Effect of incubation temperature on identification of key odorants of sewage sludge using headspace GC analysis.

Currently, headspace gas chromatography-mass spectrometry is a widely used method to identify the key odorants of sludge. However, the effect of incubation temperature on the generation and emission of key odorants from sludge was still uncertain. Thus, in this paper, headspace solid-phase microextraction gas chromatography-mass spectrometry (HS-SPME-GC-MS) and headspace gas chromatography-coupled ion mobility spectrometry (HS-GC-IMS) were carried out to analyze the volatiles emitted from the sludge incubated at different temperatures (30 °C, 50 °C, 60 °C, and 80 °C). The results indicated that the total volatile concentration of the sludge increased with temperatures, which affected the identified proportion of sludge key odorants to a certain extent. Differently from the aqueous solutions, the variation of volatile emission from the sludge was inconsistent with temperature changes, suggesting a multifactorial influence of incubation temperature on the identification of sludge odorants. The microbial community structure and adenosine triphosphate (ATP) metabolic activity of the sludge samples were analyzed at the initial state, 30 °C, and 80 °C. Although no significant effect of incubation temperature on the microbial community structure of the sludge, the incubation at 80 °C led to a noticeable decrease in microbial ATP metabolic activity, accompanied by a significant change in the proportion of odor-related microorganisms with low relative abundances. Changes in the composition and activity of these communities jointly contributed to the differences in odor emission from sludge at different temperatures. In summary, the incubation temperature affects the production and emission of volatiles from sludge through physicochemical and biochemical mechanisms, by which the microbial metabolism playing a crucial role. Therefore, when analyzing the key odorants of sludge, these factors should be considered.

Aggregation and construction mechanisms of microbial extracellular polymeric substances with the presence of different multivalent cations: Molecular dynamic simulation and experimental verification.

Interactions between cations and extracellular polymeric substances (EPS) play an important role in the formation of microbial aggregates and have key effects on the physical properties of activated sludge across wastewater and sludge treatment process. Here, a molecular model of EPS cluster in activated sludge was constructed and simulated by molecular dynamics (MD) to probe the structural properties of EPS and the interaction between EPS and prevalent multivalent cations (Ca2+, Mg2+, Al3+). Then the predicted changes in physical properties were validated against the dynamic light scattering, XAD resin fractionation and rheology test. The binding dynamics and interactions mechanisms between multivalent cations and EPS functional groups were further investigated using MD in combination with spectroscopic analysis. Results suggest that biopolymers are originally aggregated by electrostatic and intermolecular interactions forming dynamic clusters with negatively charged surface functional groups, which induced electrostatic repulsion preventing further agglomeration of biopolymer clusters. In the presence of multivalent cations, surface polar functional groups in biopolymers are connected, causing the rearrangement of EPS molecular conformation that forms larger and denser agglomerates. Reduced solvent accessible surface area, enhanced hydrophobicity, and increased binding free energy lead to a strong gel-like network of EPS. Ca2+ and Al3+ predominantly interact with functional groups in polysaccharides, promoting agglomeration of macromolecules. In contrast, Mg2+ and Al3+ disrupted the secondary structure of proteins, exposing hydrophobic interaction sites. Al3+ can better agglomerate biopolymers with its higher positive charge and shorter coordination distance as compared to Ca2+ and Mg2+, but compromised by the effect of hydration. This work offers a novel approach to explore the construction and molecular aggregation of EPS, enriching the theoretical basis for optimization of wastewater and sludge treatment.

Occurrence and influencing factors of antibiotics and antibiotic resistance genes in sediments of the largest multi-habitat lakes in Northern China.

Baiyangdian Lake is a typical and largest multi-habitat lake in the North plain of China. To understand the generation and transmission of antibiotics resistance genes (ARGs) in multi-habitat lakes, the contents of nutrients (TC, TOC, TN, TP and TS), heavy metals (Zn, Cr, Ni, Cu, Pb, As, Cd and Hg), 22 antibiotics, 16S-rRNA(16S), Class I integron (intI1) and 20 ARGs were determined. Samples were taken from the Fuhe river, river estuaries, reed marshes, living area, fish ponds and open water of Baiyangdian Lake. The results showed that quinolones were the main pollutants in six habitats, and the content range was ND-104.94 ng/g. Thereinto, aac (6') -IB, blaTEM-1, ermF, qnrA, qnrD, tetG, sul1, sul2 and tetM were detected in all the analyzed samples. The absolute abundance of sul1 was the highest (5.25 × 105 copies/g-6.21 × 107 copies/g) in most of the samples. In these different habitats, the abundance of antibiotics and ARGs in river estuary was the highest, and that in reed marshes was the lowest. There was a significant positive correlation between the abundance of heavy metals (Cu, Pb, Zn, Ni, Cd, Hg) and the absolute abundance of 11 ARGs (P < 0.01). Redundancy analysis showed that Cu, Zn, intI1, TP and macrolides were the important factors affecting the distribution of ARGs. Our finding provides a more likely driving and influencing factor for the transmission of ARGs in lakes with complex and diverse habitats.

Constructing novel hyper-crosslinked conjugated polymers through molecular expansion for enhanced gas adsorption performance.

The porous organic polymers have been considered as effective materials for gas storage and adsorption. Herein, we synthesized highly crystalline nitrogen-rich covalent triazine frameworks (CTFs) by polycondensation for preparing the novel hyper-cross-linked conjugated polymers (HCCPs) with tunable specific surface area and pore volume through coupling Friedel-Crafts reaction, in which 1,4-Bis(chloromethyl)benzene and 4,4-Bis(chloromethyl)biphenyl as the expansion molecules were pillared between the layers of CTF-HUST. This technology not only increased the specific surface area and total pore volume of CTF-HUST by 2.56 and 4.68 times, but also greatly enhanced the utilization of adsorption sites of CTF-HUST. The HCCP2-1.25 exhibited the highest surface area (1349.29 m2g-1) among these HCCPs and demonstrated excellent adsorption performance for ethyl acetate (1605.14 mg/g), ethanol (1371.49 mg/g), 1,2-Dichloroethane (1971.68 mg/g), benzene (1151.77 mg/g) and toluene (1024.28 mg/g) due to the multiple C-H…O, C-H…Cl, O-H…N and C-H…π interactions between volatile organic compounds (VOCs) and HCCPs framework. Moreover, CO2 and H2 storage capacities of the HCCP2-1.25 were 8.02 wt% and 1.54 wt%, 1.66 and 1.67 times higher than CTF-HUST, respectively. This study developed a simple and effective molecular expansion strategy to synthesize a series of novel high-surface-area porous polymers for potential applications in the environmental field.

[Distribution Characteristics and Risk Assessment of Antibiotics and Polycyclic Aromatic Hydrocarbons in the Sediments of Desilting Demonstration Area in Baiyangdian Lake].

A total of 22 antibiotics and 16 polycyclic aromatic hydrocarbons(PAHs) in sediments before and after desilting in typical areas(fish ponds and open water) of Baiyangdian Lake were analyzed using HPLC-MS/MS and GC/MS(high performance liquid chromatography and gas chromatography coupled with mass spectrometry), to evaluate their potentially risks to the ecological environment. The results showed that the contents of 22 antibiotics in Baiyangdian Lake sediments ranged from 0 to 52.89 ng·g-1, in which the quinolones content was the highest. After dredging treatment, the average content of antibiotics in Nanliuzhuang open water area decreased from 46.25 ng·g-1 to 9 ng·g-1(80.54% reduction), while the average content of antibiotic(19.07 ng·g-1) in Caiputai remained relatively stable. Therefore, the dredging treatment performed better in removing antibiotics from Naliuzhuang area. The total contents of 16 PAHs in sediments ranged from 23.79 ng·g-1 to 329.40 ng·g-1, in which Naphthalene was the highest(242.02 ng·g-1), while Fluoranthene was the lowest. The average content of PAHs in sediments in Nanliuzhuang decreased from 117.45 ng·g-1 to 50.49 ng·g-1 after dredging, while PAHs in Caiputai(57.98 ng·g-1) remained stable; the 57.01% reduction in PAHs in Nanliuzhuang open water indicated that dredging treatment exhibited stronger effects on PAHs variations in Nanliuzhuang compared to that of Caiputai. In addition, the ecological risk assessment showed that the risk of Enrofloxacin and Norfloxacin was high in area S2 of Nanliuzhuang open water, while PAHs exhibited relatively low ecological risk, in which the Naphthalene in area S1 of Fuhe river posed medium ecological risk while the remaining produced low ecological risks. The results indicated that quinolone antibiotics in sediments of the un-dredged area of Baiyangdian Lake should be monitored due to its higher ecological risk.

Understanding synergistic mechanisms of ferrous iron activated sulfite oxidation and organic polymer flocculation for enhancing wastewater sludge dewaterability.

The bound water in waste activated sludge (WAS) is trapped in extracellular polymeric substances (EPS) in the form of gel-like structure, leading to a great challenge in the sludge deep dewatering. Traditional flocculation conditioning is unable to destroy EPS and ineffective to remove the bound water in WAS. In this study, we employed integration of Fe(II)-sulfite oxidation and polyacrylamide flocculation (F/S-PAM) treatment for removing the bound water and improving sludge dewaterability under aerobic conditions. Meanwhile, the floc microstructure and EPS properties were examined to understand the mechanisms of F/S-PAM conditioning. F/S produced SO3·- radicals which could decompose the EPS in sludge, releasing bound water into free water. In addition, the formed Fe(III) from F/S led to re-coagulation of decomposed EPS, and C=O groups of tryptophan played the leading role in Fe-EPS association binding, causing transformation of the secondary structure of proteins (especially ß-sheets and α-helices). Then, the introduction of PAM caused re-flocculation of disintegrated sludge flocs, enhancing the sludge filterability. This work provides a novel and cost-effective method for efficient removal of bound water in sludge, and subsequence improvement in sludge dewaterability.

Facile synthesis of graphene-based hyper-cross-linked porous carbon composite with superior adsorption capability for chlorophenols.

In this work, we proposed a green and cost-effective method to prepare a graphene-based hyper-cross-linked porous carbon composite (GN/HCPC) by one-pot carbonization of hyper-cross-linked polymer (HCP) and glucose. The composite combined the advantages of graphene (GN) and hyper-cross-linked porous carbon (HCPC), leading to high specific surface area (396.93 m2/g) and large total pore volume (0.413 cm3/g). The resulting GN/HCPC composite was applied as an adsorbent to remove 2,4-dichlorophenol (2,4-DCP) from aqueous solutions. The influence of different solution conditions including pH, ionic strength, contact time, system temperature and concentration of humic acid was determined. The maximum adsorption capacity of GN/HCPC composite (calculated by the Langmuir model) could reach 348.43 mg/g, which represented increases of 43.6% and 13.6% over those of the as-prepared pure GN and HCPC, respectively. The Langmuir model and pseudo-second-order kinetic model were found to fit well with the adsorption process. Thermodynamic experiments suggested that the adsorption proceeded spontaneously and endothermically. In addition, the GN/HCPC composite showed high adsorption performance toward other organic contaminants including tetracycline, bisphenol A and phenol. Measurement of the adsorption capability of GN/HCPC in secondary effluent revealed a slight decrease over that in pure water solution. This study demonstrated that the GN/HCPC composite can be utilized as a practical and efficient adsorbent for the removal of organic contaminants in wastewater.

Profiling and characterization of odorous volatile compounds from the industrial fermentation of erythromycin.

Complaints caused by odors from the fermentation production of pharmaceuticals are common in China. The elimination of odor remains a challenge for the pharmaceutical industry to meet the increasingly strict environment regulations. Erythromycin is a representative antibiotic produced by microbial fermentation. The fermentation exhaust gas of erythromycin fermentation has an unpleasant odor, but the composition of the key odorants has not been identified. The major odorants from the fermentation production of erythromycin API were analyzed by electronic nose, olfactory measurements, gas chromatography-coupled ion mobility spectrometry (GC-IMS) and gas chromatography-mass spectrometry (GC-MS) analysis. Two compounds, 2-methylisoborneol (2-MIB) and geosmin, were identified as the major odorants of erythromycin fermentation. These had not been detected before using only GC-MS analysis of exhaust gas. Aldehydes, including hexanal, octanal, decanal, and benzaldehyde, also contribute to the odor. The composition analysis of odorants using the fermentation broth headspace was more efficient and reliable, considering the significant dilution effect of exhaust gas. The concentration of 2-MIB and geosmin in the fermentation broth greatly exceeded their odor thresholds. The production of major odorants started in the early fermentation stage and became significant in the middle stage (30-70 h). Due to the extremely low odor thresholds of 2-MIB and geosmin, advanced purification may require deodorization of erythromycin fermentation exhaust gas.

Catalytic pyrolysis coupling to enhanced dewatering of waste activated sludge using KMnO4Fe(II) conditioning for preparing multi-functional material to treat groundwater containing combined pollutants.

Sewage sludge, the major by-product during the primary treatment and subsequent biotreatment of wastewater, is increasingly generated around the world. KMnO4Fe(II) consists both oxidation properties of KMnO4 and flocculation ability by in-situ formed Fe(III) and is widely used in water treatment. In this study, KMnO4Fe(II) was used as chemical conditioners to synchronously improve sludge dewatering performance and catalyze the biomass pyrolysis of waste activated sludge for preparing multi-functional material to remedy arsenic containing groundwater. The results showed that the sludge dewaterability was significantly improved due to the moderate pre-oxidation of extracellular polymeric substances by KMnO4, and then the sludge particles were re-flocculated by Fe(III) generated from KMnO4Fe(II). The conditioned sludge cake was then utilized for preparing sludge-based carbon (Fe-Mn-SBC) which was systematically characterized. The surface area of Fe-Mn-SBC was characteristic of high surface area (100.08 m2/g) which had a great adsorption capacity on arsenic. Besides, Fe-Mn-SBC could effectively oxidize As(III) to As(V), and addition of low dose of H2O2 can further improve total arsenic removal due to catalytic peroxidation of Fe-Mn-SBC. Besides, it was found that the presence of humic acid could inhibit the hydroxy iron formation and compete for the active adsorption sites and then resulted in the decrease in arsenic removal, and the co-existing humic acid could also be removed by adsorption of Fe-Mn-SBC. This work proposed a novel sludge treatment process by combining enhanced sludge dewatering with catalytic pyrolysis for preparing multi-functional materials, and they are promising in treatment of water containing combined pollutants.

Cu(I)-doped Fe3O4 nanoparticles/porous C composite for enhanced H2O2 oxidation of carbamazepine.

Cu(I) doped nano-Fe3O4 were synthesized and loaded on ordered porous carbon materials using a facile co-precipitated. The synthesized catalysts were characterized by XRD, XPS, HRTEM, FESEM-EDX mapping and N2 adsorption-desorption. The results showed that the crystal unit cell of Fe3O4 was enlarged due to the implantation of small amount of Cu(I) into the Fe3O4 structure (Fe2.85Cu0.15O4). With increased Cu content, the catalyst was dominated with Cu2O and the Fe3O4 phase disappeared, the catalytic performance of Fe-Cu bimetal oxide became worse. The Cu(I)-Fe3O4/C composite was enriched with Fe(II), Fe(III) and Cu(I) sites. The prepared Cu-Fe bimetal oxide/C composite exhibited higher specific TOF and oxidation efficiency E on carbamazepine oxidation than Fe2.85Cu0.15O4 and Fe3O4. The enhanced catalytic reactivity was attributed to the synergetic effect of surface Fe and Cu species on the H2O2 activation. The dissolved metals induced catalytic reaction at pH 4.5-8.1 was ignorable. Thus, the catalytic decomposition of H2O2 by Cu-Fe3O4/C at near neutral pH was controlled by interface reactions. The CBZ in the close proximity to the interface was attacked by the generated ROS and formed urea, 2-hydroxybenzyl alcohol and other oxidative products.

One-step preparation of polyimide-inlaid amine-rich porous organic block copolymer for efficient removal of chlorophenols from aqueous solution.

A novel polyimide-inlaid amine-rich porous organic block copolymer (PI-b-ARPOP) was prepared via one-step polymerization by using different molar ratios of melamine (MA)/terephthalaldehyde (TA)/pyromellitic dianhydride (PMDA), at molar ratios of 4/3/1, 4/2/2 and 4/1/3. The copolymer contained both aminal groups belonging to ARPOP and imide groups belonging to PI, and the bonding styles of the monomers and growth orientations of the polymeric chains were diversiform, forming an excellent porous structure. Notably, MA/TA/PMDA (4/2/2) had a surface area and pore volume of 487.27 m2/g and 1.169 cm3/g, respectively. The adsorption performance of the materials towards 2,4-dichlorophenol (2,4-DCP) in ultra-pure water was systematically studied. The pH value of 7 was optimal in aqueous solution. Na+ and Cl- ions did not negatively affect the adsorption process, while humic acid (HA) slightly decreased the capacity. The equilibrium time was 40 sec, and the maximum adsorption capacity reached 282.49 mg/g at 298 K. The removal process was endothermic and spontaneous, and the copolymer could maintain its porous structure and consistent performance after regeneration by treatment with alkali. Moreover, to further assess the practical applicability of the material, the adsorption performance towards 2,4-DCP in river water was also investigated. This paper demonstrated that the PI-b-ARPOP can be an efficient and practical adsorbent to remove chlorophenols from aqueous solution.

A novel waste activated sludge multistage utilization strategy for preparing carbon-based Fenton-like catalysts: Catalytic performance assessment and micro-interfacial mechanisms.

Waste activated sludge (WAS) contains many anionic functional groups which can interact with heavy metal ions through electrostatic action and complexation reactions. The transition metals adsorbed in WAS can catalyze sludge pyrolysis in anaerobic conditions and improve structural properties of organic matter. In this work, a multistage WAS utilization process for preparing the carbon-based Fenton-like catalysis materials is proposed. More specifically, WAS is firstly used as an adsorbent for heavy metals (Cu and Ni) removal, and then complexes are converted into heterogeneous Fenton-like carbon-based catalysts through oxygen-free pyrolysis. The mechanisms of interactions between extracellular polymeric substances (EPS) and metals are investigated, and the physicochemical properties of sludge-based carbons (SBC) are comprehensively characterized using varies techniques. It is found that WAS is an excellent adsorbent for Cu and Ni removal, which is mainly due to the coordination and electrostatic interactions between EPS and heavy metals. Cu and Ni adsorbed in WAS significantly improved the porous structure of SBC. Both adsorption and catalytic oxidization of Cu/Ni-SBC contribute the removal of E2 in real wastewater. The E2 removal mechanism is explored by electron-spin resonance spectroscopy (ESR) analysis, and it is found that both of .O2- and .OH radicals are responsible for E2 degradation in Cu(II)-SBC-H2O2, while .O2- radicals contributes to E2 degradation in Ni(II)-SBC-H2O2 system, so the former performed better than the latter in total removal of E2. Besides, Cu(II) and Cu(I) are both formed in Cu(II)-SBC during the oxidation process, while only Ni(II) is found in the Ni(II)-SBC-H2O2 process, confirming that different catalytic oxidation reactions are occurred in the Cu(II)-SBC-H2O2 and Ni(II)-SBC-H2O2 processes. This study facilitates a great strategy to the sludge multi-stage circulating utilization and a better understanding about the role of the Cu/Ni existed in SBC during the estrogens removal process.

NH2Fe3O4@SiO2 supported peroxidase catalyzed H2O2 for degradation of endocrine disrupter from aqueous solution: Roles of active radicals and NOMs.

In this work, magnetic Fe3O4 was utilized to immobilize horseradish peroxidase (IM-HRP) in order to improve its stability and reusability by crosslinking method process with glutaraldehyde. The physicochemical properties of NH2Fe3O4@SiO2 and IM-HRP were characterized by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Thermo-gravimetric Analysis (TGA) and Transmission electron microscopy (TEM). The thermal stability of immobilized-HRP was considerably improved in comparison with free counterpart. The catalytic performance of IM-HRP for estrogens removal from aqueous solution was evaluated, it was found that the presence of natural organic matters (NOM) have no significant effects on E2 removal and the E2 enzyme-degradation reached around 80% when pH = 7.0 with 0.552 × 10-3 ratio of IM-HRP/H2O2. In addition, the active radicals responsible for estrogens degradation were identified with electro-spin resonance spectra (ESR). It was found that immobilization process on Fe3O4 showed no adverse effects on catalytic performance on HRP, estrogens degradation could be fitted well with pseudo-second kinetic equation. Estrogens degradation efficiency was reduced in the presence of humic substances. Both O2- and OH were detected in IM-HRP catalyzed H2O2 system and radicals quenching test indicated O2- played a more important role in estrogens removal. IM-HRP exhibited excellent stability and E2 removal efficiency could reach 45.41% after use seven times. Therefore, HRP enzymes immobilized on NH2Fe3O4@SiO2 by cross-linking method in glutaraldehyde solutions was an effective way to improve stability and reusability of HRP, and which could avoid potential secondary pollution in water environment caused by free HRP after treatment.

Transfer behavior of odorous pollutants in wastewater sludge system under typical chemical conditioning processes for dewaterability enhancement.

Chemical conditioning has been used for enhancing wastewater sludge dewaterability for many years, but the characteristics of odorous pollutants emission in sludge conditioning were still unclear. In this work, the transfer behavior of different odorous pollutants between air, liquid and solid phases under typical chemical conditioning processes for high-pressure dewatering was systematically investigated. The results indicated that that besides hydrogen sulfide (H2S) and ammonia (NH3), 21 kinds of volatile organic contaminants (VOCs) were identified and quantified by gas chromatography-mass spectrometry (GC-MS), while the concentrations and composition of odorous pollutants varied greatly for different conditioning processes. VOCs were composed by three main constituents including benzenes, halogeno benzene and hydrocarbons. According to mass balance analysis, about 50% of VOCs adsorbed within sludge extracellular polymeric substances (EPS) fraction. Since EPS was damaged and/or flocculation in different chemical conditioning processes, VOCs distributed in solid phase transformed into liquid phase and then released into air. The discrepancies in mass of odorous pollutants before and after chemical conditioning were likely to be related to chemical conversion under acidification, oxidation and precipitation in the presence of ferric ions.

Association of 17-ß Estradiol with Adipose-Derived Stem Cells: New Strategy to Produce Functional Myogenic Differentiated Cells with a Nano-Scaffold for Tissue Engineering.

The increased incidence of stress urinary incontinence (SUI) in postmenopausal women has been proposed to be associated with a reduction in the level of 17-ß estradiol (E2). E2 has also been shown to enhance the multi-differentiation ability of adipose-derived stem cells (ASCs) in vitro. However, studies on the potential value of E2 for tissue engineering in SUI treatment are rare. In the present study, we successfully fabricated myogenically differentiated ASCs (MD-ASCs), which were seeded onto a Poly(l-lactide)/Poly(e-caprolactone) electrospinning nano-scaffold, and incorporated E2 into the system, with the aim of improving the proliferation and myogenic differentiation of ASCs. ASCs were collected from the inguinal subcutaneous fat of rats. The proliferation and myogenic differentiation of ASCs, as well as the nano-scaffold biocompatibility of MD-ASCs, with or without E2 supplementation, were investigated. We demonstrated that E2 incorporation enhanced the proliferation of ASCs in vitro, and the most optimal concentration was 10-9 M. E2 also led to modulation of the MD-ASCs phenotype toward a concentrated type with smooth muscle-inductive medium. The expression of early (alpha-smooth muscle actin), mid (calponin), and late-stage (myosin heavy chain) contractile markers in MD-ASCs was enhanced by E2 during the different differentiation stages. Furthermore, the nano-scaffold was biocompatible with MD-ASCs, and cell proliferation was significantly enhanced by E2. Taken together, these results demonstrate that E2 can enhance the proliferation and myogenic differentiation of ASCs and can be used to construct a biocompatible cell/nano-scaffold. These scaffolds with desirable differentiation cells show promising applications for tissue engineering.

Electrospun poly(L-lactide)/poly(ε-caprolactone) blend nanofibrous scaffold: characterization and biocompatibility with human adipose-derived stem cells.

The essence of tissue engineering is the fabrication of autologous cells or induced stem cells in naturally derived or synthetic scaffolds to form specific tissues. Polymer is thought as an appealing source of cell-seeded scaffold owing to the diversity of its physicochemical property and can be electrospun into nano-size to mimic natural structure. Poly (L-lactic acid) (PLLA) and poly (ε-caprolactone) (PCL) are both excellent aliphatic polyester with almost "opposite" characteristics. The controlling combination of PLLA and PCL provides varying properties and makes diverse applications. Compared with the copolymers of the same components, PLLA/PCL blend demonstrates its potential in regenerative medicine as a simple, efficient and scalable alternative. In this study, we electrospun PLLA/PCL blends of different weight ratios into nanofibrous scaffolds (NFS) and their properties were detected including morphology, porosity, degradation, ATR-FTIR analysis, stress-stain assay, and inflammatory reaction. To explore the biocompatibility of the NFS we synthesized, human adipose-derived stem cells (hASCs) were used to evaluate proliferation, attachment, viability and multi-lineage differentiation. In conclusion, the electrospun PLLA/PCL blend nanofibrous scaffold with the indicated weight ratios all supported hASCs well. However, the NFS of 1/1 weight ratio showed better properties and cellular responses in all assessments, implying it a biocompatible scaffold for tissue engineering.