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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Bacterial spore with high tolerance to concentrated acid and nuclear radiation for uranium recovery from nuclear wastewater

Zhuoya Hao,Jiacheng Zhang,Qin Peng,Xuefeng Tian,Jun Zhang,Jiayi Ai,Qiqi Jia,Yihui Yuan,Ning Wang

The increasing global reliance on nuclear energy highlights the critical need for uranium recovery from nuclear wastewater. However, due to the harsh environment of concentrated acid and nuclear radiation, the development of new adsorbent for uranium recovery from nuclear wastewater is highly needed. The bacterial spore has been reported to exhibit high tolerance to these harsh environments and contain functional components with reliable uranium binding ability, while there is still no report on the use of bacterial spore for uranium recovery from nuclear wastewater. Herein, the potential of the bacterial spore for being used in uranium recovery was analyzed for the first time. The result shows that the bacterial spore realizes a high uranium adsorption capacity of 245 mg g −1 in uranium-containing aqueous environment. With a low dosage of 0.1 g L −1 , the bacterial spore achieves a high uranium removal performance of 99.03 % in simulated nuclear wastewater. Additionally, when the concentration of HNO 3 reached 12 M, the adsorption capacity can still reach 156 mg g −1 after 24 h of treatment, proving its high tolerance to concentrated acid. Moreover, after being irradiated by γ-ray with the radiation dosage of 500 kGy, the bacterial spore retains 95.94 % of the uranium adsorption capacity, indicating its high resistance to nuclear radiation. These findings indicate that the bacterial spore would be a highly potential adsorbent for the recovery of uranium from nuclear wastewater with concentrated acid and nuclear radiation.

CAS / MDL: 60-00-4 7631-99-4
研究领域: 环境科学 · 微生物学
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JOURNAL OF MEMBRANE SCIENCE · 2023 · IF 9.5

Chlorine resistant polyamide desalination membrane prepared via organic-organic interfacial polymerization

Yiman He,Yuping Zhang,Fan Liang,Yuzhang Zhu,Jian Jin

Desalination of seawater, brackish water and urban sewage is an important way to solve the global water shortage. Polyamide (PA) membranes, including reverse osmosis (RO) membrane and nanofiltration (NF) membrane, are the primary technology for seawater desalination and clean water production. However, traditional thin-film composite PA (TFC-PA) membranes prepared from interfacial polymerization (IP) of amine monomers (either piperazine or m-phenylenediamine) in water and acyl chloride monomers in organic solvent are incapable of tolerating strong acid and chlorine environment. Here, we develop a new IP process, which takes place at the immiscible interface between dimethylacetamide (DMAc) and hexane (referred to as organic/organic IP), to prepare both chlorine-resistant and acid-resistant TFC-PA membranes. Compared to conventional water/oil IP process, the organic/organic IP process can adapt more kinds of amine monomers rather than just PIP, such as tetra (4-aminophenyl) methane (TMAP), tris (4-aminophenyl) amine (TAPA), and 4,4′,4''-(1,3,5-triazine-2,4,6-triyl) triphenylamine (TTA), which we studied in this work, thereby extending the PA molecular structure and enabling the membranes with greatly improved chemical stability. Among them, the TAPM-based TFC-PA membrane exhibits a NaCl rejection of 95.9% and no obvious NaCl rejection deterioration after soaking in a high concentration of NaClO (1000 ppm, pH 7) for more than 30 h, indicating excellent chlorine resistance. The TTA-based TFC-PA membrane shows a Na 2 SO 4 rejection of 97% and remains unchanged after being exposed to a wide pH scan of 2–12. The Organic/organic IP provides a new and easy-to-operate platform for designing chlorine and acid resistant TFC-PA membranes, which will greatly improve their environmental stability as the most advanced desalination membrane at present.

CAS / MDL: 4422-95-1 5981-09-9
研究领域: 材料科学 · 环境工程 · 化学工程
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CARBON · 2015 · IF 6.196

Controllable synthesis of magnetic carbon composites with high porosity and strong acid resistance from hydrochar for efficient removal of organic pollutants: An overlooked influence

Xiangdong Zhu,Feng Qian,Yuchen Liu,Daniel Matera,Gang Wu,Shicheng Zhang,Jianmin Chen

Facile fabrication of magnetic carbon composites (MCs) via pyrolysis of hydrochar in the presence of ZnCl 2 and an iron salt has been attracting enormous interest to simultaneously realize high-surface area and magnetization. During this synthesis, the interactions between the carbon matrix and iron salts have remained unknown. In this work, a closer look was taken on iron salt interactions and their respective effect on MC characteristics. These newly fabricated MCs can provide guidance for further design of efficient MCs. It was discovered that ferric chloride (FeCl 3 ) promoted the enhancement of MC porosity, largely due to the strong reduction reaction between amorphous carbon and iron oxide (γ-Fe 2 O 3 and Fe 3 O 4 ). Various other iron salts (including ferrous oxalate (FeC 2 O 4 ), ferric citrate (FeC 6 H 5 O 7 ), and ferric sulfate (Fe 2 (SO 4 ) 3 ) were also evaluated. These compounds inhibited pore structure development, resulting from decreased carbonization seen in the composite. This phenomenon was observed from complexation reactions between Zn 2+ and the corresponding anions of these salts. Also, high Fe content and low γ-Fe 2 O 3 :Fe 3 O 4 ratios led to decreased acid resistance of the MC. Finally, higher porosity in resultant MCs resulted in larger adsorption capacity for organic pollutants (roxarsone). This study will aid in further optimization of MCs to ultimately maximum performance.

研究领域: 环境科学 · 材料科学
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Journal of Pharmaceutical Investigation · 2017 ·Vol. 48 ·期 3 ·341-350 · IF 0

Esomeprazole magnesium enteric-coated pellet-based tablets with high acid tolerance and good compressibility

Liu Jiang-Yan,Zhang Xiao-Xue,Huang Hao-Yan,Lee Beom-Jin,Cui Jing-Hao,Cao Qing-Ri

The aim of this study was to develop esomeprazole magnesium (EMZ-Mg) enteric-coated pellets and pellet-based tablets, as well as to investigate the effects of pellet size and compression method on acid tolerance, content uniformity, compressibility, and stability of preparations. This study used two types of pellet cores, namely, microcrystalline cellulose (MCC) core with a particle size of 150–300 μm and sucrose core with a particle size of 600–700 μm. Enteric-coated pellets, which consisted of a drug-free core, a drug layer, a sub-coating layer (hydroxypropyl methylcellulose, 6 cps), and an enteric-coating layer (Eudragit ® L30D-55), were prepared by using a bottom-spray fluidized bed-coating technique. Pellet-based tablets were prepared by using a direct compression method or a wet granulation method. The acid tolerances of the two types of enteric-coated pellets (MCC and sucrose cores) reached up to 98% in simulated gastric fluid (pH 1.0) within 2 h, and the dissolution rates in simulated intestinal fluid (pH 6.8) reached up to 85% of the labeled amount within 15 min. When compressed into tablets, the pellets based on MCC core (smaller particle size) displayed a significantly higher acid tolerance (up to 92%) compared with the pellets based on sucrose core (larger particle size). In addition, the MCC core-based tablets (F8), especially those prepared by using a granulation method, showed higher drug content uniformity and compressibility than the sucrose core-based tablets (F10), and no lamination phenomenon was observed during compression. The crystallinity of EMZ-Mg was altered during drug layering process, and some physicochemical interactions were observed between the drug and excipients. Moreover, the two types of enteric-coated pellets showed a relatively high stability after storage under high temperature and strong light. However, they showed poor stability under high humidity, resulting in remarkable degradation of active compound. The EMZ-Mg enteric-coated pellets and pellet-based tablets were successfully developed, and reduction in pellet size and wet granulation reduced the differences in content uniformity and better protected the pellet coating from damages during compression.

CAS / MDL: 9004-65-3 77-93-0
研究领域: 药剂学 · 药物开发
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Catalysis Science & Technology · 2019 ·Vol. 9 ·期 5 ·1108-1116 · IF 5.726

Acid-tolerant intermetallic cobalt–nickel silicides as noble metal-like catalysts for selective hydrogenation of phthalic anhydride to phthalide

Liangliang Zhang,Xiao Chen,Yujing Chen,Zhijian Peng,Changhai Liang

Chemoselective hydrogenation of phthalic anhydride is regarded as the most promising route for producing downstream high-performance phthalide. A series of intermetallic cobalt–nickel silicide catalysts embedded in a carbon matrix (CoxNi2−xSi@C) with acid-tolerance prepared by microwave-assisted chemical vapor deposition have been investigated in this reaction system. Activity measurements show a remarkable positive synergistic effect, forming a volcano-shaped plot over the nominal Co metal fraction for CoxNi2−xSi@C catalysts with a peak at x = 1.5, which corresponds to a 4.5-fold enhancement of the yield of phthalide over Co2Si@C and a 2.0-fold enhancement over the Ni2Si@C monometallic silicide catalysts, which can be correlated with the interaction of cobalt–nickel and metal–silicon bonds. In addition, the cobalt-rich bimetallic silicide exhibits an equal activity to the reference noble metal catalysts (Au, Pd, and Pt) and a significantly higher activity than transition metal catalysts. Moreover, the bimetallic silicide as an intermetallic compound catalyst has demonstrated robust acid corrosion resistance compared to the corresponding metal catalysts.

CAS / MDL: 75-78-5 610-92-4 87-41-2
研究领域: 催化化学 · 材料科学
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JOURNAL OF MOLECULAR LIQUIDS · 2020 · IF 5.065

Efficient adsorption of Cu(II) from aqueous solutions by acid-resistant and recyclable ethylenediamine tetraacetic acid-grafted polyvinyl alcohol/chitosan beads

Wentao He,Qundi Yu,Nan Wang,Xiao-kun Ouyang

Chitosan (CS)—a natural macromolecule—exhibits various limitations, such as difficult recovery, low mechanical strength, and low adsorption capacity. In this work, to address these shortcomings, polyvinyl alcohol (PVA) was mixed into chitosan beads, thereby improving the mechanical strength and acid resistance of CS. Following this, ethylenediamine tetraacetic acid (EDTA) was introduced to the surface of the mixed beads to fabricate PVA-CS-EDTA, a functionalized adsorbent. Series characterization methods are employed to study the surface morphology, chemical groups, and adsorption strengths of the adsorbents. Moreover, the effects of various adsorption conditions on Cu(II) adsorption are studied. According to the results, the adsorption of Cu(II) by the adsorbent beads follows pseudo-second-order kinetics and the Langmuir adsorption isotherm model. The maximum adsorption capacity of PVA-CS-EDTA is 127.81 mg/g, which is substantially higher than that of the CS beads. In addition, the PVA-CS-EDTA beads remain structurally intact even after treatment with an acidic solution (pH = 2). The higher adsorption capacity and acid resistance of the developed CS are promising for wide applications in the field of adsorption.

研究领域: 环境科学 · 材料科学
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Molecular Catalysis · 2023 · IF 4.6

Characterization and mutagenesis of a high-activity and highly substrate-tolerant dipeptidase for L-carnosine biosynthesis via reversed hydrolysis

Bi-Han Guan,Wu-Tong Yin,Bo-Han Cao,Chen Zhao,Jiang Pan,Jian-He Xu

L-Carnosine (L-Car) is a biologically active dipeptide with antioxidant and anti-aging effects, formed by condensation of β-alanine (β-Ala) with L-histidine (L-His), which is used widely in the pharmaceutical and cosmetic industries. Here we report a dipeptide hydrolase originating from Bacillus megaterium , designated as Bm PepD, whose synthetic activity reached 6.5 times that of Sm PepD, which is the highest active dipeptidase reported so far for L-Car biosynthesis in vitro . By site-directed saturation mutagenesis, we obtained a significantly improved variant (T171N) of Bm PepD. It showed a specific activity of 22.9 U mg −1 protein , reaching 1.4 times that of wild-type Bm PepD or 9.1 times that of Sm PepD, which is the highest ever reported among this enzyme class. After optimizing the reaction conditions of variant Bm PepD T171N , we performed the synthetic reaction of L-Car simply from the two free amino acids (0.2 M L-His and 6.5 M β-Ala), achieving a titer of 31.3 mM L-Car with a specific productivity of 283 g Car · g catalyst −1 . This work provides a highly active and substrate (β-alanine)-tolerant dipeptide hydrolase for the facile synthesis of dipeptide L-Car via reversed hydrolysis.

研究领域: 生物化学 · 酶工程 · 合成生物学
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ACS Catalysis · 2024 · IF 11.3

Ultrastable and Phosphoric Acid-Resistant PtRhCu@Pt Oxygen Reduction Electrocatalyst for High-Temperature Polymer Electrolyte Fuel Cells

Zhao An,Huanqiao Li,Xiaoming Zhang,Zhangxun Xia,Hong Zhang,Wenling Chu,Shansheng Yu,Suli Wang,Gongquan Sun

With much enhanced fuel flexibility to overcome the shortcomings of hydrogen production and storage, high-temperature polymer electrolyte membrane fuel cells (HT-PEMFCs) are still facing challenges of activity loss of oxygen reduction electrocatalyst under the working circumstance of phosphoric acid (PA) electrolyte. Dissolution and leaching of metal component of PtM (M = Cu, Co, Ni···) electrocatalysts is one of the key factors that degrade their initial resistance toward PA and hinder the accessing of activity and durability simultaneously. Here, we report an ultradurable PtRhCu@Pt/C electrocatalyst with a high mass activity of 0.90 A mg–1Pt, which only decreased by 14.4% after 30K ADT cycles in the half-cell and reaches the DOE at 2025 target (<30 mV at 0.8 A cm–2) with 27 mV voltage loss at 0.8 A cm–2 in the single-cell. After adding 0.1 M PA into the electrolyte, the half-wave potential of PtRhCu@Pt/C is negatively shifted by only 52 mV, much lower than that of commercial Pt/C (90 mV). Moreover, the HT-PEMFC assembled by this catalyst delivers a preeminent peak power density of 529 and 977 mW cm–2 under H2–air and H2–O2 conditions, respectively. Experiments and theoretical calculations reveal that the ligand effect arising from the sublayer Cu is attributed to the ability of PA resistance, while the self-healing behavior and the synergy between the PtRhCu core and the Pt shell ensures high stability.

研究领域: 材料科学 · 能源科学 · 催化化学
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CHEMOSPHERE · 2022 · IF 8.943

Preparation and application of high-performance and acid-tolerant TiO2/carbon electrocatalytic membrane for organic wastewater treatment

Chen Li,Guoqing Feng,Menghan Sun,Zonglin Pan,Xiaoqing Yan,Xinfei Fan,Chengwen Song,Tonghua Wang

Acidic organic wastewater with toxic and carcinogenic properties has long been a tough problem for industrial treatment. To break down the barrier of poor acidic stability as well as the high cost of materials and reactors, a novel strategy of utilizing a high-performance and acid-tolerant TiO 2 /carbon electrocatalytic membrane (TiO 2 /CEM) for acidic organic wastewater treatment was proposed. Study results showed that high concentrations of organic pollutants were separated and degraded by the synergistic effects of membrane separation and electrocatalytic oxidation simultaneously on the TiO 2 /CEM. The great treatment performance with membrane removal efficiency of >97.4% was obtained by treating acidic rhodamine B (RhB) dye wastewater under optimized applied voltage. Treatment experiments under various pH and electrochemical tests demonstrated the outstanding acid-tolerant property and long service life of TiO 2 /CEM. Furthermore, the feasibility of TiO 2 /CEM for industrial application and various acidic organic wastewater treatment was proved by treating typical organic pollutants (phenol, tetracycline and oil) under high acidic circumstances.

CAS / MDL: 60-54-8
研究领域: 环境科学 · 材料科学
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Nanoscale · 2018 ·Vol. 10 ·期 34 ·15932-15937 · IF 7.233

Precise mono-Cu+ ion doping enhanced electrogenerated chemiluminescence from Cd–In–S supertetrahedral chalcogenide nanoclusters for dopamine detection

Feng Wang,Jian Lin,Hongye Wang,Shansheng Yu,Xiaoqiang Cui,Asghar Ali,Tao Wu,Yang Liu

Herein, the ECL behaviors of precise mono-Cu+ ion doped Cd–In–S supertetrahedral chalcogenide nanoclusters (Cu@CdInS NCs) were investigated, and the effect of mono-Cu+ ions at the vacancy site of NCs on ECL emission performance was also elucidated. Precise mono-Cu+ ion doping not only induced new ECL emission at 596 nm with enhanced efficiency as high as 21.72% relative to [Ru(bpy)3]2+, but also improved acid tolerance of the ECL performances of NCs. In addition, a simple, fast and label-free dopamine ECL sensor with excellent selectivity was achieved.

研究领域: 分析化学 · 纳米技术 · 电化学
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MACROMOLECULAR BIOSCIENCE · 2023 ·Vol. 23 ·期 11 ·2300233 · IF 4.6

Zn2+@Polyvinylpyrrolidone and Urushiol Preparation of Nanofibrous Membranes and Their Synergistic Effect

Bing-Chiuan Shiu,Shihan Wulin,Qian-Yu Yuan,Ying Zhang,Zhicai Yu

In this study, lacquer is gathered from a lacquer tree and rotary evaporation is used to remove impurities to obtain urushiol. Next, 10 mL of anhydrous ethanol serves as the solvent for blending polyvinylpyrrolidone (PVP) at a specified content (0.7 g and 0.2–0.7 g urushiol) to form an electrospinning solution. Electrospinning is carried out with a voltage of 18 kV to prepare PVP/urushiol nanofibrous membranes. At a ratio of 7/4, the PVP/urushiol nanofibrous membranes are not eroded in 98% sulfuric acid and these membranes also demonstrate a 50–60% antibacterial effect against Staphylococcus aureus and Escherichia coli . Moreover, the antibacterial effect can be boosted to 98% with the incorporation of zinc ions. The results indicate that anhydrous ethanol can remove the sensitization of urushiol from PVP/urushiol membranes. Furthermore, animal test results indicate that when rats are in contact with PVP/urushiol anhydrous ethanol for 48 h, their skins are free from dark brown skin allergy. The presence of PVP eliminates the sensitization of urushiol, and the nanofibrous membranes demonstrate low toxicity. Hence, urushiol is the only natural material that enables PVP to withstand 98% sulfuric acid as well as acquire hydrolyzability, thereby qualify PVP as a medical material.

研究领域: 材料科学 · 纳米技术 · 生物医学工程 · 化学 · 细菌学
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Highly permeable acid-resistant nanofiltration membrane based on a novel sulfonamide aqueous monomer for efficient acidic wastewater treatment

Yang Cao,Jianquan Luo,Chulong Chen,Yinhua Wan

Thin-film composite (TFC) membrane with high permeability and selectivity is appealing in the field of industrial wastewater treatment. However, polyamide (PA) TFC membranes, the premier choice for water treatment, undergo structure deterioration when continually exposed to acidic environment. Here, we apply surface activation assisted multi-step interfacial polymerization (IP) of 3-aminobenzenesulfonamide (ABSA) and trimesoyl chloride (TMC) to prepare a poly(amide-sulfonamide) (PASA) nanofiltration (NF) membrane with strong acid resistance. Thereinto, stable sulfonamide structure of ABSA effectively prevents the direct attack of acid to the PASA layer. Importantly, the nascent PASA layer acting as a hydrophilic interlayer can promote the subsequent IP reactions to form a less defective separation layer. When the surface activation (water soaking) is carried out during the multi-step IP process, the surface smoothness and hydrophilicity as well as the water permeability of the membrane are improved. Compared to the control, the resultant NF membrane exhibits ~200% increase in water permeability (12.4 Lm −2 h −1 bar −1 ) and >95.0% Na 2 SO 4 rejection. Benefiting from the strong steric exclusion, it also has high color removal when treating model acidic dye solutions (>99.3%) or real resin elution wastewater, showing great potential in the acid reuse for decolorization resin regeneration. Moreover, such membrane owns impressive long-term stability after exposure to strong acid (20 wt% of H 2 SO 4 for 30 days), and its hydrophilic surface contributes to excellent anti-fouling performance. This acid-resistant NF membrane with high permeability and stability provides a new perspective in acidic wastewater treatment.

研究领域: 环境科学 · 化学工程 · 材料科学
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