Denitrification potential enhancement by addition of external carbon sources in a pre-denitrification process

The aim of this study is to investigate the denitrification potential enhancement by addition of external carbon sources and to estimate the denitrification potential for the predenitrification system using nitrate utilization rate （NUR） batch tests. It is shown that the denitrification potential can be substantially increased with the addition of three external carbon sources, i.e. methanol, ethanol, and acetate, and the denitrification rates of ethanol, acetate, and methanol reached up to 9.6, 12, and 3.2 mgN/（g VSS.h）, respectively, while that of starch wastewater was only 0.74 mgN/（g VSS,h）. By comparison, ethanol was found to be the best external carbon source. NUR batch tests with starch wastewater and waste ethanol were carried out. The denitfification potential increased from 5.6 to 16.5 mg NO3-N/L owing to waste ethanol addition. By means of NUR tests, the wastewater characteristics and kinetic parameters can be estimated, which are used to determine the denitrification potential of wastewater, to calculate the denitrification potential of the plant and to predict the nitrate effluent quality, as well as provide information for developing carbon dosage control strategy.

Influence of carbon on the giant magnetocaloric effect of LaFe_11.7Si_1.3

The influences of carbon on phase formation, Curie temperature, and magnetic entropy change of the NaZn13-type LaFe11.7Si1.3 were investigated. Seven carbon-containing alloys, LaFe11.7Si1.3Cx with x = 0, 0.03, 0.06, 0.10, 0.20, 0.30, and 0.50, respectively, were prepared for this investigation. Experimental results show that addition of a small amount of carbon in LaFe11.7Sil.3 is favorable for the formation of the NaZn13-type structure of LaFe11.7Si1.3Cx. The lattice constant increases with C addition and x increases in the alloy because of the introduction of C as interstitial atoms. The Curie temperature of LaFe11.7Si1.3Cx increases from 194 K to 225 K as x increases from 0 to 0.5. Large magnetic entropy changes were observed in these carbon-containing alloys LaFe11.7Si1.3Cx because of their first-order structural/magnetic transition. The maximum magnetic entropy change of 27.5 J.kg^-1K^-1 at 202 K for the 0-1.56 T magnetic field change was observed in the alloy with x = 0.06. The large magnetic-entropy changes corresponding to low magnetic field change, and the low cost of the material of LaFe11..7Si1.3Cx makes it a promising candidate to be used as magnetic refrigerants in the corresponding temperature range.

Additivity of pore structural parameters of granular activated carbons derived from different coals and their blends

A series of granular activated carbons （GACs） were prepared by briquetting method from Chinese coals of different ranks and their blends, with coal pitch as the binder. Pore structural parameters including BET specific surface area （SBEr）, total pore volume （Vr） and average pore diameter （da） were measured and cal- culated as well as process parameters such as yield of char （CY） and burn-off （B）. The relationship between the pore structural parameters of the GAC from coal blend （BC-GAC） and the ones of the GACs from corresponding single coals （SC-GACs） was analyzed, in which an index, the relative error （δ）, was presented to define the bias between fitted values and experimental values of these parameters of the BC-GACs. The results show that the BC-GAC keeps qualitatively the pore structural features of the SC-GACs; as concerned as the quantitative relationship, the pore structural parameters of the BC-GAC from coal blend consisting of non-caking coals can be obtained by adding proportionally the pore structural parameters of the SC-GACs with a less than 10%. Meanwhile, for the BC-GAC from coal blend containing weak caking bituminous coal, the δ increases up to 25% and the experimental pore size distribution differs greatly from the fitted one.

Study of control strategy and simulation in anoxic-oxic nitrogen removal process

The control strategy and simulation of external carbon addition were specially studied in an anoxic-oxic(A/O) process with low carbon: nitrogen(C/N) domestic wastewater. The control strategy aimed to adjust the flow rate of external carbon dosage to the anoxic zone, thus the concentration of nitrate plus nitrite(NOx--N) in the anoxic zone was kept closed to the set point. The relationship was studied between the NOx--N concentration in the anoxic zone(S_ NO) and the dosage of external carbon, and the results showed that the removal efficiency of the total nitrogen(TN) could not be largely improved by double dosage of carbon source when S_ NO reached about 2 mg/L. Through keeping S_ NO at the level of about 2 mg/L, the demand of effluent quality could be met and the carbon dosage could be optimized. Based on the Activated Sludge Model No.1(ASM No.1), a simplified mathematical model of external carbon dosage was developed. Simulation results showed that PI controller and feed-forward PI controller both had good dynamic response and steady precision. And feed-forward PI controller had better control effects due to its consideration of influent disturbances.

Effect of Carbon Addition on Microstructure and Properties of WC-Co Cemented Carbides

Based on a unique method to synthesize WC-Co composite powder by in-situ reactions of metal oxides and carbon, the effects of the carbon addition in the initial powders on the phase constitution, microstructure and mechanical properties of the cemented carbides were investigated. It is found that with a suitable carbon addition the pure phase constitution can be obtained in the sintered bulk from the composite powder. The mechanical properties of the cemented carbides depend on the phase constitution and the WC grain structure. To obtain the excellent properties of the WC-Co bulk, it is important to obtain the pure phase constitution from the appropriate carbon addition in the initial powders and a suitable grain size.

Soot reduction by addition of dimethyl carbonate in normal and inverse ethylene diffusion flames:Nanostructural evidence

Oxygenated fuel represents an attractive alternative as an additive for reducing soot emissions.Dimethyl carbonate（DMC） is an oxygenated compound which is a good option to reduce soot,but the detailed characteristics of soot produced from combustion of hydrocarbon fuels blended with DMC are still lacking. The present research studied the nanostructure and reactivity of soot particles in ethylene/DMC normal and inverse diffusion flames. High resolution transmission electron microscopy（HRTEM）, X-ray diffraction（XRD）, and thermogravimetric analysis（TGA）were used to analyze the nanostructure and reactivity of soot. It was found that DMC addition was effective in decreasing the average weights of soot formed in flames. The results of HRTEM images showed that soot particles obtained with DMC addition showed liquid-like material and tight bonding, and exhibited more highly disorganized layers, which give it higher reactivity than soot obtained without DMC addition. Furthermore, HRTEM was used to analyze soot fringe characteristics consisting of fringe tortuosity, fringe length, and fringe separation. XRD was used to crosscheck the results for fringe separation, and was consistent with HRTEM results. In addition, the mass loss curve of TGA experiments showed that DMC addition could enhance the reactivity of soot particles.

Effect of carbon addition on creep behavior of cast TiAl alloy with hard-oriented directional lamellar microstructure

Two TiAl alloys,Ti-47.5Al-3.7(Cr,V,Zr)and Ti-47.5Al-3.7(Cr,V,Zr)-0.1C(at.%),were prepared by cold crucible levitation melting to couple the hard-oriented directional lamellar microstructure with carbon microalloying strengthening.The creep behavior and mechanism for the improvement in creep properties by carbon addition were investigated by mechanical tests and electron microscopy characterizations.The results show that obvious improvements on the creep properties at 760°C and 276 MPa are achieved by 0.1 at.%C addition into TiAl alloy with directional lamellar microstructure,which promotes the creep strain and minimum creep rate decreasing with a large content.The minimum creep rate is reduced from 4.37×10^(-8) to 3.97×10^(-9) s^(-1),and the duration entering into creep acceleration is prolonged for more than 10 times.The mechanism for creep property improvement by 0.1%C addition is attributed to two aspects.The first one is that Ti_(2) AlC is found to be strong obstacles of 1/2[110]dislocations when moving across the lamellar interface in the carbon containing alloy.The other one is that the in terfacial dislocatio ns are effectively impeded and the release process is hindered by dynamic precipitation of Ti_(3) AlC,which is proposed to be the special mechanism for creep resistance improvement of this hard-oriented directional lamellar microstructure.

Carbon sequestration and emissions mitigation in paddy fields based on the DNDC model: A review

The DeNitrification–DeComposition(DNDC)model is a process model with a series of carbon and nitrogen biogeochemistry in agro-ecosystems.It incorporates the driving factors of the ecological environment and aims to simulate the carbon and nitrogen cycle in the terrestrial ecosystem.Furthermore,the model can be applied effectively in a paddy ecosystem.Based on an investigation and literature review,this study summarized and analyzed the impact of agricultural practices such aswatermanagement,fertilizer application,and strawincorporation on greenhouse gas emissions and soil carbon storage.After years of improvement,the DNDC model can presently be used effectively to evaluate the carbon sequestration and emissions mitigation potential of various agricultural practices.However,the related details of scientific processes of agricultural management,such as biochar incorporation and plastic mulching in paddy fields,should be added or modified and combined with experimental cases of actual agricultural practices to complete the calibration of the model,provide theoretical support for its promotion,and establish a reliable method of evaluating carbon sequestration and emissions mitigation in paddy fields.

Brønsted acid-catalyzed 1,6-hydrophosphination of propargylic para-quinone methides and aza-para-quinone methides for the rapid construction of phosphorus-substituted quaternary carbon centers

An intriguing Brønsted acid-catalyzed 1,6-hydrophosphination of in situ generated propargylic para-quinone methides(p-QMs)and aza-para-quinone methides(aza-p-QMs)with H-phosphorus oxides via dehydration/1,6-addition under ultrasonic irradiation is described.This methodology provides a rapid and green approach for the construction of diarylmethyl phosphorus oxides bearing phosphorus-substituted quaternary carbon centers in high yields(up to 98%yield)within merely 5min.This environmentally benign protocol represents a unique example of 1,6-conjugate additions of propargylic p-QMs and aza-p-QMs for site-selective C-P bond formation in an operationally simple and atom-economical manner.The use of readily available Brønsted acid catalyst,operationally simplicity,high yields,and high atom economy make this protocol very facile,practical,easily scaled-up and environmentally friendly.