Chemical looping gasification of maceral from low-rank coal: Products distribution and kinetic analysis on vitrinite

The product distribution and kinetic analysis of low-rank coal vitrinite were investigated during the chemical looping gasification(CLG)process.The acid washing method was used to treat low-rank coal,and the density gradient centrifugation method was adopted to obtain the coal macerals.By combining thermogravimetric analysis and online mass spectrometry,the influence of the heating rate and oxygen carrier(Fe2O3)blending ratio on product distribution was discussed.The macroscopic kinetic parameters were solved by the Kissinger-Akahira-Sunose(KAS)method,and the main gaseous product formation kinetic parameters were solved by the iso-conversion method.The results of vitrinite during slow heating chemical looping gasification showed that the main weight loss interval was 400–600℃,and the solid yield of sample vitrinite-Fe-10 at different heating rates was 64.30%–69.67%.When b=20℃·min^(-1),the maximum decomposition rate of vitrinite-Fe-10 was 0.312%min1.The addition of Fe2O_(3)reduced the maximum decomposition rate,but by comparing the chemical looping conversion characteristic index,it could be inferred that the chemical looping gasification of vitrinite might produce volatile substances higher than the pyrolysis process of vitrinite alone.The average activation energy of the reaction was significantly reduced during chemical looping gasification of vitrinite,which was lower than the average activation energy of 448.69 kJ·mol^(-1) during the pyrolysis process of vitrinite alone.The gaseous products were mainly CO and CO_(2).When the heating rate was 10℃·min^(-1),the highest activation energy for CH4 formation was 21.353 kJ·mol^(-1),and the lowest activation energy for CO formation was 9.7333 kJ·mol^(-1).This study provides basic data for exploring coal chemical looping gasification mechanism and reactor design by studying the chemical looping gasification process of coal macerals。

The Publication and Distribution of Chinses Standards and Other Standards-related Products

Standards Press of China (SPC), founded in October 1963, is the onlypublication center in China licensed to publish national standards, trade standards, and booksconcerned with standardization, quality, and other science and technology. The main publications areas following: 1. National standards; 2. Trade standards; 3. Standards compilation booksand guides; 4. Books concerned with standardization; 5. Books of quality management andquality certification; 6. Books of environmental management and environmental certification.

Kinetics and product distribution studies on ruthenium-promoted cobalt/alumina Fischer-Tropsch synthesis catalyst

Hydrocarbon production rates and distributions on ruthenium promoted alumina supported cobalt Fischer-Tropsch synthesis （FTS） catalyst were studied by the concept of two superimposed Anderson-Schulz-Flory （ASF） distributions.The results indicated that the characterizing growth probabilities α1 and α2 were strongly dependent on reaction conditions.By increasing the H2 /CO partial pressure ratios and reaction temperatures,deviation from normal ASF distribution decreases and the double-α-ASF distribution changes into a straight line.Based on the concept of double-α-ASF distribution,a useful rate equation for the production of hydrocarbons under industrial reaction conditions is obtained.

1-Butene isomerization and metathesis over Mo/mordenite-alumina: Factors influencing product distribution and induction period

Effects of space velocity, reaction temperature and support acidity on product distribution and induction period in 1-butene isomerization and metathesis over Mo/mordenite-alumina were investigated. As revealed by the catalytic performance results, induction period and objective product were closely related to the reaction conditions. Lower space velocity led to longer induction period and higher propene yield. The optimal reaction temperature for propene production is around 150 ~C and it shifted to 100 ~C for ethene production. 1-Butene auto-metathesis predominated in the reaction network if the support with lower degree of sodium exchanged. And propene gradually became the dominant product upon increasing the support sodium exchange degree. 6Mo/H100Na0M-30A1 catalyst with a support of full sodium exchange degree exhibited the highest propene yield.

Effect of external surface of HZSM-5 zeolite on product distribution in the conversion of methanol to hydrocarbons

The external surface of HZSM-5 zeolite was passivated by liquid siliceous deposition and by acidic sites poisoning with lepidine, respectively. Then methanol-to-hydrocarbons （MTH） reaction was investigated over the above as-prepared catalysts and the dissoluble coke on these used catalysts was analyzed by GC-MS, to study the role of the external surface of HZSM-5 in the catalytic reaction. Comparison with the experi- mental results based on parent ZSM-5 showed that the product distribution of MTH reaction was obviously influenced by the external surface. Evidences were listed as follows： （1） the final product on parent HZSM-5 showed higher aromatic selectivity, lower olefin selectivity, lower ra- tio of C2/C3＋ aliphatics and higher ratio of C3/C4＋ aliphatics than the reaction mixture produced by the sole catalysis of acidic sites in HZSM-5 channel; （2） a little of pentamethylbenzene and hexamethylbenzene in the product on parent HZSM-5, was produced via multi-methylation of methylbenzene on the external surface. The above conclusion may also be suitable for MTH reaction over other zeolites with 10-ring channel.

Product distributions of Fischer-Tropsch synthesis over Co/AC catalyst

The product distributions of Fischer-Tropsch synthesis over Co/AC catalyst are investigated under different reaction conditions in an integral fixed bed reactor.It is found that the product distributions deviate from the ASF distribution.The deviation from ASF distribution is analyzed by taking the readsorption of alkenes and the following secondary reaction into consideration.It is noted that the contents of alcohol,alkene and alkane decline with the increasing carbon number,showing a slighter declining tendency of alkanes than those of alkenes and alcohols.It is also found that high temperature,space velocity,H2/CO in feed gas and low pressure are preferential for light hydrocarbons and alcohols while against the chain propagation.The effect of space velocity on the product distributions especially on the light products is not obvious.It is noticed that low temperature,space velocity,H2/CO and high pressure lead to high contents of alcohols;high temperature,H2/CO and low space velocity lead to high contents of alkanes.The effect of pressure on the amounts of alkanes is not significant;high space velocity and low temperature,pressure,H2/CO are preferential for alkenes.

Influence of Pt/Ru anodic ratio on the valorization of ethanol by PEM electrocatalytic reforming towards value-added products

The ethanol electro-reforming process was studied over PtRu/C catalysts synthesized by the modified polyol method with different compositions.In particular,this work reports the influence of anodic Pt:Ru ratio(5:1,2:1 and 1:2)on the organic product distribution(acetaldehyde,acetic acid and ethyl acetate)and pure hydrogen generation at different current densities operation levels.Physicochemical characterization of the catalysts was made by X-ray diffraction(XRD),temperature-programmed reduction(TPR)and N_(2) adsorption-desorption measurements.XRD patterns showed that Ru is introduced into the Pt structure,forming an alloy between both metals.Also,the degree of alloy was higher by increasing the Ru amounts.From TPR profiles Pt was found to be properly reduced while Ru was both in metallic state and forming RuO2.The electrochemical behaviour of each catalyst towards ethanol electroreforming process was investigated through electrochemical techniques in a half cell and a single proton exchange membrane(PEM)cell systems.An intermediate Pt:Ru ratio was found to result in high current density and electrochemical surface area(ECSA)values along with lower amounts of adsorbed species.Also,Ru addition seems to diminish the degree of degradation of the catalyst.Based on characterization and in agreement with essays carried out in a PEM cell at mild conditions(80℃ and 1 atm),PtRu/C 2:1 anode provided the best electrocatalytic results in terms of current density(740 mA cm^(-2)),hydrogen production and selectivity toward acetic acid(up to 15%apart from acetaldehyde and ethyl acetate)while requiring the lowest energy consumption.

Catalyst-free and solvent-free oxidation of cycloalkanes(C5-C8) with molecular oxygen:Determination of autoxidation temperature and product distribution

Autoxidation of cycloalkanes （C5-C8） with molecular oxygen under catalyst-free and solvent-free conditions was conducted systematically for the first time, focusing on the autoxidation temperature and product distribution. The autoxidation of cyclopentane, cyclohexane, cycloheptane and cyclooctane occurs at 120 ℃, 130 ℃, 120 ℃, and 105 ℃ respectively, with obvious oxidized products formation. At 140 ℃, 145 ℃, 130 ℃ and 125 ℃, acceptable yields of the oxidized products could be obtained for them, and the oxidized product distributions were investigated in detail. The autoxidation of cycloalkanes follows the pseudo-first-order kinetic model and the apparent activation energies （Ea） for the autoxidation of cyclopentane and cyclohexane are 159.76 kJ. tool-1 and 86.75 kJ. mol-1 respectively. This study can act as an important reference in screen of suitable reaction temperature and comparison of the performance of various catalysts in the catalytic oxidation of cycloalkanes in the attempt to enhance the oxidized product selectivity.

Hydrocarbon Composition of Different VGO Feedstocks and Its Correlation with FCC Product Distribution

Three different types of VGO were selected and cut into various distillates by true boiling-point distillation （TBD）, and the distillates were further separated into different components （saturates, aromatics and resins） via solid phase extrac- tion （SPE）. The hydrocarbon components in saturates and aromatics were characterized on the quasi-molecular level by GC/ MS and CJC/TOF MS. Cracking reactions of VGO, their distillates, and hydrocarbon components （saturates and aromatics） were performed on an ACE （model AP） unit. Nine correlation parameters （mainly based on the previous assumption of basic structure Units, BSU） which could better reflect the structures and compositions of hydrocarbons were put forward based on the quasi-molecular level analysis data, and correlated with FCC product distribution by multi-regression method. A series of correlation formulas were obtained. The formulas were further verified by comparing experimental and calculated FCC yields emanated from two other VGO feedstocks.

UV Photolysis of N2O Isotopomers： Isotopic Fractionations and Product Rotational Quantum State Distributions

The time-dependent quantum wave packet method is used to study the dynamics of the pho- todissociation processes for the isotopomers 14N14N16O, 14N15N16O, 15N14N16O, 15N15N16O, 14N14N17O, and 14N14N18O. In general, the computed isotopic fractionation factors derived from the absorption cross sections of five heavy isotopomers are in good agreement with the experimental results. Relative to the 14NI4N16O isotopomer, the N2 rotational state distributions for the isotopically nitrogen substituted N2O are found to be entirely shifted to higher rotational states. Similar to its isotopic fractionation factors, the N2 rotational state distributions for the asymmetric isotopomers 14N15N16O and 15N14N16O are found to be observably different.

Distribution of chlorophyU a and estimation of primary productivity in the eastern waters of Balingtang Channel in summer

Oceanographical features on both sides of Balingtang Channel (17°55′-20°06′N, 122°55′-126°57′E) were comprehensively investigated on board of R/V "Experiment 3" in June. 1984. The pre-sent paper reports the chlorophyll data collected and primary productivity estimated there. Water sam-ples were taken with a glass bottle of Model HQMat the depth of 0, 10. 25, 50, 75, 100 and 150m, separately. Chlorophyll was determined according to the spectrophotometry proposed by UNESCO(1966) and calculated with the trichromatic equations of Jeffrey-Humphrey(1975). Estimations ofprimary productivity were carried out using a simplified equation (Q = 1.5) given by Cadee(1975).

Comparison of Temperature Field Distribution between Cement Preclinkering Technology and Cement Precalcining Technology

Through the comparison of calcination conditions between cement preclinkering technology and cement precalcining technology,we studied the characteristics of temperature field distribution of cement preclinkering technology systems including cyclone preheater,preclinkering furnace,and rotary kiln.We used numericalsimulation method to obtain data of temperature field distribution.Some results are found by system study.The ratio of tailcoalof cement preclinkering technology is about 70%,and raw mealtemperature can reach 1070 ℃.Shorter L/D kiln type of preclinkering technology can obtain more stable calcining zone temperature.The highest solid temperature of cement preclinkering technology is higher than 80 ℃,and high temperature region（〉1450 ℃）length is 2 times,which is beneficialfor calcining clinker and higher clinker quality.So cement preclinkering technology can obtain more performance temperature filed,which improves both the solid-phase reaction and liquid-phase reaction.

Distribution of Chlorophyll a and primary productivity in the neritic waters of Fujian Province

INTRODUCTIONThe coast zone is the area where most human activities take place and where the highest economic benefit is produced. The knowledge of the distribution and variation of primary production provides the bases as reference helping the marine exploitation and management.

Increasing Liquid Yield and Diesel Fraction in Delayed Coking Process: Mechanism of Liquid Formation

The thermal upgrading of two residual oils tory-scale continuous delayed coking unit. The goal with different characteristics was studied in a labora- was to investigate the influence of the process vari- ables such as temperature, reaction time and additive on liquid yield and products distribution. A maximum liquid yield of 73% was achieved compared to 69% with the commercial unit. This yield was even increased to 75% under the effect of an additive. The fractionation of liquid oil by simulated vacuum distillation showed a high yield of diesel （46.9%）, compared to 28% for the commercial unit.

Optimized Strategy for Layout of Crop Production Areas in Hunan Province

The optimized strategy made a comprehensive consideration of resources, technology, market orientation, production scale, industry basis and layout based on the principle of crop security and farmers’ income increasing, and determined the general planning on layout and structure optimization of future crop production ar-eas, with present crop production, market outlook, future industry development, con-cluding crop production characteristics of the 4 crop regions, and proposing function orientation and highlights.

Preparation and Cracking Performance of FCC Co-Catalyst for Enhancing Light Oil Production

In this paper, a FCC co-catalyst for enhancing the light oil production was prepared by the sol-gel method, and its effect on the performance of residue cracking catalysts was evaluated in a CCFFB reactor. The test results indicated that the liquid product yield increased obviously, after the surface of FCC equilibrium catalyst was impregnated with the co-catalyst. The yields of dry gas, slurry and coke decreased, while the diesel yield changed slightly. And the crackability of residue was increased; the rate of coke deposition on catalyst surface was decreased, with the thermal cracking reactions inhibited. All these results showed that the co-catalyst could improve the density of acid sites and change the catalyst acidity, which could promote to prolong the catalyst activity by depositing the co-catalyst on the surface of FCC equilibrium catalysts.

Mechanism of chain propagation for the synthesis of polyoxymethylene dimethyl ethers

Polyoxymethylene dimethyl ethers(PODE)were synthesized from the reaction of paraformaldehyde with dimethoxymethane(DMM)over different acid catalysts at different conditions.Products were found to follow the Schulz-Flory distribution law.The chain propagation proceeds through the insertion of an individual segment of CH2O one by one,while the simultaneous insertion of a few CH2O segments or their assembly is unlikely.Due to the restriction of this law,it is difficult to increase the selectivity to the desired products(e.g.,PODE3 4).

Hydrodeoxygenation of Phenolic Model Compounds over MoS2 Catalysts with Different Structures

Several MoS2 catalysts of different structure, prepared by in situ decomposition of ammonium heptamolybdate （AHM） and molybdenum naphthenate （MoNaph）, and by MoS2 exfoliation （TDM）, were characterized by BET, X-ray diffraction （XRD）, Energy Dispersive X-ray （EDX） and transmission electron microscopy （TEM）. The analysis showed that MoS2 structure was dependant upon the preparation procedure. The activity of the catalysts was determined by measuring the hydrodeoxygenation （HDO） of phenol, 4-methylphenol and 4-methoxyphenol using a batch autoclave reactor operated at 2.8 MPa of hydrogen and temperatures ranging from 320-370℃. By comparing the conversion, the reactivity order of the catalysts was： AHM〉TDM-D〉MoNaph〉thermal〉MoS2 powder〉 TDM-W. Also, the effect of reaction temperature on the HDO conversion was explained in terms of equilibrium of reversible reaction kinetics. The main products of the HDO for phenolic compounds were identified by gas chromatography/mass spectrometry （GC/MS）. The results showed that the product distribution and the HDO selectivity were correlated with the reaction temperature. Two parallel reaction routes, direct hydrogenolysis and combined hydrogenation-hydrogenolysis, were confirmed by the analysis of the product distribution. High temperature favored hydrogenolysis over hydrogenation for HDO of phenol and 4-methoxyphenol, whereas for 4-methylphenol the reverse was true.

Liquid chemical looping gasification of biomass:Thermodynamic analysis on cellulose

Liquid chemical looping technology is an innovation of chemical looping conversion technology.Using liquid metal oxide as the oxygen carrier during gasification process could prolong the service life of oxygen carrier and improve the process efficiency.In this paper,based on Gibbs minimum free energy method,the thermodynamic characteristics of biomass liquid chemical looping gasification were studied.Cellulose and lignin,the main components of biomass,were taken as the research objects.Bismuth oxide and antimony oxide were selected as liquid oxygen carriers.The results showed that when the temperature increased from 600℃to 900℃,the output of H_(2)and CO in the products of cellulose gasification increased from 0.5 and 0.3 kmol to 1.3 and 2.6 kmol respectively.Different ratios of oxygen carriers to gasification raw materials had the best molar ratio.The addition of steam in the system was beneficial to the increase of H_(2)content and the increase of H_(2)/CO molar ratio.Bi_(2)O_(3)and Sb_(2)O_(3)with different mass ratios were used as mixed oxygen carriers.The simulation results showed that the gasification temperature of biomass with different mixed oxygen carriers had the same equilibrium trend products.It could be seen from the results of product distribution that the influence of the mixing ratio of Bi_(2)O_(3)and Sb_(2)O_(3)on gas product distribution could be neglected.These results could provide simulation reference and data basis for subsequent research on liquid chemical looping gasification.

Characterization and catalytic performance of CeO_2-Co/SiO_2 catalyst for Fischer-Tropsch synthesis using nitrogen-diluted synthesis gas over a laboratory scale fixed-bed reactor

The surface species of CO hydrogenation on CeO2-Co/SiO2 catalyst were investigated using the techniques of temperature programmed reaction and transient response method. The results indicated that the formation of H2O and CO2 was the competitive reaction for the surface oxygen species, CH4 was produced via the hydrogenation of carbon species step by step, and C2 products were formed by the polymerization of surface-active carbon species （-CH2-）. Hydrogen assisted the dissociation of CO. The hydrogenation of surface carbon species was the rate-limiting step in the hydrogenation of CO over CeO2-Co/SiO2 catalyst. The investigation of total pressure, gas hourly space velocity （GHSV）, and product distribution using nitrogen-rich synthesis gas as feedstock over a laboratory scale fixed-bed reactor indicated that total pressure and GHSV had a significant effect on the catalytic performance of CeO2-Co/SiO2 catalyst. The removal of heat and control of the reaction temperature were extremely critical steps, which required lower GHSV and appropriate CO conversion to avoid the deactivation of the catalyst. The feedstock of nitrogen-rich synthesis gas was favorable to increase the conversion of CO, but there was a shift of product distribution toward the light hydrocarbon. The nitrogen-rich synthesis gas was feasible for F-T synthesis for the utilization of remote natural gas.