高氧气调包装对金针菇保鲜品质的影响

研究了不同气体配比条件对金针菇保鲜效果的影响。 分别用 3% O2 +97% N2 ,80% O2 +20% N2 ,80% O2 +10% N2 +10% CO2 ,80% O2 +20% CO2 气体配比充气包装金针菇,空气包装为对照组。 评定其水分损失率、呼吸强度、色差、相对电导率、多酚氧化酶(PPO)、过氧化物酶(POD)和感官指标等。 结果表明,80% O2 +20% CO2 组水分损失、颜色变化最少,PPO 酶活力、呼吸强度最低,POD 酶活力较高,感官变化最小,贮藏保鲜效果好。     

Control of nitric oxide, nitrous oxide, and ammonia emissions using microwave plasmas

The subject of this paper is mitigation of the undesirable side-effects of selective non-catalytic reduction (SNCR) and selective catalytic reduction (SCR): ammonia slip, residual NO(x), and N(2)O emissions. The use of microwave-plasma discharge within the flue gas was explored as a potential pollution-control method. The key issues addressed were: (1) N(2)O, NH(3), and NO removal efficiencies; and (2) sustaining a stable plasma at atmospheric, or close to atmospheric, pressure. In non-oxidizing atmospheres, removal efficiencies were always close to 100% for all species. In the presence of oxygen, however, appreciable amounts of nitric oxide and ammonia were formed. Methods leading to preventing these undesirable effects were examined. In a number of runs, stable plasma operation was attained at pressures close to atmospheric.     

新鲜竹笋气调保鲜技术的研究

采用O2(2%)+CO2(5%)+N2(93%),O2(80%)+CO2(5%)+N2(15%),O2(80%)+CO2(20%)气调比例包装新鲜竹笋,研究不同气调处理对竹笋保鲜效果的影响。评测竹笋在保存期间水分损失率、L 值、电导率、多酚氧化酶活力、过氧化物酶活力、抗坏血酸、感官品质的变化。结果显示,O2(80%) +CO2(20%) 组水分损失少,L值变化小,电导率上升缓慢,PPO,POD 酶活力低,抗坏血酸含量高,感官品质得分高,贮藏保鲜效果好,贮藏至15d, 仍具有良好的商品品质。     

Modulating the charge-transfer enhancement in GERS using an electrical field under vacuum and an n/p-doping atmosphere

The modulation of charger-transfer (CT) enhancement in graphene-enhanced Raman scattering (GERS) by an electric field under different atmospheres is reported. The GERS spectra of cobalt phthalocyanine (CoPc) molecules were collected by in situ Raman measurements under ambient air, vacuum, NH(3) atmosphere, and O(2) atmosphere, in which the Fermi level of graphene was modulated by an electrical field effect (EFE). The Raman scattering intensities of adsorbed molecules can be tuned to be stronger or weaker as the graphene Fermi level down-shifts or up-shifts under electrical field modulation. However, the Raman intensity modulation in GERS is seriously influenced by the hysteresis effect in graphene EFE, which makes the modulation ability small and shows strong gate voltage sweep rate dependence in ambient air. Fortunately, the hysteresis effect in graphene EFE can be decreased by performing the measurement under vacuum conditions, and thus the Raman modulation ability in GERS can be increased. Furthermore, compared with the vacuum condition, the Raman modulation ability shows an increase under an NH(3) atmosphere, while it shows a decrease under an O(2) atmosphere, which is due to the different Fermi level modulation region in different atmospheres. More interestingly, this Raman intensity modulation in GERS shows a hysteresis-like behavior that is the same as the graphene Fermi level modulation under the EFE in a different atmosphere. All these observations suggest that the Raman enhancement in GERS occurs through a charge-transfer (CT) enhancement mechanism and the CT process can be modulated by the graphene EFE. This technique will benefit the study of the basic properties of both graphene and chemical enhancement mechanism in surface-enhanced Raman spectroscopy (SERS).     

A study on N2O catalytic decomposition over Co/MgO catalysts

Different oxide supported cobalt catalysts were prepared by co-precipitation method and tested for the decomposition of nitrous oxide. Co/MgO with cobalt loading of 15% showed the best activity and a 100% N(2)O conversion was obtained at temperatures higher than 700 K. The active phase of cobalt species in Co/MgO catalysts was Co(3)O(4) highly dispersed in the matrices of MgO, based on XRD and XPS results as well as the kinetic analysis. The existence of NO, O(2) and H(2)O in reaction system showed different negative effects on N(2)O decomposition. Nevertheless, a 100% N(2)O conversion could be achieved at 800 K under simulated conditions of tail gas from nitric acid plant. Moreover, Co/MgO catalyst exhibited quite good durability and no obvious activity loss was observed in the 100 h stability test.     

Investigating the Mechanism of Hysteresis Effect in Graphene Electrical Field Device Fabricated on SiO(2) Substrates using Raman Spectroscopy

The hysteresis effect is a common problem in graphene field-effect transistors (FETs). Usually, the external doping to graphene is considered to be responsible for the hysteresis behavior, but is not yet clearly understood. By monitoring the doping of graphene and the hysteresis in graphene FETs under different atmospheres using in situ Raman spectroscopy, it is confirmed that the electrochemical doping of O(2) /H(2) O redox couple to graphene is responsible for the hysteresis effect. In addition, Raman spectra of graphene on SiO(2) substrate show stronger doping than that suspended, which indicates that SiO(2) substrate plays an important role in the doping of graphene. Herein it is proposed that the doping species (H(2) O and O(2) ) are bounded at the interface of graphene/SiO(2) substrate by hydrogen-bonds with the silanol groups on SiO(2) substrate. The dynamic equilibrium process of the charge-transfer between H(2) O/O(2) redox couple and graphene under electrical field modulation is carefully analyzed using Marcus-Gerischer theory. This work provides a clear view to the mechanism of the hysteresis effect, and is of benefit to a reliable design to suppress the hysteresis in graphene FETs.     

Spectroscopic tags using dye-embedded nanoparticles and surface-enhanced Raman scattering

Surface-enhanced Raman scattering is capable of providing rich vibrational information at the level of single molecules and single nanoparticles, but the practical applications of this enormous enhancement effect are still a challenge. Here we report a new class of dye-embedded core-shell nanoparticles that are highly efficient for surface Raman enhancement and could be used as spectroscopic tags for multiplexed detection and spectroscopy. The core-shell particles contain a metallic core for optical enhancement, a reporter molecule for spectroscopic signature, and an encapsulating silica shell for protection and conjugation. A surprising finding is that organic molecules with an isothiocyanate (-N=C=S) group or multiple sulfur atoms are compatible with silica encapsulation. In comparison with fluorescent dyes and quantum dots, enhanced Raman probes contain a built-in mechanism for signal amplification and provide rich spectroscopic information under ambient experimental conditions.     

Synthesis and characterization of gold nanoparticles coated with ultrathin and chemically inert dielectric shells for SHINERS applications

We very recently reported a new spectroscopic application for expanding the versatility of surface Raman called "shell-isolated nanoparticle-enhanced Raman spectroscopy" or "SHINERS". The most important and most difficult part of the SHINERS experiment is the effective transfer of the strong electromagnetic field from a gold core through the isolating silica or alumina shell to the probed surface. For this it is essential that the chemically inert dielectric shell be ultrathin (2-5 nm) yet pinhole-free. Herein we describe experimental and theoretical aspects of our SHINERS method in more detail. We provide a protocol for the synthesis and characterization of optimized shell-isolated nanoparticles (SHINs), and we examine the advantages of SHINERS nanoparticles over bare gold nanoparticles. We also present high-quality Raman spectra obtained from gold and platinum single-crystal surfaces in an electrochemical environment by our SHINERS technique. SHINERS is a simple and cost-effective approach that expands the flexibility of surface-enhanced Raman scattering (SERS) for an unprecedented diversity of applications in materials and surface sciences.     

Effect of substructure on crack formation and total failure of industrial alloys of the aluminium-copper-magnesium system under low-cycle fatigue conditions

On the example of pressed semifinished products made of D16 and AK4-1 type alloys of different chemical composition in the Al-Cu-Mg system in the T and T1 conditions a study has been made of the effect of a number of structural elements on the fatigue life of plane specimens with a concentrator (stress concentration factor 2.6) under low-cycle fatigue conditions. The duration of the stage to development of a fatigue crack N₀ with an area of about O.05 mm² and the overall life of specimens to total failure N_f have been determined. Tests have been carried out for low-cycle fatigue under repeated tension conditions with a cycle asymmetry factor R = O.01, frequency 5 Hz, and maximum stress in the cycle of 160 MPa. It has been established that a reduction in iron and silicon content in alloys D16, D16ch, and 1163 decreases the content in the structure of coarse particles of AlFeMnCuSi phase of variable composition and it increases the life of specimens in the naturally aged condition as a result of increasing the N₀ stage. A reduction in copper content in alloy 1163T from 4.3 to 3.9% and introduction of zirconium in an amount of 0.10%, which weakly affects N₀, increases the duration of the period of crack growth N_f-N_o by 50 kcycles. All of the alloys of the D16ch and 1163 type in the artificially aged condition have similar values of parameters N₀ and N_f with a much lower level of them in the T condition, which is explained by a change in the mechanism for crack development and its growth rate.Translated from Problemy Prochnosti, No. 1, pp. 43–49, January, 1990.     

A study on adsorption of acetonitrile on gold nanorods by non-resonant Raman measurements and density functional theory calculations

Adsorption of acetonitrile (Ac) molecules on gold (Au) nanorods has been investigated by Raman spectroscopic measurements and density functional theory (DFT) calculations. DFT calculations provide a valuable insight into the underlying structure of the metal-molecule complex. From the best agreement between the observed and the calculated Raman frequencies and also from other spectroscopic observations, we propose that Ac molecules interact with Au nanorods and form an [Ac+2Au](0)-like complex on the surface of nanostructures. The environmental effect has also been taken into consideration to explain the Raman activity of the complex.     

Atomic vapor deposition approach to In2O3 thin films

In2O3 thin films were grown by atomic vapor deposition (AVD) on Si(100) and glass substrates from a tris-guanidinate complex of indium [In(N(i)Pr2guanid)3] under an oxygen atmosphere. The effects of the growth temperature on the structure, morphology and composition of In2O3 films were investigated. X-ray diffraction (XRD) measurements revealed that In2O3 films deposited in the temperature range 450-700 degreesC crystallised in the cubic phase. The film morphology, studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM), was strongly dependent on the substrate temperature. Stoichiometric In2O3 films were formed under optimised processing conditions as was confirmed by X-ray photoelectron and X-ray excited Auger electron spectroscopies (XPS, XE-AES), as well as by Rutherford backscattering spectrometry (RBS). Finally, optical properties were investigated by photoluminescence (PL) measurements, spectroscopic ellipsometry (SE) and optical absorption. In2O3 films grown on glass exhibited excellent transparency (approximately 90%) in the Visible (Vis) spectral region.     

Electrical Conductivity of Sintered Chromia Mixed with TiO2, CuO and Mn-Oxides

The electrical conductivity of sintered Cr2O3 mixed with 2% and 5% （in molar fraction） TiO2 or CuO was investigated in the temperature range 500-900℃ in air and in At/4 vol. pct H2 atmospheres. The effect of different Mn-oxides on the electrical conductivity of Cr2O3 was also studied under the same conditions. From the conductivity measurements it is established that additions of TiO2 change the defect structure of Cr2O3 and the effect of TiO2 on the electrical conductivity is controlled by TiO2 concentration as well as temperature and O2 partial pressure of the surrounding atmosphere. The conductivity of Cr2O3 increased in air and decreased in the At/H2 atmosphere by CuO additions. The effect of CuO was discussed with possible changes in the defect concentration in Cr2O3. Mixing of Cr2O3 with different Mn-oxides at the same Mn to metal atom fraction decreased the conductivity in air and in Ar/H2 atmospheres. No clear correlation between the spinel fraction and the changes in conductivity could be found.     

Vapor phase surface functionalization under ultra violet activation of parylene thin films grown by chemical vapor deposition

Various reactive gas phase treatments have been investigated as surface functionalization dry processes with the goal to improve the wettability of parylene C films, keeping good optical properties in the visible range. The films were grown on different substrates by chemical vapor deposition with thicknesses ranging from 300 to 1630 nm. The polymer surface was treated under ultra violet (UV) irradiation at 254 nm in reactive atmospheres including He, H₂O, H₂O₂, O₂ and ambient air. The UV/O₂ treatment is the most efficient since the water contact angle decreases from 100° to 6° while the transmittance is maintained at 90% in the visible wavelengths. Furthermore it exhibits long life stability. The functionalization mechanism is discussed in relation with previous reports.     

Electrical characterisation of AlCuMo thin films prepared by DC magnetron sputtering

Thin film resistors have been manufactured to evaluate the electrical performance characteristics of AlCuMo thin films. The films were prepared on Al2O3 substrates at room temperature as a function of Mo concentration by DC magnetron sputtering and were then annealed at various temperatures in air and N2 atmospheres. The effect of annealing temperature on the electrical properties of the films was systematically investigated. Increase in Mo content produced a decrease in temperature coefficient of resistance (TCR), an increase in resistivity (r) and an improvement in long term stability (DV/V) of the films. TCR varied from negative to positive and further improvements in resistance stability of the films were also achieved through increasing annealing temperature in both air and N2 atmospheres. A temperature region is proposed where `near zero? TCR (ppm/8C) and long term stability of better than 0.2% can be realised.     

CVD synthesis of graphene nanoplates on MgO support

Synthesis of graphene directly on MgO has been carried out and the structural properties of the obtained material have been investigated. Few-layered graphene was produced by simple thermal decomposition of methane over MgO powder at 950 °C in a CVD reactor. The samples were purified by 10 N HNO₃ treatment, and studied by TEM, Raman spectroscopy, EDAX and SEM. TEM clearly indicated the formation of graphene. EDAX showed that the purified sample contained only carbon and no traces of MgO. The characteristic Raman features of graphene were also seen as D-band at 1316 cm^?1, G-band at 1602 cm^?1, and a small 2D-band at 2700 cm^?1 in the Raman spectra. The strong D-band suggests that the graphene possess large number of boundary defects. The small 2D-band indicates the formation of few-layered graphene.     

Electron Spin Resonance Studies of Nitrogen Atoms Stabilized in Impurity-Helium Condensates

Impurity-helium condensates (IHCs) created by injection of nitrogen atoms and molecules as well as rare gas (RG) atoms (Ne, Ar, and Kr) into superfluid \(^4\)He have been studied via electron spin resonance (ESR) techniques. We investigated the influence of addition of rare gas atoms (Ne, Ar, and Kr) into the condensing \(\hbox {N}_2\)–He gas mixture on the efficiency of stabilization as well as on the local and average concentrations of N atoms attainable in IHCs. Addition of Ar and Kr atoms into the condensing \(\hbox {N}_2\)–He gas mixture substantially increased the stabilization efficiency of N atoms in nanoclusters forming IHCs. Measurements of the ground-state spectroscopic parameters of nitrogen atoms show that the nanoclusters have a shell structure. Most of the N atoms reside on solid molecular layers of \(\hbox {N}_2\). These layers form on the surfaces of RG (Ar or Kr) nanoclusters.     

Role of oxygen active species in the photocatalytic degradation of phenol using polymer sensitized TiO2 under visible light irradiation

The role of dissolved oxygen, and of active species generated by photo-induced reactions with oxygen, in the photocatalytic degradation of phenol was investigated using polymer [poly-(fluorene-co-thiophene) with thiophene content of 30%, so-called PFT30] sensitized TiO2 (PFT30/TiO2) under visible light irradiation. The photoluminescent (PL) quantum yield of PFT30/TiO2 was about 30% of that of PFT30/Al(2)O(3), proving that electron transfer took place between the polymer and TiO2. The result that photocatalytic degradation of phenol was almost stopped when the solution was saturated with N(2) proved the importance of O(2). Addition of NaN(3), an effective quencher of singlet oxygen ((1)O(2)), caused about a 40% decrease in the phenol degradation ratio. Addition of alcohols caused about a 60% decrease in the phenol photodegradation ratio, indicating that the hydroxyl radicals (OH), whose presence was confirmed by electron spin resonance (ESR) spectroscopy, was the predominant active species in aqueous solution. In anhydrous solution, singlet oxygen ((1)O(2)) was the predominant species. These results indicate that oxygen plays a very important role in the photocatalytic degradation of phenol.     

Phase equilibrium of the Cu-Fe-O system under Ar,CO2 and Ar+0.5% O2 atmospheres during CuFeO2 single-crystal growth

Phase relations of CuFeO₂ during crystal growth under Ar, CO₂ and Ar+0.5% O₂ surrounding atmospheres have been investigated using scanning electron microscopy together with electron probe microanalysis and X-ray powder diffraction. CuFeO₂ was found to partially decompose into Fe₂O₃ and Cu₂O before melting and the crystal growth process was by means of Cu₂O-solvent movement. Under Ar and CO₂ atmospheres, Cu₂O was found to be further reduced to metallic copper, and under CO₂ more severe reduction of copper was observed. No copper reduction could be found under an Ar+0.5% O₂ surrounding atmosphere.     

Photochemical removal of NO(2) by using 172-nm Xe(2) excimer lamp in N(2) or air at atmospheric pressure

Photochemical removal of NO(2) in N(2) or air (5-20% O(2)) mixtures was studied by using 172-nm Xe(2) excimer lamps to develop a new simple photochemical aftertreatment technique of NO(2) in air at atmospheric pressure without using any catalysts. When a high power lamp (300 mW/cm(2)) was used, the conversion of NO(2) (200-1000 ppm) to N(2) and O(2) in N(2) was >93% after 1 min irradiation, whereas that to N(2)O(5), HNO(3), N(2), and O(2) in air (10% O(2)) was 100% after 5s irradiation in a batch system. In a flow system, about 92% of NO(2) (200 ppm) in N(2) was converted to N(2) and O(2), whereas NO(2) (200-400 ppm) in air (20% O(2)) could be completely converted to N(2)O(5), HNO(3), N(2), and O(2) at a flow rate of 1l/min. It was found that NO could also be decomposed to N(2) and O(2) under 172-nm irradiation, though the removal rate is slower than that of NO(2) by a factor of 3.8. A simple model analysis assuming a consecutive reaction NO(2)-->NO-->N+O indicated that 86% of NO(2) is decomposed directly into N+O(2) and the rest is dissociated into NO+O under 172-nm irradiation. These results led us to conclude that the present technique is a new promising catalyst-free photochemical aftertreatment method of NO(2) in N(2) and air in a flow system.