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991.
The properties, origin and analysis of carbon in silicon and its influence on the electrical characteristics of devices are investigated and reviewed. The typical carbon concentrations in electronic-grade silicon are still some 1016 cm?3. The small distribution coefficient (k0 = 0.058) causes an inhomogeneous incorporation of carbon along the crystal axis and across the crystal diameter during crystal growth. Carbon concentrations exceeding about 5 × 1016 cm?3 in float-zoned silicon can lead to the formation of process-induced defects in the fabrication of power rectifiers and thyristors. These defects which are frequently arranged in a swirl-like pattern strongly deteriorate the electrical characteristics of these devices. It is shown that carbon is involved primarily in the generation of the defect nuclei whereas the defects finally observed form via precipitation of oxygen and agglomeration of silicon interstitials. Reasons for the benign behavior of high carbon concentrations in the processing of integrated circuits are discussed. In powder device processing the formation of carbon-induced defects is safely avoided by application of silicon containing carbon less than 5 × 1016 cm?3. 相似文献
992.
Starting three weeks before mating, 12 groups of female rats were fed different amounts of linoleic acid (18∶2n−6). Their
male pups were killed when 21-days-old. Varying the dietary 18∶2n−6 content between 150 and 6200 mg/100 g food intake had
the following results. Linoleic acid levels remained very low in brain, myelin, synaptosomes, and retina. In contrast, 18∶2n−6
levels increased in sciatic nerve. In heart, linoleic acid levels were high, but were not related to dietary linoleic acid
intake. Levels of 18∶2n−6 were significantly increased in liver, lung, kidney, and testicle and were even higher in muscle
and adipose tissue. On the other hand, in heart a constant amount of 18∶2n−6 was found at a low level of dietary 18∶2n−6.
Constant levels of arachidonic acid (20∶4n−6) were reached at 150 mg/100 g diet in all nerve structures, and at 300 mg/100g
diet in testicle and muscle, at 800 mg/100 g diet in kidney, and at 1200 mg/100 g diet in liver, lung, and heart. Constant
adrenic acid (22∶4n−6) levels were obtained at 150, 900, and 1200 mg/100 g diet in myelin, sciatic nerve, and brain, respectively.
Minimal levels were difficult to determine. In all fractions examined accumulation of docosapentaenoic acid (22∶5n−6) was
the most direct and specific consequence of increasing amounts of dietary 18∶2n−6. Tissue eicosapentaenoic acid (20∶5n−3)
and 22∶5n−3 levels were relatively independent of dietary 18∶2n−6 intake, except in lung, liver, and kidney. In several organs
(muscle, lung, kidney, liver, heart) as well as in myelin, very low levels of dietary linoleic acid led to an increase in
20∶5n−3. Dietary requirements for 18∶2n−6 varied from 150 to 1200 mg/100 g food intake, depending on the organ and the nature
of the tissue fatty acid. Therefore, the minimum dietary requirement is estimated to be about 1200 mg/100 g (i.e., the level
that ensures stable and constant amounts of arachidonic acid). 相似文献
993.
K. D. Carlson A. Chaudhry R. E. Peterson M. O. Bagby 《Journal of the American Oil Chemists' Society》1990,67(8):495-498
To conduct product development research onLesquerella seed oils, we explored methods to obtain >100 g quantities of lesquerolic (14-hydroxy-cis-11-eicosenoic) acid. Preliminary experiments with open-column silica gel chromatography showed thatL. fendleri oil could be separated into 3 triglyceride (TG) fractions. The first (10%) contained nonhydroxy 16-(13%) and 18-carbon acids
(65% 18∶1,2,3). The second fraction (15%) contained monolesquerolins (39% lesquerolic acid). The major TG fraction (73%) was
mainly dilesquerolins (66% lesquerolic acid) showing that a hydroxy acid-enriched TG oil was obtainable by this procedure.
Silica gel chromatography easily separatedL. fendleri fatty acid methyl esters (FAME) into a hydroxy-free ester fraction (40–44%) consisting largely of 18∶1 (39%), 18∶2 (19%)
and 18∶3 (31%), and a hydroxy ester fraction (56–60%) that was largely methyl lesquerolate (94%) with small amounts of auricolate
(5%) (14-hydroxy-cis-11,cis-17-eicosadienoate) and traces of 18-carbon hydroxy esters. This process for isolating the hydroxy FAME ofLesquerella oil was scaled up 15-to 100-fold with a preparative high performance liquid chromatograph. Thirty-gram samples ofL. gordonii FAME were dissolved in eluting solvent, pumped onto the high performance liquid chromatography (HPLC) silica column and eluted
with 97∶3 hexane/ethyl acetate. In an 8-hr period, up to 200 g of methyl lesquerolate could be obtained with a purity >98%,
the only contaminants being methyl auricolate and methyl ricinoleate.
Presented at the AOCS meeting in Phoenix, AZ, May 1988.
The mention of firm names or trade products does not imply that they are endorsed or recommended by the U.S. Department of
Agriculture over other firms or similar products not mentioned. 相似文献
994.
T. Yokochi M. T. Usita Y. Kamisaka T. Nakahara O. Suzuki 《Journal of the American Oil Chemists' Society》1990,67(11):846-851
The fungal oil extracted fromMortierella ramanniana var.angulispora (IFO 8187) was solvent winterized in order to raise the content of γ-linolenic acid (GLA). Effects of winterization conditions
(solvent, oil concentration in the solvent and temperature) and changes of glyceride compositions were discussed. The fungal
oil was separated into four diglycerides and 17 triglycerides (TG) with high performance liquid chromatography. The predominant
species were POO, POP and LOP, whose contents were 24.4, 22.9 and 9.4% of the total TG, respectively. Ethanol at 4°C gave
the highest GLA content of 10.5% in spite of lower yield than with acetone at −20°C. The highest separation efficiency for
GLA (ηGLA) was 0.27 with acetone at −20°C and 10% oil concentration, resulting in 8.3% of GLA from the fungal oil at 5.7% LGA. In case
of lower oil concentration at 5–20%, ηGLA showed higher in the following order: acetone (−20°C)>n-hexane (−20°C)>acetone (4°C)>petroleum ether (−20°C). The winterization process also proved to be effective for the separation
of TG type, Sa2U (Sa; saturated fatty acid; U, unsaturated fatty acid) into the crystallized fraction and SaU2 into the liquid fraction. Acetone at −20°C showed higher separation efficiency for triunsaturated TG than the other solvents. 相似文献
995.
David O. Cooney 《Chemical Engineering Communications》1990,91(1):1-9
A simple method is presented for determining fluid-phase and solid-phase solute concentration profiles, and solute breakthrough curves, for fixed bed adsorbers when both the fluid-phase and solid-phase mass transfer resistances are important. The method applies to any nonlinear isotherm of the “favorable” type. Freundlich and Langmuir isotherms are used as specific examples in the present paper. Constant-pattern behavior and linear-driving-force rate laws are assumed. 相似文献
996.
Cetane numbers (C#) for the homologous series of straight-chain, saturated n-alcohols, C5−C12 and C14, were determined according to ASTM D 613. Measured C# ranged from 18.2–80.8 and increased linearly with carbon number (CN).
Regression analyses developed equations that related various physical properties or molecular characteristics of these alcohols
to calculated C#. The degree of relationship between measured and calculated C# was expressed as R2. The decreasing order of the precision with which these properties correlated with C# was: boiling point (bp)>melting point
(mp)>CN>heat of combustion (HG)>refractive index (n20
D)>density (d). This ranking was based upon R2 (0.99–0.96) and the Average % error (2.8–7.2%). C# were also determined for straight-chain homologs of saturated methyl esters
with CN of 6, 10, 12, 14, 16 and 18. C# ranged from 18.0–75.6 and increased curvilinearly with CN. Equations were also developed
that related physical properties of these esters to C#. The precision with which these properties correlated with C# was:
bp>viscosity (V)>heat of vaporization (HV)>HG>CN>surface tension (ST)>mp>n20
D>d. R2 ranged from 0.99 for bp to 0.98 for d. Equations for the alcohols were linear or quadratic, while equations for the esters
were linear, quadratic or cubic based upon statistical considerations that included a Student’s t-test. With related physical
properties and these equations, accurate predictions of C# can be made for saturated n-alcohols and methyl esters. 相似文献
997.
Many rate constants of elementary steps on single crystals have been measured. Their pre-exponential factors can now be compared to those calculated by transition state theory. Such a calculation is presented in this Letter with due attention to microscopic reversibility, standard states, and configurational entropy. 相似文献
998.
O. O. Olufajo 《Nutrient Cycling in Agroecosystems》1990,25(2):93-100
Field trials were conducted at Samaru, Nigeria over a three-year period (1986–88) to study the effects of N and P fertilization on the response of promiscuously nodulating soybean toBradyrhizobium japonicum inoculation in a ferruginous tropical soil. Phosphorus fertilization enhanced nodulation, while N fertilization had no consistent effect on nodulation. Both N and P increased dry matter production. Seed yields were not influenced by the application of N. However, P increased seed yields in two out of three years. Response of seed yield to P fertilization was significant up to 26.4 kg P ha–1.Bradyrhizobium inoculation consistently enhanced nodulation while it increased seed yield in only one out of three years. Results demonstrate that P is an important nutrient for soybean production in ferruginous tropical soils. The roles of promiscuously nodulating soybean in the maintenance of tropical soil fertility are discussed. 相似文献
999.
Geraniums (Pelargonium xhortorum Bailey) possess a pest-resistance mechanism, based on glandular trichomes and the exudate they produce, that has been shown to be effective against the two-spotted spider mite (Tetranychus urticae Koch). Using an intact plant bioassay, the effectiveness of the resistance mechanism was determined for another potential pest, the foxglove aphid (Acyrthosiphon solani Kaltenbach). Comparisons were made between plant lines previously analyzed for their degree of resistance to mites, as well as their glandular trichome density and trichome exudate production. Over 100 aphid adults were bioassayed on each of the five plant lines used in the experiment. In addition to adult aphid survival, the production and survival of nymphs was determined in this bioassay. The results indicate that plant lines that are resistant to the two-spotted spider mite are also resistant to the foxglove aphid, while lines susceptible to mites are susceptible to the aphids. To evaluate the physical impediment features of the trichome exudate, the behavior of foxglove aphid nymphs was compared on two geranium lines, one a resistant line with high trichome densities and large quantities of exudate and the second a susceptible line with few trichomes and reduced exudate. A third leaf surface type was produced by washing the exudate from resistant leaves using a mildly basic buffer solution prior to the bioassay. Aphid behavior was divided into five categories: feeding or probing, resting, wandering, struggling, and immobilized. On both susceptible leaves and resistant leaves from which the exudate had been removed by washing, the aphids settled quickly and were observed with inserted stylets during most of the observation intervals. In contrast, aphids on the unwashed resistant leaf surfaces often became ensnared in the sticky trichome exudate and had difficulty in settling to probe the leaf. Physical entrapment by glandular trichome exudate appears to be an important aspect of aphid resistance in geraniums. 相似文献
1000.
This work describes a one-step separation of rat tissue phospholipid classes by high-performance liquid chromatography (HPLC)
using a silica column and a new light-scattering detector (LSD). Complete separation of phosphatidylcholine, phosphatidylethanolamine,
diphosphatidylglycerol, phosphatidylinositol, phosphatidylserine, sphingomyelin, lysophosphatidylethanolamine, and lysophosphatidylcholine
was obtained. Direct quantification was achieved after detector calibration for each phospholipid class. The detector response
was shown to be linear within the ranges used. The LSD results agreed well with those obtained by phospholipid phosphorus
assay. The present method was applied to rat heart and rat liver phospholipid analysis. 相似文献