of micro-flotation experiments, zeta potential measurements, analysis of solution chemistry, Fourier Transform Infrared Spectrometer (FT-IR) analysis, Ultraviolet–visible spectroscopy (UV–Vis) study, and X-ray photoelectron spectroscopy (XPS) detections. PASP produced chemisorption through the coordination of O or N atoms lone pair electrons with Mo2+ on the molybdenite surface. In this process, electrostatic repulsion determines whether the mineral can come into contact with PASP.

Selective depression mechanism of polyaspartic acid and calcium oxide on arsenopyrite after copper ions activation and its effect on flotation separation performance

The arsenopyrite activated by copper ions have similar flotation properties to chalcopyrite. Polyaspartic acid (PASP) and calcium oxide (CaO) using as combination depressants for the selective separation of copper-activated arsenopyrite and chalcopyrite were carried out by micro-flotation experiments, contact angle measurements, surface adsorption capacity tests, zeta potential measurements, X-ray photoelectron spectroscopy (XPS) analyses, inductively coupled plasma-optical emission spectrometer (ICP-OES) tests and time-of-flight secondary ion mass spectrometry (ToF-SIMS) analyses, and its depression mechanism was investigated. The results of flotation experiments showed that the recovery of arsenopyrite after addition of the depressants reached only 7.80 %, while the recovery of chalcopyrite reached 94.02 %. The results of contact angles, adsorption capacity tests and zeta potential measurements showed that the PASP-CaO can selectively enhance the hydrophilicity of arsenopyrite surface, but has little effect on the chalcopyrite. XPS analyses and ICP-OES tests further verified that the depressants first eliminated the activation of copper ions and then selectively adsorbed on the surface of arsenopyrite. ToF-SIMS analyses showed that the PASP-CaO would achieve selective depression of arsenopyrite in the form of PASP, PASP-Ca complexes and Ca(OH)+, respectively. Finally, the mechanism diagram of PASP-CaO selectively depressing arsenopyrite was derived. These results will provide an excellent theoretical reference for the flotation separation of copper arsenic sulfide ore.

Polypeptide urea increases rice yield and nitrogen use efficiency through root growth improvement

ContextElucidating rice root growth and development characteristics is essential for improving nitrogen use efficiency (NUE) and grain yield (GY) of crops, particularly in light of innovations such as polyaspartic acid (PASP)–urea formulations. However, the effectiveness of PASP–urea on the morphological properties of rice roots is insufficiently explored. ObjectiveWe aimed to examine the effect of PASP–urea on root morphology properties, NUE, and grain yield of mid-season rice in southwest China. MethodsIn 2016 and 2017, a two-factor randomized block design experiment was conducted in Sichuan, China, during the rice planting season. Three N treatments: no N (control), conventional urea [CU], and polyaspartic acid–urea [PU] were administered to two rice varieties: Yixiangyou 2115 and Fyou 498. ResultsOur findings showed that grain yield and nitrogen recovery efficiency (NRE) of rice were closely related to the root surface area density (RSAD), root length density (RLD), and root volume density (RVD) of rice. Compared to the CU treatment, the PU application significantly boosted the root dry matter weight, RLD, RVD, and RSAD of both varieties by 12.00–16.87 %, 0.16–28.98 %, 12.41–37.06 %, and 8.14–33.66 % at the jointing, heading, and maturity stages, respectively. This contributed to a 0.37–15.63 % and 23.45–48.12 % increase in grain yield and NRE, respectively, in both years, and a 12.26–15.69 % increase in N partial productivity efficiency (NPPE) in 2017 by improving the effective panicle number per unit area, spikelets per panicle, and N uptake. ConclusionNRE and grain yield of rice were significantly increased by PU application by improving the rice root system. ImplicationsThe study findings offer insight on how PASP–urea application influences the root morphology of rice and its relationship with grain yield and NRE while offering novel strategies and concepts for optimizing N use in rice cultivation.

Optimization of preparation conditions and performance of a new degradable soil water retaining agent

Using polyaspartic acid (PAsp) and bentonite (BT) as the main raw materials, a new type of degradable soil water retaining agent (PAsp-AA/BT) was synthesized by microwave radiation. The optimum synthesis conditions and comprehensive properties of PAsp-AA/BT were discussed and the structure and surface characteristics of PAspsp-AA/BT were characterized by FTIR, SEM, XRD and TGA in the paper. The results showed that the optimum synthesis conditions of PAsp-AA/BT were as follows: the dosages of polyaspartic acid (PAsp), bentonite (BT), initiator potassium persulfate, crosslinking agent N,N′-methylene bisacrylamide was 5, 3, 0.3, 0.03%, respectively, the neutralization degree of acrylic acid was 75%, and the microwave power was 490W. Under this condition, the absorption ratio of the synthesized PAspsp-AA/BT in deionized water and 0.9% NaCl solution was 953 and 164 g/g, respectively. The synthesized PAsp-AA/BT had a high water absorption rate, good water retention and repeated water absorption, and the degradation rate in soil within 30 days reached 32.75%, with good degradation effect. The analysis of SEM, FT-IR, XRD and TGA showed that: the surface of PAsp-AA/BT was rough and had obvious pore structure, which was conducive to the diffusion of water molecules; polyaspartic acid, bentonite and acrylic acid were polymerized; the cross-linking structure was formed between polyaspartic acid, bentonite and acrylic acid; the product of PASP-AA/BT had good thermal stability. This study provides a new soil water retaining agent, which is helpful for the better development of soil water retaining agent research.

Polyaspartic acid modified by fluorescent carbon quantum dots as an environmentally friendly scale inhibitor for calcium sulphate

Polysuccinimide (PSI), as the precursor of polyaspartic acid (PASP), can easily react with amino (NH2) groups under mild conditions. A novel scale inhibitor, designed as PASP/N-CDs, is synthesised through the ring-opening reaction of PSI with nitrogen-doped carbon quantum dots (N-CDs). XPS, TEM, FT-IR and Raman spectroscopy are used to analyse the micro structure and spectral characteristics of synthesised inhibitors. The efficiency of PASP/N-CDs in inhibiting calcium sulphate (CaSO4) scale is tested through static scale inhibition experiments. The comparative analysis reveals a significant enhancement in the scaling resistance of PASP/N-CDs over PASP, particularly noticeable at reduced concentrations. The scale inhibition efficiency of PASP/N-CDs reaches nearly 100 % at 5 mg/L. The underlying mechanism of scale inhibition in PASP/N-CDs is investigated using SEM and XRD. It indicates that the PASP/N-CDs inhibits the formation of CaSO4 scale via a combination of chelation, adsorption, and lattice distortion.

Synthesis, scale and corrosion inhibition evaluation and mechanism of 2-aminobenzimidazole modified polyaspartic acid

With the growing public concern for environmental preservation, this work employs environmentally friendly polyaspartic acid (PASP) as the main chain, to develop a green and efficient dual-function inhibitor with scale and corrosion inhibition. The new inhibitor PASP-2-A was synthesized by grafting 2-amino-benzimidazole (2-A) containing nitrogen heterocyclic into polysuccinimide under alkaline conditions. The corrosion inhibition of carbon steel and brass was determined by static test, polarization curve and electrochemical impedance spectroscopy (EIS). It can be found that PASP-2-A had better scale inhibition performance than PASP under different conditions. The addition of 5 mg·L−1 PASP-2-A can almost 100% prevent the formation of CaCO3 scale. Molecular dynamics simulation results showed that PASP-2-A significantly destroys the crystal structure of CaCO3 scale due to the coordination between PASP-2-A and Ca2+ groups. The modified PASP scale inhibitor can prevent the growth of calcite (110) and (104) crystal faces, regulate the transformation of CaCO3 from stable calcite to more soluble spherical vaterite, making it less deposit. The electrochemical test results showed that the corrosion inhibition of PASP-2-A is greatly improved compared with PASP, and the corrosion inhibition of Q235 carbon steel increased about 40% at the dosage of 200 ppm. The corrosion inhibition efficiency of H62 brass in 3.5 wt% NaCl was 97.97% with 300 ppm PASP-2-A. Notably, due to its degradable nature, low toxicity, and affordability, PASP-2-A serves as an excellent inhibitor, exhibiting remarkable performance in both scale inhibition and corrosion inhibition. Consequently, it presents a promising avenue for further advancements in modified PASP.

The development of high‐strength, anticorrosive, and strongly adhesive polyaspartate polyurea coating suitable for pipeline spray repairs

AbstractThis study synthesized polydimethylsiloxane (PDMS)‐modified polyaspartate polyurea (PPPU) with different ratios, considering the practical performance requirements of underground water supply pipeline spray repair materials. The successful synthesis of PPPU was confirmed using Fourier transform infrared spectrometer (FTIR) spectroscopy. The influence of the ratio of the two components and the content of ‐aminopropyl terminated polydimethylsiloxane (APT‐PDMS) on the drying time and tensile performance of PPPU coatings was evaluated. Based on this evaluation, a superior ratio for PPPU coatings was proposed. Subsequently, the bonding performance, hydrophobicity, and corrosion resistance of PPPU coatings at the superior ratio were tested. The results indicate that as the mass ratio of polyaspartic acid ester to hexamethylene diisocyanate trimer increases, both the drying time and tensile strength of the coating decrease. The addition of APT‐PDMS results in a decrease in the tensile strength of PPPU, but an increase in its elongation at break. The peak value of elongation at break is achieved when the APT‐PDMS content is 5%, making the PPPU2‐1‐5 coating the superior ratio for spray application on water supply pipelines. Through experiments, it was determined that the bonding strength of the PPPU2‐1‐5 coating with cement mortar under dry and humid conditions, static water contact angle (93.4°), and corrosion resistance performance are superior to those of the unmodified polyurea coating, demonstrating its application advantages. The conclusions drawn in this study provide a theoretical foundation for the practical engineering application of PPPU.

Biopolymer Meets Nanoclay: Rational Fabrication of Superb Adsorption Beads from Green Precursors for Efficient Capture of Pb(II) and Dyes.

Renewable, green, and safe natural biopolymer-derived materials are highly desired for the purification of pollutants, but significantly improving their performance without the introduction of additional harmful chemicals remains a huge challenge. Based on the concept of "structure optimization design", environment-friendly composite beads (named SA/PASP/RE) with excellent adsorption performance and recyclability were rationally constructed through a green ionic crosslinking route, using the completely green biopolymer sodium alginate (SA), sodium salt of polyaspartic acid (PASP), and the natural nanoclay rectorite (RE) as starting materials. The nano-layered RE was embedded in the polymer matrix to prevent the polymer chain from becoming over-entangled so that more adsorption sites inside the polymer network were exposed, which effectively improved the mass transfer efficiency of the adsorbent and the removal rate of contaminants. The composite beads embedded with 0.6% RE showed high adsorption capacities of 211.78, 197.13, and 195.69 mg/g for Pb(II) and 643.00, 577.80, and 567.10 mg/g for methylene blue (MB) in Yellow River water, Yangtze River water, and tap water, respectively. And the beads embedded with 43% RE could efficiently adsorb Pb(II) and MB with high capacities of 187.78 mg/g and 586.46 mg/g, respectively. This study provides a new route to design and develop a green, cost-effective, and efficient adsorbent for the decontamination of wastewater.

Monodisperse Polyaspartic Acid Derivative Microspheres for Potential Tumor Embolization Therapy.

Polyaspartic acid derivatives are a well-known kind of polypeptide with good biocompatibility and biodegradability, and thus have been widely used as biomedical materials, including drug-loaded nano-scale micelles or macroscopic hydrogels. In this work, for the first time, monodisperse polyaspartic acid derivative microspheres with diameter ranging from 120 to 350µm for potential tumor embolization therapy are successfully prepared by single emulsion droplet microfluidic technique. The obtained microsphere shows fast cationic anticancer drug doxorubicin hydrochloride loading kinetics with high loading capacity, which is much better than those of the commercial ones. Additionally, drug release behaviors of the drug-loaded microspheres with different diameters in different media are also studied and discussed in detail. These results provide some new insights for the preparation and potential application of polyaspartic acid derivative-based monodisperse microspheres, especially for their potential application as embolic agent.