河漫滩景观植物上轻物质附积对水力糙率的影响研究

在河道漫滩景观植物是河道环境建设的需要,但在洪水期,由于垃圾、杂草、树枝等漂浮物附着积聚在漫滩植物上导致水流阻力增加对河道防洪带来消极的影响。试验采用塑料植株来模拟灌木,以柔性的天然水草模拟洪水期的漂浮物,采用概化水槽试验研究植物分布特征及水流因素对水力糙率的影响,建立河道漫滩景观植物水草附积后糙率增长率与植物分布系数、水深、流速之间的关系式。试验结果表明:水槽在未布置植物时,糙率系数约为0.009,布置植物以后,糙率系数值在0.01~0.07之间;当植物上附着水草后,糙率系数值在0.023~0.079之间,糙率增长率为11%~130%;糙率及糙率增长率与植物分布系数、淹没深度、流速等因素相关,且呈现一定的规律性。

溅射积附时金属镀层内应力的研究

本文分析了溅射积附时金属镀层内应力的起因、本质及表现形式,讨论了镀层应力、本征应力和热应力的影响因素,并对镀层粘合力进行了研究。

New method for prediction of shale gas content in continental shale formation using well logs

Shale needs to contain a sufficient amount of gas to make it viable for exploitation. The continental heterogeneous shale formation in the Yan-chang （YC） area is investigated by firstly measuring the shale gas content in a laboratory and then investigating use of a theoretical prediction model. Key factors controlling the shale gas content are determined, and a prediction model for free gas content is established according to the equation of gas state and a new petrophysical volume model. Application of the Langmuir volume constant and pressure constant obtained from results of adsorption isotherms is found to be limited because these constants are greatly affected by experimental temperature and pressures. Therefore, using measurements of adsorption isotherms and thermodynamic theory, the influence of temperature, total organic carbon （TOC）, and mineralogy on Langmuir volume constants and pressure constants are investigated in detail. A prediction model for the Langmuir pressure constant with a correction of temperatures is then established, and a prediction model for the Langmuir volume constant with correction of temperature, TOC, and quartz contents is also proposed. Using these corrected Langmuir constants, application of the Langmuir model determined using experimental adsorption isotherms is extrapolated to reservoir temperature, pressure, and lithological conditions, and a method for the prediction of shale gas content using well logs is established. Finally, this method is successfully applied to predict the shale gas content of the continental shale formation in the YC area, and practical application is shown to deliver good results with high precision.

Determination of the Real Surface Area of Palladium Electrode

Four methods, including voltammetric measurement of double layer capacitance, surface oxides reduction, under potential deposition of Cu and carbon monoxide （CO） stripping have been applied to evaluate the real surface area of a polycrystalline Pd （pc-Pd） electrode. The results reveal that the second and third methods lead to consistent results with deviations below 5%. And from the determined double layer capacitance and CO stripping charge, it is deduced that the double layer capacity unit area is 23.1±0.4μF/cm2 and the saturated CO adlayer should be ca. 0.66 ML in order to ensure that the real surface area as determined is consistent with the other two techniques. The applicability as well as the attentions when applying these techniques for the determination of the real surface area of pc-Pd electrodes have been discussed.

Modification of ACFs by chemical vapor deposition and its application for removal of methyl orange from aqueous solution

Viscose activated carbon fibers （ACFs） were characterized using specific surface area, scanning electron modified with chemical vapor deposition （CVD）. The samples were microscopy （SEM）, pore size distribution and Fourier transform infrared spectroscopy （FTIR）. Batch adsorption experiments were carried out to investigate the adsorption behavior of modified ACFs for methyl orange（MO） from its aqueous solutions. The results show that the adsorption isotherms of MO onto modified ACFs well follows the Langmuir isotherm equation. The adsorption kinetics of MO can be well described by the pseudo second-order kinetic model. The adsorption process involves the intra-particle diffusion, but is not the only rate-controlling step. Thermodynamic parameters including AG, AH and AS were calculated, suggesting that the adsorption of MO onto modified ACFs is a spontaneous, exothermic and physisorption process. FTIR result indicates that the major adsorption mechanism of modified ACFs for MO is hydrogen bond.

Treatment of Organic Wastewater Containing Cr^(3+) by a Novel Complex Process of Electrodeposition and Biofilm

A novel complex process of electrodeposition and biofilm is utilized to treat organic wastewater containing Cr 3+, and its purifying mechanism is also described in this article. In details, organic materials in wastewater are consumed as nutritious source by biofilm composed of microorganism and EPS (extracellular polysaccharide substance). While one part of heavy metal ions, such as Cr 3+, is removed by electrodeposition, the other part is adsorbed on biofilm. In contrast, experimental data of single electrodeposition or biofilm process are listed. Further, the kinetic curves of microbes cultivated or microbes acclimated by Cr 3+ to degrade glucose are provided,too. In conclusion, the experimental results indicate that initial wastewater consists of C 6H 12O 6 (500 mg·L -1), Cr 3+ (10 mg·L -1), after treated with the complex process, concentrations of C 6H 12O 6 and Cr 3+ are on the scale of 15-20 mg·L -1, and less than 1 mg·L -1, respectively. Purified water can meet the standards of industrial reused water.

Phosphorus Changes and Sorption Characteristics in a Calcareous Soil Under Long-Term Fertilization

Knowledge of phosphorus （P） behavior in long-term fertilized soils is essential for programming fertilization practices and for sustaining environmental quality. The long-term （1984-1997） effects of various fertilization treatments on P changes and sorption isotherms as well as the relationship of soil properties to P sorption and P forms were evaluated in an Ustic Isohumisol, a calcareous soil, on the Loess Plateau, China. Compared to 1984, after 13 years of crop production, total soil P in the no-P treatments （control and N treatment） decreased by 5%-7%, but in the phosphorus fertilizer alone （P）, nitrogen and phosphorus fertilizers in combination （NP）, manure alone （M）, and nitrogen and phosphorus fertilizers and manure in combination （NPM） treatments, it increased by 22%, 19%, 28%, and 58%, respectively. Residual fertilizer P was found mainly in NH4Ac-soluble P （Cas-P）, followed by NaHCO3-soluble P （NaHCO3-P）, and NH4F-soluble P （Al-P）. Phosphorus sorption in the soils with different fertilization practices fit the Langmuir equations. Phosphorus sorption capacity in the no-P treatments increased, whereas it decreased in the P-included treatments （P, NP, and NPM treatments）. Phosphorus sorption maximum （Qm） was significantly and negatively correlated to inorganic P including NaHCO3-P, Cas-P, NaOH-Na2CO3-soluble P （Fe-P）, and Al-P （P ≤ 0.01）. Moreover, long-term fertilization increased soil organic carbon in the NP, M, and NPM treatments and decreased pH in the NP and NPM treatments. Thus, the ability of the soil to release sorbed P to the environment increased under long-term P fertilization.

Lake Sediments from Dianchi Lake:A Phosphorus Sink or Source?

Dianchi Lake is a highly eutrophic lake in southwestern China where phosphorus (P) is the limiting element for eutrophication and where lake sediments play an important role in the P cycle. One hundred and eighteen sites were sampled throughout Dianchi Lake in 2002 to investigate the P loading of the lake sediments, while fresh surface sediments were studied in the laboratory to clarify its role for phosphorus. The results showed that concentrations of total phosphorus (TP) in sediments were very high, with a maximum value of 6.66 g kg-1, and decreased with sediment depth. P adsorption on surface sediments was rapid with adsorption amounts higher in acidic than in alkaline conditions. The release experiments showed that P release increased as pH rose from 7.0 to 10.5. Additionally, compared with aerobic conditions, P release was much higher under anaerobic conditions, especially with low P content in the lake water. At present, the sediments in Dianchi Lake still function as a sink for phosphorus at high P levels in lake water. However, if the external P load was reduced and P content in lake water became low, the sediment would have a large potential for P release under anaerobic conditions.

Treatment of Organic Wastewater Containing Cr3+ by a Novel Complex Process of Electrodeposition and Biofilm

A novel complex process of electrodeposition and biofilm is utilized to treat organic wastewater containing Cr 3+, and its purifying mechanism is also described in this article. In details, organic materials in wastewater are consumed as nutritious source by biofilm composed of microorganism and EPS (extracellular polysaccharide substance). While one part of heavy metal ions, such as Cr 3+, is removed by electrodeposition, the other part is adsorbed on biofilm. In contrast, experimental data of single electrodeposition or biofilm process are listed. Further, the kinetic curves of microbes cultivated or microbes acclimated by Cr 3+ to degrade glucose are provided,too. In conclusion, the experimental results indicate that initial wastewater consists of C 6H 12O 6 (500 mg·L -1), Cr 3+ (10 mg·L -1), after treated with the complex process, concentrations of C 6H 12O 6 and Cr 3+ are on the scale of 15-20 mg·L -1, and less than 1 mg·L -1, respectively. Purified water can meet the standards of industrial reused water.

Improved analytic methods for coal surface area and pore size distribution determination using 77 K nitrogen adsorption experiment

77 K nitrogen adsorption was the most widely used technique for determining surface area and pore size distribution of coal. Brunauer–Emmett–Teller(BET) and Barrett–Joyner–Halenda(BJH) model are commonly used analytic methods for adsorption/desorption isotherm. A Chinese anthracite coal is tested in this study using an improved experimental method and adsorption isotherm analyzed by three adsorption mechanisms at different relative pressure stages. The result shows that the micropore filling adsorption predominates at the relative pressure stage from 6.8E 7 to 9E 3. Theoretically, BET and BJH model are not appropriate for analyzing coal samples which contain micropores. Two new analytic procedures for coal surface area and pore size distribution calculation are developed in this work. The results show that BET model underestimates surface area, and micropores smaller than 1.751 nm account for 35.5% of the total pore volume and 74.2% of the total surface area. The investigation of surface area and pore size distribution by incorporating the influence of micropore is significant for understanding adsorption mechanism of methane and carbon dioxide in coal.

Methane adsorption-induced coal swelling measured with an optical method

In order to quantify the effect of matrix shrinkage on reservoir permeability during coalbed methane production, coal samples from Huozhou, Changzhi and Jincheng areas in Shanxi province （classified as high-volatile bituminous coal, low-volatile bituminous coal and anthracite, respectively） were collected, and adsorption-induced coal swelling in methane were determined by an optical method at 40 ℃ and pressure up to 12 MPa. All three coals showed similar behavior-that swelling increased as a function of pressure up to about 10 MPa but thereafter no further increase in swelling was observed. Swelling in the direction perpendicular to the bedding plane is greater than that parallel to the bedding plane, and the differences are about 7.77-8.33%. The maximum volumetric swelling ranges from 2.73% to 3.21 %-increasing with increasing coal rank. The swelling data can be described by a modified DR model. In addition, swelling increases with the amount of adsorption. However, the increase shows a relatively slower stage followed by a relatively faster stage instead of a linear increase. Based on the assumption that sorption-induced swelling/shrinkage of coal in methane is reversible, the permeability increases induced by coal shrinkage during methane desorption was analyzed, and the results indicate that the permeability change is larger for higher rank coal in the same unit of pressure depletion.

Surface and Hydrogen Sorption Characteristics of Various Activated Carbons Developed from Rat Coal Mine （Zonguldak） and Anthracite

Activated carbon samples were developed from coal samples obtained from a coal mine, rat （Zonguldak, Turkey） and anthracite （Siberia, Russia）, applying pyrolysis in a temperature range of 600-900 ℃ under N2 flow, and activation using chemical agents such as KOH, NH4Cl, ZnCl2 at 650 ℃. Nitrogen adsorption at low temperature （77 K） was used to characterize the activated carbon samples, and their pore structure properties including pore volume, pore diameter and pore size distribution were determined by means of the t-plots and DFT methods. The surface area values were higher for rat coal samples than for anthracite one, and for the rat coal samples treated with KOH ＋ NH4Cl ＋ ZnCl2 at 650 °C [Rat650（2）] there are highest surface area and total pore volume, 315.6 m2·g^-1 and 0.156 ml·g^-1, respectively. The highest value of the hydrogen sorption capacity was found as 0.71% （by mass） for the rat coal sample obtained by KOH ＋ ZnCl2 treatment at 650 °C [Rat650（1）].

Sorption behavior of o-nitrophenol on marine sediment

Systematic study on sorption behavior of o-nitrophenol on marine sediments was conducted. Isotherms of sorption of o-nitrophenol on marine sediments could be described by Freundlich model; and the isotherm of sorption of o-nitrophenol on HCl-treated sediment could be described by Langmuir model. The sorption behavior was affected by various factors including organic carbon content, aqueous solution salinity, temperature, and acidity. The sorption amount of o-nitrophenol increased when salinity and acidity of the aqueous solution increase, but decreased with increasing temperature. Organic carbon content in sediments had apparent effect on the behavior except for HCl-treated sediments.

Estimation of the Isotherms of Phenol on Activated Carbons and Polymeric Adsorbents under Supercritical Condition

A method named as 'volume-expanding and pressure-reducing adsorption' is proposed. It can be used to measure the isotherms under supercritical condition. The adsorption isotherms of phenol on activated carbons and polymeric adsorbents are estimated and compared respectively for the systems of 'phenol-activated carbon-supercritical fluid CO2' and 'phenol-polymeric adsorbent-supercritical fluid CO2'. The results show that the amount of phenol adsorbed on the activated carbons and the polymeric adsorbents under the supercritical condition is much less than that under the general condition, which can be utilized to develop a technology regenerating the activated carbon with supercritical fluid. Moreover, the effects of ethyl alcohol, used as the third component, on the isotherms of phenol on the activated carbons and polymeric adsorbents under the supercritical condition are also investigated.

Water vapor adsorption in activated carbon modified with hydrophilic organic salts

Five different kinds of hydrophilic organic salts were used to modify commercial activated carbon in order to prepare hydrophilic carbon materials. Properties of the samples were analyzed by surface area analyzer and SEM-EDX. The hydrophilic organic salts with different properties were introduced into activated carbon and significantly affected the properties of the samples.During adsorption experiments, the water vapor adsorption amount in modified samples increases by 0.57-17.12 times in temperature range from 303 to 323 K and at relative pressure below 0.50. Water molecules combined with surface hydrophilic groups through H-bonding exhibit good thermo stability. The effects of temperature, oxygen content and properties of the hydrophilic organic salts on water vapor adsorption were studied. It is indicated that water vapor adsorption in modified samples is mainly affected by the surface oxygen content. The carboxylate radicals in the hydrophilic organic salts greatly affect the micropore structure of the modified samples, while the metal ions in them exhibit limited influence. Different adsorption capacity of modified samples can be explained with the electronegativity of elements presented by Pauling.

Influence of Chelating Agents on Chromium Fate in Sediment

A laboratory investigation on reaction between chelating agents and chromium was conducted to evaluate the effect of chelating agents on the adsorption and desorption of chromium in sediment. The amount of adsorbed chromium(VI) in sediment decreased slightly by 5%-10% because of addition of chelating agents.Chelating agents inhibited the remodel of Cr(Ⅲ) by sediment from solutions and the inhibiting effect was in the order:citric acid > tartaric acid > EDTA, salicylic acid.No effect of chelating agents on desorption of chromium in sediment was observed.

Discrete element method for adhesion properties evaluation of deep-sea sediment from macro and micro perspectives

The adhesion between the mining machine and the deep-sea sediments will significantly affect the driving performance of the mining machine in the deep-sea environment.When the mining machine and the deep-sea sediment interaction simulation was carried out,the accuracy of the particle interaction parameters will directly affect the simulation results.This study proposed a method to systematically calibrate the interaction parameters between deep-sea sediment and grouser through the combination of experiment and simulation.The uniaxial compression test and macro adhesion test and corresponding discrete element numerical simulation were carried out,modifying the contact parameters until the simulation results are close to the experimental results.Then the micro-parameters of the JKR adhesion contact model were back calibrated with the test results,and the contact parameters between soil particle-soil particle and soil particle-metal are calibrated.Besides,the adhesion test shows that the adhesion forces were ranked in the order of 5052<STi80<TA2<TC4 under the same surface roughness,which indicates the aluminum alloy 5052 has the best anti-adhesion performance.The relationship between surface adhesion force and microscopic contact parameters was studied by discrete element numerical simulation,and the result shows that the coefficient of static friction and the coefficient of rolling friction has little effect on adhesion force.While it is mainly affected by the coefficient of restitution and surface energy,the surface adhesion force tends to decrease with the increase of the coefficient of restitution and increase with the growth of surface energy.The obtained parameters of soil particle to soil particle and soil particle to metal affecting the adhesion can contribute to the design optimization for the grouser of mining machines to decrease surface adhesion and enhance its movability and mining efficiency.

Porous g-C3N4 with enhanced adsorption and visible-light photocatalytic performance for removing aqueous dyes and tetracycline hydrochloride

Porous g-C3N4samples were obtained by simply calcining bulk g-C3N4in static air in a muffle oven.The photocatalytic performance of these samples was evaluated through the removal of aqueous organic dyes（methylene blue and methyl orange）and tetracycline hydrochloride under visible-light irradiation（λ〉420 nm）.Compared to bulk g-C3N4,porous g-C3N4exhibited much better capability for removing these contaminants,especially under visible-light irradiation,due to the enlarged specific surface area and more efficient separation of photogenerated charge carries.In particular,porous g-C3N4obtained by calcining bulk g-C3N4in air at 525℃ showed the highest visible-light-driven catalytic activity among these samples.Superoxide radical anions（·O2^-）were found to be the primary active species responsible for photodegradation.

Superior Au-adsorption performance of aminothiourea-modified waste cellulosic biomass

Waste cellulosic biomass obtains various applications due to low-cost and eco-benign characteristics.A general strategy is proposed for waste cellulosic biomass to be modified with dialdehyde functional groups as intermediates through periodate partial oxidation.Finally,aminothiourea-modified waste cellulosic biomass can be prepared through Schiff reaction.Waste corn stalk,cotton and paper as typical precursors,were used to prepare cellulosic biomass,abbreviated as AT-S,AT-C and AT-P,respectively,and their adsorption behaviors of Au(III)from the hydrochloric acid medium were investigated.The pseudo-second kinetics equation as well as the Langmuir isotherm equation can be used to depict the adsorption process,and the maximum adsorption capacities of Au(III)are21.4,19.0and3.28mol/kg for AT-S,AT-C and AT-P at298K,respectively.The adsorption capacities of Au(III)on aminothiourea modified corn stalk(AT-S)is almost357times greater than that of raw corn stalk.To the best of our knowledge,AT-S has the highest adsorption capacity towards Au(III).AT-S also displays a superior separation selectivity towards Au(III)in the presence of Cu(II),Ni(II),Co(II),Pt(VI),Pd(II)and Rh(III).Furthermore,the characterization analysis of XRD,TG,SEM,TEM and FTIR confirms that AuCl4– has been reduced to elemental Au nanoparticles and deposit onto the surface of the biomass.It shows a prospect for waste corn stalk to be used to adsorb Au(III)from liquid phase and the possible fabrication of gold nanoparticles by a general adsorption process without any reductant.

Effect of magma intrusion on the occurrence of coal gas in the Wolonghu coalfield

Chemical analysis, methane isothermal adsorption studies, and mercury porosimetry were performed on ten samples taken from the magma intrusion boundary in the Wolonghu coalfield. The physico-chemical properties of coals from the magma intrusion region are compared to those from the normal regions. The results show that the volatile content (Vad), the limiting adsorption constant (a), and the initial methane diffusion rate of samples from the magma intrusion region are generally smaller than those values from samples from the normal region. The number three coal sample from the magma intrusion region has a large vitrinite reflectance, well developed macropores, a small surface area, and weak methane adsorp- tion capacity. The number ten coal sample from the normal region has a small vitrinite reflectance, well developed micropores, a large surface area, and a strong methane adsorption capacity. The maceral of the coal samples from the magma intrusion region and the normal region are similar. The coal in the area near the magma intrusion boundary is rich in methane and is an area where coal and gas outbursts often occur.