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1.
2.
Response surface methodology is often used by researchers in different fields to determine the optimum values for controlled variables to maximize or minimize the response variables. Either maximization or minimization might be necessary depending on the response property. For example, if the response variable represents the yield of a process, maximization could be necessary; on the other hand, if the response variable is the biological oxygen demand (BOD) of an effluent the aim would definitely be minimization
Response surface methodology can be used two ways. It can be applied to the full-scale production or it can be scaled to a laboratory or the pilot plant. When applied to the full-scale production, the method is known as evolutionary operation (EVOP). EVOP is the continuous optimization of a process. The optimum conditions in a production plant can change depending on many factors such as raw material, ambient temperature, and equipment wear. Therefore, controlled variables should be optimized continuously to keep the response variable as close as possible to the maximum or minimum value. Hence, controlled variables are systematically changed around a center point to depict any shift of the response variable from the extreme. A thorough discussion of EVOP is given by Box, Evolutionary Operation: A Method for Increasing Industrial Productivity, Appl. Statist., 6, 81-101 (1957). 相似文献
Response surface methodology can be used two ways. It can be applied to the full-scale production or it can be scaled to a laboratory or the pilot plant. When applied to the full-scale production, the method is known as evolutionary operation (EVOP). EVOP is the continuous optimization of a process. The optimum conditions in a production plant can change depending on many factors such as raw material, ambient temperature, and equipment wear. Therefore, controlled variables should be optimized continuously to keep the response variable as close as possible to the maximum or minimum value. Hence, controlled variables are systematically changed around a center point to depict any shift of the response variable from the extreme. A thorough discussion of EVOP is given by Box, Evolutionary Operation: A Method for Increasing Industrial Productivity, Appl. Statist., 6, 81-101 (1957). 相似文献
3.
The aqueous leaf extracts of five different deciduous plants, namely, silver oak, flame of the forest, tanner’s senna, wattle and serviceberry, were used on their own and in combination with aluminium sulphate, stannous chloride and ferrous sulphate to dye wool by a simultaneous mordanting technique. The washing and light fastness properties of the developed shades were moderate to good. Based on the CIE 2000 spectral colour coordinate values (K/S, ΔL, Δa, Δb and ΔE), the developed shades were classified into four groups: yellow/brown, yellow, orange and dark grey. The use of aluminium sulphate gave medium shades (K/S = 8.24), while the stannous chloride and ferrous sulphate mordants provided deep shades (K/S = 30.5). Statistical analyses have shown that only the type of mordant and not the dye source significantly influenced the development of colour on wool. Hence, it was theoretically possible to use five selected leaves as a single mixture to produce four different colours on wool. 相似文献
4.
V Iyengar 《The Science of the total environment》1988,71(1):1-5
The last decade may be regarded as a crucial turning point in new developments in many areas of biological trace element research. It is slowly being recognized as a multidisciplinary science which requires a combination of biological insight and analytical awareness in planning the studies. It is also acknowledged that the complexities involved in dealing with the requirements of trace element research studies in the life sciences demand comprehensive planning of the investigations and use of a variety of techniques, thus bringing together a variety of talents. It cannot be emphasized enough that accurate analytical measurements on biologically and analytically "valid" samples hold the key for success in future biological trace element research studies. These aspects are illustrated. 相似文献
5.
Kwang‐Pill Lee Anantha Iyengar Gopalan See‐Hee Lee Ali Md Showkat Young Chang Nho 《应用聚合物科学杂志》2006,102(4):3912-3918
Conducting polydiphenylamine was used to encapsulate silica nanoparticles through the oxidative polymerization of diphenylamine in the presence of ultrasonic irradiation. The polymerization was performed in the presence of sodium lauryl sulfate as a surfactant. Experiments performed in the absence of ultrasound clearly demonstrated that the application of ultrasonication played multiple roles in the preparation of a composite of polydiphenylamine with silica nanoparticles. Ultrasonication dispersed the silica nanoparticles, converted sodium lauryl sulfate to lauryl alcohol, and augmented the dispersion of the silica‐nanoparticle/polydiphenylamine composite in an organic medium. Silica‐nanoparticle/polydiphenylamine composites were also prepared in the absence of ultrasound and/or sodium lauryl sulfate. The silica‐nanoparticle/polydiphenylamine composites were characterized with Fourier trans form infrared spectroscopy, ultraviolet–visible/near‐infrared spectroscopy, and thermogravimetric analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3912–3918, 2006 相似文献
6.
For substrates such as polyesters having limited capacity for hydrogen bonding or other specific interactions, thermodynamic compatibility of the substrate and adhesive is shown to be a key factor in promoting bondability to the substrate. Such compatibility occurs, as shown by Abere, when the cohesive energy densities (CED) or solubility parameters (δ = √CED) of substrate and adhesive are matched. Investigations with polyester film-adhesive-film model systems with the use of a variety of nonpolar (hydrocarbon) and polar (chlorinated compounds, ethers, esters) adhesives illustrate how compatibility promotes bondability to poly(ethylene terephthalate). The poor adhesion of polyester fibers to resorcinol–formaldehyde–latex (RFL) adhesives is attributed to the incompatibility of resorcinol (δ = 16.0) with the polyester (δ = 10.3). Adhesion to RFL was improved by substituting the more compatible n-hexyl resorcinol (δ = 12.5) for resorcinol in RFL adhesives. Currently, the best adhesive systems for polyester tire yarns are those (e.g., isocyanate–epoxy) involving formation of urethane polymers having matching δ values with poly(ethylene terephthalate). 相似文献
7.
Towards an Environmentally Acceptable Heterogeneous Catalytic Method of Producing Adipic Acid by the Oxidation of Hydrocarbons in Air 总被引:1,自引:0,他引:1
Raja Robert Lee Sang-Ok Sanchez-Sanchez Manuel Sankar Gopinathan Harris Kenneth D.M. Johnson Brian F.G. Thomas John Meurig 《Topics in Catalysis》2002,20(1-4):85-88
A survey is given of the catalytic methods potentially available for the production of adipic acid by the oxidation of readily available hydrocarbon precursors under environmentally benign conditions. Encouraging results are reported using H2O2 as oxidant and microporous FeAlPO-5 as catalyst at moderate temperatures. 相似文献
8.
Nanocomposites of iron oxide (Fe3O4) with a sulfonated polyaniline, poly(aniline‐co‐aminonaphthalenesulfonic acid) [SPAN(ANSA)], were synthesized through chemical oxidative copolymerization of aniline and 5‐amino‐2‐naphthalenesulfonic acid/1‐amino‐5‐naphthalenesulfonic acid in the presence of Fe3O4 nanoparticles. The nanocomposites [Fe3O4/SPAN(ANSA)‐NCs] were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X‐ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, elemental analysis, UV–visible spectroscopy, thermogravimetric analysis (TGA), superconductor quantum interference device (SQUID), and electrical conductivity measurements. The TEM images reveal that nanocrystalline Fe3O4 particles were homogeneously incorporated within the polymer matrix with the sizes in the range of 10–15 nm. XRD pattern reveals that pure Fe3O4 particles are having spinel structure, and nanocomposites are more crystalline in comparison to pristine polymers. Differential thermogravimetric (DTG) curves obtained through TGA informs that polymer chains in the composites have better thermal stability than that of the pristine copolymers. FTIR spectra provide information on the structure of the composites. The conductivity of the nanocomposites (~ 0.5 S cm?1) is higher than that of pristine PANI (~ 10?3 S cm?1). The charge transport behavior of the composites is explained through temperature difference of conductivity. The temperature dependence of conductivity fits with the quasi‐1D variable range hopping (quasi‐1D VRH) model. SQUID analysis reveals that the composites show ferromagnetic behavior at room temperature. The maximum saturation magnetization of the composite is 9.7 emu g?1. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
9.
Saturated, monoenoic and dienoic wax esters, C26−C40, have been synthesized from even-numbered fatty alcohols and acids. In homologous series of saturated esters, the increments
of melting points follow a regular trend except for those esters which have an acid moiety two carbon atoms shorter than the
alcohol moiety. These wax esters have melting points higher than interpolation would predict. Monoenoic wax esters with the
double bond in the alcohol chain have melting points about 10 C higher than their isomers with the double bond in the acid
chain. 相似文献
10.
Ali Md Showkat Kwang‐Pill Lee Anantha Iyengar Gopalan Sang‐Ho Kim Seong‐Ho Choi Sang‐Ho Sohn 《应用聚合物科学杂志》2006,101(6):3721-3729
Composites based on poly(diphenyl amine) (PDPA) and multiwall carbon nanotubes (MWNTs) were prepared by chemical oxidative polymerization through two different approaches: in situ polymerization and intimate mixing. In in situ polymerization, DPA was polymerized in the presence of dispersed MWNTs in sulfuric acid medium for different molar composition ratios of MWNT and DPA. Intimate mixing of synthesized PDPA with MWNT was also used for the preparation of PDPA/MWNT composites. Transmission electron microscopy revealed that the diameter of the tubular structure for the composite was 10–20 nm higher than the diameter of pure MWNT. Scanning electron microscopy provided evidence for the differences in the morphology between the MWNTs and the composites. Raman and Fourier transform IR (FTIR) spectroscopy, thermogravimetric analysis, X‐ray diffraction, and UV–visible spectroscopy were used to characterize the composites and reveal the differences in the molecular level interactions between the components in the composites. The Raman and FTIR spectral results revealed doping‐type molecular interactions and coordinate covalent‐type interactions between MWNT and PDPA in the composite prepared by in situ polymerization and intimate mixing, respectively. The backbone structure of PDPA in the composite decomposed at a higher temperature (>340°C) than the pristine PDPA (~300°C). This behavior also favored the molecular level interactions between MWNT and PDPA in the composite. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3721–3729, 2006 相似文献