Study on the pyroelectric properties of PLT/P (VDF-TrFE) nanocomposites

Lead lanthanum titanate (PLT) nanocrystalline powder prepared by the sol_gel process was incorporated into a polyvinylidene fluoride/trifluoroethylene (P(VDF_TrEF)) copolymer matrix to form PLT/P(VDF_TrFE) nanocomposites. The permittivities (ε) of the nanocomposites as a function of volume fraction of ceramic  were modeled using the Bruggeman model. The pyroelectric coefficients (p) and figure of merit (p/ε) were measured as functions of the poling field E. The nanocomposite has p and p/ε values higher than those of the copolymer, and has good potential in pyroelectric applications.     

葎草提取物胃肠促动作用的实验研究

目的探讨葎草提取物对胃肠运动功能的影响。方法采用胃排空、肠推进运动实验法以及离体胃、肠实验法,研究葎草提取物对胃、肠运动功能的影响。结果蒸馏水组胃内容物残留率(%)和小肠推进比(%),分别为(82.53±10.69)和(50.88±8.68);葎草水提物大、中、小剂量(10.0、7.5、5.0 g生药/kg)组,胃内容物残留率(%)和小肠推进比(%),分别为(53.83±9.89)、(48.98±9.75)、(62.75±10.56)和(60.19±7.77)、(64.98±7.41)、(58.71±6.83);葎草醇提物中、小剂量(7.5、5.0 g生药/kg)组,胃内容物残留率(%)和小肠推进比(%),分别为(73.21±8.09)、(74.19±7.71)和(57.48±6.18)、(57.42±6.62)。与蒸馏水组比较,葎草水提物大、中、小剂量(10.0、7.5、5.0 g生药/kg)组均显著降低胃内容物残留率(P0.01),明显提高小肠推进比(P0.01,P0.05);葎草醇提物中、小剂量(7.5、5.0 g生药/kg)组也明显降低胃内容物残留率(P0.05),也明显提高小肠推进比(P0.05);在降低胃内容物残留率及提高小肠推进比,葎草水提物与相同剂量的醇提物比较,差异显著(P0.01)。在离体实验中,葎草水提物给药前后肠管、胃底环状肌的收缩幅度分别为(1.20±0.06)g、(72.01±4.27)mg和(4.89±0.60)g、(211.42±6.76)mg;葎草醇提物给药前后肠管、胃底环状肌的收缩幅度分别为(0.88±0.05)g、(70.20±3.26)mg和(1.43±0.17)g、(218.75±3.13)mg。与给药前比较,葎草水提物与醇提物给药后的肠管和胃底环状肌的收缩幅度明显强于给药前(P0.01);从给药前后肠管收缩幅度差比较,葎草水提物与醇提物比较差异显著(P0.01)。结论葎草提取物具有促进胃排空、肠推进运动的作用,且水提物作用强于醇提物。     

A Large Deviation Principle for the Risk Process with Varying Premium

Let u ∈ R ,for any ω 〉 0, the processes X^ε = {X^ε（t）; 0 ≤ t≤ 1} are governed by the following random evolution equations dX^ε（t）= b（X^ε（t）,v（t））dt-εdSt/ε, where S={St; 0≤t≤1} is a compound Poisson process, the process v={v（t）; 0≤t≤1} is independent of S and takes values in R^m. We derive the large deviation principle for{（X^ε,v（.））; ε〉0} when ε↓0 by approximation method and contraction principle, which will be meaningful for us to find out the path property for the risk process of this type.     

尾巨桉化感作用对广金钱草化学成分的影响

【目的】研究尾巨桉Eucalyptus urophylla×Eucalyptus grandis对广金钱草Desmodium styracifolium(Osb.)Merr.药材化学成分的影响,探索尾巨桉-广金钱草复合经营模式的可行性。【方法】在试验田中,以不同类型和重量的尾巨桉落叶铺盖在土壤上并种植广金钱草,同时另在尾巨桉人工林中直接套种广金钱草,待药材成熟后统计其产量,并利用HPLC指纹图谱法及含量测定法检测其化学成分变化。【结果】广金钱草在尾巨桉林下种植时,产量稍有下降,但药材指纹图谱与正常种植无显著差异。【结论】广金钱草可以套种在尾巨桉人工林下。     

不同轮伐期对巨尾桉人工林碳固存的影响

【目的】深入探讨不同轮伐期对巨尾桉人工林碳固存的影响,为从应对全球气候变化的视角确定合理轮伐期提供理论依据。【方法】以轮伐期为短(7a)、中(13a)和长周期(21a)的巨尾桉人工林为研究对象,通过对不同轮伐期桉树林分生物量、碳固存、年平均固碳量的分析,揭示不同轮伐期对桉树林分碳固存的影响。【结果】巨尾桉人工林的生物量碳随着轮伐期的延长而逐渐增加,由7a轮伐期的(75.81±5.12)t·C/hm~2增至13a轮伐期的(180.11±19.97)t·C/hm~2以及21a轮伐期的(192.08±16.50)t·C/hm~2,方差分析表明,13a和21a轮伐期的总生物量碳显著高于7a轮伐期,而13a和21a轮伐期之间的差异不显著。巨尾桉人工林土壤有机碳随轮伐期延长而显著降低,由7a轮伐期的(89.99±0.35)t·C/hm~2、13a轮伐期的(85.42±0.76)t·C/hm~2下降到21a轮伐期的(74.64±0.24)t·C/hm~2。7~13a仍是巨尾桉人工林固碳能力迅速增长期,年平均总生物量碳由7a时的10.78t·C/(hm~2·a)迅速提高到13a的19.54t·C/(hm~2·a),增长81%;21a时巨尾桉人工林进入固碳能力下降期,年平均总生物量碳降至3.78t·C/(hm~2·a),固碳能力只是13a的19.34%。【结论】在南亚热带,巨尾桉人工林的最佳轮伐期确定在13a左右较为适宜,这与经济效益的最大化一致。     

Spectroscopic investigation of the interaction between human serum albumins and 10-hydroxycamptothecin

The binding reaction between 10-hydroxycamptothecin (10-HCPT) and human serum albumins (HSA) is studied by means of fluorescence spectroscopy, UV-Vis absorption spectrum, 1H NMR spectrum, and molecular simulation. The results indicate that the binding reaction of 10-HCPT and HSA is a single static quenching process, and the binding equilibrium constant for 10-HCPT binding with HSA is estimated K ₀= 4.93×10⁴ L · mol⁻¹ at 25 °C with the molar ratio of 1:1. The distance (r) and energy transfer efficiency (E) between donor (HSA) and acceptor (10-HCPT) are obtained as follows, r =3.51 nm; E =0.27. The enthalpy change (ΔH ^⦵) and entropy change (ΔS ^⦵) are calculated at different temperatures, and the hydrophobic force and shidipole force are the functions in the reaction. The results show that 10-HCPT binds within the subdomain II A of HSA by the hydrophobic force, and the 10-OH and 20-OH of 10-HCPT bind with both residue Leu-238 of HSA and Ala 291 of HSA by hydrogen bonds. Biography: LI Guizhi(1962–), female, Associate professor, research direction: organic analysis.     

不同轮伐期巨尾桉人工林的经济效益分析

【目的】探讨不同轮伐期对人工林经济效益的影响,为从经济视角科学确定人工林的合理轮伐期提供理论依据。【方法】以短(7a)、中(13a)、长(21a)轮伐期的南亚热带巨尾桉人工林为研究对象,对不同轮伐期巨尾桉人工林的蓄积量(Stand volume,SV)、营林成本、净现值(Net present value,NPV)和内部收益率(Internal rate of return,IRR)进行分析,揭示不同轮伐期对经济效益的影响。【结果】随着轮伐期的延长,巨尾桉人工林的蓄积量持续增长,7a、13a、21a轮伐期的蓄积量分别为144.95m~3/hm~2、346.97m~3/hm~2、553.69m~3/hm~2。随着轮伐期的延长,巨尾桉人工林净现值不断增加,在12a时达到最高值(30 297.61元/hm~2),之后逐渐降低,7a、21a轮伐期的净现值分别为17 239.86元/hm~2、22 008.59元/hm~2。内部收益率在13a开始趋近峰值(53.32%),明显高于7a时的39.29%。【结论】在南亚热带,巨尾桉人工林的轮伐期确定在13a左右较为适宜,既可实现经济效益最大化,又可大幅提升蓄积量。     

Efficient scalar multiplication for elliptic curves over binary fields

Scalar multiplication [n]P is the kernel and the most time-consuming operation in elliptic curve cryptosystems. In order to improve scalar multiplication, in this paper, we propose a tripling algorithm using Lopez and Dahab projective coordinates, in which there are 3 field multiplications and 3 field squarings less than that in the Jacobian projective tripling algorithm. Furthermore, we map P to（φε^-1（P）, and compute [n]（φε^-1（P） on elliptic curve Eε, which is faster than computing [n]P on E, where φε is an isomorphism. Finally we calculate （φε（[n]φε^-1（P）） = [n]P. Combined with our efficient point tripling formula, this method leads scalar multiplication using double bases to achieve about 23% improvement, compared with Jacobian projective coordinates.     

Interactively interfacial reaction of iron-reducing bacterium and goethite for reductive dechlorination of chlorinated organic compounds

The interactively interfacial reactions between the iron-reducing bacterium （Shewanella decolorationis, S12） and iron oxide （α-FeOOH） were investigated to determine reductive dechlorination transformation of chlorinated organic compounds （chloroform and pentachlorophenol）. The results showed that the interactive system of S12＋ α-FeOOH exhibited relatively high dechlorination rate. By comparison, the S12 biotic system alone had no obvious dechlorination, and the α-FeOOH abiotic system showed low dechlorination rate. The enhanced dechlorination of chloroform and pentachlorophenol in the interactive system of S12＋α-FeOOH was derived from the promoted generation of adsorbed Fe（Ⅱ） by S12. A decrease in redox potential of the Fe （Ⅲ）/Fe （Ⅱ） couple in the interactive reaction system was determined by cyclic voltammetry. Our results will give new insight into interactively interfacial reaction between iron-reducing bacterium and iron oxides for degradation of chlorinated organic compounds under anaerobic condition.     

Research of Inclusion Complexation of 4,4＇-Thiodiphenol Effected by β-Cyclodextrin in Aqueous Solutions and the Effect on Photodegradation

The inclusion behavior of 4, 4＇ -Thiodiphenol （TDP）, a typical bisphenol and endocrine disruptor, reacts with β-cyclodextrin （β-CD） in aqueous solutions has been investigated by means of UV absorption spectrum and quantum-chemical calculation with Gaussian 98 software. The results show that the inclusion behavior of TDP is quite different in acidic solutions （pH 5.9） from that in alkaline solutions （pH 10.0）. This behavior difference is attributed to the different formula structures in aqueous solutions at acidic and alkaline pH values that are demonstrated by quantum- chemical modeling and calculation. TDP forms a 1 ： 1 fl-CD inclusion complex in aqueous solutions. The equiiibrium constant K was calculated to be 553.49 L/mol at pH 5.9 and 1 318.20 L/mol at pH 10.0 respectively for the inclusion complex reaction by using the modified Benesi-Heldbrand equation. After inclusion TDP＇s structure is changed especially at the inclusion part with the bond order becoming larger, which results in inhibitive photodegradation during direct photooxidation and H2O2 assisted photooxidation.     

Photocatalytic degradation of trace-level of MicrocystinLR by nano-film of titanium dioxide

The occurrence of toxic water bloom of cyanobacte-ria algae, widely reported in eutrophic freshwater, hasbeen a serious pollution problem in recent years[1]. Mi-crocystins (MCs), the most common cyanobacteriatoxin with a cyclic heptapeptide structure (Fig…     

Existence of single-peaked solution of a semilinear elliptic problem

We discussed the Dirichlet problem of semilinear elliptic equationin (Pβ,α)D;-β△u=uε+εu,u>0,in Ω u=0, on(e),Ω where Ω(∪)RN(N≥4) is smooth and bounded domain,P=N+2/N-2,β,ε>0. We have proved that there exist positive ε0 and ε1 , such that when 0≤ε≤ε0,β>√ε1,(P0,1)has a single-peaked solution uβ, furthermore, |▽μβ|-0in the sense of measure as ε→0 and β→0.     

Surface Dissociation Properties of Short Chain Carboxyl Mercaptan Self-Assembled Monolayers by Impedance Titration

Impedance titration was used to determine the surface dissociation characteristics of short-chain carboxyl mercaptan self-assembled monolayers （SAMs）. Based on the change of the cyclic voltammetric peak current and the charge-transfer resistance, which was related to pH value of the solution, the surface pKa of mercaptoacetic acid（MA）, 3-mercaptopropionic acid（MPA） and ω-mercaptohexanic acid（MHA） self-assembled membranes, with ionic strength being 0.1 mol/L, were determined to be 5.20, 4.80, 7.40, respectively. In addition, factors such as time needed for assembling, structure of monolayers and ionic strength, which effected the surface pKa, were studied as well. Such surface pKa shifts were sufficiently explained by interactions between interfacial molecules and hydrophobicity.     

Comparison study of chitosan/β-cyclodextrin and carboxymethyl chitosan/β-cyclodextrin microspheres

To compare two microspheres of chitosan/β-cyclodextrin and carboxymethyl chitosan/β-cyclodextrin loaded theophylline as pulmonary sustained drug delivery carriers, the characteristics and ciliotoxicity were studied. The drug loadings of chitosan/β-cyclodextrin and carboxymethyl chitosan/β-cyclodextrin microspheres were 21.09% and 21.42%, and the encapsulation efficiencies were 91.40% and 92.80%. The distributions of 50% (d _0.5) of chitosan/β-cyclodextrin and carboxymethyl chitosan/β-cyclodextrin microspheres were 4.89 and 5.83 μm, respectively. Both microspheres showed spherical shape with smooth or wrinkled surfaces. FT-IR of chitosan/β-cyclodextrin microspheres demonstrated that theophylline had formed hydrogen bonds with chitosan and β-cyclodextrin, while for the carboxymethyl chitosan/β-cyclodextrin microspheres theophylline had interaction with carboxymethyl chitosan. The moisture absorption showed that an equilibrium was reached within 24 h. The two microspheres possessed better adaptability. In vitro release of theophylline from chitosan/β-cyclodextrin microspheres was slower than that from carboxymethyl chitosan/β-cyclodextrin microspheres at pH 6.8. Biography: LI Ruobao(1968–), male, Associate professor, research direction: foundation research of respiratory system.     

Investigation on chain structure of LLDPE obtained by ethylene in-situ copolymerization with DSC and XRD

Thermal segregations of LLDPE were treated with successive self-nucleation/annealing (SSA) on dif-ferential scanning calorimetry (DSC). Information on molecular heterogeneity of LLDPE was obtained. After SSA was treated, the multiple endothermic peaks were observed in the DSC thermograms during heating experiment. It is obtained that the thickness of different lamellas formed by segments of vari-ous lengths was 4―10 nm. X-ray diffraction (XRD) results showed that the crystallites dimensions of various reflections were about several dozens of nanometers. The ethylene/α-olefin copolymers and the copolymer via in-situ copolymerization were similar to each other for molecular heterogeneity and XRD characteristics, which revealed that it was possible to use the ethylene/α-olefin copolymers to simulate the copolymer via in-situ copolymerization of ethylene to simplify the complexity of the structure of the ethylene in-situ copolymer.     

Synthesis and micellization behavior of stimuli-responsive polypeptide hybrid triblock copolymer

Polypeptide hybrid triblock copolymer, poly（L-glutamic acid）-b-poly（propylene oxide）-b-poly （L-glutamic acid） （PLGA-b-PPO-b-PLGA）, was synthesized by the ring-opening polymerization of benzyI-L- glutamic N-carboxyanhydride （BLG-NCA） using poly（propylene glycol） bis（2-aminopropyl ether） as initiator, followed by the subsequent deprotection step. The obtained double hydrophilic triblock co- polymer exhibits ＂schizophrenic＂ micellization behavior in aqueous solution upon dually playing with solution pH and temperature. The multi-responsive micellization behavior of this polypeptide hybrid triblock copolymer has been thoroughly investigated by 1H NMR, laser light scattering （LLS）, tempera- ture-dependent optical transmittance, and circular dichroism spectroscopy （CD）.     

Photodegradation of <Emphasis Type="Italic">N</Emphasis>-nitrosodiethylamine in water with UV irradiation

The direct photolysis of N-nitrosodiethylamine （NDEA） in water with ultraviolet （UV） irradiation was investigated. Results showed that NDEA could be completely degraded under the direct UV irradiation. The effects of the experimental conditions, including the initial concentration of NDEA, humic acid and solution pH, were studied. The degradation products of NDEA were identified and quantified with gas chromatography-mass spectrometry （GC-MS） and high performance liquid chromatography （HPLC）. It was confirmed that methylamine （MA）, dimethylamine （DMA）, ethylamine （EA）, diethylamine （DEA）, NO2^- and NO3^- were the main degradation products. The photolysis degradation mechanism of NDEA was also discussed. As a result of N-N bond fission, NDEA was degraded by direct UV irradiation.     

Characterization of Anabaena cylindrica Solution System Using Synchronous-Scan Fluorescence Spectroscopy

The characterization of the algaeAnabaena cylindrica solution with Fe (III) was investigated using fluorescence emission and synchronous-scan spectroscopy. The ranges of concentrations of algae and Fe (III) in aqueous solutions were 5.0×10⁸ 2.5×10⁸ cell/L and 1060 μmol/L. respectively. The effective characterization method used was synchronous-scan fluorescence spectroscopy (SFS). The wavelength difference (Δλ) of 90 nm, was maintained between excitation wavelength (λen) and emission wavelength (λen). The peak was observed at about (λex) (λem) 326 nm for synchronous scan fluorescence spectroscopy. The fluorescence quenching in system of algae Fe(III)-HA was studied using synchronous-scan spectroscopy for the first time, Fe(III) was clearly the effective quencher. The relationship betweenI I (quenching efficiency) andc (concentration of Fe (III) added) was, a linear correlation for the algae solution with Fe(III). Also, Aldrich humie acid (HA) was found to be an effective quencher. Foundation item: Supported by the National Natural Science Foundation of China (20177017) and the Scientific Research Foundation of Wuhan Environmental Protection Bureau Biography: LIU Xian li(1965), male. Ph.D. Associate professor, research direction: environmental chemistry.     

3种脱蛋白方法对虎斑乌贼肌肉多糖体外抗氧化活性的影响

【目的】比较3种不同脱蛋白方法对虎斑乌贼肌肉多糖体外抗氧化活性的影响。【方法】采用Sevag法、三氯乙酸法和等电点法对经过热水浸提的虎斑乌贼肌肉多糖进行脱蛋白,同时对脱蛋白多糖的体外抗氧化活性进行研究。【结果】3种不同脱蛋白方法得到的多糖均具有一定的抗氧化能力。当多糖浓度为5 mg/mL时,Sevag法、三氯乙酸法和等电点法得到的脱蛋白多糖对1,1-二苯基-2-三硝基苯肼(DPPH)自由基的清除率分别为87.05%、42.35%和38.54%,相应的IC50值分别为1.96mg/mL、11.81mg/mL和9.84mg/mL;对羟基自由基(·OH)清除率分别为93.67%、70.80%和68.75%,相应的IC50值分别为0.67mg/mL、1.37mg/mL和2.72mg/mL;对超氧阴离子(O-2)清除率分别为72.33%、62.42%和53.33%,相应的IC50值分别为0.15mg/mL、1.56mg/mL和3.81mg/mL。多糖还原力大小分别为0.183,0.160和0.144。【结论】3种脱蛋白方法所得虎斑乌贼肌肉多糖抗氧化活性大小依次为Sevag法三氯乙酸法等电点法。