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91.
The possibility of riboflavin sensitized photo‐oxidation of polychlorinated pesticides was investigated. The dye proved to be an inefficient sensitizer for that purpose, when irradiated with visible light, in aereated aqueous solutions. A quenching of singlet and triplet excited states of the chromophore (depending on the concentrations of the quencher) is responsible for this failure in the photo‐degradation of the pesticides, which resulted easily oxidizable, via singlet oxygen mechanism, when proflavine was employed as a sensitizer. Parallel, and as a direct consequence, the rate of aerobic riboflavin photobleaching decreased drastically in the presence of the chlorophenols.

The implication of our results on the inhibition of riboflavin degradation by the presence of chlorinated phenolic pesticides in the environment, is discussed, from the point of view of a kinetic and mechanistic study.  相似文献   
92.
K Fischer  S Norman  D Freitag 《Chemosphere》1999,39(4):611-625
In order to evaluate the environmental risk potential of the polymer-additives octadecyl-3-(3.5-di-t-butyl-4-hydroxyphenyl)propionate (additive 1) and tri-(2.4-di-t-butylphenyl)phosphite (additive 2) we have studied the degradation of the 14C-labelled single components and their release from a polypropylene matrix in abiotic and biotic test systems as well as their transport behaviour in soil. The biotic degradation in waste compost, activated sludge and in soil was studied. In order to conduct release tests, waste disposal material were used as well. The abiotic degradation was effectuated by photooxidation at a catalytic surface. The highest mineralisation rates were obtained by photooxidative degradation of the two test substances. The maximum content of bounded residues was found for additive 1 in soil and for additive 2 in waste compost. In the extracts of soil and compost, the principal metabolites could be identified in the case of additive 1 as 7.9-di-t-butyl-1-oxaspiro[4.5]deca-6.9-dien-2.8-dion and in activated sludge as the methyl ester of 3-(3.5-di-t-butyl-4-hydroxyphenyl) propionic acid. Additive 2 metabolised in all degradation tests nearly completely under formation of two products. The main component was identified as tri-(2.4-di-t-butylphenyl)phosphate. Both polymer-additives were eluated from the chosen soil types. The transport behaviour of additive 1 was independent from the soil type. In all test matrices additive 1 as well as additive 2 were released from polypropylene. Because the amounts of additive 1 and 2 absorbed onto soil particles were taken into account, the highest liberation rates were found in the soil test.  相似文献   
93.
The Stylosanthes hamata SHST1 gene encodes a high-affinity sulfate transporter located in the plasma membrane. In this study the S. hamata SHST1 gene was constitutively expressed in Indian mustard [Brassica juncea (L.) Czern.] to investigate its importance for tolerance and accumulation of various oxyanions that may be transported by SHST1 and for cadmium, which is detoxified by sulfur-rich compounds. The transgenic SHST1 lines SHST1-12C and SHST1-4C were compared with wild-type Indian mustard for tolerance and accumulation of arsenate, chromate, tungstate, vanadate, and cadmium. As seedlings the SHST1 plants accumulated significantly more Cd and W, and somewhat more Cr and V. The SHST1 seedlings were less tolerant to Cd, Mo, and V compared to wild-type plants. Mature SHST1 plants were less tolerant than wild-type plants to Cd and Cr. SHST1 plants accumulated significantly more Cd, Cr, and W in their roots than wild-type plants. In their shoots they accumulated significantly more Cr and somewhat more V and W. Shoot Cd accumulation was significantly lower than in wild-type, and As levels were somewhat reduced. Compared to wild-type plants, sulfur accumulation was enhanced in roots of SHST1 plants but not in shoots. Together these results suggest that SHST1 can facilitate uptake of other oxyanions in addition to sulfate and that SHST1 mediates uptake in roots rather than root-to-shoot translocation. Since SHST1 overexpression led to enhanced accumulation of Cr, Cd, V, and W, this approach shows some potential for phytoremediation, especially if it could be combined with the expression of a gene that confers enhanced metal translocation or tolerance.  相似文献   
94.
Elevated biogenic SO2 from the oxidation of dimethylsulphide (DMS) in the marine atmosphere was measured over the North Atlantic Ocean in spring and summer 2003. Stable isotope apportionment was used to distinguish between anthropogenic and biogenic SO2 in the marine atmosphere south of Greenland. Atmospheric DMS measurements were within range of previous studies. Biogenic SO2 concentrations were as high as 82 nmol m?3 (spring geometric mean: 4 nmol m?3, σ = 17; summer geometric mean 7 nmol m?3, σ = 19) and are the highest reported values for marine biogenic SO2 in the literature. Elevated biogenic SO2 was found in air masses influenced by anthropogenic pollutants during the summer. This indicates that anthropogenic pollutants may affect the fate of oceanic emissions of sulphur compounds in the atmosphere favoring the formation of cloud condensation nuclei.  相似文献   
95.
The pH-dependent transport of eight selected ionizable pharmaceuticals was investigated by using saturated column experiments. Seventy-eight different breakthrough curves on a natural sandy aquifer material were produced and compared for three different pH levels at otherwise constant conditions. The experimentally obtained KOC data were compared with calculated KOC values derived from two different log KOW-log KOC correlation approaches. A significant pH-dependence on sorption was observed for all compounds with pKa in the considered pH range. Strong retardation was measured for several compounds despite their hydrophilic character. Besides an overall underestimation of KOC, the comparison between calculated and measured values only yields meaningful results for the acidic and neutral compounds. Basic compounds retarded much stronger than expected, particularly at low pH when their cationic species dominated. This is caused by additional ionic interactions, such as cation exchange processes, which are insufficiently considered in the applied KOC correlations.  相似文献   
96.
This paper is an examination of the range of salary levels of state, local, and multijurisdictional air pollution control agencies for specific occupational categories. It is based on a manpower and training survey of such agencies conducted by the Office of Air Programs of the Environmental Protection Agency during 1971. Since inadequate salaries have been identified as a primary obstacle in staffing air pollution control agencies, an analysis of salary levels was among the focal points for the survey.

Salaries were found to vary according to occupational category, type of agency, and size of agency. In most instances, salary levels increase as the size of the agency increases. Mean starting salaries have risen significantly since 1968, and salaries for chemists and engineers are becoming more competitive with salaries in private industry.  相似文献   
97.
Six building materials were exposed at five sites in Birmingham, Alabama, to determine the rates of soiling by different levels of suspended particulate. The exposed materials were (1) painted cedar siding, (2) concrete block, (3) brick, (4) limestone, (5) asphalt shingles, and (6) window glass. Suspended particulate levels ranged from an annual geometric mean of 60 μg/m3 at the clean site to 250 μg/m3 at the most polluted site.

Degrees of soiling were determined by measuring reflectance from the opaque surfaces and haze through the glass. Excellent dose-response relationships were obtained for the white surfaces— painted cedar siding and asphalt shingles. The degree of soiling of the paints was directly proportional to the square root of the suspended particulate dose. The shingle soiling was directly proportional to the dose. These regression equations can account for from 74 to 92% of the variability in reflectance measurements.

Similar regressions for brick can account for from 34 to 50 % of the variability. Poor correlations were obtained for concrete, limestone, and window glass.  相似文献   
98.
ABSTRACT

A multi-system, high-volume, parallel plate diffusion dénuder Brigham Young University Organic Sampling System (BIG BOSS) was tested using collocated samplers at the Pico Rivera Monitoring Station of the South Coast Air Quality Management District, South Coast Air Basin, in September 1994. Six-hr daytime and 9-hr nighttime samples were collected with a flow of about 200 L/min through each of the three systems designed to collect particles smaller than 2.5, 0.8, and 0.4 mm in a diffusion denuder sampler. Efficiency for the removal of gas phase organic compounds by the diffusion denuder was evaluated using both theoretical predictions and field measurements. Both measured and calculated data indicate high denuder efficiency for the removal of gas phase aromatic and paraffinic compounds. The precision of the BIG BOSS was evaluated using collocated samplers. The precision of determination of total carbon and elemental carbon retained by a quartz filter or of semi-volatile carbonaceous material lost from particles during sampling averaged ±7%. The precision of determination of individual organic compounds averaged ±10%. An average of 42 and 62% of the particulate organic material was semi-volatile organic compounds (SVOCs) lost from particles during sampling for daytime and nighttime samples, respectively. This “negative” sampling artifact was an order of magnitude larger than the “positive” quartz filter artifact due to adsorption of gas phase organic material. Daytime concentrations of fine particulate elemental carbon and nonvolatile organic carbon were higher than nighttime concentrations, but nighttime fine particles contained more semi-volatile organic material than daytime.  相似文献   
99.
100.
For aerosol measurements, especially those concerned with the aerosol particle size distribution, it is important to sample in isokinetic conditions. Most available instrumentation for aerosol measurements is intended for use on the ground under light wind conditions; intake air speeds rarely exceed a few meters per second. If the same instrumentation is used onboard an aircraft, the air must be decelerated 60 or more m/sec before It is sampled by individual instruments.

On The Pennsylvania State University Meteorology research aircraft, the air for all aerosol instruments is decelerated in a single isokinetic sampler located above the roof of the cabin outside the aircraft boundary layer. The air enters the sampler through a carefully designed circular intake. Its velocity is reduced as the cross section increases along a 7° conical diffuser. The expansion cone terminates in a cylindrical chamber in which the air velocity is 1/16 the aircraft speed. Behind the sampling chamber the air is accelerated in a second conical section to an end exhaust port. Exhaust porf "pumping" is used to compensate internal losses and, thus, helps preserve the isokinetic nature of the sampler.

Tubes leading to individual instruments are located in the sampling chamber and may be individually adapted to match the air sampling velocity with the local air speed inside the sampling chamber. The level of turbulence (urms/û) in the sampling section is =^0.05.

The sampler has been thoroughly wind tunnel and flight tested and successfully used in August and November, 1974, for field programs in the St. Louis and Tucson metropolitan areas, respectively.  相似文献   
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