请问“磁疗”英文怎样翻译？谢谢

asd1365409524 2006-05-16 10:10:16 617 浏览

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爱哭的小鸡 2006-05-17 00:00:00

magnetic healing/therapy

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最爱去去啊在 2006-05-17 00:00:00

magnetic therapy

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李怡憬ing 2006-05-17 00:00:00

是Magnetic Therapy --Will

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请问“磁疗”英文怎样翻译？谢谢:

英语高手帮忙翻译段英文谢谢！！: In this paper， the degradation of an azo dye Orange G (OG) on nitrogen-doped TiO2 photocatalysts has been investigated under visible light and sunlight irradiation. Under visible light irradiation， the doped TiO2 nanocatalysts demonstrated ... In this paper， the degradation of an azo dye Orange G (OG) on nitrogen-doped TiO2 photocatalysts has been investigated under visible light and sunlight irradiation. Under visible light irradiation， the doped TiO2 nanocatalysts demonstrated higher activity than the commercial Dugussa P25 TiO2， allowing more efﬁcient utilization of solar light， while under sunlight， P25 showed higher photocatalytic activity. According to the X-ray diffraction (XRD)， X-ray photoelectron spectroscopy (XPS) and UV–vis spectra analyses， it was found that both the nanosized anatase structure and the appearance of new absorption band in the visible region caused by nitrogen doping were responsible for the signiﬁcant enhancement of OG degradation under visible light. In addition， the photosensitized oxidation mechanism originated from OG itself was also considered contributing to the higher visible-light-induced degradation efﬁciency. The effect of the initial pH of the solution and the dosage of hydrogen peroxide under different light sources was also investigated. Under visible light and sunlight， the optimal solution pH was both 2.0， while the optimal dosage of H2O2 was 5.0 and 15.0 mmol/l， respectively. Azodyes， which are characterized by the presence of one or more azo bonds ( N N )， are among the most notorious widespread environmental pollutants associated with textile，cosmetic， food colorants， printing， and pharmaceutical indus-tries. Because of their non-degradability， toxicity， potential mutagenicity and carcinogenicity， wastewaters originating from these dyes production or application industries pose a major threat to the surrounding ecosystems and human beings’ health.[1–3].Environmental concerns and the need of meeting the strin-gent international standards for rejecting wastewaters has made the development of novel and cost-effective processes for the puriﬁcation of azo dyes efﬂuents an issue of major technological importance. 展开

请翻译一下这段英文1，谢谢: Materials For the present study， the matrix was ABS supplied by Formosa Co. The reinforcements were polyacrylonitrile based high strength CFs. The properties of materials used were given in Table 1. Carbon fibre surface treatment Carbon fi... Materials For the present study， the matrix was ABS supplied by Formosa Co. The reinforcements were polyacrylonitrile based high strength CFs. The properties of materials used were given in Table 1. Carbon fibre surface treatment Carbon fibres were oxidised by boiling in HNO3 under reflux for 5 h (T5120uC). Afterwards， the nitric acid oxidised fibres were washed with distilled water to neutral pH. Fibre surface composition The fibres were characterised by X-ray photoelectron spectroscopy (ESCA 300， Scienta， Sweden) to determine the level of functionalisation of the modified fibres. An initial survey scan was performed to determine the detectable elements， followed by high resolution scans. The entire X-ray photoelectron spectrum was energy referenced to the C1s peak of graphite (bending energy5284?5 eV). Composite preparation Before processing， ABS pellets and CFs were dried in a vacuum oven for 4 h at 80uC. Composites containing 0， 5， 10， 15， 20， 25 and 30 wt-% SCF were prepared by melt mixing in a co-rotating twin screw extruder (Thermoprism TSE 16 TC， L/D:24). The ABS pellets and CFs were fed from the main and side feeders respectively. The molten composite obtained from the die of the extruder was water cooled and pelletised. The extrusion conditions were arranged， as shown in Table 2. The viscosity of the melt containing CFs depends on the viscosity of the polymer matrix as well as the processing temperature. To avoid unfavourable shearing conditions， the melt temperature is kept as high as possible regarding thermal degradation. Before PA6 was blended to promote interfacial adhesion， vacuum drying of the ABS and PA6 pellets was carried out at 80uC for 4 and 12 h respectively. The 0， 10， 20 and 30 wt-% PA6 containing batches were fed through the main feeder to the twin screw extruder. The extrudate was water cooled and chopped into small pellets. The produced ABS/PA6 pellets were vacuum dried again at 80uC for 12 h. To prepare the SCF reinforced ABS/PA6 composites， the blend was introduced into the twin screw extruder from the main feeder， and SCFs were fed from the side feeder. The twin screw extruder was operated at the same processing conditions used during the blend preparation. The extrudate was again water cooled and chopped into small pellets. The extrusion grades of resin were used to make the extrudate form fully. The specimens for the mechanical characterisation experiments were moulded using a laboratory scale injection moulding machine (microinjector， model 1998; Daca Instruments) at a barrel temperature of 230uC and mould temperature of 80uC. The injection moulding machine used in this study was a laboratory type microinjector. The principle of the operation is that the preweighed (，2?5 g) raw material is loaded into the cylindrical barrel and allowed to melt at a preset barrel temperature for 1 min.Then the molten plastic is pushed through an injection tip by a piston. 展开

翻译以下英文：: The standard error of the mean (SEM) is a measure of how far your sample mean is likely to be from the true population mean. The SEM is calculated by this equation:SEM=SD/N. With large samples， the SEM is always small. By itself， the SEM i... The standard error of the mean (SEM) is a measure of how far your sample mean is likely to be from the true population mean. The SEM is calculated by this equation:SEM=SD/N. With large samples， the SEM is always small. By itself， the SEM is difficult to interpret. It is easier to interpret the 95% confidence interval， which is calculated from the SEM. 展开

高分求高人翻译植物化学英文材料，谢谢: Review Enzymatic protein hydrolysis plays a major role in various physiological processes， including digestion， and is regulated by proteinase inhibitors. Inhibitors in foods and food ingredients can reduce the absorption of free amino aci... Review Enzymatic protein hydrolysis plays a major role in various physiological processes， including digestion， and is regulated by proteinase inhibitors. Inhibitors in foods and food ingredients can reduce the absorption of free amino acids， and can impair protein hydrolysis in industrial processes. However， inhibitors can be useful tools in pest control， in the prevention and treatment of diseases such as cancers and AIDS， and in the elimination of unwanted proteinase activity in food processes. Proteinase inhibitors are also useful biochemical tools for studying proteinase classes and specificities. This article discusses how proteinase inhibition is involved in some processes of current interest to food scientists and technologists. Enzymatic protein hydrolysis is a major concern for biological scientists. The hydrolysis of proteins is catalyzed by peptide-bond-splitting enzymes (Box 1). Proteinases and peptidases are involved in the hydrolysis of protein during digestion， and have important roles in physiology and pathology. Enzymatic protein hydrolysis is controlled in several ways， including by the use of specific inhibitors (Box 2). Proteinase inhibition is a common process in nature. Proteinase-inhibitor interactions are involved in protein digestion， various physiological processes (e.g. blood coagulation， fibrinolysis， complement activation and phagocytosis)， pathological processes (e.g. cancers and hypertension) and infection Another natural method of controlling proteinase activity is the synthesis of an inactive form of the enzyme， the zymogen. Zymogens are activated， usually by the action of another proteinase， in the digestive system and also during regulatory physiological processes. When an enzyme is in its active form， proteinase inhibition is an exquisite means of enzyme control in physiological processes， which is achieved by highly specific inhibitors. The importance of the control of proteolytic activity by inhibitors in physiological processes is demonstrated by the fact that inhibitor molecules exceed 10% of the total protein in human plasma. The fact that the control of proteolysis by inhibitors is so specific makes it a valuable tool in medicine， agriculture and food technology. The human immune deficiency virus proteinase， the digestive systems of crop pests， and fish muscle proteases are some examples of targets for study. Most organisms produce proteinase inhibitors as a means to control proteolytic processes.Some organisms store huge amounts of inhibitors， for example legume seeds and some leaves. This seems to be an evolutionary response to predation. Inhibitors for digestive proteinases in food and feed Some food ingredients contain so-called antinutritive factors: lectins， phenols， and other factors， including certain proteins that inhibit proteinases. The presence of proteinase inhibitors in living tissues seems to be a natural regulatory process 展开

求翻译英文文献: 2.2. Material Characterizations. A field emission scanning electron microscope (SEM， JEOL 6701F) was used to investigate the morphologies， particle sizes of the samples. Transmission electron microscopy and elemental compositions of the ... 2.2. Material Characterizations. A field emission scanning electron microscope (SEM， JEOL 6701F) was used to investigate the morphologies， particle sizes of the samples. Transmission electron microscopy and elemental compositions of the samples were determined by JEM-2100F (JEOL) coupled with an energy-dispersive X-ray spectroscopy (EDX， Phoenix) system. Wide-angle and low-angle X-ray powder diffraction (XRD) of the as-obtained samples were recorded on a Rigaku D/max-2500 with Cu Kα radiation (λ = 1.540 56 Å) operated at 40 kV and 200 mA. Raman measurements were performed using a DXR from Thermo Scientific with a laser wavelength of 532 nm. To calculate the pore size distribution and pore volumes， the nitrogen absorption and desorption isotherms were measured at 77.3 K with an Autosorb-1 specific surface area analyzer from Quantachrome. The content of N in N-doped porous carbon was determined by NHC elemental analysis using Flash EA 1112. Thermogravimetric (TG) analysis of S/C composite was performed on TG/DTA 6300 in an N2 flow to obtain the S content in the composite. A four-contact method was applied to measure the powder electronic conductivity of porous carbons. The powder sample was pressed to disk at 4 MPa with two stainless-steel plungers， whose resistance was measured by a Keithley 2400 digital multimeter in fourwire mode. The conductivity of the sample was calculated according to the resistance and the size of the disk. Information of the surface elements was obtained by X-ray photoelectron spectroscopy (XPS) performed on the Thermo Scientific ESCALab 250Xi using 200 W monochromatic Al Kα radiation. The 500 μm X-ray spot was used for XPS analysis. The base pressure in the analysis chamber was about 3 × 10−10 mbar. All reported data of XPS binding energy are calibrated based on the hydrocarbon C 1s line at 284.8 eV from adventitious carbon. Spectra were fitted with Lorentzian−Gaussian functions and smart background using Thermo Avantage software. 展开

求助，英文文献翻译！: 2. Experimental 2.1 Materials Nano-CaCO3 particles (D50: 30−70 nm by TEM (Fig. 1) and BET: ca.17m2·g-1) were supplied by Shanghai Zhuoyue Nanotech Corporation. Methyl methacrylate (MMA， Shanghai Lingfeng Chemicals) was purified ... 2. Experimental 2.1 Materials Nano-CaCO3 particles (D50: 30−70 nm by TEM (Fig. 1) and BET: ca.17m2·g-1) were supplied by Shanghai Zhuoyue Nanotech Corporation. Methyl methacrylate (MMA， Shanghai Lingfeng Chemicals) was purified by distillation under reduced pressure; potassium persulphate (K2S2O8， initiator， Shanghai Lingfeng Chemicals) was of chemical grade. Silane coupling agent A174 (γ-methacryloxypropyltrimethoxysilane) was purchased from Shanghai Yaohua Factory. Polyvinylchloride (PVC， WS-1000S) was supplied by Shanghai Chlor-Alkali Chemical Co.， Ltd. Fig. 1 Morphology of untreated CaCO3 nanoparticles. Fig. 2 Morphology of PMMA-coated CaCO3 nanoparticles. 2.2 PMMA emulsion polymerization on CaCO3 nanoparticles 2.2.1 Surface silanation of nano-CaCO3 particles The nano-CaCO3 particles were homogeneously dispersed in ethanol (solid content 20%) by a sonication dispersion equipment. The slurry was then heated to 80°C with stirring， and the silane coupling agent A174 (5%， calculated based on the weight of nano-CaCO3 particles) was added into the slurry. After the slurry was stirred for 120 min at 80°C， it was filtered and the filter cake was then dried at 120°C in low vacuum for 120 min to obtain silanated CaCO3 powders. 展开

求助，英文文献翻译~: PMMA has good compatibility with PVC due to specific interaction of a hydrogen bonding type between carbonyl groups (C=O) of PMMA and hydrogen from (CHCl) groups of PVC (Belhaneche-Bensemra et al.， 2002; Ramesh et al.， 2002). Zhou et al... PMMA has good compatibility with PVC due to specific interaction of a hydrogen bonding type between carbonyl groups (C=O) of PMMA and hydrogen from (CHCl) groups of PVC (Belhaneche-Bensemra et al.， 2002; Ramesh et al.， 2002). Zhou et al. (2001) studied the relationship between the coating thickness of PMMA on the surface of talc and mechanical properties of PMMA-g-talc/PVC composites， and found that there existed a critical thickness. Xie (2001) found that the PMMA coating on talc improved the dispersion of talc in the PVC matrix and enhanced the interfacial adhesion between talc and PVC. There appears to be a critical coating thickness of PMMA on the talc surface for optimum toughening. Quan et al. (2002) reported improved toughness and intension of the PVC composites filled with CaCO3/ACR core-shell complex particles prepared by in-situ emulsion polymerization of acrylic ester. In the present work， PMMA coated on the surface of CaCO3 nanoparticles by in-situ emulsion polymerization was characterized by FT-IR and 1H-NMR. The effects of PMMA thickness and particle fraction on the mechanical properties of PMMA-coated CaCO3 /PVC nanocomposites were also investigated. 展开

面料色牢度 3-4级以上英文怎么翻译?谢谢!:

有关机械液压方面的英文资料及翻译，翻译的字数5000以上！谢谢！！:

数据采集的英文怎么翻译？:

翻译英文~专业类的: Whilegraphene，acarbon-basedtwo-dimensionalnanomaterials，hasreceivedanupsurgeofinterest，[1]self-assemblyofsmallorganicandorganometallicmoleculesinto2Dnanostructurescouldal... While graphene， a carbon-based two-dimensional nanomaterials， has received an upsurge of interest，[1] self-assembly of small organic and organometallic molecules into 2D nanostructures could also be harnessed to develop new classes of functional supramolecular nanomaterials.[2] In principle， quasi-2D lamellae or nanosheets are planar structures having a thickness less than 100 nm and lateral dimensions a few orders of magnitude greater than their thickness. Control over the bilateral intermolecular noncovalent interactions is anticipated to organize small molecules into regular 2D nanostructures， which has been a formidable challenge yet to be achieved. Recently， Shelnutt and co-workers obtained discrete porphyrin nanosheets reprecipitated from their solutions;[3] Sathish and co-workers constructed hexagonal C60 nanosheets using a liquid–liquid interfacial precipitation method;[4] the groups of Yao[5] and Hu[6] prepared singlecrystalline nanosheets of polycyclic aromatics using a surfactant- assisted reprecipitation and a physical vapor transporting method， respectively; and Zhang and co-workers suggested that molecules with intramolecular charge-transfer dipole moments could be grown into quasi-2D nanostructures.[7] Moreover， some amphiphiles and organogelators were found to self-organize into sheet-like nanostructures in contact with solvents.[8] Despite these advances， templateand surfactant-free synthesis of free-standing， crystalline， and optoelectronically active nanosheets from small molecules remains elusive. 展开

纳米材料英文文献加翻译:

请问高人，Profibus怎么翻译？Foundation Fieldbus怎么翻译？谢谢各位老师。: 请问高人，Profibus怎么翻译？FoundationFieldbus怎么翻译？谢谢各位老师。... 请问高人， Profibus怎么翻译？ Foundation Fieldbus怎么翻译？谢谢各位老师。展开

帮我翻译一段关于做蛋糕的英文，谢谢，急用！！！！！！高价悬赏~: heat oven as directed below (metal or glass pan).(or use cooking spray)bottom of pan.stin brownie mix water oil and eggs in medium bowl until well blended.spread in pan. bake as directed below or until toothpick inserted 2inches from of ... heat oven as directed below (metal or glass pan).(or use cooking spray)bottom of pan.stin brownie mix water oil and eggs in medium bowl until well blended.spread in pan. bake as directed below or until toothpick inserted 2inches from of pan comes out almost clean;cool.store tightly covered. 展开

怎样清洗磁疗被？在线等哦，谢谢！:

求翻译，除湿机功能按钮英文！: Z主要是模式那三个真的搞不明白。

？？？？？谁能帮我翻译几个英文——激光雷达？？？？？: 关于激光雷达的论文 1、LO 2、header board 3、inductive beams

“双辊开炼机”英文如何翻译？:

通信方面的英文文献翻译！！: 以下是文献的一部分，愿意帮忙的高手留下邮箱，我把文件发给你，若能完成，加分：SpatialCompressiveSensingApproachForFieldDirectionalityEstimation.I.INTRODUCTIONVarietyoft... 以下是文献的一部分，愿意帮忙的高手留下邮箱，我把文件发给你，若能完成，加分： Spatial Compressive Sensing Approach For Field Directionality Estimation. I. INTRODUCTION Variety of techniques for field directionality estimation were studied in literature [1]-[5]. Thus， a theoretical analysis of the relationship between the hydrophone array output and the noise field was conducted in [1]-[5]. The developed techniques were based on the array beamformer output or the crossspectral matrix between outputs of array elements [4]-[5]. The problem of a field directionality estimation in ocean， using horizontal line towed array was also addressed in literature [5]- [8]. Recently， problems of direction of arrival and field directionality estimation for moving sensors arrays have attracted renewed interest [9]-[12]. It was shown that an array motion can improve an array performance assuming temporal coherence of successive samples [10]-[11]. In [12]， the wavefield sampling method that exploits the linear relationship between the noise field and the collection of beamformer outputs over various array orientations was proposed. It was shown that the wavefield sampling (WS) method outperforms other tested methods. This algorithm was implemented via the recursive estimation method and its convergence to the unique solution was promised for a specific set of array orientations and beamformer look directions. However， a method for a proper array orientation and beamformer look direction sequence selection remains an open question. The quality of the field directionality estimation is determined by the angular resolution. The higher angular resolution is， the more accurate estimation of the far field sources， and better detection performance can be achieved. One of fundamental relations in the array signal processing is that the angular resolution is directly proportional to the number of the array elements [13]. This relation motivates the desire for longer arrays that can achieve higher resolution. Unfortunately， the requirement contradicts the implementation and installation limitations that motivate shorter arrays. Moreover， implementation of longer arrays for maneuvering platforms such as unmanned underwater vehicles (UUV) can even be impossible [14]. These contradictions motivate the quest for alternative array signal processing methods. Usually， the field directionality is modeled as a finite set of strong far-field narrow-band sources and an isotropic lowpower noise [1]. In this work， the model of the field directionality is adopted in the following way. First， the bearing angle space is uniformly sampled into a large number of discrete angles. Next， it is assumed that ether the high energy that corresponds to the far-field strong sources or the low-energy that corresponds to the isotropic noise is received at the sensor array from every of these discrete azimuth angles. 展开

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