低温CO催化氧化催化剂研究进展

对低(常)温下一氧化碳(CO)催化氧化进行了综述与讨论,介绍了各种催化体系催化反应的机理,着重分析了制备方法(共沉淀法、沉积沉淀法和溶剂化金属原子浸渍法等)、制备条件(前驱物、pH值、焙烧温度和焙烧时间等)、载体种类(金属氧化物、复合氧化物和沸石等)及助剂(Ce、Sm和La等)对催化剂在CO低(常)温催化氧化反应中的活性及稳定性的影响,并指出了今后的研究方向.     

富氧条件下NOx催化净化的研究进展

本文对富氧条件下NOx的催化净化进行了综述与探讨,着重分析了分子筛催化剂、贵金属催化剂以及金属氧化物催化剂在碳氢化合物选择性催化还原NOx反应中的活性及其影响因素,描述了催化反应的机理,并指出了今后的研究方向.     

Adsorption performance and mechanisms of mercaptans removal from gasoline oil using core-shell AC-based adsorbents

Environmental Science and Pollution Research - Sulfur compound detection such as mercaptans in liquid fuels is undesirable because sulfur is the main sourcing emission of sulfur oxide (SOx) into...     

Excimer laser fragmentation-fluorescence spectroscopy as a method for monitoring ammonium nitrate and ammonium sulfate particles

Excimer laser fragmentation-fluorescence spectroscopy (ELFFS) is shown to be an effective detection strategy for ammonium nitrate and ammonium sulfate particles at atmospheric pressure and room temperature. Following photofragmentation of the ammonium salt particle, fluorescence of the NH fragment is observed at 336 nm. The fluorescence signal is shown to depend linearly on particle surface area for laser intensities varying from 1.2 x 10(8) to 6 x 10(8) W/cm2. The 100 shot (1 s) detection limits for ammonium nitrate range from 20 ppb for 0.2 microm particles to 125 ppb for 0.8 microm particles, where these concentrations are expressed as moles of ammonium ion per mole of air. For ammonium sulfate, the 100 shot (1 s) detection limits vary from 60 ppb for 0.2 microm particles to 500 ppb for 1 microm particles. These detection limits are low enough to measure ammonium salt particles that form in the exhaust of combustion processes utilizing ammonia injection as a nitric oxide control strategy.     

选择性催化还原NO反应的研究进展

本文介绍了近年来选择性催化还原ＮＯ反应的研究进展状况，并对目前研究中存在的问题及今后研究的方向提出一些看法。     

Summary of POHC Audit Results Using VOST and Bag Methods During RCRA Trial Burns

Audit materials containing Principal Organic Hazardous Constituents (POHCs) have been developed by EPA for use by Federal, State, and Local agencies or their contractors to assess the accuracy of measurement methods used during RCRA trial burn tests. Audit materials are currently available for 27 gaseous organics in five-, six-, seven-, and nine-component mixtures at ppb levels (7 to 10,000 ppb) in compressed gas cylinders in a balance gas of nitrogen. The logic used in selecting 27 gaseous organic compounds as audit materials and how these audit materials are successfully used in performance audits is described. Stability studies indicate that all of the organics tested (with the exception of ethylene oxide and propylene oxide below 10 ppb levels) are stable enough to be used as reliable audit materials. As of January 1990, 215 performance audits have been conducted to assess the accuracy of Volatile Organic Sampling Train (VOST) and bag measurement methods during or prior to RCRA trial burn tests. A summary of the audits conducted for each POHC, the measurement system audited, and the frequency of audits is described. The audit results obtained with audit gases are generally within ±50% of the audit concentrations.     

Multipurpose Sequential Samplers

Presented is the design, construction, and field utilization of a sequential sampling system for monitoring gaseous pollutants capable of detection by “wet chemical” techniques. Also described are specially designed midget impingers and bubblers for field and laboratory use.     

Measurement of Rapid Changes of Odor Concentration by a Signal Detection Approach

For many odorous industrial gases, odor detecrability often involves such low concentrations that the sampling time factor makes physical-chemical methods of analysis impractical. However, a sensory detection method based on signal detection theory has shown itself to be well suited for such studies even at levels near the absolute threshold. Experiments undertaken to assess the method are described.     

Measurement of Exhaust Emissions in Piston And Diesel Engines by Dispersive Spectroscopy

A versatile but simple, reliable, rugged, and compact vehicle exhaust monitoring system has been developed, allowing detection of carbon monoxide (CO), carbon dioxide (COo), high and low hydrocarbons (HHC and LHC), and nitric oxide (NO). The analysis is performed by dispersive absorption spectroscopy with instrumentation designed and fabricated for this demanding industrial environment. The operation of the instrumentation is described here, as well as results for both diesel and piston engine emission testing. This equipment has been used for California 7 mode-7 cycle hot start and cold start tests, the California heavy-duty engine test cycles, EPA CVS tests reading bag samples and also continuous dilute, and finally it has been used for idle checks. Testing has been performed on production automobiles, as well as those equipped with thermal reactors or catalytic mufflers, and also both heavy-duty gasoline and diesel. engines. The instrumentation has shown very good correlation with other established techniques, and because of its sensitivity, selectivity, ruggedness, and simplicity, has been shown to be suitable for vehicle emission analysis. Applications include assembly-line testing, engine testing, certification testing, quality audit testing, emission lab testing, and research.     

Literature survey of on-line spectroscopic methods for lead determination in environmental solid samples

A review is presented where are shown the advantages involved in the use of flow injection (FI) analysis for the determination of lead in environmental solid samples by spectroscopic detectors. The FI methods proposed for the determination of lead in these samples are described and compared according to the detection technique used. Analytical data of interest and interferences are discussed for each technique.     

Sampling and analysis of particulate and gaseous polycyclic aromatic hydrocarbons from coal tar sources in the working environment

A sampling method for polycyclic aromatic hydrocarbons (PAH) in workplace atmospheres using a standard glass fiber filter with a back-up section of Amberlite XAD-2 is described. Filters and XAD are solvent-desorbed and, without further clean-up, the solutions are submitted to high performance liquid chromatographic analysis using fluorimetric detection. Recovery of PAH from XAD-2 was studied, and was found to be in the range 80–100%. The sampling method was evaluated in a coke plant, an aluminium plant and in a creosote impregnating plant. The method described is rapid and sensitive for the determination of the most important workplace PAH, and accounts for both particulate and gaseous PAH.     

Performance Audit Results for Volatile POHC Measurements

Audit materials containing principal organic hazardous constituents (POHCs) have been developed by EPA for use by federal, state, and local agencies or their contractors to assess the accuracy of measurement methods used during RCRA trial burn tests. Audit materials are currently available for 27gaseous organics in five, six, seven, and nine-component mixtures at parts-per-billion levels (7 to 10,000 ppb) in compressed gas cylinders in a balance gas of nitrogen. The criteria used for the selection of 27 gaseous organic compounds is described.

Stability studies indicate that all of the organics tested (with the exception of ethylene oxide and propylene oxide below 10 ppb levels) are stable enough to be used as reliable audit materials.

Subsequent to completion of the stability studies, 89 performance audits have been conducted with the audit materials to assess the accuracy of the Volatile Organic Sampling Train (VOST) and bag measurement methods during or prior to RCRA trial burn tests. A summary of the audits conducted for each POHC and the measurement system audited is shown in this paper. The audit results obtained with audit gases during RCRA trial burn tests are generally within ±50 percent of the audit concentrations.     

Review of advances in the thin layer chromatography of pesticides: 2008-2010

Techniques and applications of thin layer chromatography (planar chromatography) for the separation, detection, qualitative and quantitative determination, and preparative isolation of pesticides and their metabolites and other related compounds are reviewed for the period from November 1, 2008 to November 1, 2010. Analyses are described for a variety of samples types and pesticide classes. In addition to references on residue analysis, studies such as pesticide structure-retention relationships, identification and characterization of plant pesticides and synthesized pesticides, metabolism, degradation, mobility, identification of biomarkers for detection of herbicide effects in plants, and lipophilicity are covered.     

Reverse phase high performance liquid chromatographic determination of Baygon in water

A simple analytical procedure for determination of Baygon in water is described. The Baygon residues are extracted on a C18 SEP-PAK cartridge and subsequently analyzed by reverse phase high performance liquid chromatography using ultraviolet detection at 272 nm. Water samples spiked with Baygon are found to give greater than 90 percent recoveries. Concentration levels as low as 20 ppb can be easily detected by this method.     

Review of advances in the thin layer chromatography of pesticides: 2008–2010

Techniques and applications of thin layer chromatography (planar chromatography) for the separation, detection, qualitative and quantitative determination, and preparative isolation of pesticides and their metabolites and other related compounds are reviewed for the period from November 1, 2008 to November 1, 2010. Analyses are described for a variety of samples types and pesticide classes. In addition to references on residue analysis, studies such as pesticide structure-retention relationships, identification and characterization of plant pesticides and synthesized pesticides, metabolism, degradation, mobility, identification of biomarkers for detection of herbicide effects in plants, and lipophilicity are covered.     

Analytical approaches for determining human exposure to pesticides

Abstract

The presence of pesticides, both persistent and biodegradable, in the environment is a problem which is both significant and potentially dangerous to humans. An index of biodegradability is presented which is based on the correlation between environmental stability and fat solubility. Halogenated pesticides are, therefore, both more fat soluable and more resistant to biodegradation, while methylated pesticides are more water soluable and, therefore, more biodegradable. Three methods for detecting low‐levels of halogenated pesticides are presented: the Macro, the Micro “Florisil,”; and the Micro “Silica.”; A method is also presented to detect these chemicals in blood. Two methods for the detection of nonpersistent, organophosphorus and carbamate insecticides, Cholinesterase inhibition and urinary metabolites, are described. Finally, methods of monitoring human exposure through the detection of phenols, phenoxy acids, alkyl phophates, and anilines are presented.     

Response of a grassland ecosystem to air pollutants: III--The chemical climate: Vertical flux densities of gaseous species in the atmosphere near the ground

The establishment of element balances for ecosystems presupposes a knowledge of the amounts of the respective element exchanged between the ecosystem and the atmosphere near the ground by determining their vertical flux densities. Any adequate approach to calculate flux densities of gaseous species in the atmosphere has to use micrometeorological techniques. The authors applied the ratiometric method, which is described in detail. Results of flux density calculations for sulfur dioxide, nitrogen dioxide, nitric oxide and ammonia obtained during two years of measurement are discussed with regard to their role in element balances. Flux densities and deposition velocities of ozone are interpreted as functions of meteorological parameters as well as of the biological activity of the canopy. The latter is characterized by the flux density and flux-to-concentration ratio of carbon dioxide.     

Process Modifications for Air Pollution Control in Neutral Sulfite Semi-Chemical Mills

The body of information presented in this paper is directed to those individuals concerned with the air pollution control problems of the pulp and paper industry operation. Process modifications introduced at two Company mills, at Big Island, Va. and Tomahawk, Wis., where neutral sulfite semichemical pulping of hardwoods is performed at rates of 550 and 630 tons per day, respectively, are discussed. The methodology and concepts used to minimize total reduced sulfur and total sulfur oxide emissions from the recovery furnace of one of the operations are explained. In another major improvement already implemented in the Big Island Mill conventional hydrogen sulfide emissions from the sulfiting tower, on the order of 8–10 lb as sulfur per ton of pulp, have been completely eliminated by a process modification technique. Other aspects of the operations are described, and a forecast of possible emission levels for mills with a newer technology is made.     

Comparison of Hydrogen Sulfide Analysis Techniques

A summary and critique of common methods of analysis for H₂S is presented. The procedures described are: reflectance from silver plates and lead acetate-coated tiles, lead acetate and mercuric chloride paper tape, sodium nitroprusside and methylene blue wet chemical methods, infrared spectrophotometry, and gas chromatography. Pertinent details included for each method are type (continuous, semicontinuous, averaging), lower detection limit, range, known interferences and suggestions for their elimination, and appropriate instrument parameters as wavelength, flow rates, temperature, and sample size. The limitations of each technique are clearly described, as are the advantages, in such a manner as to aid the user to select proper instrumentation for his analytical requirements.     

Rapid screening for organochlorine and organophosphorus pesticides in milk using C18 and graphitized carbon black solid phase extraction cleanup

A rapid, multiresidue, solid phase extraction (SPE) technique for the isolation and gas chromatographic determination of organochlorine and moderately polar organophosphorus pesticide residues in milk is described. Milk is sonicated with an acetonitrile-acetone-methanol mixture and centrifuged. The supernatant is subjected to a cleanup using both C18 and graphitized carbon black SPE columns. The pesticide residues are determined by gas chromatography with electron capture and flame photometric detection. The method required minimal volumes of solvent and resulted in the production of minimal volumes of hazardous waste.