33 Matching Annotations
  1. Apr 2026
    1. Almost all normally developing humans learn to speak within a few years of birth and speak many times per day throughout their lives, while there is a much larger variation in musical abilities (e.g., the ability to synchronise taps to a musical beat) among normally developing humans. Most strikingly, deaf people naturally develop sign language, while there is no naturally developing “sign music” equivalent.6 Unlike Pinker’s dismissive conclusion that music is biologically “useless,” Patel’s more positive interpretation was that the “beneficial biological impact of music, while not the reason for its origin or maintenance in human societies, makes music a biologically powerful human invention or transformative technology of the mind (TTM)” (Patel, 2018; cf. Patel, 2010, 2023).

      Patel's hypothesis is interesting.

    2. more controlled and comprehensive comparisons of vocal learning and beat entrainment across species are needed to resolve this debate (see four commentaries and response accompanying Patel 2024a/2024b and Section 5.3.4 below).

      theory for my research

    3. more controlled and comprehensive comparisons of vocal learning and beat entrainment across species are needed to resolve this debate (see four commentaries and response accompanying Patel 2024a/2024b and Section 5.3.4 below).

      theory for my research

    4. the social value of music can manifest itself in bonding people together (with their children, mates, allies, etc.), as well as signaling the strength of these bonds and other qualities to competing individuals or groups

      核心theory and hypothesis

    1. 在路径 I 中,磺胺甲噁唑的异噁唑环受到 CUF/PMS 体系中活性氧物种的攻击,生成 P1、P2 和 P3。这些分解产物 P1、P2 和 P3 分别氧化为 P4 和 P5,这被视为磺胺甲噁唑的经典氧化路径[64]。根据路径 II,P6 的形成源于异噁唑环上甲基和苯环上–NH 2 的氧化,随后因 S-N 键断裂转化为 P7 和 P8[65]。在路径 III 中,磺胺甲噁唑的 S-N 键可直接被活性氧物种断裂,矿化为 P5 和 P9。接着,TP 9 的异噁唑环因羟基化被活性氧物种攻击形成 P10,随后由于·HO 与烯烃双键之间的高反应活性进一步生成 P11[66]。 此外,生成的 P9 分别通过偶联反应和异恶唑环的亲电取代进一步转化为 P12。P13 的形成可能涉及源自 P10 的–NH 2 基团的氮中心自由基与中间产物的偶联。随后,异恶唑环发生开环反应,生成 P14,后者被活性氧物种氧化为 P15。最终,这些中间产物将进一步矿化为小分子(P16、P17 和 P18)。

      Ce-UiO-66-F催化PMS降解SAs的中间产物 The intermediates of CUF/PMS system were identified by the HPLC-MS (in Figure S17), which was used to investigate the possible degradation pathway of sulfamethoxazole. As shown in Figure 13d, the degradation pathway of sulfamethoxazole could be summarized as hydroxylation, deamination, sulfonamide (S-N) cleavage and desulfonation. In pathway I, the isoxazole ring of sulfamethoxazole was attacked by ROSs in CUF/PMS to generate P1, P2 and P3. The breakdown products P1, P2 and P3 oxidized into P4 and P5, respectively, which was viewed as a classic oxidation pathway of sulfamethoxazole [64]. According to pathway II, the formation of P6 resulted from the oxidation of methyl group on the isoxazole ring and –NH2 on the benzene ring and then converted into P7 and P8 due to the broken S-N bond [65]. For pathway III, the S-N bond of sulfamethoxazole could be directly broken by ROSs to be mineralized into P5 and P9. Then, the isoxazole ring of TP 9 was attacked by ROSs to form P10 due to hydroxylation, and then further generated P11, caused by high reactivity between ·HO and olefinic double bonds [66]. In addition, the generated P9 was further converted into P12 via coupling reaction and electrophilic replacement of the isoxazole ring, respectively [67]. The formation of P13 might be involved in the coupling of N-centered radical derived from by –NH2 group of P10 and intermediate products [68]. Then, the isoxazole ring opening reaction occurred resulting in the generation of P14, which was oxidized by ROSs into P15. Finally, these intermediates would be further mineralized into small molecules (P16, P17 and P18). W. Peng, J. Liao, Y. Yan, L. Chen, C. Ge, S. Lin Enriched nitrogen-doped carbon derived from expired drug with dual active sites as effective peroxymonosulfate activator: Ultra-fast sulfamethoxazole degradation and mechanism insight Chem. Eng. J., 446 (2022), Article 137407, 10.1016/j.cej.2022.137407 View PDF View articleView in ScopusGoogle Scholar [65] Y. Chen, D. Chen, X. Bai Binary MOFs-derived Mn-Co3O4 for efficient peroxymonosulfate activation to remove sulfamethoxazole: Oxygen vacancy-assisted high-valent cobalt-oxo species generation Chem. Eng. J., 479 (2024), Article 147886, 10.1016/j.cej.2023.147886 View PDF View articleView in ScopusGoogle Scholar [66] Y. Bao, W.J. Lee, T.-T. Lim, R. Wang, X. Hu Pore-functionalized ceramic membrane with isotropically impregnated cobalt oxide for sulfamethoxazole degradation and membrane fouling elimination: Synergistic effect between catalytic oxidation and membrane separation Appl. Catal. B-Environ., 254 (2019), pp. 37-46, 10.1016/j.apcatb.2019.04.081 View PDF View articleView in ScopusGoogle Scholar [67] M. Xu, H. Zhou, Z. Wu, N. Li, Z. Xiong, G. Yao, B. Lai Efficient degradation of sulfamethoxazole by NiCo2O4 modified expanded graphite activated peroxymonosulfate: Characterization, mechanism and degradation intermediates J. Hazard. Mater., 399 (2020), Article 123103, 10.1016/j.jhazmat.2020.123103 View PDF View articleView in ScopusGoogle Scholar [68] R. Guo, Y. Wang, J. Li, X. Cheng, D.D. Dionysiou Sulfamethoxazole degradation by visible light assisted peroxymonosulfate process based on nanohybrid manganese dioxide incorporating ferric oxide Appl. Catal. B-Environ., 278 (2020), Article 119297, 10.1016/j.apcatb.2020.119297 View PDF View articleView in ScopusGoogle Scholar

    2. 在基于过硫酸盐(PMS)的非均相催化过程中,催化剂可通过相互作用(如静电作用和金属耦合)吸附 PMS 分子和污染物,随后在催化剂与 PMS 界面发生电子转移过程,导致活性位点的化学状态改变、PMS 分解及污染物降解[60]

      PMS非均相催化剂吸附PMS,污染物 X. Zhou, Q. Zhao, J. Wang, Z. Chen, Z. Chen Nonradical oxidation processes in PMS-based heterogeneous catalytic system: Generation, identification, oxidation characteristics, challenges response and application prospects Chem. Eng. J., 410 (2021), Article 128312

    3. 为评估在实际废水处理中的潜在应用,考察了 CUF/体系的抗干扰能力,这源于各种无机阴离子和有机污染物的竞争反应与清除效应。在 CUF/PMS 体系中分别添加典型无机阴离子(HCO₃⁻、HPO₄²⁻和 SO₄²⁻)及有机污染物(腐殖酸),结果如图 8c 所示。HCO₃⁻和 HPO₄²⁻对 CUF/PMS 体系的催化性能表现出积极影响,因其水解过程会干预氢离子(H⁺)与氢氧根离子(OH⁻)的比例(式 S28-S32)[46],而 SO₄²⁻对 CUF 的催化反应影响较弱。 此外,在腐殖酸存在下,磺胺甲噁唑的降解效率受到明显抑制,仅有 88.8%的磺胺甲噁唑能被去除,这归因于腐殖酸分子在活化过硫酸盐生成活性氧物种过程中产生的竞争效应。

      实际用于处理废水的各种影响 X. He, K.E. O'Shea Selective oxidation of H(1)-antihistamines by unactivated peroxymonosulfate (PMS): Influence of inorganic anions and organic compounds Water Res., 186 (2020), Article 116401,

    4. 此外,高浓度氢离子(H⁺)与磺胺甲恶唑的竞争会消耗活性氧物种(ROS)(式 S25-S26)[44],导致降解效率较低。当 pH 值从 9 增加到 11 时,溶液中反应活性高于 HSO₅⁻的 SO₅²⁻比例逐渐增加,这有利于活性氧物种的产生[45]。 此外,碱活化过一硫酸盐可归因于提高了磺胺甲噁唑的降解效率

      进一步探究PH的影响,电子互斥,碱活化PMS 44.X. Huang, W. Ren, X. Liu, C. Lin, M. He, W. Ouyang CuMgFe-LDO as superior peroxymonosulfate activator for imidacloprid removal: Performance, mechanism and effect of pH Chem. Eng. J., 441 (2022), Article 136135, 10.1016/j.cej.2022.136135 45.L. Hu, G. Zhang, M. Liu, Q. Wang, P. Wang Enhanced degradation of Bisphenol A (BPA) by peroxymonosulfate with Co3O4-Bi2O3 catalyst activation: Effects of pH, inorganic anions, and water matrix Chem. Eng. J., 338 (2018), pp. 300-310,

    5. 当浓度从 0.5 mM 提升至 1.0 mM 时,磺胺甲噁唑的降解效率从 59.1%上升至 90.9%,同时 k 值也增加了 3.4 倍,这表明产生了更多活性氧物种以氧化磺胺甲噁唑。随着初始过一硫酸盐浓度从 1.0 mM 进一步增加至 2.0 mM,观察到磺胺甲噁唑降解效率仅有微小提升,同时 k 值略有增加,这归因于过量过一硫酸盐浓度下活性氧物种的自淬灭效应

      PMS建议投加量,以及测量反应速率常数K的重要性,自淬灭效应 J. Yan, H. Liu, C. Dou, Y. Wu, W. Dong Quantitative probing of reactive oxygen species and their selective degradation on contaminants in peroxymonosulfate-based process enhanced by picolinic acid

    6. The effect of solution pH on the adsorption performance of the prepared nanoparticles was also investigated because the surface potential of adsorbents and adsorbates could be decided by their surface group under different solution pH. Owing to the sulfamethoxazole with two dissociation constants of pKa1 = 1.7 and pKa2 = 5.6, the sulfamethoxazole displayed cations forms (SMX+) at pH < 1.7, neutral ions form at 1.7 < pH < 5.6 (SMX±), and anions forms pH > 5.6 (SMX-), which would promote or inhibit adsorption performance of adsorbents

      PH影响 Y. Ma, L. Yang, L. Wu, P. Li, X. Qi, L. He, S. Cui, Y. Ding, Z. Zhang Carbon nanotube supported sludge biochar as an efficient adsorbent for low concentrations of sulfamethoxazole removal

  2. Mar 2026
    1. 通过对这些参数的系统优化,可以实现对最终缺陷结构的精确控制,既能阐明潜在的缺陷形成机制,又能获得理想的材料性能。

      Y. Luo , S. Bag , O. Zaremba , A. Cierpka , J. Andreo , S. Wuttke , P. Friederich and M. Tsotsalas , MOF Synthesis Prediction Enabled by Automatic Data Mining and Machine Learning, Angew. Chem., Int. Ed., 2022, 61 , e202200242 通过自动数据挖掘与机器学习实现 MOF 合成预测

    2. Furthermore, temperature has been unequivocally linked to defect generation, which likely stems from the thermally induced instability of Zr-O bonds between modulators and inorganic metal-oxo clusters at elevated temperatures. Consequently, higher temperatures correlate with fewer defects, thereby facilitating the detachment of modulator-capped ligands from the inorganic clusters.42,43 Following such detachment, terephthalic acid (BDC) ligands can coordinate with Zr nodes, leading to a reduction in structural defects.42

      温度与缺陷生成明确相关,这很可能源于高温下调节剂与无机金属-氧簇之间 Zr-O 键的热诱导不稳定性。因此,较高温度对应较少缺陷,从而促进调节剂封端配体从无机簇上脱离。随后,对苯二甲酸(BDC)配体可与 Zr 节点配位,导致结构缺陷减少 42.C. S. Cox , E. Slavich , L. K. Macreadie , L. K. McKemmish and M. Lessio , Understanding the Role of Synthetic Parameters in the Defect Engineering of UiO-66: A Review and Meta-analysis, Chem. Mater., 2023, 35 , 3057 —3072 43。X. Qiu and R. Wang , From construction strategies to applications: Multifunctional defective metal-organic frameworks, Coord. Chem. Rev., 2025, 526 , 216356

    3. 通过结合光谱分析与理论计算,Tan 等人发现了 UiO-66 中涉及氢键羧酸与 H 2 O 物种的独特缺陷补偿机制 41

      这反映了不同竞争物种在缺陷调控中的协同作用,然而,竞争物种间的协同机制仍不明确。 K. Tan , H. Pandey , H. Wang , E. Velasco , K.-Y. Wang , H.-C. Zhou , J. Li and T. Thonhauser , Defect Termination in the UiO-66 Family of Metal–Organic Frameworks: The Role of Water and Modulator, J. Am. Chem. Soc., 2021, 143 , 6328 —6332

    4. H 2 O/HCl 调节剂展现出竞争性成核/生长效应 39 ,而双组分体系(如 H 2 O/乙酸)则能通过协同缺陷放大实现 hcp 相形成。 40

      双组分调节 M. A. Artsiusheuski , N. P. M. Casati , A. H. Clark , M. Nachtegaal , R. Verel , J. A. van Bokhoven and V. L. Sushkevich , Controlling the Mechanism of Nucleation and Growth Enables Synthesis of UiO-66 Metal–Organic Framework with Desired Macroscopic Properties, Angew. Chem., Int. Ed., 2024, e202415919 40.X. Chen , Y. Lyu , Z. Wang , X. Qiao , B. C. Gates and D. Yang , Tuning Zr12O22 Node Defects as Catalytic Sites in the Metal–Organic Framework hcp UiO-66, ACS Catal., 2020, 10 , 2906 —2914

    5. 开创性研究通过酸蚀刻(Zn/Zr-UiO-66 至 reo 相 35 )、异质金属修饰的 SBUs 36 以及单羧酸物种 37,38 证明了缺陷的生成。

      单组分策略 X. Feng , H. S. Jena , C. Krishnaraj , D. Arenas-Esteban , K. Leus , G. Wang , J. Sun , M. Rüscher , J. Timoshenko , B. Roldan Cuenya , S. Bals and P. V. D. Voort , Creation of Exclusive Artificial Cluster Defects by Selective Metal Removal in the (Zn, Zr) Mixed-Metal UiO-66, J. Am. Chem. Soc., 2021, 143 , 21511 —21518 CrossRef CAS PubMed . X. Feng、H. S. Jena、C. Krishnaraj、D. Arenas-Esteban、K. Leus、G. Wang、J. Sun、M. Rüscher、J. Timoshenko、B. Roldan Cuenya、S. Bals 和 P. V. D. Voort,通过选择性金属移除在 (Zn, Zr) 混合金属 UiO-66 中创建专属人工簇缺陷,《J. Am. Chem. Soc.》,2021 年,第 143 卷,第 21511—21518 页 CrossRef CAS PubMed 。Journal of The American Chemical Society化学TOPESI学科分类:化学JCI 2.64IF(5) 15.6EI检索SCI升级版 化学1区SCI基础版 化学1区SCI Q1IF 15.7 S. Yuan , J. Peng , Y. Zhang and Y. Shao-Horn , Stability Trend of Metal–Organic Frameworks with Heterometal-Modified Hexanuclear Zr Building Units, J. Phys. Chem. C, 2019, 123 , 28266 —28274 CrossRef CAS . S. Yuan, J. Peng, Y. Zhang 和 Y. Shao-Horn, 异金属修饰六核锆构筑单元对金属有机框架稳定性的影响趋势, J. Phys. Chem. C, 2019, 123, 28266—28274 CrossRef CAS 。Journal of Physical Chemistry cESI学科分类:化学JCI 0.51IF(5) 3.5EI检索SCI升级版 化学3区SCI基础版 化学2区SCI Q3IF 3.2 Y. Ma , A. Li and C. Wang , Experimental study on adsorption removal of SO2 in flue gas by defective UiO-66, Chem. Eng. J., 2023, 455 , 140687 CrossRef CAS . Y. Ma、A. Li 和 C. Wang,缺陷型 UiO-66 吸附去除烟气中 SO2 的实验研究,Chem. Eng. J.,2023,455,140687 CrossRef CAS 。

    6. 这些修饰增强了分子扩散 32 并暴露出不饱和金属位点(如路易斯酸性 Zr 4+ ), 33 协同提升了吸附容量和反应动力学。综上所述,这些发现表明,此类工程化缺陷不仅解决了尺寸排阻限制,还引入了反应位点,使缺陷型 MOFs 成为先进分子分离的多功能平台。

      S. Zhuang and J. Wang , Adsorptive removal of pharmaceutical pollutants by defective metal organic framework UiO-66: Insight into the contribution of defects, Chemosphere, 2021, 281 , 130997 33.X. Feng , H. S. Jena , C. Krishnaraj , K. Leus , G. Wang , H. Chen , C. Jia and P. Van Der Voort , Generating Catalytic Sites in UiO-66 through Defect Engineering, ACS Appl. Mater. Interfaces, 2021, 13 , 60715 —60735

    7. 缺陷工程通过可控缺陷(如缺失簇/配体)策略性地引入介孔(2–50 nm),实现拓扑相变(例如 UiO-66 中从 fcu 到 reo 结构)和分级孔隙结构

      A. Jrad , G. Al Sabeh , K. Hannouche , R. Al Natour , O. Haidar , H. Sammoury , M. N. Ahmad and M. Hmadeh , Critical Role of Defects in UiO-66 Nanocrystals for Catalysis and Water Remediation, ACS Appl. Nano Mater., 2023, 6 , 18698 —18720

    8. Although extended ligands could theoretically expand porosity, practical barriers such as framework interpenetration and prohibitive synthesis costs impede scalable applications.25

      G. Cai , X. Ma , M. Kassymova , K. Sun , M. Ding and H.-L. Jiang , Large-Scale Production of Hierarchically Porous Metal–Organic Frameworks by a Reflux-Assisted Post-Synthetic Ligand Substitution Strategy, ACS Cent. Sci., 2021, 7 , 1434 —1440 延长配体扩展孔径的局限

    9. However, conventional MOFs like ZIF-8, UiO-66-NH2 and MIL-100(Fe)—widely studied for QNs' adsorption26–29—often suffer from limited micropores (<10 Å) and/or narrow pore apertures due to short ligand constraints,30 hindering mass transport of bulky pharmaceuticals.

      26.L. Zhou , N. Li , G. Owens and Z. Chen , Simultaneous removal of mixed contaminants, copper and norfloxacin, from aqueous solution by ZIF-8, Chem. Eng. J., 2019, 362 , 628 —637 27.G. Chaturvedi , A. Kaur , A. Umar , M. A. Khan , H. Algarni and S. K. Kansal , Removal of fluoroquinolone drug, levofloxacin, from aqueous phase over iron based MOFs, MIL-100(Fe), J. Solid State Chem., 2020, 281 , 121029 28.R. Yu and Z. Wu , High adsorption for ofloxacin and reusability by the use of ZIF-8 for wastewater treatment, Microporous Mesoporous Mater., 2020, 308 , 110494 29.X. Fang , S. B. Wu , Y. H. Wu , W. Yang , Y. L. Li , J. Y. He , P. D. Hong , M. X. Nie , C. Xie , Z. J. Wu , K. S. Zhang , L. T. Kong and J. H. Liu , High-efficiency adsorption of norfloxacin using octahedral UIO-66-NH2 nanomaterials: Dynamics, thermodynamics, and mechanisms, Appl. Surf. Sci., 2020, 518 , 146226 30.H. Wang , X. Pei , M. J. Kalmutzki , J. Yang and O. M. Yaghi , Large Cages of Zeolitic Imidazolate Frameworks, Acc. Chem. Res., 2022, 55 , 707 —721

    10. offer exceptional advantages for adsorption applications due to their ultrahigh surface areas (>1000 m2 g−1), tunable porosity, and tailorable functionality.18,19

      R.-R. Liang , S. Xu , Z. Han , Y. Yang , K.-Y. Wang , Z. Huang , J. Rushlow , P. Cai , P. Samorì and H.-C. Zhou , Exceptionally High Perfluorooctanoic Acid Uptake in Water by a Zirconium-Based Metal–Organic Framework through Synergistic Chemical and Physical

    11. Metal–organic frameworks (MOFs), crystalline porous materials formed by coordinated assembly of metal clusters and organic ligands,17

      C. S. Diercks , M. J. Kalmutzki , N. J. Diercks and O. M. Yaghi , Conceptual Advances from Werner Complexes to Metal–Organic Frameworks, ACS Cent. Sci., 2018, 4 , 1457 —1464

    1. Darwin’s concept of evolution as “descent with modification” emphasised branching diversification into separate lineages, which can then become adapted to diverse ecological niches without any being necessarily “more” or “less” evolved than the other (Figure 5.2B).3

      Cleared some misconception!

    2. To truly understand the evolutionary origins of musicality or language, we cannot study them independently but must compare both human song and human speech across a wide variety of species and cultures.
    3. Honing (2018) defines musicality as “a natural, spontaneously developing set of traits based on and constrained by our cognitive and biological system.

      两个研究都可以引用

  3. Dec 2022