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DSA类电极催化降解硝基苯及其动力学研究 总被引:9,自引:0,他引:9
用新兴的电化学催化系统,采用特殊工艺自制的DSA类电有作为阳极,对模拟硝基苯废水进行降解处理。结果表明,最佳试验条件为:电流密度15mA/cm^21、Na2So4浓度5g/L、pH以中性和碱性较好。在适合的条件下。硝基苯废水CODcr去除率可达到90%以上,DSA类电极能有效地催化降解硝基苯。对试验结果进行的非线性最小二乘法分析表明,硝基苯在电化学催化系统中的降解过程符合一级反应模型,在硝基苯质量浓度200mg/L、pH11.0、Na2SO4浓度10g/L、电流密度15mA/cm62的试验条件下,CODcr去除速度常数为0.0395min^-1。 相似文献
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以生化法处理有机污染物的系统为讨论对象 ,从底物负荷影响微生物生长的角度出发 ,通过对有机污染物负荷与生化反应速度之间的关系的分析 ,得出进口底物浓度的大小会影响生物反应器内微生物的量的多少 ,从而影响器内的生化反应速率的结论 ,并按照“稳定平衡”假说的设想 ,建立了修正的Michaelis -Menten公式 相似文献
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Hanen Bessaies Sidra Iftekhar Bhairavi Doshi Jamel Kheriji Mohamed Chaker Ncibi Varsha Srivastav Mika Sillanpää Bechir Hamrouni 《环境科学学报(英文版)》2020,32(5):246-261
This study focuses on the synthesis of nanocomposites named CCA and CZA that were prepared by the incorporation of cellulose(CL) in the Ca/Al and Zn/Al layered double hydroxide(LDH),respectively.These materials were then used for the uptake of As(Ⅲ)and As(V) from aqueous medium.Characterization of both nanocomposites(CCA and CZA) was done using FTIR and Raman analysis to identify the functional groups, N_2 adsorption-desorption isotherms to determine the specific surface area and pore geometry and XPS analysis to obtain the surface atomic composition.Some other characters were investigated using simultaneous TGA and DTA and elemental chemical analysis(CHNS/O).The crystallinity of the prepared nanocomposites was displayed by XRD patterns.Furthermore,the sheet-like structure of the LDHs and the irregularity of surface morphology with porous structure were observed by TEM and SEM microphotographs.Optimization of maximum adsorption capacity was adjusted using different parameters including pH,contact time and adsorbent dosage.The pseudo-second-order model was in good fitting with kinetics results.The adsorption isotherm results showed that CZA exhibits better adsorption capacity for As(Ⅲ) than CCA and the Langmuir isotherm model described the data well for both nanocomposites.Thermodynamic studies illustrated the endothermic nature of CCA and exothermic nature on CZA,as well as the fact that the adsorption process is spontaneous.A real water sample collected from well located in Gabes(Tunisia),has also been treated.The obtained experimental results were confirmed that these sorbents are efficient for the treatment of hazardous toxic species such as. 相似文献
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Jie Li Guangwei Yu Lanjia Pan Chunxing Li Futian You Shengyu Xie Yin Wang Jianli M Xiaofu Shang 《环境科学学报(英文版)》2018,30(11):20-30
In this study,used tea leaves(UTLs) were pyrolyzed to obtain used tea-leaf biochar(UTC),and then the UTC was used as an adsorbent to remove ciprofloxacin(CIP) from aqueous solutions.Batch experiments were conducted to investigate the CIP adsorption performance and mechanism.The results showed that the CIP-adsorbing ability first increased and then declined as the UTC pyrolysis temperature increased.The UTC obtained at 450°C presented excellent CIP-absorbing ability at p H 6 and 40°C.The maximum monolayer adsorption capacity was 238.10 mg/g based on the Langmuir isotherm model.The pseudo-second-order kinetic equation agreed well with the CIP adsorption process,which was controlled by both external boundary layer diffusion and intra-particle diffusion.The characterization analysis revealed that the \OH groups,C_C bonds of aromatic rings,C\H groups in aromatic rings and phenolic C\O bonds play vital roles in the CIP adsorption process,and that the N\C,N\O,O\C_O and C\OH groups of UTC were consumed in large quantities.π–π interactions,hydrogen bonding and electrostatic attraction are inferred as the main adsorption mechanisms.The present work provides not only a feasible and promising approach for UTLs utilization but also a potential adsorbent material for removing high concentrations of CIP from aqueous solutions. 相似文献
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For the first time, a series of alkynyl carbon materials(ACMs) were prepared via the mechanochemical reaction of CaC_2 with six polyhalogenated precursors, namely CCl_4,C_2Cl_6, C_2Cl_4, C_6Cl_6, C_6Br_6, and C_(14)H_4Br_(10)(ACM-1, ACM-2, ACM-3, ACM-4, ACM-5, and ACM-6,respectively) and used for the adsorptive removal of mercury from aqueous solutions.Based on preliminary investigations, the adsorption of mercury on ACM-5 was studied in depth. Specifically, the effect of p H on mercury adsorptivity, adsorption kinetics,thermodynamics, isotherms, and recyclability was studied. The adsorptivity of mercury on ACMs was found to be closely related to the hydrocarbon precursor, specific surface area of sorbent, and the alkynyl content. ACM-5 showed the best performance and is among the best raw carbonaceous sorbents reported so far, with a Langmuir saturated adsorption capacity of 191.9 mg g~(-1). The promising mercury adsorption performance mainly arises from the strong Lewis soft acid–soft base interactions between the alkynyl groups and mercury ions. The adsorption isotherms could be satisfactorily correlated with the Langmuir equation. The results show that the ACMs can be used as efficient sorbents for the removal of mercury and may also be useful for the adsorption of other heavy metals. 相似文献
119.
Highly active mesoporous TiO_2 of about 6 nm crystal size and 280.7 m~2/g specific surface areas has been successfully synthesized via controlled hydrolysis of titanium butoxide at acidic medium. It was characterized by means of XRD(X-ray diffraction), SEM(scanning electron microscopy), TEM(transmission electron microscopy), FT-IR(Fourier transform infrared spectroscopy), TGA(thermogravimetric analysis), DSC(differential scanning calorimetry) and BET(Brunauer–Emmett–Teller) surface area. The degradation of dichlorophenol-indophenol(DCPIP) under ultraviolet(UV) light was studied to evaluate the photocatalytic activity of samples. The effects of different parameters and kinetics were investigated. Accordingly, a complete degradation of DCPIP dye was achieved by applying the optimal operational conditions of 1 g/L of catalyst, 10 mg/L of DCPIP, pH of 3 and the temperature at 25 ± 3°C after 3 min under UV irradiation. Meanwhile, the Langmuir–Hinshelwood kinetic model described the variations in pure photocatalytic branch in consistent with a first order power law model.The results proved that the prepared TiO_2 nanoparticle has a photocatalytic activity significantly better than Degussa P-25. 相似文献
120.
p-Arsanilic acid(p-ASA) is widely used in China as livestock and poultry feed additive for promoting animal growth.The use of organoarsenics poses a potential threat to the environment because it is mostly excreted by animals in its original form and can be transformed by UV–Vis light excitation.This work examined the initial rate and efficiency of p-ASA phototransformation under UV-C disinfection lamp.Several factors influencing p-ASA phototransformation,namely,p H,initial concentration,temperature,as well as the presence of Na Cl,NH4+,and humic acid,were investigated.Quenching experiments and LC–MS were performed to investigate the mechanism of p-ASA phototransformation.Results show that p-ASA was decomposed to inorganic arsenic(including As(Ⅲ) and As(V))and aromatic products by UV-C light through direct photolysis and indirect oxidation.The oxidation efficency of p-ASA by direct photosis was about 32%,and those by HOU and1O2 were 19% and 49%,respectively.Cleavage of the arsenic–benzene bond through direct photolysis,HOU oxidation or1O2 oxidation results in simultaneous formation of inorganic As(Ⅲ),As(IV),and As(V).Inorganic As(Ⅲ) is oxidized to As(IV) and then to As(V) by1O2 or HOU.As(IV) can undergo dismutation or simply react with oxygen to produce As(V) as well.Reactions of the organic moieties of p-ASA produce aniline,aminophenol and azobenzene derivatives as main products.The photoconvertible property of p-ASA implies that UV disinfection of wastewaters from poultry and swine farms containing p-ASA poses a potential threat to the ecosystem,especially agricultural environments. 相似文献