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61.
62.
63.
三峡库区悬移质泥沙对磷污染物的吸附解吸特性 总被引:3,自引:0,他引:3
就三峡库区悬移质泥沙对磷污染物的吸附解吸特性从野外同步监测和室内试验研究两个方面展开研究。选取长江干流、嘉陵江和乌江共7个监测断面于2002年和2003进行野外同步监测,测试结果表明:水中的悬移质泥沙对水中各种覆存形态的磷污染物浓度具有显著影响,单位重量泥沙对磷的吸附量与水体总泥沙含量、泥沙粒径有密切关系。采集寸滩断面泥沙对磷酸盐吸附解吸特性进行室内试验研究,并根据Langmuir吸附动力学方程对吸附解吸过程进行了拟合,发现吸附速率常数k随着泥沙粒径的增加而呈递增变化,而磷酸盐初始浓度对k值的影响并不明显,同时,磷酸盐解吸量随着泥沙浓度的增加和粒径的增加呈递减变化,k值随着泥沙粒径的增加而呈递增变化,泥沙浓度对k值的影响不明显。 相似文献
64.
Competition of three bloom-forming marine phytoplankton (diatom Skeletonema costatum, and dinoflagellates Prorocentrum
minimum and Alexandrium tamarense) was studied through a series of multispecies cultures with di erent nitrate (NaNO3) and
phosphate (NaH2PO4) levels and excess silicate to interpret red tide algae succession. S. costatum outgrew the other two dinoflagellates
in nitrate and phosphate replete cultures with 10 mol/L Na2SiO3. Under nitrate limited (8.82 mol/L NaNO3) conditions, the growth
of S. costatum was also dominant when phosphate concentrations were from 3.6 to 108 mol/L. Cell density of the two dinoflagellates
only increased slightly, to less than 400 and 600 cells/mL, respectively. Cell density of S. costatum decreased with time before day
12, and then increased to 4000 cells/mL (1.5 mg/L dry biomass) at NaNO3 concentrations between 88.2 and 882 mol/L with limited
phosphate (0.36 mol/L NaH2PO4) levels. In addition, P. minimum grew well with a maximal cell density of 1690–2100 cells/mL
(0.5–0.6 mg/L dry biomass). Although S. costatum initially grew fast, its cell density decreased quickly with time later in the growth
phase and the two dinoflagellates were dominant under the nitrate-limited and high nitrate conditions with limited phosphate. These
results indicated that the diatom was a poor competitor compared to the two dinoflagellates under limited phosphate; however, it grew
well under limited nitrate when growth of the dinoflagellates was near detection limits. 相似文献
65.
Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous
silicates hybrid materials
Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water.
A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal
cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion
technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well
fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data
from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and
the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse
e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In
addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and
relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment. 相似文献
66.
Tao Zhang Qiucheng Li Lili Ding Hongqiang Ren Ke Xu Yonggang Wu Dong Sheng 《环境科学学报(英文版)》2011,23(6):881-890
Chemical precipitation to form magnesium ammonium phosphate (MAP) is an effective technology for recovering ammonium
nitrogen (NH4
+-N). In the present research, we investigated the thermodynamic modeling of the PHREEQC program for NH4
+-N
recovery to evaluate the effect of reaction factors on MAP precipitation. The case study of NH4
+-N recovery from coking wastewater
was conducted to provide a comparison. Response surface methodology (RSM) was applied to assist in understanding the relative
significance of reaction factors and the interactive effects of solution conditions. Thermodynamic modeling indicated that the saturation
index (SI) of MAP followed a polynomial function of pH. The SI of MAP increased logarithmically with the Mg2+/NH4
+ molar ratio
(Mg/N) and the initial NH4
+-N concentration (CN), respectively, while it decreased with an increase in Ca2+/NH4
+ and CO3
2??/NH4
+
molar ratios (Ca/N and CO3
2??/N), respectively. The trends for NH4
+-N removal at different pH and Mg/N levels were similar to the
thermodynamic modeling predictions. The RSM analysis indicated that the factors including pH, Mg/N, CN, Ca/N, (Mg/N) (CO3
2??/N),
(pH)2, (Mg/N)2, and (CN)2 were significant. Response surface plots were useful for understanding the interaction effects on NH4
+-N
recovery. 相似文献
67.
以冷砂黄泥和矿子黄泥为研究对象,猪粪沼渣为有机物料,分别添加0%、5%、7.5%和10%质量分数的蒙脱石,采用室内培养试验研究了蒙脱石对施有机物料土壤pH、磷形态和有效性的影响.结果表明,有机物料对两种土壤pH无显著影响,而蒙脱石使土壤pH显著提高.施加有机物料使两种土壤铝结合态磷(Al-P)含量和分布比例提高,铁结合态磷(Fe-P)含量培养后期提高、比例略有下降,闭蓄态磷(O-P)含量无明显变化、比例下降.有机物料对冷砂黄泥中钙结合态磷(Ca-P)的含量无明显影响、比例下降,却使矿子黄泥Ca-P含量和比例提高.在施加有机物料基础上添加蒙脱石后,冷砂黄泥Al-P和O-P含量和比例下降,Fe-P含量无明显变化、比例下降,Ca-P含量和比例大幅度提高;矿子黄泥Fe-P和O-P含量和比例下降,Al-P含量无明显变化、比例下降,Ca-P含量和比例大幅度提高.培养过程中,有机物料使冷砂黄泥和矿子黄泥有效磷含量分别提高了17.9%~38.0%和17.1%~33.7%,土壤磷的活化系数也显著提高,添加蒙脱石后使两种土壤有效磷含量分别降低8.8%~35.5%和1.1%~11.6%.相关分析结果表明,蒙脱石通过提高pH和Ca-P含量、降低Al-P含量降低冷砂黄泥磷的有效性,通过提高pH、降低Fe-P含量降低矿子黄泥磷的有效性,对冷砂黄泥磷有效性的影响较矿子黄泥大. 相似文献
68.
Removal of phosphate from wastewater using alkaline residue 总被引:2,自引:0,他引:2
Yubo Yan Xiaodong Liu Xiuyun Sun Fangbian M Lianjun Wang Jiansheng Li Jinyou Shen 《环境科学学报(英文版)》2014,26(5):970-980
Alkaline residue(AR) was found to be an efficient adsorbent for phosphate removal from wastewater. The kinetic and equilibrium of phosphate removal were investigated to evaluate the performance of modified alkaline residue. After treatment by NaOH(AR-NaOH), removal performance was significantly improved, while removal performance was almost completely lost after treatment by HCl(AR-HCl). The kinetics of the removal process by all adsorbents was well characterized by the pseudo second-order model. The Langmuir model exhibited the best correlation for AR-HCl, while AR was effectively described by Freundlich model. Both models were well fitted to AR-NaOH. The maximum adsorption capacities calculated from Langmuir equation were in following manner: AR-NaOH AR AR-HCl. Phosphate removal by alkaline residue was pH dependent process. Mechanisms for phosphate removal mainly involved adsorption and precipitation, varied with equilibrium pH of solution. For AR-HCl, the acid equilibrium pH( 6.0) was unfavorable for the formation of Ca-P precipitate, with adsorption as the key mechanism for phosphate removal. In contrast, for AR and ARNaOH, precipitation was the dominant mechanism for phosphate removal, due to the incrase on pH( 8.0) after phosphate removal. The results of both XRD and SEM analysis confirmed CaHPO4·2H2O formation after phosphate removal by AR and AR-NaOH. 相似文献
69.
重金属抗性解磷细菌的磷溶解特性研究 总被引:2,自引:1,他引:1
从湖南省湘西州花垣县的铅锌矿表层土壤中,筛选出两株具有重金属抗性和解磷特性的细菌T PSB1和T PSB2.通过16S rRNA基因序列比对,分别鉴定为嗜麦芽寡养单胞菌(Stenotrophomonas maltophilia)和唐菖蒲伯克霍尔德菌(Burkholderia gladioli).T PSB1和T PSB2在含有难溶性无机磷液体培养基中,其上清液的可溶性磷含量最高分别达到了402.9 mg·L-1和589.9 mg·L-1;在难溶性有机磷固体和液体培养基中,固体平板上均出现解磷圈,而液体培养基上清液中,可溶性磷含量也分别达到了2.97 mg·L-1和4.69 mg·L-1.另外,两株细菌对重金属Zn2+的抗性最高,在其浓度为2000 mg·L-1固体和液体培养基条件下均可以生长,磷溶解浓度分别为114.8 mg·L-1和125.1 mg·L-1.而在含铬和铅的浓度为1 000 mg·L-1的液体培养基中,两株细菌同样表现出重金属抗性.在Pb2+浓度为1000 mg·L-1的液体培养基中,磷溶解浓度分别达到了57.9 mg·L-1和71.7 mg·L-1;而在Cr2+浓度为1000 mg·L-1的培养基中磷溶解浓度分别为60.1 mg·L-1和98.4 mg·L-1. 相似文献
70.
不同添加剂对铅冶炼污染石灰性土壤的修复及土壤性质的影响研究 总被引:2,自引:2,他引:0
探讨了污水处理厂脱水污泥、枯草和磷矿粉对受铅冶炼污染的石灰性土壤(全Pb、Cd、Zn含量分别为2337、21.4、486 mg·kg-1,DTPA提取态Pb、Cd、Zn含量分别为1035、14.5、68.7 mg·kg-1)中重金属的稳定效果及对土壤性质的影响.其中,污泥和枯草均按200 g·kg-1(干重)的用量施用,磷矿粉按n(P)∶n(Pb)=2∶1比例施用,培养80 d.研究结果表明,单独施用污泥可使土壤DTPA-Pb含量降低18.0%(p0.05),并可显著降低土壤pH,增加土壤氮、磷有效性和电导率、DTPA-Cd、DTPA-Zn含量,其中,DTPA-Cd、DTPA-Zn含量增加比例均达到10%以上.单独施用枯草可使土壤DTPA-Pb含量降低10.7%(p0.05),土壤有机质含量增加26.4%(p0.05),对土壤其它性状影响较小.磷矿粉单独施用时对土壤性质影响较小.与污泥单独施用相比,磷矿粉与污泥配合施用时,可使土壤DTPA-Cd含量降低11.9%. 相似文献