超高压处理对多酚氧化酶活性的影响

 研究了超高压中温协同处理对砀山梨汁中多酚氧化酶活性的影响,实验压力为0.1~500 MPa,温度为20~60 ℃。此外,考察了不同pH值（3~7）和保压时间（2~34 min）超高压处理对酶活性的影响。实验结果分析表明：在处理温度为50 ℃、保压时间为10 min和梨汁pH值为5的条件下,200~300 MPa处理梨汁时多酚氧化酶被激活,活性表现最高;500 MPa时酶的活性下降到75.3%。协同温度为30 ℃处理梨汁时,酶的活性反而增大;30 ℃以后,酶活性随温度升高而迅速降低;有效协同高压处理的温度为40 ℃。随着保压时间的延长,梨汁中过氧化物酶的活性减小;18 min以前下降速度较快些,之后下降速度变缓。pH在5~6之间,酶的残留活性最大;pH值为6时,梨汁中多酚氧化酶最为耐压。     

温压协同处理黑莓β-葡萄糖苷酶失活动力学研究

 以黑莓β-葡萄糖苷酶为对象,研究其温压协同条件下的失活动力学规律,可为超高压食品处理技术的工业化和花色苷的保留提供有力的技术支持。实验压力为300~600 MPa,温度为35~55 ℃。结果表明：β-葡萄糖苷酶在温压协同条件下的失活过程为两个阶段,第一阶段用瞬时失活值描述,压力和温度影响其大小,不受保压时间影响;第二阶段将β-葡萄糖苷酶分为稳定部分和敏感部分,β-葡萄糖苷酶的失活过程用双相一级反应动力学模型描述,其失活速率常数随温度、压力的升高而增大。敏感部分和稳定部分在400 MPa、55 ℃条件下,失活速率常数K_L和K_S分别为2.777和0.047 min^-1,二者失活90%所需时间D_L和D_S分别为0.83和49.1 min。在400 MPa条件下,敏感部分的D值减少90%所需增加的温度T_Z和活化能E_a分别为23.36 ℃和81.95 kJ/mol;在45 ℃条件下D值减少90%所需增加的压力p_Z和活化体积V_a分别为1 111 MPa和-5.02 cm³/mol。     

压致硼酸盐晶态物质的非晶化现象研究

 本文用X射线衍射、Eu²⁺的发射谱与激发谱、拉曼谱以及扫描电镜（SEM）颗粒形貌，研究了常压下合成的具有正交结构的SrB₂O₄:Eu²⁺晶体在3.0~7.0 GPa压力下的晶态非晶化现象。分析结果表明，压力导致晶粒细化和晶态非晶化。晶粒尺寸由常压下的微米量级细化为几十个纳米量级，随压力的变化为：2 μm（0.1 MPa），49.4 nm（3.0 GPa），29.7 nm（5.0 GPa），25.1 nm（7.0 GPa）。晶态与非晶态体积比随压力增加而减小，分别为：70/30（3.0 GPa），63/37（5.0 GPa），57/43（7.0 GPa）。在压力下Eu²⁺是处在晶态与非晶态两种不同的低对称的环境中。纳米级晶粒是以亚晶粒形式存在于微米级大晶粒中的，压致非晶态可能组成了纳米亚晶粒的界面区。     

光纤光栅的压力传感特性研究

对聚合物封装的光纤光栅的压力敏感特性进行了实验研究,在10MPa的压力范围内,光纤光栅中心波长的相对变化与外界压力成良好的线性关系,由于聚合物基底的带动作用,两种不同聚合物封装的光纤光栅的压力灵敏度分别为-3.96×10^-5/MPa和-6.28×10^-5/MPa,提高为裸光栅的20倍和31.7倍。     

SiN掺杂提高BaMgAl10O17:Eu2+荧光粉光学性能的第一性原理研究

使用基于密度泛函理论的CASTEP软件计算了BAM:Eu²⁺(BaMgAl₁₀O₁₇:Eu²⁺)荧光粉在SiN掺杂前后的能带、态密度、吸收光谱和Mulliken布居．Eu²⁺处于BR位置光吸收更强;SiN掺杂使处于BR位置的Eu²⁺的数量上升,而处于mO位置的Eu²⁺的数量下降,抵消了SiN掺杂降低Eu的态密度对光谱的影响．所以适量掺杂的SiN提高了BAM:Eu²⁺荧光粉的吸收发射光谱强度．Si-N键和Eu-N键的Mulliken布居数分别高于Al-O键和Eu-O键, 说明Si-N键和Eu-N键的共价性分别强于Al-O键和Eu-O键．发光中心Eu²⁺局域结构共价性的增强降低了BAM:Eu²⁺镜面层的活性,这是SiN掺杂提高BAM:Eu²⁺+荧光粉光学稳定性的主要原因．     

Tm3+/Yb3+共掺碲酸盐玻璃的近红外发光及能量传递机理

采用高温熔融法制备了组分为TeO₂-ZnO-Na₂O的Tm³⁺离子单掺和Tm³⁺/Yb³⁺共掺碲酸盐玻璃,应用Judd-Ofelt理论计算分析了玻璃样品的强度参量Ω_t(t=2, 4, 6),自发辐射跃迁几率A,荧光分支比β和荧光辐射寿命τ_rad等光谱参量,测量得到了不同Yb³⁺离子掺杂浓度下玻璃样品的Tm³⁺离子上转换发光谱.结果显示,在980 nm泵浦光激励下玻璃样品发射出强烈的近红外上转换荧光.对Tm³⁺离子上转换发光分析表明,强烈的Tm³⁺离子近红外上转换发光主要来自于Yb³⁺/Yb³⁺离子间的共振能量传递以及基于单声子和双声子辅助的Yb³⁺/Tm³⁺离子间的非共振能量传递过程,并进一步计算得到了声子贡献比和能量传递系数.最后,计算分析了Tm³⁺:³F₄→³H₆能级间跃迁的1.8 μm波段吸收截面、受激发射截面和增益系数.研究表明,Yb³⁺/Tm³⁺共掺TeO₂-ZnO-Na₂O玻璃可以作为近红外波段固体激光器的潜在增益基质.     

超高压和酶抑制剂联合处理对荔枝果肉中过氧化物酶和果胶甲基酯酶的影响

 为了研究超高压与酶抑制剂联合处理对荔枝果肉中过氧化物酶（POD）和果胶甲基酯酶（PME）的影响，将荔枝（“淮枝”品种）果肉在两种酶抑制剂组合溶液（A：5 g/L柠檬酸+2.5 g/L L-抗坏血酸+5 g/L氯化钙；B：10 g/L柠檬酸+5 g/L L-抗坏血酸+10 g/L氯化钙）中分别浸泡10 min，并在100~400 MPa压力、10 ℃温度条件下处理30 min，采用分光光度法测定果肉中POD、PME的活性。结果表明：A、B两种组合处理能够明显钝化POD，但却显著激活了PME；超高压与A组合联合处理不能使POD、PME活性下降；超高压与B组合联合处理对POD、PME的影响与压力值有关系，100~300 MPa的超高压与B组合联合处理使POD活性下降，200~400 MPa的超高压与B组合联合处理则使PME活性升高。因此，超高压与酶抑制剂联合处理对荔枝果肉中POD的钝化存在一定的协同效应，且浓度越高，协同抑制效应越明显；而超高压与酶抑制剂联合处理对荔枝果肉中PME的钝化却表现出一定的拮抗性。     

红宝石Cr3+:Al2O3的电子云延伸效应及压力对电子云延伸效应影响(英文)

本文以Cr³⁺自由离子的3d电子径向波函数为基础,对Cr³⁺:Al₂O₃中的电子云延伸效应进行了理论研究,引入了电子云延伸效应系数κ,得到了Cr³⁺:Al₂O₃中Cr³⁺离子的最优化3d电子径向波函数.并研究了压力对电子云延伸效应系数κ的影响.     

Er3+/Ce3+共掺碲铋酸盐玻璃的制备及光谱特性提高研究

采用高温熔融退火法制备了系列 80TeO₂-10Bi₂O₃-10TiO₂-0.5Er₂O₃-xCe₂O₃ (x=0,0.25, 0.5,0.75,1.0 mol%)和(80-y) TeO₂-10Bi₂O₃-10TiO₂-yWO₃-0.5Er₂O₃-0.75Ce₂O₃ (y=3,6,9,12 mol%)的碲铋酸盐玻璃.测试了玻璃样品400-1700 nm范围内的吸收光谱, 975 nm抽运下的上转换发光谱和1.53 μm波段荧光谱, 以及808 nm激励下的Er³⁺离子荧光寿命和无掺杂玻璃样品的Raman光谱, 并结合Judd-Ofelt理论和McCumber理论计算了Er³⁺离子光谱参数.结果表明, 在掺Er³⁺碲铋酸盐玻璃中引入Ce³⁺离子进行Er³⁺/Ce³⁺共掺, 通过Er³⁺离子⁴I_11/2能级与Ce³⁺离子²F_5/2 能级间基于声子辅助的能量传递过程,可以有效抑制Er³⁺离子上转换发光并明显增强其 1.53 μm波段荧光;同时,在现有Er³⁺/Ce³⁺共掺玻璃组分基础上引入WO₃, 可进一步提高1.53 μm波段荧光并展宽其荧光发射谱. 研究结果对于获取优异光谱特性的宽带掺Er³⁺光纤放大器玻璃基质具有实际意义.     

Eu2+,Mn2+在BaZnP2O7中的发光及Eu2+→Mn2+能量传递

采用高温固相法合成了BaZnP₂O₇:Eu²⁺,Mn²⁺荧光粉，并对其发光性质及Eu²⁺对Mn²⁺的能量传递机理进行了研究.Eu²⁺和Mn²⁺在380 nm和670nm的发射峰分别由Eu²⁺的5d—4f跃迁和Mn²⁺的⁴T₁(^{4相似文献}   

Preparation and characterization of TiO2 photocatalysts co-doped with iron (III) and lanthanum for the degradation of organic pollutants

Titanium dioxide photocatalysts co-doped with iron (III) and lanthanum were prepared by a facile sol-gel method. The structure of catalysts was characterized by X-ray diffraction (XRD), Raman spectroscopy, UV-vis diffuse reflectance spectroscopy and X-ray photoelectron spectroscopy (XPS). The photocatalytic activities of the samples were evaluated by the degradation of methylene blue in aqueous solutions under visible light (λ > 420 nm) and UV light irradiation. Doping with Fe³⁺ results in a lower anatase to rutile (A-R) phase transformation temperature for TiO₂ particles, while doping with La³⁺ inhibits the A-R phase transformation, and co-doping samples indicate that Fe³⁺ partly counteracts the effect of La³⁺ on the A-R transformation property of TiO₂. Fe-TiO₂ has a long tail extending up the absorption edges to 600 nm, whereas La-TiO₂ results in a red shift of the absorption. However, Fe and La have synergistic effect in the absorption of TiO₂. Compared with Fe³⁺ and La³⁺ singly doped TiO₂, the co-doped simple exhibits excellent visible light and UV light activity and the synergistic effect of Fe³⁺ and La³⁺ is responsible for improving the photocatalytic activity.     

Structure and magnetic properties of Co–Ni–Li ferrites synthesized by citrate precursor method

Nanoparticles of Co_0.5Ni_0.5−2xLi_xFe_2+xO₄ with x ranging from 0.00 to 0.25 in steps of 0.05 were prepared by using citrate precursor method. The microstructure and the magnetic properties of the as-prepared nanosamples and the effect of increasing Li¹⁺ ions on their physical properties were studied. X-ray diffraction (XRD), transmission electron microscopy (TEM), particle size analyzer (PSA), Fourier transform infrared spectroscopy (FTIR) and vibrating sample magnetometer (VSM) were used to investigate the samples. The XRD analysis confirmed the cubic spinel phase formation of the prepared samples, while TEM images and PSA ensure the nanostructural features of them. The FTIR spectra reveal the presence of two prominent absorption bands v₁ and v₂ in the range of 600 and 400 cm⁻¹ which are usually attributed to the tetrahedral and octahedral complexes of the spinel lattice, respectively. The change of v₂ gradually towards lower frequency and the slightly change of v₁ were explained depending on the effect of increasing Li¹⁺ content on the bond length of B-site metal ions and the spin canting of A-site metal ions, respectively. Saturation magnetization and remnant magnetization were found to increase with adding Li¹⁺ ions up to x=0.15 and then to decrease again, while coercivity decreases monotonically by increasing Li¹⁺ ions. The change in magnetic properties by adding Li¹⁺ ions is explained as to be dependent on many factors such as crystallite size, measured density, porosity, expected cation distribution, A–B exchange interactions, and magnetocrystalline anisotropy.     

Optimization of high pressure processing parameters of Indian white prawn (Fenneropenaeus indicus)

The effect of pressure (150, 250 and 350?MPa), ramp rate (200, 400 and 600?MPa/min) and holding time (3, 6 and 9?min) on the quality indices (dependent variable) of Indian white prawn (Fenneropenaeus indicus) was optimized using response surface methodology. Box–Behnken response surface design was used with 15 runs. Second-order response surface model was fitted to the experimental data and the model adequacy was measured by R² value. The linear and quadratic effect of pressure, ramp rate and holding time was significant for tri-methylamine, total volatile base nitrogen and total plate count. Based on the ridge analysis and response surface plots, the optimum combination obtained was 250?MPa pressure, 400?MPa/min ramp rate and 6?min holding time for high pressure (HP) processing of Indian white prawn. Validation of the experiment indicated that the developed model was appropriate to predict quality indices in Indian white prawn processed by HP processing.     

High pressure-assisted encapsulation of vitamin D2 in reassembled casein micelles

For the encapsulation of vitamin D₂, native casein micelles and vitamin D₂ with or without additional Ca²⁺–P_i were treated at 600 MPa and 37 °C for 60 min. The pressure release rate was set at 20 or 600 MPa/min. Vitamin D₂ was quantified by reversed-phase high-performance liquid chromatography, and physical properties of the micelles were analysed by photon correlation spectroscopy. The results demonstrate that simultaneous application of Ca²⁺–P_i and high pressure treatment with a fast release rate significantly increased loading of vitamin D₂ per casein by 6.9-fold. The addition of Ca²⁺–P_i enhanced micelle aggregation and the vitamin was entrapped within the formed aggregates. However, high pressure treatment without Ca²⁺–P_i with a slow pressure release rate revealed similar results, increasing vitamin D₂ per casein by 6.7-fold. The vitamin D₂ loading in reassembled casein micelles is supposed to be due to hydrophobic interactions between the hydrophobic domains of the micelles.     

Spectrophotometric studies on the interaction between myricetin and lysozyme in the absence or presence of Cuor Fe

The binding of myricetin to lysozyme (Lys) in aqueous solution was investigated by fluorescence spectroscopy, ultraviolet-visible absorption spectroscopy (UV) and circular dichroism (CD) spectra under physiological conditions. There are also many metal ions present in body, thus the research about the effect of metal ions on the interaction of drugs with proteins is crucial. In this study, we have investigated the effect of both familiar metal ions Cu²⁺ and Fe³⁺ on the interaction between myricetin and Lys by using spectroscopy technique at pH 7.40, for the first time. Spectrophotometric observations are rationalized in terms of a static quenching process in a static quenching way. The cause of showing upward curvy patterns in Stern-Volmer plots was analyzed. The binding constants and binding sites of myricetin with Lys with or without Cu²⁺ and Fe³⁺ at different concentrations of myricetin were calculated. UV/vis measurements on the enzymatic activity of Lys with or without Cu²⁺ in the absence or presence of myricetin indicated that the interaction between myricetin and Lys led to a reduction in the activity of Lys. Furthermore, the effect of pH on the binding constant of myricetin with Lys was also examined.     

Effect of Pendant Group Length Upon Metal Ion Complexation in Acetonitrile by Di-Ionized Calix[4]Arenes Bearing Two Dansyl Fluorophores

A series of three di-ionizable calix[4]arenes with two pendant dansyl (1-dimethylaminonaphthalene-5-sulfonyl) groups linked to the lower rims was synthesized. Structures of the three ligands were identical except for the length of the spacers which connected the two dansyl groups to the calix[4]arene scaffold. Following conversion of the ligands into their di-ionized di(tetramethylammonium) salts, absorption and emission spectrophotometry were utilized to probe the influence of metal cation (Li⁺, Na⁺, K⁺, Rb⁺, Cs⁺, Mg²⁺, Ca²⁺, Sr²⁺, Ba²⁺, Ag⁺, Cd²⁺, Co²⁺, Fe²⁺, Hg²⁺, Mn²⁺, Pb²⁺, Zn²⁺ and Fe³⁺) complexation in acetonitrile. Upon complexation with these metal cations, emission spectra underwent marked red shifts and quenching of the dansyl group fluorescence for the di-ionized ligand with the shortest spacer. A similar effect was noted for the di-ionized ligand with an intermediate spacer for all of the metal ions, except Ba²⁺. For the di-ionized ligand with the longest spacer, the metal cations showed different effects on the emission spectrum. Li⁺, Mg²⁺, Ca²⁺ and Ba²⁺ caused enhancement of emission intensity with a red shift. Other metal cations produce quenching with red shifts in the emission spectra. Transition metal cations interacted strongly with all three di-ionized ligands. In particular, Fe³⁺ and Hg²⁺ caused greater than 99% quenching of the dansyl fluorescence in the di-ionized ligands.     

A New Fluorescent Chemosensor Detecting Co<Superscript>2+</Superscript> and K<Superscript>+</Superscript> in DMF Buffered Solution

A new fluorescent chemosensor 2-(2-thiophene)imidazo [4,5,f]-1,10-phenanthroline (L) was prepared and characterized. By adding univalent or divalent metal ions such as Na⁺, K⁺, Mg²⁺, Ba²⁺, Mn²⁺, Fe²⁺, Co²⁺, Ni²⁺, Cu²⁺, Ag⁺, Zn²⁺, Cd²⁺ and Hg²⁺ ions into the solution of L in DMF under buffered conditions with the working pH ranging from 7.0 to 8.0, we found that L could be used to detect K⁺ ratiometricly and it could also be applied to sense Co²⁺ with the phenomenon of fluorescence quenching of L. While the response behavior of L was not discernibly affected by other examined metal ions.     

Off-on Fluorescent Sensor from On-off Sensor: Exploiting Silver Nanoparticles Influence on the Organic Fluorophore Fluorescence

Turn-off fluorescence of organic fluorophore, 2-{[4-(2H-Naphtho[1,2-d][1,2,3]triazol-2-yl)-phenyl]carboxylic acid (NTPC), with metal ions (Fe³⁺, Cu²⁺, Pb²⁺) was converted into turn-on fluorescent sensor for biologically important Zn²⁺, Cu²⁺ and Fe³⁺ metal ions in aqueous solution at ppb level by exploiting strong fluorescence quenching phenomena of metal nanoparticles when organic fluorophores assembled in the vicinity of metallic surface. Amino acid attached phenolic ligands (L) were used as reducing as well as functional capping agents in the synthesis of silver nanoparticles (AgNPs). The hydrogen bonding functionality of L facilitated the assembling of NTPC in the vicinity of metallic surfaces that leads to complete quenching of NTPC fluorescence. The strong and selective coordination of L with metal ions (Zn²⁺, Cu²⁺ and Fe³⁺) separates the NTPC from the AgNPs surface that turn-on the NTPC fluorescence. HR-TEM and absorption studies confirm the metal coordination with L and separation of NTPC from the AgNPs surface. Mn²⁺ showed selective red shifting of NTPC fluorescence after 12 h with all sample. Effects of different amino acid attached phenolic ligands were explored in the metal ion sensitivity and selectivity. This approach demonstrates the multifunctional utility of metal NPs in the development of turn-on fluorescence sensor for paramagnetic heavy metal ions in aqueous solution.

Methylene blue as a DNA probe for a comparative study of Cd, Pb and Cr ions binding to calf thymus DNA

Methylene blue (MB) was developed as a sensitive DNA probe for a comparative study of Cd²⁺, Pb²⁺ and Cr³⁺ ions binding with calf thymus DNA (ctDNA). The fluorescence intensity of the MB-ctDNA system increased dramatically when heavy metal ions (Cd²⁺, Pb²⁺ and Cr³⁺ ions) were added, which indicated that some of the bound MB molecules were released from the ctDNA base pairs. To compare the binding affinity of these three different heavy metal ions with ctDNA, the relationships between the fluorescence intensity of the MB-ctDNA-M (Metal ions) system and the concentration ratio of [M]/[DNA(p)] were investigated. The results showed that the order of the binding affinity of heavy metal ions with ctDNA had the following sequence: Cr³⁺> Cd²⁺>Pb²⁺. This order was further proved by the effects of heavy metal ions on the number of MB bound to ctDNA, the measurements of binding constants of these heavy metal ions to ctDNA, and the effects of heavy metal ions on the absorption of the MB-ctDNA system. In addition, the interaction mechanisms of Cd²⁺, Pb²⁺ and Cr³⁺ ions with ctDNA were also discussed in detail. These results indicated that their interaction mechanisms are related to the concentration ratios of heavy metal ions to DNA.     

Solvatochromic Studies of Fluorescent Azo Dyes: Kamlet-Taft (π*, α and β) and Catalan (Spp, SA and SB) Solvent Scales Approach

A new metal ion-responsive azo-based fluorescent probes have been synthesized and characterized by NMR spectral techniques. Steady-state fluorometric study has been used to analyze the spectroscopic and photophysical characteristics of dye derivatives in various solvents. The fluorescence properties of these dyes are strongly solvent dependent, the wavelength of maximum fluorescence emission shifts to the red. The Kamlet-Taft and Catalan’s solvent scales were found to be the most suitable for describing the solvatochromic shifts of the absorption and fluorescence emission. The hydroxy substituted azo dye formed complexes with several metal ions (Co²⁺, Hg²⁺, Ni²⁺ and Cu²⁺) and fluorescence quenching with metal ions reveal that it can be used as a new fluorescence sensor to detect the Cu²⁺ ion.