Economic Analysis of Environmental Regulations: Lessons from VOC Standards for Paper Coating

Economic studies of proposed environmental regulations begin with estimates of compliance actions and their costs. The assumptions about compliance actions can be misleading. In economic studies pertaining to regulations for volatile organic compound emissions by Illinois paper coaters, three sources of shortcomings are particularly evident: 1) failure to appreciate linkages between regulations applying to closely allied industries; 2) emphasis on well-known technologies, despite strong evidence that they will be displaced; and 3) heavy reliance on EPA technical data, whether or not they fairly represent state or local conditions.     

Valveless Sampling of Ambient Air for Analysis by Capillary Gas Chromatography

A method for the high resolution, high sensitivity analysis of polluted air for individual organic compounds is described. Samples collected from 50 mL of ambient air at 87 K (liquid argon) are Injected without use of a valve into a silica capillary column which Is then temperature programmed from — 30°C to 180°C. Hydrocarbons (4 to 10 carbons) as well as carbonyl compounds, chlorinated compounds and terpenes can be identified and quantified. The detection limit, not strongly dependent on carbon number, is estimated to be 0.3 ppbc in a 50 mL sample. Use of small samples eliminates the need to remove water vapor, a procedure which might jeopardize sample integrity.     

Solid Absorbent Method for Sampling and Analysis of Nitrogen Dioxide in Ambient Air

A sampling and analysis system was developed for measuring concentrations of nitrogen dioxide in ambient air. Copper shot was found to be an effective absorbent for collecting samples at ambient levels. The analytical system was based on the desorption of the sample from the copper by heating in a hydrogen carrier stream. The desorbed sample was then determined by a combination of catalytic pyrolysis, which converted it to ammonia, and a Coulson Conductivity Detector. Data are presented showing overall recovery, effects of storage of collected samples, results for 24-hour sampling and interferences. Studies indicated the feasibility of the method for short time sampling as well as for 24-hour sampling periods. The detection limit was shown to be as little as 100 ng NO₂ in laboratory studies. This solid absorbent method provides a simple, convenient, and compact means for air sampling.     

Ambient Air Monitoring for Sulfur Compounds

The role of sulfur compounds in our environment has been the subject of much speculation during the past two decades. An evaluation of the effect of man-made contributions to the biogeochemical sulfur cycle requires a comprehensive examination of source magnitudes, atmospheric concentrations and removal processes. Many voids exist in our present knowledge of these parameters despite the contributions of numerous researchers. Adequate information is needed concerning the various forms of sulfur as well as other critical constituents which exist in our biosphere so that their interrelationship and role in the mechanisms of the sulfur cycle may be more fully understood.     

加强对外经济贸易的环境监管

分析了对外经济贸易环境监管中存在的问题,并在WTO和国际环境协议的背景下,提出加强对外经济贸易环境监管的对策建议.     

Analysis of VOCs in Ambient Air Using Multisorbent Packings for VOC Accumulation and Sample Drying

Abstract

Solid multisorbent packings have been characterized for trapping and release efficiency of trace (10-20 ppbv in humidified zero air) volatile organic compounds (VOCs). The use of a two-stage trapping system reduces sample water content typically by more than 95.5% while maintaining a trapping and release efficiency of 100% for 49 VOCs, including eight water-soluble VOCs. Three combinations of primary tube and focusing tube are examined in detail by using an atomic emission detector to monitor hydrogen as an indication of residual water vapor, and to monitor either chlorine, bromine, or carbon for target VOCs. Linearity of response to individual VOCs, the presence of artifacts, and a laboratory monitoring application are also discussed.     

Analysis of Ambient Concentrations of Organic Vapors with a Passive Sampler

Volatile organic compounds can contribute to the failure of electronic equipment in both switching offices and data centers. They can also be useful indicators of ventilation needs. Only within the past decade have ambient concentrations of volatile organics been measured routinely. In standard sampling approach, a pump is used to pull a known volume of air through an adsorbent. This study examines a sampling procedure that does not use a pump, but instead depends on molecular diffusion for eventual contact between the vapor phase compounds and the charcoal sorbent (passive sampling). The technique is both simpler and less expensive than active sampling with a pump. This method has been validated for low-level sampling over extended time intervals. This study demonstrates that collected amounts vary linearly with airborne concentrations for sampling intervals in excess of four weeks: even after eight weeks of sampling at typical ambient concentrations, the amount of material collected does not approach the capacity of the sorbent. The method is applicable for concentrations spanning six orders of magnitude; reproducibility averages 13 percent of the mean value; and the sensitivity is excellent (0.06 μg/m³ or roughly 0.015 ppbv for a compound with a molecular weight of 100). The procedure has already been used successfully to monitor indoor air quality at almost a dozen telephone office and data center sites.     

A Cyclone for Size-Selective Sampling of Ambient Air

A cyclone with a 47 mm after-filter has been developed for ambient air size-selective monitoring. It has been extensively evaluated with laboratory-generated aerosol. Variation of the pressure drop and 50% cut point with flow rate show that the cyclone operates in a single flow regime with a vortex in the outlet flow. The particle size cutoff curve is comparable in sharpness to a cascade impactor and is the same for solid or liquid particles. At 21.7 L/min, D ₅₀ is 2.5μm and at 15.4 L/min, D ₅₀ is 3.5 μm. Collection efficiency data for flow rates from 8 to 27 L/min fit a universal curve when plotted vs. the normalized particle diameter, (D-D ₅₀)/D ₅₀ Reentrainment of previously deposited particles is less than 1 % of the loading per day. In field tests the cyclone has proved to be a very satisfactory size-selective sampler.     

盐城市区环境空气污染原因分析及对策建议

通过对盐城市区建成空气自动监测站来的数据分析,简要说明了盐城市区环境空气质量下降的原因,并提出了改善城市大气污染的建议措施。     

Survey of Laboratory Performance Analysis of Simulated Ambient S02 Bubbler Samples

The Quality Control Branch of the Quality Assurance and Environmental Monitoring Laboratory, National Environmental Research Center, Research Triangle Park, N. C, coordinated a nationwide interlaboratory study which surveyed the ability of participating laboratories to analyze simulated ambient sulfur dioxide samples. The purposes of the study were (1) to provide participating laboratories with a means for self evaluation of their performance, and (2) to begin to acquire information which indicates the quality of ambient SO₂ data being reported.

Sample vials of sodium sulfite in mannitol were distributed to 134 laboratories throughout the country that routinely analyze for atmospheric SO₂. No restrictions were placed on the method of analysis other than that the normal absorbing solution used with the analysis be a tetrachloromercurate II solution. Each sample set contained five separate vials. Each vial, when mixed properly with absorbing reagent, simulated a 24 hour bubbler sample. The range of concentrations in each set extended from approximately the lower detectable limit of the pararosaniline method to approximately the alert level as described in Federal Regulations.     

Analysis of Complex Mixtures of Vapors in Ambient Air by Fast-Gas Chromatography

An international specialty conference cosponsored by the Air & Waste Management Association's New England Section and the WF-2, EE-5 and EP-1 technical committees was held in Boston, Massachusetts on November 7-9, 1990. The technical program consisted of 39 presentations, held in eight technical sessions, exploring a wide range of topics related to the development of cleanup criteria for contaminated soil and groundwater. Supported by 11 exhibitors, the conference was attended by more than 350 professionals from the United States and other countries. This overview by the Technical Program Chair highlights a selection of the technical presentations.     

A Comparison of Two Techniques for the Collection and Analysis of Polynuclear Aromatic Compounds in Ambient Air

A demonstration of the GHEMFIX solidification/stabilization process was conducted under the United States Environmental Protection Agency’s (EPA) Superfund Innovative Technology Evaluation (SITE) program. The demonstration was conducted in March 1989, at the Portable Equipment Salvage Company (PESC) uncontrolled hazardous waste site in Clackamas, Oregon. Waste containing lead, copper, and polychlorinated biphenyls (PCBs) from four different areas of the site were treated. Results showed substantial reduction of leachable lead and copper between the untreated waste and treated waste utilizing the EPA Toxicity Characteristics Leaching Procedure (TCLP) test. The effectiveness of this process for immobilizing PCBs could not be determined since the raw waste did not leach PCBs at high concentrations, utilizing the TCLP test. Data from other leaching tests for lead and copper would need to be utilized as input into a site specific groundwater model to determine whether solidification/stabilization would be an acceptable remedy for the site. Physical testing results indicated durability in exposed conditions.     

Are We Ready for Ambient Air Quality Standards

The legal basis for the control of air pollution has progressed from nuisance law to the statutory regulation of specific substances as the sophistication of the sciences involved has progressed. But, the control of air pollution by pursuing air pollutants one by one as evidence accumulates against them seems clearly inadequate to a technology producing new pollutants at an almost geometric rate and inappropriate to the gathering body of evidence relating air pollution to health effects. To understand the need for changed control concepts it is necessary to understand the biological problem and the evidence that has been accumulated.     

Sampling Frequency Guidance for Ambient Air Toxics Monitoring

Abstract

The U.S. Environmental Protection Agency (EPA) is in the process of designing a national network to monitor hazardous air pollutants (HAPs), also known as air toxics. The purposes of the expanded monitoring are to (1) characterize ambient concentrations in representative areas; (2) provide data to support and evaluate dispersion and receptor models; and (3) establish trends and evaluate the effectiveness of HAP emission reduction strategies. Existing air toxics data, in the form of an archive compiled by EPA’s Office of Air Quality Planning and Standards (OAQPS), are used in this paper to examine the relationship between estimated annual average (AA) HAP concentrations and their associated variability. The goal is to assess the accuracy, or bias and precision, with which the AA can be estimated as a function of ambient concentration levels and sampling frequency. The results suggest that, for several air toxics, a sampling schedule of 1 in 3 days (1:3) or 1:6 days may be appropriate for meeting some of the general objectives of the national network, with the more intense sampling rate being recommended for areas expected to exhibit relatively high ambient levels.     

Federal Regulations for New Source Performance Standards

Section 111 of the Clean Air Act Amendments of 1970 authorizes the U.S. Environmental Protection Agency (EPA) to impose emission standards (NSPS) on those stationary sources that are determined to be significant contributors to air pollution and that consequently endanger the public health or welfare. In five years EPA promulgated 19 final and 1 proposed NSPS for stationary sources. Section 112 of the Act authorizes EPA to promulgate national emission standards for hazardous air pollutants (NESHAPS). EPA promulgated three final and 1 proposed regulation under Section 112. In addition, EPA promulgated NSPS for three "designated" pollutants from specific sources under Section Hid. EPA’s use of Section 111 and 112 authority provides for a quick response emission control program compared to the relatively slow process of establishing additional ambient air quality standards and having the states adopt implementation plans (Section 109). Three court cases, argued in the U.S. Court of Appeals for the District of Columbia, established basic guidelines for future promulgation of NSPS although certain legal actions are still pending. Proposed amendments to the Clean Air Act would further broaden and strengthen EPA’s direct regulatory authority.     

Canister-Based Method for Monitoring Toxic VOCs in Ambient Air

The availability of reliable, accurate and precise monitoring methods for toxic volatile organic compounds (VOCs) is a primary need for state and local agencies addressing daily monitoring requirements related to odor complaints, fugitive emissions, and trend monitoring. The canister-based monitoring method for VOCs is a viable and widely used approach that is based on research and evaluation performed over the past several years. This activity has involved the testing of sample stability of VOCs in canisters and the design of time-integrative samplers. The development of procedures for analysis of samples in canisters, including the procedure for VOC preconcentration from whole air, the treatment of water vapor in the sample, and the selection of an appropriate analytical finish has been accomplished. The canister-based method was initially summarized in the EPA Compendium of Methods for the Determination of Toxic Organic Compounds in Ambient Air as Method TO-14. Modifications and refinements are being added to Method TO-14 in order to obtain a Statement of Work for the Superfund Contract Laboratory Program for Air. This paper discusses the developments leading to the current status of the canisterbased method and provides a critique of the method using results obtained in EPA monitoring networks.     

The Need for Representative Ambient Air Carbon Monoxide Sampling

Recent investigations have indicated that ambient air CO measurements may not reflect population exposure to CO. The lack of correlation may be due to improper siting of CO instruments, improper interpretation of air quality data, or both. Studies of population carboxy-hemoglobin levels are evaluated and compared with ambient air data.,

No significant correlation was found between median population COHb levels and reductions in CO concentrations required to meet ambient air standards when calculations used to estimate reductions were based on the second highest 8 hour average. However, calculated reductions based on annual average concentrations and a trend analysis technique correlated significantly with COHb levels in five cities from which both CAMP and COHb data were available.

Studies to determine the nature of the relationship between ambient air CO concentrations and population COHb levels are needed. The differences between the Occupational Safety and Health Act Regulations and the National Ambient Air Standards for carbon monoxide should be scrutinized to determine if a redefinition of the standards or their applicability is warranted. A reevaluation of the controls necessary to make reductions in population COHb burden may be necessary.     

Design and Operating Parameters for a Large Ambient Aerosol Chamber

Recent investigations of ambient aerosol behavior over urban areas have pointed out the need for controlled experimental data to link together field investigation results and computer simulation studies. This paper describes the design considerations, construction details and operating parameters of a large (8000 ft³) outside reaction chamber constructed in rural North Carolina. The chamber is triangular in cross-section, 20 ft wide, 20 ft high and 40 ft long, and is covered with clear 5 ml Teflon film. The outdoor location of the chamber permits the reaction volume to be exposed to the natural conditions of temperature and solar radiation. A recirculating air system allows the air in the chamber to be passed through an “absolute” fiberglas filter for adjustment of condensation nuclei concentration and also through driers for humidity adjustment. Internal fans are provided for mixing of the chamber contents without use of the recirculating system so that various degrees of turbulence can be approximated. A sampling line from the chamber passes directly to an instrument room, located directly under the chamber, where direct analyses for particle composition, concentration, and size, and gas composition and concentration are carried out. Parameters which can be varied in this system include number, size, distribution, and chemical composition of pre-existing nuclei, as well as humidity, solar radiation, temperature, and trace gas concentration and composition.