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141.
Yuri Sekimoto Tomoki Okiharu Haruka Nakajima Toshihiro Fujii Koji Shirai Hiroshi Moriwaki 《Environmental science and pollution research international》2013,20(9):6531-6538
The aim of this study is to investigate the use of keratin colloidal solution, which was obtained from wool, for the removal of Pb(II) from water. The addition of keratin colloidal solution (15 g L?1, 0.30 mL) to a Pb(II) solution (1.0 mM, 0.90 mL, pH 5.0) resulted in the formation and precipitation of a Pb–keratin aggregate. Measurement of the Pb(II) and protein concentrations in the supernatant solution revealed that 88 and 99 % of the Pb(II) and keratin protein were removed from the solution, respectively. The maximum Pb(II) uptake capacity of keratin in the colloidal solution was 43.3 mg g?1. In addition, the Pb–keratin aggregate was easily decomposed via the addition of nitric acid, which enabled the recovery of Pb(II). However, aggregation did not occur in solutions with Pb(II) concentrations below 0.10 mM. Therefore, we used a keratin colloidal solution encapsulated in a dialysis cellulose tube to remove Pb(II) from 0.10 mM solutions, which enabled the removal of 95 % of the Pb(II). From these results, we conclude that keratin colloidal solution is useful for the treatment of water polluted with Pb(II). 相似文献
142.
Arsenic accumulation in duckweed (Spirodela polyrhiza L.): a good option for phytoremediation 总被引:2,自引:0,他引:2
Some unavoidable drawbacks of traditional technologies have made phytoremediation a promising alternative for removal of arsenic from contaminated soil and water. In the present study, the potential of an aquatic macrophyte Spirodela polyrhiza L. for phytofiltration of arsenic, and the mechanism of the arsenic uptake were investigated. The S. polyrhiza L. were grown in three test concentrations of arsenate and dimethylarsinic acid (DMAA) (i.e. 1.0, 2.0 and 4.0microM) with 0 (control), 100 or 500microM of phosphate. One control treatment was also set for each test concentrations of arsenic. The PO(4)(3-) concentration in control treatment was 0.02microM. When S. polyrhiza L. was cultivated hydroponically for 6d in culture solution containing 0.02microM phosphate and 4.0microM arsenate or DMAA, the arsenic uptake was 0.353+/-0.003micromolg(-1) and 7.65+/-0.27nmolg(-1), respectively. Arsenic uptake into S. polyrhiza L. was negatively (p<0.05) correlated with phosphate uptake when arsenate was applied to the culture solutions owing to similar in the sorption mechanism between AsO(4)(3-) and PO(4)(3-), and positively (p<0.05) correlated with iron uptake due to adsorption of AsO(4)(3-) onto iron oxides. Thus, the S. polyrhiza L. accumulates arsenic by physico-chemical adsorption and via the phosphate uptake pathway when arsenate was added to the solutions. These results indicate that S. polyrhiza L. would be a good arsenic phytofiltrator. In contrast, DMAA accumulation into S. polyrhiza L. was neither affected by the phosphate concentration in the culture nor correlated (p>0.05) with iron accumulation in plant tissues, which indicates that S. polyrhiza L. uses different mechanisms for DMAA uptake. 相似文献
143.
Effect of carbon tetrachloride on sonochemical decomposition of methyl orange in water 总被引:2,自引:0,他引:2
Two types of sonicators were used for the sonochemical decomposition of methyl orange (MO) in the presence and absence of carbon tetrachloride (CCl4): One is a 45kHz ultrasonic cleaning bath (a low intensity sonicator) and the other is a 200kHz ultrasonic reactor (a high intensity sonicator). It was clearly confirmed that the rates of the sonochemical decomposition of MO increased with increasing the concentration of CCl4 in both sonicators. The enhancement effect of CCl4 was much higher in the high intensity sonicator than in the low intensity one: by the addition of 100ppm of CCl4, the decomposition ratio of MO with the high intensity sonicator became 41 times larger, while that with the low intensity sonicator became 4.8 times larger. Based on the obtained results, it was suggested that the formed cavitation phenomenon was different between sonicators. It was also suggested that the sonochemical decomposition of MO in the presence of CCl4 would be useful to evaluate the sonochemical efficiency, because the rate of MO decomposition can be effectively enhanced by the sonolysis of CCl4. 相似文献
144.
Satoshi Saitoh Albrecht Melber Hiroshi Ohbayashi Satoshi Nakai Masakuni Matsuoka Masaaki Hosomi 《Journal of Material Cycles and Waste Management》2008,10(1):71-78
We discuss the use of the Schmidt graphical method to calculate the time required to heat a polychlorinated biphenyl (PCB)-contaminated
capacitor in the vacuum thermal recycling process to the processing temperature of 400°C, and we evaluate the results of the
heating time calculation by comparing the calculated values with the corresponding experimental values. The thermal conductivity
and specific heat of the insulating paper and the carbonized paper in the capacitor were unknown, so we determined their values
from experimental data obtained during the vacuum thermal recycling process. The capacitor element is a multilamination of
aluminum foil and insulating paper, so we used an equation for a multilayer plane wall to calculate the value of the thermal
conductivity. For the thermal conductivity and specific heat of the insulating paper impregnated with PCBs, we used values
calculated from the mass ratios and thermal conductivities and specific heats of the individual materials. In addition, the
physical properties vary according to the treatment because of the evaporation of PCBs and the carbonization of the insulating
paper, so we modified the values of the thermal conductivity, specific heat, and density at the boiling point of the PCB and
the carbonization point of the insulating paper before performing the calculations. Our calculated heating times were almost
the same as, or were above, the experimental values, so we concluded that our method can be used as a simple calculation of
the heating time. 相似文献
145.
Recent detection of fluoxetine in the aquatic environment and fish suggests a possibly high accumulation of fluoxetine; however, no report is available on the bioaccumulation of fluoxetine in aquatic organisms. Since bioaccumulation of fluoxetine was probably dependent on pH near the pK(a) value of 10.1, experiments were conducted approximately at pH 7, 8, and 9. Distribution coefficients between 1-octanol and water (D(ow)), and those between synthetic membrane vesicles (liposomes) and water (D(lip-wat)) were determined at pH 7, 8, and 9. The D(ow) and D(lip-wat) values increased significantly with increasing pH. Acute toxicity tests were performed using Japanese medaka (Oryzias latipes) prior to the bioaccumulation test, and 96-h LC(50) values were 5.5, 1.3, and 0.20mgl(-1) at pH 7, 8, and 9, respectively. In the bioaccumulation test, concentrations of fluoxetine and its major metabolite, norfluoxetine, in the fish body and liver were measured. The bioconcentration factors (BCF) of fluoxetine for Japanese medaka were 8.8, 3.0x10, and 2.6x10(2) in the body and 3.3x10(2), 5.8x10(2), and 3.1x10(3) in the liver at pH 7, 8, and 9, respectively. The BCF values were lower at pH 7 and higher at pH 9 mainly because of the increase in nonionized species with significantly higher hydrophobicity than the ionized species at pH values closer to pK(a). A similar trend was obtained for the concentration of norfluoxetine in the fish but the pseudo-BCF values (the ratio of the norfluoxetine concentration in the fish and the fluoxetine concentration in test water) were higher than the BCF value of fluoxetine at all pH conditions. 相似文献
146.
Ohmichi K Komiyama M Matsuno Y Takanashi Y Miyamoto H Kadota T Maekawa M Toyama Y Tatsugi Y Kohno T Ohmichi M Mori C 《Environmental science and pollution research international》2006,13(2):120-124
Goal, Scope and Background Cadavers for gross anatomy laboratories are usually prepared by using embalming fluid which contains formaldehyde (FA) as
a principal component. During the process of dissection, FA vapors are emitted from the cadavers, resulting in the exposure
of medical students and their instructors to elevated levels of FA in the laboratory. The American Conference of Governmental
Industrial Hygienists (ACGIH) has set a ceiling limit for FA at 0.3 ppm. In Japan, the Ministry of Health, Labour and Welfare
has set an air quality guideline defining two limit values for environmental exposure to FA: 0.08 ppm as an average for general
workplaces and 0.25 ppm for specific workplaces such as an FA factory. Although there are many reports on indoor FA concentrations
in gross anatomy laboratories, only a few reports have described personal FA exposure levels. The purpose of the present study
was to clarify personal exposure levels as well as indoor FA concentrations in our laboratory in order to investigate the
relationship between them.
Methods The gross anatomy laboratory was evaluated in the 4th, 10th and 18th sessions of 20 laboratory sessions in total over a period
of 10 weeks. Air samples were collected using a diffusive sampling device for organic carbonyl compounds. Area samples were
taken in the center and four corners of the laboratory during the entire time of each session (4-6 hours). Personal samples
were collected from instructors and students using a sampling device pinned on each person's lapel, and they were 1.1 to 6
hours in duration. Analysis was carried out using high performance liquid chromatography.
Results and Discussion Room averages of FA concentrations were 0.45, 0.38 and 0.68 ppm for the 4th, 10th and 18th sessions, respectively, ranging
from 0.23 to 1.03 ppm. These levels were comparable to or relatively lower than the levels reported previously, but were still
higher than the guideline limit for specific workplaces in Japan and the ACGIH ceiling limit. The indoor FA concentrations
varied depending on the contents of laboratory sessions and seemed to increase when body cavity or deep structures were being
dissected. In all sessions but the 4th, FA levels at the center of the room were higher than those in the corners. This might
be related to the arrangement of air supply diffusers and return grills. However, it cannot be ruled out that FA levels in
the corners were lowered by leakage of FA through the doors and windows. Average personal exposure levels were 0.80, 0.45
and 0.51 ppm for instructors and 1.02, 1.08 and 0.89 ppm for students for the 4th, 10th and 18th session, respectively. The
exposure levels of students were significantly higher than the mean indoor FA concentrations in the 4th and 10th sessions,
and the same tendency was also observed in the 18th session. The personal exposure level of instructors was also significantly
higher than the indoor FA level in the 4th session, while they were almost the same in the 10th and 18th sessions. Differences
in behavior during the sessions might reflect the differential personal exposure levels between students and instructors.
Conclusion The present study revealed that, if a person is close to the cadavers during the gross anatomy laboratory, his/her personal
exposure level is possibly 2 to 3-fold higher than the mean indoor FA concentration. This should be considered in the risk
assessment of FA in gross anatomy laboratories.
Recommendation and Outlook If the risk of FA in gross anatomy laboratories is assessed based on the indoor FA levels, the possibility that personal
exposure levels are 2 to 3-fold higher than the mean indoor FA level should be taken into account. Otherwise, the risk should
be assessed based on the personal exposure levels. However, it is hard to measure everyone's exposure level. Therefore, further
studies are necessary to develop a method of personal exposure assessment from the indoor FA concentration. 相似文献
147.
Biological aerosol particles are recently gaining increased attention, but global estimates of their emissions are unclear. Traditional organic tracers for biological particles have not been able to capture the diversity of biological sources such as residential wood burning. Here, we have analyzed protein content in air particulate matter over a year in a suburban area near Shibuya, in order to identify contributions from biological sources. Aerosols were separated into five size fractions using a high-volume cascade impactor. Amino acid profiles were obtained from acid hydrolysates by high-performance liquid chromatography and were subsequently used in a receptor model for source apportionment. Results show that protein content ranged from 0.5 to 2 % throughout the year in all size fractions. We observed contributions from seasonally variable emission sources such as pollen and fallen leaves in coarse particles, larger than 7 µm, at elevated concentrations during spring and winter. We also found contributions from pollen and fallen leaves in the smallest size fraction, lower than 1.1 µm, after spring. This finding indicates that sources are broken up to smaller particles in the urban environment. Overall, our findings demonstrate that protein content can be used as marker for biological aerosol particles, and that protein amino acid composition can distinguish multiple sources. 相似文献
148.
Kumagai Shogo Hirahashi Suguru Grause Guido Kameda Tomohito Toyoda Hiroshi Yoshioka Toshiaki 《Journal of Material Cycles and Waste Management》2018,20(1):439-449
Journal of Material Cycles and Waste Management - Polyvinyl chloride (PVC)-coated poly(ethylene terephthalate) (PET) woven fibers are one of the hardest-to-recycle polymeric materials. Herein we... 相似文献
149.
Fenta Ayele Almaw Yasuda Hiroshi Shimizu Katsuyuki Haregeweyn Nigussie 《Regional Environmental Change》2017,17(4):1229-1240
Regional Environmental Change - Climate variability and human activities are two major drivers influencing changes in streamflow response of a watershed, and thus assessing their relative effect is... 相似文献
150.
Sonoko Dorothea Bellingrath-Kimura Ayaka Wenhong Kishimoto-Mo Noriko Oura Seiko Sekikawa Seichiro Yonemura Shigeto Sudo Atsushi Hayakawa Kazunori Minamikawa Yusuke Takata Hiroshi Hara 《Ambio》2015,44(1):55-66
The spatial variability of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) fluxes from forest soil with high nitrogen (N) deposition was investigated at a rolling hill region in Japan. Gas fluxes were measured on July 25th and December 5th, 2008 at 100 points within a 100 × 100 m grid. Slope direction and position influenced soil characteristics and site-specific emissions were found. The CO2 flux showed no topological difference in July, but was significantly lower in December for north-slope with coniferous trees. Spatial dependency of CH4 fluxes was stronger than that of CO2 or N2O and showed a significantly higher uptake in hill top, and emissions in the valley indicating strong influence of water status. N2O fluxes showed no spatial dependency and exhibited high hot spots at different topology in July and December. The high N deposition led to high N2O fluxes and emphasized the spatial variability. 相似文献