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1.
John Swain 《Zeitschrift fur Physik C Particles and Fields》1996,71(1):455-457
The final states for the processb→sy have been extensively discussed in the literature. Similarly-detailed analyses for the caseb→s gluon have not been performed. Generally this process is searched for in 2-body decays such as B0→K+ π ?. We present simple arguments to suggest that most of the time the quark-level process will give rise to final states with rather high multiplicities. Comments are made about the applicability of these results tob→d gluon and hadronicb→u decays. 相似文献
2.
Ultranarrow Spectral Lines via Quantum Interference 总被引:2,自引:0,他引:2
3.
Solvent isotope effects for H2O---D2O mixtures and for ionic hydration equilibria in such mixtures can be calculated from the structure difference between D2O and H2O and that between HDO and H2O and the relative amounts of the three waters. The behavior of acids in H2O---D2O mixtures is considered in detail. Dissociation constants of acetic acid are calculated over the complete range of deuterium concentrations and found to agree with the experimentally determined ones. The Gross equation for the dependence of isotope effect on mole fraction of deuterium for acid-catalyzed reaction of substrates S proceeding via SL+ transition states (L=H or D) is derived from first principles. 相似文献
4.
Pravati Swain C. Mallika R. Srinivasan U. Kamachi Mudali R. Natarajan 《Journal of Radioanalytical and Nuclear Chemistry》2013,298(2):781-796
The chemistry of the noble metal fission product, ruthenium is very complex due to the existence of many oxidation states in addition to forming a large number of co-ordination complexes. In the PUREX process for the separation of U and Pu from the spent nuclear fuels from fast breeder reactors, owing to the high volatile nature of RuO4 problems arise not only during the extraction stages but also in the treatment of high active liquid waste and subsequent vitrification. As this volatile RuO4 can deposit in cooler parts, there is an increase in the radiation field due to the presence of 106Ru. The problem is very acute in the reprocessing of fast reactor fuels due to the increased concentration of ruthenium in the spent fuel. In nitric acid medium Ru can exist in various nitroso nitrate complexes and nitroso complexes are more stable than nitrates. The nitrates are non-extractable by the solvent TBP; however, they are extractable to a higher degree by DBP (the primary degradation product of TBP). The extractability of Ru nitrates into the solvent is inhibited by high acid content, temperature and prolonged hold-up time. Nevertheless, these factors promote the volatilization of Ru as RuO4. The volatilization is enhanced by the addition of phosphate ions, but is suppressed by phosphite or hypophosphite ions. Thus, it would be advantageous if ruthenium is removed so that not only the purity of the product (Pu) is improved, but also the problem related to volatilisation can be resolved. High molecular weight amines (tertiary amines) capable of forming co-ordinate bonds are reported to be ideal extractants for Ru. Gas phase separation is an effective method for the recovery of Ru from catalysts, lead button and from other platinum group metals. Separation and pre-concentration of noble metals can be accomplished from non-metals by simple sorbents like coconut shell activated carbon to complicated chelating resins, aromatic polymers and zeolites. In the electro-oxidation of active Ru from nitroso salts, Pd was found to interfere and removal of Pd prior to oxidation of Ru is recommended. Redox catalysts such as Ag2+ and Ce4+ are found to play a prominent role in the electro-oxidation of Ru. Though, various methods and extractants are reported in the literature for the separation of Ru, R&D is being pursued for the removal of Ru during aqueous reprocessing of spent fuels using extractants and methods which are conducive to plant conditions. Hence, an exhaustive survey of literature was made and the different methods reported for the removal of Ru with emphasis towards reprocessing applications are discussed in this report as a review. Attempts made by the authors in separating Ru from simulated waste solution are also included in this review. 相似文献
5.
Alok Srivastava D. Pathania K. K. Swain Nicy Ajith R. Acharya A. V. R. Reddy H. Nayyar 《Journal of Radioanalytical and Nuclear Chemistry》2012,294(2):315-318
The phyto-accumulation efficacy of selenium (Se) from soil by chickpea plant is reported. Chickpea plants were grown in soil having different concentrations (1–4 mg kg?1) of Se. Samples of soil and different parts of chickpea plants in Se rich soil were analyzed for determination of Se concentrations by instrumental neutron activation analysis (INAA). Samples were irradiated in self-serve facility of CIRUS reactor, BARC, Mumbai at a neutron flux of the order of 1013 cm?2 s?1. The gamma activity at 264.7 keV of 75Se (119.8 d) was measured using a 45% relative efficiency HPGe detector coupled to MCA. Dependence of Se distribution in soil and plants on its spiking concentration was evaluated in this work. The Se concentrations determined in plant parts grown in control soil and in soil spiked with Se (4 mg kg?1) are in the range of 0.6–0.8 and 65–68 mg kg?1 respectively. 相似文献
6.
Marla D. Swain George P. Anderson Dan Zabetakis Rachael D. Bernstein Jinny L. Liu Laura J. Sherwood Andrew Hayhurst Ellen R. Goldman 《Analytical and bioanalytical chemistry》2010,398(1):339-348
Single-domain antibodies (sdAb) specific for botulinum neurotoxin serotype A (BoNT A) were selected from an immune llama phage
display library derived from a llama that was immunized with BoNT A toxoid. The constructed phage library was panned using
two methods: panning on plates coated with BoNT A toxoid (BoNT A Td) and BoNT A complex toxoid (BoNT Ac Td) and panning on
microspheres coupled to BoNT A Td and BoNT A toxin (BoNT A Tx). Both panning methods selected for binders that had identical
sequences, suggesting that panning on toxoided material may be as effective as panning on bead-immobilized toxin for isolating
specific binders. All of the isolated binders tested were observed to recognize bead-immobilized BoNT A Tx in direct binding
assays, and showed very little cross-reactivity towards other BoNT serotypes and unrelated protein. Sandwich assays that incorporated
selected sdAb as capture and tracer elements demonstrated that all of the sdAb were able to recognize soluble (“live”) BoNT
A Tx and BoNT Ac Tx with virtually no cross-reactivity with other BoNT serotypes. The isolated sdAb did not exhibit the high
degree of thermal stability often associated with these reagents; after the first heating cycle most of the binding activity
was lost, but the portion of the protein that did refold and recover antigen-binding activity showed only minimal loss on
subsequent heating and cooling cycles. The binding kinetics of selected binders, assessed by both an equilibrium fluid array
assay as well as surface plasmon resonance (SPR) using toxoided material, gave dissociation constants (K
D ) in the range 2.2 × 10−11 to 1.6 × 10−10 M. These high-affinity binders may prove beneficial to the development of recombinant reagents for the rapid detection of
BoNT A, particularly in field screening and monitoring applications. 相似文献
7.
Mogon Patel Anthony C. Swain Robert S. Maxwell 《Polymer Degradation and Stability》2006,91(3):548-554
Poly(m-carboranyl-siloxane) elastomers containing a mixture of di-methyl- and methylphenyl-silyl units were synthesised using the ferric chloride catalysed condensation reaction between di-chloro-diorganosilane and bis(di-methylmethoxysilyl)-m-carborane. These elastomeric materials were originally developed to have greater stability to extreme thermal environments and retain tailorable physical and chemical properties relative to comparable non-carborane containing elastomers. Prepared samples were aged either by heating in air at elevated temperatures or by gamma irradiation from a 60Co source. Multinuclear (1H, 13C and 11B) solid and solution state nuclear magnetic resonance (NMR) was used to assess degradation. This included measurements of segmental chain dynamics using a solid-echo pulse sequence reflecting changes in crosslink density and assessing changes to the carborane fragment by 11B and 1H Magic Angle Spinning (MAS) methods. Thermogravimetric measurements were also performed to assess thermal stability. Gamma radiation (to a dose of 1 MGy) was found to induce only a small degree of elastomer hardening as evidenced by a reduction in segmental chain dynamics. The carborane cage however, remained intact at these dose levels. Thermal degradation was observed to lead to oxidative crosslinking, the degree of which is dependent on temperature. At temperatures below 350 °C, only small changes in segmental dynamics were observed commensurate with only minor weight loss at this temperature. At temperatures above 350 °C, the degradation of the elastomer increased dramatically with decreased segmental dynamics and presumed partial oxidation of the carborane cage. The integrity of the m-carborane cage and the segmental dynamics were found to be significantly reduced at temperatures above 580 °C, in line with the known cage rearrangement temperature for icosahedral carboranes. 相似文献
8.
JPC – Journal of Planar Chromatography – Modern TLC - A simple normal-phase high-performance thin-layer chromatography (HPTLC) method has been developed for the quantification of... 相似文献
9.
10.
Trilochan Swain 《Journal of Thermal Analysis and Calorimetry》2012,110(2):929-935
A new inorganically template metaphosphate of Ni(II) complex has been synthesized and characterized by different measurements such as DSC, FT-IR, C?CH?CN?CS, X-RD and ICP-AES. Differential scanning calorimeter (DSC) elucidated negative specific heat of the system and has used to evaluate some thermodynamical constants like specific heat, enthalpy and entropy of that system. The specific heat capacity of the system is measured in atmospheric O2 at heating rate of 278 and 283?K?min?1. The specific heat is found both positive and negative at 278?K?min?1. 相似文献