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121.
We describe non-orientable, octagonal embeddings for certain 4-valent, bipartite Cayley graphs of finite metacyclic groups, and give a class of examples for which this embedding realizes the non-orientable genus of the group. This yields a construction of Cayley graphs for which
is arbitrarily large, where and
are the orientable genus and the non-orientable genus of the Cayley graph.Work supported in part by the Research Council of Slovenia, Yugoslavia and NSF Contract DMS-8717441.Supported by NSF Contract DMS-8601760. 相似文献
122.
Effects of temperature and moisture on dilute-acid steam explosion pretreatment of corn stover and cellulase enzyme digestibility 总被引:3,自引:0,他引:3
Melvin P. Tucker Kyoung H. Kim Mildred M. Newman Quang A. Nguyen 《Applied biochemistry and biotechnology》2003,105(1-3):165-177
Corn stover is emerging as a viable feedstock for producing bioethanol from renewable resources. Dilute-acid pretreatment
of corn stover can solubilize a significant portion of the hemicellulosic component and enhance the enzymatic digestibility
of the remaining cellulose for fermentation into ethanol. In this study, dilute H2SO4 pretreatment of corn stover was performed in a steam explosion reactor at 160°C, 180°C, and 190°C, approx 1 wt% H2SO4, and 70-s to 840-s residence times. The combined severity (Log10 [R
o
] - pH), an expression relating pH, temperature, and residence time of pretreatment, ranged from 1.8 to 2.4. Soluble xylose
yields varied from 63 to 77% of theoretical from pretreatments of corn stover at 160 and 180°C. However, yields >90% of theoretical
were found with dilute-acid pretreatments at 190°C. A narrower range of higher combined severities was required for pretreatment
to obtain high soluble xylose yields when the moisture content of the acid-impregnated feedstock was increased from 55 to
63 wt%. Simultaneous saccharification and fermentation (SSF) of washed solids from corn stover pretreated at 190°C, using
an enzyme loading of 15 filter paper units (FPU)/g of cellulose, gave ethanol yields in excess of 85%. Similar SSF ethanol
yields were found using washed solid residues from 160 and 180°C pretreatments at similar combined severities but required
a higher enzyme loading of approx 25 FPU/g of cellulose. 相似文献
123.
Wade DA Mao C Hollenbeck AC Tucker SA 《Fresenius' Journal of Analytical Chemistry》2001,369(3-4):378-384
The ability of pyridinium chloride (PC) to selectively quench alternant as opposed to nonaltemant polycyclic aromatic hydrocarbons (PAHs) in organized media is examined. PC was previously shown to be a selective quenching agent of alternant PAHs in neat polar solvents. Carboxylate-terminated poly(amido) amine (PAMAM-CT) dendrimers and anionic surfactants--sodium dodecanoate (SD), sodium octanoate (SO), and sodium dodecylsulfate (SDS)--were chosen as the solubilizing media for this study. Selective quenching of alternant PAHs is observed in the presence of the SDS and SO micelles. However, the extent of PAH quenching in SO is significantly reduced compared to PAHs dissolved in either water or SDS micelles. In the case of the smaller generation 4.5 (G4.5) PAMAM-CT dendrimers, PC was prevented from quenching both alternant and nonalternant PAHs to any appreciable extent. The dendrimer is able to "protect" the PAHs from the PC quencher that resides at the dendrimer surface. Both, SD and G5.5 PAMAM-CT precipitated out of solution with the addition of PC. Differences between traditional micelles and "unimolecular micelle" dendrimers were also examined. These studies further confirm that the PAHs did not reside in the "analogous" palisade region of the dendrimers as they do in micelles. The PAHs must reside in the outermost branches of the dendrimer, but sufficiently far enough away from the charged surface groups, where PC associated, to prevent fluorescence quenching. This work further illustrates the differences between "unimolecular micelle" dendrimers and traditional micelles. 相似文献
124.
Seeded supersonic NO beams were used to study the kinetic energy dependence of both the electronic (NO2*) and vibrational (NO23) chemiluminescence of the NO + O3 reaction. In addition the electronic CL is found to be enhanced by raising the NO internal temperature. This is shown to be due to enhanced reactivity of the NO(2Π,) fine structure component. By difference NO(2Π) is concluded to yield predominantly groundstate NO23. The excitation function for NO2* formation from NO(2Π) is of the form σ(E) = C(E/E0 - 1)n over the 3–6 kcal energy range where n = 2.4 ± 0.15, C = 0.163 Å2 and E0 = 3.2 ± 0.3 kcal/mole. Vibrational IR emission from NO23 has an energy dependence different from electronic NO2* emission, confirming that emitters are formed predominantly in distinct reaction channels rather than via a common precursor (either NO2* or NO23). The short wavelength cutoff of the CL spectra recorded at elevated collision energies E ? 15 kcal/mole corresponds to the total available energy. These and literature results are discussed in the light of general properties of the (generally unknown) ONO3 potential energy surfaces. The formation of electronically excited NO2* rather than energetically preferred O2 (1 Δg) (Gauthier and Snelling) can be rationalized in terms of surface hopping near a known intersection of potential energy surfaces more easily than by vibronic interaction in the asymptotic NO2 product. 相似文献
125.
C D Stiles W J Pledger R W Tucker R G Martin C D Scher 《Journal of supramolecular structure》1980,13(4):489-499
The platelet-derived growth factor (PDGF), which is found in serum but not in plasma, has been purified to homogeneity; it stimulates replication at a concentration of 10(-10) M. Brief treatment with PDGF causes density-inhibited Balb/c-3T3 cells to become competent to synthesize DNA; pituitary fibroblast growth factor (FGF) or precipitates of calcium phosphate also induce competence. Continuous treatment with plasma allows competent, but not incompetent, cells to synthesize DNA. A critical component of plasma is somatomedin, a group of hormones with insulin-like activity; multiplication-stimulating activity (MSA) or insulin replace plasma somatomedin in promoting DNA synthesis. We have studied the molecular correlates of competence and the role of SV40 gene A products in regulating DNA synthesis. Treatment of quiescent cells with pure PDGF or FGF causes the preferential synthesis of five cytoplasmic proteins (approximate molecular weight 29,000, 35,000, 45,000, 60,000, and 72,000 detected by SDS-PAGE under reducing conditions). Two of these competence-associated proteins (29,000 and 35,000 daltons) are insulin, or epidermal growth factor (EGF). PDGF, FGF, or calcium phosphate induce an ultrastructure change within the centriole of 3T3 cells; this ultrastructural modification of the centriole is detectable by immunofluorescence within 2 h or PDGF treatment. Plasma, EGF, or MSA do not modify the centriole. SV40 induces replicative DNA synthesis in growth-arrested 3T3 cells but does not cause this alteration in centriole structure. Gene A variants of SV40, including a mutant with temperature-sensitive (ts) T-antigen (ts A209), a deletion in t-antigen (dl 884), and several ts A209 strains containing t-antigen deletions were used to induce DNA synthesis in Balb/c-3T3 cells. Like wild type SV40, all strains induced DNA synthesis equally well under permissive or nonpermissive conditions. Addition of PDGF or plasma had little effect on SV40-induced DNA synthesis. Thus, the viral function that induces replicative DNA synthesis in Balb/c-3T3 cells. Like wild type SV40, all strains induced DNA synthesis equally well under permissive or nonpermissive conditions. Addition of PDGF or plasma had little effect on SV40-induced DNA synthesis. Thus, the viral function that induces replicative DNA synthesis in Balb/c-3T3 cells is not t and is not temperature sensitive. This SV40 gene function overrides the cellular requirement for hormonal growth factors. It does not induce transient centriole deciliation, a hormonally regulated event. 相似文献
126.
A method for the rapid and simultaneous determination of copper, nickel and lead in urine is described. Direct injections of freshly acidified and filtered (0.45-μm) urine samples were made onto a reverse-phase separator column with a guard column for sample clean-up. By complexing the metals with a dithiocarbamate ligand included in the mobile phase, the metal complexes could be detected electrochemically (copper and nickel) or spectrophotometrically (copper, nickel and lead). The procedure is shown to provide a convenient method for the determination of copper and nickel at normal to occupationally exposed levels of urinary output (electrochemical detection) after direct injection of samples. Spectrophotometric detection methods were insufficiently sensitive for direct determinations of copper and nickel at some of the lower levels found in urine. The spectrophotometric detection of lead is subject to interference by u.v.-absorbing constituents present in urine and is restricted to detection of lead in persons over-exposed to lead, unless additional clean-up procedures are applied. 相似文献
127.
Penfold J Staples E Ugazio S Tucker I Soubiran L Hubbard J Noro M O'Malley B Ferrante A Ford G Buron H 《The journal of physical chemistry. B》2005,109(38):18107-18116
The evolution of the microstructure and composition occurring in the aqueous solutions of di-alkyl chain cationic/nonionic surfactant mixtures has been studied in detail using small angle neutron scattering, SANS. For all the systems studied we observe an evolution from a predominantly lamellar phase, for solutions rich in di-alkyl chain cationic surfactant, to mixed cationic/nonionic micelles, for solutions rich in the nonionic surfactant. At intermediate solution compositions there is a region of coexistence of lamellar and micellar phases, where the relative amounts change with solution composition. A number of different di-alkyl chain cationic surfactants, DHDAB, 2HT, DHTAC, DHTA methyl sulfate, and DISDA methyl sulfate, and nonionic surfactants, C12E12 and C12E23, are investigated. For these systems the differences in phase behavior is discussed, and for the mixture DHDAB/C12E12 a direct comparison with theoretical predictions of phase behavior is made. It is shown that the phase separation that can occur in these mixed systems is induced by a depletion force arising from the micellar component, and that the size and volume fraction of the micelles are critical factors. 相似文献
128.
Penfold J Tucker I Thomas RK Staples E Schuermann R 《The journal of physical chemistry. B》2005,109(21):10760-10770
The structures of the mixed anionic/nonionic surfactant micelles of SDS/C12E6 and SDS/C12E8 have been measured by small angle neutron scattering (SANS). The variations in the micelle aggregation number and surface charge with composition, measured in D2O and in dilute electrolyte, 0.01 and 0.05 M NaCl, provide data on the relative roles of the surfactant headgroup steric and electrostatic interactions and their contributions to the free energy of micellization. For the SDS/C12E8 mixture, solutions increasingly rich in C12E8 show a modest micellar growth and an increase in the surface charge. The changes with increasing electrolyte concentration are similarly modest. In contrast, for the SDS/C12E6 mixture, solutions rich in C12E6 show a more significant increase in aggregation number. Furthermore, electrolyte has a more substantial effect on the aggregation for the nonionic (C12E6) rich mixtures. The experimental results are discussed in the context of estimates of the steric and electrostatic contributions to the free energy of micellization, calculated from the molecular thermodynamic approach. The variation in micelle surface charge is discussed in the context of the "dressed micelle" theory for micelle ionization, and other related data. 相似文献
129.
130.
Pedro Bernal Sherril D. Christian Edwin E. Tucker 《Journal of solution chemistry》1986,15(11):947-956
An automated vapor pressure apparatus has been used to obtain measurements of the vapor pressure of aqueous solutions of fluorobenzene at temperatures of 15, 25, 35, and 45°C, and in the concentration range 0 to 0.011M. The results have been interpreted to infer the dimerization constant of fluorobenzene in very dilute aqueous solutions, equivalent to the second virial coefficient of interaction between fluorobenzene molecules. The hydrophobic association of fluorobenzene molecules is thermodynamically quite similar to that of benzene at comparable temperatures and concentrations. A dimerization constant of fluorobenzene of 0.56 M–1 at 30°C and an endothermic enthalpy of association equal to 3.9 kcal-mol–1 are calculated from the measurements. 相似文献